VAERS Reports EW0153

VAERS 2634230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 19.05.2023
Impfdatum: 13.04.2021
Beginn: 05.04.2022
Tage bis Beginn: 357,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Diabetic nephropathy Hypertension Hypoxia Neuropathy peripheral

Symptomtext

NEUROPATHY 12/1/2021 NONTRAUMATIC ACUTE KIDNEY INJURY ACUTE RESPIRATORY FAILURE 9/10/2022 NONTRAUMATIC ACUTE KIDNEY INJURY ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/1/2022 NONTRAUMATIC ACUTE KIDNEY INJURY HYPOXIA 9/9/2022 NONTRAUMATIC ACUTE KIDNEY INJURY NEUROPATHY 12/1/2021 DM 2 W RENAL MANIFESTATION ACUTE RESPIRATORY FAILURE 9/10/2022 DM 2 W RENAL MANIFESTATION ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/1/2022 DM 2 W RENAL MANIFESTATION HYPOXIA 9/9/2022 DM 2 W RENAL MANIFESTATIONNEUROPATHY 12/1/2021 ACUTE RESPIRATORY FAILURE ACUTE RESPIRATORY FAILURE 9/10/2022 ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/1/2022 ACUTE RESPIRATORY FAILURE HYPOXIA 9/9/2022 ACUTE RESPIRATORY FAILURE NEUROPATHY 12/1/2021 HTN (HYPERTENSION) ACUTE RESPIRATORY FAILURE 9/10/2022 HTN (HYPERTENSION) ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/1/2022 HTN (HYPERTENSION) HYPOXIA 9/9/2022 HTN (HYPERTENSION)

Weitere VAERSDATA-Felder

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

VAERS 2627503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 87,0
Geschlecht: F
Eingang: 05.05.2023
Impfdatum: 09.04.2021
Beginn: 18.06.2021
Tage bis Beginn: 70,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure Aortic aneurysm Hyponatraemia

Symptomtext

J96.00 ACUTE RESPIRATORY FAILURE 8/8/2021 ABDOMINAL AORTIC ANEURYSM, UNSPECIFIED PART J96.00 ACUTE RESPIRATORY FAILURE 8/8/2021 HYPONATREMIA

Weitere VAERSDATA-Felder

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

VAERS 2616107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 13.04.2021
Beginn: 18.06.2021
Tage bis Beginn: 66,0
Dosis: 2
Route/Site: IM / LA

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

Epilepsy Hypotension Mental status changes Obstructive sleep apnoea syndrome Pulmonary embolism Seizure

Symptomtext

EPILEPSY, UNSPECIFIED 8/2/2021 ALTERED MENTAL STATUS, UNSPECIFIED PULMONARY EMBOLISM, UNSPECIFIED. 8/23/2021 ALTERED MENTAL STATUS, UNSPECIFIED HYPOTENSION 1/5/2022 ALTERED MENTAL STATUS, UNSPECIFIED EPILEPSY, UNSPECIFIED 8/2/2021 EPILEPSY, UNSPECIFIED PULMONARY EMBOLISM, UNSPECIFIED. 8/23/2021 EPILEPSY, UNSPECIFIED HYPOTENSION 1/5/2022 EPILEPSY, UNSPECIFIED EPILEPSY, UNSPECIFIED 8/2/2021 ADULT OBSTRUCTIVE SLEEP APNEA, MILD PULMONARY EMBOLISM, UNSPECIFIED. 8/23/2021 ADULT OBSTRUCTIVE SLEEP APNEA, MILD HYPOTENSION 1/5/2022 ADULT OBSTRUCTIVE SLEEP APNEA, MILD EPILEPSY, UNSPECIFIED 8/2/2021 SEIZURE, UNSPECIFIED PULMONARY EMBOLISM, UNSPECIFIED. 8/23/2021 SEIZURE, UNSPECIFIED HYPOTENSION 1/5/2022 SEIZURE, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2586352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CA
Alter: 65,0
Geschlecht: M
Eingang: 23.02.2023
Impfdatum: 20.04.2021
Beginn: 01.06.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: - / RA

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

Blindness unilateral Blood pressure inadequately controlled COVID-19 Cardiac function test Dizziness Fatigue Hypertension Laboratory test Myocardial infarction Tinnitus Transient ischaemic attack

Symptomtext

Since the vaccine I have had extremely loud ringing in my ears, blood pressure has been dangerously high and somewhat uncontrollable, I am dizzy a lot, suffered loss of vision in right eye on two occasions for a few seconds, constantly tired. I also suffered 2 TIA's, and a heart attack. I was doing fine prior to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 10,0
Labordaten: They are numerous. I have been in the ER twice, had several nuerological and coronary test done. I have been hospitalized twice. And I got covid 2 times post vaccine...
Aktuelle Erkrankungen: none
Vorgeschichte: Coronary artery anomaly, sarcoidosis with heart muscle and lung involvement, coronary artery disease
Andere Medikamente: Losartan, allipurinol, bisoprol, ezetimibe,
Allergien: no
Vorherige Impfungen: -

VAERS 2577347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 13.04.2021
Beginn: 01.07.2022
Tage bis Beginn: 444,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Cardioversion Chemotherapy Cough Death Dyspnoea Endotracheal intubation General physical health deterioration Hypophagia Hypoxia Intensive care Mechanical ventilation Mouth ulceration Pneumonia SARS-CoV-2 test positive Septic shock Tachycardia

Symptomtext

8/8/22 EMS transported pt to hospital with SOB and tachycardia; given medications without changes to heart rate; cardioverted without changes; septic shock; right sided pneumonia; generalized weakness, cough, poor oral intake due to mouth ulcers from chemotherapy treatment; had a positive COVID test on 7/14/22 and given Paxlovid; 8/8/22 continued to show positive COVID test; CCU; ABX; pt's condition worsened; hypoxia requiring intubation with mechanical ventilation; pt's condition continued to deteriorate; transitioned to comfort care measures; pt passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: lymphoma, COPD, duodenal ulcers, basal cell carcinoma, hyperglycemia, lichen planus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

kritisch

Staat: MN
Alter: 66,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 20.11.2021
Beginn: 22.01.2023
Tage bis Beginn: 428,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Patient expired 1/22/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Seizure disorder, thalamic lesion, essential hypertension, alcohol abuse
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2517988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 06.05.2021
Beginn: 12.10.2022
Tage bis Beginn: 524,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury COVID-19 Candida infection Computerised tomogram Condition aggravated Diabetic ketoacidosis Disease complication Dysphagia Dyspnoea Echocardiogram normal Encephalopathy Endotracheal intubation Enterobacter test positive Haemodialysis Hypotension Intensive care Klebsiella test positive Laboratory test abnormal

Symptomtext

"Patient with COVID vaccines who admitted with positive COVID PCR and COVID complications. Provider d/c note: ""Patient presented to the emergency department on 10/12/2022 with a chief complaint of shortness of breath. On arrival he was found to be COVID positive as well as be in DKA. He was intubated, placed on pressors and put in the intensive care unit. He was treated for septic shock for which infectious workup showed MSSA bacteremia as well as candida urinary tract infection. He also had MSSA, Klebsiella and Enterobacter in his sputum. He was seen by infectious disease during the course of his stay and completed a course of micafungin and meropenem in with a transition for an additional 6 weeks of oral antibiotics. He also developed an AKI during the course of his stay and did require temporary hemodialysis as well as the ureteral stent exchange with Urology. He was seen by pulmonology for his pneumonia as there was concern for lung abscess but this was not large enough to require drainage. His stay was also complicated by encephalopathy which did resolve over time. He completed his treatment for MSSA bacteremia and had a negative TEE. He will be discharged on oral Augmentin and Bactrim per Infectious Disease recommendations to complete his antibiotics. He will need a repeat CT scan outpatient with Infectious Disease. He was also found to have dysphagia during the course of his stay which resolved with eventual diet modification. Patient was tolerating diet well on day of discharge. Due to his persistent hypotension patient was placed on midodrine and blood pressure remained borderline low but stable. His kidney function eventually returned to baseline. Patient's symptoms continued to improve over the course of his stay and he will be discharged in stable and improved condition. He will need to follow-up with Infectious Disease as well as Urology. He will be discharged to facility. """

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 43,0
Labordaten: COVID Detected PCR on 10/12/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Coronary atherosclerosis LAFB (left anterior fascicular block) RBBB Coronary atherosclerosis Essential hypertension, benign Right bundle-branch block Mixed hyperlipidemia Paroxysmal atrial fibrillation Endocrine Type II diabetes mellitus with renal manifestations, uncontrolled Hyperparathyroidism due to renal insufficiency Type 2 diabetes mellitus without complication Psychological OCD (obsessive compulsive disorder) Major depression with psychotic features Urinary Stage 4 chronic kidney disease (*) Anemia of chronic renal failure CKD (chronic kidney disease) Urinary tract infectious disease Other hydronephrosis Hydronephrosis, left Other History of lumbar fusion History of nephrectomy Mechanical complication of dorsal column stimulator Ureteral stent retained Chronic bilateral low back pain Bacteremia due to methicillin susceptible Staphylococcus aureus (MSSA) Status post placement of ureteral stent
Andere Medikamente: -
Allergien: Oxycodone-acetaminophenNausea Only, Unknown Paroxetine HclAnxiety Oxycodone-acetaminophenGI Upset ParoxetineAnxiety
Vorherige Impfungen: -

VAERS 2503144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 06.05.2021
Beginn: 10.10.2022
Tage bis Beginn: 522,0
Dosis: 2
Route/Site: SYR / UN

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

Acute myocardial infarction COVID-19

Symptomtext

Hospitalization for non-STEMI (incidental COVID-19) on dates 10/10/22- 10/14/22. Treated with vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: codeine (rash), hydrochlorothiazide (rash), atorvastatin (severe myalgia), pravastatin (severe myalgia), quinapril (cough), "all generic medications"
Vorherige Impfungen: -

VAERS 2492792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: KY
Alter: 78,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 20.04.2021
Beginn: 05.03.2022
Tage bis Beginn: 319,0
Dosis: 2
Route/Site: IM / RA

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

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

Symptomtext

Patient had a breakthrough infection, positive COVID test on 12/30/2021. Patient passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Peripheral Neuropathy COPD Emphysema CAD CHF HTN Hyperlipidemia MI PAD Peripheral Arterial Occlusive DM type 2 Anemia Hypothyroidism
Andere Medikamente: Metoclopramide Melatonin Vitamin B complex Zinc Clopidogrel Atorvastatin Pantoprazole Roflumilast Glyburide Morphine Semaglutide Levothyroxine Famotidine Mirtazapine Furosemide Gabapentin Hydrocodone Aspirin Insulin detemir Insulin lispro
Allergien: Egg Fish containing products Penicillins
Vorherige Impfungen: -

VAERS 2477417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: TX
Alter: 59,0
Geschlecht: U
Eingang: 13.10.2022
Impfdatum: 02.12.2021
Beginn: 05.10.2022
Tage bis Beginn: 307,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure COVID-19 Cardiac failure congestive Condition aggravated Coronary artery disease Death Dyspnoea General physical health deterioration Pneumonia Pulmonary fibrosis Respiratory failure

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer BioNTech vaccine on 4/30/2021, 5/22/2021, and 12/02/2021. Presented w/SOB x3days. Hx of COVID-19 01/2021 c/b pulmonary disease requiring 3L NC of O2. SOB worsened; admitted to hospital; tx'd for CHF and PNA, d/c on 10L NC O2. ED 9/12, found to have acute on chronic hypoxic resp failure requiring Airvo support 2/2 progression of fibrotic lung disease from COVID-19. Severe 2-vessel CAD dx'd 9/15 plan to perform stage PCI. Cont'd to decompensate 2/2 resp status. Private was called; PCI cancelled 2/2 inability to tolerate procedure. Comfort care only, exp'd 10/05/22. Tx'd w/vanc, linezolid, zosyn, prednisone, levofloxacin,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 24,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, T2DM, HTN, HLD, Transaminitis, Glaucoma, Pulmonary fibrosis, GERD, hypothyroidism,
Andere Medikamente: dulaglutide, levothyroxine, lisinopril, prednisone, albuterol
Allergien: Amlodipine
Vorherige Impfungen: -

VAERS 2477160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 13.10.2022
Impfdatum: 04.05.2022
Beginn: 05.10.2022
Tage bis Beginn: 154,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 Chest X-ray abnormal Cough Dyspnoea Fibrin D dimer Lung opacity Oxygen saturation decreased Pneumonia Pseudomonas test positive SARS-CoV-2 test positive Sinus operation Sputum culture positive

Symptomtext

"Provider d/c note: ""63 YO male with a past medical history of CAD s/p CABG and ICD placement in 2020, s/p coronary stent placement in 07/2022, CKD stage III, DM, CHF (last echo 07/2022 EF 50-55%), bilateral cataracts 2/2 chronic steroid use, multiple skin basal cell carcinoma of the skin s/p excisions, and IGG4 deficiency on Rituximab q6 months following doctor; Who presented to the ED with complaints of difficulty in breathing, dry cough, and nasal drainage onset about 1 week ago. Covid positive. CXR result, Mild bibasilar interstitial/alveolar opacities. D-dimer 1,500, Pulm CTA ordered clear for PE. Mild bibasilar interstitial/alveolar opacities concerning for pneumonia.Admitted for Acute Respiratory insufficieny likely 2/2 pneumonia .Blood culture and sputum culture ordered. Started on cefepime and doxycycline. Schedule nebs and mucolytic. Patient improved with therapy, sputum culture showed few pseudomonas cells. Desaturation test done. He need required O2 with exertion. Continue treatment with levofloxacin at home. """

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: COVID Detected PCR on 9/27/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Hypertension Dilated cardiomyopathy class 2 heart failure with reduced ejection fraction Coronary artery disease involving coronary bypass graft of native heart without angina pectoris Ventricular tachycardia Coronary artery disease involving native coronary artery of native heart with unstable angina pectoris Chronic systolic (congestive) heart failure Hyperlipidemia Digestive GERD (gastroesophageal reflux disease) Uvular hypertrophy Pharyngeal dysphagia Endocrine Type 2 diabetes mellitus with stage 3a chronic kidney disease, without long-term current use of insulin Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin Immune and Lymphatic IgG4 deficiency Psychological Mild episode of recurrent major depressive disorder Respiratory Asthma Nasal polyposis Chronic sinusitis Chronic rhinitis DNS (deviated nasal septum) Community acquired pneumonia of left upper lobe of lung Hypoxia Urinary Chronic kidney disease, stage III (moderate) Anemia in stage 3 chronic kidney disease Benign prostatic hyperplasia with weak urinary stream Urinary retention Other Pseudolymphoma Retained myringotomy tube in left ear S/P nasal polypectomy Elevated brain natriuretic peptide (BNP) level Pancreatic mass Anemia of chronic disease Chronic fatigue IgG4 related disease Bilateral leg edema Hx of four vessel coronary artery bypass graft At high risk for injury related to fall BMI 38.0-38.9,adult Class 2 severe obesity due to excess calories with serious comorbidity and body mass index (BMI) of 39.0 to 39.9 in adult
Andere Medikamente: -
Allergien: Penicillins, Sulfa, Codeine
Vorherige Impfungen: -

VAERS 2469671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: TN
Alter: 74,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 07.04.2021
Beginn: 07.09.2022
Tage bis Beginn: 518,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Death s/p COVID-19 vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 5,0
Labordaten: Positive test 09/07/22
Aktuelle Erkrankungen: -
Vorgeschichte: coronary artery disease, atrial fibrillation, hypertension, hyperlipidemia and chronic kidney disease stage III
Andere Medikamente: Apixaban Ferrous sulfate Atorvastatin Metoprolol tartrate Acetaminophen Aripiprazole Citalopram Lumigan Alendronate
Allergien: Asprin Erythromycin Fexofenadine Shellfish
Vorherige Impfungen: -

VAERS 2469668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 17.11.2021
Beginn: 26.09.2022
Tage bis Beginn: 313,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Brain natriuretic peptide increased COVID-19 Cardiac failure Cardiac failure congestive Chest X-ray abnormal Chronic obstructive pulmonary disease Chronic respiratory failure Cough Dyspnoea Imaging procedure abnormal Lung infiltration SARS-CoV-2 test positive Skin ulcer

Symptomtext

"Patient with 3 COVID vaccines who admitted with cough and dyspnea. Provider d/c note: ""Acute respiratory insufficiency on chronic respiratory failure- etiology behind acute worsening likely multifactorial including COVID, HFpEF with infiltrates on x-ray and elevated BNP, chronic obstructive pulmonary disease. Suspect COVID with some element of CHF. - patient has been weaned to his home 2 L of supplemental oxygen -he will continue on dexamethasone at home for COVID COVID- patient received remdesivir therapy and will continue on steroids at home. He was offered the full course of remdesivir but instead preferred to go home. Risks and benefits discussed. Bilateral venous stasis ulcers with concern for bilateral cellulitis on imaging- Has PVD. - patient was treated with vancomycin and Zosyn, and will complete a course of antibiotics at home. -wound care consulted, home care has been arranged for further wound care and he will seen the wound care clinic team"""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: COIVD Detected PCR on 9/26/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular PVD (peripheral vascular disease) (*) Coronary artery disease involving native coronary artery of native heart (HFpEF) heart failure with preserved ejection fraction (*) Grade I internal hemorrhoids Essential hypertension, benign Venous insufficiency Moderate pulmonary hypertension (*) Cor pulmonale (*) Digestive Gastroparesis Diverticulosis of colon Endocrine Dyslipidemia associated with type 2 diabetes mellitus (HCC) Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (*) Integumentary Venous stasis dermatitis of both lower extremities Ulcers of both lower extremities, limited to breakdown of skin (*) Psychological Moderate episode of recurrent major depressive disorder (*) Respiratory Incidental pulmonary nodule, > 3mm and < 8mm; right OSA (obstructive sleep apnea) Asthma-COPD overlap syndrome (*) Chronic respiratory failure with hypoxia (*) Restrictive lung disease Urinary Bilateral renal cysts Other Body mass index (BMI) of 40.0-44.9 in adult (*) Low testosterone Normocytic normochromic anemia Vertigo Chronic right-sided low back pain with right-sided sciatica Lumbar disc herniation with radiculopathy History of MI (myocardial infarction)
Andere Medikamente: -
Allergien: Farxiga, trulicity, zocor
Vorherige Impfungen: -

VAERS 2417179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 22.08.2022
Impfdatum: 09.04.2021
Beginn: 20.08.2022
Tage bis Beginn: 498,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure COVID-19 Dyspnoea Osteomyelitis Positive airway pressure therapy SARS-CoV-2 test positive Tachypnoea Toe amputation

Symptomtext

Pt arrived with increased shortness of breath and acute hypoxic respiratory failure. He was recently hospitalized and discharged on 7/26 for osteomyelitis status post bilateral toe amputation, and his hospital course was complicated by AKI. Pt was found to be tachypneic and required BIPAP and was COVID positive.

Weitere VAERSDATA-Felder

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

VAERS 2405695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 06.04.2021
Beginn: 01.01.2022
Tage bis Beginn: 270,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

Per medical record, patient had a positive COVID test on 1/11/22 while patient was in nursing home. Patient was nauseated; placed on ABX and Zofran; patient passed away in the nursing home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, IBS, GERD, hiatal hernia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2367914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: TN
Alter: 51,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 07.05.2021
Beginn: 14.02.2022
Tage bis Beginn: 283,0
Dosis: 2
Route/Site: SYR / -

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

Angiogram cerebral abnormal Asthenia COVID-19 pneumonia Cerebrovascular accident Computerised tomogram head abnormal Death General physical health deterioration Hypertension Posterior reversible encephalopathy syndrome Seizure

Symptomtext

Patient admitted to Medical Center on 01/30/2022 with c/o seizure and worsening progressive debility, and placed on IV Keppra. She continued to decline and a new CT scan and CTA was done showing a new acute CVA with distribution of both the left MCA and PCA. Decision was made by family to make hospice for comfort care. Discharge diagnosis to GIP/Hospice included new acute stroke, Covid-19PNA, seizure disorder, PRES syndrome, hypertension. Patient expired on 02/26/2022.

Weitere VAERSDATA-Felder

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

VAERS 2339480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: WA
Alter: 70,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 15.04.2021
Beginn: 25.06.2022
Tage bis Beginn: 436,0
Dosis: 2
Route/Site: IM / RA

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

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

Symptomtext

Patient received Pfizer COVD vaccine on 3/25/21 and 4/15/21. On 6/25/22, patient admitted to our inpatient facility with acute respiratory failure and hypoxia secondary to COVID pneumonia. She was admitted in the med/surg unit and discharged home on 6/27/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: COVID status positive 6/25/22.
Aktuelle Erkrankungen: -
Vorgeschichte: history of kyphoscoliosis, fibromyalgia, OSA, chronic pain on chronic opiate therapy, osteoarthritis, DJD, RLS, GERD, hypertension
Andere Medikamente: albuterol inh, bisacodyl supp, Suboxone sl film, docusate, duloxetine, estradiol vag ring, fluticasone nasal sp, lactobacillus, levothyroxine, lidocaine viscous gel, linaclotide, lisinopril, methadone, modafinil, naloxone nasal sp, omeprazo
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1865612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: NJ
Alter: -
Geschlecht: M
Eingang: 18.06.2022
Impfdatum: 06.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac arrest Death Myocardial infarction

Symptomtext

died of a heart attack; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received BNT162b2 (BNT162B2), on 06Apr2021 as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "COVID 19", start date: 02Dec2020 (unspecified if ongoing), notes: He had been previously diagnosed with COVID 19 on or about 02Dec2020. The patient's concomitant medications were not reported. The following information was reported: MYOCARDIAL INFARCTION (death, medically significant) with onset 09Apr2021, outcome "fatal", described as "died of a heart attack". The patient date of death was 09Apr2021. Reported cause of death: "died of a heart attack". Clinical course: The patient received his first COVID 19 vaccine on 06Apr021. He died of a heart attack on 09Apr2021. He had been previously diagnosed with COVID 19 on or about 02Dec2020. He had no symptoms of indicating a heart issue prior to his heart attack. It has been thought by the reporter that it was important to report, in regards to efficacy and side effects of the vaccine. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Reported Cause(s) of Death: died of a heart attack

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (He had been previously diagnosed with COVID 19 on or about 02Dec2020)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2320363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: TN
Alter: 81,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 03.05.2021
Beginn: 06.01.2022
Tage bis Beginn: 248,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

1/6/22 COVID test positive; ordered by Medical Center; no medical records on this patient; pt per Death Certificate died at Hospice on 1/11/22

Weitere VAERSDATA-Felder

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

VAERS 2294517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 06.04.2021
Beginn: 22.05.2022
Tage bis Beginn: 411,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Death Electroencephalogram normal Endotracheal intubation Intensive care Meningitis Mental status changes Pyrexia SARS-CoV-2 test positive Seizure Sepsis Unresponsive to stimuli

Symptomtext

Patient presented to the ED on 5/22/22 from her LTC facility for altered mental status. On initial presentation to the ED was unresponsive and seizing. Intubated in the ED. Found to be septic, febrile, +COVID. She underwent work up for meningitis and was treated with broad spectrum antibiotics plus antiviral on admission. Neurology was consulted and she was started on keppra. EEG showed no seizure activity. Patient was admitted to the ICU, at that time further discussions had with the patient's husband. He states that she would not have wanted aggressive care, she has advanced dementia at baseline and he did not want to escalate care. He did want to wait to move to comfort measures on 5/23/22 so that he could notify family and have family see her, but did not want any additional therapy including no pressors. On 5/23/22 family was able to come see the patient, and decision was made to move to full comfort care. Patient was extubated 1743. Comfort measures maintained, and patient passed at 2003 on 5/23/2022 with her husband at bedside. Preliminary cause of death sepsis with acute respiratory failure in +COVID pneumonia patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Positive COVID PCR test 5/22/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Macrocytosis without anemia Hyperlipidemia Major neurocognitive disorder due to multiple etiologies without behavioral disturbance Diabetes mellitus due to underlying condition with diabetic polyneuropathy, without long-term current use of insulin (*) GERD (gastroesophageal reflux disease) Sepsis due to COVID-19 (*) Acute respiratory failure (*) Fever Leukocytosis Seizure-like activity (*) On mechanically assisted ventilation (*) Elevated troponin Altered mental status
Andere Medikamente: acetaminophen 500 mg Oral EVERY 6 HOURS aspirin 81 mg Oral 2 times daily, Then resume once a day dosing calcium carbonate 500 mg Oral 2 times daily cholecalciferol (vitamin D3) 1,000 Units Oral Daily cyanocobalamin (vitamin B-12) 1,000
Allergien: -
Vorherige Impfungen: -

VAERS 2281005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: TN
Alter: 67,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 03.04.2021
Beginn: 26.12.2021
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: SYR / -

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

COVID-19 pneumonia Cardio-respiratory arrest Cough Death Dyspnoea Sepsis

Symptomtext

Patient presents to ED with difficulty breathing, coughing, and dyspnea. Sepsis present upon admission secondary to Covid-PNA. Patient expired on 12/28/2021 due to cadiopulmonary arrest.

Weitere VAERSDATA-Felder

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

VAERS 2254877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: IL
Alter: 77,0
Geschlecht: M
Eingang: 27.04.2022
Impfdatum: 19.04.2021
Beginn: 19.04.2022
Tage bis Beginn: 365,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure Atelectasis COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Exposure to SARS-CoV-2 Inappropriate schedule of product administration SARS-CoV-2 test positive Walking distance test normal

Symptomtext

Patient received pfizer vaccine on 3/22/21 and 4/19/21. Presented to ER on 4/23/22. COVID positive on 4/19/22. admitted on 04/23/2022 with acute hypoxic respiratory failure secondary to COPD exacerbation prompted from COVID-19 infection. He did test positive to COVID following exposure. Chest x-ray did not show evidence of pneumonia but he had bibasilar atelectasis. He was managed medically with steroids , antibiotics and bronchodilators. .Overall doing well. Shortness of breath improved. He was weaned off oxygen. Oxygen walk test completed 04/20/2017 showed required no oxygen. He was discharged in stable condition back to facility on 04/27/2022 with plan to complete 5 more days of Decadron 6 mg daily, and azithromycin 500 mg daily for 3 more doses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 4/19/22 COVID19: positive 4/23/22 chest xray: Bibasilar atelectasis worse on the right compared to the left. This is probably not significantly changed.
Aktuelle Erkrankungen: -
Vorgeschichte: ? Arthritis ? Asthma ? Cellulitis ? Congestive heart failure (CHF) (HCC) ? COPD (chronic obstructive pulmonary disease) (HCC) ? Hypertension ? Other and unspecified alcohol dependence, in remission ? Tobacco use disorder
Andere Medikamente: acetaminophen 500 MG Tabs Commonly known as: TYLENOL 500 mg, Oral, EVERY 6 HOURS PRN albuterol (2.5 MG/3ML) 0.083% Nebu Commonly known as: PROVENTIL, VENTOLIN 2.5 mg, Nebulization, EVERY 4 HOURS PRN albuterol 108 (90 Base) MCG/ACT Aers
Allergien: nickel
Vorherige Impfungen: -

VAERS 2223023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 51,0
Geschlecht: M
Eingang: 08.04.2022
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

Anti-neutrophil cytoplasmic antibody positive vasculitis Appendicitis Autoimmune disorder Biopsy kidney Blood urine present Computerised tomogram Cystoscopy Endoscopy Laboratory test Protein urine present Pulmonary embolism Renal disorder

Symptomtext

autoimmune disease p-anca vasculitis Pulmonary Embolisms Appendicitis Kidney Disease Blood/protein in urine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: Numerous labs Endoscope Cystoscope kidney biopsy prednisone rituximab infusions CT scans
Aktuelle Erkrankungen: NA
Vorgeschichte: aortic aneurysm repair 2006
Andere Medikamente: procardia 30 mg
Allergien: cozaar
Vorherige Impfungen: -

VAERS 2216027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: TN
Alter: 79,0
Geschlecht: M
Eingang: 05.04.2022
Impfdatum: 16.04.2021
Beginn: 01.01.2022
Tage bis Beginn: 260,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

pt lives in a nursing home; had a positive COVID test on 1/11/22 in nursing home; placed on isolation; on O2 supplementation; DNR; pt passed away in the nursing home; per death certificate, the cause of death was COVID 19

Weitere VAERSDATA-Felder

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

VAERS 2209267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 03.05.2021
Beginn: 28.01.2022
Tage bis Beginn: 270,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Asthenia Blood glucose increased Brain natriuretic peptide increased COVID-19 Cardiac failure congestive Chest X-ray abnormal Computerised tomogram thorax abnormal Dyspnoea Echocardiogram normal Ejection fraction normal Fall Fatigue Glycosylated haemoglobin increased Hypoxia Left ventricular failure Oedema peripheral Pleural effusion

Symptomtext

Patient with 2 Pzifer COVID vaccinations, last dose 05/02/21, who admitted to hospital with positive COVID test noted during routine admission testing. Patient admitted for weakness, acute respiratory failure, and multiple falls and had complications potentially related to COVID. Provider d/c note: "Patient has a Hx DM, HTN, HLD, obesity - presenting to ER with high BS and Hx weakness, falls at home. She is COVID vaccinated (not boosted yet). She had a several falls over the last 2 days, no head injury. No focal arm or leg weakness, no headache. She feels her leg give out and she falls. No fever ro chills. No V,N,D. No sig cough, but has been SOB. No leg edema. She c/o fatigue. She has had slight congestion, bit no sig cough. Her BS per EMS was > 500 and her last AiC is 12.9 (Sept 2020). She was placed on 5L on route but that has been weaned down to 2L now. She tested positive for COVID. CT chest was neg for PE, and no focal PNA or covid infiltrates seen. However there is R effusion. BNP came high, and she was given Lasix IV. She was also give Rocephin and dose of Steroids. She is being admitted for hypoxia - presumed CHF, with COVID infection. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) Principal Problem: Acute Hypoxic respiratory failure - suspect this to more CHF than COVID related. No infiltrates seen on CT, other than effusion on Right. High BNP. Diuresed and did well. ECHO shows EF normal, so likely some diastolic CHF. Leg edema has resolved. . Hold off on continuing Steroids for now (uncontrolled DM). She is vaccinated for COVID x2 (not boosted). Her O2 has been stable at 2L and she needs O2. Lungs clear, with few R crackles, CXR f/u shows some effusion still. Will need outpatient eval for OSA with sleep study. Doubt this is COVID pneumonia needing steroids. CHF - As above, diuresed and doing well. Add bblocker, continue ACEi. COVID-19 virus infection - as above. not placed on steroids given DM, vaccination status and with the view that hypoxia is related to CHF. Active Problems: Type 2 diabetes mellitus without complication, without long-term current use of insulin (*) - resume metformin, glipizide. A1C is quite high - so placed on insulin. Hyperlipidemia - continue statin. Essential hypertension - continue ACEi. Monitor BP. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: COVID detected PCR on 01/28/22
Aktuelle Erkrankungen: -
Vorgeschichte: BMI 45.0-49.9, adult Hyperlipidemia Microalbuminuria Hepatic steatosis Uncontrolled type 2 diabetes mellitus with hyperglycemia (*) Gastroesophageal reflux disease without esophagitis Essential hypertension
Andere Medikamente: Aspirin Lipitor Coreg Pepcid Lasix Humalog Glucotrol Lantus Lisinopril Metformin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2209221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 05.05.2021
Beginn: 16.02.2022
Tage bis Beginn: 287,0
Dosis: 1
Route/Site: - / -

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

Asymptomatic COVID-19 Cerebral haemorrhage Computerised tomogram head abnormal Ischaemic stroke SARS-CoV-2 test positive

Symptomtext

Patient with 2 Pfizer COVID vaccinations, last dose 05/05/21, who admitted with ischemic stroke who incidentally tested detected for COVID during admission testing. No s/s of COVID per provider d/c note during stay. Provider d/c note below: "Patient is a 61 YO female who was admitted for ischemic stroke of anterior right parietal associated with L occipital subacute intraparenchymal hemorrhage. Patient was also found to have COVID 19, asymptomatic. Neurosurgery and neurology were consulted. Her repeat CT scan to monitor hemorrhage was stable and per neurosurgery no need to hold DAPT so they were resumed. She was started on high dose statin. Ordered cardiac event monitor to monitor for any cardiac arrhythmias leading to stroke. Patient will referred to vascular neurology."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 2,0
Labordaten: COVID "detected" PCR on 02/16/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Paresthesia of right upper and lower extremity CVA (cerebral vascular accident) (*)
Andere Medikamente: Aspirin Lipitor Plavix Levemir Humalog Lisinopril Oxycodone myristate Protonix
Allergien: Metal Penicillins
Vorherige Impfungen: -

VAERS 2201593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 14.04.2021
Beginn: 01.01.2022
Tage bis Beginn: 262,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cough Death Fall Fatigue General physical health deterioration Hypoxia Intensive care Pain SARS-CoV-2 test positive Subarachnoid haemorrhage

Symptomtext

pt brought to ED after a fall; subarachnoid hemorrhage; c/o fatigue, cough, body aches for the past week; initially not hypoxic; positive for COVID; monoclonal antibodies and steroids given; became hypoxic and condition worsened; O2 supplementation; transferred to MICU; O2 demands increased; given baricitinib and ABX; DNR/DNI; eventually refused to wear BiPAP; transitioned to comfort care; passed away peacefully

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, DM, mantle cell lymphoma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2184153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: FL
Alter: 59,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 06.04.2021
Beginn: 20.02.2022
Tage bis Beginn: 320,0
Dosis: 1
Route/Site: - / -

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

COVID-19 pneumonia Death

Symptomtext

Hospitalization for COVID PNA 2/20/22-3/1/22. Treated with dexamethasone, baricitinib, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily. Expired 3/1/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: History of kidney transplant
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2154882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: TN
Alter: 85,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 14.04.2021
Beginn: 01.08.2021
Tage bis Beginn: 109,0
Dosis: UNK
Route/Site: - / -

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

Arteriosclerosis COVID-19 Death Hip surgery Hypercoagulation SARS-CoV-2 test positive

Symptomtext

pt in SNF; positive for COVID after hip surgery; per death certificate, pt died in the SNF of MI, atherosclerotic heart disease, hypercoagulable state, and COVID 19

Weitere VAERSDATA-Felder

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

VAERS 1810549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: NY
Alter: 14,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 08.06.2021
Beginn: 19.07.2021
Tage bis Beginn: 41,0
Dosis: 2
Route/Site: IM / LA

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

Arrhythmia Cardiac arrest Chest pain Cytogenetic analysis Fatigue Dizziness Electrocardiogram Loss of personal independence in daily activities Nausea Implantable defibrillator insertion Myalgia Pain in jaw Paranasal sinus discomfort Resuscitation Seizure Sinusitis

Symptomtext

Initial first injection muscle soreness. Within a week post 2nd injection, my son complained of jaw pain and sinus pressure. We took him to the doctor, he was treated for sinus infection and took sudafed OTC meds. He has taken these before for years with sinus pressure. Some chest pain and fatigue developed. He thought the chest pain was due to working out. On July 19, he suffered major cardiac arrest while at a friends home. CPR was started until EMT arrived. He had to be revived 3x and was transported via helicopter to hospital where he remained for 10 days. No Myocarditis or Pericarditis but he was ruled to have an arrythmia. On July 29, he had a defibrillator installed - he is 14 years old. No prior signs of ANY heart issues and all genetic tests to date have come back with NO trace of what he suffered being present in a gene abnormality. We are still awaiting 2nd set of genes to return, but told not likely anything will be present. He was initially treated by Dr. at hospital. He is now with a new Dr. for any ongoing care. I have written to Pfizer and also CDC - I received a response 8 months ago, provided medical records and never heard back with 4 follow ups sent since. We just would like to know what happened to our son and truly believe in our hearts that this could be a reaction to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 10,0
Labordaten: I can provide all medical records as requested. It's pages of input.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxycillin
Vorherige Impfungen: -

VAERS 2115989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 15.03.2021
Beginn: 27.11.2021
Tage bis Beginn: 257,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

event occurred after 2nd vaccine; breakthrough case admission; patient expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 11/27/21 COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2088126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 20.04.2021
Beginn: 27.01.2022
Tage bis Beginn: 282,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Aortic valve incompetence Aortic valve sclerosis Arteriosclerosis coronary artery Aspartate aminotransferase increased Atelectasis Atrial fibrillation Back pain Bacterial test negative Blood culture negative Blood lactic acid normal Bronchiectasis Bundle branch block right COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Chest pain

Symptomtext

ADMITTED. Patient is an 89 y.o. male with h/o chronic pulmonary fibrosis, chronic diastolic CHF, chronic A-Fib on Coumadin, stage 3 CKD, gout and morbid obesity, presenting to the local ER on 1/27 with c/o dyspnea. He was seen by his outpatient pulmonologist earlier in the day, reporting increasing dyspnea, cough and leg swelling over the past 2 days. Cough is dry and non-productive. Dyspnea is worsened by exertion and laying flat. He reports chronic intermittent chest and back ache which has not changed significantly, and no other associated symptoms. He is prescribed home supplemental oxygen but does not typically need it. Over the past few days, he has been on the road a lot and has halved his dose of torsemide from 40 mg daily to 20 mg daily to reduce the amount of stops he'd need to take while driving. He was once on as high a dose as 60 mg daily but this has been weaned by his cardiologist with the local Clinic. Plan late last year was for cardioMEMS implantation, though this was ultimately abandoned and not pursued since due to a procedural complications. Pulmonology note from earlier today suggests plans for repeat HRCT to evaluate extent of pulmonary fibrosis and discussion regarding anti-fibrotics once past this episode of suspected volume overload. They recommended he be admitted to the hospital for IV diuresis and directed him to the ER for this purpose. In the ER, he was febrile, normotensive to moderately hypertensive, with normal HR, mild tachypnea and hypoxia to 86% on RA alone. He was placed on 2L via NC. Initial labs are notable for elevated proBNP and initial troponin, renal dysfunction, mild AST elevation with otherwise normal LFT?s, normal CBC and lactate, and positive COVID screen. BCx were collected. EKG shows rate controlled A-Fib, incomplete RBBB, and non-specific ST-T changes. CXR showed retrocardiac opacity reflective of either atelectasis or consolidation, superimposed on underlying interstitial lung disease. He was ordered IV fluids, but given less than one liter. He was ordered antibiotics, but these were not given. He will be given an initial dose of IV Lasix and dexamethasone following my conversation with his ER provider. Admission was requested for workup and management of acute hypoxic respiratory failure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: CT THORAX WITHOUT IV CONTRAST Collected: 02/04/22 1250 Order Status: Completed Updated: 02/04/22 1321 Narrative: EXAMINATION: CT Chest without IV Contrast EXAM DATE: 2/4/2022 12:12 PM TECHNIQUE: Standard protocol CT images of the chest were performed without intravenous contrast. Lack of intravenous contrast does limit assessment of the vascular structures and soft tissues. Coronal and sagittal images were reconstructed. DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Interstitial lung disease. COVID-19. COMPARISON: CT 1/28/2022 and 6/13/2021 ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: There is no mediastinal or hilar lymph node enlargement. Cardiovascular: The heart has a normal size. There is no pericardial effusion. Left subclavian cardiac device with leads in the right atrium and right ventricle. Severe coronary artery calcification. Lungs & Airways: Interval development of extensive bilateral patchy groundglass opacities, much of which have a peripheral distribution. There is a background of chronic basilar, peripheral predominant fibrotic lung disease characterized by peripheral reticulation, traction bronchiectasis, and probable honeycombing in the right lower lobe. This appears similar to the prior CT. Pleural Space: There are no pleural effusions. There is no pneumothorax. Upper Abdomen: Small hiatal hernia. Cholelithiasis. Chest Wall & Musculoskeletal: No significant abnormality. Assessment of the soft tissues and vascular structures is limited on noncontrast imaging. ____________________ Impression: 1. Interval development of extensive bilateral patchy groundglass opacities in a predominantly peripheral distribution. This likely relates to COVID-19 pneumonia given the patient's history although alternative infectious/inflammatory etiologies are possible. 2. There is a background of chronic alar predominant fibrotic lung disease in a pattern consistent with UIP. 3. Severe coronary artery calcification. Dictated by: MD on 2/4/2022 12:50 PM. Electronically signed by: MD on 2/4/2022 1:20 PM. DR CHEST SINGLE VIEW Resulted: 02/03/22 1640 Order Status: Completed Updated: 02/03/22 1642 Narrative: EXAMINATION: Single View Chest EXAM DATE: 2/3/2022 4:30 PM TECHNIQUE: Single view chest INDICATION: hypoxia COMPARISON: 1/27/2022 ENCOUNTER: Not applicable _________________________ FINDINGS: Similar enlargement of the cardiomediastinal silhouette with dual-lead pacing device. Mild central pulmonary vascular congestion. Bibasilar reticular opacities and/or atelectasis appears similar. No evidence of new consolidation or pneumothorax. Ill-definition of the CP angles which may represent trace pleural effusions. Impression: Overall similar appearance of cardiomegaly, bibasilar reticular opacities, and possibly trace effusions. CT THORAX WITHOUT IV CONTRAST Collected: 01/28/22 1805 Order Status: Completed Updated: 01/28/22 1814 Narrative: EXAMINATION: CT Chest without IV Contrast EXAM DATE: 1/28/2022 4:59 PM TECHNIQUE: Standard protocol CT images of the chest were performed without intravenous contrast. Lack of intravenous contrast does limit assessment of the vascular structures and soft tissues. Coronal and sagittal images were reconstructed. DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Chest pain or SOB, pleurisy or effusion suspected COMPARISON: High resolution chest CT 6/13/2021, nuclear medicine perfusion imaging 1/28/2022 ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: There is no mediastinal or hilar lymph node enlargement. Cardiovascular: The heart has a normal size and atherosclerotic plaque is present on the coronary arteries. There is no pericardial effusion. Cardiac support device overlies the left chest. Lungs & Airways: Bronchiectasis and ground glass and reticular opacities within the bilateral lower lobes greater within the left lower lobe. Relative sparing of the bilateral apices. These are better characterized on high resolution chest CT 6/13/2021. Pleural Space: There are no pleural effusions. There is no pneumothorax. Upper Abdomen: Cholelithiasis. Bilateral renal atrophy left greater than right Chest Wall & Musculoskeletal: There is multilevel thoracic degenerative disc disease. Assessment of the soft tissues and vascular structures is limited on noncontrast imaging. ____________________ Impression: 1. No focal consolidation or effusion. 2. Basilar peripheral round glass reticular opacities and bronchiectasis better characterized on prior high-resolution chest CT. Dictated by: MD on 1/28/2022 6:05 PM. Electronically signed by: MD on 1/28/2022 6:13 PM. NM LUNG PERFUSION ONLY Resulted: 01/28/22 1336 Order Status: Completed Updated: 01/28/22 1338 Narrative: EXAMINATION: Nuclear Medicine Pulmonary Perfusion Lung Scan Particulate EXAM DATE: 1/28/2022 1:14 PM TECHNIQUE: Radiopharmaceutical: 4.39 mCi Tc-99m MAA Route: Intravenous Images: Multiple static of the lungs INDICATION: COVID 19, lung fibrosis, elevated d-dimer COMPARISON: Prior exam dated 6/12/2021. FINDINGS: There is a suspicion of 2 segmental areas of decreased perfusion in the left lower lobe seen posteriorly worrisome for pulmonary embolism. Pacing device creates a photopenic defect overlying the left lung midportion Impression: There is a suspicion of 2 segmental areas of decreased perfusion in the left lower lobe seen posteriorly worrisome for pulmonary embolism. The orange significant findings protocol was initiated at 1/28/2022 1:34 PM. The presence of a significant findings result is to be communicated with a clinician and/or clinical staff by support staff. CV Echo Limited with Contrast Collected: 01/28/22 0815 Order Status: Completed Updated: 01/28/22 0948 Narrative: HCF LIMITED ECHOCARDIOGRAPHY REPORT Name: Study Date: 01/28/2022 MRN: Patient Location: HCF DOB: Patient Class: Inpatient Gender: Male Ordering Physician: Age: 89 yrs Referring Physician: Height: 180 cm Performed By: Weight: 142 kg Resting HR: 77 BSA: 2.5 m2 Resting BP: 155/85 mmHg Reason For Study: ., acute on chronic diastolic heart failure History/Symptoms: Pacemaker,Former Smoker,Dyspnea on exertion (DOE),Sick Sinus Syndrome,Coronary artery disease,Arrhythmia (Atrial fibrillation),Chronic kidney disease,Stent x5 Electronically signed by: MD on 01/28/2022 09:48 AM Interpretation Summary The left ventricular ejection fraction is 55%. The left ventricle is normal in size. The LV ejection fraction is normal. The right ventricle is mildly dilated. Right ventricle function is mildly decreased. Today's study was compared to one performed on 6/12/2021. The LVEF was 56% on the prior study. STUDY PERFORMED/QUALITY: AORTIC VALVE: A two-dimensional transthoracic There is mild aortic valve sclerosis. echocardiogram with color flow and The aortic valve is tricuspid. There spectral flow Doppler was performed in is no aortic valve stenosis. Trace limited views only. The technical (trivial) aortic regurgitation. quality of the exam was limited due to suboptimal acoustic windows. The MITRAL VALVE: apical views were difficult to obtain Structurally normal mitral valve. and are suboptimal in quality. Due to There is mild mitral annular limited acoustic windows, Definity was calcification. There is no mitral administered. Location: Portable. regurgitation noted. LEFT VENTRICLE: The left ventricle is normal in size. TRICUSPID VALVE: The left ventricular ejection fraction Structurally normal tricuspid valve. is 55%. The LV ejection fraction is There is trace tricuspid normal. regurgitation. The estimated right ventricular systolic pressure is 46 mmHg. LEFT ATRIUM: The left atrium is moderately dilated. RIGHT ATRIUM: The right atrium is mildly dilated. RIGHT VENTRICLE: The right ventricle is mildly dilated. Right ventricle function is mildly decreased. There is a pacemaker lead in the right ventricle. AORTA/PULMONARY ARTERY: The aortic root and ascending aorta are normal in size. Left Ventricle Tricuspid Valve EF(MOD-Avg): 55 % RVSP(TR): 46.0 mmHg EDV(MOD-sp4): 93.3 ml TR max vel: 3.08 m/sec ESV(MOD-sp4): 43.4 ml TR max PG: 38.0 mmHg SV(MOD-Avg): 51.9 ml RAP systole: 8.0 mmHg EDV(MOD-sp2): 97.0 ml ESV(MOD-sp2): 43.0 ml ______________________________________________________________________________ Reference Table: Normal Mild ModerateSevere Men LVEF > 52% 41-51% 30-40% <30% Women LVEF > 54% 41-53% 30-40% <30% Men LVIDd 4.2-5.8 5.9-6.3 6.4-6.8 >6.8 Women LVIDd 3.8-5.2 5.3-5.6 5.7-6.1 >6.1 LA Volume (ml/m^2) < 34 35-41 42-48 >48 ______________________________________________________________________________ Electronically signed by: MD on 01/28/2022 09:48 AM All sources of data reside in the Cardiology PACS EJECTION FRACTION ECHO Collected: 01/28/22 0815 Order Status: Completed Updated: 01/28/22 0948 EJECTION FRACTION ECHO 55 % DR CHEST SINGLE VIEW Collected: 01/27/22 1926 Order Status: Completed Updated: 01/27/22 1933 Narrative: EXAMINATION: Single View Chest EXAM DATE: 1/27/2022 7:10 PM TECHNIQUE: Single view chest INDICATION: Worsening shortness of breath and leg swelling. COMPARISON: Chest radiograph 8/9/2021 and chest CT 6/13/2021. ENCOUNTER: Not applicable FINDINGS: Left chest wall dual-lead pacemaker. Moderate cardiomegaly without pulmonary vascular congestion. Mild interstitial opacities in the lung bases with ill-defined retrocardiac opacity. No substantial pleural effusion or pneumothorax. _________________________ Impression: Retrocardiac opacity may reflect atelectasis or consolidation superimposed on underlying interstitial lung disease. Collected: 01/27/22 1855 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 01/27/22 2032 COVID-19 PCR Detected Influenza A PCR Not Detected Not Detected Influenza B PCR Not Detected Not Detected RSV PCR Not Detected Not Detected Respiratory Pathogens by Film Array Collected: 02/04/22 1336 Order Status: Sent Specimen: Swabbed Collection from Nasopharynx Updated: 02/04/22 1346 Peripheral Blood Culture Collected: 01/27/22 2124 Order Status: Completed Specimen: Blood, Venous Updated: 02/01/22 2300 Cult Blood Peripheral No bacteria or yeast isolated Peripheral Blood Culture Collected: 01/27/22 2053 Order Status: Completed Specimen: Blood, Venous Updated: 02/01/22 2201 Cult Blood Peripheral No bacteria or yeast isolated Sputum Culture Collected: 01/29/22 1410 Order Status: Completed Specimen: Body Fluid from Sputum Updated: 01/31/22 0736 Bacterial culture, sputum Normal Upper Respiratory Flora, no MRSA or Pseudomonas aeruginosa isolated Gram stain Many WBCs Few Gram Positive Cocci
Aktuelle Erkrankungen: STAGE 4 chronic kidney disease
Vorgeschichte: Hospital Permanent atrial fibrillation CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min Chronic heart failure with preserved ejection fraction Acute on chronic respiratory failure with hypoxia Goals of care, counseling/discussion Acute pulmonary embolus Interstitial lung disease Bacterial pneumonia Non-Hospital CHF (congestive heart failure) Coronary artery disease involving native coronary artery of native heart without angina pectoris Essential hypertension, benign Hyperlipidemia, unspecified hyperlipidemia type Hypothyroidism, unspecified type Cardiac pacemaker in situ Microscopic hematuria Sick sinus syndrome BPH (benign prostatic hyperplasia) Sleep apnea Lesion of pancreas Chronic left-sided thoracic back pain Long term (current) use of anticoagulants Dyspnea on exertion Acute respiratory insufficiency Acute respiratory failure with hypoxia
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 100 MG tablt apixaban (ELIQUIS) 5 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG enteric coated tablet atorvastatin (LIPITO
Allergien: AmlodipineRash
Vorherige Impfungen: -

VAERS 2039569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MN
Alter: 52,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 19.08.2021
Beginn: 22.12.2021
Tage bis Beginn: 125,0
Dosis: 2
Route/Site: SYR / LA

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

Acute respiratory distress syndrome COVID-19 Chemotherapy Colon cancer Death Inappropriate schedule of product administration SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 3/27, 4/17, 8/19/21 COVID-19 positive by PCR on 12/22/21 admitted to Hospital on 12/30/21-1/14/22 d/t ARDS d/t COVID-19, onset of symptoms 12/19/21. Expired on 1/14/22. Underlying malignant colon cancer, on chemo; morbid obesity

Weitere VAERSDATA-Felder

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

VAERS 1357802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: PA
Alter: 54,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 05.05.2021
Beginn: 26.05.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram pulmonary abnormal Deep vein thrombosis Dyspnoea Pulmonary embolism Ultrasound Doppler abnormal Blood test Chest X-ray Thrombosis Ultrasound scan abnormal

Symptomtext

pulmonary embolism; blood clot in right calf.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: Hospitalized for five days; numerous blood work, sonagram on leg, chest xray
Aktuelle Erkrankungen: none
Vorgeschichte: type 2 diabetes
Andere Medikamente: high blood pressure med; Type 2 diabetes med;
Allergien: -
Vorherige Impfungen: -

VAERS 2018678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: NJ
Alter: 30,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 01.05.2021
Beginn: 26.12.2021
Tage bis Beginn: 239,0
Dosis: 2
Route/Site: OT / LA

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

Anosmia Anxiety Chest pain Cough Decreased appetite Dizziness Headache Insomnia Loss of consciousness Malaise Near death experience Palpitations SARS-CoV-2 test

Symptomtext

and had a near death experience; passed out; feel ill; headache; dizziness/light headedness; loss of appetite; loss of sense of smell; sleeplessness; coughing; chest pain; anxiety; palpitation; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. The reporter is the patient. A 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 01May2021 (Lot number: EW0153) at the age of 30 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Shellfish, reaction(s): "Allergy"; Peanut, reaction(s): "Allergy"; Cashew nut, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8736, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 10Apr2021, when the patient was 30 years old, for COVID-19 Immunization. The following information was reported: NEAR DEATH EXPERIENCE (medically significant) with onset 26Dec2021, outcome "recovering", described as "and had a near death experience"; MALAISE (non-serious) with onset 26Dec2021, outcome "recovering", described as "feel ill"; LOSS OF CONSCIOUSNESS (non-serious) with onset 26Dec2021, outcome "recovering", described as "passed out "; HEADACHE (non-serious) with onset 26Dec2021, outcome "recovering", described as "headache"; DIZZINESS (non-serious) with onset 26Dec2021, outcome "recovering", described as "dizziness/light headedness"; DECREASED APPETITE (non-serious) with onset 26Dec2021, outcome "recovering", described as "loss of appetite"; ANOSMIA (non-serious) with onset 26Dec2021, outcome "recovering", described as "loss of sense of smell"; INSOMNIA (non-serious) with onset 26Dec2021, outcome "recovering", described as "sleeplessness"; COUGH (non-serious) with onset 26Dec2021, outcome "recovering", described as "coughing"; CHEST PAIN (non-serious) with onset 26Dec2021, outcome "recovering", described as "chest pain"; ANXIETY (non-serious) with onset 26Dec2021, outcome "recovering", described as "anxiety"; PALPITATIONS (non-serious) with onset 26Dec2021, outcome "recovering", described as "palpitation". The events "covid-19 positive", "covid-19 positive", "and had a near death experience", "feel ill", "passed out ", "headache", "dizziness/light headedness", "loss of appetite", "loss of sense of smell", "sleeplessness", "coughing", "chest pain", "anxiety" and "palpitation" were evaluated at the emergency room visit. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. There were no any other medications the patient received within 2 weeks of vaccination. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (26Dec2021) positive, notes: Nasal Swab. Therapeutic measures were taken as a result of vaccination failure, covid-19, malaise, loss of consciousness, headache, dizziness, decreased appetite, anosmia, insomnia, cough, chest pain, anxiety, palpitations.; Sender's Comments: Based on the temporal association between the events Near death experience, malaise, loss of Conscience, headache, Decreased Appetite, Anosmia, Insomnia, Cough, Anxiety, Palpitations , chest pain ,Dizziness, and the suspect drug BNT162B2 cannot be excluded The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: Test Date: 20211226; Test Name: Covid-19/Flu A'||CHR(38)||'B rapid; Result Unstructured Data: Test Result:Positive; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2015569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 18.05.2021
Beginn: 08.06.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / -

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

Cardiac stress test Chest X-ray Computerised tomogram Coronary arterial stent insertion Coronary artery occlusion Echocardiogram Electrocardiogram Laboratory test Myocardial infarction X-ray

Symptomtext

Initially there were no issues. 19 days later I had a LAD heart attack with only 1 artery occluded. The two arteries were clear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: 6/28 Echocardiogram/Chest XR 6/28 CV Cardiac Procedure (2 stents) 7/1 ECG 8/10 ECG 11/8 Echocardiogram 11/17 Stress Test 12/30 EKG/Xray/CT Scan/Echocardiogram Numerous lab tests between 6/27/2021 and 1/7/2022
Aktuelle Erkrankungen: slightly high cholesterol
Vorgeschichte: None
Andere Medikamente: Bisoprolol
Allergien: None
Vorherige Impfungen: -

VAERS 1982169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 05.05.2021
Beginn: 16.12.2021
Tage bis Beginn: 225,0
Dosis: 1
Route/Site: IM / AR

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

Asthenia Balance disorder Blood thyroid stimulating hormone decreased COVID-19 Cerebrovascular accident Computerised tomogram head normal Condition aggravated Fall Hyperthyroidism Hypothyroidism Inappropriate schedule of product administration Magnetic resonance imaging head normal Mental status changes Muscular weakness SARS-CoV-2 test positive Thyroid mass Thyroxine free normal Ultrasound thyroid abnormal

Symptomtext

Hospitalized 12/16/2021; COVID-19 positive 12/16/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 12/16/2021 Discharge Date: Dec 22, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Weakness [R53.1] Altered mental status, unspecified altered mental status type [R41.82] COVID [U07.1] HOSPITAL COURSE: The patient is a 62 yo woman with past medical history significant for history of left-sided brain oligodendroglioma status post resection, seizure disorder, hypothyroidism, history of CVA with chronic right leg weakness, with recent hosptialization 10/25-10/29 for weakness thought to be secondary to recrudescence of her prior CVA vs other. She was subsequently admitted at Inpatient Rehabilitation Center from 10/29-11/10/21 for ongoing right leg weakness. She was discharged in stable condition and felt she was doing well until 2 days ago. The patient was re-admitted on 12/16 due to generalized weakness, and fall as well as leftward tilting that has rapidly progresses over the past couple of days. Patient was found to have COVID-19 infection and the working diagnosis at the time of admission was acute stroke versus regarding since of prior stroke versa generalized weakness due to COVID-19 infection versus thyrotoxicosis. Patient's TSH was 0.09, free T4 was 1.9. Initial CT head was negative for acute stroke or intracranial hemorrhages. MRI of the brain was negative for acute stroke. In terms of COVID-19 infection, patient was fully vaccinated with Pfizer on 04/07 and 5/5. Has not yet received booster. She has not required any oxygen at the moment. Does not appear to be in respiratory distress. She was offered monoclonal antibodies. Patient has generalized weakness was likely is related to COVID-19 infection with associated uncontrolled hypothyroidism. The patient 's Symptoms improved after COVID was treated and Synthroid adjusted. Patient was evaluated by Endocrinology due to underlying hypothyroidism. Thyroid ultrasound revealed large right lobe thyroid nodule. Endocrinology increased her Synthroid to 112.5 mcg from 88 mcg. Endocrine will plan an outpatient right thyroid nodule FNA - scheduled 1/6/2021 at 8:20 am. Following this, will anticipate referral to General Surgery for right hemithyroidectomy vs total thyroidectomy. She will have a Repeat thyroid hormone blood test in 6 weeks. For age related osteoporosis, endocrine Recommend screening for secondary causes of decreased bone mass hyperparathyroidism, malabsorption/celiac disease, multiple myeloma, hypercalciuria w/ CMP, phosphorus, magnesium, PTH, celiac antibody cascade, SPEP/free light chains, 24h urine calcium/creatinine/sodium. This can be obtained with updated thyroid hormone blood tests in 6 weeks.Update as planned 1/2022 Patient was seen by PT/OT who initially recommended acute rehab but after evaluation they recommended subacute rehab. Her and her spouse were discouraged with this but ultimately accepted discharge to SAR but changed her mind that day so discharged home w/ HH RN and PT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Influenza A TIA (transient ischemic attack) Urinary tract infection, acute Polyneuropathy, peripheral sensorimotor axonal Localization-related partial epilepsy with complex partial seizures (HCC) Cerebellar atrophy (HCC) Hypothyroid Right thyroid nodule Sepsis (HCC) Abnormality of gait Ataxia Generalized weakness Weakness S/P vaginopexy At risk for falls Late effect of cerebrovascular accident (CVA) Age-related osteoporosis with current pathological fracture with routine healing
Andere Medikamente: atorvastatin (LIPITOR) 10 MG tablet lacosamide (VIMPAT) 100 MG tablet lacosamide (VIMPAT) 200 MG tablet levothyroxine (SYNTHROID) 75 MCG tablet melatonin 5 MG tablet
Allergien: Latex Penicillins
Vorherige Impfungen: -

VAERS 1967741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: ME
Alter: 59,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 27.04.2021
Beginn: 14.12.2021
Tage bis Beginn: 231,0
Dosis: 1
Route/Site: IM / -

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

Acute myocardial infarction Akinesia Angiogram cerebral abnormal Brain herniation Brain oedema Catheterisation cardiac abnormal Cerebral artery occlusion Computerised tomogram head abnormal Echocardiogram abnormal Ejection fraction decreased Electrocardiogram Ischaemic stroke Percutaneous coronary intervention Stent placement Troponin increased

Symptomtext

Admitted 12/14 with acute myocardial infarction, STEMI, required PCI to the left circumflex artery. Hospital course complicated by acute ischemic stroke 12/15 with severe cerebral edema and herniation syndrome

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 7,0
Labordaten: EKG troponin 8.06 12/15 Cardiac cath lab with PCI stent to circumflex 12/14 CT/CTA head/neck 12/15: left MCA occlusion, large ischemic stroke in left MCA distribution, 72cc volume of stroke CT head 12/15, 12/16, and 12/21 with progressively worsening cerebral edema related to stroke, midline shift, uncal and subfalcine herniation, and new infarct in right ACA territory due to herniation syndrome Echo 12/14: mildly reduced EF 44% basal to mid-lateral wall akinesis
Aktuelle Erkrankungen: none known
Vorgeschichte: hypertension hyperlipidemia CAD
Andere Medikamente: aspirin 81mg atorvastatin 80mg metoprolol succinate 50mg
Allergien: niacin cardizem
Vorherige Impfungen: -

VAERS 1943728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 05.05.2021
Beginn: 25.11.2021
Tage bis Beginn: 204,0
Dosis: 1
Route/Site: IM / AR

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

Angiogram abnormal Anticoagulant therapy Brain neoplasm malignant Breath sounds abnormal COVID-19 Cardiac tamponade Carotid artery occlusion Cerebral artery occlusion Cerebrovascular accident Chest discomfort Computerised tomogram thorax abnormal Condition aggravated Death Diverticulitis Dysarthria Dyspnoea Echocardiogram abnormal Facial paralysis

Symptomtext

Deceased 12/03/2021; Hospitalized 11/23/2021; COVID-19 positive 11/25/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: , MD Primary Care Physician at Discharge:, MD Admission Date: 11/23/2021 HOSPITAL COURSE: Patient presented to local HCF ED with symptoms of SOB, orthopnea, and chest pressure that had been worsening over the last three days. CT showed large pericardial effusion, bilateral small pleural effusions, and cecal diverticulitis. He was transferred to another HCF and Cardiology was consulted, recommending stat ECHO, EKG. ECHO showed large pericardial effusion with RV collapse, hemodynamically significant, early signs of tamponade. He was started on colchicine and indocin Pt was started on flagyl and levaquin for the cecal diverticulitis. Pericardiocentesis with drain placement was performed the following morning. ECHO post-procedure with trivial remaining effusion. On 11/25, patient became hypoxic (had been using lasix PRN for fluid overload) and CTA was suggestive of bilateral PE's, heparin gtt was started after significant education provided to patient and wife regarding risk for brain bleed in the setting of untreated brain metastases. Pulm was consulted and they felt that the amount of clot burden did not accurately explain his degree of hypoxia. Pt was started on HFNC. ECHO repeated and this was unremarkable. COVID re-swab (negative at admission) was positive on 11/25. Pt was started on remdesivir and dexamethasone. Pericardial drain removed 11/26. Stroke code called morning of 11/27 in the setting sudden slurred speech, left facial droop, and loss of motor/sensory function in LUE, LLE. Neurology was consulted. Stat HCT showed right MCA stroke 2/2 right ICA and MCA occlusion, not a candidate for MT due to lung cancer with brain mets. Heparin gtt stopped. Neurology recommending crani in the setting of worsening malignant edema, patient declined, hospice recommended. Patient declined escalation of care, was made DNR on 11/27. Hospice meeting on 11/28, originally planning for home with hospice, met criteria for GIP hospice on 11/29. Patient was seen per nursing request this evening as patient had expired. Upon evaluation, patient was unresponsive with wife at bedside. Patient's pupils were fixed and nonreactive to light. Patient was without heart or lung sounds upon ascultation. Patient was without pulses x4 extremities. Patient was pronounced as having expired today, 12/03/2021, at 11:36 PM. Attending Dr. notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute hypoxemic respiratory failure (HCC) Pneumonia due to COVID-19 virus Pleural effusion Metastatic non-small cell lung cancer (HCC) Lung nodule Primary lung adenocarcinoma, left (HCC) Interstitial pneumonia (HCC) Multiple subsegmental pulmonary emboli without acute cor pulmonale (HCC) Pericardial effusion Acute ischemic stroke (HCC) Constipation Lichen planus Leukocytosis Seizure (HCC) Localization-related symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus (HCC) Migraine without aura and without status migrainosus, not intractable Brain metastases (HCC) Cervical radiculopathy Neuropathy Jaw pain Pain Abnormal prostate exam Hyperlipidemia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet alectinib (ALECENSA) 150 MG capsule guaiFENesin-Codeine (GUAIFENESIN AC PO) ibuprofen (MOTRIN) 400 MG tablet levETIRAcetam (KEPPRA) 500 MG tablet Sodium Fluoride (FLUORIDEX) 1.1 % PSTE zoledronic acid (
Allergien: Environmental Penicillins
Vorherige Impfungen: -

VAERS 2566440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: -
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 22.04.2021
Beginn: 17.08.2021
Tage bis Beginn: 117,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2569050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 22.04.2021
Beginn: 26.08.2021
Tage bis Beginn: 126,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Narrative:

Weitere VAERSDATA-Felder

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

VAERS 1902060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 12.04.2021
Beginn: 14.11.2021
Tage bis Beginn: 216,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Hospital Course and Significant Findings: 81 year old woman with multiple medical problems including DM2, HTN, hypothyroidism, vaccinated against COVID 5/2021, admitted 11/14/21 with acute hypoxemic respiratory failure due to COVID. She was started on dexamethasone and remdesivir. Oxygen requirement 1-2L. Noted to be hyperglycemic and started on NPH, however patient adamantly declines to use insulin at home. At the time of hospital discharge, patient is feeling well and she is very eager to go home. Continued admission was offered to complete 5th dose of remdesivir, however patient prefers to forego this in favor of going home, which I think is reasonable given her clinical stability. She will continue dexamethasone for total of 10 days. Insulin teaching for home use was highly recommended but patient adamantly refuses to use insulin at home, she will continue metformin and check blood glucose regularly. Discussed return precautions with patient and daughter including fever, chest pain, shortness of breath, increasing oxygen requirement, hyperglycemia. They are in agreement with the discharge plan.

Weitere VAERSDATA-Felder

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

VAERS 1888289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MD
Alter: 62,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 28.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

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

Angiogram cerebral normal Arteriogram carotid normal Asthenia Cerebrovascular accident Dysarthria Echocardiogram abnormal Ejection fraction normal Gait disturbance Hemianaesthesia Magnetic resonance imaging head abnormal Mitral valve incompetence Mitral valve thickening Muscular weakness Nervous system disorder Scan with contrast abnormal Sleep disorder

Symptomtext

Began feeling weak 2 hours after vaccine administration. Awoke 4:00 a.m. (13.5 hours after vaccination) with left numbness and weakness and assumed normal side effects. Re-awoke at 8:30 a.m. with clear signs of neurologic issues and called nurse and was taken immediately to ER Hospital Center. DX: Acute right pontine CVA with associated left-side numbness with upper and lower extremity weakness, gait imbalance & slurred speech. Hospitalized 4/29 - 5/2/21. Discharge to home with PT/OT visits scheduled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: 1. MRI of brain w/ and w/o contrast documenting recent infarct w/in the right pons measuring 12 x 9 mm. No evidence of intracranial bleed. MRA of brain documents both internal carotid, anterior, middle and posterior cerebral, vertebral an basilar arteries are patent. No significant stenosis or aneurysm identified. 2. A 2D echo, EF of 60% to 65%. Right ventricle is normal size. Right ventricular systolic function is normal. Mitral valve leaflets are mildly thickened with trace mitral regurgitation. No pericardial effusion. No evidence of any intracardiac thrombus. 3. CT angiogram of the head and neck. CT angiogram of the head documents no vessel stenosis, occlusion or aneurysm identified. Unremarkable study. CT angiogram of the neck documents no evidence of dissections, stenosis, pseudoaneurysm formation or extravasation of contrast, essential unremarkable CT angiogram of the neck.
Aktuelle Erkrankungen: NK
Vorgeschichte: Diabetes Mellitis Type 2 w/o complications controlled by diet Hypercholesterolemia Hypertension Lumbar disc degeneration
Andere Medikamente: Pravastatin, Lisinopril, multivitamin, vitamin D3, vitamin B12, saw palmetto extract , certrizine
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 1864989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: IN
Alter: 34,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 06.04.2021
Beginn: 08.11.2021
Tage bis Beginn: 216,0
Dosis: 1
Route/Site: SYR / RA

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

Cerebrovascular accident Computerised tomogram Dizziness Echocardiogram Magnetic resonance imaging head Palpitations Ultrasound Doppler Ventricular extrasystoles

Symptomtext

I had a stroke on November 8th. I began having PVC heart palpitations on Aug 1. They lasted about a week. They came back for several days at a time in the weeks after. I began having dizzy or lightheaded spells in October. I then had a stroke on November 8th. I am 34 years old and was healthy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Cat scan 11/8/2021 Mri 11/8/2021 Heart Echo with bubble study 11/9/2021 Ultrasound of my leg arteries and veins 11/09/2021 Mri of veins in brain 11/09/2021 Esophageal echo of heart 11/10/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Albuterol Symbicort
Allergien: -
Vorherige Impfungen: -

VAERS 1825680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: KY
Alter: 64,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 05.05.2021
Beginn: 22.08.2021
Tage bis Beginn: 109,0
Dosis: 1
Route/Site: IM / LA

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

Death SARS-CoV-2 test Vaccine breakthrough infection

Symptomtext

Patient had breakthrough infection and deceased.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 19,0
Labordaten: COVID Antigen test on 7/25/2021.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Diabetes Mellitus, asthma, morbid obesity
Andere Medikamente: Unknow
Allergien: Codeine
Vorherige Impfungen: -

VAERS 1220292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: ME
Alter: 65,0
Geschlecht: M
Eingang: 06.10.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Aortic dilatation Blood test Computerised tomogram Echocardiogram Muscle spasms Aortic disorder Condition aggravated Pulmonary embolism Parosmia Product odour abnormal

Symptomtext

having bilateral ankle cramping and a weird smell in his nose. (pin to top)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: non
Aktuelle Erkrankungen: none
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1689119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 14.04.2021
Beginn: 18.08.2021
Tage bis Beginn: 126,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Cough Dyspnoea Dyspnoea exertional Pneumonia viral Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID-19 breakthrough case. patient with 4 days of shortness of breath progressively worsening presented initially on 8/19 at the time was not hypoxic, was discharged with monitoring system. however shortness of breath has progressively worsened to severe, worse on attempted ambulation, associated with fevers, cough, generalized weakness, so came back to ER, noted to be requiring oxygen supplementation, and also short of breath on talking, so being admitted. Admitted 8/22/21. Pfizer Covid-19 vaccine given on 3/24/21 & 4/14/21. Tested positive for covid on 8/19/21. Diagnosed and treated for acute hypoxic respiratory failure and covid viral pneumonia. Improved and discharged on 8/24/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Tested positive for covid on 8/19/21.
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, CHF, Afib, HTN
Andere Medikamente: albuterol, amiodarone, apixaban, atorvastatin, azelastine ophthalmic, cholecalciferol, clonidine, escitalopram, famotidine, hydrochlorothiazide, ipratropium nasal spray, lisinopril, meclizine, nitroglycerin sublingual, sucralfate
Allergien: Toradol
Vorherige Impfungen: -

VAERS 1591253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 20.08.2021
Impfdatum: 08.04.2021
Beginn: 07.08.2021
Tage bis Beginn: 121,0
Dosis: 2
Route/Site: - / -

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

Death

Symptomtext

Patient passed away on 08/07/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Albuterol, Calcium Vit D, lisinopril, Norvasc, Trelegy Ellipta, Lopressor, Vanicream, Protopic, Kenalog, Multi Vit, B-Complex tab
Allergien: No known alleriges
Vorherige Impfungen: -

VAERS 1573628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 16.04.2021
Beginn: 30.07.2021
Tage bis Beginn: 105,0
Dosis: UNK
Route/Site: - / -

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

Pulmonary embolism Thrombocytopenia

Symptomtext

Pulmonary emboli Thrombocytopenia, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1554286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 30.04.2021
Beginn: 31.07.2021
Tage bis Beginn: 92,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Cerebrovascular accident Facial paresis

Symptomtext

I63.9 - Stroke determined by clinical assessment I63.9 - Acute CVA (cerebrovascular accident) N17.9 - Acute kidney failure, unspecified R29.810 - Facial weakness

Weitere VAERSDATA-Felder

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

VAERS 1549468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 12.08.2021
Impfdatum: 13.04.2021
Beginn: 02.08.2021
Tage bis Beginn: 111,0
Dosis: UNK
Route/Site: - / -

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

Acute respiratory failure COVID-19 Chills Condition aggravated Diarrhoea Dyspnoea Flank pain Headache Inappropriate schedule of product administration Nausea Nephrolithiasis Pain Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

8/2/2021: presented to ED with CC of shortness of breath. Symptoms began 4 days prior to presentation, patient began experiencing shortness of breath & cough productive of white sputum, body aches, and fever/chills. Patient endorses intermittent headaches, nausea, and diarrhea for the past 2 days and intermittent left flank pain he attributes to his recurrent nephrolithiasis. Diagnosed with acute hypoxic resp failure 2/2 COVID-19 Note: patient previously vaccinated with Pfizer COVID-19 vaccine on 3/3/21 and 4/13/21. 8/12/2021: patient discharged

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: COVID PCR + 8/2/2021
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, CAD sp 3 stents, hypertension, hyperlipidemia, hypothyroidism, nephrolithiasis, anxiety, and neuropathy
Andere Medikamente: albuterol, alprazolam, azithromycin, cefdinir, clopidogrel, ferrous sulfate, gabapentin, levothyroxine, lisinopril, ondansetron, oxycodone-acetaminophen, pantoprazole, pravastatin, sucralfate
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1536538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: FL
Alter: 62,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 13.04.2021
Beginn: 27.07.2021
Tage bis Beginn: 105,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure COVID-19 Condition aggravated Pneumonia Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

7/27/21: Patient transferred to hospital from outside facility with COVID-19 infection, pneumonia and pulmonary embolism, acute hypoxic resp distress. Patient was diagnosed with COVID on 7/17. Note: Patient was previously vaccinated with Pfizer COVID-19 Vaccine, last dose in April 2021. 8/9/21: Patient is still admitted at the time of this report submission. Please note: Patient received First dose of Pfizer COVID-19 vaccine on 3/23/2021, followed by the second dose on 4/13/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: test positive for COVID-19 at outside facility on 7/17/2021
Aktuelle Erkrankungen: -
Vorgeschichte: COVID-19 dx,pneumonia and pulmonary embolism
Andere Medikamente: aspirin, azithromycin, guifenesin, ibuprofen
Allergien: Aspirin
Vorherige Impfungen: -

VAERS 1536245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: NY
Alter: 64,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 10.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: SYR / RA

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

Angiogram pulmonary Blood culture Blood lactic acid Chest discomfort Chest pain Computerised tomogram abdomen Electrocardiogram Microscopy Pulmonary embolism SARS-CoV-2 test Scan with contrast Ultrasound Doppler Urine analysis X-ray

Symptomtext

Approximately 10 days after the second dose of Pfizer covid-19 vaccine ( 4/20/21) I began experiencing tightness and pain in my chest on the right side. The pain continued and started becoming worse over the next few days and on Monday 4/26/21 I went to have it checked out at an urgent care. Xrays were taken and the physician thought it might be kidney stones so I was sent to emergency room where a right side abdomen CT scan was done. This showed negative for kidney stones so I was sent home. Three days later on Thursday 4/29 21 the pain became extreme so I went to hospital where I was admitted after testing with pulmonary embolisms and possible pnuemonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: 4/29/21 Blood cultures Electrocardiogram Covid AMp Assay of Lactic acid Urinalysis Auto w/scope CT Angio, chest, combo with and without contrast Duplex extrem veneous
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension
Andere Medikamente: Amlodipine Besylate / Benazepril HCL 10-20mg once daily Metoprolol Succinate ER 25 mg once daily Aspirin 81 mg once daily
Allergien: -
Vorherige Impfungen: -

VAERS 1515707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CO
Alter: 59,0
Geschlecht: M
Eingang: 05.08.2021
Impfdatum: 15.04.2021
Beginn: 14.07.2021
Tage bis Beginn: 90,0
Dosis: 1
Route/Site: SYR / RA

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

Anticoagulant therapy Heart rate abnormal Intracardiac thrombus Joint swelling Peripheral swelling Pulmonary embolism Pulmonary thrombosis Red blood cell count Surgery Thrombectomy Thrombosis

Symptomtext

On July 15 I had surgery to remove significant blood clots from my heart and lungs as a result from a saddle pulmonary embolism. I have done testing to eliminate Cancer, Hereditary and red blood cells; On July 15 I had surgery to remove significant blood clots from my heart and lungs as a result from a saddle pulmonary embolism. I have done testing to eliminate Cancer, Hereditary and red blood cells; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EW0153; Expiry date: unknown) via an unspecified route of administration, administered in arm right on 15Apr2021 13:00 (at age of 59-year-old) as dose 2, single for COVID-19 immunization. Medical history included chronic low back pain from multiple back surgeries and allergy to sulfa from an unknown date and unknown if ongoing. Concomitant medications included magnesium sulfate, Vitamin D Nos taken for an unspecified indication. The patient had previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EN6207; Expiry date: unknown) on 25Mar2021 at 13:00 (at age of 59-year-old) as dose 1 single for COVID-19 immunization. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. It was reported that, on July 15 patient had surgery to remove significant blood clots from his heart and lungs as a result from a saddle pulmonary embolism which was reported on 14Jul2021 (at 04:00). patient had done testing to eliminate cancer, hereditary and red blood cells for as a cause 8 days. The adverse event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The patient was hospitalized due to adverse event. Therapeutic measures were taken as a result of adverse event as patient underwent surgery (to remove significant blood clots from heart and lungs as a result from a saddle pulmonary embolism) on 15Jul2021 and unspecified medication. The outcome of events was resolving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pain back; Sulfonamide allergy
Andere Medikamente: MAGNESIUM SULFATE; VITAMIN D NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1515707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CO
Alter: 59,0
Geschlecht: M
Eingang: 05.08.2021
Impfdatum: 15.04.2021
Beginn: 14.07.2021
Tage bis Beginn: 90,0
Dosis: 2
Route/Site: - / RA

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

Anticoagulant therapy Heart rate abnormal Intracardiac thrombus Joint swelling Peripheral swelling Pulmonary embolism Pulmonary thrombosis Red blood cell count Surgery Thrombectomy Thrombosis

Symptomtext

On July 15 I had surgery to remove significant blood clots from my heart and lungs as a result from a saddle pulmonary embolism. I have done testing to eliminate Cancer, Hereditary and red blood cells; On July 15 I had surgery to remove significant blood clots from my heart and lungs as a result from a saddle pulmonary embolism. I have done testing to eliminate Cancer, Hereditary and red blood cells; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EW0153; Expiry date: unknown) via an unspecified route of administration, administered in arm right on 15Apr2021 13:00 (at age of 59-year-old) as dose 2, single for COVID-19 immunization. Medical history included chronic low back pain from multiple back surgeries and allergy to sulfa from an unknown date and unknown if ongoing. Concomitant medications included magnesium sulfate, Vitamin D Nos taken for an unspecified indication. The patient had previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EN6207; Expiry date: unknown) on 25Mar2021 at 13:00 (at age of 59-year-old) as dose 1 single for COVID-19 immunization. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. It was reported that, on July 15 patient had surgery to remove significant blood clots from his heart and lungs as a result from a saddle pulmonary embolism which was reported on 14Jul2021 (at 04:00). patient had done testing to eliminate cancer, hereditary and red blood cells for as a cause 8 days. The adverse event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The patient was hospitalized due to adverse event. Therapeutic measures were taken as a result of adverse event as patient underwent surgery (to remove significant blood clots from heart and lungs as a result from a saddle pulmonary embolism) on 15Jul2021 and unspecified medication. The outcome of events was resolving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pain back; Sulfonamide allergy
Andere Medikamente: MAGNESIUM SULFATE; VITAMIN D NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1510081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: NE
Alter: 37,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 13.04.2021
Beginn: 01.07.2021
Tage bis Beginn: 79,0
Dosis: 1
Route/Site: SYR / LA

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

Abortion spontaneous Chromosome analysis normal Exposure during pregnancy Foetal death Ultrasound antenatal screen abnormal Uterine dilation and curettage

Symptomtext

At the time of the second shot I found out I was pregnant that morning (4 weeks along). The estimated due date was January 12, 2022. The baby had a strong heartbeat at 7 weeks and at 8 1/2 weeks. However at 13 weeks had passed away due to cysts on the brain and back of the neck. Chromosome testing was done and the baby, my husband, and myself all came back without any chromosome issues. I had a miscarriage at 13 weeks after having both doses of the COVID 19 vaccine in the early month of my pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: 1,0
Labordaten: Ultrasound confirming the baby was deceased and had cysts on the brain and back of the neck was performed on 7/6/2021. Chromosomal testing was preformed on myself, my husband, and the baby on 7/8/2021. A D&C was performed to remove the baby on 7/9/2021.
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: Prenatal vitamins, Vitamin C
Allergien: Seafood and shellfish and latex
Vorherige Impfungen: -

VAERS 1502145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 26.07.2021
Impfdatum: 10.04.2021
Beginn: 21.07.2021
Tage bis Beginn: 102,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Death Pneumonia

Symptomtext

death N17.9 - Acute renal injury J18.9 - Multifocal pneumonia

Weitere VAERSDATA-Felder

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

VAERS 1502098

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 26.07.2021
Impfdatum: 17.04.2021
Beginn: 28.06.2021
Tage bis Beginn: 72,0
Dosis: UNK
Route/Site: - / -

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

Abdominal distension Death Dyspnoea Jaundice Thrombocytopenia Vaginal haemorrhage

Symptomtext

death D69.6 - Thrombocytopenia, unspecified N93.9 - Vaginal bleeding JAUNDICE BLOATED SHORTNESS OF BREATH

Weitere VAERSDATA-Felder

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

VAERS 1502062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 26.07.2021
Impfdatum: 14.05.2021
Beginn: 05.07.2021
Tage bis Beginn: 52,0
Dosis: UNK
Route/Site: - / -

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

Death Hyponatraemia Hypoosmolar state Pneumonia Thrombocytopenia

Symptomtext

death E87.1 - Hyponatremia J18.9 - Pneumonia, unspecified organism E87.1 - Hypo-osmolality and hyponatremia D69.6 - Thrombocytopenia, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1439882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: IN
Alter: 59,0
Geschlecht: M
Eingang: 18.07.2021
Impfdatum: 01.04.2021
Beginn: 01.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Abdominal pain upper Blood test Cerebrovascular accident Coronary arterial stent insertion Impaired driving ability Diarrhoea Fall Gait inability Headache Illness Intensive care Myocardial infarction Pain in extremity Peripheral swelling Pulmonary embolism Thrombosis Vomiting X-ray

Symptomtext

My father had got the covid vacacines, first one he received was in February 2021 by Hospital they didn?t put a lot number on the card, the second one he received was in April 2021, apx 3 weeks after the second vaccine both of his feet swelled the size of footballs, we went to the doctor on June 15 to Family care she wanted dad to go across the hall to see the pulmonary doctor and he wanted dad to go straight to hospital and dad couldn't drive that far because he couldn't push the gas or brake for long period of times due to his pain from the swelling on his feet it felt like blisters. So we took him to Hospital where they wanted him to go the next morning June 16, 2021 for more tests and found out that he had a blood clot in his right leg as well as his left leg and one in his lungs (Pulmonary Embolism). Then on June 28, 2021 he had a heart attack and he had to have a stint put in. Then on July 6 he got admitted again in the hospital for stomach pain. He got sent to Hospital. He is still presently in the hospital, on Friday July 16th, they think he had a stroke. We have been through so many tests, blood work, x-rays, etc. the doctors have no answers for us, their EXACT WORDS ? WE HAVE NEVER SEEN ANYTHING LIKE THIS BEFORE?. I have watched my father go through PURE MISERY and we still do not have any answers. My dad has seen so many doctors and they keep saying he is throwing blood clots and they have never seen anything like this. We are beyond mentally, physically and EMOTIONALLY exhausted. This is not fair to my dad, my mom and my family. We want answers to why this vaccine has caused all these issues. Doctor the doctor that found all the clots on dad said that his wife had the same vaccine and was having blood clots as well. We are tired of not knowing anything about this virus, vacaines, and the world is pushing for these shots and no one has any answers. For the doctors to pull us aside and tell us they are at a loss they are clueless to what is going on and none of them have ever seen anything like this. I can send more information later as we are presently in the hospital with my father now. He is in the ICU in very bad shape. I have every date written down at home, as the dates in this letter are only a few dates, I can give more info at a later time as needed.

Weitere VAERSDATA-Felder

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

VAERS 1439882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

kritisch

Staat: IN
Alter: 59,0
Geschlecht: M
Eingang: 18.07.2021
Impfdatum: 01.04.2021
Beginn: 01.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain upper Blood test Cerebrovascular accident Coronary arterial stent insertion Impaired driving ability Diarrhoea Fall Gait inability Headache Illness Intensive care Myocardial infarction Pain in extremity Peripheral swelling Pulmonary embolism Thrombosis Vomiting X-ray

Symptomtext

My father had got the covid vacacines, first one he received was in February 2021 by Hospital they didn?t put a lot number on the card, the second one he received was in April 2021, apx 3 weeks after the second vaccine both of his feet swelled the size of footballs, we went to the doctor on June 15 to Family care she wanted dad to go across the hall to see the pulmonary doctor and he wanted dad to go straight to hospital and dad couldn't drive that far because he couldn't push the gas or brake for long period of times due to his pain from the swelling on his feet it felt like blisters. So we took him to Hospital where they wanted him to go the next morning June 16, 2021 for more tests and found out that he had a blood clot in his right leg as well as his left leg and one in his lungs (Pulmonary Embolism). Then on June 28, 2021 he had a heart attack and he had to have a stint put in. Then on July 6 he got admitted again in the hospital for stomach pain. He got sent to Hospital. He is still presently in the hospital, on Friday July 16th, they think he had a stroke. We have been through so many tests, blood work, x-rays, etc. the doctors have no answers for us, their EXACT WORDS ? WE HAVE NEVER SEEN ANYTHING LIKE THIS BEFORE?. I have watched my father go through PURE MISERY and we still do not have any answers. My dad has seen so many doctors and they keep saying he is throwing blood clots and they have never seen anything like this. We are beyond mentally, physically and EMOTIONALLY exhausted. This is not fair to my dad, my mom and my family. We want answers to why this vaccine has caused all these issues. Doctor the doctor that found all the clots on dad said that his wife had the same vaccine and was having blood clots as well. We are tired of not knowing anything about this virus, vacaines, and the world is pushing for these shots and no one has any answers. For the doctors to pull us aside and tell us they are at a loss they are clueless to what is going on and none of them have ever seen anything like this. I can send more information later as we are presently in the hospital with my father now. He is in the ICU in very bad shape. I have every date written down at home, as the dates in this letter are only a few dates, I can give more info at a later time as needed.

Weitere VAERSDATA-Felder

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

VAERS 1478524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0153

kritisch

Staat: FL
Alter: 71,0
Geschlecht: M
Eingang: 16.07.2021
Impfdatum: 12.04.2021
Beginn: 14.07.2021
Tage bis Beginn: 93,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Condition aggravated Cough Decreased appetite Dyspnoea Fatigue Hyperglycaemia Malaise Metabolic acidosis Pain Pneumonia Pyrexia Renal impairment SARS-CoV-2 test positive Sepsis

Symptomtext

First dose of Pfizer COVID-19 vaccine on 3/22/2021, followed by the 2nd dose on 4/12/2021. 7/14/21: Patient arrived to ER with COVID symptoms after testing positive on 7/7/2021. Per ER records, the patient received the positive result on 7/10/21 and went to see his PCP who prescribed the patient a Zpack and cough medicine. The patient finished the Zpack but was still having body aches, shortness of breath, fever, loss of appetite, and fatigue. 7.15.21: in the ED patient found to have hyperglycemia, anion gap metabolic acidosis, worsening kidney function, and multifocal pneumonia. Diagnosed with acute hypoxic respiratory failure due to COVID-19 pneumonia, sepsis secondary to COVID pneumonia. started on remdesivir

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes, chronic kidney disease, hypertension
Andere Medikamente: carvedilol, levothyroxine, insulin lispro, lisinopril, isosorb
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 1478465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 07.05.2021
Beginn: 11.07.2021
Tage bis Beginn: 65,0
Dosis: 1
Route/Site: IM / -

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

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

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1444577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MS
Alter: 68,0
Geschlecht: M
Eingang: 02.07.2021
Impfdatum: 08.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / UN

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

Death Gait disturbance Gait inability Illness Pain in extremity Peripheral swelling

Symptomtext

My father became ill after the 2nd does and did not recover. His legs began to hurt. He found it hard to walk. He didn?t want to go to the doctor from fear of COVID. But his legs began to swell and he couldn?t walk, so he went to ER on 4/18/2021 and released on 04/20/2021. He then went to his PCP on 04/28/2021. He went to see a cardiologist who said his heart was good on 04/30/2021. He passed away on 05/06/2021 in his sleep. Please help.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: He visited Medical Center 04/18/2021. He visited PCP on 04/28/2021. He visited Dr. on 04/30/2021. DOD: 05/06/2021.
Aktuelle Erkrankungen: Emphysema/COPD
Vorgeschichte: Emphysema/COPD
Andere Medikamente: Oxygen
Allergien: N/A
Vorherige Impfungen: -

VAERS 1433778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 07.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: - / -

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

Death

Symptomtext

Patient passed away on 05/01/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Atropine sulfate, roxanol, lasix, zofran, ativan, albuterol, dulcolax, senokot, synthroid, remeron, miralax
Allergien: Codedine
Vorherige Impfungen: -

VAERS 1430080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 27.06.2021
Impfdatum: 30.04.2021
Beginn: 04.05.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / RA

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

Acute myocardial infarction Angiocardiogram Angioplasty Antinuclear antibody positive Blood test abnormal Brain natriuretic peptide increased C-reactive protein increased Cardiac failure congestive Catheterisation cardiac abnormal Cerebral artery embolism Cerebral infarction Chest X-ray Chest pain Computerised tomogram thorax normal Coronary arterial stent insertion Coronary artery dissection Coronary artery stenosis Diffusion-weighted brain MRI abnormal

Symptomtext

On April 30, 2021, I received the 2nd dose of the COVID-19 (Pfizer-BioNTech) vaccine which was 3 weeks after receiving the 1st dose. Then on May 3rd, I experienced pronounced shortness-of-breath while at work lifting objects up to 20 lbs and walking short distances of 20 to 40 m on flat ground. Then on May 4th, 2021, I went into a nearby Urgent Care Clinic (UCC) with shortness-of-breath and exertional dyspnea as the main symptoms. At the UCC blood tests were done along with EKG and chest x-ray. Blood tests revealed several results that were not within standard ranges: troponin (1.25 ng/mL), BNP (5130 pg/mL), D-dimer (1320 ng/mL FEU), and C-reactive protein (75.5 mg/L). I was told that I had congestive heart failure and NSTEMI. UCC then directed me to go to the Emergency Department (ED) at a nearby hospital. In the ED, more tests were done: EKG, CT scan chest (no blood clots were found in the lungs), and cardiac ultrasound (estimated ejection fraction 40-45%). That evening I was transferred to the main hospital for further observation and tests. Not much happened on May 5th and I was not seen by a doctor until 5pm. Then early in the morning of May 6th, I experienced chest pain which lasted between 5 and 10 minutes. I was given oral nitroglycerine. My primary care physician (PCP) and a cardiologist elected to move forward with an angiogram. On May 6th, I underwent cardiac catheterization (CC). The CC report states: (a) 2nd Diag lesion is 50% stenosed (b) Mid RCA to Dist RCA lesion is 80% stenosed,(c) RV branch lesion is 80% stenosed, (d) RPDA lesion is 80% stenosed. Likely spontaneous coronary artery dissection of the mid to distal RCA and postal to mid PDA status post PCI with 2 Xience drug-eluting stents. Post-angiogram+angioplasty tests were done, including carotid artery ultrasound (results within normal limits. No hemodynamically significant stenoses) and MRI brain (punctate foci of restricted diffusion in both cerebral hemispheres. Multiple vascular distributions w/o larger territorial infarct suggest emboli). Other blood test results were: antinuclear antibody (ANA) IFA screen (positive), BNP (8631 pg/mL). I was released from the hospital on May 8, 2021. Follow-up care included cardiac rehab therapy and consultations with the cardiologist, PCP, a neurologist and rheumatologist. Incidentally, 12 days after the angiogram and angioplasty, I experienced temporary numbness and loss of movement in my right arm which lasted no more than a minute, indicative of a transient ischemic attack (TIA). Root cause investigations focusing on SCAD and TIA are on-going.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 5,0
Labordaten: EKG, Chest x-ray, Troponin (1.25 ng/mL), BNP (5130 pg/mL), D-dimer (1320 ng/mL FEU), C-reactive protein (75.5 mg/L), CT scan chest (no blood clots were found in the lungs), Cardiac ultrasound (estimated ejection fraction 40-45%), Carotid artery ultrasound (results within normal limits. No hemodynamically significant stenoses), MRI brain (punctate foci of restricted diffusion in both cerebral hemispheres. Multiple vascular distributions w/o larger territorial infarct suggest emboli), Antinuclear antibody (ANA) IFA screen (positive), BNP (8631 pg/mL).
Aktuelle Erkrankungen: None
Vorgeschichte: Prostate cancer treated with prostatectomy.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1403515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 16.06.2021
Impfdatum: 06.04.2021
Beginn: 20.05.2021
Tage bis Beginn: 44,0
Dosis: 2
Route/Site: SYR / -

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

Acute respiratory failure Atrial fibrillation COVID-19 pneumonia Cardiac failure Chronic kidney disease Condition aggravated Ejection fraction decreased Encephalopathy Endotracheal intubation Hip fracture Hypercapnia Hypoglycaemia Influenza virus test Lung infiltration Mechanical ventilation Mitral valve incompetence Open reduction of fracture Pleural effusion

Symptomtext

77 yo male presented to the ED given unresponsiveness at SNF via EMS, found to be hypoglycemic- intubated/sedated on admission - he was recently admitted, and had prolonged hospital stay (4/30 - 5/10) after orthopedic intervention / ORIF 4/30 Rt hip Fracture- s/p. - Acute hypoxic and hypercarbic respiratory failure, on mechanical ventilation - Bibasilar infiltrates, Lt > Rt, will small bilateral pleural effusions, HCAP - COVID PNA - Small bilateral pleural effusions - Encephalopathy - A-Fib - HFrEF, EF 45%, Mild MR - Acute on CKD - UTI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: SARS-CoV-2 (COVID-19) and Influenza AB Antigens, POC: SARS CoV2 Positive (5/20/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiomyopathy, CHF, CKD, constipation, CAD, degenerative lumbar disc, depression, diabetes mellitus, DVT, GERD, gout, hyperlipemia, hypertension, hypothyroidism, history of MI, history of PE, sleep apnea, TIA
Andere Medikamente: Lexapro, ferrous sulfate, Proscar, Folate, Neurontin, insulin lispro, levothyroxine, midodrine, vitamins, solifenacin, tamsulosin, temazepam, Eliquis
Allergien: Singulair, sulfa antibiotics
Vorherige Impfungen: -

VAERS 1395445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: IL
Alter: 44,0
Geschlecht: F
Eingang: 14.06.2021
Impfdatum: 21.04.2021
Beginn: 08.06.2021
Tage bis Beginn: 48,0
Dosis: 2
Route/Site: SYR / LA

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

Anticoagulant therapy Arthralgia Computerised tomogram abnormal Deep vein thrombosis Pain in extremity Peripheral swelling Pulmonary embolism Skin discolouration Ultrasound Doppler abnormal

Symptomtext

On June 8, 2021 I noticed right shoulder/arm pain. Went to my dr on 6/9 and he ordered a port dye study (I have a Bard Power Port for iron infusions that ended in February). The port was fine, everything flowing correctly. On 6/10, my right arm was swollen and discolored. My Dr told me to go to ER. A CT scan was done and showed 2 DVTs and 1 PE. I was admitted and started on IV heparin. I was on the IV heparin until 6/13 and then was switched to oral Eloquis 10mg twice daily. It is now 6/14, and I should be discharged sometime today. I will continue to be on Eloquis for 3 - 6 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: Ultrasound 6/10/2021 CT scan 6/20/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Iron deficiency anemia
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1395416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 14.06.2021
Impfdatum: 13.04.2021
Beginn: 12.06.2021
Tage bis Beginn: 60,0
Dosis: UNK
Route/Site: - / -

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

Death Pneumonia

Symptomtext

death J18.9 - Pneumonia due to infectious organism, unspecified laterality, unspecified part of lung

Weitere VAERSDATA-Felder

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

VAERS 1232734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: NJ
Alter: 38,0
Geschlecht: M
Eingang: 11.06.2021
Impfdatum: 16.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / RA

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

Back pain Balance disorder Chest pain Dizziness Dyspnoea Blood test Cardiac function test Chest X-ray Electrocardiogram Headache Heart rate increased Hypertension Sleep disorder Pulmonary embolism SARS-CoV-2 test negative Vaccination complication Vertigo

Symptomtext

Identified PE; Pain moved to right chest; Lower Right Backpain; Breathing difficulty; Off Balance; Dizzy; This is a spontaneous report from a contactable consumer (patient). A 38-year-old male patient received the first dose of BNT162B2 (lot number: EW0153), via an unspecified route of administration in arm right on 16Apr2021 12:15 at single dose for COVID-19 immunisation. Medical history was none. Concomitant medications included vitamin b12 nos (VITAMIN B12) and colecalciferol (D3). On 18Apr2021, the patient went urgent care for breathing difficulty; On 19Apr2021, patient went ER for off balance, dizzy, and breathing difficulty and was prescribed with ibuprofin, meclazine and rest for 8 days; On 07May2021, lower right backpain started (not taken 2nd dose scheduled), on 08May2021, pain moved to right chest; On 09May2021, patient went urgent care-identified PE and admitted to hospital; On 11May2021 discharged; Under blood thinner medication (heprion). Adverse events start date of off balance, dizzy, and breathing difficulty was 18Apr2021 04:00. AEs 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). Patient was hospitalized for 3 days. Covid test post vaccination: Nasal Swab on 09May2021: Negative; Nasal Swab on 09May2021: Negative; Nasal Swab on 19Apr2021: Negative. Outcome of the events was resolving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Test Date: 20210419; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210509; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210509; 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: VITAMIN B12 [VITAMIN B12 NOS]; D3
Allergien: -
Vorherige Impfungen: -

VAERS 1388607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

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: 2
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 1382253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: ND
Alter: 55,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 14.04.2021
Beginn: 15.05.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: IM / AR

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

Asthenia Cerebrovascular accident Confusional state Facial paralysis Fatigue Lethargy Magnetic resonance imaging head abnormal Neurological symptom Speech disorder

Symptomtext

He had a stroke- sudden onset of weakness,- facial drooping, speech impairment, lethargy, and confusion obvious symptoms did resolve over 24 hour- he has some residual fatigue and questionable changes post stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: MRI did confirm CVA findings
Aktuelle Erkrankungen: none
Vorgeschichte: recent hypertension treated with medication
Andere Medikamente: levothyroxine , lisinopril, hydrochlorothiazide none
Allergien: -
Vorherige Impfungen: -

VAERS 1368670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: KY
Alter: 83,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 11.03.2021
Beginn: 02.05.2021
Tage bis Beginn: 52,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death Endotracheal intubation Hypoxia SARS-CoV-2 test positive

Symptomtext

Admitted to hospital on 5/2/2021 due to hypoxia and ultimately intubated. Family moved to comfort care and he died on 5/2/2021 at 10am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Tested positive by rapid PCR for COVID-19 on 4/21/2021.
Aktuelle Erkrankungen: COVID-19
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1173757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident Computerised tomogram Loss of consciousness Magnetic resonance imaging Unresponsive to stimuli Consciousness fluctuating Hypertension Lethargy X-ray

Symptomtext

The vaccine was given at 11:30AM by 2:15 PM she was totally unconscious and unresponsive, Was taken to the hospital, evaluated in the Emergency Room and admitted to the hospital. At 8:20 PM the charge nurse called a Stroke Alert and was taken to the Radiology Department for further testing. Dr said she had a stroke on the left side however he was not sure of the severity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: CT scans, Xrays and MRI
Aktuelle Erkrankungen: Rheumatoid Arthritis, Cardiac Disease
Vorgeschichte: Rheumatoid Arthritis, Congestive Heart Failure, CAD, Pruritus, Dizziness, Over Active Bladder, Irritable Bowel Syndrome, Vitamin Deficiency
Andere Medikamente: Linzess, Pantoprazole, Potassium, Citalopram, Furosemide, Myrbetriq, Meclizine, Amlodipine, Acyclovir, Tizanidine, Zolpidem, Losartan, Aspirin, Tramadol, Lorazepam, Prednisone,
Allergien: None
Vorherige Impfungen: the shot has made her left side weak and she had fallen and fractured her left hip on April 29, 2021. She had hip repaired on Ap

VAERS 1173757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cerebrovascular accident Computerised tomogram Loss of consciousness Magnetic resonance imaging Unresponsive to stimuli Consciousness fluctuating Hypertension Lethargy X-ray

Symptomtext

The vaccine was given at 11:30AM by 2:15 PM she was totally unconscious and unresponsive, Was taken to the hospital, evaluated in the Emergency Room and admitted to the hospital. At 8:20 PM the charge nurse called a Stroke Alert and was taken to the Radiology Department for further testing. Dr said she had a stroke on the left side however he was not sure of the severity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: CT scans, Xrays and MRI
Aktuelle Erkrankungen: Rheumatoid Arthritis, Cardiac Disease
Vorgeschichte: Rheumatoid Arthritis, Congestive Heart Failure, CAD, Pruritus, Dizziness, Over Active Bladder, Irritable Bowel Syndrome, Vitamin Deficiency
Andere Medikamente: Linzess, Pantoprazole, Potassium, Citalopram, Furosemide, Myrbetriq, Meclizine, Amlodipine, Acyclovir, Tizanidine, Zolpidem, Losartan, Aspirin, Tramadol, Lorazepam, Prednisone,
Allergien: None
Vorherige Impfungen: the shot has made her left side weak and she had fallen and fractured her left hip on April 29, 2021. She had hip repaired on Ap

VAERS 1360613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: AL
Alter: 64,0
Geschlecht: M
Eingang: 29.05.2021
Impfdatum: 30.04.2021
Beginn: 20.05.2021
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: - / -

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

Flank pain Pulmonary embolism SARS-CoV-2 test

Symptomtext

bilateral subsegmental PTEs; right flank pain under ribs; This is a spontaneous report received from a contactable HCP. A 64-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number EW0153), via an unknown route, on 30Apr2021 (at the age of 64-year-old) at single dose for COVID-19 immunisation, administered at Pharmacy/drug store. The patient was not diagnosed with COVID-19 before vaccination. Relevant medical history included hypertension (HTN), gout and osteochondritis dissecans (OCD). No relevant concomitant medications were provided. The patient did not have allergies. No other vaccine was received in four weeks. The patient presented to the emergency room (ER) with right flank pain under ribs. Found to have bilateral subsegmental pulmonary thromboembolisms (PTEs). The onset date of the events was provided as 20May2021. Both events were reported serious because requiring hospitalization for 3 days (admission date not provided) and as life-threatening conditions. The patient was treated with enoxaparin then apixaban. Nasal swab was done on 21May2021 and resulted negative. The patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number EW0172) on 21May2021 for COVID-19 immunisation. The patient was treated with enoxaparin then apixaban. The patient was recovering from the events.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of all reported events cannot be totally excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Test Date: 20210521; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Gout; Hypertension; Osteochondritis dissecans
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1358345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

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: 2
Route/Site: IM / -

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.

Weitere VAERSDATA-Felder

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 1355381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CO
Alter: 68,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 15.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram cerebral normal Antiplatelet therapy Arteriogram carotid normal Arteriosclerosis Carotid arteriosclerosis Cerebrovascular accident Computerised tomogram head abnormal Hemiparesis Magnetic resonance imaging head abnormal Meningioma White matter lesion

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient presents to emergency department three days after vaccination reporting five hours of left-sided weakness. Diagnosed with right pontine stroke, admitted to hospital, initiated anti-platelet and cholesterol-lowering medications, symptoms resolved, and patient discharged to home medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: CT brain: no large vessel territory infarct; possible right frontal lobe meningioma, severe carotid and vertebral atherosclerosis MRA neck: patent arteries of the neck MRA brain: patent intracranial arteries MR brain: right frontal convexity mass, likely meningioma; small focus of diffusion hyperintensity within the RIGHT dorsal pons that may represent an acute lacunar infarction or be artifactual
Aktuelle Erkrankungen: end-stage renal disease requiring dialysis
Vorgeschichte: hypertension, hypercholesterolemia, enlarged left atrium, DVT, type 2 diabetes mellitus, hyperparathyroidism, vertigo, tinnitus, anemia, TIAs
Andere Medikamente: amlodipine, calcium, furosemide, gabapentin, isoniazid, labetalol, lisinopril, vitamin B6, rifapentine, senna
Allergien: niacin
Vorherige Impfungen: -

VAERS 1351938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

kritisch

Staat: WA
Alter: 43,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 08.05.2021
Beginn: 10.05.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Angina pectoris Arteriogram coronary normal Blood creatine phosphokinase MB increased Echocardiogram normal Electrocardiogram normal Fibrin D dimer normal Myocardial infarction Platelet count normal Troponin increased

Symptomtext

Pt presented with angina, inital troponin normal, then rose to 5.2. Ck-MB and MB index also rose and fell consistent with MI. D-dimer was normal. EKG without clear evidence of ishcemia or pericarditis. Coronary angiogram with no culprit lesion identified (either spontaneous coronary artery dissection or thrombus). Echo did not show wall motion abnormalities or pericardial effusion. Differential for this hospitalization with NSTEMI includes myocarditis, coronary spasm, or subclinical dissection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Platelets were normal
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Lisinopril 10 mg, vitamin c, vitamin d
Allergien: nkda
Vorherige Impfungen: -

VAERS 1343126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: PA
Alter: 60,0
Geschlecht: M
Eingang: 24.05.2021
Impfdatum: 10.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: - / LA

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

Anticoagulant therapy Arteriogram coronary abnormal Arthralgia Blood test normal Chest X-ray abnormal Echocardiogram normal Infarction Pulmonary embolism Ultrasound Doppler normal

Symptomtext

On 5/18/21 AM, woke to pain in my right side under my shoulder blade. Went to ER. They performed many blood test, chest Xray, Chest CTA. Determined Pulmonary embolism and infarction. I was admitted, more blood tests, Echocardiogram, Venous Doppler study( No evidence of DVT). Released 5/20/21. Prescribed Eliquis to thin blood for easier natural clot dissolve. No Known cause of PE, yet. Follow up scheduled with my PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: All tests performed 5/18 - 5/20. Multiple blood tests including possible genetic causes for PE. to date I believe none have shown possible cause of PE. Please check with me.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, baby aspirin, Pro Biotic ( all over the counter)
Allergien: None
Vorherige Impfungen: -

VAERS 1333915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 14.04.2021
Beginn: 09.05.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Adenovirus test Atypical pneumonia COVID-19 pneumonia Chest X-ray abnormal Chlamydia test negative Coronavirus test negative Cough Dyspnoea Enterovirus test negative Human metapneumovirus test Influenza A virus test negative Influenza B virus test Lung opacity Mycoplasma test negative Respiratory syncytial virus test negative SARS-CoV-2 test positive Viral test negative

Symptomtext

COUGH ED to Hosp-Admission Discharged 5/9/2021 - 5/13/2021 (4 days) Hospital MD Last attending ? Treatment team Pneumonia due to COVID-19 virus Principal problem Hospital Course: Please refer to the admission H&P for details of presentation. In summary, patient is a 56 y.o. female with known history of moderate obesity, obstructive sleep apnea requiring CPAP at home, dyslipidemia, hypothyroidism and bronchial asthma was admitted to the hospital service for evaluation of shortness of breath and cough. Upon admission patient was found to be having Acute hypoxic respiratory failure secondary to COVID-19 pneumonia. Chest x-ray upon admission showed Patchy bilateral opacities consistent with atypical pneumonia. Patient completed 5 days course of remdesivir during hospitalization. Patient was discharged on dexamethasone.Patient received 1 unit of conversant plasma during hospitalization. Patient qualified for 2L of oxygen by nasal cannula at discharge. Patient currently feels well and is wanting to go home today. Patient is advised to follow-up with primary care physician within a span of one to 2 weeks. Currently patient is being discharged in a medically stable condition after being evaluated by our team. All the questions and concerns of the patient and family were addressed in detail at the time of discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 05/09/21 1604 Respiratory virus detection panel Collected: 05/09/21 1444 | 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 Detected Metapneumovirus Not Detected Procedure Component Value Ref Range Date/Time X-ray chest 1 view [3282303741] Resulted: 05/09/21 1347 Order Status: Completed Updated: 05/09/21 1347 Narrative: XR CHEST 1 VW PORT IMPRESSION: Patchy bilateral opacities consistent with atypical pneumonia. This nonspecific imaging pattern can be seen with Covid-19. Other considerations include but are not limited to other infectious etiologies or noninfectious etiologies. END OF IMPRESSION: INDICATION: OTHER chest pain covid positive, shortness of breath. TECHNIQUE: Portable AP view of the chest was obtained. COMPARISON: 2/28/2017 FINDINGS: The cardiac silhouette is normal in size. The mediastinal contours are within normal limits accounting for technique. There are patchy bilateral opacities atypical pneumonia. The pulmonary vascularity is within normal limits. Right pleural space: There is no pleural fluid or pneumothorax. Left pleural space: There is no pleural fluid or pneumothorax. The bone density appears to be within normal limits.
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Carpal tunnel syndrome Complex partial seizure (CMS/HCC) Lumbar radiculopathy Acute bacterial conjunctivitis of both eyes Arthralgia of both knees Epilepsy (CMS/HCC) Respiratory CPAP (continuous positive airway pressure) dependence Obstructive sleep apnea Allergic rhinitis Moderate persistent asthma without complication Pneumonia due to COVID-19 virus Digestive Obesity Vitamin D deficiency Genitourinary Symptoms, such as flushing, sleeplessness, headache, lack of concentration, associated with the menopause Musculoskeletal De Quervain's tenosynovitis Fasciculations Lipoma of upper arm Primary localized osteoarthritis of right knee Sacroiliitis (CMS/HCC) Primary osteoarthritis of both knees Tinea cruris Trapezius muscle spasm Endocrine/Metabolic Hyperlipidemia Hypothyroidism Other Soft tissue mass
Andere Medikamente: albuterol HFA (PROVENTIL;VENTOLIN) 90 mcg/actuation inhaler ascorbic acid, vitamin C, (VITAMIN C) 250 mg tablet carBAMazepine (TEGretol) 200 mg tablet cholecalciferol, vitamin D3, (VITAMIN D3) 2,000 unit tablet tablet guaiFENesin (MUCINEX)
Allergien: ClindamycinDizziness / Lightheaded
Vorherige Impfungen: -

VAERS 1332732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: WA
Alter: 62,0
Geschlecht: M
Eingang: 20.05.2021
Impfdatum: 07.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Cardiac ventricular thrombosis Cerebrovascular accident

Symptomtext

Stroke; Left ventricular thrombus in his heart; This is a spontaneous report from a contactable physician. A 62-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 07Apr2021 (Lot Number: EW0153) as UNKNOWN, SINGLE for COVID-19 immunization. Medical history included coronary artery disease (several years ago) and had a bypass (several years ago; not ongoing). The patient's concomitant medications were not reported. It was reported that the patient had a stroke on 17Apr2021 after he formed a left ventricular thrombus in his heart in Apr2021. The patient was hospitalized for the events from 17Apr2021 to 23Apr2021 and was treated with Coumadin. The outcome of the events was recovering.; Sender's Comments: Drug causality would seem unlikely for BNT162B2 vaccine since there is no plausible mechanism implicating the subject drug to the events. The reported events may be regarded as natural progression of patient's pre-existing conditions. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bypass surgery (Several years ago); Coronary artery disease (Several years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1332728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 16.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Cerebrovascular accident Computerised tomogram Loss of consciousness Magnetic resonance imaging Memory impairment Migraine Nausea Visual impairment

Symptomtext

stroke like symptoms; similar to migraines; mini-strokes; Passing Out; Blind spots in her vision; Nausea; Believes it effected her memory; stroke like symptoms; similar to migraines; mini-strokes; This is a spontaneous report received from a contactable consumer. A 59-year-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on 16Apr2021 (Lot Number: EW0153; Expiration Date: 31Jul2021) as 1ST DOSE, SINGLE for covid-19 immunisation (Age at vaccination: 59 years). Medical history included ongoing strokes, ongoing third and fourth Nerve Palsy. Concomitant medications included dabigatran etexilate mesilate (PRADAXA) taken for blood thinner; metoprolol for Stroke, Heart regulation; lovastatin taken for Stroke, Heart regulation. The patient states that she went to the Emergency Room on 17Apr2021 and then went again on either 18Apr2021 or 19Apr2021. The patient states she does not know if she was admitted or not. States that she thinks she just was in the emergency room the time that she was there. Says that after the Covid Vaccine she was having stroke like symptoms; similar to migraines; mini-strokes. She was passing out, had nausea, blind spots in her vision, and she believes it effected her memory. The events occurred on 17Apr2021. Also, she said on her first emergency room visit they did a CT Scan and on her second emergency room visit they did a MRI and both was not reported. States they told her there was no issues. The patient underwent lab tests and procedures which included CT Scan: and MRI: not reported on Apr2021. Outcome of the event vision impairment was not recovered while outcome of the event nausea was recovered on Apr2021. Outcome of the event memory impairment was recovering while outcome of the remaining events was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Date: 202104; Test Name: CT Scan; Result Unstructured Data: Test Result:Not reported; Comments: Not reported; Test Date: 202104; Test Name: MRI; Result Unstructured Data: Test Result:Not reported; Comments: Not reported
Aktuelle Erkrankungen: IIIrd nerve palsy; IVth nerve palsy; Stroke
Vorgeschichte: -
Andere Medikamente: PRADAXA; METOPROLOL; LOVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1329475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

kritisch

Staat: NJ
Alter: 59,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 07.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: - / LA

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

Blood test Pulmonary embolism SARS-CoV-2 test Thrombosis

Symptomtext

pulmonary embolism; Blood Clot; This is a spontaneous report from a contactable consumer (patient). A 59-yearold male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 07Apr2021 (Batch/Lot Number: ew0153) as 1st dose, single (at the age of 59 years) for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient has not had covid-19 prior to vaccination. The patient experienced pulmonary embolism on an unspecified date and blood clot on 22Apr2021 with outcome of not recovered. The patient was hospitalized for blood clot for 2 days. The patient underwent lab tests and procedures which included blood test: negative on 26Apr2021. Therapeutic measures were taken as a result of the events incudes blood thinner. The outcome of the event blood clot was not recovered and unknown outcome for the event pulmonary embolism. The patient was tested negative for Covid-19 on 23Apr2021 (post vaccination). No follow-up attempts are possible; information about batch number already obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Date: 20210426; Test Name: Blood test; Result Unstructured Data: Test Result:Negative; Test Date: 20210423; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1310493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CA
Alter: 89,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Death Hallucination Nausea

Symptomtext

The son came on 05/06 to receive the 2nd dose of Pfizer vaccine and informed us that his mother passed away on 04/18 after 3 days of post vaccination. A home hospice patient with Stage 5 Chronic kidney disease and Stage 4 COPD (Oxygen dependent) came in on 04/15 around 4:30 pm to receive a first dose of Pfizer. After 15 mandatory waiting in the pharmacy, she went home. Around 5:00 pm, patient told her son that she is feeling nauseated. Hospice nurse was contacted. On 4/16, patient experienced hallucination. She told her son that her fingers were disappeared. Hospice nurse was contacted. Please note that vaccine adverse event is not clearly related to vaccine, since patient was on hospice, stage 5 CKD and stage 4 COPD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: NO; CHRONIC HEALTH CONDITIONS - HOME HOSPICE CARE, STAGE 5 CHRONIC KIDNEY DISEASE, STAGE 4 COPD (O2 DEPENDENT)
Vorgeschichte: UNDER HOME HOSPICE CARE, STAGE 5 CHRONIC KIDNEY DISEASE, STAGE 4 COPD (O2 DEPENDENT)
Andere Medikamente: CYMBALTA, ALBULTEROL HFA INHALER, TRELLEGY ELLIPTA
Allergien: NO KNOWN FOOD OR DRUG ALLERGY
Vorherige Impfungen: -

VAERS 1303864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 10.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 17,0
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 on right I26.99 - Other pulmonary embolism without acute cor pulmonale

Weitere VAERSDATA-Felder

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

VAERS 1285922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew 0153

kritisch

Staat: WA
Alter: 38,0
Geschlecht: F
Eingang: 04.05.2021
Impfdatum: 12.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

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

Computerised tomogram abnormal Echocardiogram Electrocardiogram Pulmonary embolism Thrombosis Ultrasound Doppler abnormal

Symptomtext

Pulmonary embolism also blood clot in leg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: EKG, ultra sound of leg, CAT scan, echo
Aktuelle Erkrankungen: Thyroid surgery
Vorgeschichte: High blood pressure
Andere Medikamente: Primella Motropolal Atorvostatin Lisinopril
Allergien: None
Vorherige Impfungen: -

VAERS 1245223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

kritisch

Staat: ID
Alter: 24,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Circulatory collapse Fall Incoherent

Symptomtext

Patient collapsed while walking/running in the pharmacy waiting area. Patient was incoherent for several minutes. Asked if she would like ambulance called, in which she replied yes. Ambulance was called. They assessed the patient and left her at the pharmacy to recover.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Circulatory collapse
Hospital-Tage: -
Labordaten: Assessment by ambulance personnel.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: unknown
Allergien: nka
Vorherige Impfungen: -

VAERS 1240133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: AL
Alter: 65,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 20.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Recipient was found deceased the next day after receiving 1st dose pfizer vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1229335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: MA
Alter: 59,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 13.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Acute myocardial infarction Atrial fibrillation Blood culture Echocardiogram Electrocardiogram Endocarditis Staphylococcal infection Troponin I

Symptomtext

Aortic valve endocarditis with MSSA, NSTEMI, Atrial fibrillation. Patient will likely require valve replacement

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: EKG (4/15/2021) Blood cultures (4/15/2021) Transthoracic echocardiogram (4/16/2021) Transesophagic echocardiogram (4/19/2021) Troponin I (4/15/2021)
Aktuelle Erkrankungen: none
Vorgeschichte: s/p remote splenectomy after motor vehicle accident.
Andere Medikamente: losartan, metoprolol, atorvastatin, aspirin, alirocumab weekly (given on Sundays)
Allergien: none
Vorherige Impfungen: -

VAERS 1212771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: HI
Alter: 87,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Agonal respiration Bacteraemia Cardiac arrest Computerised tomogram abdomen normal Computerised tomogram pelvis Death Dyspnoea Intensive care Resuscitation Computerised tomogram thorax normal Condition aggravated Endotracheal intubation Gastrointestinal disorder Gastrointestinal haemorrhage Hepatobiliary disease Pulseless electrical activity Scan with contrast Sepsis

Symptomtext

Patient was observed for 30mins post vaccination and did not show any s/s of allergic reaction or discomfort. He went home with family after. About 12 hours post vaccination, family found patient having increased SOB and vomiting. EMS was activated. When EMS camee to home, patient was found having cardiac arrest. CPR and resuscitation started. Patient was then transferred to ER at Queens Medical Center and then ICU. Patient expired on 4/15/2021 in the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: 3/17/2021-3/22/2021 hospitalized for acute hypoxemic respiratory failure
Vorgeschichte: ESRD on peritoneal dialysis COPD Atrial fibrillation, paroxysmal HTN
Andere Medikamente: albuterol sulfate (90 mcg/actuation HFA aerosol inhaler) INHALE 2 PUFFS BY MOUTH EVERY 4 HOURS AS NEEDEDFOR SHORTNESS OF BREAT H OR WHEEZING amiodarone (100 mg tablet) TAKE 1/2 TABLET BY MOUTH EVERY DAY amoxicillin 250 mg-potassium clavulan
Allergien: Aspirin (itching)
Vorherige Impfungen: -

VAERS 1187365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

kritisch

Staat: CO
Alter: 37,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness Peripheral swelling Respiratory arrest Seizure

Symptomtext

After the vaccination, her arm started to swell up about 1 cm immediately. Benadryl was offered but the patient refused. After a couple minutes, the patient was lightheaded and dizzy. After two minutes the patient became unconscious, was not breathing, and was turning purple/blue. She then began having a seizure and was placed on to the ground. One dose of EpiPen was given to her and she regained consciousness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO ILLNESS AT THE TIME OR ONE MONTH PRIOR
Vorgeschichte: NO KNOWN HEALTH CONDITIONS
Andere Medikamente: PATIENT STATED SHE TOOK LEXAPRO AND A BIRTH CONTROL (SHE DID NOT STATE THE NAME OF THE MEDICATION.
Allergien: NO KNOWN DRUG OR MEDICATION OR FOOD ALLERGIES
Vorherige Impfungen: Tetnus, 6 years ago

VAERS 2722000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 08.12.2023
Impfdatum: 21.05.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Alanine aminotransferase increased Alanine aminotransferase normal Albumin globulin ratio Albumin urine Anion gap Antibody test Aspartate aminotransferase Bacterial test Basophil count Bilirubin urine Blood albumin Blood alkaline phosphatase Blood bilirubin Blood calcium Blood chloride Blood cholesterol Blood creatinine Blood folate abnormal

Symptomtext

blood clots; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old female patient received bnt162b2 (BNT162B2), on 21May2021 at 09:20 as dose 2, single (Lot number: EW0153) at the age of 66 years for covid-19 immunisation. The patient's relevant medical history included: "Spinal Infusion", start date: 24Jun2004 (ongoing); "Removal hardware", start date: 26Sep2008 (ongoing), notes: Became Allergic to almost everything; "Food allergy test: Almond, Beef, Chocolate, Cinnamon, Clam, Corn, crab, egg white, egg yolk, Peanut, pecan, Scallops, Shrimp" (unspecified if ongoing); "sulfa" (unspecified if ongoing); "Food allergy test: penicillin and derv" (unspecified if ongoing); "latex (Unknown)" (unspecified if ongoing); "Cardiovascular" (unspecified if ongoing), notes: Durgesic Patches - Cardiovascular; "Itching" (unspecified if ongoing), notes: Durgesic Patches - itching; "Sulfur" (unspecified if ongoing); "Histamine allergy" (unspecified if ongoing); "Hives" (unspecified if ongoing), notes: Sulfur - Cardiovascular & Hives; "nausea" (unspecified if ongoing), notes: Durgesic Patches - nausea; "Food allergy test: balsam Peru compounding powder/Balsam of Peru - Medicated lozenges, hand sanitizers, Parabens, Petroleum Jelly" (unspecified if ongoing), notes: balsam Peru compounding powder/Balsam of Peru; "Food Allergies & Chemical Sensitivities : Balsam of Peru - Medicated lozenges, hand sanitizers, Parabens, Petroleum Jelly" (unspecified if ongoing), notes: Balsam of Peru - Medicated lozenges, hand sanitizers, Parabens, Petroleum Jelly; "Food Allergies & Chemical Sensitivities : Balsam of Peru - Medicated lozenges, hand sanitizers, Parabens, Petroleum Jelly" (unspecified if ongoing), notes: Balsam of Peru - Medicated lozenges, hand sanitizers, Parabens, Petroleum Jelly; "Food Allergies & Chemical Sensitivities : Dental Medicament - Cement, Sun Flex Partial, Amalagams Filling" (unspecified if ongoing), notes: Cement, Sun Flex Partial, Amalagams Filling; "Food Allergies & Chemical Sensitivities : Denntal Medicament - Cement" (unspecified if ongoing), notes: Cement, Sun Flex Partial, Amalagams Filling; "Food Allergies & Chemical Sensitivities: Dental Medicament - Amalagams Filling" (unspecified if ongoing), notes: Cement, Sun Flex Partial, Amalagams Filling; "Food Allergies & Chemical Sensitivities : Dental Medicament - Sun Flex Partial" (unspecified if ongoing), notes: Cement, Sun Flex Partial, Amalagams Filling; "Food Allergies & Chemical Sensitivities : Latex, Velcro, Rubber Foam Chairs, Adhesive - Causes Heart Palpitation, and Burns Skin" (unspecified if ongoing), notes: Food Allergies & Chemical Sensitivities; "Food Allergies & Chemical Sensitivities : Latex, Velcro, Rubber Foam Chairs, Adhesive - Causes Heart Palpitation, and Burns Skin" (unspecified if ongoing), notes: Food Allergies & Chemical Sensitivities: Causes Heart Palpitation.; "Food Allergies & Chemical Sensitivities : Latex, Velcro, Rubber Foam Chairs, Adhesive - Causes Heart Palpitation, and Burns Skin" (unspecified if ongoing), notes: Latex, Velcro, Adhesive - Causes Heart Palpitation, and Burns Skin; "Food Allergies & Chemical Sensitivities : Rubber Foam Chairs" (unspecified if ongoing), notes: Rubber Foam Chairs; "Food Allergies & Chemical Sensitivities : Adhesive" (unspecified if ongoing), notes: Adhesive; "Food allergy test: Almond, pecan" (unspecified if ongoing); "Food allergy test: egg white, egg yolk" (unspecified if ongoing), notes: egg white, egg yolk; "Food allergy test: Peanut" (unspecified if ongoing); "Food allergy test: Shrimp" (unspecified if ongoing); "Food allergy test: Beef" (unspecified if ongoing); "Food Allergies & Chemical Sensitivities : Food coloring" (unspecified if ongoing), notes: Food coloring; "Illness/AE: Immune system Allergies", start date: 30Apr2021 (ongoing), notes: Did not have allergies before the Titanium surgery. The patient's family history included: "Food allergy test: Latex" (unspecified if ongoing), notes: Latex Allergies. There were no concomitant medications. Past drug history included: Histamin, reaction(s): "Food allergy test: Histamine"; Phenytoin, reaction(s): "Food allergy test:Phenytoin"; Cyclobenzaprine, reaction(s): "Food allergy test:cyclobenzaprine"; Codeine, reaction(s): "Food allergy test:codeine"; Oxycodone, reaction(s): "Food allergy test:oxycodone"; Hydrocodone, reaction(s): "Food allergy test:hydrocodone"; Iodine, reaction(s): "Cardiovascular"; Clarithromycin, reaction(s): "Food allergy test:clarithromycin"; Doxycycline, reaction(s): "Cardiovascular"; Codeine, reaction(s): "Cardiovascular"; Codeine, reaction(s): "insomnia"; Clarithromycin, reaction(s): "Food allergy test: clarithromycin"; Doxycycline, reaction(s): "Food allergy test: Doxycycline"; Fentanyl, reaction(s): "Food allergy test: fentanyl"; Triamcinolone, reaction(s): "Food allergy test:triamcinolone"; Ampicillin, reaction(s): "Food allergy test:ampicillin"; Tramadol, reaction(s): "Food allergy test:tramadol"; Procaine, reaction(s): "Food allergy test:procaine"; Levothyroxine, reaction(s): "Food allergy test:levothyroxine"; Coumadin, reaction(s): "Food allergy test:Coumadin"; Nickel, reaction(s): "Food allergy test: nickel"; Prednisone, reaction(s): "Food allergy test:prednisone"; Decadron, reaction(s): "Food allergy test:Decadron"; Petroleum jelly nasacort, reaction(s): "Food allergy test:Petroleum Jelly Nasacort"; Xyzal, reaction(s): "Food allergy test:Xyzal"; Petroleum jelly, reaction(s): "Food allergy test:Petroleum Jelly"; Budesonide hydrocortisone, reaction(s): "Food allergy test:budesonide hydrocortisone"; Rhinocort, reaction(s): "Food allergy test:Rhinocort"; Valium, reaction(s): "Food allergy test:Valium"; Avelox, reaction(s): "Food allergy test: Avelox"; Avelox, reaction(s): "Migraine"; Avelox, reaction(s): "insomnia"; Avinza, reaction(s): "Food allergy test:Avinza"; Avinza, reaction(s): "Night sweats"; Avinza, reaction(s): "Fever"; Avinza, reaction(s): "Insomnia"; Avinza, reaction(s): "chills"; Avinza, reaction(s): "irritability"; Avinza, reaction(s): "body pain"; Bethanechol, reaction(s): "Food allergy test:bethanechol"; Bethanechol, reaction(s): "Cardiovascular"; Bethanechol, reaction(s): "itching"; Biaxin, reaction(s): "Food allergy test:Biaxin"; Biaxin, reaction(s): "Cardiovascular"; Buspar, reaction(s): "Food allergy test:Buspar"; Dilantin, reaction(s): "Food allergy test:Dilantin"; Dilantin, reaction(s): "Nausea"; Duragesic, reaction(s): "Food allergy test:Duragesic"; Lovenox, reaction(s): "Food allergy test:Lovenox"; Lovenox, reaction(s): "Chest pain"; Lovenox, reaction(s): "Joint ache"; Lovenox, reaction(s): "Migraine"; Flexeril, reaction(s): "rash"; Flexeril, reaction(s): "Food allergy test:Flexeril"; Hydroxyzjne, reaction(s): "Food allergy test:hydroxyzjne"; Hydroxyzine, reaction(s): "Diarrhea"; Hydroxyzine, reaction(s): "Insomria"; Hyoscyamine, reaction(s): "Food allergy test:hyoscyamine"; Lyrica, reaction(s): "Food allergy test:Lyrica"; Lyrica, reaction(s): "Rash"; Lyrica, reaction(s): "Face rash"; Lyrica, reaction(s): "Diarrhea"; Methylprednisolone, reaction(s): "Food allergy test:Methylprednisolone"; Methylprednisolone, reaction(s): "Cardiovascular"; Methylprednisolone, reaction(s): "insomnia"; Gabapentin, reaction(s): "Food allergy test:gabapentin"; Novocain, reaction(s): "Food allergy test:Novocain"; Novocain, reaction(s): "Insomnia"; Paxil, reaction(s): "Food allergy test: paxil"; Paxil, reaction(s): "body rash"; Skelaxin, reaction(s): "Food allergy test:Skelaxin"; Skelaxin, reaction(s): "Facial Rash"; Triazolam, reaction(s): "Food allergy test:Triazolam"; Triazolam, reaction(s): "Itching"; Halcion, reaction(s): "Food allergy test:Halcion"; Halcion, reaction(s): "Itching"; Ampicillin, reaction(s): "Cardiovascular"; Ampicillin, reaction(s): "Itching"; Buspirone, reaction(s): "Facial rash"; Buspirone, reaction(s): "insomnia"; Coumadin, reaction(s): "Cardiovascular"; Coumadin, reaction(s): "nausea"; Coumadin, reaction(s): "leg swelling"; Coumadin, reaction(s): "migraine"; Coumadin, reaction(s): "body ache"; Coumadin, reaction(s): "pain"; Coumadin, reaction(s): "and unable to sleep due to severe leg pain"; Coumadin, reaction(s): "burning"; Detrol, reaction(s): "Itching"; Enoxaprin, reaction(s): "Swelling in legs"; Enoxaprin, reaction(s): "migraine"; Enoxaprin, reaction(s): "joint pain"; Enoxaprin, reaction(s): "tightening in the chest"; Enoxaprin, reaction(s): "fatigueless"; Enoxaprin, reaction(s): "skin rash"; Flexril, reaction(s): "Body Rash"; Hydrocodone, reaction(s): "Cardiovascular"; Hysocyamine, reaction(s): "Cardiovascular"; Hysocyamine, reaction(s): "nausea"; Levinsex, reaction(s): "Cardiovascular"; Levinsex, reaction(s): "Nausea"; Lorcet, reaction(s): "Cardiovascular"; Lorcet, reaction(s): "Rash"; Lortab, reaction(s): "Cardiovascular"; Lortab, reaction(s): "rash"; Percocet, reaction(s): "Cardiovascular"; Percocet, reaction(s): "rash"; Morphine, reaction(s): "insomnia"; Morphine, reaction(s): "irritabilit"; Morphine, reaction(s): "body pain"; Nasacort, reaction(s): "Irritates the nose"; Neurontin, reaction(s): "Insomnia"; Neurontin, reaction(s): "Clinching of the teeth"; Synthroid, reaction(s): "Cardiovascular"; Trazodone, reaction(s): "Insomnia"; Ultram for Cardiovascular; Valium, reaction(s): "Insomnia"; Valium, reaction(s): "Irritability"; Warfarin, reaction(s): "Tightness in the chest"; Warfarin, reaction(s): "Leg pain"; Warfarin, reaction(s): "Migraine"; Warfarin, reaction(s): "Teeth ache"; Warfarin, reaction(s): "Body Ache"; Warfarin, reaction(s): "Swelling in the leg"; Warfarin, reaction(s): "Muscle Weakness"; Warfarin, reaction(s): "Vein Bruise on the Legs"; Xyzal; Iodine derivatives, reaction(s): "Food allergy test: iodine derivatives"; Titanium, reaction(s): "swelling"; Titanium, reaction(s): "burning around the hip areas"; Titanium, reaction(s): "sinus condition"; Titanium, reaction(s): "back pain"; Tixocortol, reaction(s): "Food Allergies & Chemical Sensitivities : Tixocorol - Creams, Lotions, Ointments, Powders, and Fragrances with smells"; Titanium, reaction(s): "Food Allergies & Chemical Sensitivities : Titanium - Causes swelling and burning around the hip areas, sinus condition. and back pain.". Vaccination history included: covid-19 vaccine (Dose: 01 Time: 09.20, Batch/Lot number: ER8737.), administration date: 30Apr2021, when the patient was 66-year-old, for Covid-19 Immunization. The following information was reported: THROMBOSIS (medically significant), outcome "unknown", described as "blood clots". The patient underwent the following laboratory tests and procedures: Alanine aminotransferase increased (6-29): (03Jan2022) 24, notes: Units: U/L; (03Jan2022) 16, notes: U/L; Alanine aminotransferase normal (7-52): (30Mar2021) 21, notes: U/L; (03Jan2022) 2.0, notes: (calc); Albumin globulin ratio (1.0-2.8): (30Mar2021) 1.8, notes: calc; Albumin globulin ratio (1.0-2.5): (03Jan2022) 1.8, notes: (calc); (25Jul2022) 2.0, notes: (calc); Albumin urine (20-275): (03Jan2022) 97 mg/dl; (25Jul2022) 127 mg/dl; Albumin urine: (03Jan2022) 0.3 mg/dl; (25Jul2022) Less than 0.2; Anion gap: (30Mar2021) 9.4, notes: Units: mg/dL: CALC; Antibody test: (25Jul2022) 2/2; Aspartate aminotransferase (10-35): (03Jan2022) 18, notes: U/L; (25Jul2022) 20, notes: U/L; Aspartate aminotransferase (13-39): (30Mar2021) 20, notes: U/L; Bacterial test: (25Jul2022) None Seen; Basophil count (0-200): (03Jan2022) 10; Basophil count (0-200): (03Jan2022) 10 cells/uL; (25Jul2022) 21 cells/uL; Basophil count (0.0-0.2): (30Mar2021) 0.0, notes: Units: K/uL; Basophil count: (30Mar2021) 0.5 %; (03Jan2022) 0.3 %; (25Jul2022) 0.8 %; Bilirubin urine: (03Jan2022) Negative; (25Jul2022) Negative; Blood albumin (3.5-5.7): (03Jan2022) 4.2 g/dl; Blood albumin (3.6-5.1): (03Jan2022) 3.9 g/mL; (25Jul2022) 4.1 g/mL; Blood alkaline phosphatase (37-153): (30Mar2021) 76, notes: U/L; (25Jul2022) 70, notes: U/L; Blood alkaline phosphatase (20-128): (03Jan2022) 79, notes: U/L; Blood bilirubin (0.2-1.2): (03Jan2022) 1.0 mg/dl; Blood bilirubin (0.30-1.00): (30Mar2021) 0.78 mg/dl; (03Jan2022) 0.7 mg/dl; (25Jul2022) 1.0 mg/dl; Blood calcium (8.6-10.4): (30Mar2021) 8.6 mg/dl; (25Jul2022) 9.0 mg/dl; Blood calcium (8.8-10.6): (30Mar2021) 9.3 mg/dl; Blood chloride (98-110): (30Mar2021) 108 mmol/L; (25Jul2022) 107 mmol/L; Blood chloride (100-115): (03Jan2022) 107 mmol/L; Blood cholesterol (20-180): (30Mar2021) 166 mg/dl; Blood cholesterol: (25Jul2022) 172 mg/dl, notes: Less than 200 mg/dL; Blood creatinine (0.50-0.99): (03Jan2022) 0.81 mg/dl; Blood creatinine (0.50-1.05): (25Jul2022) 0.87 mg/dl; Blood creatinine (0.6-1.3): (30Mar2021) 0.9 mg/dl; Blood folate abnormal: (25Jul2022) 14.2 ng/ml; Blood glucose (97.0-140.0): (30Mar2021) 105.4 mg/dl; Blood glucose: (30Mar2021) Negative; Blood glucose (70-100): (30Mar2021) 94 mg/dl; Blood glucose (65-99): (03Jan2022) 84 mg/dl; (25Jul2022) 77 mg/dl; Blood iron (45-160): (25Jul2022) 76; Blood ketone body: (03Jan2022) Negative; (25Jul2022) Negative; Blood potassium (3.5-5.3): (15Jul2021) 4.1 mmol/L; (25Jul2022) 3.9 mmol/L; Blood potassium (3.5-5.5): (15Jul2021) 4.1 mmol/L; Blood sodium (135-145): (30Mar2021) 145 mmol/L; Blood sodium (135-146): (03Jan2022) 140 mmol/L; (25Jul2022) 142 mmol/L; Blood thyroid stimulating hormone (0.40-4.50): (25Jul2022) 3.16 MiU/L; Blood thyroid stimulating hormone (0.2700-4.2000): (30Mar2021) 1.8600 uiU/mL; Blood triglycerides (30-150): (30Mar2021) 66 mg/dl; (03Jan2022) 83 mg/dl, notes: Less than 150 mg/dL; (25Jul2022) 56 mg/dl, notes: Less than 150; Blood urea (7-25): (30Mar2021) 15 mg/dl; (03Jan2022) 17 mg/dl; Blood urea increased (7-25): (03Jan2022) 15 mg/dl; Blood urea nitrogen/creatinine ratio (6-22): (30Mar2021) 17.44, notes: Units: CALC; (03Jan2022) Not Applicable; (03Jan2022) Not applicable, notes: Not Applicable 6-22 (calc); Blood uric acid (2.5-7.0): (30Mar2021) 3.9 mg/dl, notes: Therapeutic target for gout patient : <6.0 mg/dl; Carbon dioxide (21-33): (30Mar2021) 29 mmol/L; Carbon dioxide (20-32): (03Jan2022) 28 mmol/L; (25Jul2022) 29 mmol/L; C-reactive protein: (30Mar2021) 1.2 mg/l, notes: Less than 8.0; Creatinine urine (20-275): (03Jan2022) 127 mg/dl; Eosinophil count (15-500): (03Jan2022) 99; (11Jan2023) 88; Eosinophil count (15-500): (03Jan2022) 88 cells/uL; Eosinophil count (0.1-1.0): (30Mar2021) 0.0, notes: Units: Ku/L; Eosinophil count: (30Mar2021) 1.2 %; (03Jan2022) 3.1 %; (25Jul2022) 3.4 %; Globulin (1.9-3.7): (03Jan2022) 2.2 g/dl; (25Jul2022) 2.1 g/dl; (04Jun2023) 2.1 g/dl; Globulin (1.3-4.0): (30Mar2021) 2.4 g/dl; Glomerular filtration rate: (30Mar2021) 85, notes: Ref range: greater than 60 ml/min/1.73 m2; (30Mar2021) 70, notes: Ref range: greater than 60 ml/min/1.73 m2; (03Jan2022) 76, notes: Ref range: Greater than or = 60 ml/min/ 1.73m2; (25Jul2022) 73, notes: Ref range: Greater than or = 60 ml/min/ 1.73m2; (04Jun2023) 88, notes: Ref range: Greater than or = 60 ml/min/ 1.73m2; Glucose urine: (03Jan2022) Negative; Glycosylated haemoglobin increased: (30Mar2021) 5.3, notes: Less than 5.7% of total Hgb; Glycosylated haemoglobin increased (4.3-5.6): (03Jan2022) 5.3 %; Haematocrit (35.0-45.0): (30Mar2021) 41.50 %; (03Jan2022) 38.0 %; (25Jul2022) 38.8 %; Haemoglobin (11.7-15.5): (25Jul2022) 12.8 g/dl; Haemoglobin (12.0-15.0): (unspecified date) 12.9 g/dl; (30Mar2021) 13.6 g/dl; High density lipoprotein (23-92): (30Mar2021) 59 mg/dl; (25Jul2022) 61 mg/dl, notes: Greater than OR= 50 mg/dL; Albumin Creatinin Ratio: (03Jan2022) 3, notes: Less than 30; (30Mar2021) Negative, notes: Ref range: Negative; (25Jul2022) clear, notes: Reference Range: Clear; (30Mar2021) 3, notes: Less than 3.5 optimal; (03Jan2022) 3.1, notes: Reference range: less than 5.0 (Calc); (25Jul2022) 2.8, notes: less than 5.0; (25Jul2022) None seen, notes: Reference Range: None seen/HPF Lab: # Final; (25Jul2022) 1+, notes: Reference Range: negative; Saturation (16-45): (25Jul2022) 25 %; (25Jul2022) 10-20, notes: Less than Or=5 /HPF; (03Jan2022) Normal to mildly increased, notes: Result: Less than 30 Moderately increased Result: 30-299 Severely increased. Result: Greater than Or =300; Iron binding capacity total (250-450): (25Jul2022) 302; LDL/HDL ratio: (03Jan2022) 1.8; (25Jul2022) 1.6; Low density lipoprotein: (25Jul2022) 97 mg/dl; (08May2023) 103H, notes: Reference Range: <100; (30Mar2021) 94 mg/dl; (unspecified date) 113 mg/dl, notes: Reference range: Less than 100 mg/dl (calc); (03Jan2022) 103 H, notes: Reference range: Less than 100 mg/dl (calc); Lymphocyte count (850-3900): (03Jan2022) 1834; (25Jul2022) 1453; Lymphocyte count (0.8-4.0): (30Mar2021) 46.1 %; (30Mar2021) 1.5 %; (03Jan2022) 57.3 %; (25Jul2022) 55.9 %; Mean cell haemoglobin (27.0-33.0): (30Mar2021) 30.4 pg; (03Jan2022) 30.3 pg; (25Jul2022) 30.8 pg; Mean cell haemoglobin concentration (32.0-36.0): (30Mar2021) 32.7 g/dl; (03Jan2022) 33.2 g/dl; (25Jul2022) 33.7 g/dl; Mean cell volume (80.0-100.0): (03Jan2022) 91.1; (25Jul2022) 91.6; Mean cell volume (80.0-99.0): (30Mar2021) 92.7; Mean platelet volume (7.4-10.4): (30Mar2021) 8.8; Mean platelet volume (7.5-12.5): (03Jan2022) 10.5; (25Jul2022) 10.5; Monocyte count (200-950): (03Jan2022) 339 cells/uL; (25Jul2022) 299 cells/uL; Monocyte count (0.1-1.0): (30Mar2021) 8.1 %; (30Mar2021) 0.3 %; (03Jan2022) 10.6 %; (25Jul2022) 11.5 %; Neutrophil count (1500-7800): (03Jan2022) 918 L; (25Jul2022) 738 L; Neutrophil count (1.5-7.5): (30Mar2021) 44.1 %; (30Mar2021) 1.4 %; (03Jan2022) 28.7 %; (25Jul2022) 28.4 %; Nitrite urine: (25Jul2022) Negative; Non-high-density lipoprotein cholesterol: (30Mar2021) 107 mg/dl, notes: Desirable is Less than 130 mg/dl; (03Jan2022) 120 mg/dl, notes: Reference range: Greater than (less than) 130 mg/dl (calc). Lab: TP; (25Jul2022) 111 mg/dl, notes: Less than 130; Nucleated red cells (0.00-2.00): (30Mar2021) 0.10 %; Occult blood: (25Jul2022) Negative; pH body fluid (5.0-8.0): (25Jul2022) 6.5; pH urine (5.0-8.0): (03Jan2022) 6.5; Platelet count (140-440): (30Mar2021) 211, notes: Units: K/uL; (31Jul2022) 217, notes: Units: K/uL; Platelet count (140-400): (25Jul2022) 212, notes: Thousand/uL; Platelet factor 4: (31Jul2022) 2/2; Protein total normal (6.1-8.1): (03Jan2022) 6.1 g/dl; (25Jul2022) 6.2 g/dl; Protein total normal (6.2-8.6): (30Mar2021) 6.6 g/dl; Protein urine: (25Jul2022) Negative; Red blood cell count: (25Jul2022) None Seen, notes: Reference Range: less than OR = 2/HPF; Red blood cell count (3.90-5.00): (30Mar2021) 4.48, notes: Ref range: 3.90-5.00 Units: M/uL; Red blood cell count (3.80-5.10): (30Mar2021) 4.15, notes: Reference Range 3.80-5.10 Million/uL; (31Jul2022) 4.26, notes: Ref range: 3.80-5.10 million/uL; (25Jul2022) 4.15, notes: Reference Range 3.80-5.10 Million/uL; Red blood cell sedimentation rate: (30Mar2021) 2, notes: Less than Or =30; Red cell distribution width (11.0-15.0): (30Mar2021) 13.2 %; (25Jul2022) 12.3 %; (31Jul2022) 12.7 %; Rheumatoid factor: (30Mar2021) less than 14; Specific gravity urine (1.001-1.035): (03Jan2022) 1.018; (25Jul2022) 1.018; Thyroxine (0.8-1.8): (25Jul2022) 0.9 ng/dL; Tri-iodothyronine (2.3-4.2): (25Jul2022) 3.0 pg/mL; Tri-iodothyronine (8-25): (03Jan2022) 11 mg/dl; Ultrasound testes: (15Jul2021) Blood clot, notes: Left leg Normal vascular flow; (31Jul2022) DVT, notes: Left leg Normal vascular flow; (19Sep2022) DVT, notes: Left leg Normal vascular flow; (05Dec2022) DVT, notes: Left leg Normal vascular flow; (05Dec2022) DVT, notes: Left leg Normal vascular flow; (11Jan2023) DVT, notes: Left leg Normal vascular flow; (08May2023) DVT; (04Jun2023) DVT; Urinary casts: (25Jul2022) None Seen; Urine albumin/creatinine ratio: (31Jul2022) 3, notes: Reference range: Less than 30 mcg /mg create; Urine analysis: (03Jan2022) Clear; (03Jan2022) Yellow; (25Jul2022) Yellow, notes: Reference Range: Yellow; Very low density lipoprotein: (30Mar2021) 13.20 mg/dl; Vitamin B12 (200-1100): (05Dec2022) 734 pg/mL; Vitamin D (30.00-100.00): (30Mar2021) 37.80 ng/ml; White blood cell count: (11Jan2023) None Seen, notes: Reference Range: less than OR = 5/HPF; (31Jul2022) 3.1-2.6 L, notes: Reference Range 3.8-10.8 Thousand/uL; White blood cell count (3.6-10.0): (30Mar2021) 3.3, notes: Ref range: 3.6-10 Units: K/ul; White blood cell count (3.8-10.8): (unspecified date) 3.3; (unspecified date) 3.1, notes: Thousand/uL; (25Jul2022) 2.6 L, notes: Thousand/uL; (31Jul2022) 3.2 L, notes: Thousand/uL.Clinical information: Prior vaccinations (within 4 weeks) was none. Test name: Creatinine, Ref range: 0.50-0.99 mg/dL, for patient more than 49 years of sage, the reference limit for creatinine is approximately 13 % higher for people identified as (withheld). Test name: BUN/Creatinine ratio In Range: Not Applicable, Ref range: Not Applicable 6-22 (calc). Food allergy test: Date: 20Aug2009 Histamine: 3.0, Almond: 2.0, Beef: 2.0, Chocolate: 2.0, Cinnamon: 1.0, Clam: 2.0, Corn: 1.0, Crab: 2.0, Egg White: 1.0, Egg yolk: 1.0, Peanut: 2.0, Pecan: 2.0, Scallops: 2.0, Shrimp: 2.0, Latex: 2.0. Phenytoin, cyclobenzaprine, codeine, sulfa, oxycodone, hydrocodone, penicillin and derv, iodine derivatives, clarithromycin, doxycycline, fentanyl, triamcinolone, ampicillin, tramadol, procaine, levothyroxine, latex (Unknown), Coumadin, nickel, prednisone, Decadron, Petroleum Jelly Nasacort, Xyzal, balsam Peru compounding powder, budesonide hydrocortisone, Rhino Cort, Valium, Avelox (Insomnia) (Migraine) Avinza (Night sweats) (Fever) (Insomnia), bethanechol ,Biaxin, BuSpar, Dilantin Duragesic, Lovenox (Chest pain) (Joint ache) (Migraine) Flexeril (Rash), hydroxyzine (Diarrhea) (Insomnia), hyoscyamine, Lyrica (Rash) (Diarrhea) Methylprednisolone, gabapentin, Novocain, Paxil, Skelaxin, Triazolam, Halcion. ANA IFA is a first Iino screen for detecting the presence of up to approximately 150 in various autoimmune diseases. A negative ANA IFA result suggests an AM-associated autoimmune is not present at this time. but is not definitive. If there is high clinical suspicion for Sjogren's syndrome, testing for anti-SS-A/Ro antibody should be considered. Anti-Jo-1 antibody should be considered for clinically suspected myopathies.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202300185598 same patient, different dose and AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20220103; Test Name: ALT (SGPT); Result Unstructured Data: Test Result:24; Comments: Units: U/L; Test Date: 20220103; Test Name: ALT (SGPT); Result Unstructured Data: Test Result:16; Comments: U/L; Test Date: 20210330; Test Name: ALT (SGPT); Result Unstructured Data: Test Result:21; Comments: U/L; Test Date: 20220103; Test Name: ALT (SGPT); Result Unstructured Data: Test Result:2.0; Comments: (calc); Test Date: 20210330; Test Name: A/G ratio; Result Unstructured Data: Test Result:1.8; Comments: calc; Test Date: 20220103; Test Name: Albumin/Globulin ratio; Result Unstructured Data: Test Result:1.8; Comments: (calc); Test Date: 20220725; Test Name: Albumin/Globulin ratio; Result Unstructured Data: Test Result:2.0; Comments: (calc); Test Date: 20220103; Test Name: Albumin, Random urine w/creatinine creatinine, random urine albumin, random urine albumin, random urine w/creatinine; Test Result: 97 mg/dl; Test Date: 20220725; Test Name: Albumin, Random urine w/creatinine creatinine, random urine albumin, random urine albumin, random urine w/creatinine; Test Result: 127 mg/dl; Test Date: 20220103; Test Name: Albumin, Urine; Test Result: 0.3 mg/dl; Test Date: 20220725; Test Name: Albumin, Urine; Result Unstructured Data: Test Result:Less than 0.2 mg/dl; Test Date: 20210330; Test Name: Anion gap; Result Unstructured Data: Test Result:9.4; Comments: Units: mg/dL: CALC; Test Date: 20220725; Test Name: Antibody test to Platelet factor IV; Result Unstructured Data: Test Result:2/2; Test Date: 20220103; Test Name: AST (SGOT); Result Unstructured Data: Test Result:18; Comments: U/L; Test Date: 20220725; Test Name: AST (SGOT); Result Unstructured Data: Test Result:20; Comments: U/L; Test Date: 20210330; Test Name: AST (SGOT); Result Unstructured Data: Test Result:20; Comments: U/L; Test Date: 20220725; Test Name: Bacteria; Result Unstructured Data: Test Result:None Seen; Test Date: 20220103; Test Name: Absolute Basophil; Result Unstructured Data: Test Result:10; Test Date: 20220103; Test Name: Absolute Basophil; Result Unstructured Data: Test Result:10 cells/uL; Test Date: 20220725; Test Name: Absolute Basophil; Result Unstructured Data: Test Result:21 cells/uL; Test Date: 20210330; Test Name: Basophil; Result Unstructured Data: Test Result:0.0; Comments: Units: K/uL; Test Date: 20210330; Test Name: Basophil; Test Result: 0.5 %; Test Date: 20220103; Test Name: Basophil; Test Result: 0.3 %; Test Date: 20220725; Test Name: Basophil; Test Result: 0.8 %; Test Date: 20220103; Test Name: Bilirubin; Test Result: Negative ; Test Date: 20220725; Test Name: Bilirubin; Test Result: Negative ; Test Date: 20220103; Test Name: Albumin; Result Unstructured Data: Test Result:4.2 g/dl; Test Date: 20220103; Test Name: Albumin; Result Unstructured Data: Test Result:3.9 g/mL; Test Date: 20220725; Test Name: Albumin; Result Unstructured Data: Test Result:4.1 g/mL; Test Date: 20210330; Test Name: Alkaline Phosphatase; Result Unstructured Data: Test Result:76; Comments: U/L; Test Date: 20220725; Test Name: Alkaline Phosphatase; Result Unstructured Data: Test Result:70; Comments: U/L; Test Date: 20220103; Test Name: Alkaline Phosphtase; Result Unstructured Data: Test Result:79; Comments: U/L; Test Date: 20220103; Test Name: Bilirubin; Test Result: 1.0 mg/dl; Test Date: 20210330; Test Name: Total Bilirubin; Test Result: 0.78 mg/dl; Test Date: 20220103; Test Name: Total Bilirubin; Test Result: 0.7 mg/dl; Test Date: 20220725; Test Name: Total Bilirubin; Test Result: 1.0 mg/dl; Test Date: 20210330; Test Name: Calcium; Test Result: 8.6 mg/dl; Test Date: 20220725; Test Name: Calcium; Test Result: 9.0 mg/dl; Test Date: 20210330; Test Name: Calcium; Test Result: 9.3 mg/dl; Test Date: 20210330; Test Name: Chloride; Result Unstructured Data: Test Result:108 mmol/L; Test Date: 20220725; Test Name: Chloride; Result Unstructured Data: Test Result:107 mmol/L; Test Date: 20220103; Test Name: Chloride; Result Unstructured Data: Test Result:107 mmol/L; Test Date: 20210330; Test Name: Cholesterol; Test Result: 166 mg/dl; Test Date: 20220725; Test Name: Cholesterol Total; Test Result: 172 mg/dl; Comments: Less than 200 mg/dL; Test Date: 20220103; Test Name: Creatinine; Test Result: 0.81 mg/dl; Test Date: 20220725; Test Name: Creatinine; Test Result: 0.87 mg/dl; Test Date: 20210330; Test Name: Creatinine; Test Result: 0.9 mg/dl; Test Date: 20220725; Test Name: Folate Serum; Result Unstructured Data: Test Result:14.2 ng/ml; Test Date: 20210330; Test Name: Estimated average Glucose; Test Result: 105.4 mg/dl; Test Date: 20210330; Test Name: Glucose; Test Result: Negative ; Test Date: 20210330; Test Name: Glucose; Test Result: 94 mg/dl; Test Date: 20220103; Test Name: Glucose; Test Result: 84 mg/dl; Test Date: 20220725; Test Name: Glucose; Test Result: 77 mg/dl; Test Date: 20220725; Test Name: Iron, Total; Result Unstructured Data: Test Result:76; Test Date: 20220103; Test Name: Ketones; Test Result: Negative ; Test Date: 20220725; Test Name: Ketones; Test Result: Negative ; Test Date: 20210715; Test Name: Potassium; Result Unstructured Data: Test Result:4.1 mmol/L; Test Date: 20220725; Test Name: Potassium; Result Unstructured Data: Test Result:3.9 mmol/L; Test Date: 20210715; Test Name: Potassium; Result Unstructured Data: Test Result:4.1 mmol/L; Test Date: 20210330; Test Name: Sodium; Result Unstructured Data: Test Result:145 mmol/L; Test Date: 20220103; Test Name: Sodium; Result Unstructured Data: Test Result:140 mmol/L; Test Date: 20220725; Test Name: Sodium; Result Unstructured Data: Test Result:142 mmol/L; Test Date: 20220725; Test Name: Tsh; Result Unstructured Data: Test Result:3.16 MiU/L; Test Date: 20210330; Test Name: TSH-II; Result Unstructured Data: Test Result:1.8600 uiU/mL; Test Date: 20210330; Test Name: Triglycerides; Test Result: 66 mg/dl; Test Date: 20220103; Test Name: Triglycerides; Test Result: 83 mg/dl; Comments: Less than 150 mg/dL; Test Date: 20220725; Test Name: Triglycerides; Test Result: 56 mg/dl; Comments: Less than 150; Test Date: 20210330; Test Name: Urea Nitrogen (BUN); Test Result: 15 mg/dl; Test Date: 20220103; Test Name: Urea Nitrogen (BUN); Test Result: 17 mg/dl; Test Date: 20220103; Test Name: Urea Nitrogen; Test Result: 15 mg/dl; Test Date: 20210330; Test Name: BUN/Creatinine ratio; Result Unstructured Data: Test Result:17.44; Comments: Units: CALC; Test Date: 20220103; Test Name: BUN/Creatinine ratio; Result Unstructured Data: Test Result:Not Applicable; Test Date: 20220103; Test Name: BUN/Creatinine ratio; Result Unstructured Data: Test Result:Not applicable; Comments: Not Applicable 6-22 (calc); Test Date: 20210330; Test Name: Uric Acid; Test Result: 3.9 mg/dl; Comments: Therapeutic target for gout patient : <6.0 mg/dl; Test Date: 20210330; Test Name: Co2; Result Unstructured Data: Test Result:29 mmol/L; Test Date: 20220103; Test Name: CO2; Result Unstructured Data: Test Result:28 mmol/L; Test Date: 20220725; Test Name: CO2; Result Unstructured Data: Test Result:29 mmol/L; Test Date: 20210330; Test Name: C-Reactive Protein; Result Unstructured Data: Test Result:1.2 mg/l; Comments: Less than 8.0; Test Date: 20220103; Test Name: Creatinine, random urine; Test Result: 127 mg/dl; Test Date: 20220103; Test Name: Absolute Eosinophil; Result Unstructured Data: Test Result:99; Test Date: 20230111; Test Name: Absolute Eosinophil; Result Unstructured Data: Test Result:88; Test Date: 20220103; Test Name: Absolute Eosinophil; Result Unstructured Data: Test Result:88 cells/uL; Test Date: 20210330; Test Name: Eosinophil; Result Unstructured Data: Test Result:0.0; Comments: Units: Ku/L; Test Date: 20210330; Test Name: Eosinophil; Test Result: 1.2 %; Test Date: 20220103; Test Name: Eosinophil; Test Result: 3.1 %; Test Date: 20220725; Test Name: Eosinophil; Test Result: 3.4 %; Test Date: 20220103; Test Name: Globulin; Result Unstructured Data: Test Result:2.2 g/dl; Test Date: 20220725; Test Name: Globulin; Result Unstructured Data: Test Result:2.1 g/dl; Test Date: 20230604; Test Name: Globulin; Result Unstructured Data: Test Result:2.1 g/dl; Test Date: 20210330; Test Name: Globulin; Result Unstructured Data: Test Result:2.4 g/dl; Test Date: 20210330; Test Name: eGFR; Result Unstructured Data: Test Result:85; Comments: Ref range: greater than 60 ml/min/1.73 m2; Test Date: 20210330; Test Name: eGFR; Result Unstructured Data: Test Result:70; Comments: Ref range: greater than 60 ml/min/1.73 m2; Test Date: 20220103; Test Name: eGFR; Result Unstructured Data: Test Result:76; Comments: Ref range: Greater than or = 60 ml/min/ 1.73m2; Test Date: 20220725; Test Name: eGFR; Result Unstructured Data: Test Result:73; Comments: Ref range: Greater than or = 60 ml/min/ 1.73m2; Test Date: 20230604; Test Name: eGFR; Result Unstructured Data: Test Result:88; Comments: Ref range: Greater than or = 60 ml/min/ 1.73m2; Test Date: 20220103; Test Name: Glucose; Test Result: Negative ; Test Date: 20210330; Test Name: Hemoglobin A1c; Result Unstructured Data: Test Result:5.3; Comments: Less than 5.7% of total Hgb; Test Date: 20220103; Test Name: Hemoglobin A1c; Test Result: 5.3 %; Test Date: 20210330; Test Name: Hematocrit; Test Result: 41.50 %; Test Date: 20220103; Test Name: Hematocrit; Test Result: 38.0 %; Test Date: 20220725; Test Name: Hematocrit; Test Result: 38.8 %; Test Date: 20220725; Test Name: Hemoglobin; Result Unstructured Data: Test Result:12.8 g/dl; Test Name: HGB; Result Unstructured Data: Test Result:12.9 g/dl; Test Date: 20210330; Test Name: HGB; Result Unstructured Data: Test Result:13.6 g/dl; Test Date: 20210330; Test Name: HDL Cholesterol; Test Result: 59 mg/dl; Test Date: 20220725; Test Name: HDL Cholesterol; Test Result: 61 mg/dl; Comments: Greater than OR= 50 mg/dL; Test Date: 20220103; Test Name: Albumin Creatinin Ratio; Result Unstructured Data: Test Result:3; Comments: Less than 30; Test Date: 20210330; Test Name: ANA Screen, IFA; Test Result: Negative ; Comments: Ref range: Negative; Test Date: 20220725; Test Name: Appearance; Result Unstructured Data: Test Result:clear; Comments: Reference Range: Clear; Test Date: 20210330; Test Name: Chol/HDL Ratio; Result Unstructured Data: Test Result:3; Comments: Less than 3.5 optimal; Test Date: 20220103; Test Name: Chol/HDL Ratio; Result Unstructured Data: Test Result:3.1; Comments: Reference range: less than 5.0 (Calc); Test Date: 20220725; Test Name: Chol/HDL Ratio; Result Unstructured Data: Test Result:2.8; Comments: less than 5.0; Test Date: 20220725; Test Name: Hyaline cast; Result Unstructured Data: Test Result:None seen; Comments: Reference Range: None seen/HPF Lab: # Final; Test Date: 20220725; Test Name: Leucocyte Esterase; Result Unstructured Data: Test Result:1+; Comments: Reference Range: negative; Test Date: 20220725; Test Name: Saturation; Test Result: 25 %; Test Date: 20220725; Test Name: Squamous Epithelial cells; Result Unstructured Data: Test Result:10-20; Comments: Less than Or=5 /HPF; Test Date: 20220103; Test Name: The Ada defines abnormalities in albumin excretion; Result Unstructured Data: Test Result:Normal to mildly increased; Comments: Result: Less than 30 Moderately increased Result: 30-299 Severely increased. Result: Greater than Or =300; Test Date: 20220725; Test Name: Iron Binding Capacity; Result Unstructured Data: Test Result:302; Test Date: 20220103; Test Name: LDL/HDL Ratio; Result Unstructured Data: Test Result:1.8; Test Date: 20220725; Test Name: LDL/HDL Ratio; Result Unstructured Data: Test Result:1.6; Test Date: 20220725; Test Name: LDL Cholesterol; Test Result: 97 mg/dl; Test Date: 20230508; Test Name: LDL Cholesterol; Result Unstructured Data: Test Result:103H mg/dl; Comments: Reference Range: <100; Test Date: 20210330; Test Name: LDL-calculated; Test Result: 94 mg/dl; Test Name: LDL-cholesterol; Test Result: 113 mg/dl; Comments: Reference range: Less than 100 mg/dl (calc); Test Date: 20220103; Test Name: LDL-cholesterol; Result Unstructured Data: Test Result:103 H mg/dl; Comments: Reference range: Less than 100 mg/dl (calc); Test Date: 20220103; Test Name: Absolute Lymphocyte; Result Unstructured Data: Test Result:1834; Test Date: 20220725; Test Name: Absolute Lymphocyte; Result Unstructured Data: Test Result:1453; Test Date: 20210330; Test Name: Lymphocyte; Test Result: 46.1 %; Test Date: 20210330; Test Name: Lymphocyte; Test Result: 1.5 %; Test Date: 20220103; Test Name: Lymphocyte; Test Result: 57.3 %; Test Date: 20220725; Test Name: Lymphocyte; Test Result: 55.9 %; Test Date: 20210330; Test Name: MCH; Test Result: 30.4 pg; Test Date: 20220103; Test Name: MCH; Test Result: 30.3 pg; Test Date: 20220725; Test Name: MCH; Test Result: 30.8 pg; Test Date: 20210330; Test Name: MCHC; Result Unstructured Data: Test Result:32.7 g/dl; Test Date: 20220103; Test Name: MCHC; Result Unstructured Data: Test Result:33.2 g/dl; Test Date: 20220725; Test Name: MCHC; Result Unstructured Data: Test Result:33.7 g/dl; Test Date: 20220103; Test Name: MCV; Result Unstructured Data: Test Result:91.1; Test Date: 20220725; Test Name: MCV; Result Unstructured Data: Test Result:91.6; Test Date: 20210330; Test Name: MCV; Result Unstructured Data: Test Result:92.7; Test Date: 20210330; Test Name: MPV; Result Unstructured Data: Test Result:8.8; Test Date: 20220103; Test Name: MPV; Result Unstructured Data: Test Result:10.5; Test Date: 20220725; Test Name: MPV; Result Unstructured Data: Test Result:10.5; Test Date: 20220103; Test Name: Absolute Monocyte; Result Unstructured Data: Test Result:339 cells/uL; Test Date: 20220725; Test Name: Absolute Monocyte; Result Unstructured Data: Test Result:299 cells/uL; Test Date: 20210330; Test Name: Monocyte; Test Result: 8.1 %; Test Date: 20210330; Test Name: Monocyte; Test Result: 0.3 %; Test Date: 20220103; Test Name: Monocyte; Test Result: 10.6 %; Test Date: 20220725; Test Name: Monocyte; Test Result: 11.5 %; Test Date: 20220103; Test Name: Absolute Neutrophil; Test Result: 918 l; Test Date: 20220725; Test Name: Absolute Neutrophil; Test Result: 738 l; Test Date: 20210330; Test Name: Neutrophil; Test Result: 44.1 %; Test Date: 20210330; Test Name: Neutrophil; Test Result: 1.4 %; Test Date: 20220103; Test Name: Neutrophil; Test Result: 28.7 %; Test Date: 20220725; Test Name: Neutrophil; Test Result: 28.4 %; Test Date: 20220725; Test Name: Nitrite; Test Result: Negative ; Test Date: 20210330; Test Name: Non-HDL Cholesterol; Test Result: 107 mg/dl; Comments: Desirable is Less than 130 mg/dl; Test Date: 20220103; Test Name: Non-HDL Cholesterol; Test Result: 120 mg/dl; Comments: Reference range: Greater than (less than) 130 mg/dl (calc) Lab: TP; Test Date: 20220725; Test Name: Non-HDL Cholesterol; Test Result: 111 mg/dl; Comments: Less than 130; Test Date: 20210330; Test Name: Nucleated RBC; Test Result: 0.10 %; Test Date: 20220725; Test Name: Occult Blood; Test Result: Negative ; Test Date: 20220725; Test Name: PH; Result Unstructured Data: Test Result:6.5; Test Date: 20220103; Test Name: PH; Result Unstructured Data: Test Result:6.5; Test Date: 20210330; Test Name: Platelet; Result Unstructured Data: Test Result:211; Comments: Units: K/uL; Test Date: 20220731; Test Name: Platelet; Result Unstructured Data: Test Result:217; Comments: Units: K/uL; Test Date: 20220725; Test Name: Platelet count; Result Unstructured Data: Test Result:212; Comments: Thousand/uL; Test Date: 20220731; Test Name: Antibody test to Platelet factor IV; Result Unstructured Data: Test Result:2/2; Test Date: 20220103; Test Name: Total Protein; Result Unstructured Data: Test Result:6.1 g/dl; Test Date: 20220725; Test Name: Total Protein; Result Unstructured Data: Test Result:6.2 g/dl; Test Date: 20210330; Test Name: Total Protein; Result Unstructured Data: Test Result:6.6 g/dl; Test Date: 20220725; Test Name: Protein; Test Result: Negative ; Test Date: 20220725; Test Name: RBC; Result Unstructured Data: Test Result:None Seen; Comments: Reference Range: less than OR = 2/HPF; Test Date: 20210330; Test Name: RBC; Result Unstructured Data: Test Result:4.48; Comments: Ref range: 3.90-5.00 Units: M/uL; Test Date: 20210330; Test Name: RBC; Result Unstructured Data: Test Result:4.15; Comments: Reference Range 3.80-5.10 Million/uL; Test Date: 20220731; Test Name: RBC; Result Unstructured Data: Test Result:4.26; Comments: Ref range: 3.80-5.10 million/uL; Test Date: 20220725; Test Name: Red Blood cell count; Result Unstructured Data: Test Result:4.15; Comments: Reference Range 3.80-5.10 Million/uL; Test Date: 20210330; Test Name: Sed Rate; Result Unstructured Data: Test Result:2; Comments: Less than Or =30; Test Date: 20210330; Test Name: RDW; Test Result: 13.2 %; Test Date: 20220725; Test Name: RDW; Test Result: 12.3 %; Test Date: 20220731; Test Name: RDW; Test Result: 12.7 %; Test Date: 20210330; Test Name: Rheumatoid Factor; Result Unstructured Data: Test Result:less than 14 IU/ml; Test Date: 20220103; Test Name: Specific gravity; Result Unstructured Data: Test Result:1.018; Test Date: 20220725; Test Name: Specific gravity; Result Unstructured Data: Test Result:1.018; Test Date: 20220725; Test Name: T4 Free; Result Unstructured Data: Test Result:0.9 ng/dL; Test Date: 20220725; Test Name: T3 Free; Result Unstructured Data: Test Result:3.0 pg/mL; Test Date: 20220103; Test Name: T3 Reverse, LC/MS/MS; Test Result: 11 mg/dl; Test Date: 20210715; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:Blood clot; Comments: Left leg Normal vascular flow.; Test Date: 20220731; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:DVT; Comments: Left leg Normal vascular flow.; Test Date: 20220919; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:DVT; Comments: Left leg Normal vascular flow.; Test Date: 20221205; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:DVT; Comments: Left leg Normal vascular flow.; Test Date: 20221205; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:DVT; Comments: Left leg Normal vascular flow.; Test Date: 20230111; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:DVT; Comments: Left leg Normal vascular flow.; Test Date: 20230508; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:DVT; Test Date: 20230604; Test Name: Deep vein Ultrasound; Result Unstructured Data: Test Result:DVT; Test Date: 20220725; Test Name: Hyaline Cast; Result Unstructured Data: Test Result:None Seen; Test Date: 20220731; Test Name: Albumin/creatine ratio, Random urine; Result Unstructured Data: Test Result:3; Comments: Reference range: Less than 30 mcg /mg create; Test Date: 20220103; Test Name: Appearences; Result Unstructured Data: Test Result:Clear; Test Date: 20220103; Test Name: Colour; Result Unstructured Data: Test Result:Yellow; Test Date: 20220725; Test Name: Urinalysis Reflex Colous; Result Unstructured Data: Test Result:Yellow; Comments: Reference Range: Yellow; Test Date: 20210330; Test Name: VLDL Cholesterol; Test Result: 13.20 mg/dl; Test Date: 20221205; Test Name: Vitamin B12; Result Unstructured Data: Test Result:734 pg/mL; Test Date: 20210330; Test Name: Vitamin D, 25-Hydroxy; Result Unstructured Data: Test Result:37.80 ng/ml; Test Date: 20230111; Test Name: WBC; Result Unstructured Data: Test Result:None Seen; Comments: Reference Range: less than OR = 5/HPF; Test Date: 20220731; Test Name: White blood cell count; Result Unstructured Data: Test Result:3.1-2.6 L; Comments: Reference Range 3.8-10.8 Thousand/uL; Test Date: 20210330; Test Name: White blood cell count; Result Unstructured Data: Test Result:3.3; Comments: Ref range: 3.6-10 Units: K/ul; Test Name: White blood cell count; Result Unstructured Data: Test Result:3.3; Test Name: White blood cell count; Result Unstructured Data: Test Result:3.1; Comments: Thousand/uL; Test Date: 20220725; Test Name: White blood cell count; Result Unstructured Data: Test Result:2.6 L; Comments: Thousand/uL; Test Date: 20220731; Test Name: White blood cell count; Result Unstructured Data: Test Result:3.2 L; Comments: Thousand/uL
Aktuelle Erkrankungen: Immune system disorder (Did not have allergies before the Titanium surgery); Removal of surgical hardware (Became Allergic to almost everything); Spinal fusion
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy (Adhesive); Allergy (balsam Peru compounding powder/Balsam of Peru); Allergy to chemicals (Food Allergies & Chemical Sensitivities); Allergy to chemicals (Cement, Sun Flex Partial, Amalagams Filling); Allergy to chemicals (Balsam of Peru - Medicated lozenges, hand sanitizers, Parabens, Petroleum Jelly); Allergy to dental material (Cement, Sun Flex Partial, Amalagams Filling); Allergy to metals (Cement, Sun Flex Partial, Amalagams Filling); Allergy to nuts; Cardiovascular disorder (Durgesic Patches - Cardiovascular); Cement dust allergy (Cement, Sun Flex Partial, Amalagams Filling); Egg allergy (egg white, egg yolk); Food allergy; Hives (Sulfur - Cardiovascular & Hives); Itching (Durgesic Patches - itching); Latex allergy (Latex Allergies); Latex allergy; Meat allergy; Nausea (Durgesic Patches - nausea); Palpitation (Food Allergies & Chemical Sensitivities: Causes Heart Palpitation.); Paraben allergy (Balsam of Peru - Medicated lozenges, hand sanitizers, Parabens, Petroleum Jelly); Peanut allergy; Penicillin allergy; Reaction to food coloring (Food coloring); Rubber sensitivity (Rubber Foam Chairs); Skin burning sensation (Latex, Velcro, Adhesive - Causes Heart Palpitation, and Burns Skin); Specific allergy (drug); Sulfonamide allergy; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: Food allergy test: Shrimp
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2633544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 64,0
Geschlecht: M
Eingang: 18.05.2023
Impfdatum: 21.03.2021
Beginn: 13.07.2022
Tage bis Beginn: 479,0
Dosis: 2
Route/Site: UN / UN

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

Acute left ventricular failure Arrhythmia Atrial fibrillation COVID-19 COVID-19 pneumonia Cardiac failure congestive Cardiomyopathy Chest X-ray abnormal Condition aggravated Cough Dyspnoea Echocardiogram abnormal Ejection fraction decreased Electrocardiogram QRS complex normal Electrocardiogram abnormal Hypertension Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

COVID BREAKTHROUGH: 65-year-old fully vaccinated and booster. Initially tested positive on June 8th, had a repeat test 2 weeks later,and approximately June 22nd which was negative. He states that since then he has had progressive cough with associated shortness of breath. He states last night he was unable to really sleep well because of the cough and shortness of breath. Once in the ED, patient was found to be hypertensive with a blood pressure of 175/137, WBC was normal, patient was afebrile. Patient was given nebulizers, ceftriaxone, azithromycin, Decadron for presumed post viral pneumonia. Patient denies current fever, nausea, vomiting, diarrhea. Shortness of breath,-established problem, stable. LVEF by echo 35-40%, Atrial fibrillation-established problem, stable,HTN-established problem, stable, Hypercholesterolemia-established problem, stable , Acute systolic CHF exacerbation, POA, Cardiomyopathy newly diagnosed, and Pulmonary edema.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 2,0
Labordaten: chest x-ray which the ED physician thought this was post COVID pneumonia.Chest x-ray was actually read as vascular congestion. EKG: NORMAL AXIS. ATRIAL FIBRILLATION RATE 91. NO ST ELEVATIONS ORT TWAVE INVERSIONS. QTC 450MS. NORMAL QRS. NO PREVIOUS STUDT FOR COMPARISON. ABNORMAL RHYTHM ECG
Aktuelle Erkrankungen: unknown
Vorgeschichte: hypertension, hyperlipidemia, morbid obesity
Andere Medikamente: Atorvastatin, Glimepiride, Lisinopril, Insulin, MetFORMIN, insulin, lispro, cyanocobalamin, apixaban, cholecalciferol, Omega-3, multivitamin, Toprol-XL, Symbicort,albuterol CFC, ZITHROmax, Lasix, Spironolactone, Omnicef
Allergien: iodine
Vorherige Impfungen: -

VAERS 2584857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: OR
Alter: 70,0
Geschlecht: M
Eingang: 21.02.2023
Impfdatum: 20.04.2021
Beginn: 13.05.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: IM / -

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

Deep vein thrombosis

Symptomtext

DVT and PE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia, Hashimoto Thyroidosis, impaired fasting glycemia
Andere Medikamente: Levothyroxine, Vitamin D, Vitamin C
Allergien: -
Vorherige Impfungen: -

VAERS 2519952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 13.04.2021
Beginn: 13.06.2021
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Fibrin D dimer Gait disturbance Mobility decreased Pain in extremity Peripheral swelling Sleep disorder Thrombosis Ultrasound Doppler abnormal

Symptomtext

I woke up at 5AM with pain in my outer left thigh and swelling. The pain would subside when walking or moving around and increase when sitting down. By 6PM I was limping and swollen from my toes to my belly button, I went to the ER which could not admit me due to the beds being full with COVID-19 patients, a blood profile was done which was inconclusive so I was told to follow up with my doctor as soon as possible. I woke up that night at 2:30AM with my left side so swollen I could not get out of bed and when I did or was able to get out of bed I was unable to use my left leg. I went to a Vascular specialist who performed an Ultrasound where a blood clot was discovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: D Dimer inconclusive. Ultrasound showed blood clot.
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Venous Insufficiency
Andere Medikamente: Baby aspirin
Allergien: None
Vorherige Impfungen: 48 hours after my vaccine my calves doubled in size at two toes on my left foot and two toes on my right foot turned purple. I w

VAERS 1376399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CA
Alter: -
Geschlecht: M
Eingang: 24.11.2022
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Chest pain Echocardiogram normal Electrocardiogram abnormal Full blood count Magnetic resonance imaging heart Troponin Troponin increased Echocardiogram Myocarditis Magnetic resonance imaging normal Respiratory viral panel SARS-CoV-2 test Ultrasound chest

Symptomtext

myocarditis; has occasional similar chest pain for brief periods; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A male patient received BNT162b2 (BNT162B2), in Jun2021 as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for COVID-19 immunization. The following information was reported: CHEST PAIN (non-serious) with onset 2021, outcome "not recovered", described as "has occasional similar chest pain for brief periods"; MYOCARDITIS (hospitalization) with onset Jun2021, outcome "recovered" (2021). The patient was hospitalized for myocarditis (start date: Jun2021, hospitalization duration: 4 day(s)). Patient on restricted activities for six months. He is mostly okay now but has occasional similar chest pain for brief periods The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

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

VAERS 1376399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: -
Geschlecht: M
Eingang: 24.11.2022
Impfdatum: 01.06.2021
Beginn: 01.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Blood test Chest pain Echocardiogram normal Electrocardiogram abnormal Full blood count Magnetic resonance imaging heart Troponin Troponin increased Echocardiogram Myocarditis Magnetic resonance imaging normal Respiratory viral panel SARS-CoV-2 test Ultrasound chest

Symptomtext

myocarditis; has occasional similar chest pain for brief periods; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A male patient received BNT162b2 (BNT162B2), in Jun2021 as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for COVID-19 immunization. The following information was reported: CHEST PAIN (non-serious) with onset 2021, outcome "not recovered", described as "has occasional similar chest pain for brief periods"; MYOCARDITIS (hospitalization) with onset Jun2021, outcome "recovered" (2021). The patient was hospitalized for myocarditis (start date: Jun2021, hospitalization duration: 4 day(s)). Patient on restricted activities for six months. He is mostly okay now but has occasional similar chest pain for brief periods The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

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

VAERS 2312684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 08.06.2022
Impfdatum: 08.04.2021
Beginn: 17.05.2021
Tage bis Beginn: 39,0
Dosis: 2
Route/Site: - / RA

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

Muscle spasms Thrombosis

Symptomtext

After caller had his 2nd shot last year caller developed 2 blood clots in 1 leg; Caller's legs have been cramping since caller got the vaccine; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), on 08Apr2021 as dose 2, single (Lot number: EW0153) at the age of 60 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (NDC number, lot number, expiration date: ER6213, Dose and route: Unknown, Dose: 1), administration date: 18Mar2021, when the patient was 59-year-old, for COVID-19 immunization, reaction(s): "Cramping". The following information was reported: THROMBOSIS (medically significant) with onset 17May2021, outcome "recovered" (Nov2021), described as "After caller had his 2nd shot last year caller developed 2 blood clots in 1 leg"; MUSCLE SPASMS (non-serious) with onset 17May2021, outcome "unknown", described as "Caller's legs have been cramping since caller got the vaccine". The events "after caller had his 2nd shot last year caller developed 2 blood clots in 1 leg" and "caller's legs have been cramping since caller got the vaccine" required physician office visit. Therapeutic measures were taken as a result of thrombosis, muscle spasms. Clinical Course : Caller is calling about the Pfizer COVID-19 vaccine. After caller had his 2nd shot last year caller developed 2 blood clots in 1 leg, which was caller's right leg. Doctor said they have never seen that before. Caller is having the same symptoms now going on in caller's left leg and caller had to go to the emergency room. Caller clarifies he did not go to the emergency room, caller went to urgent care. Just came back from urgent care and they wanted caller to go to the emergency room, but caller hasn't gone to the emergency room yet. Caller's legs have been cramping since caller got the vaccine. Caller actually went last month to urgent care and it was 7 o'clock and they sent a note for caller to go to the emergency room because the ultrasound person that checks for blood clots was gone. Caller waited a month, went back to the urgent care when the ultrasound person was supposed to be there and the ultrasound person was too busy. Don't get Healthcare. Caller has been having these symptoms for like 2 months now in both legs, now both legs are cramping and aching, but left leg is hurting more and burning more, very good burning sensation, probably where the clots are. Going to go to the emergency room later tonight. Caller is sitting up with legs in the air on pillows right now because legs are hurting so bad, has legs 4 feet up in the air, has been doing this the past 2 months, helps caller's legs. Vaccination Facility Type: Clinic set up in the mall. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2277857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 59,0
Geschlecht: M
Eingang: 15.05.2022
Impfdatum: 03.08.2021
Beginn: 09.05.2022
Tage bis Beginn: 279,0
Dosis: 1
Route/Site: IM / RA

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

Intensive care

Symptomtext

Unknown. Unable to contact this case as he remains in ICU, admitted 05/09/2022.

Weitere VAERSDATA-Felder

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

VAERS 2270807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 18.03.2021
Beginn: 06.03.2022
Tage bis Beginn: 353,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dizziness Head injury SARS-CoV-2 test positive Syncope

Symptomtext

03/06/22 presents to EC ED for "lightheadedness and one episode of syncope with head injury". PMHx of "obesity, CAD, HTN, HLD, T2DM (not on insulin), COPD, asthma, history of inhalation injury, and OSA (CPAP at night)"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 03/06/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2254614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AL
Alter: 61,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 15.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Blood test CSF test Computerised tomogram Diarrhoea Dizziness Electroencephalogram Hashimoto's encephalopathy Lumbar puncture Magnetic resonance imaging Malaise Nausea Pain Syncope Vomiting

Symptomtext

The day after the vaccination I was violently ill with nausea, vomiting, diarrhea, and massive body aches. These subsided about 24 hours post injection. Six weeks after injection I began have dizzy and fainting spells. I went to my PCP and was referred to a neurologist. After many tests I was diagnosed with Steroid-Responsive Encephalopathy Hashimoto.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood work; Spinal tap for CSF; EEG; MRI; CT-Scan
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; Prolapsed Heart Valve
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2238638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: RI
Alter: 64,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 06.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Dizziness Fatigue Headache Lymphadenopathy Malaise Nervousness Presyncope Tremor

Symptomtext

4/7/2021: I woke up with a headache and went back to sleep. I woke up around 10:45am and felt well. Got dressed and went downstairs. Around 11:15 I started to feel unwell. I felt shaky. I went back upstairs, I had chills, was shaking, felt like I was going to faint. I felt dizzy. I got back into bed and felt extremely fatigued. I did not feel like I was going to pass out anymore. Then I just slept, I would wake up momentarily, then would go back to sleep. I slept until about 6:30 the next morning. I felt well on 4/8/2022. On 4/9/2022, I had swollen glands on the right side of my throat and under both armpits. After that, I was fine, and had no more effects. I had the Booster and did fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Obesity
Andere Medikamente: Multivitamin Flovent
Allergien: None
Vorherige Impfungen: -

VAERS 2236076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 52,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 08.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Balance disorder Ear discomfort Ear pain Facial discomfort Facial paralysis Fatigue Feeding disorder Fluid intake reduced Headache Herpes zoster Insomnia Magnetic resonance imaging normal Pain

Symptomtext

I started having headache and lasted for about a week. I couldn't sleep and very painful. 4/25/2021 My left ear started to feel wet. This is when I went to doctor and identified as shingles. I couldn't eat or drink and by 4/28/2021 my face started to paralyze so my doc ordered an MRI on 4/29/2021. I cannot work because balance and was feeling fatigue and tired. Even today, my face is still partially paralyzed and feel uncomfortable and mild pain in hear and/or ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: 4/29/2021 MRI (stroke possible but came back as normal).
Aktuelle Erkrankungen: None
Vorgeschichte: HBP; HCL; Seasonal Allergies
Andere Medikamente: Azilsartan; Rosuvastatin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2225217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 37,0
Geschlecht: F
Eingang: 09.04.2022
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anxiety Fatigue Pain Panic attack SARS-CoV-2 test Thrombosis

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 37 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Apr2021 10:45 (Lot number: EW0153) at the age of 37 years as dose 1, single for Covid-19 immunisation. Patient received bnt162b2 Dose 2 (Lot number: EW0153) in arm left on administration date 30Apr2021. Relevant medical history included: "Known Allergies: Sulfa" (unspecified if ongoing) and other medical history was none. The patient's concomitant medications were not reported. The following information was reported: THROMBOSIS (medically significant) with onset 09Apr2021, outcome "not recovered", described as "Blood Clogs"; ANXIETY (non-serious) with onset 09Apr2021, outcome "not recovered", described as "Anxiety"; PANIC ATTACK (non-serious) with onset 09Apr2021, outcome "not recovered", described as "Panic Attacks"; FATIGUE (non-serious) with onset 09Apr2021, outcome "not recovered", described as "Tiredness"; PAIN (non-serious) with onset 09Apr2021, outcome "not recovered", described as "Body Pain". The events "blood clogs", "anxiety", "panic attacks", "tiredness" and "body pain" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (28Dec2021) negative, notes: Nasal Swab; (04Jan2022) positive, notes: Nasal Swab; (12Jan2022) positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of thrombosis, anxiety, panic attack, fatigue, pain. Patient had not received any other vaccine in four weeks. Patient had not received any other medications in two weeks. Patient did not experienced Covid prior vaccination. Sender's Comments: As there is limited information in the case provided, the causal association between the Reported events and the suspect drug cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20211228; Test Name: Covid test; Test Result: Negative; Comments: Nasal Swab; Test Date: 20220104; Test Name: Covid test; Test Result: Positive; Comments: Nasal Swab; Test Date: 20220112; Test Name: Covid test; Test Result: Positive; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1262506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 21,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 26.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Confusional state Dizziness Dyspnoea Fatigue Flushing Hypotension Loss of consciousness Hyperhidrosis Lethargy Syncope Unresponsive to stimuli

Symptomtext

Shortness of breath a couple minutes after the shot. Loss of consciousness soon after for around 5 minutes. Blood pressure measured to be 60/30 and dizziness after regaining consciousness. Epinephrine administered and 911 called after a few minutes of sustained low blood pressure and dizziness. After lying down for around 5 more minutes for a total of around 15 minutes, started to feel better.

Weitere VAERSDATA-Felder

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

VAERS 2181904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 01.05.2021
Beginn: 01.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Asthenopia Burning sensation Chest discomfort Chills Dizziness Feeling abnormal Hypoaesthesia Hypoaesthesia oral Pain in extremity Presyncope Thirst Vascular test

Symptomtext

she felt very strange; her chest became tight; lightheadedness shortly after her 2nd shot and also during day; Also reported numbness around bottom lip and chin; Also reported numbness around bottom lip and chin; Also reported chills the first night of the 2nd shot; eyes having a heavy feeling; felt very thirsty; burning /stabbing sensation (day after her 2nd shot) in inside of left thigh which stops her in her tracks; burning /stabbing sensation (day after her 2nd shot) in inside of left thigh which stops her in her tracks; She felt like she was going to faint but didn't; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 64 year-old female patient received bnt162b2 (COMIRNATY-Pfizer COVID 19 Vaccine-Solution for injection), administration date May2021 (Lot number: EW0153) at the age of 63 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose:1st, she did perfectly fine with the first dose), for COVID-19 immunization, reaction(s): "No reaction on previous exposure to vaccine". The following information was reported: FEELING ABNORMAL (non-serious) with onset May2021, outcome "unknown", described as "she felt very strange"; CHEST DISCOMFORT (non-serious) with onset May2021, outcome "unknown", described as "her chest became tight"; DIZZINESS (non-serious) with onset May2021, outcome "unknown", described as "lightheadedness shortly after her 2nd shot and also during day"; PRESYNCOPE (non-serious) with onset 2021, outcome "unknown", described as "She felt like she was going to faint but didn't"; HYPOAESTHESIA (non-serious), HYPOAESTHESIA ORAL (non-serious) all with onset May2021, outcome "recovered" (May2021) and all described as "Also reported numbness around bottom lip and chin"; ASTHENOPIA (non-serious) with onset 2021, outcome "unknown", described as "eyes having a heavy feeling"; THIRST (non-serious) with onset 2021, outcome "unknown", described as "felt very thirsty"; PAIN IN EXTREMITY (non-serious), BURNING SENSATION (non-serious) all with onset 2021, outcome "not recovered" and all described as "burning /stabbing sensation (day after her 2nd shot) in inside of left thigh which stops her in her tracks"; CHILLS (non-serious) with onset May2021, outcome "unknown", described as "Also reported chills the first night of the 2nd shot". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: states had pfizer covid vaccine; she did perfectly fine with the first dose however with the 2nd dose she received in May, 'all kinds of very strange things happened'. States within 15 mins of receiving the 2nd dose, she felt very strange and her chest became tight. Also reported lightheadedness shortly after her 2nd shot and also during day. She felt like she was going to faint but didnt. Also reported numbness around bottom lip and chin; eyes having a heavy feeling and felt very thirsty. Reports burning /stabbing sensation (day after her 2nd shot) in inside of left thigh which stops her in her tracks. She felt like someone took a hot pick and stabbed her with it (inside of her left thigh). She has to wait for it to go away. States her numbness resolved/disappated after the first day however the burning/stabbing pains in her thigh she still has but occurs intermittently. Also reported chills the first night of the 2nd shot. Two months after her second shot, her dr. did a vascular study to rule out blood clot ( there was no blood clot). Asking if other people reported these other type of sxs? states she wants to get the booster but is afraid of landing in the hospital. States she talked to her dr. but he wouldn't give any answers. DOB: (withheld). She has talked to some people who have gotten the booster and they report that the booster is worse than the 2nd dose. Her dr. said her side effects weren't normal side effects. Adds that her husband felt crappier than she did after the first dose but with the 2nd shot he felt ok and the booster was fine. states she talked to 6 different people. COVID-19 Vaccine was a Pfizer product. No follow-up attempts are possible. No further information is expected. Follow-up(13Jan2022): New information received from a contactable consumer (patient) reported for herself that updated Information: Lot Number added for Suspect Drug and additional information. Follow-up (19Jan2022): Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 202107; Test Name: vascular study; Result Unstructured Data: Test Result:No blood clot
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1919630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 49,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 15.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Dyspnoea Pain in extremity Painful respiration Pulmonary thrombosis Thrombosis Ultrasound scan Weight Weight increased X-ray

Symptomtext

he only had a sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A 49 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 15Oct2021 (Lot number: FF2593) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, Anatomical Location: Left arm, Lot Number: EP7534 or ED7534), administration date: 19Mar2021, when the patient was 49 years old, for COVID-19 Immunization, reaction(s): "had a sore arm"; Bnt162b2 (Dose: 2, Anatomical Location: Left arm, Lot Number: EW0153, Time the Vaccination maybe anywhere between noon and 15:00), administration date: 09Apr2021, when the patient was 49 years old, for COVID-19 Immunization, reaction(s): "he had blood clots in his lungs", "rounding up his weight to 205lbs", "had a broken rib", "labored breathing and couldn't hardly breathe"; Flu shot (He mentions he got the flu shot, but he did that on a separate day, it was not on either days he received the COVID-19 vaccine.). The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "he only had a sore arm". Additional Information:NDC number,Expiry Date of Pfizer BioNTech COVID-19 vaccine was unknown.Other Products,Patient History and Investigation Assessment was no.The reporter had both doses of the Pfizer BioNTech COVID-19 vaccine and also had the booster dose. Once he was done with all of his vaccines, he states he was rushed to hospital because he had blood clots in his lungs. The reporter knows with the Moderna vaccine, this could possibly be a side effect, but wanting to know if blood clots could be a side effect to the Pfizer vaccine. He stated really can't find anything about it. The agent requests the reporter be transferred to Agency after speaking with Safety.Upon transfer, the reporter clarifies that after the two vaccinations, had the blood clots. Then, had the booster dose later. He clarifies further the blood clots occurred in between his first two doses and the booster dose.He verifies since then he has received his booster dose.He has never taken medicines.He was given the Tylenol 3 and pain pills but this was used to treat the pain. After he was diagnosed with blood clots, his doctor has him on the blood thinner, Eliquis, going forward and he may be on it for the rest of life, they have to monitor the blood clots and see. Emergency Room and Physician Office visit was yes.He was told if he had any significant bruising or anything like that, to come back to the hospital. He paid a crazy bill but basically just said he was fine and everything looks good. He was told they didn't see anything they were looking for and to pay attention to it. He didn't go back. He didn't have any problems or similar pains. He was told if he did, to go back to the ER because the urgent care didn't have the equipment to do the ultrasound, but the ER didn't even do an ultrasound when he went. The caller explains he was never admitted into the hospital, he was just seen in the ER two consecutive days in a row for the same reason. The reporter states the clot was unidentified. It was like he had a broken rib, he had labored breathing and couldn't hardly breathe. It was like he had this stabbing pain inside his body when he took a breath. They did all kinds of test and the first visit, he was not sent home with any pain pills. After the pain pills wore off that they had given him that day, he went back a second time and went through the same process except they were able to identify the issue and he was given pain pills and extra strength Tylenol. He clarifies he didn't have to use the pain pills, the extra strength Tylenol kicked the pain.The reporter clarifies went to the ER the first time and they were almost going to admit him into the hospital but didn't because they didn't have any beds or rooms to put him in, it was crazy.The next day, it was the same thing, went to the ER, but he didn't have any testing done like they did before, they basically just gave him pain pills. Patient told them he wasn't leaving without pain pills because he was dying. The reporter clarifies that he didn't even take the pain pills he just took the Tylenol 3 and the pain went right away after taking the Tylenol 3. He was waiting for the pain to come back, but it didn't. He guesses the clots dissipated or went away or something.The doctor in the ER said the clots were unprovoked because they did x-rays and ultrasounds in his legs and couldn't find out where the blood clot began. He doesn't know if the doctor was speaking out of turn. The reporter didn't think at the time it could be from the vaccine, but then someone told him happened with the Moderna vaccine. He never had blood clots ever before so it concerns him that it had something to do with the vaccination. He doesn't think its coincidental, he all of a sudden got this after getting the vaccine. AE(s) following prior vaccinations was none.Patient's Medical History (including any illness at time of vaccination) was none. The reporter states did see his primary care physician who did a medical workup, but there was not anything alarming. There was nothing really relevant otherwise his primary care would have told him. Everything seemed to be fine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1307084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TX
Alter: 22,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 06.05.2021
Beginn: 09.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram pulmonary normal Arteriogram coronary normal Catheterisation cardiac Chest X-ray Chest pain Myocarditis SARS-CoV-2 antibody test Troponin increased Early repolarisation syndrome Echocardiogram normal Ejection fraction decreased Ejection fraction normal Electrocardiogram ST segment elevation Fatigue Fibrin D dimer normal Pain Pericarditis Peripheral vascular disorder

Symptomtext

Fatigue, followed by dull, pleuritic left anterior chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: Troponin 1513, 6056, d-dimer normal, CXRR, NAD, ECG: diffuse ST elevation that might be early repolarization vs. early pericarditis, frequent PVDs, . chest CTA : no PTE, echo normal EF, no pericardial effusion. Left heart catheterization for ongoing chest pain with normal LVEF 50-55%. Normal coronary arteriograms.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2132218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 64,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 15.05.2021
Beginn: 30.10.2021
Tage bis Beginn: 168,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Hypoxia Syncope

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 2104973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 80,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 23.03.2021
Beginn: 17.01.2022
Tage bis Beginn: 300,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Diverticulitis Hospitalisation SARS-CoV-2 test positive

Symptomtext

Patient hospitalized for perforated diverticulitis 1/17/22-1/26/22. Tested positive for COVID 1/17/22. No evidence of respiratory failure.

Weitere VAERSDATA-Felder

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

VAERS 2092232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 20.12.2021
Beginn: 31.01.2022
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Emphysema Pain Respiratory distress Respiratory failure SARS-CoV-2 test positive Wheezing

Symptomtext

Patient was admitted for worsening respiratory failure and respiratory distress. Does have COPD and chronically wears 2-4 L nasal cannula at baseline. Did test positive for COVID-19 Chest x-ray did not show acute intrathoracic process but did show significant emphysematous changes. At most required 3 L nasal cannula to maintain oxygenation. Had significant pan expiratory and inspiratory wheezes. Received remdesivir and Solu-Medrol. Also received bronchodilator therapy. Had drastic improvement in her wheezing and her shortness of breath. Weaned to her baseline oxygenation of 2 L nasal cannula. COPD Exacerbation in addition to COVID. Discharged home 2/2/22. Previously vacc: Pfizer 3/18/21, 4/8/21, 12/20/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 3,0
Labordaten: COVID 19 PCR + 1/31/22
Aktuelle Erkrankungen: -
Vorgeschichte: COPD on home O2, sleep apnea, hypertension, hyperlipidemia, diabetes, obesity, anxiety, peripheral neuropathy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2088522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TN
Alter: 56,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 20.04.2021
Beginn: 13.05.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: IM / RA

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

Blood test Chest X-ray Chills Computerised tomogram kidney abnormal Malaise Nephrolithiasis Pain Pyrexia Renal stone removal Scan with contrast abnormal Shock Surgery Ureteral stent insertion

Symptomtext

May 13, 2021 feel unwell shotting pain contact doctor, he called in broad spectrum antibotic took 2 pills - Nitro Furantoin Mono-MCR and later during the night she bad chills, fever highest 104.2 and did not know she was in shock and and continued to try to resolve her fever and next moring 05/14/2021 husband call the physician and phyician was caller stronger medicine, Cephalexime 1 -2 tablets before going to the hospital. CT scan with contrast and did a chest x-ray, saw the kidney stone and and blood work done and based on thosed findings sent to check up for surgery. Was sent to a larger hospital :30 minutes away call Hospital that surgery insert a stient into uritia vein from kidney to the blatter. Sent her home to take the prescribed antobotic 10 days and removal of the kidney stone on 05/25/2021. Kidney stone emergency room went into shock and because antibotic was

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shock
Hospital-Tage: 1,0
Labordaten: CT scan with contrast and did a chest x-ray, blood work done, surgery insert a stient into uritia vein from kidney to the blatter.
Aktuelle Erkrankungen: No
Vorgeschichte: Thyriod , Pre- Diabetic , Depression and Sleep Abpinia
Andere Medikamente: Levothyronine 50mg, Liothyronine 15mc, Bupropion xcl 150mg, once a days, Gapatentin 600mg per day, Metformin 500mg twice daily, Hormone replacement Estodiol 2mg, Progestone 400mg, Testirone Lipo derm, one click a day equavilent to 5mg
Allergien: Sulfa drugs, almond or spinach
Vorherige Impfungen: -

VAERS 2082611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 70,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 08.04.2021
Beginn: 30.01.2022
Tage bis Beginn: 297,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Hospitalisation Infection

Symptomtext

This patient was admitted to Hospital on 1/30/2022 for COVID related symptoms. This is considered a breakthrough case.

Weitere VAERSDATA-Felder

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

VAERS 2068568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NH
Alter: 65,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 11.05.2021
Beginn: 31.05.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: SYR / -

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

Dizziness Feeling hot Hyperhidrosis Loss of consciousness Seizure

Symptomtext

On 5/31/21 He had a seizure which lasted approximately 2 minutes. Myself (wife) and 2 friends witnessed the whole thing. He complained of being extremely hot and sweating profusely and extremely dizzy. He was unconscious for approx 8 or 9 minutes. I called the paramedics who took vitals and his blood pressure. By the time they got there, he was awake but still on the floor. They found nothing. They told him that his body had to ?reset?, whatever that means. He refused to go to the hospital since it was a holiday and didn?t want to spend the entire day there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vit D3, Lisinopril
Allergien: N/A
Vorherige Impfungen: -

VAERS 2065642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 12.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: - / RA

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

Pain Thrombosis

Symptomtext

On the 8th day I was not able to get out of bed, I had a lot of paint all over my body but the worse was on my both knees and joints. My husband had to carry me to the rest room to the living room. I when to the hospital where they told me I had to blood cloth on my both knees.

Weitere VAERSDATA-Felder

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

VAERS 2052237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 01.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

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

Malaise Presyncope Seizure Sinusitis Unresponsive to stimuli

Symptomtext

The facility was located in a parking garage. My daughter received the injection and we drove up to the 2nd floor to park and wait the 15 minutes for observation. Before we even parked she began not feeling well. As I was parking pulling in to park she said she felt like she was going to pass out. I told her to put her chair back and I parked. I got out to walk over to the passenger side of the car and when I opened her door she kicked out and hit me in the leg. When I looked inside the car she was having a seizure. She was arched back with her hands clenched in fists against her chest and her legs kicked out several times kicking under the dash. She was unresponsive and I called for the nurses on site. When I went to the backseat I continued calling her name and got no response. The nurses arrived and began calling her name. She then came out of the seizure. They checked her vitals and brought her juice. We stayed for an additional 30 minutes of observation. I mentioned this episode to a Dr at her Pediatrician's office and she said she had not heard of anyone having a seizure. My daughter recently was diagnosed with a sinus infection on 1/10/22 and I described this experience to her because I had my daughter scheduled for the booster. She advised me to report this and not have my daughter get the booster.

Weitere VAERSDATA-Felder

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

VAERS 2038470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 16.01.2022
Impfdatum: 26.12.2021
Beginn: 16.01.2022
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / LA

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

Intensive care Ischaemic stroke Thrombectomy

Symptomtext

acute ischemic stroke. pt was admitted to the ICU and is currently being treated. pt was taken emergently to IR for mechanical thrombectomy. also received alteplase.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: squamous cell carcinoma treated with radiation
Andere Medikamente: none known
Allergien: -
Vorherige Impfungen: -

VAERS 2034937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 11.06.2021
Beginn: 11.01.2022
Tage bis Beginn: 214,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Blood creatinine increased COVID-19 Dyspnoea Fatigue Haematocrit decreased Haemoglobin decreased Lung opacity Oxygen saturation decreased Pleural effusion Pneumonia Pulmonary oedema SARS-CoV-2 test positive Superinfection

Symptomtext

74 y.o. female admitted 1/11/2022 with PMH significant for COPD on 2 L home O2 continuously, diastolic CHF, chronic cor pulmonale, OSA, HTN, and dyslipidemia who presents to ED with complaint of shortness of breath. Patient notes she started feeling more tired and short of breath 2 or 3 weeks ago, similar to how she felt when she was diagnosed with CHF in 2002 with dyspnea on exertion and orthopnea. Yesterday, patient became increasingly short of breath and her daughter called her PCP to have her seen today. On the way to her appointment patient became extremely short of breath and her daughter brought her to the ED. Patient denies any known exposure to COVID-19 or other illness, cough, change in taste or smell, fever or chills, or N/V/D. Of note, she states she got her COVID booster yesterday, 1/10/2022, at pharmacy. In the ED, patient was placed on a nonrebreather at 10 L. No documentation of O2 sat on admission. CT angio was negative for PE, but did show mid and lower lung opacifications of bronchopneumonia superimposed upon interstitial pulmonary edema, trace left pleural effusion. Patient's COVID test came back positive. Of note, patient's creatinine is elevated at 1.24 beyond baseline of 0.95. She also has a low H&H, 9.6/31.8. During physical exam, patient desatted into the low 70s after talking and had to be placed back on nonrebreather after being on 5 L NC. She will be admitted to hospital medicine for further evaluation and treatment.

Weitere VAERSDATA-Felder

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

VAERS 2032271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 85,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 07.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Chest pain Computerised tomogram Lung disorder Thrombosis

Symptomtext

2 wks after the vaccine he started to not wanting to do anytime, lack of energy. He woke up one morning with knife sharp pains under his chest he went to the ER and found out he had blood clots in his lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: yes ct-scan
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 1519998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 51,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 15.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Abdominal discomfort Abdominal distension Chronic inflammatory demyelinating polyradiculoneuropathy Colonoscopy Condition aggravated Abdominal pain Abnormal loss of weight Ataxia Balance disorder Blood test Burning sensation Burns third degree Chest X-ray Computerised tomogram Computerised tomogram thorax Endoscopy Fall Guillain-Barre syndrome

Symptomtext

Determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse; Determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse; Had huge difficulty eating; felt super bloated like was going to explode; The caller could not feel hands or feet; lost 54 pounds since Apr2021; stomach has shrank; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 15Apr2021 09:30 (Lot number: EW0153) at the age of 51 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st dose of covid vaccine, Vaccine Name: Adult Pfizer Covid 19 Vaccine, Lot Number: ER8727, Expiry Date: Unknown, Anatomical Location: Right arm, No. of Previous Doses: First dose), administration date: 25Mar2021, when the patient was 50 years old, for COVID-19 Immunization, reaction(s): "The caller received the first dose Adult Pfizer Covid 19 Vaccine with zero effects"; Flu vaccine (Flu vaccine received a year and a half ago.), administration date: 2020, for Immunization. The following information was reported: CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY (medically significant), CONDITION AGGRAVATED (non-serious) all with onset 16Apr2021, outcome "not recovered" and all described as "Determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse"; EATING DISORDER (non-serious) with onset Apr2021, outcome "unknown", described as "Had huge difficulty eating"; ABDOMINAL DISTENSION (non-serious) with onset Apr2021, outcome "unknown", described as "felt super bloated like was going to explode"; FEELING ABNORMAL (non-serious) with onset Apr2021, outcome "unknown", described as "The caller could not feel hands or feet"; WEIGHT DECREASED (non-serious) with onset Apr2021, outcome "unknown", described as "lost 54 pounds since Apr2021"; ABDOMINAL DISCOMFORT (non-serious) with onset Apr2021, outcome "unknown", described as "stomach has shrank". The events "determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse", "determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse", "had huge difficulty eating", "felt super bloated like was going to explode", "the caller could not feel hands or feet", "lost 54 pounds since apr2021" and "stomach has shrank" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: colonoscopy: (2021) unknown results; endoscopy: (2021) unknown results; investigation: (16Apr2021) chronic inflammatory demyelinating polyneuropathy; (2021) neuropathy; nerve stimulation test: (16Apr2021) chronic inflammatory demyelinating polyneuropathy; weight: (Apr2021) lost 54 pounds. Therapeutic measures were taken as a result of chronic inflammatory demyelinating polyradiculoneuropathy, condition aggravated, eating disorder, abdominal distension, feeling abnormal, weight decreased. Clinical indication: Had huge difficulty eating: Had huge difficulty eating. The caller states this difficulty eating began in Apr2021 when the caller felt so bloated. The caller could not eat anything because would make feel more bloated. The caller had issues where did not eat for a while and stuff so the caller lost 54 pounds since Apr2021. The caller previously weighed 198 or 199 pounds. Had huge difficulty eating: The caller states the difficulty eating is still going on a little bit. The size of the callers stomach has shrank and the caller cannot eat as much food. DSU Agent asked if difficulty eating has improved, worsened or persisted and the caller replied a couple of callers friends force the caller to eat whether the caller is hungry or not. Thought the Adult Pfizer Covid 10 Vaccine would feel cold, the caller never recalled being cold: The caller also states Adult Pfizer Covid 19 Vaccine has to be stored at subzero temperatures. The caller thought the Adult Pfizer Covid 19 Vaccine would feel cold, the caller never recalled being cold. Maybe the Adult Pfizer Covid 19 Vaccine the caller received was left out too long. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): NO, the only vaccine the caller has received prior to the Adult Pfizer Covid 19 Vaccine was the Flu vaccine received a year and a half ago. Determined had neuropathy: On 16Apr2021, the day after the caller received the second dose Adult Pfizer Covid 19 Vaccine, the caller developed all kinds of medical issues that the caller first thought were gastric related. After every single possible test it was determined the caller had neuropathy. The caller went through a course of different testing, brain wave testing and secondary nerve testing. It was determined that the Adult Pfizer Covid 19 Vaccine caused the caller to have chronic inflammatory demyelinating polyneuropathy. GBS is acute and CIDP is chronic. Patient Assistance Octagam: The caller states the neurologist prescribed Octagam, which is a human immunoglobulin infusion. The caller goes three days in a row every month to receive the Octagam infusion for total of 9 months. The caller woke up the morning of 16Apr2021 and felt super bloated like was going to explode. The caller was sent to the gastroenterologist. The caller had a colonoscopy and endoscopy. The caller tried 15 different kinds of medicine, and nothing worked. The caller was told there was nothing more could be done for the caller and the caller had neuropathy. The caller could not feel hands or feet. The caller states the neuropath has gotten worse and worse. The caller tried 15 different kinds of medicine, and nothing worked; The caller states: Omeprazole, which is for heart burn gas release and stuff like that. The caller then says caller still takes Omeprazole sometimes and would prefer to not provide this information. Cholestyramine: Lot:2905684; expiration: 31Dec2021. The caller states has not taken Cholestyramine in a while. Dose: 1 packet by mouth twice a day, supposed to help break down food, 9 gram pouch, 60 packet count. Was to take two a day for a months supply. Creon:36,000 unit capsule, take two capsules by mouth with each meal, one by mouth with each snack, count: 500,lot: 1142090; Expiration: 14Dec2022 Ondansetron: 4mg tablet, 15 lot: unknown, medication in a bottle from the pharmacy, Expiration: 21Jun2022 Cefalexin: 500mg capsule, the label is worn off here but looks like 30 count. Label is part worn off and does not know if was wet or not, cannot read information. Unable to provide NDC/lot/expiration. The medication is in a bottle from the pharmacy. Clindamycin: 300mg capsule/ 1 by mouth 3 times daily, 30 count, Expiration: 22Jul2022 Pantoprazole DR: 40mg tablet, 30 count, instructions to take 1 tablet per day ,Expiration: 21Jun2022 Gabapentin: 600mg, takes three times a day :indication: DSU Agent asked indication and caller stated supposed to take 1 in morning and 1 in middle of day and one at bed time ,began taking: Jun2021 ,expiration: 22Nov2022 Dicyclomine: 10mg capsule, 30 count. Supposed to take 1 by mouth four times a day as needed, expiration: 12Nov2022 Sucralfate: 1gm tab, count size 60 ,supposed to take 1 tablet twice a day on empty stomach ,expiration: 16Jun2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Colonoscopy; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: Endoscopy; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210416; Test Name: Brain Wave testing; Result Unstructured Data: Test Result:chronic inflammatory demyelinating Polyneuropathy; Test Date: 2021; Test Name: every single possible test; Result Unstructured Data: Test Result:neuropathy; Test Date: 20210416; Test Name: Secondary Nerve Testing; Result Unstructured Data: Test Result:chronic inflammatory demyelinating Polyneuropathy; Test Date: 202104; Test Name: Weight; Result Unstructured Data: Test Result:lost 54 pounds
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1519998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 51,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 15.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / RA

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

Abdominal discomfort Abdominal distension Chronic inflammatory demyelinating polyradiculoneuropathy Colonoscopy Condition aggravated Abdominal pain Abnormal loss of weight Ataxia Balance disorder Blood test Burning sensation Burns third degree Chest X-ray Computerised tomogram Computerised tomogram thorax Endoscopy Fall Guillain-Barre syndrome

Symptomtext

Determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse; Determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse; Had huge difficulty eating; felt super bloated like was going to explode; The caller could not feel hands or feet; lost 54 pounds since Apr2021; stomach has shrank; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 15Apr2021 09:30 (Lot number: EW0153) at the age of 51 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st dose of covid vaccine, Vaccine Name: Adult Pfizer Covid 19 Vaccine, Lot Number: ER8727, Expiry Date: Unknown, Anatomical Location: Right arm, No. of Previous Doses: First dose), administration date: 25Mar2021, when the patient was 50 years old, for COVID-19 Immunization, reaction(s): "The caller received the first dose Adult Pfizer Covid 19 Vaccine with zero effects"; Flu vaccine (Flu vaccine received a year and a half ago.), administration date: 2020, for Immunization. The following information was reported: CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY (medically significant), CONDITION AGGRAVATED (non-serious) all with onset 16Apr2021, outcome "not recovered" and all described as "Determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse"; EATING DISORDER (non-serious) with onset Apr2021, outcome "unknown", described as "Had huge difficulty eating"; ABDOMINAL DISTENSION (non-serious) with onset Apr2021, outcome "unknown", described as "felt super bloated like was going to explode"; FEELING ABNORMAL (non-serious) with onset Apr2021, outcome "unknown", described as "The caller could not feel hands or feet"; WEIGHT DECREASED (non-serious) with onset Apr2021, outcome "unknown", described as "lost 54 pounds since Apr2021"; ABDOMINAL DISCOMFORT (non-serious) with onset Apr2021, outcome "unknown", described as "stomach has shrank". The events "determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse", "determined had neuropathy/chronic inflammatory demyelinating polyneuropathy/neuropath has gotten worse and worse", "had huge difficulty eating", "felt super bloated like was going to explode", "the caller could not feel hands or feet", "lost 54 pounds since apr2021" and "stomach has shrank" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: colonoscopy: (2021) unknown results; endoscopy: (2021) unknown results; investigation: (16Apr2021) chronic inflammatory demyelinating polyneuropathy; (2021) neuropathy; nerve stimulation test: (16Apr2021) chronic inflammatory demyelinating polyneuropathy; weight: (Apr2021) lost 54 pounds. Therapeutic measures were taken as a result of chronic inflammatory demyelinating polyradiculoneuropathy, condition aggravated, eating disorder, abdominal distension, feeling abnormal, weight decreased. Clinical indication: Had huge difficulty eating: Had huge difficulty eating. The caller states this difficulty eating began in Apr2021 when the caller felt so bloated. The caller could not eat anything because would make feel more bloated. The caller had issues where did not eat for a while and stuff so the caller lost 54 pounds since Apr2021. The caller previously weighed 198 or 199 pounds. Had huge difficulty eating: The caller states the difficulty eating is still going on a little bit. The size of the callers stomach has shrank and the caller cannot eat as much food. DSU Agent asked if difficulty eating has improved, worsened or persisted and the caller replied a couple of callers friends force the caller to eat whether the caller is hungry or not. Thought the Adult Pfizer Covid 10 Vaccine would feel cold, the caller never recalled being cold: The caller also states Adult Pfizer Covid 19 Vaccine has to be stored at subzero temperatures. The caller thought the Adult Pfizer Covid 19 Vaccine would feel cold, the caller never recalled being cold. Maybe the Adult Pfizer Covid 19 Vaccine the caller received was left out too long. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): NO, the only vaccine the caller has received prior to the Adult Pfizer Covid 19 Vaccine was the Flu vaccine received a year and a half ago. Determined had neuropathy: On 16Apr2021, the day after the caller received the second dose Adult Pfizer Covid 19 Vaccine, the caller developed all kinds of medical issues that the caller first thought were gastric related. After every single possible test it was determined the caller had neuropathy. The caller went through a course of different testing, brain wave testing and secondary nerve testing. It was determined that the Adult Pfizer Covid 19 Vaccine caused the caller to have chronic inflammatory demyelinating polyneuropathy. GBS is acute and CIDP is chronic. Patient Assistance Octagam: The caller states the neurologist prescribed Octagam, which is a human immunoglobulin infusion. The caller goes three days in a row every month to receive the Octagam infusion for total of 9 months. The caller woke up the morning of 16Apr2021 and felt super bloated like was going to explode. The caller was sent to the gastroenterologist. The caller had a colonoscopy and endoscopy. The caller tried 15 different kinds of medicine, and nothing worked. The caller was told there was nothing more could be done for the caller and the caller had neuropathy. The caller could not feel hands or feet. The caller states the neuropath has gotten worse and worse. The caller tried 15 different kinds of medicine, and nothing worked; The caller states: Omeprazole, which is for heart burn gas release and stuff like that. The caller then says caller still takes Omeprazole sometimes and would prefer to not provide this information. Cholestyramine: Lot:2905684; expiration: 31Dec2021. The caller states has not taken Cholestyramine in a while. Dose: 1 packet by mouth twice a day, supposed to help break down food, 9 gram pouch, 60 packet count. Was to take two a day for a months supply. Creon:36,000 unit capsule, take two capsules by mouth with each meal, one by mouth with each snack, count: 500,lot: 1142090; Expiration: 14Dec2022 Ondansetron: 4mg tablet, 15 lot: unknown, medication in a bottle from the pharmacy, Expiration: 21Jun2022 Cefalexin: 500mg capsule, the label is worn off here but looks like 30 count. Label is part worn off and does not know if was wet or not, cannot read information. Unable to provide NDC/lot/expiration. The medication is in a bottle from the pharmacy. Clindamycin: 300mg capsule/ 1 by mouth 3 times daily, 30 count, Expiration: 22Jul2022 Pantoprazole DR: 40mg tablet, 30 count, instructions to take 1 tablet per day ,Expiration: 21Jun2022 Gabapentin: 600mg, takes three times a day :indication: DSU Agent asked indication and caller stated supposed to take 1 in morning and 1 in middle of day and one at bed time ,began taking: Jun2021 ,expiration: 22Nov2022 Dicyclomine: 10mg capsule, 30 count. Supposed to take 1 by mouth four times a day as needed, expiration: 12Nov2022 Sucralfate: 1gm tab, count size 60 ,supposed to take 1 tablet twice a day on empty stomach ,expiration: 16Jun2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Colonoscopy; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: Endoscopy; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210416; Test Name: Brain Wave testing; Result Unstructured Data: Test Result:chronic inflammatory demyelinating Polyneuropathy; Test Date: 2021; Test Name: every single possible test; Result Unstructured Data: Test Result:neuropathy; Test Date: 20210416; Test Name: Secondary Nerve Testing; Result Unstructured Data: Test Result:chronic inflammatory demyelinating Polyneuropathy; Test Date: 202104; Test Name: Weight; Result Unstructured Data: Test Result:lost 54 pounds
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2013714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 14.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

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

Syncope

Symptomtext

Syncope after 2nd dose the following day, no seizure, no trauma sustained

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypothyroid
Vorgeschichte: hypothyroidism
Andere Medikamente: focalin, sertraline, spironolactone and minocycline (for acne) and unithroid
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1997996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 60,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 03.05.2021
Beginn: 24.12.2021
Tage bis Beginn: 235,0
Dosis: 1
Route/Site: SYR / -

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

Fatigue Intensive care Polymerase chain reaction positive Pyrexia Somnolence

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1997956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: ID
Alter: 18,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 19.04.2021
Beginn: 03.06.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: - / RA

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

Heart rate increased Laboratory test Syncope Tachycardia

Symptomtext

Fainted after second dose of vaccine, on April 19, 2021 treated by on-site paramedic. Was referred to Emergency Room. On June 3, 2021 after noticing an abnormally high heart rate I went to an Urgent Care clinic. The attending physician immediately sent me to the local Emergency Room. I was admitted, and the ER and the Dr and staff ran a multitude of tests, including those to determine enlarged heart, blood clots, etc. that might be associated with the Pfizer COVID-19 vaccine. I was discharged without a definitive diagnosis and was referred to my general physician with The Clinic. Dr. ordered a heart monitor, and she prescribed Propranolol, but that did not work, so a few weeks later, Dr. prescribed Metoprolol, which I have been on for the past 6 months. I am now living in another area and since my condition has not improved, my GP has referred me to a Cardiac Specialist with a local health care facility. PLEASE NOTE: The sticker that the Vaccine clinic placed on my COVID-19 Vaccination Record Card has two overlapping Pfizer Lot numbers! I have a photo of the card if you would like to see it. So I really don't know which lot number I received for my second dose on April 19, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 1,0
Labordaten: Admitted to Emergency Room on June 3, 2021 for excessively high heart rate that was detected by clinic Urgent Care Provider.
Aktuelle Erkrankungen: none
Vorgeschichte: NONE at the time of vaccine, 5 weeks after the Pfizer second dose Tachycardia was diagnosed in the Emergency Room
Andere Medikamente: none
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1989327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: VA
Alter: 52,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 10.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Blood test normal Chest discomfort Computerised tomogram normal Electrocardiogram normal Facial paralysis Hypoaesthesia Magnetic resonance imaging abnormal Muscular weakness Pain Urine analysis normal X-ray normal

Symptomtext

After week 2 after the vaccination, I felt pain, chest tightness, and numbness. (04/26) Went to Urgent care and had a urine test to see if it was a kidney stone (normal) and without finding anything they referred me to ER. There they took EKG, CT scan, X-Ray, and Blood panel and did not find any reason for the pain or numbness. No treatments and only one pill for the pain in office. 05/01 Had a new issue where it seems I was having some kind of stroke. Returned to ER and after a physical and MRI and found it was Bell's Palsy. Advised a set of massage exercises to restore face droop on right side. As of 12/29 still have muscle issues on right side of face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 04/26 EKG(normal), CT scan(normal), X-Ray(normal), Blood panel(normal) 05/01 MRI(Confirmed Bell's Palsy)
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal Allergy
Andere Medikamente: Lisinopril, Tylenol, B-12, Spring Valley MultiVitamin, Centrum for Men
Allergien: NKA
Vorherige Impfungen: -

VAERS 1981100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 27,0
Geschlecht: F
Eingang: 26.12.2021
Impfdatum: 04.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RL

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

Blood test normal Chest discomfort Condition aggravated Discomfort Dizziness Echocardiogram abnormal Electrocardiogram normal Hypertension Loss of consciousness Malaise Palpitations Supraventricular tachycardia Tremor Vertigo

Symptomtext

I have been experienceing pressure, discomfort, tightness in the chest since the second vaccination. I passed out with extreme vertigo and my vitals dropped right after the second shot, then went to the hospital, and I was sick for 5 days afterwards. I have had ongoing issues with irregularly high blood pressure and heavy palpitations, feeling very dizzy, shaking, and periodic severe discomfort.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -EKG normal -Echo Cardiogram: SVT Supraventrical tachycardia -Bloodwork Negative
Aktuelle Erkrankungen: vertigo lightheaded chest discomft pain pressure passing out fainting palpatations congenital heart defect vitals drop and spike
Vorgeschichte: congenital heart defect arrythmia tachycardia right bundle branch block vertigo epilepsy cpti autoimmimune d asthma
Andere Medikamente: no
Allergien: dairy v
Vorherige Impfungen: -

VAERS 1919663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

schwer

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 12.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Asthenia Cardiac disorder Fatigue Feeling abnormal Gastrointestinal disorder Illness Lung disorder Migraine SARS-CoV-2 test Syncope Vomiting

Symptomtext

Fainting; Weakness beyond control; Migraines; puking; Heart issues; Brain fog; Digestive issues; Major fatigue; Lung problems; Sick all the time; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 12Apr2021 10:00 (Lot number: Ew0153) at the age of 50 years as dose 2, single and administration date 12Mar2021 10:00 (Lot number: Er2613) as dose1, single for covid-19 immunisation. Relevant medical history included: "Rheumatoid arthritis failed c spine surgery" (unspecified if ongoing). No known allergies. Concomitant medication(s) included: LEVOTHYROXINE SODIUM; VALACYCLOVIR HCL; FLUOXETINE. Other medications in two weeks also included Clariti (unspecified). No other vaccine in four weeks. The following information was reported: SYNCOPE (disability, medically significant), outcome "not recovered", described as "Fainting"; ASTHENIA (disability, medically significant), outcome "not recovered", described as "Weakness beyond control"; MIGRAINE (disability, medically significant), outcome "not recovered", described as "Migraines"; VOMITING (disability, medically significant), outcome "not recovered", described as "puking"; CARDIAC DISORDER (disability, medically significant), outcome "not recovered", described as "Heart issues"; FEELING ABNORMAL (disability, medically significant), outcome "not recovered", described as "Brain fog"; GASTROINTESTINAL DISORDER (disability, medically significant), outcome "not recovered", described as "Digestive issues"; FATIGUE (disability, medically significant), outcome "not recovered", described as "Major fatigue"; LUNG DISORDER (disability, medically significant), outcome "not recovered", described as "Lung problems"; ILLNESS (disability, medically significant), outcome "not recovered", described as "Sick all the time". The events "fainting", "weakness beyond control", "migraines", "puking", "heart issues", "brain fog", "digestive issues", "major fatigue", "lung problems" and "sick all the time" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: negative, notes: Blood n nasal test. Therapeutic measures were taken as a result of syncope, asthenia, migraine, vomiting, cardiac disorder, feeling abnormal, gastrointestinal disorder, fatigue, lung disorder, illness. Ae treatment: They can't figure me out she was a hot mess. The patient had no covid prior vaccination. Ae resulted in: Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Disability or permanent damage].

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Nasal swab; Test Result: Negative ; Comments: Blood n nasal test
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Rheumatoid arthritis
Andere Medikamente: LEVOTHYROXINE SODIUM; VALACYCLOVIR HCL; FLUOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 1887751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 48,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 21.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Fatigue Feeling abnormal Impaired driving ability Loss of consciousness Loss of personal independence in daily activities Myalgia Pain Pelvic pain Weight Weight increased

Symptomtext

did errands, a minor portion of what she would normally do, and just collapsed afterwards; Achy/Everything hurts/Overall body aches; Unable to drive; walking either up or down her stairs and felt like she had been horseback riding for a week/was a wreck; had just done the worst leg day ever, everything in her pelvis and her gluteus maximus aches; had just done the worst leg day ever, everything in her pelvis and her gluteus maximus aches; Has gained 15-20 pounds; literally does not leave the house/did errands, a minor portion of what she would normally do, and just collapsed afterwards; Too fucking tired to go to the doctor; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient received BNT162b2 (Pfizer BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number: EW0153, Expiration date and NDC number was unknown), via an unspecified route of administration, administered in right arm on 21Apr2021 as dose 2, single (at the age of 48-year-old) for COVID-19 immunization. Patient medical history included some neurological things (other than some neurological things she was perfectly healthy, fit, and very active prior to these events). No further information provided by the caller on the neurological things she has mentioned. Patient had no relevant family medical history. Patient had no prior vaccinations (within 4 weeks). Patient had no additional vaccines administered on same date of the Pfizer suspect. Historical vaccine included patient received BNT162b2 (Pfizer BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number: ER8732, Expiration date and NDC number was unknown), via an unspecified route of administration on 31Mar201 as dose 1, single (at the age of 48-year-old) for COVID-19 immunization and stated she was fine. The patient concomitant medications included unspecified medications she has unspecified medications, but they were not relevant to these events. Patient stated that prior to the second vaccine, patient was healthy and active. On 22Apr2021, right after the second dose, the next day, patient had been achy, unable to drive, she does not go anywhere, and everything hurts, was walking either up or down her stairs and felt like she had been horseback riding for a week, had just done the worst leg day ever, everything in her pelvis and her gluteus maximus aches. Patient stated that particular pain comes and goes, but the overall body aches were consistent. Patient used to be 140 pounds and has gained between 15-20 pounds. Patient stated that she orders groceries and cooks for her family, even big pots were too much for her and stated that she literally does not leave the house. Patient stated that she left one week ago, last Friday (13Aug2021), and did some errands, patient stated that she did just a minor portion of what she would normally do and just collapsed afterwards. Patient stated that she was too fucking tried to go to the doctor and just drags from one pair of pajamas to the next. Patient stated that her girlfriend was with her today (20Aug2021) and patient has been being told that she needs to at least call and report her symptoms. Patient stated that she does not look like herself, she was a wreck, and she was not even fucking joking, stated before this she was healthy. Patient had no emergency room and physician office visit for the events. No relevant tests were performed for the events. Patient stated that she was in the process of getting a new primary care provider since hers was so lazy and stated that she had a new one lined up, but when she went for her appointment, they had retired. The outcome of did errands, a minor portion of what she would normally do, and just collapsed afterwards was unknown and not recovered for rest of the events. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210422; Test Name: Weight; Result Unstructured Data: Test Result:Has gained 15-20 pounds; Comments: Increased
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Neurological disorder NOS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1876418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CT
Alter: 53,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 12.04.2021
Beginn: 08.05.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: SYR / LA

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

5-hydroxyindolacetic acid in urine Activated partial thromboplastin time Activated protein C resistance test Angiogram Angiogram cerebral Antinuclear antibody Antiphospholipid antibodies Antithrombin III Aphasia Beta-2 glycoprotein antibody Blood chromogranin A Blood cortisol Blood fibrinogen Blood glucose Blood homocysteine Blood iron Blood magnesium Blood osmolarity

Symptomtext

Ischaemic stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 2,0
Labordaten: May 21, 2021: Osmolatiy, urine; urea nitrogen, urine, random; creatinine, random urine; sodium, random urine w/o creat; tpe and RH recheck; CBC with auto differential; basic metabolic panel; 9 drug toxicology panel, urine, No Conf. (YH); Type & screen; hepatic function panel; POCT perform urine pregnancy; MRI brain W WO IV Contrast; COVID Testing- Viral RNA (PCR/NAAT); Basic Metabolic Panel; osmolality; troponin T; May 22, 2021: troponin T; CTA Head Neck W and/or WO IV Contrast; Lipid panel; TSH, 3rd generation w/Reflex to FT4; Troponin T; LDL cholestoerol, direct; cortisol; comprehensive metabolic panel; CBC with auto differential; hemoglobin A1C; post glucose; Echo 2D complete Bubble Study w Doppler and CFI if Ind Image Enhancement and or 3D; post glucose; protein C activity; antithrombin activity; activated protein C resistance; Lupus anticoagullant; homocysteine; cardiolipin AB (IgA, IgA, IgM); Beta-2 glycoprotein 1 ABS, IGG, IGA. IGM; ANA IFA Screen W/ REFL to Titer and Pattern, IFA; sodium; ANA Titer and Pattern W/RFLX (BH GH); special coagulation MD interpretation (Lab Oderable only) (GH YH); partial thromboplastin time; Protime and INR; Protein S Activity; sodium May 23, 2021: Basic Metabolic panel; magnesium; CBC Without Differential; sodium June 8, 2021: US LT Dop Upper extremity venous July 28, 2021: Factor VII Activity; 5 HIAA nQuantitative, urine, random w/creatinine (BH GH L Q NH); chromogranin A; ferritin; iron & TIBC; fibrinogen; c reactive protein (CRP); sedimentation Rate (ESR); extractable Nuclear antigen ABS Group; Factor IX activity; Factor XI activity; Factor XII activity; PT/INR and PTT (BH GH L YH); prothrombin gene mutation; special coagulation MD interpretation (lab orderable only) (GH YH); Von Wilebrand Factor Antigen; July 31, 2021: 5-HIAA (Serotonin), urine, 24 hour; pancreatic elastase, fecal; ova and parasite *There are additional tests, including heart monitor, additional GI tests, additional bloodwork for hematology; additional bloodwork for immunology, but this form won't allow me to add them in. Form auto-adjusts back to the top of this section each time that I try to add in additional tests. **Item #5: ischaemic stroke may have occurred prior to 5/8/2021; I had commonly reported adverse events following the first and second does of the COVID-19 vaccine, most notably fatigue, but also some body aches, small fever. Sometime after the second dose (within the week of May 2, 2021), I got a headache that lasted for one week that I didn't realize may have been connected to the vaccine. It was accompanied by pain in or around my eye and sometimes with difficulty with vision. Therafter, I experienced extreme fatigue, difficulty with organizing thought and word finding; gross motor flailing (uncontrolled movements), and fine motor control issues when cocentrating that would result in larger uncontrolled gross motor movements.
Aktuelle Erkrankungen: None
Vorgeschichte: IBS, Hypogammaglobulinemia IgA and IgG
Andere Medikamente: occasional vitamins (daily, iron)
Allergien: Shellfish
Vorherige Impfungen: commonly reported fever, chills, body aches; 53 yrs.; 02/08/2021; Shingrix MCG Intramuscular Susp. Rec.

VAERS 1870704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 13.05.2021
Beginn: 08.09.2021
Tage bis Beginn: 118,0
Dosis: 1
Route/Site: ID / LA

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

Anticoagulant therapy Anxiety Blood test Chest X-ray Deep vein thrombosis Emotional distress Impaired work ability Thrombosis Ultrasound scan

Symptomtext

Blood clot that turned into DVT and PE on 09/24/2021 was admitted into hospital for 2 days. Blood thinniers -Eloquis. Lost of wages. Emotional, mental, physical duress and angusih due to the configuration of my leg. I will never be normal again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 2,0
Labordaten: ultrasounds, chest xrays, blood work
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1868405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 57,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 01.05.2021
Beginn: 01.10.2021
Tage bis Beginn: 153,0
Dosis: 1
Route/Site: IM / LA

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

Chest pain Painful respiration Pericarditis

Symptomtext

5 months after 2nd dose, I had mild symptom of pericarditis that lasted about 3 hours. Mild, constant sharp pain on left side of chest while inhaling. Took acetaminophen and pain subsided and did not reoccur. Self-diagnosed and treated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Losartan 25mg Allopurinol 100mg
Allergien: None
Vorherige Impfungen: -

VAERS 1354841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Anaphylactic reaction Heart rate Swollen tongue Chest discomfort Lip swelling

Symptomtext

she experienced anaphylactic reaction as her tongue swelled; she experienced anaphylactic reaction as her tongue swelled; This is a spontaneous report from a contactable consumer (patient). A 58-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 12Apr2021 (9:30 am or 10:00 am ) (Batch/Lot Number: EW0153) age at vaccination of 58-years-old, as single dose, for covid-19 immunisation. Medical history included ongoing asthma, coccidioidomycosis from an unknown date and unknown if ongoing, scar from an unknown date and unknown if ongoing (lungs are scared), tachycardia from an unknown date and unknown if ongoing (Fast resting heartrate). The patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 22Mar2021 (Batch/Lot Number: EN6207) age at vaccination of 58-years-old, as single dose, for covid-19 immunisation. Concomitant medication included metoprolol succinate (TOPROL) taken for tachycardia from an unspecified start date and ongoing. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient stated that, on 12Apr2021,15-20 minutes after getting the second dose of the vaccine, she experienced anaphylactic reaction as her tongue swelled. The event did not result in emergency room nor physician Office visit. She had to get a Benadryl shot and they were measuring her heartrate. The patient recovered from anaphylactic reaction on 12Apr2021 while outcome of swollen tongue was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: heartrate; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Medical History/Concurrent Conditions: Scar (lungs are scared); Tachycardia (Fast resting heartrate); Valley fever
Andere Medikamente: TOPROL
Allergien: -
Vorherige Impfungen: -

VAERS 1354841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Heart rate Swollen tongue Chest discomfort Lip swelling

Symptomtext

she experienced anaphylactic reaction as her tongue swelled; she experienced anaphylactic reaction as her tongue swelled; This is a spontaneous report from a contactable consumer (patient). A 58-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 12Apr2021 (9:30 am or 10:00 am ) (Batch/Lot Number: EW0153) age at vaccination of 58-years-old, as single dose, for covid-19 immunisation. Medical history included ongoing asthma, coccidioidomycosis from an unknown date and unknown if ongoing, scar from an unknown date and unknown if ongoing (lungs are scared), tachycardia from an unknown date and unknown if ongoing (Fast resting heartrate). The patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 22Mar2021 (Batch/Lot Number: EN6207) age at vaccination of 58-years-old, as single dose, for covid-19 immunisation. Concomitant medication included metoprolol succinate (TOPROL) taken for tachycardia from an unspecified start date and ongoing. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient stated that, on 12Apr2021,15-20 minutes after getting the second dose of the vaccine, she experienced anaphylactic reaction as her tongue swelled. The event did not result in emergency room nor physician Office visit. She had to get a Benadryl shot and they were measuring her heartrate. The patient recovered from anaphylactic reaction on 12Apr2021 while outcome of swollen tongue was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: heartrate; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Medical History/Concurrent Conditions: Scar (lungs are scared); Tachycardia (Fast resting heartrate); Valley fever
Andere Medikamente: TOPROL
Allergien: -
Vorherige Impfungen: -

VAERS 1804232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 16.04.2021
Beginn: 03.08.2021
Tage bis Beginn: 109,0
Dosis: 2
Route/Site: SYR / LA

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

Agitation Blood test Breast pain Chest X-ray Dizziness Electrocardiogram Hypertension Hypoaesthesia Impaired work ability Pain in extremity Thrombosis Ultrasound scan

Symptomtext

On August 3, 2021 - I awoke feeling light headed and dizzy. I felt very agitated. The agitation would not subside. I went and had breakfast and got ready for work. By 10:00 am I decided it was not usual for me. I had pain in the upper right arm and my hand was numb. I went to the ER to report the symptoms. Several tests were done. Blood clot in my upper right arm - on that same day 8-3. I had never had a blood clot before. I had never high blood pressure before. It was bouncing over150/and over 90 for the bottom number. I usually have low blood pressure. I felt it. They gave me baby aspirin and oral blood thinners. They asked me to return to another office when they realized it was not heart attack. I had follow up appt with doctor at 8/6/2021 - I was given Xarelto 20 mg twice a day and Lisinopril (20 mg) with Hydrochlorothiazide - 12.5 mg - one tablet a day. 14 days later, Prescription was changed. Reduced Xarelto to 15 mg and once a day; and kept the Lisinopril the same. I am still taking these now. Low salt; low carb (DASH) diet; drink water every day. I am going to the restroom a lot. I was feeling better this week, I was watching the Dodger game and I could feel additional pains on my right breast and my blood pressure went up 159/80 and then it would drop to 135 with exercise a lot of water a lot of rest. I am restricted from driving distance and from travel right now. I am not working anymore. I had to retire due to the stress of my job and this adverse event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: ER - Blood tests - to look for the chemical whether I had a heart attack or not; they did a Scan; electro-cardiogram; chest xray; Subsequently, they put me in the donut to look at my lungs to see if they were clear and then an ultrasound of my arm. They found only the blockage in my right arm. No additional blockages.
Aktuelle Erkrankungen: no
Vorgeschichte: Overweight (have lost weight since the diagnosis); pre-diabetic
Andere Medikamente: no
Allergien: Codeine - nausea
Vorherige Impfungen: -

VAERS 2638060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 36,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Full blood count normal Laboratory test normal Liver function test normal Syncope Tinnitus

Symptomtext

Narrative: Several minutes after receiving the first Covid vaccination patient felt hot heard ringing in the ears and felt like he was going to pass out. Patient informed staff and they put him on a stretcher and transported him to the Emergency Room. Patient did not pass out and his symptoms passed quickly after lying down. Patient history and physical consistent with vasovagal/neurocardiogenic syncope. He was observed in ED for resolution of symptoms. He remained stable and was discharged home. Impression - Neurocardiogenic syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: September 27, 2021 CBC, Chem 19 & LFTs all WNL.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1783412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: GA
Alter: 41,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 21.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Fear Hypoaesthesia Injection site pain Mobility decreased Monoplegia Paralysis Pyrexia

Symptomtext

About 8-10 hours after 2 nd dose , I had normal soreness at injection site but then developed high fever 104.2 , chills , and my left hand was stuck in bent position, I was unable to use my left hand it was completely numb for 2 days . Very scary felt like I was paralyzed on the left arm and hand .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: N/A
Vorherige Impfungen: -

VAERS 1768250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 07.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / AR

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

Computerised tomogram abnormal Knee operation Syncope Thyroid mass Thyroid operation

Symptomtext

I had knee surgery and fainted after it. I had to get a CAT scan to rule out blood clots and they found I had a mass on the right side of my thyroid. It was about 5.7cm and it grew to like 6.4cm by the time it was taken out. I had the surgery on Monday 10/4/2021. They also did blood work to figure out to see if the rest of my thyroid is functional. Right now I am on pain management.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: CAT scan- mass on the right side of my thyroid.
Aktuelle Erkrankungen: None
Vorgeschichte: PTSD; Fibromyalgia; Depression; Arthritis
Andere Medikamente: Hydrochlorothiazide; Allergy medicine; Tramadol; Magnesium; Vitamin D; Mix vitamins.
Allergien: Bee venom; Contrast dye
Vorherige Impfungen: -

VAERS 1453781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Acupuncture Blood test abnormal Burning sensation Fibrin D dimer increased Formication Deep vein thrombosis Immune system disorder Limb discomfort Synovial cyst Tinnitus Headache Hemiparesis Hypertension Inflammation Insomnia Migraine Muscle contractions involuntary Muscle spasms

Symptomtext

Sudden throbbing calf pain, muscle spasms, fasciculations, tinnitus, migraine, eyes out of focus, vibrating of left side of body with burning sensation in feet and toes. Sudden feeling of popcorn popping all over body in veins. Internal vibrations continue 5 months later on left side, tremor in left hand and weakness in left arm and left leg. Left side of head hurts frequently--feeling of worms crawling in there and pain to the touch. Insomnia is awful.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Numerous blood tests showing very high inflammation, high blood pressure, kidney dysfunction, so many things ! 9/7 Ultrasound for DVT on 4/20. High d-dimer and possible micro clotting of blood. Telehealth call diagnosed me with Small Fiber Neuropathy, New neurologist locally put me on Gabapentin. Continued High inflammation is consistent with MCAS and being treated with antihistamines and acupuncture.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism and Diabetes Insipidus
Andere Medikamente: Synthroid, Cytomel and Desmopressin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1453781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Acupuncture Blood test abnormal Burning sensation Fibrin D dimer increased Formication Deep vein thrombosis Immune system disorder Limb discomfort Synovial cyst Tinnitus Headache Hemiparesis Hypertension Inflammation Insomnia Migraine Muscle contractions involuntary Muscle spasms

Symptomtext

Sudden throbbing calf pain, muscle spasms, fasciculations, tinnitus, migraine, eyes out of focus, vibrating of left side of body with burning sensation in feet and toes. Sudden feeling of popcorn popping all over body in veins. Internal vibrations continue 5 months later on left side, tremor in left hand and weakness in left arm and left leg. Left side of head hurts frequently--feeling of worms crawling in there and pain to the touch. Insomnia is awful.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Numerous blood tests showing very high inflammation, high blood pressure, kidney dysfunction, so many things ! 9/7 Ultrasound for DVT on 4/20. High d-dimer and possible micro clotting of blood. Telehealth call diagnosed me with Small Fiber Neuropathy, New neurologist locally put me on Gabapentin. Continued High inflammation is consistent with MCAS and being treated with antihistamines and acupuncture.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism and Diabetes Insipidus
Andere Medikamente: Synthroid, Cytomel and Desmopressin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1741497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AR
Alter: 61,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 27.04.2021
Beginn: 27.05.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Condition aggravated Dyspnoea Fatigue Lymph node pain Lymphadenopathy Pericarditis Pyrexia

Symptomtext

I have a history of Recurrent Idiopathic Pericarditis. On Thursday, 05/27/2021, thirty days after receiving the 2nd COVID-19 vaccine, I started having symptoms of pericarditis which included shortness of breath, pain in center of chest (worse when lying down), fatigue, and fever of 99.8. I started taking Advil and Tylenol, and quit treadmill exercising. On Tuesday, 06/01/2021, symptoms had not improved--I restarted the Recurrent Idiopathic Pericarditis Treatment Protocol--800mg Ibuprofen 3 times daily for 2-4 weeks for recurrence, Colchicine 0.6mg daily for 6 months for recurrence, and a proton pump inhibitor for gastric protection. (See Continuation Page) I visited my Cardiologist on Wednesday, 06/02/2021--no labs were drawn since this was my 7th episode of recurrent idiopathic pericarditis in three years, and the symptoms were not severe compared to my last episode of pericarditis, The symptoms resolved within 2 weeks of treatment. Addendum: I also had swollen lymph nodes under both arms and a very large painful/swollen lymph node under the right arm (the first vaccine dose was given in the right arm). The lymph noted swelling starting approximately 4-5 days after the first COVID vaccine. The lymph nodes were still swollen when I received the second vaccine dose 21 days later--therefore, I decided to receive the second dose in the opposite arm (my left arm). The lymph nodes remained swollen for weeks after the second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Recurrent Idiopathic Pericarditis
Andere Medikamente: Levothyroxine, Lipitor, Centrum Silver MVI, Vitamin D3
Allergien: Sulfa drugs, Neomycin, Bacitracin
Vorherige Impfungen: -

VAERS 1694843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 10.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: - / LA

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

Blood pressure measurement Blood test Computerised tomogram Heart rate decreased Heparin resistance Cardiac monitoring Cytogenetic analysis Echocardiogram Electrocardiogram Hypotension Magnetic resonance imaging Portal vein embolism Ultrasound scan Portal vein thrombosis SARS-CoV-2 test

Symptomtext

Blood clot in left portal vein to liver.; Low blood pressure; slowed heart rate; This is a spontaneous report from a contactable consumer (patient). A 32-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 10Apr2021 15:30 (Batch/Lot Number: EW0153) (at the age of 32 years) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included hypothyroidism from an unknown date and unknown if ongoing. There were no known allergies. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1, administered in Arm Left on 20Mar2021 04:30 PM (Batch/Lot Number: PAA165969) (at the age of 32 years) for covid-19 immunisation. There was no other vaccine in four weeks. There was no other medication in two weeks. The patient's concomitant medications were none. The patient experienced blood clot in left portal vein to liver, low blood pressure, slowed heart rate, all on 16Apr2021 04:00. The outcome of events was recovered. The patient was hospitalized for 7 days. Events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization. The events required treatment (Mri, ct scan, ultrasound, heparin drip, blood test, as reported). There was no COVID prior vaccination. Patient was tested for COVID (Nasal swab) on 05May2021 with test results of negative. The patient underwent lab tests and procedures which included blood pressure measurement: unknown, blood test: unknown, computerised tomogram: unknown, heparin resistance: unknown, magnetic resonance imaging: unknown, sars-cov-2 test: negative, ultrasound scan: unknown, all on 05May2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Portal vein embolism
Hospital-Tage: 7,0
Labordaten: Test Date: 20210505; Test Name: Blood Pressure; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: Blood Test; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: CT Scan; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: heparin drip; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: MRI; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210505; Test Name: Ultrasound; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1694843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 28.09.2021
Impfdatum: 10.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / LA

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

Blood pressure measurement Blood test Computerised tomogram Heart rate decreased Heparin resistance Cardiac monitoring Cytogenetic analysis Echocardiogram Electrocardiogram Hypotension Magnetic resonance imaging Portal vein embolism Ultrasound scan Portal vein thrombosis SARS-CoV-2 test

Symptomtext

Blood clot in left portal vein to liver.; Low blood pressure; slowed heart rate; This is a spontaneous report from a contactable consumer (patient). A 32-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 10Apr2021 15:30 (Batch/Lot Number: EW0153) (at the age of 32 years) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included hypothyroidism from an unknown date and unknown if ongoing. There were no known allergies. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1, administered in Arm Left on 20Mar2021 04:30 PM (Batch/Lot Number: PAA165969) (at the age of 32 years) for covid-19 immunisation. There was no other vaccine in four weeks. There was no other medication in two weeks. The patient's concomitant medications were none. The patient experienced blood clot in left portal vein to liver, low blood pressure, slowed heart rate, all on 16Apr2021 04:00. The outcome of events was recovered. The patient was hospitalized for 7 days. Events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization. The events required treatment (Mri, ct scan, ultrasound, heparin drip, blood test, as reported). There was no COVID prior vaccination. Patient was tested for COVID (Nasal swab) on 05May2021 with test results of negative. The patient underwent lab tests and procedures which included blood pressure measurement: unknown, blood test: unknown, computerised tomogram: unknown, heparin resistance: unknown, magnetic resonance imaging: unknown, sars-cov-2 test: negative, ultrasound scan: unknown, all on 05May2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Portal vein embolism
Hospital-Tage: 7,0
Labordaten: Test Date: 20210505; Test Name: Blood Pressure; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: Blood Test; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: CT Scan; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: heparin drip; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: MRI; Result Unstructured Data: Test Result:Unknown; Test Date: 20210505; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210505; Test Name: Ultrasound; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1221330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AR
Alter: 39,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Angiogram normal Cardiac imaging procedure abnormal Chest pain Dyspnoea Echocardiogram Angiogram Arthralgia Back pain Chills Body temperature increased Chest discomfort Cold sweat Discomfort Echocardiogram abnormal Ejection fraction Ejection fraction decreased Electrocardiogram Headache

Symptomtext

Myocarditis; This literature-study case was reported in a literature article and describes the occurrence of MYOCARDITIS (Myocarditis) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MYOCARDITIS (Myocarditis) (seriousness criterion medically significant). At the time of the report, MYOCARDITIS (Myocarditis) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Ejection fraction: 52 % (normal) 52 %. On an unknown date, Troponin I: 13 ng/ml (High) 13 ng/mL. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered MYOCARDITIS (Myocarditis) to be possibly related. No concomitant medication was reported. This analysis shows that myocarditis related to COVID-19 vaccine has an overall fast recovery with no short-term complications. Out of 15 patient 1 patient had subtle apical septal and apical lateral hypokinesis with a LVEF of 52%. No treatment medication was reported This literature-study case was reported in a literature article and describes the occurrence of Myocarditis in a 39-year-old male patient who received both dosis of mRNA-1273. Based on reporter?s causality , a causal relationship cannot be excluded. This case was linked to MOD-2021-317848, MOD-2021-317975, MOD-2021-317977, MOD-2021-317978 (Patient Link).; Sender's Comments: This literature-study case was reported in a literature article and describes the occurrence of Myocarditis in a 39-year-old male patient who received both dosis of mRNA-1273. Based on reporter?s causality , a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Name: left ventricular ejection fraction; Result Unstructured Data: 52 %; Test Name: Peak cardiac troponin I; Result Unstructured Data: 13 ng/mL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1221330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AR
Alter: 39,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

Angiogram normal Cardiac imaging procedure abnormal Chest pain Dyspnoea Echocardiogram Angiogram Arthralgia Back pain Chills Body temperature increased Chest discomfort Cold sweat Discomfort Echocardiogram abnormal Ejection fraction Ejection fraction decreased Electrocardiogram Headache

Symptomtext

Myocarditis; This literature-study case was reported in a literature article and describes the occurrence of MYOCARDITIS (Myocarditis) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MYOCARDITIS (Myocarditis) (seriousness criterion medically significant). At the time of the report, MYOCARDITIS (Myocarditis) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Ejection fraction: 52 % (normal) 52 %. On an unknown date, Troponin I: 13 ng/ml (High) 13 ng/mL. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered MYOCARDITIS (Myocarditis) to be possibly related. No concomitant medication was reported. This analysis shows that myocarditis related to COVID-19 vaccine has an overall fast recovery with no short-term complications. Out of 15 patient 1 patient had subtle apical septal and apical lateral hypokinesis with a LVEF of 52%. No treatment medication was reported This literature-study case was reported in a literature article and describes the occurrence of Myocarditis in a 39-year-old male patient who received both dosis of mRNA-1273. Based on reporter?s causality , a causal relationship cannot be excluded. This case was linked to MOD-2021-317848, MOD-2021-317975, MOD-2021-317977, MOD-2021-317978 (Patient Link).; Sender's Comments: This literature-study case was reported in a literature article and describes the occurrence of Myocarditis in a 39-year-old male patient who received both dosis of mRNA-1273. Based on reporter?s causality , a causal relationship cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Name: left ventricular ejection fraction; Result Unstructured Data: 52 %; Test Name: Peak cardiac troponin I; Result Unstructured Data: 13 ng/mL
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1723876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

schwer

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 07.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dysmenorrhoea Heavy menstrual bleeding Lymphadenopathy Menstruation irregular Thrombosis

Symptomtext

Enlarge lymphatic tissue Abdominal pain Irregular/heavy/blood clotting like/painful menstrual cycle Enlarged lymphatic tissue and abdominal pain occurred the following day. The other symptoms occurred shortly after. I was prescribed several medications to treat these symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1696392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 26,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 15.04.2021
Beginn: 13.08.2021
Tage bis Beginn: 120,0
Dosis: 2
Route/Site: SYR / LA

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

Bell's palsy Illness Pathogen resistance Pharyngitis streptococcal

Symptomtext

Bell?s palsy on the left side of my face. This started a few months after the vaccine so not sure if it?s a side effect, but figured I should report it anyways. So far the Bell?s palsy has lasted about a month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Was not sick at time of vaccination. However I was sick the month leading up to the Bell?s palsy. I had an antibiotic resistant form of strep throat and then had an allergic reaction to amoxicillin. First Vaccination (Pfizer) was on 3/25/2021 at 8:15am. Second Vaccination was on 4/15/2021 at 8:15am.
Vorgeschichte: Crohn's Disease and Asthma.
Andere Medikamente: Concerta, Ritalin, Lexapro, Oral Birth Control. Prednisone, Amoxicillin
Allergien: Amoxicillin (results in a full body rash/hives)
Vorherige Impfungen: -

VAERS 1661219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 35,0
Geschlecht: M
Eingang: 01.09.2021
Impfdatum: 11.04.2021
Beginn: 01.07.2021
Tage bis Beginn: 81,0
Dosis: 2
Route/Site: - / RA

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

Bell's palsy Lip disorder Muscle rigidity

Symptomtext

This is a spontaneous report from a contactable consumer, the patient. A 35-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number: EW0153), via an unspecified route of administration, in the arm right on 11Apr2021 10:00 as dose 2, single (at the age of 35-years-old) for covid-19 immunization. Medical history included blood cholesterol increased and seasonal allergy. Concomitant medications included LIPITOR, CoQ 10, and FISH OIL. The patient previously took bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number: EP7534), via an unspecified route of administration, in the arm right on 19Mar2021 as dose 1, single (at the age of 35-years-old) for covid-19 immunization. On 01Jul2021, the patient's upper lip was not moving correctly when he speak. Patient's upper lip felt rigid and not malleable when he speaks. Patient worried this was a case of bell's palsy. The patient seeing a doctor for the first time on 24Aug to evaluate this. Therapeutic measures were not taken for the events. The patient did not have covid prior to vaccination and did not tested for covid post vaccination. The patient visited the doctor or other healthcare professional office. The outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol; Seasonal allergy
Andere Medikamente: LIPITOR; COQ 10; FISH OIL
Allergien: -
Vorherige Impfungen: -

VAERS 1658778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IA
Alter: 31,0
Geschlecht: M
Eingang: 31.08.2021
Impfdatum: 09.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / RA

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

Headache Hypertension Malaise Pain Presyncope

Symptomtext

About a week after getting the first vaccine does, I started having massive headaches. I've never had a headache before in my life. The searing pain was accompanied by very high blood pressure and near fainting. I thought I was dying and I have no health insurance so I could never get it checked out. It has continued for months now, randomly hitting me from time to time a few times a week. I can feel my blood pressure rise and my had hurt. I have to lay down for about half an hour and let it pass. I was healthy before the vaccine, I've never experienced anything like this before, so I am confident it was caused by the vaccine. Like I said, I don't have insurance so I have just been dealing with it myself...

Weitere VAERSDATA-Felder

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

VAERS 1647244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: -
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Pericarditis

Symptomtext

he ended up in the hospital with Paracydis/The side effect listed should be: Pericarditis; This is a spontaneous report from a Pfizer-sponsored program reported by a contactable consumer (patient). A male patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution injection; Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution injection; Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. On an unspecified date, after the 2nd dose the patient ended up in the hospital with pericarditis which was supposedly a common side effect of the vaccine. The patient wanted to know what Pfizer recommends and if this should be reported. The outcome of the event was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

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

VAERS 1647119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 15.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: OT / LA

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

Chest pain Myocarditis Pericarditis

Symptomtext

This is a spontaneous report received from a contactable Physician received via COVID-19 Adverse Event Self-Reporting Solution (COVAES). A 32-year-old female patient (non-pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 intramuscular, administered in Arm Left on 15Apr2021 (at 32 years old, not pregnant) (Batch/Lot Number: EW0153) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history was not reported. Concomitant medication included TRI-SPRINTEC. The patient experienced suspected myocarditis or pericarditis, chest pain all on 20Apr2021 with outcome of not recovered. Treatment given for all events was colchicine. No covid prior vaccination. Not covid tested post vaccination. No follow-up attempts are needed. No further information is expected. Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the events myocarditis and pericarditis and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the product is evaluated as part of 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, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 1646991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 24.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Back pain Blood test Body temperature Computerised tomogram Confusional state Disorientation Dizziness Dyspnoea Fall Guillain-Barre syndrome Headache Heart rate Heart rate increased Hypokinesia Hypoxia Intervertebral disc displacement Limb discomfort Lumbar puncture

Symptomtext

spinal discs had collapsed and it felt like his sciatic nerve was being pinched off; spinal discs had collapsed and it felt like his sciatic nerve was being pinched off; diagnosed with Guillian Barre; lost all feeling from the waist down/he became totally paralyzed from the neck down; lost all feeling from the waist down/he became totally paralyzed from the neck down; hypoxia/pulse oximeter read 60%/oxygen saturation dropped; pulse oximeter showed a heart rate of 188 beats per minute; when he was sleeping his oxygen levels went into the 80s/oxygen saturation dropped; unable to move his lower extremities; back pain; not breathing properly; disoriented; light headed; been without sleep for 36-38 hours; woke up and had no clue he was in his house; went to stand up and fell over; having complaints of a headache; fever; couldn't move of the bed; This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose, via an unspecified route of administration, administered in arm left on 24Apr2021 12:00 (Batch/Lot Number: EW0153) at the age of 68 years old, as single dose for covid-19 immunisation. Medical history included chronic back problems, cervical stenosis, spinal stenosis, previous back surgeries, prostate cancer, chronic obstructive pulmonary disease (COPD) with lung disorder, heart attack, urinary tract infection, pinched nerves, chicken pox virus, Covid 19 virus infection. The patient was receiving steroids for his spinal stenosis. About every other week he would be taking steroids. The urgent care prescribed steroids many times to calm down his spinal stenosis and also his lung problems. The doctor was calling his lung problems exacerbated COPD due to the Covid 19 virus. He doesn't recall the names of any steroid prescribed. He reports he took some in a pack and some as injections. He estimates 5 different steroid pills and injections. The patient previously took shingles vaccine for immunisation and he ended up in bed for 3 days with 103 degree Fahrenheit temperature and he could hardly move. The patient also previously took a pneumonia vaccine for immunisation. There was no other vaccine in four weeks. The patient experienced diagnosed with Guillian barre, lost all feeling from the waist down/he became totally paralyzed from the neck down, hypoxia/pulse oximeter read 60%, pulse oximeter showed a heart rate of 188 beats per minute, complaints of a headache in Apr2021, fever in Apr2021, couldn't move of the bed in Apr2021, unable to move his lower extremities, back pain, not breathing properly, spinal discs had collapsed and it felt like his sciatic nerve was being pinched off, when he was sleeping his oxygen levels went into the 80s/ oxygen saturation dropped, disoriented, light headed, without sleep for 36-38 hours, woke up and had no clue he was in his house, went to stand up and fell over. The patient was hospitalized twice for lost all feeling from the waist down/he became totally paralyzed from the neck down, diagnosed with Guillian barre from an unknown date to 05Aug2021 (the last discharged date, 2 admissions lasting about 5 days each). Clinical course: 4-5 hours later started having complaints of a headache, fever, and couldn't move of the bed. The patient was unable to move his lower extremities and has been out of the ER and Urgent Care 2-3 times a week since receiving the Pfizer Covid-19 vaccine. The patient was diagnosed with Guillian Barre and has a medical history of cervical stenosis, spinal stenosis, pinched nerves, and back surgery. The patient has been treated for Guillian Barre on two separate occasions with dyspnea and was now on home oxygen. The patient has also been diagnosed with exacerbation of COPD and started on steroids (via injections five times and pill). Caller was also given an infusion of bamlanivimab. He stated he has never had a problem with vaccines before until about a year ago, prior to the Covid 19 virus, he had the shingles vaccine and he ended up in bed for 3 days with 103 degree Fahrenheit temperature and he could hardly move. He did talk to his doctor about getting the second shingles vaccine and she advised him not to. He would not have even gotten the shingles vaccine except he was concerned about his mother in law. He reports both he and his wife had the chicken pox virus. He states that the flu virus will target that area, meaning his back. So he expected that with the Covid 19 vaccine. Meaning, he expected to have side effects related to his back, since he had chronic back problems. He called the advice nurse line and she advised him to receive the Covid 19 vaccine. His mother in law who is 85 years old and his wife, who he almost lost, both survived the Covid 19 virus. He thought for the best protection he should get the Covid 19 vaccine. Four to five hours after receiving the Covid 19 vaccine he experienced severe headaches, fever for 4 days, and he couldn't move off the bed. He reported his wife and mother in law returned 15 days later for their second Covid 19 vaccines but he held off because he had a planned surgery for his neck. When probing for information related to his wife and mother in law, he stated he did not have their Covid 19 vaccine information cards. He reported his neck surgery was expedited because he had been to the emergency department multiple times after receiving the Covid 19 vaccine for not breathing properly and severe back pain. He stated the doctor's kept treating his history of spinal stenosis and pinched nerves. He was told his spinal discs had collapsed and it felt like his sciatic nerve was being pinched off. He was treated for 3 months, after receiving the Covid 19 vaccine, for his chronic back history and not for anything caused by the Covid 19 vaccine. Seventeen days ago he couldn't use his legs so he took an ambulance to the hospital. He spent 3 or 4 days in the hospital. He was seen by neurosurgery who evaluated him for possible emergency surgery. The neurosurgeon did motor tests and told him that his problem could not be surgically fixed. He was discharged and was told to follow up for more testing like nerve conduction. Twenty four hours after being discharged from the hospital he lost all feeling from his waist down. He stated he had prostate cancer and wanted to get on the schedule to get the prostate cancer out of his body so he called his prostate doctor's surgical coordinator. He mentioned his symptoms to the coordinator who asked him if he had been treated for Guillian-Barre syndrome. He clarified he had prostate cancer prior to receiving the Covid 19 vaccine. He called the hospital and mentioned his symptoms of losing feeling from the waist down and he was told to get to the hospital so a spinal tap could be done. The spinal tap results were not conclusive. He became totally paralyzed from the neck down. By midnight that day he had started treatment for Guillian-Barre syndrome. He spent 5 days in the hospital getting treatment. He was then discharged from the hospital and he was able to walk out. Three days after being discharged he had a relapse and went back to the hospital by ambulance. A neurologist was called back in and he was restarted on a 5 day campaign of plasma, he doesn't know the name, he stated the plasma is from healthy people's immune systems and it was given to him to stop any attack on his spinal column. This last hospitalization was last week and he was discharged on Thursday, 05Aug2021. He doesn't recall all the dates of his doctor's appointments, urgent care visits, emergency room visits or the exact dates of his hospitalizations. He also reportd that while in the hospital every time he dozed off he would set off the monitors. The nurse would come in his room and reset the monitor and put him on oxygen just in case he fell asleep. When he was awake his oxygen level was 95-97% but when he was sleeping his oxygen levels went into the 80s. He was told his motor nerves aren't healed from the Guillian-Barre syndrome. When he got home from this hospitalization, he was able to get an earlier appointment for his neurologist because Guillian-Barre is a very scary disease. He laid down on the couch at 2:35PM trying to relax and get rest before seeing his neurologist. While laying down he experienced hypoxia. He felt disoriented and light headed. He told his wife, who works from home, that he was going to the urgent care because his pulse oximeter showed a heart rate of 188 beats per minute and an oxygen level of 97%. The doctor at the urgent care was confused. While laying on the gurney at the urgent care his oxygen level dropped and his heart rate dropped. When he got off the gurney and walked the length of the urgent care, the pulse oximeter went up in oxygen saturation. The minute he was resting again his oxygen saturation dropped. He does have a history of COPD. He was told to go to the emergency room so he could have oxygen sent to his house. He explained to the urgent care doctor that he also had an appointment with his neurologist that day. He went to the appointment with his neurologist and explained what was happening with his oxygen level and the neurologist advised him to get the oxygen. The urgent care doctor said she was going to follow up with him and she did call while he was having dinner. She advised him again to go back to the emergency department to get the home oxygen ordered and delivered. He went to a different hospital, at 8:00PM that night. While at hospital he was put on the oxygen monitor and nothing was wrong. He was discharged at 3:53AM the next morning. He went home and didn't get to go to sleep and he got a phone call from the oxygen distributor. The urgent care doctor was able to get his oxygen ordered. He was sitting in his garage in 101 degree heat waiting for the oxygen to show up. At this point he had been without sleep for 36-38 hours. His wife told him to come inside the house and he fell asleep. After he fell asleep, he woke back up and he had no clue he was at his house. He went to stand up and he fell over. He put the pulse oximeter on and it read 60%. He took several big breaths and his oxygen went into the 80s. About that time the oxygen showed up. While he was sitting down having the oxygen hooked up, his oxygen levels went back to the 93-94% range. As much as he researched the Covid 19 vaccine, all brands of the Covid 19 vaccine, no where did he see Guillian Barre listed as a side effect. He's confused as to why this information isn't out there. His neurologist told him the Guillian Barre was caused by the Covid 19 vaccine. He asked about getting the second Covid 19 vaccine and he was advised not to get the second dose. He provides the following information in a historical context. His mother in law broke her femur on 16Dec2020. When his mother in law was discharged, the patient asked for a Covid 19 virus test to be done on his mother in law before he picked her up. Her rapid test came back negative. He picked her up and brought her home on 15Jan2021. He and his wife were the caregivers until his mother in law recovered completely. Seven days after picking his mother in law up from rehab, he was not feeling good, his wife wasn't feeling good. He received a call at that point that his mother in law's Covid 19 virus test was positive. He told his wife to go to the drive thru Covid 19 virus testing site because she was feeling bad. The caller went to the urgent care and he was tested for the Covid 19 virus. He had some elevated cardiac enzymes with that blood work so he was sent to the emergency department for a possible heart attack. He was placed in the Covid 19 ward at the hospital and was tested again for the Covid 19 virus. He adds this information because with some blood work he did have Covid 19 antibodies show up. This occurred prior to him receiving the Covid 19 vaccine in Jan2021. He reported when he was seen in the emergency room in the beginning he wasn't being treated for anything Covid 19 vaccine related. He was being treated for his chronic back pain with Fentanyl and Morphine. He was in the urgent care or emergency room 2 to 3 times a week because of not breathing well or extensive back pain after receiving the Covid 19 vaccine. The urgent care and emergency room doctor's were also treating his COPD and supposed allergies brought on by his previous Covid 19 virus infection. The outcome of the event Guillian-Barre was not recovered, of the other events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Name: body temperature; Result Unstructured Data: Test Result:101 degree; Test Name: body temperature; Result Unstructured Data: Test Result:103 Fahrenheit; Test Name: CAT scan; Result Unstructured Data: Test Result:Unknown results; Test Name: heart rate; Result Unstructured Data: Test Result:188 beats per minute; Test Name: pulse rate; Test Result: 60 %; Test Name: spinal tap; Result Unstructured Data: Test Result:Unknown results; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Test Name: oxygen; Result Unstructured Data: Test Result:80s; Test Name: oxygen; Result Unstructured Data: Test Result:80s; Test Name: oxygen; Result Unstructured Data: Test Result:dropped; Test Name: oxygen; Result Unstructured Data: Test Result:pulse oximeter went up; Test Name: oxygen saturation; Test Result: 97 %; Test Name: oxygen saturation; Result Unstructured Data: Test Result:95-97 %; Test Name: oxygen saturation; Test Result: 60 %; Test Name: oxygen saturation; Result Unstructured Data: Test Result:93-94 %; Test Date: 202101; Test Name: Covid 19 antibodies; Result Unstructured Data: Test Result:Covid 19 antibodies show up; Test Name: Covid 19 virus test; Test Result: Negative ; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back surgery; Cervical spinal stenosis; Chronic back pain; COPD (with lung disorder); COVID-19; Heart attack; Pinched nerve; Prostate cancer; Shingles; Spinal stenosis; Urinary tract infection
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1646913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Blood pressure increased Blood pressure measurement Chest pain Dizziness Dyspepsia Feeling hot Heart rate Heart rate increased Hepatic enzyme increased Hyperhidrosis Inflammation Investigation Thrombosis

Symptomtext

extreme heartburn; Blood work showed an inflammatory response; elevated liver enzymes; Sweating; I go to ER to check for blood clots, even though it felt like heartburn; 1 minute after the shot, immediate pain and heat radiating from my chest.; 1 minute after the shot, immediate pain and heat radiating from my chest.; dizzy; BP and HR were very high; BP and HR were very high; This is a spontaneous report from a contactable Consumer or other non-HCP (patient). A 43-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EW0153), dose 2 via an unspecified route of administration, administered in Arm Left on 13Apr2021 at 14:00 (at the age of 43-year-old) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included Thyroid/Hashimoto from an unknown date and unknown if ongoing. The patient had Known allergies to Penicillin. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included Levothyroxine sodium (SYNTHROID); Clonazepam (KLONOPIN); Escitalopram oxalate (LEXAPRO) and Buspirone hydrochloride (BUSPAR), all taken for an unspecified indication, start and stop date were not reported. The patient previously took his first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: ER8727), via an unspecified route of administration, administered in Arm Left on 13Mar2021 at 14:00 (at the age of 43-year-old) as single for covid-19 immunisation and experienced fatigue, tired and weakness for about a week. The patient previously took Levaquin and experienced allergy. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. On 13Apr2021, at 14:00 one minute after the shot, the patient experienced immediate pain and heat radiating from my chest, Sweating, dizzy, blood clots, BP (blood pressure) and HR (heart rate) were very high, Blood work showed an inflammatory response and elevated liver enzymes. On 14Apr2021 (on Day 02), the patient experienced extreme heartburn. The clinical details of the events as follows: one minute after the shot, immediate pain and heat radiating from my chest, Sweating and dizzy. Paramedics on site had him sit and took vitals. BP and HR were very high. Over a period of 10-15 minutes these symptoms subsided. Some lingering chest pain remained for over a week. On Day 2, extreme heartburn. Dr. recommended, and he went to ER to check for blood clots, even though it felt like heartburn. On day 3, ended up in ER heartburn lasted for 24 hours. OTC medications did not work. Hospital concluded it was likely heartburn. Blood work showed an inflammatory response and elevated liver enzymes. This lasted for 6 weeks. Blood work was repeated several times during and after this period. Developed high BP or if he had underlying minor hypertension (even though going to doctors frequently his BP was on average 120/80) it was exacerbated. Average BP was 145/95 plus/minus 10 points (usually on the higher end) Currently taking 2 medication to regulate BP. The events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient underwent lab tests and procedures which included blood pressure measurement: high, blood pressure measurement: 120/80, heart rate: high on an unspecified date in 2021. The patient received treatment "cocktail" for heartburn from ER and unspecified BP medications. The case was non-Serious. The events did not result in death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating and Congenital anomaly/birth defect. The outcome of the events was not resolved. No follow-up attempts are needed. No further information is expected.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood Pressure; Result Unstructured Data: Test Result:High; Test Date: 2021; Test Name: Blood Pressure; Result Unstructured Data: Test Result:120/80; Test Date: 2021; Test Name: Heart rate; Result Unstructured Data: Test Result:High; Test Date: 2021; Test Name: Blood work; Result Unstructured Data: Test Result:showed an inflammatory response and elevated liver
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's thyroiditis; Penicillin allergy
Andere Medikamente: SYNTHROID; KLONOPIN; LEXAPRO; BUSPAR
Allergien: -
Vorherige Impfungen: -

VAERS 1646050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AR
Alter: 59,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 30.07.2021
Beginn: 30.07.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Arrhythmia Electrocardiogram Loss of consciousness

Symptomtext

12 hours later was walking from one room to another and completely collapsed with short period of unconsciousness; Heart arrhythmia issues slowly subsided; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Right on 30Jul2021 11:15 (Lot Number: EW0153) as dose number unknown, single (at 59 years old) for COVID-19 immunisation. Medical history included hypertension. Concomitant medications included amlodipine; levothyroxine sodium (SYNTHROID); potassium, all taken for an unspecified indication, start and stop date were not reported. The patient experienced 12 hours later was walking from one room to another and completely collapsed with short period of unconsciousness on 30Jul2021 12:00 PM with outcome of unknown, heart arrhythmia issues slowly subsided on 30Jul2021 12:00 PM with outcome of recovering. The clinical course was reported as follows: 12 hours later was walking from one room to another and completely collapsed with short period of unconsciousness. ECG indicated multiple events. Went to ER the next day. Admitted to hospital with multiple tests. Heart arrhythmia issues slowly subsided. No treatment required. The patient was hospitalized for the events for 1 days. Prior to vaccination, the patient was not diagnosed with COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: Test Date: 20210730; Test Name: ECG; Result Unstructured Data: Test Result:indicated multiple events
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high
Andere Medikamente: AMLODIPINE; SYNTHROID; POTASSIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1645700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 53,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 15.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: - / RA

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

Blood pressure increased Blood pressure measurement Eating disorder Feeling abnormal Headache Human seminal plasma hypersensitivity Hypersensitivity Loss of consciousness Palpitations

Symptomtext

heart palpitations; states she can't have sex with her husband because she is allergic to his sperm; feeling bad; can't eat a lot of foods and supplements and chemicals and everything; blood pressure goes up; she was melting and felt she may pass out; allergic reaction; Her head starts pounding; This is a spontaneous report from a contactable consumer reported for herself. This 53-year-old female patient received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0153) via an unspecified route of administration in the right arm on 15Apr2021 at age of 53 years old as single dose for covid 19 immunization. Medical history was unknown. Concomitant medications were none. The patient previously received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6208) in the right arm on 15Mar2021 at age of 53 years old for covid 19 immunization. The patient had no additional vaccines administered on same date of the Pfizer suspect. The patient had no prior Vaccinations (within 4 weeks), she had not had the cold vaccine this year. In May2021, she started having a reaction that was an allergy and still had the allergies today and was waiting for them to go away and it was unbearable and she cannot go outside in the heat and had a reaction. She cannot have intercourse with her husband because she was allergic to his sperm. She had a lot of allergies to food substances, a lot of foods and chemicals and everything. Her reported symptoms started around mid-May 2021 and her head started pounding and she started to have head pressure and the worst symptom was heart palpitations and sometimes her blood pressure went up because she measured it at home and it went up when she was not feeling well; stated she had a like a feeling of that she was melting and did not know how to explain it and felt she will pass out and that began around mid May2021 and then the symptoms also were she was allergic to the things she already mentioned earlier in the call; stated she had no names or lot numbers of the products she was allergic to and she was also allergic to her husband's sperm and it was around that same time but she figured out this later. The patient stated she needed help and nobody or her HCP or allergist cannot do anything and stated the first appointment with her HCP is on 31Aug2021 and he and the nurse told her they did not work with vaccine patients. She can complete the report but her head started pounding and she did not know if they can help her and was aware they do not offer medical advice or treatment recommendations and would be referred to her HCP. The patient stated her reported symptoms were the same and it had been going on more than two months already. With the heat, she cannot go outside and stayed in the head three minutes and then started feeling bad. She had not had treatment for the reported events. Before the vaccine, she was always a very sensitive person but not as close as it was right now and she was a very sensitive person; no further details provided by the caller. The events did not required a visit to Emergency Room. No Physician Office required, the patient was trying to see her HCP and her HCP had no appointment and can't see her. Outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 202105; Test Name: blood pressure; Result Unstructured Data: Test Result:blood pressure goes up
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1617813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 30,0
Geschlecht: F
Eingang: 22.08.2021
Impfdatum: 16.04.2021
Beginn: 03.05.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / LA

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

Computerised tomogram normal Electroencephalogram normal Generalised tonic-clonic seizure Magnetic resonance imaging normal Partial seizures Seizure

Symptomtext

Seizures, starting on 5/3 with focal seizures occurring all day although I didn't realize that was what was happening, 2 tonic clonic seizures the following day. Symptoms may have started as early as 4/27 with some of the focal seizure symptoms. No head trauma, no family history of epilepsy, no illicit drug use. Seizures resolved with treatment with Keppra, one dose increase required to resolve all symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: 1,0
Labordaten: CT scan, MRI -nothing abnormal found 5/4/2021. EEG within normal after being medicated with anticonvulsants 5/5 & 7/16
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Excedrin
Allergien: Sulfa antibiotics
Vorherige Impfungen: -

VAERS 1591606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 20.08.2021
Impfdatum: 14.04.2021
Beginn: 26.06.2021
Tage bis Beginn: 73,0
Dosis: 2
Route/Site: IM / RA

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

Cardiac failure Coagulopathy Intensive care Malaise Organ failure

Symptomtext

General malaise at beginning , mixed reports from doctors, By end of week one was admitted to ICU for heart failure, blood clotting following remainder of organs were failing. First admitted to hospital, after 6 days flown to another hospital, were he is still

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 47,0
Labordaten: He has been in ICU for 47 days
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1579186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TN
Alter: 50,0
Geschlecht: F
Eingang: 17.08.2021
Impfdatum: 27.04.2021
Beginn: 10.07.2021
Tage bis Beginn: 74,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy Blood test Breast mass Computerised tomogram Computerised tomogram thorax Facial paralysis Guillain-Barre syndrome Immunoglobulin therapy Laboratory test Magnetic resonance imaging Trigeminal neuralgia Vth nerve injury

Symptomtext

On 7/10/21 I started experiencing excruciating trigeminal right face nerve pain and facial dropping. Went to ER on 7/11/21 where I was accessed as stroke patient but diagnosed as bilateral bell's palsey after MRI and CT scan was done. I was admitted and all kinds of tests and labs were done that I can provide from medical records. I was discharged on 7/13/21 with prednisone to take. I had set back on 7/19/21 with the trigeminal nereve pain again and went to medical facility where I was advised by doctor to go to hospital. I went on 7/20/21 to the ER where I was then admitted as inpatient with bilateral bell's palsey and trigeminal nerve damage. i was inpatient until discharged on 7/28/21. while there MRI, CT scan, chest CT, all kinds blood work and lab were done. Every test possible was done for the bell' s palsey and all were negative. I was diagnosed with bilateral bell's palsey, guillian barre syndrome and the CT chest showed a new left brest nodule. All side effects from the Pfizer vaccine. I was told by the neuro team that they only had 1 case in research they could compare me to and that I was extremely rare case. I was given IVIG treatment and I was discharged on 7/28/21 and sent home with prednisone and trileptal for the trygeminal nerve pain. On 7/30/21 I had severe allergic reaction to the trileptal medication and was taken back to ER where an ambulance then transported me back to another medical facility. I was admitted and discharged on 8/1/21 an medication changed to cymbalta. I have all medical records needed that i can provide. s

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 12,0
Labordaten: too many to list....I am happy to provide all medical records from both medical facilities where I was seen.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, blood pressure
Andere Medikamente: Atorvastatin, Vitamin D, Gabapentin, Metformin, Omeprozole, Rybelsus, Telmisartan
Allergien: Trileptal
Vorherige Impfungen: -

VAERS 1574318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: OR
Alter: 31,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Facial paralysis Magnetic resonance imaging normal

Symptomtext

Bell's Palsy- right side. Drooping started in eyebrow, progressed to mouth and cheek. went to urgent care 4/6/2021, prescribed prednisone and rest, sent home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI (negative for any tumors) - 6/30/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia, migraines, asthma, adhd
Andere Medikamente: Duloxetine, Adderall, vitamin D
Allergien: Penicillin, Sulfa
Vorherige Impfungen: -

VAERS 1534861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 07.08.2021
Impfdatum: 15.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Facial paralysis Seizure Speech disorder

Symptomtext

Siezure April 28th garbled talk right side facial drooping

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: emergency room, put on keppra
Aktuelle Erkrankungen: meningioma removed March 23 2021
Vorgeschichte: none
Andere Medikamente: none
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1181889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: RI
Alter: 32,0
Geschlecht: F
Eingang: 06.08.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Dizziness Dysgeusia Feeling hot Flushing Heart rate Presyncope Tachycardia Heart rate increased Urticaria

Symptomtext

Immediate metallic taste, lightheadedness, warm sensation head to toe, almost passing out (did not pass out, was always conscious ), tachycardia, flushed skin, this lasted 5 minutes. It did subside.; Immediate metallic taste, lightheadedness, warm sensation head to toe, almost passing out (did not pass out, was always conscious ), tachycardia, flushed skin, this lasted 5 minutes. It did subside.; Immediate metallic taste, lightheadedness, warm sensation head to toe, almost passing out (did not pass out, was always conscious ), tachycardia, flushed skin, this lasted 5 minutes. It did subside.; almost passing out (did not pass out, was always conscious); tachycardia, flushed skin this lasted 5 minutes. It did subside. Later that day had localized hives that went away; tachycardia, flushed skin this lasted 5 minutes. It did subside. Later that day had localized hives that went away; localized hives that went away; This is a spontaneous report from a contactable consumer. A 32-year-old non-pregnant female patient (not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number: EW0153) via an unspecified route of administration administered in left arm on 06Apr2021 12:00 Pm (at the age of 32-years-old) as a single dose for covid-19 immunisation. Medical history included autoimmune disorder. Concomitant medication(s) included mycophenolate mofetil (CELLCEPT [MYCOPHENOLATE MOFETIL]) taken for an unspecified indication, start and stop date were not reported. patient had known allergies Penicillin, shellfish, contrast dye. Prior to the vaccination, the patient was not 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 06Apr2021 12:00 Pm, the patient experienced Immediate metallic taste, light-headedness, warm sensation head to toe, almost passing out (did not pass out, was always conscious), tachycardia, flushed skin, this lasted 5 minutes. It did subside. Later that day had localized hives that went away. No treatment received for adverse events. The outcome of the event flushed skin was recovered on 06Apr2021 12:05 and other events were recovered on unspecified date on 2021. No follow up attempts are possible. Information about lot/batch number cannot be requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder; Contrast media allergy; Penicillin allergy; Shellfish allergy
Andere Medikamente: CELLCEPT [MYCOPHENOLATE MOFETIL]
Allergien: -
Vorherige Impfungen: -

VAERS 1526242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 46,0
Geschlecht: M
Eingang: 04.08.2021
Impfdatum: 10.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / -

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

Fall Guillain-Barre syndrome Lumbar puncture Magnetic resonance imaging Muscular weakness Quadriplegia Wheelchair user

Symptomtext

Four falls. Extreme upper and lower weakness. quadriplegia. Hospitalized for one month. Diagnosed with AIDP/GBS. Given IV's. In wheelchair currently since April.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 30,0
Labordaten: Spinal tap. Mri's for knee.
Aktuelle Erkrankungen: Was rehabilitating from triple bypass surgery performed on 02/09/21.
Vorgeschichte: II Diabetes with previous heart attack in 02/21, Neuromusclar disease,
Andere Medikamente: tabletvit C/vit E ac/lut/copper/zinc (PRESERVISION LUTEIN ORAL), aspirin 81 MG enteric coated tablet, atorvastatin 40 MG tablet, gabapentin 300 MG capsule, lamoTRIgine 100 MG tablet, sertraline 100 MG tablet, lithium 300 MG CR tablet, los
Allergien: None
Vorherige Impfungen: -

VAERS 1498378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MD
Alter: 43,0
Geschlecht: M
Eingang: 23.07.2021
Impfdatum: 12.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test abnormal Computerised tomogram abnormal Dyspnoea Heart rate increased Myocardial strain Thrombosis

Symptomtext

I start having SOB and fast heartbeat around the end of April. It got worst through May. I went to the ER They did blood work, that came back abnormal. So, they did a CT scan, it show that a had pulmonary embolism, which confirmed that I had a blood clot. The blood clot caused a strain on my right side of my heart. I am not taking blood thinners. I have never had blood clots before the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: blood work CT scan
Aktuelle Erkrankungen: asthma
Vorgeschichte: asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1496329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 64,0
Geschlecht: F
Eingang: 23.07.2021
Impfdatum: 07.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dyspnoea exertional Echocardiogram normal Electrocardiogram ST segment elevation Pericarditis Pleuritic pain SARS-CoV-2 test negative Troponin

Symptomtext

DX: Pericarditis S/S: Syspnea on exertion, acute Chest Pain Pt c/o sudden onset of chest pain and dyspnea, pleuritic chest pain 64 yr old female healthy with acute onset of chest pain with elevated troponin, ST segment changes, normal ECHO supports diagnosis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: Vitals: Temp: 37.7C Resp: 18 HR: 106 BP: 108/68 O2: 100 EKG: diffuse ST segment elevation 04/10/2021 ECHO: normal Troponin: 04/10/2021 abnormal- 0.103 ng/mL Reference Range :<0.05 ng/mL Highest level: 04/11/2021 COVID-19: 04/10/2021 Negative
Aktuelle Erkrankungen: NA-Data Received from ESSENCE report pulled at State Level. Details are limited.
Vorgeschichte: NA-Data Received from ESSENCE report pulled at State Level. Details are limited.
Andere Medikamente: NA-Data Received from ESSENCE report pulled at State Level. Details are limited.
Allergien: NA-Data Received from ESSENCE report pulled at State Level. Details are limited.
Vorherige Impfungen: -

VAERS 1484590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 62,0
Geschlecht: F
Eingang: 19.07.2021
Impfdatum: 08.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Chills Electric shock sensation Hyperhidrosis Hypoaesthesia Muscle spasms Muscular weakness Neuralgia Pain Pain in extremity Peripheral coldness

Symptomtext

Alternating chills and sweating. Cold toes that could not be warmed up with heating pad. Eventually, ?fluttering? sensation in legs (worse at night) and sometimes in stomach and arms, repeated hypnic jerks at night, numbness in extremities, shooting ?electric-like? pain in hand, fingers and toes. Nerve-like pain in arms and legs. Extreme weakness arms and legs. Burning sensation in hips. Pain in right leg and thigh. Pain in shoulders radiating down arm mostly on the right side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Myofascial pain
Andere Medikamente: Hydroxychloroquine (had just started taking 2 days prior to second vaccine), clonazepam, Protonix, Pepcid, omega-3, multi vitamin, vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 1461770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: MS
Alter: 14,0
Geschlecht: F
Eingang: 10.07.2021
Impfdatum: 08.07.2021
Beginn: 08.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: patient fainted within 15 minutes of receiving first dose of pfizer covid vaccine. patient immediately gained conciousness

Weitere VAERSDATA-Felder

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

VAERS 1223409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 07.07.2021
Impfdatum: 14.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Blood test Lumbar puncture Paralysis Cardiac disorder Chest pain Disability Dyspnoea Electrocardiogram Feeling cold Hypoaesthesia Muscular weakness

Symptomtext

Paralyzed 13 hours later; She reports her daughter has to use braces and a wheelchair and is unable to work; Left arm goes numb, cannot feel hot or cold; Shortness of breath; Always feels cold; Chest pain; Does not have full strength in her legs/both of her daughter's hands are weak, but the left hand is extremely weak; Heart issues; This is a spontaneous report received from a contactable consumer (patient's mother reported for her daughter). A 33-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), first dose via an unspecified route of administration, administered in left arm on 14Apr2021 between 11:00-11:30 (at the age of 33-year-old) as a single for COVID-19 immunization.The patient did not had any medical history (including any illness at time of vaccination). Concomitant medications were reported. There were no patient's family medical history relevant to adverse event. It was reported that, doctors have done two MRIs and a spinal tab and she was healthy and there was no doctor visits nothing before the vaccine. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No previous immunization with the Pfizer vaccine considered as suspect. On 15Apr2021, the patient was paralyzed. It was reported that the patient received the Pfizer COVID-19 injection on 14Apr2021 between 11:00-11:30 and was paralyzed 13 hours later. She was taken to hospital. The mother stated her daughter did not have full strength in her legs, left arm goes numb, cannot feel hot or cold, has shortness of breath, always feels cold, and chest pain. She reported a cardiologist saw something on an EKG and that her daughter has also seen a neurologist and several other doctors.The mother said her daughter has been on the local news about her reaction.She reported her daughter has to use braces and a wheelchair and is unable to work. She stated there have been other people she was aware of with this same type of reaction, including a girl and a guy. Reporter stated she has several questions since her daughter has no feeling in one leg, no feeling in part of the other leg and one hand is very weak. Reporter stated so when this all happened the media reached out and they put a stop to that, but her daughter did do an interview to a local station and will possibly do an interview with a mainstream media.Reporter stated apparently there are several cases for this. Reporter asked for the ones that have experienced the paralyzed event where are they going, how are they doing because her daughter has a baby and was needing information on even what treatments to take. Reporter stated it has been reported and they received a letter saying the paralyzed was a side effect to the first initial shot. Reporter stated her concern is they need to get and want to get treatment so she can get back to walking and Pfizer should be able to provide this information. Reporter stated the paralyzed was not reported with Pfizer and also stated her daughter has no feeling at all-in-one leg, then the other leg she has feeling from hip to knee but no feeling knee to foot, both of her daughter's hands are weak, but the left hand is extremely weak. Adverse events resulted in visit to emergency room taken by ambulance to general hospital and paralyzed required visit to physician office. Reporter stated her daughter got to Hospital and was there on Friday, Saturday, Sunday and on Monday she was transported to Clinic since it was more suit for her daughter.Reporter stated her daughter was taken to one hospital and taken to another Clinic on Monday and left Thursday where she was taken to acute rehab. The reporter stated her daughter has been in and out of the hospital and was still having issues 2 months after the Pfizer COVID-19 vaccine injection. Reporter stated the patient was showing signs of improvement but nowhere near how she was prior to vaccine. They told her it was a side effect from the shot. She was finally getting to feel back but now, was having heart issues. Treatment included medicine that was an injection for blood clots in the hospital, but she does not believe she was given any oral medication for her being paralyzed. Reporter confirmed that her daughter did not have a blood clot and the blood clot injection was for prevention. Reporter stated her daughter has not had the second dose.The patient was recovering from paralysis and outcome for the other events was reported as unknown. Information about batch/Lot number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: Test Result:No results; Comments: something
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1443142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: VA
Alter: 17,0
Geschlecht: M
Eingang: 02.07.2021
Impfdatum: 29.06.2021
Beginn: 29.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fall Loss of consciousness

Symptomtext

A few minutes after receiving vaccination, patient stood up and passed out falling face first to the floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Patient was transported to emergency dept. by emt.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin C and Vitamin D supplementation
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1441902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 02.07.2021
Impfdatum: 05.04.2021
Beginn: 27.06.2021
Tage bis Beginn: 83,0
Dosis: 2
Route/Site: SYR / LA

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

Erythema Induration Thrombosis Varicophlebitis

Symptomtext

On left feet under knee and up swelling vain, red and hard when I touch, really painful. Looks for me like thrombosis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Liver cirrhosis
Vorgeschichte: Aortic aneurysm Vascular disorder
Andere Medikamente: Metroprolol 75?2 Losartan 25
Allergien: -
Vorherige Impfungen: -

VAERS 1429445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 02.07.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chest pain Myocarditis Electrocardiogram Electrocardiogram abnormal

Symptomtext

myocarditis; Chest pain; This is a spontaneous report from a contactable consumer (Reporter's girlfriend). This is report 3 of 3. A female patient of an unspecified age received first dose of bnt162b2 (Pfizer-BioNTech Covid-19, Solution injection; Batch/Lot Number: EW0153), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced myocarditis starting about 5 days after Covid Vaccine first dose. The patient never went back for the second dose because the chest pain was so intense. It took the patient about 4 weeks for adverse event to go away. The patient was treated and have moved on but maybe patient was a little bit healthier than the next person would be. Caller was concerned that they had gotten bad batches. Caller wanted to know how many vaccines are in each batch. Caller verified that she believes the third character in Lot number is the letter O, not the numeral zero. Caller questioned if the vaccine Lot numbers are sequentially in order, like numerically; and if there is a particular number of batches manufactured for each Lot number: like are there 10,000 or 100 of one Lot number manufactured, and then they make the next batch of the next Lot number. She called the CDC to ask those questions, but CDC did not know the answers. Caller reported she and her girlfriends experienced adverse events after Pfizer Covid Vaccine and they all kind of joked and said it must have been the Pfizer Covid Vaccine. They finally compared their cards and their vaccines Lot numbers were all within digits of each other. Caller feels it is worthwhile to look into it. They are all fine, but it might be an issue of bad batches of Lot numbers of the Pfizer Covid Vaccine. They all recovered; but if there is a bad batch Pfizer needs to know this. This patient and her girlfriends were in different locations for their Pfizer Covid Vaccine doses; they just all happened to sit down together and compare their cards. If all of the sudden it is asked why are these people who weren't in the same locations experiencing these adverse events, it might be worthwhile to consider if those Lot numbers were bad batches. She also asked if someone ends up in the emergency room or urgent care are they at the emergency room or urgent care required to report the information; or is it just for the patient to report it. What is the protocol they are supposed to do on the emergency room or urgent care's side. Caller was unwilling to complete the report. Further details for report and vaccine supplemental form not provided. The outcome of event was recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1438049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: VA
Alter: 21,0
Geschlecht: M
Eingang: 30.06.2021
Impfdatum: 30.06.2021
Beginn: 30.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling abnormal Syncope

Symptomtext

After patient received first Pfizer Covid 19 vaccine approximately 5 minutes after, the patient fainted, he was dazed for about 2 to 3 minutes and then awoke. He completely recovered after approximately 10 minutes. Refused care of EMS and stated he was fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Patient stated a history of fainting during immunizations from his teenage years.

VAERS 1433927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AR
Alter: 14,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 29.06.2021
Beginn: 29.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

After receiving first PFIZER brand COVID-19 vaccine patient had a syncope episode in clinic. After leaving exam room, while walking to appointment desk, patient stated that she may have stood up too fast and needs to sit down. Nurse sat patient in near by nurse chair. Patient then closed eyes and became limp. With the help of, RMA, LPN and patient's mom patient was assisted to a supine position on the floor with patient's head and neck supported the entire time. Within 3-5 seconds patient's eyes opened and she began speaking clearly AAAx3. Cool rags placed on forehead. Patient supported in this position for about 3-5 minutes then assisted to a seated position. Cup of water and sucker given. Patient actively talking with nursing staf and mom. After several more minutes patient assisted and ambulated to exam room. Patient on exam table in supine position for aprox 15 mins then seated for 15 mins before arrived. Patient cleared for discharged per. Patient ambulated to vehicle without difficulty. Mom advised to call with any questions or concerns. VSS b/p 97/59 HR60 Pox 96-100% , LPN Care Coordinator

Weitere VAERSDATA-Felder

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

VAERS 1416823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: ND
Alter: 20,0
Geschlecht: M
Eingang: 22.06.2021
Impfdatum: 19.06.2021
Beginn: 19.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 1414428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: ME
Alter: 33,0
Geschlecht: F
Eingang: 21.06.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Alice in wonderland syndrome Bowel movement irregularity Consciousness fluctuating Diarrhoea Dizziness Dizziness exertional Dyspnoea Fall Fatigue Gait inability Hypersomnia Hypopnoea Impaired driving ability Limb discomfort Migraine Photopsia Somnolence Syncope

Symptomtext

On the 9th of April about 3:40pm about 10 minutes after the vaccine I felt faint and waived the Doctor over because of my allergy to contrast dye I was in a section of people to be watched but I called my Dr. before the vaccine and he said I could get the vaccine. So I waived someone and they put me on a stretcher and I was in and out of consciousness for around 90 minutes so I fainted and from that point I experienced Alice In Wonderland Syndrome for the next 3-4 weeks. This is something I have since I was a child but I only get it when i have a fever so the difference is that I had no fever and was stuck in Alice In Wonderland mode so it wasn't safe to drive. The next day april 5th and I started having diarrhea and haven't had a regular bowel movement until this day. It hasn't gone away. That day also April 10th I started having breathing problems where my breathing was very shallow and it was the first time i called my Dr and asked for an appointment but at that time there wasn't enough lab work to know what was going on. Later that week around 12/13th I started having extreme fatigue and dizziness with trouble going up and down the stairs and stuck in Alice In Wonderland mode so i fell down a lot. I had trouble walking and walking my dog and started getting migraines without head pain with little lights flashing and circles that expanding, having a lot of those for several weeks but no head pain so it was odd. My last symptom before my second vaccine between 23/26 I started to feel that my limbs were really heavy and I was sleeping a lot and had a really hard time getting up in the morning and short of breath and still tired after sleeping 11 hours and that's when I got my 2nd vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: I don't believe so but to be honest I don't remember.
Aktuelle Erkrankungen: 1 month prior I had pneumonia from Feb-April
Vorgeschichte: I have Celiac disease; nerve damage; PTSD; OCD
Andere Medikamente: Abrazame; Fluvoxamine; Androgen Testosterone
Allergien: Celiac; anaphylaxis to IV contrast dye; immediate vomiting reaction to oxycodone
Vorherige Impfungen: -

VAERS 1409708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NC
Alter: 54,0
Geschlecht: F
Eingang: 18.06.2021
Impfdatum: 08.04.2021
Beginn: 25.05.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: - / RA

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

Bell's palsy Facial paralysis

Symptomtext

Bell's palsy over one month later. Right side facial paralysis.; Bell's palsy over one month later. Right side facial paralysis.; This is a spontaneous report from a contactable consumer. A 55-years-old female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection. Lot Number: EW0153), dose 2 via an unspecified route of administration, administered in right arm on 08Apr2021 at 11:00 (at the age 54-years-old) as 2nd single dose for COVID-19 immunization. Patient's medical history included hypothyroidism and patient had known allergies gluten, bee or wasp venom. Patient took 1st dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EN6207) administered in right arm on 11Mar2021; administration time at 11:00 AM. Patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Patient did not receive any other medication within 2 weeks prior to the COVID-19 vaccine. The patient had not been tested for COVID-19 nor before neither since the vaccination. Facility where the most recent COVID-19 vaccine was administered at Pharmacy or Drug Store. Patient's concomitant medications were not reported. The patient experienced bell's palsy over one month later and right side facial paralysis on 25May2021 at 12:00. The treatment medications include prednisone and Valtrex. The outcome of the event was not resolved. Follow-up attempts are needed. Further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to grains (Known allergies Gluten, bee or wasp venom); Allergy to venom (bee or wasp venom); Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1392857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IL
Alter: 20,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 07.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: UN / -

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

Electroencephalogram normal Generalised tonic-clonic seizure Laboratory test normal Neurological examination normal

Symptomtext

Generalized tonic clonic seizure on 4/15/2021. Follow up neuro exam and EEG were normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: 1,0
Labordaten: Normal lab eval and EEG
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1392656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 07.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Deep vein thrombosis Iliac vein occlusion Pelvic venous thrombosis Peripheral vein occlusion Thrombolysis Vascular operation Venogram abnormal

Symptomtext

Patient with significant right leg DVT requiring thrombolysis by vascular surgery. She will need to continue on anticoaggulants outpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 5,0
Labordaten: MRV pelvis on 6/9: Complete occluding thrombosis beginning in the right groin of the right venous system, the common femoral vein is occluded as are the right internal and external iliac veins and numerous smaller unnamed pelvic veins. Thrombus extends into and occludes the right common iliac although a left to the level of the expected anastomosis with the left system to form the IVC. There is no evidence of thrombus in the IVC. On the left side, clot is seen occluding several left-sided unnamed pelvic veins, thrombosis extends into the left internal iliac vein which is occluded, thrombus extends into the left common iliac which contains nonoccluding thrombus leading up to just proximal to the formation of the IVC. The left external iliac and the common femoral vein on the left side are patent.
Aktuelle Erkrankungen: None
Vorgeschichte: repaired gastroschisis, left thoracic outlet syndrome surgery, POTS (postural orthostatic tachycardia syndrome), and tension headaches
Andere Medikamente: Xulane 150-35 mcg/ 24 hour patch ( birth control), Lexapro, Midodrine, Mag-Ox, Corlanor
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1381854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 38,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 05.04.2021
Beginn: 04.06.2021
Tage bis Beginn: 60,0
Dosis: 2
Route/Site: IM / AR

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

C-reactive protein increased Cardiac imaging procedure abnormal Catheterisation cardiac normal Chest pain Dyspnoea Dyspnoea exertional Echocardiogram abnormal Ejection fraction decreased Electrocardiogram ST segment elevation Electrocardiogram abnormal Myocarditis Red blood cell sedimentation rate increased SARS-CoV-2 antibody test Troponin increased Ventricular tachycardia

Symptomtext

Chest pain, SOB, DOE Pt presented to hospital - transferred to university hospital - underwent LHC which was clean - Troponin rose to 2.23 - ESR, CRP elevated - active chest pain, EKG w/ diffuse ST elevation - myopericarditis - Cardiac MRI - colchicine/ibuprophen - developed NSVT, required beta blockade

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 5,0
Labordaten: ESR -42 6/8/21 CRP 82 6/8/21 Troponin 2.23 6/8/21 Covid Spike Protein Domain Antibody >250 6/7/21 Echo: 1. Normal global left ventricular systolic function. 2. Left ventricular ejection fraction, by visual estimation, is 55 to 60%. 3. Trivial pericardial effusion.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1381143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MS
Alter: 17,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Blood test Computerised tomogram Echocardiogram Electrocardiogram Pericarditis

Symptomtext

Heart problems; Diagnosed him with pericarditis that's the inflammation of the heart; This is a spontaneous report from a contactable consumer. A 17-year-old male patient (reporter's brother) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EW0153), via an unspecified route of administration on an unspecified date (at 17-year-old) as 2ND DOSE, SINGLE DOSE for COVID-19 immunisation. Medical history was reported as none and no concomitant medications. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number unknown), via an unspecified route of administration on an unspecified date (at an unspecified age) as 1st dose, single for COVID-19 immunisation. On an unspecified date after the second dose of vaccine, the patient had heart problem and doctor diagnosed him with pericarditis that's the inflammation of the heart. Lab test: He went under test after he had the symptoms multiple EKGs, multiple blood test, CT scan, and he also did ultrasound for his heart. Treatment: For the side effects he took some Motrin, for the heart problems the cardiologist told him to take some Motrin, it's Ibuprofen and that's for the side effects. The outcome of the event was unknown. Information on the batch/lot number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Name: multiple blood test; Result Unstructured Data: Test Result:Unknown results; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown results; Test Name: ultrasound for his heart; Result Unstructured Data: Test Result:Unknown results; Test Name: Multiple EKGs; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1374451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 04.06.2021
Impfdatum: 27.03.2021
Beginn: 27.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Seizure

Symptomtext

R56.9 - Unspecified convulsions

Weitere VAERSDATA-Felder

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

VAERS 1372592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 38,0
Geschlecht: M
Eingang: 03.06.2021
Impfdatum: 10.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Dizziness Electrocardiogram Immediate post-injection reaction Syncope

Symptomtext

Immediately after the shot, I began to feel light headed. The first time I felt like I was going to faint was 04/11/2021 within 24 hours of getting the shot. I began to feel lightheaded over the next few weeks. On May 2, 2021, I collapsed and fainted

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG, etc
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: Lisinipril-HCTZ 10 - 12.5 MG Tab
Allergien: None
Vorherige Impfungen: -

VAERS 1371264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: VA
Alter: 45,0
Geschlecht: M
Eingang: 03.06.2021
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Muscle tightness Peripheral swelling Thrombosis Ultrasound Doppler abnormal

Symptomtext

-tightness in inner thigh- day or so after first dose -tightness in calf worsened over the course of a couple weeks -swelling and soreness in calf gradually increased until doctor visit -doctor visit and ultrasound found multiple blood clots in mid thigh and calf -doctor prescribed blood thinner -continued swelling and tightness in thigh and calf

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: doctor visit and ultrasound on 5/24 found multiple blood clots in left leg
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: zinc - 50mg tablets
Allergien: chlorhexadine
Vorherige Impfungen: -

VAERS 1365206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AL
Alter: 38,0
Geschlecht: M
Eingang: 01.06.2021
Impfdatum: 22.04.2021
Beginn: 09.05.2021
Tage bis Beginn: 17,0
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 head Electrocardiogram Facial paralysis Magnetic resonance imaging

Symptomtext

1st shot 4/22/2021 No immediate adverse reaction. Sudden facial paralysis on left side started aprox 2? weeks later (5/9/2021). Hospital diagnosed me with Bells Palsy on 5/10/2021 after I went to the emergency room . The bells palsy has corrected itself and now I owe $13,872.05 to the hospital because I have no insurance and cannot afford to pay it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI Brain with and without contrast 5/10/21 CT Head without contrast 5/10/21 MRA head without contrast 5/10/21 EKG 5/10/21 Blood tests (not sure what tests) 5/10/21 All tests were negative or normal. They couldnt find any physical reason that was causing the bells palsy.
Aktuelle Erkrankungen: Iritis
Vorgeschichte: none
Andere Medikamente: Prescribed to Buprenorphine & Clonazepam for 9yrs prior to vaccination
Allergien: None
Vorherige Impfungen: -

VAERS 1361002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: ND
Alter: 13,0
Geschlecht: F
Eingang: 30.05.2021
Impfdatum: 29.05.2021
Beginn: 29.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Nausea Syncope Dizziness Tremor

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Additional Details: Patient sat down in waiting room right after her first COVID shot & seemed fine. She suddenly started to shake & looked dizzy. She said she just felt nauseated. We called ambulance & they checked her vitals & everything was normal. Her mother said she reacted this way to last HPV shot last year. She went home & we called her later in the day & she was feeling fine.

Weitere VAERSDATA-Felder

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

VAERS 1360892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MS
Alter: 52,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 05.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dry eye Eye pain Facial paralysis Hypoaesthesia Nausea Pain Skin irritation Tenderness Tinnitus

Symptomtext

Day after shot, right side facial paralysis Then changed to numb feeling around right eye and ache behind eye ?Pulling? at right eye Tightness of scalp Ear ringing Tenderness/pain, right side of head Dry eye Nausea (comes and goes)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Ear infection diagnosed 4/16
Vorgeschichte: Bipolar disorder Generalized Anxiety Disorder Depression Agoraphobia Hypothyroidism/Hashimotos GERD/LPR
Andere Medikamente: Lamictal (15 years) Synthroid (5 years) Wellbutrin (2 months and haven previously taken) Protonix (1 month) Pepcid (2 months) Xanax
Allergien: Penicillin family (reaction to shot) Alpha-gal (mammal meat) Mild reaction per allergy tests to milk, egg and peanuts but never noticed a real life reaction.
Vorherige Impfungen: -

VAERS 1321674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 03.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Loss of consciousness Vomiting

Symptomtext

passed out; vomited; This is a spontaneous report from a contactable consumer (patient). A 17-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm left on 03May2021 15:30 (Batch/Lot Number: EW0153) as 2nd dose, single for COVID-19 immunisation. The patient had no relevant medical history. She had no allergies to medications, food, or other products. Concomitant medication included fluoxetine taken for an unspecified indication within 2 weeks of vaccination. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in right arm on 12Apr2021, 03:30 PM (Batch/Lot Number: EW0153) as 1st dose, single for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. She was not diagnosed with COVID-19 prior to vaccination. On 04May2021 12:00, the patient passed out and vomited at the same time while in a sitting position. The were no additional side affects once the episode passed. The event resulted in doctor or other healthcare professional office/clinic visit. Events were reported as non-serious. No treatment was received. Outcome of the events was recovered in May2021. The patient had not been tested for COVID-19 since the vaccination. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: None
Andere Medikamente: FLUOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 1321674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 03.05.2021
Beginn: 04.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Loss of consciousness Vomiting

Symptomtext

passed out; vomited; This is a spontaneous report from a contactable consumer (patient). A 17-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm left on 03May2021 15:30 (Batch/Lot Number: EW0153) as 2nd dose, single for COVID-19 immunisation. The patient had no relevant medical history. She had no allergies to medications, food, or other products. Concomitant medication included fluoxetine taken for an unspecified indication within 2 weeks of vaccination. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in right arm on 12Apr2021, 03:30 PM (Batch/Lot Number: EW0153) as 1st dose, single for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. She was not diagnosed with COVID-19 prior to vaccination. On 04May2021 12:00, the patient passed out and vomited at the same time while in a sitting position. The were no additional side affects once the episode passed. The event resulted in doctor or other healthcare professional office/clinic visit. Events were reported as non-serious. No treatment was received. Outcome of the events was recovered in May2021. The patient had not been tested for COVID-19 since the vaccination. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: None
Andere Medikamente: FLUOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 1358428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 23,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 07.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain upper Alanine aminotransferase increased Aspartate aminotransferase increased Blood test C-reactive protein increased Epstein-Barr virus test Headache Liver function test abnormal Loss of consciousness Malaise Mean platelet volume increased Pain Pain in extremity SARS-CoV-2 antibody test positive Serum ferritin decreased Somnolence

Symptomtext

Headaches beginning Apr 21-25 Pain through right thigh Apr 24 Headache Bursts on right side of head began Apr 26- now Drowsy beginning Apr 26-now 1 sec blackout while sitting up on Apr 26 Side pain in upper right abdominal area beginning May 13 General malaise continues everyday Shooting leg pain continues through right thigh

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Bloodwork was done on 2 separate occasions at primary physician office. April 27 and April 30. AST and ALT levels are high (87 and 83, respectively) MPV level slightly high (12.6) Ferritin level low (10) CRP level high (systemic inflammation, 11.5) Covid antibody test indicates I have the antibodies (level=14.54) Epstein Barr Panel high levels, however this is indicative of my past mononucleosis years ago. Because of the poor liver function tests and pain in upper right abdominal, I have set an appointment to see a GI specialist on July 21.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Fluoxetine, birth control
Allergien: -
Vorherige Impfungen: -

VAERS 1358387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 48,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 28.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyskinesia Eye movement disorder Seizure Skin tightness Tearfulness

Symptomtext

The patient let us know that she had had a seizure after the first COVID shot and that she has them after every vaccine. This has happened since she was a little girl. The patient was visibly nervous before the vaccine was administered. During her observation time following the vaccine administration, she let provider know that she could feel her left arm tightening up. Provider provided the patient with an ice pack for her neck to try to calm her down. The patient asked for us to not call a rapid response yet and that "I'm trying to calm myself down." observed the patient's left hand starting to grasp and the patient became tearful so asked the patient if she was okay. The patient stated she was okay. Provider asked her to let her know if she felt like she was going to have a seizure. About a minute later, the patient let provider know she felt one coming. Provider called the RRT as the clinic Team Lead, let the patient know she was going to recline her in the chair she had been vaccinated in. Seconds after the chair was reclined, the patient's eyes started to roll back in her head and her eyelids started to flutter. Within about 10 seconds, the patient was jerking up and down in the chair. The clinic staff ensured the patient was safe until the arrival of the RRT. As the RRT arrived, the patient's seizure ended. The patient became alert to talk to the team that arrived to the clinic. She refused being seen by the ED. The clinic staff agreed to monitor her vitals until she felt comfortable to leave. After around 30 minutes after the seizure, the patient was in good spirits and stated she would like to stand and see how she felt. The patient stood up and walked around for a moment before saying she was ready to leave. Provider checked the patient out, and she left the clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Seizures after vaccination
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Every vaccine in her lifetime that she can remember

VAERS 1356079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 18,0
Geschlecht: F
Eingang: 28.05.2021
Impfdatum: 18.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Electrocardiogram abnormal Myocarditis Troponin increased Palpitations

Symptomtext

Myocarditis

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Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Elevated troponin (2.8), abnormal ECG.
Aktuelle Erkrankungen: None
Vorgeschichte: PCOS
Andere Medikamente: norgestimate-ethinyl estradiol
Allergien: Kiwi, Amoxicillin
Vorherige Impfungen: -

VAERS 1355284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WV
Alter: 40,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 18.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / RA

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

Deafness Dizziness Fatigue Feeling cold Loss of consciousness Memory impairment Mobility decreased Tinnitus

Symptomtext

I became very light headed and passed completely out. I do not remember anything leading up to this or while it was happening. When I came too, I couldn't hear, had ringing in my ears, couldn't walk on my own, and my husband said I was very cold. Two days later and i still have dizzy spells and extreme fatigue.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zyrtec, Losartan, Hydrochlorothiazide
Allergien: Tree Nuts
Vorherige Impfungen: -

VAERS 1349546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 22,0
Geschlecht: M
Eingang: 26.05.2021
Impfdatum: 05.05.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Body temperature Chest pain Dyspnoea Haemorrhage Laboratory test Pyrexia Viral myocarditis

Symptomtext

Bleeding; Shortness of breath; Chest pain; Fever of 102; Viral myocarditis; This is a spontaneous report from a contactable consumer (parent). A 22-year-old male patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration assuming left arm, at age 22 years, on 05May2021 (Batch/Lot Number: EW0153) as 2ND DOSE, SINGLE for COVID-19 immunization. The patient's medical history was reported as no. Concomitant medications were not reported. Patient historically took first dose of BNT162B2 at age 22 years on 14Apr2021 for COVID-19 immunization. Reporter's son unfortunately appeared was hospitalized for adverse reaction (bleeding) and the physician told reporter to report this. Patient had has viral myocarditis of heart on an unspecified date on May2021 after he got his second dose on 05May2021. On 06May2021, patient started having symptoms of shortness of breath, chest pain and fever of 102 (unit: unknown) after the second dose, so he went to emergency room. Then on Friday , 07May2021, he ended up with bleeding, so admission date is 07May2021 and he is still in the hospital at the time of reporting, they don't know how long. Patient also underwent lab test and procedure that includes laboratory test on May2021, 2 weeks before, patient was fine until the second dose. The outcome of the events was unknown.

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Praegender Schweregrund: Viral myocarditis
Hospital-Tage: -
Labordaten: Test Date: 20210506; Test Name: Fever; Result Unstructured Data: Test Result:102; Test Date: 202105; Test Name: laboratory test; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1348476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 59,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Seizure

Symptomtext

PATIENT WITH HISTORY OF SEIZURES WENT INTO A SEIZURE ABOUT 5 MINUTES AFTER ADMINISTRATION. PATIENT ALSO HAD SEIZURE WITH 1ST DOSE.

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

VAERS 1347321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MA
Alter: 27,0
Geschlecht: M
Eingang: 25.05.2021
Impfdatum: 10.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Myocarditis Troponin

Symptomtext

Acute Myocarditis requiring hospitalization

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Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: troponin peaked at 2.01
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Albuterol, inhaled fluticasone
Allergien: Cat dander
Vorherige Impfungen: -

VAERS 1346873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: ME
Alter: 27,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 10.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Fainted. Past history of fainting episodes. Drank water and felt better.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Oxygen 98%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1346865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: ME
Alter: 27,0
Geschlecht: F
Eingang: 25.05.2021
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

Paraesthesia Syncope

Symptomtext

felt faint with tingling in arms. Drank water, rested able to go home

Weitere VAERSDATA-Felder

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

VAERS 1323477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: GA
Alter: 46,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 14.04.2021
Beginn: 10.05.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: - / RA

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

Computerised tomogram Dyspnoea Thrombosis Pulmonary thrombosis SARS-CoV-2 test

Symptomtext

I started having shortness of breath and went to the emergency room. It was determined I had blood clots in both lungs based on a CT Scan; This is a spontaneous report from a contactable consumer (patient). A 46-years-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Right on 14Apr2021 (Lot Number: EW0153) as 2ND DOSE,SINGLE for covid-19 immunisation. Medical history included Sleep apnoea. No other vaccine in four weeks. No COVID prior vaccination. Concomitant medication(s) included phentermine hydrochloride (LOMAIRA); fluoxetine; loratadine (CLARITIN); diphenhydramine and Charlotte24 (unspecified). The patient previously took morphine and tetracycline and experienced drug allergy. Patient took the first dose of bnt162b2 (lot number EN6207) in right arm on 17Mar2021 for covid-19 immunisation. The patient started having shortness of breath and went to the emergency room on 10May2021. It was determined she had blood clots in both lungs based on a CT Scan. AE 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 hospitalized for two days. Patient received blood thinners as treatment. The patient had covid test type post vaccination nasal swab on 14May2021 with negative result. The outcome was recovering.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: 2,0
Labordaten: Test Date: 20210510; Test Name: CT scan; Result Unstructured Data: Test Result:blood clots in both lungs; Test Date: 20210514; Test Name: Nasal swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sleep apnoea
Andere Medikamente: LOMAIRA; FLUOXETINE; CLARITINE; DIPHENHYDRAMINE
Allergien: -
Vorherige Impfungen: -

VAERS 1323477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: GA
Alter: 46,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 14.04.2021
Beginn: 10.05.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / RA

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

Computerised tomogram Dyspnoea Thrombosis Pulmonary thrombosis SARS-CoV-2 test

Symptomtext

I started having shortness of breath and went to the emergency room. It was determined I had blood clots in both lungs based on a CT Scan; This is a spontaneous report from a contactable consumer (patient). A 46-years-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Right on 14Apr2021 (Lot Number: EW0153) as 2ND DOSE,SINGLE for covid-19 immunisation. Medical history included Sleep apnoea. No other vaccine in four weeks. No COVID prior vaccination. Concomitant medication(s) included phentermine hydrochloride (LOMAIRA); fluoxetine; loratadine (CLARITIN); diphenhydramine and Charlotte24 (unspecified). The patient previously took morphine and tetracycline and experienced drug allergy. Patient took the first dose of bnt162b2 (lot number EN6207) in right arm on 17Mar2021 for covid-19 immunisation. The patient started having shortness of breath and went to the emergency room on 10May2021. It was determined she had blood clots in both lungs based on a CT Scan. AE 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 hospitalized for two days. Patient received blood thinners as treatment. The patient had covid test type post vaccination nasal swab on 14May2021 with negative result. The outcome was recovering.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: 2,0
Labordaten: Test Date: 20210510; Test Name: CT scan; Result Unstructured Data: Test Result:blood clots in both lungs; Test Date: 20210514; Test Name: Nasal swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sleep apnoea
Andere Medikamente: LOMAIRA; FLUOXETINE; CLARITINE; DIPHENHYDRAMINE
Allergien: -
Vorherige Impfungen: -

VAERS 1296331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: RI
Alter: 64,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 09.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Anxiety Body height Contusion Disease recurrence Fatigue Pain in extremity Peripheral swelling Feeling abnormal Lethargy Macule Mobility decreased Pain Patient elopement SARS-CoV-2 test Sluggishness Tendonitis Thrombosis Vaccination site pain

Symptomtext

This is a spontaneous report from a contactable consumer (patient) and a physician. A 64-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 09Apr2021 in the afternoon around 2 or 3 o clock (Batch/Lot Number: EW0153) as 2ND DOSE, SINGLE for covid-19 vaccination. The vaccination was done in her building, a medical team came to them. She lives in subsidized housing. The patient's medical history included tendonitis; juvenile idiopathic arthritis from Dec 1969 and ongoing; lupus nephritis from 1989 (diagnosed ten years after SLE); systemic lupus erythematosus (SLE) from Dec 1979; discoid lupus; proliferative kidney disease stage 3; sjogren's; raynaud's; arthritis (since she was 13); bursitis; oral necrosis (this was from being on a calcium drug that they give menopausal women, it was out of her head right now when reporting. She could not think of the name. The drug was supposed to promote bone growth and keep her from getting osteoporosis); menopausal (because of chemo she started menopause at 42); vulvar lichen sclerosus; filamentary keratosis from 2015 and ongoing (this was since either Feb 2015 or Mar 2015); kidney cysts(one is benign and one is being watched); liver hepatic hemangioma; allergies (Allergies to aspirin, penicillin, dextrose IV, Biaxin, Levaquin, Cipro, band-aid adhesive, zofran, sulfa topical. The sulfa is a topical as opposed to being the sulpha with a ph.); adeno conjunctivitis from Jan2015 and ongoing (she had a really bad case of this in JAN 2015 and had to quarantine for three weeks. She lost her vision, she could not see for three days. She got a fever. It left her with a filament thing. It is just delightful. It is viral and really bad. She got it at her eye doctors office when she was there for an annual visit. She sometimes had to go there 3 times to have filament growing on her eye scrubbed off. It is wicked painful. It is quite an adventure.); she used to be three quarters but she shrunk a little; has been a couch potato for a year, it comes with the territory with lockdown and being depressed; she is immunocompromised and catches many things and is high risk She feels like a sitting duck; had issues on her palm of hands; had issues on her breasts, and chest; and various problems. Family Medical History Relevant to adverse events was none. No other vaccinations within four weeks prior to the first administration date of the suspect vaccine. No other vaccines administered on same date with the Pfizer vaccine considered as suspect. Concomitant medications included vitamin b complex (B-COMPLEX 100) 100 as dose did not clarify units, has been on for years; hydroxyzine embonate (HYDROXYZINE PAM) Dosage 25 mg, she did not remember indication, may be allergies, if she is around a cat, she takes it prophylactically; acetylsalicylic acid (ASPIRIN) low strength, 81 mg twice a week, has been on for decades, nephrologist put her on it in the 90's and She did not remember why, he said it preserves kidney function or it is good for overall health; pentoxifylline ongoing at 400 mg, 3 a day, she has been on for years, her vascular doctor prescribed; prednisone dosage:1 mg, she takes and alternates between 6 and 7 mg, If she takes lower than that, she is a "narcoleptic" (as reported, did not clarify); rosuvastatin Dosage:10 mg, frequency not specified, it is a nightly thing; fish oil (SUPER OMEGA 3) overall supplement that was suggested by former nephrologist at some point some; estradiol (YUVAFEM) Dosage:10 micrograms for menopause, vaginal dryness; there was no variable in her medication routine, she is on a long list of medications (she could not remember, one was blood pressure, with the last administration she was worked up and her blood pressure would not come down, she also takes Tylenol as needed), she provided the details as she knows them, but did not know full details for all of her medications. There was nothing new to her routine except like when Prilosec was taken off the market, she got a different medication for it. She has been on all of these for long term maintenance. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 19MAR2021 (at the age of 64-year-old)(Batch/Lot Number: ER2613) for covid-19 vaccination, adverse events following prior vaccinations: none; and flu vaccine for immunization in last fall, 2020. She has a history of obscure side effects to medication, things that people have never heard of and she is the 1 in a million that has ever had these problems. The patient previously took ondansetron (ZOFRAN), ("a chemotherapy treatment", given before chemotherapy), which gave her a homicidal migraine and they had to give her ice packs for her head; 9 rounds of "Cytox" (Cytoxin or Cytoxan) she was not sure how this was spelled, and chemotherapy (9 rounds of chemo); azathioprine (IMURAN), she does not know if it was spelled Immuran or Imuran; prednisone a number of years and she said to her rheumatologist, "it did not make sense on an intellectual basis that the prednisone being effective in her body as it was once" and he said he would give her IMURAN which is given to kidney patients to cause less of a reaction with the organ, and patient mentioned she had barely an immune system after all these years on prednisone, she went through 3 rounds of steroids; Heparin IV, which made her arm feel on fire on the inside, which they would not give her a flush when she had IV treatment; Dextrose IV made her skin feel hot and itchy, her mouth felt like she put something in that had been soaking in rubbing alcohol; ciprofloxacin (reported as "Cipro"), she had a bad reaction to Cipro, she was given after she was bit by a dog on her calves, she knew it was attached to and is "hurting her calves the rest of her life/the podiatrist said if it has not gone away, she is kind of stuck" (as reported, not specified). The patient just wanted to give Pfizer a full picture of what she was dealing with and she is an unusual case. She added that chemo was in the 90s and that is when all of the medication reactions she mentioned were. She absolutely does not have any of the information about the products she mentioned she had previous reactions to. Every time they did "this", it "hurt" and she asked them not to do it anymore. She asked them to not do dextrose anymore with the chemo because it feels like it is on fire, and she asked them to mix it with saline. She did not have any additional information, did not have the NDC, LOT, expiration date, or manufacturer for any of these medications she reported historical adverse events on. The patient reported that she got her 2nd shot of the Pfizer covid vaccine on 09Apr2021. She has soreness at the site, more-so several hours after getting the vaccine (09Apr2021). Just her arm felt sore within moments after the second vaccine, but she did not get this after the first. She rested and took it easy that weekend. There was Sore, Tired, general lethargy, and fatigue (Apr2021): when she looked online, it really only told her what everyone knows about that you might be sore and tired and she had all that, she thought she was through with all of that. She had no chills, just general lethargy and fatigue. She was sluggish and tired and not herself that weekend (Apr 2021). She stayed home so it is difficulty to say. Her arm was definitely sore. For sluggishness and fatigue, she said that she has been a couch potato for a year, it comes with the territory with lockdown and being depressed, so it is difficult to decide if it is health or physically induced or a emotional base. She did not knowingly spike a fever, no chills or sweats. And on Monday (did not clarify dates but states it was Monday after 09APR2021, throughout the weekend she took it easy), she noticed with her foot, she had difficulty getting out of bed could not put weight on her right foot. She was alarmed. She stayed home and rested and did a lot of napping and taking it slow. It is still difficulty and moving certain ways hurts more if she flexes. She has a known history of tendonitis so she wore her brace in the meantime. She thought maybe she had tendonitis in both ankles and this was similar so maybe it was a different set of tendons. She would wear a brace, and eventually it will get better in time. She also was wearing braces like compression socks that toes stick out of. She thought she had tendonitis and that is what she has done in the past. It has been a month and she is not better. This was her left foot, most of the pain was focused on the sole of her foot towards the outer edge. That is where it started. Then it migrated over time. That was weird and had her worried. It was all in her arch in the initial spot. She notes it is not like the tendonitis she had the first time. She does not want to be an alarmist or have her doctor think she is a hypochondriac she waited. She was then rubbing her foot, the right one, and noticed it was tender on the top of her foot just like the left one. There was sore. There was pain in right foot, pain in feet. Pain in feet, her left foot had most of the pain on the top and bottom and a lot of it is along the outer part of her sole of the foot. In her right foot, the pain is mostly at the fleshy part below her toes and on top of her foot. The pain moved around into the other foot for about a month so she went to the podiatrist yesterday (06May2021) and doctor did x-rays. The night before (05May2021), the opposite leg had a line of black and blue dots on her right calf that went up her leg, she did not notice this until Wednesday (05May2021) evening because she never examines it. She soaped up a washcloth and she knew where her parts are in the bath. Her mind wanders and she was not looking. She happened to be wearing something where her legs were not covered and that is how she knew. It did not hurt. It was strange, looking like bruising in a line. The doctor said it was all like one vein and he cold feel it. She can not feel it, but he could. The doctor told her these could be clots. She still has them. Doctor said the other leg where she had the pain was only soft tissue pain. Doctor found that every place that hurt when he touched it and it still hurts where he had touched it. She was told she does not have arthritis and she has had arthritis since she was 13. The doctor did not know what it is. It was her left foot constantly, and the right foot hurt off and on during that period. The left for sure was kind of a dull ache and throbbing. The right was only a little bit. The left was worse. It appeared to be soft tissue that was hurting and he said there are so many side effects of this new vaccine and to maybe try heat or ice. Ever since the patient left doctor's office until now (the time of reporting) she did not known if she need to be concerned, that if she does not know what it is, can ice or heat make it worse? She did not know the next steps. Treatment, she tried to keep it elevated because that can not hurt but that is about it. She has not done heat and ice because if the doctor does not know what it is, how does he know it will not make it worse. He asked if she could take aspirin and she said no she is allergic to aspirin. Tylenol she does not take often, only when she feels like she needs it and she has not been doing it often. When she stays off it, it does not hurt as much as when she is walking. She wanted to know if she should be worried and she wanted to add (report this) to the database if this is a side effect and if Pfizer has ever heard of this before. There was also tired, general lethargy, and fatigue. At this point when reporting, she is single and lives alone, and said that "God forbid something happens, there is nobody to say let's get you to a hospital". She heard about blood clots on the news. When they said blood clot yesterday, it was a red warning light going on and a siren. At the time of reporting it was Friday and she did not know that if she need to rush to the hospital. Her primary care physician (PCP) said she had never heard of this and to call Pfizer. The patient asked if she is one of a small group of people this has happened to. She asked if she should not worry and it will go away or should she get to a hospital. She thought she had a problem with her feet (foot problem) but her podiatrist does not know what was going on. She communicated with her physician office today and she said she has never heard of this. She wanted to know if her symptoms have been heard of and if she should go to the hospital. The events did not require a visit to emergency room. The patient underwent lab tests and procedures which included: height as "5 and three quarters of an inch feet (5'0.75")" on an unspecified date; rapid COVID-19 test on 06May2021: negative; regular COVID-19 test on 06May2021: negative; x-ray on 06May2021 to make sure she did not break anything: unknown results. She also went because she had not done it in a year and she had something from the health department saying to get tested weekly for the virus (clarified that she was talking about the COVID tests as what she went and got done). The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Name: height; Result Unstructured Data: Test Result:5 and three quarters of an inch feet; Comments: 5 and three quarters of an inch feet (5'0.75"); Test Date: 20210506; Test Name: rapid COVID test; Test Result: Negative ; Test Date: 20210506; Test Name: regular COVID test; Test Result: Negative ; Test Date: 20210506; Test Name: x-rays; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: Juvenile rheumatoid arthritis; Keratosis (filamentary keratosis; this was since either Feb2015 or Mar2015); Viral conjunctivitis (adeno conjunctivitis/It is viral and really bad)
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (since she was 13); Body height decreased (she used to be three quarters but she shrunk a little); Breast disorder female (issues on her breasts, and chest); Bursitis; Cyst of kidney (one is benign and one is being watched); Depression (has been a couch potato for a year, it comes with the territory with lockdown and being depressed); Discoid lupus erythematosis (discoid lupus); Drug allergy (aspirin, penicillin, dextrose IV, Biaxin, Levaquin, Cipro, band-aid adhesive, zofran, sulfa topical); Hemangioma of liver; Immunocompromised; Kidney disorder (proliferative kidney disease stage 3); Lupus nephritis (diagnosed ten years after SLE); Menopausal (because of chemo she started menopause at 42); Musculoskeletal disorder (issues on her palm of hands); Necrosis mouth (this was from being on a calcium drug that they give menopausal women); Raynauds; Sjogren's; Systemic lupus erythematosus; Tendonitis; Vulval lichen sclerosus et atrophicus
Andere Medikamente: B-complex 100; HYDROXYZINE PAM; ASPIRIN; PENTOXIFYLLINE; PREDNISONE; ROSUVASTATIN; SUPER OMEGA 3 [FISH OIL]; YUVAFEM; PRILOSEC [OMEPRAZOLE]
Allergien: -
Vorherige Impfungen: -

VAERS 1337910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: VA
Alter: 20,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 21.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: Fainted, recovered within seconds. Gave water and monitored-Severe

Weitere VAERSDATA-Felder

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

VAERS 1337129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AL
Alter: 13,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 18.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Loss of consciousness Syncope

Symptomtext

Vasovagal syncope with full passing out the following day after the vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, allergic rhinitis/conjunctivitis, eczema
Andere Medikamente: Albuterol, Zyrtec, Azelastine eye drops, topical Hydrocortisone
Allergien: None
Vorherige Impfungen: -

VAERS 1334666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WV
Alter: 48,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Presyncope

Symptomtext

Vasovagal reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EMS assessment refusal of transport.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1332375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 38,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 14.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

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

Ageusia Bell's palsy Dizziness Facial paralysis Headache Magnetic resonance imaging Metabolic function test Nausea Photophobia

Symptomtext

I started having a headache the same day non stop, nausea and light dizziness, sensitivity to bright lights and a week after the vaccine I lost my sense of taste on my right side of my mouth. April 25th I woke up to my right side of my face paralyzed and rushed to the ER. I was diagnosed with Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI and POCT CHEM 8
Aktuelle Erkrankungen: N/A
Vorgeschichte: Migraines
Andere Medikamente: Multivitamin One a Day, vitamin D and collagen+biotin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1321779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MT
Alter: 48,0
Geschlecht: M
Eingang: 16.05.2021
Impfdatum: 04.05.2021
Beginn: 09.05.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / LA

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

Atelectasis Back pain Computerised tomogram abnormal Fibrin D dimer increased Insomnia Pulmonary infarction Thrombosis

Symptomtext

On May 9th I began to experience severe pain in my back extending down my left side. The pain was severe enough to prevent sleeping that night. The pain continued throughout May 10th becoming worse with deep breaths or any type of internal strain (cough, sneeze, etc). That evening, I took two Tylenol and later two Ibuprofen and was able to sleep. The pain persisted for the next week, slowly improving but not fully going away. On May 15th I conducted a telemedicine appointment and was advised to go to either Urgent Care or the ER. I chose the ER at Hospital. A D-Dimer test showed elevated results and a CT scan was ordered. The CT revealed blood clots in my right lung, specifically "Subpleural conslidation in the posterior basilar segment the right lower lobe is present, compatible with pulmonary infarct. Question additional pulmonary infarct in the lateral basilar segment the lower right lobe. Probable atelectasis in the left lung base." MD prescribed Eliquis @ 10mg 2x daily and I was discharged with a referral to .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: D-Dimer, CT scan "Helical axial images were performed after the administration of IV contrast with multiple reconstructions. Coronal MIP images through the chest were also generated. CT dose-reducing technique was utilized." Contrast was "75 mL Isovue 370"
Aktuelle Erkrankungen: None
Vorgeschichte: Early stage cardiovascular disease (mild calsification)
Andere Medikamente: Vitamin D3 (5000 IU) 1x daily; Aspirin 81mg 1x daily
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1320351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 75,0
Geschlecht: F
Eingang: 15.05.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Anaphylactic reaction

Symptomtext

Anaphylaxis reaction (itching, rash, tingling, insomnia); This is a spontaneous report from a contactable Nurse. This 75-years-old female Nurse (patient) reported herself that she received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Lot number and expiration date unknown), via an intramuscular route of administration, administered in arm left on 09Apr2021 09:45 at age of 75-year-old at a single dose for COVID-19 immunization. Medical history included ongoing hypertension and patient was diagnosed with high blood pressure probably 30 years ago. Patient reported that she was put on amlodipine because her other blood pressure medication wasn't keeping her blood pressure down. patient unable to provide details for blood pressure medication she took before amlodipine, ongoing reflux gastritis patient reported that she was diagnosed with acid reflux 25 years ago, ongoing osteoporosis patient was diagnosed with osteoporosis 3.5 years ago, ongoing scoliosis patient was diagnosed with scoliosis as a child when she was 11 years old. Patient reported that she had surgery 3.5 years ago and her spine was fused from T3 to her coccyx. Patient reported that when she was diagnosed with scoliosis, the doctors back then said that surgery was too drastic. Patient reported that an orthopedic back specialist advised her parents not to let anyone touch the caller, ongoing blood cholesterol increased patient was diagnosed with high cholesterol a year and a half ago, hysterectomy from an unknown date and unknown if ongoing Caller reported that she had a hysterectomy when she was 40. Family Medical History Relevant: Caller reported that she has a grandson that has a severe reaction to tree nuts. Caller reported that her grandson is the only one in her family that she knows of that has a severe allergy to something specific. The patient did not have a history of any previous allergies to specific products or any conditions indicative of an allergy. Concomitant medications included calcium taken for hysterectomy from an unspecified start date and ongoing, esomeprazole taken for reflux gastritis from an unspecified start date and ongoing, Atorvastatin taken for blood cholesterol from an unspecified start date and ongoing, losartan potassium taken for blood pressure measurement from an unspecified start date and ongoing, amlodipine besylate taken for blood pressure measurement from an unspecified start date and ongoing, alendronate sodium taken for osteoporosis from an unspecified start date to Apr2021. Calcium: Caller reported that she has been taking Calcium for years. Fosamax: Caller reported that her doctor cancelled the Fosamax because it was causing a problem with reflux, burning and so forth. Caller reported that her physician is trying to get her one something that is given by an infusion once a year to replace the Fosamax. Caller reported that she took the Fosamax in the morning with water, no food, and didn't lay down afterward. Caller reported that she knew that it would cause problems if she laid down after taking the Fosamax. Fosamax Product Info: NDC: 69097-224-16, Lot Number: GC00501, Expiration Date: Apr2023. Caller reported that she used another medication for 2 years before Fosamax that was given via injection that can only be given for 2 years. Losartan: Caller reported that she was on another blood pressure medication and the pharmacy called and told the caller to stop taking that blood pressure medicine. Caller reported that the pharmacy informed her that they had gotten reports that her blood medication was bad medication. Caller reported that she received the medication and phone call from the Pharmacy. Caller reported that the pharmacy instructed her not to take any more of the blood pressure medication and to go back to her doctor and have him prescribe something else. Caller reported that the pharmacy informed her that the product had something in it that is not good for your health. Caller was queried for details on her old blood pressure medication. Caller reported that she threw the medication in the trash because the pharmacy explained that it could be deadly to her health. Caller unable to provide details of the blood pressure medication she took before Losartan. Scoliosis: Caller reported that her brother found out that there are surgeons that are taking care of scoliosis in older patients at the hospital. Caller reported that she had the surgery done and it has allowed her to have her life back because she was going down very fast in what she could do. Caller reported that the pain was just too much at times. Caller reported that her quality of life was poor and now it's very good. Caller reported that she didn't go to see her physician for the rash or itching, she just took Benadryl and waited it out. The patient did not receive any recent vaccines for any other conditions prior to the event being reported, the patient did not receive any recent vaccines for SARS-CoV2 other than Pfizer BIONTECH COVID-19 Vaccine prior to the event being reported, the patient did not received any other vaccines around the time of the Pfizer BIONTECH COVID-19 Vaccine vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced anaphylaxis reaction, (itching all over just severely from head to toe, small rash on back, lips tingle a little) on 09Apr2021, patient itching so bad she couldn't sleep. Patient reported that she received her first dose of the Pfizer Covid-19 vaccine on 09Apr2021. She was supposed to have her second dose of the Covid-19 vaccine today, 07May2021, but she called and cancelled the appointment. The lady that gave the caller the Covid-19 vaccine called her wondering why she had cancelled her appointment. Patient had a reaction from the first dose of the Covid-19 vaccine where she was itching all over just severely from head to toe. Patient was miserable and took Benadryl. Patient reported that the Benadryl helped her get to sleep. Patient reported that she also had a small rash on her back that she put Benadryl cream on. Patient reported that the rash lasted 2 days or so. Patient reported that she has a little itching now but it's nothing, the itching could be just normal for her. Patient reported that for 2 days the itching was not normal at all, it was severe itching. Patient reported that she didn't know if she should even have the second dose of the Covid-19 vaccine following her reaction to the first dose. Patient reported that she called the pharmacist who instructed the caller to call her physician. Caller reported that she called her physician and he informed the Patient that there is not enough information for him to be able to tell the caller what she should do. Caller reported that she asked her physician if she took a Benadryl before she went to get the second dose of the Covid-19 vaccine and took someone with her to the vaccination facility, would that be enough. Patient reported that her physician informed her that he would definitely recommend that the caller take Benadryl if she gets the second dose of the COVID-19 vaccine, but would not tell the caller whether or not she should get the second dose. Patient reported that she didn't know how long you had to decide to get the second dose of the Covid-19 vaccine or not. Caller reported that someone told her that you have 3 weeks after the first dose of the Covid-19 vaccine and 3 weeks after you're supposed to have the second dose. Caller inquired how much longer she has to decide whether or not to get the second dose of the Covid-19 vaccine. Patient reported that the itching began about 5 hours after she received the first dose of the Covid-19 vaccine on 09Apr2021 and the itching was severe for at least 2 days. Patient he has itched a little here and there, patient is always out in the yard doing something. Patient nose itched so bad that she couldn't stand it, not having any trouble with breathing and lips tingled a little and she wondered if that was just from itching. Patient was trying to use her knowledge to figure all of this out on her own. Caller reported that's all she could figure out and it was mainly severe itching. Patient had no swelling of the lips and no difficulty swallowing or breathing. Patient couldn't sleep due to the itching, so she would say that the itching was at least almost definitely medically significant, patient reported that it wasn't life or death, the itching was just annoying. Patient was constantly just scratching her head a little and she feels a little itchy at places. Patient did not know if in the past she has been itchy before but she doesn't think that she has. Small rash on back: Caller reported that when the severe itching began, there was one place on her back that she started scratching. Caller reported that she had her husband look at her back and he informed her that there was a little rash back there. Patient reported that her husband stated the rash was probably about 5 inches but only maybe 2 inches the other way. Caller reported that the rash was not a big area. Patient didn't have her husband look at the rash after that. Caller reported that when she took Benadryl orally, the itching stopped and she just let it go. Caller reported that she did have her husband look the other day and the rash was no longer there, itching, rash, tingling, insomnia was diagnosis as anaphylaxis. The patient did not required medical intervention, the patient did not visit in the Emergency Department or physician office, not hospitalized and not admitted to an Intensive Care Unit. Seriousness of the event was reported as always serious, medically significant. The outcome of event was recovering. Additional information has been requested.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the event anaphylactic reaction and the suspect drug BNT162B2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high (Caller reported that she was diagnosed with high blood pressure probably 30 years ago. Caller reported that she was put on amlodipine because her other blood pressure medication wasn't keeping her blood pressure down. Caller unable to provide details for blood pressure medication she took before amlodipine.); High cholesterol (Caller reported that she was diagnosed with high cholesterol a year and a half ago.); Osteoporosis (Caller reported that she was diagnosed with osteoporosis 3.5 years ago.); Reflux gastritis (Caller reported that she was diagnosed with acid reflux 25 years ago.); Scoliosis (Caller reported that she was diagnosed with scoliosis as a child when she was 11 years old. Caller reported that she had surgery 3.5 years ago and her spine was fused from T3 to her coccyx. Caller reported that when she was diagnosed with scoliosis, the doctors back then said that surgery was too drastic. Caller reported that an orthopedic back specialist advised her parents not to let anyone touch the caller.)
Vorgeschichte: Medical History/Concurrent Conditions: Hysterectomy (Caller reported that she had a hysterectomy when she was 40.)
Andere Medikamente: CALCIUM; ESOMEPRAZOLE; ATORVASTATIN; LOSARTAN "AGP"; AMLODIPINE BESYLATE; FOSAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 1320052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 20,0
Geschlecht: F
Eingang: 15.05.2021
Impfdatum: 29.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Blood glucose Dizziness Syncope

Symptomtext

fainted; very light-headed; This is a spontaneous report from a contactable consumer (patient). A 20-year-old female patient (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EW0153) via an unspecified route of administration at left arm on 29Apr2021 10:45 (20-year-old at time of vaccination), at single dose, for COVID-19 immunization. The patient's medical history included anxiety, ADHD, and allergies to amoxicillin. Concomitant medications in two weeks included amfetamine aspartate/ amfetamine sulfate/ dexamfetamine saccharate/ dexamfetamine sulfate (ADDERALL) and Vitamin D3. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EW0153) via an unspecified route of administration at left arm on 07Apr2021 10:30 (20-year-old at time of vaccination), at single dose, for COVID-19 immunization. There was no other vaccine in four weeks. The patient was very light-headed and fainted on 29Apr2021 15:45. Adverse events resulted in Emergency room/department or urgent care. Prior to vaccination, the was not patient diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Therapeutic measures were taken as a result of the events and included "Ruled out heart issue, checked blood sugar level". The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: blood sugar level; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD; Anxiety; Drug allergy
Andere Medikamente: ADDERALL; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 1317346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MD
Alter: 26,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

Patient got his vaccine and was waiting in the waiting area and about five minutes later, he temporary loss consciousness for about a minutes. After about a minute, he full regained consciousness and EMS was called. He was taken to the hospital for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: No known drug reactions
Vorherige Impfungen: -

VAERS 1317009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 20.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Confusional state Feeling abnormal Head injury Loss of consciousness

Symptomtext

Support staff checking in patients outside the building witnessed a patient passing out at the top of the walkway. One person ran inside to get the clinic coordinator. She immediately asked staff to call EMS and she ran out to assess the situation. The patient was lying on his side motionless. She attempted to rouse the patient and assess if CPR was needed. The patient opened his eyes and looked dazed and confused. He rolled on his back. He began to verbally respond and apologized for passing out. He stated that this happens to him frequently when he gets an immunization or blood drawn. He had abrasions and a small contusion on the left side of his face in the temple region with a small amount of blood and dirt from hitting the sidewalk. She was joined by NP and NP along with 2 medical assistants. While waiting to EMS to arrive, campus police came on the scene to help direct EMS whenever they arrived. Vitals were taken BP 140/70 HR 62 2:30 PM . An ice pack was applied to his head. Additional information on the patient?s identity was acquired. Patient was alert and oriented. Patient had his cellphone and attempted to call his wife with no answer. He also sent her a text. EMS arrived on the scene. Patient?s wife called and she apprised her of the situation as EMS assessed the patient. After their examination, EMS declined to transport the patient due to the patient's narrative of this situation occurring frequently. They advised him to follow-up with his MD and left the scene. Clinic staff and campus police stayed on the scene until the patient?s wife arrived. She was advised to take him immediately to the ED to be assessed for a head injury. Wife drove patient to hospital. She called the patient later that evening. Patient stated he was thoroughly examined for a potential head injury and was cleared. He was given information on interventions he can try to use to avoid a severe vasovagal incident in the future. Patient was cleared to get his second dose of COVID-19 vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1313726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: GA
Alter: 50,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Dyspnoea Pharyngeal swelling

Symptomtext

Anaphylactic reaction. treatment with EpiPen. patient treated with own EpiPen. EMT called and was retreated with EpiPen. Also given Benadryl by RPh on duty. given IM Benadryl by EMT. Throat swelled up and pt has trouble breathing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Benadryl,
Allergien: latex, morphine, iodine, silicone, avocado,
Vorherige Impfungen: -

VAERS 1313038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 53,0
Geschlecht: M
Eingang: 13.05.2021
Impfdatum: 20.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Musculoskeletal stiffness Thrombosis Vaccination site bruising Vaccination site discolouration Vaccination site erythema Vaccination site pain

Symptomtext

possible thrombosis reaction; Unexpected bruising near injection site.; Bruise was purple and red splotches and has now progressed to mostly yellow/discoloration; Bruise was purple and red splotches and has now progressed to mostly yellow/discoloration; minimal pain/stiffness following the shot; minimal pain/stiffness following the shot; This is a spontaneous report from a contactable consumer (patient). A 53-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at the age of 53-year-old via an unspecified route of administration, administered in Arm Left on 20Apr2021 11:15 (Lot Number: EW0153) at 1st dose, single for covid-19 immunisation. The patient medical history was not reported. The patient received no 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 had not been tested for COVID-19. Concomitant medication included famotidine (PEPCID AC). The patient previously took flu shot in Oct2020, prilosec [omeprazole magnesium] for seasonal allergy and experienced drug hypersensitivity. The patient experienced unexpected bruising near injection site. Bruise was the size of the bandaid, approximately 1" x 2". Bruising had persisted for more than a week now. The patient had never experienced bruising like this with other vaccines. He would like to rule out possible thrombosis reaction before second shot. He did not have bruising at any other locations other than the injection site. Bruise was purple and red splotches and has now progressed to mostly yellow. He believed the discoloration was a reaction to the vaccine and not the result of the needle. The shot itself was painful but patient felt minimal pain/stiffness following the shot. The event start date was on 20Apr2021. No treatment was received. The outcome was unknown.

Weitere VAERSDATA-Felder

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

VAERS 1311270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 27.03.2021
Beginn: 10.04.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / LA

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

Abnormal uterine bleeding Headache Seizure Vaginal haemorrhage

Symptomtext

R56.9 - Unspecified convulsions N93.9 - Abnormal uterine and vaginal bleeding, unspecified VAGINAL BLEEDING HEADACHE

Weitere VAERSDATA-Felder

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

VAERS 1310823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 30,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 10.05.2021
Beginn: 10.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Chills Dizziness Feeling hot Headache Hyperhidrosis Loss of consciousness Nausea Pain

Symptomtext

I was fine throughout the morning of 5/10 with mild body aches developing in the afternoon. The body aches worsened in the evening and were then accompanied by cold chills throughout the body and a moderate headache, especially an occasional sharp pain in the lower right side of the back my skull. As I tried to make my way to bed at 8:30 pm, I got extremely lightheaded and nauseous and ended up passing out for a second and falling to the floor. The lightheadedness and nausea lasted for about 15 minutes before finally passing. I took Advil at this point and went to bed. Throughout the night, my body alternated between cold chills and burning up, profusely sweating. A mild headache persisted throughout the night. I took Advil again in the morning of 5/11. I continued to have minor body aches and a slight headache throughout most of the day, including the same occasional sharp pain in the lower right of the skull, but no more chills, lightheadedness, or nausea. All side effects subsided by the morning of 5/12.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Spironolactone 150 mg daily Syeda birth control daily Onexton topical gel daily Adapalene topical gel daily
Allergien: None
Vorherige Impfungen: -

VAERS 1309533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 11.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / RA

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

Asthenia Balance disorder Blood pressure increased Blood pressure measurement Dizziness Musculoskeletal stiffness Nausea Nervousness Presyncope Tremor Vaccination site pain

Symptomtext

weakness; Right arm sore at injection site; Body started shaking uncontrollably; she felt faint; she felt like she was going to pass out; feeling off kilter; nauseous; a stiffness in the back of her neck; she checked her blood pressure and it elevated; Felt jumpy; This is a spontaneous report from a contactable consumer (patient) via Medical Information team. A 66-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EW0153) via an unspecified route of administration, administered into right arm on 11Apr2021 as 1st dose, single for COVID-19 immunization. The patient's medical history was not reported. Concomitant medications include vitamins and supplements (unspecified). On 14Apr2021, patient felt jumpy. On 15Apr2021, patient felt faint, she felt like she was going to pass out as she was feeling off kilter, she was nauseous, had a stiffness in the back of her neck, she checked her blood pressure and it was elevated. On an unspecified date, she experienced weakness, right arm sore at injection site and her body started shaking uncontrollably. Outcome of events was unknown. No follow-up attempts are needed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20210415; Test Name: blood pressure measurement; Result Unstructured Data: Test Result:elevated
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1305747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 54,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 24.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Chest pain Chills Headache Loss of consciousness Nausea Pain

Symptomtext

was going to blackout; Body aches; headache; chills; nausea; Chest pain; This is a spontaneous report from a contactable consumer reported for self. A 54-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 2 via an unspecified route of administration, administered in Arm Left on 24Apr2021 20:30 (Batch/Lot Number: EW0153) as 2nd dose, single for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Medical history included Heart murmur. Prior to vaccination, the patient did not diagnose with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient's concomitant medications were not reported. Historical vaccine included the first dose of BNT162B2 via an unspecified route of administration, administered in Arm Left on 01Apr2021 (Batch/Lot Number: EP7533) as 1st dose, single for COVID-19 immunization. On 25Apr2021 16:00, the patient experienced body aches, headache, chills, nausea and chest pain, chest pain was severe with chills, felt like she was going to blackout, her husband propped her up in bed, gave Advil and a cool rag for her head, temp was 98.3 Fahrenheit. Outcome of the events were unknown. Follow up attempts needed. Further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210425; Test Name: temp; Result Unstructured Data: Test Result:98.3 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart murmur
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1304126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: FL
Alter: 80,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 04.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / RA

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

Bell's palsy Blood pressure increased Facial paralysis

Symptomtext

patient experienced partial paralysis of face, left face. was taken to the hospital, ruled out a stroke.. diagnosed bell's palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: patient was taken to the hospital 04/30/2021. patient had elevated blood pressure.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1302548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 45,0
Geschlecht: M
Eingang: 10.05.2021
Impfdatum: 01.05.2021
Beginn: 05.05.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Deep vein thrombosis Fibrin D dimer increased Pain in extremity Ultrasound scan abnormal

Symptomtext

Deep vein thrombosis (DVT). Woke up on 4th day after vaccine (May 5, 2021) with pain in calf. Swelling continued to get worse. Went to an emergency room just over one week after vaccine (May 8, 2021) and was diagnosed with DVT in the lower left calf (after D Dimer test and ultrasound). No family history of clotting issues. And no personal history of clotting issues. Currently on Rivaroxaban (Xarelto), 15 mg twice per day. Will be on for at least 3 months (moving to 20 mg once per day after the first 21 days).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: D-dimer (May 8, 2021) - High (exact numbers from hospital not available to me) Ultrasound (May 8, 2021) - Confirmed DVT
Aktuelle Erkrankungen: Gout
Vorgeschichte: Hypothyroidism, GERD
Andere Medikamente: Levothyroxine, prilosec
Allergien: -
Vorherige Impfungen: -

VAERS 1299197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

schwer

Staat: MO
Alter: 51,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / LA

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

Chest pain Computerised tomogram thorax Pain in extremity Thrombosis Ultrasound scan

Symptomtext

I had an ultrasound done on my leg where a blood clot was found. I had a chest CT performed where several clots were found; Two days after my vaccine I began having severe pain in my right leg in the calf area and pain in my chest when I took a deep breath or coughed. Over the weekend it got worse and worse, on Tuesday th; Pain in my chest; This is a spontaneous report from a contactable consumer (patient). A 51-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in left arm on 14Apr2021 13:00 (Batch/Lot Number: Ew0153) (at the age of 51 years old) as single dose for COVID-19 immunization. The patient medical history was not reported. Concomitant medications included duloxetine; trazodone; pregabalin (LYRICA); oxycodone hydrochloride, oxycodone terephthalate, paracetamol (PERCOCET [OXYCODONE HYDROCHLORIDE;OXYCODONE TEREPHTHALATE;PARACETAMOL]); and meloxicam, all taken for an unspecified indication, start and stop date were not reported. The patient previously took vancomycin and daptomycin and experienced drug allergy to these medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 16Apr2021 09:00, two days after the vaccine, the patient began having severe pain in his right leg in the calf area and pain in his chest when he took a deep breath or coughed. Over the weekend, it got worse and worse, on Tuesday 20Apr2021, the patient had an ultrasound done on his leg where a blood clot was found. He had a chest computerized tomography (CT) performed where several clots were found. The event resulted in doctor or other healthcare professional office/clinic visit. The treatment included blood thinners. No COVID prior vaccination and not COVID tested post vaccination. The case was assessed as non-serious by the reporter. The outcome of the event was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210420; Test Name: Chest CT; Result Unstructured Data: Test Result:Several clots were found; Test Date: 20210420; Test Name: Ultrasound; Result Unstructured Data: Test Result:Blood clot was found
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: DULOXETINE; TRAZODONE; LYRICA; PERCOCET [OXYCODONE HYDROCHLORIDE;OXYCODONE TEREPHTHALATE;PARACETAMOL]; MELOXICAM
Allergien: -
Vorherige Impfungen: -

VAERS 1299106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: MA
Alter: 49,0
Geschlecht: F
Eingang: 08.05.2021
Impfdatum: 06.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: - / LA

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

Deep vein thrombosis Erythema Investigation Limb mass Pain Swelling Tenderness Ultrasound scan

Symptomtext

2 weeks after vaccine noticed pain; Swelling; Tenderness; redness; lump on left leg; Superficial clot and other DVT clot found; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female consumer received his first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), from lot ew0153 as single dose via unknown route at the left arm on 06Apr2021 11:30, at the age of 49 years, for COVID-19 immunization. The patient was not pregnant. Medical history included, in 1996 while on oral contraceptives had a blood clot in left leg. Prescribed Coumadin for year. Went off, bad leg swelling occurred. Prescribed compression stocking. Genetic test discovered Factor V Leiden mutation heterozygous. Since 1996-1998, have had bad swelling in left leg but no further clotting. Last time ultrasound was needed to confirm leg was just bad swelling was approximately 2007. No other clotting since around 1996-1998. Concomitant medications were not reported. On evening 20Apr2021, 2 weeks after vaccine, noticed pain, swelling, tenderness, redness and lump on left leg. Went to doctor on 21Apr2021. Ultrasound performed. Superficial clot and other DVT clot found. Prescribed Xarelto. The outcome of the events was reported as recovering. No covid prior vaccination and the patient was not tested for covid post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Test Name: Genetic test; Result Unstructured Data: Test Result:Factor V Leiden mutation heterozygous; Comments: Genetic test discovered Factor V Leiden mutation heterozygous; Test Date: 2007; Test Name: Ultrasound; Result Unstructured Data: Test Result:bad swelling; Comments: Last time ultrasound was needed to confirm leg was just bad swelling was approximately 2007
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1296627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 07.05.2021
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Bell's palsy

Symptomtext

Bells Palsy of left side of face developed starting the day after shot #2 and getting worse over the course of a week

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: went to Urgent Care and ER and both did physical exam to make sure it was not a stroke and both diagnosed Bell's Palsy on 4/22
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, seasonal allergies
Andere Medikamente: Claritin, Lexapro, QVair, flonase
Allergien: nickel allergy
Vorherige Impfungen: -

VAERS 1417243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MN
Alter: 20,0
Geschlecht: M
Eingang: 06.05.2021
Impfdatum: 30.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arteriogram coronary normal Back pain Chest pain Chills Echocardiogram normal Electrocardiogram repolarisation abnormality Fibrin D dimer Hyperhidrosis Laboratory test normal Myocarditis Painful respiration Pyrexia SARS-CoV-2 test negative Tobacco user Troponin increased

Symptomtext

Please see attached file. Physician Addendum, Specialty: Internal Medicine Cardiovascular Disease, Date of Service: 5/4/2021 10:08 AM, INPATIENT DISCHARGE SUMMARY, Admission Date: 5/3/2021, Discharge Date: 5/4/2021, HOSPITAL SUMMARY, Discharge Diagnosis, Principal Problem: Other acute myocarditis, Active Problems: Chest pain, Tobacco use, Resolved Problems: * No resolved hospital problems. * Reason for Hospitalization, Acute myocarditis after COVID vaccination, Hospital Course - Patient is a very pleasant 20-year-old man without prior medical history who was transferred here from emergency department for further management of chest pain. Patient received his second COVID-19 vaccination on Friday, April 30, 2021 (Pfizer). Later in the evening on Friday, he developed constitutional symptoms, including fever/chills/sweats as well as severe back pain. These symptoms subsided by the following morning but later in the day on May 1, 2021, he developed significant substernal chest pain. The chest pain persisted throughout the weekend. It was worse when he took a deep breath in and also had a positional component. He identified no other aggravating or alleviating factors. When his pain had not resolved, he presented to the emergency department early in the morning on May 3, 2021. On arrival to the outside hospital emergency department, his electrocardiogram was unremarkable, aside from early repolarization abnormality. His troponin was significantly elevated to 7.3. His COVID test was negative. All other lab work was unremarkable, including an undetectable D-dimer. He was transferred here for further management of chest pain and troponin elevation. On arrival here, we completed a CT coronary angiogram, which showed no evidence for coronary stenosis and normal origin of the coronary arteries from the aortic root. An echocardiogram showed preserved left ventricular systolic function and no valvular heart disease. It was, overall, an unremarkable echocardiogram. His troponin was trended and peaked at 7.3. A follow-up troponin after that was 6.4. His presentation is presumed to be related to acute myocarditis secondary to the COVID vaccination. We are obtaining a cardiac MRI as an outpatient on May 4, 2021 (the day after discharge). He will be provided with a one-month supply of colchicine, which he will take daily. We attempted to start him on both Toprol XL and losartan, but we had to discontinue the Toprol XL due to bradycardia (heart rates in the 40-to-50 beats per minute range, increasing only up to 60 beats per minute with activity). He will, therefore, be discharged only on losartan. We will plan to obtain a repeat cardiac MRI in 3-6 months. If that study is favorable, the losartan could be discontinued. Finally, patient had a trip planned with his family to celebrate his 21st birthday in the near future. This trip would obviously involve heavy alcohol consumption. Because alcohol is a cardiotoxin, I advised against such a trip until he has more time to recover from his myocarditis (I also reminded him that heavy alcohol consumption in general is not advised). I provided him a letter that they can use as they cancel their travel plans and seek reimbursement. DISCHARGE EXAM - Admission Weight: Weight: 66.8 kg (147 lb 3.2 oz), Discharge Weight: Weight: 66 kg (145 lb 9.6 oz); Physical Exam: BP 102/65 (BP position: Lying) | Pulse (!) 47 | Temp 98.7 degrees F (37.1 degrees C) | Resp 16 | Ht 175.3 cm (69") | Wt 66 kg (145 lb 9.6 oz) | SpO2 99% | BMI 21.50 kg/m2; GENERAL: well developed, well nourished, in no apparent distress, appears stated age; CHEST: breath sounds are symmetric & normal, no rales or rhonchi; CARDIOVASCULAR: normal rate and rhythm with S1 and S2, there is no S3 or S4 noted, no murmurs or gallops; HEAD: normocephalic, atraumatic; EYES: EOMI, conjunctivae pink, scleral nonicteric; NECK: veins are flat, no bruits, no thyromegaly; LYMPH: no cervical adenopathy; ABDOMEN: no tenderness, masses or hepatosplenomegaly; EXTREMITIES: no edema, cyanosis or clubbing, good distal pulses upper & lower extremities bilaterally; MUSCULOSKELETAL: joints and gait normal; SKIN: warm and dry, normal color, no rashes or lesions; NEURO: awake, alert & oriented; PSYCH: mood pleasant, affect appropriate; Physical Condition at Discharge - Patient's condition is good . Patient was seen by me on the day of discharge. Consultants - None; Procedures performed - See Hospital Course. Pertinent imaging - See hospital course. Test Results Pending at Discharge - Unresulted Labs, No orders found from 4/20/2021 to 5/5/2021. Unresulted Pathology, No orders found from 4/20/2021 to 5/5/2021. Unresulted Imaging, No orders found from 4/20/2021 to 5/5/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: Cardiac MRI: pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1291457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 06.05.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Head injury Loss of consciousness Syncope

Symptomtext

AFTER VACCINATION, PATIENT HAD A BLACK OUT/FAINTING SPELL DURING HER 15 MINUTES OBSERVATION AT THE PHARMACY. PATIENT STATED SHE FELL DOWN AND BUMP THE BACK OF HER HEAD. PATIENT ABLE TO GAIN CONCIOUSNESS AND DENIED EMERGENCY HELP. PATIENT SAT AT THE PHARMACY WAITING AREA FOR APPROXIMATELY 45 MINUTES BEFORE SOMEONE PICKS HER UP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1290033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 28.04.2021
Beginn: 05.05.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram cerebral normal Angiogram normal Anion gap decreased Blood alkaline phosphatase increased Blood calcium decreased Blood glucose normal Computerised tomogram head normal Confusional state Facial paralysis Headache Hemiparesis Intensive care Ischaemic stroke Nausea Platelet count normal

Symptomtext

At 1030on 5/5/21 the patient developed right-sided facial droop, and right arm and leg weakness. These were accompanied by headache and confusion (unable to state year of birth/age). No intracranial bleed was noted on head CT and NIHSS was 5. Glucose WNL and BP 146/72. Patient received alteplase to treat suspected ischemic stroke. Patient received ondansetron pre-hospital for nausea, and received Norco and a fluid bolus. Patient is being admitted to ICU for monitoring after alteplase administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: 5/5/21: Non-contrast head CT: No acute intracranial abnormality CTA head and neck: no acute intracranial abnormality or flow limiting stenosis of the major arteries of the head and neck Platelets: 183 Glucose: 114 Calcium: 8.3 Anion gap: 8 Alk phos: 127
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, GERD, obesity, hyperlipidemia, OSA, malignant neoplasm on thyroid gland, vitamin D deficiency
Andere Medikamente: Albuterol inhaler, Vitamin C, aspirin, atorvastatin, Fioricet, calcium-vitamin D, carvedilol, citalopram, isosorbide mononitrate ER, levothyroxine, multivitamin, omeprazole
Allergien: NKA
Vorherige Impfungen: -

VAERS 1288402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MS
Alter: 21,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Bell's palsy Headache Hypoaesthesia oral Pain Pain in extremity

Symptomtext

Bell's palsy; tongue went numb; body aches; regular sore arm; headache; This is a spontaneous report from a contactable consumer reporting for herself. A 21-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number EW0153/expiration date: not provided), via an unspecified route of administration, on 15Apr2021 10:45 (at the age of 21 years old) as a single dose in the right arm for COVID-19 IMMUNIZATION. Relevant medical history and concomitant medication were none. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 15Apr2021, the patient experienced regular sore arm, headache. On 16Apr2021, the patient experienced body aches. On 17Apr2021, the patient's tongue went numb. On 20Apr2021, the patient experienced Bell's palsy and described it as getting worse. The outcome of the event regular sore arm was recovered on 16Apr2021. The outcome of the event body aches was recovered on 19Apr2021. The outcome of the events headache, tongue went numb and Bell's palsy was not recovered.

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: -
Allergien: -
Vorherige Impfungen: -

VAERS 1209216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MD
Alter: 56,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 08.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Hypoaesthesia Paraesthesia Peripheral swelling Thrombosis Skin discolouration Ultrasound scan

Symptomtext

blood clot at upper right chest underneath collar bone; Swollen right arm and fingers; tingling and numbness in arm; numbness in arm; headaches; This is a spontaneous report from a contactable consumer (patient). A 56-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) dose 1 via an unspecified route of administration, administered in Arm Left on 08Apr2021 04:00 (Lot Number: EWO153) as SINGLE DOSE for covid-19 immunisation. Medical history included Implantable cardioverter defibrillator insertion from 2005. Concomitant medication in two weeks included verapamil 120 mg. No other vaccine in four weeks. No Covid prior vaccination. No Covid tested post vaccination. No Known allergies. On 12Apr2021, the patient experienced blood clot at upper right chest underneath collar bone. Swollen right arm and fingers with tingling and numbness in arm. Also, suffering from occasionally headaches. The patient was relatively heathy with no know blood clot issues. Events resulted in Doctor or other healthcare professional office or clinic visit. Unknown if treatment was received for events. The outcome of events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Implantable cardioverter defibrillator insertion
Andere Medikamente: VERAPAMIL
Allergien: -
Vorherige Impfungen: -

VAERS 1286893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AS
Alter: 31,0
Geschlecht: F
Eingang: 03.05.2021
Impfdatum: 10.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Agitation Disorientation Dysarthria Incontinence Pyrexia Seizure Vomiting

Symptomtext

At 22 hr mark, had a seizure and began vomiting. Vomiting continued throughout the day. No fever or other adverse symptoms besides the vomiting. Went to bed at 10pm with low grade fever (100). Had a complicated seizure at 10:56pm, incontinent, grossly disoriented and agitated, garbled language. Called 911. Then drove my daughter to local hospital, to ED, just prior to midnight. Discharged 4/12/21 (about 3 hrs at ED)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: IV saline bag, tylenol, toradol, ativan, Klor-Con M20
Aktuelle Erkrankungen: none
Vorgeschichte: recovering from post-infectious dysmotility gastroparesis
Andere Medikamente: Nothing at time of vaccination; routine seizure meds prior to
Allergien: no
Vorherige Impfungen: -

VAERS 1248217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: LA
Alter: 34,0
Geschlecht: F
Eingang: 02.05.2021
Impfdatum: 25.03.2021
Beginn: 15.04.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / RA

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

Angiotensin converting enzyme Antinuclear antibody negative Blood test normal Borrelia test negative C-reactive protein normal Asthenia Facial paralysis Hemiparesis Hypoaesthesia Lumbar puncture CSF cell count normal CSF immunoglobulin G index CSF myelin basic protein normal CSF protein normal CSF test normal CSF white blood cell differential Computerised tomogram normal Differential white blood cell count normal

Symptomtext

One day after the shot I experienced redness and swelling of the arm where it was administered. Day two I started experiencing tingling and twitching of the face. Day three I had to go to the ER because of facial droop. The doctor said possible bell palsy and sent me home to follow up with normal doctor. Day four I went to normal doctor and by end of the day ended up in the ER with facial droop and body tremors. I was admitted into the hospital for day 5 through day 7 where I had CT scan, MRI and spinal tap. We are still awaiting the test results but I am still experiencing side effects. My speech is now being effected along with the body tremors. I am waiting to get set up with PT, OT and speech therapy to start that process but we are unsure of the test results at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 3,0
Labordaten: 4/20/21 - T3 Free Test, MRI Brain W/WO contrast, MRI Cervical Spine Demyelinating W W/O contrast 4/21/21 - CBC W/Auto Diff, Comprehensive Metabolic Panel, MS Profile Blood Collection, ACE, CSF, MS Profile, WNV Antibodies, CSF Saint Louis Encephalitis AB Panel IGG and IGM CSF, West Nile Virus PCR CSF, VDRL CSF, Myelin Basic Protein CSF, Lyme AB IGM Immunoblot CSF, Lyme Disease AB IGG Immunoblot CSF, Protein CSF, Glucose CSF, CSF Cell Count with Diff, IGG Index CSF, Vitamin D, RNP Antibody, Rheumatoid Factor, ANA, C-Reactive Protein, Sedimentation Rate Manual So far all test have come back in the normal range
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Adderall 25 mg
Allergien: none
Vorherige Impfungen: -

VAERS 1248217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: LA
Alter: 34,0
Geschlecht: F
Eingang: 02.05.2021
Impfdatum: 25.03.2021
Beginn: 15.04.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: SYR / RA

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

Angiotensin converting enzyme Antinuclear antibody negative Blood test normal Borrelia test negative C-reactive protein normal Asthenia Facial paralysis Hemiparesis Hypoaesthesia Lumbar puncture CSF cell count normal CSF immunoglobulin G index CSF myelin basic protein normal CSF protein normal CSF test normal CSF white blood cell differential Computerised tomogram normal Differential white blood cell count normal

Symptomtext

One day after the shot I experienced redness and swelling of the arm where it was administered. Day two I started experiencing tingling and twitching of the face. Day three I had to go to the ER because of facial droop. The doctor said possible bell palsy and sent me home to follow up with normal doctor. Day four I went to normal doctor and by end of the day ended up in the ER with facial droop and body tremors. I was admitted into the hospital for day 5 through day 7 where I had CT scan, MRI and spinal tap. We are still awaiting the test results but I am still experiencing side effects. My speech is now being effected along with the body tremors. I am waiting to get set up with PT, OT and speech therapy to start that process but we are unsure of the test results at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 3,0
Labordaten: 4/20/21 - T3 Free Test, MRI Brain W/WO contrast, MRI Cervical Spine Demyelinating W W/O contrast 4/21/21 - CBC W/Auto Diff, Comprehensive Metabolic Panel, MS Profile Blood Collection, ACE, CSF, MS Profile, WNV Antibodies, CSF Saint Louis Encephalitis AB Panel IGG and IGM CSF, West Nile Virus PCR CSF, VDRL CSF, Myelin Basic Protein CSF, Lyme AB IGM Immunoblot CSF, Lyme Disease AB IGG Immunoblot CSF, Protein CSF, Glucose CSF, CSF Cell Count with Diff, IGG Index CSF, Vitamin D, RNP Antibody, Rheumatoid Factor, ANA, C-Reactive Protein, Sedimentation Rate Manual So far all test have come back in the normal range
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Adderall 25 mg
Allergien: none
Vorherige Impfungen: -

VAERS 1278328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 21,0
Geschlecht: M
Eingang: 01.05.2021
Impfdatum: 01.05.2021
Beginn: 01.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fall Presyncope Somnolence

Symptomtext

Found patient on floor, awake but drowsy. Patient was able to speak, appeared to have had a vagal response. Patient was laid flat on back, legs raised, given glucose, apple sauce and water. Vital Signs stable. Patient denied having a seizure, also later denied EMS service

Weitere VAERSDATA-Felder

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

VAERS 1203274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WI
Alter: 18,0
Geschlecht: M
Eingang: 01.05.2021
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: ja

Feeling abnormal Pallor Syncope Loss of consciousness Seizure Somnolence Vomiting

Symptomtext

Loss of consciousness; Seizure; Drowsiness, couldn't stay awake; Vomiting; This is a spontaneous report from a contactable consumer (patient). An 18-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on the left arm on 12Apr2021 (11:30) as a single dose, with route of administration unspecified, for COVID-19 immunization at the pharmacy/drug store. Medical history included peanut and penicillin allergy. The patient's concomitant medications were not reported. On12Apr2021 (11:45), the patient had loss of consciousness; seizure; drowsiness/could not stay awake; and vomiting. The events had resulted in an emergency room/department for urgent care, and were assessed as serious (medically significant). The patient was hospitalized in Apr2021 due to loss of consciousness. The patient had received epinephrine (EPIPEN) as treatment for the reported events. The outcome of the events was recovered in Apr2021. The patient did no have COVID-19 prior to the vaccination, and had not been tested post-vaccination. Information on the lot/batch number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Peanut allergy; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1274726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 57,0
Geschlecht: M
Eingang: 30.04.2021
Impfdatum: 15.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / RA

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

Body temperature increased Chills Dizziness Pyrexia Syncope

Symptomtext

Fever/chills, low temperature (up to 100.2F), feeling faint (fainting one time); symptoms lasted for 3 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Home instant COVID test taken 4/27/21--negative
Aktuelle Erkrankungen: -
Vorgeschichte: Factor V blood clot mutation
Andere Medikamente: low-dose aspirin
Allergien: scallops
Vorherige Impfungen: -

VAERS 1271415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 31,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 29.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Pt fainted, but she was awake, we lifted her leg for about 10 minutes and drank some water, sat down for about 5 minutes, then got fainted again ( still conscious and awake) , then again laid back on the floor by the pharmacist and able to talk and relax, 911 was called (after her second incident) they checked her vitals, all were normal , pt stayed in the store for about 1 and 1/2 hours and was well before left for home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: flu vaccine at around age 21, fainted but was conscious and went back normal

VAERS 1269714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 22,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 10.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Fatigue Head injury Loss of consciousness Malaise Migraine Nausea Pain Syncope

Symptomtext

passed out; fainted; migraine; feel body aches; fatigue; felt incredibly ill; nauseous; hitting head; This is a spontaneous report from a contactable consumer (patient). A 22-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EW0153), via an unspecified route of administration, administered in Right Arm on 10Apr2021 11:30 (at age of 22 years old) at single dose for COVID-19 immunisation. Medical history included Seasonal allergies, asthma, Known allergies: peanuts (mildly). Concomitant drug was Yes. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: ER8727) on 20Mar2021 11:30AM (at 22 years old) at Left arm at single dose for COVID-19 immunisation. No other vaccine in four weeks. No COVID prior vaccination. No COVID tested post vaccination. A few hours after second dose, on 10Apr2021 02:00PM, patient developed a migraine and began to feel body aches and fatigue. The next morning, patient felt incredibly ill. Shortly after rising, patient became severely nauseous and fainted, hitting head; patient became conscious and passed out again before being taken to the ER (Emergency room). All AE resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Treatment (IV and anti-nausea med. administered) received for all events. The outcome of the events was Recovering. Information on the lot/batch number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts (peanuts (mildly)); Asthma; Seasonal allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1268291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MT
Alter: 45,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 28.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Malaise Pallor Secretion discharge Seizure

Symptomtext

On cell phone at approximately 1120AM in monitoring area; per volunteer MD and volunteer RN, pt voice louder, was observed leaning forward in chair. Pt stated not feeling well and noted to have moist pale skin. Assisted to floor at approx. 1123, feet elevated. Pt had full body seizure with oral secretions at approximately 1125; O2 applied, airway/limbs and head were protected. VS at 1125 160/100, HR 93, O2 sat 99%. EMS called at 1127, pt seizure approx. 1 minute. Pt aroused, oriented to name, place, requested mom be called. Mom called at, she denied seizure hx. Pt VS monitored at 1130 99% sat, 96 HR, 160/115, EMS arrived at 1135 sat 99%, HR 81, transported to ED with EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none, denied seizure hx
Vorgeschichte: none
Andere Medikamente: Diloxitine, Lamotrigine
Allergien: none
Vorherige Impfungen: -

VAERS 1267398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: ME
Alter: 20,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 10.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

NEAR SYNCOPE BP 120/81mmHg HR 64 bpm O2 SAT 99%

Weitere VAERSDATA-Felder

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

VAERS 1263911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 13.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / RA

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

Craniocerebral injury Full blood count normal Guillain-Barre syndrome Headache Hypoaesthesia Immediate post-injection reaction Immunoglobulin therapy Laboratory test normal Limb discomfort Lyme disease Magnetic resonance imaging head abnormal Magnetic resonance imaging neck Pain Paraesthesia Pyrexia Skin tightness Troponin normal Urine analysis normal

Symptomtext

Presents to ED after her second COVID-19 vaccination on 4/13/2021. Immediately thereafter she had fever, body aches, headaches, and her feet felt tight. The symptoms gradually declined. On 4/19/2021 she developed stocking glove numbness that began to ascend up her legs. Her calf's feel like they are being squeezed. She has paresthesia's currently, she describes them as prickly and needlelike. Labs, urinalysis, CBC, and chemistries unremarkable, troponin negative. Probable AIDP given history and examination. IVIG and steroids given. Guillain Barre syndrome suspected. MRI brain and cervical spine performed to eval for CNS pathology. MRI brain: No acute intracranial formalities. No evidence of mass or infarct. However noted to several bilateral Supratentorial T2/FLAIR hyperintense foci mostly in the centrum semi vale and optic radiations. These are nonspecific foci and should be correlated for demyelinating disease, small vessel disease, traumatic brain injury, Lyme disease, chronic migraine etiologies. MRI cervical spine was unremarkable. Patient DC'ed in stable condition and told to F/U with neurology clinic.

Weitere VAERSDATA-Felder

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

VAERS 1262655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 22,0
Geschlecht: M
Eingang: 27.04.2021
Impfdatum: 27.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood pressure measurement Body temperature Heart rate Seizure like phenomena Tremor

Symptomtext

Patient experienced seizure like activity 10 minutes after receiving the vaccine. Patient tensed up and became unresponsive. He was slightly shaking. This lasted for under a minute (RN estimated 20-30 seconds). Has had one seizure in the past as a child. Currently not taking any medications for this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: In ED, blood pressure 134/78, temp 99.3 and HR 82 about 10 minutes after the event.
Aktuelle Erkrankungen: -
Vorgeschichte: ADHD
Andere Medikamente: None known, verified not on any medications for seizures.
Allergien: No known allergies per patient.
Vorherige Impfungen: -

VAERS 1261791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 58,0
Geschlecht: M
Eingang: 27.04.2021
Impfdatum: 11.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Bell's palsy

Symptomtext

Bells Palsy; This is a spontaneous report from a contactable consumer reporting for husband. A 58-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number EW0153/expiration date: 31Jul2021), via an unspecified route of administration, on 11Apr2021 (at the age of 58 years old) as a single dose in the left arm for COVID-19 IMMUNIZATION. The patient previously patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number EM8727/expiration date: 31Jul2021), via an unspecified route of administration, on 21Mar2021 (at the age of 58 years old) as a single dose for COVID-19 IMMUNIZATION. Relevant medical history included ongoing hypertension, when he was about 45, probably 10 years and was recovering from leukemia onset 2 years ago, in 2019 and he has been recovering from leukemia since about 2020; the patient had an ongoing history of being a little overweight, with onset unknown other than over 10 years ago. Concomitant medication included nebivolol hydrochloride (BYSTOLIC) 10mg tablet taken by mouth once daily for hypertension. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 12Apr2021, late afternoon the patient experienced swelling in his face, couldn't blink, drooping and was diagnosed with Bells Palsy which required an emergency room visit. He was not admitted to the hospital for this event, was kept under observation only in the emergency room on 12Apr2021. He was given some medication and then discharged. Bell's Palsy affected his right side of his face. The outcome was improved, the pain was a little less; but he still does not have, nothing works on the right side of his face. His right eye does not blink, eyebrow does not move, and he still can't speak very good. Treatment was received for the event. The outcome of the events Bells Palsy was recovering. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension (when he was about 45, probably 10 years); Overweight (Onset unknown other than over 10 years ago.)
Vorgeschichte: Medical History/Concurrent Conditions: Leukemia (Recovering from Leukemia since about 2020)
Andere Medikamente: BYSTOLIC
Allergien: -
Vorherige Impfungen: -

VAERS 1258866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AL
Alter: 25,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 26.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Seizure

Symptomtext

PATIENT HAS HISTORY OF SEIZURES. SEIZURE ACTIVITY X 4 MINUTES. PATIENT IS ALERT AND ORIENTED X 4. BP 141/64, HR 46, O2S 98%. 911 WAS CALLED AND EMS ARRIVED AT 10:52. PATIENT WAS TRANSPORTED TO HOSPITAL AT 10:53.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: ?
Aktuelle Erkrankungen: ?
Vorgeschichte: PATIENT HAS HISTORY OF SEIZURES HOWEVER, STATED NOT ON MEDICATION.
Andere Medikamente: ?
Allergien: ?
Vorherige Impfungen: -

VAERS 2005216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TX
Alter: 44,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Gaze palsy Joint contracture Loss of consciousness Seizure

Symptomtext

Patient was given the COVID19 Pfizer vaccine. The patient felt very dizzy 5 minutes after so we had him lay on the floor. Seconds later the patient passed out. His eyes were rolling and hands clenching as if he was having a seizure. About less than a minute later the patient became responsive again. Patient has no history of seizures. Emergency services was called and the patient was evaluated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: mitral valve prolapse
Andere Medikamente: flonase nasal spray
Allergien: shellfish, kiwi fruit
Vorherige Impfungen: -

VAERS 1256950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: WA
Alter: 18,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 25.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Nausea Syncope Urinary incontinence

Symptomtext

Patient fainted after waiting for 10 minutes. He did not lose consciousness. He responded to RPH commands. He did not have shortness of breath, rash, inflammation. He urinated himself after falling. He remained laying on the ground for 20 minutes, after which he stood up and had recovered from the dizziness/nausea. Patient and parents did not wish for 911 to be called or to go the hospital. They agreed to call 911 if patient has any further symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1251780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: 16.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Deep vein thrombosis Electrocardiogram normal Joint swelling Oedema peripheral Pain in extremity Thrombosis Ultrasound Doppler abnormal

Symptomtext

4/16/21 Second Dose received. 4/17 and 4/18 noticed light swelling in ankles. No other effects. 4/19 - Emailed my Cardiologist about swollen ankles. Didn?t think about the vaccine as a potential cause. He scheduled an Echocardiogram for May. 4/20 to 4/22 - Edema is ankles and lower legs with pain on bottom left. Tried heat and elevation with no relief. 4/23 - Called Advice Nurse with recommendation to go to ER. ER determined a blood clot in left leg at the left posterior tibial vein measured at 6.3cm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 1,0
Labordaten: 4/23/21 - Called Advice Nurse with recommendation to go to ER. ER determined a blood clot in left leg at the left posterior tibial vein measured at 6.3cm. Test verified via Ultrasound on both legs. EKG performed with no issues. I am on blood thinners now. Blood clots could be life threatening if not treated. I am her I tune to my body and immediately knew something wasn?t right.
Aktuelle Erkrankungen: None
Vorgeschichte: Cardiac Arrest May 2020 believed to be due to a Ruptured Cord that occurred due to a Prolapsed Valve.
Andere Medikamente: 25 Mg Metoprolol
Allergien: None
Vorherige Impfungen: -

VAERS 1249768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: VA
Alter: 43,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: 20.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Menstrual disorder Thrombosis

Symptomtext

I passed a number of large blood clots (the size of a walnut) from my body on the two days after I received the shot. The day that I got the shot coincided with the day that I got my period, so I was already menstruating when the clots passed from my body. The clots were much larger than normal, and much more frequent. I passed almost a half dozen large clots. By the third day, my menstruation flow started to subside (the first two days tend to be heavier days for me). I did not pass any large clots on the third day going forward.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Claritin the day before and after vaccination.
Allergien: None
Vorherige Impfungen: -

VAERS 1248519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CO
Alter: 29,0
Geschlecht: M
Eingang: 23.04.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Drug hypersensitivity Skin laceration Syncope

Symptomtext

pt received vaccine, told to wait 15 minutes. went to the restroom here in the store, had fainted in the bathroom. He came back to the pharmacy reported the event to the pharmacy, Upon evaluating him he had a small cut on the back of the head. One of our techs noticed a person from fire rescue in the store shopping she called him over he initially evaluated the patient and called for his emts to come and assess the pt. I know the took the pt out of the store on a gurney. they just wanted to assess him in a more private area (in the ambulance), we were in the middle of a clinicwith lots of people around. Unkown what transpired past that.

Weitere VAERSDATA-Felder

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

VAERS 1248487

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: AL
Alter: 21,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope Tonic posturing

Symptomtext

PATIENT WITH SYNCOPE EPISODE WITH TONIX POSTURE NOTED. PATIENT AROUSED TO VERAL STIMULATION POST EPISODE. VITAL SIGNS WERE 99/56, HEART RATE 63, RESPIRATIONS 20, OXYGEN 98%. CLEAR BILATERAL BREATH SOUNDS. NO INCREASE OF SHORTNESS OF BREATH NOTED. WATCH AN ADDITONAL 15 MINUTES.

Weitere VAERSDATA-Felder

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

VAERS 1246638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 18,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Electrocardiogram Eye movement disorder Loss of consciousness Muscle twitching Posture abnormal

Symptomtext

She received the shot walked a couple steps had a blank stare on face sat her in a chair where she sat for a couple seconds and just stared at me then head jerked and right hand curled and eyes rolled back into head. tried shaking her to respond she passed out .She came to opened eyes wasn't speaking but followed my command to spit out gum then again went limp with head shaking and hands twitching. Got her to the ground with help and called 911. She laid on ground then came to . She did not remember incident but was responding appropriately to questions. drank orange juice and placed ice bag under neck while laying. By the time paramedics arrived she was awake and appropriate. Pulse ox, blood sugar and EKG normal. Blood pressure was low but not unusual for her. Prior to shot she was well hydrated and had eaten. After being checked out by paramedics we denied need to go to hospital and she did walk out on her own. Observed her closely over night and had no further symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG, Pulse Ox, Blood sugar all normal
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1246376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 25,0
Geschlecht: M
Eingang: 23.04.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cold sweat Dizziness Erythema Loss of consciousness Pallor Skin warm

Symptomtext

About 5 to 10 minutes after receiving vaccine (during observation period), patient became dizzy, lightheaded and his skin was very pale and clammy. His hands were red and warm to the touch. About 3 to 5 minutes after symptoms started, he passed out for about 10 seconds, but came to on his own. EMS was called and he was checked- out by paramedics, his blood pressure and blood sugar were all within normal range. They observed him for 5 to 10 minutes after which he signed a "refusal" to be transported to ER. He stated he was feeling better and would continue to self-monitor at home with his girlfriend.

Weitere VAERSDATA-Felder

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

VAERS 1246359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MA
Alter: 29,0
Geschlecht: M
Eingang: 23.04.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bradycardia Hypotension Syncope

Symptomtext

Syncope with bradycardia and Hypotension BP 70/40 HR 44 O2sat 95%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Taken to local Hospital by ambulance.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1246227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MS
Alter: 34,0
Geschlecht: M
Eingang: 23.04.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Flushing Hyperhidrosis Syncope

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Mild, Additional Details: Under pharmacist observation for 45 minutes , fainted and light-headed 5 minutes, given bottle water for hydration . no other symptoms and fine after 45 minutes of observation

Weitere VAERSDATA-Felder

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

VAERS 1244304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 62,0
Geschlecht: M
Eingang: 22.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Loss of consciousness Pallor Unresponsive to stimuli

Symptomtext

The patient passed out while sitting in the waiting area about 15 minutes after the vaccine was given. They were pale but became responsive very quickly after the fall. After about 20 more minutes the patient was able to stand up and felt "all better". The paramedics were called and assessed the patient before the patient left.

Weitere VAERSDATA-Felder

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

VAERS 1243802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 22.04.2021
Impfdatum: 21.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypotension Loss of consciousness Syncope

Symptomtext

Syncopal episode with loss of consciousness. Hypotensive (79/49). EMS called to evaluate. Pt refused transport. Sx resolved after 20 minutes.

Weitere VAERSDATA-Felder

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

VAERS 1242881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 21,0
Geschlecht: M
Eingang: 22.04.2021
Impfdatum: 21.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction Nausea Presyncope

Symptomtext

Patient stated that he felt "faint", a "head rush", nauseous, and dizzy immediately after his vaccination. No shortness of breath, itching, or swelling of throat or face. Vitals signs stable. Symptoms consistent with vasovagal response. Symptoms resolved after about an hour.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Not reported
Vorgeschichte: MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE, IN PARTIAL REMISSION SEIZURE, UNSPECIFIED GENDER DYSPHORIA
Andere Medikamente: Not reported
Allergien: Cephalosporins (rash), Augmentin (rash, swelling), ceftriaxone (rash), omnicef (rash)
Vorherige Impfungen: -

VAERS 1242241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Loss of consciousness

Symptomtext

Within a couple minutes of the vaccination, patient said she felt like she was going to pass out. The pharmacist took her to a chair to sit down. Within a few seconds, the patient collapsed out of the chair, fell in the floor. She was out for about 15-20 seconds then came around. 911 was called immediately when patient collapsed from the chair. Patient was taken to the hospital for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none known
Aktuelle Erkrankungen: none known
Vorgeschichte: none known
Andere Medikamente: none known
Allergien: biaxin, augmentin
Vorherige Impfungen: -

VAERS 1240162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 17.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Blood glucose Syncope

Symptomtext

patient experienced multiple syncope episodes after her second dose of the pfizer vaccine, she mentioned she was pretty anxious before the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Paramedics were called, the they took her vitals and blood sugar levels
Aktuelle Erkrankungen: not sure
Vorgeschichte: asthma and diabetes marked on her form
Andere Medikamente: n/a
Allergien: don't know, i was not the pharmacist that administered the vaccine
Vorherige Impfungen: -

VAERS 1239294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TN
Alter: 44,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 19.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / RA

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

Blood test Erythema Induration Peripheral swelling Skin warm Thrombosis Ultrasound scan

Symptomtext

I started having right leg swelling. I noticed a small red spot on my medial side of my knee. I had this for about a week and then the swelling went down. A few days later, I had redness, skin was warm to touch, and hardness developing where the red spot was. I went to urgent care and the NP sent me to the ER for a possible blood clot. I had a venous study done in the ER and it was determined I had a superficial blood clot and was started on ASA 325 mg daily x7 days. I followed up with a vascular doctor and it was determined the clot was worse and had clotted all the way up the vein into my thigh. It remains superficial in nature at this time. I was started on Xarelto 10 mg daily x1 month. I follow up with vascular in 1 month to make sure the clot is dissolving. I was instructed to Follow up with either the doc or go to the ER with worsening symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasounds and blood work
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic kidney disease - IGA nephropathy Tachycardia
Andere Medikamente: Tylenol pm Clonazapam Omeprozole Bisoprolol Tizanidine HRT drops
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1239084

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge EW0153

schwer

Staat: -
Alter: 17,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 21.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood pressure measurement Dizziness Loss of consciousness Pallor Syncope Vital signs measurement

Symptomtext

Patient stated she felt dizzy and faint and then passed out for about 5 seconds. Appeared pale, but quickly was alert and oriented. BP's 108/68 and 102/70. HR 68, pulse ox 98%

Weitere VAERSDATA-Felder

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

VAERS 1239005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 57,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 17.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Cardiac monitoring Chest X-ray Electrocardiogram Fatigue Fibrin D dimer Full blood count Injection site pain International normalised ratio Lipase Metabolic function test N-terminal prohormone brain natriuretic peptide Nausea Oxygen saturation Oxygen therapy Pyrexia Syncope Thirst Troponin

Symptomtext

On 4/18/21 the day after receiving my second Pfizer vaccine. I awoke fatigued and with a sore right arm and fever of about 99. The fatigue increased, and then included extreme thirst despite drinking plain water throughout the morning and early afternoon, then I experienced slight nausea, then syncope after attempting to sit for a few moments, after having been resting (in a prone position) around 1 pm. My husband was unable to revive me - he says my eyes were open but I was not responsive so he called 911. I regained consciousness after receiving saline via IV and then was taken to the ER for follow up testing, then released a few hours later - around 4 pm. It it likely relevant to know I had passed out from fever brought on by flu during the very harsh flu season a few years before, at the onset of influenza, although vaccinated that year for flu.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: ER doctor: Hospital Lab tests: CBC w/ differential CK, Comprehensive metabolic panel, d-dimer, lipase, manual differential, PTT, Protime INR Troponin Urinalysis, proBNP, ecg 12 lead, x-ray chest, oxygen therapy, pulse oximetry, cardiac monitoring
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine (average: 2-4 per month)
Andere Medikamente: Daily: Vitamin D, Vitamin B2 (200 mg daily), Magnesium Citrate (400mg daily), Hemp Oil, Vegan B12; Advil as needed for headaches.
Allergien: None
Vorherige Impfungen: -

VAERS 1238681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 10.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Discomfort Facial paralysis Full blood count Preauricular cyst

Symptomtext

Patient developed pain in R preauricular area on the day following vaccine. Discomfort continued and on the following day patient noted mild droop of R side of face, decreased blinking of R eyelid. Diagnosed with Bell's Palsy, treated with prednisone 60mg for 5 days, then 40mg for 5 days. Patient undergoing ongoing treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CBC, ESR, CRP, Lyme test all negative
Aktuelle Erkrankungen: None
Vorgeschichte: Occasional exacerbation of seasonal allergic rhinitis
Andere Medikamente: None known
Allergien: No known drug or food allergies.
Vorherige Impfungen: -

VAERS 1235756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IA
Alter: 17,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Loss of consciousness

Symptomtext

Lost consciousness approximately 3 minutes after receiving first dose of vaccine. was feeling fine after vaccine until they stood up.; This is a spontaneous report received from a contactable consumer (patient). A 17-year-old female patient (non-pregnant) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: EW0153, expiration date unknown), via unspecified route of administration in left arm on 05Apr2021 at 11:30 AM at a single dose for COVID-19 immunization. The medical history was not reported. Patient did not receive any other vaccine in four weeks. No allergies to medications, food, or other products No known allergies. Concomitant medications included birth control pills (other medications in two weeks). On 05Apr2021 at 11:30 AM, the patient lost consciousness approximately 3 minutes after receiving first dose of vaccine and was feeling fine after vaccine until they stood up. Treatment included the emergency room/department or urgent care, treatment was EKG, concussion test. No covid prior vaccination. There was no covid test performed post vaccination. The patient considered the event as non-serious. The patient recovered from the event on 05Apr2021. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

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

VAERS 1235719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 12.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test abnormal Deep vein thrombosis Fibrin D dimer increased Musculoskeletal discomfort Peripheral swelling Thrombosis Ultrasound scan

Symptomtext

left arm swelling started from 4/18, extended from upper arm to lower arm in the afternoon. went to Urgent care on 4/19 morning, the NP reviewed my blood report and referred me to do ultrasound and also ask me to go to ER if the swell extend. as the swell extend, i went to ER in the afternoon. blood test shows high D-dimer and then ultrasound finds blood clot in the vessel near left neck. diagonised to be Deep Vein Thrombosis. no family history of such problem. in the hospital, they gave me a shot of blood thinner and also prescript oral blood thinner to be take at home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: 4/20 blood test D-dimer high 1.31 4/20 ultrasound. DVT
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1233286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 20,0
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 18.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Hyperhidrosis Loss of consciousness Syncope

Symptomtext

After administering vaccine, patient stated he was very anxious - has a history of needle phobia. He then stated he was going to faint and I assisted him to the floor. He temporarily lost consciousness ( less than 20 seconds). He appeared diaphoretic. He regained consciousness and appropriately responded to my inquiries. I assisted him to a chair where he sat for 3 - 4 minutes then said he was feeling better and wanted to leave. His mother was in the waiting room and took custody. She confirmed she was present due to this happening before.

Weitere VAERSDATA-Felder

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

VAERS 1232825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

schwer

Staat: MI
Alter: 56,0
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 01.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: - / -

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

Computerised tomogram Full blood count Laboratory test Magnetic resonance imaging Seizure

Symptomtext

Seizure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: CT and MRI with contrast 4/17/21 CBC Chemistry panel
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Allegra, Trazodone 100mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 1232125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: OH
Alter: 25,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 18.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Differential white blood cell count Dizziness Full blood count Headache Nausea Seizure

Symptomtext

small seizure, headache, nausea, dizzy, lightheaded

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: CBC with Diff
Aktuelle Erkrankungen: -
Vorgeschichte: Epilepsy, high cholesterol, anxiety
Andere Medikamente: Onfi, Atorvastatin, Escitalopram
Allergien: coconut, lamictal, diladud, soft soap
Vorherige Impfungen: -

VAERS 1230268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 36,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Hyperhidrosis Loss of consciousness Skin abrasion Skin laceration

Symptomtext

Patient was sitting in waiting area and became very diaphoretic and dizzy. Patient collapsed to the floor witnessed by family member and nurse. Within 5-10 seconds patient jumped off floor confused but alert. Left eyebrow had 3cm cut with blood coming from his eyebrow. A small abrasion to the left lateral nose was noted. Patient was assisted to the chair and was alert and oriented x3. EMS was notified and came out to evaluate patient. Vitals were as followed b/p 100/64, HR 51, O2 98%. Cold compress was placed on patients neck. Pressure placed on laceration. Minimum bleeding noted to area. Patient refused to be taken by EMS to the hospital and stated that he would be taken by his accompanied family member. Vitals upon leaving were B\P 115/65, HR 79, O2 99% and alert and oriented x3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Laceration on left eyebrow was cleaned and pressure was applied to site to stop bleeding.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1229869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 18.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient fainted and fell on the floor. Patient was awake and oriented on the floor. Vitals taken, BP 100/52,pulse 72, respiration 12. EMS called. Patient transported to hospital for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1229556

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 41,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood electrolytes normal Dizziness Facial paralysis Full blood count normal International normalised ratio normal Myasthenia gravis Paraesthesia oral Prothrombin time normal

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient experienced worsening left-sided facial droop, dizziness, tongue heaviness, and weakness within minutes after reciving vaccine. Vital signs within normal ranges except for blood pressure 141/06. Patient observed and monitored, diagnosed by neurology with myasthenia flare, and discharged to home ambulating independently and stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: CBC, electrolytes, PT/INR all within normal ranges
Aktuelle Erkrankungen: parvovirus and myasthenia gravis flare
Vorgeschichte: idiopathic angioedema, postural orthostatis tachycardia syndrome, hypotension, Paynaud's disease vitamin D deficiency, MTHFR mutation, nasal polyp, gastroparesis, chronic idiopathic constipation, irritable bowel syndrome, renal cyst, iron deficiency anemia, Ehlers-Danlos syndrome, lupus, occipital neuralgia, back pain, peripheral neuralgia, maigraine, neuropathy, Lamber-Eaton syndrome, asthma, chonric idiopathic urticaria
Andere Medikamente: acetaminophen, fremanezumab-vfrm, albuterol, buprenorphine (Belbuca), cetirizine, vitamin D3, ivabradine, diphenhdramine, Epi-Pen, eszopiclone, famotidine, fluticasone, IVIG, mycophenolate, ondansetron, prednisone, pyriostigmine, rimegepant
Allergien: silicone adhesive tape, iodinated contrast media, iron dextran, pregabalin, NSAIDs, octyl 2-cyanoacrylate, celecoxib, hydroxychloroquine, promethazine, sulfa, trazodone
Vorherige Impfungen: -

VAERS 1229461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 30,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 05.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Angiogram Asthenia Blood count normal Blood pressure decreased Computerised tomogram normal Cyst Fatigue Haemoglobin decreased Heavy menstrual bleeding Oligomenorrhoea Pain Pain in extremity Pregnancy test negative Pyrexia Thrombosis Transfusion Ultrasound scan normal Uterine leiomyoma embolisation

Symptomtext

I had my first dose of Covid 19 Pfizer vaccine on the 5th of April, 2021 at 1pm. I had sore arm and was fatigued which was expected. However, the day I had my vaccine was also the day my menstrual cycle started and just to assure myself I informed the pharmacist and asked if that was okay and they said it shouldn?t be a concern. I was doing fine until toward the end of day 3. I was expecting my period to stop as it always does on 3rd day but I started bleeding heavier that day there after. It didn?t worry me much until I started discharging huge blood clots as big as an apple 2 times every after 30 mins from that moment. I rushed to the ER later that night(still bleeding heavily with blood clots every now and then) but I was not admitted since my vitals and the blood counts were normal at that moment. I went back home and hoped the bleeding would stop but again with on pain or fever what so ever I kept bleeding all day. This is my 5th day of bleeding. Then on Sunday morning, I still kept bleeding heavy and I was too weak that I went back to the ER again. This time , (day 6) I got admitted because I have had lost a lot of blood and I needed blood transfusion. My HB dropped from 11.3 to 6.7 and it went further down to 5 something. I got 3 units of blood transfusion in the ER. They did ultrasound, CT scans(with and without contrast) and still couldn?t figure out the cause of the bleeding. My uterus showed no problems but my body was not even responding to Tranexamic acid to stop the bleeding. So the doctor proceeded with an angiogram and did an emergency uterine artery Embolization to stop the blood supply to the uterus. The bleeding stopped there after and I started regaining my vitals. However, the cause of the bleeding still remains unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: pregnancy - negative ct scans and ultrasounds all said nothing. They found a cyst but it wasn't the cause of the bleeding. uterine atery embolization
Aktuelle Erkrankungen: none
Vorgeschichte: none ( Brain AVM in 2019- resolved)
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1229235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CT
Alter: 60,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Hypotension Syncope

Symptomtext

Patient had syncopal episode falling from seated position in chair 10 minutes after vaccination. Pt had low BP and was transported to the hospital

Weitere VAERSDATA-Felder

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

VAERS 1229165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CT
Alter: 60,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Syncope

Symptomtext

Patient had syncopal episode 10 minutes after being vaccinated and fell off the chair from a seated position. Blood pressure was low and patient was transported to the hospital for evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1225944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: FL
Alter: 18,0
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 17.04.2021
Beginn: 17.04.2021
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 Pallor

Symptomtext

Patient was given vaccine. A couple of minutes after the vaccine, during observation period, patient was in and out of consciousness, feeling faint, and was very pale. Fire rescue was called and all vitals were fine. Patient opted out of leaving with fire rescue and decided to go home.

Weitere VAERSDATA-Felder

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

VAERS 2042704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: -
Geschlecht: F
Eingang: 17.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Loss of consciousness Rash macular

Symptomtext

Patient received pfizer vaccine around 1:10-1:20pm 4-14-2021. Patient found passed out but became alert when we called to her. Patient had some red blotches on arms and was given 25mg benedryl and some water. Patient remained in store for about 1 hour and was then driven home by a friend.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: 2
Allergien: -
Vorherige Impfungen: -

VAERS 1223750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 17.04.2021
Impfdatum: 17.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Loss of consciousness

Symptomtext

Patient received Pfizer vaccine and was standing with parents during his suggested 15 minute wait time. During this time, parents noted that he "passed out" but they caught him. He then gained consciousness immediately and sat down to be monitored by pharmacists on duty. His vitals were checked immediately. O2 saturation was 97-99. Blood pressure 138/83mmHg with HR of 81. Patient had trouble breathing for 2 minutes. O2 saturation did not change. After 2 minutes, he breathing improved and patient was calm.

Weitere VAERSDATA-Felder

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

VAERS 1222698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: MD
Alter: 50,0
Geschlecht: F
Eingang: 17.04.2021
Impfdatum: 17.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Tremor

Symptomtext

The patient felt dizzy/ was shaking a couple minutes after receiving the Pfizer Covid-19 vaccine and then passed out/ was unconcious for about 30 seconds, while still shaking and breathing. She regained consciousness, but still felt dizzy/ sweaty. Emergency services were called and evaluated the patient, who left under her own will.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood pressure and heart rate.
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroidism
Andere Medikamente: per patient - thyroid medication
Allergien: No
Vorherige Impfungen: -

VAERS 1222141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MI
Alter: 22,0
Geschlecht: M
Eingang: 17.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Fall Loss of consciousness Nausea

Symptomtext

Patient fall unconcious on the chair for couple of second and felt nauseated. moved patient to the floor laying on the back and feet elevated. Called 911 for paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1222103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MI
Alter: 32,0
Geschlecht: M
Eingang: 17.04.2021
Impfdatum: 17.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Loss of consciousness

Symptomtext

Patient had dizziness and fall forward on the chair unconciously. Made the patient to lay on the back with legs on the chair until paramedicals arrived

Weitere VAERSDATA-Felder

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

VAERS 1221029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 26,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient felt lightheaded, then passed out.

Weitere VAERSDATA-Felder

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

VAERS 1220829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IA
Alter: 39,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Hypotension Loss of consciousness Pallor

Symptomtext

The patient received the shot at approximately 4:30 pm. About 10 minutes later, the patient reported feeling faint and was sweating. He sat down and became very pale. The nurse, took his blood pressure and it was low. He started to shake and appeared to lose consciousness. We laid him on the floor and nurse again took his blood pressure. It did not register and he did not respond to her voice. At this point, I called 911 and requested EMS. The EMS arrived shortly and the patient had regained consciousness. They took his vitals and transported him to the hospital to check him over.

Weitere VAERSDATA-Felder

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

VAERS 1220756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 37,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Fall Hyperhidrosis Loss of consciousness Musculoskeletal stiffness Seizure like phenomena

Symptomtext

While RN BSN CCM was conducting educational facts about the covid 19 vaccination. Observed patients body went stiff and fell backwards in sitting position in his chair and started to exhibit seizure like symptoms in his chair for approximately 8-10 seconds. RRT called immediately and arrived 1 minuted after. Pt had beads of sweat dripping off forehead. Temp obtain 86.6. Sp02 95% Attempted to obtain BP vitals but machine did not complete cycle before pt blacked out again. ED transferred at 1055.

Weitere VAERSDATA-Felder

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

VAERS 1219590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: RI
Alter: 19,0
Geschlecht: M
Eingang: 16.04.2021
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: ja Erholt: ja

Anaphylactic reaction Dizziness Hypotension Pallor

Symptomtext

patient developed anaphylactic symptoms, hypotensive, dizziness, facial paleness. Epi-pen and 1 liter NS administered. Patient brought to ED, medicated with diphenhydramine and ondansetron. sent home from ED after approx 4 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: BP was 66/31 during ADR
Aktuelle Erkrankungen: none
Vorgeschichte: ADHD
Andere Medikamente: Adderall XR, Epi-Pen, Guanfacine
Allergien: amoxicillin, doxycycline, smoked marijuana same day of vaccine.
Vorherige Impfungen: -

VAERS 1217599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CT
Alter: 18,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium

Weitere VAERSDATA-Felder

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

VAERS 1216643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Vital signs measurement

Symptomtext

Patient fainted about 5 minutes after receiving vaccine. Pharmacist checked patient and she had a pulse. Patient quickly gained conscious and laid down on the floor. Patient said she usually faints when she receives a vaccine or has her blood drawn. Pharmacist checked patient's blood pressure and pulse, within normal range.

Weitere VAERSDATA-Felder

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

VAERS 1214147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Abdominal pain upper Blood pressure increased Chest pain Dyschezia Anaphylactic reaction Dysphagia Throat tightness Dysuria Hypoaesthesia Oxygen consumption decreased Pain Pain in extremity Peripheral coldness Pyrexia Renal pain Skin discolouration Swelling face

Symptomtext

Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe

Weitere VAERSDATA-Felder

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

VAERS 2087606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TN
Alter: 20,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 04.04.2021
Beginn: 04.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Immediate post-injection reaction Loss of consciousness Syncope

Symptomtext

Patient received dose #1 of COVID vaccine shot was given and when bandage was applied, Pt had episode of fainting. Pt was not provided acute treatment. Pt was out for 10 seconds.

Weitere VAERSDATA-Felder

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

VAERS 1215942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MI
Alter: 22,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 08.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Body temperature abnormal Chills Fatigue Headache Influenza virus test negative Loss of consciousness Pain SARS-CoV-2 test negative

Symptomtext

Seven days of side effects, including fatigue, body aches, headaches, chills, and body temperature issues. After one week, still getting severe headaches on the eighth day which is today 4/15/21. Passed out after vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: On Monday April 12th rapid COVID and flu tests negative.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1215406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Reported being light headed exit monitor walking client to the cot. Client fainted assisted to the floor. Client quickly came responsive and was assisted to get in wheelchair. Taken to a private monitoring room. b/p 118/50 PSO2 100% pulse 84. Respirations even and unlabored. Skin pink warm and dry. 3:53 Given water and a snack. Stated she felt 80% better. 3:57 stated she was ready to go, no further symptoms. informed to seek medical attention with any further problems.

Weitere VAERSDATA-Felder

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

VAERS 1215393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Presyncope

Symptomtext

Patient started experience syncope symptom after the vaccine administration and during the waiting period (15 minutes). She started feeling light headedness on her chair and tipping over to the floor. Her father who arrived with her to the vaccination had come to the rescue, and together with the pharmacist on duty, helped situating her on the floor. Paramedic was also called to ensure the patient safety but left shortly after since the patient had recovered nicely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Not disclosed
Vorgeschichte: None
Andere Medikamente: Not disclosed
Allergien: No known allergy
Vorherige Impfungen: -

VAERS 1214737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

syncope. collapsed from sitting position. emergency services called and arrived. administered aid. stabilized patient but he and wife refused further emergency services. left on his own recognizance

Weitere VAERSDATA-Felder

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

VAERS 1212938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

schwer

Staat: WA
Alter: 43,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Disorientation Dysphagia Heart rate increased Throat tightness

Symptomtext

Mild/moderate anaphylactic reaction lasting about 45 minutes, trouble swallowing, fast pulse, disorientation, tight throat. Epinephrine not used.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Mild cold
Vorgeschichte: -
Andere Medikamente: Wellbutrin, naltrexone, vitamin d
Allergien: Soy, corn, wheat, shellfish, erythromycin, latex, lidocaine / benzocaine
Vorherige Impfungen: -

VAERS 1212209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 49,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 13.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Electrocardiogram Hyperhidrosis Laboratory test normal Loss of consciousness Malaise Urine analysis

Symptomtext

Felt dizzy and not well- at work. Put head down between legs and next thing I remember is laying on the floor (having passed out for at least one minute). Tried to sit up and passed out again. When I woke up the second time (unknown duration) I was sweating over entire body and remained on the ground. Waited ten minutes until someone found me. EMT was called. Normal heart rate, blood pressure, EKG at scene. All blood work was within normal range. Hematocrit 12.1, blood glucose level 102 1.5 hours after episode. Spent approximately 5 hours under care of either EMT or emergency room care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: CBC and cardiac blood biomarker analysis (2X), urinalysis, EKG, continuous pulse oximeter and blood pressure monitoring
Aktuelle Erkrankungen: Longer period one month prior, but not excessive bleeding.
Vorgeschichte: None
Andere Medikamente: Viorele Tablets, GNC Women's Multivitamin
Allergien: No known
Vorherige Impfungen: -

VAERS 1212066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 10.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Dizziness Fatigue Gait disturbance Lethargy Nausea Pain Syncope Unresponsive to stimuli Vertigo

Symptomtext

Systemic: Body Aches Generalized-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: difficulty walking had to call 911-Severe, Systemic: Nausea-Severe, Systemic: Weakness-Severe, Additional Details: per Nurse, pt developed severe vertigo and pt had developed weakness and lead to difficulty walking

Weitere VAERSDATA-Felder

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

VAERS 1211042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 29,0
Geschlecht: M
Eingang: 14.04.2021
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: unbekannt Erholt: ja

Fall Lip injury Loss of consciousness

Symptomtext

As patient was sitting for 15 minute waiting period after receiving Pfizer COVID-19 vaccine, patient lost consciousness. He fell from a sitting position and bumped his lip on a shelf. Patient quickly regained consciousness after less than 1 minute. Helped him sit back into a chair. Patient reiterated he was "okay" but began to lose consciousness again, then woke up after less than 30 seconds. Checked blood pressure with his consent which was 116/64, pulse 64. Medics arrived shortly for additional testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood pressure 116/64, pulse 64
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 1210346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: VA
Alter: 44,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 09.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Computerised tomogram Haemorrhage Hypertension Pain Thrombosis Ultrasound scan

Symptomtext

Hemorrhage like bleeding, soaked up 4 maxi pads within a 30 minute span. Expelled Blood clots the size of apples. Went to ER. Blood loss and clots resembled the look of a miscarriage, but pregancy test, can back negative. Multiply tests were ran. This carried on from 1:30 to 8pm, when fentaNYL and omipaque was given for pain. Blood Pressure was also high 154/119 and temp 99.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: CT scans, Ultra sound, Several blood test
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Wellbutin
Allergien: none
Vorherige Impfungen: -

VAERS 1210056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Hyperhidrosis Syncope

Symptomtext

After administration of the COVID-19 1st dose, patient fainted and was caught by his father. Patient then sat on a chair while pharmacy staff monitored patient. Approximately 5 minutes after the incident, patient continue to experience sweating and weakness.

Weitere VAERSDATA-Felder

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

VAERS 1209758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 26,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
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

While client was in observation, she feels lightheaded and past out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood pressure was taken , 125/80
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1209574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 24,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Confusional state Fall Syncope

Symptomtext

MINUTES AFTER RECEIVING VACCINE, PATIENT FELL AND WOKE UP CONFUSED. POSSIBLE SLIGHT SYNCOPE. PATIENT SEEMED FINE AFTER SITTING DOWN AGAIN. PATIENT TOLD TO WAIT 30 MINUTES LONGER AND TO CONTACT SOMEONE ELSE TO DRIVE HIM HOME. OFFERED TO CALL 911, BUT PATIENT DECLINED AND SAID HE FELT FINE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Nicotine products
Allergien: No
Vorherige Impfungen: -

VAERS 1208992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 25,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Nausea Syncope

Symptomtext

Pt received his first Pfizer vaccine and completed all screening questions and passed them. Pt was given the vaccine and approx. 1-2 minutes after he stated he was nauseated and then had a syncopal episode where he fell on his knees and side but was caught before hitting his head. Pt came to in 5-10 seconds and was treated by ER team and taken to the ER for evaluation d/t being hypotensive. Pt was doing well when transferred.

Weitere VAERSDATA-Felder

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

VAERS 1208012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 60,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 12.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal discomfort Asthenia Body temperature increased Cold sweat Dizziness Electric shock sensation Myalgia

Symptomtext

Body muscle aches. Cold sweats. Weak upset stomach. Raised body temperature 99.7 and dissyness and brain zaps.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Depression
Andere Medikamente: Paxil 40mg daily and Atorvastatin 40mg daily
Allergien: None
Vorherige Impfungen: -

VAERS 1207087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MA
Alter: 18,0
Geschlecht: F
Eingang: 14.04.2021
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

Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild

Weitere VAERSDATA-Felder

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

VAERS 1206363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Seizure

Symptomtext

Within a few seconds of receiving vaccine, patient had a seizure last approx 10 sec. Code blue called, transferred to ED for evaluation. Stable and discharged home following event. Mom later reported previous hx of seizure following vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: 9 years of age per mom; vaccine unknown

VAERS 1423349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 19,0
Geschlecht: F
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: ja

Condition aggravated Dizziness Syncope

Symptomtext

1. lightheadedness 2. syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: patient has history of syncope
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1205928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Blood pressure measurement Fall Loss of consciousness Syncope

Symptomtext

Syncope and dizziness, BP 125/75, HR73, RR16. Patient experienced syncope and fell to floor from chair. Regained consciousness after ~3 seconds. Vital signs stable, released in stable condition

Weitere VAERSDATA-Felder

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

VAERS 1205555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 18,0
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: ja

Syncope

Symptomtext

patient fainted but has history of fainting with vaccines

Weitere VAERSDATA-Felder

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

VAERS 1205522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CO
Alter: 21,0
Geschlecht: F
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

Syncope

Symptomtext

patient fainted but usually faints with vaccines

Weitere VAERSDATA-Felder

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

VAERS 1205471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CO
Alter: 16,0
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

Syncope

Symptomtext

patient fainted,

Weitere VAERSDATA-Felder

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

VAERS 1205380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: MD
Alter: 17,0
Geschlecht: F
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

Syncope

Symptomtext

patient fainted after receiving vaccine - her dad was with her here in the pharmacy and stated that this was typical of her when getting blood drawn/needles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none that we know of
Vorgeschichte: none that we know of
Andere Medikamente: none that we know of
Allergien: nkda
Vorherige Impfungen: -

VAERS 1204493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 27,0
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

Anxiety Loss of consciousness

Symptomtext

patient passed out several minutes after receiving vaccine. he was very anxious before and during the vaccination. He came to in under a minute, waited in the store for approx. 20 minutes before leaving.

Weitere VAERSDATA-Felder

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

VAERS 1203993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MA
Alter: 24,0
Geschlecht: M
Eingang: 13.04.2021
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: unbekannt

Dizziness Hyperhidrosis Nausea Syncope Vomiting

Symptomtext

PT OBSERVED IN CLINIC. 20 MINUTES POST VACCINE PT REQUESTED TO LAY DOWN.PT HAD SYNCOPAL EPISODE. TO STRETCHER.CAT CALLED. PT DIAPHORETIC. VITALS #1 BP 81/51 HR 39 SPO2 99% 9:19 PT C/O NAUSEA #2 BP 90/60 HR 67 SPO2 99% 9:20#3 100/65 HR 61 SPO2 99% 9:25 #4 103/64 HR 65 SPO2 100% 9:32#5 106/60 HR 69 SPO2 99% 9:35 PT STATES NAUSEA, VOMITTING AND DIZZINESS HAS RESOLVED.PT NEEDED TO USE RESTROOM, ACCOMPANIED TO RESTROOM. PT NO LONGER COMPLAINED OF ANY SYMPTOMS. LAST VITALS SIGNSAFTER AMBULATING TO THE RESTROOM 109/72 HR 56 SPO2-99%

Weitere VAERSDATA-Felder

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

VAERS 1203789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: PA
Alter: 36,0
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 Dyspnoea Erythema Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

patient was given the vaccine,he was fine until he started walking around the store then he felt faint and returned to the pharmacy. we sat him in a chair,he was sweaty.white and started to slowly faint to the floor. His face got very red and his breathing sounded labored ,we placed him on the floor and he passed out briefly but came back to in about 3 minutes,very quickly he came back and his color returned and he knew where he was and answered all of our questions.We called 911 for an ambulance and when the ambulance crew arrived he was talking and feeling better.He had a gatoraid and sat up and answered all the questions everyone asked and his color was restored and he stood up and was feeling well enough to leave

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: his blood pressure was checked and that was all
Aktuelle Erkrankungen: not known
Vorgeschichte: takes high blood pressure medication
Andere Medikamente: UNKNOWN
Allergien: sulfa antibiotics
Vorherige Impfungen: -

VAERS 1203537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 13.04.2021
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

Fluid replacement Malaise Seizure

Symptomtext

Patient was with Medical Examiner. She was reviewing his allergies (PCN, bee stings) and discussed with patient need to wait 30 minutes after vaccine for observation. She then gave him pfizer vaccine. Within 1 minute of giving vaccine, patient began to have seizure. He was assisted to ground by MD and RNs at vaccination site. He was assessed and assisted to remain safe throughout seizure, 911 called and arrived on scene. Meanwhile, caregiver with patient stated seizures are "normal" for him and he has 4-5 a day. She reported that in line he was not feeling well and had precursors to seizure. Patient had reported to MD that he felt fine today and did not report seizure history to her previous to giving vaccine. It was also later reported that he had a seizure the night before as well. IVF were started by RN's. When emergency services arrived, patient was recovering and refusing to go to ER - against medical advice. He was assisted back into wheelchair by emergency services personnel. Patient was alert, and oriented and able to make decision not to go to emergency room. Patient left facility with caregiver in private vehicle. Patient was instructed to contact his primary care physician and let them know what happened and ask if 2nd dose of pfizer is appropriate for him. Patient was also instructed if MD wants him to get 2nd dose to go to a more controlled setting then Mass vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Seizure Disorder, Diabetes Type 2, Hypertension
Vorgeschichte: Seizure Disorder, Diabetes Type 2, HTN, GERD, Major Depressive disorder, Anxiety Disorder, Heart Disease, Enlarged prostrate, incontinence, Chronic pain
Andere Medikamente: -
Allergien: Penicillins, Bee Stings
Vorherige Impfungen: -

VAERS 1203181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 19,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Confusional state Dizziness Hypoacusis Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Additional Details: a few minutes after the patient took the vaacine she started getting lightheaded and she came to the pharmacy counter and passed out there. i carried the patient and sat her straight in a chair. i gave her water and orange juice. patient was confused and not aware of her surrounding and said she barely could hear. once she drank the OJ she felt better. took her vitals everything was fine. pt said she felt all good

Weitere VAERSDATA-Felder

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

VAERS 1202803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: MA
Alter: 22,0
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: ja Erholt: nein

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 1202567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: WV
Alter: 41,0
Geschlecht: F
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: ja Erholt: nein

Loss of consciousness Seizure

Symptomtext

Patient was intially responsive.. After waiting approximately 5 minutes patient informed staff at pharmacy that she felt like she was going to have a seizure. Patient moved to floor from chair. Was conscious for about 5 more minutes. Lost consciousness during seizure (approximately 2-3 minutes). Emergency medical personnel was called at that time. Patient regained consciousness and went with EMS to hospital for further testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: seizures
Andere Medikamente: Unknown
Allergien: latex
Vorherige Impfungen: -

VAERS 1202467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 57,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 11.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Anaphylactic reaction Influenza like illness Pruritus Urticaria

Symptomtext

2nd dose - In addition to the flu like symptoms routinely reported I had also had anaphylaxis approx. 24 hours after the shot. It happened between 6-11 pm on 4/12 (the day after receiving the vaccine at 6 pm on 4/11). It did not impact my breathing, but I had itchy welts and hives over most of my trunk and arms and upper legs. I took a Claritin and it helped relieve the symptoms. After the 1st dose on 3/20/2021 I also experienced mild rash like symptoms and hives for several weeks following the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1202335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 31,0
Geschlecht: F
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 Feeling hot Hyperhidrosis Loss of consciousness Tunnel vision

Symptomtext

Within five minutes was feeling dizzy, hot, vision started to tunnel. Suddenly broke into a sweat and then lost consciousness in a seated position. Nurses came over, laid me on my side, took blood pressure and pulse, and loosened flannel shirt/jacket. After about 10 minutes started to regain mental clarity. After 30 minutes was driven home by husband.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: multivitamin, loratadine (generic Claritin)
Allergien: none known
Vorherige Impfungen: -

VAERS 1202244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: AR
Alter: 55,0
Geschlecht: F
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: unbekannt Disable: unbekannt ER: ja Erholt: nein

Nausea Syncope

Symptomtext

Nausea with Syncope lasted longer than 10 seconds

Weitere VAERSDATA-Felder

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

VAERS 1182917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 56,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Erythema Hypertension Migraine Laboratory test Rash Oral mucosal blistering Oropharyngeal pain Pruritus Pyrexia Syncope

Symptomtext

Rash all over, redness, fever, chest pain and heaviness, fainting, severe itching, sore throat with blisters in mouth, Migraine, and HBP. Treatment: ER-IV Solu-medrol X1, Pepcid x1, Fiorcet x1, Toradol x1, Caffeine pill by mouth.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Migraines
Vorgeschichte: Migraines, Lupus, Asthma, Glaucoma, Blind
Andere Medikamente: Sertraline , Synthryoid , Multi Vit, Calcium Citrate
Allergien: Ibuprofen, Benadryl, Trazadone, Amoxicillin, Cephlasporins
Vorherige Impfungen: -

VAERS 1199550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 12.04.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Head injury Loss of consciousness Syncope Tremor

Symptomtext

Patient received the Pfizer COVID vaccine at around 4:50pm and while under observation he began to feel dizzy. He eventually passed out and became unconscious (5:00pm). Unfortunately he hit the ground with his head after he became unconscious. He also appeared to begin shaking while unconscious. He regained consciousness after about 20 seconds and was immediately fully alert. He stated he had no history of losing consciousness in the past. He was then taken to a nearby hospital via ambulance for evaluation and required staples to address the cut. He was discharged from the hospital around 8:00pm.

Weitere VAERSDATA-Felder

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

VAERS 1198707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NE
Alter: 20,0
Geschlecht: F
Eingang: 12.04.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Pallor Presyncope Vomiting

Symptomtext

Vasovagal reaction, pale, did not faint, but very light headed. Threw up.

Weitere VAERSDATA-Felder

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

VAERS 1198690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: RI
Alter: 19,0
Geschlecht: M
Eingang: 12.04.2021
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: ja Erholt: ja

Anaphylactic reaction Blood pressure decreased Blood pressure measurement Cyanosis Hypoacusis Vision blurred

Symptomtext

Anaphylaxis. Turned gray, diaphoretic, blurred vision, difficulty hearing. Blood pressure quickly dropped to 66/31. Perfusion was 5 seconds. Received EpiPen (0.3mg Epinephrine) x1. BP better but slow to return to baseline. To Emergency Room for 4 hours observation. While in ED, received IV Benadryl and IV Zofran. Condition improved by the end of 4 hour observation so discharged with an EpiPen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin (hives), Doxycycline (drug induced lupus)
Vorherige Impfungen: -

VAERS 1197370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: FL
Alter: 38,0
Geschlecht: M
Eingang: 12.04.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Nausea Syncope Vomiting

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1196655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 26,0
Geschlecht: F
Eingang: 12.04.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

pt fainted shortly after the vaccine was given, we tapped her shoulder and called her name and she came to and she was given water.. called 911 she denied going to the hospital...her friend drove her home after 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Low BP stated after fainting then waking up from the vaccination
Vorgeschichte: Low BP
Andere Medikamente: Unknown
Allergien: No
Vorherige Impfungen: pt said not all the time

VAERS 1195867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IA
Alter: 25,0
Geschlecht: M
Eingang: 12.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dehydration Hyperhidrosis Loss of consciousness Pallor Presyncope

Symptomtext

Pt was sitting in chair approximately 15 minutes following receiving the vaccine. he became unconscious, pale and sweaty. I checked and he had a pulse and was breathing and we called 911. I was able to yell at him and he regained consciousness and could tell me his name, date of birth and other info. He was able to grab my hand and squeeze. he said he he had been dehydrated and had had covid before. we gave him Gatorade and he felt better. paramedics checked him out and said most likely a vasovagal response. pt refused transport to hospital. his mother came and got him and was going to monitor

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 1195458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: PA
Alter: 50,0
Geschlecht: M
Eingang: 11.04.2021
Impfdatum: 10.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Bell's palsy Blood test Chest X-ray Computerised tomogram Electrocardiogram

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA Diagnosed with Bell?s palsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Ct scan. EKG. Chest Xray. Bloodwork. 4/11/21
Aktuelle Erkrankungen: None
Vorgeschichte: Sinus issues. Had two sinus surgeries and continued sinus issues.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1192904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 11.04.2021
Impfdatum: 10.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Mild, Additional Details: Pt felt lightheaded after receiving vaccine. Instructed to sit for a few minutes before heading to the post vaccination area. Pt fainted within 10 secs onto the immunizer (me). Asked for help to move pt to a lying down position. Upon lifting pt up, her body/arms seized up. Asked someone to call 911 and I went to grab an epipen just incase. Within 5 secs, patient woke up, so did not admin epi. Pt was alert but did not know what happened. Pt refused ambulance, left after 30 min, was feeling ok.

Weitere VAERSDATA-Felder

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

VAERS 1192856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: FL
Alter: 27,0
Geschlecht: M
Eingang: 11.04.2021
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

Dizziness Flushing Hyperhidrosis Hypotension Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Additional Details: Sycope episode

Weitere VAERSDATA-Felder

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

VAERS 1192541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 24,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Fainting and dizziness about four hours later

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Myalgic encephalomyelitis, postural orthostatic tachycardia syndrome, irritable bowel syndrome
Andere Medikamente: Adderall XR, Effexor XR, Abilify, Junel FE, multivitamin, fiber gummies, fish oil, electrolyte supplements, probiotic
Allergien: Lactose, gluten, avocado, watermelon
Vorherige Impfungen: -

VAERS 1192277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CO
Alter: -
Geschlecht: M
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

Hyperhidrosis Nausea Palpitations Paraesthesia Syncope

Symptomtext

Patient fainted about 5 minutes after getting vaccine. He gained consciousness right away. He complained of heart palpitations, sweating, hand tingling, and nausea.

Weitere VAERSDATA-Felder

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

VAERS 1191100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: WA
Alter: 27,0
Geschlecht: M
Eingang: 10.04.2021
Impfdatum: 10.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

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

Presyncope

Symptomtext

vasovagal reaction

Weitere VAERSDATA-Felder

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

VAERS 1191086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: WA
Alter: 49,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 10.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

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

Presyncope

Symptomtext

vasovagal reaction-mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: denies
Vorgeschichte: nnone
Andere Medikamente: Tamoxifen
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1190011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: FL
Alter: 37,0
Geschlecht: M
Eingang: 10.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient fainted about 1 and 1/2 hours after receiving the vaccine @ a grocery store. After waking up, he drank water and was able to feel better.

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 1189561

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge EW0153

schwer

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 10.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Chills Dizziness Fall Flushing Hyperhidrosis Injection site erythema Paraesthesia Syncope Tremor

Symptomtext

Site: Redness at Injection Site-Mild, Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Medium, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: patient reported not having eaten since previous day in the afternoon, briefly experienced syncope and fell out of chair that he was seated in while waiting 15 min after given first dose of covid shot, patient waited full amount of time and felt fine after 15 min

Weitere VAERSDATA-Felder

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

VAERS 1186479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MD
Alter: 46,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Pharyngeal swelling Throat irritation Dysphagia Feeling abnormal Paraesthesia oral

Symptomtext

Was taken by ambulance diagnoses anaphylaxis Throat swelling itching you get swelling was released after 4 hours with meds given iv steroids iv Benadryl

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: All blood work ekg
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol
Andere Medikamente: Rovostatin
Allergien: Bee Sulfur based drugs
Vorherige Impfungen: -

VAERS 1381470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: -
Geschlecht: M
Eingang: 09.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Loss of consciousness Refusal of treatment by patient Syncope

Symptomtext

Before I gave the vaccine to patient, I asked if he had why allergy or allergic reaction to any vaccine , and his was "No". I asked if he has any health condition that we should be aware off, his answer is "No". patient did not mention that he passed out (fainted) before after his blood drawn 10 years ago until after the incident. (after receiving covid vaccine). Patient refused us to call ambulance or medical help. Patient was told to sit down and was offered some water to drink. I asked if patient was OK, he said he was ok. I told patient to let his family member know to pick him up in case he cannot drive home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: -
Allergien: shrimp, beer, ibuprofen, tetracyclin
Vorherige Impfungen: blood drawn

VAERS 1187971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 23,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Blood glucose normal Chest pain Dyspnoea Hyperventilation Muscle twitching Throat tightness Tremor Vomiting

Symptomtext

23 yo FM who received first dose of Pfizer vaccine and then was noted to have shortness of breath and complaining tongue closing sensation immediately after at Vaccine Clinic --I was called to evaluate the patient. When I arrived patient was laying down on a chair with a friend, shaking with seizure like activity but alert and oriented to person place and time. Upon my arrival she was shaking, vomited x 1 and then complained about chest pain. Vitals upon my arrival: HR 58, o2 100% RR appeared to be around 22-24 (hyperventilating) BP 88 systolic (manual)--repeated by medics upon arrival minutes later 110/72. Given throat closing sensation, vomiting, shortness of breath I advised to call 911 and ordered Epinephrine x 1 which was given by RN immediately. Pt was then placed on the grown chin up, she continued to shake throughout entire body but continued to be alert and oriented. Medics then arrived on seen, started an IV, glucose by medics 84, IVF started by medics. Pt was transported to ER via medics. Pt is not a patient, last visit 2017. Pt did state she has hx of POTS and DRESS syndrome to Lamictal. Reports taking cetirizine this AM, Zofran and Oxycodone and Baclofen (prescribed by external PCP?). Prior to transport to ER pt continued to be alert oriented, but shaking and twitching throughout her body. MD verbally communicated to patient to not receive the 2nd dose given her severe anaphylaxis like reaction to the first dose of the vaccine. Pt can be referred to allergist after ER follow up by PCP. Denied pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gender dysphoria, Postural orthostatic tachycardia syndrome
Vorgeschichte: -
Andere Medikamente: Baclophen, Cetirizine, zofran, oxycode, baclophen
Allergien: Lamictal
Vorherige Impfungen: -

VAERS 1187946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Dizziness Loss of consciousness

Symptomtext

We are a Pharmacy. Today, April 9, 2021, we had a patient. She was scheduled for her first dose of the Pfizer vaccine at 9:30 am. The pharmacy manager gave her the vaccine inside the store at around 9:30 am. She was accompanied by her husband. After the shot, she sat down in one of the chairs in front of the pharmacy to wait for the mandatory 15 minutes wait for any reactions. At 9:43 am, we noticed that she was looking a bit dizzy. As we were approaching her, she slid down the chair and became unconscious. Luckily her husband was right beside her and caught her before she fell. Pharmacy manager then helped her husband to quickly lay her down flat on her back. The husband asked to call 911. The pharmacy technician was there to assist and she called 911. The patient regained consciousness roughly around 30 seconds after she fainted. She was alert and breathing normally. We asked again if they wanted us to continue calling 911. They said yes. Roughly 5 mins later, the paramedics came and assisted the patient. The sugar was good, blood pressure was good, temperature was good. They asked her if she wanted to go to the hospital. The patient denied. The paramedics left and the patient stayed for more time at the pharmacy and eventually left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood sugar (finger stick) 90 Temperature 98 F
Aktuelle Erkrankungen: No
Vorgeschichte: NO
Andere Medikamente: No
Allergien: NO
Vorherige Impfungen: -

VAERS 1187931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Body temperature increased Fall Head injury Loss of consciousness

Symptomtext

The patient was seemed OK after I gave her the shot. She came in with her mother who was in the vaccination room with her while I gave the shot. I told them to stay in the store at least 15 to 30 minutes after receiving the first dose. They walked out the vaccination room and I returned to the dispensing area. The mother immediately came up to the pharmacy dispensing window to ask for an ice pack because her daughter passed out on the floor and hit her head. I got the ice pack and went to the patient to see if she was OK. She was lying down on her back. The mother took the ice pack and rested it under the patients head. I checked her pupils and checked her pulse. Those vitals were normal. I asked the patient if she could tell me her name and what day of the week this was. She answered correctly. I took her temperature on her forehead and it was elevated to 100.4 - I re-checked her temperature again in 3 minutes and it was 99. The patient was able to get up to a chair a few minutes later, and then they left after 15 minutes and the patient seemed OK.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1187779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Disorientation Syncope

Symptomtext

Patient was reported to have fainted in an aisle about 10 minutes after administration of the vaccine. Upon arriving the patient was conscious but appeared to be disoriented, sitting in a chair. 911 was called and a police officer responded; patient was evaluated and EMT services were called in afterwards.

Weitere VAERSDATA-Felder

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

VAERS 1186942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: GA
Alter: 40,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Cold sweat Loss of consciousness Nausea Pallor

Symptomtext

patient has mitral insufficiency and vasovagal syncope. hit a vein and sight of blood and needle almost caused her to pass out. she was sitting on floor, very nauseous, blacking out, cold sweats, and palpitations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: mitral insufficiency and vasovagal syncope
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1186901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CT
Alter: 26,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Patient received first dose Pfizer covid without incident. Upon sitting in waiting area post vaccination, patient experienced syncope and fell off chair to floor. Patient regained consciousness within moments and was verbally conversing with staff. EMS was called and responded. Patient was given blood pressure check. patient declined any other medical treatment. Patient left without further incident.

Weitere VAERSDATA-Felder

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

VAERS 1186342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 07.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Fall Loss of consciousness Pain Pallor

Symptomtext

Patient became unconscious and fell in the family room around 8 am. She seemed to have a very low blood pressure and was very pale. She had pain on her right side due to the fall. She gradually improved over the day after taking twice 400 mg Ibuprofen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: vitamins
Allergien: none known
Vorherige Impfungen: -

VAERS 1184187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 22,0
Geschlecht: F
Eingang: 09.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Flushing Hyperhidrosis Loss of consciousness Syncope

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Weakness-Severe, Additional Details: Patient was give vaccine and fainted a couple minutes after sitting

Weitere VAERSDATA-Felder

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

VAERS 1184178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 25,0
Geschlecht: M
Eingang: 09.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood pressure decreased Chills Dizziness Feeling cold Hypotension Loss of consciousness Presyncope Syncope Tremor

Symptomtext

Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Systemic: Hypotension-Severe, Systemic: Shakiness-Severe, Systemic: Weakness-Medium, Additional Details: Within 15 minutes of receiving the vaccine, pt BP dropped to 97/47 and 37 BPM. Pt was put to lay down on their back with their feet elevated, and their BP and BPM returned to normal levels. Within 15 min from then, pt complained of feeling chills and was strongly shaking. 911 was called w/ pt and relative consent. Pt later left home, returning to normal. Seemed like vasovega response

Weitere VAERSDATA-Felder

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

VAERS 1183469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 17,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

A few minutes after receiving the vaccine, the patient fainted in the pharmacy wait area. She woke up a few seconds later and was alert. She was able to answer questions like "what is your name?" "where are your?" " etc. She denied a history of fainting but did say she fainted once about 8 years ago. She remained seated in the pharmacy waiting area for another 30 minutes and said she felt fine. She denied feeling dizzy, short of breath, and any allergic reaction symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None known
Vorgeschichte: none known
Andere Medikamente: Unknown
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1182814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 08.04.2021
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: ja

Loss of consciousness Muscle contractions involuntary

Symptomtext

Passed out in chair after vaccination, then muscles contracted for 5 seconds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: UNKOWN
Vorgeschichte: UNKOWN
Andere Medikamente: UNKNOWN
Allergien: NONE REPORTED OTHER THAN REACTION IN THE PAST TO VACCINES
Vorherige Impfungen: Did not disclose which vaccine

VAERS 1182554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 08.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Hyperhidrosis Presyncope

Symptomtext

Pt became light headed, diaphoretic and confused and had a near syncopal episode approximately 5 minutes after vaccine administration. Pt states history of passing out post injections/blood work. Pt vitals evaluated and Pt refused transport to ED.

Weitere VAERSDATA-Felder

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

VAERS 1181485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 27,0
Geschlecht: M
Eingang: 08.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Seizure Thirst

Symptomtext

Patient received immunization and felt fine after sitting in chair for a few seconds. Pt got up and went to waiting area and was sitting down in chair during the 15 minute observation window. Pt passed out and slumped/fell out of chair on patients left side. I was called out by the person monitoring the waiting area to see pt in fetal position on their left side seizing. The seizing lasted for about 15 seconds and then stopped. PT was motionless for a few more seconds and then came around and said "I'm back". The pt was given a bottle of water because he said he was thirsty. In the meantime the paramedics were called and arrived. They checked his BP and Blood Glucose. After several minutes they took the pt out on a gurney for further evaluation, there was a question as to whether or not pt hit his head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cyclic Vomiting Syndrome pt also reported having had a seizure when 10 years old
Andere Medikamente: Celexa
Allergien: None
Vorherige Impfungen: pt fainting, felt dizzy after previous vaccinations

VAERS 1180734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: MO
Alter: 18,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Syncope Vomiting

Symptomtext

Patient vomited immediately after vaccination. She sat for approximately 7 minutes with an ice pack before asking to walk somewhere to lay down. About 100 feet in to the walk, she fainted. She was being supported on both sides by pharmacist and het boyfriend, so she went to the ground gently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: All vaccines since age 7

VAERS 1180093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: ME
Alter: 23,0
Geschlecht: F
Eingang: 08.04.2021
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Loss of consciousness Syncope

Symptomtext

Patient had a synoptic episode approximately 10 minutes after receiving the vaccine. She fell and quickly regained consciousness. She recovered in a chair in about 15 minutes. She denied any injuries and did not require any emergency services.

Weitere VAERSDATA-Felder

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

VAERS 1179457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: FL
Alter: 30,0
Geschlecht: M
Eingang: 08.04.2021
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: ja

Hypotension Injection site pain Nausea Paraesthesia Syncope Tremor Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Fainting / Unresponsive-Medium, Systemic: Hypotension-Medium, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium

Weitere VAERSDATA-Felder

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

VAERS 1178401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: NJ
Alter: 16,0
Geschlecht: M
Eingang: 07.04.2021
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Seizure

Symptomtext

This patient has a history of epilepsy. He received the vaccine approximately 1pm. This is a minor who was here with his father. At approximately 1:10pm we were alerted that he started to seize. 911 was called. The father had him on the floor. He came out of the seizure prior to EMS arriving. Once they arrived, the parent declined ambulance transportation to the hospital and said he would call his physician.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: The patient has a history of Epilepsy.
Andere Medikamente: Levetiracetam
Allergien: Pollen
Vorherige Impfungen: -

VAERS 1178153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CA
Alter: 21,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 03.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

patient fainted for 30 sec the regained consciousness

Weitere VAERSDATA-Felder

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

VAERS 1177608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: UT
Alter: 19,0
Geschlecht: M
Eingang: 07.04.2021
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Feeling abnormal Limb injury Loss of consciousness Vision blurred

Symptomtext

Pfizer shot given. Patient felt ok immediately after shot, but approximately 5 minutes later told his mom he felt weird. He passed out and was helped to a sitting position. When I was called out to the lobby patient was still feeling a little lightheaded but he was conscious and breathing normally. He sustained a small cut on his hand which we cleaned up promptly. Patient told mom he felt like his vision was blurry. Mom wanted him checked out so I called emergency help.

Weitere VAERSDATA-Felder

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

VAERS 1177455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 07.04.2021
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: ja Erholt: ja

Dizziness Loss of consciousness

Symptomtext

Patient felt dizzy and black out for about 30 seconds. Patient was alert and talking in one minute.

Weitere VAERSDATA-Felder

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

VAERS 1177122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: IN
Alter: 17,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Chest pain Dizziness Loss of consciousness Paraesthesia

Symptomtext

Patient passed out. tingling in finger. light headedness. chest pain related to anxiety. occurred after about 15 minutes

Weitere VAERSDATA-Felder

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

VAERS 1177028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CT
Alter: 29,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Loss of consciousness Malaise

Symptomtext

told the immunizer before hand that she gets faint with vaccines/needles. The immunizer administered the vaccine and asked the individual if they were all right after. She said she was. She waited in the waiting room and then started feeling ill. She ended up passing out on the floor.

Weitere VAERSDATA-Felder

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

VAERS 1176686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: FL
Alter: 18,0
Geschlecht: F
Eingang: 07.04.2021
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: nein

Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium

Weitere VAERSDATA-Felder

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

VAERS 1175981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: ME
Alter: 47,0
Geschlecht: M
Eingang: 07.04.2021
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: ja

Fall Loss of consciousness Presyncope

Symptomtext

While standing at the check out desk, patient experienced dizziness with fall and loss of conciousness for ~30 seconds. He was not observed to hit his head and reported no headache or feeling of brusing of his head Treatment Administered: Cold Compress and Sips of Water Treatment Comments: Patient was taken to the observation area where he was observed for 40 minutes. He reported resoluation of any dizziness and reported prior vasovagal events from other vaccinations/blood draws.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: prior vasovagal reactions to needles/blood draws/
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1175938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IN
Alter: 18,0
Geschlecht: F
Eingang: 07.04.2021
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: ja Erholt: nein

Dizziness Head injury Seizure Syncope

Symptomtext

Pt received vaccine and approximately 5 minutes later pt got light headed fainted and hit head on the floor of the waiting room. Pt begun to seize for approximately 30 seconds then regained consciousness. Pt was stabilized and monitored. 9-1-1 contacted immediately and handled pt care once they arrived.

Weitere VAERSDATA-Felder

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

VAERS 1173991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: CO
Alter: 24,0
Geschlecht: M
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Malaise Syncope

Symptomtext

Pt Stated that he was not feeling well after the vaccination and wanted water. While getting him a bottle of water pet had Fainted and was out for 10 seconds before he regained consciousness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none pt did not want medical help after IMZ and was told to stay for a bit longer to make sure he was ok.
Aktuelle Erkrankungen: None reported
Vorgeschichte: none reported
Andere Medikamente: None reported
Allergien: None reported
Vorherige Impfungen: -

VAERS 1173939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TN
Alter: 16,0
Geschlecht: M
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Asthenia Cold sweat Dizziness Heart rate irregular Hyperhidrosis Loss of consciousness Nervousness Pain in extremity Pallor Tremor

Symptomtext

Patient was nervous upon receipt of vaccine. It was an unscheduled (expiring) dose. Per parent, he had fallen asleep outside vaccine room and they had to wake him up to get vaccine. I gave immunization and asked him to stay for 15 minutes afterwards. His Mom ran to consult window to notify staff patient was passing out. I was sanitizing vaccine room so I immediately ran to him and his Dad and I caught him as he was slumping over. He was shaking really hard, weak, and clammy. He was coherent b/c I asked him his name but did not have clear recollection of timing of vaccine. He was very pale in color. His Mom grabbed him a Gatorade and he seemed very thirsty as he was drinking. He mentioned he felt dizzy and that both arms were hurting and the arm I gave vaccine in felt like he had sweat dripping off it. (I felt his arm and it did not). I grabbed an instant cold pack and placed on his neck to help cool him off. His color returned over the 30 minutes. I asked parents if they wanted me to call ambulance but they wanted to wait and see how he responded. He looked at his iPhone data and his heart rate had spiked. Unclear if right before vaccine or right after but I believe he mentioned it went up to 120 when Mom said his normal resting heart rate was 60. He ate some gold fish and seemed to perk up and have a few funny conversations showing his personality. I explained to him very important to let parents know if he experienced any other side effects after leaving. He was able to stand up and walk out of RX with parents.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: None listed on VAR
Andere Medikamente: Unknown
Allergien: No
Vorherige Impfungen: -

VAERS 1173853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: AZ
Alter: 26,0
Geschlecht: M
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope Taste disorder

Symptomtext

Patient sat down for the 15 minute observation period, after about 3-5minutes fainted, falling face forward. Episode lasted less than 2 minutes, sat up and stated felt better. Patient stated they have fainted before and tasted blood however mouth had no signs of bleeding. 911 was called and came within 5 -10 minutes. Patient left with first responders

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient stated history of syncope
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1173833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CA
Alter: 35,0
Geschlecht: M
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Nausea Pallor Paraesthesia Somnolence Syncope Vomiting

Symptomtext

Vaccine Reaction: Nauseated, Syncope and sweating Description of Event: Pt found in observation chair, sweaty and nauseous and had about a 1 minute syncopal episode observed by OBS RN. Pt slow to arouse post syncope. Able to ambulate 2 steps and placed on gurney. Taken outside of the building by exit doors. Pt sleepy and sweaty, placed on vital sign machine. Dr. and multiple RN's with patient. Pt remained slightly nauseous at 1033. Pt had eaten breakfast and denies any medical history or meds. 1035 attempt sips of water, 1038 we called his girlfriend to come be with him and drive him home. Pt felt like he couldn't get enough air at 1038, we removed both of his masks at this time. Pt was sweaty again, but oxygen sats were 100%. 1056 GF arrived. 1106 we attempt to sit up patient slightly and he gets lightheaded and request to lie flat again. Sips of water causes nausea. Dr. remains at BS with patient. Pt began feeling a whole body tingle, encouraged to take nice slow easy breaths. 1111 took a bite of granola bar. 1143 tried sitting up again, gets lightheaded and laid back down. 1154 Dr. back at bedside. 1200 Pt cold bath blanket put on patient. Pt had periods of being slightly pale during observation period and dry mucuous membranes.Pt refusing to try water or granola bar at this time. 1205 pt began to vomit stomach contents.1212 Dr. back at BS to evaluate patient. Pt feels slightly better, taking sips of water. 1220 pt has been able to lay with head up on his left side now for 20 mins. Dr. offered to send patient to ER to get IVF and be checked out, pt began to perk up and wanted to go home. Orthostatic VS done and remain stable. GF is agreeable to take patient home and monitor him, she is not going in to work today. Pt taken to car via wheelchair, assisted in car, able to walk a few steps. Advised by Dr. to eat a salty meal and drink plenty of fluids and rest. Go to ER if symptoms worsen. Also advised by this RN to follow up with his PCP and let them know of his syncope with vaccine. Pt also advised if he dose get the second vaccine to let them know up front he faints and will be given vaccine in reclining chair.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: denied any medical issues
Andere Medikamente: denies any daily meds
Allergien: denied
Vorherige Impfungen: -

VAERS 1173312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 42,0
Geschlecht: M
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Fall Feeling hot Hyperhidrosis Nausea Syncope Tremor

Symptomtext

Patient was given first dose of Pfizer COVID-19 vaccine. I counseled the patient on side effects and asked him to wait 15 minutes afterwards in our waiting area. After about 5 minutes, the patient starting complaining of feeling dizzy. We asked him to sit back in the chair and brought him a bottle of water. I asked the patient if he had eaten today and he replied no. I offered a snack and also a glucose tablet to help with shakiness. As I went to get a bottle of glucose tablets off the shelf, the patient fainted and fell out of his chair. I immediately ran to get an Epipen while my technicians called for a Code White and 911. I was about to inject the patient with the Epipen when he came to about 10 seconds later. He said he was really hot, sweaty, dizzy, and nauseous. Paramedics and AP arrived to evaluate him and take a statement. Patient left on his own will and received a ride home from his mother-in-law, who is an associate at our store.

Weitere VAERSDATA-Felder

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

VAERS 1173064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 37,0
Geschlecht: M
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Syncope

Symptomtext

Patient was asked to remain in store for 15 minutes after immunizing and was seated in lobby at pharmacy. After about 5 minutes patient said he stood up to tell pharmacy he was feeling dizzy and he fainted and fell down. Pharmacy immunizing technician immediately attended to patient as well as store management. Pharmacist called 911 and monitored patient. Patient did not require CPR, he was awake after a few seconds. We had patient remain face down on the floor and still on the floor talking to him until paramedics arrived. Paramedics arrived about 5 minutes after calling 911. Patient was taken to the ER by paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: None/ Unkown
Allergien: No know drug allergies
Vorherige Impfungen: -

VAERS 1172910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TX
Alter: 16,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

Patient passed out for about 2 minutes upon receiving immunization. The patient was caught by her father and placed in a seated position. As the pharmacist went to call for assistance, the patient's father realized that she was awake again. The whole incident occurred within a few minutes. We had the patient sit in observation for 30 minutes, and we gave her water.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1171614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: IA
Alter: 17,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test normal Dizziness Electrocardiogram normal Loss of consciousness

Symptomtext

patient lost consciousness approximately 3 minutes after receiving vaccine, appeared to be fine immediately following vaccine, was speaking coherently to nurse, stood up under own power, became dizzy and lost consciousness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG, standard blood work, all normal
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: birth control pills
Allergien: none
Vorherige Impfungen: -

VAERS 1171582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: SC
Alter: 26,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 06.04.2021
Beginn: 06.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Fainted and fell out of chair

Weitere VAERSDATA-Felder

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

VAERS 1170124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: CO
Alter: 16,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fall Syncope

Symptomtext

Pt was sitting down, and mother was standing by patient. Pt fainted and fell out of chair, Did not hit head per mother. Patient was awake and aware right away and sitting up. EMS came to evaluate patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None Known
Aktuelle Erkrankungen: None known
Vorgeschichte: None Known
Andere Medikamente: None Known
Allergien: no
Vorherige Impfungen: -

VAERS 1169156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

schwer

Staat: VA
Alter: 19,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope Tinnitus

Symptomtext

Patient didn't think she fainted. Thought she fell asleep. However, a customer saw her phone and personal items fall. She did state she has a history of fainting from taking blood, so it's possible she fainted. She was feeling light headed and woozy and her ears were ringing just before the episode. I asked her if she wanted me to call 911 and she said no because when it had happened in the past, she had been fine. I took her blood pressure and it was 95/52. She waited in the area till 12:25 and I took her blood pressure again and it was 115/60. She did not have any other incindent. She left with her companion. I called her at 1:27p. She had arrived home and was still doing ok.

Weitere VAERSDATA-Felder

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

VAERS 1168697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

schwer

Staat: TN
Alter: 16,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

Syncope and vomiting. Symptomatic treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: No significant illness/injuries
Andere Medikamente: Sertraline 25mg, Proactive Acne topical, Fluticasone nasal spray
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1167131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

schwer

Staat: FL
Alter: 31,0
Geschlecht: M
Eingang: 04.04.2021
Impfdatum: 04.04.2021
Beginn: 04.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Electrocardiogram Hyperhidrosis Hypotension Syncope

Symptomtext

Passed out, low blood pressure, extreme sweating

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG, monitoring, low blood pressure on 4/4
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vivance and adderall
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2678030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 30.08.2023
Impfdatum: 04.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Balance disorder Crohn's disease Fatigue SARS-CoV-2 test Tremor

Symptomtext

Hand tremors; weakness in hands; Chronic fatigue; unbalanced; Crohn's disease came out of remission; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old male patient received BNT162b2 (BNT162B2), on 04Apr2021 as dose 2, single (Lot number: EW0153) at the age of 56 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Type two diabetes" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "Crohn's disease" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "Known allergies: Black pepper" (unspecified if ongoing); "Known allergies: lactose" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Cephalexin, reaction(s): "Known allergies: Cephalexin". Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: Unknown. EP7534, Location of injection: Arm Left), administration date: 23Mar2021, when the patient was 56-year-old, for COVID-19 Immunization; Humira, reaction(s): "Known allergies: Humira". The following information was reported: FATIGUE (hospitalization, disability) with onset 25Apr2021, outcome "not recovered", described as "Chronic fatigue"; CROHN'S DISEASE (hospitalization, disability) with onset 25Apr2021, outcome "not recovered", described as "Crohn's disease came out of remission"; TREMOR (hospitalization, disability) with onset 25Apr2021, outcome "not recovered", described as "Hand tremors"; BALANCE DISORDER (hospitalization, disability) with onset 25Apr2021, outcome "not recovered", described as "unbalanced"; ASTHENIA (hospitalization, disability) with onset 25Apr2021, outcome "not recovered", described as "weakness in hands". The patient was hospitalized for tremor, asthenia, fatigue, balance disorder, crohn's disease (hospitalization duration: 4 day(s)). The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative, notes: Nasal Swab. Therapeutic measures were taken as a result of tremor, asthenia, fatigue, balance disorder, crohn's disease. Clinical course: No other vaccine in four weeks, no vaccination before. AE treatment: IV fluids, antibiotics, colonoscopy, blood tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: 4,0
Labordaten: Test Name: COVID-19 Test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Crohn's disease; Food allergy; High cholesterol; Hypertension; Lactose intolerance; Type 2 diabetes mellitus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 49,0
Geschlecht: U
Eingang: 13.07.2023
Impfdatum: 20.04.2021
Beginn: 16.04.2023
Tage bis Beginn: 726,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Angiogram pulmonary abnormal Ankylosing spondylitis Aphonia Asthenia Blood creatinine Blood thyroid stimulating hormone normal Blood urea COVID-19 Glycosylated haemoglobin normal Leukocytosis Lung opacity Oropharyngeal pain Pneumonia bacterial Pneumonitis Procalcitonin increased Productive cough Pulmonary mass

Symptomtext

Assessment and Plan Patient is a 51 y.o. male patient of Physician No with history of diabetes, ankylosing spondylitis presented to Hospital with fevers, weakness. Covid-19 Virus Infection Pneumonia Gram negative suspected Sepsis Date of onset of symptoms: 04/14 Symptoms present on admission: Yes, sore throat, productive cough, loss of voice, fever. Fever of 101.5 with tachycardia and leukocytosis of 17K on arrival. Date of covid positive test: 04/16 Imaging: CTPA with RLL clustered nodular opacity Oxygen requirements on admission: none Current oxygen requirements: none Medical therapy: Not a candidate for steroids/remdesivir. Paxlovid X5 days Consultants following: ID Anticipated special isol Anticipated special isolation end date: 04/23. Discharged with azithromycin and cefdinir AKI Creatinine 1.98, BUN 16. Likely secondary to sepsis in the setting of metformin, indomethacin use.(Patient also received contrast study). Improving creat, 1. today Hold indomethacin at dishcarge Diabetes type 2 On metformin at home Hold metformin, A1C 6.6 SSI Ankylosing spondylitis On chronic indomethacin. Given AKI would recommend discontinuation of indomethacin. Discussed with PCP. Thyroid nodule Right thyroid lobe nodule measuring 3.8 cm noted on CTPA study. TSH wnl. Recommend thyroid ultrasound as outpatient. Clustered nodular opacities in the right lower lobe Likely inflammatory, on abx. Elevated procalcitonin. Follow-up CT chest recommended in 6 weeks as outpatient. F/U with PCP.

Weitere VAERSDATA-Felder

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

VAERS 2653137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 06.07.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / AR

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

Dyspnoea Mobility decreased Pyrexia Speech disorder Tremor

Symptomtext

Patient experienced a severe fever and violent body tremors throughout the entire body, resulting in speech, movement, and breathing difficulties.

Weitere VAERSDATA-Felder

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

VAERS 2652367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 61,0
Geschlecht: M
Eingang: 04.07.2023
Impfdatum: 06.04.2021
Beginn: 30.06.2021
Tage bis Beginn: 85,0
Dosis: 1
Route/Site: SYR / LA

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

Acute myeloid leukaemia Condition aggravated Cytogenetic analysis Fatigue Nausea Next-generation sequencing

Symptomtext

Leukemia, AML, He is day ~21 Decitabine and day 14 VEnclexta for now confirmed t-AML. NGS and cytogenetics returned complex cytogenetics with RUXN1-MECOM fusion t(3;21) TET2 x 2 DNMT3A and RUNX1 genes. THis is all c/w treatment-related AML. Besides fatigue and minimal nausea, he has no focal complaints. No fever, on LVQ ppx due to severe NTP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: See recent hospital notes. He is day ~21 Decitabine and day 14 VEnclexta for now confirmed t-AML. NGS and cytogenetics returned complex cytogenetics with RUXN1-MECOM fusion t(3;21) TET2 x 2 DNMT3A and RUNX1 genes. THis is all c/w treatment-related AML. Besides fatigue and minimal nausea, he has no focal complaints. No fever, on LVQ ppx due to severe NTP.
Aktuelle Erkrankungen: None
Vorgeschichte: Leukemia in remission since November 2016
Andere Medikamente: Losartan, Metropplol
Allergien: None
Vorherige Impfungen: -

VAERS 2638353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

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: 2
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 2617554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 19.04.2023
Impfdatum: 13.04.2021
Beginn: 11.05.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: IM / LA

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

Aortic arteriosclerosis Hypotension Urinary retention

Symptomtext

HYPOTENSION 5/28/2021 ATHEROSCLEROSIS OF AORTA HYPOTENSION 5/28/2021 URINARY RETENTION

Weitere VAERSDATA-Felder

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

VAERS 2599437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 24.01.2022
Beginn: 16.03.2023
Tage bis Beginn: 416,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Chronic obstructive pulmonary disease Condition aggravated Hypoxia SARS-CoV-2 test positive

Symptomtext

Brief Summary of Hospital Stay: 80-year-old female with a history of chronic obstructive pulmonary disease, HTN, T2DM who was admitted for acute hypoxia 2/2 to COVID-19 infection and likely COPD exacerbation. She was given a course of Remdesivir for 2 days, Ceftriaxone, and Prednisone. She was feeling better at time of discharge. She was sent home on 2L of oxygen. She was discharged to finish 2 more days of antibiotics with Cefdinir, and 7 more days of Prednisone. She was found to have soft BP's inpatient and was told to hold HCTZ until she sees PCP. She was discharged on home oxygen. She needs to follow with PCP for management of care after inpatient stay.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: Positive COVID PCR test 3/16/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 18.02.2023
Impfdatum: 18.02.2022
Beginn: 20.07.2022
Tage bis Beginn: 152,0
Dosis: 2
Route/Site: IM / AR

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

Biopsy Biopsy skin Blood test Dizziness Dry eye Dry mouth Dyspnoea Echocardiogram Electrocardiogram Exercise tolerance decreased Fatigue Hypotension Laboratory test Magnetic resonance imaging head Musculoskeletal discomfort Palpitations Paraesthesia Tilt table test

Symptomtext

Have had a number of fluctuating symptoms that started in July. Extreme fatigue, unable to exercise. tingling hands/feet, low blood pressure, racing heartbeat, shortness of breath, dizzy. Phantom sensations in back / shoulder, dry mouth and eyes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG in ER 7/21/2022, echocardiogram 8/1/2022, Tilt table test 9/27/2022, cortisol 10/11/2022, Breathing test 9/29/2022, qsart 11/30/2022, fat pad biopsy 12/12/2022, multiple blood tests, bone scan 11/14/2022, 24-hour urine test 11/14/2022, brain MRI 11/17/2022, skin biopsy 2/3/2022
Aktuelle Erkrankungen: Not ill at time of vaccination
Vorgeschichte: None
Andere Medikamente: Women's One a Day multivitamin, occasional Calcium, occasional Iron supplement
Allergien: Bactrum
Vorherige Impfungen: -

VAERS 2575128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: WA
Alter: 40,0
Geschlecht: F
Eingang: 03.02.2023
Impfdatum: 10.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / RA

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

ACTH stimulation test abnormal Adrenal insufficiency COVID-19 Cardiovascular autonomic function test Dizziness Echocardiogram normal Exercise tolerance decreased Fatigue Headache Heart rate increased Hypotension Magnetic resonance imaging head normal Nasal congestion Pain Postural orthostatic tachycardia syndrome Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

After dose 2 of COVID-19 vaccine I began having symptoms never experienced before. My symptoms were fatigue, exercise intolerance, lightheaded, high heart rate, and low blood pressure. I did several tests at the cardiologists. I ended up in the Fall of 2021 doing autonomics testing, a tilt table test. I met the criteria for POTS, Postural Orthostatic Tachycardic Syndrome. I was diagnosed with thyroid disease. I began taking levothyroxine. There was concern for my cortisol. Fall of 2022 I went through testing for Adrenal Insufficiency. My body no longer produces cortisol. ACTH Stimulation test fall of 2022. I am now on steroids for my lifetime. I now carry an emergency kit with an injectable steroid in case of accident or high stress situation. I am also on fludrocortisone. Even though I met the criteria for POTS, it's likely that what I had all along was Adrenal Insufficiency. Also, on February 1, 2023, I tested positive for COVID-19. This was after dose 4 on 12/26/2022. My symptoms were nasal congestion, headache, wet cough, slight fever, fatigue and mild body aches. I didn't visit the doctor for care. I did home remedies for comfort. This is day 3 and I feel about the same.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Autonomics Testing, a tilt table test; abnormal, POTS, Fall of 2022; ACTH Stimulation test fall of 2022, abnormal, Adrenal Insufficiency; ECHO cardiogram, normal, 2021; MRI on the brain, normal, 2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Amoxicillin; penicillin
Vorherige Impfungen: -

VAERS 2572812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NY
Alter: 83,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 01.05.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Cardiac failure Dyspnoea Feeding disorder Gait inability Illness Weight Weight decreased

Symptomtext

She got really sick after the second dose; Said cause of death was her heart; She had lost 60 lbs; Winded / difficulty breathing; Unable to walk; By the time she passed away, she was not able to eat much; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). An 83-year-old female patient received BNT162b2 (BNT162B2), in May2021 as dose 2, single (Lot number: EW0153) at the age of 83 years for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "Depression" (unspecified if ongoing); "Had issues with her heart five years ago" (unspecified if ongoing); "Did a stent about 5 years ago" (unspecified if ongoing). Patient never got Covid. The patient took concomitant medications, including a lot of mediation for high blood pressure, antidepressants; taking six medicines by the time she died. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: EN6203), administration date: Apr2021, when the patient was 83 years old, for Covid-19 immunization. The following information was reported: ILLNESS (death, hospitalization), outcome "fatal", described as "She got really sick after the second dose"; CARDIAC FAILURE (death, medically significant), outcome "fatal", described as "Said cause of death was her heart"; WEIGHT DECREASED (medically significant), outcome "unknown", described as "She had lost 60 lbs"; DYSPNOEA (non-serious), outcome "unknown", described as "Winded / difficulty breathing"; GAIT INABILITY (non-serious), outcome "unknown", described as "Unable to walk"; FEEDING DISORDER (non-serious), outcome "unknown", described as "By the time she passed away, she was not able to eat much". The patient underwent the following laboratory tests and procedures: Weight: had lost 60; over 200; probably around 250, notes: before getting the vaccines. The patient date of death was 01Nov2021. Reported cause of death: "She got really sick after the second dose", "Heart failure". No autopsy was performed. Clinical course of events: The reporter believes that the patient's death was in regards to the second Covid-19 vaccine. Within two weeks of taking the second dose, patient was winded, unable to walk, and had difficulty breathing. The patient never had trouble walking before, but her legs became completely useless. In another couple of weeks, she had lost 60 lbs. She was a pretty heavy woman and started losing weight rapidly. By the time she passed away, she was not able to eat much. They were just giving her water and putting ice on her lips. After she got sick, she was hospitalized numerous times. She was getting so sick. She was admitted to the hospital and had a stay in a nursing home. Felt bad, so had her bought back home from the nursing home and a week after that she passed away in the house. She was hospitalized like three times. Unsure of the dates. Never took an autopsy. Doctor said cause of death was her heart. Doctor came to that conclusion without an autopsy. Heart failure was put on the death certificate.; Reported Cause(s) of Death: Heart failure; She got really sick after the second dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Weight; Result Unstructured Data: Test Result:had lost 60 lbs; Test Name: Weight; Result Unstructured Data: Test Result:over 200 lbs; Test Name: Weight; Result Unstructured Data: Test Result:probably around 250 lbs; Comments: before getting the vaccines
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Depression; Heart disorder; Stent placement
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2561960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: VA
Alter: 38,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 23.09.2022
Beginn: 25.09.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / AR

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

Arthralgia Dyspnoea Heart rate increased Hypertension Palpitations

Symptomtext

extreme heart palpataions, racing pounding heart felt throughout my body and visibly noticeable, Joint pains that worsened following the last vaccine 09/23/2022 started after the first vaccine 2021.shortness of breath. My heart rate was so high that i went to local emergency dept and my resting heart rate was 175 beats per minute, blood pressure has been high ever since. Seeing a cardiologist tomorrow for an echocardiogram and a holter monitor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Joint pain from first vaccine 03/2021
Andere Medikamente: flu vaccine
Allergien: NO
Vorherige Impfungen: folowwing the first covid vaccines I had joint pains

VAERS 2558196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 20.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Blood pressure increased Blood pressure measurement Chest discomfort Dizziness Feeling hot Menstruation irregular Palpitations SARS-CoV-2 test Vertigo

Symptomtext

my head felt on fire and I felt I was going to faint; felt I was going to faint/dizziness; developed irregular menses; vertigo; chest tightness; elevated blood pressure; palpitations; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 20Apr2021 at 11:30 as dose 2, single (Lot number: EW0153) at the age of 43 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Peanuts" (unspecified if ongoing); "Known allergies: latex" (unspecified if ongoing); "Psoriasis" (unspecified if ongoing). Concomitant medication(s) included: TYLENOL. Vaccination history included: BNT162b2 (dose lot number=EN6198, dose administration time=11:00 AM, dose number=1, dose vaccine location=Arm Left), administration date: 30Mar2021, when the patient was 43-year-old, for COVID-19 immunization. The following information was reported: CHEST DISCOMFORT (non-serious) with onset 20Apr2021 at 11:00, outcome "unknown", described as "chest tightness"; MENSTRUATION IRREGULAR (non-serious) with onset 20Apr2021 at 11:00, outcome "unknown", described as "developed irregular menses"; BLOOD PRESSURE INCREASED (non-serious) with onset 20Apr2021 at 11:00, outcome "unknown", described as "elevated blood pressure"; DIZZINESS (non-serious) with onset 20Apr2021 at 11:00, outcome "unknown", described as "felt I was going to faint/dizziness"; FEELING HOT (non-serious) with onset 20Apr2021 at 11:00, outcome "unknown", described as "my head felt on fire and I felt I was going to faint"; PALPITATIONS (non-serious) with onset 20Apr2021 at 11:00, outcome "unknown"; VERTIGO (non-serious) with onset 20Apr2021 at 11:00, outcome "unknown". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of feeling hot, dizziness, menstruation irregular, vertigo, chest discomfort, blood pressure increased, palpitations. Additional information: Prior to vaccination the patient was not diagnosed with COVID- 19, Since the vaccination, patient has been tested for COVID-19. The patient received Tylenol within 2 weeks of vaccination. Within 20 minutes her head felt on fire and she felt she was going to faint. Since then, she developed irregular menses, vertigo, dizziness, chest tightness. Four days after she had elevated blood pressure, palpitations. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Serious: No. Hospitalization Prolonged: No.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:I had elevated blood pressure; Test Date: 20210901; Test Name: Covid; Test Result: Positive ; Comments: Positive; Test Date: 20211220; Test Name: Covid; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts; Latex allergy; Psoriasis
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 2548163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0153

moderat

Staat: NY
Alter: 19,0
Geschlecht: F
Eingang: 02.01.2023
Impfdatum: 01.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: SYR / LA

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

Chills Dizziness Echocardiogram Exercise tolerance decreased Fatigue Feeling abnormal Heart rate increased Humidity intolerance Orthostatic intolerance Pain Postural orthostatic tachycardia syndrome Pyrexia Skin discolouration Tachycardia Temperature intolerance Tilt table test

Symptomtext

High heart rate, hands turned purple, high fever, dizziness,chills, body aches, orthostatic intolerance. All within 1 day of dose. Diagnosed with POTS thereafter. Medications have helped tachycardia but continue to have brain fog, fatigue, exercise intolerance, heat/humidity intolerance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postural orthostatic tachycardia syndrome
Hospital-Tage: -
Labordaten: Tilt table test June 2021; echocardiogram June 2021.
Aktuelle Erkrankungen: -
Vorgeschichte: MALS
Andere Medikamente: -
Allergien: Cephlasporins
Vorherige Impfungen: -

VAERS 2543563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 03.06.2021
Beginn: 27.10.2022
Tage bis Beginn: 511,0
Dosis: 2
Route/Site: - / -

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

Arthritis Bronchitis COVID-19 Carpal tunnel syndrome Coronary artery disease Diabetes mellitus inadequate control Electrocardiogram QT prolonged Gastrooesophageal reflux disease Glycosylated haemoglobin increased Hepatic steatosis Hyperlipidaemia Hypertension Obesity Oedema peripheral SARS-CoV-2 test positive Vision blurred Vitamin D deficiency

Symptomtext

DATE OF ADMISSION: 10/27/2022 DATE OF DISCHARGE: 11/04/2022 DISCHARGE DIAGNOSIS: PRIMARY DIAGNOSIS: Acute COVID infection. SECONDARY DIAGNOSES: Acute bronchitis secondary to COVID, right eye blurred vision?, QT prolongation (455 milliseconds), hepatic steatosis, arthritis, obesity, gastroesophageal reflux disease, hyperlipidemia, bilateral leg edema, hypertension, carpal tunnel syndrome, vitamin D deficiency, coronary artery disease, uncontrolled diabetes mellitus (A1c 13.8).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 10/27 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC--detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2508382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 15.04.2021
Beginn: 01.04.2022
Tage bis Beginn: 351,0
Dosis: 1
Route/Site: SC / RA

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

Arthralgia Fatigue Heart rate increased Inflammation Migraine Pain in extremity Palpitations Tinnitus

Symptomtext

Severe fatigue last from 4/21, migraines 1-2 weekly since 4/21, i Increase heart rate and palpitations.lasting 2 weeks .inflammation and pain bilat knees, hands and feet. tinnitus chronic now since 4/21

Weitere VAERSDATA-Felder

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

VAERS 2443014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 25.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Alopecia Arthritis Cognitive disorder Feeling abnormal Gait disturbance Hot flush Laboratory test Myalgia Onychoclasis Pain Palpitations Paraesthesia Seborrhoeic dermatitis Tremor

Symptomtext

When I was given the shot my body went into a severe shaking uncontrollable for an hour and then other problems began by May all of these problems began -muscle pain. cognitive problems, heart palpitation, hot flashes, wobbly with my legs and couldn't walk felt like a puppet trying to pick up something from the floor, tinging in my hands, My nails cracked and Hair started falling. Since getting the virus in June 2022 some of these systems began to disappear like the fogginess feel better. Test for auto immune have increase. My finger have developed Arthritis. I felt my whole body was being attacked .I developed Seborrheic Dermatitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: I had to see a Heart dr, trying to work with a a rheumatologist for the pain. Dermatologist.
Aktuelle Erkrankungen: I was fine and my medical issues were all controlled. I was walking from 2 to 3 miles a day.
Vorgeschichte: I have essential tremors. Delayed Bleeding clotting disorder. Arthritis.
Andere Medikamente: Primidone 50 mg 2x a day, Zyrtec, Motrin, 400, Albuterol inhaler PRN, B12 Shots, vitamin D2 1250 MCG, Lorazapam.5 PRN at night.
Allergien: Tetracycline
Vorherige Impfungen: -

VAERS 2426700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IN
Alter: 58,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram head normal Culture urine Dizziness Glomerular filtration rate Headache Injection site pain Loss of personal independence in daily activities Metabolic function test Mobility decreased Red blood cell sedimentation rate Urine analysis

Symptomtext

The site was sore, similar to tetanus shots I have received. Within a couple days my flu-like symptoms I had before lessened, but what I experienced was a raging headache like I have never experienced in my life. It felt like the left side of my head was about to split open. I had to remain in bed and was unable to move to do normal activities without feeling like I would either faint, or that my head would explode inside. After about two weeks of this, I could not stand it any more and I finally called my doctor. He was unavailable but I did have a telehealth visit with a nurse practitioner in his office. After some discussion, and my age, and my symptoms (splitting, non-ending headache), she referred me to the ER. They performed a CT scan which was read almost immediately after its completion. No problems were seen on the scan. My headache subsided a day or two after that and I got on with life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: All on April 23: CT head/brain without contrast on Friday, April 23, 6:05 p.m.; URINALYSIS W REFLEX TO CULTURE; ESTIMATED GLOMERULAR FILTRATION RATE; COMPREHENSIVE METABOLIC PANEL; SEDIMENTATION RATE
Aktuelle Erkrankungen: I was dealing with a mild flu at the time, but was tested for COVID the prior week via a rapid nasal swab test and the test was negative. I was dealing with mild flu symptoms.
Vorgeschichte: none
Andere Medikamente: multivitamin, vitamin C, AREDS 2 eye supplement, 82mg aspirin
Allergien: none
Vorherige Impfungen: -

VAERS 2414745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CO
Alter: 62,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Gastric disorder Migraine Pyrexia

Symptomtext

Migraines, stomach issues and fever.

Weitere VAERSDATA-Felder

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

VAERS 2370531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MI
Alter: 97,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 06.04.2021
Beginn: 12.07.2022
Tage bis Beginn: 462,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive Vaginal haemorrhage

Symptomtext

07/12/22 presents to ED for "vaginal bleeding and shortness of breath". PMHx of "anemia, right total knee arthroplsaty, pancytopenia, malignant lymphoma, arthritis, cellulitis, obesity, gait instability, MI, myelodysplastic syndrome, and coronary artery disease"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 07/12/22 SARS-CoV-2 (COVID-19) by detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2359492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 79,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 14.04.2021
Beginn: 21.12.2021
Tage bis Beginn: 251,0
Dosis: 2
Route/Site: IM / -

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

Chills Cough Diarrhoea Dizziness Dyspnoea Hypoxia Inappropriate schedule of product administration Inflammatory marker decreased Ischaemic cerebral infarction Malaise Oxygen saturation decreased Pain Productive cough Pyrexia Vomiting Walking distance test abnormal

Symptomtext

Pfizer Dose 1 3/12/21 (EN6204) Pfizer Dose 2 4/14/21 (EW0153) COVID Positive 1/4/22 1/4/22: Patient is a 80 year old female with past history of CVA, hypertension, hyperlipidemia, and GERD who was admitted with shortness of breath, cough, diarrhea and found to have partial hypoxemia. History is obtained from chart review as well as discussion with the patient and the ED provider. Patient does have a history of CVA and was admitted from September 1st until September 3rd of this year. That time she was found to have a acute right frontal lobe ischemic infarct. Patient states she has no residual deficits from that time. She does take 81 mg of aspirin per day. Patient started feeling ill about 3 weeks ago. She has had worsening shortness of breath as well as sputum production which she described as being pain. Does get more short of breath when she tries to lie flat. She has had some fevers and chills as well as vomiting and diarrhea. Also having dizziness with walking. She has had 2 COVID-19 shots but no booster. Her daughter did test positive for COVID-19 today. Patient did have some desaturations at rest as well as with exertion in the ER and is currently on 2 L. She denies any chest pain or abdominal pain. 1/7/22: past history of CVA, hypertension, hyperlipidemia, and GERD who was admitted with shortness of breath, cough, diarrhea and found to have partial hypoxemia.Patient started feeling ill about 3 weeks ago. She has had worsening shortness of breath as well as sputum production which she described as being pain. Does get more short of breath when she tries to lie flat. She has had some fevers and chills as well as vomiting and diarrhea. Also having dizziness with walking. She has had 2 COVID-19 shots but no booster. She had exposure to her daughter who is COVID positive. she was being managed with IV steroids, IV antibiotics and IV remdesivir on admission. Her symptoms improved decline in inflammatory markers but patient was on 2L oxygenation which seems to be the plateau. She had an oxygen walk test which showed she requires 3L with exertion and no oxygen at rest. Will discharged on covid supportive treatments, PO decadron and PO levofloxacin as well as COVID safe home program.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CVA HTN HLD GERD
Andere Medikamente: aspirin 81 mg PO QD atenolol 25 mg PO QD atorvastatin 80 mg PO QD guaifenesin 1200 mg PO BID pantoprazole 40 mg PO QD
Allergien: lisinopril - cough pneumococcal 23 vaccine - swelling sulfa drugs - unknown
Vorherige Impfungen: -

VAERS 2357360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 04.07.2022
Impfdatum: 14.04.2022
Beginn: 23.04.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / RA

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

Colitis Condition aggravated Swelling

Symptomtext

For the initial vaccination I had head swelling and migraines and for the booster shot, mild head swelling and colitis flare

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Saw neurologist in June (2022) and started steroids for colitis flare shortly after booster shot
Aktuelle Erkrankungen: None at the time but I have colitis and it flared up shortly after the booster.
Vorgeschichte: ICS and colitis
Andere Medikamente: glutathione, Vitamin D, multi vitamin, probiotic and elmiron
Allergien: Canno take advil or motrin, and sensitivity to gluten
Vorherige Impfungen: -

VAERS 2347849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 66,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 24.04.2021
Beginn: 10.01.2022
Tage bis Beginn: 261,0
Dosis: 2
Route/Site: IM / -

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

Angiogram pulmonary abnormal Asthenia Blood test abnormal Bronchiectasis Bronchiolitis C-reactive protein COVID-19 COVID-19 pneumonia Chest X-ray normal Chills Dyspnoea Fibrin D dimer increased Hyponatraemia Hypoxia Inappropriate schedule of product administration Leukopenia Productive cough SARS-CoV-2 test positive

Symptomtext

Pfizer dose 1 3/20/21 (ER2613) Pfizer Dose 2 4/24/21 (EW0153) COVID Positive 1/14/22 1/13/22: A 67-year-old female with a past medical history of COPD not on home oxygen, type 2 DM with neuropathy, hyperlipidemia and history of aorto-femoral bypass surgery comes to ED complaining of cough and shortness of breath. Patient states that since last week she has been feeling weak with cough and shortness of breath. Cough is productive with small amounts of mucoid sputum. The last couple of days she is feeling more short of breath and also feels chills. Two days ago she did give home COVID test and it was reported positive. Patient lives alone, no sick contacts. She states she took 2 doses of COVID-19 vaccine, but not booster. In the ED, temp was 19.9 degree F, pulse ox 94% on room air, vital signs stable. Blood work is significant for mild leukopenia and mild hyponatremia, mild lesion CRP and elevated D-dimer.. Chest x-ray negative for infiltrate. CT angio chest is done and is reported negative for pneumonia or infiltrate, positive for chronic bronchiectasis and bronchiolitis. She was given IV dexamethasone 6 mg, IV ceftriaxone, IV Zithromax and the duo nebs in the ED. patient was placed on nasal cannula oxygen for comfort, no documented hypoxia. COVID-19 PCR pending. 1/16/22: 67-year-old female with a history of COPD admitted for COVID-19 pneumonia and acute hypoxia. Patient was managed with IV remdesivir, dexamethasone, antibiotics in addition to other supportive treatment on re-evaluation today she feels fine with complete resolution of hypoxia. She will be discharged on pre-admission medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD DM type 2 neuropathy HLD h/o aorto-femoral bypass surgery
Andere Medikamente: aspirin 81 mg PO QD atorvastatin 20 mg PO QD bupropion XL 150 mg PO QD calcium carbonate 500 mg PO BI cyclobenzaprine 10 mg PO TID PRN diclofenac 50 mg PO TID vitamin D 50,000 units PO Q3days gabapentin 300 mg PO TID metformin 500 mg PO QD
Allergien: NKA
Vorherige Impfungen: -

VAERS 2344735

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 81,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 14.04.2021
Beginn: 07.03.2022
Tage bis Beginn: 327,0
Dosis: 2
Route/Site: IM / -

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

Anticoagulant therapy Body temperature increased COVID-19 Dyspnoea Dyspnoea exertional Electrocauterisation Endoscopy upper gastrointestinal tract abnormal Fatigue Gait disturbance Gastrointestinal ulcer Haemoglobin decreased Helicobacter test negative Inappropriate schedule of product administration SARS-CoV-2 test positive Transfusion

Symptomtext

Pfizer Dose 1 3/17/21 (EN6205); Pfizer Dose 2 4/14/21 (EW0153); COVID Positive 3/8/22; 3/8/22: 82-year-old lady presented to the emergency room with complaint of generalized fatigue and shortness of breath with activity that started yesterday evening. The patient reports having difficulty ambulating because of increasing shortness of breath. She denies fever. She denies cough. The patient was treated for COVID 10 days ago and stated that after treatment she was feeling just all right with no issues. She denies diarrhea. In the emergency room, she was noted to have a hemoglobin of 6. She denies abdominal discomfort. She stated that she was on dexamethasone, and she continued taking her Plavix as usual. 3/13/22: Patient is an 82-year-old female with a history of coronary artery disease with the hospital with a chief complaint of generalized fatigue and shortness of breath. On initial lab evaluation the patient's hemoglobin was found to be 6.8. Patient was transfused with 2 units of blood. Gastroenterology team was consulted and patient had an upper endoscopy performed which revealed 2 ulcerations which were about 0.5 cm x 2 cm arm and the other one was 1.5 cm 1 cm long. Both of these ulcers were found to be not moving and both were cauterized. H pylori samples were taken. H pylori is negative. Patient's hemoglobin remained stable during her hospitalization. Patient is to be discharged with Protonix 40 mg p.o. b.i.d. Patient was instructed not to take Plavix and dexamethasone. It is okay to take aspirin should follow-up with primary care physician in 1 week. Also the low-grade temp of 100.8? F recorded in the patient's chart but according to the nurses report the patient was wearing a few layers of blanket. Patient was discharged from the hospital in a hemodynamically stable state. Patient will follow-up with PCP in 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CDA; GERD; Depression; OA; Asthma; HTN.
Andere Medikamente: Albuterol; Ascorbic Acid; Aspirin; Cholecalciferol; Citalopram; Copidogrel; Cyanocobalamin Donepezil; Breo Ellipta; Furosemide; Gabapentin; Isosorbide Mononitrate ER; Lorazepam; Metoprolol Tartrate; KCl; Rabeprazole; Ranolazine; Rosuvastat
Allergien: Codeine - Gastritis
Vorherige Impfungen: -

VAERS 2331645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 85,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 16.04.2021
Beginn: 16.05.2022
Tage bis Beginn: 395,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 Dyspnoea Mental status changes

Symptomtext

Hospitalization for altered mental status, shortness of breath that led to COVID-19 diagnosis on dates 5/16/2022-6/10/2022. Treated with Duoneb inhaler, vitamin C 1000mg daily, Vitamin D3 25mcg daily, dexmethasone 6mg IV daily, zinc sulfate 50mg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 26,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: amlodipine, lisinopril, metoprolol
Vorherige Impfungen: -

VAERS 2327304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 67,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 23.04.2021
Beginn: 02.01.2022
Tage bis Beginn: 254,0
Dosis: 2
Route/Site: IM / -

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

Arthralgia Back pain Blood culture negative Blood gases COVID-19 Chest X-ray abnormal Computerised tomogram head normal Computerised tomogram spine Confusional state Electrocardiogram normal Exercise lack of Fall Full blood count Head injury Inappropriate schedule of product administration Inflammatory marker test Joint injury Magnetic resonance imaging head normal

Symptomtext

Pfizer Dose 1 4/1/21 (EN6198) Pfizer Dose 2 4/23/21 (EW0153) COVID Positive 1/2/22 1/2/22: Patient is a pleasant 67-year-old male with past medical history of intellectual/cognitive impairment comes in with chief complaint of mechanical fall. Patient is not very good historian history is primarily obtained from chart review. Patient with cognitive impairment at baseline reportedly EMS was called as patient had ground level fall ambulating to restroom, patient fell forward on his knees no loss of consciousness. Patient endorse bilateral knee and hip pain in low back pain, ordered lead did strike his head. His caretakers sister-in-law who lives with him reports frequent falls at baseline usually able to assist back to chair or sitting position however after this current fall patient was unable to follow directions and was confuse not understanding what was being asked of him which is a new finding. Patient usually stays at home and only leaves the house for essential visits. Was going to therapy at home could ambulate and of block. Stationary bike otherwise sedentary. In the emergency department blood work and imaging were obtained. Chem panel, blood gases, tox screening, hemogram, UA without acute derangement. In addition CT head, C-spine repeating negative for acute derangement. plain film imaging of femur pelvis on lumbar spine without acute derangement. EKG reportedly negative. Chest x-ray concerning for possible pneumonia. Patient received Rocephin emergency department request was made to admit to medical service for further treatment evaluation. At bedside patient is lying comfortably in bed denies any lightheadedness, dizziness, vision change, chills, fever, nausea, vomiting, diarrhea, chest pain, palpitations, abdominal pain, paresthesia, swelling of extremities, pain or discomfort of joint her extremities. Reports compliance with all medications provided on home unclear on recent change. Unclear on sick contact, unclear on COVID-19 vaccination status. Denies tobacco, alcohol, marijuana/recreational drug use. Attempted to obtain family history a however patient is unable to provide further insite. 1/5/22: Mechanical fall History of recurrent falls Community-acquired pneumonia COVID-19 positive - imaging studies as noted. MRI negative, for CVA. Further imaging no acute deformity or derangement.Therapy home health as outpatient. falls may be mechanical versus infectious etiology from COVID. - as per chest x-ray, no leukocytosis no respiratory distress, low-grade temps. Empirically treat with Rocephin/doxycycline Blood cultures remain negative for 48 hours. Vitamin-C, D, zinc Doxycycline. these can be continued on dispo for course.. Inflammatory markers reviewed currently does not qualify for remdesivir, dexamethasone. - patient did not require oxygen during hospitalization. However patient did have falls at home and mental status changed from baseline according to family. Family strongly requested O2 walk prior to discharge for this purpose. I felt because of this it wasn't unreasonable to get an O2 walk prior to disposition even if patient was not requiring supplemental oxygen-- O2 walk orders placed. Respiratory therapy provider called me and refused to do oxygen for home going walk even after multiple verbal request were made, along with formal order in Cerner-- order was discontinued unilaterally without physician consent even after unique circumstances were conveyed. In addition RT provider stated that she would convey to nursing to do oxygen walk if needed, however I spoke to patient's floor nurse who notified me that this was never done and no O2 walk for home going was done as stipulated in discharge orders prior to patient leaving facility. Rule out CVA- - MRI is negative, suspect mechanical/metabolic/ infectious related. Cognitive impairment - baseline. Family member/ sister-in-law primary caregiver. All ED And RTC precautions were provided to patient, in writing patient endorse understanding. Further precautions provided to patient's family along with quarantined

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: intellectual impairment obesity spleen enlargement
Andere Medikamente: APAP 650 mg PO Q4h PRN albuterol 2 puffs Q6h PRN sertraline 100 mg PO BID
Allergien: latex- unknown laundry soap - unknown
Vorherige Impfungen: -

VAERS 2321935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 59,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 07.04.2021
Beginn: 15.06.2022
Tage bis Beginn: 434,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 pneumonia Tachypnoea

Symptomtext

admitted for COVID-19 pneumonia.the patient is requiring 2 L of oxygen via nasal cannula, and is tachypneic with respiratory rate above 30, patient will benefit from remdesivir

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2317406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 57,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 07.04.2021
Beginn: 10.06.2022
Tage bis Beginn: 429,0
Dosis: 2
Route/Site: IM / -

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

Dyspnoea Laboratory test abnormal Pain in extremity

Symptomtext

presents with symptoms of shortness of breath and bilateral leg pain. Sx onset: 6/10/22. Positive Test: 6/11/22.

Weitere VAERSDATA-Felder

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

VAERS 2296357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 07.04.2021
Beginn: 07.04.2022
Tage bis Beginn: 365,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Arthritis Grip strength decreased Impaired driving ability Injected limb mobility decreased Injection site pain Limb discomfort Loss of personal independence in daily activities

Symptomtext

I received my first Pfizer vaccine when they were first available to the public (April 7,2021). My shoulder was in pain soreness at the injection site. I got the shot in my nondominated arm because I knew it was going to be some discomfort. On April 28 I went to get the second dose and I asked the nurse was it weird that my arm was still in sooo much pain 3 weeks later. The nurses didn't think that there was any correlation to the pain in that arm, so I received the second dose in left arm as well. The pain was nonstop and in July I noticed that the weird arm discomfort hadn't resolved. And I had a hard time doing daily activities driving's. Picking things up or even opening doors. I really find it strange because I am young to have issues with range of motion and baring weight. I have let this go on for a while because I thought that over time it would just go away but it hasn't. In December my arm was showing some improvement I was able to move my arm parallel to my shoulder like above my head without pain. My arm was better with the range of motion. I met with my PCP (April 12,2022) and she refereed me to an Ortho doctor. I saw the Ortho doctor on May 2,2022, he referred me to physical therapy which starts on Tue May 31,2022. I was also given a shot of cortisone. Rotator cuff and bursa was in flamed and mad as my Orto doctor described which is why I was limited with range of motion and having so much discomfort.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Mirena Birth control
Allergien: None that I know of
Vorherige Impfungen: -

VAERS 2286954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 71,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 11.04.2021
Beginn: 07.12.2021
Tage bis Beginn: 240,0
Dosis: 2
Route/Site: IM / -

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

Angiogram pulmonary abnormal Blood lactic acid COVID-19 Cancer in remission Chills Chronic granulomatous disease Computerised tomogram abdomen abnormal Cough Diarrhoea Dyspnoea Enteritis Fibrin D dimer Hypoxia Intestinal dilatation Lung infiltration Nausea Pyrexia SARS-CoV-2 test positive

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 3/21/21 (ER8730) Pfizer Dose 2 4/11/21 (EW0153) COVID Positive 12/10/21 12/10/21: This is a 71-year-old male with history of tobacco use and prostate cancer status post radiation in remission who presented with shortness of breath and cough. Patient reports that his symptoms started 3 days ago. He has been having fever, chills, shortness of breath, cough, nausea, vomiting and diarrhea. He is vaccinated against COVID-19 and had 2 shots. He denies chest pain or dizziness. He has history of prostate cancer and underwent radiation therapy in the past and follows at the University of Iowa and was told that he is currently in remission. In the emergency department, patient was found to be hypoxic and was put on 2 L of O2 via nasal cannula. Labs showed a lactic acid of 2.1, D-dimer of 1.15. Patient had a positive rapid COVID-19 antigen test. CT abdomen and pelvis with IV contrast showed mild small bowel dilatation suggesting enteritis. CT angiography of the chest was negative for pulmonary embolism but it showed bilateral patchy infiltrates and chronic granulomatous disease. Patient received nebulizer treatments and a dose of IV azithromycin, Rocephin and Solu-Medrol. 12/14/21: Albuterol HFA q.6 hours P.o. azithromycin course P.o. Decadron course P.o. vitamin-C, vitamin-D and zinc sulfate Patient requires 1 L of O2 with activity Hemodynamically stable for discharge Will discharge home Follow-up with PCP in 3-5 days Patient agrees with plan of care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: tobacco use prostate CA s/p radiation
Vorgeschichte: tobacco use prostate CA s/p radiation
Andere Medikamente: acetaminophen-hydrocodone 325-5 mg PO Q4h PRN tamsulosin 0.4 mg PO QD
Allergien: NKA
Vorherige Impfungen: -

VAERS 2286948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 79,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 14.04.2021
Beginn: 28.11.2021
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Bundle branch block left COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Decreased appetite Dyspnoea Dyspnoea exertional Electrocardiogram abnormal Epigastric discomfort Fatigue Hypophagia Hypoxia Inappropriate schedule of product administration Lung opacity Nausea Pneumonia

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 3/19/21 (EN6208) Pfizer Dose 2 4/14/21 (EW0153) COVID Positive 11/28/21 Discharged home 11/30/31 Hospitalized 11/28/21-11/30/21 12/8/21: The patient vaccinated for COVID-19, diagnosed with COVID-19 pneumonitis on November 28 and she was admitted to the hospital and observed and discharged home, for the last 3 days she had progressive shortness of breath with sputum productive cough and episodes of chills with epigastric discomfort and nausea and occasional vomiting and unable to tolerate p.o. intake last 24 hours with generalized weakness and fatigue, she does have dyspnea with minimal exertion while she is walking within her room and her home. She is known to be asthmatic and was using her inhalers at home 2-3 times within 24 hours within the last 3 days without resolution in her cough and shortness of breath. No wheezing noted test. At baseline she does not use any oxygen. At emergency she was hypoxic and require 3 L of oxygen to maintain SpO2 above 94%, her EKG show sinus rhythm with old left bundle branch block, troponin unremarkable, proBNP mildly elevated. Chest x-ray reviewed personally and show vascular congestion and linear opacities. At emergency she received Zofran and IV fluid. 12/10/21: She is a 79-year-old female recently admitted to hospital for severe COVID-19 infection complicated with pneumonia and hypoxia was discharged on 3 L of oxygen but came back to the emergency room on 12/08/2021 because of persistent SOB, nausea and poor appetite. She was admitted and commenced on usual management for COVID-19 infection including restarting remdesivir, dexamethasone, IV antibiotics in addition to other supportive management. On re-evaluation this morning she feels much better except for mild nausea. She has a good appetite. Her Sao2 on room air is 100%. She will be discharged home on pre-admission medications. She will follow-up with the PCP in 1-2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: HLD asthma GERD obesity depression anemia
Vorgeschichte: HLD asthma GERD obesity depression anemia
Andere Medikamente: albuterol 2 puffs Q4h PRN atorvastatin 40 mg PO HS Symbicort 2 puffs inh BID calcium-vitamin D PO QD cranberry 250 mL PO QD dicyclomine 10 mg PO TID PRN fluoxetine 40 mg PO QD fluticasone nasal spray both nares QD lansoprazole 30 mg PO QD m
Allergien: anabolic steroids - itching contrast dye - unknown detrol - unknown nitrofurantoin - unknown sulfadiazine - unknown vancomycin - unknown
Vorherige Impfungen: -

VAERS 2260126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 73,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 14.04.2021
Beginn: 04.11.2021
Tage bis Beginn: 204,0
Dosis: 2
Route/Site: IM / -

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

Abdominal pain Acute kidney injury Asthenia Blood creatinine increased Blood culture negative Bradycardia C-reactive protein normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Diarrhoea Dyspnoea Dysstasia Fall Fatigue Head injury Hyperkalaemia Hypotension

Symptomtext

COVID vaccine breakthrough case Pfizer Dose 1 3/17/21 (EN6208) Pfizer Dose 2 4/14/21 (EW0153) COVID Positive 11/9/21 11/9/21: 73-year-old woman who presented with complaints of generalized weakness and diarrhea. She reports insidious onset of symptoms approximately 4-5 days ago with daily diarrhea, having 10-10 anti lose watery bowel motions daily. She reports associated nausea and abdominal cramping, denies vomiting, fever or chills. She denies any similar symptoms in household contacts, denies dietary indiscretions or recent travel. She reports antibiotic use within the last 30-90 days. She presented to the emergency department where laboratories remarkable for acute kidney injury, Hyperkalemia and lactic acidosis. She has not had any further watery bowel motions since presentation to the emergency department. She has been admitted to hospitalist services for further treatment and evaluation. 11/16/21: A 73-year-old woman with a history of chronic hypoxic respiratory failure on 3 L of home oxygen, chronic kidney disease, hypertension, hypothyroidism, type 2 diabetes mellitus, presented complaints of generalized weakness and diarrhea. In the emergency room, patient was noted to have volume depletion with acute kidney injury and lactic acidosis and hyperkalemia which was corrected. She was done IV fluids for hydration. COVID-19 screen returned positive. Chest x-ray done on presentation revealed diffuse airspace disease. Patient was managed with IV dexamethasone, IV antibiotic therapy with ceftriaxone and azithromycin. Pulmonary was consulted to assist with management. She was started on Actemra and remdesivir. She had worsening oxygen requirement, requiring up to 8 L of oxygen. She had bradycardia rate remdesivir and this was discontinued. Patient had resolution of diarrhea, resolution of lactic acidosis and improvement in acute kidney injury back to her baseline. She has improved, has been weaned to 3 L of oxygen. Patient assessed by Physical therapy with recommendations for skilled nursing facility. Patient is being discharged to a skilled nursing facility. 11/26/21: A 73-year-old lady presented to the emergency room with complaint of generalized fatigue. The patient reports that she was just discharged from Hospital yesterday. Before yesterday on November 24. On arriving home, she had a fall hitting her head. Today, she is experiencing weakness and has been unable to stand by herself since discharged from the hospital, and had had about 4 recent falls. The patient denies shortness of breath. She normally uses 2 L of oxygen at baseline. She was treated for COVID-19 pneumonia and discharged 10 days ago after completing a course of remdesivir, steroid, dexamethasone, as well as empiric antibiotic therapy. She currently denied any chest pain. 11/30/21: Creatinine improved from 2.06 to 1.3, within baseline. UA is unremarkable. Blood cultures negative. COVID-19 positive. CRP was 0.3. Portable chest x-ray was reviewed. A 73-year-old lady presented to the emergency room with history of generalized fatigue, shortness of breath. After thorough review, the patient was noted to be hypotensive, bradycardic, likely related to metoprolol. The patient also was noted to have an AKI. The patient was hydrated. Metoprolol was eventually discontinued as she also had a baseline of left bundle branch block. The patient's condition has improved. Her blood pressure has remained steady. The patient, however, is deconditioned and will be discharged to skilled nursing facility for further conditioning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: HTN CHF COPD emphysema DM type 2 hypothyroidism chronic renal insufficiency depression HTN urinary incontinence
Vorgeschichte: HTN CHF COPD emphysema DM type 2 hypothyroidism chronic renal insufficiency depression HTN urinary incontinence
Andere Medikamente: aspirin 81 mg PO QD azelastine 1 spray BID Symbicort 2 puffs BID calcium-vitamin D 600-200 unit sPO BID escitalopram 20 mg PO QD fluticasone nasal spray QD PRN furosemide 20 mg PO QD gabapentin 100 mg PO TID insulin degludec 36 units SQ QD
Allergien: atorvastatin - itching, flush niacin - flush pregabalin - upset stomach
Vorherige Impfungen: -

VAERS 1354433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 20.04.2021
Beginn: 30.04.2022
Tage bis Beginn: 375,0
Dosis: 2
Route/Site: IM / LA

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

Achenbach syndrome Laboratory test Burning sensation Mobility decreased Pain Pain in extremity Paraesthesia COVID-19 Chills Exposure to SARS-CoV-2 Malaise SARS-CoV-2 test positive Peripheral swelling

Symptomtext

Late afternoon April 30th 2022, I had chills, general unwell feeling. My husband had been on the phone with his breakthrough COVID-19 case so I wasn't too concerned. The chills would come and go away, it wasn't horrible so I treated with Tylenol. The next day I tested positive and had 99.8 temperature. I took Tylenol and Benadryl and extra vitamins. Symptoms persist today and are mild to moderate. I feel a little better than yesterday. Oxygen is 98, 99.6 temp so I'm not feeling too bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: At home COVID-19 test, positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroid; Hashimoto's
Andere Medikamente: Multivitamin; Vitamin D; Magnesium; Krill Oil; COQ10
Allergien: No; Gluten Sensitive
Vorherige Impfungen: -

VAERS 1354433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 20.04.2021
Beginn: 30.04.2022
Tage bis Beginn: 375,0
Dosis: 2
Route/Site: SYR / LA

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

Achenbach syndrome Laboratory test Burning sensation Mobility decreased Pain Pain in extremity Paraesthesia COVID-19 Chills Exposure to SARS-CoV-2 Malaise SARS-CoV-2 test positive Peripheral swelling

Symptomtext

Late afternoon April 30th 2022, I had chills, general unwell feeling. My husband had been on the phone with his breakthrough COVID-19 case so I wasn't too concerned. The chills would come and go away, it wasn't horrible so I treated with Tylenol. The next day I tested positive and had 99.8 temperature. I took Tylenol and Benadryl and extra vitamins. Symptoms persist today and are mild to moderate. I feel a little better than yesterday. Oxygen is 98, 99.6 temp so I'm not feeling too bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: At home COVID-19 test, positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroid; Hashimoto's
Andere Medikamente: Multivitamin; Vitamin D; Magnesium; Krill Oil; COQ10
Allergien: No; Gluten Sensitive
Vorherige Impfungen: -

VAERS 2253275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 21.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Fatigue Hypersensitivity Lip swelling Pain Paraesthesia Skin swelling Swelling face Swollen tongue

Symptomtext

I had a severe allergic reaction. The next morning, I woke up and my tongue, lips and the rest of my face was swollen and puffy. I also had tingling in my left hand and arm. I received the vaccine in my left arm, so I wonder if it's correlated. I went to my doctor and was advised to take Benadryl and Zyrtec for 3 days. Periodically, I still have tingling from my face, arms and hands. My left side has been most effected. And I feel fatigued and achy during these times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: My Dr's: (Privacy); Neurologist
Aktuelle Erkrankungen: None
Vorgeschichte: Defibrillator-from past Cardiac Arrest; Celiac Disease
Andere Medikamente: None
Allergien: Latex; Morphine
Vorherige Impfungen: -

VAERS 2252315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 21.04.2021
Beginn: 23.09.2021
Tage bis Beginn: 155,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Joint effusion Joint lock Magnetic resonance imaging joint Magnetic resonance imaging normal Mobility decreased Pain Walking aid user X-ray normal

Symptomtext

Note, I do not believe this is related to my receipt of Covid-19 vaccine, but am reporting in case there is any possibility it could have been an adverse event (5 months after vaccination.) My left knee locked in a bent position, after sitting on the ground with legs under/to the side of me. I was unable to straighten left leg without pain for 5 days. I used crutches during that time. I iced the knee and used ibuprofen in case the cause was inflammation. Urgent care visit X-ray was normal (i.e., no torn patella or other physical issue.) MRI a week later was also normal (only slight effusion.) I have had a finger in my left hand (middle finger) also lock in a bent position on occasion, but all other instances of locked/bent joints have resolved in under 10 minutes before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 9/24/21, X-ray at Priority Urgent care, normal 9/30/21, MRI at, also normal (slight effusion noted.)
Aktuelle Erkrankungen: None
Vorgeschichte: Higher than desired cholesterol; not currently on prescription meds
Andere Medikamente: Calcium 600 mg +D Fish oil 1000 mg Mature multivitamin Aspirin, 81 mg/day Vitamin C, 1500 mg/day Vitamin D, 5000 , 3x per week Super B complex 3x per week B-12, methyl form, 4 x per week Zinc 50 mg, 3 per week Glucomannan, about 2 g per day
Allergien: None known
Vorherige Impfungen: -

VAERS 2246045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MA
Alter: 36,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 13.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: SYR / AR

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

Condition aggravated Uveitis

Symptomtext

Uveitis flare up

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic uveitis, rosacea
Andere Medikamente: None
Allergien: Monistat, diflucan
Vorherige Impfungen: -

VAERS 2238801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: WA
Alter: 52,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 10.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Back pain Blood test COVID-19 Chest pain Hepatic enzyme increased Pain Pancreatic enzymes increased Panic attack SARS-CoV-2 test positive

Symptomtext

I had a pain in my back and right shoulder, I went to the doctor and testing was done. The results showed high levels of liver enzymes. I had chest pain and what felt like a panic attack. I had a follow-up and the results showed I had high levels of pancreas enzymes. I did a home test and I tested positive for COVID, I only had symptoms of body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood panel
Aktuelle Erkrankungen: None
Vorgeschichte: MTHFR Gene Mutation
Andere Medikamente: Fish Oil, Vitamin D, Mushroom Supplement, Ashwagandha, Vitamin C
Allergien: Quinoa
Vorherige Impfungen: -

VAERS 2238696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 22.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / -

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

Fatigue Migraine Somnolence

Symptomtext

Extreme exhaustion, hard time staying awake. As well as I had migraines for the next few days after that. It took a while for it to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Lupus; Rheumatoid Arthritis
Andere Medikamente: Methotrexate; Embrel
Allergien: Gluten; Straight Penicillin
Vorherige Impfungen: MMR vaccine.

VAERS 2225443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: VA
Alter: 67,0
Geschlecht: F
Eingang: 10.04.2022
Impfdatum: 01.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: IM / LA

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

Atypical pneumonia Blood potassium abnormal Cluster headache Cough Dyspnoea Ear, nose and throat examination abnormal Exercise tolerance decreased Fatigue Magnetic resonance imaging normal Malaise Migraine Scan with contrast Thyroid disorder Vomiting X-ray

Symptomtext

Daily migraines that caused vomiting. Fatigue and shortness of breath. I was going to the gym to lift weights 2 times a week and going for 2-3 miles walks with my husband every week also. the shots took that away! I also developed a cough that my GP sent me to an ENT doctor, and he said that I had cluster migraines and did not address the cough. At times the cough the cough was so bad that I thought I would die. This went on and I was sent to a Nuru and had MRI done and it was clear, I have had 4 different migraine medicines. Also developed walking phenonium and took 2 rounds of antibiotics and steroids. I still suffer from migraines and a cough. Still have shortness of breath. I wish to get my health back and exercise again with my husband. I owned a fitness club and enjoyed good health before trusting in these shots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atypical pneumonia
Hospital-Tage: -
Labordaten: MRI MRI with contrast X-rays X-rays again off the scale potassium levels off the scale thyroid levels
Aktuelle Erkrankungen: low thyroid, hasimoto
Vorgeschichte: fibromyalgia from Lyme disease
Andere Medikamente: thyroid meds Xanax
Allergien: -
Vorherige Impfungen: -

VAERS 1322990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 36,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 17.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Ear inflammation Feeding disorder Gait inability Gastritis Computerised tomogram head normal Computerised tomogram thorax normal Diarrhoea Dizziness Ear discomfort Ear swelling Fatigue Injection site pain Nasal congestion Palpitations Impaired work ability Vertigo Weight

Symptomtext

could not work for 8 months; Severe vertigo; Sever stomach inflammation; Sever inner ear inflammation nerve system; heart palpitations; lost 25 lbs in two weeks couldn't eat or walk; lost 25 lbs in two weeks couldn't eat or walk; suffer severe anxiety; lost 25 lbs in two weeks couldn't eat or walk; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 17Apr2021 11:00 (Batch/Lot number: unknown) at the age of 36 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: IMPAIRED WORK ABILITY (hospitalization, disability) with onset 17Apr2021 11:00, outcome "not recovered", described as "could not work for 8 months"; VERTIGO (hospitalization, disability) with onset 17Apr2021 11:00, outcome "not recovered", described as "Severe vertigo"; GASTRITIS (hospitalization, disability) with onset 17Apr2021 11:00, outcome "not recovered", described as "Sever stomach inflammation"; EAR INFLAMMATION (hospitalization, disability) with onset 17Apr2021 11:00, outcome "not recovered", described as "Sever inner ear inflammation nerve system"; PALPITATIONS (hospitalization, disability) with onset 17Apr2021 11:00, outcome "not recovered", described as "heart palpitations"; WEIGHT DECREASED (hospitalization, disability), FEEDING DISORDER (hospitalization, disability), GAIT INABILITY (hospitalization, disability) all with onset 17Apr2021 11:00, outcome "not recovered" and all described as "lost 25 lbs in two weeks couldn't eat or walk"; ANXIETY (hospitalization, disability) with onset 17Apr2021 11:00, outcome "not recovered", described as "suffer severe anxiety". The patient was hospitalized for impaired work ability, vertigo, gastritis, ear inflammation, palpitations, weight decreased, feeding disorder, anxiety, gait inability (hospitalization duration: 7 day(s)). The events "could not work for 8 months", "severe vertigo", "sever stomach inflammation", "sever inner ear inflammation nerve system", "heart palpitations", "lost 25 lbs in two weeks couldn't eat or walk", "lost 25 lbs in two weeks couldn't eat or walk", "suffer severe anxiety" and "lost 25 lbs in two weeks couldn't eat or walk" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: weight: lost 25 lbs, notes: lost 25 lbs in two weeks. It was unknown if therapeutic measures were taken as a result of impaired work ability, vertigo, gastritis, ear inflammation, palpitations, weight decreased, feeding disorder, anxiety, gait inability. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient had not received any other vaccine within 4 weeks prior to the COVID-19 vaccine. Severe vertigo, Severe stomach inflammation, Severe inner ear inflammation nerve system, heart palpitations,7 times in the hospital, lost 25 lbs in two weeks couldn't eat or walk, could not work for 8 months. Still suffering. Seeming all types of doctors and still seeing doctors. Body not the same, suffer severe anxiety. The lot number for bnt162b2 was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 7,0
Labordaten: Test Name: Body weight; Result Unstructured Data: Test Result:lost 25 lbs; Comments: lost 25 lbs in two weeks
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: AR
Alter: 47,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 14.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: - / LA

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

Acoustic stimulation tests Allergy test Antinuclear antibody Arthritis Blood glucose Arthralgia Diarrhoea Dizziness Dyspepsia Ear pain Blood test Computerised tomogram Electronystagmogram Headache Inflammatory marker test Laboratory test Flushing Hypoaesthesia

Symptomtext

Dizziness/vertigo, palpitations, head pain, tinnitus, ear pain, diarrhea, heartburn, sudden weight loss, knee joint inflammation, blurry vision, vision change, eye floaters

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Lab tests for anemia, glucose, etc, blood pressure, heart rate, VNG for vestibular, BPPV and Physical Therapy for vestibular, hearing, CT scan, eye exam and vision test for Neuro Optometric Rehab, allergy skin testing, inflammation lab tests, ANA for autoimmune, lab tests for Vitamin D and B12
Aktuelle Erkrankungen: -
Vorgeschichte: Atypical Ductal Hyperplasia- benign
Andere Medikamente: Tamoxifen, Zyrtec
Allergien: -
Vorherige Impfungen: -

VAERS 2179434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: AR
Alter: 47,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 14.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: SYR / LA

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

Acoustic stimulation tests Allergy test Antinuclear antibody Arthritis Blood glucose Arthralgia Diarrhoea Dizziness Dyspepsia Ear pain Blood test Computerised tomogram Electronystagmogram Headache Inflammatory marker test Laboratory test Flushing Hypoaesthesia

Symptomtext

Dizziness/vertigo, palpitations, head pain, tinnitus, ear pain, diarrhea, heartburn, sudden weight loss, knee joint inflammation, blurry vision, vision change, eye floaters

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Lab tests for anemia, glucose, etc, blood pressure, heart rate, VNG for vestibular, BPPV and Physical Therapy for vestibular, hearing, CT scan, eye exam and vision test for Neuro Optometric Rehab, allergy skin testing, inflammation lab tests, ANA for autoimmune, lab tests for Vitamin D and B12
Aktuelle Erkrankungen: -
Vorgeschichte: Atypical Ductal Hyperplasia- benign
Andere Medikamente: Tamoxifen, Zyrtec
Allergien: -
Vorherige Impfungen: -

VAERS 2218412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: VA
Alter: 64,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 09.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / AR

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

Atrial tachycardia Cardiac monitoring abnormal Cardiac stress test abnormal Echocardiogram abnormal Heart rate irregular

Symptomtext

Ten days after the vaccine, I was in my yard working, I started feeling my heart beating irregularly. I am a nurse, I listened to my heart with a stethoscope and I could hear it. I waited to Monday to see my PCP. By then it was back to normal. This lasted about 3 days. I went to a cardiologist and wore a heart monitor, stress test, echocardiogram. It came back with atrial tachycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial tachycardia
Hospital-Tage: -
Labordaten: Heart monitor, stress test, Echocardiogram
Aktuelle Erkrankungen: -
Vorgeschichte: Allergies, Bicuspid Aortic valve disease
Andere Medikamente: None
Allergien: Avelox, Lamisil, Flagyl, Fosamax
Vorherige Impfungen: -

VAERS 2213652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 12.04.2021
Beginn: 27.12.2021
Tage bis Beginn: 259,0
Dosis: 2
Route/Site: IM / LA

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

Bronchitis COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received two doses COVID 19 Vaccine in Apr/May 21. The patient tested positive for COVID 19 on 27 Dec 21 and was admitted to the hospital with chest pain and COVID bronchitis. The patient was treated with dexamethasone, nitroglycerin, and scheduled for nuclear stress test. The patient was discharged on 28 Dec 21.

Weitere VAERSDATA-Felder

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

VAERS 2204304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: OH
Alter: 16,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 16.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Acoustic stimulation tests normal Arthritis Condition aggravated Ear infection Temporomandibular joint syndrome Tinnitus

Symptomtext

Symptoms began day after vaccination. Because of TMD condition, susceptible to tinnitus. Symptoms have not subsided 1 year later and are bilateral.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 5/25/2021 ? Hearing found normal
Aktuelle Erkrankungen: None
Vorgeschichte: Temporomandibular Joint Dysfunction?Anterior Disc Displacement (left and right). No ringing in ears until after vaccination. Has not subsided. Received severe ear infection and inflammation in the TMD disc 1 week after vaccination.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2194893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 53,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 06.04.2021
Beginn: 21.03.2022
Tage bis Beginn: 349,0
Dosis: 1
Route/Site: IM / LA

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

Anaemia Blood iron increased Condition aggravated Hypothyroidism Mean cell volume increased Red blood cell count decreased

Symptomtext

Comprehensive metabolic panel performed with low RBC, high mean RBC and high Iron levels. Indications of anemia and increased symptoms of Hypothyroidism despite treatment with levothyroxine 150mcg 6 days/week

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: RBC Count 3.91 million/uL Mean RBC volume 105.9 fL Mean RBC Iron 35.5pg Tested 3/18/22
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Tirosint, Xtend Life CX-80, Xtend Life Omega 3, Ikaria Beauty Collagen
Allergien: None
Vorherige Impfungen: -

VAERS 2194103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

moderat

Staat: IA
Alter: -
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 09.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Paraesthesia

Symptomtext

[Pfizer Biontech Covid 19 Vaccine] use for COVID-19 under Emergency Use Authorization (EUA):Pfizer Blontech ] use for COVID-19 under Emergency Use Authorization The patient experienced tingling sensations all after receiving his second dose.

Weitere VAERSDATA-Felder

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

VAERS 1289721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: PA
Alter: -
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 14.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Anaesthesia Asthenia Blood pressure measurement Body temperature Cardiovascular evaluation Cough Ear, nose and throat examination Generalised anxiety disorder Heart rate Hypoaesthesia Pain Paraesthesia Insomnia Investigation Major depression Neck pain Neurological examination Ophthalmological examination

Symptomtext

she just felt little sore; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP) from medical information team. The reporter is the patient. A female patient received bnt162b2 (BNT162B2), administration date 14Apr2021 11:10 (Batch/Lot number: unknown) as dose number unknown, single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN (non-serious), outcome "unknown", described as "she just felt little sore". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1289721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

moderat

Staat: PA
Alter: -
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 14.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Anaesthesia Asthenia Blood pressure measurement Body temperature Cardiovascular evaluation Cough Ear, nose and throat examination Generalised anxiety disorder Heart rate Hypoaesthesia Pain Paraesthesia Insomnia Investigation Major depression Neck pain Neurological examination Ophthalmological examination

Symptomtext

she just felt little sore; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP) from medical information team. The reporter is the patient. A female patient received bnt162b2 (BNT162B2), administration date 14Apr2021 11:10 (Batch/Lot number: unknown) as dose number unknown, single for covid-19 immunization. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN (non-serious), outcome "unknown", described as "she just felt little sore". No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1243953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 16.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Antinuclear antibody Arthralgia Axillary pain Back pain Blood creatine phosphokinase Blood thyroid stimulating hormone Blood thyroid stimulating hormone increased Computerised tomogram Fibromyalgia Full blood count Burning sensation Condition aggravated Pain Gait disturbance Glycosylated haemoglobin increased Inflammation Inflammation scan Investigation

Symptomtext

TSH, a test for thyroid function, which was 9.7 ulU/mL; inflammation; Fibromyalgia; The pain was in her armpits, shoulder, back, hips and ankles/ calves; The pain was in her armpits, shoulder, back, hips and ankles/ calves; The pain was in her armpits, shoulder, back, hips and ankles/ calves; She could hardly walk; Joint and muscle pain/ The pain was in her armpits, shoulder, back, hips and ankles/ calves; Joint and muscle pain; Pain in her cheeks; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) . A 57 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Apr2021 (Lot number: EW0153) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Fibromyalgia", start date: 09Dec2014, stop date: Feb2015, notes: Pertinent Details: Triggered by contrast dye injected prior to CT scan. Family history included: "lung cancer" (unspecified if ongoing), notes: father died of lung cancer at age 70; "pneumonia" (unspecified if ongoing), notes: mother died of pneumonia at age 78. Concomitant medication(s) included: MIRTAZAPINE taken for fibromyalgia, start date: Feb2015 (ongoing). The following information was reported: ARTHRALGIA (non-serious) with onset 18Apr2021, outcome "not recovered", described as "Joint and muscle pain/ The pain was in her armpits, shoulder, back, hips and ankles/ calves"; MYALGIA (non-serious) with onset 18Apr2021, outcome "not recovered", described as "Joint and muscle pain"; PAIN (non-serious) with onset 17Apr2021 17:00, outcome "not recovered", described as "Pain in her cheeks"; FIBROMYALGIA (non-serious) with onset 18Apr2021 08:00, outcome "not recovered", described as "Fibromyalgia"; AXILLARY PAIN (non-serious), BACK PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 18Apr2021, outcome "not recovered" and all described as "The pain was in her armpits, shoulder, back, hips and ankles/ calves"; GAIT DISTURBANCE (non-serious) with onset 18Apr2021, outcome "not recovered", described as "She could hardly walk"; BLOOD THYROID STIMULATING HORMONE INCREASED (non-serious) with onset 22Oct2021, outcome "recovered", described as "TSH, a test for thyroid function, which was 9.7 ulU/mL"; INFLAMMATION (non-serious) with onset May2021, outcome "unknown", described as "inflammation". The events "joint and muscle pain/ the pain was in her armpits, shoulder, back, hips and ankles/ calves", "joint and muscle pain", "fibromyalgia" and "the pain was in her armpits, shoulder, back, hips and ankles/ calves" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of arthralgia, myalgia, fibromyalgia, pain in extremity, gait disturbance, blood thyroid stimulating hormone increased. Therapeutic measures were not taken as a result of pain. Additional information: It was reported that prior to receiving the Pfizer vaccine the morning of 16Apr2021, patient was in good health, and her fibromyalgia, which was triggered in Dec2014 by contrast dye injected for a CT scan, had been under control since 2015 with 30 mg of Mirtizapine. Approximately 17:00 on 17Apr2021, she began feeling pain in her cheeks. By the next morning, the same pain that she felt in the early days of fibromyalgia returned. Two days later she began feeling joint and muscle pain, and nearly 7 months later it has not gone away. She has been to 4 doctors and taken several medications to no avail. The pain was in her armpits, shoulders, back, hips and ankles/calves. She was in so much pain that she could hardly walk or do any strenuous activities. Following discussions with her doctor, 75 mg of Lyrica was added to her medication, and the Mirtazapine was increased to 45 mg. However, there was not much improvement. In late May, patient first saw Doctor, a rheumatologist. He ordered many of the same tests as (withheld) primary care physician, Dr. The test results were normal except for sedimentation rate, a test for inflammation, which was 61 mm/hr, and TSH, a test for thyroid function, which was 9.7 ulU/mL. Dr. prescribed 25 mcg of levothyroxine, and Dr. prescribed 15 mg of prednisone to be tapered down to 5 mg over three weeks. She has further reduced her prednisone dose to 2.5 mg and maintained it over the past four months, and she stopped taking Lyrica. The prednisone had some benefit in terms of pain reduction, and the levothyroxine has brought (withheld) TSH level within the normal range. Subsequent sedimentation rate results have been up and down, with values as low as 31. Results of sedimentation test indicated high levels of inflammation but the most recent test on 22Oct was 84 mm/hr. After seven months, (withheld) still has pain that she didn't have when she received the first injection on 16Apr. She has not received a second vaccine dose because of the pain she experienced (and continues to experience). She is justifiably unhappy that she got the vaccine at all.. All other tests were normal. Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EW0181 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EW0181, fill lot EP8732, and bulk formulation lot EP8613. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EN6203 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. and product type. The final scope included the reported finished goods lot EN6203, fill lot EN5336, and the formulated drug product lot EN5324. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. The final scope included the reported finished goods lot EL3247, fill lot EL3230, and the formulated drug product lot EL3223. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20210521; Test Name: ANA TITER; Result Unstructured Data: Test Result:Normal; Test Date: 20210521; Test Name: CK; Result Unstructured Data: Test Result:Normal; Test Date: 20211022; Test Name: TSH; Result Unstructured Data: Test Result:9.7 uiU/mL; Test Date: 20211022; Test Name: TSH ABNORMAL TO FREE T4; Result Unstructured Data: Test Result:Normal; Test Date: 20210709; Test Name: TSH RFX ON ABNORMAL TO FREE T4; Result Unstructured Data: Test Result:Normal; Test Date: 20210811; Test Name: TSH RFX ON ABNORMAL TO FREE T4; Result Unstructured Data: Test Result:Unknown Results; Test Date: 20210521; Test Name: TSH RFX ON ABNORMAL TO FREE; Result Unstructured Data: Test Result:Normal; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown results; Comments: contrast dye injected for Ct scan; Test Date: 20210521; Test Name: Complete blood count; Result Unstructured Data: Test Result:Normal; Test Date: 20210709; Test Name: HGB A1C WITH EAG ESTIMATION; Result Unstructured Data: Test Result:Normal; Test Date: 202105; Test Name: Inflammation test; Result Unstructured Data: Test Result:61mm/hr; Test Date: 20210521; Test Name: CYCLIC ClTRUL PEPTIDE AB, IGG; Result Unstructured Data: Test Result:Normal; Test Date: 20210921; Test Name: NUSWAB VAGINITIS PLUS (VG+); Result Unstructured Data: Test Result:Normal; Test Date: 20210521; Test Name: LIPID PANEL; Result Unstructured Data: Test Result:Normal; Test Date: 20210521; Test Name: COMPREHENSIVE METABOLIC PANEL; Result Unstructured Data: Test Result:Normal; Test Date: 202105; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:61 mm/hr; Test Date: 20210521; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:Normal; Test Date: 20210811; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:High level of inflammation; Test Date: 20211022; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:84 mm/hr; Test Date: 20210521; Test Name: COVID-19 AB IgG; Result Unstructured Data: Test Result:03; Test Date: 20210603; Test Name: COVID-19 AB IgG; Result Unstructured Data: Test Result:4; Test Date: 20210709; Test Name: COVID-19 AB IgG; Test Result: Positive ; Test Date: 20210709; Test Name: SARS-COV-2 (COVID-19) Antibody IgG; Result Unstructured Data: Test Result:Normal; Test Date: 20200330; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20200804; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20210619; Test Name: COVID-19 Test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fibromyalgia (Pertinent Details: Triggered by contrast dye injected prior to CT scan); Lung cancer (father died of lung cancer at age 70); Pneumonia (mother died of pneumonia at age 78)
Andere Medikamente: MIRTAZAPINE
Allergien: -
Vorherige Impfungen: -

VAERS 1243953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 16.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Antinuclear antibody Arthralgia Axillary pain Back pain Blood creatine phosphokinase Blood thyroid stimulating hormone Blood thyroid stimulating hormone increased Computerised tomogram Fibromyalgia Full blood count Burning sensation Condition aggravated Pain Gait disturbance Glycosylated haemoglobin increased Inflammation Inflammation scan Investigation

Symptomtext

TSH, a test for thyroid function, which was 9.7 ulU/mL; inflammation; Fibromyalgia; The pain was in her armpits, shoulder, back, hips and ankles/ calves; The pain was in her armpits, shoulder, back, hips and ankles/ calves; The pain was in her armpits, shoulder, back, hips and ankles/ calves; She could hardly walk; Joint and muscle pain/ The pain was in her armpits, shoulder, back, hips and ankles/ calves; Joint and muscle pain; Pain in her cheeks; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) . A 57 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 16Apr2021 (Lot number: EW0153) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Fibromyalgia", start date: 09Dec2014, stop date: Feb2015, notes: Pertinent Details: Triggered by contrast dye injected prior to CT scan. Family history included: "lung cancer" (unspecified if ongoing), notes: father died of lung cancer at age 70; "pneumonia" (unspecified if ongoing), notes: mother died of pneumonia at age 78. Concomitant medication(s) included: MIRTAZAPINE taken for fibromyalgia, start date: Feb2015 (ongoing). The following information was reported: ARTHRALGIA (non-serious) with onset 18Apr2021, outcome "not recovered", described as "Joint and muscle pain/ The pain was in her armpits, shoulder, back, hips and ankles/ calves"; MYALGIA (non-serious) with onset 18Apr2021, outcome "not recovered", described as "Joint and muscle pain"; PAIN (non-serious) with onset 17Apr2021 17:00, outcome "not recovered", described as "Pain in her cheeks"; FIBROMYALGIA (non-serious) with onset 18Apr2021 08:00, outcome "not recovered", described as "Fibromyalgia"; AXILLARY PAIN (non-serious), BACK PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 18Apr2021, outcome "not recovered" and all described as "The pain was in her armpits, shoulder, back, hips and ankles/ calves"; GAIT DISTURBANCE (non-serious) with onset 18Apr2021, outcome "not recovered", described as "She could hardly walk"; BLOOD THYROID STIMULATING HORMONE INCREASED (non-serious) with onset 22Oct2021, outcome "recovered", described as "TSH, a test for thyroid function, which was 9.7 ulU/mL"; INFLAMMATION (non-serious) with onset May2021, outcome "unknown", described as "inflammation". The events "joint and muscle pain/ the pain was in her armpits, shoulder, back, hips and ankles/ calves", "joint and muscle pain", "fibromyalgia" and "the pain was in her armpits, shoulder, back, hips and ankles/ calves" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of arthralgia, myalgia, fibromyalgia, pain in extremity, gait disturbance, blood thyroid stimulating hormone increased. Therapeutic measures were not taken as a result of pain. Additional information: It was reported that prior to receiving the Pfizer vaccine the morning of 16Apr2021, patient was in good health, and her fibromyalgia, which was triggered in Dec2014 by contrast dye injected for a CT scan, had been under control since 2015 with 30 mg of Mirtizapine. Approximately 17:00 on 17Apr2021, she began feeling pain in her cheeks. By the next morning, the same pain that she felt in the early days of fibromyalgia returned. Two days later she began feeling joint and muscle pain, and nearly 7 months later it has not gone away. She has been to 4 doctors and taken several medications to no avail. The pain was in her armpits, shoulders, back, hips and ankles/calves. She was in so much pain that she could hardly walk or do any strenuous activities. Following discussions with her doctor, 75 mg of Lyrica was added to her medication, and the Mirtazapine was increased to 45 mg. However, there was not much improvement. In late May, patient first saw Doctor, a rheumatologist. He ordered many of the same tests as (withheld) primary care physician, Dr. The test results were normal except for sedimentation rate, a test for inflammation, which was 61 mm/hr, and TSH, a test for thyroid function, which was 9.7 ulU/mL. Dr. prescribed 25 mcg of levothyroxine, and Dr. prescribed 15 mg of prednisone to be tapered down to 5 mg over three weeks. She has further reduced her prednisone dose to 2.5 mg and maintained it over the past four months, and she stopped taking Lyrica. The prednisone had some benefit in terms of pain reduction, and the levothyroxine has brought (withheld) TSH level within the normal range. Subsequent sedimentation rate results have been up and down, with values as low as 31. Results of sedimentation test indicated high levels of inflammation but the most recent test on 22Oct was 84 mm/hr. After seven months, (withheld) still has pain that she didn't have when she received the first injection on 16Apr. She has not received a second vaccine dose because of the pain she experienced (and continues to experience). She is justifiably unhappy that she got the vaccine at all.. All other tests were normal. Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EW0181 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EW0181, fill lot EP8732, and bulk formulation lot EP8613. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EN6203 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. and product type. The final scope included the reported finished goods lot EN6203, fill lot EN5336, and the formulated drug product lot EN5324. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. The final scope included the reported finished goods lot EL3247, fill lot EL3230, and the formulated drug product lot EL3223. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20210521; Test Name: ANA TITER; Result Unstructured Data: Test Result:Normal; Test Date: 20210521; Test Name: CK; Result Unstructured Data: Test Result:Normal; Test Date: 20211022; Test Name: TSH; Result Unstructured Data: Test Result:9.7 uiU/mL; Test Date: 20211022; Test Name: TSH ABNORMAL TO FREE T4; Result Unstructured Data: Test Result:Normal; Test Date: 20210709; Test Name: TSH RFX ON ABNORMAL TO FREE T4; Result Unstructured Data: Test Result:Normal; Test Date: 20210811; Test Name: TSH RFX ON ABNORMAL TO FREE T4; Result Unstructured Data: Test Result:Unknown Results; Test Date: 20210521; Test Name: TSH RFX ON ABNORMAL TO FREE; Result Unstructured Data: Test Result:Normal; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown results; Comments: contrast dye injected for Ct scan; Test Date: 20210521; Test Name: Complete blood count; Result Unstructured Data: Test Result:Normal; Test Date: 20210709; Test Name: HGB A1C WITH EAG ESTIMATION; Result Unstructured Data: Test Result:Normal; Test Date: 202105; Test Name: Inflammation test; Result Unstructured Data: Test Result:61mm/hr; Test Date: 20210521; Test Name: CYCLIC ClTRUL PEPTIDE AB, IGG; Result Unstructured Data: Test Result:Normal; Test Date: 20210921; Test Name: NUSWAB VAGINITIS PLUS (VG+); Result Unstructured Data: Test Result:Normal; Test Date: 20210521; Test Name: LIPID PANEL; Result Unstructured Data: Test Result:Normal; Test Date: 20210521; Test Name: COMPREHENSIVE METABOLIC PANEL; Result Unstructured Data: Test Result:Normal; Test Date: 202105; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:61 mm/hr; Test Date: 20210521; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:Normal; Test Date: 20210811; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:High level of inflammation; Test Date: 20211022; Test Name: SEDIMENTATION RATE. AUTOMATED; Result Unstructured Data: Test Result:84 mm/hr; Test Date: 20210521; Test Name: COVID-19 AB IgG; Result Unstructured Data: Test Result:03; Test Date: 20210603; Test Name: COVID-19 AB IgG; Result Unstructured Data: Test Result:4; Test Date: 20210709; Test Name: COVID-19 AB IgG; Test Result: Positive ; Test Date: 20210709; Test Name: SARS-COV-2 (COVID-19) Antibody IgG; Result Unstructured Data: Test Result:Normal; Test Date: 20200330; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20200804; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20210619; Test Name: COVID-19 Test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fibromyalgia (Pertinent Details: Triggered by contrast dye injected prior to CT scan); Lung cancer (father died of lung cancer at age 70); Pneumonia (mother died of pneumonia at age 78)
Andere Medikamente: MIRTAZAPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2123959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 60,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 07.04.2021
Beginn: 17.02.2022
Tage bis Beginn: 316,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea Haemoptysis SARS-CoV-2 test positive Fibrin D dimer increased Imaging procedure abnormal

Symptomtext

admit 2/17/2022-2/18/2022 Vital signs stable, afebrile and saturating well on room air. COVID positive, vaccinated and boosted. is in no acute distress. Her cardiopulmonary exam is largely unremarkable. Her D-dimer is mildly positive and she has been found to be COVID positive as well. readmit 2/27/2022 diagnosed with COVID-19 and was subsequently admitted overnight for further evaluation. Imaging was concerning for aspiration pneumonia but there was no evidence of a pulmonary embolism. She was ultimately discharged home on 2/18/22 in a stable condition with a course of Augmentin and plans for outpatient remdesivir treatment Admin Location (Facility)-(Privacy) 11/18/2021-3rd vaccine, Pfizer

Weitere VAERSDATA-Felder

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

VAERS 2123959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 60,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 07.04.2021
Beginn: 17.02.2022
Tage bis Beginn: 316,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Dyspnoea Haemoptysis SARS-CoV-2 test positive Fibrin D dimer increased Imaging procedure abnormal

Symptomtext

admit 2/17/2022-2/18/2022 Vital signs stable, afebrile and saturating well on room air. COVID positive, vaccinated and boosted. is in no acute distress. Her cardiopulmonary exam is largely unremarkable. Her D-dimer is mildly positive and she has been found to be COVID positive as well. readmit 2/27/2022 diagnosed with COVID-19 and was subsequently admitted overnight for further evaluation. Imaging was concerning for aspiration pneumonia but there was no evidence of a pulmonary embolism. She was ultimately discharged home on 2/18/22 in a stable condition with a course of Augmentin and plans for outpatient remdesivir treatment Admin Location (Facility)-(Privacy) 11/18/2021-3rd vaccine, Pfizer

Weitere VAERSDATA-Felder

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

VAERS 2147222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: -
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 23.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea Investigation Lethargy Maternal exposure during pregnancy White blood cell count White blood cell count increased X-ray

Symptomtext

pregnant while vaccinated; lethargic; high white blood cell; breathing issue; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the parent. A 39 week-old female patient was exposed to bnt162b2 (BNT162B2), transplacental (mother's route: intramedullar) administered in arm left, administration date 23Apr2021 (Lot number: EW0153, Expiration Date: Jul2021) as dose 1, single and transplacental (mother's route: intramuscular) administered in arm left, administration date 14May2021 (Lot number: EW0172, Expiration Date: Aug2021) as dose 2, single for covid-19 immunisation. The mother of the patient was 34 years old at the time of vaccination. The mother's relevant medical history included: "Migraines" (unspecified if ongoing). Date of last menstrual period of the mother: 06Jan2021. The mother was 15 weeks pregnant at the time of exposure to bnt162b2; 3 weeks pregnant to ascorbic acid, calcium, colecalciferol, cyanocobalamin, folic acid, iron, nicotinamide, pyridoxine hydrochloride, retinol, riboflavin, thiamine hydrochloride, tocopherol, zinc, colecalciferol, folic acid, paracetamol. The mother is expected to deliver a baby(s) on 12Oct2021. Concomitant medication(s) included: PRENATAL S, start date: 31Jan2021 (ongoing); B12 [CYANOCOBALAMIN], start date: 2020 (ongoing); VIT D [COLECALCIFEROL], start date: 01Feb2021; IMITREX, start date: 2010 (ongoing); BIOTIN, start date: 2020 (ongoing); B6, start date: 2020 (ongoing); FOLIC ACID, start date: 31Jan2021 (ongoing); TYLENOL, start date: 31Jan2021 (ongoing); MAXALT, start date: 2010; ZYRTEC [CETIRIZINE HYDROCHLORIDE], start date: 2021; MAGNESIUM, start date: 2021; ACYCLOVIR [ACICLOVIR], start date: 2015. Drug taken by the father: CAFFEINE, start date: 2009; ADVIL [IBUPROFEN], start date: 2019; CBD OIL, start date: 2018; WELLBUTRIN, start date: 2021; ZOLOFT, start date: 2021. Family history of mother: Mother: Lung cancer; Father: Diabetic. Outcome of Infant included:Other neonatal problem/abnormality (neonatal illness), X-ray + High white blood cell, Follow up X-rays ER Visit due to being lethargic. Normal, some breathing issues The first week No resolved. The following information was reported: MATERNAL EXPOSURE DURING PREGNANCY (hospitalization) with onset 2021, outcome "unknown", described as "pregnant while vaccinated"; LETHARGY (hospitalization) with onset 2021, outcome "unknown", described as "lethargic"; WHITE BLOOD CELL COUNT INCREASED (medically significant) with onset 2021, outcome "unknown", described as "high white blood cell"; DYSPNOEA (non-serious) with onset 2021, outcome "unknown", described as "breathing issue". The event "lethargic" was evaluated at the emergency room visit. The baby was delivered full-term, via vaginal route, delivery date 05Oct2021. The baby weighed 3990.8 grams. APGAR Score was 1, 5. The patient underwent the following laboratory tests and procedures: investigation: normal; white blood cell count: high; x-ray: unknown results.; Sender's Comments: We cannot totally exclude the causal association of reported events in relation to BNT162B2 based on temporal relation and exposure to the vaccine. Case will be reassessed pending new information. 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-2021466066 mother case;US-PFIZER INC-202200301415 same patient (baby), different product/event (Maternal / Paternal EDP)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Ante-natal check-up; Result Unstructured Data: Test Result:normal; Test Name: White blood cell; Result Unstructured Data: Test Result:High; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PRENATAL S; B12 [CYANOCOBALAMIN]; VIT D [COLECALCIFEROL]; IMITREX; BIOTIN; B6; FOLIC ACID; TYLENOL; MAXALT; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; MAGNESIUM; ACYCLOVIR [ACICLOVIR]; CAFFEINE; ADVIL [IBUPROFEN]; CBD OIL; WELLBUTRIN; ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 2147007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 45,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 14.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Mobility decreased Myalgia

Symptomtext

Muscle pain in my left arm and shoulder; Limited movement; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 14Apr2021 16:15 (Lot number: EW0153) at the age of 45 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: MYALGIA (non-serious) with onset 15Apr2021, outcome "not recovered", described as "Muscle pain in my left arm and shoulder"; MOBILITY DECREASED (non-serious) with onset 15Apr2021, outcome "not recovered", described as "Limited movement". Therapeutic measures were not taken as a result of myalgia, mobility decreased. Additional information: Facility type vaccine was reported as Pharmacy or Drug Store. No known allergies. No other vaccine in four weeks. No other medications in two weeks. Patient had not been diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination. Patient reported that he still have muscle pain in arm and shoulder. No issues with the 2nd dose. Adverse event start time was 12:00 AM. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2146640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 30,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 24.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Migraine Pain in extremity Somnolence

Symptomtext

A sore arm; Migraine; Slept most; 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 30 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Apr2021 (Lot number: EW0153) at the age of 30 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "A sore arm"; MIGRAINE (non-serious), outcome "unknown", described as "Migraine"; SOMNOLENCE (non-serious), outcome "unknown", described as "Slept most". Additional Information: After receiving her second dose she began to experience the "normal" side effects on Saturday evening into Sunday. She states that after her first dose of the vaccine she experienced a sore arm, a migraine and slept most of the day. She did not experienced any sort of chest tightness after her first dose. She would like to know if there is any information regarding chest tightness as a side effect for the Pfizer COVID-19 vaccine No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2134438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NC
Alter: 45,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 10.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Chills Lymph node pain Lymphadenopathy Mobility decreased Ultrasound scan abnormal

Symptomtext

I had bad chill without fever. For 48 hrs Swollen lymph node under my left arm side of a ping pong ball. It was extremely sore painful to touch and I couldn't move it. I went to the Dr a week after when it wasn't going away. They sent me to do an ultrasound. Just confirm swollen lymph node. It can last six week and it was normal side affect. I went sent home afterward. Recommended to take Tylenol. It resolve on its own after 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Ultrasound
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Nuvaring, Celexa
Allergien: None
Vorherige Impfungen: -

VAERS 2131445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 61,0
Geschlecht: M
Eingang: 22.02.2022
Impfdatum: 07.04.2021
Beginn: 08.02.2022
Tage bis Beginn: 307,0
Dosis: 2
Route/Site: IM / LA

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

Mobility decreased

Symptomtext

Hospitalized for respite care on 2/8 as unable to get out of bed and put on Hospice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pancreatic cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 01.07.2021
Beginn: 11.07.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

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

Abortion spontaneous COVID-19 Cardiac stress test Electrocardiogram Heart rate irregular Blood test normal Chest X-ray normal Chest discomfort Dyspnoea Electrocardiogram normal Feeling abnormal Heart rate increased Laboratory test normal Palpitations Sleep disorder Heavy menstrual bleeding Hyperhidrosis Laboratory test

Symptomtext

Irregular heartbeat- pounding, racing, profuse sweating even in the middle of the night. Still going on months later positive covid post vaccine, , Mentrual disregualtion, painful, heavy bleeding-prolonged several days, miscarriage post vaccine (november)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Symptoms began post 2nd dose-7/18/21 ER visit, subseguent x-rays, lab work,ekg,stress test, dx possible heart blockage, ref to cardiology and pulmonology. Tests within normal limits
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: postnatal vit,Vit B, Mag,calcium,iron,cod liver oil,D3, probio
Allergien: soy, latex
Vorherige Impfungen: -

VAERS 2126476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: OH
Alter: 23,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Axillary pain Mobility decreased Peripheral swelling

Symptomtext

Extreme discomfort in armpit of right arm; Swollen and hard to lift arm; Swollen and hard to lift arm; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 23 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 23Apr2021 14:15 (Lot number: EW0153) at the age of 23 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Spice allergy" (unspecified if ongoing), notes: Known allergies: cinnamon; "Dermatitis contact" (unspecified if ongoing), notes: Known allergies: adhesive; "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: Penicillin; "Attention deficit hyperactivity disorder" (unspecified if ongoing), notes: ADHD; "Mast cell activation syndrome" (unspecified if ongoing), notes: MCAS; "Postural orthostatic tachycardia syndrome" (unspecified if ongoing), notes: POTS; "Ehlers-Danlos syndrome" (unspecified if ongoing). Concomitant medication(s) included: STRATTERA; LORATADINE; VITAMIN D [VITAMIN D NOS]; ZINC. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: ER8730, Administration time:14:15), administration date: 02Apr2021, when the patient was 23 years old, for COVID-19 immunisation. The following information was reported: AXILLARY PAIN (non-serious) with onset 23Apr2021 18:00, outcome "not recovered", described as "Extreme discomfort in armpit of right arm"; PERIPHERAL SWELLING (non-serious), MOBILITY DECREASED (non-serious) all with onset 23Apr2021 18:00, outcome "not recovered" and all described as "Swollen and hard to lift arm". Therapeutic measures were not taken as a result of axillary pain, peripheral swelling, mobility decreased. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.The patient reported, the first shot did not hurt her armpit that way. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No therapeutic measures were not taken as a result of the events. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Attention deficit hyperactivity disorder (ADHD); Dermatitis contact (Known allergies: adhesive); Ehlers-Danlos syndrome; Mast cell activation syndrome (MCAS); Penicillin allergy (Known allergies: Penicillin); Postural orthostatic tachycardia syndrome (POTS); Spice allergy (Known allergies: cinnamon)
Andere Medikamente: STRATTERA; LORATADINE; VITAMIN D [VITAMIN D NOS]; ZINC
Allergien: -
Vorherige Impfungen: -

VAERS 2126128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 28,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 16.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Loss of personal independence in daily activities Tremor

Symptomtext

Tremble/ shake in the thumb on my right hand; Severe enough to interfere with any function of my right hand; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 28 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 16Apr2021 11:00 (Lot number: EW0153) at the age of 28 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "migraines" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). Family history included: low level tremble in hands does occur periodically" (unspecified if ongoing). Concomitant medication(s) included: PROPRANOLOL; CETIRIZINE HCL. Past drug history included: Propranolol, reaction(s): "low blood pressure", notes: low blood pressure (side effect of propranolol). Vaccination history included: Bnt162b2 (Product: COVID 19, Brand: Pfizer, Lot number: EN5318, Administration date: 29Mar2021, Administration time: 09:00 AM, Dose number: 1, Vaccine location: Right arm), administration date: 29Mar2021, when the patient was 28 years old, for Covid-19 Immunization. The following information was reported: TREMOR (non-serious) with onset 17Apr2021 12:00, outcome "recovering", described as "Tremble/ shake in the thumb on my right hand"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 17Apr2021 12:00, outcome "recovering", described as "Severe enough to interfere with any function of my right hand". Therapeutic measures were not taken as a result of tremor, loss of personal independence in daily activities. additional information: some low level tremble in hands does occur periodically and is common in patients family but does not interfere with function and patient haven't seen a physician for the issue. Patient did not receive other vaccine in four weeks. Adverse events Lasted roughly 2 hours beginning 25 hours post injection. Patient was not tested for covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine; Penicillin allergy; Tremor of hands
Andere Medikamente: PROPRANOLOL; CETIRIZINE HCL
Allergien: -
Vorherige Impfungen: -

VAERS 2125973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 59,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Confusional state Headache Hypokinesia Malaise Migraine Nausea Wrong technique in product usage process

Symptomtext

the insertion of the medication was truly excruciating; headache; nausea; not feeling well; confused as to how to get home (less than 2 miles!); weak; full blown migraine; stayed in bed all day; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2, solution for injection), administered in arm left, administration date 13Apr2021 09:45 (Lot number: EW0153) at the age of 59 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "hashimotos thyroiditis" (unspecified if ongoing); "depression" (unspecified if ongoing); "sarcoid" (unspecified if ongoing), notes: sarcoid (lungs); "Known Allergies: CORN" (unspecified if ongoing); "Known Allergies: gluten" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Codeine, reaction(s): "Known Allergies: codeine". The following information was reported: WRONG TECHNIQUE IN PRODUCT USAGE PROCESS (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "the insertion of the medication was truly excruciating"; HEADACHE (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "headache"; NAUSEA (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "nausea"; MALAISE (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "not feeling well"; CONFUSIONAL STATE (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "confused as to how to get home (less than 2 miles!)"; ASTHENIA (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "weak"; MIGRAINE (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "full blown migraine"; HYPOKINESIA (non-serious) with onset 13Apr2021 10:00, outcome "recovering", described as "stayed in bed all day". Therapeutic measures were not taken as a result of wrong technique in product usage process, nausea, malaise, confusional state, asthenia, hypokinesia. Therapeutic measures were taken as a result of headache, migraine. Additional information: No other vaccine in four weeks. The patient had other medications in two weeks. The patient did not have covid prior vaccination. The patient was not tested for covid post vaccination. The needle insertion was fine, but the insertion of the medication was truly excruciating. Almost had him stop. Before she even left the store started developing headache and a little nausea. When got into car was not feeling well and was confused as to how to get home (less than 2 miles). When got home went straight to bed because felt weak and had headache. Headache worsened during the night (took Ibuprofen 800 mg). Had full blown migraine by 14th and stayed in bed all day. Took 2 doses of Rizatriptan on 14th and 1 dose this a.m. (15th). Finally feeling better, though still a little nauseous. Interestingly, arm not really ever sore, except if the patient pushed on area. Would not really even say had "sore arm" - but the insertion of the medication was excruciating. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to grains; Depression; Sarcoid (sarcoid (lungs)); Thyroiditis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2119899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 06.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / RA

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

Ageusia Anosmia Arthralgia Dyspnoea Haemoptysis Headache Myalgia

Symptomtext

Shortness of breath, lack of taste and smell, coughing up blood and headaches. Having muscle and joint pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: yes
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure, thyroid
Andere Medikamente: amlodipine, levothyroxine, propranolol, hydrocholthyroize, lormortragen, labaxine, seroquel
Allergien: penicillin and bees
Vorherige Impfungen: -

VAERS 2119333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 06.04.2021
Beginn: 12.11.2021
Tage bis Beginn: 220,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain Anticoagulant therapy Asthenia Blood glucose increased COVID-19 Condition aggravated Dyspnoea Full blood count Hyperglycaemia Hyperkalaemia Pelvic haematoma SARS-CoV-2 test positive

Symptomtext

Patient vaccinated with Pfizer, last dose 04/06/21, who admitted to the hospital with a positive COVID test. Provider discharge summary below: "71 year old female who presented to the ED on 11/12/21 due to shortness of breath and weakness and was noted to be covid positive. She was started on COVID directed therapies and her symptoms continued to improve. Her stay was complicated by the development of an anterior pelvic hematoma without any active bleeding evident so no intervention was required. Her plavix and DVT prophylaxis were held with improvement in her symptoms. Her CBC remained stable and her abdominal pain substantially improved. She will have to follow up with her PCP for a CBC tomorrow and possible re-initiation of plavix. She also continued to have elevated blood sugars due to steroids that were initiated for COVID treatment. Her home medications were held and she required higher doses of insulin. She will be sent home with her home regimen in addition to prandial insulin and instructions to take her blood sugar 4x daily. She only has 1 additional day of steroids. Her PO medications were restarted on discharge. The patient also did have notable hyperkalemia during her stay. Her ARB was discontinued and her HCTZ dose was increased per nephrology recommendations with improvement, she will have a BMP checked tomorrow outpatient and her family physician/nephrologist can adjust BP medications as necessary. On day of discharge she was in improved and stable condition, she was still requiring O2 so she will be sent home with home O2 and home care."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 10,0
Labordaten: COVID "detected" test on 11/11/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism Type 2 diabetes mellitus with peripheral neuropathy Hyperlipidemia DEPRESSION HYPERTENSION GERD Umbilical hernia Stage 3b chronic kidney disease Osteoarthritis involving multiple joints Pain, Lumbar EDEMA WEIGHT GAIN (abnormal) Hoarseness MURMUR Seborrhea Neuropathy, Diabetic Snoring ADHD Gout Morbid obesity (*) Anemia Multiple joint pain Hyperkalemia History of CVA (cerebrovascular accident) Vitamin D deficiency Uncomplicated opioid dependence (*) Hyperparathyroidism, secondary (*) OSA (obstructive sleep apnea)
Andere Medikamente: Precose Tylenol Albuterol Zyloprim Plavix Cardizem Empagliflozin Vitamin D2 Zetia Pepcid Lasix Hydrodiuril Norco Novolog Lantus Protonix Actos Micardis
Allergien: Atenolol Benicar Hct [Olmesartan-hydrochlorothiazide] Cortizone-10 [Hydrocortisone] Crestor [Rosuvastatin] Lipitor [Atorvastatin] Lovastatin) Penicillins Pravastatin: Muscle Symptoms Relafen [Nabumetone]: Rash Victoza [Liraglutide]
Vorherige Impfungen: -

VAERS 2116371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 25.03.2021
Beginn: 10.02.2022
Tage bis Beginn: 322,0
Dosis: UNK
Route/Site: IM / RA

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

Acute kidney injury Blood creatinine increased Blood urea increased COVID-19 COVID-19 pneumonia Chemotherapy Computerised tomogram kidney abnormal Computerised tomogram thorax abnormal Cough Fatigue Hydronephrosis Laboratory test abnormal Lung opacity Nephrolithiasis SARS-CoV-2 test positive

Symptomtext

76 y/o female with history of nephrolithiasis, Follicular cell lymphoma currently on treatment, DM II who p/w AKI. The patient was sent over from by Dr due to abnormal labs with AKI. Patient has no history of CKD that is known. In the ER, patient had Cr 6.7 with BUN 44. CT scan shows an 8mm stone with moderate left hydronephrosis. The patient also had ground glass opacities in the lung c/w covid pna. The patient has had a cough for about a week and has been tired. Covid swab came back positive after I saw the patient. Her daughter is in the room with her and notes she has started to have a cough as well. The patient denies sob or fevers. She notes she has a history of nephrolithiasis with prior lithot lithotripsy also noting she has had stenting in the past but caused discomfort. Dr. in the ER has discussed the patient with Dr of nephrology and Dr of urology. Admission requested. Histories Past Medical History: -DM II non-insuln dependent -HTN -angiosarcoma of the breast -Follicular cell lymphoma currently under treatment, last chemotherapy was in Oct, was supposed to receive chemo again today but sent here due to abnl labs (missed Dec chemo for Christmas). 02/16/2022 - currently inpatient of COVID stepdown unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 92,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 06.04.2021
Beginn: 11.02.2022
Tage bis Beginn: 311,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Computerised tomogram thorax abnormal Decreased appetite Dyspnoea Mobility decreased Oxygen saturation decreased Pneumonia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 03/16/2021. 93 y/o with PMHx AFIB, CHF, HTN, HLD, Hypothyroid, Urinary Retention, CKD stage 3 presents to ER via EMS with c/o worsening generalized weakness and SOB. Pt was initially diagnosed with Covid on 02/02/2022. Per family pt is now unable to get OOB, has decreased appetite so brought to ED for evaluation. Afebrile, Room air sat initially normal but dropped to 83%, O2 placed on 5L NC. CT chest suspicious for multi-focal PNA. Pt started on IV steroids and ABX.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Per MD note-pt tested positive for Covid19 on 02/02/2022 and on 02/11/2022-records unavailable.
Aktuelle Erkrankungen: -
Vorgeschichte: AFIB, CHF, HLD, HTN, Hypothyroid, CKD stage 3, urinary retention
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2112940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IL
Alter: 28,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 02.05.2021
Beginn: 18.11.2021
Tage bis Beginn: 200,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray Electrocardiogram Electrocardiogram ambulatory Hypertension Laboratory test Palpitations Tachycardia

Symptomtext

Began having episodes of racing heart in October 2021. Multiple times per day, unexplained. On 11/18/2021 had an episode of sustained tachycardia (heart rate up to 180's) and HTN (180/120). Presented to emergency department for this episode. No etiology identified. Continue to have multiple episodes of tachycardia throughout the day. Cardiology appointment pending.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Lab work, EKG, Chest X-ray, Holter monitor
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: oral contraceptive- had been on for >10 years
Allergien: none
Vorherige Impfungen: -

VAERS 2108250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

moderat

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 05.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: - / LA

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

Condition aggravated Dizziness Feeling abnormal Headache Nausea Sleep disorder Vomiting

Symptomtext

nauseous; headache; dizzy; vomited on and off/was throwing up bile by 6 am; could not lay down or close my eyes; felt horrible; could not lay down or close my eyes without it getting worse; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Apr2021 18:00 (Lot number: ew0153) at the age of 32 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Allergy: avocados and apples" (unspecified if ongoing), notes: Known allergies= Avocados and Apples. Concomitant medication(s) included: ADDERALL. Vaccination history included: Bnt162b2 (Dose: 1, Lot no: En6206, Time: 04:00 PM, Anatomical location: Left arm), when the patient was 32 years old, for COVID-19 immunization. The following information was reported: NAUSEA (non-serious) with onset 08Apr2021 04:00, outcome "not recovered", described as "nauseous"; HEADACHE (non-serious) with onset 08Apr2021 04:00, outcome "recovering", described as "headache"; DIZZINESS (non-serious) with onset 08Apr2021 04:00, outcome "recovering", described as "dizzy"; VOMITING (non-serious) with onset 08Apr2021 04:00, outcome "recovering", described as "vomited on and off/was throwing up bile by 6 am"; SLEEP DISORDER (non-serious) with onset 08Apr2021 04:00, outcome "recovering", described as "could not lay down or close my eyes"; FEELING ABNORMAL (non-serious) with onset 08Apr2021 04:00, outcome "recovering", described as "felt horrible"; CONDITION AGGRAVATED (non-serious) with onset 08Apr2021 04:00, outcome "recovering", described as "could not lay down or close my eyes without it getting worse". The event "nauseous" was evaluated at the physician office visit and emergency room visit. The events "headache", "dizzy", "vomited on and off/was throwing up bile by 6 am", "could not lay down or close my eyes", "felt horrible" and "could not lay down or close my eyes without it getting worse" were evaluated at the physician office visit. Therapeutic measures were taken as a result of nausea, headache, dizziness, vomiting, sleep disorder, feeling abnormal, condition aggravated. Additional Information: Patient did not taken other vaccine in four weeks. Patient taken other medication in two weeks. Patient taken treatment with Ondansetron. No COVID test was done on post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy (Known allergies= Avocados and Apples)
Andere Medikamente: ADDERALL
Allergien: -
Vorherige Impfungen: -

VAERS 1195996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MA
Alter: 44,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 07.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dizziness Hypoaesthesia oral Paraesthesia oral Frustration tolerance decreased Hypoaesthesia Paraesthesia

Symptomtext

numbness on her tongue and lips, like a tingling numbness; numbness on her tongue and lips, like a tingling numbness; numbness on her tongue and lips, like a tingling numbness; upsetting and frustrating/ States she is frustrated; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. A 44 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Apr2021 15:10 (Lot number: EW0153, Expiration Date: 31Jul2021) at the age of 44 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Cold urticaria" (ongoing). Concomitant medication(s) included: ANTIHISTAMINE ALLERGY RELIEF taken for cold urticaria.The following information was reported: HYPOAESTHESIA ORAL (non-serious), PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 07Apr2021 15:20, outcome "recovered" (08Apr2021) and all described as "numbness on her tongue and lips, like a tingling numbness"; FRUSTRATION TOLERANCE DECREASED (non-serious) with onset 2021, outcome "unknown", described as "upsetting and frustrating/ States she is frustrated". Therapeutic measures were not taken as a result of hypoaesthesia oral, paraesthesia, hypoaesthesia, frustration tolerance decreased. Additional information: She had vaccine on Wednesday and vaccine administrator massaged her arm after injection, and asked if this negatively effects her vaccine, she thought it was odd but did not think much of it, afterwards she experienced a reaction. She called her doctor and he said it might have been because of the administration of it and when she looked into it, it said not to massage the arm before the vaccine is delicate. She called the pharmacy and they said she should not have done that, they said if anything may be the vaccine does not reach full efficacy, and that was really upsetting and frustrating to her especially after this past year, she was frustrated. The patient had none treatment, she was on an antihistamine chronically for Cold Urticaria, which is an allergy to cold, she was taking that before and after the vaccine. The AE(s) did not require a visit to Emergency Room or Physician Office. Prior Vaccinations (within 4 weeks), AE(s) following prior vaccinations, Family Medical History Relevant to AE(s) was None. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cold urticaria.
Vorgeschichte: -
Andere Medikamente: ANTIHISTAMINE ALLERGY RELIEF.
Allergien: -
Vorherige Impfungen: -

VAERS 2092837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 87,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 13.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Cardiac monitoring Cardiac stress test Chest pain Dizziness Dyspnoea Electrocardiogram Palpitations

Symptomtext

Light headed, shortness of breath, extreme weakness, chest pain, heart palpitations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG , Nuclear Stress Test, Heart monitor for 30 days
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Losartan Potassium, Amlodipine Besylate, Atorvastatin, Omeprazole, Metformin Hydrochloride, Multivitamin/ mineral
Allergien: Vioxx Celebrex Daypro Penicillin Sulfa drugs Hydroco/APAP APAP/Codeine Sumycin
Vorherige Impfungen: -

VAERS 1281509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: RI
Alter: 40,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 08.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

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

Anti-RNA polymerase III antibody Antinuclear antibody Arthralgia Electromyogram Feeling cold Blood test Pain Peripheral coldness Ultrasound scan Joint stiffness Laboratory test Limb discomfort Magnetic resonance imaging Musculoskeletal stiffness Paraesthesia Raynaud's phenomenon Skin lesion X-ray

Symptomtext

one of her feet is cold as a popsicle but it was not cold to the touch/one of her feet that was frozen like a popsicle; stiffness/tightness in her lower legs in her knees and below her knees; discomfort in her lower leg; here were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that also led to pins and needles in her leg that "felt like bugs"; soreness with pain and discomfort in her lower leg; She had tightness in her lower legs in her knees and below her knees.; soreness with pain; this led to pins and needles in her legs like she had jumping bugs on her legs; cold feeling in her feet was Raynaud's; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Pharmacist) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200194189 (Pfizer). A 40 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 08Apr2021 (Lot number: EW0153) at the age of 40 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Anxiety", start date: 2017 (ongoing). Family history included: "rheumatoid arthritis" (unspecified if ongoing), notes: Family Medical History Relevant to AE(s): Mom has severe rheumatoid arthritis. Concomitant medication(s) included: ZINC taken for supplementation therapy (ongoing); VITAMIN D NOS taken for supplementation therapy (ongoing); MULTIVITAMIN [VITAMINS NOS] (ongoing). The following information was reported: FEELING COLD (non-serious) with onset 09Apr2021, outcome "not recovered", described as "one of her feet is cold as a popsicle but it was not cold to the touch/one of her feet that was frozen like a popsicle"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 2021, outcome "unknown", described as "stiffness/tightness in her lower legs in her knees and below her knees"; LIMB DISCOMFORT (non-serious) with onset 2021, outcome "unknown", described as "discomfort in her lower leg"; SKIN LESION (non-serious) with onset 2021, outcome "unknown", described as "here were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that also led to pins and needles in her leg that "felt like bugs""; ARTHRALGIA (non-serious) with onset 2021, outcome "unknown", described as "soreness with pain and discomfort in her lower leg"; JOINT STIFFNESS (non-serious) with onset 2021, outcome "unknown", described as "She had tightness in her lower legs in her knees and below her knees."; PAIN (non-serious) with onset 2021, outcome "unknown", described as "soreness with pain"; PARAESTHESIA (non-serious) with onset 2021, outcome "unknown", described as "this led to pins and needles in her legs like she had jumping bugs on her legs"; RAYNAUD'S PHENOMENON (non-serious) with onset 2021, outcome "unknown", described as "cold feeling in her feet was Raynaud's". The events "one of her feet is cold as a popsicle but it was not cold to the touch/one of her feet that was frozen like a popsicle", "stiffness/tightness in her lower legs in her knees and below her knees", "discomfort in her lower leg", "here were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that also led to pins and needles in her leg that "felt like bugs"", "she had tightness in her lower legs in her knees and below her knees.", "soreness with pain", "this led to pins and needles in her legs like she had jumping bugs on her legs" and "cold feeling in her feet was raynaud's" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of feeling cold, limb discomfort, skin lesion, arthralgia, joint stiffness, pain, paraesthesia. Additional information: The patient did not take any other vaccine in four weeks prior COVID -19 vaccine. The patient stated that one of her feet was cold as popsicle but it was not cold to the touch. It was also did spread to the other foot and there were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that were also led to pins and needles in her leg that felt like bugs. The patient had horrible side effects that started after the first dose. The patient started with one of her feet that was frozen like a popsicle, but was not cold to the touch, but was warm to the touch. It was very bothersome and felt like it was freezing. It spread to the other foot. The coldness continued and the other symptoms started showing up too. The patient had tightness in her lower legs in her knees and below her knees. The patient had tightness, stiffness, soreness and pain and discomfort. The patient led pins and needles in her legs like she had jumping bugs on her legs. The patient not had this before vaccine. Most of the symptoms were in her lower legs. The patient received steroid after the summer thinking it was a inflammatory response from getting the vaccine. All of the tests were not negative. The patient had a ultrasound, MRI, X-ray and lab work. The patient stated that it has to be a response to the vaccine. The patient said that her physician said that the odds were very high that it was because of the vaccine. she said that the cold feeling in her feet was Raynaud's, but she did not have any of the rash, of the discoloration in her feet, hands or fingertips that go along with Raynaud's. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101733211 Same reporter/patient/drug, different dose/event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210412; Test Name: ANA titer; Result Unstructured Data: Test Result:1.80; Comments: +ANA; Test Date: 20210521; Test Name: Lyme Ab; Result Unstructured Data: Test Result:0.2; Test Date: 20211122; Test Name: EMG; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: Lab work; Test Result: Negative ; Comments: All of tests were negative; Test Date: 2021; Test Name: MRI; Test Result: Negative ; Comments: All of tests were negative; Test Date: 2021; Test Name: ultrasound; Test Result: Negative ; Comments: All of tests were negative; Test Date: 2021; Test Name: X-ray; Test Result: Negative ; Comments: All of tests were negative
Aktuelle Erkrankungen: Anxiety
Vorgeschichte: Medical History/Concurrent Conditions: Rheumatoid arthritis (Family Medical History Relevant to AE(s): Mom has severe rheumatoid arthritis.)
Andere Medikamente: ZINC; VITAMIN D NOS; MULTIVITAMIN [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1281509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: RI
Alter: 40,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 08.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Anti-RNA polymerase III antibody Antinuclear antibody Arthralgia Electromyogram Feeling cold Blood test Pain Peripheral coldness Ultrasound scan Joint stiffness Laboratory test Limb discomfort Magnetic resonance imaging Musculoskeletal stiffness Paraesthesia Raynaud's phenomenon Skin lesion X-ray

Symptomtext

one of her feet is cold as a popsicle but it was not cold to the touch/one of her feet that was frozen like a popsicle; stiffness/tightness in her lower legs in her knees and below her knees; discomfort in her lower leg; here were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that also led to pins and needles in her leg that "felt like bugs"; soreness with pain and discomfort in her lower leg; She had tightness in her lower legs in her knees and below her knees.; soreness with pain; this led to pins and needles in her legs like she had jumping bugs on her legs; cold feeling in her feet was Raynaud's; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Pharmacist) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200194189 (Pfizer). A 40 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 08Apr2021 (Lot number: EW0153) at the age of 40 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Anxiety", start date: 2017 (ongoing). Family history included: "rheumatoid arthritis" (unspecified if ongoing), notes: Family Medical History Relevant to AE(s): Mom has severe rheumatoid arthritis. Concomitant medication(s) included: ZINC taken for supplementation therapy (ongoing); VITAMIN D NOS taken for supplementation therapy (ongoing); MULTIVITAMIN [VITAMINS NOS] (ongoing). The following information was reported: FEELING COLD (non-serious) with onset 09Apr2021, outcome "not recovered", described as "one of her feet is cold as a popsicle but it was not cold to the touch/one of her feet that was frozen like a popsicle"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 2021, outcome "unknown", described as "stiffness/tightness in her lower legs in her knees and below her knees"; LIMB DISCOMFORT (non-serious) with onset 2021, outcome "unknown", described as "discomfort in her lower leg"; SKIN LESION (non-serious) with onset 2021, outcome "unknown", described as "here were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that also led to pins and needles in her leg that "felt like bugs""; ARTHRALGIA (non-serious) with onset 2021, outcome "unknown", described as "soreness with pain and discomfort in her lower leg"; JOINT STIFFNESS (non-serious) with onset 2021, outcome "unknown", described as "She had tightness in her lower legs in her knees and below her knees."; PAIN (non-serious) with onset 2021, outcome "unknown", described as "soreness with pain"; PARAESTHESIA (non-serious) with onset 2021, outcome "unknown", described as "this led to pins and needles in her legs like she had jumping bugs on her legs"; RAYNAUD'S PHENOMENON (non-serious) with onset 2021, outcome "unknown", described as "cold feeling in her feet was Raynaud's". The events "one of her feet is cold as a popsicle but it was not cold to the touch/one of her feet that was frozen like a popsicle", "stiffness/tightness in her lower legs in her knees and below her knees", "discomfort in her lower leg", "here were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that also led to pins and needles in her leg that "felt like bugs"", "she had tightness in her lower legs in her knees and below her knees.", "soreness with pain", "this led to pins and needles in her legs like she had jumping bugs on her legs" and "cold feeling in her feet was raynaud's" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of feeling cold, limb discomfort, skin lesion, arthralgia, joint stiffness, pain, paraesthesia. Additional information: The patient did not take any other vaccine in four weeks prior COVID -19 vaccine. The patient stated that one of her feet was cold as popsicle but it was not cold to the touch. It was also did spread to the other foot and there were also tightness, stiffness and soreness with pain and discomfort in her lower leg and knees that were also led to pins and needles in her leg that felt like bugs. The patient had horrible side effects that started after the first dose. The patient started with one of her feet that was frozen like a popsicle, but was not cold to the touch, but was warm to the touch. It was very bothersome and felt like it was freezing. It spread to the other foot. The coldness continued and the other symptoms started showing up too. The patient had tightness in her lower legs in her knees and below her knees. The patient had tightness, stiffness, soreness and pain and discomfort. The patient led pins and needles in her legs like she had jumping bugs on her legs. The patient not had this before vaccine. Most of the symptoms were in her lower legs. The patient received steroid after the summer thinking it was a inflammatory response from getting the vaccine. All of the tests were not negative. The patient had a ultrasound, MRI, X-ray and lab work. The patient stated that it has to be a response to the vaccine. The patient said that her physician said that the odds were very high that it was because of the vaccine. she said that the cold feeling in her feet was Raynaud's, but she did not have any of the rash, of the discoloration in her feet, hands or fingertips that go along with Raynaud's. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101733211 Same reporter/patient/drug, different dose/event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210412; Test Name: ANA titer; Result Unstructured Data: Test Result:1.80; Comments: +ANA; Test Date: 20210521; Test Name: Lyme Ab; Result Unstructured Data: Test Result:0.2; Test Date: 20211122; Test Name: EMG; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: Lab work; Test Result: Negative ; Comments: All of tests were negative; Test Date: 2021; Test Name: MRI; Test Result: Negative ; Comments: All of tests were negative; Test Date: 2021; Test Name: ultrasound; Test Result: Negative ; Comments: All of tests were negative; Test Date: 2021; Test Name: X-ray; Test Result: Negative ; Comments: All of tests were negative
Aktuelle Erkrankungen: Anxiety
Vorgeschichte: Medical History/Concurrent Conditions: Rheumatoid arthritis (Family Medical History Relevant to AE(s): Mom has severe rheumatoid arthritis.)
Andere Medikamente: ZINC; VITAMIN D NOS; MULTIVITAMIN [VITAMINS NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 2087616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 06.04.2021
Beginn: 19.01.2022
Tage bis Beginn: 288,0
Dosis: 2
Route/Site: - / -

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

Anticoagulant therapy COVID-19 Chest X-ray normal Chest discomfort Cough Dyspnoea Fall Inappropriate schedule of product administration SARS-CoV-2 test positive

Symptomtext

Patient is fully vaccinated. 63yo M with PMHx of neurosarcoidosis, HLD and vertigo presents with shortness of breath. Reports he tested positive for COVID 2 days ago and since that time has been having cough, worsening shortness of breath and chest discomfort. No history of heart attack, stroke or blood clots. Does not wear oxygen at home. Reports he had a fall a few days ago. No LOC, head trauma or blood thinner use. In the ER, he was placed on oxygen and given steroids and robitussin with significant improvement in his symptoms. CXR was negative for focal infiltrate. DVT prophylaxis with Lovenox. Discharged home.

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

VAERS 1184416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 08.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure measurement Bone pain Confusional state Disorientation Dizziness Chest discomfort Chest pain Nausea Nervousness Dyspnoea Flushing Hyperhidrosis Fatigue Feeling cold Hypertension Muscle tightness Nasopharyngitis Hyperventilation

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Hyperventilation-Mild, Additional Details: paramedics were called to assess pt, no further action was determined to be necessary

Weitere VAERSDATA-Felder

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

VAERS 2065803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: KY
Alter: 68,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 14.06.2021
Beginn: 20.01.2022
Tage bis Beginn: 220,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Alanine aminotransferase normal Aspartate aminotransferase increased Blood creatinine increased Blood glucose normal Blood potassium normal Blood sodium decreased COVID-19 Decreased appetite Diarrhoea Dyspnoea Fatigue Haematocrit normal Haemoglobin normal Hypotension Nausea Platelet count normal SARS-CoV-2 test positive

Symptomtext

The patient presents to ED with a 5-day history of fatigue, shortness of air, nausea, anorexia, and diarrhea. His wife noted that his blood pressure was 77/53 which prompted ED evaluation. On arrival he was found to be hypotensive which improved slightly with fluid bolus (2 L) to 81/49. Oxygen saturation was found to be 89% which improved to 96-97% after application of 2 L by nasal cannula. He was found to be Covid-19 positive, and with acute kidney injury (creatinine 2.46). Significant labs: Glucose 103, sodium 129, potassium 4.4, creatinine 2.46, AST 46, ALT 24, WBCs 10.74, Hgb 16.5, HCT 47.6, platelets 173. Thus far the patient has received 2 doses of Pfizer vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2065431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 12.04.2021
Beginn: 24.01.2022
Tage bis Beginn: 287,0
Dosis: UNK
Route/Site: - / -

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

Atrial fibrillation Bundle branch block COVID-19 COVID-19 pneumonia Chills Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Electrocardiogram abnormal SARS-CoV-2 test positive Sepsis Vaccine breakthrough infection

Symptomtext

Breakthrough COVID . Patient fully vaccinated with booster. Patient is 74 yo F who came to ED with c/o SOB, cough and chills for a few days. ED workup inluded EKG of afib with BBB, supplemental oxygen, IV abx, IV fluids. Treated for Covid Pneumonia with sepsis, COPD exacerbation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Covid Test + 1/24/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Diabetes, diabetic neuropathy, osteopenia, CHF, afib, COPD
Andere Medikamente: -
Allergien: Codeine, DIlaudid
Vorherige Impfungen: -

VAERS 2062803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 60,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 09.04.2021
Beginn: 13.09.2021
Tage bis Beginn: 157,0
Dosis: 2
Route/Site: IM / -

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

Blood pressure increased COVID-19 Complication of device insertion Dyspnoea Endotracheal intubation Erythema Gastrointestinal tube insertion Hyperhidrosis Hypoxia Mechanical ventilation Oxygen saturation decreased Pruritus SARS-CoV-2 test positive Sinusitis Swollen tongue Tachypnoea Tracheostomy Vaccine breakthrough infection

Symptomtext

COVID Breakthrough Case Pfizer Dose 1 3/19/21 ER8730 Pfizer Dose 2 4/9/21 EW0153 CV+ 9/14/21 9/14/21 60-year-old male with type 2 diabetes mellitus, hypertension, hyperlipidemia, obstructive sleep apnea presented with shortness of breath. Patient is currently intubated and unable to provide history,his story is obtained from chart review and phone interview with patient's wife. Wife reports patient was having sinus infection and took 1st dose of his antibiotics Augmentin and Tussionex. He came to her saying he is having shortness of breath, his neck and face was red and itching. She drove him to the emergency room, on arrival to the ED patient was tachypneic, diaphoretic with erythema involving his face and abdomen and swollen tongue. He was given multiple rounds of epinephrine with some improvement in his breathing , also received IV Benadryl, Solu-Medrol and ketamine. Intubation was attempted but unsuccessful, patient was being bagged in the meantime. Cricothyroidotomy was not successful. Patient was hypoxic with oxygen saturation in to low 30s. Surgeon placed ET tube through the incision already made of increasing size tubes and subsequently tracheostomy was completed and secured prior to transfer. Oxygenation improved, on transfer patient has elevated blood pressure with normal heart rate and was on mechanical ventilator at the time of my evaluation. Patient was following commands and moving his upper extremities and grimaces with and NG-tube placement. Patient does not have any known allergy for penicillins, pain medications, is currently on enalapril for hypertension.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 9,0
Labordaten: see above
Aktuelle Erkrankungen: TDM HTN HLD Obstructive sleep apnea Glaucoma Blindess in right eye Morbid Obesity Allergic rhinitis
Vorgeschichte: TDM HTN HLD Obstructive sleep apnea Glaucoma Blindess in right eye Morbid Obesity Allergic rhinitis
Andere Medikamente: acetaminophen 325 mg 2 Q4H prn mild pain/fever Albuterol 2 puffs Q6H allopurinol 100 mg oral tablet QD amLODIPine 5 mg oral tablet 1BID Combigan 0.2%-0.5% ophthalmic solution 1 gtt into both eyes Q12H famotidine 20 mg HS guaifenesine
Allergien: ACEI - angioedema Amoxicillin-clavulanate - Anaphylactic shock Tussionex PennKinetic - Angioedema
Vorherige Impfungen: -

VAERS 2062334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 38,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 07.04.2021
Beginn: 12.01.2022
Tage bis Beginn: 280,0
Dosis: 1
Route/Site: - / -

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

Chills Cough Musculoskeletal chest pain Nasal congestion Oropharyngeal pain Sinus congestion Upper-airway cough syndrome

Symptomtext

sore throat (has improved), cough, nonproductive cough, chills, sinus congestion (Improving), nasal congestion, post nasal drainage, some pain in ribs. starting 1/12/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: ?Omega 3 550 MG Capsule as directed Orally ?Probiotic - Capsule as directed Orally ?Vitamin D 400 UNIT Capsule 1 capsule Orally Once a day
Allergien: none
Vorherige Impfungen: -

VAERS 2047772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 74,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 20.05.2021
Beginn: 18.01.2022
Tage bis Beginn: 243,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Cough Dyspnoea Lung opacity SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st vaccine received on 04/29/2021. 74 y/o with PMH IBS, Fibromyalgia, GERD, Type 2 DM, OSA, HTN, HLD, DVT, Pulm fibrosis presents to ED via EMS for c/o SOB, Cough x2 weeks. CXR worsening diffuse interstitial opacities, requiring O2 at 4L NC-sats 93%, afebrile. Started on IV ABX, IV Steroids and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19-Detected on 01/18/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: IBS, Fibromyalgia, GERD, Arthritis, glaucoma, Type 2 DM, OSA, HTN, HLD, DVT, pulm fibrosis, conduction disorder heart
Andere Medikamente: -
Allergien: Codeine, Donnatal, Grass, Morphine
Vorherige Impfungen: -

VAERS 2035796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 49,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 07.04.2021
Beginn: 10.01.2022
Tage bis Beginn: 278,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 3/17, 4/7/21 COVID-19 positive by PCR on 1/10/22 admitted to hospital 1/10-1/12/22 for pneumonia d/t COVID 19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2029033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CO
Alter: 35,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 03.04.2021
Beginn: 03.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Blood test Condition aggravated Dizziness Dysarthria Dysstasia Epstein-Barr virus infection Fatigue Feeling abnormal Hypothyroidism Impaired work ability Influenza like illness Injection site erythema Injection site pain Injection site swelling Loss of personal independence in daily activities Myalgia Oropharyngeal pain

Symptomtext

I had Flu-like symptoms and severe muscle aches about 12 hours after the second dose. I was very fatigued. I had redness, swelling and pain at the injection site. It lasted for two days. After they subsided I had much more fatigue than I normally had with my condition. I have also had a lot of Brain Fog and I have trouble articulating. I feel like I have a sore throat and congestion every day. I have had Chronic Fatigue since I had Epstein Barr Virus. It has been 15 years but I was able to work and do normal household activities. It has been eight months and my Fatigue is still debilitating. I can only stand for about one minute without feeling weak. I am unable to stand to shower. I can no longer do housework and I cannot work. Any kind of exertion makes me think I am going to faint. I was diagnosed with Hypothyroidism within three months of getting my second dose and I am taking Levothyroxine for that. I have been unable to get my EBV symptoms and fatigue under control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood Work Immunologist, Scheduled for consultation 04/18/2021:
Aktuelle Erkrankungen: N/A
Vorgeschichte: Depression, Back Pain and Muscle Pain ? Chronic Fatigue Syndrome/ caused by Epstein Barr Syndrome
Andere Medikamente: Duloxetine, Gabapentin Famotidine, Montelukast Women's 1 Multivitamin, Vitamin D3 Turmeric
Allergien: Penicillin, Mosquitos Dog and Cat allergies Seasonal Allergies
Vorherige Impfungen: -

VAERS 2027255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 09.04.2021
Beginn: 11.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Dyspnoea Electrocardiogram Heart rate Heart rate increased SARS-CoV-2 test

Symptomtext

Difficulty in breathing; increased heart rate; 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 30 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 09Apr2021 (Lot number: EW0153) at the age of 30 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Seafood allergy" (unspecified if ongoing). Concomitant medication(s) included: VITAMIN D NOS; VITAMIN C [ASCORBIC ACID]. Vaccination history included: Bnt162b2 (lot number: ED6955, dose number: 1, vaccine location: Left arm), administration date: 19Mar2021, when the patient was 30 years old, for COVID-19 Immunization, reaction(s): "No reaction reported". The following information was reported: DYSPNOEA (non-serious) with onset 11Apr2021, outcome "recovered" (2021), described as "Difficulty in breathing"; HEART RATE INCREASED (non-serious) with onset 11Apr2021, outcome "recovered" (2021), described as "increased heart rate". The events "difficulty in breathing" and "increased heart rate" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of dyspnoea, heart rate increased. Additional information: The patient was not received other vaccine in four weeks. No covid prior vaccination. Patient was covid tested post vaccination. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20210411; Test Name: Heart rate; Result Unstructured Data: Test Result:increased; Test Date: 20210428; Test Name: Covidn test/Nasal swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seafood allergy
Andere Medikamente: VITAMIN D NOS; VITAMIN C [ASCORBIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 1222943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NJ
Alter: 50,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram Magnetic resonance imaging Transient ischaemic attack Vestibular disorder Dizziness Headache Hypertension

Symptomtext

TIA Mini stroke; vestibular dysfunction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: CT Scan MRI
Aktuelle Erkrankungen: -
Vorgeschichte: Fatty Liver IBS
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1222943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NJ
Alter: 50,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Computerised tomogram Magnetic resonance imaging Transient ischaemic attack Vestibular disorder Dizziness Headache Hypertension

Symptomtext

TIA Mini stroke; vestibular dysfunction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: CT Scan MRI
Aktuelle Erkrankungen: -
Vorgeschichte: Fatty Liver IBS
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2019638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 48,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 20.04.2021
Beginn: 08.01.2022
Tage bis Beginn: 263,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Dyspnoea Exposure to SARS-CoV-2 Lung disorder SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st Vaccine received on 03/30/2021. 48 y/o with PMHx of Asthma, CHF, COPD, DVT, DM, OSA, CKD presents to ED with c/o increasing SOB since yesterday. Recent exposure to +family members. Room air sat 87% requiring O2 @5L NC. CXR low lung volumes. Started on IV steroids and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19- detected on 01/08/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, CHF, COPD, DM, OSA, CKD, DVT
Andere Medikamente: -
Allergien: Heparin
Vorherige Impfungen: -

VAERS 2010792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: OK
Alter: 58,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 07.07.2021
Beginn: 03.01.2022
Tage bis Beginn: 180,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Diarrhoea Dyspnoea Renal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

01/03/22: RN, CONGESTION, DIARRHEA, COUGH, KIDNEY PAIN, AND SOB.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/03/22: POSITIVE POC SARS COVID RAPID ANTIGEN.
Aktuelle Erkrankungen: GERD
Vorgeschichte: HTN, Edema, Obesity, Panic Disorder, Hyperlipidemia, Dm2, Osteoarthritis, GERD
Andere Medikamente: Metoprolol, Metformin, Omeprazole, Potassium Chloride, Furosemide, Acetaminophen, Promethazine, Azo, Crestor, Cholecalciferol
Allergien: MORPHINE, PENICILLIN
Vorherige Impfungen: -

VAERS 2010219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 05.04.2021
Beginn: 28.12.2021
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Chest pain Dyspnoea Muscle spasms SARS-CoV-2 test positive

Symptomtext

12/28/2021: Event occurred after 2nd vaccine. 64-year-old gentleman presents the emergency department for evaluation of shortness of breath. Patient denies any productive cough, fevers, chills, nausea vomiting. He did have some mild left-sided chest pain associated with this. Symptoms resolved. Patient also notes that he had cramping in his left calf today which is atypical for him.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: 12/28/2021: SarsCov2- positive
Aktuelle Erkrankungen: unknown
Vorgeschichte: He does have insulin-dependent diabetes hyperlipidemia and hypertension.
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2006506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 53,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 09.04.2021
Beginn: 01.01.2022
Tage bis Beginn: 267,0
Dosis: 1
Route/Site: - / -

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

Ageusia Anosmia Cough Diarrhoea Dyspnoea Ear pain Nasal congestion Oropharyngeal pain

Symptomtext

Nonproductive cough, nasal congestion, ear pain, diarrhea, sore throat, shortness of breath, loss of taste, and loss of smell. All starting 1/1/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: G2P2. Diverticulitis. Seasonal allergies. Gestational Diabetes. panic attacks seeing psychiatrist. Normal colonoscopy 9/2017 repeat 5 year.
Andere Medikamente: metFORMIN HCl 500 MG Tablet 1 tablet with a meal Orally Once a day, Multivitamins Capsule Orally, Citracal + D, Levothyroxine Sodium 88 MCG Tablet 1 tablet in the morning on an empty stomach Orally Once a day, Eliquis 5 MG Tablet 1 tablet O
Allergien: PENICILLIN DRUGS: rash - Allergy, Spironolactone: muscle pain
Vorherige Impfungen: -

VAERS 2006217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: AR
Alter: 63,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 22.03.2021
Beginn: 27.12.2021
Tage bis Beginn: 280,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Balance disorder Blood bicarbonate normal Blood glucose normal Blood pH normal Blood sodium decreased COVID-19 Carbon dioxide decreased Cough Dizziness Dyspnoea Headache Hypoxia Nausea PO2 decreased Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Chief Complaint pt arrives to triage with HA, fever, cough, off balance states +covid on Monday. Patient is a 63 y/o female who presented with complaints of cough, fever, headache, and dizziness for the past week. Patient symptoms started on 12/26, she was diagnosed with COVID19 on 12/27. Patient reports persistent symptoms of dizziness, cough, and fevers 101.7 at home. She has had associated nausea and vomiting. She received 2 doses of the Pfizer vaccine in April, no booster. Due to persistent symptoms with no improvement she presented to the emergency department. Upon arrival patient was noted to be hypoxic with pulse ox in the 90s on room air. Routine lab work with Na 133, CO2 21, glucose 135. ABG pH 7.45, oCO2 35, pO251, HCO3 24.4 on room air. Patient has been placed on 2L O2 via NC. Hospitalist service asked to admit. Currently on COVID Stepdown unit (01/05/2021). Progress note of 01/05/2022: Subjective Feeling somewhat better, cough still bothersome. On 5L, unable to turn down to 4 without dropping. Energy level improving. Review of Systems Constitutional: Negative. Respiratory: Shortness of breath, Cough. Cardiovascular: Negative. Gastrointestinal: Negative. Genitourinary: Negative. Musculoskeletal: Negative. Integumentary: Negative. Neurologic: Negative. ROS reviewed as documented in chart Objective VS/Measurements Vital Signs( 01/03/22 11:55:56 to current ) VITAL SIGN LAST CHARTED MINIMUM MAXIMUM Blood Pressure 149/69 (01/04 11:11) 104/50 (01/04 05:00) 149/69 (01/04 11:11) Heart Rate 46 (01/04 11:40) 46 (01/04 11:40) 74 (01/03 15:15) Respirations 18 (01/04 11:40) 11 (01/04 08:00) 25 (01/03 17:16) Temperature 97.4 (01/04 08:15) 96.8 (01/04 05:00) 98.7 (01/03 17:16) SpO2 90 (01/04 11:40) 88 (01/04 00:00) 96 (01/04 10:00) Oxygen Flow Rate 5 (01/04 11:40) 4 (01/04 11:30) 6 (01/04 09:00) Weight 94.1 (01/04 11:29) 94.1 (01/04 11:29) 94.1 (01/04 11:29)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/27/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthma Condition aggravated Dyspnoea Wheezing

Symptomtext

Narrative: He has history of asthma since childhood. ASTHMA IS UNCONTROLLED BASED ON CHART REVIEW. He also has anaphylaxis to multiple tree nuts and was intubated once. Onset of sx after COVID19 Pfizer vaccine was at 5hrs, used EpiPen b/c he felt SOB and wheezing. Sx thought likely due to uncontrolled asthma rather than the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1992314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: RI
Alter: 49,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 09.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: SYR / LA

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

Cardiac stress test Chest discomfort Dyspnoea Echocardiogram normal Electrocardiogram ambulatory abnormal Hypotension Ventricular extrasystoles

Symptomtext

Premature ventricular contractions Tightening of chest Inability to take deep breaths Chronic Low Blood pressure : 90/50

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: June 29, 2021: Halta Monitor - 24hrs ; 300 PVCs Aug 10, 2021: Stress Test - PVCs recorded Aug 17, 2021: Echocardiogram - ?normal?
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1989290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 06.04.2021
Beginn: 16.10.2021
Tage bis Beginn: 193,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain COVID-19 Colitis Decreased appetite Dyspnoea Nausea Productive cough SARS-CoV-2 test positive

Symptomtext

62-year-old female with past medical history of COPD, chronic pain syndrome, arthritis presented to the emergency department complaining of productive cough, shortness of breath, abdominal pain with nausea and poor appetite for the past few days. Pt + for COVID on 10/16/2021. Treatment: oxygen, albuterol, breo, DX also with colitis with acute abdominal pain, treatment: antibiotics. Discharged to home.

Weitere VAERSDATA-Felder

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

VAERS 1989267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 52,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 07.04.2021
Beginn: 23.12.2021
Tage bis Beginn: 260,0
Dosis: 2
Route/Site: IM / -

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

Chest discomfort Dyspnoea Hypoxia

Symptomtext

Hospitalized for dyspnea, substernal chest discomfort and new hypoxia.

Weitere VAERSDATA-Felder

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

VAERS 1979374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NJ
Alter: 67,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 26.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test Cardiac stress test Chest pain Electrocardiogram Electroencephalogram Magnetic resonance imaging

Symptomtext

Chest pains. Cardiologist ruled out any heart problems with several tests

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Stress test, nuclear test, ekg, egg, mri, blood panel
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure
Andere Medikamente: Bupropion Amloidapene
Allergien: No
Vorherige Impfungen: -

VAERS 1975332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NJ
Alter: 37,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 05.05.2021
Beginn: 07.06.2021
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: SYR / UN

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

Biopsy heart Catheterisation cardiac Chest discomfort Echocardiogram Electrocardiogram Fluid intake reduced Haematemesis Hypophagia Palpitations

Symptomtext

Intense ?coffee grind vomit? 12 days no food/water Chest racing Feeling of hollowness in chest Zofran for a few crackers during two separate 15 days total hospitalization 6/7/15 hospital and 10/28-11/2 other hospital No fluid while hospitalized had iv and now I have no veins left from weeks with many iv

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 15,0
Labordaten: Catherazation and biopsy of heart 6/14 Ultrasound, ekg, 6/10 EKG/Ultrasound 10/30
Aktuelle Erkrankungen: No
Vorgeschichte: Bipolar 1
Andere Medikamente: Lithium Haldol
Allergien: No
Vorherige Impfungen: Hives from chicken pox booster

VAERS 1971975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 24.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Anxiety Arthralgia Back pain Chills Decreased appetite Erythromelalgia Fatigue Feeling abnormal Head discomfort Heart rate increased Hypoaesthesia Insomnia Muscle tightness Muscle twitching Musculoskeletal stiffness Myalgia Night sweats Paraesthesia

Symptomtext

Tachycardia within 15 minutes of injection. Within 2 weeks, the following symptoms developed: numbness and tingling all over body; tightness/stiffness (compression, banding, wrapped in tape feeling) and constricting feeling in ankles, knees, forearms, abdomen, forehead/temple; joint and muscle pain; backache; head pressure (makes head feel heavy, squeezing inside); fatigue; elevated heartrate when standing or walking; burning skin; anxiety attacks (adrenaline rushes); insomnia; night sweats; loss of appetite; rapid weight loss; mild tinnitus in left ear; tremors in left hand; random twitches throughout the body; feeling of internal vibration/humming/buzzing; erythromelalgia; chills; low fever; cold hands/feet

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: COVID-19 (Pfizer), tachycardia, numbness in arms and legs

VAERS 2529520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 28.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Back pain Headache Hypoaesthesia Injected limb mobility decreased Injection site pain Myalgia Neck pain Paraesthesia Pyrexia

Symptomtext

Headache, Myalgia, Arthralgia, Fever, Severe headache and back pain, pain in the back of neck, unable to lift Left arm (injection site) pain at injections site, numbness and tingling L side of body.

Weitere VAERSDATA-Felder

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

VAERS 1946715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 09.04.2021
Beginn: 21.05.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal discomfort Allergy test Anxiety Blood test Cardiac monitoring Cardiac stress test Chest X-ray Decreased appetite Dyspnoea Electrocardiogram Flushing Gastrointestinal disorder Hot flush Laboratory test Nodule Palpitations Panic attack Paraesthesia

Symptomtext

Started with Heart Palpitations. Shortness of breath. Extreme anxiety and panic attack symptoms lasting for hours and days(now months) with no prior history. Flushing (hot flash type) Tingling. Loss of appetite. Lower GI issues. Stomach discomfort, knots, just below breast bone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 05/2021 Chest XRay, EKG, Blood work. 05/2021 ER Chest XRay, EKG 06/2021 Cardiologist- 24 hr Heart monitor. Stress and Rest Testing. with Scans. 06/2021 Family Physician - Consult/followup 7/2021 Allergist - allergy testing, asthma testing 7/2021 ER - Chest XRay, EKG. Blood Test 7/2021 Cardiologist - follow up 8/2021 Home water tested 8/2021 Family physician. Follow up from July visit 2 day/24 hr testing. Blood Test. 9/2021 Endocrinologist. Consult 9/2021 Family physician - Occult testing
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Lisinopril. Potassium, Baby Aspirin, Vitamin D
Allergien: Penicillin. Codeine.
Vorherige Impfungen: -

VAERS 1923680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: PA
Alter: 62,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 15.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / RA

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

Acoustic stimulation tests normal Computerised tomogram normal Condition aggravated Ear, nose and throat examination Tinnitus Vestibular function test normal

Symptomtext

After the first vaccine noticed tinnitus in both ears when second Pfizer shot given I waited til September 27,2021 got second Pfizer and the tinnitus got worse have seen ENT and had audiology testing no hearing loss and also CT scan of inner ear canal for vestibular reason also had a whole vestibular testing done by Dr including rotation chair and VESTIBULAR-EVOKED MYOGENIC Tests and caloric testing all findings normal So I can only attribute this ringing to the Pfizer first and second shot very annoying

Weitere VAERSDATA-Felder

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

VAERS 1923290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 57,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 20.04.2021
Beginn: 29.11.2021
Tage bis Beginn: 223,0
Dosis: 1
Route/Site: - / -

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

Chills Dyspnoea exertional Headache Nasal congestion Pain Productive cough Pyrexia Respiratory tract congestion

Symptomtext

fever-highest at 100.2 oral temp, body aches, productive cough , headache-slight, shortness of breath with exertion, nasal congestion, chest congestion, chills, starting 11/29/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Left shoulder impingement . Myalgias. GERD. A.fib; s/p ablation 2019.
Andere Medikamente: ?PriLOSEC OTC 20 MG Tablet Delayed Release 1 tablet Orally Once a day, Notes: PRN ?Metoprolol Tartrate 25 MG Tablet 1.5 tablet with food Orally once a day ?Aspirin 81 MG Tablet Chewable 1 tablet Orally once a day ?Atorvastatin Calc
Allergien: none
Vorherige Impfungen: -

VAERS 1905721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0153

moderat

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 30.09.2021
Beginn: 07.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Arthralgia Inappropriate schedule of product administration Muscle tightness Neck pain Pain Pain in extremity Paraesthesia SARS-CoV-2 test

Symptomtext

Severe right shoulder, neck and arm pain; Severe right shoulder, neck and arm pain; Severe right shoulder, neck and arm pain; Muscle tightness; Aches; Finger tingling; Dose 1: 07Apr2021, Dose 2: 30Sep2021; This is a spontaneous report from a contactable reporter (consumer). The reporter is the patient. A 30 year-old female patient (not pregnant) received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in right arm, administration date 30Sep2021 at 12:00 (Batch/Lot number: 506780) at the age of 30 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "COVID-19". Concomitant medications were not reported. Vaccination history included: BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, DOSE 1, SINGLE, Lot Number: EW0153, Anatomical site: Left Arm, Route of administration: Unspecified, Administration time: 12:00), administration date: 07Apr2021, when the patient was 30 years old, for COVID-19 immunisation. The following information was reported: ARTHRALGIA (non-serious), NECK PAIN (non-serious), PAIN IN EXTREMITY (non-serious), MUSCLE TIGHTNESS (non-serious), PAIN (non-serious), PARAESTHESIA (non-serious) all with onset 01Oct2021 at 06:00, outcome "not recovered", and all described as "severe right shoulder, neck and arm pain, muscle tightness, aches and finger tingling.'' The events severe right shoulder, neck and arm pain, muscle tightness, aches and finger tingling were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of arthralgia, neck pain, pain in extremity, muscle tightness, pain and paraesthesia. Additional Information: The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to the vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. Therapeutic measures were taken as a result of arthralgia, neck pain, pain in extremity, muscle tightness, pain and paraesthesia and included treatment with chiropractor, cupping and acupuncture.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210711; Test Name: Nasal swab; Test Result: Negative ; Comments: Binax
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 1920628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 35,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 13.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: - / -

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

Anxiety Condition aggravated

Symptomtext

Sometime in may I started to experience severe anxiety. I didn't see any doctor. I am being treated for anxiety as of now. I had to take more of the Alprazolam .5mgs as needed used it every day, and I rarely used. I was using it at least once a day or twice a day. It lasted about a week, closer to two weeks. I however do feel like things have gone back to how they were before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, high cholesterol anxiety and depression. Migraine headaches.
Andere Medikamente: I take Trazadone 50mgs twice a day Alprazolam .5mgs as needed Atorvastatin 10mgs once a day Bupropion xl 150mgs once a day Losartan 25 mgs once a day 100mgs once a day Desvenlasaxine Tenatoprazole40mgs once a day Propranolol 120mgs o
Allergien: Two Allergies Imitrex Fluorescein and just seasonal allergies.
Vorherige Impfungen: -

VAERS 1916945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NJ
Alter: 80,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 28.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Dehydration Delirium Feeling hot Food refusal Pyrexia Screaming

Symptomtext

Patient had a high fever and, in my opinion, became delirious- refused to eat and/or drink and was screaming obscenities and for me to get away from him - I had a thermometer and bottle of fluid which he refused- a couple of hours later (I believe this was on the 30th of April), he accepted the thermometer, left it in his mouth for about 15 seconds and through it on the table at which point it had already reached 99.9 degrees - his back and neck were burning hot - he was dehydrated and refused hospital care - by Friday morning, he was much better and able to eat and drink as he normally would

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: None - he refused hospital care and refused to call doctor
Aktuelle Erkrankungen: Rheumatoid arthritis - cervical spinal stenosis
Vorgeschichte: Rheumatoid arthritis - cervical spinal stenosis
Andere Medikamente: Methrotrexate, Anora inhaler, folic acid, prednisone
Allergien: -
Vorherige Impfungen: -

VAERS 1908475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: SC
Alter: 67,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 07.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Adjusted calcium Alanine aminotransferase Anion gap Aspartate aminotransferase Basophil count Basophil percentage Blood albumin Blood alkaline phosphatase Blood bilirubin Blood calcium Blood chloride Blood creatinine Blood glucose Blood potassium Blood sodium Blood urea Body temperature Carbon dioxide

Symptomtext

Major rash; itched and hurt a lot/ brokeout her arm; Dermatologist felt it had a system allergy; Dehydration/ Got too dehydrated; sick/ nausea; high fever/fever got up to 103/ fever set in; Booster; Felt pretty bad; The initial safety information received was reporting only non-serious adverse drug reaction. Upon receipt of follow-up information on 15Nov2021, this case now contains serious adverse reactions. Information processed together. This is a spontaneous report received from a contactable consumer for a Pfizer-sponsored program (159558). The reporter is the patient. A 67 year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), administered in arm, administration date 07Oct2021 at noon (Lot number: EW0153) at the age of 67 years as dose 3 (booster), single for COVID-19 immunization. The vaccination facility type was reported as the doctor's office/urgent care. Relevant medical history included: "Extreme dry eyes", start date: 30Sep2021 (unspecified if ongoing); "Hashimoto's thyroid disease" (ongoing); "Type II diabetes" (ongoing); "Cholesterol" (ongoing); "High Blood Pressure" (ongoing); "Arrhythmia heart" (ongoing); "osteoporosis" (ongoing); "Osteopenia" (ongoing); "did have issues with potassium phosphate (intolerance)" (unspecified if ongoing); "Weakened immune system" (unspecified if ongoing); "Sleep apnea" (unspecified if ongoing); "bradycardia" (unspecified if ongoing); "patient was receiving numerous vaccines for a cruise and to update, but still got sick on cruise", start date: 07Dec2019 (unspecified if ongoing), notes: felt like all symptoms of COVID-19. Concomitant medications included: PREDNISOLONE ACETATE taken for extreme dry eyes, start date: 30Sep2021, stop date: 26Oct2021 [stopped due to blood pressure (BP) issues]; SYNTHROID taken for her thyroid (ongoing); METFORMIN taken for diabetes (ongoing); CRESTOR taken for her cholesterol (ongoing); TOPROL taken for high blood pressure (ongoing); LISIPRIL taken for high blood pressure (ongoing); FLECAINIDE ACETATE taken for arrhythmia heart (ongoing); XANAX (ongoing); CALCIUM + VIT D taken for osteopenia (ongoing); "Prolea" (Ongoing) every 6 months for osteoporosis; and "Prelasec" (Ongoing). Vaccination history included: BNT162B2 (DOSE 1, SINGLE, Batch/Lot number: EL9262, anatomical site of injection: arm), administration date: 22Jan2021 at noon, when the patient was 66 years old, for COVID-19 immunization, reaction "felt a little ill"; BNT162B2 (DOSE 2, SINGLE, Batch/Lot number: EM9809, anatomical site of injection: arm), administration date: 12Feb2021 at noon, when the patient was 66 years old, for COVID-19 immunization, reactions: "Dehydration", "dry heaves", "Nausea", and "very sick with high fever/fever got up to 103"; Flu shot (anatomical site of injection: arm, once a year), administration date: 20Sep2021, reaction: "No reaction"; Zoster recombinant, administration date: 10Sep2019, reaction: "fatigue", "fever", "felt like an infection" [very similar reaction, ended up in emergency room (ER) twice]; Flu vaccine, reactions: "very sick", "high fever/fever got up to 103"; Shingles vaccine, reactions: "very sick", "high fever/fever got up to 103"; German measles vaccine, reactions: "very sick", "high fever/fever got up to 103"; Zoster live, administration date: 2014, reaction: "No reaction" (no reaction at all to other vaccines on list even the Zoster live in 2014); German measles vaccine, administration date: 1978, reaction: "had a full case and was in hospital 2 weeks" (was told she was the only one who had a reaction). The following information was reported: IMMUNISATION (medically significant) with onset 07Oct2021, outcome "unknown", described as "Booster"; DEHYDRATION (medically significant) with onset 08Oct2021, outcome "unknown", described as "Dehydration/ Got too dehydrated"; NAUSEA (non-serious) with onset 08Oct2021, outcome "unknown", described as "sick/ nausea"; PYREXIA (non-serious) with onset 07Oct2021, outcome "unknown", described as "high fever/fever got up to 103/ fever set in"; FEELING ABNORMAL (non-serious) with onset Oct2021, outcome "unknown", described as "Felt pretty bad"; RASH PRURITIC (non-serious) with onset 11Oct2021, outcome "unknown", described as "Major rash; itched and hurt a lot/ brokeout her arm"; HYPERSENSITIVITY (non-serious) with onset 11Oct2021, outcome "unknown", described as "Dermatologist felt it had a system allergy". The events "booster", "dehydration/ got too dehydrated", "sick/ nausea", "high fever/fever got up to 103/ fever set in" were evaluated at the emergency room visit. The events "major rash; itched and hurt a lot/ brokeout her arm" and "dermatologist felt it had a system allergy" were evaluated at the physician office visit. The patient called, because she wanted to see if there was potassium phosphate in the three shots of the Pfizer Covid vaccine, with first dose she felt a little ill and with second dose and booster, she ended up in ER very sick with high fever, drank a lot of fluids, fever got up to 103, also reacted that way to flu vaccine and shingles vaccine and the German measles vaccine. She drank buttermilk once and ended up in ER for four hours, because it contained potassium phosphate. There was nothing out of ordinary regarding patient's medical history. The patient made sure it was well before getting vaccine and did not take it at same time as flu vaccine. For the adverse events, the patient reported on 2nd vaccine, the patient started to have dehydration, dry heaves, and nausea on 13Feb2021 at around 2AM, which required visit to ER and for which the patient was admitted to ICU for approximately 3hrs. The patient recovered after 3 days with treatment of intravenous (IV) Tylonol/moltrin/nausea medications in IV, 2 antibiotics in IV, and steroid. For the 3rd booster, the patient started to have event on 08Oct2021 at midnight close to 09Oct2021, which required visit to ER and for which the patient was admitted to ICU for approx. 3hrs. Treatment included IV mix, Tylenol+Moltrin, and anti-nausea medications. The reactions started later with arm breaking out also, for which the patient stayed in bed for 2 days. There were no major problems with 1st dose COVID-19 vaccine. There was brokeout on her arm on 11Oct2021 after vaccine on 07Oct2021; top to elbow, and was still feverish. Dermatologist felt it had a system allergy to 2nd and 3rd vaccine, but not sure. For Covid 19 vaccine #1 in Jan2021, it had only mild symptoms. For Covid 19 vaccine #2, about 8-10 hrs after vaccine, the patient had fever over 102, worked hard at reducing fever. The patient got dehydrated very easily. For Covid 19 vaccine #3, on 07Oct2021, the patient was fine for first 9-10 hrs then fever set in. The patient was in ER 24 hrs later, after working hard at reducing it on her own; got too dehydrated. The patient felt pretty bad for about a week. She rested as much as possible. There was major rash from vaccine on 11Oct2021; it itched and hurt a lot. The patient was not sure if preservatives or salts, but she did have issues with potassium phosphate (intolerance). Possibly, doses could be reduced to half after 1st vaccine to top off 1st vaccine felt like vaccine overload. The patient was asking if antibodies test would show if she was protected enough at the point they need another vaccine. The patient did want to stay protected and protect others. The patient underwent the following laboratory tests and procedures: adjusted calcium: 9 mg/dl; alanine aminotransferase: 61 IU/l, notes: Normal; anion gap: 9, notes: Normal; aspartate aminotransferase: 68 IU/l, notes: High (H); basophil count: 0 k, notes: Nornal; basophil percentage: 0.3 %, notes: Normal; blood albumin: 3.8 g/dl, notes: Normal; blood alkaline phosphatase: 73 IU/l, notes: Normal; blood bilirubin: 0.5 mg/dl; blood calcium: 8.8 mg/dl, notes: Low(L); blood chloride: 99 mEq/l, notes: Low (L); blood creatinine: 0.8 mg/dl, notes: Normal; blood glucose: 141 mg/dl, notes: High (H); blood potassium: 4.1 mEq/l, notes: Normal; blood sodium: 136 mEq/l; 135 mEq/l, notes: Low (L); blood urea: 15 mg/dl, notes: Normal; body temperature: 103, notes: fever got up to 103; carbon dioxide: 27 mEq/l, notes: Normal; creatinine renal clearance: 81.8 ml/min; 66.4 ml/min, notes: Normal; eosinophil count: 0 k, notes: Normal; eosinophil percentage: 0.5 %, notes: Normal; glomerular filtration rate: >60, notes: N/A; haematocrit: 39.7 %, notes: Normal; haemoglobin: 126 g/dl, notes: Normal; immature granulocyte count: 0.03 k, notes: Normal; immature granulocyte count: 0.5 %, notes: High (H); lymphocyte count: 0.5 k, notes: Normal; lymphocyte percentage: 7.5 %, notes: Low (L); mean cell haemoglobin: 27 pg, notes: Normal; mean cell haemoglobin concentration: 31.7 g/dl, notes: Low (L); mean cell volume: 85.2 fl, notes: Normal; mean platelet volume: 11.5 fl, notes: Normal; monocyte count: 0.7 k, notes: Normal; monocyte percentage: 11.9 %, notes: Normal; neutrophil count: 4.9 k, notes: Normal; neutrophil percentage: 79.3 %, notes: High (H); platelet count: 175k, notes: Normal; protein total normal: 7.5 g/dl, notes: Normal; red blood cell count normal: 4.66m, notes: Normal; red cell distribution width: 14.1 %, notes: Normal; red cell distribution width: 43.8 fl, notes: Normal; white blood cell count normal: 6.1 k, notes: Normal. Therapeutic measures were taken as a result of dehydration, nausea, pyrexia, feeling abnormal, rash pruritic, hypersensitivity. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Name: CORRECTED CALCIUM; Test Result: 9 mg/dl; Test Name: SGPT/ALT; Result Unstructured Data: Test Result:61 IU/l; Comments: Normal; Test Name: ANION GAP; Result Unstructured Data: Test Result:9; Comments: Normal; Test Name: SGOT/AST; Result Unstructured Data: Test Result:68 IU/l; Comments: High (H); Test Name: BASOPHIL #; Result Unstructured Data: Test Result:0 k /mm3; Comments: Nornal; Test Name: BASOPHIL %; Test Result: 0.3 %; Comments: Normal; Test Name: ALBUMIN; Result Unstructured Data: Test Result:3.8 g/dl; Comments: Normal; Test Name: ALKALINE PHOSPHATASE TOTAL; Result Unstructured Data: Test Result:73 IU/l; Comments: Normal; Test Name: TOTAL BILIRUBIN; Test Result: 0.5 mg/dl; Test Name: CALCIUM; Test Result: 8.8 mg/dl; Comments: Low(L); Test Name: CHLORIDE; Result Unstructured Data: Test Result:99 mEq/l; Comments: Low (L); Test Name: CREATININE; Test Result: 0.8 mg/dl; Comments: Normal; Test Name: GLUCOSE; Test Result: 141 mg/dl; Comments: High (H); Test Name: POTASSIUM; Result Unstructured Data: Test Result:4.1 mEq/l; Comments: Normal; Test Name: CORRECTED SODIUM; Result Unstructured Data: Test Result:136 mEq/l; Test Name: SODIUM; Result Unstructured Data: Test Result:135 mEq/l; Comments: Low (L); Test Name: BLOOD UREA NITROGEN; Test Result: 15 mg/dl; Comments: Normal; Test Name: Body temperature; Result Unstructured Data: Test Result:103; Comments: fever got up to 103; Test Name: CARBON DIOXIDE; Result Unstructured Data: Test Result:27 mEq/l; Comments: Normal; Test Name: EST CRCL/COCKCROFT-GAULT/ABW; Result Unstructured Data: Test Result:81.8 ml/min; Test Name: EST CRCL/COCKCROFT-GAULT/IBW; Result Unstructured Data: Test Result:66.4 ml/min; Comments: Normal; Test Name: EOSINOPHIL #; Result Unstructured Data: Test Result:0 k /mm3; Comments: Normal; Test Name: EOSINOPHIL %; Test Result: 0.5 %; Comments: Normal; Test Name: GLOMERULAR FILTRATION BY MDRD; Result Unstructured Data: Test Result:>60; Comments: N/A; Test Name: HEMATOCRIT; Test Result: 39.7 %; Comments: Normal; Test Name: HEMOGLOBIN; Result Unstructured Data: Test Result:126 g/dl; Comments: Normal; Test Name: IMMATURE GRANULOCYTES #; Result Unstructured Data: Test Result:0.03 k /mm3; Comments: Normal; Test Name: IMMATURE GRANULOCYTES %; Test Result: 0.5 %; Comments: High (H); Test Name: LYMPHOCYTE #; Result Unstructured Data: Test Result:0.5 k /mm3; Comments: Normal; Test Name: LYMPHOCYTE %; Test Result: 7.5 %; Comments: Low (L); Test Name: MEAN CELL HGB; Test Result: 27 pg; Comments: Normal; Test Name: MEAN CELL HGB CONCENTRATION; Result Unstructured Data: Test Result:31.7 g/dl; Comments: Low (L); Test Name: MEAN CELL VOLUME; Result Unstructured Data: Test Result:85.2 fL; Comments: Normal; Test Name: MEAN PLATELET VOLUME; Result Unstructured Data: Test Result:11.5 fL; Comments: Normal; Test Name: MONOCYTE #; Result Unstructured Data: Test Result:0.7 k /mm3; Comments: Normal; Test Name: MONOCYTE %; Test Result: 11.9 %; Comments: Normal; Test Name: NEUTROPHIL #; Result Unstructured Data: Test Result:4.9 k /mm3; Comments: Normal; Test Name: NEUTROPHIL %; Test Result: 79.3 %; Comments: High (H); Test Name: PLATELET COUNT; Result Unstructured Data: Test Result:175k /mm3; Comments: Normal; Test Name: TOTAL PROTEIN; Result Unstructured Data: Test Result:7.5 g/dl; Comments: Normal; Test Name: RED BLOOD CELL; Result Unstructured Data: Test Result:4.66M /mm3; Comments: Normal; Test Name: RDW COEFFICIENT OF VARIATION; Test Result: 14.1 %; Comments: Normal; Test Name: RDW STANDARD DEVIATION; Result Unstructured Data: Test Result:43.8 fL; Comments: Normal; Test Name: WHITE BLOOD CELL; Result Unstructured Data: Test Result:6.1 k /mm3; Comments: Normal
Aktuelle Erkrankungen: Arrhythmia; Blood cholesterol abnormal; Blood pressure high; Hashimoto's thyroiditis; Osteopenia; Osteoporosis; Type II diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Bradycardia; Dry eyes; Immunocompromised; Intolerance to excipients; Sickness (felt like all symptoms of COVID-19); Sleep apnea
Andere Medikamente: PREDNISOLONE ACETATE; SYNTHROID; METFORMIN; CRESTOR; TOPROL; LISIPRIL; FLECAINIDE ACETATE; XANAX; CALCIUM + VIT D
Allergien: -
Vorherige Impfungen: -

VAERS 1897479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 57,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 13.04.2021
Beginn: 23.11.2021
Tage bis Beginn: 224,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 Dehydration Nausea Vomiting

Symptomtext

Hospital admission nausea, vomiting, and dehydration post op now with COVID on admit.

Weitere VAERSDATA-Felder

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

VAERS 1890565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 62,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 07.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Condition aggravated Hyperaesthesia Nerve conduction studies normal Neurological examination Pain in extremity Paraesthesia Vitamin B6 increased

Symptomtext

5 days after the injection (April 12) I noticed pain/tingling in both hands and both feet. In addition, some places on hands and feet were very sore to the touch. Symptoms increased over the next week; visited primary care Dr on April 21. Symptoms escalated and visited ER on April 24. Consulted with pain specialist May 4, neurologist May 6 and had nerve conductivity tests May 13.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: May 13: Nerve conductivity tests negative. Lots of blood tests over a several month period of time and the only interesting finding was elevated levels of vitamin B6. Those levels have returned to normal although symptoms persist. Symptoms being managed by Lyrica 25mg three times per day.
Aktuelle Erkrankungen: None
Vorgeschichte: Low level pain in hands and feet caused by negative reaction to Cipro
Andere Medikamente: Fish oil, Metagenics Ultra Prostagen, D3, Magnesium
Allergien: Sulfa antibiotics, Cipro, Doxycline
Vorherige Impfungen: -

VAERS 1881361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: CA
Alter: 25,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 19.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / AR

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

Blindness Magnetic resonance imaging Ophthalmic migraine Ultrasound scan Visual field defect

Symptomtext

Occular migranes and roving scotomas causing partial blindness for 7 out of 30 days. Strongest symptoms during days directly after vaccine injection. No history of similar symptoms prior. Emergency medical care received at a Medical Center (out of state). Checked for retinal detachment with ultrasound (no retinal detachment found). Further medical care received at another Medical Center (with neurologist) who ordered an MRI (taken at a local imaging center) that was inconclusive. Then a visit with an Eye care Dr. locally was ordered to have an fMRI with contrast taken to investigate possible causes of the migranes and scotomas. This fMRI was not taken because symptoms had subsided and medical costs were becoming unwieldy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ophthalmic migraine
Hospital-Tage: -
Labordaten: Emergency medical care received at a Medical Center (out of state) 04/26/2021. Checked for retinal detachment with ultrasound (no retinal detachment found). Further medical care received at another Medical Center (with neurologist) who ordered an MRI (taken at a local Imaging center) that was inconclusive. Then a visit with a local Eye care Dr.) on 06/03/2021 was ordered to have an fMRI with contrast taken to investigate possible causes of the migranes and scotomas. This fMRI was not taken because symptoms had subsided and medical costs were becoming unwieldy.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1880639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: MN
Alter: 93,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 24.03.2021
Beginn: 14.04.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: UN / UN

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

Chest pain Malaise Mental status changes Pyrexia

Symptomtext

Hospitalized for mental status changes with chest pain, fever, and malaise.

Weitere VAERSDATA-Felder

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

VAERS 1877574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

moderat

Staat: PA
Alter: 40,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Electrocardiogram Electrocardiogram ambulatory abnormal Full blood count Heart rate abnormal Metabolic function test Palpitations Ventricular extrasystoles

Symptomtext

palpitations after first dose made MUCH worse after second dose, heart rate issues, frequent PVCs noted in Holter monitor, chest pain, heart races after exercise (frighteningly so) The Problem has not been resolved yet, I?m still suffering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CBC and Basic Metabolic panel on 10/13/21, in office ECG ON 10/13/21, 24 hour Holter monitor on 10/20-21/21, repeat CBC on 11/15/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None, not sure if I took daily supplements that time
Allergien: None
Vorherige Impfungen: -

VAERS 2574895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 17.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blood bicarbonate normal Blood fibrinogen increased Blood gases Blood pH normal COVID-19 COVID-19 pneumonia Diarrhoea Dyspnoea Fatigue Fibrin D dimer normal Nasal congestion PCO2 normal PO2 decreased Procalcitonin normal Red blood cell sedimentation rate increased SARS-CoV-2 test positive Serum ferritin increased

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/25, Pfizer, dose #1 03/18, Pfizer, dose #2 09/17, Pfizer, dose #3 09/01 pt admit to medicine cc: 3-4 weeks watery diarrhea, SOB, generalized weakness, and nasal congestion dx: COVID PNA los: 8 days 09/01 pt cc: fatigue, dyspnea exposure: unknown 09/01 ABG result: i-pH 7.41, i-PC02 35.1, i-P02 53, i-HCO3 22.2 09/01 FIBRINOGEN 515 09/01 TROPONIN I <0.016 09/01 DDIMER 0.25 09/01 FERRITIN 998.7 09/02 FIBRINOGEN: 528 09/02 DDIMER: 0.43 09/02 ESR 60 09/03 FIBRINOGEN: 414 09/03 DDIMER: 0.53 09/03 ESR 39 09/04 FIBRINOGEN: 359 09/04 DDIMER: 0.66 09/04 ESR 31 09/05 FIBRINOGEN: 308 09/05 DDIMER: 0.96 09/05 ESR 21 09/06 FIBRINOGEN: 258 09/06 DDIMER: 25.90 09/06 ESR 27 09/06 DDIMER 0.69 09/07 FIBRINOGEN: 271 09/07 DDIMER: 0.84 09/07 ESR 23 09/07 procalcitonin <0.05 09/08 FIBRINOGEN: 261 09/08 DDIMER: 0.76 09/08 ESR 18 09/09 ESR 16 09/09 DDIMER 0.69 09/13 clinically resolved 09/17 COVID swab, result: detected 09/17 SARS-COV-2 Variant Sequencing result: pending

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: 09/01 ABG result: i-pH 7.41, i-PC02 35.1, i-P02 53, i-HCO3 22.2 09/01 FIBRINOGEN 515 09/01 TROPONIN I <0.016 09/01 DDIMER 0.25 09/01 FERRITIN 998.7 09/02 FIBRINOGEN: 528 09/02 DDIMER: 0.43 09/02 ESR 60 09/03 FIBRINOGEN: 414 09/03 DDIMER: 0.53 09/03 ESR 39 09/04 FIBRINOGEN: 359 09/04 DDIMER: 0.66 09/04 ESR 31 09/05 FIBRINOGEN: 308 09/05 DDIMER: 0.96 09/05 ESR 21 09/06 FIBRINOGEN: 258 09/06 DDIMER: 25.90 09/06 ESR 27 09/06 DDIMER 0.69 09/07 FIBRINOGEN: 271 09/07 DDIMER: 0.84 09/07 ESR 23 09/07 procalcitonin <0.05 09/08 FIBRINOGEN: 261 09/08 DDIMER: 0.76 09/08 ESR 18 09/09 ESR 16 09/09 DDIMER 0.69 09/17 COVID swab, result: detected 09/17 SARS-COV-2 Variant Sequencing result: pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1869707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 15.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain upper Arthralgia Chest discomfort Dyspnoea Fatigue Gastrointestinal pain Nausea Stress cardiomyopathy Vomiting

Symptomtext

Tiredness, joint pain, severe stomach and intestinal pain, tightness in chest, nausea and vomiting, labored breathing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I went to my digestive diseases doctor and it was decided that it could have been my gallbladder. My gallbladder function was tested at 27% four years prior to this. A gallbladder surgery was scheduled for 04-26-2021 and while being put under anesthesia I had a stress cardiomyopathy and was hospitalized for four days.
Aktuelle Erkrankungen: none
Vorgeschichte: I was having episodes of tightness and pain in chest and between shoulder blades, tiredness and difficulty breathing. Went to the Hospital on November 17, 2020 and given tests for heart problems and they found none.
Andere Medikamente: Multi Vitamin, MSM 2000mg (methylsufonylmeyhane) Vitamin D-325mcg
Allergien: Neomycin, Astorvastatin, Peanuts, Bee stings
Vorherige Impfungen: Shingles vaccine, swelling, redness of arm, tiredness, joint pain, sore throat, aches. Patient was 69 yrs old. Received on or ab

VAERS 1849690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 72,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 15.09.2021
Beginn: 01.09.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Asthenia Back pain Chest pain Dyspnoea Fatigue Malaise Muscular weakness Pain

Symptomtext

Extreme fatigue, SOB especially with exertion, ?dull ache in chest and into back & shoulders, ?dragging?. Lack of energy, muscle weakness, joint pain, general malaise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None at this time.
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia, diabetes, heart issues, skin cancer
Andere Medikamente: Certrazine, asa, coenzyme Q-10, gemfibrozil,sertraline, ezetimibe, Novolog, Tresiba
Allergien: PCN, multiple insulins (except the ones currently taking), and statins.
Vorherige Impfungen: 72 03/01/21, 03,23,21 Pfizer vaccines

VAERS 1849418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: IA
Alter: 65,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 09.04.2021
Beginn: 12.08.2021
Tage bis Beginn: 125,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Chest X-ray abnormal Cough Dyspnoea Pain Pneumonia Post-acute COVID-19 syndrome Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Pfizer Dose 1 3/19/21 (ER8730) Pfizer Dose 2 4/9/21 (EW0153) COVID Positive 8/15/21 8/15/21: The patient presents with difficulty breathing and cough. The onset was just prior to arrival. The course/duration of symptoms is constant. Degree at onset moderate. Degree at present none. The Exacerbating factors is none. The Relieving factors is none. Risk factors consist of none. Prior episodes: none. Therapy today: beta-agonist albuterol. Associated symptoms: cough. Patient was tested positive for COVID on Thursday August 12th, 2021 and was given the news the next day. Patient states that he has had problems with cough, congestion trouble breathing body aches and pains due to the COVID. Patient has had both shots and is diabetic and is currently on doxycycline. Patient states his main concern is that he is having trouble breathing. Patient takes an albuterol inhaler and states that did not help much. 8/17/21:Patient was admitted from the ER on August 15th, 2021 with bilateral pneumonia due to post COVID syndrome. Patient states that when he would walker try to do anything exertion he would cough become short of breath very easy. The chest x-ray showed a bilateral pneumonia patient states he feels much better with IV antibiotics and breathing treatments. Patient did not require oxygen during his hospital stay and states that he was able to walking cooperate with his treatment feels comfortable going home at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: see above
Aktuelle Erkrankungen: asthma BPH CKD degenerative joint disease diabetes fatty liver HLD HTN obesity
Vorgeschichte: asthma BPH CKD degenerative joint disease diabetes fatty liver HLD HTN obesity
Andere Medikamente: albuterol 2 pufs QID PRN amlodipine 5 mg PO QD aspirin 81 mg PO QD atorvastatin 40 mg PO QD vitamin D 400 units PO QD fluticasone nasal spray both nostrils QD hydrochlorothiazide 50 mg PO QD insulin aspart 30 units SQ AC insulin glargine 85
Allergien: gemfibrozil - rash latex - rash lisinopril - cough
Vorherige Impfungen: -

VAERS 2578671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 01/26, Pfizer, dose #1 02/17, Pfizer, dose #2 09/30, Pfizer, dose #3 08/24 pt cc: rhinorrhea, dyspnea exposure: unknown 08/24 COVID swab, result: detected 09/14 COVID swab, result: not detected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 08/24 COVID swab, result: detected 09/14 COVID swab, result: not detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2599284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Mobility decreased Myalgia

Symptomtext

Myalgia INABILITY TO MORE THE LEFT ARM Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes 10 YEARS AGO A FLU VACCINE; POSSIBLY DUE TO LATEX, INFLAMMATION OF THE SITE

VAERS 2577014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 28.09.2021
Beginn: 21.08.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Ageusia Anosmia COVID-19 Chills Diarrhoea Dyspnoea Fatigue Headache Myalgia Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/16, Pfizer, dose #1 03/08, Pfizer, dose #2 09/28, Pfizer, dose #3 08/21 pt cc: chills, diarrhea, fatigue, fever, headache, loss of taste or smell, myalgias, rhinorrhea, dyspnea exposure: unknown 08/24 COVID swab, result: detected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 08/24 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1843011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: WA
Alter: 21,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 09.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

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

Asthenia Fatigue Lymphadenopathy Nausea Pain Pyrexia Tremor

Symptomtext

For about 4 days after I received this vaccination (my second dose) I experienced extreme weakness, shaking joints, nausea, swollen lymph nodes, body aches, and a fever reaching up to 103 degrees. Looking back I wish I would have gone into urgent care or something but I didn't think they could do much for me and it eventually subsided so I felt as if I had a bad cold that lingered for weeks. As of now, I am still experiencing body aches, fatigue, and my lymph nodes are still swollen specifically in my neck (they can sometimes be seen pulsing).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma diagnosed at age 18
Andere Medikamente: Venlaflaxine, iron supplements, vitamin c, women's multi vitamin
Allergien: mucinex/other cough medicines
Vorherige Impfungen: I had a rash after recieving the chick pox vaccine in kindergarten and again when I received the booster at 18

VAERS 1840245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 01.05.2021
Beginn: 29.10.2021
Tage bis Beginn: 181,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Confusional state Cough Dizziness Dyspnoea Fatigue Mobility decreased Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID first dose 4/3/2021. Patient is a fully vaccinated 66-year-old male with past medical history of Parkinson's, CVA with residual right-sided weakness, DM 2, HTN, and anxiety/depression who presents with generalized weakness. Patient with 9 day history of positive COVID test and symptoms including but not limited to nonproductive cough, congestion, slight fever, fatigue, SOB, confusion, and dizziness. For the past 3 days patient has been increasingly fatigued unable to get out of bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID + 10/20/2021
Aktuelle Erkrankungen: -
Vorgeschichte: BPH, diabetes, constipation, hypertension, parkinson's disease, stroke
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1840058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: PA
Alter: 41,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 14.04.2021
Beginn: 16.10.2021
Tage bis Beginn: 185,0
Dosis: 1
Route/Site: IM / LA

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

Bronchitis COVID-19 Chills Cough Diarrhoea Dyspnoea Exposure to SARS-CoV-2 Fatigue Headache Nausea Oropharyngeal pain Pain Paranasal sinus discomfort Pyrexia SARS-CoV-2 test positive Sinus pain Viral upper respiratory tract infection Vomiting

Symptomtext

10/18/2021 Urgent Care - CRNP Exposure to SARS-associated coronavirus + Cough ? Sore Throat ? Fever ? Fatigue ? Shortness of Breath Patient was seen today for cough, sore throat, fever, fatigue and shortness of breath. Diagnoses and all orders for this visit: Exposure to SARS-associated coronavirus - POCT COVID-19 PCR Patient presented to the urgent care with cough, sore throat, fever fatigue and shortness of breath for 1 to 2 days. Patient was vaccinated for COVID-19. Covid point-of-care test was run during this visit. Most likely viral upper respiratory infection/bronchitis. Placed the patient on 5-day course of prednisone and albuterol inhaler. Also prescribed Tessalon Perles. Informed patient presents to improve in the next 2 to 3 days to follow-up with her PCP. I notified the patient that she is positive for COVID-19 and that she needs to stay quarantine for 10 days. Informed the patient that her symptoms become life-threatening such as increased shortness of breath or difficulty breathing that she needs to go to the ER for further evaluation. Patient Education There are no Patient Instructions on file for this visit. History Chief Complaint Patient presents with ? Cough sx's started yesterday ? Sore Throat ? Fever pt reports temp of 101.2 yesterday ? Fatigue ? Shortness of Breath Patient is a 41 y.o. female HPI Pt presents with concerns of possible Covid 19. Pt reports the following symptoms that started 2 days ago. Sinus pain and pressure No Fever/ chills Yes Headache Yes Body aches Yes Cough Yes Sob Yes Sore throat Yes Nausea/ vomiting/ diarrhea. No Loss of taste or smell No Medications used:No Tolerating fluids:Yes Tolerating. solids:Yes Smoke exposure:No Exposed to someone who tested positive for COVID 19: No History of asthma, bronchitis, pneumonia. Yes Pt works at school district ED Discharged 10/18/2021 (2 hours) Hospital ED, MD COVID-19 & fatigue Patient is a 41 y.o. female with hx of Addison's disease, migraines, fibromyalgia, anxiety, asthma, POTS presenting to the ED with fatigue, body aches, nausea, cough. Patient is a symptoms started just yesterday. Woke up and had some body aches and chills with some increasing fatigue and a sore throat. Sore throat has since subsided, but has since developed cough. Went to urgent care earlier today where she did have a COVID-19 test that did return positive. Patient was immunized x2 doses of Pfizer in April and May. States that she does have a bit of shortness of breath, but cough continues. Given her history of pots and Addison's disease is, is concerned for the reaction her body may face and states that she gets dehydrated very easily. States that her p.o. intake has been significantly decreased over the past 24 hours, but denies any vomiting or diarrhea. Work-up largely reassuring. Patient does feel bit better after IV fluids. Otherwise cleared for discharge and advised to follow primary care provider. Offered monoclonal about infusion given possible immunosuppression given history of Addison's disease on chronic steroids, but she does not wish to have this done at this time. She has been vaccinated otherwise has reassuring vital signs including pulse oximetry. Again advised to follow primary care provider given strict precautions. She voices understanding agreed with plan.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 10/18/2021 0911 POCT COVID-19 PCR Collected: 10/18/21 0911 | Final result | Specimen: Swab from Nares POC COVID-19 PCR Detected Abnormal Lot # 1000285223 Point of Care COVID-19 PCR Testing Method Cepheid Lot Expiration Date 8/21/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Fibromyalgia Orthostatic syncope Migraine without status migrainosus, not intractable, unspecified migraine type Carpal tunnel syndrome on left Intractable migraine with aura without status migrainosus Respiratory Asthma, mild intermittent Asthma Circulatory Tachycardia Pre-syncope POTS (postural orthostatic tachycardia syndrome) Genitourinary Genital herpes simplex Ovarian cyst, left Musculoskeletal Arthritis Endocrine/Metabolic Hypothyroidism due to Hashimoto's thyroiditis Adrenal insufficiency (Addison's disease) Hashimoto's thyroiditis Hematologic Inguinal lymphadenopathy Infectious/Inflammatory COVID-19 Other Anxiety Insomnia
Andere Medikamente: Outpatient Medications albuterol HFA (VENTOLIN HFA) 90 mcg/actuation inhaler clindamycin (CLEOCIN) 2 % vaginal cream cyclobenzaprine (FLEXERIL) 5 mg tablet dexAMETHasone (DECADRON) 4 mg/mL injection DULoxetine (CYMBALTA) 20 mg capsule
Allergien: Sertraline HclNausea And Vomiting, Palpitations AmoxicillinRash AzithromycinDiarrhea, Nausea Only Percocet [Oxycodone-acetaminophen]Nausea and Vomiting
Vorherige Impfungen: -

VAERS 1839903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: ME
Alter: 52,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 07.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Anxiety Arthralgia Asthenia Condition aggravated Depression Fatigue Hyperarousal Injection site pain Post-traumatic stress disorder

Symptomtext

PTSD response with severe anxiety, depression, and hyperarousal. Pain at injection site, joint pain systemic, weakness, exhaustion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: PTSD
Vorgeschichte: Asthma, PTSD
Andere Medikamente: Fluoxetine 40mg qd, Loratadine 10 mg qd, Simvastatin 40mg dq, Androgel 1.62% 4 pumps qd, doTERRA PB Assist qd, doTERRA TerraZyme 2 qd, doTERRA xEOmega 2 qd, doTERRA OnGuard+ prn, doTERRA Alpha CRS+ 2 qd, doTERRA Microplex VMz 2 qd, doTERRA
Allergien: PCN (never verified-advised not to take as a child), animal dander, hay, pollen, adhesives such as bandages, Neosporin, wool, & other environmental allergens.
Vorherige Impfungen: -

VAERS 1839327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 03.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chest pain Discomfort Myalgia Pain Speech disorder

Symptomtext

Severe body aches and pressure on my body; Severe body aches and pressure on my body; Muscle pain in the chest and in the upper back in the shoulders; Having a lot of trouble being able to talk; really hurts my chest; This is a spontaneous report from contactable consumer. This consumer (patient) reported that: A patient of an unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Lot Number: EW0153) via an unspecified route of administration on an unspecified date as dose 1, single for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced severe body aches and pressure on my body, muscle pain in the chest and in the upper back in the shoulders, having a lot of trouble being able to talk and really hurts my chest. The patient received first dose Pfizer Covid-19 Vaccine on Monday about 4-5 days ago 16:15 in the afternoon. The patient was still experiencing severe body aches and pressure on body, muscle pain in the shoulders and in the chest and especially in the upper back in the shoulders and in the chest and was wondering if that was normal for 5 days away. The patient was having a lot of trouble being able to talk. It really hurts the patient's chest. The outcome of the events was unknown. Information on Lot/Batch number was available. Additional information has been requested. No Follow-up attempts completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1837055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: PA
Alter: 82,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 15.04.2021
Beginn: 15.10.2021
Tage bis Beginn: 183,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain COVID-19 Chest pain Cough Diarrhoea Dizziness Dyspnoea Exposure to SARS-CoV-2 Musculoskeletal stiffness Nausea Rash SARS-CoV-2 test positive Upper respiratory tract infection Vomiting

Symptomtext

Office Visit 10/18/2021 Urgent Care PA-C Family Medicine Exposure to COVID-19 virus +1 more Dx Cough Reason for Visit 10/18/2021 Chief Complaint Patient presents with ? Cough mild , exposure to covid HPI Assessment/Plan Pt was seen today for cough. Diagnoses and all orders for this visit: Exposure to COVID-19 virus - COVID-19 PCR URI, acute Pt is a 82 y.o. male Presents with slight cough x 3 days. Symptoms are stable .Patient has tried cough suppressant with moderate relief. Patient denies fever/chills, ST, nausea/vomiting, diarrhea, abdominal pain, rash, neck stiffness, chest pain, shortness of breath, dizziness. +covid exposure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/18/2021 1428 COVID-19 (SARS CoV-2 RNA, RT-PCR) Collected: 10/18/21 1428 | Final result | Specimen: Swab from Nares COVID-19 SARS CoV-2 RNA Detected Abnormal 10/18/2021 1428 COVID-19 PCR Collected: 10/18/21 1428 | Final result | Specimen: Swab from Nares
Aktuelle Erkrankungen: -
Vorgeschichte: Digestive Tubular adenoma of colon
Andere Medikamente: finasteride (PROSCAR) 5 mg tablet fluticasone propionate (FLONASE) 50 mcg/actuation nasal spray fluticasone propionate (FLONASE) 50 mcg/actuation nasal spray lisinopril (PRINIVIL,ZESTRIL) 2.5 mg tablet primidone (MYSOLINE) 50 mg tablet
Allergien: NKA
Vorherige Impfungen: -

VAERS 1835761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: -
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 04.05.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Chest pain

Symptomtext

kind of pain in chest; This is a spontaneous report received from a contactable consumer. A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EW0153) via an unspecified route of administration at left arm on 04May2021 as dose 2, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EW0171) via an unspecified route of administration at left arm on 13Apr2021 as dose 1, single for COVID-19 immunisation. The patient had kind of pain in chest and reporter wanted to know these side effects were severe. Reporter confirmed that side effects were after taking the second dose. The outcome of event was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1835733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: NJ
Alter: 85,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 20.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Blood pressure increased Hypersensitivity Tachycardia

Symptomtext

rapid heartbeat; blood pressure rising; she did take the first shot and her allergies were not as bad; This is a spontaneous report from a contactable consumer (patient herself). An 85-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot number: EW0153, Expiry date was not reported), via an unspecified route, administered in left arm on 20Apr2021 at 11:00 (Age at vaccination 85-year-old) as DOSE 1, SINGLE for COVID-19 immunization. The vaccination facility type was pharmacy or drug store. Medical history included asthma (asthma was bad this year since the beginning of Jan2021) to an unknown date and arthritis from an unknown date and unknown if ongoing. Concomitant medications included prednisone ongoing, been taking for maybe 4 or 5 years for asthma and arthritis, formoterol fumarate (SYMBICORT) taken for asthma, start and stop date were not reported. The patient experienced rapid heartbeat, blood pressure rising on 20Apr2021, and she did take the first shot and her allergies were not as bad on an unspecified date in Apr2021. It was reported that she did take the first shot and her allergies were not as bad. The asthma did not get bad because of the vaccine. The asthma had been bad this year since the beginning of January. Patient stated that the symptom she experienced was a rapid heartbeat. She had a thing that she puts her finger in and her heart rate went over 100 and it was about 110. Her blood pressure was rising on 20Apr2021 and so she took an extra half of blood pressure medication, and she took a medication called Librium that she takes for her nerves, 2 pills that were 5mg each and so her heart racing only lasted an hour in a half and she laid down and it subsided. Rapid heartbeat started about an hour after she got home and once it went away which it lasted about hour in a half and was annoying and scary, but it finally went away after she laid down and took medicine. she felt was relevant to the blood pressure that was rising and rapid heartbeat she experienced after receiving the COVID 19 vaccine. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient received treatment for rapid heartbeat and blood pressure rising. The clinical outcome of the event she did take the first shot and her allergies were not as bad was unknown and rest of the events was resolved on 20Apr2021. No follow-up attempts are needed. No further information is expected.

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Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Asthma (asthma was bad this year since the beginning of Jan2021)
Andere Medikamente: PREDNISONE; SYMBICORT
Allergien: -
Vorherige Impfungen: -

VAERS 1835687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: TN
Alter: 62,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Body temperature COVID-19 Chills Fatigue Headache Lethargy Migraine Nausea Oral herpes Photosensitivity reaction Pyrexia Sinus pain Vaccination site pain Vomiting

Symptomtext

light sensitive; fever; lethargic; Fever blister; she vomited once; Tiredness; Chills; headache; Sinus pain; sensitive to light like with a migraine; Nausea; injection site pain; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 62-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number: EW0153), via an unspecified route of administration, administered in Arm Left on 19Apr2021 (at the age of 62-years-old) as DOSE 1, SINGLE for covid-19 immunization. Medical history included gastro oesophageal reflux disease, blood cholesterol increased, hypertension, hypothyroidism, gout from an unknown date and unknown if ongoing, gall bladder out in Nov2019, She was taking Prilosec after her gallbladder was out and transitioned to Esomeprazole, covid-19 in 12Jan2021, she has also had shingles, tetanus, and plans to get her second pneumonia vaccine. Concomitant medications included levothyroxine sodium (LEVOTHYROXINE SODIUM) taken for hypothyroidism from 1995 and ongoing, esomeprazole (ESOMEPRAZOLE) taken for gastro oesophageal reflux disease from Jun2019 and ongoing; pravastatin sodium (PRAVASTATIN SODIUM) taken for blood cholesterol increased from Jan2004 and ongoing; acetylsalicylic acid (BABY ASPIRIN) taken for cardiac disorder from 2004 to an unspecified stop date; valsartan (VALSARTAN) taken for hypertension from Mar2020 to an unspecified stop date; allopurinol (ALLOPURINOL) taken for gout from Dec2019 to an unspecified stop date. The patient reported that she had the Pfizer Covid vaccine Monday 19Apr2021 and she had all of the side effects normally listed such as tiredness, headache but more like a migraine because she became light sensitive, injection site pain, and later in call mentioned sinus pain, fever, nausea, chills, and sensitivity to light. She noted that she did not have swollen lymph nodes or diarrhea that is listed. Patient described the tiredness was so extreme it was to the point of being lethargic and that it was for 30 hours off and on because she slept until the next day. She describes all of these symptoms as way worse than when she had COVID. Today is the first day that she has got out for an hour to run quick errands. She was less functional with the vaccine than she was with COVID. She reports that she tested positive for COVID 12Jan2021. The patient stated that she was told that you needed to wait 90 days from when you test positive for COVID until you get your first shot and that she actually waited 97 days. She was wondering if she had antibodies and was the shot made it harder on her body. It was reported that the patient started out real bad as shaky chills. Her chills might started in the middle of the night Monday night, 19APR2021, as she woke up during the night thinking she was cold, but her awareness of it was Tuesday morning about 6am. She reported that she had the vaccine around 2pm and it was about 16 hours later when she experienced chills. She reported the chills lasted a few hours and then went away later when she had fever. She reports her normal temp was 97.6 and that it went up to 98.8 or 98.9 at one time. The patient also had injection site pain did not bother her because she had been getting flu shots for 20 years. She described her injection site pain as it started the same night she got her vaccine, Monday, 19Apr2021 and felt like her previous vaccines with usual muscle soreness. She notes that she gets the flu shot every year and she has also had shingles, tetanus, and plans to get her second pneumonia vaccine and she know what to expect with that. Tuesday and Wednesday the light bothered her. She reported that she got headaches all the time and she was not sure if it was because the weather changed and also mentioned menopause or hypothyroid as possibilities for some symptoms. She reports her headaches on Tuesday and Wednesday were stronger than usual ones and that she has migraines too. She explained that the headache was a couple of times Tuesday but all night Wednesday and that she had sinus pain as well. She reported that hot wet cloths helped with the sinus pain. She reported the tiredness started 20Apr2021 and was ongoing. She clarified that it was severe on Tuesday and reported it was noon on Wednesday when she felt more like herself. Right now the tiredness was not extreme. The patient described that the tiredness was so extreme it was to the point of being lethargic and that it was for 30 hours off and on because she slept until the next day. All of these symptoms were as way worse than when she had COVID. She was trying to get her stamina up. She can do a few things, but then has to rest. The patient had tiredness and she took Tylenol, but tried not to because she heard it was best not to. She reported that she took Tylenol Gel Caps Rapid Release 500mg gel capsules, NDC: 50580-488-10, Expiry: Sep2022. She took 2 at the time. She only probably took them two or three times on Tuesday and Wednesday. She might have taken it once on Thursday and it took the edge off the headache because she was still had waves of the headache. The patient was sensitive to light like with a migraine: did not want to keep her eyes open. The light was too bright. When the sun was coming in the room it bothered her eyes. She threw up her evening medications Tuesday night. She did not try taking it anymore that day. She takes Levothyroxine in the morning. Her nausea started Tuesday, she vomited once Tuesday night. Tuesday all she could eat was one of those little cups of jello that you get at the store and gingerale that made it worse. She sipped on water. On Tuesday evening when she was taking most of her medicines and she was taking more Tylenol she drank too much water and immediately it came back on her. She reports the nausea was strong on Tuesday and gradually improved and by Thursday was completely gone. Yesterday she noticed fever blisters. Her immune system took a knocking down. She used Abreva to treat them. She clarified that today they were worse. She thought she caught it in time because she could only see a little red spot, but as the day continued there are five little blisters. She described them as 5 little blisters that sting. She had hoped that the Abreva would stop them immediately but it didn't. She clarified that the injection site pain was still there but not noticeable unless you touch it. The patient did not have chills or a fever now. The Tylenol resolved the fever. Headache had resolved on 21Apr2021. The patient was concerned about the second COVID Vaccine because her symptoms were so bad after the first shot and that she heard that if you have already had COVID that you have antibodies and you may not need to take the second shot. She heard of people giving plasma 6 months after having COVID and having antibodies. She was not sure if Pfizer or the CDC know that. The patient underwent lab tests and procedures which included covid-19 was positive on 12Jan2021, normal temp is 97.6 and that it went up to 98.8 or 98.9 at one time on 20Apr2021. The outcome of headache, sensitive to light like with a migraine recovered on 21Apr2021, chills on 20Apr2021, nausea on 22Apr2021, fever and lethargic on unspecified date, unknown for light sensitivity, vomited, Sinus pain, not recovered for fever blister and recovering for injection site pain and tiredness. No follow-up attempts are needed. No further information is expected.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20210420; Test Name: normal temp; Result Unstructured Data: Test Result:98.8 or 98.9; Comments: normal temp is 97.6 and that it went up to 98.8 or 98.9 at one time; Test Date: 20210112; Test Name: COVID; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Gallbladder removal (She was taking Prilosec after her gallbladder was out and transitioned to Esomeprazole); GERD; Gout; High cholesterol; Hypertension; Hypothyroidism; Shingles (she has also had shingles, tetanus, and plans to get her second pneumonia vaccine); Tetanus (she has also had shingles, tetanus, and plans to get her second pneumonia vaccine)
Andere Medikamente: LEVOTHYROXINE SODIUM; ESOMEPRAZOLE; PRAVASTATIN SODIUM; BABY ASPIRIN; VALSARTAN; ALLOPURINOL
Allergien: -
Vorherige Impfungen: -

VAERS 1832253

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge EW0153

moderat

Staat: WA
Alter: 16,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 28.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Electrocardiogram Palpitations

Symptomtext

Racing heart rate even when lying down. Normal resting heart rate is less than 60, she was over 150bpm. Bilateral blood pressures were equal, no other symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Followup appointment with cardiologist and EKG
Aktuelle Erkrankungen: N/a
Vorgeschichte: Asthma
Andere Medikamente: Miralax, multi-vitamin
Allergien: N/a
Vorherige Impfungen: -

VAERS 1831328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 40,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 04.05.2021
Beginn: 08.05.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Chest pain Dyspepsia Lymphadenopathy

Symptomtext

Heartburn; Pain in my chest; Swollen lymph nodes; This is a spontaneous report from a contactable consumer (Patient). A 40-year-old male received second dose of BNT162B2 (PFIZER-BIONTECH m-RNA COVID-19 VACCINE, formulation: Solution for injection, Lot number: EW0153 and expiry date was not reported), via an unspecified route of administration into left arm on 04May2021 (At the age of 40-year-old) as Dose 2, single for COVID-19 immunization. Medical history included High Blood pressure. Concomitant Medications were none. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number: EW0171 and expiry date: not reported) via an unspecified route of administration into left arm on 13Apr2021 as dose 1, single (At the age of 39-year-old) for COVID-19 immunization. On 08May2021 (last night from reporting) after taking second dose of vaccine, the patient complained of two problems: One was swollen lymph nodes and other was like pain in his chest. The patient thought it was heartburn and took unspecified treatment for it. The lymph node was what gone now feel anymore, now it's not like that. The patient did not undergo any laboratory tests. Outcome of Swollen lymph nodes was recovering, and outcome for Heartburn and chest pain was not recovered. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Linked Report(s) : -PFIZER INC-2021531972 same reporter and drug, different patient and event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1829322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 18.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Decreased appetite Dizziness Dyspnoea Headache Inappropriate schedule of product administration Nausea Throat irritation

Symptomtext

Patient presents to health care clinic for COVID Pfizer booster reaction. Received booster on 10/18/2021. Reports she made an appointment on employee health website. States she received the booster without knowing it was too early. States she received Dose 1 on July 7, 2021, and dose 2 on July 18, 2021. Patient states since receiving the booster she has had severe headaches that come and go, throat burning constantly, light headedness when ambulating, loss of appetite with nausea constantly, chest pressure that comes and goes. Reports she gets lightheaded when standing for a long period of time. Patient states she ?gets winded when ambulating for a long time.? Patient states her boss told you her she received the booster too early. Patient states due to continuing to have these symptoms she came to employee health for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: sent to ER for evaluation 10/29/2021 for possible adverse reaction of COVID vaccine and to rule out cardiac processes
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: PCN, vancomycin, Phenergan, Reglan
Vorherige Impfungen: -

VAERS 1827855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0153

moderat

Staat: PA
Alter: 36,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Asthenia Chest pain Cold sweat Dysgeusia Feeling abnormal Feeling cold Headache Hyperhidrosis Lymph node pain Lymphadenopathy Menstrual disorder Musculoskeletal stiffness Nausea Vaccination site pain Vaccination site warmth

Symptomtext

got period; injection site very hot to the touch; arm very sore at injection site; gland/lymph node in arm pit of injected arm was swollen and sore; gland/lymph node in arm pit of injected arm was swollen and sore; sweating profusely; freezing but clammy; freezing but clammy; Feeling run down; headache; nauseous; body stiffness, neck stiff; chest ache; blah feeling; menthol taste/feeling again but fine otherwise; This is a spontaneous report from a contactable consumer (patient). This consumer reported that a 36-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EW0153), via an unspecified route, administered in arm right on 12Apr2021 at 05:30 PM (age at vaccination was 36 year) as dose 2, single for covid-19 immunization. Medical history included asthma from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient was not pregnant at the time of vaccination. No other vaccines were recieved within 4 weeks prior to covid-19 vaccine. The patient previously took dilaudid and experienced allergy and bnt162b2 (Batch/Lot Number was not reported), via an unspecified route, administered in arm right on 19Mar2021 at 08:15 AM (age at vaccination was 36 year) as dose 1, single for covid-19 immunization and experienced menthol taste/feeling in mouth/throat, had to start supplementing formula bc milk production dropped drastically. On 12Apr2021, the patient experienced feeling of menthol taste but was fine otherwise. On 13Apr2021, freezing but clammy, freezing but clammy, feeling run down, headache, nauseous, body stiffness, neck stiff, chest ache, sweating profusely and blah feeling. On 14Apr2021, arm very sore at injection site, gland/lymph node in arm pit of injected arm was swollen and sore and injection site very hot to the touch. On 28Apr2021, got period. On 13Apr2021, the menthol feeling had gone when the patient woke up. At around 01:15 she started feeling run down, freezing but clammy, headache, nauseous, body stiffness (like the patient was in a bad accident), chest ache. The patient felt asleep around 3, woke up around 5:30 sweating profusely but feeling mostly normal just a headache, blah feeling and stiff neck. On 14Apr2021, the patient woke up at 5:30 freezing again, arm was very sore at injection site and gland/lymph node in arm pit of injected arm was swollen and sore. 5:40 pm noticed injection site very hot to the touch. On 15Apr2021, the patient woke up feeling totally normal, injection site not hot at all, arm was still a little sore where injection was and arm pit was still sore. On 28Apr2021, the patient got her period even though she was nursing which she have never had. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient was not tested for COVID-19. The outcome of the event injection site very hot to the touch was recovered on 15Apr2021; menthol taste/feeling again but fine otherwise was recovered on 13Apr2021; while outcome of all other events was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthmatic
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1823967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0153

moderat

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 09.04.2021
Beginn: 09.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Chills Dyspnoea Headache Malaise Pain Pyrexia

Symptomtext

severe chills; fever; all over body aches; shooting pain in joints and back of head; headache/shooting pain in back of head; shortness of breath; general malaise; This is a spontaneous report from a contactable consumer (patient). This 34-year-old female patient (non pregnant) received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Batch/Lot Number: Ew0153) on 09Apr2021at 10:30 via an unspecified route of administration in the left arm as DOSE 2, SINGLE for COVID-19 immunisation (age at vaccination:34-years-old). The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccination. The patient did not have Covid prior vaccination neither covid tested post vaccination. The patient's other medical history included: OCD, and complex PTSD. Patient reported known allergy to Nickel. Patient took Celexa and lorazepam within 2 weeks of vaccination. Previously the patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Batch/Lot Number: En6207) on 19Mar2021at 10:15 via an unspecified route of administration in the left arm as DOSE 1, SINGLE for COVID-19 immunisation. Patient did not have any past drug history.On 09Apr2021, at 22:00 the patient experienced severe chills, fever, all over body aches, shooting pain in joints and back of head, headache, shortness of breath, and general malaise. Patient did not receive any treatment for the events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Nickel sensitivity; Obsessive-compulsive disorder; Post-traumatic stress disorder (other medical history complex ptsd)
Andere Medikamente: CELEXA [CELECOXIB]; LORAZEPAM
Allergien: -
Vorherige Impfungen: -