VAERS Reports pfizer EL9267

VAERS 2719939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 47,0
Geschlecht: M
Eingang: 01.12.2023
Impfdatum: 24.02.2021
Beginn: 05.01.2022
Tage bis Beginn: 315,0
Dosis: 2
Route/Site: IM / UN

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

Acute respiratory failure COVID-19 Dyspnoea Infection Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient tested positive for Covid-19 a few days PTA. Patient started to have worsening SOB and came to the ER when his o2 sat was 85%. Patient was diagnosed with acute hypoxic respiratory failure due to pneumonia secondary to Covid-19 infection. Patient received steroids, vitamin supplements, antibiotics, Remdesivir. Patient was discharged home with home o2.

Weitere VAERSDATA-Felder

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

VAERS 2716122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 79,0
Geschlecht: F
Eingang: 21.11.2023
Impfdatum: 13.02.2021
Beginn: 09.01.2022
Tage bis Beginn: 330,0
Dosis: 2
Route/Site: IM / UN

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

Asthenia COVID-19 COVID-19 pneumonia Dementia Hypophagia Mental status changes Pulmonary embolism Toxic encephalopathy

Symptomtext

presents with generalized weakness. Admitted with COVID-19 pneumonia And acute pulmonary embolus. Patient noted to have altered mental status thought to be due to toxic metabolic encephalopathy in the setting of COVID-19. Seen by infectious disease and treated with remdesivir, antibiotics and steroids. She was started on Eliquis for pulmonary embolus. Respiratory status has improved and she is stable on room air. Patient had poor p.o. intake likely related to dementia and COVID. Seen by dietitian and started on Clinimix. Diet has improved some and she is eating Less than 50% of 2 meals daily.. She was started on mirtazapine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2713672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 85,0
Geschlecht: M
Eingang: 14.11.2023
Impfdatum: 23.02.2021
Beginn: 17.12.2021
Tage bis Beginn: 297,0
Dosis: 2
Route/Site: IM / UN

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

Acute respiratory failure Asthenia COVID-19 Dyspnoea Fatigue Fibrin D dimer increased Hypoxia Liver function test increased SARS-CoV-2 test negative

Symptomtext

Comes in with worsening SOB and weakness, dyspnea, fatigue. Acute respiratory failure with hypoxia (HCC) -- patient with recent COVID, however repeat COVID testing here has been negative. Continued Lovenox for positive D dimer, Patient seen for respiratory complaints and thought to have COVID. He did require oxygen for a short while. He was able to be weaned down and did not qualify for home oxygen. He had mild elevation in his LFTs which improved during admission. D-dimer was high but he was negative for blood clot. He had a positive blood culture for a contaminant. He was covered with antibiotics while in hospital. Patient felt better was really wanting to go home. He was discharged on oral antibiotics

Weitere VAERSDATA-Felder

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

VAERS 2701433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 71,0
Geschlecht: M
Eingang: 25.10.2023
Impfdatum: 12.02.2021
Beginn: 23.01.2022
Tage bis Beginn: 345,0
Dosis: 2
Route/Site: IM / UN

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

Acute respiratory failure COVID-19 Cough Dyspnoea Hypoxia

Symptomtext

Patient presented to the ER with progressively worsening cough and SOB. Patient was diagnosed with acute respiratory failure with hypoxia secondary to Covid-19. Patient received IV steroids, remdesivir, 1 dose of tocilizumab, antibiotics. Patient was weaned down to 2L of oxygen by time of discharge. Patient was discharged home with home oxygen.

Weitere VAERSDATA-Felder

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

VAERS 2695501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 80,0
Geschlecht: M
Eingang: 13.10.2023
Impfdatum: 10.02.2021
Beginn: 22.01.2022
Tage bis Beginn: 346,0
Dosis: 2
Route/Site: IM / UN

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

Abdominal wall haematoma Acute kidney injury Acute respiratory failure Anticoagulant therapy COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest wall haematoma Chronic kidney disease Dialysis Dyspnoea Hypotension Hypoxia Intensive care Renal impairment SARS-CoV-2 test positive Shock

Symptomtext

Presented to hospital with progressively worsening SOB, tested positive for covid-19. CXR showing Covid PNA. Admitted for acute respiratory failure with hypoxia secondary to Covid-19, AKI on CKD-4. Patient was transferred on 1.30.22 for worsening renal function and dialysis needs. Oxygen requirements remained consistently high through entire length of stay - unable to wean off. Was transferred to ICU for hypotensive shock, chest/abdominal wall hematoma development while on Heparin gtt. Family agreed to comfort care on 2.8.22. Patient was not a candidate for Remdesivir due to renal function. Treated with IV Steroids and Baricitinib at hospital.

Weitere VAERSDATA-Felder

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

VAERS 2673536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: FL
Alter: 78,0
Geschlecht: M
Eingang: 18.08.2023
Impfdatum: 30.09.2021
Beginn: 02.07.2023
Tage bis Beginn: 640,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure COVID-19 pneumonia

Symptomtext

7/2/2023 - 7/13/2023 (11 days) admitted with Covid 19 pneumonia and acute respiratory failure with Hypoxia IV Decadron & Remdesivir EL9263 1/23/2021 EL9267 2/15/2021 30155BA 9/30/2021

Weitere VAERSDATA-Felder

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

VAERS 2672375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 16.08.2023
Impfdatum: 15.02.2021
Beginn: 28.01.2022
Tage bis Beginn: 347,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission/ patient expired after 2 vaccines Pfizer 1/21/21 lot# EL9261; Pfizer 2/15/21 lot# El9267

Weitere VAERSDATA-Felder

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

VAERS 2660897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 86,0
Geschlecht: M
Eingang: 26.07.2023
Impfdatum: 21.02.2021
Beginn: 07.01.2022
Tage bis Beginn: 320,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Asthenia COVID-19 pneumonia Cough Dyspnoea

Symptomtext

Presented complaining of worsening shortness of breath, cough and generalized weakness. Dx w/ COVID-19 PNA complicated by acute hypoxemic respiratory failure; tx w/steroids, O2, zinc; weaned off O2 for dc home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2656726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El9267

kritisch

Staat: AZ
Alter: 79,0
Geschlecht: M
Eingang: 16.07.2023
Impfdatum: 04.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

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

Chest X-ray Computerised tomogram thorax Death Full blood count Hypertension Prostate cancer Pulmonary hypertension

Symptomtext

Developed prostate cancer, pulmonary hypertention, death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 5,0
Labordaten: Ct thorax Chest xrays Cbc
Aktuelle Erkrankungen: Copd, emphysema, stage 3 kidneyn developed cancer prostate, high blood pressure pulmonary hypertension from vaccine
Vorgeschichte: -
Andere Medikamente: First vaccination pfizer EK5730 01/04/2021 The day after 1st dose became very sick with flu like symptoms. Went to er. At a local HCF. Was told pt. had pneumonia. And because of his copd and emphysema he would need oxygen. Pt. was not on o
Allergien: Lyrica
Vorherige Impfungen: -

VAERS 2641099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: FL
Alter: 77,0
Geschlecht: M
Eingang: 05.06.2023
Impfdatum: 03.12.2021
Beginn: 02.05.2023
Tage bis Beginn: 515,0
Dosis: 1
Route/Site: IM / -

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

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

Symptomtext

Hospitalization: 5/2/2023 - 5/7/2023 (5 days) Presentation to the ED: acute respiratory failure with hypoxia COVID + date: 5/2/23 Treatment: Remdesivir Discharge to: home. EL9267 2/15/2021 EW0186 5/24/2021 FJ1620 12/3/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: BPH, HLD, LUNG CA, RA, AAA, CKDii
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2606579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 03.03.2021
Beginn: 28.03.2023
Tage bis Beginn: 755,0
Dosis: 1
Route/Site: - / -

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

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

Symptomtext

Pt admitted on 3/20 for NSTEMI and possible evolving community acquired pneumonia. Pt was tested for COVID on admission and was negative. Pt was retested for COVID prior to discharge on 3/28 and was positive. RN stated that pt had developed a worsening cough.

Weitere VAERSDATA-Felder

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

VAERS 2599124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 19.03.2023
Impfdatum: 23.02.2021
Beginn: 21.02.2023
Tage bis Beginn: 728,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy COVID-19 Chest X-ray normal Colectomy Computerised tomogram abdomen Condition aggravated Coronary arterial stent insertion Coronary artery disease Duodenal ulcer Faeces discoloured Full blood count abnormal Glycosylated haemoglobin increased Haematochezia Haemoglobin decreased Haemostasis Hypomagnesaemia Hypophosphataemia

Symptomtext

Patient is a 88 y.o. male patient of MD with history of CAD s/p stents, hypertension, hyperlipidemia, type 2 DM, chronic anemia presented with melena and black tarry stool Acute on chronic anemia d/t ABLA with hemorrhagic shock Iron deficiency anemia Colon adenocarcinoma Presented with melena mixed with bright red blood S/p right hemicolectomy with ileocolic anastomosis on 2/9 per Dr. CT a/p on admission with post-surgical changes. Non-acute Initial CBC with Hgb 6.1 (from 7.4 week prior). Only improved to 6.5 after 2uPRBCs EGD 2/22 with 2 duodenal ulcers, hemostasis via epinephrine Has required 6 total units of PRBCs (5 units prior to EGD) Cont IV PPI bid, carafate Holding Plavix as risks > benefits (DES in 12/05/2022). Per cardiology recommendation 11/2022: Continue aspirin 81 mg daily indefinitely and clopidogrel for 3 months On empiric H pylori coverage Clinically UGIB is resolving. BMs normalizing, no further tachy response. Hgb 7.5-8, stable over last few days Surgery following, recommending to hold ASA for 14 days and then resume Acute hypoxic respiratory failure d/t COVID-19 infection AHRF multifactorial. Post-op resp insufficiency, poor O2 carrying capacity, COVID Tested positive 2/26. Symptom onset 2/26. Wife also positive. Vaccinated x2 Required 4L NC initially, , now down to room air CXR without vascular congestion or consolidation Cont supplemental O2 to maintain goal SpO2 > 92% Decadron 6mg daily for 10 days Hold off on Remdesivir Hypomagnesemia Hypophosphatemia Replaced. CAD s/p PCI of LAD with DES 12/09/2022 Per cardiology note from December patient was advised to continue DAPT for at least 3 months but according to patient was later instructed to stop aspirin and continue Plavix. Continue statin Holding plavix Hypertension Held home blood pressure meds on admission as blood pressure soft. Will restart Hyperlipidemia Continue statin Type 2 DM -A1c not at goal A1C 9.1 on 1/24/2023 on metformin, glipizide and pioglitazone at home Continue sliding scale and every 4 hours checks Lantus increased for hyperglycemia due to steroids. Nocturnal Hypoxia Suspect OSA Recommend outpatient sleep study Chronic urinary retention Has indwelling Foley catheter, will f/u with Dr Continue Flomax Severe protein caloric malnutrition

Weitere VAERSDATA-Felder

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

VAERS 2597093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 17.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Acute cardiac event Balance disorder Cerebrovascular accident Computerised tomogram abnormal Dizziness Exercise tolerance decreased Hemiparesis Hypogeusia Hyposmia Insomnia Lethargy Memory impairment Mobility decreased Muscle strength abnormal Nausea Pallor Sleep disorder Vertigo

Symptomtext

I woke up between midnight and 2:00AM with nausea and vomiting for hours. I thought that I had food poisoning at first. I also experienced severe dizziness with weakness on my right side. I had issues getting out the bed. Between 5:00 am and 6:00 am, my husband had to help me get out of the bed and to the bathroom. I was pale and lethargic. I took an 500mg aspirin around 2:30am- 3:00am. I had loss of balance, and the room was spinning. By 8:30am - 9:00am, we called to see a physician. I didn't get to see a physician till noon and was admitted to the emergency room for 12 hours. My physician said I had a cardiac event and gave me medication to stabilize it. I went to get a CT scan the next day where I was told I had a minor stroke. I have since then limited taste and smell on the right side. I also have occasional memory lapses. I don't have the same kind of muscle strength. I have muscle weakness on the left side. I can only sleep for about three to four hours. I also don't have the stamina I use to have.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Feb2021 - CT scan - Mild Stroke
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hyperthyroid; Anemic
Andere Medikamente: Macrobid; Tylenol; Ibuprofen; Naproxen
Allergien: Novocaine; Chromic; Thimerosal; Fish; Some Antibacterial Soap
Vorherige Impfungen: I am allergic to Thimerosal that is found in Flu shots.

VAERS 2574373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 86,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 12.02.2021
Beginn: 23.11.2022
Tage bis Beginn: 649,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Confusional state Death SARS-CoV-2 test positive

Symptomtext

. HAD BEEN ADMITTED 7-31-22 FOR CONFUSION AT HOSPITAL, TESTED + FOR COVID 8-16-22 AND WAS TRANSFERRED TO ANOTHER HOSPITAL ON 8-31-22 WHERE SHE REMAINED UNTIL 9-9-2022 DECEASED ON 11-23-2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PARAOXYSMAL AFIB, HTN, HYPERLIPIDEMIA, GERD, ANEMIA, there may be others
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2574294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 90,0
Geschlecht: M
Eingang: 02.02.2023
Impfdatum: 12.02.2021
Beginn: 11.12.2022
Tage bis Beginn: 667,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

This death was reported to us and we do not have a date of covid test. He had old records from that reported he had had covid in the past. I do not have the dates. I have no records of his covid illness. He passed at his residence .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: NONRHEUMATIC AORTIC INSUFFICIENCY, POORLY CONTROLLED DIABETES MELLITUS, CHRONIC KIDNEY DISEASE STAGE 3, HTN, HYPERLIPIDEMIA, CHRONIC AFIB, MILD lvh, BPH, GERD, DIASTOLIC DYSFUNCTION AND SYSTOLIC CONGESTIVE HEART FAILURE, HISTORY OF COVID,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 79,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 04.10.2021
Beginn: 02.08.2022
Tage bis Beginn: 302,0
Dosis: 1
Route/Site: IM / LA

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

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

Symptomtext

Patient had breakthrough infection and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID test on 7/12/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2566731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 77,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 21.11.2021
Beginn: 23.06.2022
Tage bis Beginn: 214,0
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 and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Positive COVId test on 6/19/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: COPD Bladder Cancer CAD
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2543554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 27.12.2021
Beginn: 24.10.2022
Tage bis Beginn: 301,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction COVID-19 Influenza virus test positive Respiratory syncytial virus test positive SARS-CoV-2 test positive

Symptomtext

Date of Admission: 10/24/2022 Date of Discharge: 10/27/2022 Admission Diagnosis: STEMI (ST elevation myocardial infarction) Myocardial infarction acute Hospital Principal Problem (Discharge Diagnoses): Acute ST elevation myocardial infarction (STEMI) of inferior wall

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: 10/24 Covid-19, Flu, RSV by NAA, Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 69,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 10.02.2021
Beginn: 02.03.2022
Tage bis Beginn: 385,0
Dosis: UNK
Route/Site: IM / LA

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

Abdominal pain COVID-19 COVID-19 pneumonia Cardiac arrest Death Dialysis Hyperkalaemia Mechanical ventilation Respiratory failure SARS-CoV-2 test positive

Symptomtext

tested positive for covid on 2-4-22 , deceased on 3-2-22 . Admitted at local hospital on 2-13-22 with resp failure, covid pneumonia and abd pain. Notes show she was transferred to alternate hospital by air ambulance and underwent cardiac arrest. on mech ventilation, hyperkalema and for dialysis. sx resp failure, cardiac arrest and hyperkalemia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, FORMER SMOKER, HTN
Andere Medikamente: -
Allergien: CEFDINIR, MORPHINE, OXYCODONE
Vorherige Impfungen: -

VAERS 2469974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 94,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 29.09.2021
Beginn: 13.02.2022
Tage bis Beginn: 137,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient had a positive COVID test on 1/31/2022 and passed away on 2/13/2022.

Weitere VAERSDATA-Felder

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

VAERS 2469694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 07.10.2021
Beginn: 26.09.2022
Tage bis Beginn: 354,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Oropharyngeal pain Procalcitonin increased SARS-CoV-2 test positive

Symptomtext

Provider d/c note: Pt is a 89 YO male with a PMHx of pacemaker for afib, HTN, T2 DM, and BPH who presented with sore throat and was diagnosed with acute hypoxic respiratory failure 2/2 COVID-19 pneumonia. Pt finished 5 days of remdesivir and was started on decadron, which he will finish 10-day course at home. Due to elevated procalcitonin and concern for superimposed bacterial infection, Pt was started unasyn and azithromycin (received Zosyn and azithromycin on 9/26) and transitioned to Augmentin. Will take 3 more doses of Augmentin after discharge. Pt initially required up to 6L NC, which were weaned to 2L NC. Pt discharged to home with home O2 in stable condition. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: COVID Detected PCR on 9/26/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia, unspecified BENIGN ESSENTIAL HYPERTENSION (401.1) Chronic combined systolic and diastolic CHF (congestive heart failure) (*) Atrial fibrillation (*) Tachy-brady syndrome (*) Digestive DISEASES OF ESOPHAGUS, REFLUX ESOPHAGITIS (530.11) Endocrine Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin Integumentary DERMATITIS, OTHER ATOPIC (691.8) Respiratory Allergic rhinitis Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxia (*) Gram-negative pneumonia (*) Urinary Stage 3a chronic kidney disease (*) Other Gout HYPRTRPHY PROSTATE BNG W/O URINARY OBST/LUTS (600.00) Arthropathy of ankle and foot Disorder of bone and cartilage S/P placement of cardiac pacemaker RSV infection Unsteady gait
Andere Medikamente: -
Allergien: Ancef, Crestor, Lipitor
Vorherige Impfungen: -

VAERS 2460667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 26.08.2021
Beginn: 20.09.2022
Tage bis Beginn: 390,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure COVID-19 Chest pain Death Dyspnoea Fatigue Metabolic encephalopathy Pyrexia SARS-CoV-2 test positive

Symptomtext

"Patient with 3 COVID vaccines who admitted to hospital with COVID detected PCR and complications of COVID who subsequently died of COVID complications. Hospice provider consult note (patient died prior to admission to hospice): ""86 YO female with a past medical history of mild chronic obstructive pulmonary disease, prior lung cancer status post LUL resection, scleroderma, Sjogren's syndrome. Followed with Dr. outpatient. Presented with fever, dyspnea and chest pain and admitted with diagnosis of COVID-19 and acute hypoxic respiratory failure. She continued worsening inpatient with increased oxygen requirement. Care service is now asked to see the patient for goals of care. At time of initial consult she is on high-flow nasal cannula oxygen 40 liters/minute at 90%. Per family report she is much more greatly fatigued today than previously. She has asked several family members to just let me go and I do not want to do this anymore. IMPRESSIONS / PLAN: Care Issues: Conversion to comfort directed end of life care 1. Medical decision making capacity: At the time of our consult the patient has limited ability for participation and medical decision making due to being in extremis. Recent history of encephalopathy over past few days. Neurology had evaluated as multifactorial metabolic encephalopathy. There are documents. Medical power of attorney 1. Is husband 2. Is daughter 2. Goals of Care: medical team had several meetings with family members today. First meeting today involved daughter, with myself and medical care chaplain. We shared some of the prognostic information from consultants and primary medical team. Shared likely end of life trajectory given her acute on chronic respiratory failure. Shared the ethics of decision making involving the patient's previously expressed personal wishes, including stating that she wanted to stop with aggressive care. Discussed a reasonable plan for symptom management and the burdens and benefits of symptom management at end of life, including down and off titration of high-flow nasal cannula oxygen. Another meeting was held this afternoon with myself, again daughter, and brothers. The patient's husband, is present however he prefers to stay at the wife's bedside. Comfort-directed End of Life care 3. Code Status: No CPR/DNI/comfort 4. Psychosocial and Spiritual Support: Chaplain was present at family meeting today and religious priest was called by hospital chaplain this afternoon 5. medical care follow up : medical Care will help to place comfort care orders. Also placed hospice referral order and asking liaison to get hospice consent signed. We can begin the process of admitting. Family has already agreed to that plan.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: COIVD Detected PCR on 9/15/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular; HTN (hypertension); Carotid artery plaque; Digestive; Gastroesophageal reflux disease without esophagitis; Endocrine; Hypothyroidism; Integumentary; Skin cancer; basal cell; Respiratory; Primary cancer of left upper lobe of lung (*); Moderate COPD (chronic obstructive pulmonary disease) (*); Acute respiratory failure with hypoxia (*); Urinary; Chronic renal failure, stage 3a (*); Other Sjogren's disease (*) Personal history of malignant; neoplasm of bronchus and lung; History of nonmelanoma skin cancer; History of lymphoma Chronic insomnia; Generalized OA; Osteoporosis; Anxiety; MGUS (monoclonal gammopathy of unknown significance); History of malignant neoplasm of head and neck; Invasive ductal carcinoma of breast, left (*); Postmenopausal; Immunocompromised (*); Metabolic encephalopathy.
Andere Medikamente: -
Allergien: Latex; Adhesive
Vorherige Impfungen: -

VAERS 2449295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: OH
Alter: 82,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 13.01.2021
Beginn: 09.03.2021
Tage bis Beginn: 55,0
Dosis: 2
Route/Site: SYR / -

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

Blood test Blood urine present Choking Computerised tomogram Death Dysphagia Dyspnoea Electrocardiogram Haemorrhage Incontinence Laboratory test Swallow study Thrombosis

Symptomtext

Shortness of breath, hard to breathe, chocking, inability to swallow, incontinence, blood clot, blood in urine, and death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 20,0
Labordaten: Several test - too many to list all dates. In and out of hospital 4 times. In patient lasting 4-7 days. FInal days included bleeding in hospital from 9/5/21 to 9/13/21 with death on 9/19/21. CT Scan, EKG, blood work, barium swallow
Aktuelle Erkrankungen: None
Vorgeschichte: Neuropathy
Andere Medikamente: Gabapentin Aspirin Areds 2
Allergien: n/a
Vorherige Impfungen: -

VAERS 2446485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 72,0
Geschlecht: M
Eingang: 15.09.2022
Impfdatum: 25.10.2021
Beginn: 20.07.2022
Tage bis Beginn: 268,0
Dosis: 1
Route/Site: SYR / LA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual received Pfizer vaccine on 02/12/2021, 03/05/2021, and 10/25/2021. They tested positive for COVID-19 on 07/20/2022 at the nursing home at which they were a resident. They experienced an episode of acute respiratory arrest and were diagnosed with COVID-19 pneumonia. They died later on the same day, on 07/20/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type II Diabetes, Coronary Artery Disease, COPD, Mixed Vascular and Neurodegenerative Dementia, Hypertension The individual was a resident of the nursing home indicated in the Address portion of this form.
Andere Medikamente: -
Allergien: Flovastatin (reaction: hair loss) Simvastatin (reaction: hair loss)
Vorherige Impfungen: -

VAERS 2433731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 60,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 12.02.2021
Beginn: 19.08.2022
Tage bis Beginn: 553,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Anaemia COVID-19 Death Dyspnoea Endotracheal intubation General physical health deterioration Haemorrhage Hypokalaemia Liver function test increased Metabolic acidosis Pneumonia SARS-CoV-2 test positive Sepsis Thrombocytopenia

Symptomtext

tested + covid 8-14-22; to er with shortness of breath, had covid 19 sepsis pneumonia, anemia , thrombocytopenia, hypokalemia and elevated lfts. H/o metastatic breast cancer. and ITP. admitted for remdesivir, decadron vitamins electrolyte replacement . Required intubation and developed acute kidney injury and etabolic acidosis and contined to decline. 8/19/22 had bleeding issues and it was decided to place her on comfort measures and expired 8-19-22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: metastatic breast cancer, diabetes mellitus, anxiety/depression, GERD, ITP , htn, vit D deficiency
Andere Medikamente: -
Allergien: allergy to aspirin -rash; penicillins - rash; carisoprodol soma - joint pain
Vorherige Impfungen: -

VAERS 2426525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 83,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 12.02.2021
Beginn: 26.07.2022
Tage bis Beginn: 529,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Balance disorder Blood creatine phosphokinase increased COVID-19 Death Disease complication Fall Humerus fracture Mallory-Weiss syndrome Respiratory distress SARS-CoV-2 test positive Upper gastrointestinal haemorrhage

Symptomtext

He had been weedeating a few days before and fell and broke humerus a few days before coming to ER for weakness and another fall. He had appt with ortho apparently. He lost balance and slid into the floor and was brought in due to this fall and weakness and had elevated cpk due to fall and laying in the floor. He incidentally tested + for covid in ER. Admitted 7-17-22. He developed resp distress and had Upper GI bleed felt to be Mallory Weiss tear and expired 7-26-22 and it was felt that he had complications from the covid. Tx rem D and decadron

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: chronic anemia, chronic kidney disease, diabetes mellitus, BPH , diabetic nephropathy, GERD, h/o Malignant neoplasm prostate, h/o vitamin D deficiency
Andere Medikamente: -
Allergien: nkda
Vorherige Impfungen: -

VAERS 2424250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 80,0
Geschlecht: F
Eingang: 30.08.2022
Impfdatum: 09.02.2021
Beginn: 05.07.2022
Tage bis Beginn: 511,0
Dosis: 1
Route/Site: UN / RA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

date of death 07-05-2022, tested + 6-18-22

Weitere VAERSDATA-Felder

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

VAERS 2424187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 75,0
Geschlecht: M
Eingang: 30.08.2022
Impfdatum: 10.02.2021
Beginn: 18.02.2022
Tage bis Beginn: 373,0
Dosis: 1
Route/Site: UN / UN

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

Acute myocardial infarction Acute respiratory failure COVID-19 Death Endotracheal intubation Pneumonia

Symptomtext

Date of death 02/18/2022; hosp notes covid 19; stemi; acute resp failure, intubated in ER , pneumonia; admit 2-4-22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, htn, cva, functional quadriplegia, CVD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2419369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: FL
Alter: 75,0
Geschlecht: M
Eingang: 24.08.2022
Impfdatum: 28.09.2021
Beginn: 14.08.2022
Tage bis Beginn: 320,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cardiovascular disorder Chronic obstructive pulmonary disease Condition aggravated Death Dyspnoea Intensive care Lung neoplasm malignant Productive cough SARS-CoV-2 test positive White blood cell count increased

Symptomtext

Hospitalization: Admitted 8/14/22, discharged 8/22/22 Presentation to the ED: Shortness of breath. elevated white blood cell count. COVID-19 + date: 08/14/22 Treatment: Patient was admitted from the ED to the ICU. He had a productive cough. Patient was treated for lung cancer, COPD, and cardiovascular problems. He was prescribed vancomycin, but was not given COVID prophalyxis. Discharge: deceased on 08/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: c.difficle collitis, hypertension, hyperlipidemia, COPD, GERD, dementia, lung cancer.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2418258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 82,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: 12.02.2021
Beginn: 23.12.2021
Tage bis Beginn: 314,0
Dosis: 1
Route/Site: UN / LA

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

Death

Symptomtext

deceased 12/23/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: had three covid vaccines, third was 9/28/2021 and had flu shot 9/16/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2415931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 66,0
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 10.02.2021
Beginn: 05.12.2021
Tage bis Beginn: 298,0
Dosis: 1
Route/Site: UN / LA

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

Death

Symptomtext

deceased on 12/05/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: pancreatic cancer s/p chemo 12-1-21; chronic renal failure, morbid obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2393236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 91,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 03.03.2021
Beginn: 24.07.2022
Tage bis Beginn: 508,0
Dosis: 1
Route/Site: - / -

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

Acute myocardial infarction COVID-19 Hypoxia Joint dislocation SARS-CoV-2 test positive

Symptomtext

Pt found to be COVID positive after being transferred from ED due to right hip dislocation and NSTEMI. Pt had no symptoms at that time, but did develop hypoxia a day later.

Weitere VAERSDATA-Felder

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

VAERS 2368929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 15.12.2021
Beginn: 19.06.2022
Tage bis Beginn: 186,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Angiogram pulmonary abnormal Anticoagulant therapy Apathy Asthenia Bladder catheterisation Bowel movement irregularity COVID-19 COVID-19 pneumonia Catheter removal Cellulitis Chest X-ray normal Compulsive hoarding Computerised tomogram abdomen abnormal Condition aggravated Culture Culture urine positive Depression

Symptomtext

Provider Summary "71 year old male living alone with past medical history significant for obesity, Type 2 diabetes mellitus, longstanding nicotine dependence, hypothyroidism following iodine therapy, hearing loss, alcoholism in remission, prostate cancer status post prostatectomy (recently found to have elevated PSA again) and poor compliance presented with difficulty urinating and having bowel movements, generalized weakness and a significant yeast infection in his groin and perineum. He was noted to have fevers, lymphopenia and lactic acidosis concerning for sepsis. He was also found to be + for COVID 19. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) Sepsis with lactic acidosis, lymphopenia and fevers with possible fungal/bacterial cellulitis Admitting provider presumed sepsis due to fungal cellulitis with possible superimposed bacterial infection. Patient was cultured up and started on IV Vancomycin, Zosyn and Fluconazole. He was continued on IV Vancomycin for possible cellulitis. He was later thought to have a UTI with an abnormal UA and was started on IV Ceftriaxone. Urine culture grew multiple different strains of bacteria with low CFU and without significant urinary symptoms other than retention, UTI was not felt to not be a valid diagnosis. Cellulitis was improving and patient was switched to Cephalexin to complete a five day course of treatment. Both Cephalexin and Fluconazole were discontinued with resolution of candidal infection and cellulitis. Acute respiratory failure with hypoxia in setting of COVID 19 pneumonia, viral sepsis and pulmonary embolism Patient developed an oxygen requirement escalating to need for 5 liters by nasal cannula with patient on no supplemental oxygen at home. Initial CXR was unremarkable. Checked D-dimer which was greater than 3000. With suspicion for pulmonary embolism, obtained CT Angio of Chest which showed pulmonary emboli in the segmental branches of the pulmonary arteries in the RUL, RML, RLL and lingula. It also showed peripheral infiltrated suspicious for COVID 19 pneumonia. Patient was started on Decadron 6 mg daily as well as IV Heparin for pulmonary emboli. He was given scheduled Albuterol, symptom and supportive care with aggressive pulmonary toilet. He was encouraged to use prone positioning. Over time, patient's respiratory status improved remarkably and he was weaned off supplemental oxygen. His IV Heparin was transitioned to Eliquis. Patient had significant hyperglycemia on Decadron and with resolution of hypoxia and most respiratory symptoms, Decadron was stopped after 7 days. Type 2 diabetes with hyperglycemia in setting of infection and steroid use - Patient with HgbA1C of 7.4 prior to admission on Metformin only. Patient developed significant hyperglycemia in the 300s on decadron. He received aggressive Insulin titration and eventually was on Lantus 40 units at night with Humalog prandial 10 units before meals with aggressive sliding scale. Patient was very resistant to considering Insulin at home. Decadron was discontinued and patient was transitioned off Insulin back on to home Metformin with addition of Glipizide. Depression, hoarding behavior and lack of motivation Patient was willing to trial Bupropion targeting his depression. The hope is that it would have a secondary benefit of promoting smoking cessation Nicotine dependence - 3 packs of small cigars daily Patient was counseled regarding benefits of smoking cessation but was not interested Generalized weakness with debility PT and OT were consulted and recommended home care with therapies on discharge Gross hematuria with anticoagulation after temporary Foley catheter placement Improved with removal of catheter Recommend follow-up this issue with Urology in addition to the elevated PSA with history of prostate cancer status post remote prostatectomy Abnormal rectosigmoid colon thickening on CT - recommend referral to GI for colonoscopy as an outpatient Issues Requiring Follow Up: (Who, what, when, and how communicated?) Follow-up pulmonary embolism and resolution of COVID 19 pneumonia with PCP, recommend three to six months of anticoagulation with follow-up with hematology; follow-up with Urology for elevated PSA with history of prostate cancer and gross hematuria; follow-up with GI for abnormal recto-sigmoid wall thickening"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: Positive PCR COVID test 6/24/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes mellitus type 2 in obese (Chronic) 9/19/2012 Hyperlipidemia (Chronic) 9/19/2012 History of prostate cancer 7/10/2014 Chronic lumbar pain (Chronic) 7/21/2015 Current smoker 7/21/2015 Bilateral leg edema (Chronic) 7/21/2015 Hard of hearing 7/21/2015 Hypothyroidism following radioiodine therapy (Chronic) 8/4/2015 History of Graves' disease (Chronic) 8/4/2015 Dilated cardiomyopathy secondary to neuromuscular disorders 4/2/2016 Morbid obesity with BMI of 45.0-49.9, adult (Chronic) 4/2/2016 Vitamin D deficiency 4/2/2016 Mild cognitive impairment 4/4/2016 Venous stasis ulcer limited to breakdown of skin without varicose veins (HCC) 5/18/2016 Cellulitis 5/29/2020 Chronic obstructive pulmonary disease 3/25/2021 Comedone 6/20/2021 Venous stasis ulcer of right calf limited to breakdown of skin without varicose veins 6/25/2021 Recurrent major depressive disorder 1/26/2022
Andere Medikamente: apixaban 5 mg (74 tabs) Dspk, Take 2 tablets by mouth twice daily for 7 days then 1 tablet by mouth twice daily 5 mg Oral 2 times daily atorvastatin calcium 40 mg Oral NIGHTLY blood sugar diagnostic Check glu qday blood-glucose meter
Allergien: None
Vorherige Impfungen: -

VAERS 2357959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 66,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 31.08.2021
Beginn: 14.10.2021
Tage bis Beginn: 44,0
Dosis: 1
Route/Site: SYR / UN

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiac arrest Death Dyspnoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/17/2021, 03/10/2021, and 08/31/2021. They tested positive for COVID-19 twice on 10/14/2021. They were also admitted to hospital on 10/14/2021 after presenting to emergency department with a primary complaint of shortness of breath. The individual experienced complications of acute kidney injury, cardiac arrest, acute hypoxic respiratory failure, COVID-19 pneumonia, and acute respiratory distress syndrome. After aggressive treatments did not improve their condition, they were transitioned to comfort care and died on 10/25/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: Two positive COVID-19 tests on 10/14/2021 despite being vaccinated and boosted.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Immunosuppression, Obesity, Chronic Kidney Disease, Hypertension, Type II Diabetes, Atrial Fibrillation, kidney transplant recipient approx 14 years before the adverse event, hypothyroidism.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2324280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 20.06.2022
Impfdatum: -
Beginn: 14.06.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Blood creatinine increased Blood gases abnormal Blood lactic acid Blood pH decreased Blood potassium increased Brain natriuretic peptide increased COVID-19 Carbon dioxide decreased Death Dyspnoea Endotracheal intubation Haemoglobin normal Hyperglycaemia Hypervolaemia Hypotension Hypoxia Influenza virus test negative

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Rec'd Pfizer Vaccines 1/23/2021 and 2/13/2021. Presented to ED 6/10 w/SOB x 1 wk. Recently vacationed. On 6/4, he developed URI sx and went to outside ER where he tested negative for COVID, but + for flu. Prescribed tamiflu and doxycycline x 5days. SOB worsened; readmitted to outside ED where he was intubated for resp dist and transferred to facility. In the ED, afebrile w/HR ranging 90s-100s, and hypotensive requiring levo. Req'd Vent settings of 100/20. Labs significant for BSG 325, Cr 4.0 (baseline around 2.5),cont K 5.9, CO2 20, procal 0.09, trop 0.75, BNP 1000, Lactate 2.5, ABG with pH 7.28, pCO2 46. Hgb normal WBC 12.4. COVID+, flu negative. CTA without PE but w/multifocal PNA. Admitted to ICU. During stay, pt experience uncontrolled hyperglycemia which was tx'd multiple times with lokelma,insulin, ca glu, and bicarbonate. Volume overloaded but unable to diurese given his shock and pressor requirements. Cont'd to decompensate with hypotension and hypoxia. Transitioned to DNR/COT status. Tx'd with remdesivir, cefepime, and decadron. Pt expired on 6/14/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: COVID + 6/10/22; This sample was analyzed using the SARS assay platform using PCR or equivalent Nucleic Acid Amplification(NAA)technology
Aktuelle Erkrankungen: -
Vorgeschichte: T2DM,HLD,HTN, Morbid Obesity, CKD stage 4, gout, GERD, EtOH use, OSA
Andere Medikamente: acarbose, amlodipine, aspirin, atorvastatin, carvedilol, vitamin D3, vitamin B-12, jardiance, febuxostat, furosemide, glipizide, hydralazine, lisinopril, omega 3, omeprazole, actos, semaglutide, sodium bicarbonate, terazosin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2316608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: FL
Alter: 100,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Cerebrovascular accident

Symptomtext

within 24 hours of this vaccine, the patient had a stroke; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An 101-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Mar2021 as dose 2, single (Lot number: EL9267) at the age of 100 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. There were no known allergies. No covid prior vaccination. Vaccination history included: BNT162b2 (Prev dose lot number: EL9269, Prev dose administration date: 25Feb2021, Prev dose dose number 1, Prev dose vaccine location: Left arm), administration date: 25Feb2021, when the patient was 100-year-old, for Covid-19 Immunization. No other vaccine was taken in four weeks. The following information was reported: CEREBROVASCULAR ACCIDENT (death, disability, medically significant) with onset 19Mar2021, outcome "fatal", described as "within 24 hours of this vaccine, the patient had a stroke". Therapeutic measures were not taken as a result of cerebrovascular accident. No covid tested post vaccination. The patient date of death was 22Mar2021. Reported cause of death: "within 24 hours of this vaccine, the patient had a stroke". It was not reported if an autopsy was performed. The patient was not tested covid post vaccination.; Reported Cause(s) of Death: within 24 hours of this vaccine, the patient had a stroke

Weitere VAERSDATA-Felder

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

VAERS 2315377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 10.06.2022
Impfdatum: 11.02.2021
Beginn: 10.05.2022
Tage bis Beginn: 453,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

Patient is fully vaccinated and boosted. COVID positive test 5/10/2022 on admission to hospital.Admitting DX: general weakness, fever, COVID. Acute respiratory failure. Patient presented with shortness of breath and hypoxic from covid-19 infection with suspected pneumonia. ID and pulmonary were consulted. He was treated with 3 day course of IV remdesivir, IV steroids. He clinically improved and was discharged home once cleared by pulmonary.

Weitere VAERSDATA-Felder

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

VAERS 2304971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 01.06.2022
Impfdatum: 01.10.2021
Beginn: 26.05.2022
Tage bis Beginn: 237,0
Dosis: 2
Route/Site: IM / LA

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

Benign prostatic hyperplasia COVID-19 Carotid artery stenosis Cerebellar infarction Cerebral infarction Cerebrovascular accident Condition aggravated Dizziness Fall Glaucoma Head injury Hyperchloraemia Hyperglycaemia Lipase increased Lower urinary tract symptoms Magnetic resonance imaging head abnormal SARS-CoV-2 test positive Troponin increased

Symptomtext

"87 YO male with h/o hypertension and BPH who presented to the ER for evaluation of acute onset vertigo and projectile vomiting. At approximately 5:30 p.m. today, he sat down while eating dinner and developed acute onset vertigo characterized as room spinning sensation with subsequent projectile vomiting. He went to go lay down, which was followed by patient falling off the bed and hitting his left forehead. He notes chronic dizziness, but this was different from any other episode. He denies any previous history of CVA or TIA. He denies any history of epilepsy. He follows with a doctor for carotid artery stenosis. Hospitalist team asked to admit for further monitoring. MRI brain obtained revealed multiple cerebellar infarcts. Teleneurology consulted and recommend DAPT for 21 days with Plavix 75mg Monotherapy indefinitely. He is to obtain TEE to assess for vegetations and atrial appendages. He is to wear Zio monitor to assess for arrhythmia with results sent to our cardiology team. He is to follow with Neurology and PCP as able. He is discharged home in stable condition. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: Positive COVID PCR test 5/26/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Suspected cerebral infarction due to unspecified occlusion or stenosis of right vertebral artery (*) 5/26/2022 Essential hypertension (Chronic) 5/31/2016 Mixed hyperlipidemia (Chronic) 6/21/2017 Microscopic colitis (Chronic) 11/25/2017 Syncope 11/25/2017 Stage 3 chronic kidney disease (Chronic) 11/25/2017 Carotid artery stenosis (Chronic) 2/17/2018 History of melanoma Unknown Hyperglycemia 5/26/2022 Hyperchloremia 5/26/2022 Vertigo as late effect of cerebrovascular accident (CVA) 5/26/2022 Elevated lipase 5/26/2022 Elevated troponin 5/26/2022 Vertebral artery dissection, right 5/26/2022 Benign prostatic hyperplasia with lower urinary tract symptoms 5/26/2022 COVID-19 5/26/2022 Glaucoma 5/26/2022
Andere Medikamente: aspirin 81 mg Oral Daily atorvastatin calcium 40 mg TAKE 1 TABLET NIGHTLY calcium citrate/vitamin D3 1 tablet Oral Daily cinnamon bark 300 mg Oral Daily clopidogrel bisulfate 75 mg Oral Daily cranberry fruit extract,cranberry,cranberry
Allergien: Severity Reactions Comments Orange Juice Medium Swelling Any orange Benadryl [diphenhydramine Hcl] Low Other (See Comments) Urinary retention
Vorherige Impfungen: -

VAERS 2290907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 74,0
Geschlecht: M
Eingang: 23.05.2022
Impfdatum: 17.02.2021
Beginn: 14.09.2021
Tage bis Beginn: 209,0
Dosis: 2
Route/Site: SYR / UN

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

Acute kidney injury Atrial fibrillation COVID-19 COVID-19 pneumonia Death Enterococcal infection Pneumonia pseudomonal SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Pfizer product on 01/27/2021 and 02/17/2021. They first tested positive for COVID-19 on 09/14/2021 at a clinic. They presented to emergency department on 09/17/2021 but it seems they were not admitted to hospital at that time. They were admitted to hospital on 09/28/2021 and an additional COVID-19 test was positive on this day. They were found to be having multiple complications and co-occurring conditions, including COVID-19 pneumonia, Psudomonas Pneumonia, Enterococcus Pneumonia, Acute Kidney Failure, and A-fib. A third COVID-19 test on 10/15/2021 was also positive. They remained hospitalized until their death on 10/22/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 24,0
Labordaten: Positive COVID-19 tests x3 despite being vaccinated, on 09/14/2021, 09/28/2021, and 10/15/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Melanoma, malignant neoplasm of colon, adenocarcinoma of unknown primary site with mesenteric node involvement (post-chemotherapy and on 5-FU maintenance), psoriatic arthritis, coronary artery calcification, hypertension, iron deficiency anemia, hyperkalemia, hypomagnesemia, cardiac murmur, osteoarthritis, carotid artery stenosis, parathyroidectomy
Andere Medikamente: -
Allergien: Omeprazole (reaction not listed) Duloxetine (reaction not listed) Lisinopril (reaction: cough)
Vorherige Impfungen: -

VAERS 2248225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 66,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 17.03.2021
Beginn: 01.09.2021
Tage bis Beginn: 168,0
Dosis: 1
Route/Site: SYR / LA

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

Arrhythmia Blood culture positive COVID-19 Cardiac arrest Cardio-respiratory arrest Cardiogenic shock Death Hypoxia Malaise Pulmonary oedema Respiratory failure Resuscitation SARS-CoV-2 test positive Scrotal gangrene Staphylococcus test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/05/2021 and 03/17/2021. They became symptomatic on 08/31/2021 and first tested positive for COVID-19 on 09/01/2021. They presented to emergency department on 09/01/2021. They were admitted to hospital on 09/01/2021 and discharged 09/02/2021. They presented to emergency department again on 09/08/2021 but were not admitted to hospital at this time. They presented to emergency department again on 09/15/2021 after blood culture results from a sample collected 09/08/2021 were positive for staph auricularis. They were admitted to hospital this time, on 09/15/2021. A second COVID-19 test was positive on 09/16/2021. They were discharged 09/21/2021. They were then re-admitted 09/21/2021 and found to be having multiple complications and issues including: scrotoal gangrene, respiratory failure, hypoxia, and mild pulmonary edema. The individual code blue'd while in the hospital on 09/26/2021 and per the wishes of the next of kin, CPR was discontinued. It was determined the individual had suffered a cardiac arrest, either due to a fatal arrhythmia or cardiogenic shock. Date of death was 09/26/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: Positive COVID-19 tests on 09/01/2021 and 09/16/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: End-Stage Renal Disease (on dialysis), COPD (on oxygen), Type II Diabetes, Coronary Artery Disease, Hypertension, Chronic Respiratory Failure, previous myocardial infarction
Andere Medikamente: -
Allergien: Sertraline (reaction: visual impairment)
Vorherige Impfungen: -

VAERS 2236032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 06.10.2021
Beginn: 07.04.2022
Tage bis Beginn: 183,0
Dosis: 2
Route/Site: IM / AR

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

Angiogram cerebral normal Arteriogram carotid normal COVID-19 COVID-19 pneumonia Cerebrovascular accident Chest X-ray abnormal Cognitive disorder Computerised tomogram head normal Device malfunction Dyspnoea Dyspnoea exertional Electrocardiogram ST-T change Fatigue Hypotension Hypoxia Laboratory test Lung infiltration Malaise

Symptomtext

Hospitalized 04/07/2022-04/11/2022; COVID-19 positive 04/07/2022; fully vaccinated plus booster BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 4/7/2022 Discharge Date: 4/11/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] Pneumonia due to COVID-19 virus [U07.1, J12.82] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 85 y.o. male admitted with worsening dyspnea from COVID-19..Patient was previously vaccinated for COVID-19. Initially, he developed symptoms on March 8th. Had positive COVID test on March 12. At that time felt he was recovered from the illness and was doing better. Over the previous 2-3 weeks prior to admission he had significant worsening of of symptoms including shortness of breath, increasing fatigue, malaise, body aches, intermittently productive cough with yellow sputum, and exertional dyspnea. In recent weeks, seen by his primary care provider and given antibiotics for suspected bacterial pneumonia. In addition, patient was admitted to Hospital April 1st for suspected acute CVA. No evidence of acute brain CVA/ injury noted. Positive COVID test again noted at that time. Chest x-ray-April 1st, showed stringyand patch infiltrates. Patient was discharged home. Emergency department patient was tachycardic mildly hypotensive and on 2 L per nasal cannula. Chest x-ray appearance was consistent with COVID-19 pneumonia. Patient was outside the window of and the severe but admitted to hospital and placed on IV Decadron. During hospitalization oxygenation initially worsen to up to 6 L per nasal cannula. Patient was given gentle diuresis with good results. Patient's oxygenation started to improve and over a 2 day. Patient went from 6 L per nasal cannula to room air. Prior to discharge patient did have a home oxygen evaluation and maintain adequate oxygen saturations are 97%. Patient is being discharged to home. He will complete a 10 day course of steroids. Patient should follow up with his primary care physician in 1 week. Patient was evaluated by Occupational therapy and Physical therapy prior to discharge in May had no further recommendations. Patient states he is doing well and is anxious for discharge to home. Discharge instructions were explained all patient's questions were answered. Course the patient has worsening shortness of breath worsening cough developed high fevers chills or feels his clinical condition is deteriorating in any way he should call his primary care physician or return to the emergency department immediately for further evaluation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: Admission to Facility on 04/01/2022: Hospital Course: This is a 85 y.o., male patient with a history of rheumatoid arthritis, obstructive sleep apnea, hyperlipidemia, coronary artery disease with pacemaker, hypertension, GERD, COPD, who was admitted to Facility on 4/1/2022 with speech disturbance. He originally presented to Hospital with the complaint. Patient went to bed in his normal state of health at 9 PM on March 31, 2022. Upon waking up in the morning patient was noted to have some difficulty getting certain words out. At Facility the patient did have a CT of the head which was without acute intracranial abnormality. In addition, the patient did have a CT angiogram of the head and neck with perfusion imaging which again were without abnormality. Secondary to inability to get further neuroimaging the patient was sent to University of Facility for further evaluation. Follow up CT head without obvious infarct. Family at bedside shares the patient has had issues with shortness of breathing for the last two years. They report the patient's pacemaker was reportedly "not working" at Facility and he was said to have ST-changes. Family continues to report the patient is not as cognitively sharp as he normally is. Of note, the patient was diagnosed with COVID in March while away. They just recently returned. Cardiology was consulted to the case. Due to hypotension episodes, multiple blood pressure medications were changed by cardiology. His device was interrogated and his outside EKGs were reviewed. Patient was felt to be quite stable from a cardiology standpoint. Cardiology was also asked to assist in the case as there were reports of intermittent feelings of possible fever and due to the concern that chronic methotrexate use may be masking normal symptoms of infection. Extensive infectious workup was completed which was unrevealing. Internal medicine team did think there may be a component of COVID sequelae contributing to the patient's alteration in mental status. PT/OT/SLP evaluated the patient, home therapies were recommended but the patient/family declined. Case management/social work followed for discharge needs/disposition planning. On 4/3/2022, the patient was stable for discharge to home.
Vorgeschichte: Pneumonia due to COVID-19 virus Acute exacerbation of chronic obstructive airways disease Obstructive sleep apnea Pulmonary congestion Acute hypoxemic respiratory failure due to COVID-19 CAD (coronary artery disease) Gastric ulcer with hemorrhage, unspecified chronicity AICD (automatic cardioverter/defibrillator) present Atrial fibrillation Morbid obesity Protein-calorie malnutrition, moderate Anemia Acute blood loss anemia Fatigue associated with anemia Iron deficiency anemia BPH (benign prostatic hyperplasia) Rheumatoid arthritis
Andere Medikamente: acetaminophen (TYLENOL) 650 MG extended release tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amoxicillin (AMOXIL) 500 MG capsule ascorbic acid (VITAMIN C) 500 MG tablet cholecalciferol (VITAMI
Allergien: Promethazine
Vorherige Impfungen: -

VAERS 2228581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 10.02.2021
Beginn: 20.12.2021
Tage bis Beginn: 313,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

Patient with 2 Pfizer COVID vaccinations, last dose 02/10/21, who admitted to hospital with complications from COVID. Provider D/C note below: "Brief Summary of Hospital Stay: Patient had a Fall at home without suffering any injuries but due to Weakness generalized she could not get up off the floor. When evaluated she was found to have evidence or Acute respiratory insufficieny with hypoxia. The respiratory disturbance and weakness appear to be due to a COVID 19 infection. Though the patient was vaccinated she may not have had as robust response due immunosuppression from METHOTREXATE and PREDNISONE she takes for Adult-onset Still's disease. She was started on DECADRON (course continued at discharge) and REMDESIVIR (course not completed). Patient's weakness improved quickly and she did well with physical therapy. Her oxygen requirements were improving rapidly as well. She was discharge with supplemental oxygen but suspect she will not need support for long."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: PCR detected COVID test on 12/20/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia, unspecified CAD (coronary artery disease), autologous vein bypass graft Adult-onset Still's disease Paroxysmal atrial fibrillation Hypothyroidism Menopausal and postmenopausal disorder Diverticulosis of sigmoid colon Right knee DJD Anemia in chronic kidney disease (CODE) Iron deficiency anemia secondary to inadequate dietary iron intake Intestinal malabsorption
Andere Medikamente: -
Allergien: Amoxicillin: Rash Clarithromycin: Rash Metronidazole: Rash
Vorherige Impfungen: -

VAERS 2223223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 25.02.2021
Beginn: 11.10.2021
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Dyspnoea Hypoxia

Symptomtext

Pt presented to ED 10/11 w/ c/o SOB & hypoxia; reports dx w/ COVID-19 7 days prior to presentation; pt admitted for acute resp failure w/ hypoxia & COVID-19 PNA; 10/11 - tx w/ decadron, levaquin; 10/12 - added Vit C, zithromax, rocephin, Vit D3, Protonix, Zinc; originally required 3L O2 but weaned to RA prior to discharge.

Weitere VAERSDATA-Felder

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

VAERS 2206744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 75,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 28.09.2021
Beginn: 25.01.2022
Tage bis Beginn: 119,0
Dosis: 2
Route/Site: SYR / RA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 01/28/2021, 02/18/2021, and 09/28/2021. They tested positive for COVID-19 via antigen test on 01/25/2022. They presented to emergency department o 01/21/2022, and twice on 01/27/2022. The last emergency department visit, they were brought over to ED from the dialysis unit due to extraordinarily low blood pressure. They were admitted to hospital. They were discharged back to skilled nursing facility on 01/27/2022 on hospice care. The individual died on 01/29/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 2,0
Labordaten: Positive COVID-19 test despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary Artery Disease, Hyperlipidemia, Hypertension, Peripheral Vascular Disease, previous history of femoral aneurysm, end-stage renal disease (was on dialysis at the time of the adverse event). Previous history of abdominal aortic aneurysm; The individual was a resident of a skilled nursing facility at the time of the adverse event.
Andere Medikamente: -
Allergien: Morphine, Oxycodone, Fentanyl
Vorherige Impfungen: -

VAERS 2196589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 79,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 11.02.2021
Beginn: 18.03.2022
Tage bis Beginn: 400,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Asthenia COVID-19 Cardiac failure congestive Condition aggravated Cough Death Dyspnoea Dyspnoea exertional Encephalopathy Endotracheal intubation Pneumonia Positive airway pressure therapy SARS-CoV-2 test positive Shock

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccine on 1/21/21 and 2/11/21. COVID + 2/17/22 and 3/12/22. Presented 3/11/22 shortness of breath x3/days, dyspnea exertion, associated cough, no hemoptysis and generalized weakness. Admitted for CHF exacerbation c/b acute hypoxic resp failure. Became more hypoxic the following morning and placed on BiPAP. Course c/b NSTEMI, acute encephalopathy, intubated 3/17/22, secondary pneumonia and shock. Placed on comfort care. Treated with remdesivir (2/22), ceftriaxone, doxycycline, cefepime, vacomycin, and zosyn. Pt expired on 3/18/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 7,0
Labordaten: 3/12/22 - This sample was analyzed using the Roche LIAT SARS assay platform.
Aktuelle Erkrankungen: -
Vorgeschichte: T2DM, CAD, CHF, HTN, aortic valve replacement with TAVR on 9/2018, pacemaker placement with electrophysiology
Andere Medikamente: tylenol, insulin glargine, insulin lispro, irbesartan, allopurinol, amlodipine, aspirin, atorvastatin, carvedilol, vitamin D3, clopidogrel, dexamethasone, docusate, escitalopram, folic acid, gabapentin, glucosamine, isosorbide mononitrate,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2184337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 77,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 03.03.2021
Beginn: 03.03.2022
Tage bis Beginn: 365,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Blood gases abnormal COVID-19 Cough Death Dyspnoea Endotracheal intubation Hypovolaemic shock Hypoxia Oxygen saturation decreased Rectal haemorrhage SARS-CoV-2 test positive

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Received PfizerVaccine on 2/13/21 and 3/03/21. Presented to ED c/o SOB shortness and cough x/1 wk. Admitted for acute hypoxic respiratory failure due to COVID-19 and requiring high-flow O2. Course c/b rectal bleeding and hypovolemic shock; tx'd w/Phenylphrine. ABG showed severe hypoxia requiring intubation but patient requested DNR status. Tx'd with IV vancomycin, Rocephin and doxycycline. His oxygenation continued to decline, transitioned to comfort care. Pt expired 3/03/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: 3/02/22-This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification(NAA)technology.
Aktuelle Erkrankungen: -
Vorgeschichte: BCC, PSA, HTN, hypothyroid, prostate cancer, OSA, CHF
Andere Medikamente: vitamin C, vitamin d3, clindamycin, clotrimazole/betamethasone, furosemide, levothyroxine,magnesium, melatonin, multivitamin, omerga 3, potassium chloride, sildenafil, tadalfil, ubidecarenone,
Allergien: gabapentin, codeine, nabumetone
Vorherige Impfungen: -

VAERS 2173931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 72,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 10.03.2021
Beginn: 31.12.2021
Tage bis Beginn: 296,0
Dosis: 1
Route/Site: SYR / LA

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

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

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/17/2021 and 03/10/2021. Symptom onset date is not available, but they tested positive for COVID-19 on 12/31/2021 and were admitted to hospital on the same day (12/31/2021). They were discharged to a skilled nursing facility on 01/05/2022 to continue palliative care (no CPR). They died later the same day, on 01/05/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 6,0
Labordaten: Positive COVID-19 test on 12/31/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Congestive Heart Failure, Ventricular Tachycardia, Severe Persistent Asthma, Hypertrophic Cardiomyopathy, Implantable Cardioverter-Defibrillator in place, Coronary Artery Disease, Hypothyroidism, Sleep Apnea, Type II Diabetes, Hypertension, Chronic use of anticoagulation medication, Diastolic Heart Failure, Benign hypertensive heart and kidney disease with Stage 4 chronic kidney disease, paroxsmal A-fib, previous episode of sudden cardiac arrest approx 10 years previous
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2167997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 75,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 13.02.2021
Beginn: 26.02.2022
Tage bis Beginn: 378,0
Dosis: 2
Route/Site: IM / RA

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

Acidosis Acute kidney injury Acute respiratory failure COVID-19 COVID-19 pneumonia Death Encephalopathy Haemofiltration Intensive care Intestinal ischaemia Intestinal perforation Mechanical ventilation Renal transplant Viral test

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccine on 1/23/21 and 2/13/21. Admitted 2/23/22 with Covid at local hospital c/b AKI needing CRRT. Transferred to ICU 2/2 renal transplant. Admitted w/acute hypoxic respiratory failure 2/2 Covid PNA and acute encephalopathy. MRI 2/26/21 w/perforated bowel 2/2 right colonic ischemia. Acutely decompensated with a large increase of vasopressor needs and refractory acidosis despite maximized ventilation techniques and CRRT. Transitioned to comfort care and expired on 2/26/22. Treated with vancomycin and Merem at hospital. Treated with vacomycin, cefepime, micafungin, and Cresemba.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 2/23/22: The sample was analyzed using one or a combination of Real-Time PCR based methods and multiplex reagents.
Aktuelle Erkrankungen: -
Vorgeschichte: OSA, DM2, HTN, obesity, diabetic nephropathy with ESRD s/p kidney transplant in 2015 and HLD (Hypersensitivity lung disease)
Andere Medikamente: amitriptyline, aspirin, atorvastatin, calcium carbonate, duloxetine, ezetimibe, famotidine, furosemide, gabapentin, insulin glargine, insulin regular, melatonin, metoprolol, montelukast, mycophenolate, oxybutynin, prednisone, tacrolimus, ta
Allergien: Saccharin
Vorherige Impfungen: -

VAERS 2162523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 72,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 22.01.2021
Beginn: 23.09.2021
Tage bis Beginn: 244,0
Dosis: 2
Route/Site: SYR / LA

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

Acute kidney injury Acute respiratory failure COVID-19 pneumonia Chest tube insertion Hyperkalaemia Lactic acidosis Left ventricular failure Pneumothorax Pulseless electrical activity Septic shock

Symptomtext

Acute hypoxic respiratory failure MV 9-21-21 severe COVID 19 pneumonia septic shock right-sided pneumothorax s/p chest tube 14 F pigtail 9-21-21 pulseless electrical activity of the heart diastolic heart failure acute kidney injury lactic acidosis-improved hyperkalemia

Weitere VAERSDATA-Felder

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

VAERS 2158187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 74,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 10.03.2021
Beginn: 08.01.2022
Tage bis Beginn: 304,0
Dosis: 1
Route/Site: SYR / RA

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

Acute myocardial infarction COVID-19 Cardiac arrest Death Dyspnoea exertional Hypoxic-ischaemic encephalopathy SARS-CoV-2 test positive Syncope Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/17/2021 and 03/10/2021. They did not have a known specific symptom onset, but became suddenly short of breath while walking and collapsed. They presented to emergency department and were admitted to hospital on 01/08/2022; they tested positive for COVID-19 upon this hospital admission. It was determined that the individual had complications of anoxic encephalopathy, cardiac arrest, and an acute myocardial infarction. Given poor prognosis, the individual was transitioned to comfort care and died on 01/12/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 4,0
Labordaten: Positive COVID-19 test on 01/08/2022 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Type II Diabetes, Obesity, Hypertension, Coronary Artery Disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 81,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 12.03.2021
Beginn: 14.01.2022
Tage bis Beginn: 308,0
Dosis: 1
Route/Site: UN / UN

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

Acute respiratory failure Angiogram pulmonary abnormal Atelectasis Body height decreased Bronchial wall thickening Bronchiolitis COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chills Death Dyspnoea Fatigue Gram stain negative Hyperkalaemia Lung infiltration Malaise Pleural effusion

Symptomtext

1/5/22 82-year-old male presents from nursing home by EMS with history of DNR, Parkinson's, CLL, A. fib presents emergency room with complaints of increased shortness of breath and fever/chills, malaise and fatigue. Presents by ambulance who gave him a neb treatment in route and placed on nasal cannula oxygen. He was recently admitted for approximately 1 week and discharged 2 days ago after admission for pneumonia with respiratory difficulty requiring supplemental oxygen and steroid treatment. No significant abdominal pain vomiting diarrhea or GI symptoms. No chest pressure palpitations or near syncope. 1/13/22 82-year-old male with past medical history of chronic lymphocytic leukemia, Parkinson's disease, MI, CVA, hypertension, A. fib on Eliquis and GERD who presented with worsening dyspnea after recently being discharged from Hospital with COVID PNA. He was treated for respiratory failure. Pulmonology was consulted and patient was given bronchodilators, cefepime/vanc, mucinex, solumedrol, ZnSO4. The patient repeatedly made comments to staff and the family indicating a desire to be allowed to die. Hospice was consulted. His family has met with hospice and wishes to honor his wishes. He was discharged to hospice scatter bed and expired at time and date listed above. Parkinson's disease, MI, CVA, hypertension, A. fib on Eliquis and GERD who presented with worsening dyspnea after recently being discharged from hospital with COVID PNA. He was treated for respiratory failure. Pulmonology was consulted and patient was given bronchodilators, cefepime/vanc, mucinex, solumedrol, ZnSO4. The patient repeatedly made comments to staff and the family indicating a desire to be allowed to die. Hospice was consulted. His family has met with hospice and wishes to honor his wishes. He was discharged to hospice scatter bed and expired at time and date listed above. Admission date: 1/13/2022 Date of death: 1/14/2022 Time of death: 6:55 AM Principal Problem: Hospice care (1/13/2022) POA: Not Applicable Acute respiratory failure with hypoxia (1/5/2022) POA: Yes Chronic lymphocytic leukemia (2/6/2012) POA: Yes Chronic kidney disease (6/30/2016) POA: Yes Benign prostatic hyperplasia (5/23/2019) POA: Yes Parkinson's disease (5/1/2005) POA: Yes History of cerebrovascular accident (1/1/2008) POA: Not Applicable Gastroesophageal reflux disease (10/24/2011) POA: Yes Atrial fibrillation (5/1/2019) POA: Yes Coronary artery disease involving native coronary artery (6/21/2018) POA: Yes Post-acute COVID-19 syndrome (12/29/2021) POA: Not Applicable HCAP (healthcare-associated pneumonia)/gram-negative pneumonia (1/8/2022) POA: Yes Hyperkalemia (1/11/2022) POA: No Admit date: 1/5/2022 Discharge date: 1/13/2022 Discharged Condition: Good Hospital Course: From initial H&P: "82-year-old male with past medical history of chronic lymphocytic leukemia, Parkinson's disease, MI, CVA, hypertension, A. fib on Eliquis and GERD who presented to ED with increasing shortness of breath and fever. Of note, patient was recently admitted to Hospital for Covid PNA and discharged on 1/3/2022. However patient reports increasing dyspnea with O2 sats in 80s on 4L NC and temp of 100.5. Patient is a DNR." He was treated for the following: Respiratory failure/COVID, treating for HCAP: pulmonology following. Giving scheduled and PRN bronchodilators, cefepime/vanc, mucinex, solumedrol, ZnSO4. - r required CLL: WBC >72K on 1/10 and suspect some elevation related to CLL. Parkinson's: continue sinemet A fib: anticoagulated on eliquis Hyperkalemia: BPH: flomax The patient repeatedly made comments to staff and the family indicating a desire to be allowed to die. Hospice was consulted. His family has met with hospice and wishes to honor his wishes. He will be discharged to hospice scatter bed. Discharge Diagnoses: Principal Problem: Acute respiratory failure with hypoxia Active Problems: Chronic lymphocytic leukemia Chronic kidney disease Benign prostatic hyperplasia (5/23/2019) Parkinson's disease (5/1/2005) History of cerebrovascular accident (1/1/2008) Gastroesophageal reflux disease (10/24/2011) Atrial fibrillation (5/1/2019) Coronary artery disease involving native coronary artery (6/21/2018) Post-acute COVID-19 syndrome (12/29/2021) HCAP (healthcare-associated pneumonia)/gram-negative pneumonia (1/8/2022) Hyperkalemia (1/11/2022) Additional information for Item 12: Balance problems R/T PARKINSON'S USES CANE W/AMBULATION o Blood dyscrasia o Carpal tunnel syndrome on right REPAIRED 5/1/18 o Cerebrovascular accident 6/30/2016 o CVA (cerebral vascular accident) 05/2008 "SLOW TO FIND WORDS" PER PT o Diffuse large B-cell lymphoma of lymph nodes of neck 1/26/2017 o Fatigue due to treatment o GERD (gastroesophageal reflux disease) DAILY OMEPRAZOLE o History of cancer chemotherapy 2017 R/T EAR SQUAMOUS CA & ORAL CHEMO R/T NON HODGKINS LYMPHEMA o History of shingles ABD-BACK , APPROX 2013 o HTN (hypertension) TOPROL BID-CARDIOLOGIST o Hx of therapeutic radiation 2016 & 2017 H/O R/T SQUAMOUS CELL CA/LEFT EAR o Infection of prosthetic joint 7/25/2016 o Intestinal malabsorption, unspecified 12/29/2021 o Low vitamin D level 12/28/2021 o Myocardial infarction "SILENT" o Non-Hodgkin's lymphoma 1998 ONCOLOGIST o Osteoarthritis S/P LTHR 2016 , HANDS o Osteoradionecrosis of temporal bone 3/28/2018 o Parkinson disease 05/2005 o SCC (squamous cell carcinoma) 2/27/2018 o Squamous cell cancer of skin of earlobe, left 2016 o Tremor RIGHT HAND & LEG R/T PARKINSON'S PER PT 1/8/22 XR Chest 1 Vw IMPRESSION: Progressive right perihilar and unchanged bibasilar infiltrates, suspicious for pneumonia 12/29/21 CT Angiogram Chest For PE IMPRESSION: 1.No evidence of pulmonary embolism 2.Smooth intralobular septal thickening with mild bronchial wall thickening at the lung bases may relate to mild interstitial pulmonary edema versus bronchiolitis 3.Trace effusions with bibasilar atelectasis 4.Further loss of height at the known L1 compression deformity in comparison to 2017. Please note that all CT scans at this facility use dose modulation, iterative reconstruction, and/or weight based dosing when appropriate to reduce radiation dose to as low as reasonably achievable Additional information for Item 9: amantadine (SYMMETREL) 100 MG capsule Take 100 mg by mouth 2 (two) times daily. apixaban (ELIQUIS) 5 MG tablet Take 1 tablet by mouth 2 (two) times daily. Aspirin (ASPIR-81 PO) Take 81 mg by mouth daily atorvastatin (LIPITOR) 40 MG tablet carbidopa-levodopa (SINEMET) 25-100 MG Take by mouth 4 (four) times daily Melatonin 1 MG/4ML LIQD 15 mg. metoprolol, TOPROL-XL, 50 MG 24 hr tablet Take 1 tablet by mouth daily. omeprazole (PRILOSEC) 20 MG capsule Take 20 mg by mouth daily. tamsulosin (FLOMAX) 0.4 MG CAPS TAKE 1 CAPSULE BY MOUTH ONCE DAILY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: 12/28/21 COVID-19 Result Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Balance problems R/T PARKINSON'S USES CANE W/AMBULATION o Blood dyscrasia o Carpal tunnel syndrome on right
Andere Medikamente: amantadine (SYMMETREL) 100 MG capsule Take 100 mg by mouth
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2148525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: GA
Alter: 78,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 26.02.2021
Beginn: 16.11.2021
Tage bis Beginn: 263,0
Dosis: 2
Route/Site: SYR / LA

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

Cerebrovascular accident Computerised tomogram normal Hypoaesthesia oral Magnetic resonance imaging abnormal

Symptomtext

On Nov 16th, my mouth started feeling numb so my son took me to the doctor. They gave me a CT scan but told me I didn't have a stroke. I went back the next day and was still told I didn't have a stroke. They sent me home w/ prednisone. A few days later, I checked myself into hospital and stayed over night and had another MRI which revealed I had a small stroke. They put me on aspirin and Lipitor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Aspirin, a lot of vitamins.
Allergien: Codeine
Vorherige Impfungen: Sore arm from flu vaccine.

VAERS 2134430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 81,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 31.08.2021
Beginn: 09.02.2022
Tage bis Beginn: 162,0
Dosis: 1
Route/Site: IM / LA

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

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

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 2134408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 56,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 14.08.2021
Beginn: 06.02.2022
Tage bis Beginn: 176,0
Dosis: 2
Route/Site: IM / UN

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 COVID-19 pneumonia Death Deep vein thrombosis Dyspnoea Endotracheal intubation Positive airway pressure therapy Pulmonary embolism SARS-CoV-2 test positive Sepsis

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/27/2021, 2/16/2021 and 8/14/2021. Presented to ED 2/11/22 c/o SOB, O2 sats in 30s on arrival. Admitted for acute hypoxemic resp failure 2/2 covid PNA. Oxygenation demands escalated to Bipap w/eventual intubation on admission day 2. Received inhaled epoprostenol and one day of remdesivir. Started on empiric antibiotics. Large DVT resulting in Phlegmasia cerulea dolens dx'd 2/12/22 c/b multiple PEs on CTA and sepsis. 2/13/22 pressor requirements increased with MAPs below 60 tx'd w/3 pressors. Transiioned to comfort care, expired 2/14/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: 2/11/2022 COVID Positive using the Roche LIAT SARS assay platform
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, Crohn's, Hypertension, Irritable Bowel Syndrome, Osteoporosis, Osteoarthritis of spine
Andere Medikamente: Acetaminophen, Alprazolam, Amoxicillin-Clavulanate, Arginine, Biotin, Bupropion, Cholecalciferol, Cholestyramine, Lomotil, Descovy, Flonase, Folic Acid, Furosemide, Gabapentin, Ganciclovir, Norco, Loperamide, Metaxolone, Methotrexate, Multi
Allergien: Aspirin, Ciprofloxacin, Sulfonamides
Vorherige Impfungen: -

VAERS 2134377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 16.02.2021
Beginn: 24.11.2021
Tage bis Beginn: 281,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory failure Asthenia COVID-19 Cardiac telemetry normal Hypotension Hypoxia SARS-CoV-2 test positive Syncope

Symptomtext

Provider hospital summary "Patient is a 85 y/o male w/ history of prostate cancer on Xtandi, Hypertension, CKD III, hyperlipidemia presented 11/24 with weakness, syncope, hypotension, hypoxia and known history of COVID 19 infection. He is admitted for acute hypoxic respiratory insufficiency and debility. During his hospitalization stay, he received IV Regeneron and was monitored closely. His oxygen requirement has been minimal and did not need O2 supplementation at discharge. Orthostatic hypotension test was negative and no evidence of arrhythmia on telemetry were revealed. No further presyncope or syncopal episode noted while inpatient after holding all anti-hypertensive medications. He was able to ambulate in the room and work with therapy without difficulties. All his anti hypertensive except his diuretic was restarted on discharge. He is advised to discuss re initiation of his diuretic with is PRIMARY CARE PHYSICIAN."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: Positive COVID PCR Test 11/20/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia Stage 3a chronic kidney disease (*) Essential hypertension, benign COVID-19 Debility Syncope Severe protein-calorie malnutrition (*)
Andere Medikamente: ascorbic acid 500 mg Oral Daily benzonatate 100 mg Oral EVERY 8 HOURS PRN cholecalciferol (vitamin D3) 5,000 Units Oral Daily enzalutamide 40 mg TAKE 4 CAPSULES DAILY famotidine 10 mg Oral 2 times daily hydrochlorothiazide 25 mg Oral D
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2129231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 80,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 10.02.2021
Beginn: 03.09.2021
Tage bis Beginn: 205,0
Dosis: 2
Route/Site: UN / UN

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

Angioplasty Asthenia COVID-19 pneumonia Cardiac arrest Cough Death Dialysis Encephalopathy Fall Hypoxia Pyrexia Respiratory distress Syncope Thromboembolectomy Unresponsive to stimuli

Symptomtext

Presents for generalized weakness & fall, cough/fever. Admit for COVID pneumonia & syncope. Tx: remdesivir, tocilizumab, steroids, abx, embolectomy/angioplasty. Patient stabilized with improved repiratory and mental status, then developed sudden severe encephalopathy and respiratory distress. Family confirmed DNR status, dialysis attempted but patient became hypoxic and unresponsive; developed asystole. Expired on hospital day 12.

Weitere VAERSDATA-Felder

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

VAERS 2116882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 73,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 10.03.2021
Beginn: 28.08.2021
Tage bis Beginn: 171,0
Dosis: 1
Route/Site: SYR / UN

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

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

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/17/2021 and 03/10/2021. They presented to emergency dept on 08/28/2021 for shortness of breath and were admitted to hospital the same day. They also tested positive for COVID-19 via PCR test on 08/28/2021. After several days of treatment, the individual was placed on comfort care due to poor prognosis, due to the significant underlying medical conditions. They remained hospitalized until their death on 09/01/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: Positive COVID-19 test on 08/28/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Metastatic stage IV lung cancer; Acute on chronic systolic CHF exacerbation; Pancytopenia; Diabetes mellitus type 2
Andere Medikamente: Metformin (1,000 mg tablet, twice a day); aspirin; Lipitor; Breztri Aerosphere; cholecalciferol; citalopram ; Coreg; cyanocobalamin; ergocalciferol; folic acid; gabapentin; glipiZIDE; magnesium oxide; mirtazapine; ondansetron ; potassium ch
Allergien: -
Vorherige Impfungen: -

VAERS 2110309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WI
Alter: 74,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 08.04.2021
Beginn: 25.01.2022
Tage bis Beginn: 292,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 Gastroenteritis Escherichia coli Lethargy Myxoedema coma SARS-CoV-2 test positive

Symptomtext

75 year old female with history of HFpEF, CKD III, HTN, HLD, DM II, OSA, obesity, and papillary thyroid carcinoma s/p postsurgical (2007) hypothyroidism who presents with worsening generalized weakness and lethargy and was found to have myxedema coma in setting of known COVID infection. Recent admission (records obtained today). Treated for enteropathic E.coli with Cipro/Flagyl, planned total of 7 days from discharge on 1/21. COVID positive on 1/18

Weitere VAERSDATA-Felder

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

VAERS 2110226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 71,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 25.02.2021
Beginn: 31.08.2021
Tage bis Beginn: 187,0
Dosis: 2
Route/Site: UN / UN

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

Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Cough Death Dyspnoea Endotracheal intubation General physical health deterioration Hypoxia Illness Intensive care Pyrexia SARS-CoV-2 test positive

Symptomtext

presented with SOB x 5 days, fever, hypoxia, cough; + Covid; admit with Covid PNA; tx with singulair, maxipime, steroid, remdesivir, zinc, actemra, zyvox, merrem, vanc; maintained on high flow O2 initially; moved to ICU 9/14; intubated; COVID ARDS- FiO2 @ 70% currently.Despite all measures, she continued to deteriorate and became moribund on 11/5/2021. After a long battle with her illness, her family felt that she had fought enough and opted for comfort measures. She was pronounced deceased on 11/5/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 67,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2082980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 79,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 12.03.2021
Beginn: 27.01.2022
Tage bis Beginn: 321,0
Dosis: 1
Route/Site: IM / UN

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Death Dyspnoea Endotracheal intubation Fungaemia Intensive care Respiratory distress SARS-CoV-2 test positive Staphylococcal bacteraemia

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 2/14/21, 3/6/2021, and 9/19/2021. Covid + 1/8/22, Presented to ED 1/13/22 c/o SOB. Placed on HFNC in ED, admitted for acute hypoxemic respiratory failure due to Covid PNA transferred to ICU 1/14/22 due to O2 needs. Intubated 1/15/21. Developed staph epi bacteremia and fungemia during admission. Treated with remdesivir, baricitnib,zosyn, tobramycin, vancomycin, ambisome, micafungin, corticosteroids. Extubated on 1/25/22 leading to respiratory distress but pt declined reintubation. Status changed to DNR on 1/26/22. Expired on 1/27/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: 1/11/21 Covid + Nasopharyngeal from nasopharynx
Aktuelle Erkrankungen: C. diff diarrhea
Vorgeschichte: bliateral lung transplant, afib, DM2, anxiety disorder, HTN
Andere Medikamente: acetominophen, apixaban, ascobic acid,buspirone, calcium citrate/vitamin D3, Vitamin B12, dilitiazem, ferrous sulfate, furosemide, gabapentin, levothyroxine, magnesium oxide, mycophenolate mofetil, pantoprazole, polyethylene glycol, potassi
Allergien: Ciprofloxacin, codeine, levofloxacin, latex, linezolid
Vorherige Impfungen: -

VAERS 2062720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 81,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 10.02.2021
Beginn: 12.01.2022
Tage bis Beginn: 336,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 Condition aggravated Death Fatigue Hepatic cirrhosis Lung opacity Oxygen saturation abnormal Renal impairment Respiratory disorder Respiratory failure SARS-CoV-2 antibody test negative SARS-CoV-2 test positive Sepsis

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/20/2021 and 2/10/2021. Presented to Emergency Department for fatigue and weakness. Family states tested positive for COVID on 1/10/2021. Admitted for renal dysfunction, hypoxic respiratory failure due to COVID-19, sepsis, and cirrhosis. Received supplemental oxygen, steroids, antibiotics and albumin. Sudden worsening of oxygenation status the morning after admission. Supplemental O2 was increased but respiratory status worsened. Expired 1/14/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 2,0
Labordaten: 1/11/2022: COVID positive; 1/13/2022: SARS CoV2 Nucleocapsid Antibodies negative; 1/13/2021: Chest x-ray revealed patchy interstitial and airspace opacities bilaterally
Aktuelle Erkrankungen: -
Vorgeschichte: lupus, Sjogren's, primary biliary cholangitis, cirrhosis, gastric varices, chronic kidney disease, Iliotibial, syndrome, alopecia, anemia, arthritis, osteopenia, osteroporosis
Andere Medikamente: dronabinol, K-dur, fosamax, align, citracal plus, nexium 65 FE, Norco, tussionex, medrol dosepack, lopressor, zofran, sodium bicarbonate, zanaflex, urso, vitamin E
Allergien: Amoxicillin, nitrofurantoin, bactrim, penicillins, sulfa
Vorherige Impfungen: -

VAERS 2058559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 15.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / UN

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

Cardiac arrest Cardiac pacemaker insertion Electrocardiogram Loss of consciousness Pulse absent Sinus node dysfunction

Symptomtext

On 2/26/2021, I passed out on kitchen floor at 7:45 am, and was looking straight up with no movement. Husband shook and I snapped out of it and was taken to ER. While monitored in ER around 8:30am, pulseless for 20 seconds and heart restarted on own. Pacemaker was determined to be needed. Pacemaker was inserted during that morning. Sick Sinus Syndrome was the diagnosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 2,0
Labordaten: 2/26/2021, took EKG at ER. Then was monitoring me for bp, oxygen levels and cardiac in ER when my heart stopped for 20 seconds. Diagnosed as Sick Sinus Syndrome requiring pacemaker.
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Gerd, rectal cancer four year survivor
Andere Medikamente: Prilosec,hydrochlorazide
Allergien: mangoes,aspirin,oxycodone,percodan,tramadol
Vorherige Impfungen: -

VAERS 2054548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 75,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 08.09.2021
Beginn: 04.01.2022
Tage bis Beginn: 118,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Cough Death Dyspnoea Endotracheal intubation Mechanical ventilation Pneumonia pseudomonal

Symptomtext

Pfizer COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/20/2021, 2/10/2021 and 9/08/2021. on 1/4/2022. Presented to ED with complaints of cough and shortness of breath, admitted for acute hypoxic respiratory failure due to COVID-19 and Pseudomonas pneumonia. She was intubated 1/5 and extubated on 1/10, treated w/steroids, vancomycin and cefepime, remained on NIV without ability to wean. Expired on 1/15.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cataracts, DIabetes, Hemorrhoids, Hypertension, Hypothyroidism, Lung transplant 2005, Hyperlipidemia, Migraine, Sacral wound present for 3 months.
Andere Medikamente: Alendronate, Aspirin, Azithromycin, Carvedilol, Cetrizine, Diphenoxylate-atropine, ezetimibe, Fenofibrate, hydralazine, insulin aspart, levothyroxine, losartan, Multivitamin, Mycophenolate, Omeprazole, Oxybutynin, Prednisone, Sirolimus, Bac
Allergien: Adhesives, Levofloxacin, Penicillin, Banana, Grapefruit
Vorherige Impfungen: -

VAERS 2034916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WI
Alter: 89,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 20.01.2021
Beginn: 12.02.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: - / RA

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

COVID-19 Death

Symptomtext

Death related to COVID 19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Complications of Type 2 DM; OSC: COVID-19; CKD Stage 4; HTN; PVD; dementia; recent orbital cellulitis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2027888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 16.02.2021
Beginn: 10.01.2022
Tage bis Beginn: 328,0
Dosis: 2
Route/Site: - / -

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

Anaemia Arthralgia Asthenia COVID-19 COVID-19 pneumonia Death Delirium Diabetic neuropathy Dyspnoea Gait disturbance Gastrooesophageal reflux disease Genital candidiasis Hypomagnesaemia Hypoxia Interstitial lung disease Lymphoedema Metapneumovirus pneumonia Metatarsalgia

Symptomtext

Patient with 2 doses of Pfizer vaccine, last dose February of 2021. Admitted through ED from facility with hypoxia and dyspnea found to have COVID pneumonia. Continued to decompensate during stay, requested comfort measures only. Died on 01/10/22 of COVID related complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: COVID positive test on 01/03/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (hypertension) (Chronic) 9/10/2012 Hyperlipidemia LDL goal <70 (Chronic) 9/10/2012 Vitamin D deficiency 11/7/2012 Ex-smoker 5/30/2013 Microalbuminuria due to type 2 diabetes mellitus 3/24/2016 History of motor vehicle accident 2017 wit multiple fractures, trach and PEG 7/27/2017 Shortness of breath 12/5/2017 Chronic congestive heart failure 12/8/2017 Sleep apnea 12/8/2017 Type 2 diabetes mellitus with insulin therapy (Chronic) 3/22/2018 Carotid stenosis (Chronic) 8/3/2018 Balance problem 1/21/2019 Constipation 7/17/2019 Coronary artery disease (Chronic) Unknown PAF (paroxysmal atrial fibrillation) (Chronic) 2/3/2020 S/P AVR Bioprosthetic valve (Chronic) 2/17/2020 Non-seasonal allergic rhinitis due to pollen 2/17/2020 Stage 3b chronic kidney disease (Chronic) 2/17/2020 Long term (current) use of anticoagulants 2/28/2020 Nocturnal hypoxia (Chronic) 2/28/2020 Human metapneumovirus pneumonia 2/28/2020 Delirium due to known physiological condition 2/28/2020 Gastroesophageal reflux disease without esophagitis 2/28/2020 Hypomagnesemia 2/28/2020 Neuropathy 2/29/2020 Diabetic polyneuropathy associated with type 2 diabetes mellitus 2/29/2020 Anemia 2/29/2020 Candidiasis of scrotum 2/29/2020 ILD (interstitial lung disease) 5/28/2021 Arthralgia of left knee 9/15/2021 Metatarsalgia, left foot 9/15/2021 Left foot drop 9/15/2021 Lymphedema of left lower extremity 9/15/2021 Post-traumatic osteoarthritis of left foot 9/15/2021 Gait difficulty 9/15/2021 Debility 11/16/2021 Morbid obesity with BMI of 40.0-44.9, adult (Chronic) 1/8/2022
Andere Medikamente: Amiodarone, aspirin, albuterol, lipitor, Symbicort, Spiriva, Lasix, Neurontin, Lantus, Humalog, Veltassa, Lopressor, Seroquel,
Allergien: Bee and yellow jacket stings (anaphylaxis) Pollens and ragweed (runny nose, watery eyes, sneezing)
Vorherige Impfungen: -

VAERS 2010852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 59,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 15.03.2021
Beginn: 04.12.2021
Tage bis Beginn: 264,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 COVID-19 pneumonia Condition aggravated Death Hypogammaglobulinaemia Lymphoma SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/22/2020 and 03/15/2021. They became symptomatic on 11/23/2021 and tested positive on 12/04/2021. They were seen in an emergency department on 12/05/2021. They were admitted to hospital on 12/05/2021 and remained hospitalized until their death on 12/20/2021. Death Certificate details are as follow: Part I Cause of Death A: COVID 19 Pneumonia Part II Other Significant Conditions: Lymphoma, Hypogammaglobulinemia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 15,0
Labordaten: Positive COVID-19 test despite being fully vaccinated against COVID-19.
Aktuelle Erkrankungen: -
Vorgeschichte: Lymphoma (under treatment), Hypogammaglobulinemia, Hypertension, Hypothyroidism, Fibromyalgia, Osteoporosis, history of papillary urothelial carcinoma, asthma
Andere Medikamente: -
Allergien: Ketorolac (severe, hives and swelling), Penicillins (severe, hives and swelling), Sulfa (moderate, hives and swelling), Lisinopril (mild, cough), Chlorthalidone (moderate, hyponatremia), Etodolac (severe, itching and rash), Sumatriptan (severe, hives and swelling), Losartan (mild, cough), Levofloxacin (severe, hives), Ibuprofen (severe, hives)
Vorherige Impfungen: -

VAERS 2005958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 10.02.2021
Beginn: 04.11.2021
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Anticoagulant therapy Atrial fibrillation COVID-19 COVID-19 pneumonia Cardiac failure congestive Chronic left ventricular failure Death Dyspnoea Endotracheal intubation Pyrexia SARS-CoV-2 test positive Sepsis Troponin increased

Symptomtext

Pt is a know COPD and dementia who presented with severe sepsis with COVID pneumonia with acute respiratory failure. Pt is COVID + on 11/4/2021 at admission. Pt admitted with atrial fibrillation with RVR, SOB, elevated troponin, fever, COVID and acute chronic respiratory failure with hypoxia. Treatment IV cardizem, Lovenox, IV Decadron, Breo inhaler, albuterol nebulizer, Metoprolol with chronic systolic congestive heart failure. Pt required intubation, pressors, broad-spectrum IV antibiotics. Patient developed acute kidney injury. Patient Expired.

Weitere VAERSDATA-Felder

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

VAERS 2005802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 10.02.2021
Beginn: 03.11.1954
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Blood pressure decreased COVID-19 Death Dyspnoea Endotracheal intubation Pulse absent SARS-CoV-2 test positive

Symptomtext

67-year-old female who presented to ED with worsening SOB. Pt tested + for COVID on 11/3. Comorbidities of COPD and obesity. Patient also had diabetes. The patient presented on November 4th and progressively worsened throughout stay. Treatment with decadron, remesivir and proning. She continually required more and more oxygen and then she was required to be intubated. On 11/13, the patient lost her pulse early in the morning and this was after her pressures continually decreased despite multiple pressors. Pt expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 12.02.2021
Beginn: 05.03.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: DEATH FOLLOWING 1 DOSE OF COVID VACCINE 02/12/2021 COVID vaccine dose #1 03/05/2021 Patient died at hospital (no records provided or reason given) Patient did not have reaction immediately following vaccine, did not have prior infection with COVID. Patient was seen in ED a few days prior to receiving covid vaccination (2/8-2/9) and was sent home with possible pneumonia, advised to follow up as outpatient. Received most of his medical care through other sources, saw his PCP once per year, in April. Likely that vaccine did not contribute to death, but was combination of advanced age (72 y/o) and comorbidities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NO LABS FROM FACILITY SINCE 2018 OTHER FACILITY: 02/08/2021 Labs: Gluc 149, HH 3.89/12.4, TROPONIN NEG X 2 EKG-NO ISCHEMIC CHANGES GALLBLADDER ULTRASOUND: "Cholelithiasis with no sonographic evidence of acute cholecystitis. Surgery consulted and stated pt can follow up outpt for consideration of elective cholecystectomy. pt was able to tolerate diet with no nausea or vomiting no chest pain, pt is stable for dc to fu with PCP, surgery and cardiology in outpt. CTA a/p: Sigmoid diverticulosis but no acute diverticulitis. Gallstones within the gallbladder associated with mild distention. No surrounding inflammatory changes. CXR-IMPRESSION: Opacity left lung base near the costophrenic recess could be due to atelectasis or pneumonia.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1989293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WI
Alter: 67,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 06.03.2021
Beginn: 18.12.2021
Tage bis Beginn: 287,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

fully vaccinated covid related death

Weitere VAERSDATA-Felder

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

VAERS 1984740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WI
Alter: 95,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 04.03.2021
Beginn: 20.12.2021
Tage bis Beginn: 291,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Fully vaccinated Covid-19 related death.

Weitere VAERSDATA-Felder

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

VAERS 1982153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 14.02.2021
Beginn: 15.12.2021
Tage bis Beginn: 304,0
Dosis: 2
Route/Site: IM / RA

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

Acute kidney injury Acute respiratory failure Bacteraemia Bacterial test positive Blood culture positive Blood urine present Breath sounds absent COVID-19 Cardiac arrest Cardiac failure Condition aggravated Death Deep vein thrombosis Dyspnoea Endotracheal intubation Heart sounds abnormal Impaired quality of life Laboratory test abnormal

Symptomtext

Deceased 12/16/2021; Hospitalized 12/15/2021; COVID-19 positive 12/15/2021; fully vaccinated BRIEF OVERVIEW: Admission Date: 12/15 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Severe sepsis (HCC) [A41.9, R65.20] Acute respiratory failure with hypoxia (HCC) [J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Patient is an 86 year old male with past medical history significant for non-hodkin's lymphoma, CAD, CABG in 1992, COPD, DMT2 who presented to the ED 12/15 with altered mental status and SOB. He was in respiratory distress upon arrival to ED and was intubated. Found to be COVID positive. He developed septic shock requiring Epi, NE, and vasopressin. Blood cultures positive for GPCs in pairs and chains. Strep pneumo urine antigen negative. UA positive for blood, bacteria, leukocytes. He was started on broad spectrum antibiotics. Labs were notable for AKI, elevated troponin, leukocytosis, thrombocytopenia. On 12/16am, patient developed pulseless VT. ROSC after ~7 minutes. US 12/16 showing right peroneal vein DVT. GOC discussion with family 12/16: All family in agreement that patient would never be happy with a quality of life where he was dependent on machines or others to help hi live. He would never want to be confined to a nursing home. If he could not go back to the quality of life he had before admission, he would not want to continue care. Given heart failure/cardiac arrest, circulatory shock, acute renal failure, bacteremia, underlying lymphoma that cannot be treated at present time, and COVID requiring a ventilator, family is requesting DNR with plans to transition to comfort care this afternoon after daughter arrives. All family in agreement. Dr. present for length of goals of care discussion (see separate note) and in agreement with plan. On follow up, all children and spouse present and in agreement to withdraw care. Patient has one brother who family has been keeping updated and in agreement with whatever patient's spouse and children decide. Family tearful but appropriate. Dr. updated. I was called by nurse for signs of death. On exam, no heart or lung sounds auscultated for 2 minutes. No palpable pulse for two minutes. No discernible chest rise or fall. No spontaneous movements. Pupils fixed and dilated. No response to noxious stimuli. Time of death 1615. Dr. updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma Acute respiratory failure with hypoxemia (HCC) Chronic bronchitis (HCC) Hypertension Coronary artery disease, s/p 4V CABG age 58. LBBB (left bundle branch block) Acute on chronic combined systolic and diastolic congestive heart failure (HCC) Cardiomyopathy, ischemic COVID-19 virus infection, noted 12/15/2021 Septic shock (HCC), with urinary tract infection Non Hodgkin's lymphoma (HCC), with thrombocytopenica, noted 10/2021 Severe thrombocytopenia (HCC) Iron deficiency anemia Renal insufficiency, secondary to shock Malignant neoplasm of prostate (HCC) Right thyroid nodule Multinodular goiter Hyperlipidemia Type 2 diabetes mellitus without complication, without long-term current use of insulin (HCC) Melanoma (HCC) Hx of squamous cell carcinoma of the anal canal Personal history of radiation therapy
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acyclovir (ZOVIRAX) 800 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler carvedilol (COREG) 25 MG tablet citalopram (CELEXA) 20 MG tablet Contour Test Stri
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1947790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 03.03.2021
Beginn: 05.12.2021
Tage bis Beginn: 277,0
Dosis: 2
Route/Site: IM / AR

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

Acute kidney injury Acute respiratory failure COVID-19 Chest X-ray abnormal Cough Fatigue Lung opacity SARS-CoV-2 test positive Tachycardia

Symptomtext

Hospitalized 12/5/2021; COVID-19 positive 12/5/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider at Discharge: MD Admission Date: 12/5/2021 Discharge Date: 12/07/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: AKI (acute kidney injury) (HCC) [N17.9] Acute respiratory failure with hypoxia (HCC) [J96.01] Acute hypoxemic respiratory failure due to COVID-19 (HCC) [U07.1, J96.01] COVID [U07.1] HOSPITAL COURSE: Patient is a 71-year-old male who presented to the emergency department with fatigue and cough. In the emergency department, patient was tachycardic and found to be hypoxemic on room air and placed on supplemental oxygen. Chest x-ray showed minimal hazy and streaky opacities seen in the inferior lateral left lung which can be seen with COVID 19 pneumonia. Patient was positive for COVID-19. He was admitted. He was started on Decadron and remdesivir. Patient improved during his hospital stay. He was able to be weaned from supplemental oxygen. PT/OT evaluated patient recommended home with assist. Patient was recommended to increased testing of blood sugars at home while on Decadron into call PCP with elevated sugars. Patient was recommended follow-up with primary care physician. He was discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSA (obstructive sleep apnea) Pulmonary nodule MVP (mitral valve prolapse) Dilated aortic root (HCC) Acute deep vein thrombosis (DVT) of tibial vein of left lower extremity (HCC) Vitamin D deficiency Fatty liver Olecranon bursitis Unspecified convulsions (HCC) Chronic back pain Migraine Other psychoactive substance dependence, in remission (HCC) Chronic headache disorder Tremor, essential Unspecified dementia without behavioral disturbance (HCC) Polymyalgia rheumatica (HCC) Sensorineural hearing loss (SNHL) of both ears Stage 3 chronic kidney disease (HCC) Diabetes mellitus without complication (HCC) Hyperlipidemia, unspecified Type 2 diabetes mellitus without complications (HCC) Elevated prostate specific antigen (PSA) Squamous cell carcinoma in situ of skin Osteopenia Major depressive disorder, single episode, unspecified Episode of recurrent major depressive disorder (HCC)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler alendronate (FOSAMAX) 35 MG tablet ARIPiprazole (ABILIFY) 5 MG tablet aspirin-acetaminophen-caffeine (EXCEDRIN MIGRAINE) 250-250-65 MG per tablet atorvast
Allergien: Ambien [Zolpidem Tartrate] Tegretol [Acid Red #17] Penicillins Ambien [Red Dye] Butorphanol Dilantin [Fd&c Yellow #1] Minocycline Nsaids Other Penicillin [Aspartame] Phenytoin Stadol [Butorphanol Tartrate] Tegretol [Carbamazepine-fd&c Yell #6-propyl Glycol] Toradol
Vorherige Impfungen: -

VAERS 1936547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 82,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 17.02.2021
Beginn: 15.05.2021
Tage bis Beginn: 87,0
Dosis: 2
Route/Site: SYR / UN

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

Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Condition aggravated Death Intensive care Malaise Malnutrition Rheumatoid arthritis SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of COVID-19 breakthrough disease after which a death occurred. The individual was vaccinated with the Pfizer product on 01/27/2021 and 02/17/2021. The individual became symptomatic on 04/10/2021 and was admitted to hospital on 04/11/2021. PCR tests on 04/11/2021 and 04/18/2021 were both positive. They were discharged from hospital on 04/13/2021 and then re-admitted on 04/18/2021 and left against medical advice on 04/21/2021. The individual had contact with the health department on 04/21/2021 regarding release from isolation and the individual reported that they had recovered from their illness and were no longer experiencing symptoms; based on the individual's self-report, they were released from isolation. The individual was then re-admitted on 04/23/2021 which required ICU admission. They were discharged to an out-of-state advanced care hospital on 05/13/2021, and died at that out-of-state facility on 05/15/2021. Death certificate details as follows: Part I Cause of Death A: Acute Respiratory Distress Syndrome B: Sequela of COVID 19 Viral Pneumonia C: Rheumatoid Arthritis D: Severe Protein Calorie Malnutrition Part II Other Significant Conditions: Urothelial Carcinoma

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 29,0
Labordaten: Positive COVID-19 tests x2 despite being fully vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid Arthritis, Severe Protein Calorie Malnutrition (listed on the death certificate, unclear if this was a chronic or acute condition), Urothelial Carcinoma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 23.03.2021
Beginn: 26.11.2021
Tage bis Beginn: 248,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Anticoagulant therapy COVID-19 pneumonia Condition aggravated Leukocytosis SARS-CoV-2 test positive Sputum culture

Symptomtext

Hospitalized 11/26/2021-still admitted currently; COVID-19 positive 11/26/2021; fully vaccinated ASSESSMENT / PLAN: Patient is a 79 y.o. male with a past medical history of atrial fibrillation who is admitted with COVID-19 pneumonia. Symptoms started on 11/21/2021, patient started outpatient dexamethasone on 11/23/2021. Patient has had 2 doses of Pfizer vaccine, last in March. Admitted on 5 L nasal cannula. Acute hypoxic respiratory failure COVID-19 pneumonia Plan - currently on 5 L nasal cannula - dexamethasone to complete 10 day course (12/2), remdesivir to complete 5 day course (end 11/30) - strict I&Os, daily weights - no current indication patient needs diuresis at this time. Appears euvolemic on exam. - no need for additional cap coverage at this time, would not hesitate to start this with further workup if there is concerns for clinical worsening - Lovenox for DVT prophylaxis - wean oxygen as able 12/4/2021 note: Acute hypoxic respiratory failure COVID-19 pneumonia Leukocytosis Leukocytosis likely secondary to steroids. No indication for diuresis at this time. No indication for CAP coverage at this time, with Procal wnl. Decreased from HFNC 50% to 45% at 40 L, without increased work of breathing. Plan - dexamethasone 6mg / day, x 10 day (end 12/2) - remdesivir x 5 day, (end 11/30) - the patient has completed both dexamethasone and remdesivir and has had no significant improvement. Will trial high-dose Solu-Medrol per recent studies demonstrating benefit with Solu-Medrol 250 mg daily for 3 days followed by 14 day course of prednisone 40 mg daily. Pepcid for GI ppx - Oxygen therapy - wean high-flow nasal cannula, as tolerated - strict I&Os, daily weights - encourage self proning - Sputum culture, pending Dispo: Patient likely to be inpatient for multiple in-patient days secondary to COVID-19 pneumonia Care Management note 11/6/2021: Discharge Coordination/Progress: RA completed. Wife is in agreement with Mission Point Cedar Springs referral for SAR. MP is unable to take patient until patient is using 4L or less of oxygen. Using HFNC 50%, 40L.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pneumonia due to COVID-19 virus Atrial fibrillation, persistent (HCC
Andere Medikamente: diltiazem (DILACOR XR) 240 MG 24 hr capsule tadalafil (CIALIS) 20 MG tablet
Allergien: NKA
Vorherige Impfungen: -

VAERS 2562001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 90,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 11.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 32,0
Dosis: 1
Route/Site: IM / LA

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

Adverse reaction Death Incomplete course of vaccination

Symptomtext

Narrative: 89 year old male, received first dose of COVID-19 vaccine (Pfizer) on 2/11/2021. Contacted medicine team 3/11/2021 with complaint of a "bad reaction" and still recovering. Declined scheduled second dose (due 3/4/2021). No other updates from patient. Expired 3/15/2021.

Weitere VAERSDATA-Felder

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

VAERS 2561994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 11.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / LA

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

Anticoagulant therapy Death

Symptomtext

Narrative: 76 year old male, received first dose of COVID-19 vaccine on 2/11/2021. PMH HTN, CAD s/p NSTEMI and CABGX4, HFrEF and HLD. Spoke with pharmacy/anticoagulation on 2/16/2021. No further medical notes. Patient expired 2/28/2021.

Weitere VAERSDATA-Felder

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

VAERS 2559296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 16.02.2021
Beginn: 22.03.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: IM / LA

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

Bacteraemia COVID-19 Cardiac failure congestive Cough Death Dyspnoea exertional Incomplete course of vaccination Malaise Peripheral swelling Pneumonia SARS-CoV-2 test positive

Symptomtext

Narrative: 76 year old male received first dose of COVID-19 vaccine (Pfizer) on 2/16/2021. Patient was admitted to emergency room on 2/11/2021 from rehab, skilled nursing facility with pneumonia and CHF. He was on treatment for bacteremia and presented with dyspnea on exertion & leg swelling. Patient had symptoms for 2 weeks prior, worsening and associated with non-productive cough. Patient tested positive for COVID-19 on 3/11/2021, never received second dose of COVID-19 vaccine and expired 3/22/2021.

Weitere VAERSDATA-Felder

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

VAERS 2557233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 11.02.2021
Beginn: 23.05.2021
Tage bis Beginn: 101,0
Dosis: 1
Route/Site: IM / LA

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

Death Dyspnoea Incomplete course of vaccination Mental status changes Tumour excision Urosepsis

Symptomtext

Narrative: Pt is 75 y/o male with a PMH of initial diagnosis of small cell lung cancer and most likely metastatic colorectal adenocarcinoma had received the first dose of Pfizer COVID-19 vaccination on 2/11/2021. Pt was then admitted at a local hospital since 3/1 for surgery to remove tumor. Pt was then seen by non-facility ER on 4/14 and 5/14 for SOB and AMS. On the admission for 5/14, patient was found to be uroseptic. Pt never received 2nd dose of COVID-19 vaccination. Pt passed away 5/23/2021.

Weitere VAERSDATA-Felder

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

VAERS 2557231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 24.02.2021
Beginn: 06.04.2021
Tage bis Beginn: 41,0
Dosis: 1
Route/Site: IM / RA

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

Anticoagulant therapy Death Loss of consciousness Lower gastrointestinal haemorrhage Pallor Rectal haemorrhage

Symptomtext

Narrative: 88 year old male, received first dose of COVID-19 vaccine (Pfizer) on 2/24/2021. Admitted to hospital on 2/26/21 for lower GI bleed while on warfarin, BRB per rectum, becoming pale and losing consciousness. d/c to home, received hospice care. Patient expired 4/6/21, facility received message the following day.

Weitere VAERSDATA-Felder

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

VAERS 1920680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 13.09.2021
Beginn: 28.11.2021
Tage bis Beginn: 76,0
Dosis: 2
Route/Site: IM / AR

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

Acute respiratory failure Angiogram normal Asthenia Blood culture Blood gases normal Blood lactic acid COVID-19 Chest X-ray normal Computerised tomogram abdomen Confusional state Diarrhoea Dyspnoea Fall Fatigue Feeling abnormal Hypophagia Mental status changes Pain

Symptomtext

Hospitalized (11.28.21 - still currently admitted); COVID-19 positive (11.28.21); Fully vaccinated plus BOOSTER HISTORY OF PRESENT ILLNESS: Patient is a 71 y.o. male PMH of splenic B cell lymphoma, Hx of LLE DVT (was on eliquis and off receiving chemo, cholangitis sepsis in 10/2021, type II DM, HTN, who presented to ED with his wife with complaints of progressive confusion and AMS concerns, as well as weakness. Most of hx is collected from the wife who is bedside, but patient does add to it. They state patient has received his flu shot on 11/21/21, and was doing well, but on Wed 11/23 started to feel worse, tired, fatigued, and at this time has rec'd tx in office. He cont to have progressive weakness, per wife also has had fevers >101F, and a fall - was not witnessed (unsure if he hit his head, not on blood thinners). He has been having diarrhea on and off. Not eating much. Due to all above, his wife decided to bring him to the ED. In ED work up as above noted positive covid test, but most of rest work up neg, blood cult pending, given zosyn, and decadron in ED, and IVF per sepsis protocol. On my eval, patient sleepy, but responds appropriately, he just had benadryl as he is allergic to contrast, so had been pretreated for imaging. He states he feels poorly, achy, tired, had mild SOB, no cough, and no pain anywhere. Has on and off diarrhea as mentioned, and no other sx. will give remdesevir and cont dexamethasone, might need compassionate use of Regeneron (as patient is high risk of getting worse and getting re-current covid infx, due to inability to amount good antibody response), will re-assess tomorrow and see the O2 needs. No obvious infectious process per imaging, will re-image later today post hydration to assess for PNA -- CXR ordered., in the mean time vanc/zosyn, and follow up on cultures. Supportive care and monitor closely

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: Sepsis Covid - 19 infection Acute hypoxic respiratory failure - patient has had covid - 19 vaccine and booster - s/p 30ml/kg IVF given in ED, cultures obtained and started on zosyn - UA negative - Blood cult obtained - cont to monitor - covid -19 swab positive - lactic 1.1 -- > 0.8 - ABG 7.38/39/23 -- no concerns - CXR neg - CTA angio abd/pelvis (had complains of diarrhea) no acute findings - CTA angio thorax - no PE or infection, noted emphysema - cont O2 supplement - will obtain procal and cont zosyn for now - discussed with ID, cont abx, and as above, might need compassionate use of Regeneron, will re-address tomorrow, if hypoxic, will need compassionate use, if hypoxia resolves, then will be able to give. - ID will be following
Aktuelle Erkrankungen: NA
Vorgeschichte: MRSA (methicillin resistant Staphylococcus aureus) infection At risk for falls SIRS (systemic inflammatory response syndrome) Lymphoma Febrile neutropenia Weakness Septic shock Anemia Thrombocytopenia Histoplasmosis Mucositis due to chemotherapy Tachyarrhythmia Metabolic acidosis, NAG, bicarbonate losses AKI (acute kidney injury) Encounter for counseling for are management of patient with chronic conditions and complex health needs using nurse-based model Cholangitis Major depressive disorder, recurrent episode, moderate Acquired hypothyroidism Essential hypertension Immune thrombocytopenic purpura Other non-follicular lymphoma, extranodal and solid organ sites Nonfamilial hypogammaglobulinemia Panlobular emphysema
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acyclovir (ZOVIRAX) 400 MG tablet butalbital-acetaminophen-caffeine 50-325-40mg (FIORICET, ESGIC) per tablet escitalopram (LEXAPRO) 20 MG tablet fluconazole (DIFLUCAN) 100 MG tablet HYDROcodone-acetamin
Allergien: RituximabShortness of Breath, Palpitations, Other Contrast Dye [Ivp Dye, Iodine Containing]Hives
Vorherige Impfungen: -

VAERS 1920193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 87,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 15.03.2021
Beginn: 14.09.2021
Tage bis Beginn: 183,0
Dosis: 1
Route/Site: IM / LA

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

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

Symptomtext

Had breakthrough infection and passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Positive COVID-19 test on 9/10/2021
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Coronary artery disease Hypertension Dyslipidemia
Andere Medikamente: Unknwon
Allergien: None known
Vorherige Impfungen: -

VAERS 1905950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 15.03.2021
Beginn: 18.11.2021
Tage bis Beginn: 248,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Ageusia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Condition aggravated Cough Decreased appetite Dyspnoea exertional Headache Laboratory test normal Respiratory tract congestion SARS-CoV-2 test positive Transaminases increased

Symptomtext

Hospitalized 11/21/2021; COVID-19 positive 11/18/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider: MD Admission Date: 11/21/2021 Discharge Date: Nov 23, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute respiratory failure with hypoxia (HCC) [J96.01] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 72-year-old female with a past medical history of dyslipidemia, depression, obesity, OSA who presented secondary to a chief complaint of headache, loss of taste, decreased appetite, coughing congestion. She also started noting shortness of breath with exertion. She received both doses of Pfizer vaccine in March 2021. When EMS arrived she was 80% on room air. She was placed on 4 L nasal cannula. In the emergency department she was otherwise hemodynamically stable. Her labs were unremarkable. Her chest x-ray showed findings consistent with COVID-19 infection. She was known to be COVID positive on 11/18/2021. She was admitted for COVID-19 pneumonia. She was started on Decadron and was out of the window for remdesivir and monoclonal antibodies. She weaned to 3 L nasal cannula with activity per Pulmonary rehab evaluation. She was noted to have mildly elevated transaminases secondary to COVID-19. She had improvement of her symptoms and was discharged home on 11/23/2021 with home oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSA (obstructive sleep apnea) Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxia (HCC) Essential hypertension PAD (peripheral artery disease) (HCC) Duodenitis Colon polyps Class 1 obesity with serious comorbidity and body mass index (BMI) of 33.0 to 33.9 in adult, unspecified obesity type Unspecified severe protein-calorie malnutrition (HCC) Senile nuclear cataract, bilateral Lattice degeneration of both retinas Posterior vitreous detachment, bilateral Dyslipidemia
Andere Medikamente: aspirin 81 MG tablet atorvastatin (LIPITOR) 10 MG tablet B Complex-C (SUPER B COMPLEX) TABS benzonatate (TESSALON) 100 MG capsule Cholecalciferol (VITAMIN D3) 1000 UNITS TABS dexamethasone (DECADRON) 6 MG tablet famotidine (PEPCID) 20 MG ta
Allergien: Codeine PCN
Vorherige Impfungen: -

VAERS 1905648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 15.03.2021
Beginn: 17.11.2021
Tage bis Beginn: 247,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Angiopathy Aspiration Asthenia Asymptomatic COVID-19 Asymptomatic bacteriuria Blood culture negative Blood lactic acid normal Bradycardia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic kidney disease Condition aggravated Drug level Gait disturbance Hypotension

Symptomtext

Hospitalized 11/23/2021-currently still admitted; COVID-19 positive 11/17/2021; fully vaccinated ASSESSMENT / PLAN: Patient is an 89 year old male with past medical history significant for CKD stage 3, chronic afib not on anticoagulation, CAD, chronic combined systolic and diastolic heart failure, and HTN. He was recently admitted 11/17 - 11/20 with fever and AKI. COVID positive but without respiratory symptoms. Discharged in prn 2L nasal cannula (felt to be more related to underlying OSA than COVID). ED reported patient was brought in for SOB although patient denied this. He was noted to have difficulty with ambulation in the ED and then became hypotensive requiring vasopressors. Labs were significant for AKI on CKD, troponin 301, procal .28, and mild leukocytosis. UA was unremarkable. Chest XR diffuse bilateral infiltrates (COVID vs bacterial pneumonia vs vascular congestion). He was started on vancomycin and Zosyn. NE weaned off shortly after arrival to ICU. Sepsis: Etiology likely pneumonia given chest XR findings COVID positive 11/17 (but patient reports no symptoms) Procalcitonin mildly elevated at .28 LA WNL Blood cultures NGTD Legionella and strep pneumo pending MRSA screen pending Sputum culture ordered NE for MAP >65mmHg, weaned off shortly after arrival to ICU Vancomycin and Zosyn for empiric coverage COVID: Vaccinated in March COVID positive 11/17 Has denied current symptoms Chest XR with bilateral infiltrates Decadron 6mg daily 11/29/2021 note: Assessment & Plan: # Septic Shock (Resolved) # Aspiration PNA Presented 11/23 with fever and hypotension and presumed respiratory etiology. Placed on vasopressors Norepi (11/24) and weaned the same day. UA unremarkable. Started on Zosyn and Vancomycin while in ICU and Vancomycin discontinued as MRSA screen negative. Strep pneumonia and legionella antigen negative. Unable to provide sputum sample ---follow peripheral blood cultures x2 (11/23) and no growth to date, maintain MAP >65 ---IV Zosyn (3.375 mg q6 day #6) and continue for now given worsening hypoxia and plan for 5-7 days ---SLP consulted and recommending NPO until respiratory status improves, aspiration precautions ---consult nutrition and likely if respiratory status not improved by tomorrow will need CorPak # COVID-19 PNA with Acute Hypoxic Respiratory Failure Admitted to hospital (11/17-11/20) with fever and AKI. Treated with UTI at the time with Fosfomycin. Tested positive for COVID-19 (11/17). CXR (11/23) with diffuse bilateral airspace opacities (worsening when compared to prior). Remdesivir (11/18-11/19), Decadron (11/17-11/20). States he is vaccinated against COVID-19, received 2 vaccines a couple months ago. ---Decadron (6 mg IV daily day #6 - did receive prior to hospitalization), ---continous pulse oximetry, hold on further lasix at this time given given NPO status Discharge Coordination/Progress: Pt is currently on high flow O2, per nursing pt continues to aspirate Plan: Pt to d/c when medically stable, to return to assisted living

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: Discharge Physician: Doctor Primary Care Physician: Doctor Date of Admission: 11/17/2021, Hospital Day: 4 Discharge Date: 11/20/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness AKI (acute kidney injury) COVID-19 virus infection COVID-19 HOSPITAL COURSE: 89-year-old male past medical history CKD stage 3, peripheral tibial disease, chronic combined systolic and diastolic CHF, permanent atrial fibrillation, coronary artery disease presents with weakness. In the emergency department, patient noted to be febrile. COVID-19 PCR positive. UA with evidence of increased WBC and was administered IV fosfomycin. Patient also noted to have AKI on CKD stage 3. He was not hypoxic and did not require supplemental oxygen. Hospitalist service consulted for admission further evaluation. Patient asymptomatic was not continued on antibiotics for abnormal finding on UA as likely asymptomatic bacteriuria. Medications were renally dosed. Patient was administered gentle IV fluid monitor closely given COVID-19 status. He had improvement of AKI with return to baseline CKD. PT/OT evaluated and initial advised SAR after additional days recommendations were updated to return to assisted living with PT/OT. Case management/MSW consulted to arrange for outpatient services and discharge planning. Patient was noted to be slightly bradycardic and digoxin was held with digoxin levels within normal limits. Bradycardia resolved and was continued on home medications. Respiratory therapy performed home oxygen evaluation as patient had on and off 1-2 L nasal cannula 1-2 L at night possibly related to underlying OSA. Respiratory therapy performed home oxygen evaluation patient did not qualify for continuous supplemental oxygen. Patient has a known establish order for supplemental oxygen 2 L p.r.n which he may continue. Patient clinically improved and hemodynamically stable for discharge. Discussed plan of care discharge with patient including outpatient follow-up PCP within 7 days. Patient voiced understanding was agreeable with plan of care discharge.
Vorgeschichte: Acute kidney injury Permanent atrial fibrillation Cardiomyopathy, ischemic Essential hypertension with goal blood pressure less than 140/90 Stage 3a chronic kidney disease Pressure injury of right foot, stage 3 COVID-19 virus infection Septic shock Chronic pain Coronary artery disease due to lipid rich plaque Dyslipidemia BPH (benign prostatic hyperplasia) GERD (gastroesophageal reflux disease) Lumbar spinal stenosis DJD (degenerative joint disease) Radicular syndrome of left leg-severe Congestive heart failure, NYHA class 2, chronic, combined PSA elevation Closed nondisplaced fracture of lateral malleolus of left fibula with routine healing Pressure injury of right ankle, stage 3 Physical deconditioning PAD (peripheral artery disease)
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet aluminum, magnesium & simethicone (ANTACID) 200-200-20 MG/5ML SUSP suspension aspirin 81 MG tablet atorvastatin (LIPITOR) 10 MG tablet benzonatate (TESSALON) 100 MG capsule bisacodyl (DULCOLAX) 10 MG su
Allergien: Valium Levofoxacin Morphine Fentanyl
Vorherige Impfungen: -

VAERS 1885399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 14.02.2021
Beginn: 11.11.2021
Tage bis Beginn: 270,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Asthenia Brain natriuretic peptide normal C-reactive protein abnormal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Hypoxia Mental status changes Pleural effusion Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

Hospitalized 11/11/2021; COVID-19 positive 11/11/2021; fully vaccinated Discharge Summary MD (Physician) ? ? General Medicine BRIEF OVERVIEW: Discharge Provider MD Primary Care Provider: MD Admission Date: 11/11/2021 Discharge Date: Nov 13, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] Altered mental status, unspecified altered mental status type [R41.82] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 87 yo who presented with progressive weakness, dyspnea and cough. In the ED patient tested positive for COVID-19 PNA requiring 2 liter of oxygen via NC. He was admitted to the medicine service. # Acute Respiratory Insufficiency with Hypoxia Secondary to COVID-19 PNA He was noted to be fully vaccinated but no booster, 2nd dose of Pfizer vaccine received in March. Reported symptoms initially started 11/10. CXR on admission was notable for left lateral airspace disease and mildly on peripheral of right mid lung, with interstitial edema and trace pleural effusion bilaterally per radiology read. COVID-19 PCR positive (11/11/21). BNP testing was found to be unremarkable. He was treated with Decadron and Remdesivir. He completed 3 days of Decadron while hospitalized with not ed improvement in CRP and was able to wean to room air at rest. Pulmonary was consulted and provided oxygen for home (1 liter to be worn with activity). Weakness improved and patient was found to be independent with activity while hospitalized. He was discharged home in stable condition on decadron to complete therapy in hopes of weaning oxygen off completely. He was provided discharge instructions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Essential hypertension, benign Venous insufficiency of both lower extremities Mild aortic stenosis Mild tricuspid regurgitation Obesity Neuropathic spondylopathy of lumbar spine (HCC) COVID-19 Chronic bilateral low back pain with bilateral sciatica Nonexudative senile macular degeneration of retina Hyperopia Lumbar cord compression (HCC) Benign prostatic hyperplasia Peyronie's disease Hypogonadism male Mixed hyperlipidemia Osteoarthritis Erectile dysfunction History of basal cell carcinoma (BCC) Insomnia History of small bowel obstruction Personal history of colonic polyps Restless legs syndrome (RLS) History of rheumatic fever as a child Primary osteoarthritis involving multiple joints Degenerative disc disease, lumbar
Andere Medikamente: Cholecalciferol (VITAMIN D3) 1000 UNITS CAPS clonazePAM (KLONOPIN) 0.5 MG tablet cyanocobalamin 1000 MCG tablet cyclobenzaprine (FLEXERIL) 10 MG tablet dexamethasone (DECADRON) 6 MG tablet furosemide (LASIX) 40 MG tablet Ibuprofen-diphenhyd
Allergien: Codeine Seasonal
Vorherige Impfungen: -

VAERS 1882915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WI
Alter: 77,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 22.02.2021
Beginn: 16.11.2021
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

fully vaccincated, complications of covid death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM; a-fib; PVD; CAD; HTN; HLD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1700626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 17.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / AR

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

Acute lung injury Acute respiratory distress syndrome Acute respiratory failure Adverse drug reaction Alkalosis hypochloraemic Endotracheal intubation Extra dose administered Laboratory test normal Anticoagulant therapy Bladder catheterisation Blood creatine increased Bronchoalveolar lavage Bronchoscopy Chest X-ray Computerised tomogram Death Chest X-ray abnormal Chills

Symptomtext

Believe that this may be a duplicate report. Patient has died (9.24.21); Hospitalized (8.31.21); Fully Vaccinated including 3rd dose (immunocompromised) Preliminary cause of death listed as Respiratory Failure. Severe acute hypoxemic respiratory failure. Multifactorial from severe acute lung injury and severe ACR (temporally related to third COVID vaccine received on 8/17/21) as well as bilaterally pulmonary embolism. Intubated 9/4/21. Tracheostomy 9/14/21. Infectious studies negative to date. COVID Ab negative on 9/9/21. Submitted to VAERS on 9/15/21 per Dr. HOSPITAL COURSE: Patient is a 73 y.o. female with a past medical history of veno-occlusive dx and ILD s/p bilateral lung transplant (09/2020), high risk EBV status, A. Fib not on anticoagulation, HTN and OSA. She received her 3rd dose of the COVID vaccine on 8/17/21. Admitted 8/31/21 for fatigue, dyspnea, nonproductive cough, subjective fevers and chills, and hypoxia. Recent bronch by transplant team identified A2 acute cellular rejection associated with declining lung function (FEV1 down 10% from best). On 9/4/21 she was transferred to the MICU for worsening hypoxemia with increased work of breathing. CT chest showed bilateral PE and subsequent doppler showed DVT in Right posterior tibial and Left peroneal veins. She received targeted thrombolytic therapy with IR and was continued on a heparin drip. She was started on broad spectrum antibiotics, pulse dose steroids and continued with her transplant medications and prophylaxis. 9/5 Continued low volume protective ventilation, some vent dyssynchrony improved with sedation on propofol. Had acute reaction to thymoglobulin, resolved with tylenol and benadryl- continued with pretreatment. 9/6 Weaning PEEP, remains on low dose sedation buit awake and alert. Continued diuresis with Lasix. Restarted home metoprolol and diltiazem for hypertension. BAL with GPC and GNR; MRSA nares negative- d/c vancomycin and continued on cefepime. 9/7 Tolerated PEEP 10 overnight, weaned down this morning with good oxygenation but CXR shows worsening bilateral effusions. Plan to increase diuresis and maintain current ventilator settings. Holding further thymo doses given leukopenia and thrombocytopenia. Insulin increased for steroid induced hyperglycemia. 9/8 CXR improved, stable respiratory status, net positive fluid balance. Sedation weaned. Passed SBT but had increased WOB after requiring increased FiO2 and PEEP. Plan to diurese with increased lasix and trial tomorrow. Better glucose control with increased insulin. Having multiple bowel movements after aggressive regimen yesterday, now held. 9/9 SBT overnight but switched to pressure control for increased work of breathing and perceived shortness of breath. Repeat SBT failed with similar issues after 10 minutes, returned to pressure support. Met fluid net negative goal, continue diuresis. Increased insulin for hyperglycemia. Awake and interactive on the vent. Transplant team restarted valgancyclovir. 9/10 Episodes of desaturation requiring 100% FiO2 for resolution. CXR unchanged and meeting negative fluid goal. Bedside bronch shows clear airways, BAL collected for culture and testing. Concern worsening respiratory status is related to cellular rejection with no clear infectious source and otherwise medically optimized. Transplant and infectious disease following. Thymoglobulin continues to be on hold. Complaints of suprapubic pain, Foley exchanged and UA collected, no signs of infection. 9/11 remains intubated and sedated. ID concern for possible PTLD given increased LFTs and Cre, CT A/P with nonspecific findings. Transplant team continues to hold thymoglobulin as EBV viral load has increased. Scheduled insulin increased for hyperglycemia. 9/12 Continues to have episodes of desaturations, requiring increased FiO2 for recovery. Fluid balance ever after 60 lasix TID yesterday, increasing Cre and contraction alkalosis. Lasix BID and one time diamox. Transplant team to restart thymoglobulin today and possible repeat bronchoscopy with biopsy later this week. Due to persistent ventilator requirements, tracheostomy was performed. This allowed for weaning of the patient's sedation in the patient tolerated minimal pressure support with low peak pressures. Over the next 2 weeks, the patient had persistent high FiO2 recover min in PEEP requirement chest x-ray remained more or less unchanged without improvement in her infiltrates likely secondary to her acute cellular rejection. There was continual effort made to keep the patient as dry as tolerated to remove any component of fluid overload from her respiratory failure. Similarly, repeat cultures, BAL, cell free DNA sequencing, and universal PCR were all sent without any evidence of infectious etiology for the patient's respiratory failure. Due to continued aggressive immunosuppression, rituximab was administered prophylactically to prevent PTLD in the setting of the patient's EBV positive donor status. Finally, the decision was ultimately made to sedate and paralyze the patient to help achieve optimal lung protective ventilation as the patient had been generating excessive tidal volumes of her own volition while on pressure support ventilation. Unfortunately, despite all these changes, the patient's ARDS continued to worsen, her lung compliance continue to decrease, and her O2 requirement continued to increase. Given the patient's overall worsening respiratory failure, conversation was had between the transplant team and family regarding consideration of ECMO. Due to the overall poor prognosis given the ongoing cellular rejection, family did not feel that this measure was consistent with the patient's wishes, and did opt to make the patient comfort care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Lung transplant status, bilateral (HCC) Severe pulmonary arterial systolic hypertension (HCC) OSA on CPAP Respiratory failure (HCC) Goals of care, counseling/discussion Active advance directive on file PVOD (pulmonary veno-occlusive disease) (HCC) Right ventricular dysfunction Anemia AF (paroxysmal atrial fibrillation) (HCC) Steroid-induced hyperglycemia Venous (peripheral) insufficiency Basal cell papilloma Astigmatism Anxiety Lipoma Benign neoplasm of eyelid Closed fracture of proximal end of left fibula Constipation Corneal epithelial and basement membrane dystrophy Diverticulitis Edema Gastroesophageal reflux disease Hearing loss Idiopathic osteoarthritis Insomnia Osteopenia of multiple sites Other complications of lung transplant (HCC) Post-transplant lymphoproliferative disorder (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acyclovir (ZOVIRAX) 200 MG capsule ALPRAZolam (XANAX) 0.25 MG tablet azithromycin (ZITHROMAX) 250 MG tablet calcium citrate-vitamin D (CITRACAL) 315-250 MG-UNIT tablet cholecalciferol (VITAMIN D3) 25 MC
Allergien: AspirinAnaphylaxis PenicillinsRash Tetanus ToxoidsSwelling, Other Dermatitis Antigen DiltiazemConfusion Diphtheria,pertussis,tetanus
Vorherige Impfungen: -

VAERS 1857473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 74,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 05.03.2021
Beginn: 09.11.2021
Tage bis Beginn: 249,0
Dosis: 1
Route/Site: IM / UN

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

Anxiety Death Hypoxia Intensive care Mechanical ventilation Pulse absent Pulseless electrical activity Respiratory failure Resuscitation

Symptomtext

Pt initially admitted to the covid medical floor with respiratory failure. She was on nasal cannula which rapidly progressed to high flow cannula. Pt was struggling with anxiety which did contribute to her increasing oxygen requirements and repetitive hypoxic events. Decision was made to transfer her to the ICU on 11/2/2021 given that she was unable to come off NIV. Once on ventilator, Pt required maximum ventilator settings and eventually even nitric oxide. Despite all interventions, Pt rapidly deteriorated on 11/9/2021. Husband and grandson arrived to bedside. Pt went into PEA, CPR was performed. She was able to regain a pulse for a few minutes then again went pulseless. CPR was performed until husband requested all efforts to be terminated. Pt was pronounced deceased @ 1135 on 11/9/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1857465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 76,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 17.02.2021
Beginn: 05.08.2021
Tage bis Beginn: 169,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Death

Symptomtext

DX WITH COVID 07/27/2021; VACCINATED WITH PRIMARY SERIES; PATIENT EXPIRED ON 08/05/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD CHF CRONIC RESPIRATORY FAILURE CHRONIC A-FIB
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1849876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 79,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 15.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / UN

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

Acidosis Cardiac arrest Delirium Endotracheal intubation General physical health deterioration Hypotension Hypoxia Illness Intensive care Mechanical ventilation

Symptomtext

Pt was initially admitted to the medical COVID floor where he was initiated on Dexamethasone and Remdesivir therapies. His hypoxemia continued to worsen and he required initiation of noninvasive positive pressure ventilation and was eventually transferred to the ICU on 10/28/2021 for ongoing care and management in the setting of refractory hypoxemia. His ICU course was initially complicated by delirium. His condition continued to worsen and was intubated on 10/30/2021 in the setting of impending respiratory/cardiac arrest. He began to experience increasing hypotension as well and required initiation of vasopressors. Given the history of heart failure with reduced ejection fraction, cardiologist was consulted and Pt was additionally placed on Dobutamine. He had worsening acidemia despite optimization of ventilator settings and required initiation on renal replacement therapy on 11/02/2021. Unfortunately, he continued to decompensate and on the evening of 11/04/2021, the patient did suffer of a cardiac arrest. Unfortunately Pt did succumb to his critical illness on the evening of 11/04/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1840437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Chills Coma Headache Nausea SARS-CoV-2 test positive Tremor Vomiting

Symptomtext

14-16 hours after the shot with severe chills, jackets on, and heated blanket. The shakes, headache, vomiting, and it didn't hit until the 14-15th hour. I saw a doctor and I wanted to make sure if it was part of the COVID-19 shot. I was in bed for the first shot for 2 weeks. I was really sick and nauseous. Symptoms lasted about two weeks. This time it was a few days less. COVID-19 positive in April 2020, Coma for 5 months from 4/26/2020 - 08/2020. Coded 3 times during coma and was in hospice 3 times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Numbness from COVID-19 Lost hearing Lung damage History from a lot of surgeries Prior to COVID-19 I was pretty healthy.
Andere Medikamente: Hydrochlorothiazide 12.5 mg Lopressor 50mg Singular 10mg Amlodipine 10mg Trazodone 100mg Simvastatin 40mg Celexa 40mg
Allergien: Sulfa Medication
Vorherige Impfungen: -

VAERS 2491058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 22.01.2021
Beginn: 03.08.2021
Tage bis Beginn: 193,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 pneumonia Cough Death Dyspnoea Endotracheal intubation Headache Intensive care Pain Syncope

Symptomtext

Narrative: Presented to ER on 7/31/21 s/p syncope. Since syncopal episode had increased SOB, cough, headache and body aches. Dx with Acute Hypoxic Respiratory Failure due to COVID-19 Pneumonia and admitted as inpatient, transferred to MICU 7/25/21, and eventually intubated. Treated with Remdesivir x 5 days (completed 7/28/21), dexamethasone x 10 days (completed 8/1) and provided supportive care with supplemental O, vitamin C, zinc, benzonatate, and acetaminophen. Patient expired on 8/3/2021. Co-morbidities included cardiac arrhythmia, pacemaker placement, hx laryngeal cancer, obesity, chronic obstructive sleep apnea, and spondyloarthropathy (treated with tofacitinib + sulfasalazine).

Weitere VAERSDATA-Felder

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

VAERS 1825563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 26.03.2021
Beginn: 20.10.2021
Tage bis Beginn: 208,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Anaemia Anticoagulant therapy Anticoagulation drug level above therapeutic Asthenia COVID-19 COVID-19 pneumonia Computerised tomogram head normal Condition aggravated Death Decreased appetite Endotracheal intubation Fall Gait disturbance Gastrointestinal endoscopic therapy Gastrointestinal polyp haemorrhage International normalised ratio increased Mental status changes

Symptomtext

Deceased (10.23.21); Hospitalized (10.20.21); COVID-19 positive (10.20.21); fully vaccinated Primary Care Physician at Discharge Admission Date: 10/20/2021 Date of Death: 10/23/21 Time of Death: 5:47 PM Preliminary Cause of Death: Pneumonia due to COVID-19 virus DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Supratherapeutic INR Acute on chronic anemia Acute respiratory failure due to COVID-19 HOSPITAL COURSE: 86yo Afib on coumadin, trip/fall on 10/20, admitted to IM for INR-7.3, recent GIB (9/13 EGD with coag, 10/1 21 friable polyps resected for oozing and need for anticoagulation), found to be COVID + (full vax with Pfizer and booster), symptoms of weakness, poor appetite since 10/14, 10/22 Azith/Rocephin started for CAP, pt mentation declining, taking off his oxygen, not following commands, early AM 10/23 pt removed oxygen, went into PEA arrest. ROSC obtained after 15min. Intubated, cooled to prevent fever, no target temp. CT head done and NEG, EEG ordered however son came in to see patient, held a family mtng and decided to go comfort care. Therefore pt was extubated this afternoon, sedation off and passed away peacefully.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: 10.1.21: Procedure: ENDOSCOPIC MUCOSAL RESECTION (EMR), UPPER GI. Friable bleeding gastric polyps. Multiple friable polyps in the stomach. Benign appearing. These were treated by cold BAS (band and slough) EMR.
Vorgeschichte: Rheumatic aortic insufficiency Rheumatic mitral insufficiency CHF (congestive heart failure) Permanent atrial fibrillation Elevated prostate specific antigen (PSA) Cardiomyopathy, nonischemic HDL deficiency VT (ventricular tachycardia) Cardiac resynchronization therapy defibrillator (CRT-D) in place Mixed hyperlipidemia Essential hypertension Macular degeneration Orthostatic hypotension Diabetes mellitus type 2 with complications GERD (gastroesophageal reflux disease) S/P aortic valve replacement S/P mitral valve repair Exudative age-related macular degeneration, unspecified laterality, unspecified stage Hemiplegia and hemiparesis following cerebral infarction affecting left non-dominant side Thoracic aortic aneurysm, without rupture Supratherapeutic INR Shock Acute respiratory failure with hypoxia Cardiac arrest COVID-19 AKI (acute kidney injury)
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet aspirin 81 MG tablet Blood Glucose Monitoring Suppl MISC carvedilol (COREG) 25 MG tablet Ferrous Sulfate (IRON) 325 (65 Fe) MG TABS glucose blood VI test strips (ONE TOUCH ULTRA TEST) strip insulin glar
Allergien: Lipitor [Atorvastatin] Statins [Hmg-coa-r Inhibitors]Myalgia
Vorherige Impfungen: -

VAERS 1821632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 11.03.2021
Beginn: 04.07.2021
Tage bis Beginn: 115,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Death Thrombocytopenia

Symptomtext

death N17.9 - Acute kidney failure, unspecified D69.6 - Thrombocytopenia (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1126981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: ND
Alter: 56,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 20.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Blood test Computerised tomogram Dyspnoea Fibrin D dimer Hypoaesthesia Computerised tomogram head Deep vein thrombosis Laboratory test Pulmonary embolism Ultrasound scan Pain in extremity Pulmonary thrombosis Thrombosis

Symptomtext

blood clots and lung clots; blood clots and lung clots; severe pain in the right arm; Numbness; short of breath walking; Pulmonary embolism; This is a spontaneous report from a contactable consumer (patient). This 56-year-old female patient received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9267) via an unspecified route of administration in the right arm on 20Feb2021 as single dose for COVID-19 immunization. Medical history included Acid Reflux, allergic to Penicillin's, Sulfa, Wasp and Bee strings. Concomitant medications were unknown. The patient was reporting on having blood clots after receiving the Pfizer-BioNTech COVID-19 Vaccine. She had been on the ER. She had also been prescribed Eliquis. The patient received apixaban (ELIQUIS, tablet, strength: 5 mg, lot number: 1796053, expiration date: Sep2023) oral from Mar2021 at 5 mg twice a day for blood clots. The patient was asking for compensation and was given with the Legal Team's address. She wanted to know statistical information on how often blood clots happen after receiving the vaccine and if this was a common side effect. The patient wanted to know details about the side effects of the Pfizer-BioNTech COVID-19 Vaccine, specifically what was fatigue. The patient had the Pfizer covid BioNtech vaccine last year and developed blood clots. She was put on Eliquis. The doctor then took her off Eliquis saying she didn't need it anymore. When she was off of Eliquis she developed clots again and so she was put on Eliquis again. The patient stated that she worked in a healthcare setting before but she was retired. The patient stated that she had reported it to VAERS. During the call she also said that with Eliquis she had been paying a lot out of pocket, and she had been to the ER a couple times and would like compensation. The patient complained that the help for Eliquis was all based on income, they made too much and would not qualify for it, this was one more hurdle she guesses. The patient stated that she had only gotten the first dose of the Pfizer covid vaccine, and she was instructed to not get it anymore. The blood clot began about 2-4 days on Feb2021 after getting the first dose. Initially she had trouble with her leg, but she never expected a blood clot, she had babied it forever, she was thinking to herself how did she pull a muscle and not know. She had elevated the leg. Finally she was at a (withheld) one day and she picked something up and her lower calf felt like big jello just jumped above into the knee into the upper part of the leg and thigh. It was so painful, and she was in the middle of this at withheld. The patient clarified stating that she needed to back up a bit. It was in the lower calf, she didn't know when but she got severe pain in the right arm, and it went numb for a bit but then it went away into the shoulder, back and neck area it was aching. She was still making excuses telling herself maybe she was sitting in the recliner and her head was getting tilted not thinking that it was a blood clot. The clot jumped from the lower leg into the upper leg, luckily she made it home, and that's when they thought it was a clot and said she has got to go to the ER. She went to ER, the doctor there did a scan, they did scans all over, she was there for 5 hours, and they were about to discharge her home but that's when the finally the report from the scans came and that's when they told her she absolutely had a blood clot. The next day, she was short of breath walking from her bedroom to the chair, and so they went back to the ER and told her she had bilateral clots in the lungs confirming that when she went to ER again it was a pulmonary embolism. She then went for blood work follow up. She told her Primary care and brought all her records and primary Care said to stay on Eliquis. She then went to a doctor that did vein work, Dr (withheld) said that he thought the D Dimer test wasn't spiking any more and since there's no family history of clots and since it's more harmful than a benefit to stay on Eliquis he told her to stop the Eliquis. In 10 days she was back with blood clot and lung clots Feb2021. Now today that vein doctor, sent her to her primary care, the patient stated that she will ask her if she can see a hematologist. Next week she will see the Vein doctor again, because he said he wanted to scan the leg again. She called her insurance because she thought back on the Eliquis since Mar2021, she had all these appointments of this illness, and test. The patient stated that she was seen in a clinic, it all started at a clinic, they were the people that initially saw her, when she went to the ER first. The patient clarified that she had only made ER visits in which she would be at the hospital for 5 hours or so, but she was never admitted to the hospital. She was just at the facility 5 hours each time. Eliquis was started in Mar2021 when she first went to the ER. The covid vaccine was given in the right arm and the Right leg was where she had the problem to start with. She was very healthy, she swam and walked. With this blood thinner she didn't know if being on this forever will change what she can do, she didn't want an injury. The patient had had a lot of blood work and CT scans. Prior to ending the call, caller states that she would like to be reimbursed for medical procedure, tests, appointment, her insurance, and Eliquis. Outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown result; Test Date: 2021; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown result; Test Date: 2021; Test Name: D Dimer test; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (oesophageal); Allergic reaction to bee sting; Allergic reaction to wasp sting; Penicillin allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1804826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: SD
Alter: 60,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 10.03.2021
Beginn: 08.09.2021
Tage bis Beginn: 182,0
Dosis: 1
Route/Site: UN / LA

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

Acute respiratory distress syndrome Acute respiratory failure COVID-19 pneumonia Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough disease that resulted in death. Death Certificate details are as follows: Part I Cause of Death A: Acute Respiratory Failure B: Adult Respiratory Distress Syndrome C: COVID 19 Pneumonia Part II Other Significant Conditions: Acute Kidney Failure, Sepsis, Encephalopathy, Atrial Fibrillation, Coronary Artery Disease The patient was admitted to the hospital on 09/08/2021. It is unknown if they were having symptoms, but the patient did receive diagnoses of both pneumonia and ARDS so it seems that respiratory symptoms were likely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 19,0
Labordaten: Positive COVID-19 test on 09/09/2021 despite being fully vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Acute Kidney Failure, Sepsis, Encephalopathy, Atrial Fibrillation, Coronary Artery Disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1798229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 92,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 12.02.2021
Beginn: 19.10.2021
Tage bis Beginn: 249,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

PATIENT EXPIRED ON 10/19/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN HLD GERD DM II AFIB DEPRESSION
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1798201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 66,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 16.02.2021
Beginn: 19.10.2021
Tage bis Beginn: 245,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

PATIENT EXPIRED ON 10/19/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COAL WORKERS PNEUMO SMALL CELL LUNG CANCER, LEFT LOBE URINARY BLADDER CANCER
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1788377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 17.03.2021
Beginn: 09.08.2021
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain upper Alopecia Anxiety Blood test normal Body temperature abnormal Depression Diarrhoea Dizziness Dysstasia Feeling of despair Gait disturbance Impaired work ability Insomnia Near death experience Palpitations Peripheral swelling Postural orthostatic tachycardia syndrome Stress

Symptomtext

Noticed hair loss and hand swelling between March-August 2021. On August 9, 2021, I had an overwhelming sensation that I was going to faint while walking, I also had stomach pain and diarrhea. In the following week, I was taken to the Emergency Department 4 times; my heart felt like it was racing, I got extremely lightheaded, I could not walk straight, I needed to hold on to something sturdy within my range to hold myself up, felt like I was dying. Doctors performed EKG, routine blood work and results were normal so they did not know what was wrong with me and would just give me IV fluid and discharge me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: I had blood work done for autoimmune disorders, poison testing, results would come back normal. Finally, in September 2021, a Tilt Table Test was performed on me and I was told I meet the criteria for Post Orthostatic Tachycardia Syndrome. I can't stand or walk for more than a few minutes before I get lightheaded and feel faint. I experience an adrenaline reaction, diarrhea, temperature irregularities, and insomnia. This situation is causing me stress, I am anxious, depressed, feeling hopeless. Prior to this, I was healthy, attending the gym 3 days a week, and did not suffer from any illness. I will be forced to resign from a per diem position as a pharmacy technician because I can't perform the duties (standing/walking, delivering medications throughout the hospital).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Natures Bounty Biotin, Vitamin D3, cyanocobalamin injection once a month, Ozempic 2mg once a week.
Allergien: Allergic to raw fruits and vegetables (Alder, Birch, Ragweed) No allergies to medications
Vorherige Impfungen: -

VAERS 1785213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 70,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 17.02.2021
Beginn: 12.10.2021
Tage bis Beginn: 237,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Pt died after being diagnosed with COVID-19 on Sep 29, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Type 2 Diabetes, severe obesity, Hypertension
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1784983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: GA
Alter: 70,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 23.03.2021
Beginn: 24.08.2021
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death

Symptomtext

Hospitalized twice: 8/23-9/7 and 9/20-9/28. Patient died due to COVID-19. Patient was fully vaccinated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Lung Disease, Diabetes, Chronic Renal Disease, Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1775694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: ID
Alter: 65,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 22.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

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

Blindness unilateral Cerebrovascular accident Computerised tomogram head Echocardiogram Electrocardiogram Laboratory test Lymphadenopathy Magnetic resonance imaging head Retinal artery occlusion Skull X-ray Ultrasound Doppler

Symptomtext

Retinal artery occlusion-Stroke in eye. Permament vision lose in left eye. Left under arm lymphnodes swelled for 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: 3/3/2021-eye exam w/ Retina Specialist 3/3/2021-ER visit MRI brain, CT brain, EKG, Rad head scan, lab work 4/9/2021-Ultrasound of heart, Ultrasound of carotid arteries
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Bayer Aspirin, Atorvasyatin Calcium, Patoprazole, Escitalopram
Allergien: N/A
Vorherige Impfungen: -

VAERS 1774925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 83,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: 15.03.2021
Beginn: 07.10.2021
Tage bis Beginn: 206,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Cardio-respiratory arrest Death Resuscitation

Symptomtext

Patient was admitted and being treated for covid. She was receiving maximal therapy (see my progress note from today), but unfortunately underwent a cardiopulmonary arrest. Patient started to be resuscitated, but discussions with family revealed that she did not want to be put on a machine. She was made a DNR and comfort medications (morphine) were administered given pain of CPR. Patient passed shortly after stopping CPR.

Weitere VAERSDATA-Felder

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

VAERS 1772188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WI
Alter: 98,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 20.03.2021
Beginn: 30.08.2021
Tage bis Beginn: 163,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Fully vaccinated COVID-19 death

Weitere VAERSDATA-Felder

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

VAERS 1772155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 09.02.2021
Beginn: 09.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Cerebrovascular accident Fatigue Headache Hemianaesthesia Pain Seizure

Symptomtext

severe headache, fatigue, body aches, left side numbness, and seizures

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: stroke
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes
Andere Medikamente: Renexa
Allergien: -
Vorherige Impfungen: flu vaccine

VAERS 1768915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 13.02.2021
Beginn: 12.09.2021
Tage bis Beginn: 211,0
Dosis: 1
Route/Site: UN / UN

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

Acute kidney injury COVID-19 COVID-19 pneumonia Chest X-ray abnormal Death Dyspnoea Endotracheal intubation Lung opacity Mechanical ventilation Paralysis Prone position Respiratory failure SARS-CoV-2 test positive Shock

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/23/2021 and 2/13/2021. Patient presented to the emergency department with complaints of shortness of breath and admitted for COVID pneumonia. Patient progressed to respiratory failure requiring intubation on 9/16/2021. Despite lung protective mechanical ventilation, paralysis, proning, inhaled pulmonary vasodilators, steroids, broad spectrum antibiotics, and remdesivir, her respiratory failure progressively worsened. On 9/25/2021 patient developed acute renal failure with worsening shock. Family elected to pursue comfort care at that time. Patient was extubated on 9/25/2021, and expired at 2107 on 9/25/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: COVID test positive on 9/12/2021; CXR: Bilateral lower lobe opacities and consolidation on 9/12/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism, hyperlipidemia, diabetes, hypertension, bipolar disorder, gastroesophageal reflux disease, depression allergic rhinitis
Andere Medikamente: atorvastatin 40 mg nightly, bupropion 150 mg daily, lexapro, 20 mg daily, levothyroxine 75 mcg daily, losartan 100 mg daily, pantoprazole 40 mg daily, risperidone 1 mg
Allergien: Penicillin, lactose
Vorherige Impfungen: -

VAERS 1768915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 13.02.2021
Beginn: 12.09.2021
Tage bis Beginn: 211,0
Dosis: 2
Route/Site: UN / UN

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

Acute kidney injury COVID-19 COVID-19 pneumonia Chest X-ray abnormal Death Dyspnoea Endotracheal intubation Lung opacity Mechanical ventilation Paralysis Prone position Respiratory failure SARS-CoV-2 test positive Shock

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/23/2021 and 2/13/2021. Patient presented to the emergency department with complaints of shortness of breath and admitted for COVID pneumonia. Patient progressed to respiratory failure requiring intubation on 9/16/2021. Despite lung protective mechanical ventilation, paralysis, proning, inhaled pulmonary vasodilators, steroids, broad spectrum antibiotics, and remdesivir, her respiratory failure progressively worsened. On 9/25/2021 patient developed acute renal failure with worsening shock. Family elected to pursue comfort care at that time. Patient was extubated on 9/25/2021, and expired at 2107 on 9/25/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: COVID test positive on 9/12/2021; CXR: Bilateral lower lobe opacities and consolidation on 9/12/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism, hyperlipidemia, diabetes, hypertension, bipolar disorder, gastroesophageal reflux disease, depression allergic rhinitis
Andere Medikamente: atorvastatin 40 mg nightly, bupropion 150 mg daily, lexapro, 20 mg daily, levothyroxine 75 mcg daily, losartan 100 mg daily, pantoprazole 40 mg daily, risperidone 1 mg
Allergien: Penicillin, lactose
Vorherige Impfungen: -

VAERS 1753482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: GA
Alter: 83,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 17.02.2021
Beginn: 01.09.2021
Tage bis Beginn: 196,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 Death

Symptomtext

Death due to COVID-19. Details unknown

Weitere VAERSDATA-Felder

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

VAERS 1753250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 18.03.2021
Beginn: 31.08.2021
Tage bis Beginn: 166,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Anticoagulant therapy Anxiety Arthralgia Blood culture negative Bursitis COVID-19 COVID-19 pneumonia Coronary artery thrombosis Culture negative Death Dyspnoea Endotracheal intubation General physical health deterioration Hypervolaemia Intensive care Laboratory test normal

Symptomtext

Deceased (9.26.21); Hospitalized due to COVID-19 (9.2.21); COVID-19 positive (8.31.21); Fully vaccinated Admission Date: 9/2/2021 Died 9/26/21 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] Pneumonia due to COVID-19 virus [U07.1, J12.82] Acute hypoxemic respiratory failure (HCC) [J96.01] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 65 y.o. female with a PMHx of COPD not on home oxygen, HTN, Hypothyroid, RA on immunomodulator therapy who was admitted for AHRF secondary to Covid pneumonia. Completed 4 days of dexamethasone, 3 days of remdesivir so far. Bcx, other infectious work-up have been negative. Going intermittently between HFNC and BiPAP, stays relatively comfortable without additional work of breathing. She has been responding well to once/day diuresis. Multiple conversations at that time were held with the patient, who has elected to be DNR/DNI - okay with vasopressor medications if needed. After transfer out of the ICU she completed dexamethasone, remdesivir, diuresis as needed- she developed an AkI that resolved. She was able to alternate between HFNC and BiPAP but developed hypoxia despite continuous BiPAP at 100%. She was readmitted to the ICU on 9/11 and was unsure of her code status to be DNR or FULL. Overnight she remained on continuous BiPAP with O2 sats in the high 80s. A CTA to rule out PE was unable to be performed given her respiratory status, U/S showed no signsof DVT. On 9/12 Patient had increased work of breathing and anxiety, especially with repositioning and requested to be FULL CODE and was electively intubated for hypoxic respiratory failure 2/2 COVID-19 PNA. Following intubation, the patient did develop worsening urine output and AKI. She ultimately was started on CRRT for volume overload. With volume overload, her O2 requirement did improve somewhat, but she still had significant ventilatory needs due to her COVID-19 pneumonia. Patient also had persistent tachycardia during her hospital stay. Her serotonergic medications were held to rule out serotonin syndrome, repeat cultures were obtained without any growth, and extremity ultrasounds were performed which did show equivocal left coronal DVT. Patient was started on heparin drip for this possible DVT. Due to the persistent high ventilatory needs, goals of care were discussed with the family. It was agreed that tracheostomy tube placement was not in line with the patient's goals of care, and due to her persistent refractory hypoxemia requiring high ventilatory needs, plan was made to transition patient to comfort care on Monday, 09/27/2021. On Sunday 9/26 patient had acute worsening in clinical status with decreasing oxygen levels. Based on patient's families wishes for the patient to be with her husband upon passing the patient was made comfort care and passed away at 1108 AM. Date of Death: 9/26/21 Time of Death: 11:08 AM Preliminary Cause of Death: COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: 8.11.21: Office visit - plans to schedule - rotator cuff repair 8.16.21: Office visit - left hip pain (trochanteric bursitis, lumbar radiculopathy) COVID-19 positive 8.31.21
Vorgeschichte: Rheumatoid arthritis involving multiple sites (HCC) Fibromyalgia HTN (hypertension) Tremor, essential Fatigue Morbid obesity (HCC) OSA (obstructive sleep apnea) Nocturnal hypoxemia Knee pain OA (osteoarthritis) of knee S/P total knee arthroplasty Pinguecula of both eyes Myopia of both eyes Hypothyroidism, unspecified type Bilateral hip joint arthritis Need for vaccination Screening, lipid Obesity hypoventilation syndrome (HCC) Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxia (HCC) Obesity hypoventilation syndrome (HCC)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 1 MG tablet atenolol (TENORMIN) 100 MG tablet benzonatate (TESSALON) 100 MG capsule busPIRone (BUSPAR) 10 MG tablet DULoxetine (CYMBALT
Allergien: Dilaudid
Vorherige Impfungen: -

VAERS 1745226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 93,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 17.02.2021
Beginn: 27.09.2021
Tage bis Beginn: 222,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

Patient died at home under hospice care. Hospice notes submitted into database.

Weitere VAERSDATA-Felder

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

VAERS 1744956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WI
Alter: 82,0
Geschlecht: M
Eingang: 29.09.2021
Impfdatum: 27.01.2021
Beginn: 28.09.2021
Tage bis Beginn: 244,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Death

Symptomtext

fully vaccinated-covid death

Weitere VAERSDATA-Felder

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

VAERS 1741219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 79,0
Geschlecht: M
Eingang: 28.09.2021
Impfdatum: 18.02.2021
Beginn: 15.09.2021
Tage bis Beginn: 209,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory distress syndrome Acute respiratory failure Atrial fibrillation Bradycardia COVID-19 Chronic kidney disease Condition aggravated Death Dyspnoea Electroencephalogram normal Endotracheal intubation Fibrin D dimer increased Hyperkalaemia Magnetic resonance imaging abnormal Malnutrition Metabolic encephalopathy Microangiopathy SARS-CoV-2 test positive

Symptomtext

Pt wife tested positive for COVID-19. Pt tested positive 9/15/21. Presented to ED 9/17/21 with SOB. Intubated upon arrival. Terminal extubation on 9/22/21. Deceased 9/23/21. Discharge Dx: Sepsis d/t COVID-19. Acute hypoxemic resp failure, Moderate ARDS, Acute metabolic encephalopathy, Elevated d-dimer, Afib, Bradycardia, CKD Stage 3a, moderate protein calorie malnutrition, hyperkalemia. HO smoking, afib, hyperlipidemia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: MRI: chronic microangiopathic disease but no evidence of anoxic injury EEG: no seizure activity
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1736780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 90,0
Geschlecht: M
Eingang: 27.09.2021
Impfdatum: 05.03.2021
Beginn: 05.09.2021
Tage bis Beginn: 184,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia COVID-19 Chills Cough Death Diarrhoea General physical health deterioration Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 2/12/2021 and 3/5/2021. Presented to ED on 9/5/2021 with complaints of generalized weakness, cough, body aches, diarrhea, as well as subjective fever and chills. Weakness has been progressing over 1 week. Patient treated with dexamethasone, remdesivir, ceftriaxone, azithromycin. Increasing O2 needs on 9/8. On 9/15 patients condition deteriorated, and using high flow O2 80% 50 L. Patient expired on 9/16/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: COVID-19 positive test on 9/6/2021 using PCR or equivalent Nucleic Acid Amplification (NAA)technology.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, CHF, Diabetes
Andere Medikamente: Ascorbic acid 500 mg QD, Atorvastatin 40 mg QD, Carvedilol
Allergien: Penicillin (Swelling), Streptomycin (Swelling)
Vorherige Impfungen: -

VAERS 1731846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 20.01.2021
Beginn: 29.04.2021
Tage bis Beginn: 99,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Death Extubation Intensive care Respiratory distress SARS-CoV-2 test positive

Symptomtext

On 04/29/21 pt. presented to EC in respiratory distress via EMS; "Hx of CHF, NSCLC with mets to brain"; subsequently admitted to ICU; Palliative extubation was carried out on 05/05/21, which is when patient diet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 04/29/21 SARS-CoV-2 (COVID-19) by NAA - DETECTED
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1727005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 23.09.2021
Impfdatum: 24.02.2021
Beginn: 21.09.2021
Tage bis Beginn: 209,0
Dosis: 2
Route/Site: IM / RA

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

Alanine aminotransferase increased Aphasia Aspartate aminotransferase increased Blood calcium decreased Blood sodium decreased Colonoscopy abnormal Communication disorder Condition aggravated Cough Diverticulum COVID-19 COVID-19 pneumonia Cardiac telemetry Cerebrovascular accident Chest X-ray abnormal Faeces discoloured Gastritis erosive Gastrointestinal tube insertion

Symptomtext

Hospitalized (9.21.21); COVID-19 positive (9.21.21); Fully Vaccinated HISTORY OF PRESENT ILLNESS: Pt is a 86 y.o. female with a past medical history of recent stroke, recurrent GI bleeding, HTN, AAA, hx of MI, hypotension, and rectal cancer. She presents today with worsening cough and rectal bleeding . Secondary to patient's recent stoke, she is aphasic and unable to communicate a history or ROS. Daughter is present and able to assist with history. Daughter states that since she was discharged on 9/18/21, patient has developed a cough that has been progressively worsening. Patient did receive her COVID vaccine. She did notify the facility of this and requested a CXR for concern of aspiration pneumonia, although she is unsure if the x-ray was completed. In addition to her cough, daughter notes that staff has been noticing blood per rectum that started today (9/21/21). She denies noticing any fevers/chills or episodes of vomiting. Patient was recently discharged from the hospital on 9/18/21 for an acute left MCA stroke with residual right-sided hemiparesis. She was started on dual antiplatelet therapy with ASA and Plavix with known risk of recurrent bleeding , NJ tube was placed. Prior to this, patient was admitted on 8/31 for treatment of an upper GI bleeding, where she received a 2U transfusion then asa an plavix held . Pt presented to the ED on 9/21/21 for increased coughing with possible aspiration, as well as melena/maroon stools . On initial presentation, patient was slightly hypotensive and tachycardic. Basic labs were performed which revealed a hbg of 8.7 slightly down from most recent of 9.6 , Na2+ of 124, Ca2+ of 7.5, and mildly elevated AST/ALT. COVID test was positive which is a new finding . No hypoxia observerd CXR was performed and revealed right upper lobe airspace disease, suspicious for pneumonia. ASSESSMENT / PLAN: * GI bleed Assessment & Plan - Suspect upper GI bleed. Melena/maroon stool noted by ED staff. Positive occult testing. History of GI bleeds requiring transfusions. Recently admitted 8/31 for upper GI bleed and 2U transfusion. - EGD performed on 5/22/21 revealed a large hiatal hernia and minor erosions. Colonoscopy performed 9/2/21 friable tissue and scattered diverticula. - Initial hbg of 8.7 and hct 26. Down from Hbg of 9.6 on 9/17/21. - Trend H&H's q 6 hours. Transfuse if Hbg < 7. - IV Protonix - Obtain type and screen. - NPO diet. - Hold ASA/Plavix. Avoid NSAID Use. - Frequent vital sign monitoring - Establish IV access x2 Gi consultation prn Pneumonia due to COVID-19 virus Assessment & Plan - COVID pneumonia vs. Aspiration pneumonia?: Normal WBC, procalcitonin WNL, and mildly elevated AST/ALT are consistent with COVID pneumonia over aspiration. Being at high risk for aspiration and infiltrate in right upper lobe will tx with Rocephin / azithromycin for now - Sxs onset ~ 9/18 with (+) test on 9/21/21. - CXR performed in ED reveals right upper lobe airspace disease, suspicious for pneumonia. - Patient is not currently hypoxic on room air, therefore is not a candidate for Remdesivir or steroid treatment. - Patient is a candidate for MAB treatment , covid team contacted at tx ordered - Trend d-dimer, CRP, and CMP's. - Maintain SpO2 > 89%. Supplemental oxygen as needed. - Continuous pulse ox and tele monitoring - PRN antitussives. All medications via J tube Acute CVA (cerebrovascular accident) (HCC) Assessment & Plan History of on 9/10: Acute left MCA distribution infarct involving the left corpus striatum and left frontal lobe. - Residual right-sided hemiparesis and aphasia. - Hold ASA and Plavix secondary to suspected GI bleeding putting at increased risk of recurrent cva

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: 8.31.21: ED to hospital admission - GI bleed, hypertension - aspirin held 9.10.21: ED to hospital admission - Acute CVA (stroke) COVID-19 positive 9.21.21
Vorgeschichte: Non-Hospital Coronary artery disease Abdominal aortic aneurysm (AAA) without rupture Large hiatal hernia Iron deficiency anemia History of rectal cancer Diarrhea Abnormal CT of the abdomen Symptomatic bradycardia Upper GI bleeding History of GI bleeding Dysphagia due to recent cerebrovascular accident (CVA)
Andere Medikamente: Outpatient Medications acetaminophen (TYLENOL) 32 MG/ML suspension aspirin buffered,CaCarb-MgCarb-MgO, (BUFFERIN) 325 MG tablet atorvastatin (LIPITOR) 10 MG tablet bisacodyl (DULCOLAX) 10 MG suppository clopidogrel (PLAVIX) 75 MG tablet cya
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1719659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 79,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 10.02.2021
Beginn: 19.09.2021
Tage bis Beginn: 221,0
Dosis: 2
Route/Site: IM / LA

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

Death

Symptomtext

PATIENT EXPIRED ON 09/19/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM COPD GERD FORMER SMOKER
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1719634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 78,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 12.02.2021
Beginn: 06.09.2021
Tage bis Beginn: 206,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

PATIENT EXPIRED ON 09/06/2021

Weitere VAERSDATA-Felder

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

VAERS 1718885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 21.03.2021
Beginn: 10.09.2021
Tage bis Beginn: 173,0
Dosis: 1
Route/Site: IM / AR

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

Acute respiratory failure Anticoagulant therapy Atrial fibrillation COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Evidence based treatment Fibrin D dimer increased Full blood count Headache Hypoxia Lung opacity Nasopharyngitis Procalcitonin decreased Respiratory tract congestion Rhinorrhoea

Symptomtext

Hospitalized (9.11.21 - present); COVID-19 positive; Fully Vaccinated History of Present Illness Patient is a 85 y.o. male with a history of HTN, paroxysmal atrial tachycardia and prostate cancer s/p prostatectomy who presents today with cough and shortness of breath. Symptoms started about a week ago and patient thought he had a mild head cold with congestion, rhinorrhea, and headaches. His symptoms continued throughout the week, but he noted they were "up and down" and he initially felt he was improving. However, he then began to have more shortness of breath and coughing. He tested positive for COVID on 9/10. Shortness of breath worsened, prompting ED presentation. Initially planned for monoclonal antibodies, but he then became hypoxic and was placed on 3 L NC. CXR showing bilateral groundglass opacities suggestive of COVID. WBC 14.3. He was given decadron and hospitalists were asked to admit for further care. Chief complaint COVID-19 Assessment and Plan Covid-19 pneumonia Acute respiratory insufficiency with hypoxia - symptom onset about 1 week ago - (+) PCR 09/10 - fully vaccinated with Pfizer (2/25/21 and 3/25/21) - Chest xray consistent with COVID pneumonia - started on decadron - start remdesivir - supportive measures - prone positioning - daily labs Leukocytosis - WBC 14.3 - will check procal - trend CBC - hold off on antibiotics for now Progress note 9.20.21: This is a 85 y.o. who has a past medical history significant for remote history of Prostate Cancer s/p Resection, HTN, who presented to the ED 9/11 with dyspnea, testing positive for COVID on 9/10, was admitted for hypoxia and started on dexamethasone/remdesevir 9/11, and empiric antibiotics on 9/13. His oxygen requirement has worsened and Pulm/Crit Care was asked to see for his respiratory failure. He ultimately worsened and required transfer to the MICU. D-Dimer significantly elevated, superficial clots seen in upper extremities. Key Plan for Today September 20: Continue high-flow nasal cannula oxygen/non-rebreather face mask At high risk for requiring intubation/mechanical ventilation Begin amiodarone for atrial fibrillation with RVR Decadron day 10/14 tentative course Continue empiric heparin drip given superficial clots and markedly elevated D-dimer Status post empiric ceftriaxone/azithromycin through September 17 Fluid balance -400/24 hours -- > goal even to negative fluid balance, as tolerated Advanced diet, as tolerated Add Pepcid, given steroids and anticoagulation Acute respiratory failure with hypoxia Assessment & Plan 2/2 COVID Pneumonia despite vaccination. Question additional issues, maybe some reticular changesin the bases bilaterally - Continue HFNC + NRB Mask and wean for goal sats>90%. At significant risk of decompensation requiring intubation - Completed empiric antibiotics, started 9/13 for 5d course. Procal is low - UE dopplers with superficial clots, question PE given elevated D-Dimer, starting empiric heparin gtt. Echo Pending. Hold on CTPE for now given tenuous status - Continue intermittent lasix for euvolemia Pneumonia due to COVID-19 virus Assessment & Plan - despite vaccination, very ill, no evidence of immunocompromise. Tested positive 9/10 - Continue dexamethasone, started 9/11, expecting 10d course, will extend depending on his trajectory - s/p remdesevir 5d, started 9/11

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Hospital Osteoarthritis of left hip Paroxysmal atrial tachycardia Essential hypertension COVID-19 Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxia Acute thrombosis of superficial vein of both upper extremities Obesity Non-Hospital Malignant neoplasm of prostate-RRP 9/2005,Gleason 3+3=6, pT2a, negative margins, nerve sparing Epididymal head cyst. Palpable area appears correspond to a more prominent left epididymal head cyst measuring 10 mm Meniere's disease Status post total hip replacement, left
Andere Medikamente: Outpatient Medications cephALEXin (KEFLEX) 250 MG capsule metoprolol succinate-XL (TOPROL-XL) 25 MG 24 hr tablet Psyllium (METAMUCIL FIBER PO) triamterene-hydrochlorothiazide (MAXZIDE) 37.5-25 MG per tablet
Allergien: Penicillins Rash Celecoxib Rash Sulfa Drugs Swelling
Vorherige Impfungen: -

VAERS 1708241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: GA
Alter: 72,0
Geschlecht: M
Eingang: 17.09.2021
Impfdatum: 01.03.2021
Beginn: 26.07.2021
Tage bis Beginn: 147,0
Dosis: 2
Route/Site: - / -

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

Death Exposure to SARS-CoV-2 Mechanical ventilation Renal failure Unresponsive to stimuli

Symptomtext

PUI is at Ave. PUI was fully vaccinated however wife indicated why she was out of town he was exposed by someone and upon her return he was found non-responsive. He currently is in critical condition on a ventilator and currently experiencing kidney failure. Prognosis is not good. Patient died.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 20,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease, Chronic renal disease, Hypertension, Immunosuppressive condition
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1700099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 15.09.2021
Impfdatum: 18.03.2021
Beginn: 03.09.2021
Tage bis Beginn: 169,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Alpha tumour necrosis factor Aspergillus infection Aspergillus test COVID-19 COVID-19 pneumonia Candida infection Computerised tomogram thorax abnormal Condition aggravated Diarrhoea Dyspnoea Endotracheal intubation Immunodeficiency Intensive care Myalgia Pain Productive cough Pulmonary mass

Symptomtext

Hospitalized (9.2.21 - still admitted); COVID-19 positive (8.30.21; 9.3.21); fully vaccinated HISTORY OF PRESENT ILLNESS: Patient is a 59 y.o. male who presents today with 7 day history of fever, muscle aches, dyspnea, diarrhea, productive cough and body aches. Patient has a history of RA and is currently on Humira, Plaquenil and Sulfasalazine. He follows with rheumatology. Patient states he has been full vaccinated with Pfizer COVID-19 vaccination (completed in March) and denies any tobacco use. He states he possible contracted virus possible at a wedding and his wife also is currently being admitted for COVID-19. He tested positive on 8/30 but due to progressive symptoms presented to the ED today. ASSESSMENT / PLAN: # Acute Hypoxic Respiratory Failure Secondary to COVID-19 PNA -symptom onset 8/27 and tested positive on 8/30 per patient (unable to locate in EMR) -fully vaccinated with Pfizer vaccination (completed in March 2021) & CXR personally reviewed -continuous pulse oximetry and target oxygen saturation >90% -decadron 6 mg daily x 10 days, Remdesivir and monitor LFT's and renal function -check CRP and if >75 and not improving with decadron consider Tocilizumab -maintain net negative fluid balance (fluid restriction, 20 mg PO lasix daily) -given immunocompromised state high risk for secondary bacterial PNA -check pro-calcitonin and will cover with IV Rocephin (1 gm daily) for now -if pro-calcitonin negative and improving consider discontinuation of antibiotics Aspergillus fumigatus Assessment & Plan Presented with respiratory failure secondary to COVID pneumonia. Course complicated with increasing oxygenation requirement as result was subsequently brought to the intensive care unit and intubated on 09/11. Remains afebrile since completion of antibiotic therapy for 5 days empirically with Rocephin/azithromycin on 09/07. Furthermore, sputum cultures obtained on 09/11-aspergillus fumigatus and 0 9/12-identified isolated fungal species with Candida. He is a high risk for fungal pneumonia in the setting of COVID -19 along with this history of immune suppression with TNF alpha inhibitor/humeral for his rheumatoid arthritis and CT evidence of subpleural nodules in bilateral lung fields, left greater than right are all reasonable indications in the clinical setting to initiate antifungal therapy. Monotherapy with IV Voriconazole loaded with 6 mg/kg IV BID on 09/14. Plan: -Will Follow: Fungitell, Aspergillus serum antigen, Repeat Sputum Cx with Aspergillus PCR -Continue Voriconazole 4mg/kg BID for atleast 7 days. Stop dates placed. Will transition to orally when able. Anticipate total duration of therapy 6-12 weeks, will reassess the need of chronic prophylaxis oral therapy. -Will check through levels 4-7 days into the therapy with goals serum concentration 1-5.5 mcg/ml. And trough level 1-1.5 mcg/kg. Trough level check ordered for 09/17 am.. -Daily CMP to monitor for hepatotoxicity and nephrotoxicity -Agree with holding DMARDs * Pneumonia due to COVID-19 virus Assessment & Plan Vaccinated fully with Pfizer vaccine in March 2021 (immune compromised); Sx onset 08/27, tested positive 8/30 admitted on 09/02. Has finished appropriate 5 day therapy with remdesivir, dexamethasone from 09/02-09/11 x 9 days. CAP coverage completed w/ Rocephin/Azithromycin 09/02-09/07

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Hospital Pneumonia due to COVID-19 virus Rheumatoid arthritis Acute hypoxemic respiratory failure due to COVID-19 Aspergillus fumigatus
Andere Medikamente: Hospital Medications L1 acetaminophen (TYLENOL) tablet 1,000 mg L1 acetaminophen (TYLENOL) tablet 500 mg artificial tears ophthalmic ointment 3.5 g L2 chlorhexidine (PERIDEX) 0.12 % solution 15 mL L2 chlorhexidine (PERIDEX) 0.12 % solution
Allergien: NA
Vorherige Impfungen: -

VAERS 1689320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 69,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 13.02.2021
Beginn: 16.08.2021
Tage bis Beginn: 184,0
Dosis: 2
Route/Site: IM / LA

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

Agonal respiration Arthralgia Atrial fibrillation COVID-19 Cough Death Endotracheal intubation Fatigue Hypotension Hypoxia Intensive care Mechanical ventilation Nausea Positive airway pressure therapy Respiratory distress Syncope Ventricular dyssynchrony

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer BioNTech Vaccine on 1/23/2021 and 2/13/2021. Presented to ED on 8/16 with complaints of syncope and right shoulder pain. Patient had been diagnosed with COVID on 8/13, with his main symptoms being fatigue/tiredness, cough, nausea. On 8/27, patient was agonal breathing (after he removed his bipap); patient was intubated and placed on mechanical ventilation and moved to ICU. On 8/29, patient became more hypoxic in respiratory distress with dyssynchronous hypotensive Afib with RVR. Patient received decadron x 6 days, baricitnib x 8 days, doxycycline x 7 days, Micafungin started on 8/26, started vancomycin and meropenem on 8/28. Patient expired on 8/29/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, T2DM with stage 3 CKD, Non- Hodgkin's Lymphoma, HLD, HTN
Andere Medikamente: atorvastatin 40mg 1/2 tab daily, escitalopram 10mg 1/2 tab daily, metoprolol XL 100mg daily, rybelsus 7mg 1 tab daily before meal
Allergien: Cefuroxime Axetil
Vorherige Impfungen: -

VAERS 1685242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 09.09.2021
Impfdatum: 19.02.2021
Beginn: 31.08.2021
Tage bis Beginn: 193,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Cerebrovascular accident Death Endotracheal intubation Extubation Hypoaesthesia Paraesthesia

Symptomtext

54-year-old female who was diagnosed with Covid several weeks prior presented to outside hospital due to facial numbness/tingling. She was found to have evidence of MCA stroke and was given TPA, she was transferred here for further management. Upon arrival here she was found to have evidence of bilateral MCA strokes, given that the patient was intubated and there is no likelihood of meaningful recovery goals of care discussions were had with neurology and the recommendation was to proceed with comfort care measures. The patient was extubated and transitioned to comfort care measures. Patient expired on 8/31/2021, cause of death was bilateral MCA strokes.

Weitere VAERSDATA-Felder

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

VAERS 1685183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 74,0
Geschlecht: F
Eingang: 09.09.2021
Impfdatum: 08.04.2021
Beginn: 20.08.2021
Tage bis Beginn: 134,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 pneumonia Death Dyspnoea Heart rate decreased Oxygen saturation decreased Procalcitonin increased Tachypnoea X-ray abnormal

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccine on 03/11/2021 and 04/08/2021. On 8/20/2021, pt presented to ED with increasing shortness of breath. Pt was admitted to a hospital on 8/17/2021 and diagnosed with COVID-19 pneumonia. She was discharged on 8/20/2021 with 4 L NC oxygen. Once discharged patient began to desaturate to 80% and called EMS. Patient was transported to ED and placed on HFNC 50/40 then titrated up to 60/60 and then later 70/60. Her lab work demonstrated elevated procalcitonin and her x-ray demonstrated a multifocal pneumonia. She was given dexamethasone, Rocephin and remdesivir. On morning of 8/25/21 she was noted to be significantly tachypneic with RR to 40s and slightly altered. Despite ongoing treatment, she declined. Patient expired on 8/25/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: morbid obesity, HTN, moderate persistent asthma, OSA, HLD, allergic rhinitis, long term systemic steroid user
Andere Medikamente: Trelegy Ellipta 100-62.5-25mcg 1 puff daily, lisinopril 10mg daily, prednisone 10mg daily, albuterol 2 puffs q4hours prn, atorvastatin 20mg daily, cetirizine 10mg daily, fluticasone 2 sprays each nostril daily, Floranex 100 million cell gra
Allergien: Aleve, Fentanyl
Vorherige Impfungen: -

VAERS 1685126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 83,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 05.03.2021
Beginn: 02.09.2021
Tage bis Beginn: 181,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Nursing notes have been submitted into system, death summary is not available yet.

Weitere VAERSDATA-Felder

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

VAERS 1636612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 12.02.2021
Beginn: 21.08.2021
Tage bis Beginn: 190,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 pneumonia Hypercapnia Alanine aminotransferase increased Angiogram pulmonary abnormal Anion gap Aspartate aminotransferase increased Bilevel positive airway pressure Blood albumin decreased Blood alkaline phosphatase increased Blood bilirubin normal Blood calcium normal Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea increased

Symptomtext

Acute respiratory failure with hypoxia and hypercapnia (HCC), Pneumonia due to COVID-19

Weitere VAERSDATA-Felder

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

VAERS 1662426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 15.03.2021
Beginn: 17.08.2021
Tage bis Beginn: 155,0
Dosis: 2
Route/Site: IM / UN

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

Bilevel positive airway pressure Blood gases abnormal COVID-19 Carbon dioxide decreased Cardio-respiratory arrest Cellulitis Chills Culture wound positive Death Dyspnoea Encephalopathy Fall Fibula fracture Generalised oedema Hypophagia Lethargy Malaise Oedema

Symptomtext

Patient hospitalized; positive for COVID-19 (after vaccinated); patient expired / died in hospital. DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Cellulitis of left leg [L03.116] Cellulitis [L03.90] Cellulitis of left lower extremity [L03.116] HOSPITAL COURSE: Patient is a 66-year-old female with past medical history significant for multiple medical comorbidities including severe peripheral arterial disease, chronic obstructive pulmonary disease, pulmonary hypertension, history of TAVR, history of TIA, morbid obesity, OSA/CPAP, diabetes on insulin, CKD 3B, chronic diastolic heart failure, peripheral edema, chronic pain, ongoing tobacco abuse recent fall resulting in a right fibular fracture presents to hospital on 08/23 from subacute rehab facility due to worsening lower extremity pain, lethargy, chills, decreased oral intake for about 5 days prior to presentation and was incidentally noted to be COVID positive. Patient also recently had a hospital stay from 07/28 to 8/3 due to a right fibular fracture and was fitted with a cam boot with instructions to weight bear as tolerated. Patient was admitted with working diagnosis of acute encephalopathy and lower extremity cellulitis on the left and asymptomatic COVID-19 infection. Encephalopathy: Felt to be related to polypharmacy including sedating medications namely gabapentin, Norco and possibly also related to infection. VBG with CO2 of only 44. With supportive treatment alone, her encephalopathy improved over the next 24-48 hours and resolved completely. Only Norco was restarted. Gabapentin was planned to be discontinued due to ineffectiveness. Cellulitis: Patient was noted to have left leg cellulitis associated with changes consistent with venous stasis and edema. Patient was started on Ancef initially but surface cultures obtained at the time of admit showed MRSA and hence vancomycin was added on top. Ancef was discontinued on 08/24 with plans to continue vancomycin and eventually switch over to doxycycline to completed 10 day course. Cellulitis gradually was improving; COVID-19 infection: Incidentally noted at rehab on 08/22, patient without much respiratory symptoms and continued on 3 L baseline oxygen and hence no particular treatment was initiated. Right fibular fracture: due to previous fall/recent hospital stay at which time orthopedics recommended non operative management with a Cam boot and weight-bearing as tolerated. Patient had not had a chance to follow-up with orthopedics and hence consult was obtained here. Repeat x-ray showed improvement and possible healing, Orthopedics recommended continuation of Cam boot with weight-bearing as tolerated in outpatient follow-up. Peripheral arterial disease: With extensive nature of peripheral arterial disease noted on previous imaging studies with plans for following up with vascular surgery at Metro Hospital with upcoming plans for angiography/angioplasty. There was no concern for acute ischemia on exam. Anasarca, acute on chronic diastolic congestive heart failure with significant weight gain compared to previous hospital stay. Daughter did mention that subacute rehab did not really pay close attention to her salt intake and weight gain and she had gained significant amount await (close to 20 kilos) and hence aggressive IV Lasix/diureses were started. Her renal function mostly was holding in spite of aggressive diureses and slow weight loss. This was also noted in the lower extremities with improvement in the edema. On 08/28, during my interview patient had a unremarkable night, used her BiPAP in the night, noticed that she was slightly more short of breath ( while she had taken off her CPAP mask, had not put her oxygen on yet), a short while later when she was helped to the bedside commode for urination, patient became acutely short of breath, appeared unwell and lost her pulse is. All code was called and resuscitation efforts were continued for 29 minutes and and unsuccessful in obtaining ROSC, pronounced at 11:35 a.m.. Suspicion was that she may have had a PE or seizure (she did have seizures during resuscitation). Daughter was notified, discussed with a little bit later when she arrived at bedside. Not a ME case, daughter did not want autopsy; Death certificate signed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: Hospitalized 7.28.21; COVID positive; COPD (chronic obstructive pulmonary disease) (HCC) Uncontrolled type 2 diabetes mellitus with diabetic neuropathy, with long-term current use of insulin (HCC); Morbid obesity (HCC); Chronic hypoxemic respiratory failure (HCC) NSTEMI (non-ST elevated myocardial infarction) (HCC); Right fibular fracture; PAD (peripheral artery disease) (HCC)
Vorgeschichte: CAD (coronary artery disease); Severe aortic stenosis; Coronary artery disease involving native heart; Lung nodule; COPD (chronic obstructive pulmonary disease) (HCC); Choledocholithiasis; Acute kidney injury superimposed on CKD (HCC); Poor dentition Uncontrolled type 2 diabetes mellitus with diabetic neuropathy, with long-term current use of insulin (HCC); Morbid obesity (HCC); Postoperative anemia due to acute blood loss Paresthesias; Acute on chronic diastolic congestive heart failure, NYHA class 3 (HCC); Constipation; Acute on chronic diastolic heart failure (HCC); Chronic hypoxemic respiratory failure (HCC); Chronic kidney disease, stage III (moderate Essential hypertension, benign; OSA on CPAP Chronic narcotic dependence (HCC); Chronic right-sided low back pain with right-sided sciatica Hypothyroidism; Acute kidney injury (HCC); NSTEMI (non-ST elevated myocardial infarction) (HCC); Right fibular fracture; PAD (peripheral artery disease) (HCC); Cellulitis of left leg COVID-19; History of stroke; History of aortic stenosis; Tobacco abuse; Venous stasis ulcer of other part of left lower leg with fat layer exposed with varicose veins (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet; albuterol HFA (PROAIR HFA) 108 (90 Base) MCG/ACT inhaler; aspirin EC 81 MG enteric coated tablet; atorvastatin (LIPITOR) 80 MG tablet; bumetanide (BUMEX) 1 MG tablet; buPROPion (WELLBUTRIN XL) 300 MG 2
Allergien: Thiopental Anaphylaxis; Adhesive Rash
Vorherige Impfungen: -

VAERS 1656531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

kritisch

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 30.08.2021
Impfdatum: 08.03.2021
Beginn: 11.08.2021
Tage bis Beginn: 156,0
Dosis: 2
Route/Site: SYR / UN

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

Acute respiratory failure COVID-19 Death Infection

Symptomtext

breakthrough Covid infection, acute resp failure, patient died

Weitere VAERSDATA-Felder

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

VAERS 1656237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 80,0
Geschlecht: F
Eingang: 30.08.2021
Impfdatum: 05.03.2021
Beginn: 29.08.2021
Tage bis Beginn: 177,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chest pain Death Dyspnoea Nausea Oxygen saturation decreased Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient is a 81 y.o. female with history of COPD/emphysema on oxygen at home who presents with shortness of breath, chest pain, and nausea. She states her symptoms started this past Thursday. They progressively worsened with time. She normally wears 2 L of oxygen at home at night at baseline. However, her oxygen needs have had to increased since this past Thursday and she was up to 10 L oxygen at home today prior to coming to the emergency department. She came to the emergency department on Saturday 08/21/2021 and was positive for COVID-19. She did not require any more oxygen to be admitted at that time. She did have her COVID-19 vaccine and was fully vaccinated well over a month ago. She denies any other complaints today. Of note, she states only 1 of her lungs is working at 100% as the other 1 is being collapse by an uneven diaphragm. She had a car accident recently and had a ruptured sternum with diaphragmatic rupture. Hospital Course: Patient was treated for COVID-19 protocol. Unfortunately, her respiratory status continued to decompensate. She began telling staff that she was ?done ?and ?ready to go to the lord.? After difficult discussion, patient elected to make herself comfort measures only. Aggressive measures were discontinued and her family was allowed to visit say goodbye. She passed away 08/29/2021 at 1007. May she rest in peace.

Weitere VAERSDATA-Felder

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

VAERS 1641664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 83,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 25.02.2021
Beginn: 02.03.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: SYR / LA

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

Aortic thrombosis COVID-19 Dyspnoea Fatigue Flank pain Memory impairment Mobility decreased Pain Pulmonary embolism Pulmonary thrombosis Pyrexia SARS-CoV-2 test positive Thrombosis Venous thrombosis limb

Symptomtext

I was tired and achy, running a fever. Then it progressed to where I was having difficulty breathing and pain in both sides. It got to the point where I could not get out of bed. My granddaughter called the ambulance. I believe I had pneumonia. They did some tests and I had blood clots in both lungs, one in my leg, and one in my aortic valve. Once I was in the ambulance I do not remember much. I do not remember which tests they did but they were a lot. I was admitted to the hospital on 03/06/2021 and discharged 03/09/2021. I was treated by Doctor L. They treated me for pulmonary embolism, acute vein thrombosis of right vein, thrombosis of aorta. They sent me home with some oxygen machines. For one week I had home health care. I do not need the oxygen anymore. Last week my granddaughter tested positive for Covid, so I took the test and it was positive. I was feeling fine just some aches and pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: All kind of tests- I had blood clots in both lungs, one in my leg, and one in my aortic valve. Covid test- positive
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes
Andere Medikamente: Lisinopril, Atorvastatin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1628789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 24.08.2021
Impfdatum: 12.02.2021
Beginn: 09.08.2021
Tage bis Beginn: 178,0
Dosis: 2
Route/Site: IM / UN

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

Anticoagulant therapy Blood loss anaemia COVID-19 Cerebrovascular accident Death Deep vein thrombosis Endotracheal intubation General physical health deterioration Hypotension Retroperitoneal haematoma SARS-CoV-2 test positive Shock haemorrhagic Unresponsive to stimuli

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA Patient received Pfizer-BioNTech COVID Vaccines on 1/20/2021 and 2/12/2021. Presented to ED on 8/9/21 from acute rehab with complaints of unresponsiveness at Rehab. PMH of CVA (2019). 2 weeks prior to admission patient with admitted to hospital and diagnosed with pontine stroke. Patient was scheduled for TEE and underwent routine COVID test and tested positive. Pt caregivers reported patient showed no respiratory symptoms prior to this admission. During this stay patient was treated with empiric antibiotics, Decadron for 10 days and Lovenox for treatment of a DVT and discharged to acute rehab. Upon arrival to ED pt was hypotensive, intubated and found to have a large retroperitoneal hematoma. Pt was also started on Cefepime, Vancomycin, and Doxycycline. Patient diagnosed with acute hemorrhagic shock and, acute blood loss anemia. Patient continued to decline and family decided to withdraw care and initiate comfort care. Patient expired on 8/10/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CVA(2019), AFib (on Eliquis), pulmonary sarcoidosis, Gout, Kidney stones, HLD, CKD 3, coronary arteriosclerosis in native artery
Andere Medikamente: apixaban 5mg BID; Polycitra 1,100-334 mg/5mL TID; escitalopram 10mg daily; gabapentin 100mg TID
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1628050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 93,0
Geschlecht: M
Eingang: 24.08.2021
Impfdatum: 05.03.2021
Beginn: 25.07.2021
Tage bis Beginn: 142,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain COVID-19 COVID-19 pneumonia Chest X-ray abnormal Convalescent plasma transfusion Death Pyrexia SARS-CoV-2 test positive

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA Patient received Pfizer-BioNTech COVID Vaccines on 2/12/2021 and 3/5/2021. Patient presented to ED on 7/25/21 and diagnosed with COVID-19 pneumonia. Associated symptoms included fever and abdominal pain. X-ray showed development of patchy bilateral alveolar airspace. While in the hospital, patient was treated with remdesivir, ceftriaxone, and azithromycin. On 7/27/21, patient received 1 unit of convalescent plasma transfusion. He was discharged on 7/28/2021. Patient expired on 8/5/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Afib (on Eliquis), CAD s/p PCI to RCA (2010), HTN, HLD, colon cancer s/p colostomy, CKD, and Alzheimer's dementia
Andere Medikamente: apixaban 2.5 mg, cholecalciferol (vitamin D3) 1K units, esomeprazole magnesium 20 mg, loratadine 10 mg, melatonin 5 mg, memantine HCl/donepezil HCl 28-10 mg, multivitamin, simvastatin 40 mg
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1586737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 19.08.2021
Impfdatum: 11.02.2021
Beginn: 17.07.2021
Tage bis Beginn: 156,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram abnormal Asthenia COVID-19 Chest X-ray abnormal Computerised tomogram thorax abnormal Death Diarrhoea Dizziness Dyspnoea Endotracheal intubation Hypophagia Hypoxia Intensive care Leukocytosis Lung opacity Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient tested positive for COVID-19 on 7/24. She felt well for the first week following the test but then started to have symptoms including dizziness, SOB, weakness, diarrhea, and decreased PO intake. She was started on prednisone 5 mg PO on 8/5 and presented to urgent care on 8/10 because her symptoms continued to worsen. She went to an outside hospital ED and was hypoxic to 91% requiring NC. CXR and CTA chest at that time showed diffuse ground glass opacities. She was administered dexamethasone 6 mg IV and 1 L of normal saline. She arrived to the hospital on 8/11 satting well on 4L of nasal cannula. She continued on dexamethasone. Thereafter, her oxygen requirements escalated to max high flow nasal cannula on 8/13 and 8/14. She received tocilizumab 8 mg/kg IV x 1 on 8/14 and transferred to the medical intensive care unit. On 8/15, she was having oxygen desaturations to the 70s and 80s and was intubated. Over the next 24 hours, she developed increasing pressor requirements, was spiking fevers, and started on iNO. She was started on vancomycin and cefepime and her leukocytosis progressed to >200. The patient was made DNR and passed on 8/17.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: CLL
Vorgeschichte: CLL Rheumatoid arthritis Hypogammaglobulinemia R foot stress fracture of R 2nd metatarsal Osteopenia Iron deficiency anemia GERD
Andere Medikamente: Rituximab 1600 mg subcut every 8 weeks Tretinoin 0.025% topical cream at bedtime 3 times per week Ventolin HFA 2 puffs by mouth every 4 hours PRN SOB/wheezing Acyclovir 400 mg PO BID Estradiol 10 mcg tablet vaginally 1-2 times per week Famo
Allergien: Cheese (anaphylaxis) Sulfa (anaphylaxis) Carrageenan, corn-containing products, cor syrope, dextrose, geltain, ketchup, lecithin, mayonnaise, molasses, mustard, rennet, sulfites, wine spirit (swelling)
Vorherige Impfungen: -

VAERS 1577657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: KY
Alter: 93,0
Geschlecht: M
Eingang: 17.08.2021
Impfdatum: 22.02.2021
Beginn: 15.08.2021
Tage bis Beginn: 174,0
Dosis: 2
Route/Site: IM / RA

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

Death General physical health deterioration

Symptomtext

Overall, critical condition with poor outcome. Discussed with patient's daughters 8/13. I explained that the patient is deteriorating gradually and I agrees with comfort measures. On 8/14, discussed with the patient's son at bedside, all questions answered. I also called the POA updated on the patient current condition. Family will meet today and update us on their plan of care. Addendum 3 PM on 8/14: Family had a meeting about goals of care, all questions answered. Family decided to proceed with comfort measures. Will add Ativan and Morphine. Will continue high flow oxygen as per family request. Will continue to monitor. Discussed with the RN. Expired peacefully 8/15/2021

Weitere VAERSDATA-Felder

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

VAERS 1535895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: AZ
Alter: 80,0
Geschlecht: F
Eingang: 09.08.2021
Impfdatum: 17.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 43,0
Dosis: 2
Route/Site: SYR / LA

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

Brain scan abnormal Death Haemorrhage intracranial

Symptomtext

Brain Bleed, Hemorrhage (Intracranial Hemorrhage). Death

Weitere VAERSDATA-Felder

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

VAERS 1502131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 26.07.2021
Impfdatum: 19.02.2021
Beginn: 18.05.2021
Tage bis Beginn: 88,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Chest pain Death Thrombocytopenia

Symptomtext

death N17.9 - Acute kidney failure, unspecified D69.6 - Thrombocytopenia, unspecified chest pain

Weitere VAERSDATA-Felder

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

VAERS 1500649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: NC
Alter: 67,0
Geschlecht: M
Eingang: 24.07.2021
Impfdatum: 16.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Blister Decreased appetite Dizziness Dyspnoea Hernia Herpes zoster Myocardial infarction Neuralgia Pruritus Rash Weight Weight decreased

Symptomtext

Hernia; Shortness of breath; Lightheaded; losing weight; appetite had decreased; itching; Heart attack; He had a bad case of shingles and needed something for nerve pain, the nerve pain was bad.; Shingles; They put tegaderm on his stomach and he developed blisters.; Rash on his arms and legs; This is a spontaneous report from a contactable consumer. A 67-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2, administered in Arm Left on 16Feb2021 at age of 67 years old (Lot Number: EL9267) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included Cholesterol and Hernia. Concomitant product included ongoing ASPIRIN [ACETYLSALICYLIC ACID] at 81mg tablet once a day by mouth given his age to help from getting blood clots. None additional vaccines administered on same date of the Pfizer suspect. None prior Vaccinations within 4 weeks. He did not have high blood pressure and was not a diabetic. The only thing he took was an aspirin and cholesterol pill and his cholesterol was better than hers, she does not know the name of the cholesterol pill he took, states it begins with r, unknown dose, and he took half a pill once a day by mouth, every night. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 26Jan2021 at age of 67 years old at as DOSE 1, SINGLE (Lot: EL8982) for covid-19 immunisation and experienced Shingles. After he got the second dose, he developed a rash on 20Feb2021 on his arms and legs. He went to the doctor and they gave him a steroid and something for itching. He did not think anything about the shot. On 25Mar2021 he had hernia surgery done and they put tegaderm on his stomach and he developed blisters. He had about 12 blisters on his stomach. He has had tegaderm dressings in the past and never broke out. He developed shingles on 22Apr2021. He had a heart attack and died 15May2021. No autopsy done. She had to do CPR on him at home. She is looking for answers. Her husband complained of shortness of breath and being lightheaded. She met a younger man that also developed shingles after the Pfizer covid vaccine. Her husband had a lot more shingles compared to the young man. Her husband had shingles that looked like clusters. Her husbands shingles was terrible and she has pictures of that. Her husband was doing fine before he took the shot. She knows the shot has caused people to get shingles, have heart attacks and all other stuff. She is not going to ask if it can happen, because she knows it can. She mentions something about a family member that put it in and something in regards to things happening after the shot but she did not provide further clarification. He started losing weight after the shot. He was normally 168 lbs and died at about 158 lbs. His appetite had decreased. She had to get him off the bed and put him on the floor to do cpr. Reports his shingles had cleared up on 6May2021 and they were scabbed up but he was left with severe pain. He called the doctor the Monday before he died and told him that he had a bad case of shingles and needed something for nerve pain, the nerve pain was bad. The doctor sent him medicine and the medication came in the day he died, and never took the medication. He died that Saturday and she has his death certificate that states the cause of death . The paramedics tried cpr as well. AEs require a visit Emergency Room. No physician office. Outcome of the event Heart attack was fatal. Outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.; Reported Cause(s) of Death: Cardiac arrest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Name: weight; Result Unstructured Data: Test Result:168 lbs; Test Name: weight; Result Unstructured Data: Test Result:158 lbs
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood cholesterol abnormal; Hernia
Andere Medikamente: ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 1474730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: CA
Alter: 94,0
Geschlecht: M
Eingang: 15.07.2021
Impfdatum: 18.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Asthenia Death Dyspnoea Gait inability

Symptomtext

Within two hours of the vaccine, my father was unable to walk, suffered severe weakness, and had severe shortness of breath. The weakness, inability to walk, and shortness of breath lasted in a severe state for 48 hours. After that, he continued to be unable to walk, suffered weakness and had shortness of breath until he died. He never recovered the strength and vitality he had prior to the 2nd vaccine. That 2nd shot shortened his life and killed him.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Patient was under palliative care at the time. They gave us a nebulizer to help with his breathing.
Aktuelle Erkrankungen: None
Vorgeschichte: Parkinsons disease
Andere Medikamente: 1. Carbidopa/Levodopa 25-250mg, 4x daily (continued on other p #2 Entacapone 200 mg, 3x daily; #3 Levothyroxine 0.025mg, 1x daily; #4 Combigan eye drops 0.2%/0.5%.
Allergien: Hay fever
Vorherige Impfungen: -

VAERS 1474388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: NE
Alter: 59,0
Geschlecht: M
Eingang: 15.07.2021
Impfdatum: 18.02.2021
Beginn: 12.03.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Deep vein thrombosis Pulmonary embolism Ultrasound Doppler abnormal

Symptomtext

DVT/PE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Positive CTA chest; Doppler US legs
Aktuelle Erkrankungen: nothing
Vorgeschichte: polycythemia; hx lymphoma, asplenia; COPD; GERD, Gout,
Andere Medikamente: Metoprolol, amlodipine, levothyroxine, citalopram, allopurinol, omeprazole, hydroxyurea, atorvastatin, Flomax, albuterol
Allergien: NKMA
Vorherige Impfungen: -

VAERS 1466134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: AZ
Alter: 70,0
Geschlecht: M
Eingang: 13.07.2021
Impfdatum: 23.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Myocardial infarction

Symptomtext

Heart Attack-Mild/Heart Attack; This is a spontaneous report from a contactable consumer (patient). A 70-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot number: EL9267) via an unspecified route of administration in left arm on 23Feb2021 at 12:00 (at the age of 70-year-old) as single dose for COVID-19 immunization. Patient had no medical history and concomitant medications were not reported. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot number: EL8982) via an unspecified route of administration in left arm on 03Feb2021 (at the age of 70-year-old) as single dose for COVID-19 immunization and experienced severe heart burn and was overall not feeling well. On 24Feb2021, at 17:00, the patient experienced mild heart attack. Adverse event resulted in visit to emergency room and physician office. Patient was admitted to the hospital in response to the event. Patient received the treatment in response to the event which included stent implant (Surgery: stent). Surgery was not planned before taking the vaccination. Outcome of the event was resolved on an unspecified date on 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
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 1464271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 12.07.2021
Impfdatum: 10.03.2021
Beginn: 22.06.2021
Tage bis Beginn: 104,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Death

Symptomtext

death N17.9 - Acute kidney failure, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1412823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: AZ
Alter: 71,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 01.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / LA

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

Abdomen scan Anaemia Bacterial test Biopsy bone Blood culture Blood test Brain stem stroke Cerebellar stroke Muscle atrophy Cardiac monitoring Cerebrovascular accident Computerised tomogram Culture stool Culture urine Electroencephalogram Fungal test Haemoglobin decreased Lumbar puncture

Symptomtext

Strokes in the medulla and cerebellum; Strokes in the medulla and cerebellum; anemia with high levels of ferritin; anemia with high levels of ferritin; persistent fever; complete muscle atrophy; This is a spontaneous report received from a contactable consumer or other non hcp. A 71-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/lot number: EN6202) via an unspecified route of administration in Arm Left on 01Mar2021 (age at vaccination 71years old) as dose 2, single for covid-19 immunisation. Medical history included herpes zoster from an unknown date and unknown if ongoing other medical history: History of Shingles and medically controlled blood pressure, surgery from an unknown date and unknown if ongoing He's had multiple scans, blood tests, surgeries, and biopsies, biopsy from an unknown date and unknown if ongoing He's had multiple scans, blood tests, surgeries, and biopsies. The patient did not have known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medication(s) included amlodipine (AMLODIPINE); losartan potassium (LOSARTIN); hydrochlorothiazide (HYDROCHLOROTHIAZIDE). For all these concomitant products start and stop date and indication were not reported. Since the vaccination, the patient had not been tested positive for COVID-19. The patient received historical vaccine first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number: EL9267) via an unspecified route of administration in Arm Left on 10Feb2021(age at vaccination 71years old) as single dose for covid-19 immunisation. The patient experienced strokes in the medulla and cerebellum, anemia, anemia with high levels of ferritin, persistent fever, complete muscle atrophy on 19Mar2021.The patient Reported Events as Strokes in the medulla and cerebellum. Hemoglobin struggles to stay above 7. Multiple blood transfusions. He's developed anemia with high levels of ferritin, persistent fever, with no sign of inflammation or infectious disease. He also has complete muscle atrophy. He's had multiple scans, blood tests, surgeries, and biopsies. 3 months, 2 hospitals, and multiple physician and specialist intervention with no determinization of diagnosable cause of symptoms. The patient received any treatment for the adverse events reported as unknown. The patient was hospitalized for strokes in the medulla and cerebellum, anemia with high levels of ferritin, persistent fever for 91 days. The patient underwent lab tests and procedures which included blood test: unknown on unspecified date. He's had multiple scans, blood tests, scan: unknown on unspecified date. The clinical outcome of the event reported as not recovered. Follow up attempt is excepted. Further information is requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 91,0
Labordaten: Test Name: Blood tests; Result Unstructured Data: Test Result:Unknown; Comments: He's had multiple scans, blood tests,; Test Name: multiple scans; Result Unstructured Data: Test Result:Unknown; Comments: He's had multiple scans, blood tests,
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Biopsy (He's had multiple scans, blood tests, surgeries, and biopsies.); Blood pressure inadequately controlled (other_medical_history: History of Shingles and medically controlled blood pressure); Shingles (other_medical_history: History of Shingles and medically controlled blood pressure); Surgery (He's had multiple scans, blood tests, surgeries, and biopsies.)
Andere Medikamente: AMLODIPINE; LOSARTIN; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1431234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 23.02.2021
Beginn: 10.04.2021
Tage bis Beginn: 46,0
Dosis: UNK
Route/Site: - / -

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

Death Pneumonia

Symptomtext

Death J18.9 - Pneumonia, unspecified organism

Weitere VAERSDATA-Felder

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

VAERS 1431178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 09.03.2021
Beginn: 12.06.2021
Tage bis Beginn: 95,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury Death Hyponatraemia Hypoosmolar state Seizure like phenomena Subarachnoid haemorrhage Thrombocytopenia

Symptomtext

Death SAH (subarachnoid hemorrhage) Observed seizure-like activity Hypo-osmolality and hyponatremia Acute kidney failure, unspecified Thrombocytopenia, unspecified

Weitere VAERSDATA-Felder

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

VAERS 1416816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: OH
Alter: 31,0
Geschlecht: M
Eingang: 22.06.2021
Impfdatum: 17.02.2021
Beginn: 03.05.2021
Tage bis Beginn: 75,0
Dosis: 1
Route/Site: IM / RA

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

Cardiomyopathy Death Depressed level of consciousness Lethargy

Symptomtext

Woke that morning very lethargic and hard to arouse. Mom states had been doing very well, exercising and losing weight. States he felt good up until that day. DEATH

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Death certificate states cardiomyopathy
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: None
Allergien: unknown
Vorherige Impfungen: -

VAERS 1391343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 93,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 23.02.2021
Beginn: 02.06.2021
Tage bis Beginn: 99,0
Dosis: UNK
Route/Site: - / -

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

Cerebrovascular accident

Symptomtext

I63.9 - Stroke determined by clinical assessment (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1376559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: OH
Alter: 42,0
Geschlecht: F
Eingang: 06.06.2021
Impfdatum: 05.03.2021
Beginn: 31.05.2021
Tage bis Beginn: 87,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident Computerised tomogram Hemiparesis Laboratory test Magnetic resonance imaging

Symptomtext

Event - stroke without known precursors Treatment- currently in inpatient rehab Outcome - unknown if I will regain full use of right side 3 days at hospital and now currently in inpatient rehab with unknown discharge date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: 4 CTs MRI Lab work
Aktuelle Erkrankungen: n/
Vorgeschichte: Asthma Ulcerative Colitis
Andere Medikamente: Advair 230-21 ProAir Xyzal
Allergien: Nuts Codeine Expectorant Some decongestants
Vorherige Impfungen: -

VAERS 1374122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

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

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

Death Pneumonia

Symptomtext

death J18.9 - Pneumonia, unspecified organism

Weitere VAERSDATA-Felder

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

VAERS 1364866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: AZ
Alter: 65,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 18.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Blood test abnormal Cardiomegaly Computerised tomogram thorax abnormal Dyspnoea Echocardiogram abnormal Fibrin D dimer increased Plasminogen activator inhibitor type 1 deficiency Pulmonary embolism

Symptomtext

Couldn?t breath, Ambulance to ER, Blood Test and Chest CT showed multiple pulmonary embolisms in both lungs, hospital stay for 3 days, multiple IV doses of Heparin, Echocardiogram showed enlarged right side of heart, released with script for Eliquis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Chest CT Scan and D dimer blood tests showed Pulmonary embolisms in both lungs 02/20/21 Multiple Blood Tests 02/20-02/23/21 Multiple Blood Tests by Hematologist revealed previously unknown PAI1/4G 03/05/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension, Hypothyroid, Sleep Apnea, Myeloid Hypoplasia, Chronic Low IgM, Diverticulosis
Andere Medikamente: Synthroid 112 mcg, Amlodipine 5 mg, Diovan 160 mg, Bupropion 300 mg, Trazodone 75 mg, Potassium Citrate, Hydroxyzine 25 mg (1/4 pill as needed), Vitamins C and D and multi, Calcium, Allegra, Glucosamine/Chondroitin
Allergien: Penicillin, Latex, Adhesives, Codeine (Intolerance)
Vorherige Impfungen: -

VAERS 1362402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 90,0
Geschlecht: M
Eingang: 31.05.2021
Impfdatum: 15.03.2021
Beginn: 05.05.2021
Tage bis Beginn: 51,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Death Hyponatraemia Hypoosmolar state

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 1355397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 27.05.2021
Impfdatum: 23.01.2021
Beginn: 21.04.2021
Tage bis Beginn: 88,0
Dosis: 2
Route/Site: SYR / RA

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

Acute respiratory failure Blood culture COVID-19 COVID-19 pneumonia Chest X-ray Electrocardiogram normal Hypoxia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Positive COVID-19 test on April 24th, and on April 28, 2021. Hospitalization on April 28th with Pneumonia due to COVID-19 virus, COVID, Hypoxia, Acute respiratory failure with hypoxia (HCC)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: COVID-19 test Positive ECG 12 lead, ECG ED Preliminary Interpretation XR Chest 1 Vw Portable Blood Culture, aerobic & anaerobic
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1316829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 09.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Acute myocardial infarction Chest pain

Symptomtext

Non-ST elevation (NSTEMI) myocardial infarction chest pain

Weitere VAERSDATA-Felder

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

VAERS 1307366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 24.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

Pulmonary embolism

Symptomtext

I26.99 - Pulmonary embolism

Weitere VAERSDATA-Felder

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

VAERS 1303400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 10.05.2021
Impfdatum: 19.02.2021
Beginn: 22.04.2021
Tage bis Beginn: 62,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction

Symptomtext

This 79 year old female received the Covid shot on 2/19/21 and went to the ED and admitted on 4/22/21 with the following diagnoses listed below. I21.4 - Non-ST elevation (NSTEMI) myocardial infarction

Weitere VAERSDATA-Felder

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

VAERS 1289390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 19.02.2021
Beginn: 28.03.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: SYR / UN

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

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

Symptomtext

Patient hospitalized and died of pneumonia caused by COVID-19 after being fully vaccinated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: COVID-19 PCR positive test on 3/28/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1241404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 20.04.2021
Impfdatum: 10.02.2021
Beginn: 25.03.2021
Tage bis Beginn: 43,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Atypical pneumonia Chest X-ray abnormal Cough Death Dyspnoea Headache Hypoxia Malaise Nasal congestion Neck pain Pain Pneumonia Respiratory tract congestion

Symptomtext

WEAKNESS, SHORTNESS OF BREATH, NASAL CONGESTION, DEATH Narrative: Patient died after COVID vaccine dose #1 01/07 visit for chemo, stable 01/21 visit for chemo, stable 01/27 hematology visit d/t rash, likely heat rash 02/09 chemo for multiple myeloma, reports fatigue but no dyspnea 02/10 COVID vaccine dose #1 03/02 chest xray with concern for bilateral pneumonia, treated with antibiotics 03/08 pt having pain in back of the neck 03/09 pt having shortness of breath, transported to hospital with persistent generalized weakness with body ache and shortness of breath; diagnosis: atypical pneumonia, viral vs. bacterial, acute dyspnea with hypoxia, nonproductive cough, chest congestion, headache, and malaise 03/25 pt passed away COVID vaccination not likely contributor to patient's death, but is more likely due to advanced age (83 y/o) and comorbidities, especially active multiple myeloma, receiving chemo. No immediate reaction after first vaccination. Hospitalized a month after vaccine and illness persisted, leading to patient's passint. No COVID infection documented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: 3/2/21 VITALS BP 159/72, PULSE 96, R 18, O2 SAT 95%
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1231330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 20.02.2021
Beginn: 13.04.2021
Tage bis Beginn: 52,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure Anaemia Asthenia Blood lactic acid increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Dizziness Dyspnoea exertional Haemoglobin decreased Hypotension Lung opacity Pneumonia Pulmonary embolism SARS-CoV-2 test positive Sepsis White blood cell count increased

Symptomtext

Pt presented to ED at the recommendation of the PCP for low hemoglobin where he reported having increased generalized weakness for the past month, dyspnea on exertion, occasional lightheadedness. On arrival to ED was found to be hypotensive, with elevated WBC count, mildly elevated lactic acid level, and anemic at Hgb 7.5. An incidental finding of a positive COVID-19 nasal swab was found despite receiving Pfizer COVID vaccinations on 1/30/21 and 2/20/21. Pt admitted for additional management of sepsis, hypotension potentially secondary to COVID-19 infection and/or RLL developing pneumonia. Pt currently still hospitalized with worsening acute respiratory failure due to COVID and acute pulmonary embolism.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 4/13/21: Positive COVID nasal swab CXR (4/18): worsening bilateral alveolar opacities compatible with pt's known COVID pneumonia
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, CAD, AFib, kidney disease, diabetes, hypertension
Andere Medikamente: carvedilol, clopidogrel, aspirin, atorvastatin, metformin
Allergien: morphine
Vorherige Impfungen: -

VAERS 1227961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: UT
Alter: 92,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 16.02.2021
Beginn: 07.03.2021
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: - / RA

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

Pulmonary embolism

Symptomtext

Pulmonary Embolism in right lung; This is a spontaneous report from a contactable consumer (patient). A 92-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EL9267), via an unspecified route of administration, administered in right arm on 16Feb2021 at 12:45 PM at the age of 92-years-old as single dose for COVID-19 immunization. Facility type vaccine was reported as Other. The patient had no other vaccine in four weeks. The patient's medical history included known allergies to penicillin and sulfa drugs. Concomitant medications included fluoxetine, cyanocobalamin (B12-VITAMIN), and fish oil (OMEGA 3); all taken for unspecified indications, start and stop dates were not reported (reported as other medications in two weeks). The patient previously took potassium iodate and experienced allergies. The patient previously received the first dose of BNT162B2 in the right arm on 26Jan2021 at 12:45 PM (lot number: EL9261) at the age of 92-years-old for COVID-19 immunization. The patient experienced pulmonary embolism in right lung on 07Mar2021 at 09:00 AM. The event resulted in emergency room/department or urgent care, hospitalization, life threatening illness (immediate risk of death from the event). The patient was hospitalized for pulmonary embolism in right lung for 2 days in 2021. The patient received treatment for the event which included heparin. The patient had no COVID prior the vaccination and was not tested for COVID post vaccination. The outcome of the event was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Sulfonamide allergy
Andere Medikamente: FLUOXETINE; B12-VITAMIN; OMEGA 3 [FISH OIL]
Allergien: -
Vorherige Impfungen: -

VAERS 1212474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 20.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Cough Death Hypotension Mental status changes Respiratory failure Syncope

Symptomtext

Death R05 - Cough J96.90 - Respiratory failure R55 - Syncope R41.82 - Altered mental status I95.9 - Hypotension M25.551 - Right hip pain Z79.01 - On apixaban therapy

Weitere VAERSDATA-Felder

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

VAERS 1208724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 23.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

death

Weitere VAERSDATA-Felder

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

VAERS 1207286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 17.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 1201256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 18.02.2021
Beginn: 06.03.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: SYR / LA

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

Cerebrovascular accident Computerised tomogram Magnetic resonance imaging

Symptomtext

Stroke 13 days after 2nd injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Cat scan MRI
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Wellbutrin
Allergien: Cipro
Vorherige Impfungen: -

VAERS 1200805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 20.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 40,0
Dosis: 2
Route/Site: IM / LA

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

Death Infection Pyrexia Vomiting

Symptomtext

FEVER VOMITING ISOLATION-INFECTIOUS DISEASE Death

Weitere VAERSDATA-Felder

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

VAERS 1143055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 29.03.2021
Impfdatum: 09.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / RA

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

Cardiac arrest Death

Symptomtext

CARDIAC ARREST DEATH

Weitere VAERSDATA-Felder

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

VAERS 1142210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: FL
Alter: 92,0
Geschlecht: F
Eingang: 28.03.2021
Impfdatum: 17.02.2021
Beginn: 16.03.2021
Tage bis Beginn: 27,0
Dosis: 2
Route/Site: IM / LA

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

Brain stem ischaemia Cerebrovascular accident Cognitive disorder Computerised tomogram Echocardiogram Electrocardiogram Injury Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging Memory impairment Speech disorder Transient ischaemic attack

Symptomtext

TIA 3/16/2021 and moderate stroke on 3/18/2021 resulting in ischemic area left temporal and occipital lobe. Injury affecting speech, memory, and cognitive abilities. unable to live independently as prior to the event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: CT, MRI, EKG, Echo cardiogram, various lab work from 3/16 - 3/20/2021
Aktuelle Erkrankungen: chronic hypertension, well controlled, hypothyroidism, osteoporosis
Vorgeschichte: hypertension
Andere Medikamente: Bystolic, Diazide, Olmesartan, Synthroid, Eliquis, Prolia, Nitrofurantoin. Prevavision, Multi vitamin, Calcium
Allergien: Penicillin, Clonidine, Tetanus immunization
Vorherige Impfungen: tetnus, as a child, date unknown

VAERS 1123805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: TX
Alter: 75,0
Geschlecht: F
Eingang: 22.03.2021
Impfdatum: 12.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / UN

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

Acute respiratory failure Asthenia Chills Confusional state Death Hypoxia Pyrexia SARS-CoV-2 antibody test positive SARS-CoV-2 test positive

Symptomtext

Admitted on 2/17/2021 with acute respiratory failure with marked hypoxia. Noted to have fever & chills, weakness and acute confusion ~ 3 days prior to admission. Placed on NIPPV, steroids, convalescent plasma and antibiotics. Patient died 2/24/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: COVID 19 PCR + 2/17/2021 COVID antibody (total) + 2/20/2021
Aktuelle Erkrankungen: ESRD s/p renal transplant 2010, DM, HTN, CAD, HLD, GERD, Hypothyroidism
Vorgeschichte: ESRD s/p renal transplant 2010, DM, HTN, CAD, HLD, GERD, Hypothyroidism
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG qd aspirin (Aspir-Low) 81 MG qd B complex-vitamin C-folic acid (NEPHRO-VITE) 0.8 MG qd cyanocobalamin (VITAMIN B-12) 1000 MCG qd folic acid (FOLVITE) 1 MG qd furosemide (LASIX) 40 MG bid insulin degludec 30 Uni
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1123137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: AZ
Alter: 71,0
Geschlecht: M
Eingang: 22.03.2021
Impfdatum: 19.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: - / RA

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

Myocardial infarction

Symptomtext

massive heart attack; This is a spontaneous report from a contactable consumer or (patient's daughter-in-law). A 71-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number EL9267) via an unspecified route of administration at single dose in right arm on 19Feb2021 3:30PM for COVID-19 immunisation. Medical history included diabetes, high blood pressure. Concomitant medications included meloxicam at 15 mg one tablet per day in morning by mouth, metformin at 1000 mg twice daily by mouth, hydrochlorothiazide, valsartan (VALSARTAN + HIDROCLOROTIAZIDA) at 320 mg/12.5 mg once a day in morning by mouth, all from unspecified date and ongoing for unknown indication. On 03Mar2021, the patient experienced massive heart attack with outcome of unknown. The event required a visit to the emergency room. The patient was hospitalized for massive heart attack from 03Mar2021 to ongoing. Reporter stated that "Patient is in the hospital right now as he had a massive heart attack on Wednesday 03Mar2021. She reports they do not think its an adverse event related to the COVID-19 vaccine because 3 of his 4 valves were clogged, but she did fill out a form online with the state of (state withheld). The patient's second COVID-19 vaccine was rescheduled to 13Mar2021 and she is asking if the second COVID-19 vaccine can be rescheduled to the 31Mar2021, since the patient will have a long recovery. She's not sure how far they can go with the scheduling of the second vaccine before the 1st one will expire and he will have to start the series all over again".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Diabetes
Andere Medikamente: MELOXICAM; METFORMIN; VALSARTAN + HIDROCLOROTIAZIDA
Allergien: -
Vorherige Impfungen: -

VAERS 1104720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 20.02.2021
Beginn: 11.03.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

death

Weitere VAERSDATA-Felder

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

VAERS 1095705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 20.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Death Respiratory distress

Symptomtext

RESPIRATORY DISTRESS death

Weitere VAERSDATA-Felder

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

VAERS 1085673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: NM
Alter: 88,0
Geschlecht: M
Eingang: 09.03.2021
Impfdatum: 23.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Patient died 2/26/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: GLUCOSE INTOLERANCE HYPOTENSION
Vorgeschichte: NSTEMI - Non-ST segment elevation MI Diabetes mellitus Hypothyroid Hyperlipidemia CHF - Congestive heart failure Benign essential hypertension Chronic obstructive lung disease Osteoarthritis Obstructive sleep apnea of adult Chronic kidney disease Impaired fasting glucose Electrocardiogram abnormal
Andere Medikamente: 1) ALBUTEROL 100/IPRATRO 20MCG 120D PO INHL INHALE 1 ACTIVE PUFF BY MOUTH FOUR TIMES A DAY . FOR BREATHING. 2) BUDESONIDE 160/FORMOTER 4.5MCG 120D INH INHALE 2 ACTIVE PUFFS BY MOUTH TWICE A DAY FOR BREATHING. R
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1085200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: VA
Alter: 35,0
Geschlecht: F
Eingang: 09.03.2021
Impfdatum: 16.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: OT / LA

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

Blood test Cerebrovascular accident Investigation Magnetic resonance imaging SARS-CoV-2 test

Symptomtext

Patient had 4 mm left frontal lobe stroke without any other known etiology on testing (heme, cardio, neuro consulting/workup); This is a spontaneous report from a contactable physician. A 35-year-old female patient (no pregnancy) received the first dose of BNT162B2 (Pfizer-BIONTECH Covid-19 Vaccine, lot number: EL9267), intramuscularly at site of left arm at 16:30 on 16Feb2021 at single dose for COVID-19 immunisation. Medical history included hypothyroidism and autism spectrum disorder (ASD) (closed 12 years ago with NO sequelae). Concomitant medication included levothyroxine and valacyclovir [valaciclovir], both received within two weeks of vaccine. The patient had 4 mm left frontal lobe stroke without any other known etiology on testing (heme, cardio, neuro consulting/workup) at 13:15 on 20Feb2021. The patient was hospitalized for this event for 2 days. The adverse event resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, hospitalization, life threatening illness (immediate risk of death from the event), disability or permanent damage. The patient received treatment (Multiple MRI/MRI, TTE AND TEE, blood studies/holter study, new medicatinos) for adverse event. No covid prior vaccination. Covid was tested post vaccination. Covid test type post vaccination was blood test, covid test name post vaccination was Ig M/IgG with negative result on 24Feb2021. Covid test type post vaccination was Nasal Swab, covid test name post vaccination was Rapid with negative result on 24Feb2021. No known allergies. No other vaccine received in four weeks. The outcome of event was recovered/resolved with sequel.; Sender's Comments: Limited information does not allow a medically meaningful assessment for the event Stroke for BNT162B2. Details regarding the clinical symptoms, relevant test results, treatment medications and clinical course are not provided. At this time, the case is handled as related for reporting purposes. The case will be re-evaluated if more information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: Test Date: 20210224; Test Name: Blood test; Test Result: Negative ; Comments: covid test name post vaccination was Ig M/IgG; Test Name: blood studies/holter study; Result Unstructured Data: Test Result:unknown results; Test Name: Multiple MRI/MRI; Result Unstructured Data: Test Result:unknown results; Test Date: 20210224; Test Name: Nasal Swab; Test Result: Negative ; Comments: covid test name post vaccination was Rapid
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autism spectrum disorder (closed 12 years ago with NO sequelae); Hypothyroidism
Andere Medikamente: LEVOTHYROXINE; VALACYCLOVIR [VALACICLOVIR]
Allergien: -
Vorherige Impfungen: -

VAERS 1075289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: OH
Alter: 76,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 12.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Acute myocardial infarction Asthenia Blood bicarbonate normal Blood chloride normal Blood creatinine increased Blood glucose normal Blood potassium decreased Blood sodium normal Blood urea increased Brain natriuretic peptide increased COVID-19 Chest X-ray abnormal Haematocrit decreased Haemoglobin decreased Influenza A virus test negative Influenza B virus test Influenza virus test negative Loss of personal independence in daily activities

Symptomtext

Patient was vaccinated tihe Pfizer #1 2/12/21. Started feeling weak 2/13 and presented to ED on 2/14. Was admitted to Hospital. Found to be COVID +, required O2 per NC 2-3 L for approx 24 hours. Was found to have NSTEMI. Was transferred for speciality/cardiology care at General Hospital. Was on heparin gtt. Cardiology-no intervention. Was not treated for COVID and was discharged to home on 2/16. Was unable to care for himself at home and was readmitted with in hours. He has failed discharge twice and is being now discharged to SNF

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: 1/30/21 Nasal swab -Negative for SARS-CoV-2, Influenza A & B CXR showed patchy bibasilar opacities 2/14/21 Nasal swab-Positive SARS-CoV-2, negative influenza A/B, WBD 6.2, Hgb 11.7, Hct 36.5, Plt 254, Na 138, K+ 3.4, Cl- 104, HCO3 28, BUN 26, Cr 1.34, gluc 177, Troponin 708 (=<45) BNP 2575 2/14/21 CXR No significant change compared to prior examination (1/30/21) may be related to atelectasis and/or residual PNA
Aktuelle Erkrankungen: Diagnosed with PNA 1/30/21. Treated with prednisone and Augmentin. Covid test negative at that time but did have a know exposure in his home (grandson tested positive 1/28/21)
Vorgeschichte: chronic HFpEF CAD HTN HLD COPD w/asthma type 2 DM morbid obesity chronic LBP w/sciatica BPH
Andere Medikamente: Anoro 100/62.5/2.5 one puff daily Albuterol med neb QID prn ASA 81mg daily Carvedilol 6.25mg BID Benadryl 25mg QHS prn Furosemide 80mg BID Gabapentin 600mg TID Glimepiride 4mg daily Losartan 100mg daily omeprazole 20mg daily saxagliptin/met
Allergien: NKA
Vorherige Impfungen: -

VAERS 1075234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: AZ
Alter: 71,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 19.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: SYR / RA

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

Coronary artery bypass Laboratory test Myocardial infarction

Symptomtext

Massive Heart Attack

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Tests started on 3/3/2021 Having Coronary Artery Bypass Graft Surgery to repair 3-4 Passages
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes High blood pressure
Andere Medikamente: Meloxicam 15mg once morning. Metformin hcl 1000 mg twice daily Valsartan hctz 12.5mg once morning.
Allergien: Latex
Vorherige Impfungen: -

VAERS 1046722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: WY
Alter: 67,0
Geschlecht: M
Eingang: 22.02.2021
Impfdatum: 11.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / AR

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

Cardiac arrest Cardiac disorder Chills Death Diaphragmatic spasm Toxicologic test

Symptomtext

No symptoms or signs on the day 1st dose of vaccine was received (2/11/2021). 3 days later, (2/14/2021) patient experienced chills for approximately 6 hours, followed by severe (visible) chest spasms, and then cardiac arrest. 911 was called upon witnessing chest spasms, but cardiac arrest/death occurred before patient could be transported to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: County coroner verified that they conduct toxicology reports on all deaths. Contact Funeral Home for details/follow up if needed.
Aktuelle Erkrankungen: UTI
Vorgeschichte: Congestive Heart Failure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1044891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 21.02.2021
Impfdatum: 26.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Glaucoma Vision blurred

Symptomtext

Four days after 1st vaccine woke up with blurry vision and ophthalmologist diagnosed me with Glaucoma on Monday Feb.1, 2021. My eye pressure was at 42. Day after 2nd vaccine my blurry vision doubled. Saw ophthalmologist again who confirmed it was due to the vaccine due to no other issues or changes on my body or health.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Glaucoma
Hospital-Tage: -
Labordaten: Ophthalmologist saw me numerous times after both times and prescribed different oral medications and drops. I continue to have the problem and don?t know if this will be temporary or permanent. I?m also continuing with the medications. I?m quite disturbed.
Aktuelle Erkrankungen: Shingles
Vorgeschichte: Fibromyalgia Arthritis Herniated Discs
Andere Medikamente: Liothyronine 10mcg 1xD Levothyroxine 50mcg 1xD Nifedipine XL 30mg 1xD Clonazepam 2mg 1xD Quetiapine 50 mg 1to2 at bedtime Kepra 1,000 mg at bedtime Zyrtec 10mg 1xD Liquid Vit. D 2,000 IU 1 drop B12 with L-5 MTHF 1,000 mcg 1xD Potassium 99mg
Allergien: Need to eat lactose and gluten free.
Vorherige Impfungen: -

VAERS 1060522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: -
Alter: 87,0
Geschlecht: M
Eingang: 19.02.2021
Impfdatum: 17.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / RA

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

Death Feeling abnormal Injection site pain Malaise

Symptomtext

death Narrative: 86 year old MALE with PMH of Afib s/p AICD/PPM, HFrEF (EF< 20% 10/2019), DM2, HTN, HLD, BPH, Depression. Was stable and feeling well when he was administered Covid-19 vaccine on 02/17/2021- Pfizer COVID-19 Vaccine 0.3 ml IM. MVX (Manuf); PFR; Lot#; EL9267; Exp Date:05/31/2021 Administration Anatomic site: Right Deltoid; Pt was monitored for 30 minutes after administration and had no adverse effects. He was called later in the day and reports he feels well and has had no adverse reactions, he endorsed his arm is a little sore at injection site. ON 02/19/2021- his dghter found him on the floor, next to his bed, dead. She reported on 2/19/2021- that she was out with him to dinner on 2/18/2021, and he stated he did not feel well, that his insides did not feel right. He proceeded to have dinner and 2 drinks. HE was doing ok, when she took him home.

Weitere VAERSDATA-Felder

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

VAERS 1025579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

kritisch

Staat: LA
Alter: 76,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Atrial fibrillation Cardioversion Death Fall Life support Cardiac arrest Pulse absent Resuscitation Screaming Ventricular fibrillation

Symptomtext

Patient received the COVID vaccine in the morning. She was at home for about an hour after, when she "screamed" and fell out of her chair. Family members called 911. Patient was in cardiac arrest upon arrival. Upon arrival to ED, they performed ACLS for 42 minutes with no pulse for 25 minutes. Patient received 450 of amiodarone, epinephrine 7x, and bicarb 2x with IO access in R femur.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: CAD, COPD, DM2, emphysema, Heart Failure, HTN
Vorgeschichte: DM2, CAD, HTN, RA
Andere Medikamente: Unknown from encounter record
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2703515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 27.10.2023
Impfdatum: 18.02.2021
Beginn: 01.06.2021
Tage bis Beginn: 103,0
Dosis: 2
Route/Site: - / -

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

Blood pressure increased Cardiac disorder Catheterisation cardiac Computerised tomogram Dyspnoea Emphysema Myocarditis Peripheral swelling

Symptomtext

myocarditis; Blood pressure it was 240 over 180; Leg swollen to my knees; heart was swollen; Mild emphysema; Shortness of breath with exertion; This is a spontaneous report received from a contactable reporter(s) (Nurse). A 66-year-old male patient received bnt162b2 (BNT162B2), on 18Feb2021 as dose 2, single (Lot number: EL9267) at the age of 65 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "had quit smoking" (unspecified if ongoing), notes: so he had quit smoking about 3 months before the event. There were no concomitant medications. Vaccination history included: bnt162b2 (DOSE 1, SINGLE, LOT#: EL3249, Expiration date: Reporter stated, "It is not on the paper. It does not have an expiration date."), administration date: 28Jan2021, when the patient was 65-year-old, for COVID-19 Immunization. The following information was reported: DYSPNOEA (non-serious) with onset Jun2021, outcome "unknown", described as "Shortness of breath with exertion"; BLOOD PRESSURE INCREASED (hospitalization) with onset Oct2021, outcome "unknown", described as "Blood pressure it was 240 over 180"; PERIPHERAL SWELLING (non-serious) with onset Oct2021, outcome "unknown", described as "Leg swollen to my knees"; EMPHYSEMA (non-serious) with onset Oct2021, outcome "unknown", described as "Mild emphysema"; CARDIAC DISORDER (non-serious) with onset Oct2021, outcome "unknown", described as "heart was swollen"; MYOCARDITIS (hospitalization, medically significant) with onset Oct2021, outcome "unknown". The event "myocarditis" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood pressure increased: 240, notes: over 180; Catheterisation cardiac: Unknown results; Computerised tomogram: Unknown results. Therapeutic measures were taken as a result of myocarditis, blood pressure increased, dyspnoea, peripheral swelling, cardiac disorder, emphysema. Clinical course: Reporter stated, "I am calling to report a possible reaction that my husband had to his COVID Vaccine. Currently they did not spell out an adverse reaction like I thought they did at the hospital at the time of event. I want to make sure that it was recorded now. I am reporting an adverse reaction that my husband had to his COVID Vaccine. Yes, he was hospitalized. So, at the time that he was hospitalized we were not aware that the COVID Vaccine was linked to myocarditis and my husband had an event in Oct2021 after he had received two COVID Vaccines. He did not have anything on it prior to these event. He woke up and he started having some shortness of breath. A few months before the event no chest pain but he thought it was because of his smoking and he quit smoking and so he had quit smoking about 3 months before the event and in the middle of the night he woke me up and said I just get up to go to the bathroom and my left leg swollen to my knees. So, I took his blood pressure it was 240 over 180 and so I took couple of Aspirin and took him to the car and take him to the hospital. When we go to the hospital they ran cath test and one of them was Heart Cath they said that his coronary arteries were big and wide open, his valves were perfect but his heart was swollen. So, they kept him for a week and took 11 liters of fluid of him. He had an ejection fraction of 10%. They sent him home with LifeVest and the cardiologist who gave the Heart Cath said, he had no chest pain he said no none. He was not sick at all prior to this event he said no I never missed a day at work and then I never had any illnesses. I started getting a little bit more short of breath and sprain, I had smoked for years about 5 years ago, I switched from cigarettes to Cigars. He have had a CAT scan of his lungs to evaluate his lungs and they said he had mild emphysema and that is when he had switched from cigarettes to cigars. When he was in hospital, they gave some Lasix and 'diuretic' and started him on a bunch of other medications for his heart failure. My husband legs was swollen and he had no infection prior month. Months prior, he was healthy with no infections or anything. He was completely healthy. He had gone to work the night before or the day before and woke up at 3'O clock in the morning and had swollen legs. I do have to tell you one more thing that because we were not aware at that time that the COVID-19 was causing the myocarditis, he did not consider the COVID-19 as a culprit possible and so he did receive the another COVID Vaccine in December. He took the COVID Vaccine on 03Dec2021and it was again the COVID-19 Pfizer Vaccine that he had 3 doses of that. The first dose was 28Jan2021. The second dose was 28Feb2021 and the third dose was 03Dec21 and when we had the Heart Cath the doctor said I say this is probably cause by bed rest when you sit at all and we said no he has been healthy for last six months and he said I don't, I expect him to get for recovery is what he said. When his coronary arteries being perfect and his valves being perfect he said there is nothing wrong in his heart. He started feeling out better but shortness of breath in about Jun2021. His age is 68 years." Third Dose LOT#: FJ1620. Expiration date: Reporter stated, "On that stuff it does shows the expiration date. 31May2022 (31May2022). He was on no medications and have no diagnosis of any disease. He has no lab work done in last two weeks. In Jun2021 and it was very mild shortness of breath. It was Shortness of breath with exertion. He has some very mild shortness of breath with exertion and it is like it does not have any shortness of breath anymore. Yes, He is on Entresto, dose is 97/103, he takes one tablet twice a day. He is on Metoprolol Succinate ER 50, twice a day. He is on 'Xeljanz' (Not clarified) 10 milligrams once a day and Spironolactone 25 milligrams, once a day and he is on Lasix 10 milligrams, one tablet PRN (As needed). It does not say on his vaccine card where they gave the shot. All of them were in arm and I do not know which one of it. Previous medication. He was on no medication prior to the event. He got the Flu Vaccine on 20Oct2022." The patient took no vaccine on same date with Pfizer COVID Vaccine.; Sender's Comments: Based on the available information and the known product safety profile, a causal relationship between the reported event Myocarditis and suspect product cannot be excluded. Based on the available information, a causal relationship between the reported event Blood pressure increased and suspect product 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: Myocarditis
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:240; Comments: over 180; Test Name: cath test; Result Unstructured Data: Test Result:Unknown results; Test Name: CAT scan; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Ex-smoker (so he had quit smoking about 3 months before the event.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2685696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MN
Alter: 40,0
Geschlecht: F
Eingang: 24.09.2023
Impfdatum: 22.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: UN / LA

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

Blindness Dyskinesia Dyspnoea Dyspnoea exertional Electric shock sensation Exercise tolerance decreased Facial pain Herpes simplex test positive Hypoaesthesia Impaired work ability Laboratory test normal Loss of personal independence in daily activities Muscle spasms Muscle twitching Pain in extremity Palpitations Screaming Skin swelling

Symptomtext

I received the vaccine in Feb. and March of 2021. That summer, I climbed a flight of stairs and noticed my heart was pounding and I was out of breath. After this continued, I asked doctors about it and I was dismissed. Within several more months I started twitching involuntarily. Even my eye balls would twitch in their sockets. I could visually see my muscles having spasms throughout my body. My skin would raise up and down. My feet and hands began to fall asleep on their own accord. I would get zaps in my face and feet so painful I would yell out in pain. I lost vision and have lived with a significant reduction in my vision. The overall impact on my body took away my ability to work out like I used to. Just the other day I gasped for air and almost threw up after just a short workout trying to push it like I used to. My life got taken away from me. I "all of a sudden" tested positive for herpes two. EVEN THOUGH I was negative (I have the test) when I got the vaccine and I had NO new partners. The stupid thing triggered my T cells to malfunction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Like the majority of people, my tests come back normal. But, my history before and after speaks for itself. So do my medical charts that prove this.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Buproprion XL 150 mg every other day.
Allergien: -
Vorherige Impfungen: -

VAERS 2597187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 13.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Ischaemic stroke Neoplasm malignant

Symptomtext

Ischemic stroke; Cancer; 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 78-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Sep2022 as dose 5 (booster), single (Lot number: GH9694) for covid-19 immunisation; BNT162b2 (BNT162B2), as dose 1, single (Lot number: EL9267), as dose 2, single (Lot number: EN6203), as dose 3 (booster), single (Lot number: EW0164) and as dose 4 (booster), single (Lot number: FL3198) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: ISCHAEMIC STROKE (medically significant), outcome "unknown", described as "Ischemic stroke"; NEOPLASM MALIGNANT (medically significant), outcome "unknown", described as "Cancer". The patient was asking whether it was okay to receive the Pfizer COVID vaccine if you have had a ischemic stroke. She heard there was a second booster dose out and wanted to know if it was okay to get it. She stated she asked her primary care doctor and she could not give her an answer and went to the health department where she got the "last 3 shots." The "3 prior" shots she got at where she had her cancer taken care of. None of them could give her any advice. She had all the Pfizer COVID vaccines and had no reaction from them (as reported). Read on the net about a warning on taking Pfizer COVID 19 shot if had a certain stroke, the stroke the patient had called ischemic stroke. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2559199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 69,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 11.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 79,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac electrophysiologic study Cardiac flutter Cardiac monitoring Cardiac stress test Echocardiogram Electrocardiogram Implantable cardiac monitor insertion Magnetic resonance imaging heart Myocarditis Ventricular tachycardia

Symptomtext

Spring / summer of 2021 after first vaccine doses, started noticing occasional chest flutters. After many tests including a heart mri at facility, myocarditis was identified as possible / probable cause. Started on metoprolol 12.5 mg daily June 2022 - 3 days after receiving the 4th covid vaccine, I experienced a Ventricular Tachycardia event. An study was performed at Hospital in July 2022 and a specific reason for the VT was not identified. I had an ICM implanted and have not experienced any further cardiac events. Background I have CLL and started being treated with Acalabrutinib about the same time the initial heart flutters were felt (spring/summer 2021). Both Acalabrutinib and Covid vax are possible causes. Numerous tests - EKG, echocardiogram (hospital), heart mri and stress test. After MRI, cardiologist diagnosed as myocarditis and Rx metoprolol. In fall of 2021, I switched from Acalabrutinib into a clinical trial for an experiment BTK inhibitor LP-168. for my CLL. Dr is my oncologist and most familiar with this entire situation. In spring of 2022, I experienced some dizziness clinical trial personnel ordered a heart holster to determine if I was having any heart rhythm problems. A couple days into wearing this holster (6/13/22) , a VT event was recorded early in the morning when I was asleep. i did not notice anything. The EV event lasted 19 sec with a max heart rate of 157 and resolved itself. The VT occurred 3 days after having received the 4th Covid vax dose. Despite an study, the exact cause of the VT event has not been determined. There was no apparent permanent heart wiring issues from the study. It is not clear if the heart issues (myocarditis and VT event) were caused by the covid vax or something else. Some other factors which may be relevant: - I have a farm and am quite active outside in spring. It is possible I was experiencing some dehydration which was causing the dizziness and may have caused the VT. I try to drink lots of water but it had been purified bottled water. After discussion with my Drs, I started drinking Smart Water which has some of the essential nutrients added. When I started using Smart Water, the dizziness decreased. I am not sure if I started drinking the Smart Water before or after the VT event. - As noted, I have been taking an experimental BTK inhibitor LP-168 for my CLL. There had not been any issues with heart rhythm with this drug but to be cautious, I discontinued using it until the study could not identify any cause. My oncologist did not believe the LP-168 caused the issue and I restarted the drug. I also had an ICM implanted to monitor my heart rhythm. 6+ months later, there have not been any VT or other cardiac events recorded. - The VT event occurred at night when I was asleep. Earlier in the day, I was cleaning an area under a cracked shower pan which had become moldy. I was exposed to the mold and to an anti-mold agent. - I have sleep apnea and use a CPAP. My CPAP reports do not show any significant abnormal events on the day of the VT. - I have a lot of sinus congestion issues and routinely go to sleep with a Halls cough drop in my mouth. I don't know that I did but it is possible that I choked momentarily on the cough drop. - Throughout the night, I change sleeping positions several times - back, right side, left side. Other conditions and drugs: I am 71, obese, have several chronic conditions - OSA, high blood pressure, cholestrol. I take various medications to address the issues above. These include: Mucinex, Flonase (50 mcg), azelastine .15% nasal spray to address sinus congestion lisinopril 20 mg (blood pressure) lovastatin 20 mg (cholesterol) levothyrozine 50 mg (throid) valtrex 500 MG (shingles prevention) LP-168 100 mg (cll clinical trial med) metoprolol 25 mg (heart) sildenafil 50 mg (rarely used and don't remember using it during any of the events) I listed all of the covid vaccine doses above. Dates of each dose are as follows: Dose 1 - 2/11/21 Dose 2 - 3/4/21 Dose 3 - 10/1/21 Dose 4 - 6/10/22 (VT event occurred 3 days later) I participated in an study to determine antibodies created by the covid vax. I tested after the first 3 doses and did not record any antibodies. It is difficult to say definitively that the covid vax caused my cardiac issues but it is certainly one of the possible causes.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG, echo cardiogram, heart mri, stress test, heart monitor, study
Aktuelle Erkrankungen: -
Vorgeschichte: cll, high blood pressure, cholesterol, obstructive sleep apnea, obesity, chronic sinus congestion
Andere Medikamente: Mucinex, Flonase (50 mcg), azelastine .15% nasal spray to address sinus congestion lisinopril 20 mg (blood pressure) lovastatin 20 mg (cholesterol) levothyrozine 50 mg (throid) valtrex 500 MG (shingles prevention) LP-168 100 mg (cll clinica
Allergien: none
Vorherige Impfungen: -

VAERS 2537298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

schwer

Staat: FL
Alter: 54,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 05.01.2020
Beginn: 05.04.2022
Tage bis Beginn: 821,0
Dosis: 2
Route/Site: IM / LA

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

Autoimmune disorder Bartonellosis Dysbiosis Electric shock sensation Haematological infection Laboratory test Lyme disease Malignant melanoma Muscle twitching Post viral fatigue syndrome Tongue disorder

Symptomtext

1) Myalgic Encephamyolitis, 2) Reactivated Lyme Disease, 3) Furry Tongue Disease, 4) Bartonella Blood Infection 5) Melanoma skin cancer 6) Muscle Twitching and Electric Shocks 7) Auto Immune Disease 8) Gut Dysbiosis

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Lab 6/22
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Statins
Vorherige Impfungen: Flu Shot 2018 Quad

VAERS 2462823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 03.02.2021
Beginn: 25.05.2021
Tage bis Beginn: 111,0
Dosis: 2
Route/Site: - / LA

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

Guillain-Barre syndrome SARS-CoV-2 test

Symptomtext

Guillen Barre; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Feb2021 as dose 2, single (Lot number: EL9267) at the age of 70 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: OZEMPIC. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: EL8982, Location of injection: Arm Left), administration date: 22Jan2022, when the patient was 71-year-old, for Covid-19 Immunization. No other vaccine in four weeks. No known allergies. No covid prior vaccination. The following information was reported: GUILLAIN-BARRE SYNDROME (prolonged hospitalization, disability, life threatening) with onset 25May2021, outcome "not recovered", described as "Guillen Barre". The event "guillen barre" required emergency room visit. In June 2022. Hospital for Guillen Barre Aug2022 hospital again for Guillen Barre Sep2022 diagnosed with CIDP chronic form of Guillen Barre. Ae treatment included: lvlG. The event resulted in: Emergency room/department or urgent care, Hospitalization, Prolongation of existing hospitalization (vaccine received during existing hospitalization), Life threatening illness (immediate risk of death from the event), Disability or permanent damage. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06Jan2022) Positive, notes: Nasal Swab. Therapeutic measures were taken as a result of guillain-barre syndrome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Test Date: 20220106; Test Name: Wars corona virus 2Ag; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: OZEMPIC
Allergien: -
Vorherige Impfungen: -

VAERS 2284748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 21.12.2021
Beginn: 07.05.2022
Tage bis Beginn: 137,0
Dosis: 1
Route/Site: IM / AR

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

Blood culture Bradycardia Brain natriuretic peptide increased COVID-19 Clostridium test negative Cough Culture urine Diarrhoea Dyspnoea Echocardiogram Emotional distress Gait disturbance Intensive care International normalised ratio increased Positive airway pressure therapy Pyrexia SARS-CoV-2 test positive Tachypnoea

Symptomtext

Hospitalized (05/07/2022-05/18/2022); COVID-19 positive 05/07/2022; fully vaccinated plus booster BRIEF OVERVIEW: Primary Care Physician at Discharge: MD Hematologist/Oncologist: Admission Date: 5/7/2022 Discharge Date: 05/18/2022 Patient's Discharge Disposition: Rehab in stable condition. Hospital course: 87 y/oM with pmHx bacterial endocarditis s/p MVR and ICD placement in 2007, CAD (50% occlusion of LAD), combined systolic and diastolic CHF with most recent EF 40%, multiple myeloma on Revlimid and bortezomib + decadron, afib on coumadin admitted with acute hypoxic respiratory failure and hypotension. Patient currently lives with his daughter. EMS was called after an episode of coughing and vomiting for which he became very dyspneic and distressed. He presented to the ED on NRB, tachypneic, febrile, and bradycardic. Labs confirmed + UA, + COVID-19 PCR, BNP 4,100, INR 3.1. BiPAP was initiated, patient received 2L IVF, blood and urine culture cultures obtained, and he was given a dose of ceftriaxone and azithromycin. Despite IVF he was started on NE and admitted to the ICU. Upon arrival, NE was weaned from .08 down to .02 and he was stable on BiPAP with normal RR. He was started on remdesivir and decadron, abx broadened to vancomycin and zosyn. He was able to wean off BiPAP and NE. Repeat ECHO stable. Patient evaluated by SLP and diet ordered. On 5/8, patient improved and able to transfer out of the ICU. Spoke with oncology service who accepted the patient under Dr. The patient completed a course of abx with Zosyn on 5/12, Remdesivir on 5/11, and a 10 day course of dexamethasone on 5/16. He developed diarrhea during his admission but was c diff neg. He was started on scheduled Imodium and PRN Lomotil. Diarrhea was starting to improve by time of discharge. PT/OT evaluated and recommended SAR. Staff assisted with arranging and the patient was able to discharge to a facility via ambulance. The patient was eating and ambulating with assistance at the time of discharge. Discharge medications and follow up as listed below. Answered all questions and the patient was comfortable with the discharge plan

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Posttraumatic respiratory failure (HCC) Acute hypoxemic respiratory failure due to COVID-19 (HCC) SBE (subacute bacterial endocarditis) CHF (congestive heart failure) Hypotension, unspecified CAD (coronary artery disease) Atrial fibrillation, persistent (HCC) Occlusion of right femoral artery (HCC) Cardiac pacemaker in situ Acute cystitis Macrocytic anemia Multiple myeloma not having achieved remission (HCC) Multiple myeloma (HCC) hx of CVA (cerebral infarction) Dementia without behavioral disturbance, unspecified dementia type (HCC) Obstructive uropathy Urinary retention Hypercholesteremia Severely underweight adult Shock (HCC) S/P MVR (mitral valve replacement) Statin intolerance Closed displaced fracture of fifth cervical vertebra with routine healing, unspecified fracture morphology, subsequent encounter Long term (current) use of anticoagulants History of total hip replacement History of endocarditis Closed rib fracture At risk of decubitus ulcer At risk for falls Scoliosis Traumatic rhabdomyolysis (HCC)
Andere Medikamente: acyclovir (ZOVIRAX) 400 MG tablet benzonatate (TESSALON) 100 MG capsule CALCIUM PO cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) capsule cyanocobalamin 1000 MCG tablet dexamethasone (DECADRON) 4 MG tablet diphenoxylate-atropine (LOMOTIL) 2.
Allergien: Sulfadiazine Heparin Lipitor Statins Sulfa drugs
Vorherige Impfungen: -

VAERS 2266001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 06.05.2022
Impfdatum: 18.10.2021
Beginn: 28.04.2022
Tage bis Beginn: 192,0
Dosis: 2
Route/Site: IM / RA

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

Anticoagulant therapy Aortic dissection Aortic intramural haematoma COVID-19 COVID-19 pneumonia Chest X-ray abnormal Deep vein thrombosis Dyspnoea exertional Hypertension Positive airway pressure therapy Productive cough Pulmonary oedema Respiratory distress SARS-CoV-2 test positive

Symptomtext

Admission Date: 4/28/2022 Discharge Date: 5/4/2022 Condition on discharge: Stable Patient is a 87 y.o. male with PMH of HTN, Paroxysmal afib on Eliquis, complete heart block s/p AICD placement, recent admission on 3/20 for (type B aortic dissection with intramural hematoma and subsequently admitted to cardiothoracic surgery for continued management. Over course of hospital stay patient developed DVT and was started on Eliquis. Patient was subseqntly treated and realeased on 3/29. He presented to the ED on 4/28 with worsening exertional dyspnea and productive cough. Patient arrived to the ED in respirtaroy distress satting to the 80s in nonrebreather. Patient was started on BIPAP and improved. A chest xray showed pulmonary edema. Patient was subsequently admitted to the hospitalist medicine team for further medical management. Patient also found to be positive for COVID-19 pneumonia. Patient treated with 5 days of IV remdesivir and 7 days of Decadron. He should finish 4 more days of po Decadron 6 mg daily. He was weaned to RA, and did not require any home O2 at discharge. He was evaluated by PT/OT and was discharged home with HHC. Patient was also found to be hypertensive to systolic blood pressure to the 200s and placed on a nitroglycerin drip. Patient weaned off nitroglycerin drip as blood pressure improved with BiPAP and IV Lasix. Cardiology consulted increased hydralazine for improved blood pressure control. Of note spoke with outpatient vascular surgery team no need for inpatient CT angiogram thorax they have arranged outpatient follow-up for repeat imaging and follow-up visit with vascular surgery has been scheduled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Personal history of colonic polyps PVC (premature ventricular contraction) Cardiac pacemaker in situ Obstructive sleep apnea on CPAP Permanent atrial fibrillation (HCC) Essential hypertension Closed comminuted intertrochanteric fracture of proximal end of right femur (HCC) Closed comminuted intertrochanteric fracture of right femur, initial encounter (HCC) Hip fracture (HCC) Mitral regurgitation Primary osteoarthritis of right hip Complete heart block (HCC) Non-sustained ventricular tachycardia (HCC) Intramural aortic hematoma (HCC) Deep vein thrombosis (DVT) of left upper extremity (HCC) Counseling regarding advance care planning and goals of care Hyponatremia Dissecting aneurysm of thoracic aorta, Stanford type B (HCC) Acute hypoxemic respiratory failure (HCC) Pneumonia due to COVID-19 virus Acute pulmonary edema (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 10 MG tablet amoxicillin (AMOXIL) 500 MG tablet apixaban (ELIQUIS) 5 MG TABS ascorbic acid (VITAMIN C) 500 MG tablet Carboxymethylcellulose Sodium (REFRESH TEARS OPTH) choleca
Allergien: Lisinopril Swelling, Edema
Vorherige Impfungen: -

VAERS 2250640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: GA
Alter: 50,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 13.04.2021
Beginn: 23.08.2021
Tage bis Beginn: 132,0
Dosis: 2
Route/Site: SYR / -

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

Angiogram Angiogram cerebral abnormal Back pain Computerised tomogram head abnormal Headache Magnetic resonance imaging abnormal Magnetic resonance imaging head abnormal Myositis Scan with contrast abnormal Sigmoid sinus thrombosis Transverse sinus thrombosis Venogram abnormal

Symptomtext

Patient developed worsening chronic upper back pain. Myositis was revealed on MRI dated 5/6/2021. Patient went on to develop a severe HA in August 2021. Was diagnosed wit thrombosis of the left transverse and sigmoid sinus in 12/2021 after multiple MRI's were performed erroneously without contrast despite ordering provider's instruction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sigmoid sinus thrombosis
Hospital-Tage: 1,0
Labordaten: May 6, 2021 MRI right shoulder October 29, 2021 CT head without contrast, MRI stroke protocol without contrast, MRV brain without contrast December 17, 2021 MRI brain with and without contrast, December 30, 2021 CT angiogram head, February 13, 2022 CT head without contrast, February 19, 2022 CT head without contrast, March 22, 2022 MRV brain with and without contrast, MRI angiogram head with and without contrast
Aktuelle Erkrankungen: constipation, diarrhea
Vorgeschichte: Polyarthralgia, hemorrhoids, essential tremor, lipoma, hyperlipidemia, depression, degenerative disc disease, hypertension, Ehler's Danlos
Andere Medikamente: Albuterol, Xanax, Zoloft, metoprolol, Norco, ondansetron, Cymbalta, vitamin D 5000 international units, multivitamin, marijuana
Allergien: Morphine, Phenergan, Percocet
Vorherige Impfungen: -

VAERS 2209237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 13.10.2021
Beginn: 14.02.2022
Tage bis Beginn: 124,0
Dosis: 1
Route/Site: - / -

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

Anticoagulant therapy Aortic stenosis Atrial fibrillation Blood creatine phosphokinase increased COVID-19 Fall Magnetic resonance imaging head normal Muscular weakness Pain in extremity SARS-CoV-2 test positive Syncope Thrombolysis Transient ischaemic attack Ventilation/perfusion scan abnormal

Symptomtext

Patient up to date of COVID pfizer vaccinations who tested detected for COVID during hospital admission during routine testing after admission for a fall. No respiratory symptoms during stay. Provider discharge note below: "Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) the patient presented after unwitnessed syncopal episode at home, falling suspended by pressure placed under both arms for a few hours. R arm was weak after so came to the ED. CPK elevated significantly, improved some after gentle IVF given CHF/AS. Weakness/pain in R upper extremity improved significantly during admission. stroke pathway in ED showed CT perfusion which initially had occlusion then re-canulized during procedure, likely representing TIA with thrombolysis. MRI brain negative. Neurology saw and stated no need for aspirin. She had new onset atrial fibrillation rapid ventricular response treated with increased metoprolol and addition of digoxin. Eliquis was started after risk v benefit discussion. Syncope probably from severe aortic stenosis. Cardiology consulted, will plan on initiating outpatient TAVR planning once improved from current illness. Patient/family wished to discharge and consider proceeding with TAVR as outpatient, but wanted to go home today. covid without hypoxia."

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Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: COVID "detected" PCR on 02/14/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Silent myocardial ischemia NYHA class 1 heart failure with reduced ejection fraction (*) Hypertension Venous stasis of lower extremity Microalbuminuria Low back pain Aortic stenosis, moderate Chronic systolic heart failure (*) Stage 3 chronic kidney disease (*) Arthritis of knee Peripheral vascular disease (*) History of CVA (cerebrovascular accident) HFrEF (heart failure with reduced ejection fraction) (*) Atrial fibrillation (*) Orthostatic hypotension
Andere Medikamente: Eliquis Lipitor D3 Lanoxin Zestril Tylenol PM Toprol XL Multivitamin Fish oil
Allergien: Amoxicillin Penicillin
Vorherige Impfungen: -

VAERS 2194551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 21.02.2021
Beginn: 29.09.2021
Tage bis Beginn: 220,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 COVID-19 pneumonia Dehydration Fall Nausea Presyncope Syncope

Symptomtext

Presents for vasovagal syncope & fall from bed. Admit for sycope from nausea/dehydration in setting of COVID. Dx with COVID pneumonia x7days PTA. Tx: supportive (was already started on Prednisone while in rehab facility). DC back to rehab.

Weitere VAERSDATA-Felder

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

VAERS 2119733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 12.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Bell's palsy Blood test Facial paralysis Magnetic resonance imaging

Symptomtext

I woke and the right side of my face was paralyzed for 2 months. I was diagnosed with Bell's Palsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Blood work, normal. MRI normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Graves' disease
Andere Medikamente: Vitamin D; vitamin C
Allergien: Penicillin; sulphur; steroids'
Vorherige Impfungen: -

VAERS 2115844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: TX
Alter: -
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 12.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / AR

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

Brain natriuretic peptide normal COVID-19 Cardiac imaging procedure abnormal Chest pain Echocardiogram normal Ejection fraction decreased Electrocardiogram normal Interleukin level increased Myocarditis Pericardial effusion Pleural effusion Troponin normal Vaccination failure Vaccine breakthrough infection

Symptomtext

Per patient report he developed chest pain and effort intolerance and underwent ED evaluation at Hospital and understood he had vaccine induced myocarditis. He reported multiple cardiac imaging studies demonstrating reduced LVEF. He was treated with Entresto and had recovery of LV function. When he was seen by Dr in Jan 2022 he had normal ECG, echocardiography LVEF but an elevated ST2 level. Troponin and BNP were normal. He had no clinical signs of heart failure at that time but did have mild pleural pericardial symptoms were treated with prednisone and colchicine. On January 18, 2022 he had mild COVID-19 breakthrough infection with failure of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Per patient report multiple cardiac imaging tests in 2021 demonstrating reduced LVEF. January 2022, ST2 elevated.
Aktuelle Erkrankungen: Migraine headaches
Vorgeschichte: Migraine headaches
Andere Medikamente: Emgality Pen 120 mg/mL subcutaneous pen injector Inject 1 mL every month by sub-q route for 28 days.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2085360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 12.02.2021
Beginn: 05.01.2022
Tage bis Beginn: 327,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chills Cough Diarrhoea Exposure to SARS-CoV-2 Influenza A virus test negative Influenza B virus test Loss of consciousness Mental status changes Presyncope Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

/5/2022 Chief Complaint: Chills, mental status changes and near syncope Source of Information: Patient and Available medical record History of Present Illness: This is a 79y.o. male with past medical history of dementia, diabetes, and hypertension who presents to the ED via EMS for concern of coronavirus. Per EMS run sheet, squad found patient over toilet coughing, with 2 other family members with him who recently tested positive for Covid. Patient had not tested for Covid yet. Patient is a poor historian and states that his symptoms have been chills, as well as loss of consciousness-approximately "half a dozen times". He is unable to characterize the events leading up to his loss of consciousness or what he was doing at the time of these events. He denies any fevers, cough, sore throat, chest pain, shortness of breath, wheezing, palpitations, abdominal pain, nausea, vomiting, constipation, weakness in arms or legs. He endorses 1 month history of diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 8,0
Labordaten: Contains abnormal data Covid-19, Flu, RSV by NAA Order: 1279134471 Status: Final result Visible to patient: Yes (not seen) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 01/05/22 12:33 PM Last Resulted: 01/05/22 1:46 PM
Aktuelle Erkrankungen: ? Dementia ? Diabetes ? Diabetes mellitus, type II ? H/O prostate cancer 2008 ? High cholesterol ? Hypertension ? Hypothyroid
Vorgeschichte: ? Dementia ? Diabetes ? Diabetes mellitus, type II ? H/O prostate cancer 2008 ? High cholesterol ? Hypertension ? Hypothyroid
Andere Medikamente: alfuzosin (UROXATRAL) 10 MG PO TABLET SR 24 HR take 10 mg by mouth once daily. buPROPion (WELLBUTRIN XL) 300 MG PO TABLET SR 24 HR take 300 mg by mouth once daily. citalopram (CELEXA) 40 MG PO Tab take 40 mg by mouth once daily. donep
Allergien: none
Vorherige Impfungen: -

VAERS 2065797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 81,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 09.03.2021
Beginn: 13.01.2022
Tage bis Beginn: 310,0
Dosis: 1
Route/Site: IM / -

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

Alanine aminotransferase increased Aspartate aminotransferase increased Asthenia Atrial fibrillation Blood alkaline phosphatase normal Blood lactic acid Blood urea increased Brain natriuretic peptide increased COVID-19 Chest X-ray abnormal Condition aggravated Dizziness Electrocardiogram abnormal Hepatic enzyme increased Influenza like illness Lung infiltration Lung opacity Pulmonary oedema

Symptomtext

Pt presented to ED 1/16/22 for flu-like symptoms, worsening weakness and dizziness. - ED workup significant for fever T-max 101?, HR 148, RR 22, elevated BUN 35, elevated troponin 70 (baseline 29-31) and BNP elevated 12,916, elevated liver enzymes with alk-phos 119, AST 56 and ALT 45. Normal lactic acid 1.7 - EKG reveals atrial fibrillation with rapid ventricular response and diltiazem 20 IV x1 given in the ED.- Chest x-ray with bilateral opacities concerning for pulmonary edema versus bilateral infiltrates. - COVID-19 positive (son and DIL both positive) - COVID + 1/16/22. Received Pfizer vaccine 2/15/21 & 03/09/21. Discharged 1/21/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 5,0
Labordaten: COVID-19 PCR + 1/16/22
Aktuelle Erkrankungen: -
Vorgeschichte: chronic anemia, heart failure, CAD, dementia, hyperlipidemia, hypertension, hypothyroidism, a-fib
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2065286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 18.02.2021
Beginn: 10.10.2021
Tage bis Beginn: 234,0
Dosis: 1
Route/Site: - / LA

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

Balance disorder Blindness unilateral Cardiac monitoring normal Cerebral thrombosis Computerised tomogram head normal Computerised tomogram normal Echocardiogram Echocardiogram normal Laboratory test Magnetic resonance imaging head abnormal Ophthalmological examination Retinal artery thrombosis Vertigo Visual impairment

Symptomtext

9/18/21- Patient dev. vertigo for 2 days (1st time ever) 10/10/21 - Patient lost 1/2 of eyesight in left eye due to ARTERIAL RETINA CLOT (permanently). 10/27/21- Patient's G.P. ordered MRI/MRA of head. Diagnosis was an Acute Cerebral Thrombosis discovered in her Brain. Patient was hospitalized for 3 days subjected to numerous tests. To date there have been no lasting effects other than a slight imbalance from the acute brain thrombosis. Patient has a permanent partial loss of SIGHT IN Left EYE. Second vaccine given 3/11/21 lot # EN6205 Left Arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral thrombosis
Hospital-Tage: 3,0
Labordaten: 10/10/21 Ophthalmologist tested eyes @ office 10/27/21-10/29/21 - MRI/MRA- Blood clot in head. ECHO Heart- (Negative) CAT Scan of Carotid + Head (Negative) Babble Cardiac- (Negative) Monitor for A-Fib in Hospital (Negative) TEE-ECHO Cardiac (Negative) A-Fib @ home for 2 weeks (Negative)
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Atorvastatin, Venlafaxine, Cetirizine, Pepcid, Xanax, COQ10, Calcium+D
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1988658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 76,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.01.2021
Beginn: 28.12.2021
Tage bis Beginn: 335,0
Dosis: 2
Route/Site: IM / LA

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

Diarrhoea Dyspnoea Fatigue Syncope

Symptomtext

Hospitalized for syncope, shortness of breath, fatigue and diarrhea. On 2 L of nasal oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension and hypothyroid
Andere Medikamente: Hydrochlorothiazide, levothyroxine, metoprolol, oxybutynin, pantoprazole, vitamin B 12 1000 mcg daily
Allergien: Keflex
Vorherige Impfungen: -

VAERS 1943791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 15.03.2021
Beginn: 02.12.2021
Tage bis Beginn: 262,0
Dosis: 1
Route/Site: IM / AR

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

Asthenia Blood pressure orthostatic normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram head abnormal Computerised tomogram spine Condition aggravated Dizziness Echocardiogram normal Fall Head injury Hypophagia Musculoskeletal chest pain Nausea Respiratory failure SARS-CoV-2 test positive Skin laceration

Symptomtext

Hospitalized 12/2/2021; COVID-19 positive 12/2/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: * Primary Care Provider: MD Admission Date: 12/2/2021 Discharge Date: Dec 8, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: SAH (subarachnoid hemorrhage) [I60.9] Generalized weakness [R53.1] Syncope, unspecified syncope type [R55] COVID-19 [U07.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 79-year-old male, presents to the hospital on 12/2 after he fell at home, syncope. Patient apparently was feeling weak on Thanksgiving Day and was walking to his bathroom and fell backwards hitting his head on the bathtub. Patient had been diagnosed with COVID-19 on the day prior to fall, he started to feel lightheaded, dizzy and nauseated after urinating and then proceeded to fall. Patient had his laceration on the scalp on the left side stapled with 4 staples (which have to be removed in about a week post discharge through PCP office.) Chest x-ray showed COVID pneumonia CT C-spine without any acute pathology but CT head questioned a possible subarachnoid hemorrhage. Trauma felt that he did not needed official consultation. Syncope: This is felt to be related to his poor oral intake secondary to his struggles with ongoing COVID infection. Orthostatics were negative. Echocardiogram was unremarkable. Bilateral carotid ultrasound were also normal. Patient tolerated out of bed activity, PT/OT recommending home with physical therapy. Subarachnoid hemorrhage: This was suspected on initial CT however not seen and repeat CT. COVID-19 pneumonia: Associated with hypoxic respiratory failure. Patient was previously vaccinated. Patient will finish 10 day course of dexamethasone. He was arranged with home oxygen at the time of discharge. Patient did complain of left-sided rib pain, however her rib view chest x-ray was negative for any rib fracture. Lidocaine provided some relief. Recommended him to follow-up with PCP in 1 week to have the staples removed and also discuss further need of oxygen. Because syncope was felt to be related to generalized weakness, poor oral intake driving restriction was felt not to be needed. More over patient had negative orthostatics while at hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Generalized weakness Scalp laceration
Andere Medikamente: amLODIPine (NORVASC) 5 MG tablet cetirizine (ZYRTEC) 10 MG tablet dexamethasone (DECADRON) 6 MG tablet lidocaine (LIDODERM) 5 % patch losartan (COZAAR) 50 MG tablet Multiple Vitamins-Minerals (CERTAVITE SENIOR/ANTIOXIDANT) tablet raNITIdine
Allergien: NKA
Vorherige Impfungen: -

VAERS 1928068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 23.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: - / RA

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

Blindness unilateral Cardiac stress test Computerised tomogram head Echocardiogram Magnetic resonance imaging Retinal artery occlusion Thrombosis

Symptomtext

a total central artery occlusion of the left eye cause by a blood clot which has resulted in permanent blindness of the left eye; a total central artery occlusion of the left eye cause by a blood clot which has resulted in permanent blindness of the left eye; a total central artery occlusion of the left eye cause by a blood clot which has resulted in permanent blindness of the left eye; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 68 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 23Feb2021 09:30 (Lot number: EL9267) at the age of 68 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Hypertension" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "depression" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "osteoarthritis" (unspecified if ongoing); "sleep apnea" (unspecified if ongoing). Prior to vaccination the patient was not diagnosed with COVID-19. No known allergies. Concomitant medications included: CYMBALTA; ATIVAN; CELEBREX; DIAZIDE [GLICLAZIDE]; LIPITOR; LISI. Vaccination history included: Bnt162b2 (1st dose, lot EL3249, at 05:30 AM, in right arm), administration date: 26Jan2021, when the patient was 68 years old, for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The following information was reported: RETINAL ARTERY OCCLUSION (hospitalization, disability, medically significant, life threatening), THROMBOSIS (hospitalization, disability, medically significant, life threatening), BLINDNESS UNILATERAL (hospitalization, disability, medically significant, life threatening) all with onset 28Feb2021 21:30, outcome "recovered with sequelae" and all described as "a total central artery occlusion of the left eye cause by a blood clot which has resulted in permanent blindness of the left eye". The patient was hospitalized for retinal artery occlusion, thrombosis, blindness unilateral (hospitalization duration: 4 day(s)). The events "a total central artery occlusion of the left eye cause by a blood clot which has resulted in permanent blindness of the left eye" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures in ICU: cardiac stress test: (Feb2021) unknown results; computerised tomogram head: (Feb2021) unknown results; echocardiogram: (Feb2021) unknown results; magnetic resonance imaging: (Feb2021) unknown results. Since the vaccination the patient had not been tested for COVID-19.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine can not be excluded for the reported events of retinal artery occlusion, thrombosis, blindness unilateral. 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: Thrombosis
Hospital-Tage: 4,0
Labordaten: Test Date: 202102; Test Name: Stress test; Result Unstructured Data: Test Result:Unknown results; Test Date: 202102; Test Name: CT of brain; Result Unstructured Data: Test Result:Unknown results; Test Date: 202102; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Unknown results; Test Date: 202102; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Depression; High cholesterol; Hypertension; Osteoarthritis; Sleep apnea
Andere Medikamente: CYMBALTA; ATIVAN; CELEBREX; DIAZIDE [GLICLAZIDE]; LIPITOR; LISI
Allergien: -
Vorherige Impfungen: -

VAERS 1870919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 06.04.2021
Beginn: 03.11.2021
Tage bis Beginn: 211,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 Chest pain Computerised tomogram abdomen abnormal Computerised tomogram head normal Computerised tomogram spine Computerised tomogram thorax abnormal Constipation Culture positive Dyspnoea Echocardiogram normal Intraductal papillary mucinous neoplasm Lung opacity Magnetic resonance cholangiopancreatography Magnetic resonance imaging head normal Myocardial necrosis marker normal Neck pain Oedema peripheral

Symptomtext

Hospitalized (11.9.21); COVID-19 positive (11.3.21); Fully Vaccinated Admission Date: 11/9/2021 Discharge Date: Nov 13, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Syncope and collapse [R55] Debility [R53.81] Chest pain in adult [R07.9] COVID-19 [U07.1] BRIEF HISTORY OF PRESENTING ILLNESS: 78-year-old female with a past medical history significant for fibromyalgia who presents after suffering a syncopal event while going to the restroom at home. Upon awakening, the patient states she felt some sharp chest pain. She decided to present to the emergency department. In the emergency department the patient was found to be hemodynamically stable. Labs are obtained and remarkable for a white blood cell count of 12000. Cardiac enzymes were checked and found remained relatively flat at 27 and 28. CT of the head unenhanced shows no acute process. CT of the cervical spine showed no acute process. CT PE study showed no evidence of PE but ground-glass opacities were noted with some reactive adenopathy. CT of the abdomen pelvis with IV contrast was obtained and this showed no acute intra-abdominal process but the patient was found to have a 7 mm low attenuating anterior pancreatic lesion concerning for cyst versus neoplasm. Patient was thought to warrant admission to the hospital. The patient was found culture positive had no symptoms and did receive monoclonal antibody therapy and remained on room air throughout her hospital stay. Patient had no recurrent syncopal or presyncopal events while hospitalized. She had negative orthostatic vital sign and to evaluate for study likely posterior stroke, she did go for MRI of the head with and without contrast and this did not show any acute pathology. The etiology behind the patient's symptomatology was uncertain. She did undergo further imaging in the form of echocardiogram and this did not show any evidence of shunt or any significant valvular pathology or focal wall motion abnormalities. After being seen by PT and OT, the patient did not seem to have any requirements that would steer her toward subacute rehab facility placement, therefore she was thought to be appropriate for discharge home with outpatient physical therapy as desired. Of note, the patient did have an incidental finding of a pancreatic mass and MRCP suggested an intraductal papillary mucinous neoplasm. Recommendation based on imaging was for the patient have 1 year follow-up imaging in the form of MRCP for surveillance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: 10.12.2021 - ED - edema of both lower extremities; neck pain - LEG SWELLING (Increased bilateral lower and upper extremity swelling; neck swelling is new; increased SOB; started a month ago and has become worse; also feeling constipated) and SHORTNESS OF BREATH 11.3.21 - COVID swab - positive 11.8.21 - monoclonal antibody infusion
Vorgeschichte: Hypertension Fibromyalgia Arthritis Hyperlipidemia Ulcerative colitis, unspecified Headache Pre-procedure lab exam Recurrent UTI Gross hematuria Hypertensive urgency Speech disturbance Dysarthria COVID-19 Asthenia
Andere Medikamente: acetaminophen (TYLENOL 8 HOUR) 650 MG tablet amLODIPine (NORVASC) 5 MG tablet ANTIVERT PO atorvastatin (LIPITOR) 40 MG tablet B COMPLEX VITAMINS ER PO bisacodyl (DULCOLAX) 5 MG enteric coated tablet Calcium 500 MG TABS carBAMazepine XR (TEG
Allergien: DemerolSwelling Benadryl [Diphenhydramine]Swelling KeflexSwelling Ketek [Telithromycin] LisinoprilItching, Rash Moxifloxacin Hcl In NaclSwelling Sulfa Drugs
Vorherige Impfungen: -

VAERS 1828032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 17.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Blood test Chills Electric shock sensation Investigation Pernicious anaemia Vitamin B12 Vitamin B12 decreased

Symptomtext

Shivering electrical current /it goes throughout the patient's body all the way up to her chest. Caller reported that the patient says the feeling is around her heart.; All of the patient's body is really shivering; Patients B12 was low.; She was found to have pernicious anemia; This is a spontaneous report from a contactable consumer (patient's husband) reported his wife. A 71-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267), via an unspecified route, administrated in left arm on 17Feb2021 (at the age of 71-year-old) as dose 2, single for COVID-19 immunization at clinic. The patient's medical history included ongoing diabetes (diagnosed with diabetes a long time ago, years already, many years), ongoing fibromyalgia (diagnosed with fibromyalgia a long time ago), ongoing neuropathy (her neuropathy has been going on for years and was hand in hand with her diabetes), stroke from an unknown date in May2019 to an unknown date (she had a stroke about 2 years ago), ongoing depression and anxiety (diagnosed with depression and anxiety awhile back, years ago); ongoing really bad problems with back and (years of back problems with a lot of pain). She needs to go back and see her pain medicine doctor and neurologist to see what the next step was. It was definitely recommended for her to have surgery, but he was in a wheelchair, and they don't know how surgery will deal with her condition, ongoing acid reflux (for years). Concomitant medications included amlodipine taken for blood pressure; apixaban (ELIQUIS) taken for Blood clots after stroke; aspirin [ACETYLSALICYLIC ACID] taken for Blood clots after stroke; atorvastatin {LIPITOR (ATORVASTATIN)} taken for cholesterol (she had been on Eliquis, aspirin, Lipitor; started taking them after her stroke); cyanocobalamin (B-12) taken for vitamin B12 deficiency; duloxetine hydrochloride (CYMBALTA) taken for depression, anxiety; gabapentin taken for an unspecified indication; hydrocodone bitartrate, paracetamol (NORCO) taken for Problems with back really bad; hydrochlorothiazide, losartan potassium (LOSARTAN HCTZ) taken for an unspecified indication; metformin hydrochloride (GLUCOPHAGE) taken for an unspecified indication; omeprazole taken for acid reflux; solifenacin succinate (VESICARE) taken for Bladder control; insulin human, insulin human injection, isophane (NOVOLIN 70/30) taken for an unspecified indication; oxymetazoline hydrochloride (CLARITIN ALLERGIC) taken for allergies; the patient has been taking the over the counter sleeping aid from Costco; all were from an unknown date to ongoing (she had been on Eliquis, aspirin, Lipitor, B-12, Cymbalta, gabapentin, Norco, Losartan HCTZ, Glucophage, Omeprazole, Vesicare, Novolin 70/30, Claritin and Costco for awhile). The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9262), via an unspecified route, administrated in left arm on 27Jan2021 (at the age of 71-year-old) as dose 1, single for COVID-19 immunization. On an unknown date in Feb2021, the patient experienced shivering electrical current /it goes throughout her body all the way up to her chest. Reporter reported that she said the feeling was around her heart, all of her body was really shivering. In 2021, her B12 was low, she was found to have pernicious anemia. She was experiencing the electrical current feeling off and on. She began feeling like there was an electrical current going through her body soon after receiving the second dose of the COVID-19 vaccine but he could not say if it was a day or two or right away and that's why she thinks it might be related to the vaccine. It was stated at the end of the day it might not be related. It was reported that all of her blood work, all results were normal in exception of her B12 was low and that the patients B12 was low because she had not taken her B-12 injection for 2-3 months. She had usually administered B-12 shot but because of her reaction to the COVID-19 vaccine, the reporter was hesitant to give her the B-12 shot. It was reported that he decided to take a break from giving her the B-12 injections and then found out on a blood test that her B-12 was low. It was reported that it was probably because she had been neglected for taking injections. It was reported that they now back on schedule and he gives her injection at the beginning of the month, so she just received her Jul2021 dose of B-12. The patient underwent lab tests and procedures which included on an unknown date in 2021 blood test: normal, investigation: unknown, vitamin B12: low. As a result of Electric shock sensation, shivering patient went to emergency room visit and physician office visit. Therapeutic measures were taken as a result of patients B12 was low and she was found to have pernicious anemia. The clinical outcome of events "Patients B12 was low" and "She was found to have pernicious anemia" was unknow, while the outcome of the remaining events was not recovered at the time of reporting. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: Run tests; Result Unstructured Data: Test Result:Unknown; Test Date: 2021; Test Name: B12 test; Result Unstructured Data: Test Result: Low.
Aktuelle Erkrankungen: Acid reflux (esophageal); Anxiety depression; Back disorder; Diabetes; Fibromyalgia; Neuropathy.
Vorgeschichte: Medical History/Concurrent Conditions: Stroke.
Andere Medikamente: AMLODIPINE; ELIQUIS; ASPIRIN [ACETYLSALICYLIC ACID]; LIPITOR [ATORVASTATIN]; B-12; CYMBALTA; GABAPENTIN; NORCO; LOSARTAN HCTZ; GLUCOPHAGE FORTE; OMEPRAZOLE; VESICARE; NOVOLIN 70/30; CLARITIN ALLERGIC.
Allergien: -
Vorherige Impfungen: -

VAERS 1818688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 01.02.2021
Beginn: 18.06.2021
Tage bis Beginn: 137,0
Dosis: 2
Route/Site: SYR / LA

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

Arterial stent insertion Cavernous sinus thrombosis Headache Nausea Optic nerve disorder

Symptomtext

The symptoms was severe headache and nausea. I had a blood clot in my main artery. The neurosurgeon put in a stent. It impact the the nerve in my left eye for 3 months and now it has started to open up again. They diagnosed it as Cavernous Sinus Thrombosis. I am still in recovery from it.

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Praegender Schweregrund: Cavernous sinus thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Obese
Andere Medikamente: Revusatin 10mg
Allergien: None
Vorherige Impfungen: -

VAERS 1712911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: 16.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Diarrhoea Dizziness Electric shock sensation Paraesthesia Urticaria Headache Hypersensitivity Illness Paraesthesia oral Pruritus Rash Vaccination site urticaria

Symptomtext

her lips were "tingling"; she had one hive appear where she received her shot but it disappeared within a minute; gastrointestinal issues such as diarrhea; terrible headache; Rash; non-severe allergic reactions; Itching; really sick a few days right after; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient reported for herself that she received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL9267, NDC number: Not Provided, expiry date: Unknown) via an unspecified route of administration on 16Mar2021 (age at vaccination was 37 years) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient normally takes Zyrtec for seasonal allergies but states she did not take it before her first dose of the vaccine because patient was worried about a potential reaction. The patient states that when she received her first dose, within 25 minutes on an unspecified date in Mar2021, her lips were "tingling" but states that went away after a minute. on an unspecified date in Mar2021, the patient then reports that 30 hours later she had one hive appear where she received her shot but it disappeared within a minute. The patient then reports that 48 hours later another hive appeared on the shoulder of the same arm that she received her shot in, but states that it also went away in a minute. on an unspecified date in 2021, she also had GI issues such as diarrhea for like five days afterwards and also had a "terrible headache" but states she was more so concerned about her symptoms with the lips and the hives. The patient knows that things such as rash, itching, and hives were reported after a dose of the vaccine on an unspecified date in 2021 and were considered to be non-severe allergic reactions. The patient called the third day after the shot as she was really sick a few days right after the shot. The report was non-serious. Outcome of the event her lips were "tingling" and Vaccination site urticaria was resolved on an unspecified date in Mar2021 and outcome was unknown for remaining events. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1704164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: GA
Alter: 73,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 22.03.2021
Beginn: 12.07.2021
Tage bis Beginn: 112,0
Dosis: 2
Route/Site: IM / AR

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

Ageusia Anosmia COVID-19 Chills Cough Diarrhoea Dyspnoea Fatigue Headache Intensive care Oropharyngeal pain SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID-19 case with symptom onset 7/12/2021: chills, sore throat, cough, sob/difficulty breathing, headache, diarrhea, loss of smell/taste, tired. Hospitalized 7/19/2021-7/24/2021. ICU Admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: 07/15/2021 PCR+ COVID-19 test at pharmacy 4424; 07/19/2021 PCR+ COVID-19 test, 08/10/2021 PCR+ COVID-19 test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1700686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: IL
Alter: 76,0
Geschlecht: M
Eingang: 15.09.2021
Impfdatum: 01.09.2021
Beginn: 13.09.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram Brain natriuretic peptide increased Catheterisation cardiac normal Chest pain Computerised tomogram thorax Electrocardiogram ST segment elevation Extra dose administered Hypotension Myocarditis Pericarditis Pleuritic pain Troponin increased

Symptomtext

This was the patients third dose given at the time of his flu shot. Pt woke up on 9/13 with CP rated at 7/10. Pain was pleuritic but also found to have inf ST elevation on EKG. Ruled out for PE and given EKG and elevated troponin he was taken to the cath lab. No CAD. Trop contiued to rise overnight and he became hypotensive down t to the 70sys range. This responded to fluids and the next day he was feeling better. BNP was elevated to > 7,000 and trop HS peaked at 809 ng/L(443 to 809 to 601) The pt was treated for pericarditis and the next day he improved. Before waiting for a formal echo or MRI he left the hospital AMA. Suspected pericarditis/ Myocarditis picture

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: CT for PE Angiogram Planned for Echo and likely cardiac MRI but he left AMA. Will try to get pt evaluate for outpt follow up.
Aktuelle Erkrankungen: none but got the
Vorgeschichte: hx of Cataracts Hyperlipemia
Andere Medikamente: Simvastatin 40mg Vit B12 Also got flu shot at the same time.
Allergien: none
Vorherige Impfungen: -

VAERS 1694488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 13.09.2021
Impfdatum: 11.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Heavy menstrual bleeding Hypertension Laboratory test Lymphadenopathy Mammogram abnormal Migraine Palpitations Thrombosis Ultrasound Doppler abnormal Ultrasound breast abnormal Ultrasound scan vagina

Symptomtext

Blood clots, high blood pressure, migraines, heart palpitations, swollen lymph nodes under arm and in left breast, heavy menstrual cycles. I have to now take a blood thinner, water pill, blood pressure pill, and migraine medicine. I have to have follow ups with hematology, rheumatology, my PCP, my OB/GYN, and have been referred to another facility for further appointments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: I had a mammogram and ultrasound done to confirm swollen lymph nodes in my arm and breast. I had ultrasounds done in my leg to confirm blood clots. I have had repeated labs done. I also had a vaginal ultrasound done for the heavy bleeding.
Aktuelle Erkrankungen: None
Vorgeschichte: None prior to vaccine
Andere Medikamente: Protonix
Allergien: None
Vorherige Impfungen: -

VAERS 1670546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: WI
Alter: 65,0
Geschlecht: F
Eingang: 03.09.2021
Impfdatum: 16.02.2021
Beginn: 29.08.2021
Tage bis Beginn: 194,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Dyspnoea exertional Endotracheal intubation Fatigue Hypoxia Intensive care Lung consolidation Lung opacity Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt completed Pfizer COVID-19 vaccine series on 1/26/21 and 2/16/21. Pt was transferred to reporting hospital by medical flight transport for ICU. Pt initially admitted to outside hospital on 8/29/21 with shortness of breath, dyspnea with exertion, productive cough, fevers, fatigue and noted to be hypoxic. Symptoms started on 8/22 after a recent trip. She was intubated on 9/1 due to worsening hypoxia and fatigue. COVID PNA with ARDS. Pt is currently admitted.

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Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: -
Labordaten: COVID PCR NP swab positive 8/27/21 Chest X-ray 9/2/21 Re-demonstration of diffuse bilateral interstitial and alveolar airspace opacities with consolidation greatest within the periphery of the mid to lower right lung, consistent with Covid-19 pneumonia. The right basilar airspace disease appears mildly worse compared to the exam from earlier today but there some improved aeration of the right upper lobe.
Aktuelle Erkrankungen: asthma, obesity
Vorgeschichte: Asthma, obesity (BMI 50), HLD, Hypothyroidism, Chronic low back pain due to degenerative scoliosis of lumbar spine
Andere Medikamente: Albuterol 108, aspirin 81mg, tessalon, Calcium-Vitamin D, Coenzyme Q10, Voltaren 75mg, Levaquin 750mg, metaformin, ditropan-XL, KCL, Pravachol, zoloft, Vitamin D3
Allergien: Codeine, Niacin
Vorherige Impfungen: -

VAERS 1636760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: GA
Alter: 69,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 15.02.2021
Beginn: 17.08.2021
Tage bis Beginn: 183,0
Dosis: 2
Route/Site: SYR / UN

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

COVID-19 Chronic obstructive pulmonary disease Condition aggravated Hypoxia Intensive care Respiratory disorder

Symptomtext

The case is in the ICU for respiratory issues/hypoxia caused by Covid and exacerbated by COPD.

Weitere VAERSDATA-Felder

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

VAERS 1632337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: GA
Alter: 75,0
Geschlecht: F
Eingang: 25.08.2021
Impfdatum: 22.01.2021
Beginn: 07.02.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / LA

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

Bell's palsy Diplopia Dysphagia Ear discomfort Extraocular muscle paresis Face and mouth X-ray Facial paralysis

Symptomtext

Double vision started 5 days before 2nd dose, Dr, new prescription with prism correction, weakness in eye muscle Bells palsy 6 days after 2nd dose, Dr, 2/18.21 prescribed Methylpredisolone, left side of face drawn down and trouble swallowing, second round of meds again on 5/29/21when symptoms became strong again. Some time during this time frame my ears began stopping up and popping. I will be seeing an ENT on 8/30/21.I have also seen an allergist to try to pinpoint the cause of these symptoms. The Bells Palsy continues to pull daily but particularly when talking too long or eating something cold like ice cream.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: sinus X-rays
Aktuelle Erkrankungen: -
Vorgeschichte: Crohn's Diabetes type 2 Renauds Osteoporosis Hashimoto's Degenerative Disk Disease GERD High BP Spinal Cord Stimulator
Andere Medikamente: Ramipril 5mg 1/day Rosuvastatin 20mg 1/day Synthroid 75mcg 1/day Pantoprazole 40mg 1/day Diclophenac 50mg 2/day Multi Vitamin Centrum Silver 1/day Temazepam 15mg as needed Glipizide 5mg 2/day Prolia 2/yearly Vitamin E 400 iu 1/day Calcium
Allergien: Codeine
Vorherige Impfungen: -

VAERS 1587403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 19.08.2021
Impfdatum: 10.02.2021
Beginn: 01.06.2021
Tage bis Beginn: 111,0
Dosis: 2
Route/Site: IM / AR

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

Asthenia Blood pressure increased Cardiac imaging procedure abnormal Catheterisation cardiac normal Chest discomfort Chest scan Coronary artery occlusion Disorientation Electrocardiogram normal Feeling hot Malaise Myocarditis Nausea Pain Troponin increased Ultrasound scan normal

Symptomtext

On 6/1/2021 at about 1:00PM, I was on a bike ride with my wife. I had a lack of energy, and I had mild pressure in my chest. It wasn't painful, but it felt irregular. I didn't feel well, but I continued riding, because I didn't think my symptoms were serious. Later that evening, I went to a barbecue. I was able to socialize, but I felt mildly nauseous and achy; I thought that maybe I was coming down with something. At 1:00 on 6/2/2021, I woke up feeling hot, nauseous, and a little disoriented. I had pressure in my chest. I checked my blood pressure, which was elevated, and I decided to go to the ER hospital in city. The ER personnel noticed my troponins were elevated. They admitted me as an inpatient and ran a series of tests that included an EKG, a cardio catheter, a chest scan, and an ultrasound. They found that my heart was functionally and structurally sound. However, when they did an MRI, they discovered that the soft tissue of my heart my inflamed (myocarditis). They also discovered a 40-50% blockage in the left anterior descending artery. I was released from the hospital on 6/4/2021, and I was given atorvastatin and an aspirin. I was also advised to not physically exert myself for 2 months. On 8/1/2021, I went back to same ER for the same symptoms as before. The troponins were elevated, but not as much as the first time. I was prescribed colchicine and advised to continue resting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: I underwent an EKG, a cardiocatheter, a chest scan, and an ultrasound. Through these tests, they found my heart was structurally and functionally sound. I also underwent an MRI, through which they discovered I had myocarditis. The cardiologist in charge of my care was doctor, who can be reached at phone number.
Aktuelle Erkrankungen: None
Vorgeschichte: Gout in right foot
Andere Medikamente: Lisinopril; allopurinol; omega 3 fish oil supplement; magnesium supplement
Allergien: None
Vorherige Impfungen: -

VAERS 1573999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

schwer

Staat: CA
Alter: 82,0
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 22.01.2021
Beginn: 04.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / RA

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

Dysarthria Facial paralysis Ischaemic stroke Muscular weakness Thrombosis

Symptomtext

Ischemic stroke, two clots in left brain. Results: right hand weakness, right side of face sagging, slurred speech.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: MRI, CT Scan, x-ray
Aktuelle Erkrankungen: none
Vorgeschichte: long term lower back pain
Andere Medikamente: Telmisartan, hydrochlorothiazide, simvastatin, 81 mg aspirin
Allergien: none
Vorherige Impfungen: -

VAERS 1569061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 65,0
Geschlecht: M
Eingang: 15.08.2021
Impfdatum: 06.03.2021
Beginn: 06.08.2021
Tage bis Beginn: 153,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Fatigue Infection Intensive care SARS-CoV-2 test positive

Symptomtext

Patient required hospitalization due to breakthrough infection. He received the Pfizer vaccine (2nd dose in series) on 03/06/21. Hospitalized from 08/06/21 - 08/14/21. Below is copied from discharge summary: Patient is a 65 y/o CM with PMH significant for COPD, PAH, HTN, HLD who presented to ER on 8/6 for concerns of SOB. He (and his wife) were vaccinated for covid in Feb March 2021. He was seen by his pulm due to SOB, cough, fatigue on monday 8/2 and tested pos for covid at that time. His pulm gave him a course of oral abx and steroids and he has completed them but was not feeling any better. He checks his sats regularly at home and found a reading of 64% on 5l NC o2 so called EMS. Upon arrival to ER he required escalation to HFNC 90%/ 60 l flow and ICU was consulted due to O2 req. Patient was discharged on 08/14/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 8,0
Labordaten: SARS-COV-2, NAA, Detected 08/06/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis Hyperlipidemia Hypertension COPD PAH
Andere Medikamente: amLODIPine-benazepril (LOTREL) 10-40 MG PO Capsule Take 1 capsule by mouth daily. TAKE ONE CAPSULE BY MOUTH ONCE DAILY 7/5/18 atorvastatin (LIPITOR) 40 MG PO Tablet Take 1 tablet by mouth nightly at bedtime. 7/5/18 celecoxib (CeleBR
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1536079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 12.02.2021
Beginn: 02.08.2021
Tage bis Beginn: 171,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive Syncope

Symptomtext

Patient presented to emergency department on 8/3/2021 following a syncopal episode at home. He was experiencing shortness of breath for approximately 1 week and was found to be COVID-19 positive on 8/2/2021 prior to his presentation. During admission, he was asymptomatic for COVID-19 and was not treated for infection. He was discharged on 8/5/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: COVID-19 positive on 8/2/2021
Aktuelle Erkrankungen: None known
Vorgeschichte: Anxiety, coronary artery disease, depression, heart failure, dyslipidemia, hypertension, mitral valve stenosis, paroxysmal atrial fibrillation
Andere Medikamente: atorvastatin (LIPITOR) 80 MG tablet carbamide peroxide (DEBROX) 6.5 % otic solution furosemide (LASIX) 40 MG tablet lisinopril (PRINIVIL) 5 MG tablet metoprolol tartrate (LOPRESSOR) 50 MG tablet venlafaxine (EFFEXOR XR) 75 MG XR capsule war
Allergien: None Known
Vorherige Impfungen: -

VAERS 1065133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 02.08.2021
Impfdatum: 12.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Bell's palsy Facial paralysis

Symptomtext

A few hours later after my second vaccine 02-12-2021, my whole face drooped. On 02-11-2021 I was having a weird taste on the left side of my tongue. I went to the ER where I was diagnosed with Bell's Palsy. I made a follow up appointment with a neurologist. My symptoms of Bell's palsy only lasted three weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity
Andere Medikamente: Trazadone, Levothyroxine, Cholesterol pill
Allergien: Novocain ( I get panic attackes)
Vorherige Impfungen: -

VAERS 1465394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: NV
Alter: 57,0
Geschlecht: F
Eingang: 12.07.2021
Impfdatum: 20.01.2021
Beginn: 19.03.2021
Tage bis Beginn: 58,0
Dosis: 2
Route/Site: IM / RA

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

Blood test Cognitive disorder Guillain-Barre syndrome Magnetic resonance imaging Memory impairment

Symptomtext

Guillen Barre, Short term cognitive memory issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 12,0
Labordaten: Blood, MRI, Neurology consults
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Atorvastatin 20 mg / Folic Acid 1mg / Levothyroxine 0.175 mg
Allergien: none
Vorherige Impfungen: -

VAERS 1461916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El9267

schwer

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 10.07.2021
Impfdatum: 22.02.2021
Beginn: 20.04.2021
Tage bis Beginn: 57,0
Dosis: 1
Route/Site: SYR / LA

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

Anticoagulant therapy Asthenia Deep vein thrombosis Fatigue Laboratory test Pyrexia

Symptomtext

developed 2 DVT clots in left groin taken to Er and put on Heperin drip for 3 days No previous history of blood clot Also developed 101? Fever and intense fatigue and weaknesssee

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 4,0
Labordaten: available in online portal at hospital
Aktuelle Erkrankungen: Bakers cyst, arthritis
Vorgeschichte: heart block/pacemaker , her 2 breast cancer in remission, ibs, arthritis
Andere Medikamente: carvedilol, prilosec, losartin, lorazapam, B12, vit D, Lexapro, melatonin, mlodapine, magnesium, acetapheninam, Flonase, flexibility, loratidinebakers c
Allergien: -
Vorherige Impfungen: -

VAERS 1458353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 08.07.2021
Impfdatum: 08.07.2021
Beginn: 08.07.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Dysstasia Fibrin D dimer increased Gait disturbance Intervertebral disc protrusion Loss of consciousness Magnetic resonance imaging Pain Pain in extremity Ultrasound Doppler normal X-ray

Symptomtext

Woke up on May 24, 2021 at around 445 am in excruciating pain very localized on my left thigh. The pain was o intense I could walk sit or stand. Was take to the hospital by ambulance where I passed out from the numerous times. I explained the pain as burning as if my thigh was about to explode. They gave me lots of different medicine a scan where we were told it was my L5 or potential constipation. A few days passed and I went to several stat cares with no answers. About 7 days later I went to the Care Clinic where they tested me for my Fdimer and it proved elevated so they did a dopplor test with no visible clots. I was sent home with more medicine and a few days later ended up in the emergency room at Spohn South where I kept passing out from the pain. After some more x-rays and exams we were told that I had my l2 L3 bulging and that I need to see a spine specialist. Sent me home with more medicine. I was told to called Dr. at The bone and Joint office and Dr. saw me and gave me steroids and more pain meds. 2 weeks later no change I was barely able to walk and I finally got in to see the right Dr. which was Dr. he evaluated me ran his own exam and MRI and after 2 weeks he along with other s doctor determined it was a side affect due to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estradiol 0.5 daily
Allergien: CODIEN
Vorherige Impfungen: -

VAERS 1360491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 9267

schwer

Staat: VA
Alter: 77,0
Geschlecht: M
Eingang: 03.07.2021
Impfdatum: 11.02.2021
Beginn: 25.03.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal distension Asthenia COVID-19 Chest pain Costochondritis Dyspnoea SARS-CoV-2 test Inflammatory marker increased Painful respiration Pericardial effusion Pleurisy Pneumonia Presyncope Pyrexia Weight increased Wheezing

Symptomtext

Visit summaries/notes attached on below visits 3/25/2021 ER with chest pain, worse with deep breath; diagnosis costochondritis 4/14/2021 ER with chest pain, painful breathing, wheezing, weakness, fever (101.3 rectal). 4 pound weight gain overnight. Differential diagnoses costochondritis, pleurisy, pneumonia, COVID-19; admitted to hospital.Discharged 4/16. 4/25/2021 admitted to hospital; chest pain, shortness of breath, weakness, bloat, inflammation markers high, mild pericardial effusion, near syncope.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 5,0
Labordaten: see attached
Aktuelle Erkrankungen: none
Vorgeschichte: Parkinson's Disease; high blood pressure (controlled); high cholesterol(controlled); prostate cancer(recent PSA 0.0)
Andere Medikamente: see attached
Allergien: Penicillin, Bactrim
Vorherige Impfungen: -

VAERS 1360491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: VA
Alter: 77,0
Geschlecht: M
Eingang: 03.07.2021
Impfdatum: 11.02.2021
Beginn: 25.03.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: - / LA

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

Abdominal distension Asthenia COVID-19 Chest pain Costochondritis Dyspnoea SARS-CoV-2 test Inflammatory marker increased Painful respiration Pericardial effusion Pleurisy Pneumonia Presyncope Pyrexia Weight increased Wheezing

Symptomtext

Visit summaries/notes attached on below visits 3/25/2021 ER with chest pain, worse with deep breath; diagnosis costochondritis 4/14/2021 ER with chest pain, painful breathing, wheezing, weakness, fever (101.3 rectal). 4 pound weight gain overnight. Differential diagnoses costochondritis, pleurisy, pneumonia, COVID-19; admitted to hospital.Discharged 4/16. 4/25/2021 admitted to hospital; chest pain, shortness of breath, weakness, bloat, inflammation markers high, mild pericardial effusion, near syncope.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 5,0
Labordaten: see attached
Aktuelle Erkrankungen: none
Vorgeschichte: Parkinson's Disease; high blood pressure (controlled); high cholesterol(controlled); prostate cancer(recent PSA 0.0)
Andere Medikamente: see attached
Allergien: Penicillin, Bactrim
Vorherige Impfungen: -

VAERS 1095603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 20.06.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Blood pressure orthostatic Dizziness Dysstasia Echocardiogram Electrocardiogram Feeling abnormal Feeling hot Palpitations Electrocardiogram ambulatory Feeling of body temperature change Gait disturbance Heart rate increased Impaired driving ability Laboratory test Presyncope Tachycardia Tremor Vertigo

Symptomtext

4 min. after injection - dizziness, presyncope, tachycardia/heart was pounding out of chest , waves of being hot followed by waves of being freezing cold, tremors/ uncontrolled shakiness. This would come on, then pass, then come on again for several hours after vaccine. Was monitored by EMS for 2 ish hours after vaccine. Unable to drive home. The constant immediate reaction slowly subsided but continue to have episodes of this exact reaction - and they continue to this date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Primary care office visit - ordered lab work and 30 days cardiac holter monitor Emergency room visit x 2, due to episodes continuing and worsening tachycardia - labs, orthostatic blood pressure, heart rate monitoring, EKG. Questionable POTS? Given BP medication. Second ER visit - labs, echo done, resting HR was extremely high / tachycardia - given beta blocker 25 mg 2x a day. At this point i couldn?t stand or walk without being tachycardic. Electrical cardiology appointment - followed up with cardiologist and symptoms weren?t improving - upped beta blocker dose to 50mg 2x a day. Tachycardia slowly subsided due to beta blocker. Currently still on beta blocker, lowered dose 25mg 2 x a day to keep from being tachycardic. Reccurent dizziness has occurred and seeks Chiropractic care and exploring acupuncture to help relieve vertigo.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1407166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: GA
Alter: 84,0
Geschlecht: M
Eingang: 17.06.2021
Impfdatum: 25.02.2021
Beginn: 19.04.2021
Tage bis Beginn: 53,0
Dosis: 2
Route/Site: SYR / UN

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

Acute kidney injury Amnesia Asthenia COVID-19 Endotracheal intubation Hypoxia Intensive care Metabolic acidosis Multiple organ dysfunction syndrome Pyrexia SARS-CoV-2 test positive Shock Urinary tract infection

Symptomtext

84 y/o M PMHx of non-hodgkin's lymphoma, adenocarcinoma of the colon (1996) and type 2 DM, presented ED 4/17 with complaints of weakness x 1 week. He reported some Memory loss but denied fever/chills, coughing, dyspnea or fever. Admitted for UTI. On 4/19 patient developed fever, tested positive COVID, started on decadron and remdesivir, pulmonology consulted. 5/1 increasing O2 requirements, prompting transfer to ICU. Mental status improved. 5/3: Fluctuant FiO2 requirements. Transferred to the floor and back to the ICU for hypoxemia. Intubated 5/7. Pt with worsening AKI, metabolic acidosis and shock in the evening of 5/8. Daughter on 5/9 and pt made a DNR. Worsening shock, metabolic acidosis and MODS. Decision to dc to hospice

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 24,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: 84 y/o M PMHx of non-hodgkin's lymphoma, adenocarcinoma of the colon (1996) and type 2 DM, presented ED 4/17 with complaints of weakness x 1 week. He reported some Memory loss but denied fever/chills, coughing, dyspnea or fever. Admitted for UTI. On 4/19 patient developed fever, tested positive COVID, started on decadron and remdesivir, pulmonology consulted. 5/1 increasing O2 requirements, prompting transfer to ICU. Mental status improved. 5/3: Fluctuant FiO2 requirements. Transferred to the floor and back to the ICU for hypoxemia. Intubated 5/7. Pt with worsening AKI, metabolic acidosis and shock in the evening of 5/8. Daughter on 5/9 and pt made a DNR. Worsening shock, metabolic acidosis and MODS. Decision to dc to hospice
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1390740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: GA
Alter: 72,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 16.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction Dizziness Feeling abnormal Investigation Pain

Symptomtext

she was having an anaphylactic reaction; feeling so bad; It was pained all over; she got a woozy after the vaccine; This is a spontaneous report from a contactable consumer (patient). A 72-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267), via an unspecified route of administration, administered in Arm Left on 16Feb2021 11:30 as 1ST DOSE, SINGLE DOSE for covid-19 immunisation. Medical history included ongoing diabetes, ongoing blood pressure high, coronary artery disease, spinal stenosis, arthritis, Penicillin allergy (doesn't have the product that was back in 1969, Drug hypersensitivity), bee sting, shrimp, ongoing cholesterol, ongoing hypertension. Concomitant medication included insulin aspart (NOVOLOG) taken for diabetes; insulin detemir (LEVEMIR) taken for diabetes, candesartan taken for hypertension; nifedipine (PROCARDIA [NIFEDIPINE]) taken for hypertension; carvedilol taken for hypertension; rosuvastatin calcium (CRESTOR) taken for cholesterol; aspirin [acetylsalicylic acid] (ASPIRIN [ACETYLSALICYLIC ACID]); vitamin c [ascorbic acid] (VITAMIN C [ASCORBIC ACID]); and colecalciferol (VITAMIN D [COLECALCIFEROL]). The patient previously took epipen for stung by a bee (stuck that EpiPen in her thigh). The patient experienced she was having an anaphylactic reaction, feeling so bad on 17Feb2021, she got a woozy after the vaccine and it was pained all over on 16Feb2021. Patient stated she received the first dose of the vaccine on 16Feb2021. Caller states she had a severe reaction so dramatic that she has decided that she is not going to take the second dose of the vaccine. When she went in they asked if she had an allergy. She said bee sting, Penicillin, and shrimp. They responded and told her if she had a reaction they had an EpiPen there for her. She has not had an EpiPen injection since 1987. She did not remember what it was like. Back in 1987, she got stung by a bee. She felt so bad. She felt that if she closed her eyes she would die. Her daughter called 911 and they came, but they did not have the EpiPen. Her son called her family doctor who came over with the EpiPen. He said she was having a severe reaction to the bee sting. He saved her life. When she went in on Tuesday she got a woozy after the vaccine. It was not near as bad as what she experienced in 1987. She stayed there 45 minutes and they brought her water and a bagel. She drank the water but did not eat the bagel. She went home and was fine all night. The next morning about 8AM, she started feeling so bad. She felt worse than she did in 1987. She felt like she was going to die if she closed her eye. It did not dawn on her that she was having an anaphylactic reaction. Her friend sent her a text that had four versions of a scripture. The scripture said has different plans for her. She read that to herself and started to feel better. She attributed it to saving her life. She told her cardiologist she is 72 years old and has underlying conditions and she does not want to go through that again. In 1987 the doctor came in the house and the fireman was already there. The doctor came over to her and he just stuck that EpiPen in her thigh. Everything in the body went to the top of her head. She felt like if she could open her head she could let the pain and everything out. Feeling so bad: It lasted for about 15 to 30 minutes. Then caller clarified her friend texted her at 9:26AM, so it may have lasted an hour to an hour and a half. She ached all over. Her body felt dead. It was pained all over. Everything was trapped inside her head. She went to the cardiologist and all her numbers were fine. She told him she was not going to take another shot. She is going to go back for a stress test because she has been diagnosed with coronary artery disease. She has an appointment with her primary care doctor, on 10Mar2021 and will see what he has to say. Time the Vaccination Was Given: her appointment was at 11:30AM. History of all previous immunization with the Pfizer vaccine considered as suspect was none. Additional Vaccines Administered on Same Date of the Pfizer Suspect was none. The adverse events require a visit to Physician Office, She felt better and decided not to take the other shot. She ran it by her doctors. She has an appointment. She has not cancelled it yet. She wants to find out what the ramifications would be if she did not take the second one. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Adverse events following prior vaccinations: She does not have a spleen. She has had her flu shot. She has not had the shingles vaccination. It is not time for Pneumovax. She keeps up and follows her doctors. The patient underwent lab tests and procedures which included numbers: unknown results. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Name: numbers; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: Blood cholesterol abnormal; Blood pressure high; Diabetes; Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Bee sting; Coronary artery disease; Penicillin allergy (doesn't have the product that was back in 1969,Drug hypersensitivity); Seafood allergy; Spinal stenosis
Andere Medikamente: NOVOLOG; LEVEMIR; CANDESARTAN; PROCARDIA [NIFEDIPINE]; CARVEDILOL; CRESTOR; ASPIRIN [ACETYLSALICYLIC ACID]; VITAMIN C [ASCORBIC ACID]; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1308683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 10.02.2021
Beginn: 08.04.2021
Tage bis Beginn: 57,0
Dosis: 2
Route/Site: SYR / LA

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

Bell's palsy

Symptomtext

Right side facial Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: ER visit to main hospital on 4/8/21. No tests were performed; the attending physician said I had a "textbook case of Bell's Palsy ".
Aktuelle Erkrankungen: N/a
Vorgeschichte: Asthma, kidney stones
Andere Medikamente: Xanax, Wellbutrin, Lexapro, Buspar, Zyrtec, Advil, prenatal vitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1296134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 07.05.2021
Impfdatum: 09.02.2021
Beginn: 30.03.2021
Tage bis Beginn: 49,0
Dosis: 1
Route/Site: SYR / LA

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

Angiogram Ischaemic stroke Magnetic resonance imaging

Symptomtext

Isochemic Stroke- Plavix, Lipitor, PT, OT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: -
Labordaten: MRI, CTA
Aktuelle Erkrankungen: none
Vorgeschichte: Gerd
Andere Medikamente: Myrbetriq 50mg, Omeprozole 40 mg, Lexapro 10 mg, multi vitamin, ASA 81 mg, Zyrtek -OTC
Allergien: none known
Vorherige Impfungen: -

VAERS 1288299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 67,0
Geschlecht: M
Eingang: 05.05.2021
Impfdatum: 15.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Blood test Cardiac stress test Computerised tomogram Dizziness Echocardiogram Electrocardiogram Investigation Magnetic resonance imaging Presyncope Vertigo

Symptomtext

he had a very lightheaded episode that was much more vertigo-like where things were spinning; I had almost a very light headache where I almost fainted; he had a very lightheaded episode that was much more vertigo-like where things were spinning; he had a very lightheaded episode that was much more vertigo-like where things were spinning; This is a spontaneous report from a contactable consumer. This 67-year-old male consumer reported that: Patient characteristics - Weight (kg): 95.25 Height (cm): 183 Sex: MALE Reaction(s)/Event(s) Reaction/event as reported by primary source- Very, very lightheaded episode where he almost passed out Term highlighted by the reporter: YES Date of start of reaction/event: Feb2021 Outcome of reaction/event at the time of last observation: UNKNOWN Reaction(s)/Event(s) Reaction/event as reported by primary source: Very lightheaded episode that was much more vertigo-like where things were spinning Outcome of reaction/event at the time of last observation: RECOVERING/RESOLVING Results of tests and procedures for investigation of the patient Date: Feb2021 Test: EKGs Result: Normal More information available: NO Results of tests and procedures for investigation of the patient Date: Feb2021 Test: MRIs of his head Result: Normal More information available: NO Results of tests and procedures for investigation of the patient Date: Feb2021 Test: echocardiograms of his heart Result: Normal More information available: NO Results of tests and procedures for investigation of the patient Date: 17Mar2021 Test: VNG test- Videonystagmography Result - Unknown, not resulted yet More information available: NO Results of tests and procedures for investigation of the patient Date: 10Mar2021 Test: Nuclear stress test Result: Normal More information available: NO Results of tests and procedures for investigation of the patient Date: 10Mar2021 Test: Exercise stress test Result: Normal More information available: NO Results of tests and procedures for investigation of the patient Date: Feb2021 Test: Blood work Result: Normal More information available: NO Drug(s) Information Characterization of drug role: (SUSPECT) Proprietary medicinal product name: Pfizer-BioNTech COVID-19 Vaccine Batch/lot number: EL9263 Dosage text: Unknown strength/volume/dose injection to left arm shoulder before 12:00 Pharmaceutical form (Dosage form): Injection Indication for use in the case: Vaccination) Date of start of drug: (26Jan2021 Date of last administration: 15Feb2021 Drug(s) Information Characterization of drug role - CONCOMITANT Proprietary medicinal product name: Amlodipine Dosage text: 5mg taken daily Indication for use in the case: Blood pressure Drug(s) Information Characterization of drug role: CONCOMITANT Proprietary medicinal product name: Esomeprazole Dosage text: 40mg taken daily Drug(s) Information Characterization of drug role: CONCOMITANT Proprietary medicinal product name: Centrum Silver for people over 50 years Dosage text: Once daily Narrative case summary and further information Submitted by Call Centre 1 Ref: #; ININ:# Selected Report Type: Initial Is report related to a study or programme? No Is the patient also the reporter? Yes Reporter type: Consumer or other non health professional Specify Consumer or other non health professional: Patient Dates for Very, very lightheaded episode where he almost passed out: (From: Feb2021 To: Unknown) Dates when patient was in hospital for Very, very lightheaded episode where he almost passed out: Feb2021 to Feb2021 Dates for Very lightheaded episode that was much more vertigo-like where things were spinning: (From: Feb2021 To: Ongoing) Is Pfizer-BioNTech COVID-19 Vaccine a Pfizer product? Yes Pfizer-BioNTech COVID-19 Vaccine manufacturer: Pfizer-BioNTech Dates for Pfizer-BioNTech COVID-19 Vaccine: (Start: 26Jan2021 Stop: 15Feb2021) NDC number of Pfizer-BioNTech COVID-19 Vaccine: Unknown Expiry Date of Pfizer-BioNTech COVID-19 Vaccine: Unknown Pfizer-BioNTech COVID-19 Vaccine: Dosage previously discontinued/treatment completed Other Products: Yes Dates for Concomitant Products Amlodipine: (Start: Unspecified Stop: Ongoing) Additional Information for Concomitant Products Amlodipine: Taken for years. Dates for Concomitant Products Esomeprazole: (Start: Unknown Stop: Ongoing) Additional Information for Concomitant Products Esomeprazole: Taken for years. Why was the patient taking Concomitant Products Esomeprazole (Verbatim): Acid reflux Dates for Concomitant Products Centrum Silver for people over 50 years: (Start: Unknown Stop: Ongoing) Additional Information for Concomitant Products Centrum Silver for people over 50 years: Taken for years. Why was the patient taking Concomitant Products Centrum Silver for people over 50 years (Verbatim): Multivitamin Patient History: No Investigation Assessment: Yes Additional Context: This consumer is the patient who has been administered both first and second doses of Pfizer-BioNTech COVID-19 Vaccines. About 8-11 days after first dose of Pfizer-BioNTech COVID-19 Vaccine he had a very, very lightheaded episode where he almost passed out. About 8-11 days after second dose of Pfizer-BioNTech COVID-19 Vaccine he had a very lightheaded episode that was much more vertigo-like where things were spinning. He clarified he thinks one event was like 8 days and the other was like 10 days after the vaccine doses were administered, but is not sure, so left it as about 8-11 days. Consumer is not sure if the events are Pfizer-BioNTech COVID-19 Vaccine related, but they never happened to him before those doses were administered. He does not know if this is vaccine related or just coincidence that they popped up at the same time as the vaccine doses. He does not know if events could be age related, the medical community can't figure it out so he is trying to get information on if events could be related to the vaccines. Patient: Age at onset: Over the age of 65 years. Reporter: Address: Unknown. Primary: Further address details/Email: Unknown. Very, very lightheaded episode where he almost passed out: Onset about 8-11 days after first dose was administered, maybe 09Feb2021 or 10Feb2021. He went to the emergency room on the date of event onset and was admitted to hospital from about 13:00 that day, overnight and discharged about 17:00-18:00 the following day. While in hospital he had EKGs of his head-verified this information with caller repeatedly; MRIs of his head; CTs of his head; and echocardiograms of his heart. All of those tests came back ok, nothing abnormal on results. They recommended he have a stress test done which was not performed until after the second reported event following second dose of Pfizer-BioNTech COVID-19 Vaccine. Very lightheaded episode that was much more vertigo-like where things were spinning: Onset was about 8-11 days after second dose of Pfizer-BioNTech COVID-19 Vaccine was administered. He has never had vertigo in his life before event. He went back to the emergency room on date of onset of this event, but was not admitted to the hospital at that time; was only in the emergency room about 5-6 hours. While in the emergency room he had CT scans of his head, MRIs of his head and EKGs and everything looks good, nothing abnormal on results. Outcome: He still has ongoing very lightheaded episodes for a good part of the day. Those episodes usually last about 30 minutes and occur multiple times daily but are not really severe like the 2 initial events were following the first dose and then the second dose. Pfizer-BioNTech COVID-19 Vaccine: First dose: 26Jan2021 Lot: EL9263 NDC/Expiry: Unknown, this is not on CDC vaccine record card. Dose: Unknown strength/volume/dose injection to left arm shoulder before 12:00 Second dose: 15Feb2021 Lot: EL9267 NDC/Expiry: Unknown, this is not on CDC vaccine record card. Dose: Unknown strength/volume/dose injection to left arm shoulder before 12:00 - verified with reporter that details were same for both first and second doses. This completed his prescribed therapy. Regarding concomitant products and other medical conditions caller reported he really had no issues going on prior to onset of these events. Regarding other testing/investigations done relative to these events: He had a nuclear stress test and exercise stress test, both performed on 10Mar2021 he believes and results of those tests were they both came back good, family doctor emailed him the results which were normal. He has gone to the ENT-ear, nose and throat doctor where he had a balance test done which he referred to also as a VNG test-Videonystagmography done on 17Mar2021. He will get results of balance test on Wednesday, 24Mar2021. He had blood work done the first time he was in the emergency room when he was admitted to the hospital in Feb2021; they took his blood 3-4 times while he was there overnight and blood work results all came back normal. He is not sure what they were testing for, but thinks they were looking for stroke type things because event almost made him pass out. They did not draw more blood the second emergency room visit. Follow-up (23Mar2021): This is a follow-up spontaneous report from a contactable consumer. This consumer reported that: Reaction(s)/Event(s) MedDRA version for reaction/event term LLT - N/A Reaction/event in MedDRA terminology (LLT) - Medical Information Potential AE Drug(s) Information Characterization of drug Role: 1 (SUSPECT) Proprietary medicinal product name : PFIZER-BIONTECH COVID-19 VACCINE Active Substance Information :Active Drug substance names PFIZER-BIONTECH COVID-19 VACCINE Narrative case summary and further information: Originating AE Request: REQ-# Attachments: 1 Contact HCP: N/A Patient Age: 67 Reporter Subtype: Patient PQC Present: No AE Present: Yes PQC Details: Request Name: REQ-# Product:PFIZER-BIONTECH COVID-19 VACCINE Question: AUTO-CALLBACK REQUEST 23Mar2021 10:06AM Caller received both doses of the Pfizer-BioNtech Covid-19 vaccine (1st dose 26Jan2021, 2nd dose 15Feb2021). About ten days after the first dose he had a very lightheaded episode and he almostfainted, he went to ER and had an MRI of his head, a CT scan, a CT scan with contrast and also an echocardiogram, they were relating this to a strokelike symptom however the results were normal, also his blood test results were fine. He went to his HCP and he was schedules to get a nuclear stress test and an exercise stress test, his results came back normal; before this tests he received the second dose on 15Feb2021 and 10 days later he had again a very bad episode in his house he had a lot of vertigo, he felt the walls were moving so he went back to ER and had another EKG and CT scan, his heart was ok, so they suspected it was vertigo. He has daily episodes that las a few minutes were he feels lightheaded. He went to an otolaryngologist ("ear and nose doctor") to see if this was vertigo and had a balance test done. Caller states he had never this symptoms before, his vaccination card has the lot number for both doses, he hasn't changed his medications or habits and it's odd that this happened 9-10 days after both doses of the vaccine. He would like to know if this has been reported before as a side effect related to the vaccine. Caller states that he already called Safety twice, report #. Potential duplicate E-transmitting to DSU. Response:Spoke from attached documents. Referred caller to his HCP. Request Name: REQ-# Product:PFIZER-BIONTECH COVID-19 VACCINE Question: Caller received both doses of the Pfizer-BioNtech Covid-19 vaccine (1st dose 26Jan2021, 2nd dose 15Feb2021). About ten days after the first dose he had a very lightheaded episode and he almost fainted, he went to ER and had an MRI of his head, a CT scan, a CT scan with contrast and also an echocardiogram, they were relating this to a strokelike symptom however the results were normal, also his blood test results were fine. He went to his HCP and he was schedules to get a nuclear stress test and an exercise stress test, his results came back normal; before this tests he received the second dose on 15Feb2021 and 10 days later he had again a very bad episode in his house he had a lot of vertigo, he felt the walls were moving so he went back to ER and had another EKG and CT scan, his heart was ok, so they suspected it was vertigo. He has daily episodes that las a few minutes were he feels lightheaded. He went to an otolaryngologist ("ear and nose doctor") to see if this was vertigo and had a balance test done. Caller states he had never this symptoms before, his vaccination card has the lot number for both doses, he hasn't changed his medications or habits and it's odd that this happened 9-10 days after both doses of the vaccine. He wanted to know if his information will help somebody else who may experience the same symptoms, and is his information could be useful for Pfizer. Follow-up (23Mar2021): This is a follow-up spontaneous report from a contactable consumer. This consumer reported that: Patient Details Sex - Male Height - 183 cm Or 6 feet Weight -95.25 kg Or 210 pounds Is the patient also the reporter? Yes Age - 67 Years Reporter Details Reporter type: Consumer or other non health professional Primary / Prescribing Healthcare Professional Info (the) Event Details I have been having some strange things; it's symptom like I never had before I had almost a very light headache where I almost fainted It might be stroke like symptom I continued to have some light headed symptoms but nothing real bad; continued to have symptoms which was not normal for me I had another episode; this was much more vertigo like or the room is spinning and the walk and things are moving Products Suspect products: Covid Vaccine Is this a Pfizer product? Yes NDC number: Unknown UPC number: Unknown Lot Number: EL9267 Expiry date: Unknown History Concomitant Products Other Products Yes Omeprazole Indication - Acid reflux Multivitamin Amlodipine Dosage 5 MG Indication Blood pressure Additional Context: Consumer stated, "I have been having some symptoms but I did call into one of your number yesterday and they told me call back and try to get into you but they did gave me some case number in case help you, they did an open internet case# and I will give you that number if you like it. It's # (Hence follow-up was checked). Well I have been having some strange things that I don't know if its Covid shot related but it's symptom like I never had before. After I had received the first shot, I had almost a very light headache where I almost fainted. We went to ER, they were sort of testing, it might be stroke like symptom and they did a MRI of my brain and they did CT scan of my brain and CT scan contrast. They did micro cardiogram, some EKGs and work. All of those come back normal. So I spent the night in hospital, they sent me the next day. I continued to have some light headed symptoms but nothing real bad but continued to have symptoms which was not normal for me. After I had my shot about 10 days after the second shot, I had another episode. This was much more vertigo like or the room is spinning and the walk and things are moving. I did go back to ER again just in case there was something going on. They tested again another CT scan and EKG and everything looked normal and they said it sounded like a vertigo related. I told him I had shot about 10 days after each shot, the symptoms hit me. Because of the first episode my family doctor ordered some other testing done, and they did stress test of my heart, a nuclear stress test and an exercise stress test of my heart and both came back normal. But I am continuing to have the light headed, the episodes just about daily. Sometimes they last for 30 minutes or more, multiple times a day. Sometimes I have a good day but I have those light headed episodes and I never had it before I got the shot. I am also going ENT- ear, nose and throat doctor to check on vertigo stuff and they did some testing last week and I am supposed to get the result tomorrow on what they found about vertigo test but I never had vertigo or light headed or anything before the shot. So I don't know if anybody else is reporting this but I had 2 sorts of severe episodes both of them 10ish days after each shot and I am continuing to have light headed episodes but not severe as those 2 but I had light headed dizzy episodes daily, since the Covid vaccine. I want to report it, so you guys have a report file and other people reporting it. I guess I sort of want to know if you guys were having any other report or something like this. So that I know it might be related to the shot. I am still working with my ENT and I tried to figure out if it's vertigo. If it's not vertigo then they have really run all sorts of test and if it's not vertigo we don't know if Covid shot triggered the vertigo or not. Let me know, we don't know. So they have ran 30,000 dollar test on me and so far all my tests are coming back normal." Consumer was informed about the role of Pfizer Drug Safety and Pfizer Medical Information. Consumer was provided with the contact# for Pfizer Medical Information as # and requested to dial the Option 3 and informed about timings as Monday to Sunday from 8 am to 8 pm EST. Consumer stated, "I already did, and that's what I just dialed. I just dialed that number and option no. 3, I just dialed. That's the no. I dialed that's #and pressed option number 3. Can you forward this call to that department?" Call could not be transferred because of some technical issue. When probed for exact date of AE, "Consumer stated, hang up one second. Let me pull my card out. I think it's all I that other file that I gave but I'll give it you again. I received my first shot on January 27 of this year and I had the first episode February 10th, then I received my second shot on February 25th of this year and I believe it was march 4th, I think when I had those episodes. Those are the 2 episodes. I had smaller episodes daily but they were two bad episodes." When probed for Physician's details, Consumer stated, "It was distributed from a count location." When probed for LOT#, Consumer stated, "Hang up one second. I haven't told you one thing, my second shot was February 15 not 25. I was looking at my visa card. My first shot was EL9263 and my second shot was EL9267." Expiration date of vaccine: Consumer stated, "I doesn't have that." Dose of vaccine: Consumer stated, "It did not write that on card." When probed for anatomical site of vaccine administration, Consumer stated, "Left arm shoulder." Lab Test: Consumer stated, "Every year I go and get my yearly test in which they had my blood work and my glucose levels are always good, cholesterol level as always good. All my other tests come back as normal." (Further not clarified hence not captured in tab) Treatment: Consumer stated, "The hospital was, the emergency room gave me something for dizziness that I am no longer taking. They gave me something for dizziness when I was there but I am no longer taking it. So I am really taking nothing. This time I am working with ENT i.e. ear, nose and throat doctor, they are doing vertigo type testing but they got nothing, the results are supposed to be back tomorrow. I don't know what test they are going to show, if they do show vertigo there will be some treatments to help me. But we don't know what brought these episodes on, other than timing wise it was during the Covid shot. And I never had anything like that and I am not blaming it on the Covid shot. That was the only thing changed in my lifestyle. There might be a possibility, because that's the only thing changed, my medication has not changed, diet doesn't changed. Nothing is changed other than I got Covid." Consumer stated, "Can you give me report#." Reportum# was provided as # #Is there a product complaint to report?No Is there a medical information request?Yes Please describe the medical information request Consumer stated, "I have been having some symptoms but I did call into one of your number yesterday and they told me call back and try to get into you but they did gave me some case number in case help you, they did an open internet case# and I will give you that number if you like it. It's 4NW3L5MR (Hence follow-up was checked). Well I have been having some strange things that I don't know if its Covid shot related but it's symptom like I never had before. After I had received the first shot, I had almost a very light headed where I almost fainted. We went to ER, they were sort of testing, it might be stroke like symptom and they did a MRI of my brain and they did CT scan of my brain and CT scan contrast. They did micro cardiogram, some EKGs and work. All of those come back normal. So I spent the night in hospital, they sent me the next day. I continued to have some light headed symptoms but nothing real bad but continued to have symptoms which was not normal for me. After I had my shot about 10 days after the second shot, I had another episode. This was much more vertigo like or the room is spinning and the walk and things are moving. I did go back to ER again just in case there was something going on. They tested again another CT scan and EKG and everything looked normal and they said it sounded like a vertigo related." Consumer was informed about the role of Pfizer Drug Safety and Pfizer Medical Information. Consumer was provided with the contact# for Pfizer Medical Information as #and requested to dial the Option 3 and informed about timings as Monday to Sunday from 8 am to 8 pm EST. Consumer stated, "I already did, and that's what I just dialed. I just dialed that number and option no. 3, I just dialed. That's the no. I dialed that's # and pressed option number 3. Can you forward this call to that department?" Call could not be transferred because of some technical issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 20210310; Test Name: Nuclear stress test; Result Unstructured Data: Test Result:Normal; Test Date: 202102; Test Name: echocardiograms of his heart; Result Unstructured Data: Test Result:Normal; Test Date: 202102; Test Name: EKGs; Result Unstructured Data: Test Result:Normal; Test Date: 202102; Test Name: EKGs; Result Unstructured Data: Test Result:Normal; Test Date: 20210317; Test Name: VNG test-Videonystagmography; Result Unstructured Data: Test Result:Unknown, not resulted yet; Test Date: 202102; Test Name: MRIs of his head; Result Unstructured Data: Test Result:Normal; Test Date: 202102; Test Name: MRIs of his head; Result Unstructured Data: Test Result:Normal; Test Name: CT scan of my brain; Result Unstructured Data: Test Result:unknown result; Test Date: 202102; Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Test Date: 20210310; Test Name: Exercise stress test; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (esophageal); Blood pressure abnormal
Andere Medikamente: AMLODIPINE; ESOMEPRAZOLE; CENTRUM SILVER ADULTS 50+; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1219410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 9267

schwer

Staat: MI
Alter: -
Geschlecht: U
Eingang: 05.05.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Antinuclear antibody negative Blood bilirubin increased Blood lactate dehydrogenase increased Central nervous system lesion Cerebral thrombosis Contusion Platelet count Platelet count decreased Thrombosis Headache Hepatitis viral test negative Magnetic resonance imaging head abnormal Plasmapheresis SARS-CoV-2 test negative

Symptomtext

clots; I received the pfizer vaccine and within 2 weeks had bruising; low platelets; This is a spontaneous report from a contactable consumer, the patient. This patient of unspecified age and gender received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: UNKNOWN) via unspecified route on unspecified date as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient reported that he/she received the vaccine and within 2 weeks had bruising, low platelets and clots (unspecified date). Lab data included platelets: low on unspecified date. The clinical outcomes of bruising, low platelets and clots were unknown. The lot number for the vaccine, BNT162b2, was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral thrombosis
Hospital-Tage: -
Labordaten: Test Name: Platelets; Result Unstructured Data: Test Result:low
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1284737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: KY
Alter: 37,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 19.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood test Dizziness Heart rate Hyperhidrosis Palpitations Syncope

Symptomtext

dizziness/dizzy/almost felt like fainting; felt like fainting; racing heart; sweating; This is a spontaneous report from contactable consumers (one is the patient). A 37-year-old male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration in the left arm on 19Feb2021 13:00 [also reported as 26Feb2021 12:45 PM] (Lot Number: EL9267; Expiration Date: May2021) as a single dose for covid-19 immunisation. Medical history included drug penicillin allergies and low testosterone ongoing since 2018. Concomitant medication included testosterone cipionate (TESTOSTERONE CYPIONATE) for low testosterone, start and stop date were not reported. The patient previously took amoxicillin but had allergies. The patient reported that a few minutes after his first vaccination (19Feb2021), he experienced a racing heart, dizziness, sweating, and almost felt like fainting. A couple waves of this hit him and subsided after 10-15 minutes. The events required emergency room visit. The patient has not been covid tested post vaccination. The patient was not diagnosed with covid prior vaccination. The patient has his blood checked twice/year all normal levels (unspecified date). The patient mentioned that he became slightly dizzy after receiving his first COVID-19 vaccine and he was not nervous or scared prior to or following receiving the vaccine. He also does not have history or problems receiving other vaccines or blood draws when he received the second vaccine, he felt normal for a couple minutes although he would feel "something" thought his body immediately after the injection. A few minutes went suddenly, he became very dizzy or short of breath, EMS was on standby at this site, so they advised him to sit on the floor. They connected heart /02 monitor to him (2021), and his heart rate was very highly (around 130 BPM) or then it would swing widely to less than 50 BPM. During these swings, he would get very dizzy or faint. This happened multiple times starting from less severe to severe with fainting, to finally going away, unfortunately after 30 minutes or so when the heart rate swings were observed, EMS administered Epinephrine and Benadryl in IV form. He was taken to a hospital via ambulance where he was later discharged after no issue in observation. The events tachycardia, dizziness and fainting were considered serious with seriousness criterion of hospitalization/prolongation of hospitalization and important medical event. The outcome of the events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Blood test; Result Unstructured Data: Test Result:All normal levels; Comments: Blood is checked twice/year; Test Date: 2021; Test Name: heart rate; Result Unstructured Data: Test Result:very highly; Comments: very highly (around 130 BPM) or then it would swing widely to less than 50 BPM
Aktuelle Erkrankungen: Testosterone low
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: TESTOSTERONE CYPIONATE
Allergien: -
Vorherige Impfungen: -

VAERS 1274746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: AK
Alter: 42,0
Geschlecht: F
Eingang: 30.04.2021
Impfdatum: 02.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: SYR / LA

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

Bell's palsy Herpes zoster

Symptomtext

I came down with shingles and then bell's palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Doctor visits entailing visual diagnosis
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid disease
Andere Medikamente: progestrone and synthroid
Allergien: tylenol and cipro
Vorherige Impfungen: -

VAERS 1270795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: IL
Alter: 81,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 12.02.2021
Beginn: 07.03.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: IM / RA

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

Chills Electroencephalogram normal Extremity contracture Muscle contracture Muscle spasms Muscle tightness Seizure

Symptomtext

She got the vaccine, and had no reactions at all other than perhaps a chill. About 2-3 weeks later on 3/7/21 she started experiencing what they are calling muscle confusions. She feels a tapping sensation on her biceps and triceps and then starts with muscle cramps running down her right arm creating her fingers to cringe or come together or contract. This then travels down to her right leg to her quadriceps which cramps and convulse and travels to her calves which tighten up like a Charlie Horse and down her toes to where they contract as well. They are intermittent, scattered and sporadic. Sometimes she will get 2-3 a day, and then none at all and then a few days later a couple more. These contractions last 3-5 minutes. She had COVID back in April of 2020 and was hospitalized until August of 2020 with that. During that time she was on a ventilator for 60 days and on a breathing tube and coded and was out for about 30 minutes. She had an EEG of her brain in September and told that she was fine. her neurologist felt she should have another one due to these symptoms, and she had that and everything was normal. The doctor prescribed 500 mg twice a day of Levetiracetam. The seizures kind of regress a little and then they came back and he upped that medication to 1000 mg twice a day. The seizures still continue and have continued but is still taking the medication. He felt that she should know see an epileptic specialist and they have an APT for 5/27/21. These episodes are exhausting and wear her out. She was going to PT due to the weakness from being in the hospital for so long, and now she is fearful if she is going to fall and uses a walker and is having a setback in that progress. She is to continue therapy at home for now and to follow up with the Epilepsy specialist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: As above.
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes.
Andere Medikamente: Vitamin D, iron, Metformin, Omeprazole, Trazadone, Losartan, Melatonin, Vitamin C, Vitamin B12, calcium.
Allergien: None.
Vorherige Impfungen: -

VAERS 1265968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 12.02.2021
Beginn: 05.04.2021
Tage bis Beginn: 52,0
Dosis: 2
Route/Site: - / RA

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

Computerised tomogram thorax Deep vein thrombosis Fatigue Oropharyngeal pain Pain in extremity Peripheral swelling Ultrasound scan

Symptomtext

This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose via an unspecified route of administration (injection), administered in the right arm on 12Feb2021 at 13:00 (batch/lot number: EL9267) as a single dose for COVID-19 immunization. Medical history included rheumatoid arthritis from 1991 and ongoing (diagnosed 30 years ago; doctor said that he didn't know if she has RA because she's taken all of those infusions and it may just be severe osteoarthritis), ongoing thyroid (disorder), thyroid was removed, knee replacement left leg from 2020 (she had knee replacement last year on her left knee), Achilles tendon tear - reported that she had to have surgery last to repair her right Achilles tendon as it tore, cholesterol (abnormal) from 1991 and ongoing (diagnosed with cholesterol problems 30 years ago), ongoing depression (diagnosed with depression a couple years ago), ongoing sleep problems (experienced sleep problems for a long time), blood pressure (abnormal) from 2013 and ongoing (diagnosed with blood pressure problems 8 years ago), physical therapy, lymphedema, and unable to recall exact dates. There was no family medical history. No prior vaccinations (within 4 weeks). Concomitant medications included amitriptyline taken to help her sleep from an unspecified start date and ongoing (she has been taking this medication for years and years); folic acid taken for arthritis from an unspecified start date and ongoing (she has been taking this medication for years and years); levothyroxine taken for thyroid, start and stop date were not reported (she has been taking this medication for years and years); chlordiazepoxide (LIBRIUM) taken for sleep from an unspecified start date and ongoing (she has been taking this medication for years and years); losartan taken for blood pressure from an unspecified start date and ongoing (she has been taking this medication for years and years); meloxicam taken for arthritis from an unspecified start date and ongoing (began taking for 10 or 15 years after switching from celecoxib); metoprolol taken for blood pressure from an unspecified start date and ongoing (she has been taking this medication for years and years); omeprazole taken for stomach from an unspecified start date and ongoing (helps her stomach with all of the medications she has to take); pravastatin taken for cholesterol from an unspecified start date and ongoing (she has been taking this medication for years and years); desvenlafaxine succinate (PRISTIQ) taken for depression from an unspecified start date and ongoing (she started taking over a year ago, a year and a half or maybe two years ago); levothyroxine sodium (SYNTHROID) taken since thyroid was removed from an unspecified start date and ongoing (she has been taking since 15 years ago, for a long time); temazepam taken to help her sleep from an unspecified start date and ongoing (she has been taking this medication for years and years); cholecalciferol (VITAMIN D3) taken for an unspecified indication from an unspecified start date and ongoing (she has been taking this medication for years and years). The patient previously took BNT162B2 first dose on 21Jan2021 via injection in the right arm (lot number: EL3047 or EL3247; expiration date unknown) for COVID-19 immunization; and celecoxib (CELEBREX). The patient experienced extensive deep vein thrombosis on 06Apr2021; leg pain and feet swollen/ leg was like a balloon/ leg started to swell on 05Apr2021; throat hurts and tired on an unspecified date. The patient was calling about the Pfizer Covid-19 vaccine. She reported that she and her husband received both doses of the Pfizer Covid-19 vaccine. She received her first dose of the Covid-19 vaccine on 21Jan2021 and her second dose on 12Feb2021. She reported that she has had no complications before such as blood clots or problems with her blood or anything. She reported that on Monday, 05Apr2021, her leg started to swell. She reported that on the following day, 06Apr2021, her leg was so swollen that she couldn't put it down. She reported that she went to the emergency room on 06Apr2021 and was found to have an extremely extensive deep vein thrombosis. She reported that she was calling to complete a safety report. She stated that she doesn't want a deep vein thrombosis to happen to anyone else if her thrombus was from the Covid-19 vaccine. She reported that she and her husband thought they were so lucky as they had no side effects whatsoever following the Covid-19 vaccine doses. She reported that she was not saying that the deep vein thrombosis was from the Covid-19 vaccine but she has never had any blood or clotting problems in her life. Throat hurts: She reported that she thinks that when she was intubated, that whoever intubated her caught her tongue and cut it. She reported that she and her son and husband had been seeing news stories about the (Company name) vaccine. She reported that she has friends that were waiting for the (Company name) vaccine. She reported that her son wanted to send a text message so that others could be aware of the problems they might have. Leg pain: She reported that she went to the dentist on 05Apr2021 and was fine. She reported that when she got home from the dentist, her husband asked if she wanted to the take dog for walk. She reported that she put a leash on her dog and walked to the end of her driveway and said to her husband that she couldn't walk because her leg hurt so much. She reported that she had 2 surgeries last year, a knee replacement in her left leg and an Achilles tendon repair in her right leg. She reported that when she was released from physical therapy that the therapist told the caller that she might have lymphedema. She reported that the physical therapist directed her to go to a clinic that had no doctor where the clinic staff wanted her to buy a (dollar)10,000 piece of equipment to pump up her legs in the morning and at night. She reported that she came home from the clinic and called the podiatrist that repaired her Achilles tendon. She reported that she went to see the podiatrist that day and that the podiatrist ordered an ultrasound. She reported that a vascular surgeon called her regarding the ultrasound and stated that there was nothing wrong with the veins in her legs. She reported that the surgeon stated that they could tell there was nothing wrong with the her because her feet weren't swollen and instructed her to follow up in 9 months. She reported that on 05Apr2021, she went back into her house after experiencing the leg pain. She reported that her feet were not swollen and she was not that concerned. She reported that she thought maybe she was just tired and laid down. She reported that when she woke up the next morning, 06Apr2021, that her feet were like balloons. She reported that her son called a friend of his who was an orthopod. She reported that her son's friend instructed her son to take her to the emergency room, recommending that they bypass a certain hospital. She reported that she went to the emergency room on 06Apr2021. She reported that the emergency room staff did an ultrasound as soon as the caller arrived. She reported that the emergency room staff called the vascular surgeon. She reported that the vascular surgeon stated that if he had been in the caller's hospital room 5 minutes earlier that the would have done the surgery then, but that he had to lay her on her stomach to perform the surgery and she had eaten some cookies and drank diet soda. She reported that on the following day, 07Apr2021, the vascular surgeon put a scope in her vein and pulled out the clot. She reported that the physician was extremely concerned because the clots were very extensive. Leg pain: She reported that the leg pain was still ongoing. She reported that it hurts when she walks. She reported that she doesn't know if the leg pain has gotten worse. She reported that her leg pain on 06Apr2021 was excruciating and off the charts. Feet swollen: She reported that the swelling in her feet has maybe gotten slightly better. She reported that her feet were wrapped tightly with ace bandages. Leg swollen like a balloon: She reported that her leg was still swollen but it's gotten better, maybe about 90%. Extensive deep vein thrombosis: She reported that the deep vein thrombosis was removed on 07Apr2021 from her left leg. She reported that she was at end of her life and she had trips planned. She reported that she had a trip planned recently to go to Las Vegas with her daughter. She reported that her daughter was not able to take the trip, and stated she didn't know what would have happened if she had experienced the blood clot while in Las Vegas. She reported that she received both doses of the Covid-19 vaccine in her right arm, as she was in the car and her husband was driving. First dose: Date: 21Jan2021; Lot Number: She reported the lot number as EL3047, then stated that the handwriting was hard to read and that the lot number was either EL3247 or EL3047. She stated when reporting on her history that she has no concept of time and was unable to recall exact dates. She reported that while in the emergency room and during admission, the hospital staff did labs, but she has no idea what the results were. Vaccination facility type was drive through clinic at (clinic name). Vaccine administered at military facility: No. The adverse events leg pain, swelling in feet and leg, extensive deep vein thrombosis required a visit to the emergency room. Did not require a visit to the physician's office. The patient was hospitalized for 6 days for extensive deep vein thrombosis from 06Apr2021 to 12Apr2021. The patient underwent lab tests and procedures which included CT scan of chest: normal on an unspecified date, ultrasound: there was nothing wrong with the veins in her legs on an unspecified date, ultrasound: unknown results on an unspecified date. The outcome was not recovered for the event leg pain; recovering for the event feet swollen/ leg was like a balloon/ leg started to swell; and unknown for the rest of the events.; Sender's Comments: Reported events are assessed as intercurrent medical conditions probably associated to patients underlying conditions and are therefore unlikely related to BNT162B2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 6,0
Labordaten: Test Name: CT scan of chest; Result Unstructured Data: Test Result:normal; Test Name: Ultrasound; Result Unstructured Data: Test Result:there was nothing wrong with the veins in her legs; Test Name: Ultrasound; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: Blood cholesterol abnormal (diagnosed with cholesterol problems 30 years ago); Blood pressure abnormal (diagnosed with blood pressure problems 8 years ago); Depression (diagnosed with depression a couple years ago); Rheumatoid arthritis (diagnosed 30 years ago); Sleep problem (experienced sleep problems for a long time); Thyroid disorder.
Vorgeschichte: Medical History/Concurrent Conditions: Achilles tendon repair; Achilles tendon rupture (had to have surgery last to repair her right Achilles tendon as it tore); Forgetfulness; Gastric disorder; Knee replacement (left leg; last year on her left knee); Lymphedema; Physical therapy; Thyroidectomy.
Andere Medikamente: AMITRIPTYLINE; FOLIC ACID; LEVOTHYROXINE; LIBRIUM; LOSARTAN; MELOXICAM; METOPROLOL; OMEPRAZOLE; PRAVASTATIN; PRISTIQ; SYNTHROID; TEMAZEPAM; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 1258192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: LA
Alter: 63,0
Geschlecht: M
Eingang: 26.04.2021
Impfdatum: 17.03.2021
Beginn: 13.04.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram pulmonary normal Chest pain Echocardiogram Electroconvulsive therapy Pericarditis

Symptomtext

Acute pericarditis, severe chest pain, colchicine 0.6 mg tablet 2 times per day for 10 days, asprin 81 mg

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Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: CT angiogram pulmonary - negative ECT 12 lead ECHO Complete
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: propranolol 10 mg,, multi vitamin, omeprazole , claritin
Allergien: none
Vorherige Impfungen: -

VAERS 1246783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 23.04.2021
Impfdatum: 22.01.2021
Beginn: 07.04.2021
Tage bis Beginn: 75,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Respiratory distress SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Pt tested positive for COVID after receiving both vaccines. Pt developed respiratory distress requiring supplemental oxygen.

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: COVID + on 4/7/21
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, A-Fib, CHF, Peripheral vascular occlusive disease
Andere Medikamente: Duoneb, lipitor, flomax, nitrostat, xalatan, trelegy ellipta,
Allergien: -
Vorherige Impfungen: -

VAERS 1229099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: GA
Alter: 27,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 13.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 34,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Deep vein thrombosis Erythema Feeling hot Muscle strain Pain in extremity Swelling Ultrasound Doppler Weight bearing difficulty X-ray limb

Symptomtext

On day 3 following, 2nd dose of Pfizer vaccine, he had right sided calf pain. Initially thought to be recurence of strain injury, although no history of trauma or obvious trigger. Pain conitnued to worsen and had different characteristics than original strain symptoms. Continued to worsen to point wher eunable to weight bear and swollen, hot and red. Saw orthopedist who refered to vascular surgeon, and on day 13 was officially diagnosed with large DVT extending form tibeal & peroneal, popliteal up to the femoral veins. Has no known clotting defects. Currently under evaluation with hematologist who recommended anticoagulants for remainder of his life.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Xrays of right extremity Ultra sound of right leg 4/7/2021 Labwork by hematologist pending (4/15/2021)
Aktuelle Erkrankungen: calf strain
Vorgeschichte: mild intermittent asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1162662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: AK
Alter: 16,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 02.04.2021
Beginn: 02.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Syncope

Symptomtext

Syncopy episode about 10 minutes after receiving second dose of pfizer vaccine

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lamotrigine
Allergien: no Known Allergies
Vorherige Impfungen: -

VAERS 1162085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: AZ
Alter: 66,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Anxiety Bell's palsy Dyspnoea Fear Hypoaesthesia Oral herpes

Symptomtext

short of breath; fear and anxiety or from the vaccine; fever blisters; fear and anxiety or from the vaccine; like bells palsy; numbness of the right side of her face from her jaw to her ear and up to her right eye; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EL9267), via an unspecified route of administration, on 26Feb2021 (received at the age of 66-years-old), at a single dose for COVID-19 immunization. Medical history included cold sores, 2 knee surgeries, and ADD (Attention deficit hyperactivity disorder) from an unspecified date and ongoing (diagnosed at 30-years-old). Concomitant medications included methylphenidate hydrochloride (RITALIN), amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL) and other regular medication. The patient received first dose of Pfizer BioNTech vaccine and developed numbness of the right side of her face from her jaw to her ear and up to her right eye on 26Feb2021. It felt like she had received a lidocaine injection. Her doctor said this can happen with RNA vaccines, affect the 7th cranial nerve and develop Bell's Palsy. She was prescribed Valacyclovir 1mg and has taken it for 3 days. She wants to know what the other Bell's Palsy cases were like. She wants to know what their treatments were. Her doctor said it was okay to receive her second dose at 8am on 20Mar2021 but she wants to do her due diligence and see if there is a case report or study on these patients that developed this side effect. The patient further explained that she had her first dose on 26Feb2021 and was she was there for the 15 minutes for observation. On her way home, the right side of her mouth and the right side of her nostril were numb like Novocaine that you get at the dentist. She said that the numbness traveled up the right side of her jaw to her ear and then over to her right eye. When she got home, she told her daughter and she said that she thought it was because she volunteered all day and was worn out and anxious (26Feb2021). She said that she slammed water and ate crackers and after about a 1.5 hours she started to feel better. She said that she then she called her physician and the doctor told her that it was flaring the nerve root like bells palsy and that it is a RNA Virus. She said that she was placed on some medication for it, but was wondering if she should get the second dose of the vaccine. She said that the doctor asked her if she had previously had cold sores and she said yes. The caller said that her doctor said that it is exactly what that is. The patient stated that she was also short of breath on an unspecified date, but thought it was from fear and anxiousness. She does not know if it was from fear and anxiety or from the vaccine. She said that the doctor told her to take the medication 3 days before and 3 days after her second dose. She clarified that the doctor put her on Valacyclovir HCl 1Gm tablets 1 a day. She said that she broke out with fever blisters on 02Mar2021. She really did not think anything of it until speaking with friends in the medical field and they told her to follow up with this. She added that the fever blisters are healing and only a tiny bit left. It is at the scab and end of healing. Outcome of numbness of the right side of her face from her jaw to her ear and up to her right eye was recovered on 26Feb2021. Outcome of fever blisters was recovering. Outcome of other events was unknown.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: ADD (diagnosed at 30-years-old)
Vorgeschichte: Medical History/Concurrent Conditions: Cold sores; Knee surgery NOS
Andere Medikamente: RITALIN; ADDERALL
Allergien: -
Vorherige Impfungen: -

VAERS 1150873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 22.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: - / -

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

Anaphylactic reaction Blood pressure measurement Rash

Symptomtext

Anaphylactic reaction: full body rash; Anaphylactic reaction: full body rash; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration at 69-year-old on 22Feb2021 (lot number: EL9267, expiration date unknown), at single dose for COVID-19 immunization. Medical history included cardiac disease, triple bypass operation, diabetes, thyroid, high blood pressure, known allergies: penicillin. The patient was not diagnosed with COVID prior vaccination. The patient's concomitant medications were not reported. The patient did not receive other vaccine in four weeks. On 01Mar2021 the patient experienced anaphylactic reaction: full body rash. The event resulted in doctor or other healthcare professional office/clinic visit. The COVID was not tested post vaccination. The patient received treatment for the events, included unspecified medications. The outcome of the events was not recovered.

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Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:high
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Bypass surgery; Cardiac disorder; Diabetes; Penicillin allergy; Thyroid disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1131639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 24.03.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood pressure increased Dizziness Electrocardiogram Feeling cold Headache Hyperhidrosis Somnolence Syncope

Symptomtext

After 10 minutes of receiving shot I felt a cold surge in my left arm and felt lightheaded. I felt sweaty, weak and faint. The EMTs quickly came to my side and administered my blood pressure and oximeter. When I continued to feel lightheaded they took me to a back room and hooked me up to an EKG with electrodes throughout my body. They retook my blood pressure and told me that my blood pressure had risen to 180/90 earlier! After sitting for a while they took it again and read 160/80. They told me to get it checked again, asked if I need go to ER, Walk-in or doctor. They walked me out to my husband, who was waiting in car. I went home and slept for 11/2 hours. Took my blood pressure the next day 3 times and averaged in the low 120s.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood pressure after vaccine- rose from 139/70 to 180/90 After sitting a few minutes - retook blood pressure - down to 160/80 Next day ( took 3x)- averaged in low 120s Headache next day (3/10/21) Fatigue
Aktuelle Erkrankungen: non
Vorgeschichte: hypoglycemia asthma hypertension
Andere Medikamente: non
Allergien: penicillin
Vorherige Impfungen: Shingles #1 - January 2021

VAERS 1127741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 23.03.2021
Impfdatum: 20.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Injection site pain Pain Pyrexia Respiratory distress

Symptomtext

Injection site soreness shortly after administration. Fever started by 7:30 a.m. on 3/21/21, Fever reduced after taking Advil. By 7:00 p.m. 3/21/21, fever returned and achiness and respiratory distress started. Asthma medication administered, but only helped for a couple minutes at a time. An additional dose of Mucinex also administered. Respiratory distress increased if lying down. Respiratory distress eased by 8:00 a.m.. on 3/22/21.

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Liddle's Syndrome (rare genetic kidney disease) Asthma High blood pressure High cholesterol Pre-diabetes
Andere Medikamente: Amiloride Indapamide Amlodipine Besylate Atovastatin Vitamin D2 Zinc Vitamin C Mucinex
Allergien: Prednisone
Vorherige Impfungen: Dose 1 of above vaccine produced lightheadedness within 2 minutes of administration. Eased within an hour.

VAERS 1127665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: AK
Alter: 25,0
Geschlecht: M
Eingang: 23.03.2021
Impfdatum: 03.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Computerised tomogram Full blood count Metabolic function test Toxicologic test Urine analysis

Symptomtext

On 3/21/21 his neck started bothering him and progressed into him not being able to use half of his face. He was transported to Local Hospital. Where he was diagnosed with Bell's Palsy. He was given a treatment of Prednisone. He was seen again by the Facility provider on 3/23/21 where the prednisone was continued on a tapered dose. Acyclovir was also added to the treatment.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CT Scan, CBC, CMP, urinalysis, toxicology
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Fish
Vorherige Impfungen: -

VAERS 1126974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: LA
Alter: 67,0
Geschlecht: F
Eingang: 23.03.2021
Impfdatum: 23.02.2021
Beginn: 04.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / RA

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

Bell's palsy

Symptomtext

PATIENT STATED WENT TO ED ON 3/4/2021 2 WEEKS AFTER 1ST DOSE OF COVID VACCINE WITH "FLARE UP OF BELL,S PALSY" TO RIGHT SIDE OF HER FACE. FOLLOWED UP WITH PRIMARY CARE PHYSICIAN AND WAS STARTED ON PREDNISONE.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1123878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 34,0
Geschlecht: F
Eingang: 23.03.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Cough Dyspnoea

Symptomtext

Anaphylaxis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: No labs. Just gave me albuterol, epinephrine, benadryl, and toradol I believe. It all happened really quickly so I don't remember everything.
Aktuelle Erkrankungen: Non-alcoholic fatty liver
Vorgeschichte: N/A. Currently lost over 20 lbs for the non-alcoholic fatty liver
Andere Medikamente: High EPA Omega-3, Chromium Picolinate Previous days: hepato support max, calcium pyruvate, high EPA omega, Vitamin D2 (50,000 IU once per week on Sundays.), Cardio metabolic vitamins & minerals, chromium Picolinate, alpha lipoic acid (all
Allergien: Zithromax, Percocet, hot dogs, cats, feathers, sausage
Vorherige Impfungen: -

VAERS 1102813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 15.03.2021
Impfdatum: 11.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / RA

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

Deep vein thrombosis Incomplete course of vaccination Ultrasound Doppler abnormal

Symptomtext

Developed an Acute nonoocclusive DVT in left leg 10 days after my first vaccine. Decided to decline my second vaccine. I do have a history of having blood clots, but last one was 32 years ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: vas venous duplex lower ext lt 02/26/21 13:13 acute nonocclusive DVT
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, High Blood Pressure, High Colestertol
Andere Medikamente: Losartan Potassium 50 mg -pm Cmega Q Plus 200 mg , CoQ 10 200mg, Vitamin C 500 mg, D3 2000mg
Allergien: None
Vorherige Impfungen: -

VAERS 1083750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: KY
Alter: 71,0
Geschlecht: M
Eingang: 09.03.2021
Impfdatum: 21.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

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

Condition aggravated Gait disturbance Loss of consciousness Vertigo

Symptomtext

passed out; This will drive me nuts all day; I don't feel comfortable walking in my own house; I got up this morning with the feeling of vertigo; getting little worse, worse than they were; This is a spontaneous report from a contactable Consumer. A 71-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, NDC number of Covid-19 Vaccine: 592671000-1, Expiry Date of Covid-19 Vaccine: 31May2021, Lot: EL9267), via an unspecified route of administration on 21Feb2021 13:24 at single dose for covid-19 immunisation. The patient medical history were none. Concomitant drug received. Patient stated, "Yes, I am on Inhalation Pump so, I take it went for one when I need it, I just had that was just little while ago, it wasn't (Incomplete sentence). The patient stated, "I got my second shot (Covid-19 Vaccine by Pfizer) Sunday about 1:30(13:24 PM) it says on the piece of paper, and I was fine all day Sunday, Monday(22Feb2021), I got up this morning with the feeling of vertigo, which I have had in the years of the past okay, all day, got out of shower from the bathroom out here and get some coffee, and I sat down I went to get up and the vertigo hit and I almost fall over, now I went into the shower and I dropped the wash cloth on the floor, so I went down to pick it up and again almost passed out, almost immediately, and I sat and I get in the kitchen for some toast and I said well let me see what happens here and sat down eating some toast and when I got up to put dirty dishes in the sink, I almost again passed out, now I just got up to get the check I have to write to the gentleman right here who is working for me and just before that I got the same thing now I don't like it, how are these supposed to last, is what I want to know because I can't, this will drive me nuts all day, I can't go anywhere, I can't drive anywhere, yeah I don't feel comfortable walking in my own house. Right now, I have to say I am feeling them getting little worse, worse than they were." No treatment. Outcome was not recovered.

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
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1082754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: AZ
Alter: 69,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 16.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Intensive care Laboratory test Nerve compression Peripheral artery occlusion Poor peripheral circulation Thrombectomy

Symptomtext

two days after receiving the vaccination my left arm went numb. the next am i went to urgent care and they said pinched nerve - no improvement so went to ER on Monday morning. It was determined that the arteries in my left arm were completely blocked and I was not getting any blood flow to limb. Sent from ER and within hours an emergency throbectomy was performed to save my left arm/hand. Spent a couple days in ICU, total 5 in hospital. Doctors DO NOT KNOW if COVID 19 vaccine could have caused or be partially responsible so they advised me to file a report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: Numerous tests performed before and after surgery during 5 days at hospital.
Aktuelle Erkrankungen: Sinus / respiratory infection prior
Vorgeschichte: diabetes, rheumatoid arthritis, asthma
Andere Medikamente: pls contact for list of meds - or i will attach if allowed on this website
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1082675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 12.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / -

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

Chills Dehydration Headache Hyponatraemia Hypophagia Lactic acidosis Loss of consciousness Nausea Pain Syncope Vomiting

Symptomtext

Patient received first Pfizer COVID-19 vaccine on 1/20/2021 and second dose on 2/12/2021. Patient had minor symptoms such as body aches with both vaccine doses which resolved. Patient then stated she started to experience headache, nausea, and body aches, decreased oral intake, and chill starting on 2/18/2021. On 2/20/2021 patient had several loss of consciousness episodes. Patient presented to the Emergency Department on 2/21/2021 with a chief complaint of syncope, nausea, and vomiting and subsequently admitted to the hospital for potential sepsis, syncope, hyponatremia, dehydration, lactic acidosis. (Continued on second page)

Weitere VAERSDATA-Felder

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

VAERS 1081748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 18.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / LA

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

Balance disorder Chills Dysgeusia Fatigue Feeling abnormal Headache Hyperhidrosis Hypoaesthesia Somnolence Syncope

Symptomtext

groggy; Headache; metallic taste; sweating; shivering; feeling like I was going to either have vertigo spell or throw up; balance unsteady; feeling numbness in left arm; Exhausted/tired; feeling faint; This is a spontaneous report from a contactable consumer reported for herself. A 45-year-old female patient (No Pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL9267), left arm on 18Feb2021 14:15 at single dose for COVID-19 immunisation. Medical history included overweight, pre-diabetic. The patient did not diagnose with COVID-19. No allergies to medications, food, or other products.The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Other medications the patient received within 2 weeks of vaccination included multivitamin. Shot on Thursday. No problem on Friday. Headache Saturday morning 20Feb2021 06:30 AM. After dinner on 20Feb2021, she had a metallic taste in her mouth started sweating and feeling faint then started shivering and feeling like she was going to either have a vertigo spell or throw up. Ballance unsteady. Drank water got into bed and then she started feeling numbness in her left arm. Exhausted and tired. Sunday tired and groggy. Monday still tired and groggy. Events were non serious. Since the vaccination, the patient has not been tested for COVID-19. No treatments were received. Outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Overweight; Pre-diabetic
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1081452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 08.03.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray Electrocardiogram Full blood count Metabolic function test Musculoskeletal chest pain Presyncope Resuscitation Syncope Troponin

Symptomtext

64-year-old male with a history of hypertension, melanoma, vasovagal events from previous needles presenting to the emergency department today for vasovagal episode. Patient was across the street receiving his first dose of Covid vaccine. At that time patient had a syncopal episode. According to EMS they indicate that nursing there was unable to feel pulse and began CPR. They did multiple rounds of compressions and patient woke up. They are bringing patient in today for further evaluation of syncope versus cardiac arrest. Patient does endorse that he has chest wall pain from where they were doing compressions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Orders been placed for CBC, BMP, troponin, EKG, 2 view chest x-ray and will plan to observe patient for 2 to 3-hour timeframe here in the emergency department. Patient also has outpatient lab work scheduled for next week including lipid panel, PSA, A1c, TSH. Due to patient having vasovagal episodes after needle pokes will obtain lab work here at this time as he already has IV started.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: Unknown

VAERS 1043542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Chest pain Dizziness Dyspnoea Throat tightness

Symptomtext

anaphylactic reaction; This is a spontaneous report from a non-contactable consumer. A female patient of an unspecified age received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) , via an unspecified route of administration on an unspecified date at single dose for covid-19 immunisation . The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced anaphylactic reaction on an unspecified date, which caused Emergency room/department or urgent care. Therapeutic measures were taken as a result of anaphylactic reaction included unspecified treatment. The outcome of event was recovered. No follow-up attempts are possible. information about lot/batch number cannot be obtained.

Weitere VAERSDATA-Felder

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

VAERS 1051938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: WA
Alter: 40,0
Geschlecht: F
Eingang: 06.03.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Anxiety Aphasia Asthenopia Bradyphrenia Computerised tomogram head Confusional state Dizziness Electrocardiogram Fatigue Impaired work ability Hyperhidrosis Pallor Seizure Laboratory test Loss of consciousness Migraine Seizure like phenomena Tinnitus

Symptomtext

8 minutes after the administration of the vaccine (while in the observation area) I started to feel really off (dizzy, anxious, ringing in right ear). I ended up becoming unconscious with seizure like activity. They rushed me to the ER and kept me for 6 hours with lots of testing. XRay, blood test, CT of head, EKG, Urine test...all came back normal. Doctor said it was likely a reaction to the vaccine. I am 40 years old with no history of seizures or allergic reactions to vaccines. The week following I experienced confusion, migraines, dizziness, slow cognitive processing, eye strain, word finding difficulties, and exhaustion. I had to take a week off of work to recover. This is the second week and I am still experiencing headaches and occasional dizziness/eye strain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: All tests were performed in the ER: XRay, blood test, CT of head, EKG, Urine test
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity, Hypothyroidism, hypertension, anemia
Andere Medikamente: Levothyroxine, Citalopram, Buspar, Wellbuterin, blood pressure meds, water pill, iron, Vitamin D, fish oil, stool softners,
Allergien: None
Vorherige Impfungen: -

VAERS 1293800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 12.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Asthenia COVID-19 Dehydration Fall Hepatic enzyme increased Hyponatraemia Intensive care unit acquired weakness Pyrexia Sepsis

Symptomtext

weakness, fall Narrative: Pt with history of CAD (s/p PCI mid and prox RCA in 2006, on ASA/Plavix; CABG, AVR), afib, GERD, HTN, HLD, hypothyroidism, BPH, diverticulosis, aortic stenosis, small fiber neuropathy (since 2010), lumbar stenosis at S1. Also, pt presented to outside ED on 12/26/20 for increasing falls and weakness over one week and was admitted to outside hospital 12/26/20 for generalized weakness, dehydration, hyponatremia all secondary to covid 10 infection. Hospital course included sepsis due to covid 19, elevated liver enzymes, acute kidney injury. Pt discharged 12/29/2021. After first COVID vaccine 2/12/2021, patient experienced fever x 1 day, weakness, and fall. Presented to outside ED 2/13/21 abd was admitted for critical illness myopathy 2/2 recent COVID infection +/-COVID vaccination. Pt was discharged 2/18/2021.

Weitere VAERSDATA-Felder

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

VAERS 1075927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: 22.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Rash

Symptomtext

Anaphylactic reaction: full body rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiac disease; diabetes; thyroid; high blood pressure
Andere Medikamente: -
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1073830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

schwer

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dysgeusia Euphoric mood Headache Pallor Rash Syncope Tunnel vision

Symptomtext

funny taste in mouth, felt buzzed, headache, confused, tunnel vision, pale, fainted, rash on torso

Weitere VAERSDATA-Felder

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

VAERS 1073258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OK
Alter: 87,0
Geschlecht: F
Eingang: 04.03.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cold sweat Dizziness Dyspnoea Flushing Loss of consciousness Malaise Seizure

Symptomtext

After receiving the vaccine client became flushed, clammy, labored breathing, LOC, and had seizure like activity. After she came to, she c/o not feeling good and lightheaded. She was taken by ambulance to the hospital. Husband said they ran several tests. She continues to sleep a lot and is sore all over.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: none
Vorgeschichte: Alzheimer's,
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1069209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: LA
Alter: 63,0
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 25.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Eye discharge Eye irritation Eye swelling Facial paralysis

Symptomtext

Was notified by nurse at clinic that Patient started having right eye dripping, swelling and burning starting on Monday 3/1/21. Patient went to see her Family Dr. with complaint of right side drooping starting today 3/3/2021. She was sent to the ED at Hospital for evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1063796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 01.03.2021
Impfdatum: 23.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Dyspepsia Full blood count Metabolic function test Nausea Syncope

Symptomtext

Pt presented to the ED after a syncopal episode at home. Pt was on the toilet having a bowel movement when he developed sudden-onset nausea, light-headedness, and dizziness. He felt that he was going to pass out and his daughter came into the room and helped him. He did not lose consciousness or hit his head. Symptoms resolved "several minutes later." Pt complains of new-onset heartburn. Pt states that the symptoms he felt during the episode were similar to the sensation he felt during a heart attack he had several years ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: CBC and CMP completed in ED. Notable abnormalities: calcium 8.2, total protein 5.4, albumin 3.2, RBC 3.6, hemoglobin 11.7, hematocrit 35.2, platelet 117. High-sensitivity troponin completed and was negative.
Aktuelle Erkrankungen: -
Vorgeschichte: vascular disease, thrombocytopenia, syncope (8/7/2019), skin cancer, rheumatoid arthritis, hyperlipidemia, HTN, heart failure, follicular lymphoma, emphysema, COPD, CAD, atrial fibrillation, anemia, bladder cancer
Andere Medikamente: symbicort, coreg, lisinopril, plavix, lipitor, albuterol, cyanocobalamin, tylenol, aspirin, dulcolax, plaquenil
Allergien: iodine, IVP dye (iodine containing)
Vorherige Impfungen: -

VAERS 1062771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 9267

schwer

Staat: AZ
Alter: 23,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blindness transient Heart rate increased Hyperhidrosis Loss of consciousness Nausea Pallor Physical capacity evaluation Urinary incontinence

Symptomtext

Within 10 minutes of receiving the vaccine, developed "blackening" vision and then lost consciousness. Uncertain about time of loss of consciousness. Other symptoms included pallor, fast heart rate, sweating, nausea and loss of bladder function. No treatment required, seen in the ED and recovered without treatment. Because she was driving a car at the time, she rear-ended the car in front of her and the airbags deployed. Underwent evaluation for motor vehicle accident as well in the ED with no injuries noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG - per report normal blood glucose 87
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Progesterone containing IUD in place
Allergien: none
Vorherige Impfungen: -

VAERS 1062239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: SC
Alter: 72,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 08.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Cough Diarrhoea Loss of consciousness Oropharyngeal pain Rhinorrhoea

Symptomtext

Passed out; Constant running nose; Cough; bad cough; Sore throat; Diarrhea; This is a spontaneous report from a contactable consumer. A 72-years-old female patient received the second of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot number: EL9267, Expiration Date May2021, via an unspecified route of administration on 08Feb2021 (at the age of 72 years old) as SINGLE DOSE in the left arm for COVID-19 vaccination. The patient's medical history and concomitant medications were not reported. Historical information included BNT162B2 dose 1 for COVID-19 vaccination.The patient developed the sore throat on 09Feb2021, Cough; bad cough on 10Feb2021, constant running nose on 11Feb2021. On 11Feb2021, the patient passed out in the bathroom floor, had an ambulance here. Patient still coughing a little, not as badly. The patient experienced diarrhea in Feb2021. Treatment for all events included cetirizine (ZYRTEC), Triamcinolone (NASACORT), pseudoephedrine (SUDAFED), dextromethorphan hydrobromide, guaifenesin, paracetamol, pseudoephedrine hydrochloride (DAYQUIL). Outcome of the events Passed out, Sore throat, Constant running nose, Diarrhea was unknown. Outcome of the events Cough; bad cough was not recovered

Weitere VAERSDATA-Felder

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

VAERS 1059672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: ID
Alter: 50,0
Geschlecht: F
Eingang: 27.02.2021
Impfdatum: 17.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Ankle fracture Concussion Dizziness Fall Impaired work ability Open reduction of fracture Syncope

Symptomtext

Dizziness, that turned into a Syncopal event, resulting in a fall, that resulted in a broken ankle and concussion. Transported to nearest hospital, I had to have emergency surgery on left ankle, by Dr. A plate and screws were placed in my ankle to stabilize the break. I am being treated and monitored by my general doctor for the concussion. I am currently non-weight bearing on my ankle, for a minimum of 2-4 weeks. I am unable to work due to the ankle break and concussion, for an undetermined amount of time. I am scheduled to meet with Dr. on the 4th of March, at which time he stated he will want to begin physical therapy, once the break has reached an adequate stage of healing. I will be re-evaluated by my general Dr. for the concussion in 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Protonix, Gabapentin
Allergien: Eggs, Codeine
Vorherige Impfungen: -

VAERS 1052747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 24.02.2021
Impfdatum: 09.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / UN

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

Angiogram pulmonary normal Atelectasis Atrial fibrillation Brain natriuretic peptide normal Chest X-ray abnormal Diaphragmatic paralysis Differential white blood cell count normal Dyspnoea Laboratory test normal Magnetic resonance imaging spinal Pleural effusion Procalcitonin normal SARS-CoV-2 test negative Troponin White blood cell count normal

Symptomtext

Patient presented to hospital with increasing SOB, dyspnea on 2/22/21 (vaccine dose on 2/9/21). Patient is still currently admitted to monitor respiratory status and has been diagnosed with unilateral diaphragmatic paralysis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diaphragmatic paralysis
Hospital-Tage: -
Labordaten: No other clear etiologies for acute respiratory failure. CTPA (2/22/21) negative for acute PE, CXR (2/23/21) demonstrated small R pleural effusion and small LLL atelectasis. Patient has been afebrile since admission. Labs were normal: WBC normal, troponin undetectable, procalcitonin undetectable, BNP normal. Rapid COVID negative for acute infection negative x 2. Pulmonology and neurology have been consulted without further understanding for cause of illness. MRI spine pending at the time of this report.
Aktuelle Erkrankungen: No active illnesses prior to vaccination
Vorgeschichte: Hypothyroidism
Andere Medikamente: Atorvastatin 40mg daily, levothyroxine 62.5mcg daily, lorazepam 0.5mg BID prn anxiety (rarely used)
Allergien: No known allergies to food, drug, or otherwise
Vorherige Impfungen: -

VAERS 1051783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OK
Alter: 63,0
Geschlecht: F
Eingang: 24.02.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Agitation Anaphylactic reaction Anxiety Cardiac monitoring Dizziness Irritability Throat tightness

Symptomtext

Pt complained of throat tightness and being lightheaded beginning at 1127 hours (5 minutes after vaccine). She arrived at emergency/symptoms reporting station at 1129 hours. She denied tongue swelling, denied rash, denied difficulty speaking. No rash was seen by medics either. Pt did not have wheezing or stridor. Medics on scene and student medics under the direction of Medics, placed the patient on the monitor. Her HR was stable in the 70s and her sats were 99-100% on room air, with a strong pulse and RR of 16. The pt became more anxious and demanded that someone assist her with her Epi pen administration. RN explained sxs of anxiety and sxs of anaphylaxis. Pt became agitated and again remained adamant that medics give her Epi. At 1132 hours a student medic under the direction of Medics administered the pts own epi pen to her. Vitals signs after epi were HR of 88, BP of 170/97, RR 22, sats 100% . A transport unit was called as precaution and to potentially transport. Pt appeared to have an increase in agitation as indicated by her speech with medics being short and her stating that she was "irritated" with "everyone talking", that she "can't hear everyone all at the same time", that this is just "too much" and waving her hands in the air. Pt was transported to the ER via Medics for continued care and follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Medics and ER treatments
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, Bipolar, anxiety, and hypothyroidism
Andere Medikamente: Lisinopril, Levothyroxine, Wellbutrin, another unknown mood stabilizer
Allergien: No allergies to meds, no allergies to foods, carries an epi pen for hx of anaphylactic reaction to bee or wasp stings
Vorherige Impfungen: -

VAERS 1045120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: AZ
Alter: 41,0
Geschlecht: F
Eingang: 21.02.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Epistaxis Hypoaesthesia Myalgia Paraesthesia Thrombosis

Symptomtext

extreme muscle pain for 24 hrs . started immediately as minimal and increase to extreme within 3 hrs. face felt numb for about 20 minutes after receiving shot that lasted 15-20minutes. there was a tingling sensation present during the numbness in the center of my forehead. possibly related: experienced light nosebleed day after shot. three days after shot experienced a heavy nosebleed with very large clotting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: gastroesophageal reflux disease
Vorgeschichte: asthma
Andere Medikamente: -
Allergien: penicillin. miralax, septocaine or lidocaine (were both present in shot administered so not sure), morphine
Vorherige Impfungen: age 41, extreme pain in right arm that set in within a few hours and lasted about 24 hrs before minimizing, slight numbness and

VAERS 1043956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

schwer

Staat: PA
Alter: 80,0
Geschlecht: M
Eingang: 21.02.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
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-Medium

Weitere VAERSDATA-Felder

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

VAERS 1042623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: ID
Alter: 45,0
Geschlecht: F
Eingang: 19.02.2021
Impfdatum: 19.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Dizziness Presyncope

Symptomtext

felt faint - ?vasovagal rxn

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Vital signs
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: nka/nkda
Vorherige Impfungen: flu shot - in her 20s

VAERS 1041936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 19.02.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Dizziness Hyperhidrosis Nausea Syncope

Symptomtext

Exactly 12 hours after the shot, I experienced a severe wave of nausea, dizziness, faintness, and body sweats that lasted 15 minutes. It gradually subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity, diabetes 2
Andere Medikamente: Pramipexole, Lisinopril, Lebothyroxine, Rosuvastatin, Gabapentin, Vitamin D, Vitamin B12
Allergien: Codiene, Statins
Vorherige Impfungen: -

VAERS 1039359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 88,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 18.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Seizure

Symptomtext

Patient was sitting in observation area after vaccination when she began seizing. Patient was taken to the emergency department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Primary Hypertension, Hypercalcemia, Hyponatremia, Pre-diabetes, Adrenal adenoma, Osteoarthrosis, Meralgia paresthetica.
Andere Medikamente: Biotin, Calcium D3, decadron, Colace, Dyazide, Lutein Epinephrine (Bee stings), Magnesium, Netiorikikm Multivitamin, Benicar, Potassium, Metamucil, Vitamin C, Coumadin.
Allergien: ACE Inhibitors, Benicar, Celecoxib, Fentanyl, Oranges, Oxycodone, Statins, Sulfa
Vorherige Impfungen: -

VAERS 1039051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: PA
Alter: 84,0
Geschlecht: F
Eingang: 18.02.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Dysphagia Dyspnoea Throat tightness

Symptomtext

Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Difficulty Breathing-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 1033043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: WY
Alter: 57,0
Geschlecht: M
Eingang: 16.02.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Bell's palsy Condition aggravated Ear pain Eye inflammation Facial paralysis Neck pain

Symptomtext

Onset of Bell's Palsy; facial drooping on left side, sore behind left ear and down left side of neck Prednisone 20 mg 3 times per day for 7 days; Valacyclovir 1 g 3 times per day for 7 days; Eye is not as inflamed as it was previously; Patient and his wife feel that symptoms are drastically improving as of this report which is 4 days after the onset of the Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Patient has history of Bell's Palsy 5 years ago. No lab work or imaging tests were performed.
Aktuelle Erkrankungen: None
Vorgeschichte: Type II Diabetes Mellitus
Andere Medikamente: Lantis, Metformin, Jardia
Allergien: None
Vorherige Impfungen: -

VAERS 1028779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: MI
Alter: 25,0
Geschlecht: F
Eingang: 14.02.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Pain Pain in extremity Presyncope Pyrexia

Symptomtext

Arm soreness began 7PM on 2/11. Vasovagal syncope episode at 2:25AM on 2/12; triggered by combination of arm soreness, body aches, and low-grade fever. Senses returned back to normal within 5-10 minutes. Consistent low-grade fever from 1AM on 2/12 until 6PM on 2/13. Treated with 1000mg liquid acetaminophen every 6 hours per manufacturer instructions. Notable ache in legs (akin to Restless Leg Syndrome) from 3AM on 2/12 until around 9AM on 2/13. Urge to move calmed by acetaminophen. Highest recorded fever: 99.5?F at 9AM on 2/12. Fever subsided as of 6PM on 2/13.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Microgestin Fe 1/20 Tabs Sertraline 100mg
Allergien: None
Vorherige Impfungen: -

VAERS 1026374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 65,0
Geschlecht: F
Eingang: 12.02.2021
Impfdatum: 12.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Blood glucose decreased Dysarthria Lethargy Slow speech Syncope Unresponsive to stimuli

Symptomtext

Syncopal episode, unresponsive. Able to arouse but slow, garbled speech. Transferred from chair to cot. BP 128/68, HR 95. Lethargic, oriented x3/3. Called EMS. Blood glucose 49, glucagon, juice and crackers given. Refused transfer to ED. Boxed lunch provided. Emergency contact called. Refused ride home. Observed for total of 1hr15minutes. Awake, A&O x3/3, steady gait when sent home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood glucose 49.
Aktuelle Erkrankungen: COVID-19 one month prior
Vorgeschichte: Asthma, prediabetes
Andere Medikamente: Albuterol
Allergien: None
Vorherige Impfungen: -

VAERS 1020714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

schwer

Staat: OH
Alter: 25,0
Geschlecht: M
Eingang: 10.02.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
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 COVID-19 vaccination,. Clinic personal assessed and EMS on site. Patient refused transfer to medical facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: nka
Vorherige Impfungen: Patient states he always faints when he receives an injection.

VAERS 2718380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 85,0
Geschlecht: M
Eingang: 28.11.2023
Impfdatum: 16.02.2021
Beginn: 02.11.2021
Tage bis Beginn: 259,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 COVID-19 pneumonia Leukocytosis Oxygen saturation decreased Pneumonia SARS-CoV-2 test positive

Symptomtext

Patient was recently diagnosed with COVID no 19 1 week ago patient was being managed by PCP and was started on p.o. steroids and p.o. doxycycline however this morning patient was complaining of feeling weak EMS was called patient was found to be desaturating at 90% on room air and patient was immediately placed on non-rebreather mask with improvement saturations and brought into the ER. In ER patient noted to have leukocytosis and left lower lobe pneumonia COVID-19 came back positive and he is now being admitted for further management worker COVID-19 related pneumonia. During his hospitalization patient initially required 2 L nasal cannula oxygen however his down to room air now patient is being treated empirically with antibiotics for pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2714040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 87,0
Geschlecht: M
Eingang: 15.11.2023
Impfdatum: 12.02.2021
Beginn: 01.02.2022
Tage bis Beginn: 354,0
Dosis: 2
Route/Site: IM / UN

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

Angiogram peripheral COVID-19 COVID-19 pneumonia Dyspnoea Lethargy Limb injury Peripheral arterial occlusive disease Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient developed right foot wound and was referred to Dr. for peripheral arterial disease. Patient underwent right lower extremity angiogram 2 weeks ago and upon follow-up visit on February 1st, 2022 he was noted to be lethargic, febrile and having shortness of breath. Patient was subsequently sent to the ER for further evaluation. Patient had tested positive prior to admission for Covid-19 at NH. Patient was diagnosed with Covid-19 pneumonia. Patient was able to wean off oxygen. Patient received IV antibiotics. Patient was discharged back to SNU

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2713687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 80,0
Geschlecht: M
Eingang: 14.11.2023
Impfdatum: 13.02.2021
Beginn: 09.02.2022
Tage bis Beginn: 361,0
Dosis: 2
Route/Site: IM / UN

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

Atrial fibrillation COVID-19 Dyspnoea Pneumonia SARS-CoV-2 test positive

Symptomtext

Presented to the ED with SOB, found to be COVID positive, small PE, patient was started on empiric IV antibiotics, steroid therapy with Decadron, infection Disease consulted, he was also seen by Cardiology due to associated atrial fibrillation with RVR new onset, most likely triggered by pneumonia, patient was started on heparin anticoagulation and later switched to Eliquis with loading dose for 1 week then switch to 5 mg b.i.d.

Weitere VAERSDATA-Felder

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

VAERS 2689859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 03.10.2023
Impfdatum: 11.02.2021
Beginn: 29.12.2021
Tage bis Beginn: 321,0
Dosis: 2
Route/Site: IM / UN

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

Blood creatinine increased Catheter placement Chest X-ray abnormal Cough Dyspnoea Haemodialysis Intentional removal of drug delivery system by patient Mental status changes Serum ferritin increased White blood cell count increased

Symptomtext

Ferritin 1590; 1/4 On 1 L - but keeps pulling of NC dry cough. Cr 6.4. Last day of azithromycin; 1/5 comfortable on room air. Patient now agreed to dialysis 1/6 s/p HD. Daughter noted improving mental status and breathing. 1/7 breathing okay. Dry coughing. 1/8 no diarrhea, on room air. 1/9 continuing on room air, WBC elevated 13.7 - from line placement, chest x-ray better, blood culture today and monitor WBC. No phlebitis noted 1/10 in HD today. WBC 11.6. Remain on room air, past speech evaluation 1/11 stable on RA, WBC approaching Normal. D/c Airborne plus Isolation at this point. HD placement Pending approval .1/12 last day of Decadron. Daughters reporting back to baseline mental status

Weitere VAERSDATA-Felder

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

VAERS 2681259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267 -- --

moderat

Staat: FL
Alter: 90,0
Geschlecht: M
Eingang: 12.09.2023
Impfdatum: 26.09.2021
Beginn: 11.09.2023
Tage bis Beginn: 715,0
Dosis: 1
Route/Site: - / -

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

COVID-19 pneumonia Dyspnoea

Symptomtext

93-year-old gentleman who is being admitted for shortness of breaths secondary to COVID 19 pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, CVA and dyslipidemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2679577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 77,0
Geschlecht: F
Eingang: 06.09.2023
Impfdatum: 11.02.2021
Beginn: 20.01.2022
Tage bis Beginn: 343,0
Dosis: 2
Route/Site: IM / UN

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

Chest X-ray abnormal Cough Dyspnoea Lung infiltration

Symptomtext

Presented with SOB/cough; CXR: Patchy infiltrates within the lung bases bilaterally; Tx with zithromax, rocephin, remdesivir, decadron; initially increased FIO2 to 6LPM but back down to 3 LPM at discharge;

Weitere VAERSDATA-Felder

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

VAERS 2679176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 05.09.2023
Impfdatum: 18.02.2021
Beginn: 25.01.2022
Tage bis Beginn: 341,0
Dosis: 2
Route/Site: IM / UN

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

Chest X-ray abnormal Cough Dyspnoea Haemoptysis Pleural effusion Pyrexia

Symptomtext

Presented with hemoptysis/dyspnea, fever, cough; CXR: bil pleural effusions TX: Lasix, Steroids, doxycycline, zinc,

Weitere VAERSDATA-Felder

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

VAERS 2677482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 86,0
Geschlecht: F
Eingang: 29.08.2023
Impfdatum: 13.02.2021
Beginn: 30.01.2022
Tage bis Beginn: 351,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 COVID-19 pneumonia Hypotension Hypoxia

Symptomtext

Arrived w/ known COVID infection, hypoxia and hypotension. Fully vaccinated plus booster. Admitted for COVID pna. Received O2, zithromax, steroids, Merrem, Rocephin, vit c. DC to rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2673659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 16.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Chest pain Hypothyroidism Infection Metabolic syndrome Painful respiration Palpitations Peripheral venous disease Postural orthostatic tachycardia syndrome

Symptomtext

Hypothyroidism; Palpitations; Anterior Wall chest Pain with respiration; Anterior Wall chest Pain with respiration; Chronic peripheral venous insufficiency; Metabolic syndrome; Pots; Late effect of infectious disease; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Feb2021 as dose 2, single (Lot number: EL9267) at the age of 53 years, in arm right for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Yes" (unspecified if ongoing), notes: Known allergies: Yes. Concomitant medication(s) included: SERTRALINE; ZOLOFT. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: Unknown. EL 9262, Location of injection: Arm Left), administration date: 26Jan2021, when the patient was 52-year-old, for Covid-19 immunization. The following information was reported: CHEST PAIN (disability), PAINFUL RESPIRATION (disability) all with onset 17Feb2021 at 20:00, outcome "not recovered" and all described as "Anterior Wall chest Pain with respiration"; PERIPHERAL VENOUS DISEASE (disability) with onset 17Feb2021 at 20:00, outcome "not recovered", described as "Chronic peripheral venous insufficiency"; HYPOTHYROIDISM (disability, medically significant) with onset 17Feb2021 at 20:00, outcome "not recovered"; INFECTION (disability) with onset 17Feb2021 at 20:00, outcome "not recovered", described as "Late effect of infectious disease"; METABOLIC SYNDROME (disability) with onset 17Feb2021 at 20:00, outcome "not recovered"; PALPITATIONS (disability) with onset 17Feb2021 at 20:00, outcome "not recovered"; POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (disability) with onset 17Feb2021 at 20:00, outcome "not recovered", described as "Pots". The events "hypothyroidism", "palpitations", "anterior wall chest pain with respiration", "chronic peripheral venous insufficiency", "metabolic syndrome", "pots" and "late effect of infectious disease" required physician office visit. It was reported that AE resulted in Doctor or Other healthcare professional office/clinic visit, Disability or permanent damage. Therapeutic measures were not taken as a result of hypothyroidism, palpitations, chest pain, painful respiration, peripheral venous disease, metabolic syndrome, postural orthostatic tachycardia syndrome, infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Known allergies: Yes)
Andere Medikamente: SERTRALINE; ZOLOFT
Allergien: -
Vorherige Impfungen: -

VAERS 2670894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 72,0
Geschlecht: M
Eingang: 14.08.2023
Impfdatum: 28.09.2021
Beginn: 01.08.2023
Tage bis Beginn: 672,0
Dosis: 1
Route/Site: - / -

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

Asthenia COVID-19 Cough Dyspnoea Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

presents to the hospital with generalized weakness and shortness of breath. Patient also tested positive for COVID-19. No hypoxemia present. No sepsis present. C/o some shortness of breath, generalized body aches, subjective fever on admission. Endorses cough and sore throat. Saturating well on room air at this time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: depression, fatty liver, hyperlipidemia, hypertension, TIA, complete heart block presents
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2670097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 75,0
Geschlecht: M
Eingang: 11.08.2023
Impfdatum: 28.09.2021
Beginn: 15.07.2023
Tage bis Beginn: 655,0
Dosis: 1
Route/Site: - / -

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

Blood alkaline phosphatase increased Blood lactic acid COVID-19 Chest X-ray abnormal Cough Dyspnoea Fibrin D dimer increased Hypoxia Inflammatory marker increased Legionella test Leukocytosis Lung opacity SARS-CoV-2 test positive Streptococcus test negative Systemic inflammatory response syndrome Tachypnoea Troponin increased

Symptomtext

Presents hospital with worsening cough and shortness of breath In the emergency department patient was found (+) sirs (tachypnea; leukocytosis -10.75); acute hypoxia saturating well on 2 L nasal cannula; lactic acid (1.6); elevated alkaline phosphatase (217); elevated troponin (23); elevated D-dimer (2.37); elevated acute phase reactant; (-) Legionella and strep; respiratory PCR shows (+) COVID-19; chest x-ray independently reviewed and patient has opacities diffused in both lungs concerning for atypical pneumonia COVID-19 pneumonia patient was initially treated with remdesivir, IV antibiotics, which he completed a course of ceftriaxone and discontinued off of further antibiotics per ID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -hypertension -GERD -CKD 3 -HLD -thyroid nodule -overweight -nicotine dependence -multiple myeloma-on chemotherapy -im
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2668490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 74,0
Geschlecht: M
Eingang: 09.08.2023
Impfdatum: 11.02.2021
Beginn: 06.01.2022
Tage bis Beginn: 329,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 pneumonia

Symptomtext

Admitted for pna d/t COVID-19; tx w/IV dexamethasone, zinc, steroid and O2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2623964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 21.09.2022
Beginn: 26.04.2023
Tage bis Beginn: 217,0
Dosis: 2
Route/Site: - / -

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

Anticoagulant therapy Asthenia Atrial fibrillation Bladder mass Blood creatinine increased CHA2DS2-VASc-score COVID-19 Computerised tomogram head normal Condition aggravated Culture urine positive Escherichia test positive Fall Gout Heart rate increased Infection Renal ischaemia SARS-CoV-2 test positive Sepsis

Symptomtext

Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) This is a 86 yr old male with PMHx of CKD-3, gout, persistent Afib, HTN, HLD and BPH who presented for generalized weakness and falls. CT head was negative. UA showed evidence of infection and Ucx grew 2 strains of E coli so he was started on ceftriaxone. He had a CT urogram which showed 2 new bladder masses. Urology was consulted and said workup can be done outpt. He follows with Urology at other facility and he will decide if he wants to follow up with them or stay here for the workup. During his stay he developed a gout flare and was started on a steroid taper along with colchicine. His heart rate was elevated so Toprol dose was increased. PT/OT recommended SNF. Pt was stable on discharge. He will be discharged. Sepsis 2/2 UTI - elevated wbc and HR - sepsis resolved - Ucx growing E coli 2 strains - continue cefdinir 300mg BID for 3 more days New bladder masses Hx of bladder cancer - s/p TURBT - CT urogram showed 2 new bladder masses - follow up with Urology outpt for workup Elevated Cr on CKD-3 - baseline Cr 1.4 - likely due to poor perfusion in setting of infection - resolved Gout flare - evidence of polyarticular disease with tophi - continue prednisone 40mg for 3 days, then 30mg for 3 days then 20mg for 3 days - start colchicine 0.6mg every other day - start allopurinol 100mg daily on 5/6/23 - referral placed to Rheumatology Afib with RVR - CHADS-VASc- 3 - continue Eliquis 2.5mg BID - increased Toprol to 100mg daily, monitor HR and may need dose reduced HTN - continue HCTZ 12.5mg daily, lisinopril 10mg nighlty and Toprol HLD - continue atorvastatin 20mg daily BPH - s/p HoLEP Issues Requiring Follow Up: (Who, what, when, and how communicated?) Follow up with PCP and Urology. Referral placed to Rheumatology. Complete 3 more days of antibiotics. Complete steroid taper. Start colchicine and allopurinol. Toprol dose increased, monitor HR for dose adjustments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: COVID positive PCR 4/13/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2590292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 02.03.2023
Impfdatum: 02.09.2021
Beginn: 15.02.2023
Tage bis Beginn: 531,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/15/23 presents to ED for "shortness of breath". PMHx of "CAD s/p CABG, atrial fibrillation on AC, SSS s/p PPM, HTN, HLD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/15/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2586340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 23.02.2023
Impfdatum: 22.10.2021
Beginn: 04.01.2023
Tage bis Beginn: 439,0
Dosis: 1
Route/Site: - / -

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

Abdominal pain COVID-19 Computerised tomogram abdomen abnormal Condition aggravated Constipation Enema administration Explorative laparotomy Fluid intake reduced Internal hernia Intestinal strangulation Mental status changes Nausea Pain Physical deconditioning SARS-CoV-2 test positive Small intestinal anastomosis Small intestinal resection Urinary tract infection

Symptomtext

"Patient with history of COVID vaccines who was hospitalized and had a COVID detected PCR during stay. Provider d/c note: ""82 y/o female patient with PMH significant for HTN, hyperlipidemia, Sjogren's syndrome, malignant lung ca, CVA, pessary placement, recurrent UTI, who presents with complaint of moderate, constant, non-radiating, dull abdominal pain associated with nausea and vomiting which started this morning. She vomited once since the onset of pain. Patient denies any food triggers but admits to constipation since midnight last night. Patient's spouse at bedside who states that he tried to treat the pain with otc medications without relief. He also tried to use fleet enema for constipation with no relief either. Denies fever, chills, chest pain, shortness of breath, melena, dysuria, urinary urgency, low back pain, loss of appetite, weakness, dizziness, headaches. Admits to lack of fluid intake. Spouse also reports patient's recurrent UTI with no urinary symptoms but presence of altered mental status. Patient is a, a & o x 3, coherent, in no acute distress. Still complains of mild generalized abdominal pain but denies nausea or vomiting currently. CT showed suspicion for a possible strangulated hernia in addition to possible ischemic colitis and she was taken to the OR for exploratory laparotomy. She underwent an open small bowel resection with anastomosis secondary to internal hernia containing strangulated small bowel. She tolerated surgery and recovery well receiving antibiotics for both this and a UTI. She did well with rehab initially and gradual increase in food and was recommended to return home however at the time of discharge was incidentally found to be covid positive. Patient sustained deconditioning and therapy recommendations changed to Pine Ridge however patient consistently worked with PT/OT during isolation period and was ultimately strong enough to return home. She will follow up with Surgery in the outpatient setting. She will also receive PT/OT and home care at home."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 19,0
Labordaten: Covid PCR detected on 01/13/2023.
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Mild mitral and aortic regurgitation Hypertension, essential, benign High cholesterol Respiratory Sleep apnea Dyspnea on exertion Malignant neoplasm of lower lobe of right lung (HCC) Urinary Urge incontinence Renal insufficiency Other Enlarged lymph nodes History of primary malignant neoplasm of lung Status post bilateral minimally invasive L3-4 decompressions of stenosis/Left L3-4 far lateral minimally invasive diskectomy on 11/2/15 Unsteady gait History of lung cancer Hemiplegia and hemiparesis following cerebral infarction affecting right dominant side (HCC) Insomnia Benign essential tremor Sjogren's syndrome (*) Hyperproteinemia Metabolic encephalopathy Weakness History of CVA (cerebrovascular accident
Andere Medikamente: artificial tears,hypromellose, (GENTEAL) 0.3 % drop Place 1 drop into both eyes 4 (four) times daily as needed (dry eyes). aspirin 81 mg EC tablet Take 1 tablet by mouth daily. atorvastatin (LIPITOR) 40 mg tablet Take 1 tablet by mouth da
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2566839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 60,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 03.03.2022
Beginn: 26.12.2022
Tage bis Beginn: 298,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

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

Weitere VAERSDATA-Felder

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

VAERS 2560337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 9267

moderat

Staat: AZ
Alter: 59,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 26.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest pain Computerised tomogram Cough Ear discomfort Hyperhidrosis Laboratory test Neck pain Pain Pyrexia

Symptomtext

Sweats, cough, fever, chest pain after 10 days, the pain travelled from my chest to the neck, to the left head by the left ear, with feeling of pressure behind the ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EQG, CT scan, and blood work
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: B-Complex, Calcium, Vit D., Turmeric, Brain Power
Allergien: Tetracycline and wheat
Vorherige Impfungen: on my second shot, had fever, sweats, and cough for two weeks.

VAERS 2558700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 14.02.2021
Beginn: 16.12.2022
Tage bis Beginn: 670,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

12/16/22 presents to ED for "chest pain". PMHx of "CAD s/p CABG, bradycardia s/p PPM, HTN, dyslipidemia, hypertrophic cardiomyopathy, CVA, and rheumatoid arthritis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/16/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 22.01.2021
Beginn: 13.12.2022
Tage bis Beginn: 690,0
Dosis: 2
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Tachycardia

Symptomtext

12/13/22 presents to ED for "tachycardia". PMHx of "CLL, history of breast cancer s/p mastectomy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: 12/13/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 22.01.2021
Beginn: 28.11.2022
Tage bis Beginn: 675,0
Dosis: 2
Route/Site: - / -

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

Dyspnoea

Symptomtext

11/28/22 presents to ED for "shortness of breath". PMHx of "A. fib, breast cancer, lung cancer, hypothyroidism, GERD"

Weitere VAERSDATA-Felder

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

VAERS 2548821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 03.03.2021
Beginn: 02.01.2023
Tage bis Beginn: 670,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Dyspnoea Pneumonia Respiratory symptom

Symptomtext

Pt has had increased difficulty breathing for 3 days and is on home oxygen. She has COPD and has been giving herself 4 nebulizer treatments per day without improvement. She has had upper respiratory symptoms. She is found to have COVID-19 and pneumonia.

Weitere VAERSDATA-Felder

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

VAERS 1944302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 19.01.2021
Beginn: 04.12.2021
Tage bis Beginn: 319,0
Dosis: 2
Route/Site: - / -

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

Dyspnoea Fatigue

Symptomtext

12/04/21 presents to ED for "sob and fatigue". PMHx of "renal transplant, CAD, AFib"

Weitere VAERSDATA-Felder

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

VAERS 1944302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 19.01.2021
Beginn: 04.12.2021
Tage bis Beginn: 319,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Fatigue

Symptomtext

12/04/21 presents to ED for "sob and fatigue". PMHx of "renal transplant, CAD, AFib"

Weitere VAERSDATA-Felder

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

VAERS 1944302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 19.01.2021
Beginn: 04.12.2021
Tage bis Beginn: 319,0
Dosis: UNK
Route/Site: - / -

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

Dyspnoea Fatigue

Symptomtext

12/04/21 presents to ED for "sob and fatigue". PMHx of "renal transplant, CAD, AFib"

Weitere VAERSDATA-Felder

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

VAERS 2539114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 20.01.2021
Beginn: 07.10.2022
Tage bis Beginn: 625,0
Dosis: 2
Route/Site: - / -

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

Atelectasis COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Gamma radiation therapy to lung Lung consolidation Pneumonia SARS-CoV-2 test positive White blood cell count increased

Symptomtext

A 81y.o. female with history of non-small cell lung cancer diagnosed in 8/20/2021-s/p radiation therapy, gamma knife on 6/11/2021, completed 5 fractions of palliative radiation therapy on 714 2 right chest wall nodule currently on Keytruda for every 3 weeks, COPD, hyperlipidemia, hypertension. Patient presented with cough, shortness of breath.Labs showed white count of 24.3. Chest x-ray showed large area of right upper lobe consolidation likely combination of atelectasis and pneumonia COVID-19 was negative was started on vancomycin and cefepime, azithromycin pulmonary was consulted started on prednisone for COPD exacerbation..patient completed antibiotics, steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 10/16 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2537327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 16.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain upper Arthralgia Asthenia Blood test Chest pain Condition aggravated Dysphagia Dyspnoea Fatigue Malaise Migraine Movement disorder Muscle disorder Musculoskeletal chest pain Musculoskeletal stiffness Myalgia Neck pain Pain

Symptomtext

After my second dose, within 8 hours I had muscle construction throughout my body, fever, severe migraine, extreme fatigue. Within a few days I could not move my head, lymph nodes in my neck, trouble from pain lifting my head. I was in bed 13 days and over three months I was having chronic fatigue, rashes, muscle pain from my hips to my feet with stiffness, difficulty breathing, pain in my thorax, heart racing, vertigo. Four months later rt upper quadrant pain, crossing over under my ribs. Difficulty swallowing pain in my neck. I spoke with a different doctor office 1 month post second vaccine was told to take Motrin and warm packs and that was all. I?ve never regained my energy and still have body stiffness and arthritis type symptoms and overall unwell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None doctors were not believing me. Now have a doctor that told me no more vaccines after this doctor, 2nd. Doctor did blood work.
Aktuelle Erkrankungen: Fibromyalgia, migrain disorder, a previous flu vaccine injury
Vorgeschichte: Fibromyalgia, migraine disorder, flu vaccine injury
Andere Medikamente: Topomax, Wellbutrin, sertaline, multivitamin, D3
Allergien: Gluten, thermisol, pcn, clindamycin, lorcet
Vorherige Impfungen: Influenza 2011

VAERS 2511881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 23.02.2021
Beginn: 02.11.2022
Tage bis Beginn: 617,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt to ED 11/2 for shortness of breath. Pt COVID+ 11/2. 11/3 started on remdesivir & decadron. 11/4 pt left hospital, discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: COPD with acute exacerbation (CMS/HCC) ...
Andere Medikamente: aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) ...
Allergien: None
Vorherige Impfungen: -

VAERS 2511881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 23.02.2021
Beginn: 02.11.2022
Tage bis Beginn: 617,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt to ED 11/2 for shortness of breath. Pt COVID+ 11/2. 11/3 started on remdesivir & decadron. 11/4 pt left hospital, discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: COPD with acute exacerbation (CMS/HCC) ...
Andere Medikamente: aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) ...
Allergien: None
Vorherige Impfungen: -

VAERS 2511670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 11.11.2021
Beginn: 27.10.2022
Tage bis Beginn: 350,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Dyspnoea Hypervolaemia Pneumonia bacterial Renal replacement therapy SARS-CoV-2 test positive Sepsis

Symptomtext

Patient with 3 COVID vaccines who admitted with positive COVID PCR and dypsnea. Provider d/c note: "Brief Summary of Hospital Stay: Presented with acute fluid overload after missing dialysis and was found to have acute Covid 19 with suspected sepsis due to bacterial pneumonia. He required low flow oxygen initally but was able to return to room air. He was treated with Augmentin and doxycyline empirically until 11/3. Patient had profound weakness and was not able to return home. Needed subacute rehab in additon to his ongoing renal replacement therapy 3x weekly. Waiting for placement was the main issue for the past 13 days of admit."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 19,0
Labordaten: COVID Detected PCR on 10/27/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular HTN (hypertension), benign AVF (arteriovenous fistula) Hyperlipidemia Retinal vein occlusion Orthostatic hypotension Essential hypertension with goal blood pressure less than 130/80 Digestive Diverticulosis Endocrine Secondary renal hyperparathyroidism Type 2 diabetes mellitus with diabetic neuropathy, without long-term current use of insulin Diabetic neuropathy Diabetic retinopathy Musculoskeletal Diaphragmatic eventration Respiratory AR (allergic rhinitis) Pneumonia Urinary ESRD on hemodialysis Renal mass, right ESRD (end stage renal disease) Clear cell renal cell carcinoma, right Clear cell renal cell carcinoma, left Other Proteinuria BPH Elevated PSA ED Vitamin D deficiency Elevated alkaline phosphatase level Overweight (BMI 25.0-29.9) History of nephrectomy Polyarthralgia Gout of multiple sites due to renal impairment Dizziness Abnormal stress test Other constipation Asthenia Dyslipidemia Presence of artificial right eye COVID-19
Andere Medikamente: -
Allergien: Ace Inhibitors
Vorherige Impfungen: -

VAERS 2507297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 37,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 02.02.2021
Beginn: 19.10.2022
Tage bis Beginn: 624,0
Dosis: 2
Route/Site: IM / UN

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

Bed rest COVID-19 Endotracheal intubation Hypoaesthesia Hypotension Lethargy Paraesthesia SARS-CoV-2 test positive

Symptomtext

Pt to ED 10/18 for numbness and tingling in R leg. Pt COVID+ 10/19. 10/20 pt to complete 3 d course of remdesivir. 10/21 pt is intubated, hypotensive. 10/23 Pt lethargic, oriented x4. 10/27 Pt is alert and oriented x4; able to follow commands, on RA with no respiratory difficulties noted. 10/29 pt on bedrest, aox4, room air. 10/30 Pt A&Ox4 and VSS on room air. Pt discharged 11/1.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 15,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Hepatic steatosis ...
Andere Medikamente: amLODIPine (NORVASC) 10 MG PO Tab apixaban ...
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2507258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 24.02.2021
Beginn: 19.09.2022
Tage bis Beginn: 572,0
Dosis: 1
Route/Site: - / -

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

Anxiety COVID-19 Confusional state Dyspnoea SARS-CoV-2 test positive

Symptomtext

09/19/22 presents to ED for "anxiety, confusion, SOB". PMHx of "anxiety, depression, and a colon cancer treated in 1998 with surgery and chemotherapy, and recently diagnosed with breast CA on Letrozole"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/20/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 24.09.2021
Beginn: 13.09.2022
Tage bis Beginn: 354,0
Dosis: 1
Route/Site: - / -

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

Anal incontinence Asthenia Back pain Blood gases Blood magnesium decreased COVID-19 Chest X-ray normal Cough Echocardiogram normal Erythema Foot fracture Headache Hypocapnia Hypoxia Mobility decreased Nasal congestion Nausea Pyrexia

Symptomtext

"Patient with 3 COVID vaccines, but not up to date, who admitted to hospital with complications of COVID and positive PCR test. Provider d/c note: ""Patient is a 77 year-old male with a history of DM2 on an insulin pump, HTN, and dyslipidemia who presented to the ED on 9/13/22 with a 2-3 day history of worsening weakness, nasal congestion, cough, and fever. History is obtained from the patient and his daughter, who report that he last felt well about 3 days prior to admission, when he developed nasal congestion. The next day he noted weakness which progressively became worse until he could not get out of his chair, prompting him to call EMS. On admission he endorsed frontal HA and nausea without vomiting. No chest pain, diarrhea, abdominal pain, new back pain (stable back pain from osteoarthritis), dysuria, or hematuria. He was in a motorcycle accident at the end of July which resulted in a fracture to his left foot and a large abrasion over his left shin. He has been following with ortho and undergone 2 courses of antibiotics and reports that the fracture has healed, but his daughter noticed increasing redness of his left foot over the 2 days prior to admission. After he was admitted to the floor he had 2 episodes of emesis and fecal incontinence. Required increased O2 up to 6L NC. ABG revealed hypoxia and hypocapnia. No significant change on CXR. He was treated with IV antibiotics and steroids and he elected to discontinue his insulin pump while inpatient. His blood glucose was managed with accuchecks and insulin. He was seen by the physical therapy team who assessed that he was ready for discharge. He experienced a run of 19 v tach. An echocardiogram was ordered which showed no acute abnormalities. His magnesium was just below the normal range, and was repleted with IV supplementation. His clinical status improved and he was deemed stable for discharge on 9/18/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 7,0
Labordaten: COVID Detected PCR on 9/13/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension; Ventricular tachycardia; Endocrine; Type 1 diabetes mellitus with hyperglycemia (*); Respiratory; Sinobronchitis; Acute respiratory failure due to COVID-19 (*); Urinary; Right ureteral stone; Other; Primary osteoarthritis of right knee; History of total knee arthroplasty, left; Insulin pump in place; Sprain of medial collateral ligament of right knee; Closed nondisplaced fracture of cuboid of left foot; Closed nondisplaced fracture of second metatarsal bone of left foot; Left leg cellulitis.
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2460589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 15.12.2021
Beginn: 11.09.2022
Tage bis Beginn: 270,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain upper Aortic valve incompetence Atrial fibrillation Blood sodium decreased Bradycardia COVID-19 Chest pain Condition aggravated Decreased appetite Echocardiogram abnormal Ejection fraction normal Electrocardiogram QT prolonged Hypokalaemia Hypomagnesaemia Hyponatraemia Hypophagia Hypophosphataemia Nausea

Symptomtext

"Patient with 3 COVID vaccines who admitted to hospital with complications from COVID and COVID detected PCR. Provider d/c note: ""85-year-old female presenting to the emergency department with epigastric pain that radiates to her sternum. This has been going on for 2 days. She is COVID positive via home test and has been started on Paxlovid. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) See below note for details re: this current hospitalization. Hospital Course: No notes on file These were her acute medical issues addressed: Covid infection - 19 infection tested 9/11/22 - Holding paxlovid - No resp complaints, no hypoxia. - Vaccinated x 3 doses. Last booster dose 12/2021 - 10 days out from her first symptoms at discharge. A Fib with slow ventricular response, rates in 40-60'ss Hx of HTN Hx of PVC Diastolic heart failure Prolonged QTc - Echo 4/25/22: EF 70%, trace AR, mild - mod TR, RVSP 42mmHg - Held home Norvasc, chlorthalidone, Toprol, Valsartan given bradycardia and low normal BP on admission. - resume Norvasc, ARB at discharge. - continue to hold Chlorthalidone at DC. DC Toprol due to bradycardia. - Consult cardiology: Seen by Dr and Dr. She has declined PPM placement at this time. - on Pradaxa for chronic AF. Anorexia, nausea, resolved - General diet - Zofran prn, consider compazine if QTc prolonged. - may have contributed to hyponatremia. Hyponatremia - Sodium 108 on admission, corrected with IVF and salt tablets - Poor PO intake (COVID) +/- chlorthalidone use likely the main mechanism. Also may have had a component of SIADH, given nausea the preceding days. - no encephalopathy. Mentation maintained. -- IV NS + NaCl tabs. -- Na 129 at discharge. Hypomagnesemia Hypokalemic Hypophosphatemia - replace as needed DC home today with Home Health RN Will hold BB and Chlorthalidone at discharge."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 7,0
Labordaten: COVID Detected PCR on 9/11/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Varicose veins PVC (premature ventricular contraction) Pure hypercholesterolemia Hypertension Atrial fibrillation (*) AI (aortic insufficiency) MR (mitral regurgitation) Chronic diastolic heart failure (*) Chronic atrial fibrillation (*) Coronary artery disease of native artery of native heart with stable angina pectoris (*) Digestive Cholelithiasis Nausea and vomiting Psychological Episode of anxiety Urinary Urinary tract infection with hematuria Other CTS (carpal tunnel syndrome) Sensorineural hearing loss, asymmetrical Subjective tinnitus Dyslipidemia Hyponatremia
Andere Medikamente: -
Allergien: Readi-cat, Bactrim Cephalosporins, Dtp Toxoids Adsorbed, Penicillins, Pravastatin, Tetanus, Cephalexin, Sulfa
Vorherige Impfungen: -

VAERS 2459651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 87,0
Geschlecht: M
Eingang: 24.09.2022
Impfdatum: 15.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / RA

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

Abdominal pain Body temperature Chest pain Chills Pyrexia

Symptomtext

temperature of a 102 that got up too; he had very bad chills; aches in his chest and abdomen; aches in his chest and abdomen; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An 87-year-old male patient received BNT162b2 (BNT162B2), on 15Sep2022 as dose number unknown (booster), single (Lot number: EL9267) at the age of 87 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: DONEPEZIL; FAMOTIDINE; GABAPENTIN; ATORVASTATIN; HYDROCHLOROTHIAZIDE; TRAZODONE. Vaccination history included: Covid-19 vaccine (Primary immunization complete, Manufacturer unknown), for Covid-19 immunization. The following information was reported: CHEST PAIN (non-serious), ABDOMINAL PAIN (non-serious) all with onset 2022, outcome "recovered" and all described as "aches in his chest and abdomen"; CHILLS (non-serious) with onset 2022, outcome "recovered", described as "he had very bad chills"; PYREXIA (non-serious) with onset 2022, outcome "recovered", described as "temperature of a 102 that got up too". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, chills, chest pain, abdominal pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: temperature; Result Unstructured Data: Test Result:102; Comments: he has a temperature of a 102 that got up too
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: DONEPEZIL; FAMOTIDINE; GABAPENTIN; ATORVASTATIN; HYDROCHLOROTHIAZIDE; TRAZODONE
Allergien: -
Vorherige Impfungen: -

VAERS 2426598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 28.09.2021
Beginn: 29.07.2022
Tage bis Beginn: 304,0
Dosis: 1
Route/Site: - / -

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

Bladder outlet obstruction Bladder scan COVID-19 COVID-19 pneumonia Chronic obstructive pulmonary disease Cough Dyspnoea Hypoxia SARS-CoV-2 test positive Sputum culture Transaminases increased Urogram abnormal

Symptomtext

Patient with COVID vaccinations who admitted with hypoxia and complications of COVID. Provider d/c note: "Patient is a 73-year-old male with a past medical history Myofibrillar myopathy type 1-type of muscular dystrophy, history of abnormal stress test 2003 who presents with cough, shortness of breath. Diagnosed with COVID pneumonia, monitor for signs of superimposed bacterial pneumonia, hold antibiotics at this time. Sputum culture shows normal oral flora.. Continue dexamethasone x 10 days. Patient is no longer hypoxic so remdesivir stopped, consider restarting if patient becomes hypoxic again. CT urogram negative for hydronephrosis but shows some chronic outlet obstruction. Start Flomax, bladder scans. Chronic obstructive pulmonary disease changes also noted. Elevated transaminases, possibly secondary to remdesivir? Improving. Consider outpatient CMP." Discharged to acute rehab unit for physical therapy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: COVID detected PCR on 07/29/22
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes mellitus without complication (*) Anxiety, generalized HTN (hypertension) Hyperlipidemia Muscular dystrophy (*)
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1692772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 01.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: SYR / RA

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

Asthenia Balance disorder Dizziness Electronystagmogram Gait disturbance Chills Lethargy Pyrexia Vertigo Headache Hemiparesis Impaired driving ability Laboratory test abnormal Loss of personal independence in daily activities Mobility decreased Nausea Nervous system disorder

Symptomtext

I woke up with vertigo. Unable to leave my bed for many days. I went to one ENT for treatments for about 2 months. I was prescribed Valium so I could function. I then went to another ENT and had many tests done. I then went to a Sensory Occupational Therapist. This started April 2021 through July 2022. I could open my eyes, I was dizzy, nauseous, walked into furniture and walls. Could not drive my car. Could not take a walk because I felt as if I was going to fall off the sidewalk. All physical activities stopped. Debilitating! Never had headaches or dizziness until this vaccine entered my system.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Videonystagmography-I lost 83% of my balance on my right side. Positive Fukuyama stepping test (movement to the right) indicates abnormality. Positive vertebral artery test with head left. The left-beating nystagmus observed during the up gaze is consistent with a central nervous system abnormality. The left-beating nystagmus observed in supine, lateral left and lateral right positions is a non localizing finding. The caloric unilateral weakness on the right of 83% indicates the presence of a right peripheral (nerve or end-organ) vestibular lesion. The 39% directional preponderance to the left is consistent with aforementioned left-beating observed throughout testing and is secondary to the right unilateral weakness.
Aktuelle Erkrankungen: No illnesses-I was fine until I got the vaccination.
Vorgeschichte: N/A
Andere Medikamente: 30 mg Armour Thyroid 5mg Buspirone Gummy vitamins
Allergien: Shellfish Sulfa Cipro Antibiotics SHT-3 Penicillin-body rash
Vorherige Impfungen: -

VAERS 2399365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 01.12.2021
Beginn: 29.07.2022
Tage bis Beginn: 240,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Ageusia Asthenia COVID-19 Chills Diarrhoea Dyspnoea Fatigue Headache Myalgia Nausea Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Patient admitted to hospital 7/29/2022 on Observation Status with complaints of weakness, increased fatigue, subjective fever, chills, chronic n/v, diarrhea, lack of taste, epigastric pain, sob, myalgias, HA, sore throat. Patient was tested for COVID-19 and was positive on 7/29/2022.

Weitere VAERSDATA-Felder

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

VAERS 2322136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 89,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 10.05.2022
Beginn: 06.06.2022
Tage bis Beginn: 27,0
Dosis: 2
Route/Site: UN / UN

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

Atrial fibrillation COVID-19 Cardiomyopathy Chest X-ray abnormal Dyspnoea Electrocardiogram Laboratory test Palpitations Pleural effusion Troponin increased

Symptomtext

Patient was seen in ED due palpitations and dyspnea. She was recently diagnosed with COVID-19. She was COVID vaccinated and boosted. She presented with A. fib with RVR. Troponin was elevated at 116 and suspected to be myocardial strain from the underlying atrial fibrillation with rapid ventricular response. Diltiazem bolus and drip administered. chest x-ray note s small bilateral pleural effusions. Patient was admitted to hospital for further evaluation and treatment The Health department has no further information. No known outcome. Contact Provider for any additional information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Lab work ECG XRay chest
Aktuelle Erkrankungen: unknown
Vorgeschichte: benign head tremor, anemia, hypertension, hyponatremia, hypomagnesemia,
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2321955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 09.02.2021
Beginn: 09.05.2022
Tage bis Beginn: 454,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Chest pain Cough Hypertension Nasopharyngitis Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Pt to ED 5/9 c/o chest pain and hypertension. Pt states she was on antibiotics last week for a "cold", only c/o cough and congestion currently. COVID test positive. Pt with no resp distress, no audible wheezes, no acute distress, A&OX3. Pt discharged home with self care no apparent distress noted 5/9.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: pneumonia, Melena Diabetes ... Type 2 diabetes mellitus Spondylosis Spondylolisthesis Hypertension Meralgia paresthetica of left side Postlaminectomy syndrome of lumbosacral region Chronic lymphocytic leukemia, Rai stage I Anemia HTN (hypertension) Hyperlipidemia Acute kidney injury Hypogammaglobulinemia Obesity (BMI 30-39.9) COVID-19 virus infection
Andere Medikamente: Accu-Chek Guide INVITRO test strip Accu-Chek Softclix Lancets XX Misc acetaminophen (TYLENOL) 325 MG PO Tab albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln BD Pen Needle Nano 2nd Gen 32G X 4 MM XX Misc Bloo
Allergien: Iodinated diagnostic agents, iodine, shellfish
Vorherige Impfungen: -

VAERS 2318788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 23.02.2021
Beginn: 16.03.2022
Tage bis Beginn: 386,0
Dosis: 1
Route/Site: IM / UN

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

COVID-19 Chest discomfort Chest pain Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt to ED 3/16 c/o cough, chest pain, shortness of breath for the past week. COVID+ upon adm 3/16. Pt A&Ox4, speech is clear, respirations are regular and unlabored, skin is warm and dry. Pt reported chest heaviness, denied need for pain intervention. Pt on room air. 3/17 Pt continued complaint of chest pain that dissipates over time. 3/18 pt still on room air, expressed no further needs. Pt discharged to home 3/18.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Other chest pain Chest pain Coronary artery disease of bypass graft of native heart with stable angina pectoris
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln amLODIPine (NORVASC) 2.5 MG PO Tab apixaban (ELIQUIS) 5 MG PO Tab aspirin 81 MG PO Chew Tab atenolol (TENORMIN) 25 MG PO Tab atorvastatin (LIPITOR) 40 MG PO T
Allergien: Bupivacaine-lidocaine [Lidocaine Hcl-bupivacaine Hcl]Anaphylaxis/Shock CephalexinHives Contrast [Iodinated Diagnostic Agents]Swelling, lips/throat/tongue Fish Oil Hives IodineSwelling, lips/throat/tongue LidocaineAnaphylaxis/Shock Novocain [Procaine]Anaphylaxis/Shock PenicillinsHives Sulfa AntibioticsSwelling, lips/throat/tongue Sulfamethoxazole-trimethoprimSwelling, lips/throat/tongue ErythromycinUnable to specify DexamethasoneUnable to specify DicyclomineUnable to specify EzetimibeUnable to specify NiacinUnable to specify ProtamineUnable to specify PseudoephedrineUnable to specify TrimethobenzamideUnable
Vorherige Impfungen: -

VAERS 2315384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 10.06.2022
Impfdatum: 10.02.2021
Beginn: 10.05.2022
Tage bis Beginn: 454,0
Dosis: 2
Route/Site: - / -

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

Anxiety COVID-19 Chest X-ray normal Chest pain Chills Cough Electrocardiogram abnormal Fatigue SARS-CoV-2 test positive Sinus bradycardia

Symptomtext

Patient is fully vaccinated and boosted twice. COVID positive on 5/10/2022.72-year-old male who presents complaining of chest pain that is since resolved. Patient tested positive for COVID earlier today and was getting his infusion at Dr's office. States that he thinks that his chest pain was brought on by anxiety. States that he is multiple needles and developed chest pain. Symptoms resolved. He was given aspirin in route. He does have a history of CABG. Positive for chills, fatigue, cough and chest pain. BP 153/85 | Pulse 60 | Temp 98.8 ?F (37.1 ?C) | Resp 18 | Ht 198.1 cm (6' 6") | Wt 99.8 kg (220 lb) | SpO2 97% EKG: sinus bradycardia, no signs of ischemia and no infarction. Medications: fluid and Nitro. CXR: acutely unremarkable radiograph of the chest.Left AMA.

Weitere VAERSDATA-Felder

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

VAERS 1512835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: PA
Alter: 70,0
Geschlecht: M
Eingang: 26.05.2022
Impfdatum: 05.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Fatigue Mobility decreased Weight decreased Arthrofibrosis Musculoskeletal stiffness Oral discomfort Peripheral swelling SARS-CoV-2 test Skin burning sensation

Symptomtext

Arthrofibrosis; locking both shoulders overnight/locking right wrist, thumb, and all fingers; Swollen hands and feet; Burning inside mouth; Burning facial skin; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old male patient received BNT162b2 (BNT162B2), on 05Mar2021 at 14:45 as dose 2, single (Lot number: EN6204) at the age of 70 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Arrhythmia" (unspecified if ongoing); "Hiatal Hernia" (unspecified if ongoing); "Arthritis" (unspecified if ongoing); "Known allergies: Sulphuric base Rx" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, Prev dose lot number=EL9267, Prev dose lot unknown=False, Prev dose administration date=12Feb2021, Prev dose administration time=12:00PM, Prev dose vaccine location=Right arm), administration date: 12Feb2021, when the patient was 70-year-old, for COVID-19 immunization. The following information was reported: ARTHROFIBROSIS (disability, medically significant) with onset 19Mar2021 at 08:00, outcome "not recovered"; SKIN BURNING SENSATION (disability, medically significant) with onset 19Mar2021 at 08:00, outcome "not recovered", described as "Burning facial skin"; ORAL DISCOMFORT (disability, medically significant) with onset 19Mar2021 at 08:00, outcome "not recovered", described as "Burning inside mouth"; PERIPHERAL SWELLING (disability, medically significant) with onset 19Mar2021 at 08:00, outcome "not recovered", described as "Swollen hands and feet"; MUSCULOSKELETAL STIFFNESS (disability, medically significant) with onset 19Mar2021 at 08:00, outcome "not recovered", described as "locking both shoulders overnight/locking right wrist, thumb, and all fingers". The events "arthrofibrosis", "locking both shoulders overnight/locking right wrist, thumb, and all fingers", "swollen hands and feet", "burning inside mouth" and "burning facial skin" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (09Jul2021) Negative, notes: Nasal Swab; (08Apr2022) Negative, notes: Nasal Swab. Therapeutic measures were taken as a result of arthrofibrosis, musculoskeletal stiffness, peripheral swelling, oral discomfort, skin burning sensation. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20210709; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20220408; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arrhythmia; Arthritis; Asthma; Hiatal hernia; Penicillin allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2271032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TN
Alter: 35,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 19.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: IM / AR

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

Cardiac monitoring Cardiac stress test Chest X-ray Chest pain Dyspnoea Fatigue Laboratory test Magnetic resonance imaging heart Tachycardia

Symptomtext

Difficulty breathing, random chest pains, tachycardia, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Heart Monitor Laboratory tests Chest xray Cardiac MRI Stress Test
Aktuelle Erkrankungen: Covid-19, Dec 2020
Vorgeschichte: Low Back Pain
Andere Medikamente: Concerta-18mg/daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 2270842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 19.01.2021
Beginn: 22.02.2022
Tage bis Beginn: 399,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Confusional state Hypotension Hypoxia SARS-CoV-2 test positive

Symptomtext

02/22/22 presents to ED for "hypoxia, hypotension as well as confusion". PMHx of "Alzheimer dementia"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: 02/22/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1666317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 69,0
Geschlecht: M
Eingang: 29.04.2022
Impfdatum: 17.02.2021
Beginn: 07.08.2021
Tage bis Beginn: 171,0
Dosis: 2
Route/Site: - / -

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

COVID-19 pneumonia Oxygen saturation decreased COVID-19 Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID -19 Breakthrough: I was admitted to the hospital for 17 days, I had a high fever and low oxygen. I tested positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 17,0
Labordaten: None.
Aktuelle Erkrankungen: No
Vorgeschichte: Type II Diabetes; Hypertension
Andere Medikamente: Lisinopril, Lovaza, Crestor, Synthroid, Metformin, Jardiance, Baby Aspirin, Senior Vitamin, Vitamin-D3 and Glucosamine
Allergien: Penicillin; sulfa; nystatin
Vorherige Impfungen: -

VAERS 1666317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 69,0
Geschlecht: M
Eingang: 29.04.2022
Impfdatum: 17.02.2021
Beginn: 07.08.2021
Tage bis Beginn: 171,0
Dosis: 2
Route/Site: SYR / AR

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

COVID-19 pneumonia Oxygen saturation decreased COVID-19 Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID -19 Breakthrough: I was admitted to the hospital for 17 days, I had a high fever and low oxygen. I tested positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 17,0
Labordaten: None.
Aktuelle Erkrankungen: No
Vorgeschichte: Type II Diabetes; Hypertension
Andere Medikamente: Lisinopril, Lovaza, Crestor, Synthroid, Metformin, Jardiance, Baby Aspirin, Senior Vitamin, Vitamin-D3 and Glucosamine
Allergien: Penicillin; sulfa; nystatin
Vorherige Impfungen: -

VAERS 2254656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 06.12.2021
Beginn: 25.04.2022
Tage bis Beginn: 140,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram spine Computerised tomogram thorax abnormal Condition aggravated Fall Gait disturbance COVID-19 Cerebral cavernous malformation Chest X-ray normal Computerised tomogram abdomen abnormal Computerised tomogram head abnormal Haemangioma of bone Haemoglobin decreased Intracranial mass Lip injury Magnetic resonance imaging head abnormal Neutropenia Retroperitoneal mass SARS-CoV-2 test positive

Symptomtext

Hospitalized 04/25/2022-04/26/2022; COVID-19 positive 04/25/2022; fully vaccinated plus booster BRIEF OVERVIEW: Admission Date: 4/25/2022 Discharge Date: 4/26/2022 DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is an 87 y.o female, hx of HTN, dyslipidemia, seizures, breast cancer s/p mastectomy, who presented to the ED following a mechanical fall. Previously known family members recently tested positive for COVID. Also noted to have unsteady gait. In the emergency department, she was noted have a laceration above her left lateral are broad left upper lip which was repaired. She was found to be COVID positive. She underwent a CT head which showed a right uncal mass. She also underwent a CT cervical spine which showed a C4 vertebral body lesion favored to represent a hemangioma. X-ray of her ribs and knee showed no acute abnormality. The case was discussed with Neurosurgery who recommended MRI of the brain. Due to her history of breast cancer, it was also recommended to obtain a CT of the chest abdomen and pelvis. She was admitted for further evaluation and management. CT of the chest abdomen and pelvis showed a retroperitoneal mass which was unchanged from previous examination in 2019 with a stable appearance of the remainder of the abdomen and pelvis. She also was noted to have a chronic T12 vertebral compression fracture. She underwent MRI of the brain which showed a 1.5 cm right mesial temporal lobe lesion most consistent with a cavernous hemangioma. Imaging was reviewed by Neurosurgery and recommended outpatient follow-up with no acute surgical intervention. She was seen by PT/OT who recommended home with assist and outpatient therapies. She was discharged home in stable condition. Of note, hemoglobin drop from 11.3 to 9.9 without overt bleed, suspect dilutional with IVF given. Also with chronic mild neutropenia that could be contributed to her lamictal. Recommend follow up with PCP to discuss further.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (hypertension), benign Nonrheumatic aortic valve stenosis Mild concentric left ventricular hypertrophy (LVH) Benign hypertensive heart and CKD, stage 3 (GFR 30-59), w CHF Carotid disease, bilateral Chronic diastolic heart failure Disorder of arteries and arterioles, unspecified Cavernous hemangioma of brain Rectocele COVID-19 Anemia in chronic kidney disease Seizure, petit mal Benign essential tremor Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus Cystocele with prolapse Hyperlipidemia, unspecified Mass of psoas muscle Osteoporosis HX OTHER MEDICAL S/P mastectomy Wedge compression fracture of T11 vertebra Basal cell carcinoma (BCC) of scalp Age-related osteoporosis without current pathological fracture Age-related osteoporosis without current pathological fracture Hx of breast cancer Unsteady gait when walking Lip laceration
Andere Medikamente: aspirin 81 MG chewable tablet Cholecalciferol (VITAMIN D3) 2000 units CAPS docusate (COLACE) 100 MG capsule lamoTRIgine (LAMICTAL) 100 MG tablet lisinopril (PRINIVIL,ZESTRIL) 10 MG tablet
Allergien: Actonel Alendronic Acid Bisphosphonates Evista Fosamax Pfizer
Vorherige Impfungen: -

VAERS 2254527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 18.02.2021
Beginn: 05.04.2022
Tage bis Beginn: 411,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

4/4/22 PMH of COPD, A-fib (not on AC), DVT, TBI, and HTN -- presenting for worsening SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 4/5/2022 COVID-19 by NAA -- Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2235977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 67,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 12.02.2021
Beginn: 14.04.2022
Tage bis Beginn: 426,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 pneumonia

Symptomtext

COVID pna, receiving IV steroids, Sx onset 4/7, presented to ED on 4/14, ED boarder currently On RA

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CLL Hx
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 04.10.2021
Beginn: 02.04.2022
Tage bis Beginn: 180,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased COVID-19 Chest discomfort Dyspnoea Fatigue Hypoxia Paranasal sinus discomfort Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Hospitalized (4.2.22 - present); COVID_19 positive (4.2.22); fully vaccinated PLUS booster BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 4/2/2022 Discharge Date: 04/06/2022 Presenting Problem: COVID-19 in immunocompromised patient Immunosuppression medications: Cyclosporine (goal 50-100) No recent changes Discharge Disposition: home health care svc Changes in Medications at Discharge: Decadron 6 mg daily for 6 days (to total 10 days) Hydralazine increased to 75 mg tid from 50 mg tid DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is a 80 y.o. male with past medical history of CAD and ICM leading to inotrope dependent, end-stage heart failure s/p OHT 4/17/2007, PVD, DM2, hypertension, hyperlipidemia, CKD3 and hx tobacco abuse (quit in 1970). He presented to the ED 4/2 with shortness of breath, found to be COVID positive. He reported symptoms starting Thursday 3/31 of congestion, rhinorrhea, sinus pressure, and fatigue. Then he developed SOB and chest tightness. In the ED, he was hypoxic, placed on 2L NC, unable to wean so he was admitted to AHF service for COVID in immunocompromised patient. ID was consulted to help manage; he was treated with remdesivir 5 doses and decadron. Of note, his BPs were elevated while admitted, he admitted to not taking some doses of hydralazine while at home when he felt ill. After few doses of home hydralazine dose in the hospital, his BPs remained elevated and hydralazine was increased from 50mg tid to 75mg tid. After a few doses of remdesivir and decadron, his symptoms improved and he did not require oxygen. On 4/6 he was stable for discharge. No change in his immunosuppression medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Shingles (herpes zoster) polyneuropathy Gout Hypomagnesemia Hypercholesterolemia Lumbar spondylosis Status post heart transplant 4.17.2007 Essential hypertension, benign Obesity (BMI 30.0-34.9) Dyslipidemia History of diabetes mellitus, type II Gastroesophageal reflux disease without esophagitis Aftercare following organ transplant Immunosuppressed status Chronic kidney disease, stage 3
Andere Medikamente: amoxicillin (AMOXIL) 500 MG capsule aspirin 325 MG tablet clindamycin-benzoyl peroxide (BENZACLIN) gel colchicine (COLCRYS) 0.6 MG tablet cycloSPORINE modified, GENGRAF, (GENGRAF BRAND) 25 MG capsule dexamethasone (DECADRON) 6 MG tablet dil
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2647642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: SC
Alter: 71,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 06.03.2021
Beginn: 10.11.2021
Tage bis Beginn: 249,0
Dosis: 1
Route/Site: - / LA

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

Atrial fibrillation Cancer screening Cardiac pharmacologic stress test Chest X-ray Computerised tomogram thorax Dysstasia Electrocardiogram Exercise test Fatigue Gait disturbance Inflammation Mobility decreased Peripheral swelling Scan myocardial perfusion Weight decreased X-ray

Symptomtext

Hospitalization for Afib for 5 days. Weight loss, fatigue and inflamation lost 30 pounds within 8 weeks and was unable to make a fist with his hands because of swelling. Also swelling in his feet. Found difficulty to walk and stand.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 5,0
Labordaten: November 10 - 16 was hospitalized November 26, 2021 x-ray 2 views December 06, 2021 EKG using at least 12 leads, November 11, 2021 x-ray of chest, December 13, 2021 Low dose CT scan of chest for lung cancer screening, December 14, 2021 exercise or drug-induced heart and blood vessel stress test November 11, 2021 nuclear medicine study of vessels of heart using drugs or exercise multiple studies, December 20, 2021 routine EKG using at least 12 leads including interpretation and report, December 03, 2021 Cyanocobalamin (vitamin B-12).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Olmesartan
Allergien: None
Vorherige Impfungen: -

VAERS 2209213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 05.11.2021
Beginn: 03.02.2022
Tage bis Beginn: 90,0
Dosis: 2
Route/Site: - / -

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

Atrial fibrillation COVID-19 Cardioversion Dyspnoea Echocardiogram abnormal Electrocardiogram normal Glomerular filtration rate decreased Hypoxia Pneumonia Polyuria Renal impairment SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient up to date on Pfizer COVID vaccinations who admitted to the hospital with positive COVID test and complications likely related to COVID. Provider discharge note below: "Patient developed increased shortness of breath, admitted with hypoxia though it should be noted that he was recently started on home oxygen @ 2 L/m and the hypoxia was noted on room air. The hypoxia may be due to several factors. He may have had some mild Pneumonia due to COVID-19 virus as he was found to be positive for COVID infection but with diuresis he was saturating well on room air. He had been started on steroids but since he was not truly hypoxic related to the COVID infection and was risk for fluid retention and exacerbation of his heart he was continued on steroids at discharge. He also has a history of Ischemic dilated cardiomyopathy (EF 20% Echo 12/2021) with AICD (automatic cardioverter/defibrillator) present and may have Acute on chronic systolic (congestive) heart failure though just recently had his diuretic dose increased at last hospitalization. He was started on intravenous FUROSEMIDE while monitoring CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min with solitary kidney. At admission patient noted to have a decreased GFR (21 to 13) likely due to recent increase in TORSEMIDE dose. Discussed with Dr of cardiology and at discharge his dose was reduced to previous regimen of 10 mg twice daily. Paroxysmal atrial fibrillation on APIXABAN, AMIODARONE and had cardioversion prior to admission. Note that the patient is nearly eighty and has renal dysfunction and likely should be on the lower dose of 2.5 mg twice daily. Elevated troponin values with negative delta, no acute findings on electrocardiogram. No chest pain. Likely demand phenomena. Hypertension Controlled. Pure hypercholesterolemia ROSUVUSTATIN Gout ALLOPURINOL Issues Requiring Follow Up: Recommend follow up basic metabolic panel to monitor renal function. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: COVID "detected" PCR on 02/03/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Pure hypercholesterolemia Ischemic dilated cardiomyopathy AICD (automatic cardioverter/defibrillator) present Paroxysmal atrial fibrillation Pulmonary hypertension (*) CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min Gout Benign prostatic hyperplasia Coronary artery disease with angina pectoris, unspecified vessel or lesion type, unspecified whether native or transplanted heart (*) DDD (degenerative disc disease), lumbar Primary osteoarthritis of right shoulder History of prostate cancer Degenerative disc disease, lumbar NYHA class 2 heart failure with reduced ejection fraction (*) History of renal cell carcinoma Left bundle branch block
Andere Medikamente: Zyloprim Pacerone Eliquis Zyrtec Farxiga Toprol XL Multivitamin Crestor Demadex Vitamin E
Allergien: Shellfish: swelling
Vorherige Impfungen: -

VAERS 2198808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Arthritis Blood pressure increased Condition aggravated Dyspnoea Dysstasia Fatigue Gait disturbance Hot flush Insomnia Magnetic resonance imaging Menopause Muscle injury Night sweats Osteoarthritis Sitting disability Skeletal injury Skin indentation Skin laceration

Symptomtext

It has accelerative of my body degenerative. It flare up my arthritis and my thumb had a grove in it now. It has caused me to get tendonitis all over my body. It caused me to go back into menopaused. It has caused my skin to thinning, wear it tears layers of skin just from a little pump. My skin looks like a 100 year old person now. It has really messed with my thermo-balance. It hurts to seat, stand, to walk and sleep. I have hot flashes so bad. I am always tired as well. I also have night sweats really bad. I been to several specialist. I had x-rays, MRI, and blood work. It shows that my vitamin D is gone completely. I been sent to physical therapy due to the tears in my muscle and bone just from the pump. It shows that my joint are degenerative at a rapid rate. My blood pressure has been evaluated as well. I have also had weight gain since the shot. I also keep getting SOB but they said that my heart is fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: X-ray MRI Blood work
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism, Arthritis, Degenerative bone
Andere Medikamente: Mega, Synthroid, Amlodipine
Allergien: Levaquin, Lesotho, Eggplant
Vorherige Impfungen: -

VAERS 2196702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 21.01.2021
Beginn: 03.01.2022
Tage bis Beginn: 347,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dizziness Palpitations SARS-CoV-2 test positive

Symptomtext

01/03/22 presents to EC ED for "palpitations and lightheadedness". PMHx of "PAF (not on AC), HTN, DM type II"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 01/03/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 67,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 23.02.2021
Beginn: 25.04.2021
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: SYR / UN

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

Aspiration pleural cavity Blood test Cardiac valve disease Chest X-ray abnormal Cough Dyspnoea Echocardiogram abnormal Electrocardiogram abnormal Electrocardiogram ambulatory abnormal Heart rate irregular Inappropriate schedule of product administration Mobility decreased Pain Peripheral swelling Pleural effusion Pneumothorax Respiratory tract congestion Tricuspid valve replacement

Symptomtext

01/26/2021 1st vaccination; 02/23/2021 2nd vaccination; 04/25/2021 Started to experience irregular HR; 04/27/2021 Went back to cardiologist. Fitted for Holter monitor. Resulted to PVCs, irregular. 06/05/21 Daughter graduation. Upon return, experienced SOB, coughing, congestion. Put on antibiotics for 10 days. Off for 10 days. Then put back on them and I did not get better at all. I struggled all summer with the SOB with no answers. 08/03/2021 Went to cardiologist for SOB. No answers. Didn't feel heart related. 08/16/2021 PCP ordered chest x-ray. Result=moderate pleural effusion, collapsed lung. 09/03/2021 I couldn't even walk up a flight of stairs. They drained the fluid around the lungs. I felt good for a day. Then the pain was back. 09/08/2021 Blood panel ordered. 09/14/2021 Cardiologist appt. Lower extremities were swollen; put on Lasix and echo on heart; "the valves do not look good". Put on monitor for a TEET test of the heart. They found that heart valve, 'pig valve', was torn. I had had that valve for 10 years. My daughter was getting married in October, opted to operate till after wedding. 10/14/2021 Valve replacement; TVIR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: EKG; Echo; blood panel
Aktuelle Erkrankungen: N/A
Vorgeschichte: *09/12/2011 heart valve replacement; *MDS - I have had for about 12 years
Andere Medikamente: Eye drop Bromiste, Cialis, Toprol 25mg 1 tablet a day
Allergien: N/A
Vorherige Impfungen: -

VAERS 2196294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 19.02.2021
Beginn: 15.03.2022
Tage bis Beginn: 389,0
Dosis: 2
Route/Site: - / -

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

Acute psychosis Angiogram pulmonary normal Bipolar disorder COVID-19 Cough Fibrin D dimer increased Pain Rhinorrhoea SARS-CoV-2 test positive Tachycardia Wheezing White blood cell count increased

Symptomtext

Patient iss fully vaccinated and boosted. Covid positive test at home but PCR Covid negative in ER. + wheezing with dry cough, runny nose, body aches. CTA PE protocol chest/no PE. Patient seen by psychiatrist in ER with plan of inpatient psych for bipolar with acute psychosis. D Dimer 539. Tachycardia. WBC 10.8. Pt on room air. The patient was not a candidate for any treatment, especially the patient was on room air. discharged home

Weitere VAERSDATA-Felder

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

VAERS 2192102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 72,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 10.02.2021
Beginn: 27.08.2021
Tage bis Beginn: 198,0
Dosis: 1
Route/Site: SYR / LA

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

Acute kidney injury Anaemia Chronic kidney disease Colitis Gallbladder cancer metastatic Hypotension Lower gastrointestinal haemorrhage Mental status changes Sepsis

Symptomtext

metastatic gallbladder cancer, sepsis, hypotension, altered mental status, acute on chronic renal insufficiency, colitis, lower GI bleed, and anemia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 24,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: metastatic gallbladder cancer
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2190241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 08.12.2021
Beginn: 16.03.2022
Tage bis Beginn: 98,0
Dosis: 2
Route/Site: - / -

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

Aortic valve disease Atrial fibrillation COVID-19 Catheterisation cardiac abnormal Dyspnoea Dyspnoea at rest Dyspnoea exertional Echocardiogram abnormal Infusion Polyuria SARS-CoV-2 test positive Systolic dysfunction

Symptomtext

Patient up to date on COVID vaccines who admitted to hospital with A fib and tested detected for COVID during facility admission testing. Provider discharge summary below: "90 YO year old female with a history of Afib on Eliquis, severe aortic stenosis, and hypertension who presented to the Spectrum Health - ED on 3/16/2022 with progressive shortness of breath. Patient has had worsening shortness of breath over the past 1-2 months. Started out as dyspnea on exertion and has progressed to dyspnea at rest. She has been seen by cardiology and her PCP over the past month. Adjustments have been made to both her Amiodarone and Lasix. Prior to admission she was on Amiodarone 200mg and Lasix 20mg bid. She had an echocardiogram on 3/16/22 which revealed greatly reduced systolic dysfunction, at which point she was directed to the emergency department. On admission, cardiology was consulted and she was started on gentle diuresis. Right/Left catheterization was performed by Dr. on 3/18/22. It revealed no obstructive coronary disease, but did demonstrated an aortic valve area of 0.5 cm2. Cardiology now recommending to start process of TAVR work up - can be done as outpatient. Patient scheduled to follow-up with the valve clinic on 3/24/22. Of note, following the procedure, patient slipped into atrial fibrillation, though she later converted back into normal sinus rhythm following an amiodarone infusion. Issues Requiring Follow Up: (Who, what, when, and how communicated?) PCP - Diagnosed with incidental COVID. Not hypoxic - no treatment initiated. Was diagnosed with a 30-day supple of Metoprolol per cardiology recommendations. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: PCR detected test 03/16/22.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (hypertension) Primary osteoarthritis of right knee Beta-thalassemia Stage 3b chronic kidney disease Microcytic anemia - multifactorial Dyslipidemia Osteoporosis, post-menopausal HX: breast cancer Asthma Atrial flutter with rapid ventricular response Severe aortic stenosis Anemia in stage 3b chronic kidney disease (*) Iron deficiency anemia due to chronic blood loss Acute heart failure with reduced ejection fraction and diastolic dysfunction (*) Paroxysmal atrial fibrillation (*)
Andere Medikamente: Eliquis Os-CAL Pacerone Iron Lasix Lopressor Multivitamin Klor-Con Preservision vitamin
Allergien: Ancef [Cefazolin] Terazosin Mushroom Flavor Sulfadiazine Fosamax [Alendronate]
Vorherige Impfungen: -

VAERS 2176484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 18.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Cerebral disorder Condition aggravated Feeling abnormal Hypoacusis Tinnitus

Symptomtext

Experiencing tinnitus, a ringing and buzzing in her ears; It is driving her nuts; She does not hear as well as she used to; Doctor said it is in her brain, and that really bugs the caller; the symptoms started around March or February and have worsened; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 18Feb2021 (Lot number: EL9267) at the age of 74 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (1st Dose, Lot: EL9262., Location: Arm Right), administration date: 24Jan2021, for COVID-19 Immunization. The following information was reported: TINNITUS (non-serious) with onset Feb2021, outcome "not recovered", described as "Experiencing tinnitus, a ringing and buzzing in her ears"; FEELING ABNORMAL (non-serious) with onset Feb2021, outcome "unknown", described as "It is driving her nuts"; HYPOACUSIS (non-serious) with onset Feb2021, outcome "unknown", described as "She does not hear as well as she used to"; CEREBRAL DISORDER (non-serious) with onset Feb2021, outcome "unknown", described as "Doctor said it is in her brain, and that really bugs the caller"; CONDITION AGGRAVATED (non-serious) with onset Feb2021, outcome "unknown", described as "the symptoms started around March or February and have worsened". The events "experiencing tinnitus, a ringing and buzzing in her ears", "it is driving her nuts", "she does not hear as well as she used to", "doctor said it is in her brain, and that really bugs the caller" and "the symptoms started around march or February and have worsened" were evaluated at the physician office visit. Additional information: States that she has been experiencing tinnitus, a ringing and buzzing in her ears since her injections; since the last one on 18Feb2021. She spoke to her primary care physician who said it is tinnitus. Caller states she has never had that before and believes it was caused by the vaccine. States it is driving her nuts. It is so loud sometimes, especially at night. Says she does not hear as well as she used to. States that she has to say what did you say to people over and over. Caller says she may need to go to a hearing doctor since she never had this problem until recently. No Emergency Room visit. There was physician Office visit. Caller states that she was unfortunately told there is no cure for this. States that is a shame, she wishes they had a cure. Wishes that Pfizer would have a cure now for these reactions. States she feels strongly her symptoms were caused by the vaccines. States it is getting worse. The doctor told her that it is in her brain and that really bugs her. Caller denies any other medical conditions, medications, labs, testing, or treatments relevant to these events. States she is otherwise healthy. 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): None. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2176399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NY
Alter: -
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 01.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Palpitations

Symptomtext

getting terrible heart palpitations; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 92 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date Feb2021 (Lot number: EL9267) as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Lot number: EL9264, 1st dose), administration date: Jan2021, when the patient was 91 years old, for Covid-19 immunization. The following information was reported: PALPITATIONS (non-serious), outcome "not recovered", described as "getting terrible heart palpitations". Therapeutic measures were taken as a result of palpitations. Additional information: Therapeutic measures were taken as a result of events with Magnesium. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2162715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 20.02.2021
Beginn: 04.07.2021
Tage bis Beginn: 134,0
Dosis: 2
Route/Site: IM / RA

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

Atrial fibrillation COVID-19 Cardioversion Dyspnoea Electrocardiogram Fatigue Headache Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had sore throat, running nose, low-grade fever, headache, SOB, and fatigue that lasted for about 6 days. On July 27th, I tested positive for COVID-19. About 6 weeks later, I develop Atrial fibrillation. I went to the ER and they did EKG and Electronical Cardio version.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG Electronic Cardio version
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: just regular medicine
Allergien: Sofia
Vorherige Impfungen: -

VAERS 2154621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 10.02.2021
Beginn: 05.02.2022
Tage bis Beginn: 360,0
Dosis: 2
Route/Site: - / -

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

Anxiety Chest X-ray normal Computerised tomogram thorax normal Dyspnoea Echocardiogram normal Electrocardiogram normal Palpitations Sleep disorder Troponin

Symptomtext

Patient is fully vaccinated. 50-year-old female presented to the hospital with a chief complaint of heart palpitation and anxiety. The patient sometimes wake up at night gasping for air. EKG showed no signs of ischemic cardiac event. Cardiac troponin negative. CT chest, no acute abnormality. Her 2D echocardiogram was normal. CXR: No acute cardiopulmonary process. Medications: atorvastin, Vitamin D, B-12, Motrin and zoloft. Discharged home.

Weitere VAERSDATA-Felder

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

VAERS 2151954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: LA
Alter: 38,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 22.02.2021
Beginn: 28.02.2022
Tage bis Beginn: 371,0
Dosis: 2
Route/Site: SYR / LA

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

Palpitations

Symptomtext

I was trying to do water aerobics as usual (3x a week for over a year), and my heart started pounding when it never did that before. I took it easy for the rest of the workout and was careful to monitor my heartrate during workouts over the next few months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: obesity, hypothyroidism
Andere Medikamente: Levothyroxin, Atorvostatin, Lisinopril/Hydrochlorothiazine, Wellbutrin
Allergien: None
Vorherige Impfungen: -

VAERS 2148589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 28.02.2022
Impfdatum: 12.02.2021
Beginn: 29.01.2022
Tage bis Beginn: 351,0
Dosis: 2
Route/Site: IM / -

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

Cough Dyspnoea Mental status changes SARS-CoV-2 test

Symptomtext

altered mental status and cough, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) by NAA, Micro 1/29/2022
Aktuelle Erkrankungen: -
Vorgeschichte: heart block, sepsis, hypertension, arrhythmia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2146448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: RI
Alter: 80,0
Geschlecht: M
Eingang: 26.02.2022
Impfdatum: 02.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Arthralgia Condition aggravated

Symptomtext

left shoulder still hurts since the injections/ It has seemed to get worse. There are days where it really hurts him. He he can feel it; shoulder pain in the arm of injection; 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 81 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Mar2021 09:45 (Lot number: EL9267) at the age of 80 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Myeloma" (ongoing), notes: He was diagnosed with both of those 10 years ago.; "Melanoma" (ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, First vaccine Lot: EL3247; Left arm), administration date: 09Feb2021, when the patient was 80 years old, for Covid-19 immunization, reaction(s): "The arm pain started maybe a couple of days after the first dose". The following information was reported: CONDITION AGGRAVATED (non-serious) with onset Mar2021, outcome "not recovered", described as "left shoulder still hurts since the injections/ It has seemed to get worse. There are days where it really hurts him. He he can feel it"; ARTHRALGIA (non-serious) with onset Mar2021, outcome "not recovered", described as "shoulder pain in the arm of injection". Therapeutic measures were taken as a result of condition aggravated, arthralgia. Additional information: There was no additional vaccines administered on same date of the Pfizer Suspect. There was no emergency room visit or physician's office visit due to the adverse events. No prior vaccinations (within 4 weeks) was administered. Agent reports that ever since, he has been having shoulder pain in the arm of injection which is his left arm for both doses. Agent reports that it hurts some days more than others and sometimes he can't lift his arm over his head. He has tried hot and cold presses on it and it didn't help. it happened after the second dose. He does not have a regular doctor, only has a cancer doctor. It isn't painful, but it hurts. He can't lift his left arm as high as his right. No prescribing doctor. He doesn't have primary care. He has tried hot and cold therapy. He has given it time. He thinks he has given it plenty of time since the injection for it to get better. There are days where he can't lift his arm over his head. He does have two types of cancer. He has Myeloma, blood cancer, and Melanoma, skin cancer. Follow-up attempts completed. No further information expected..

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Melanoma; Myeloma (He was diagnosed with both of those 10 years ago.)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2110504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 65,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Capsular contracture associated with breast implant Condition aggravated Induration Lymph node pain Lymphadenopathy Magnetic resonance imaging abnormal Medical device site pain Medical device site swelling Sleep disorder

Symptomtext

The next morning, I noticed swelling and hardening of my lymph nodes in my left armpit. A lot of tenderness. It lasted probably a week. Each day being a little better than the first day. After about maybe 2 weeks after the shot, I noticed that my left breast implant felt hard. It was swollen and it was very painful. I got an MRI to see what was going on and I went and saw Dr. (plastic surgeon). The swelling of the implant, it was swelling on the top of the implant. She was not familiar with this happening to anyone else. They were shocked when they saw my breast in the office. When sleeping at night, it would be so painful it would wake me up. Right breast remained normal during these health events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MRI- showed that I did have capsular contracture in my left breast
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure High Cholesterol
Andere Medikamente: Simvastatin 40mg 1xday Valtrex 500mg 1xday Irbesartan 150mg 1xday Progesterone 100mg 1xday Estradiol patch 0.0375mg 2xweekly Align probiotic Vitamin C 500mg 2xday Vitamin D3 50mg 2xday Calcium 500mg 1xday
Allergien: One episode with Dilaudid after surgery
Vorherige Impfungen: 1st COVID Pfizer vaccination on 01/21/2021 - The next morning, I noticed swelling and hardening of my lymph nodes in my left arm

VAERS 2110235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 25.02.2021
Beginn: 31.08.2021
Tage bis Beginn: 187,0
Dosis: 2
Route/Site: UN / UN

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

Acute kidney injury Arthralgia Asthenia COVID-19 COVID-19 pneumonia Chills Coagulopathy Hypoxia Rhabdomyolysis

Symptomtext

Presented for weakness, chills, Arthralgia. MD states no PMH. Admit for severe COVID PNA, hypoxia, rhabdo and coagulopathy d/t COVID. Tx w/O2, steroid, abx, no remdesivir d/t AKI. DC to acute rehab on 2L O2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2110232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 84,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 11.02.2021
Beginn: 05.09.2021
Tage bis Beginn: 206,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 COVID-19 pneumonia Cough Dyspnoea

Symptomtext

Presented w/SOB, cough. COVID in August w/no improvement. Admit for COVID PNA. Hx of HTN, CAD. Tx w/O2, abx, Vit C, D, zinc, neb, remdesivir. Disposition:She will be discharged today to home with hospice

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 24,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2107222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 16.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Body temperature Chills Diarrhoea Disorientation Dizziness Headache Pyrexia SARS-CoV-2 test Tremor

Symptomtext

weakness; diarrhea; bad headaches; woozy; disorriented; fever/fever up to 102; chills; uncontrollable shaking for next 6 hours; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Feb2021 10:00 (Lot number: EL9267) at the age of 65 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "aprox. 4 year remission from Non Hodgkins Lymphoma" (unspecified if ongoing), notes: aprox. 4 year remission from Non Hodgkins Lymphoma. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose number: 1, Administration time: 10:00 AM, vaccine location: Left arm, lot number: EL9262,), administration date: 26Jan2021, when the patient was 65 years old, for COVID-19 immunization. The following information was reported: DIZZINESS (non-serious) with onset 16Feb2021, outcome "recovered" (Feb2021), described as "woozy"; DISORIENTATION (non-serious) with onset 16Feb2021, outcome "recovered" (Feb2021), described as "disorriented"; PYREXIA (non-serious) with onset 16Feb2021, outcome "recovered" (Feb2021), described as "fever/fever up to 102"; CHILLS (non-serious) with onset 16Feb2021, outcome "recovered" (Feb2021), described as "chills"; TREMOR (non-serious) with onset 16Feb2021, outcome "recovered" (Feb2021), described as "uncontrollable shaking for next 6 hours"; ASTHENIA (non-serious) with onset 17Feb2021, outcome "recovered" (Feb2021), described as "weakness"; DIARRHOEA (non-serious) with onset 17Feb2021, outcome "recovered" (Feb2021), described as "diarrhea"; HEADACHE (non-serious) with onset 17Feb2021, outcome "recovered" (Feb2021), described as "bad headaches". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of dizziness, disorientation, pyrexia, chills, tremor, diarrhoea, headache. Additional information: Reaction/event as reported by primary source: 1 hour after, woozy & disorriented. 3 hrs after: sudden onset of fever & chills, uncontrollable shaking for next 6 hours. On second day, fever up to 102, weakness and diarrhea, bad headaches. 3rd & 4th day : Headache, weakness & continued diarrhea. On 5th day weak but improved.Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination the patient has not been tested for COVID-19. Patient did not received any other vaccines within 4 weeks prior to COVID vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20210906; Test Name: Temperature; Result Unstructured Data: Test Result:102; Test Date: 20210906; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Non-Hodgkin's lymphoma (aprox. 4 year remission from Non Hodgkins Lymphoma.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2099037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 71,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 22.01.2021
Beginn: 06.02.2022
Tage bis Beginn: 380,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Chest X-ray abnormal Chills Cough Dyspnoea Fatigue Nausea Oropharyngeal pain Pneumonia Pyrexia Respiratory tract congestion Respiratory tract infection Wheezing

Symptomtext

C/O weakness, started about 3-4 days ago. Brought on by respiratory infection, has had cough and congestion. Pt having chills, fever, fatigue, congestion, sore throat, cough, sob, wheezing and nausea. Chest Xray shows pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, A Fib, DM, COPD, CKD
Andere Medikamente: -
Allergien: Insulins, Nubain, SSRI
Vorherige Impfungen: -

VAERS 2089210

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El9267

moderat

Staat: AZ
Alter: 62,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 01.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: IM / AR

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

Abdominal pain upper Blood calcium Cardiac stress test Catheterisation cardiac Chest X-ray Chest discomfort Chest pain Cystitis Dyspepsia Endoscopy abnormal Gastritis Laboratory test abnormal Nausea Pneumonia Troponin increased Vomiting

Symptomtext

After 2nd injection: Extreme upper gastric pain, heavy chest pain , nausea, vomiting, Resulted in an ER visit. Troponen level slightly elevated -no other cardiac symptoms . Resulted in Cardac Cath procedure- and endoscopy. Endoscopy revealed inflamed stomach mucosa. After booster: Again extreme upper gastric pain and burning. nausea/vomiting. chest pain. ER visit. result was pneumonia, cystitis and abnormal tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: cardiac cath stress test calcium test Endoscopy chest X-rays
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: colostipol
Allergien: no
Vorherige Impfungen: -

VAERS 2085337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OK
Alter: 64,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 23.02.2021
Beginn: 31.03.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: SYR / LA

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

Herpes zoster Paraesthesia Rash Rash erythematous Rash vesicular

Symptomtext

Metoprolol was prescribed by my doctor on March 29th 2021, March 31st of 2021, I began to feel tingling sensation on my left lower abdomen, I then actually broke out and got some sort of red rash from the 31st. Everyday moving forward the area became blistered and painful, my physician put me on steroids and and antiviral, and this spanned for many weeks until they became to subside. No flare ups after the shingles went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma, Heart Arrhythmia
Andere Medikamente: Q-var ready haler 80mcg, Premarin Hormone Replacement .45, Probiotic, Calcium, Biotin 1000 mcg
Allergien: Aspirin, sulfasalazine
Vorherige Impfungen: -

VAERS 2071970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 38,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 23.02.2021
Beginn: 26.01.2022
Tage bis Beginn: 337,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

Patient presented to the ED on 1/26/22 with chest pain. She tested positive for COVID on 1/26/22. She is currently on 4L of nasal canula Oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: COVID+ by PCR on 1/26/22
Aktuelle Erkrankungen: -
Vorgeschichte: Down syndrome, CHF, Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2047566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 17.02.2021
Beginn: 08.12.2021
Tage bis Beginn: 294,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain Chest X-ray normal Chills Cough Diarrhoea Dyspnoea Dyspnoea exertional Gallbladder disorder Imaging procedure abnormal Pain Pyrexia

Symptomtext

Patient is fully vaccinated. COVID + on 12/8/2021. ED visit on 12/8/2021. Pt c/o abdominal pain, diarrhea, sob that is worse with exertion, bodyaches X5 days.60-year-old male with history of diabetes, hypertension, CVA, myocardial infarction presents to the ED complaining of COVID 19 symptoms. Patient states that he has been experiencing diffuse body aches, intermittent fevers, chills, and mild shortness of breath for the past 3-4 days.Patient denies any history of DVT/PE. Positi ve for cough too. BP 111/65 | Pulse 58 | Temp 97.9 ?F (36.6 ?C) (Oral) | Resp 16 | Ht 182.9 cm (6') | Wt 92.5 kg (204 lb) | SpO2 94% | BMI 27.67 kg/m? CXR: Chest appears as stated without evidence of a suspicious pleural or parenchymal abnormality.Imaging revealed gallbladder sludge without any evidence of acute cholecystitis. Treatment: Toradol, potassium bicarbonate. His oxygen saturation has remained stable throughout his time on room air. Patient will be discharged at this time and has been advised to follow-up with his primary care physician and general surgery soon as possible. He was given strict return precautions. Discharged.

Weitere VAERSDATA-Felder

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

VAERS 2047483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

moderat

Staat: KY
Alter: 80,0
Geschlecht: U
Eingang: 19.01.2022
Impfdatum: 27.01.2021
Beginn: 25.02.2021
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 Computerised tomogram thorax Cough Decreased appetite Dyspnoea Dyspnoea exertional Gait disturbance Hypotension Illness SARS-CoV-2 test positive Weight decreased

Symptomtext

Pt fully vaccinated and admitted inpatient for COVID. * Final Report * General Admission H&P * Chief Complaint 1/17/2022 11:50 EST COVID +, increased SOB History of Present Illness 80-year-old male who is well-known to me he has a complex past medical history which include aortic stenosis congestive heart failure ventricular tachycardia with AICD placement paroxysmal atrial fibrillation COPD polymyalgia rheumatica hypertension hyperlipidemia and diabetes. Patient first developed symptoms on January 1. I did a home COVID test on January 4 which was positive he had another COVID test on January 5 was positive. His prednisone dose was increased to 20 mg a day for 5 days starting on January 10. He was having a cough shortness of breath and weakness he was also prescribed Robitussin-AC at that time. He is not eating he has lost more than 11 pounds since he has been sick he is very weak. He gets out of breath with minimal exertion such as walking across the room. He was seen in the office today and although he was feeling little bit better he was very weak and needed assistance getting up and walking. He was noted to have low blood pressure. As there were no beds for direct admission he was referred to the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CT of chest 1/17/22 Covid PCR 1/17/22
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Active Problems (6) AICD (automatic cardioverter/defibrillator) present CAD (coronary artery disease) High cholesterol HTN (hypertension) MI (myocardial infarction) Pacemaker
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 2039269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: PR
Alter: 41,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 17.02.2021
Beginn: 01.06.2021
Tage bis Beginn: 104,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Dizziness Headache Laboratory test Tachycardia

Symptomtext

Severe headaches, tachycardia that persists at rest, dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Laboratory in process.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Tachycardia, severe headaches and dizziness
Vorherige Impfungen: Influenza

VAERS 2032002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 11.02.2021
Beginn: 26.11.2021
Tage bis Beginn: 288,0
Dosis: 2
Route/Site: - / -

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

Atrial fibrillation COVID-19 Chest X-ray abnormal Heart rate increased Pleural effusion Pneumonia SARS-CoV-2 test positive

Symptomtext

01/11/2022: event occurred after 2nd vaccine. 87-year-old male who comes with mom today for elevated heart rate. Patient was at his primary care office for a routine follow-up after being discharged from the hospital few weeks ago and was noted to be in A. fib RVR there. He states that he has been wearing 2 L nasal cannula since being discharged after his COVID illness. Patient was COVID-positive on 11/26 and was feeling better however still requiring 2 L nasal cannula throughout the day. Denies any fever, syncope, headache, vomiting, chest pain, shortness breath, abdominal pain, diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 2,0
Labordaten: 01/11/2021: Chest xray:IMPRESSION: Persistent bilateral pneumonia and trace left pleural effusion.
Aktuelle Erkrankungen: unknown
Vorgeschichte: CAD, hypertension
Andere Medikamente: Unknown
Allergien: NSAIDS, iodine
Vorherige Impfungen: -

VAERS 2014172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 17.11.2021
Beginn: 02.01.2022
Tage bis Beginn: 46,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Asthenia COVID-19 Chronic obstructive pulmonary disease Condition aggravated Cough Malaise Oxygen saturation decreased Pneumonia SARS-CoV-2 test positive Sputum discoloured

Symptomtext

Hospitalized 1/2/2022; COVID-19 positive 1/2/2022; fully vaccinated plus booster BRIEF OVERVIEW: Discharge Provider:, MD Primary Care Provider: MD Admission Date: 1/2/2022 Discharge Date: Jan 6, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COPD with acute exacerbation (HCC) Community acquired pneumonia of right lower lobe of lung COVID-19 HOSPITAL COURSE: Patient is a 85 y.o. female who presented with cough, weakness. Patient has a history of COPD, chronic respiratory failure on 3L NC at baseline, Hx pseudomonas pneumonia, chronic diastolic CHF, hypothyroid. Patient's symptoms started on 12/31 with a cough and malaise. Per patient, she was having severe coughing up a greenish sputum so she called her pulmonologist who started the patient on Levaquin 2 days ago, she was able to take 2 doses, but then began having pain in both her ankles, and called her pulmonologist again who recommended she come to the emergency department for IV antibiotics. Patient took a COVID test at home which was positive. She was admitted to HCF and maintained on cefepime/azithromycin. Oxygen weaned to baseline 4L. Patient continued to improve though would desaturate to low 80's with activity. Local rehab consult was placed who recommended patient remain on 4 L nasal cannula at rest, with activity she will need to increase to 5-6 L.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (Chronic Obstructive Pulmonary Disease), Very severe. Chronic obstructive pulmonary disease, unspecified COPD type (HCC) Bronchiectasis with acute exacerbation (HCC) Hypoxemia requiring supplemental oxygen, since 2007 Chronic sinusitis of both maxillary sinuses Pneumonia Acute on chronic respiratory failure with hypoxia (HCC) Chronic deep vein thrombosis (DVT) of femoral vein of right lower extremity (HCC) Paroxysmal atrial fibrillation (HCC) Pulmonary hypertension due to lung diseases and hypoxia (HCC) Chronic diastolic congestive heart failure (HCC) Obesity, BMI 33. Diverticulosis GERD (gastroesophageal reflux disease) COVID-19 Tobacco abuse, in remission. 30 pack years. Hyperlipidemia Hypoxemia, chronic Dyslipidemia Hypothyroidism Immunoglobulin deficiency, noted 9/2010. Osteoarthritis Osteoarthritis of lumbar spine Cyst of finger Insomnia Mild cognitive impairment
Andere Medikamente: albuterol HFA (PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet B Complex Vitamins (VITAMIN B COMPLEX) tablet budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler busPIRone (BUSPAR) 7.5 MG tablet cetirizine (ZYR
Allergien: Oxycodone
Vorherige Impfungen: -

VAERS 2010367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 17.02.2021
Beginn: 07.11.2021
Tage bis Beginn: 263,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Dyspnoea Dysuria Fatigue Malaise Pollakiuria Productive cough Pyrexia SARS-CoV-2 test positive Tachycardia Urinary tract infection

Symptomtext

COVID positive on 11/7/2021. 69-year-old female presents to the ED complaining of generalized weakness, slight shortness of breath, cough with white sputum production, fatigue, myalgias, dysuria and frequency. Vital signs show patient is febrile with fever of 101.6 and tachycardic but no hypotension noted. Patient meets SIRS criteria, initiated sepsis bundle with 30 cc/kg and Rocephin for antibiotic coverage. Patient also given Tylenol for fever control. Patient while in the ED has not been hypoxic with O2 sat dropping below 88%, after fluid, Tylenol and antibiotic administration states feels much better. Patient was discharged with Keflex for antibiotic coverage for UTI, given pulse oximeter prescription with strict return precautions to the ED if become hypoxic or if fever continues to get worse and is not controlled with Tylenol.

Weitere VAERSDATA-Felder

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

VAERS 2006135

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 10.02.2021
Beginn: 04.11.2021
Tage bis Beginn: 267,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Anticoagulant therapy COVID-19 Cough Dialysis device insertion Dyspnoea Electrocardiogram normal SARS-CoV-2 test positive Troponin increased

Symptomtext

70-year-old male known to us with past medical history significant for CAD s/p stenting, hyperlipidemia, complete heart block, hypertension, type 2 diabetes mellitus history of pacemaker, CHF with an EF of 35% was previously noted to have sustained V. tach on his pacemaker interrogation underwent an upgrade of his previous pacemaker to a biventricular ICD on September 27, 2021.Patient is COVID positive on 11/4/2021. He presented to the hospital due to shortness of breath and cough. In addition he had slightly elevated troponins and had been trending down. EKG was negative for ACS. Hospital course: remdesivir and dexamethasone for COVID. Oxygen therapy, bronchodilator treatment, Lovenox for anticoagulation. Acute renal failure. Dialysis catheter placed. Set up HD as outpatient. Pt discharged to home.

Weitere VAERSDATA-Felder

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

VAERS 2001423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 09.10.2021
Beginn: 23.12.2021
Tage bis Beginn: 75,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram pulmonary abnormal Aspiration C-reactive protein increased COVID-19 Colon adenoma Colonoscopy abnormal Fibrin D dimer increased Hyperchlorhydria Hypoxia Infection Large intestine polyp Pneumonia Pneumonia aspiration Pyrexia SARS-CoV-2 test positive Vomiting White blood cell count increased

Symptomtext

Hospitalized (12.23.21); COVID-19 positive (12.23.21); Fully vaccinated plus booster Admission Date: 12/23/2021 Discharge Date: 12/24/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Aspiration pneumonia of both lungs due to gastric secretions, unspecified part of lung COVID-19 Aspiration pneumonia of left lower lobe due to vomit HOSPITAL COURSE: Patient is a 51 y.o. female who presents today with acute hypoxemia and aspiration pneumonia. Patient had elective colonoscopy done earlier today. Following the procedure she was acutely hypoxemic requiring 5 L of oxygen. She had been totally asymptomatic prior to this procedure in regards to any respiratory symptoms or COVID symptoms. COVID test was done after procedure and was noted to be positive. Patient is fully vaccinated and has had booster. In the emergency department it was noted that she had elevated dimer so CT angiogram was done which revealed evidence of left lower lobe pneumonia indicative of likely aspiration pneumonia. Decision was made to admit patient to inpatient this time. She is placed on IV Rocephin and oral doxycycline at this time. Continue supplemental oxygen. Placed on oral Decadron. She was not placed on remdesivir at this time. Overnight patient's clinical condition improved. She was transitioned to room air as maintain adequate oxygen saturations on room air. Patient has mild increase in white blood cell count overnight but most likely secondary to receiving a dose of Decadron. Fevers have improved. Since infection is most likely secondary to aspiration patient will be discharged on a 5 day course of antibiotic. With elevated D-dimer and markedly elevated CRP patient will complete a full course of Decadron. Patient has been instructed to hold her estrogen replacement therapy in till follows up with primary care physician. She was also instructed to isolate for 10 days. Around other people patient should wear a mask. Patient also instructed if she has worsening shortness of breath especially with activity feels her clinical condition is deteriorating anyway she should return to the emergency department immediately for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 12.23.21: Colonoscopy. 1 of the polyps was adenomatous. Recommend repeat colonoscopy in 5 years
Vorgeschichte: NA
Andere Medikamente: ARIPiprazole (ABILIFY) 5 MG tablet atorvastatin (LIPITOR) 40 MG tablet buPROPion (WELLBUTRIN XL) 150 MG 24 hr tablet buPROPion (WELLBUTRIN XL) 300 MG 24 hr tablet cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) tablet escitalopram (LEXAPRO) 1
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1995516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NM
Alter: 78,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 11.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Arthralgia Cardiac function test Chest X-ray Computerised tomogram abdomen Computerised tomogram thorax Cough Drug ineffective Dyspnoea Feeling abnormal Full blood count Joint range of motion decreased Lipids Malaise Muscle spasms Suspected COVID-19 Swelling Tendonitis X-ray limb

Symptomtext

Probably had COVID; Probably had COVID; Severe joint pain again/Joint pain mainly in the ankles, Achilles, and knees; Couldn't raise her shoulders; Swelled up; Terribly short of breath; Tendinitis all over/Tendonitis in her ankles, shoulder and knees/Tendonitis is mainly now in her ankles; Felt ill; Cough; Feeling bad; Hand cramped; This is a spontaneous report received from a contactable consumer from medical information team. The reporter is the patient. A 79-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection), via an unspecified route of administration, administered in the left arm, administration date 11Feb2021 (Lot number: EL9267) at the age of 78 years as dose 2, single for COVID-19 immunization. Relevant medical history included: "Obesity" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing); "Aortic aneurysm" (unspecified if ongoing); "Triple bypass" (unspecified if ongoing); "COVID-19" (unspecified if ongoing); "Sleep apnea" (unspecified if ongoing); "Terrible joint pain" (unspecified if ongoing); "Productive cough" (unspecified if ongoing); "Tendinitis" (unspecified if ongoing); "Hand cramped" (unspecified if ongoing); "Couldn't raise her shoulders" (unspecified if ongoing); "Knees and ankles hurts so bad" (unspecified if ongoing). Concomitant medications included: ADVAIR; LIPITOR taken for high cholesterol; PHENYTOIN; PROTONIX [OMEPRAZOLE]; and VITAMIN D3. Past drug history included: Levaquin, reaction: tendinitis, notes: she developed tendonitis in her ankles, shoulder and knees and it has been 6 months; Aspirin; Tylenol; Ibuprofen; and Mucinex. Vaccination history included: BNT162B2 (dose 1, single; lot: EL9261), administration date: 21Jan2021, when the patient was 78 years old, for COVID-19 immunization; and FLU VACCINE. The following information was reported: The patient reported that in 01Oct2019 (as reported), she was told that COVID was here, and she was from (redacted). She was held over in (redacted) for about 5 hours and then she home to (redacted). About three to four days later, she developed some kind of cough, productive, she felt awful and had to put herself on oxygen around the clock. She was taking Tylenol, Ibuprofen, Advair, Aspirin, and Mucinex. These events occurred before taking the vaccine. Two weeks later, she good enough to go see her doctor. The doctor told her that she had some kind of a terrible virus (not clarified further). The doctor put her on Levaquin, as empirically as per the doctor (though that it will not do any good to the patient but she needed to be treated empirically). Within four days, she developed what she called tendinitis in her ankles, shoulders and knees, she couldn't raise her shoulders, her hand cramped, and she couldn't and hardly get out of bed because her knees and ankles hurst so bad. The pain lasted for about six months and finally in the spring of 2020, she went for physical therapy for about 3 months and got better. On 21Jan2021, the patient her first Pfizer vaccine and then on 11Feb2021 she took the second vaccine. The patient did not receive any other vaccines prior to the COVID-19 vaccine. Shortly after that, she developed severe joint pain again, that she can't seem to get over, it was in her Achilles tendon and her knees, and then she swelled up like all through May and June. She just got terribly short of breath. After getting the second shot, all the previous symptoms after her trip to (redacted) came back again. In June, she had a cardiac test and it was negative. She had to be put on salt-restricted and fluid-restricted diet, and she was taking big doses of Lasix, and she had seen a nephrologist with it. She saw a pediatrist who gave "left" to her shoes and said that she could either have either surgery or ice and Ibuprofen, but she can't take Ibuprofen. The patient didn't have any heart issues but she still got a tendinitis all over and she didn't know how to get rid of it. The patient was feeling bad and felt ill. The tendonitis was mainly now in her ankles. She saw a pulmonologist on Friday (unspecified date) who said and thought that the patient probably had COVID, the patient had reaction because of already having COVID with getting the shot. The patient had lots of lab word done in the past year. She have had a lipid panel, a complete blood count (CBC), chest X-rays, computerized tomogram (CT)s of her chest and abdomen, and X-rays of her knees and feet. Therapeutic measures were taken as result of event "probably had COVID". The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 202106; Test Name: Cardiac test; Test Result: Negative ; Test Date: 2021; Test Name: Chest X-ray; Result Unstructured Data: Test Result:unknown results; Test Date: 2021; Test Name: CT abdomen; Result Unstructured Data: Test Result:unknown results; Test Date: 2021; Test Name: CT chest; Result Unstructured Data: Test Result:unknown results; Test Date: 2021; Test Name: CBC; Result Unstructured Data: Test Result:unknown results; Test Date: 2021; Test Name: Lipid panel; Result Unstructured Data: Test Result:unknown results; Test Date: 2021; Test Name: X-rays of knees and feet; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Aortic aneurysm; Arthralgia; Bypass surgery; COVID-19; Cramp in hand; High cholesterol; Joint pain; Joint range of motion decreased; Obesity; Productive cough; Sleep apnea; Tendinitis
Andere Medikamente: ADVAIR; LIPITOR; PHENYTOIN; PROTONIX [OMEPRAZOLE]; VITAMIN D3
Allergien: -
Vorherige Impfungen: -

VAERS 1989022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 67,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 30.08.2021
Beginn: 26.12.2021
Tage bis Beginn: 118,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

Patient admitted as inpatient on 12/26 due to COVID-19 pneumonia. Patient was tested for COVID-19 and was positive on 12/26.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Nortriptyline
Vorherige Impfungen: -

VAERS 2526347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 21.01.2021
Beginn: 26.06.2021
Tage bis Beginn: 156,0
Dosis: UNK
Route/Site: IM / LA

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

Blood creatinine increased Cough Dyspnoea Dyspnoea exertional Exposure to SARS-CoV-2 Fatigue Headache Pyrexia Renal impairment

Symptomtext

Narrative: Patient presented with complaints of fever/fatigue/cough/shortness of breath. -Patient has been having several COVID-19 complaints such as headache, fatigue, cough, shortness of breath particularly on exertion. Symptoms have been occurring for appx 1 week. Patient's longterm partner was recently admitted to Medical Center for PNA which she was found to be COVID19 positive. Patient's partner was having a cough for appx 3-4 weeks and was worsening the last several days. -No complaints of anosmia, loss of appetite, diarrhea, CP, pleuritic CP -Patient had Pfizer COVID19 PNA vaccination in Jan/Feb 2021 -Patient has former tobacco hx 1ppd for 30 years in past and Substance abuse history including cocaine, IV heroin, marijuana Admitted to hospital, administered oxygen and dexamethasone and supportive care. Remdesevir administered once renal functino improved to Cr<1.5. Discharged home after revovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 01.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: SYR / AR

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

Central nervous system lesion Condition aggravated Fatigue Inflammation Intervertebral disc disorder Magnetic resonance imaging abnormal Nausea Relapsing-remitting multiple sclerosis

Symptomtext

I got my first vaccine on 2/3/2021, my second dose on 2/24/1986. I was being monitored for MS following a bad case of viral meningitis where I had optic neuritis and MRI showed one other lesion. This was attributed to the viral infection. I was monitored for the development of MS, but had been told this was pretty unlikely. (80/20 chance was the number I was told). I went through a pregnancy and everything was completely stable in terms of MS. After my first dose I was fine but felt a little funny feeling on my face that went away after a week or so. I attributed this to a reactivation of a feeling I had during viral meningitis. After the second dose I felt alright. My main side effect was nausea and fatigue. I was due for my final monitoring MRI for MS on 03/22/2021. They found two new lesions. One an active lesion on my c2 location on my spine. I was given a week of prednisone to calm inflammation. I believe that the vaccine?s inflammatory aspect caused my predisposition to MS to be activated giving me the new lesion and pushing me over into full RRMS. I was not on any medication for MS prior to this new discovery in March. The timing is so close that it is hard not to connect the two. My neurologist told me that he thinks the vaccine likely trigger the c2 lesion. Although he can?t figure out the other lesion I developed on my frontal lobe (which has now shrunk my half). I have not gotten a booster yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Vaccine 2/24/2021 MRI 3/22/2021 at ARA Imaging in (LOCATION)
Aktuelle Erkrankungen: Was fine at the time of vaccine and leading up to the vaccine.
Vorgeschichte: I had recovered from viral meningitis in October 2019. Had a clinically isolated viral lesion in my brain and a case of optic neuritis from viral meningitis. I then had a second pregnancy that went smoothly other than gestational diabetes. No new lesions or anything after pregnancy (scanned October 2020 by MRI)
Andere Medikamente: Vitamin d 10,000 iu L-lysine Prenatal gummy vitamin Magnesium
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1967746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

moderat

Staat: KY
Alter: 71,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 24.01.2021
Beginn: 20.12.2021
Tage bis Beginn: 330,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

ED with SOA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: myelofibrosis, splenomegaly,stage III kidney disease, hypertension, permanent atrial fibrillation, pancytopenia, obstructive sleep apnea, GERD.
Andere Medikamente: home prednisone; thalidomide.
Allergien: -
Vorherige Impfungen: -

VAERS 1967624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 24.08.2021
Beginn: 12.12.2021
Tage bis Beginn: 110,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Atelectasis COVID-19 Chemotherapy Chest X-ray abnormal Cough Dyspnoea Hypertension Lung opacity Pyrexia SARS-CoV-2 test positive Wheezing

Symptomtext

Hospitalized 12/12/2021; COVID-19 positive 12/12/2021; fully vaccinated plus booster BRIEF OVERVIEW: Primary Care Physician at Discharge: MD Hematologist/Oncologist: Dr. Admission Date: 12/12/2021 Discharge Date: 12/14/2021 Patient's Discharge Disposition: Home in stable condition. Discharge summary: This is a 80 y.o. year old patient who was admitted on 12/12/2021 with PMH of HLD, Hx DVT, and multiple myeloma on active tx with DaraCarfilzomib who presented to Hospital with symptoms of weakness, cough, and fever. Patient fully vaccinated including booster. COVID testing however in the emergency department was positive. Chest x-rays done in the emergency department on 12/12/2021 which showed minor atelectasis or opacity of the left lung base. All other infectious workup remained negative during this admission. Patient was started on Rocephin and azithromycin in the emergency room empirically however after negative further infectious workup in no further fevers, it was determined that antibiotics were no longer indicated. Patient was given monoclonal antibody in the emergency department however despite requiring no supplemental oxygen, patient was admitted for further evaluation and treatment of patient's shortness of breath because after receiving monoclonal antibody, patient subsequently became severely hypertensive, short of breath and had wheezing. Following this reaction, patient was given albuterol, dexamethasone and Benadryl for possible reaction. Chest x-ray was repeated at that time to ensure no pulmonary edema and this was negative and stable compared to previous chest x-ray. Patient was given remdesivir and dexamethasone in emergency department and throughout the duration of this admission (two doses of remdesivir given). Patient continued to remain on room air and having completely recovered from suspected reaction, it was determined clinically stable to discharge home off antibiotics or steroids per my discussion with Dr. Patient continued to eat, drink, void and ambulate on his own during this admission as per home baseline. Patient eager to discharge home today though did have significant concerns about infecting his wife. We did discuss safety measures and quarantine recommendations at great length. Patient is aware that he may not present back to our office until 10 days of quarantine has elapsed but should call with questions/concerns. We are pushing his chemotherapy out until 12/22/21. During this admission, patient was evaluated by the physical therapy team and felt that patient was stable to return home with outpatient services. Physical therapy was consulted for outpatient care upon discharge. Prior to discharge today, patient denies new, worsening or changes in ROS at this time, including no fevers/chills/sweats, no CP/SOB/DOE, no abd pain/N/V/D, and no neuro changes. Patient eating/drinking/voiding well and ambulating as tolerated. Patient will plan to follow up in our office as per below. Patient's discharge medications were discussed and new prescriptions were sent to patient's requested pharmacy prior to discharge as per generated list below. Patient is aware to call our office should further questions or concerns arise following this discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Obstructive sleep apnea (adult) (pediatric) Pneumonia due to COVID-19 virus Hypertension DVT (deep venous thrombosis) Esophageal reflux Arthritis Multiple myeloma in remission Drug-induced polyneuropathy Pure hypercholesterolemia, unspecified Anticoagulant long-term use Staphylococcus aureus bacteremia History of recurrent deep vein thrombosis (DVT) Personal history of malignant neoplasm of prostate Personal history of other venous thrombosis and embolism Presence of left artificial knee joint S/P total knee arthroplasty, left
Andere Medikamente: acyclovir (ZOVIRAX) 400 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler B Complex Vitamins (VITAMIN B COMPLEX PO) benzonatate (TESSALON) 100 MG capsule dexamethasone (DECADRON) 4 MG tablet DUL
Allergien: NKA
Vorherige Impfungen: -

VAERS 1962409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 53,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 13.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Fatigue Gait disturbance Injected limb mobility decreased Limb discomfort Muscle spasms Muscle twitching Pain in extremity Pruritus Rash Rash erythematous Tendon pain

Symptomtext

Feb. 13, 2021 could not lift left arm for 2 days, left upper arm spasms/twitching continued. March 2-6, 2021 left leg lower spasms on back side. March 10 left leg aches, limp. March 13 rash noticed on 3 areas on back of left leg rash bumps white itch. March 15 upper left arm twitches, left leg Achilles tight, rash red, left foot pulsating. Symptoms ongoing for 2 1/2 months including fatigue, then random symptoms. Some of Treatment: rash ointment, bloodwork, chiropractor visits, GABAnol supplement

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None Chiropractor for adjustments periodically
Andere Medikamente: No medication Vitamins; multi-vitamin, Vitamin D, vitamin C Supplements: probiotics
Allergien: None
Vorherige Impfungen: -

VAERS 1947652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 85,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 18.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Condition aggravated Gastric cancer Nausea Obstruction gastric SARS-CoV-2 test positive Vomiting

Symptomtext

Patient tested positive while admitted. Been admitted since 11/18/21.Complex medical history including chronic atrial fibrillation, hypertension, DM2, esophagitis with gastritis, gastric cancer with gastric outlet obstruction, cervical myelopathy, pseudogout, osteopenia, aspiration pneumonitis, urinary retention, admitted with nausea and vomiting, found to have gastric cancer with outlet obstruction. A facility was consulted to assist with goals of care, now providing comfort-focused care at end of life

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: acetaminophen
Allergien: Tetracycline, Niaspan [Niacin]
Vorherige Impfungen: -

VAERS 1947607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 10.02.2021
Beginn: 18.11.2021
Tage bis Beginn: 281,0
Dosis: 2
Route/Site: - / -

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

COVID-19 pneumonia Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Hypoxia SARS-CoV-2 test positive

Symptomtext

COVID vaccinated (2 doses) patient admitted through ED with shortness of breath. Provider discharge note below: "70 YO female with COPD presented with dyspnea, admitted with hypoxia due to covid pneumonia. Placed on solumedrol for COPD exacerbation, remdesivir for covid. Improved, not requiring supplemental O2 since yesterday.""

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: COVID "detected" test on 11/13/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipemia Essential hypertension, benign COPD (chronic obstructive pulmonary disease) (*) GERD (gastroesophageal reflux disease) Tobacco use disorder DM (diabetes mellitus) (*) Screening for colorectal cancer Diverticulosis of large intestine without hemorrhage
Andere Medikamente: Albuterol, Atorvastatin, Symbicort, Jardiance, Nexium, Amaryl, Losartan, Fish oil, Januvia, Spiriva, Zanaflex, Desyrel
Allergien: Vicodin
Vorherige Impfungen: -

VAERS 1943775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 70,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 18.02.2021
Beginn: 12.12.2021
Tage bis Beginn: 297,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 pneumonia

Symptomtext

Patient admitted for COVID PNA

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic airway obstruction High cholesterol or triglycerides High blood pressure disorder
Andere Medikamente: Fluticasone-Umeclidin-Vilant, albuterol sulfate HFA, atorvastatin, clopidogrel, diphenhydrAMINE, fluticasone, furosemide, losartan, melatonin, metoprolol succinate XL, omeprazole, potassium chloride, and tamsulosin
Allergien: NSAID, Penicillin
Vorherige Impfungen: -

VAERS 1939804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 51,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 12.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Back pain Chest pain Electrocardiogram Fatigue Heart rate increased Neuropathy peripheral Palpitations SARS-CoV-2 test Systemic lupus erythematosus

Symptomtext

The day after the injection I experienced heart palpitations, fast heart rate, tired legs, and back pain. It worsened over the day over the next day. I went to urgent care a few days after the injection. I received a COVID test, EKG, and was sent to the emergency room to rule out blood clot. I also experienced pain over my sternum. I went to the local hospital and was told to follow up with a cardiologist. I was prescribed a "cardiac cocktail" and beta blockers to lower my heart rate. I started to experience neuropathy in my left leg. I saw my cardiologist May 2021. I was diagnosed with vaccine induced Lupus due to all of the symptoms and joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 Test; EKG
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: NP Thyroid
Allergien: Compazine
Vorherige Impfungen: -

VAERS 1935600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 22.01.2021
Beginn: 27.11.2021
Tage bis Beginn: 309,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia COVID-19 Dyspnoea exertional SARS-CoV-2 test positive

Symptomtext

11/27/21 presents to ED for "left shoulder pain" "more SOB on exertion". PMHx of "CAD, asthma, HTN, HLD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 11/28/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 09.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal X-ray Anal abscess Balance disorder COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram abdomen abnormal Cough Diarrhoea Fatigue Ileus Lung opacity Nausea Pain Pyrexia SARS-CoV-2 test positive Small intestinal obstruction Vomiting

Symptomtext

Hospitalized 11/26/2021-still currently hospitalized; COVID-19 positive 11/26/2021; fully vaccinated plus booster ASSESSMENT Principal Problem: AKI (acute kidney injury) (HCC) Active Problems: Uncontrolled type 2 diabetes mellitus with hyperglycemia (HCC) Chronic atrial fibrillation PLAN Covid-19 Pneumonia Vaccinated, received booster (11/9) Symptom onset about 2.5 weeks ago with body aches, fatigue, fever, cough, balance difficulties CXR with multifocal opacities non specific but compatible with Covid pneumonia Oxygen saturation normal on room air Not candidate for MAB Continue to monitor, check CRP, D-dimer, daily labs 12/4/2021 notes: Nausea/Vomiting/Diarrhea. Due to colonic ileus, distal SBO CT abdomen and pelvis on admit: showed colonic ileus but no bowel obstruction AXR report reviewed from 11/27 findings consistent with ileus. Possible partial obstruction. Repeat CT abd/pelvis on 11/30 with distal SBO. Gastric Grafton completed on 12/02/2021 without evidence of obstruction. Patient advance diet to solids and had return of nausea and emesis. His appetite returned today Covid-19 Pneumonia. Improving from a respiratory standpoint as symptoms started 2.5 weeks prior to admit Vaccinated, received booster (11/9) Symptom onset about 2.5 weeks ago with body aches, fatigue, fever, cough, balance difficulties Finished COVID isolation CXR with multifocal opacities non specific but compatible with Covid pneumonia Oxygen saturation normal on room air Not candidate for MAB, Decadron or remdesivir due to timing of symptoms and lack of hypoxia Dispo: Patient unable to tolerate full diet, will limit to liquids today. Appreciate GI and DGMS inputs 12/7/2021 note: ASSESSMENT / PLAN: Nausea vomiting resolved Partial small-bowel obstruction, colonic ileus resolved Patient currently tolerating soft diet Patient is stooling, no nausea or vomiting. Plan - Continue slow advancement of diet as tolerated COVID-19 pneumonia Fully vaccinated Asymptomatic, did not require treatment Off of severe respiratory isolation PT/OT recommends SAR Plan for Home patient considering sore hopeful complete resolution of SBO likely in 1-2 days Can likely DC on oral antibiotics to complete 7 days of treatment for anal abscess

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Uncontrolled type 2 diabetes mellitus with hyperglycemia (HCC) Chronic atrial fibrillation AKI (acute kidney injury) (HCC) Hypercholesterolemia Essential hypertension Degenerative joint disease (DJD) of hip Bilateral lower extremity edema Foraminal stenosis of lumbar region Obesity (BMI 30.0-34.9) Solitary kidney, acquired
Andere Medikamente: apixaban (ELIQUIS) 5 MG TABS atorvastatin (LIPITOR) 40 MG tablet Blood Glucose Monitoring Suppl MISC Insulin Pen Needle (BD ULTRA-FINE MINI PEN NEEDLE 5 MM X 31G) LANTUS SOLOSTAR 100 UNIT/ML pen-injector levothyroxine (SYNTHROID) 25 MCG tab
Allergien: Ampicillin Aspirin Penicillins Vancomycin
Vorherige Impfungen: -

VAERS 1929348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 10.02.2021
Beginn: 05.11.2021
Tage bis Beginn: 268,0
Dosis: 2
Route/Site: - / -

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

Angiogram cerebral normal Arteriogram carotid normal Asthenia COVID-19 Chest X-ray normal Computerised tomogram head normal Computerised tomogram neck Fall Mobility decreased Muscular weakness SARS-CoV-2 test positive

Symptomtext

Fully vaccinated patient who admitted through ED after a fall. Upon admission was noted to be COVID positive. Provider d/c note: "Patient with three days of generalized weakness leading to a Fall at home from which he could not get himself up and was found on the floor by his son. He had reported that his right leg ""gave out"" and when evaluated in emergency department he was felt to be weak about right hip flexor so he was evaluated for a stroke. He has a history of ischemic multifocal multiple vascular territories stroke noted in 2016 and In 2018 had 3 cm right frontal lobe hematoma. Unclear if his right leg weakness is a residual from these events. His CT head and computed tomography angiogram head/neck negative for acute findings. An MRI brain was requested but patient declined. He has been improving with physical therapy and the patient is going to have further subacute rehab at an extended care facility. He was incidentally was found to have a COVID-19 virus infection (a caregiver had tested positive). The patient has been vaccinated and has no new respiratory symptoms (has chronic cough) and chest film without findings consistent with viral pneumonia though some finding noted in upper lung on CT neck.. He did complete a course of REMDESIVIR and DECADRON. He was able to be weaned down to room air. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 12,0
Labordaten: COVID detected test 11/05/21.
Aktuelle Erkrankungen: -
Vorgeschichte: Essential hypertension GERD (gastroesophageal reflux disease) Stage 3 chronic kidney disease Dyslipidemia, goal LDL below 70 Diet controlled diabetes mellitus, type II Debility Type 2 diabetes mellitus with stage 3 chronic kidney disease, without long-term current use of insulin (*) Hx of ischemic multifocal multiple vascular territories stroke Embolic strokes involving all vascular territories Renal cyst, left Elevated prostate specific antigen (PSA) Hemorrhagic stroke (*)
Andere Medikamente: Tylenol, aspirin, hydrodiuril, Mag-Ox, Melatin, Protonix, Zocor
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1917082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 03.03.2021
Beginn: 02.09.2021
Tage bis Beginn: 183,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac stress test Chest X-ray Chest pain Computerised tomogram thorax Dyspnoea Echocardiogram Fatigue Fibrin D dimer Palpitations

Symptomtext

chess Pains, Heart papitations, shorness of breath, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: CT scasn Chess, Xray Chess. E cocardiogram, heart stress test, D dimer test. all done at the ER 0n 09/092021 and 09/10/2021.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: sumatriptan. Acyclovir
Allergien: unknowed
Vorherige Impfungen: -

VAERS 1916651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 12.02.2021
Beginn: 28.11.2021
Tage bis Beginn: 289,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

patient presented to the emergency department with shortness of breath. he has copd patient was found to be covid-19 positive on 10/22/21 patient was admitted for treatment of covid-19 with bamlanivimab, dexamethasone,etesevimab patient was discharged to home on 10/28/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: patient was tested positive outside for covid-19 on 10/22/21
Aktuelle Erkrankungen: none known
Vorgeschichte: Ulnar neuropathy Carpal tunnel syndrome COPD (chronic obstructive pulmonary disease) COPD exacerbation COPD with emphysema, verys evere based on PFT COPD, severe (HCC) with severe emphysema Smoker, for 51 yrs, started 2 PPD ,down to pack of less a day SIRS (systemic inflammatory response syndrome) Respiratory failure COVID-19 Acute exacerbation of chronic obstructive pulmonary disease (COPD)
Andere Medikamente: albuterol (VENTOLIN HFA) 108 (90 BASE) MCG/ACT HFA inhaler albuterol (VENTOLIN) (2.5 mg/3 mL) 0.083% nebulizer solution ALPRAZolam (XANAX) 0.25 MG tablet amlodipine-benazepril (LOTREL) 5-20 mg capsule benzonatate (TESSALON) 100 MG capsu
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1913243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 91,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 10.02.2021
Beginn: 29.10.2021
Tage bis Beginn: 261,0
Dosis: 2
Route/Site: - / -

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

Blood pressure decreased COVID-19 Cardiac failure Cardiac failure acute Cardiac failure congestive Condition aggravated Cor pulmonale Dyspnoea Left ventricular failure Oedema peripheral Polyuria Pulmonary hypertension SARS-CoV-2 test positive

Symptomtext

Fully vaccinated patient who tested positive for COVID during facility placement testing upon discharge. Provider discharge note below. Patient discharged back to facility as symptoms were improved even though positive COVID test was detected as facility currently in outbreak status and is likely source of infection. "92-year-old female with a past medical history of severe pulmonary hypertension, chronic left knee staph orthopedic hardware infection, squamous cell carcinoma of the scalp and neck on immune treatment who presents with shortness of breath. Found to be in heart failure exacerbation. She was treated for CHF, diastolic acute on chronic, Cor Pulmonale with severe Puln HTN - and diuresed well on IV lasix 80mg TID. She sees Dr. and was on demadex 20mg which was increased to 40mg on DC. BP was soft, so her Bblocker dose was reduced. Lungs are clear on Dc and no longer has leg edema. Advised to watch fluid intake, salt intake. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: COVID detected test 11/02/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid factor positive Osteopenia Grave's disease Erosive osteoarthritis Essential hypertension Primary osteoarthritis involving multiple joints Status post total hip replacement, bilateral Postablative hypothyroidism Dyslipidemia Primary osteoarthritis of right knee Basal cell carcinoma of skin of scalp and neck Nonrheumatic aortic valve stenosis Recurrent squamous cell carcinoma of skin Open wound of scalp Neoplastic malignant related fatigue Encounter for antineoplastic chemotherapy and immunotherapy Frequent falls Effusion of left knee joint Septic arthritis of knee, left (*) Iron deficiency anemia Atrial flutter (*) On apixaban therapy Acute pain of left knee Drug-induced constipation Acute on chronic combined systolic and diastolic heart failure (*) Closed fracture of tibial plateau, left, sequela Hypoxia Acute on chronic right-sided heart failure (*) Respiratory insufficiency Nursing home resident Chronic heart failure with preserved ejection fraction (*) Infected hardware in left leg (*) H/O staphylococcal infection Long-term current use of antibiotics for prevention of recurrent infection Paroxysmal atrial fibrillation (*) Hypomagnesemia
Andere Medikamente: Tylenol, Proventil, Eliquis, Aspirin, Keflex, iron, boost, neurontin, synthroid, lisinopril, mag-ox, toprol XL, multivitamin, miralax, K-dur, senna, torsemide.
Allergien: Norco [Hydrocodone-acetaminophen]Confusion Flexeril [Cyclobenzaprine]Muscle Symptoms Lipitor [Atorvastatin]Muscle Symptoms Pravachol [Pravastatin]Muscle Symptoms Welchol [Colesevelam]Muscle Symptoms Zetia [Ezetimibe]Muscle Symptoms
Vorherige Impfungen: -

VAERS 1904155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WV
Alter: 27,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 05.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Heart rate irregular Thyroid disorder Vaginal haemorrhage Visual impairment

Symptomtext

Spotting - for over 6 months continues nonstop. Irregular heartbeat- ranging from 200-40. Constant chest pain. Eye sight continually getting worse. Thyroid issues. I was healthy with non of those issue until I record the vaccine. It prevents me from working out since my chest hurts so bad. Doctors say it?s a side effect and don?t know why. Same with star spotting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: April 2021
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: Slow Fe - vitamin D - fish oil
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 1901890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 46,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 18.02.2021
Beginn: 20.11.2021
Tage bis Beginn: 275,0
Dosis: 2
Route/Site: UN / UN

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

Arthralgia Blood chloride decreased Blood creatinine normal Blood sodium decreased Blood urea normal COVID-19 Chest X-ray abnormal Chills Cough Diarrhoea Dyspnoea Fatigue Haemoglobin normal Hypoxia Lung infiltration Myalgia Nausea Pyrexia

Symptomtext

Patient discharged after (4) inpatient admission from 11/20-11/24/2021. Patient is a 47 y.o. female with past medical history significant for HTN, HLD, migraines, GERD, depression and anxiety who presents today with chills, fever and cough in setting of known Covid 19 infection. The patient reports first developing fatigue and cough 8 days ago. She has been experiencing intermittent chills and fever over the last five days. She took an at home Covid 19 test which was positive, later confirmed by a PCR. She complains of diffuse myalgias and joint pain. She has also been having loose stool. This morning, the patient woke up with chills and a temperature of 103.8F with nausea, vomiting and shortness of breath, at which time she presented to the ED. The patient is vaccinated. In the ED, the patient was febrile (T102.7F), tachycardic (HR 107), tachypneic (RR 28) and hypoxic requiring 2LNC. Baseline lab work showed sodium 131, chloride 97, BUN 11, Cr 0.74, WBC 7.19, Hgb 13.5. CXR showed probable left lower lobe infiltrate. The patient received tylenol. IV Rocephin, IV doxycyline, IV decadron, IV toradol, IV morphine and IV zofran while in the ED. She will be admitted for further management.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: DR CHEST SINGLE VIEW [350942986] Resulted: 11/20/21 0945 Order Status: Completed Updated: 11/20/21 0947 Narrative: EXAMINATION: Single View Chest EXAM DATE: 11/20/2021 8:43 AM TECHNIQUE: Single view chest INDICATION: COVID x 8 days, increasing fevers, cough COMPARISON: August 15, 2020 ENCOUNTER: Initial _________________________ FINDINGS: Cardiac size is within normal limits for the radiographic technique. Lungs are symmetrically expanded but there is an abnormal increase in density in the left retrocardiac area which could represent infiltrate. There are no pleural effusions. _________________________ Impression: Probable left lower lobe infiltrate.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic migraine without aura, with intractable migraine, so stated, with status migrainosus
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler atorvastatin (LIPITOR) 40 MG tablet dexamethasone (DECADRON) 6 MG tablet diphenhydrAMINE (BENADRYL) 50 MG capsul
Allergien: AdhesiveOther Erythromycin Sulfa Drugs Vancomycin
Vorherige Impfungen: -

VAERS 1897838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 24.02.2021
Beginn: 20.11.2021
Tage bis Beginn: 269,0
Dosis: 2
Route/Site: IM / AR

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

Anticoagulant therapy Asthenia Blood folate normal Blood thyroid stimulating hormone COVID-19 Dyspnoea exertional Fall Monoclonal antibody unconjugated therapy Physical deconditioning SARS-CoV-2 test positive Thyroxine normal Vitamin B12 normal

Symptomtext

Hospitalized 11/20/21-still currently admitted; COVID-19 positive 11/20/21; fully vaccinated ASSESSMENT / PLAN: Patient is an 85yo male with PMH that includes dementia, HTN, HLD, hypothyroidism who is presents with weakness and was found to be COVID positive. #COVID-19 COVID positive on 11/20/21. Received Pfizer vaccine x 2 in February. Symptoms include dyspnea on exertion, unclear date of onset. Stable on RA. - Order CXR - Lovenox - Decadron, remdesivir not indicated, may consider if worsening respiratory status - Consider MAB 11/22/2021 note: COVID-19 Recent increased weakness and falls most likely due to COVID-19 infection or potentially deconditioning. B12/folate WNL. TSH elevated at 9.6, T4 WNL less likely to be due to hypothyroidism. Plan -Monoclonal antibody being administered today -does not qualify for other COVID treatments as patient on room air -PT/OT ordered -Consult to care manager -PMR consult- recommend SAR or home with assistance 11/24/2021 Note: Discharge Coordination/Progress: Patient's spouse requests to take patient home today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Benign essential hypertension Dementia (HCC) History of malignant neoplasm of prostate Hyperlipidemia
Andere Medikamente: amlodipine-benazepril (LOTREL) 5-20 MG per capsule atorvastatin (LIPITOR) 40 MG tablet donepezil (ARICEPT) 10 MG tablet enzalutamide (XTANDI) 40 MG tablet levothyroxine (SYNTHROID) 175 MCG tablet Relugolix (ORGOVYX) 120 MG TABS
Allergien: NKA
Vorherige Impfungen: -

VAERS 1897438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 14.02.2021
Beginn: 14.11.2021
Tage bis Beginn: 273,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

11/14/21 presents to ED for "chest pain x 4 days". PMHx "DM2 and atrial fibrilliation"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/14/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1894824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 21.01.2021
Beginn: 10.11.2021
Tage bis Beginn: 293,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea Fatigue Pyrexia SARS-CoV-2 test positive

Symptomtext

11/10/21 presents to EC ED for "dyspnea, fatigue and fevers". PMH "of multiple myeloma on monoclinal ab infusions"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/10/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1886443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 78,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 18.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: SYR / LA

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

Cardiac murmur Echocardiogram Electrocardiogram Hypertension Hypotension

Symptomtext

Prior to the vaccination I did not have HBP. Several weeks after vaccination, around 03/01/2021, I was going to routine doctor appointment and I notice my BP was suddenly high. The BP was up and down for a month and a half after the vaccine. My blood pressure was very high 160/98. I went to see a Cardiologist and he immediately said I had HBP and put me on medication. He sent me for a bunch of test. My BP was spiking up and down. I thought it was white coat syndrome or the tightness of the cuff. I did not want to take my HBP medication. I was afraid to take the medication when my BP was very low. I did not know what was going on. The doctor suggested I track my BP for two weeks. The results were suggested I did not have HBP. After I had the 3rd booster vaccine, a couple of weeks later I had the same HBP results again-190/105. It was worse after the 3rd dose, instead of spiking up and down. It was spiking up. I have a heart murmur that I did not have before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Tracking BP for 2 weeks 05/24/2021 Echo without contrast and an LVEF Echo US Renal Artery Bilateral VAS Lab-Left Ventricle is normal in size/Mitral Valve-Trace Mitral Valve Regurgitation 06/18 ECG Complete with Interpretation VET- Normal Sinus Rhythm possible Atrial Enlargement Borderline ECG
Aktuelle Erkrankungen: No
Vorgeschichte: Mild COPD Mild emphysema Smoker
Andere Medikamente: HRT Hormone Replacement Therapy
Allergien: Codeine Percodan Novacaine
Vorherige Impfungen: When I was a child in grade school. It was when they put 5 needles in your arm - it got infected

VAERS 1885249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 03.03.2021
Beginn: 18.11.2021
Tage bis Beginn: 260,0
Dosis: 1
Route/Site: - / -

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

COVID-19 pneumonia Vomiting

Symptomtext

Pt has chronic kidney disease stage IV and diabetes mellitus type 2. He comes to the hospital due to vomiting and is found to have COVID pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 72,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 25.02.2021
Beginn: 09.08.2021
Tage bis Beginn: 165,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 COVID-19 pneumonia Hypoxia Nausea Vomiting

Symptomtext

Dx w/ COVID 5 days PTA. Was admitted for one night after initial dx, then sent home. RTER for N/V and hypoxia, dx w/ COVID pna. Fully vaccinated 3/2021. O2, azithro/rocephin, steroids. Did not require remdesivir or plasma. Weaned to RA. Discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1847157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NV
Alter: 76,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 10.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Tremor

Symptomtext

tremor to right hand 2 weeks after 1st dose of Pfizer COVID 19 vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none, referring today to neurology
Aktuelle Erkrankungen: Pneumonia
Vorgeschichte: Type 2 DM, htn, hyperlipidemia
Andere Medikamente: Finasteride, lisinopril, ASA, CoQ10, Pravastatin, trilipix, trulicity, glipizide, doxycycline ( for PNA), glipizide, omeprazole
Allergien: ampicillin
Vorherige Impfungen: -

VAERS 1843309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 12.02.2021
Beginn: 02.11.2021
Tage bis Beginn: 263,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient presented difficulty breathing and generalized weakness. Patient is still inpatient, being treated with aspirin, tylenol, pantoprazole, and dexamethasone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: Covid test was positive
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hypertension, end-stage renal disease, congestive heart failure, coronary-artery disease
Andere Medikamente: Unknown
Allergien: Statins, Penicillin
Vorherige Impfungen: -

VAERS 1836492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 80,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 23.02.2021
Beginn: 28.10.2021
Tage bis Beginn: 247,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia COVID-19 Cough Fall Musculoskeletal chest pain Oropharyngeal pain Paranasal sinus hypersecretion SARS-CoV-2 test

Symptomtext

an 81 y.o. female with Hx lymphoma, recurrent UTIs, who presents to the hospital for evaluation of right hip pain. This morning she went into the garage to get something and her slipper came loose and she tripped and fell with immediate right hip pain. Her pain was improved with IV morphine given in the ED but she feels it is starting to wear off. Of note approximately 10/22 she and her husband at bedside developed sore throat, sinus drainage, cough. They took over-the-counter Robitussin and analgesics with improvement of symptoms, however her cough was at some point bad enough to cause sore ribs. At this time she denies any acute respiratory symptoms, change in taste/smell. They did stop at their nearby pharmacy for field testing on the way in because they were suspicious that had COVID-19. COVID-19 infection ?Symptom onset reported 10/22 ?Requiring 2 L/min NC in the ED to maintain O2 sat at 90%, denies any history of tobacco use/pulmonary disease ?Obtain CTA of the chest, if evidence for Covid will initiate therapy due to hypoxia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1826469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 05.03.2021
Beginn: 24.10.2021
Tage bis Beginn: 233,0
Dosis: 2
Route/Site: IM / AR

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

Asthenia Blood sodium COVID-19 COVID-19 pneumonia Condition aggravated Diarrhoea Hyponatraemia Hypovolaemia Metabolic function test SARS-CoV-2 test positive Urinary tract infection Vaginal infection

Symptomtext

Hospitalized (10.24.21); COVID-19 positive (10.24.21); Fully vaccinated Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 10/24/2021 Discharge Date: 10/25/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hyponatremia [E87.1] Generalized weakness [R53.1] Diarrhea, unspecified type [R19.7] COVID-19 [U07.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is an 81-year-old female who presents with complaints of diarrhea and weakness. The patient tested positive for COVID on admission which is likely the cause of her diarrhea. Patient was also noted to be hyponatremic on presentation. Patient's hyponatremia was likely secondary to hypovolemia. With IV fluid administration the patient's sodium return to a normal range. The patient was feeling significantly better and reported improvement of her diarrhea. She was tolerating a normal diet and eager to be discharged home today. We discussed recommendations for follow-up including a repeat BMP. Questions have been answered to the patient's satisfaction and she is being discharged home in stable and improved condition. The patient recovered faster than anticipated leading to a faster than anticipated discharge Plus another ED visit on 10.26.21 - for COVID-19 and acute lower urinary tract infection

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 10.15.21: ED - vaginal infection ; infected pessary
Vorgeschichte: GERD (gastroesophageal reflux disease) Diverticulosis PMR (polymyalgia rheumatica) Vitamin D deficiency Presbyopia Chronic low back pain Pelvic floor weakness Encounter for therapeutic drug monitoring Essential hypertension Controlled type 2 diabetes mellitus without complication, without long-term current use of insulin Paroxysmal atrial fibrillation DM II (diabetes mellitus, type II), controlled Insomnia Mixed hyperlipidemia Anxiety disorder Irritable bowel syndrome with diarrhea Pessary maintenance Midline cystocele Rectocele Urge incontinence Vaginal atrophy Mild CAD Gastrointestinal hemorrhage associated with intestinal diverticulosis Atrial fibrillation with RVR Acute on chronic anemia COVID-19 Hyponatremia Diarrhea of presumed infectious origin Weakness
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ALPRAZolam (XANAX) 0.5 MG tablet Calcium Acetate, Phos Binder, (CALCIUM ACETATE PO) cholecalciferol (CHOLECALCIFEROL) 1000 units famotidine (PEPCID) 40 MG tablet Ferrous Sulfate (IRON) 325 (65 Fe) MG TA
Allergien: Augmentin [Amoxicillin-pot Clavulanate]Joint Pain GabapentinDizziness Lisinopril [Ace Inhibitors]Cough Reglan [Metoclopramide]Agitation Pravastatin
Vorherige Impfungen: -

VAERS 1825211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 14.02.2021
Beginn: 20.10.2021
Tage bis Beginn: 248,0
Dosis: 2
Route/Site: IM / UN

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

Appetite disorder Arthralgia Asthenia Atelectasis Atrial fibrillation COVID-19 Chest X-ray abnormal Chills Condition aggravated Cough Dizziness Electrocardiogram ST segment abnormal Electrocardiogram abnormal Exposure to SARS-CoV-2 Fatigue Hiatus hernia Hypertension Loss of personal independence in daily activities

Symptomtext

Patient is an 88M with h/o CAD, A-Fib on chronic Eliquis, HTN, HLD, NIDDM, CKD, seizure disorder on chronic AED, chronic anemia, GERD, gout and OSA, who presents today with generalized weakness and progressive inability to attend to ADL's. He lives at home with his spouse, who was recently diagnosed with COVID. He has symptoms of fatigue, intermittent subjective fever and chills, appetite change, dry cough, myalgias/arthralgias and lightheadedness. In the ER, he was afebrile, hypertensive, tachycardic and tachypneic, saturating normally on baseline 2L via NC. CXR shows no acute processes with mention of moderate sized HH. EKG shows rate-controlled A-Fib with non-specific ST changes, but no e/o ACS. COVID PCR + He received monoclonal antibody 10/22 and was started on decadron 6 mg daily for persistent fevers. His fevers resolved. He was weaned to home O2 requirement. He was medically stable for discharge. PT/OT recommends SAR

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: Results Procedure Component Value Ref Range Date/Time DR CHEST 2 VIEWS FRONTAL AND LATERAL Resulted: 10/21/21 0009 Order Status: Completed Updated: 10/21/21 0011 Narrative: EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 10/20/2021 11:18 PM TECHNIQUE: Frontal and lateral views INDICATION: Weakness, covid positive.. COMPARISON: Chest radiographs 3/25/2021, 11/3/2019, 12/12/2017. ENCOUNTER: Not applicable _________________________ FINDINGS: The heart size is within normal limits. Moderate hiatal hernia. No pulmonary vascular distention. Smaller scarring and/or atelectasis at the left lung base. No focal consolidation. No pleural effusion or pneumothorax. Left humeral head surgical anchors. _________________________ Impression: 1. No acute cardiopulmonary findings. 2. Moderate hiatal hernia. I have personally viewed the images, discussed the findings with MD, reviewed the interpretation, and agree.
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory Asthma OSA (obstructive sleep apnea) Circulatory Coronary artery disease involving native coronary artery of native heart without angina pectoris Permanent atrial fibrillation (HCC) Essential hypertension Mild to moderate aortic stenosis Chronic diastolic heart failure Digestive GERD (gastroesophageal reflux disease) Organoaxial gastric volvulus Esophageal dysphagia Infectious/Inflammatory COVID-19 Hematologic Chronic iron deficiency anemia Hypochromic microcytic anemia Nervous Seizure disorder (HCC) Late onset Alzheimer's dementia without behavioral disturbance (HCC) Genitourinary Type 2 diabetes mellitus with stage 3b chronic kidney disease Stage 3a chronic kidney disease (HCC) Endocrine/Metabolic Gout Dyslipidemia Other Spinal stenosis of lumbar region Seasonal allergies Osteoarthritis Status post placement of bare metal stent to RCA, 08/09/2015 Insomnia Paraesophageal hiatal hernia Bilateral leg edema Driving safety issue Generalized weakness
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 300 MG tablet apixaban (ELIQUIS) 2.5 MG tablet aspirin 81 MG tablet benzocaine-menthol (CEPAC
Allergien: Tiotropium Bromide [Tiotropium] Oxycontin [Oxycodone] SpirivaOther
Vorherige Impfungen: -

VAERS 1823808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 23.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

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

Abdominal discomfort Blood glucose Blood glucose decreased Dizziness Eating disorder symptom Musculoskeletal chest pain Vomiting

Symptomtext

Little discomfort in the ribs; Sore ribs; Dizziness; Blood sugar going down; I am feeling like reluctant to put food in my mouth and because it does not seem to be agreeing with me; I got horribly sick to my stomach and it cause me to throw up; I got horribly sick to my stomach and it cause me to throw up; This is a spontaneous report from a contactable consumer (patient) or other non-health care professional. A 71-year-old female patient received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EL9267) via an unspecified route of administration on 23Feb2021 (at the age of 71-year-old) as dose 2, single for covid-19 immunization. Medical history included type 1 diabetes mellitus from an unknown date and unknown if ongoing. The patient's concomitant medications patient stated as yes, she took a lot of medication, well there was awful lot of them.".Historical vaccine included BNT162B2 (solution for injection) via an unspecified route of administration, administered on 02Feb2021 as dose 1 single for COVID-19 immunization. On 24Feb2021 the patient got horribly sick to her stomach and it cause her to throw up, on an unspecified date she experienced little discomfort in the ribs; sore ribs, dizziness, blood sugar going down, she felt like reluctant to put food in her mouth and because it does not seem to be agreeing with her. The patient underwent lab tests and procedures which included blood glucose: going down on an unspecified date. No treatment received for blood sugar as the patient stated her blood sugar was fine. Outcome of the events Little discomfort in the ribs; Sore ribs, Felt like reluctant to put food in her mouth and because it does not seem to be agreeing with her were not resolved, outcome of the event Blood sugar going down was resolving and Outcome of rest of all the events were unknown. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: Test Name: blood sugar; Result Unstructured Data: Test Result:going down
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type 1 diabetes mellitus (Relevant medical history: Patient Medical comments : Type 1 Diabetes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1815516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 66,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 15.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Echocardiogram Electrocardiogram ambulatory Fatigue Hypotension Tachycardia Vaccine positive rechallenge

Symptomtext

I experience 5 days of debilitating tachycardia and low blood pressure and fatigue with the first shot. The same happened with the second shot but it lasted for weeks.

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Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Echocardiogram, Cardiogram and holster monitor for one week
Aktuelle Erkrankungen: None. Perfectly fit
Vorgeschichte: GERD, Osteoporosis, Elevated Cholesterol
Andere Medikamente: Tamoxifen, Protonix
Allergien: Sulfa antibiotics, NSAIDS, Aspirin
Vorherige Impfungen: -

VAERS 1814897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 22.01.2021
Beginn: 12.10.2021
Tage bis Beginn: 263,0
Dosis: 2
Route/Site: - / -

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

Dyspnoea Laboratory test abnormal

Symptomtext

SOB

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 13,0
Labordaten: Positive on admission 10.11.21
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, diabetes, heart disease, high cholesterol and blood pressure
Andere Medikamente: Levothyroxine, pravachaol, metformin, lantus, uoloric, pepcid, daily aspirin
Allergien: -
Vorherige Impfungen: -

VAERS 1812790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood test Computerised tomogram thorax Dyspnoea Electrocardiogram Oxygen saturation SARS-CoV-2 test Spirometry X-ray

Symptomtext

Strong dyspnea; This is a spontaneous report from a contactable consumer (patient). A 60-year-old adult male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EL9267 and Expiration date was unknown), via an unspecified route of administration in left arm on 11Feb2021 at 17:00 (at the age of 60-year-old) as dose 1, single for COVID-19 immunisation. The patient medical history included none and concomitant medications was not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. The patient had no Known Allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. On 11Feb2021 at 23:00, the patient had experienced Strong dyspnoea for 3 days after 1st dose starting first night. Then disappeared. The patient had visited urgent care, Primary doctors, Pulmonologist. Adverse event resulted in doctor or other healthcare professional office/clinic visit/Emergency room/department or urgent care. The patient did not receive any treatment for AE and no Hospitalization prolonged. Since the vaccination, the patient has been tested for COVID-19. Covid test type post vaccination was reported as Nasal Swab. On 13Apr2021, the patient underwent Covid 19 rapid diagnostic test and the result of covid test was reported as negative. The patient underwent lab tests and procedures which included blood test: ok, computerised tomogram thorax: negative, electrocardiogram: negative, oxygen saturation: ok, spirometry: normal, x-ray: negative in 2021. Outcome of the event was not recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood test; Result Unstructured Data: Test Result:Ok; Test Date: 2021; Test Name: Contrast chest CT scan; Test Result: Negative ; Test Date: 2021; Test Name: ECG; Test Result: Negative ; Test Date: 2021; Test Name: Oxygen; Result Unstructured Data: Test Result:Ok; Test Date: 20210413; Test Name: Covid 19 rapid diagnostic test; Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 2021; Test Name: Spirometry; Result Unstructured Data: Test Result:Normal; Test Date: 2021; Test Name: X-ray; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1810766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 15.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Feeling abnormal Insomnia Migraine Pain Vomiting

Symptomtext

unable to sleep at night; She felt like she wanted to die; migraines; very achy; throwing up,; This is a spontaneous report from a contactable consumer (patient). A 65-years-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL9267), via an unspecified route on 15Feb2021 at 11:30 (at the age of 65-years) as dose 1, single in the left arm for covid-19 immunisation. The patient medical history included irritable bowel syndrome. The patient concomitant medications were not reported. The patient previously received pneumonia vaccine on 04Jan2021. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient experienced migraines, very achy, throwing up unable to sleep at night on 17Feb2021. Patient stated 10 days later I'm still having migraines, I feel like dying. She started having daily migraines. She has had a problem with migraines off and on for 4 years. She was also very achy. She wishes she could throw up. She doesn't sleep at night. She is concerned that this will happen with the second dose. The pain with the migraine is so bad. The migraines started at noon. She felt like she wanted to die. They start every afternoon. The feeling of wanting to throw up comes and goes. It is not constant. It comes in cycles. Last night she took two Ibuprofen because she could not take it anymore. The outcome of the events migraines was not recovered, very achy was recovering and other events was unknown. 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: Irritable bowel syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1795339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 12.02.2021
Beginn: 10.10.2021
Tage bis Beginn: 240,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Chest X-ray abnormal Cough Diarrhoea Dyspnoea Fatigue Lung opacity Nausea Pneumonia viral SARS-CoV-2 test positive Vomiting

Symptomtext

Patient developed symptomatic infection on 10/10 and tested positive for covid on 10/17/21. Symptoms include loss of smell or tast, nausea, vomiting, diarrhea. SOB, fatigue, cough. Patient's husband also sick with covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CXR on 10/17 showed patchy airspace opacities bilateral, supicious for viral pneumonia SARS-CoV-2 (COVID-19) by NAA, Micro Detected on 10/17/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1791437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 74,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 22.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

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

Hot flush Paraesthesia

Symptomtext

Slight hot flash; Back,butt and down right thigh feel like a thousand needles are pricking skin; This is a spontaneous report from a contactable consumer, the patient. A 74-year-old non-pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9267) via an unspecified route of administration on 22Feb2021 at 08:15 (at the age of 74-years-old) as a single dose for COVID-19 immunisation. Medical history included atrial fibrillation (Afibrulation), chronic obstructive pulmonary disease (COPD), chronic sinusitis and penicillin allergy. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included celecoxib (CELEBREX), salbutamol (ALBUTEROL), theophylline (MANUFACTURER UNKNOWN), estrogens conjugated/medroxyprogesterone acetateprempro (PREMPRO) and gabape (MANUFACTURER UNKNOWN); all from an unknown date and unknown if ongoing for an unknown indication. The patient previously took codeine (MANUFACTURER UNKNOWN) and experienced drug allergy. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL8982) via an unspecified route of administration in the left arm on 01Feb2021 at 08:30 AM for COVID-19 immunisation. On 23Feb2021 at 20:00, the patient experienced a slight hot flash, then the patient's back, butt and down her right thigh felt like a thousand needles were pricking her skin which was hurt for about 5 to 10 seconds. Therapeutic measures were taken as a result of the events and included treatment with unspecified pain medication. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events slight hot flash and back, butt and downright thigh felt like a thousand needles pricking the skin were not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation (Afibrulation); Chronic obstructive pulmonary disease (COPD); Chronic sinusitis; Penicillin allergy
Andere Medikamente: CELEBREX; ALBUTEROL [SALBUTAMOL]; THEOPHYLLINE; PREMPRO
Allergien: -
Vorherige Impfungen: -

VAERS 1788107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 18,0
Geschlecht: M
Eingang: 15.10.2021
Impfdatum: 23.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / AR

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

Chest X-ray Chest discomfort Chest pain Dyspnoea Electrocardiogram Ultrasound scan

Symptomtext

Delayed onset of chest tightness and labored breathing (2 days after shot).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Went to pediatrician on or around Feb. 25 due to chest pain. They found nothing wrong (and chest X-ray okay). Continued to have chest tightness and labored breathing. By Feb 26 (or maybe the 25th?), he couldn't walk ten feet without feeling incredibly winded. We went to the ER on or around Feb. 26, and they gave him a series of tests (EKG, ultrasound, gave him an IV, etc.), finding nothing. But this was an 18-year old athlete who couldn't walk in to the ER on his two feet--he had to go in a wheelchair because he felt so winded.
Aktuelle Erkrankungen: None
Vorgeschichte: Moderate asthma
Andere Medikamente: Zyrtec, Nasonex, Pulmicort
Allergien: Peanuts. Previous hives from Tamiflu and Keflex
Vorherige Impfungen: -

VAERS 1775504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 05.03.2021
Beginn: 06.10.2021
Tage bis Beginn: 215,0
Dosis: 1
Route/Site: IM / LA

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

Atypical pneumonia COVID-19 Chest X-ray abnormal Fall Malaise Pneumonia Pyrexia Rib fracture SARS-CoV-2 test positive Traumatic haemothorax

Symptomtext

initial presentation for fall w/ rib fx, hemo/PTX. developed symptomatic covid symptoms, fevers, PNA,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atypical pneumonia
Hospital-Tage: -
Labordaten: CXR: + atypical PNA, PCR + 10.6.2021
Aktuelle Erkrankungen: none
Vorgeschichte: DM, HTN, HLD, emphysema, osteopenia, hiatal hernia
Andere Medikamente: ASA, atorvastatin, vit D, glimepiride, insulin lispro, metoprolol, naproxen, olmesartan, HCTZ, stagliptin
Allergien: metformin
Vorherige Impfungen: -

VAERS 1773904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 09.10.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Dry mouth Dyspnoea Sleep apnoea syndrome

Symptomtext

Had like an episode of sleep apnea; My mouth was real dry; I was sleeping and it was like I couldn't breathe; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL9267), via an unspecified route on unspecified date as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On unspecified date, the patient experienced like an episode of sleep apnea, mouth was real dry and patient stated that she was sleeping and it was like she couldn't breathe. Patient stated, "I am going to take the second vaccine today from the Pfizer for the COVID and I don't know, I had not reported this but before, like I said I don't know if this is the side effect or not of the first one but after I took the first one, maybe about a week later or so I had like an episode of sleep apnea and my mouth was real dry, I was sleeping and it was like I couldn't breathe you know and I had that in the past a long time ago and stuff. It happened twice." The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1770764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 40,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Chest discomfort Contusion Dysphagia Dyspnoea Feeling abnormal Flank pain Headache Pain Pain in extremity Pyrexia Vaccination site pain

Symptomtext

pain above left hip but in the center of her body; felt like a bruise/ states it was a dull bruise feeling; Left Arm Hurting; shoulder to fingertip; Body Aches; Brain Fog/ does not feel good feeling; left arm hurt from shoulder to fingertip/ arm soreness; had flashes of headaches accompanied by chest tightness and heaviness with a little shortness of breath; had flashes of headaches accompanied by chest tightness and heaviness with a little shortness of breath; had flashes of headaches accompanied by chest tightness and heaviness with a little shortness of breath; feeling like forgot how to swallow/ front of her mouth would move but the back was not swallowing; injection site pain; fever; This is a Follow-up spontaneous report from a Pfizer sponsored program. A contactable consumer (patient) reported that a 40-year-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection, Lot Number: EL9267), via an unspecified route of administration, administered in left arm on 01Mar2021 18:30 (at the age of 40-year-old) as dose 1, single for covid-19 immunisation. The patient's medical history included in the last year or two she developed an anaphylactic allergy to a weird spice in Indian food; scary 2 years for creepy allergies. Concomitant medications were not reported. On 01Mar2021, the patient had a strange side effect to the vaccine: She states she had body aches, she does not feel good feeling, her left arm hurt from shoulder to fingertip, and she had flashes of headaches accompanied by chest tightness and heaviness with a little shortness of breath as well as feeling like forgot how to swallow, nothing in her throat was swollen. States the front of her mouth would move but the back was not swallowing, states it was odder than anything. The patient had injection site pain. States she thought she should check if reactions are worse with the second dose of the vaccine. The next day on 02Mar2021 she reports pain above left hip but in the center of her body. The area was about the size of a golf ball that expanded and covered a larger area over the next few days and it felt like a bruise. states it was a dull bruise feeling. She also reports the following side effects: arm soreness, and brain fog. States her symptoms were mostly in the afternoon. The injection site pain lasted until the 04Mar2021. The patient experienced fever on an unknown date in 2021. Should I have any concerns about proceeding with a second vaccination?. The patient clarified that forgot how to swallow: it happen 2 times very close to one another. States that it took 15-20 seconds of telling her body how to swallow and it happened once more where it took another 15-20 sec to figure out how to make her body work then it was gone. The patient also states that someone she knows just died from it. She verified from the coronavirus, not the vaccine. States they lost someone close to them. States that is what pushed her to get the vaccine. States she is supposed to go there [withheld] again today for second vaccine. Caller states that in the last year or two she developed an anaphylactic allergy to a weird spice in Indian food. She states it is one of reasons why she wanted to call. She states this has been a scary 2 years for creepy allergies. Discovering an allergy with an anaphylactic reaction is not fun. Prior Vaccinations (within 4 weeks): None. AE(s) following prior vaccinations: None. Family Medical History Relevant to AE: None. No AEs require a visit to Emergency Room and Physician Office. The outcome of the event fever was unknown. The outcome of forgot how to swallow was recovered on 01Mar2021. The outcome of Vaccination site pain, body aches, Pain in arm and bruise was recovered on 04Mar2021. The outcome of the event Dysphagia was recovered on 01Mar2021. The outcome of all the other events was recovered on 05Mar2021. 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: Allergy (scary 2 years for creepy allergies); Anaphylactic reaction to food (in the last year or two she developed an anaphylactic allergy to a weird spice in Indian food)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1770654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Bone pain Circumstance or information capable of leading to medication error Condition aggravated Myalgia Pain Vaccination site pain

Symptomtext

Has a question about a possible interaction with Naproxen and the COVID vaccine; her muscles and joint pain are worse /her pain was worse; Injection site pain; Legs, back, shoulders, and pretty much everything hurts; stronger muscle and bone pain; stronger muscle and bone pain; This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL9267), via an unspecified route of administration on 10Feb2021 12:36 (at the age of 73-year-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included diabetes, arthritis, blood pressure. Concomitant medication(s) included metformin 500 mg twice a day taken for diabetes mellitus, start and stop date were not reported; lisinopril 10 mg once a day taken for blood pressure, start and stop date were not reported. The patient experienced stronger muscle and bone pain after the injection on 10Feb2021. She was due for her second dose on 03Mar2021. She had started taking Naproxen 500 mg twice daily and was wondering if there was a possible interaction with the vaccine. If so, when should she stop taking the medicine and when should she resume after receiving the second dose. She had read some place that Naproxen, an NSAID, might reduce the effectiveness of the COVID Vaccine. She was in such pain after the COVID Vaccine. Right afterwards her muscles and joint pain were worse. She needed to take Naproxen. Wanted to know how long she can be on Naproxen before her second dose. Her back and legs were in pain. She thought she could use heat pads. Tylenol does not work at all for muscle pain. She wanted to know if that was detrimental to the vaccine. She reported that injection site was not hurting after two days. Injection site was painful starting 11Feb2021 and she could lift her arm. After two days it subsided. The rest of her was not good. Her legs, back, shoulders, and pretty much everything hurts. Pain was terrible on 11Feb2021. She could not say she never had back pain before the COVID vaccine because she has arthritis. Her arthritis was under control. For some reason after the COVID Vaccine, her pain was worse. Started the Wednesday after the COVID vaccine and has continued. She said she has regular arthritis and not rheumatoid arthritis. The patient willingly took Naproxen. She stated asking her doctor for Prednisone would probably be worse. Stated sometimes doctors prescribed Prednisone and then has to be tapered off. Definitely read that Prednisone has an interaction and lowers the effectiveness of the COVID vaccine. She confirmed that she has not been prescribed Prednisone. The patient received treatment for stronger muscle and bone pain. The outcome of event vaccination site pain was recovering, stronger muscle and bone pain and for all other events was unknown. 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: Arthritis; Blood pressure abnormal; Diabetes
Andere Medikamente: METFORMIN; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1767625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: LA
Alter: 43,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Ankylosing spondylitis Anti-cyclic citrullinated peptide antibody negative Antinuclear antibody Antinuclear antibody negative Arthralgia Blood creatine normal Blood uric acid normal C-reactive protein increased Double stranded DNA antibody Fatigue Headache Immunology test Liver function test normal Migraine Muscle strength abnormal Red blood cell sedimentation rate normal Rheumatoid factor negative Spinal X-ray abnormal

Symptomtext

At about midnight after the first dose of the covid vaccine that I received on 2/11/2021 at 8:00am, I experienced a migraine and pain in my spine, shoulders, hips and knees that kept me up trembling in excruciating pain. I was sore and fatigued 2 days after. At about 2:00pm after the second dose of the covid vaccine that I received on 3/4/2021 at 8:00am, I experienced fatigue, headaches, and the same excruciating pain in my spine, shoulders, hips, and knees. The fatigue and pain in my spine and joints after the two shots never went away. I also noticed a rapid regression in my muscle strength in my arms and legs at the gym. I went to my PCP on 3/5/2021 and he ordered labs that were completed on 3/11/2021. He noticed that my ANA screen was negative, my sed rate was negative, but my C-reactive protein was abnormal and wanted it repeated. On April 7,2021 my C-reactive protein level was even higher, to which he referred me to a Rheumotologist. After my referral finally went through, I was able to see the Rheumotologist on July 6, 2021. He ordered labs that were completed on July 16, 2021. My ANA screen came back positive with a titer of 1:80 and the pattern was Nuclear, Speckled, and my HLA-B27 was positive. On my follow up appointment on 8/12/2021 at 10:45am he told me that my labs and symptoms are consistant with Ankylosing Spondylitis. He ordered X-rays on my spine and hips to determine the damage as well as my treatment plan. On 8/26/2021 at 2:30pm, I went to my follow up appointment and was prescribed Humira shots that I will now have to take for the rest of my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 3/11/2021: C-reactive protein=9.4 High, Sed Rate by modified Westergren=2 Normal, ANA screen=negative. Complete metabolic panel normal with elevated AST=45 and ALT=36. 4/7/2021: 4/7/2021: C-reactive protein=9.7 high, sed rate=2 normal. 7/16/2021: ANA screen, IFA=positive, DNA (DS) Antibody=neg, SM Antibody=neg, SM/RNP Antibody=neg, Sjogren's antibody (SS-A)=neg , Sjogren's antibody (SS-B)=neg, ANA titer=1:80 high, ANA pattern=nuclear, speckled, HLA-B27=postive, creatine=0.89 normal, uric acid=5.3 normal , Hepatic function panel normal (including AST & ALT both normal), sed rate=2 normal, Cyclic citrullinated peptide=<16 neg, Rheumatoid factor=<14 neg, C-reactive protein=4.7 normal.
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: armour thyroid, lo loestrin Fe, albuterol, duexis, Viibryd
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1767357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: 26.02.2021
Beginn: 10.03.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: - / LA

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

Dyspnoea Exercise lack of Lung disorder

Symptomtext

Decreased lung capacity.; Not able to exercise; getting short of breath after only one minute of any type of physical activity.; This is a spontaneous report from a contactable consumer (patient). A 47-years-old male patient reported for himself that he received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL9267), via an unspecified route of administration, administered in arm left on 26Feb2021 at 01:00 PM (age at vaccination was 47-year-old) as dose 2, single for COVID-19 immunisation at health clinic facility. No other vaccines were received within four weeks of vaccination. No other medications were received witFhin 2 weeks of vaccination. The patient's medical history was not reported. The patient had known allergies with Codein. The patient's concomitant medications were not reported. The patient previously took first dose of bnt162b2 (Batch/Lot Number: EL9265), via an unspecified route of administration, administered in arm left on 29Jan2021 at 05:30 PM (age at vaccination was 47-year-old) as dose 1, single for COVID-19 immunisation. On 10Mar2021 at 12:00 PM, the patient experienced decreased lung capacity. Not able to exercise without getting short of breath after only one minute of any type of physical activity. The events resulted in visit to doctor or other healthcare professional office/clinic visit. No treatment was received. Prior to vaccination, the patient was diagnosed with COVID-19 and since the vaccination, the patient was not tested for COVID-19. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1753625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 89,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 19.02.2021
Beginn: 29.09.2021
Tage bis Beginn: 222,0
Dosis: 2
Route/Site: IM / LA

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

Asymptomatic COVID-19 Atelectasis Chest X-ray abnormal Dyspnoea Hypoxia Lung opacity Pneumonia Productive cough SARS-CoV-2 test positive Surgery Traumatic lung injury

Symptomtext

Patient was fully vaccinated against COVID 19 on 2/19/21. Patient was found to be asymptomatic COVID positive prior to a surgery on 9/17/21. Upon surgical follow-up in clinic, patient was symptomatic with productive cough, dyspnea and hypoxemia requiring 2L nasal cannula 02. Patient was admitted to reporting hospital on 9/29/21 and remains hospitalized at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 PCR swab positive 9/17/21 9/29/21 Chest X-ray Compared to 7/21/2020, lungs are underinflated with left basilar opacity, either atelectasis or localized organizing pneumonia pattern of lung injury resulting from SARS-CoV-2 infection. No pleural effusion or pneumothorax. Heart size and mediastinal contours are unchanged.
Aktuelle Erkrankungen: Anemia, osteopenia, obesity aortic stenosis, hypercholesterolemia, HTN, GERD, Deep vein thrombosis (2/21/2021), Chrons, C-diff infections
Vorgeschichte: Bladder cancer status post radical cystectomy with urostomy, bilateral lymph node dissection and ileal conduit urinary diversion last year complicated by recent vaginal cuff dehiscence with small bowel perforation status post exploratory laparotomy with partial small bowel resection, primary anastomosis and vaginal cuff repair, recent left lower extremity group C Streptococcus cellulitis complicated by sepsis, history of recurrent C. difficile colitis including recently, recently diagnosed COVID-19 infection, history of recurrent DVT anticoagulated on apixaban, history of Crohn's disease, history of limited breast cancer, hypertension, hypercholesterolemia, history of vitamin B12 deficiency and chronic anemia
Andere Medikamente: Eliquis 5mg, vitamin C 500mg, Calcium, cyanocobalamin, ferrous sultate 325mg, lasix 20mg, melatonin, lialda 1.2g, Multivitamin, prilosec 20mg, KCl 10 meQ, florajen3, Verapamil 240mg, vitamin D3, zinc sulfate, levothyroxine 25mg, mycostatin
Allergien: Sultamethoxazole-trimethoprim
Vorherige Impfungen: -

VAERS 1752326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: IN
Alter: 74,0
Geschlecht: M
Eingang: 01.10.2021
Impfdatum: 27.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: - / LA

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

Dyschezia Dyspnoea Fatigue Gait disturbance Headache Palpitations

Symptomtext

This is a spontaneous report from a contactable other HCP (reported for himself). A 74-year-old male patient received the 2nd dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot#: EL9267), at the vaccination age of 74, via an unspecified route of administration, left arm, on Feb 27, 2021, single dose, for COVID-19 immunization. The patient's medical not reported. Prior to the vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not tested for COVID-19. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccination. No allergies reported. The patient received other medications in two weeks. On Mar 3, 2021, at 04:00, patient experienced shortness of breath, tiredness, racing heart, headache and had hard time going to bathroom to defecate; with outcome of recovered Mar 2021. No follow-up attempts possible. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1749594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 30.09.2021
Impfdatum: 16.02.2021
Beginn: 04.08.2021
Tage bis Beginn: 169,0
Dosis: 2
Route/Site: - / -

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

Angiogram pulmonary abnormal COVID-19 COVID-19 pneumonia Dyspnoea Fibrin D dimer increased Hypoxia Laboratory test normal Lung disorder Oxygen saturation decreased Pulmonary fibrosis SARS-CoV-2 test negative SARS-CoV-2 test positive Superinfection Tachycardia

Symptomtext

"Fully vaccinated patient admitted for COVID originally on 08/11/21. Following note taken from pulmonology's dischage summary after second admission/discharge: ""78 yo M, hx of AAA, T2DM, prostate cancer, and recent COVID PNA, who came in with SOB. He was admitted 8/7-8/11 for similar symptoms, found to be COVID positive, received dexamethasone and remdesivir, completing his course. On admission, he was tachycardic, satting in the low 90's on 2.5 L NC, but quickly desatted to the 70's when ambulating on 4 L. His D-dimer was elevated but the rest of his labs were unremarkable. A CTA showed moderate bilateral airspace disease suggestive of evolving COVID-like changes with no PE. COVID test was negative. He was suspected to have a superimposed infection, received antibiotics and finished his course of Zosyn. He continued to require oxygen, eventually requiring high flow nasal canula, at one point. Pulmonology was consulted, and they determined that he likely had pulmonary fibrosis 2/2 post-COVID syndrome. He was given Solu-medrol during his stay. His symptoms slowly improved, and he was eventually brought down to 4 L NC at rest, requiring more with ambulation. On discharge day, he desatted to mid-70's on 6 L going up 2-3 steps on the stairs. We discussed with the patient what he wished to do knowing that information, and he still maintained that he wished to go home. He understood the risks of going home when he was hypoxic with ambulation and increased oxygen. He has stairs at home, but is willing to take breaks when going up stairs. He was advised to come back if he became short of breath at rest even with his current level of oxygen. """

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 33,0
Labordaten: COVID positive swab on 08/07/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Mixed dislipidemia, class 2 severe obesity, osteoarthosis, history of malignancy of prostate, abdominal aortic aneurysm, GERD, hypovitaminosis vit D, type 2 diabetes
Andere Medikamente: -
Allergien: Latex, statins
Vorherige Impfungen: -

VAERS 1730526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge El9267

moderat

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 19.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: OT / RA

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

Chills Dizziness Migraine Pain

Symptomtext

Chills; migraine; dizziness; body aches; This is a spontaneous report from a contactable healthcare professional (patient). A non-pregnant 45-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot number: El9267), intramuscularly, administered in right arm on 19Feb2021 at 15:30 (age at vaccination was 45-year-old) as dose number unknown, single for COVID-19 immunization. The patient's medical history included ulcerative colitis. Concomitant medications were not reported. The patient did not receive any other vaccine within 4 weeks. Prior to vaccination, the patient has not been diagnosed with COVID-19 and post vaccination, the patient has not been tested for COVID-19. The facility type where COVID-19 vaccine was administered was reported as workplace clinic. On 20Feb2021, the patient experienced chills, migraine, dizziness, and body aches. No therapeutic measures were taken as a result of the events. The outcome of the events was unknown. 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: Ulcerative colitis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1722910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 31.03.2021
Beginn: 21.09.2021
Tage bis Beginn: 174,0
Dosis: 1
Route/Site: UN / UN

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

Acute kidney injury COVID-19 pneumonia Hypothermia Rhabdomyolysis Troponin increased

Symptomtext

Hospitalization - pneumonia due to COVID-19 virus; non-traumatic rhabdomyolysis; acute kidney injury; hypothermia; elevated troponin

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1715241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 20.09.2021
Impfdatum: 09.03.2021
Beginn: 12.08.2021
Tage bis Beginn: 156,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Asymptomatic COVID-19 Condition aggravated SARS-CoV-2 test positive

Symptomtext

Pt is 66 yo male s/p Pfizer vaccination: dose 1 on 2/16/2021 and dose 2 on 3/9/2021. Pt has a history of metastatic prostate cancer to the bone, HCV, alcohol abuse, chronic abdominal pain and lower back pain. During time of vaccination, cancer managed with Eligard every 3 months. Last treatment before vaccination on 1/11. He presents to the hospital with worsening abdominal pain and admitted on 8/12 for pain management. Upon admission, patient tested positive for COVID-19 and was asymptomatic. No therapy for COVID management needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: Novel Coronavirus PCR- SARS-COV-2 Detected (8/12/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1712418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: LA
Alter: 60,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 23.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Dyspnoea

Symptomtext

shortness of breath; Weakness; This is the spontaneous report from a contactable consumer (patient). A 60-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number- EL9267) via an unspecified route of administration in arm left on 23Feb2021 01:30 PM (age at vaccination was 60 years) as dose 1, single for COVID-19 immunisation. The patient's medical history included ongoing asthma, she had asthma in the past but she had outgrown it. When she would get sinuses or a minor infection she would have little issue then. She used to have trouble breathing before but not like this. She never took any medication for the asthma, she is not on any medications or nebulizer treatments. The patient's concomitant medications were not reported. She did take vitamins and protein before the vaccine for a few days because thats what she read, She work in organic gardening and so she takes mostly organic stuff. She did not take other products. The patient stated that she got her first Pfizer Covid- 19 dose last 23Feb2021 and the next day she experienced weakness and shortness of breath on 24Feb2021 on 06:00 AM. The breathing was worse, but the weakness was not as bad, the weakness was better, it was like she could not do anything. It was reported that she was still having side effects. She read up a lot about the vaccine. she read that side effect usually last the first 2-3 days, but this is her 6th day, was it normal. When this all first began, when she heard about the shot, she heard that its suppose to be in the second shot that there would be side effects not the first. She does land scaping so she was pretty active and yesterday(28Feb2021) all she did was cuttings, she didnt do digging or anything but still got worn out and yesterday was the 5th day. It's like she just cant catch her breath. She did not take Tylenol, because she read that she was not suppose to. The outcome of weakness was resolving and for shortness of breath was not resolved. No follow-up attempts were possible. No further information was expected.

Weitere VAERSDATA-Felder

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

VAERS 1712377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 55,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 27.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Body temperature increased Dizziness Fatigue Paraesthesia Paraesthesia oral Pruritus Skin warm Somnolence Vaccination site pain Vaccination site pruritus

Symptomtext

Sore and very itchy Injection Site; Sore and very itchy Injection Site; Itching and Tingling around mouth and eyes; Itching and Tingling around mouth and eyes; feeling pins & Needles and Tingling all over my body; Dizzy; Tired; Sleepy; low-grade temperature; Forehead was warmer than usual; This is a spontaneous report from a contactable pharmacist (patient herself). A 55-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267), via an unspecified route of administration, administered in left arm on 27Feb2021 13:45 (age at vaccination: 55 years) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history included Hashimoto's, glaucoma and hazelnut allergy. Concomitant medication(s) included levothyroxine sodium tablets and brimonidine tartrate (ALPHAGAN) eye drops. On 27Feb2021 15:45, 2 hours after the vaccination, the patient was dizzy, tired, sleepy, low-grade temperature. On 27Feb2021, the patient's forehead was warmer than usual. On 28Feb2021, the patient was sore and very itchy at injection site, itching and tingling around mouth and eyes, feeling pins and needles and tingling all over her body. The patient received Hydrocortisone 1 percent Cream, Tylenol and Claritine as treatment for the adverse events. The patient did not have any other vaccine in four weeks. The patient was not diagnosed with covid-19 prior to vaccination nor was tested since vaccination. The outcome of all the events was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy (known allergies: Hazelnut); Glaucoma (Other medical history: Glaucoma); Hypothyroidism (Other medical history: Hashimoto's)
Andere Medikamente: LEVOTHYROXINE SODIUM; ALPHAGAN
Allergien: -
Vorherige Impfungen: -

VAERS 1364194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 39,0
Geschlecht: F
Eingang: 18.09.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Abdominal discomfort Diarrhoea Fatigue Feeling abnormal Headache Migraine Pyrexia Vaccination site pain

Symptomtext

low grade fever; fatigue; intermittent head aches; some upset stomach; diarrhea; a foggy/spacey feeling in my head; Arm pain near injection; This is a spontaneous report from a contactable other HCP (patient). A 39-years-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EL9267), via an unspecified route of administration, administrated in Right arm on 22Feb2021 13:00 (age at the time of vaccination 39-years-old), as a single dose for COVID-19 immunization. The patient's medical history included hypothyroidism, and hyperthyroidism, Hypothyroidism subsequent to radioactive thyroid ablation for Hyperthyroidism. The patient's concomitant medications included Levothyroxine Sodium (for many years). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: EL9265), via an unspecified route of administration, administrated in Right arm on 29Jan2021 14:00 (age at the time of vaccination 39-years-old), as a single dose for COVID-19 immunization. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination. Patient had no known allergies. On 22Feb2021 20:00, the patient experienced Arm pain near injection; on 23Feb2021 low grade fever, fatigue, intermittent head aches, some upset stomach, diarrhea, and a foggy/spacey feeling in my head. Patient did not received treatment as a result of adverse events. The outcome for all the events was not recovered. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hyperthyroidism (Hypothyroidism subsequent to radioactive thyroid ablation for hyperthyroidism); Hypothyroidism (Hypothyroidism subsequent to radioactive thyroid ablation for hyperthyroidism)
Andere Medikamente: LEVOTHYROXINE SODIUM
Allergien: -
Vorherige Impfungen: -

VAERS 1068639

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge el9267

moderat

Staat: FL
Alter: 72,0
Geschlecht: M
Eingang: 18.09.2021
Impfdatum: 01.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Mobility decreased Sleep disorder

Symptomtext

Left shoulder in so much pain, unable to use due to pain; This is a spontaneous report from a contactable consumer (patient). A 72-year-old male patient received bnt162b2 ((PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number was not reported), via an unspecified route of administration, administered in Arm Left on 01Mar2021 12:30 at the age of 72-year-old as dose 2, single for covid-19 immunisation. The patient medical history was none and no known allergies. The patient previously received bnt162b2 ((PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number was not reported), via an unspecified route of administration, on unspecified date as dose 1, single for covid-19 immunisation. The patient was not diagnosed with covid prior to vaccination and patient was not tested for COVID-19 post vaccination. Concomitant medications included tamsulosin, atorvastatin, oxybutynin taken for an unspecified indication, start and stop date were not reported. The patient experienced left shoulder in so much pain, unable to use due to pain on 03Mar2021 08:00. The patient did not receive any treatment in response to the events. The outcome of the vent was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained. 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: TAMSULOSIN; ATORVASTATIN; OXYBUTYNIN
Allergien: -
Vorherige Impfungen: -

VAERS 1704217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 16.09.2021
Impfdatum: 08.03.2021
Beginn: 10.09.2021
Tage bis Beginn: 186,0
Dosis: UNK
Route/Site: - / -

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

Angiogram pulmonary abnormal Atelectasis COVID-19 Chest discomfort Dyspnoea Inappropriate schedule of product administration Lung disorder Lung opacity Productive cough Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

First dose 2/12/2021 84-year-old male seen in office 9/7/2021 for clearance for upcomming knee surgery. presents to the emergency department complaining of shortness of breath yesterday morning. He began having congestion and cough with sputum production approximately 1 week ago with increasing dyspnea and chest pressure. CTA of the chest completed which demonstrated ground-glass opacities was a continuation most pronounced in the left lower lobe likely due atelectasis or air trapping tested positive for COVID-19. Tested positive for COVID-19 three weeks ago but was vaccinated with the second dose in April of 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: COVID test 9/10/2021
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, CAD, pre diabetes, overweight, hyperlipidemia,
Andere Medikamente: -
Allergien: penicillins
Vorherige Impfungen: -

VAERS 1704064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 13.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: SYR / RA

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

Blood pressure decreased Blood test normal Cardiac monitoring abnormal Cardiac stress test normal Condition aggravated Dizziness Echocardiogram Electrocardiogram normal Extrasystoles Fatigue Ultrasound scan normal Vertigo X-ray normal

Symptomtext

Heart skipping (extra beats) multiple times in a row, light-headed, room spins on standing, fatigue, blood pressure drop All this began around April 9th. By April 12th, early that morning, I called my doctor who had me come in immediately. When I got there it was so severe, he was fearful of a possible heart attack and sent me to the ER. The ER sent me home and the issues continued for me. On 6/4 I was sent to the ER again for the same issues. On 6/7 I saw a cardiologist. He did an ultrasound and found no problems with blood flow or the valves.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 4/12/21 - The ER kept me on a heart monitor and, did an EKG and ran blood tests to check for possible deficiencies. All test results came back as normal but blood pressure continued to be lower than normal and I was sent home. 6/4/21 - The ER did EKG, X-rays and blood work. All tests came back normal except blood pressure was still very low (sometimes as low as 79/59 and I was sent home once again and appointment was made for a cardiologist. Prescribed Metoprolol 1X/day and told to check my BP daily, wear compression socks at night, try to get more salt in my diet. 6/7/21 - Cardiologist did an ultrasound. The valves were working fine and blood flow was good. 6/9/21 - Cardiologist did a stress test and it was normal. 6/10/21 - A heart monitor was placed to be worn for 2 weeks - results were fine, other than the extra beats which began to slow down, with the Metoprolol. Blood pressure continues to be lower than normal.
Aktuelle Erkrankungen: GERD with Chronic Reflux Cough
Vorgeschichte: GERD with Chronic Reflux Cough; Osteoporosis; Low Blood Pressure; Possible Mitral Valve Prolapse was diagnosed years ago but recent cardiologist said I do not have prolapse and the recent episodes I had are not valve related issues.
Andere Medikamente: Famotidine 40mg 2X/day; Vitamin D3 Supplement; Vitamin B12 Supplement; Melatonin Supplement
Allergien: None
Vorherige Impfungen: -

VAERS 1704022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 44,0
Geschlecht: M
Eingang: 16.09.2021
Impfdatum: 27.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Chest pain

Symptomtext

Persistent (i.e., 24/7 but fluctuates in degree of severity) chest pain (believe it was more concentrated in center of chest early but appears to have migrated a bit to upper left side of chest) dating back from around the time of vaccinations (did not immediately connect the two - and only perhaps linking the pain to the vaccinations now as a result of seeing publicity about the potential for heart inflammation - as pain was very mild early on). Have taken some anti-heartburn OTC medication at medical professional's direction, but that has not been an effective solution as pain has continued. Not overwhelmingly crippling pain, just persistent and concerning. Have not had a chance to see a specialist for full-blown evaluation/diagnosis yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 1 diabetic
Andere Medikamente: Novolog; statin
Allergien: Egg (including flu vaccine)
Vorherige Impfungen: Flu Vaccine 30+ years ago, presumably adverse reaction to egg allergy

VAERS 1701905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injected limb mobility decreased Pain Pain in extremity

Symptomtext

From Feb. 20th through Aug. 14th unable to lift anything with left arm & constant sharp pain in upper left arm - felt like it was frozen also because I couldn't raise my arm up or move it backward without sharp pains & inability to move the arm. From Aug. 15th through today (Sept. 16th) have been able to move arm, but still cannot raise my arm up without pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: CRPS type II in lower extremities, allergic rhinitis, osteoporosis, arthritis
Andere Medikamente: Singulair, Xyzal, Fluticasone, Azylastine, Calcium, Vitamin D, Vitamin B12, Prevalite, Prolia, Gabapentin
Allergien: Penicillin, Boniva, mold & mildew, tree pollen, dust, cats
Vorherige Impfungen: -

VAERS 1950966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL 9267

moderat

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 13.09.2021
Impfdatum: 02.02.2021
Beginn: 02.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Condition aggravated Hypersensitivity Laboratory test White blood cell disorder

Symptomtext

1) increase in mast cell /allergy Sx's - starting xolair, prednisone to keep reactions down 2) Abrupt ^ BP sustained months when had normal BP life long

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: BP testing
Aktuelle Erkrankungen: mast cell, COPD
Vorgeschichte: COPD on continuous O2
Andere Medikamente: many - on antihistamines for mast cell
Allergien: many due to mast cell.
Vorherige Impfungen: -

VAERS 1694940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 13.09.2021
Impfdatum: 18.02.2021
Beginn: 01.09.2021
Tage bis Beginn: 195,0
Dosis: 2
Route/Site: IM / LA

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

Adult failure to thrive COVID-19 Chest X-ray normal Condition aggravated Cough Fall Feeling abnormal Head injury Loss of personal independence in daily activities Musculoskeletal chest pain Rib fracture SARS-CoV-2 test positive

Symptomtext

Hospitalized; COVID-19 positive (9.1.21); (fully vaccinated) Admission Date: 9/1/2021 Discharge Date: 9/5/21 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Failure to thrive in adult At high risk for falls COVID-19 virus detected HOSPITAL COURSE: Patient is a 83 yo male with history of Parkinson's disease and mild dementia, CAD s/p CABG, HTN, and mild intermittent asthma. Patient presented from home on 9/1 due to inability to care for himself. He was recently admitted from 8/12-8/17 for rib fractures after a fall at home. He discharged and returned home, but was having trouble caring for himself so returned to the ED 8/31. At that time, he was discharged directly to a Long term care facility, but did not stay after he discovered he would be living in a room with five other residents. Upon returning home with his son, he again was unstable and had a near fall, leading to his return to the ED. He notes ongoing right sided rib pain as well as an unproductive cough for two weeks. In the ED, he had a low grade temp of 100.3 with VS otherwise stable. COVID PCR was tested and positive. CXR unremarkable. He was unable to be discharged from ED due to COVID, so he was placed under observation. PT/OT evaluated patient and initially recommended subacute rehab versus home with assistance. However, the following day patient had improved and PT OT recommended return to home with assist. As family had concerns with patient returning to live on his own, set up multiple resources for home care. Patient appears to have decision making capacity and ultimately preferred to go home, reporting that he would not have been agreeable to a long-term care facility including assisted living. Patient did not develop any symptoms from COVID. He is without any complaints at time of discharge and denies any rib pain. Family updated prior to discharge and in agreement with plan

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Fall, hit head 8.12.21; rib fractures Parkinson's Disease Confusion / weakness / failure to thrive
Vorgeschichte: Chronic right rotator cuff tear Dyslipidemia Osteoarthritis Constipation Benign prostatic hyperplasia with lower urinary tract symptoms, symptom details unspecified Arthritis of wrist, degenerative, left Synovial cyst left wrist Essential hypertension Parkinsons disease Moderate persistent asthma without complication S/P total knee arthroplasty, left Abdominal aortic aneurysm (AAA) without rupture Dementia associated with other underlying disease without behavioral disturbance Recurrent falls NSTEMI (non-ST elevated myocardial infarction) Coronary artery disease involving native coronary artery CHF NYHA class II (symptoms with moderately strenuous activities), chronic, diastolic S/P CABG (coronary artery bypass graft) Closed fracture of multiple ribs of right side with routine healing Depression Gastroesophageal reflux disease without esophagitis Vitamin D deficiency Failure to thrive in adult COVID-19 virus detected Inadequate social support
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet carbidopa-levodopa (SINEMET) 25-100 MG per tablet chl
Allergien: Environmental Sneezing Penicillins Rash
Vorherige Impfungen: -

VAERS 1694316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 73,0
Geschlecht: M
Eingang: 13.09.2021
Impfdatum: 10.03.2021
Beginn: 10.06.2021
Tage bis Beginn: 92,0
Dosis: 2
Route/Site: SYR / RA

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

Computerised tomogram thorax abnormal Pneumonia

Symptomtext

Double pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: CAT Scan.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension; Cholesterol; Herpes.
Andere Medikamente: Atorvastatin; Hydrochlorothiazide; Valacyclovir; Lisinopril; Aspirin; Vitamin D; Fish Oil.
Allergien: None.
Vorherige Impfungen: -

VAERS 1692389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: UT
Alter: 93,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 12.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Blood pressure measurement Fatigue Hypertension

Symptomtext

This is a spontaneous report from a contactable consumer reported for mother and contactable consumer reported for herself. A 93-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EL9267; Expiration date was not reported), via an unspecified route of administration, administered in Arm Right on 12Feb2021 14:00 (at the age of 93-years-old) as DOSE 2, SINGLE for covid-19 immunisation at other facility. Patient was not pregnant at the time of vaccination. Medical history included high blood pressure, acid reflux disease from an unknown date and unknown if ongoing. Concomitant medication(s) included valsartan (VALSARTAN); omeprazole (OMEPRAZOLE); calcium (CALCIUM); colecalciferol (VITAMIN D [COLECALCIFEROL]) taken for an unspecified indication, start and stop date were not reported. The patient previously took CLEOCIN [CLINDAMYCIN HYDROCHLORIDE] and experienced allergy. The patient previously took first dose of BNT162B2 (Batch/Lot number: EL3247) in right arm on 22Jan2021 16:30 (at the age of 93-years-old) for covid-19 immunisation and experienced feeling washed out. The patient experienced high blood pressure, feeling very washed out as well on unspecified date in Feb2021. The patient underwent lab tests and procedures which included blood pressure measurement: 171/91. The event was stated as not serious. Three days after the second injection her blood pressure spiked on 16Feb2021 (reported as today) at 171/91 and feeling very washed out as well. No other vaccines within 4 weeks prior to the COVID vaccine. No treatment received for the adverse event. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Clinical outcome of events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210216; Test Name: Blood pressure; Result Unstructured Data: Test Result:171/91; Comments: second injection my blood pressure has spiked today at 171/91
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (oesophageal); Blood pressure high
Andere Medikamente: VALSARTAN; OMEPRAZOLE; CALCIUM; VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1376497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Biopsy skin abnormal Blood test Condition aggravated Eczema Eosinophilic pustular folliculitis Rash pruritic Rash Rash erythematous Skin weeping Ultrasound scan Urticaria

Symptomtext

signs of eosinophilic pustular folliculitis; Angry itchy rashes all over face and now body; This is a spontaneous report from a contactable consumer or other non hcp. A 37-years-old non-pregnant female patient received first dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EL9267) via an unspecified route of administration in Arm Left on 12Mar2021 13:00 (age at vaccination:37 Years) as DOSE 1, SINGLE for covid-19 immunisation (at hospital). Patient was not pregnant at the time of vaccination, patient didn't receive other vaccines within 4 weeks prior to vaccination, patient received other medications was birth control within 2 weeks of vaccination. Medical history included eczema from an unknown date and unknown if ongoing, herpes zoster from an unknown date and unknown if ongoing, allergy to plants (Birch tree allergy) from an unknown date and unknown if ongoing known allergies: Birch tree allergy. On 12Mar2021 16:00 the patient experienced signs of eosinophilic pustular folliculitis, angry itchy rashes all over face and now body. Patient had physician office visit for the events. Therapeutic measures were taken as a result of signs of eosinophilic pustular folliculitis, angry itchy rashes all over face and now body was topical steroids. Patient was not diagnosed with COVID-19 prior to vaccination, patient was not tested with COVID-19 to post vaccination. The outcome of the events eosinophilic pustular folliculitis, rash pruritic was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to plants (known allergies: Birch tree allergy); Eczema; Shingles.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1376497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 11.09.2021
Impfdatum: 12.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Biopsy skin abnormal Blood test Condition aggravated Eczema Eosinophilic pustular folliculitis Rash pruritic Rash Rash erythematous Skin weeping Ultrasound scan Urticaria

Symptomtext

signs of eosinophilic pustular folliculitis; Angry itchy rashes all over face and now body; This is a spontaneous report from a contactable consumer or other non hcp. A 37-years-old non-pregnant female patient received first dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EL9267) via an unspecified route of administration in Arm Left on 12Mar2021 13:00 (age at vaccination:37 Years) as DOSE 1, SINGLE for covid-19 immunisation (at hospital). Patient was not pregnant at the time of vaccination, patient didn't receive other vaccines within 4 weeks prior to vaccination, patient received other medications was birth control within 2 weeks of vaccination. Medical history included eczema from an unknown date and unknown if ongoing, herpes zoster from an unknown date and unknown if ongoing, allergy to plants (Birch tree allergy) from an unknown date and unknown if ongoing known allergies: Birch tree allergy. On 12Mar2021 16:00 the patient experienced signs of eosinophilic pustular folliculitis, angry itchy rashes all over face and now body. Patient had physician office visit for the events. Therapeutic measures were taken as a result of signs of eosinophilic pustular folliculitis, angry itchy rashes all over face and now body was topical steroids. Patient was not diagnosed with COVID-19 prior to vaccination, patient was not tested with COVID-19 to post vaccination. The outcome of the events eosinophilic pustular folliculitis, rash pruritic was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to plants (known allergies: Birch tree allergy); Eczema; Shingles.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1689247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 76,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 22.02.2021
Beginn: 06.09.2021
Tage bis Beginn: 196,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax abnormal Cough Dyspnoea Endotracheal intubation Lung disorder SARS-CoV-2 test positive

Symptomtext

Patient was fully vaccinated with Pfizer COVID-19 vaccine on 1/29/21 and 2/22/21. Patient admitted to reporting hospital on 9/6/21 as a transfer from Hospital. Admitting diagnosis is worsening COVID pneumonia requiring intubation. Patient was reported to arrive at ER after having 10-14 days of symptoms relating to cough. Over the last 5 to 6 days she then began having progressive difficulty breathing. Pt is still currently admitting at another hospital.

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 11,0
Labordaten: COVID PCR positive 8/31/21 Chest Xray 9/6/21 ET tube tip lies at the level the mid trachea. The heart size and vascularity are within normal limits. Bilateral patchy airspace disease is present, most pronounced in the lung bases. This had an organizing pneumonia pattern on prior CT. There is no pneumothorax or pleural effusion.
Aktuelle Erkrankungen: Polycythemia Vera, OSA on CPAP, H. pylori, HTN, Microscopic ischemic colitis
Vorgeschichte: Polycythemia Vera, OSA on CPAP, chronic low back pain, H. pylori gastritis, HTN, Microscopic Ischemic Colitis, JAK2 V6 17F+
Andere Medikamente: Aspirin 81mg, Lasix 20 mg, ruxolitinib phosphate (Jakafi), tessalon
Allergien: Penicillins, Hydrocodone
Vorherige Impfungen: -

VAERS 1689152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 22.03.2021
Beginn: 09.09.2021
Tage bis Beginn: 171,0
Dosis: 1
Route/Site: UN / UN

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

COVID-19 COVID-19 pneumonia

Symptomtext

Hospitalization - pneumonia due to COVID-19 virus

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1685095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 87,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 27.01.2021
Beginn: 10.08.2021
Tage bis Beginn: 195,0
Dosis: 2
Route/Site: SYR / UN

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

Ageusia Anosmia COVID-19 Cough Decreased appetite Dyspnoea Fatigue Oxygen saturation decreased SARS-CoV-2 test positive

Symptomtext

Patient started with symptoms on Friday 8/6/21. They decided to test him on Tues 8/10/21 and he came back positive on Wed 8/11/21. Patient has a history of COPD, CHF, Diabetes, Prostate Cancer, CVA. He started with SOB, cough, loss of taste and smell and now is very fatigued, has a loss of appetite and has low O2 saturation. Employee of clinic denied that he has any stomach concerns (no vomiting or diarrhea). His O2 sat has been in the high 70's and they are concerned about him. They may look into if he has pneumonia, as he has not had a chest xray, however they have already prescribed antibiotics, steroids, ivermectin, and vitamins C, D, and Zinc

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes Mellitus COPD Cardiovascular disease Hypertension Immunosuppressive condition
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1683031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 39,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 12.02.2021
Beginn: 13.08.2021
Tage bis Beginn: 182,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Migraine

Symptomtext

I have been getting intermittent migraines (I have tracking data of dates, severity, and possible triggers) for over a year. During this specific incident, the pain was in a different location, and didn't respond to any of my usual tricks to get it to clear. I tried to resolve on my own at home for about 4 days before seeking medical care. It took me an additional week to actually be able to get medical care. With help from a pharmacist I was able to get it manageable and saw my doctor for a new migraine prescription on August 26th. I have had intermittent headaches since then.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma - diagnosed July 2020 after chronic bronchitis caused by unknown upper respiratory infection in January of 2020. Anemia - lifelong
Andere Medikamente: Symbicort BID, Claritin SID, Tylenol as needed.
Allergien: Allergic to doxycycline, sulfa based drugs, Pseudocholinesterase deficiency syndrome leads to anesthesia concerns.
Vorherige Impfungen: -

VAERS 1683017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 73,0
Geschlecht: M
Eingang: 08.09.2021
Impfdatum: 21.01.2021
Beginn: 31.07.2021
Tage bis Beginn: 191,0
Dosis: 2
Route/Site: SYR / UN

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

Chest X-ray Cough Dehydration Headache Hypotension Nasopharyngitis Respiratory tract congestion

Symptomtext

PUI's symptoms started with a cold-like symptoms - congestion, cough, headache.The doctors at the urgent care where they tested sent PUI to Hospital for chest x-ray due to cough and smoking hx. Wife states PUI stayed 1 night in the hospital due to dehydration and low Blood pressure and was discharged the next day.

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Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Current Smoker
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1682456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 14.02.2021
Beginn: 31.08.2021
Tage bis Beginn: 198,0
Dosis: 2
Route/Site: IM / RA

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

Bronchiectasis COVID-19 Computerised tomogram thorax abnormal Condition aggravated Cough Haemoptysis Imaging procedure abnormal Lung infiltration Pneumonia pseudomonal Sputum culture positive Sputum increased

Symptomtext

Hospitalized 8.30.21; COVID-19 positive 8.31.21; fully vaccinated Admission Date: 8/30/2021 Discharge Date: 09/06/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Pneumonia of both lungs due to Pseudomonas species, unspecified part of lung [J15.1] Pseudomonal pneumonia [J15.1] Bronchiectasis [J47.9] HOSPITAL COURSE: Patient is a 74 y.o. who has a past medical history significant for long-standing severe bronchiectasis of unclear etiology, heart failure with reduced ejection (NICM) complicated by severe aortic stenosis (for which she is currently undergoing evaluation for TAVR), atrial flutter on chronic Eliquis, and chronic anemia. She was admitted 8/30 for presumed exacerbation of her chronic bronchiectasis, with recent sputum cx having grown multi-drug resistant Pseudomonas aeruginosa. Historically, she has hx of isolation of multiple morphotypes of Pseudomonas, as well as hx of Burkholderia and Citrobacter in the past. She was admitted on the recommendation of her primary pulmonologist. She had failed 2 rounds of ciprofloxacin this month and was still having increased sputum production, cough. She grew pseudomonas again 8/19 but was resistant to oral agents. She was started initially on meropenem but after beign seen by ID was transitioned to ceftazidime which she tolerated well. CT thorax showed new foci of patchy and nodular infiltrates. Film array incidentally returned positive with COVID-19. She did have ongoing hemoptysis but NOT massive and was controlled. SHe was seen by pulmonology and ID throughout her course. Hemoptysis improved and stabilized. She was back to her baseline 2L O2. ID recommended continuing ceftaz through 9/14. SHe had a midline placed on 9/6 and was discharged home in stable condition with home visiting nurses and infusion setup to start at 1700 today. Her eliquis was resumed and she was told to monitor for further hemoptysis. PCP was messaged to have their staff set up a follow up appointment, even if virtual. ROS Patient feels good today. Ready to go home. Excited to get home. No new symptoms. Coughing improving slowly. No further significant hemoptysis. No fevers no chills. Breathing easier. CONSULTS / RECOMMENDATION: pulm ID INPATIENT PROCEDURES: Midline placed 09/06/2021

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: Hospitalized 8.30.21; COVID-19 positive 8.31.21; fully vaccinated Possible respiratory infection (treated with antibiotics) 8.3.21 (bronchiectasis) admitted to hospital 6/19/21 - 7/4/21 due to aortic valve stenosis. Nauseous; increased SOB; hemoptysis; hypoxia
Vorgeschichte: NICM (nonischemic cardiomyopathy) Osteoporosis GERD with moderate hiatal hernia and patulous esophagus, likely contributing to occult aspiration DA (degenerative arthritis) Bronchiectasis without complication Hemoptysis Normocytic anemia History of anal cancer s/p chemoradiation 7/2015 Overflow incontinence Transient Loss of sensation Tibial plateau fracture, right, closed, initial encounter COVID-19 virus infection Acquired hypothyroidism Hypomagnesemia Encounter for monitoring long-term proton pump inhibitor therapy Syncope Aortic root enlargement Diastolic dysfunction Aortic valve stenosis Iron deficiency Hypoxia Acute systolic heart failure Atrial flutter Adrenal insufficiency Other specified anxiety disorders Bronchiectasis with acute lower respiratory infection Acute on chronic respiratory failure with hypoxemia Unspecified severe protein-calorie malnutrition
Andere Medikamente: acetaminophen (TYLENOL 8 HOUR ARTHRITIS PAIN) 650 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization Amikacin Sulfate Liposome (ARIKAYCE) 590 MG/8.4ML SUSP amiodarone (PACERONE) 200 MG tablet amitriptyline (ELAVIL) 25 MG table
Allergien: Allergies Bactrim Codeine Demerol Levaquin Meperidine Mobic [Meloxicam] Narcotics Pain Medications Pulmozyme [Dornase Alfa] Sulfa Drugs Nausea Only Penicillins Nausea and Vomiting
Vorherige Impfungen: -

VAERS 1678791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 70,0
Geschlecht: M
Eingang: 07.09.2021
Impfdatum: 11.02.2021
Beginn: 01.09.2021
Tage bis Beginn: 202,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Asthma COVID-19 Chronic obstructive pulmonary disease Dizziness Encephalopathy Headache Leukocytosis Malaise Mobility decreased Pyrexia Renal failure

Symptomtext

Patient presented to Hospital on 9/1/2021 with complaints of fever, weakness, headache, and malaise. He was recently hospitalized at hospital on 8/27-8/29/2021 for Covid-19 viral infection with associated general weakness and mild encephalopathy that resolved, mild COPD/asthma exacerbation, leukocytosis worsened with steroid-induced therapy, and mild renal insufficiency. He was discharged on oral prednisone and Levaquin for 7 days. He was recommended to continue isolation precautions through 9/4/2021 and follow-up with his PCP in 1 week. The patient had no complaints of illness or discomfort on Sunday and Monday. However, when he awoke on Tuesday (8/31/21) morning he had a fever of 102 and a pounding headache. He felt weak and dizzy. When he awoke on Wednesday (9/1/21) he continued to feel the same. He presented to Hospital outpatient services for Casirivimab-imbevimab 1200 mg infusion. During that time he was afebrile with T-max 100.0 and vital signs were stable. Wednesday evening at home, he developed a recurrent headache and febrile conditions. He then proceeded to call EMS as he was unable to get out of his chair.

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

VAERS 1678770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Cardiac stress test abnormal Chills Echocardiogram normal Electrocardiogram ambulatory normal Electrocardiogram normal Laboratory test Pain Palpitations Tremor

Symptomtext

After my second dose and between 11pm to 11:30pm, I got chills to my body, teeth were rattling against each other. My body was extremely shaking and the symptoms lasted till about 12:30am. I placed warm blankets and finally my chills and body aches eased off. At about 2am to 2:30 on 02-12-2021. woke up racing heart beat and pounding heart. I again felt exploding feeling in my chest. I contacted my PCP on Friday 02-12-2021 and reported the symptoms. The chills were vaccine related and probably related with the vaccine. I saw the cardiologist on 02-23-2021; he did an EKG in office and also ordered a 3D echocardiogram, a nuclear stress test and also a 24 hour event holter monitor was placed which I wore for two solid weeks. I took the holter off on 03-08-2021. On 03-17-2021 had echocardiogram and on 03-26-21; nuclear and echocardiogram were normal. Paroxysmal atrial fibrillation showed on the nuclear test. The cardiologist placed me on blood thinner medication because he is trying to avoid any chance of stroke. My doctor does not know if this is related to the vaccine and the timing is interesting. I feel today do not have any transient blood spikes and I am taking Eliquis 5mg twice a day. I am scheduled to see my cardiologist on October 1st 2021 to repeat exams, holter monitor. I also can not sleep due to the tinnitus since my first vaccine. I took OTC Tylenol PM to help me fall asleep. The tinnitus in my ears have not gone away and my doctor tells me I will have this for rest of my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Lab work; was normal. EKG; normal, nuclear stress test, holter monitor
Aktuelle Erkrankungen: -
Vorgeschichte: Under active thyroid since 1980; I take levothyroxine 50 mg since 1990.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1675331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 33,0
Geschlecht: M
Eingang: 05.09.2021
Impfdatum: 10.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / AR

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

Blood thyroid stimulating hormone Cardiac telemetry Chest X-ray Chest pain Computerised tomogram Dizziness Dyspnoea Echocardiogram Full blood count Lipids Metabolic function test Palpitations Sedative therapy

Symptomtext

Chest pain, heart palpitations, lightheaded, shortness of breath. No specific treatment plan. I was told to drink more water and work on my cholesterol and not lift heavily for weight lifting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 12-lead 07/07/2021, EKG 12-lead 07/29/2021, Echocardiogram 08/12/2021, Lipid Panel 08/13/2021, CBC 08/17/2021, Comprehensive Metabolic Panel, 08/17/2021, TSH 08/17/2021, Event Monitor - Mobile Telemetry (MCOT) 08/18/2021, X ray chest single view 08/25/2021 CAT Scan with sedation 09/10/2021. Some sort of sleep test in the near future.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multi-vitamin, turmeric 1200 mgs, Omega-3 1000 mgs, Glucosamine and chondroitin supplement, L-glutamine 5-10 grams 5 X week, creatine monohydrate 5-10 5 X week, whey protein 25 grams,
Allergien: Raw cherries and raw apples.
Vorherige Impfungen: -

VAERS 1673622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 04.09.2021
Impfdatum: 09.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Dyspnoea

Symptomtext

I was having difficulty in breathing and short of breath; This is a spontaneous report from a contactable consumer or other non hcp (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection, Lot Number: EL9267) via an unspecified route of administration on 09Feb2021 as dose 1, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that "the patient had the first Pfizer shot (clarified as Covid 19 vaccine) on 09Feb2021 and the next day on 10Feb2021 was having difficulty breathing and short of breath and went to urgent care and they gave patient a shot of he/she think (statement incomplete) and they put patient on a breathing machine and patient was wondering if he/she should go get the second shot on 02Mar2021". The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1670466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 03.09.2021
Impfdatum: 10.02.2020
Beginn: 03.04.2021
Tage bis Beginn: 418,0
Dosis: 1
Route/Site: SYR / RA

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

Abdominal discomfort Blood parathyroid hormone increased Blood potassium decreased Bowel movement irregularity Calcium ionised decreased Chills Diarrhoea Feeding disorder Heart rate increased Nausea Tremor

Symptomtext

Experienced gastro events and the only thing different that I had done was the vaccine shot. I experienced nausea, rapid heart beat, chills and shaking. This went on for three days before going to emergency room. I was afraid to eat due to getting sick. I also would not have a bowel movement for 5 or more days, then would have diarrhea for 2 days. I would have the nausea, rapid heart beat, chills and shaking at least 2 days a week. I switched up my diet thinking it might be what I was eating and still had the same results. This has gone on since April 2021. I cannot definitely say it was the vaccine shot, but it has been the only thing different that I have done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Blood test, which showed high calcium Ionized at 1.30 mmol/L, high PTH at 99.5 PG/ML and low potassium at 3.1 mmo/L
Aktuelle Erkrankungen: none
Vorgeschichte: rheumatoid arthritis, premature atrial beats
Andere Medikamente: Amlodipine Besylate, L-Thyroxine, Estradiol, Methotrexate, Pravastatin, Tolterodine Tart, Losartan/HTCZ, Folic Acid, Enbrel, Myrbetriq, Bayer aspirin, D3
Allergien: IVP contrast dye
Vorherige Impfungen: -

VAERS 1666355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 02.09.2021
Impfdatum: 18.03.2021
Beginn: 26.08.2021
Tage bis Beginn: 161,0
Dosis: 1
Route/Site: IM / UN

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

C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Decreased appetite Dyspnoea Fibrin D dimer increased Haemodialysis Lung infiltration Platelet count decreased Productive cough Pyrexia SARS-CoV-2 test positive Thrombocytopenia

Symptomtext

Hospitalized; COVID-19 positive (8.26.21) - after being fully vaccinated Admission Date: 8/26/2021 Discharge Date: 8/30/2021 Active Hospital Problems Diagnosis Date Noted POA ? Pneumonia due to COVID-19 virus 08/26/2021 Yes ? ESRD (end stage renal disease) on dialysis (HCC) 07/31/2019 Yes HOSPITAL COURSE: 68 year old man with hx of CAD, pacemaker in place, NIDDM2, HTN, ESRD on HD on compassionate dialysis program. He was dialyzed on 8/23/21 and felt well. Developed cough, sputum, shortness of breath over the past 3 days. He developed a fever. Denied any weight gain or pedal edema or chest pain. His appetite has been down. He presented to the ER on 8/26/21. In the ER, he had a fever 38, 76 bpm, 95% on RA, CXR showed bilateral infiltrates, COVID PCR was positive. He will be admitted for further treatment of COVID pneumonia. CRP 64.6. D-dimer 1130. He is previously vaccinated, Pfizer COVID-19 vaccine: 3/18/2021, 2/23/2021. He was started on Decadron 6 mg po daily and received 5 doses, he needs 5 more days. Should stay in isolation until he finish Decadron 6 mg daily. He was evaluated by the dr. and was found to needs 2 l/m at all times. Airway Oxygen will deliver portable tank to room for DC home. ESRD on hemodialysis, he had 2 hemodialysis while in hospital. Should continue compassionate hemodialysis as before. He had mild thrombocytopenia with Plt. Count of 110 at discharge. PCP to follow.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Cough -- > found to be COVID-19 positive 8.26.21 Multiple hospital admissions: ESRD; dialysis; hyperkalemia; SOB; leg / facial swelling; uremia
Vorgeschichte: Anemia of chronic disease ESRD needing dialysis (HCC) Hypertension Hyperlipidemia Monoclonal gammopathy of unknown significance Non-proliferative diabetic retinopathy, severe, both eyes (HCC) Stage 5 chronic kidney disease on chronic dialysis (HCC) Daytime sleepiness Subepithelial esophageal mass Cardiac pacemaker in situ Dependence on renal dialysis (HCC) Right kidney mass End stage renal failure on dialysis (HCC) ESRD (end stage renal disease) on dialysis (HCC) ESRD on hemodialysis (HCC) Peripheral neuropathy Renal mass Chronic heart failure with preserved ejection fraction (HCC) Coronary artery disease Diabetes mellitus type 2, insulin dependent (HCC) Acute respiratory failure (HCC) ESRD needing dialysis (HCC) Counseling regarding advance care planning and goals of care Clear cell carcinoma of right kidney (HCC) Appendicitis ESRD needing dialysis (HCC) Debility Other constipation Goals of care, counseling/discussion ESRD needing dialysis (HCC) Pneumonia due to COVID-19 virus
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet aspirin EC 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet benzonatate (TESSALON) 100 MG capsule carvedilol (COREG) 25 MG tablet dexamethasone (DECADRON) 6 MG tablet diphenhydrAMINE-Zinc
Allergien: Captopril Swelling, Angioedema, Throat swelling Penicillins Hives Adhesive Tape Rash Norco [Hydrocodone]
Vorherige Impfungen: -

VAERS 1661423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OK
Alter: 79,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 23.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Asthenia Body height Body temperature Chills Pain Pyrexia Tremor Vaccination site pain Weight

Symptomtext

Weakness; Shaking; Generalized aching; Injection site pain; Chills; Fever; This is a spontaneous report form a contactable consumer (Patient) reported that. A 79-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in Arm Right on 23Feb2021 11:15 (Batch/Lot Number: EL9267; Expiration Date: May2021) as SINGLE DOSE for covid-19 immunization(Age at vaccination 79 years). The patient past Medical history included gastroesophageal reflux disease from an unknown date and unknown if ongoing Blood pressure high (Caller says that she was put on a blood pressure medication 10-15 years ago for this). The concomitant medication was none. Caller says that she was fine that afternoon she had her second dose, which was at 11:15AM. She says that later she hurt bad and could barely move, had a fever of 101-102 degrees Fahrenheit on unspecified date in Feb2021, and nothing else. She says that the pain with her muscles had never hurt like that before, which went on that night and the next day she is better, today she is kind of weak and feels knocked out today. She says her arm was sore but that was not bad, she exercised it and it was fine. She says she just ached and throbbed all over, and couldn't lay any way comfortably, she got hot and had chills and shakes that went on a big part of the night to the next day on 23Feb2021. She says that last night she slept well and feels better she is just beat and kind of weak. Caller says that she has been taking Tylenol then finally took Advil, which she doesn't like to take Advil because she has stomach problems, but they brought her fever down and she feels better. Caller says that she doesn't have those medications with her to provide UIPC/LOT/EXP she says she recently got them, and they were relatively new on the store shelf. No further details provided about the Tylenol or Advil. The event outcome was Unknown for weakness and recovering for rest of the events. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:5 feet 8 inches and a quarter tall.; Test Date: 202102; Test Name: fever; Result Unstructured Data: Test Result:101-102 Fahrenheit; Comments: had a fever of 101-102 degrees Fahrenheit; Test Name: weight; Result Unstructured Data: Test Result:145-146 lbs
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (esophageal) (Caller says she has that real bad, she has had it off and on for 20 years.); Blood pressure high (Caller says that she was put on a blood pressure medication 10-15 years ago for this.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1120401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Asthenia Body temperature Chills Headache Lymph node pain Basophil count increased Chest pain Lymphadenopathy Magnetic resonance imaging abnormal Magnetic resonance imaging Malaise Myalgia Nausea Pruritus Mean cell volume decreased Pain Pyrexia Sleep disorder

Symptomtext

Lymph nodes under arm hurt; Fever; Chills; Muscle aches and pain; Truly feeling lousy; Headache; Itchy but no hives; nausea; Weak; This is a spontaneous report from a contactable consumer (patient herself). A 68-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267), via an unspecified route of administration, administered in right arm on 23Feb2021 10:00 (age at vaccination: 68 years) as DOSE 2, Single for covid-19 immunisation. The patient's medical history included ongoing just diagnosed with ductal carcinoma in situ breast cancer (recently had mri with contrast). The patient's concomitant medications were not reported. The patient did not have no known allergies. The patient's historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unknown date as DOSE 1, single. The patient did not have any other vaccine in four weeks. On 23Feb2021 22:15, the patient experienced lymph nodes under arm hurt, fever, chills, muscle aches and pain, truly feeling lousy, headache, itchy but no hives, nausea and weak. The patient received Tylenol as treatment for the adverse events. On 23Feb2021, the patient's body temperature was 100 and on an unknown date, magnetic resonance imaging with unknown result. The patient did not have covid prior vaccination nor was tested since vaccination. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210223; Test Name: Body temperature; Result Unstructured Data: Test Result:100; Test Name: MRI; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer in situ (Just diagnosed with ducal carcinoma in situ breast cancer.. recently had mri with contrast.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1120401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Asthenia Body temperature Chills Headache Lymph node pain Basophil count increased Chest pain Lymphadenopathy Magnetic resonance imaging abnormal Magnetic resonance imaging Malaise Myalgia Nausea Pruritus Mean cell volume decreased Pain Pyrexia Sleep disorder

Symptomtext

Lymph nodes under arm hurt; Fever; Chills; Muscle aches and pain; Truly feeling lousy; Headache; Itchy but no hives; nausea; Weak; This is a spontaneous report from a contactable consumer (patient herself). A 68-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267), via an unspecified route of administration, administered in right arm on 23Feb2021 10:00 (age at vaccination: 68 years) as DOSE 2, Single for covid-19 immunisation. The patient's medical history included ongoing just diagnosed with ductal carcinoma in situ breast cancer (recently had mri with contrast). The patient's concomitant medications were not reported. The patient did not have no known allergies. The patient's historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unknown date as DOSE 1, single. The patient did not have any other vaccine in four weeks. On 23Feb2021 22:15, the patient experienced lymph nodes under arm hurt, fever, chills, muscle aches and pain, truly feeling lousy, headache, itchy but no hives, nausea and weak. The patient received Tylenol as treatment for the adverse events. On 23Feb2021, the patient's body temperature was 100 and on an unknown date, magnetic resonance imaging with unknown result. The patient did not have covid prior vaccination nor was tested since vaccination. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20210223; Test Name: Body temperature; Result Unstructured Data: Test Result:100; Test Name: MRI; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer in situ (Just diagnosed with ducal carcinoma in situ breast cancer.. recently had mri with contrast.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1658597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: SC
Alter: 81,0
Geschlecht: F
Eingang: 31.08.2021
Impfdatum: 18.02.2021
Beginn: 23.06.2021
Tage bis Beginn: 125,0
Dosis: 2
Route/Site: SYR / RA

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

Blood pressure increased Blood test Computerised tomogram Decreased appetite Feeling abnormal Headache Magnetic resonance imaging head normal Migraine Nausea Sinusitis Sleep disorder Vision blurred

Symptomtext

I woke up with a headache all over the head. Head felt like it was going to explode. I took 2 extra strength Tylenol. I took another Tylenol before I went to bed. I had trouble sleeping. June 24th woke up with a headache and thought it might be blood pressure so didn't take anything that day. Went to bed with headache and took Tylenol at bedtime and still had trouble sleeping. Next day the same thing. The 26th headache was worse and not much sleep and called my PCP but they weren't open. 27th was feeling really bad, no appetite, blurry vision, nauseated, blood pressure getting really high and headache really bad. Called daughter and went to the ER 200/88. They ran some tests and gave me a bag of fluid and IV cocktail, and headache eased up from what they gave me and sent me home. They diagnosed it as migraines. I got home and ate soup and crackers and the headache returned but my blood pressure eased up. The headache continued and then I went to my PCP she treated for sinus infection and headache didn't go away. They gave me migraine medication and I took 2 doses and it didn't go away. In the main time Doctor's are still trying to figure out what's going on. Neurologist thinks it's a migraine she gave me 10 pills, I took the Ubravely and I took 6 pills and it didn't help. So I stopped taking it and called the Neurologist back. Still having the headache for 2 months. DPHT is what the Neurologist thought it could be and put me on Topamax which I've been taking and hasn't helped. Sept. 15th I go back to the Neurologist. Currently no one knows what's causing the persistent headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: CT scan, MRI of the brain which came out normal, bloodwork
Aktuelle Erkrankungen: No, I was perfectly healthy
Vorgeschichte: Affib; Breast cancer 20 years ago
Andere Medikamente: Eliquis; Losartan; Pacerone; Temazepam; Loratadine; Melatonin; Multivitamin; Probiotic every other day
Allergien: Not that I know of. Only Cayenne pepper
Vorherige Impfungen: -

VAERS 1652704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 18.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: OT / LA

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

Asthenia Dizziness Erythema Feeling hot Headache Migraine Myalgia Nausea Peripheral swelling Photophobia SARS-CoV-2 test Tinnitus Visual impairment

Symptomtext

Severe, debilitating, crushing, headache; debilitating; migraine-type; vision issues; sensivity to light; noise; arm swelling; hot; red; nausea; dizziness; muscle aches; This is a spontaneous report from a contactable consumer or other non-HCP. A 65-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267; Expiration Date: 31May2021), intramuscular, administered in Left Arm on 18Feb2021 as DOSE 2, SINGLE (at the age of: 65-year-old) for covid-19 immunization. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution injection, Lot number: EL3247) intramuscular, administered in Left Arm on 20Jan2021 (at the age of: 65-year-old) for covid-19 immunization. Medical history included psoriatic arthropathy from 1980 and ongoing, fibromyalgia, covid-19 from Feb2020 and she believes she had covid-19 in Feb2020. There were no concomitant medications. The patient previously took statins and experienced drug hypersensitivity, bnt162b2 for covid-19 immunization. Facility where the most recent COVID-19 vaccine was administered is mentioned as Hospital. Vaccine was not administered at Military facility. Other vaccine in fourweeks as Pfizer COVID 19 on 04Feb2021. Prior to vaccination, Unknown about the patient was diagnosed with COVID-19 and since the vaccination, the patient has been not tested for COVID-19. On 20Feb2 021 the patient experienced severe, debilitating, crushing, headache, debilitating, migraine-type, vision issues, sensivity to light, noise, arm swelling, hot, red, nausea, dizziness, muscle aches. The patient underwent lab tests and procedures which included sars-cov-2 test: had covid-19 on Feb2020 I believe I had covid-19 in Feb2020. Therapeutic measures were taken as Pain med, office visits, MRIs as a result of severe, debilitating, crushing, headache. The outcome of event severe, debilitating, crushing, headache was not recovered while outcome of rest all events unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 202002; Test Name: COVID-19; Result Unstructured Data: Test Result:had covid-19; Comments: I believe I had covid-19 in Feb2020
Aktuelle Erkrankungen: Psoriatic arthritis
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (I believe I had covid-19 in Feb2020); Fibromyalgia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1648479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 65,0
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

Had some tingling down my left arm into my thumb and hand. Little bit of numbness in thumb; Had some tingling down my left arm into my thumb and hand. Little bit of numbness in thumb; This is a spontaneous report from a contactable other hcp. A 65-years-old male patient received first dose of bnt162b2 (BNT162B2, Pfizer-BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number EL9267), via an unspecified route of administration, administered in Arm Left on 25Feb2021 15:30 as DOSE 2,SINGLE for covid-19 immunisation (Age at vaccination 65 years). The patient medical history and concomitant medications were not reported. On 25Feb2021 15:30 patient experienced had some tingling down my left arm into my thumb and hand. little bit of numbness in thumb. Therapeutic measures were taken as a result of events includes ice on hand. No other vaccine in four weeks. The outcome for both events was recovered on an unspecified date in 2021. No follow up attempts are needed. Information on Lot/batch cannot be requested. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1647901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 14.02.2021
Beginn: 15.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Cough Dyspnoea Feeling abnormal

Symptomtext

Shortness of breath; Cough; Feel moody; This is a spontaneous report from a contactable Other-HCP (patient). A 37-year-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot Number: EL9267), via an unspecified route of administration, administered in left arm on 14Feb2021 05:00 (age at the time of vaccination 37-years-old) as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient had no known allergies. On 15Feb2021, the patient experienced shortness of breath, cough, and feel moody. No covid prior vaccination. Covid tested post vaccination was unknown. The outcome for all the events was unknown. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1646831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 18.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Blood pressure abnormal Chills Dizziness Hypertension Pain Pyrexia SARS-CoV-2 test Vomiting

Symptomtext

by Sun. 31Jul, I checked myself into a hospital and my blood pressure was 207/94. I was given medication for BP, but it is still very erratic.; Suddenly on 25Jul I began vomiting which lasted into that night; For the next 5 days I remained very dizzy; The day after that shot I had fever, chills and soreness.; The day after that shot I had fever, chills and soreness.; The day after that shot I had fever, chills and soreness.; This is a spontaneous report from a contactable consumer (patient). This is the first of two reports with events experienced under the second dose. A 73-year-old female patient not pregnant received second dose of bnt162b2 (BNT162B2), via an unspecified route of administration, administered in Arm Left on 18Feb2021 14:15 (Lot Number: EL9267) as single dose (at age of 73-year-old) for covid-19 immunisation. Medical history included allergies to sulfa and penicillin, sjogren's syndrome, hypo thyroid. Concomitant medication received within 2 weeks of vaccination included levothyroxine sodium (SYNTHROID). The patient previously took first dose of bnt162b2 (BNT162B2) for covid-19 immunisation on 21Jan2021 03:15 PM in Left arm, lot number: EL9263 (at age of 73-year-old) and experienced pain in extremity (first vaccine shot 21Jan2021, her arm was very sore for 3 days), she previously received amoxicillin, clavulanic acid (AUGMENTIN) and experienced drug hypersensitivity. Facility where the most recent COVID-19 vaccine was administered: Public Health Clinic. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient stated that her blood pressure had been 110/70 her whole life. Her first vaccine shot was on 21Jan2021, her arm was very sore for 3 days. Patient had her second shot on 18Feb2021. The day after that shot (19Feb2021) she had fever, chills and soreness. Suddenly on 25Jul2021 at 09:30 she began vomiting which lasted into that night. For the next 5 days she remained very dizzy, on 31Jul2021 patient checked herself into a hospital and her blood pressure was 207/94, she was given medication for blood pressure (BP), but it was still very erratic. The patient was hospitalized for blood pressure was 207/94, vomiting and dizziness for 2 days. Events blood pressure was 207/94, vomiting and dizziness resulted in Emergency room/ department or urgent care, hospitalization and they were treated with blood pressure and anti vomiting medications. Since the vaccination, the patient has been tested for COVID-19, on 31Jul2021 with Nasal Swab and result was negative. Patient had not recovered from blood pressure was 207/94 and dizziness, she recovered on unknown date from Vomiting, while outcome of the other mentioned events was unknown. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101025465 same patient/reporter, different vaccine dose/AE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 2,0
Labordaten: Test Name: my blood pressure was 207/94; Result Unstructured Data: Test Result:110/70; Test Date: 20210731; Test Name: my blood pressure was 207/94; Result Unstructured Data: Test Result:207/94; Test Date: 20210731; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Penicillin allergy; Sjogren's syndrome; Sulfonamide allergy
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1256360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 13.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

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

Blood test Body temperature Chest X-ray Fatigue Gait disturbance C-reactive protein increased Headache Immunoglobulins Pain Loss of personal independence in daily activities Magnetic resonance imaging Pain in extremity Red blood cell sedimentation rate increased X-ray Red blood cell count decreased Synovial cyst Total complement activity test Tremor

Symptomtext

extreme tiredness; trouble walking; legs are sore but not related to muscle or bone/legs are sore in her inner thigh area; Things like bending over, putting her shoes and socks on and going up steps are hard for her to do.; This is a spontaneous report from a contactable consumer or other non-health care professional (patient). A 57-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL9267; Expiration Date: 31May2021), via an intramuscular route of administration (at the age of 57-years), on 13Feb2021 at 08:30 as dose 1,.single for COVID-19 immunisation and co-suspect as adalimumab (HUMIRA, Batch/Lot number was not reported), via an subcutaneous route of administration an unspecified date at unspecified dose for an unspecified indication and received apremilast (OTEZLA, Batch/Lot number was not reported), via an unspecified route of administration from Mar2021 to Jul2021, at unspecified dose for an unspecified indication. Medical history included ongoing asthma had maybe 15 years , allergy to vaccine from 2018 to an unknown date. The patient concomitant medications were not reported. The patient previously took pneumococcal vaccine and experienced cellulitis, Arm swelled up, pneumococcal vaccine and experienced fever. On 13Feb2021, the patient experienced extreme tiredness, trouble walking, legs are sore but not related to muscle or bone/legs are sore in her inner thigh area and things like bending over, putting her shoes and socks on and going up steps are hard for her to do. The adverse events resulted in physician office visit. After her first dose she experienced that same day, extreme tiredness, trouble walking, and leg soreness in her inner thigh area. He doctors told her it is not related to her muscle or bones. After her second dose the doctor did a lab test and tested her SED rate. It resulted at 60 and is supposed to be 5. Her inflammatory response is very high. She saw a rheumatologist and that doctor repeated the SED rate and it resulted an even higher number. The rheumatologist believes she has autoimmune disease. As of today, no one medically knows what to do with her. Caller asking do you know of any physicians that are dealing with symptoms of Covid-19 for example, has lower back pain and unable to do daily activities been reported after receiving the Pfizer Covid-19 Vaccine? Still having trouble putting shoes on going up steps. She was calling about the Covid 19 vaccine. She received the first dose on 13Feb2021 and that same day, later in the evening she was extremely tired and had trouble walking. Her legs are sore but not related to muscle or bone. Her legs are sore in her inner thigh area. Things like bending over, putting her shoes and socks on and going up steps are hard for her to do. She went to her doctor in Mar2021 and her sedimentation rate was 60 and it's normally supposed to be 5 so her inflammatory numbers were really high. Her doctor prescribed a steroid and referred her to a rheumatologist. The rheumatologist repeated the blood work and her sedimentation rate kept going up higher. The rheumatologist believed the caller has an autoimmune disease. The rheumatologist prescribed another steroid because the caller's legs were hurting again. The caller was signed up for Otezla but that medication takes a long time for approval from insurance so she was finally approved and took the Otezla. It was supposed to be in her system for 40 days to know if it's going to work. The Otezla did not work. She was prescribed another round of steroids and is now trying to get Humira. Her blood work now shows she is anemic. She has pain in her lower back. She does not think that her doctor know what to do with her. She has a full time job working with special education kids and she was very concerned over how can she go back to work. Her doctor wanted to prescribe an opioid but she does not want to take that and to become addicted to something like that. She was asking for some kind of direction or guidance. She is hoping to find a doctor that deals with adverse events from the Covid 19 vaccine. She wascalled the (name)and the CDC but no one can help her. She reports she used to work in housekeeping at Hospital. She had to quit because of the Covid 19 pandemic because she was immune compromised. She quit prior to receiving her Covid 19 vaccines. She received her second Covid 19 vaccine on 06Mar2021 in the right arm but was not 100% certain. Lot# EN6205, Expiry 30Jun2021, NDC not known. First Covid 19 vaccine information is in the suspect product field. When probing anatomical location of her first Covid 19 vaccine she wants to say she received it in the left arm but was not 100% sure. She received the second vaccine in the other arm thinking maybe that would cure her. After receiving her second Covid 19 vaccine she reports her symptoms and side effects stayed about the same. When probing for medical history and concomitant medications she reports she does not think her medications are relevant, she has been on her medications for years. She reports the rheumatologist did an X-ray of her hips and her knees and her chest. She had an MRI done of her spine. The MRI was about 2 weeks ago. The chest X-ray was sometime last week. Her hips and knees were X-rayed on 10May2021. When probing for adverse events following other vaccines she reports she had an allergic reaction to the pneumonia vaccine. She states one doctor called it an allergic reaction but the emergency room doctor called it cellulitis. She reports her arm swelled up and she had a fever of 103 degrees Fahrenheit. That happened in 2018. NDC/Lot/Expiry not known. When probing for information regarding the Otezla, she reports she tried it maybe in Mar2021. She had to take it for 40 days before she could see results. She has been off of it for maybe 2 or 3 weeks now. Description of Product Complaint: Description of complaint: The caller was signed up for Otezla but that medication takes a long time for approval from insurance so she was finally approved and took the Otezla. It was supposed to be in her system for 40 days to know if it was going to work. The Otezla did not work. Caller stated that she would just like to add additional information to her previous encounter in case her Rheumatologists calls she would like her blood work information included in the file. Patient was speaking about the Pfizer COVID-19 Vaccine she had her first dose on 13Feb2021 and her second on 06Mar2021. She stated they are thinking that her pain that she was having is being cause by her blood being out of wack. Spontaneous report by a consumer of a 57-year-old female with events of non-serious trouble walking, things like bending over, putting shoes and socks on and going up steps were hard to do, allergic reaction to pneumonia vaccine/cellulitis, autoimmune disease, sedimentation rate kept going up higher, inflammatory numbers were really high, Otezla did not work, anemic, pain in lower back, arm swelled up, fever and legs hurting/legs were sore but not related to muscle or bone/legs were sore in inner thigh area with Humira (Adalimumab). On unknown dates, the patient experienced autoimmune disease, sedimentation rate kept going up higher, inflammatory numbers were really high, anemic, pain in lower back, arm swelled up, fever and allergic reaction to pneumonia vaccine/cellulitis. in 2018, the patient experienced allergic reaction to pneumonia vaccine/cellulitis. in 2021, the patient experienced Otezla did not work. on 13Feb2021, the patient experienced trouble walking, things like bending over, putting shoes and socks on and going up steps were hard to do and legs hurting/legs were sore but not related to muscle or bone/legs were sore in inner thigh area. Pfizer BioNTech covid-19 vaccine (Tozinameran) and Otezla (Apremilast) were also considered suspect. The patient underwent lab tests and procedures which included blood work: unknown results, sedimentation rate: 60 on unspecified date, body temperature: 103 fahrenheit on unspecified date in 2018, chest x-ray: unknown results on Jul2021, MRI of spine: unknown results on an unspecified date in Jul2021, knee x-ray: unknown results, hip x-ray: unknown results on 10may2021. The vaccine facility type was reported as university of toledo mass vaccination site for faculty members. The patient was taking Covid 19 vaccine to prevent the Covid 19 virus. The clinical outcome for the events was reported as not recovered. Causality for HUMIRA: The reporter's causality for the event(s) of trouble walking, things like bending over, putting shoes and socks on and going up steps were hard to do onset 13Feb2021, allergic reaction to pneumonia vaccine/cellulitis onset in 2018, autoimmune disease, sedimentation rate kept going up higher, inflammatory numbers were really high, otezla did not work, anemic, pain in lower back, arm swelled up, fever, legs hurting/legs were sore but not related to muscle or bone/legs were sore in inner thigh area and allergic reaction to pneumonia vaccine/cellulitis unknown onset was not provided. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Date: 2018; Test Name: body temperature; Result Unstructured Data: Test Result:103 Fahrenheit; Test Date: 202107; Test Name: Chest X-Ray; Result Unstructured Data: Test Result:Unknown results; Test Date: 202107; Test Name: MRI of spine; Result Unstructured Data: Test Result:Unknown results; Test Name: sedimentation rate; Result Unstructured Data: Test Result:60; Test Date: 20210510; Test Name: Knee X-Ray; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210510; Test Name: Hip X-Ray; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: Asthma (Had maybe 15 years)
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to vaccine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1256360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 13.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Body temperature Chest X-ray Fatigue Gait disturbance C-reactive protein increased Headache Immunoglobulins Pain Loss of personal independence in daily activities Magnetic resonance imaging Pain in extremity Red blood cell sedimentation rate increased X-ray Red blood cell count decreased Synovial cyst Total complement activity test Tremor

Symptomtext

extreme tiredness; trouble walking; legs are sore but not related to muscle or bone/legs are sore in her inner thigh area; Things like bending over, putting her shoes and socks on and going up steps are hard for her to do.; This is a spontaneous report from a contactable consumer or other non-health care professional (patient). A 57-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL9267; Expiration Date: 31May2021), via an intramuscular route of administration (at the age of 57-years), on 13Feb2021 at 08:30 as dose 1,.single for COVID-19 immunisation and co-suspect as adalimumab (HUMIRA, Batch/Lot number was not reported), via an subcutaneous route of administration an unspecified date at unspecified dose for an unspecified indication and received apremilast (OTEZLA, Batch/Lot number was not reported), via an unspecified route of administration from Mar2021 to Jul2021, at unspecified dose for an unspecified indication. Medical history included ongoing asthma had maybe 15 years , allergy to vaccine from 2018 to an unknown date. The patient concomitant medications were not reported. The patient previously took pneumococcal vaccine and experienced cellulitis, Arm swelled up, pneumococcal vaccine and experienced fever. On 13Feb2021, the patient experienced extreme tiredness, trouble walking, legs are sore but not related to muscle or bone/legs are sore in her inner thigh area and things like bending over, putting her shoes and socks on and going up steps are hard for her to do. The adverse events resulted in physician office visit. After her first dose she experienced that same day, extreme tiredness, trouble walking, and leg soreness in her inner thigh area. He doctors told her it is not related to her muscle or bones. After her second dose the doctor did a lab test and tested her SED rate. It resulted at 60 and is supposed to be 5. Her inflammatory response is very high. She saw a rheumatologist and that doctor repeated the SED rate and it resulted an even higher number. The rheumatologist believes she has autoimmune disease. As of today, no one medically knows what to do with her. Caller asking do you know of any physicians that are dealing with symptoms of Covid-19 for example, has lower back pain and unable to do daily activities been reported after receiving the Pfizer Covid-19 Vaccine? Still having trouble putting shoes on going up steps. She was calling about the Covid 19 vaccine. She received the first dose on 13Feb2021 and that same day, later in the evening she was extremely tired and had trouble walking. Her legs are sore but not related to muscle or bone. Her legs are sore in her inner thigh area. Things like bending over, putting her shoes and socks on and going up steps are hard for her to do. She went to her doctor in Mar2021 and her sedimentation rate was 60 and it's normally supposed to be 5 so her inflammatory numbers were really high. Her doctor prescribed a steroid and referred her to a rheumatologist. The rheumatologist repeated the blood work and her sedimentation rate kept going up higher. The rheumatologist believed the caller has an autoimmune disease. The rheumatologist prescribed another steroid because the caller's legs were hurting again. The caller was signed up for Otezla but that medication takes a long time for approval from insurance so she was finally approved and took the Otezla. It was supposed to be in her system for 40 days to know if it's going to work. The Otezla did not work. She was prescribed another round of steroids and is now trying to get Humira. Her blood work now shows she is anemic. She has pain in her lower back. She does not think that her doctor know what to do with her. She has a full time job working with special education kids and she was very concerned over how can she go back to work. Her doctor wanted to prescribe an opioid but she does not want to take that and to become addicted to something like that. She was asking for some kind of direction or guidance. She is hoping to find a doctor that deals with adverse events from the Covid 19 vaccine. She wascalled the (name)and the CDC but no one can help her. She reports she used to work in housekeeping at Hospital. She had to quit because of the Covid 19 pandemic because she was immune compromised. She quit prior to receiving her Covid 19 vaccines. She received her second Covid 19 vaccine on 06Mar2021 in the right arm but was not 100% certain. Lot# EN6205, Expiry 30Jun2021, NDC not known. First Covid 19 vaccine information is in the suspect product field. When probing anatomical location of her first Covid 19 vaccine she wants to say she received it in the left arm but was not 100% sure. She received the second vaccine in the other arm thinking maybe that would cure her. After receiving her second Covid 19 vaccine she reports her symptoms and side effects stayed about the same. When probing for medical history and concomitant medications she reports she does not think her medications are relevant, she has been on her medications for years. She reports the rheumatologist did an X-ray of her hips and her knees and her chest. She had an MRI done of her spine. The MRI was about 2 weeks ago. The chest X-ray was sometime last week. Her hips and knees were X-rayed on 10May2021. When probing for adverse events following other vaccines she reports she had an allergic reaction to the pneumonia vaccine. She states one doctor called it an allergic reaction but the emergency room doctor called it cellulitis. She reports her arm swelled up and she had a fever of 103 degrees Fahrenheit. That happened in 2018. NDC/Lot/Expiry not known. When probing for information regarding the Otezla, she reports she tried it maybe in Mar2021. She had to take it for 40 days before she could see results. She has been off of it for maybe 2 or 3 weeks now. Description of Product Complaint: Description of complaint: The caller was signed up for Otezla but that medication takes a long time for approval from insurance so she was finally approved and took the Otezla. It was supposed to be in her system for 40 days to know if it was going to work. The Otezla did not work. Caller stated that she would just like to add additional information to her previous encounter in case her Rheumatologists calls she would like her blood work information included in the file. Patient was speaking about the Pfizer COVID-19 Vaccine she had her first dose on 13Feb2021 and her second on 06Mar2021. She stated they are thinking that her pain that she was having is being cause by her blood being out of wack. Spontaneous report by a consumer of a 57-year-old female with events of non-serious trouble walking, things like bending over, putting shoes and socks on and going up steps were hard to do, allergic reaction to pneumonia vaccine/cellulitis, autoimmune disease, sedimentation rate kept going up higher, inflammatory numbers were really high, Otezla did not work, anemic, pain in lower back, arm swelled up, fever and legs hurting/legs were sore but not related to muscle or bone/legs were sore in inner thigh area with Humira (Adalimumab). On unknown dates, the patient experienced autoimmune disease, sedimentation rate kept going up higher, inflammatory numbers were really high, anemic, pain in lower back, arm swelled up, fever and allergic reaction to pneumonia vaccine/cellulitis. in 2018, the patient experienced allergic reaction to pneumonia vaccine/cellulitis. in 2021, the patient experienced Otezla did not work. on 13Feb2021, the patient experienced trouble walking, things like bending over, putting shoes and socks on and going up steps were hard to do and legs hurting/legs were sore but not related to muscle or bone/legs were sore in inner thigh area. Pfizer BioNTech covid-19 vaccine (Tozinameran) and Otezla (Apremilast) were also considered suspect. The patient underwent lab tests and procedures which included blood work: unknown results, sedimentation rate: 60 on unspecified date, body temperature: 103 fahrenheit on unspecified date in 2018, chest x-ray: unknown results on Jul2021, MRI of spine: unknown results on an unspecified date in Jul2021, knee x-ray: unknown results, hip x-ray: unknown results on 10may2021. The vaccine facility type was reported as university of toledo mass vaccination site for faculty members. The patient was taking Covid 19 vaccine to prevent the Covid 19 virus. The clinical outcome for the events was reported as not recovered. Causality for HUMIRA: The reporter's causality for the event(s) of trouble walking, things like bending over, putting shoes and socks on and going up steps were hard to do onset 13Feb2021, allergic reaction to pneumonia vaccine/cellulitis onset in 2018, autoimmune disease, sedimentation rate kept going up higher, inflammatory numbers were really high, otezla did not work, anemic, pain in lower back, arm swelled up, fever, legs hurting/legs were sore but not related to muscle or bone/legs were sore in inner thigh area and allergic reaction to pneumonia vaccine/cellulitis unknown onset was not provided. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Date: 2018; Test Name: body temperature; Result Unstructured Data: Test Result:103 Fahrenheit; Test Date: 202107; Test Name: Chest X-Ray; Result Unstructured Data: Test Result:Unknown results; Test Date: 202107; Test Name: MRI of spine; Result Unstructured Data: Test Result:Unknown results; Test Name: sedimentation rate; Result Unstructured Data: Test Result:60; Test Date: 20210510; Test Name: Knee X-Ray; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210510; Test Name: Hip X-Ray; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: Asthma (Had maybe 15 years)
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to vaccine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1641683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 79,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 11.02.2021
Beginn: 24.08.2021
Tage bis Beginn: 194,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chills Cough Diarrhoea Dyspnoea Fatigue Headache Myalgia Nausea Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Taste disorder Wheezing

Symptomtext

Patient presented to hospital on 8/24/2021 with a 3-day history of worsening shortness of breath, wheezing, and fatigue. She is COVID-19 vaccinated but tested positive for COVID-19 in the ED. She also has subjective fevers, chills, headache, and change in taste that also started 3 days ago. Her headache is bifrontal, throbbing which she rates as 10/10, not responsive to acetaminophen. She reports nausea, sore throat, nonproductive cough, diarrhea, and muscle aches that started 3 weeks ago. Patient was admitted to the hospital for management of COVID-19 illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: 8/24/21: CORONAVIRUS SARS COV 2 PCR (RESP) - positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1641554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 60,0
Geschlecht: M
Eingang: 27.08.2021
Impfdatum: 20.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 40,0
Dosis: 2
Route/Site: IM / RA

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

Dyspnoea Fatigue

Symptomtext

I had exhaustion and shortness of breath during small distances. I got to the restroom, and I get winded. I also get winded and tired taking a shower I have gone to the doctor, and they do not know what is going on.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetic, Muscular Dystrophia
Andere Medikamente: Bacolsen, Cetirizine, Doxazosin, Hydrocodone, Insulin, Victoza, Lisinopril 1xday Mexiletine, Pentoprtarzol.
Allergien: Celebrex
Vorherige Impfungen: -

VAERS 1636852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 26.08.2021
Impfdatum: 20.02.2021
Beginn: 23.07.2021
Tage bis Beginn: 153,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal discomfort Ageusia Anosmia COVID-19 Chest X-ray abnormal Chest pain Chills Dehydration Dry mouth Dysgeusia Exposure to SARS-CoV-2 Facial pain Fatigue Headache Loss of personal independence in daily activities Mobility decreased Nasopharyngitis Pain in jaw

Symptomtext

I was fully vaccinated the last dose dates Feb 20th 2021. My husband and I were in our home from June 30th until now. I got sick with the symptoms of a cold and my cheeks and jaw hurt in the middle of the night. So I woke up feeling congested and had a headache and fever. I was surprised I might be getting a bad head cold. Then I thought maybe it is just allergies so I took allergy medicine that day. The second day I continued to have a headache, sinuses, and jaw hurting. And on and of fever and chills of about 100. Allergy medicine wasn't touching it. The third day I thought I should have a covid test since a friend of ours here (unvaccinated got COVID) So I got a rapid test three days later at urgent care and it was positive. They could not tell me if it was Delta but I assumed it was. I was pretty shocked. The nurse told me to go home, treat it like a cold but if my oxygen levels were low or my chest hurt to go to the emergency room. My husband got it the next day. For the first week, I had bad cold symptoms and was fatigued. Fever on and off, up to 101. Mostly laid around, could not work or do much of anything else. The second week I felt worse instead of better. More fatigue, dry mouth, fever still, weird stomach pressure at night-not pain-just all my organs feeling the pressure. Once it was so bad I wanted to scream! So I ended up going to the emergency room Thursday eve (a week later from first symptoms) as I was feeling worse not better and I couldn't break my temp 102 with Tylenol anymore. And my chest hurt. After going home (4 hours in emergency) I got better on the steroids but just laid around, really incapable of extending much energy on household tasks or normal activities. Very fatigued, slept a lot. Lost my smell and taste for about 6 days. At times my mouth tasted metal. I did eventually get both back, though I can't smell as well. My chest cleared up and I am back to walking 45 mins a day, being on a stair stepper, and swimming 20 laps morning and night. I do still seem to need a nap every day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: The emergency doc gave me fluids as I was dehydrated and some pain meds. and did a chest x-ray where he told me I had the beginnings of pneumonia. He sent me home with a prescription for 5 days of steroids and told me if my oxygen levels dropped under 92 to call him. The steroids messed with my sleep but helped.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Verpamil and mult-vitamins
Allergien: No
Vorherige Impfungen: -

VAERS 1623492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: SC
Alter: 77,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 14.02.2021
Beginn: 01.04.2021
Tage bis Beginn: 46,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Gait disturbance Mobility decreased Somnolence Vertigo Visual impairment

Symptomtext

I had sudden onset of vertigo and I had my visual perception was constantly going from right to left over and over again. I also was extremely sleepy. That lasted for a day and a half. I woke up with it because it persisted for a day and a half those 3 problems. I called my Doctor and they sent me a prescription for dizziness and it did not help at all. I couldn't walk without assistance for a day and a half, I could only sit with my eyes closed or lay down. I didn't go to the hospital because I couldn't walk across the room and I was out of town at that time. It cleared in about a day and a half. I saw Dr. when I returned home on July 28th. And Cardiologist July 21st. And Dermatologist July 22nd.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I will have an MRI of the brain and Brain Scan this coming Friday.
Aktuelle Erkrankungen: No
Vorgeschichte: Klonopin for insomnia and anxiety
Andere Medikamente: Losartan 100mg/daily; Prilosec 20mg/daily
Allergien: No
Vorherige Impfungen: -

VAERS 1617518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 85,0
Geschlecht: M
Eingang: 22.08.2021
Impfdatum: 18.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Asthenia Injected limb mobility decreased Injection site pain

Symptomtext

Extreme pain in right shoulder and injection site. Limited mobility in shoulder. No strength, cannot lift arm up. This situation still exists 6 month later. Saw family doctor in May of 2021 and again in August. Referred to Orthopedic surgeon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Seeing an Orthopedic surgeon on September 2, 201.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1591615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: IL
Alter: 70,0
Geschlecht: F
Eingang: 20.08.2021
Impfdatum: 13.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: SYR / RA

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

Cardiac stress test Chest X-ray Chest discomfort Chills Cough Dyspnoea Dyspnoea exertional Echocardiogram abnormal Ejection fraction decreased Electrocardiogram Heart rate increased Laboratory test Oxygen saturation decreased Pneumonia Pyrexia Sleep disorder Sluggishness

Symptomtext

February 27th -- 2 weeks after vaccine number 2, I awoke at 2 am shaking with chills, a fever of 103, shortness of breath, high heart rate, low oxygen saturation rate, coughing and a feeling of heaviness on my chest. Later in the day, my primary care physician's on-call doctor told me to call 911 and go to the ER, assuming this must be COVID. Hospital ER diagnosed pneumonia but I didn't believe it. March 17th, I visited my primary care physician after drawing blood in the lab, doing another chest X-ray and an echocardiogram. March 18th, the echocardiogram report filed showed reduction in ejection fraction to about 30-35 percent (from what had been a normal 55 to 60% before the vaccines). Cardiology started a beta blocker drug and I was referred on to pulmonology and gastroenterology for additional testing. May 9th, the exact same symptoms occurred at around 2 am, which necessitated another visit to the ER, again with the same pneumonia diagnosis. Still don't believe I had pneumonia but did go through two rounds of two different antibiotics each. Just had my 2nd echo a few weeks ago and the ejection fraction is up to 40, but cardiologist doesn't "like the way the heart" looks. All of these medical visits and explorations are in an effort to truly understand what has happened to my body -- I am slow and sluggish, can't walk more than 4 blocks without being winded, and of course am staying alone in my high-rise apartment most of the time. I still believe this is vaccine related myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: February 27th -- ER visit -- lab work, chest X-ray, EKG, physical exam March 17th -- primary care physician visit -- lab work, chest X-ray, echocardiogram, physical exam Additional PET stress test in nuclear diagnostics and a second echo a few weeks ago Pulmonology visit with 3rd chests X-ray GI physician scheduled next week for an examination of the esophogus and stomach
Aktuelle Erkrankungen: GERD, asthma, PT for left rotator cuff soreness
Vorgeschichte: idiosyncratic cardiomyopathy, GERD, asthma
Andere Medikamente: atorvastatin 40 mg 1/day; fluticasone propionate 50 mcg, 1/day both nostrils; lisinopril 5 mg 1/day; omega-3 fatty acids fish oil 1,000 mg 1/day; omeprazole 20 mg 2/day; proventil HFA 90 mcg as needed; rifaxim 200 mg, 1/day; metoprolol 25
Allergien: narcotics, H2 blockers, pneumococal vaccine #1
Vorherige Impfungen: first pneumocal

VAERS 1586913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 87,0
Geschlecht: M
Eingang: 19.08.2021
Impfdatum: 10.02.2021
Beginn: 07.08.2021
Tage bis Beginn: 178,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 Chest X-ray normal Cough Dyspnoea SARS-CoV-2 test positive Sputum retention Thrombocytopenia

Symptomtext

8/10/2021 - presents to ED with cough, SOB and weakness for a couple days - Started decadron and remdesivir, requiring 2 to 3L O2 8/12/2021 - on room air, still coughing a lot and difficult to experctorate mucous 8/14/2021: pt stable and on room air, thrombocytopenia stable

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: COVID pos 8/9/21 and 8/10/21 8/10/21: lungs clear of any new damage
Aktuelle Erkrankungen: none
Vorgeschichte: Chronic Renal Failure stage 3, COPD, Hyperlipidemia, Hypothyroidism, Pulmonary fibrosis, Asthma, Arthritis, BPH, atherosclerosis, diverticulitis
Andere Medikamente: Aspirin, cholestyramine, fluticasone/salmeterol, levothyroxine, Omega 3, vitamin E, fluticasone
Allergien: Aspirin (no problem with 81mg), penicillin's
Vorherige Impfungen: -

VAERS 1582698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 67,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 16.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain upper Computerised tomogram abnormal Condition aggravated Diarrhoea Irritable bowel syndrome Lymphadenopathy Ultrasound scan abnormal

Symptomtext

I went to the doctor and I noticed that my IB became very active I was having a lot of stomach cramping and diarrhea and she said that it might be an immune response to the vaccine. I saw a GI doctor and explained what was going on and she agreed that it might be an immune response. Shortly after that I notice and enlarged lymph node on the left side of my neck. They sent me for an ultrasound and that suggested to the doctor to get a CAT scan. They said that it showed I had an enlarged lymph node in the post triangular portion of the neck. The doctor just said to keep an eye on the lymph node. They just changed my medication from hyoscyamine to Bentyl and Imodium to try and make sure the diarrhea became under control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: ultrasound- suggested to get a CAT scan CAT scan- enlarged lymph node in the post triangular portion of the neck CAT scan of abdomen- normal
Aktuelle Erkrankungen: None
Vorgeschichte: Irritable bowel syndrome
Andere Medikamente: Hyoscyamine; Famotidine; Claritin; Simvastatin; baby aspirin; fiber tablet; multi vitamin
Allergien: Flagyl; Cipro
Vorherige Impfungen: -

VAERS 1578398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 46,0
Geschlecht: M
Eingang: 17.08.2021
Impfdatum: 25.02.2021
Beginn: 25.07.2021
Tage bis Beginn: 150,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 COVID-19 pneumonia Convalescent plasma transfusion Inflammatory marker test Malaise SARS-CoV-2 test positive

Symptomtext

Admit for COVID pneumonia; tested positive 7 days PTA. Completed vaccine in Feb 2021. Treated w/ zpack PTA. He had his Pfizer vaccine. Despite tested positive and got sick. However his COVID19 IgG antibodies were negative. Was treated with convalescent plasma. Was given Remdesivir for 5 days. Was started on high dose steroids, empiric abx. Over the course of hospitalization his inflammatory markers improved. O2 requirements came down from 4 to 2 liters. Was eventually sent home on Oxygen with steroid taper.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1574588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 67,0
Geschlecht: M
Eingang: 16.08.2021
Impfdatum: 22.02.2021
Beginn: 06.08.2021
Tage bis Beginn: 165,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram abnormal Chills Cough Dyspnoea Fatigue Myalgia Pneumonia viral Pyrexia

Symptomtext

Hospitalization - He notes fever, chills, fatigue, myalgias, cough, and shortness of breath. CTA demonstrates bilateral viral pneumonitis. No other known aggravating or alleviating factors. No other associated symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, DM2, HTN, GERD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1130632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 11.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / LA

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

Biopsy Biopsy bone marrow Biopsy muscle Blood test normal Carpal tunnel syndrome Blood creatine phosphokinase increased Hypoaesthesia Magnetic resonance imaging Pain in extremity Paraesthesia Condition aggravated Electrocardiogram normal Hypertension Mononeuropathy multiplex Nerve stimulation test Neuropathy peripheral Peroneal nerve injury Peroneal nerve palsy

Symptomtext

I had no adverse event with the 1st dose of the Pfizer vaccine. On 2/11/2021, I received the 2nd dose vaccine. On 2/19/2021, I woke up with hypertension 220/115 and excruciating pain in right arm and went to the ER (Hospital). They did EKG, blood work and X-ray and everything came back normal. I was discharged with a referral to see my PCP to follow up. They did not treat me for my arm pain. Please note that I got my vaccine in my left arm and the pain is on the opposite side of my body. On 3/1/2021, I woke up with excruciating pain in my right arm. I went to the ER and they did a sonogram and did not find anything. I was prescribed Orphenadrine- a muscle relaxer. I did go see an orthopedic who did an x-ray but pain continued. At this time, I was starting to lose feeling in the 3 digits of my right hand (thumb, index, middle finger). I was prescribed a 6 day pack of steroid. It did help with pain in my arm but once I was off steroids, the pain came back. I was referred to a neck and spine specialist. I did go see neck and spine and they recommended physical therapist. I also went to see a rheumatologist who recommended me to do a nerve test. It was determined from the nerve test that I had carpal tunnel syndrome and decompressed peroneal nerve in my right knee. On 4/15/2021, I developed dropped foot in my right foot and I had no control of my right foot. I have neuropathy of the right side of my body and have no control of my right foot and right arm. I did see finally see a neurologist and he recommended me to be admitted to the hospital to run tests and be monitored (Hospital). I was admitted 4/20/2021 -4/27/2021 and had a bunch of tests done. I was finally diagnosed with poly neuropathy, mononeuritis multiplex and right drop foot. I was put on high doses of prednisone for treatment and I am currently on prednisone. Test performed when I was admitted: doppler test, MRI, x ray, bloodwork, bone marrow biopsy, muscle and nerve biopsy, From 2/12/2021 to April 2021 , I have seen 18 doctors related to adverse events to the vaccine. I am still suffering from the adverse event and have not fully recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: 7,0
Labordaten: doppler test, MRI, X- ray, bloodwork, bone marrow biopsy, muscle and nerve biopsy
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Clonidine; losartan; orphenadrine
Allergien: compazine
Vorherige Impfungen: -

VAERS 1554085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 12.02.2021
Beginn: 10.08.2021
Tage bis Beginn: 179,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Chest X-ray normal Condition aggravated Fatigue Hypertension SARS-CoV-2 test positive

Symptomtext

patient presented with generalized fatigue x 2-3 days, along with increased hypertension w BP reportedly in 200's. Patient tested positive for COVID on 8/12. pt has hx of Alzheimer, HTN, and CKD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: COVID: SARS-CoV-2 (COVID-19) by NAA, Micro detected; on 8/12/21. CR on 8/11 showed no acute cardiopulmonary process.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1553829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 67,0
Geschlecht: M
Eingang: 13.08.2021
Impfdatum: 03.03.2021
Beginn: 07.04.2021
Tage bis Beginn: 35,0
Dosis: 2
Route/Site: SYR / UN

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

Acute left ventricular failure Blood sodium decreased COVID-19 COVID-19 pneumonia Dyspnoea HIV infection Haemoptysis Hyperlipidaemia Hypertension Hypertensive heart disease Hypokalaemia Hyponatraemia Hypoosmolar state Mitral valve incompetence Pneumonia SARS-CoV-2 test positive Tricuspid valve incompetence Type 2 diabetes mellitus

Symptomtext

PUI went to the ED with shortness of breath and suspected covid pneumonia on 4/6/21. Tested positive for covid on 4/7. He was discharged on 4/13. Main diagnosis was hypertensive heart disease with heart failure (acute left systolic heart failure). Other diagnoses included acute systolic congestive heart failure, hypo-osmolar hyponatremia (low blood sodium), hemoptysis, type 2 diabetes without complication (on insulin long term), pneumonia, coughing up blood (hemoptysis), HIV infection, hypertension, hyperlipidemia, hypokalemia, mitral and tricuspid valve disorders (regurgitation). He also has a history of tuberculosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes cardiovascular disease Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1553720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 09.03.2021
Beginn: 04.08.2021
Tage bis Beginn: 148,0
Dosis: 1
Route/Site: IM / UN

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

Ageusia Back pain COVID-19 Chills Cough Dyspnoea Exposure to SARS-CoV-2 Headache Nausea Non-cardiac chest pain Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

This is a 72-year-old female with past medical history of hyperlipidemia, coronary artery disease status post CABG x4, anxiety, depression, multiple sclerosis, immunocompromised. She came to the hospital with a chief complaint of progressive worsening cough and shortness of breath over the last 10 days. Initially tested positive about 4 days after starting to have symptoms. Was prescribed azithromycin as an outpatient by her primary care physician. Her son initially tested positive for COVID-19 after which the patient started having symptoms as well due to exposure. The patient was having significant worsening of the shortness of breath over the weekend and had a very severe heada 8/11/2021 tested positive This is a 72-year-old female with past medical history of hyperlipidemia, coronary artery disease status post CABG x4, anxiety, depression, multiple sclerosis, immunocompromised. She came to the hospital with a chief complaint of progressive worsening cough and shortness of breath over the last 10 days. Initially tested positive about 4 days after starting to have symptoms. Was prescribed azithromycin as an outpatient by her primary care physician. Her son initially tested positive for COVID-19 after which the patient started having symptoms as well due to exposure. The patient was having significant worsening of the shortness of breath over the weekend and had a very severe headache so she decided come to the hospital for further evaluation and treatment. Patient was also having some cough, chest pain associated with cough, back pain, fevers, chills, nausea, vomiting, loss of taste. Denies any abdominal pain, burning or painful urination or diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hyperlipidemia, coronary artery disease status post CABG x4, anxiety, depression, multiple sclerosis, immunocompromise
Andere Medikamente: Metoprolol Succinate ER
Allergien: -
Vorherige Impfungen: -

VAERS 1534811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 47,0
Geschlecht: M
Eingang: 07.08.2021
Impfdatum: 02.04.2021
Beginn: 01.06.2021
Tage bis Beginn: 60,0
Dosis: UNK
Route/Site: SYR / LA

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

Blood test Electroencephalogram Magnetic resonance imaging Panic attack Tremor

Symptomtext

Subsequent panic attacks and left hand tremor. Patient has had an MRI, EEG, blood work, and is scheduled to meet with a neuropsychologist later this month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Some memory loss issues
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1532104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WI
Alter: 75,0
Geschlecht: M
Eingang: 06.08.2021
Impfdatum: 21.01.2021
Beginn: 01.08.2021
Tage bis Beginn: 192,0
Dosis: 2
Route/Site: IM / LA

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

Cough Dyspnoea Fatigue

Symptomtext

COUGH, SOB, AND FATIGUE

Weitere VAERSDATA-Felder

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

VAERS 1531479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 88,0
Geschlecht: M
Eingang: 06.08.2021
Impfdatum: 13.02.2021
Beginn: 05.08.2021
Tage bis Beginn: 173,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Dyspnoea Fatigue Infection SARS-CoV-2 test positive

Symptomtext

COVID-19 Breakthrough--Patient admitted to hospital with generalized weakness, shortness of breath, cough for 2 days. Feeling fatigue and weakness for 2 days PTA. SpO2 93% on room air, Not currently requiring supplemental O2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 8/5 SARS-CoV-2 detected
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, h/o CABG, CKD 3, HTN
Andere Medikamente: unknown
Allergien: nifedipine, metoprolol
Vorherige Impfungen: -

VAERS 1526318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 04.08.2021
Impfdatum: 12.02.2021
Beginn: 27.06.2021
Tage bis Beginn: 135,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Cough Feeling abnormal Impaired work ability Malaise Mobility decreased SARS-CoV-2 test positive Throat irritation Urinary tract infection

Symptomtext

June 6th - I got sick. I talked to my doctor and I had a test done on Friday - negative result for COVID. My daughter in law had home tests. I was positive for COVID on Sunday - Sunday was when I had the symptoms. I had a scratchy throat; I didn't feel good. It felt like a building fell on me with not feeling good. I didn't get out of bed too much for the first three days. Fourth day, I was still no energy but I got up and showered. . I talked to doctor on Monday (video call). He said I had the Delta Variant - I was sick for 4 days. I still have cough and low energy. I am without fever. My vitals - I got a blood pressure cuff - and oxygen monitor - my levels stayed where they needed to be without going to ER. I also developed a UTI infection (not tested but based on symptoms) which added to my being sick - I developed that on my fifth day. I got medication for that. After the 14 days, (got a negative test after the two weeks) - at Beaumont Urgent Care in Dearborn. I work from home and I still didn't feel good to do that. I still have the cough but not as bad. My energy level is not good - I have to take a nap after work. For COVID I was given to take Zinc and Vit D and I took OTC ThoroughFLU.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID - tests - three
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Levothyroxine; Atorvastatin; Omeprazole; Metformin; Baby aspirin; Biotin; B12; Vit with no iron; Sambucas; Vit C
Allergien: no
Vorherige Impfungen: -

VAERS 1525796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 04.08.2021
Impfdatum: 01.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Insomnia Sleep disorder Tinnitus

Symptomtext

I have had mild tinnitus since 2004. I never had a problem with it interfering with falling asleep. Since March 2021 it has become sever to the point I need to take Valium or Ambien to sleep 3-4 times a week. Prior to March 2021 I only need to take one or 2 of those medications once a month. The sever tinnitus not only causes me to difficulty falling asleep it is with me all day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: GERD Mild Tinnitus
Vorgeschichte: Same as above Severe Tinnitus began in March 2021 and continues
Andere Medikamente: Omeprazole, Atorvastatin, Valium, Ambien, B12, Turmeric, Biotin, D3
Allergien: Sulfa medications Cefdinir
Vorherige Impfungen: -

VAERS 1518628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 11.02.2021
Beginn: 18.02.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / RA

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

Antinuclear antibody Autoimmune disorder C-reactive protein normal Chapped lips Condition aggravated Eczema eyelids Lip swelling Stomatitis Throat irritation

Symptomtext

autoimmune flare up including swollen, chapped, cracked lips; raw throat; sores in mouth; eczema on eyelids starting one week after vaccine and continuing to today; treatment with antihistamines (Zyrtec, Zantac, Benadryl)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Drawn on 07/27/2021 and 07/28/2021: Anti-Nuclear Antibodies (ANA) 1:320; C-Reactive Protein (CRP) 0.9
Aktuelle Erkrankungen: none
Vorgeschichte: managed Hashimotos Disease, managed high blood pressure
Andere Medikamente: 150 ug synthroid, 37 mg metoprolol, vitamin D&K, Adrenotone, methyl B12, zinc
Allergien: sulfa, Bactrim, Claritin, Diflucan, Lisinoprol-HCTZ, penicillins
Vorherige Impfungen: -

VAERS 1518079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 31.07.2021
Impfdatum: 10.02.2021
Beginn: 10.05.2021
Tage bis Beginn: 89,0
Dosis: 2
Route/Site: - / LA

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

Blood test Cardiac failure Dyspnoea Investigation Lymphoedema Renal failure SARS-CoV-2 antibody test SARS-CoV-2 antibody test negative Urine analysis Visual impairment

Symptomtext

Heart failure; Kidney failure; Difficulty breathing; lymphedema in the right arm; she has low vision and has trouble seeing things; test showed that she had no antibodies against COVID19; This is a spontaneous report from a contactable consumer, the patient. A 76 years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL9267, Expiry Date: unknown), via an unspecified route of administration on arm left on 10-FEB-2021 08:50 (age at vaccination: 76 years) as DOSE 2, 0.3 ML SINGLE for COVID-19 immunization. The reported verbatim indication was reported as She was 76 years old and she does not want to die of Covid. The patient medical history included kidney disease, COPD, Asthma, Fibromyalgia, A- Fib, Cholesterol, Spinal stenosis, GERD (Gastrooesophageal reflux disease), heart damage and blood pressure, congestive heart failure to deal with edema, sleep. Historical vaccines included Pneumonia vaccine, Flu vaccine. Prior Vaccinations (within 4 weeks)or any other vaccinations within four weeks prior to the first administration date of the suspect vaccine was reported as none. Adverse events following prior vaccinations was reported as none. Family Medical History Relevant to Adverse events was reported as none and family members have had Covid and has 2 friends that have died of Covid. The patient Concomitant medications included Carvedilol(Generic for Coreg) taken for heart damage and blood pressure from an unknown date, Lisinopril taken for heart damage and blood pressure from an unknown date, Furosemide taken for congestive heart failure to deal with edema from an unknown date, Atorvastatin taken for Cholesterol from an unknown date, salbutamol(ALBUTEROL HFA) taken for unspecified indication from an unknown date, Alprazolam taken for sleep from an unknown date, fluticasone furoate, umeclidinium bromide, vilanterol trifenatate (TRELEGY ELLIPTA) taken for unspecified indication from an unknown date, Duloxetine (which is also Cymbalta) taken for Fibromyalgia from an unknown date, Diclofenac sodium taken for Spinal stenosis from an unknown date, Omeprazole taken for GERD from an unknown date, colecalciferol(VIT D3) taken for unspecified indication from an unknown date, Fluticasone taken for unspecified indication from an unknown date. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL3249), via an unspecified route of administration on arm left on 20Jan2021 (at the age of 76 years) as DOSE 1, 0.3 ML SINGLE for COVID-19 immunization. On 10May2021, the patient experienced Difficulty breathing, Kidney failure, Heart failure. On an unspecified date, the patient experienced lymphedema in the right arm. It was reported that Caller states she has low vision and has trouble seeing things. The patient was hospitalized from 10May2021 to Unspecified as a result of Difficulty breathing, Kidney failure, Heart failure. The events Difficulty breathing, kidney failure, heart failure resulted in Emergency Room (admitted for 39 days) and physician office (many times). The lab tests included test: Blood test: Unknown result, Investigation: Unknown result, Urine analysis: Unknown result on an unknown date; Test: SARS-CoV-2 antibody test, result: Negative on 10May2021; Test: SARS-CoV-2 antibody test (Sars-Cov-2 anti spike) was collected 28May2021, result: negative (with no serological evidence) on 01Jun2021. It was reported that she had several tests because she just spent 39 days in the hospital. They did blood work pretty much every day. They did urinalyses, bladder scans, all those kind of things. Was brought in to the ER 10May2021 and was admitted to the hospital for 39 days. She spent part of the time in rehab and then was re-admitted to the hospital and then back home after 39 days. Was admitted for congestive heart failure, kidney failure and difficulty breathing. The breathing was exacerbated that day, she has COPD and asthma. All of those thing worsened to the point where she was in serious trouble and needed to be admitted to the hospital. It was reported as there was product complaint. Therapeutic measures were taken as a result of Heart failure, kidney disease, lymphedema in the right arm and treatment included They put her on IV Lasix to get rid of the fluid build up and take the burden off of her heart and kidneys. The clinical outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 39,0
Labordaten: Test Name: BLOOD WORK; Result Unstructured Data: Test Result:Unknown result; Test Name: Bladder scans; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210510; Test Name: Sars Covid spike test; Result Unstructured Data: Test Result:Negative; Comments: She has had since, a Sars Covid spike test and has no antibodies; Test Date: 20210601; Test Name: SARS-CoV-2 antibody test; Result Unstructured Data: Test Result:negative; Test Name: urinalyses; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Atrial fibrillation; Blood cholesterol abnormal; Blood pressure abnormal; Congestive heart failure; COPD; Edema; Fibromyalgia; GERD; Heart disorder; Kidney disorder; Sleep disorder; Spinal stenosis
Andere Medikamente: CARVEDILOL; LISINOPRIL; FUROSEMIDE; ATORVASTATIN; ALBUTEROL HFA; ALPRAZOLAM; TRELEGY ELLIPTA; DULOXETINE; DICLOFENAC SODIUM; OMEPRAZOLE; VIT D3; FLUTICASONE
Allergien: -
Vorherige Impfungen: -

VAERS 1512862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 62,0
Geschlecht: M
Eingang: 29.07.2021
Impfdatum: 26.02.2021
Beginn: 27.07.2021
Tage bis Beginn: 151,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

covid-19 infection with pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: COVID-19 nasal swab = positive on 7/27/21
Aktuelle Erkrankungen: pyelonephritis
Vorgeschichte: Healthcare associated bacterial pneumonia ? Pneumonia of right lower lobe due to infectious organism ? HCAP (healthcare-associated pneumonia) ? Acute GI bleeding ? Pneumonia of left lower lobe due to infectious organism ? COVID-19 virus infection ? COVID-19 virus detected ? ARF (acute renal failure) (CMS/HCC) ? Generalized weakness ? CP (cerebral palsy) (CMS/HCC) ? Acute respiratory failure with hypoxia and hypercapnia (CMS/HCC) ? Aspiration pneumonia due to vomitus (CMS/HCC) ? Acute deep vein thrombosis (DVT) of proximal end of left lower extremity (CMS/HCC) ? Acute pulmonary embolism without acute cor pulmonale (CMS/HCC) ? Pyelonephritis ? Acute gangrenous cholecystitis ? Aspiration pneumonia of right lung due to gastric secretions (CMS/HCC) ? UTI (urinary tract infection) ? Septic shock (CMS/HCC) ? Type 2 MI (myocardial infarction) (CMS/HCC) ? Anemia, chronic disease ? Paroxysmal A-fib (CMS/HCC) ? Chronic diastolic congestive heart failure (CMS/HCC) ? Personal history of venous thrombosis and embolism ? Closed intertrochanteric fracture of left femur (CMS/HCC) ? Closed intertrochanteric fracture of left femur, initial encounter (CMS/HCC) ? COPD (chronic obstructive pulmonary disease) (CMS/HCC) ? Colostomy in place (CMS/HCC) ? PEG (percutaneous endoscopic gastrostomy) status (CMS/HCC) ? Aspiration pneumonia (CMS/HCC) ? Shortness of breath ? Acute on chronic respiratory failure with hypoxia (CMS/HCC) ? Hypernatremia ? Elevated troponin ? Alkalosis, metabolic ? Acute metabolic encephalopathy ? Aspiration pneumonia (CMS/HCC) ? Hemoptysis ? Stage 3a chronic kidney disease (CMS/HCC) ? Hypothyroidism ? Hematemesis
Andere Medikamente: Maalox albuterol apixaban ondansetron quetiapine guaifenesin aquaphor nystain furosemide folic acid vitamin B-12 dulcolax miralax multivitamin lansoprazole midodrine
Allergien: compazine
Vorherige Impfungen: -

VAERS 1512499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: KY
Alter: 77,0
Geschlecht: F
Eingang: 29.07.2021
Impfdatum: 29.01.2021
Beginn: 26.07.2021
Tage bis Beginn: 178,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

COVID PNA requiring hospitalization and oxygen + remdesivir & dexamethasone

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: COVID-19 nasal swab positive on 7/13/2021
Aktuelle Erkrankungen: none
Vorgeschichte: History of pulmonary embolism ? Chronic kidney disease, stage III (moderate) ? CHF (congestive heart failure) ? Hyperlipidemia ? Hypertension ? Hypothyroidism ? IDA (iron deficiency anemia) ? Status post mitral valve replacement ? Status post aortic valve replacement ? Pulmonary hypertension ? Atrial fibrillation ? Chronic anticoagulation
Andere Medikamente: aspirin, 81 mg, Oral, Daily atorvastatin, 40 mg, Oral, Daily cefTRIAXone, 1 g, Intravenous, Q24H dexamethasone, 6 mg, Intravenous, BID isosorbide mononitrate, 60 mg, Oral, Daily levothyroxine, 25 mcg, Oral, Q AM metoprolol tartrate, 25 mg,
Allergien: none
Vorherige Impfungen: -

VAERS 1509025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 23,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 25.02.2021
Beginn: 01.07.2021
Tage bis Beginn: 126,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain upper Ageusia Anosmia Aphonia Asthenia COVID-19 Chest discomfort Chest pain Chills Cough Decreased appetite Diarrhoea Drug ineffective Dyspnoea Fatigue Feeling abnormal Feeling cold Hyperhidrosis

Symptomtext

Really lethargic and fatigued; Tested positive for the Covid virus; Tested positive for the Covid virus; Can't taste or smell; Can't taste or smell; Horrible stomach ache; Diarrhea; Exhausted/really lethargic and fatigued; Felt ill, run down and not herself; Voice was gone and was very cracky; Did not feel good; Throat sore and vocal cords hurting; Throat sore and vocal cords hurting; Freezing cold and had the chills; Freezing cold and had the chills; Woke up in a puddle of sweat and hair was soaking wet and dripping; Nose really runny and super congested; Nose really runny and super congested; Deep cough/a little cough; Feels nauseas; Her energy was very low; She thought she caught the flu and was not thinking that it was Covid; freezing and shaking; She didn't have an appetite the first couple of days; She felt horrible in her chest and it was hard to breathe; Chest sore and felt like pressure on her chest; Chest sore and felt like pressure on her chest; This is a spontaneous report from a Pfizer sponsored program by a contactable consumer (patient). This 24-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration Arm Left on 25Feb2021 14:00 at age of 23 year-old (Lot: EL9267) as DOSE 1, SINGLE, Arm Left on 19Mar2021 11:00 at age of 23 year-old at DOSE 2, SINGLE (Lot # EN6208) for covid-19 immunisation. Medical history included none. Concomitant Products included ongoing lisdexamfetamine mesilate (VYVANSE) Has been taking since grade 10 at Believes it is 40mg, once daily for Attention deficit hyperactivity disorder. No prior vaccinations within 4 weeks.On 09Jul2021, she tested positive for Covid-19. States that she does not know the exact strain that it was. She is trying to get genome sequencing done so that they can find out. She has one but, she is (withheld) and has a PCP back home. She hasn't given them any info about her having Covid yet. She hasn't called her physician. She saw someone in the clinic. She hasn't told them yet, so she wants to call them first. In the clinic, they assumed it was as sinus infection and the prescribed her with Amoxicillin. She was taking it last week when she didn't know that she had it yet. She is still taking it right now. They gave her nasal spray and she did that for 2 days completely and it is clear now. She had every possible symptom she can think of. On Tuesday, 06Jul2021, she woke up with a horrible stomach ache and diarrhea. When she got to campus, she was more exhausted on 06Jul2021 and just felt ill and run down, not herself on 06Jul2021. Her voice was so gone. She did not feel good on 06Jul2021. She felt like that is probably because she took the vaccine while she was sick. She had all this work to do, so she went through it. She took her Vyvanse medication instead of resting and it almost masked the symptoms but, she felt ok for an hour, then all of a sudden she had to go to bed because she felt so sick. She just thought it was food she had eaten because of her birthday. She had eaten cake and a whole lot of junk food. She usually eats really healthy. She went to clinic that morning to see patients. She also had no voice and it was very crackly/ Voice was gone and was very cracky on 06Jul2021. Her throat didn't hurt, it was just very sore and her vocal chords were hurting on 06Jul2021. It hurt to talk. Those were the only 2 symptoms she had the first day. She felt ill, fatigued and her body started to hurt and she felt really tired. She came home and didn't feel like she usually did. She just felt really sick. She could taste and smell, it was all still there. She is still getting the runs though out the day. She was with family and 2 friends and did not pass anything on to them. They are all vaccinated. That night, she was exhausted and went to bed early, then she was freezing cold, had the chills but didn't take her temperature in Jul2021. She took Nyquil and Dayquil. She woke up again at night and was freezing and shaking and Woke up in a puddle of sweat and hair was soaking wet and dripping in Jul2021. She felt horrible. She thought she caught the flu and was not thinking that it was Covid in Jul2021. That day, she kind of tried to get though school and do work online. She was feeling really crummy. All of those symptoms, she had the next couple of days. Then her Nose really runny and super congested in Jul2021. her throat didn't really hurt but she had a kind of deep cough in Jul2021. This was the last night before she saw the doctor. She had tried going for testing the day before but the lines were 3 hours. She booked a test and a doctor's appointment for the next day because she thought she caught the cold or flu. One night, she woke up again and it was the same, with chills and sweat but, her chest was really sore. It felt like pressure on her chest in Jul2021. It felt not normal, like it was maybe a variant. She was super contagious and vaccines may not be fully effective against them. She felt horrible in her chest and it was hard to breathe in Jul2021. When going up and down the stairs, she would get really tired and was out of breath. She tested at the Drive through. It was a nasal swab in each nostril. That night, 08Jul2021, when she had dinner, she couldn't taste anything or smell anything on 08Jul2021. She thought, it must be Covid. The next day, she went to the clinic and saw a Nurse Practitioner. She made her put her head down to see if there was pressure in the sinuses. She tested her breathing and her lungs, everything was clear. She didn't really think it was Covid. She put her on amoxicillin and has been taking that ever since. She tested positive (09Jul2021) was when she was starting to feel better but really, she was still tired and exhausted. Her energy was very low in Jul2021. She was only really sick for 3 full days. On Saturday, she was really lethargic on 10Jul2021 and fatigued. She knew she was getting better, just not 100 percent. When she knew that it was Covid, if it wasn't for the vaccine, she didn't think she would be able to tough it out. She still can't taste or smell at the moment. She is in self isolation. She feels completely normal. If she hadn't gotten the Covid test, she would have never thought that it was Covid. She feels 90% right now. She is back to studying. Horrible stomach ache and Diarrhea: Did not last very long, would say, like 30 minutes and then it passed. Still has diarrhea every morning but it may because of the amoxicillin. Lethargy and fatigue and all of the other symptoms: They were all on 6Jul2021, 7Jul2021 and 8Jul2021. On 9Jul2021, she started to get better. Treatment included Before Friday, when she saw the Nurse practitioner on 9Jul2021, she started taking the Flonase. She only did it a couple of times. It was fluticasone propionate, Flonase nasal spray and Sodium chloride nasal spray, 1 spray in each nostril. She only did it 3 times since she got it. Her nose was really runny through out the time and super congested. The only thing is that her stomach feels a little nauseous and has a little cough. Her cough has gotten way better, so much better. The nausea/ Feels nauseas didn't happen that often in Jul2021. She didn't have an appetite the first couple of days in Jul2021. Just today, she is a little nauseated but, it may not be Covid. No Emergency Room and Physician Office. She went to the clinic. She barely had any symptoms from the second dose. She looks like she has Covid and it is not good. Was tested prior to getting the vaccine and was negative. Outcome of the event Tested positive for the Covid virus, Nose really runny and super congested, Nose really runny and super congested was unknown. Outcome of the event hard to breathe, Exhausted/really lethargic and fatigued, Felt ill, run down and not herself, Voice was gone and was very cracky, Did not feel good, Throat sore and vocal cords hurting, Freezing cold and had the chills, Woke up in a puddle of sweat and hair was soaking wet and dripping, Deep cough/a little cough, Really lethargic and fatigued, Chest sore and felt like pressure on her chest, Feels nauseas, Her energy was very low, She thought she caught the flu and was not thinking that it was Covid, freezing and shaking, She didn't have an appetite the first couple of days was recovering. Outcome of the event Horrible stomach ache was recovered in Jul2021. Outcome of the event Diarrhea, Can't taste or smell was not recovered. (Parent) Evaluation Comment: Pfizer withheld reviewed this complaint and agrees with the site assignment, investigation decision, classification, sub-classification, and priority. The reported lot number is valid and an investigation will be performed. QA Review & Rationale: The complaint and its classification have been reviewed. No immediate containment actionis required. The complaint, its priority, and its classification have been reviewed and determined to be appropriate. A full investigation will be performed. This is a complaint for lack of effect of lot EN6208 of the PFIZER-BIONTECH COVID-19 VACCINE INJECTABLE. The initial scope of this investigation is limited to the reported finished goods lot EN6208 pending review of lot genealogy. The investigation will include a review of the returned complaint sample (if received) and reserve samples, if necessary. Conclusion: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE INJECTABLE lot EN6208 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot EN6208, fill lot EN5338, and the formulated drug product lot EN5329. 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 an adverse event requested by safety with the use of the PFIZER-BIONTECH COVID-19 VACCINE lot EL1283 was investigated. The investigation included reviewing the manufacturing and packaging batch records, retained reference samples, deviation investigations and an analysis of the complaint history for the reported lot and product type. The final scope was expanded to the reported finished goods lot EL1283, fill lot EL1281, and the bulk formulated drug product lot EL1279. A complaint sample or photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. The complaint was not confirmed. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: tested; Result Unstructured Data: Test Result:tested her breathing and her lungs, everything was; Comments: tested her breathing and her lungs, everything was clear.; Test Name: Covid-19; Test Result: Negative ; Test Date: 20210709; Test Name: Covid-19; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: VYVANSE
Allergien: -
Vorherige Impfungen: -

VAERS 1507970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: LA
Alter: 63,0
Geschlecht: F
Eingang: 28.07.2021
Impfdatum: 27.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dry skin Dyspnoea Erythema Paraesthesia Swelling face Urticaria

Symptomtext

her faced swelled on both sides where her sinuses are at; Skin roughness; the side of her left thigh had a tingling sensation; she had the tingling sensation in the bottom part of her butt cheeks for the first 2-3 days after getting the COVID-19 Vaccine; her left thigh had welted up; her left thigh had turned red; she had shortness of breath immediately after she had the COVID-19 Vaccine, and the shortness of breath lasted about 10-15 minutes; This is a spontaneous report from a contactable consumer (patient). A 63-years-old female patient received BNT162B2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL9267, Expiration date and NDC number was unknown), via an unspecified route of administration, administered in left arm on 27Feb2021 at 13:45 hours as dose 1, single (at the age of 63-years-old) for COVID-19 immunisation. Medical history included shrimp allergy for about 7-8 years, patient stated that the shrimp allergy mysteriously started, clarifying she never had a problem with eating shrimp before that time. She said she had ordered a plate of grilled shrimp with pepper and onions, and when she started to eat the shrimp, her lips and face started swelling, she had not touched shrimp again since that time, blood pressure high for about 7-8 years, obesity for about as long as her high blood pressure (7-8 years). She said her weight had fluctuated up and down over time, but she had been obese for probably at least 7 years, gastrooesophageal reflux disease (GERD) (all from an unknown date and unknown if ongoing). Family medical history was not reported. No relevant tests were performed. Patient had no prior vaccinations (within 4 weeks). Patient had no history of all previous immunization with the Pfizer vaccine considered as suspect. Patient had no chills, fever, or arm soreness after getting her COVID-19 vaccine. There were no concomitant medications. On 27Feb2021, patient had shortness of breath immediately after she had the COVID-19 vaccine, and the shortness of breath lasted about 10-15 minutes. Patient clarified for the last year she had a problem with GERD. Patient stated that at certain times when she eats, she had shortness of breath and a rapid heartbeat. She said she went to her doctor, and her doctor doesn't know why her shortness of breath and rapid heartbeat keeps happening when she eats. Patient stated that she does not had shortness of breath or a rapid heartbeat every time she eats. Patient stated that she had ate lunch before she got her first COVID-19 vaccine shot. Patient stated that she was not sure if the shortness of breath she experienced after the COVID-19 Vaccine was from the vaccine, itself, or her GERD. On 27Feb2021, patient had her faced swelled on both sides where her sinuses are at. Patient clarified that she could tell there was a difference in her face because the skin got rough up underneath her eyes. Patient had "2 little puffs" right where her sinuses begin, and noticed when she touched her skin, her skin wasn't smooth right there. Patient had no itching with the skin roughness. Patient clarified facial swelling was only for the first hour after getting the COVID-19 vaccine. On 27Feb2021 (noticed later in the day or evening), patient experienced on side of her left thigh had a tingling sensation and had welted up and turned red. Patient clarified that she noticed later in the day or evening, her left leg felt funny, and she felt welts on her left thigh. Patient had her husband look at her left thigh, and her husband said her left thigh had turned red and he could see welts. Patient still had the tingling sensation from time to time in her left thigh. Patient also had the tingling sensation in the bottom part of her butt cheeks for the first 2-3 days after getting the COVID-19 vaccine. Patient stated that the tingling sensation stopped in her butt cheeks (or the bottom part of her rear-end). Patient used her husband's prescription triamcinolone 0.1% itch cream (NDC Number: 45802-064-36, Lot Number: either 6FTO444 or 6FT0444, Expiration Date: May2018) and she was unable to read the Lot Number, he had used for a bad rash on one of his legs. She said her husband thought the prescription itch cream may help her left thigh redness and welts. Patient stated that cream worked good and she hadn't welted up since using the triamcinolone 0.1% cream. Patient stated that her left thigh was still getting the tingling sensation on and off. Patient took an allergy pill, Equate Brand Loratadine 10mg tablet, and couldn't read the NDC Number. Patient stated she needed to put glasses on to read the Loratadine NDC Number. Patient stated that she had to use her cell phone camera to take a picture of the Loratadine NDC Number and blow the picture up to read the NDC Number (NDC Number: 49035-612-95, Lot Number: either 9EE2445A (listed above the Expiration Date) or 612952EF3 (listed below the Expiration Date), Expiration Date: Feb2021). Patient was scheduled to have her next Pfizer COVID-19 vaccine dose on Saturday (20Mar2021). Patient stated that she had some reaction to her first COVID-19 vaccine dose. Patient was wondering because she had a reaction to the first COVID-19 vaccine dose, if she needed to take the second COVID-19 vaccine shot, or what she needed to do. Patient had no emergency room and physician office visit for all the events. The outcome of her faced swelled on both sides where her sinuses are at, Skin roughness, had the tingling sensation in the bottom part of her butt cheeks for the first 2-3 days after getting the COVID-19 Vaccine, her left thigh had welted up, her left thigh had turned red, had shortness of breath immediately after she had the COVID-19 Vaccine was recovered on an unspecified date of 2021, shortness of breath lasted about 10-15 minutes was recovered on 27Feb2021, recovering for the side of her left thigh had a tingling sensation. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (high blood pressure for about 7-8 years.); GERD; Obesity (obesity for about as long as her high BP (7-8 years), weight had fluctuated up & down over time); Shellfish allergy (shrimp allergy for about 7-8 years, had a plate of grilled shrimp, her lips & face started swelling.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1493635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 86,0
Geschlecht: M
Eingang: 22.07.2021
Impfdatum: 15.02.2021
Beginn: 13.07.2021
Tage bis Beginn: 148,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 pneumonia

Symptomtext

Hospitalized for COVID-19 pneumonia

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1192491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MD
Alter: 71,0
Geschlecht: M
Eingang: 18.07.2021
Impfdatum: 15.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Psoriasis Rash Skin lesion Vaccine positive rechallenge Pruritus Rash pruritic

Symptomtext

Rash on face; Red patch on neck and both arms; Burning and itching on face; Multiple red patches on neck and both arms - red and itching; This is a spontaneous report from a contactable consumer, the patient. A 71-year-old male patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: UNKNOWN) in the left arm on 15Feb2021 at 10: 45 (at the age 0f 71-years-old) as a single dose for COVID-19 immunisation. The patient also received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: UNKNOWN) in the left arm on 08Mar2021 at 10:15 (at the age 0f 71-years-old) as single dose for COVID-19 immunisation. The patient's medical history included psoriasis (mild - skin) and not psoriatic arthritis. The patient had a known allergy to BACTRIM (sulf drugs). The patient did not receive any concomitant medications. The patient had not received any other vaccines within 4 weeks prior to the COVID-19 vaccination. Prior to vaccination the patient was not diagnosed with COVID-19. Since vaccination, the patient had not tested for COVID-19. On 24Feb2021, the patient experienced rash with swelling, burning and itching on face and multiple red patches on neck and both arms which was red and itching. The events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures taken as a result of rash with swelling on face, burning and itching on face, red patch on neck and both arms, red patches itching included prednisone tablets (MANUFACTURER UNKNOWN) and cortisone ointment (MANUFACTURER UNKNOWN). The clinical outcome of the events rash with swelling on face, burning and itching on face, red patch on neck and both arms, red patches itching was recovering. No follow-up attempts are needed; information about lot/ batch number cannot be obtained.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Psoriasis ((mild - skin), not psoriatic arthritis)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1478196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: ID
Alter: 65,0
Geschlecht: F
Eingang: 16.07.2021
Impfdatum: 10.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal loss of weight Blood test Chills Condition aggravated Dehydration Mobility decreased

Symptomtext

1st shot - like I had a light case of the flu 2nd shot - almost totally incapacitated, in bed for 3 days, extremely dehydrated and had to get IV fluids at doctor's office, lost 20 pounds in 14 days, kept getting chills.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Tons of blood work...
Aktuelle Erkrankungen: Small reaction to 1st Pfizer on 2/17/21 at 0930am, in bed for a few days.
Vorgeschichte: No chronic issues until I contracted Covid 10/28/2019 in Vietnam, light case with dark urine for a few days. Until May 2020 had dark urine every 2 months, but otherwise OK. Had flu shot on 9/20/2020...ambulanced to ER with suspected heart attack. X-ray did not show fluid in lung, CT scan did. D-dimer was more than double the upper limit. Things were better until the Pfizer vaccines 2/17/21 and 3/10/21...
Andere Medikamente: Multivitamins, hydroxychloroquine
Allergien: None
Vorherige Impfungen: -

VAERS 1470796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 74,0
Geschlecht: M
Eingang: 14.07.2021
Impfdatum: 21.02.2021
Beginn: 02.03.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

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

Cellulitis Condition aggravated Erythema Peripheral swelling Ultrasound scan

Symptomtext

Redness and swelling of the right lower leg. Diagnosed with cellulitis. Prescribed an antibiotic and discharged.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Vital signs checked. Ultrasound. 03/05/2021
Aktuelle Erkrankungen: None.
Vorgeschichte: Chronic Lymphoid Leukemia.
Andere Medikamente: Alfuzosin HCL 10mg. Vitamin B complex. L-tryptophan.
Allergien: Dairy, eggs, garlic, snakebite serum
Vorherige Impfungen: Pain and swelling of right lower leg. Severe. Age 74. Pfizer Biotech Lot # EL 9263. Cellulitis diagnosed.

VAERS 1467059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 13.07.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
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 Heart rate increased Incomplete course of vaccination Lip blister Oral herpes Respiratory tract oedema Swollen tongue

Symptomtext

Approximately two hours after the shot, a cold sore/blister popped up on my bottom lip. Within minutes, I felt my tongue begin to swell and then my airway began to swell/constrict and it was difficult to breathe. This caused my heart rate to increase and I was forced to lie down. I took an antihistamine and monitored my oxygen and had to remain lying down for about two hours. I then began to feel better. I did not have to use an Epi pen. I still felt dizzy with an increased heart rate and some difficulty breathing from time to time that evening, but it was better than the initial reaction. After that I had two incidents within the month after the shot of feeling like it was difficult to breathe again. Since April, I have not had any more incidents of difficulty breathing/constricted airway/heart racing. I was advised not to get the second dose due to my reaction. I informed my doctor of the reaction and then went for a doctor's visit a couple of months later to get a full check up due to the two other incidents of difficulty breathing after the vaccine and to make sure everything seemed okay.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: None.
Vorgeschichte: fibromyalgia, IBS
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1460377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: AZ
Alter: 71,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 14.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Balance disorder Dysarthria Fatigue Hypoaesthesia Laboratory test Nervous system disorder Paraesthesia Vision blurred

Symptomtext

right side,,,,, nerve tingling and numbness blurry eyes fatigue unbalanced slurred speech

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: numerous tests went to emergency room and was admitted for 24 hours when the tests were done
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: 81 mg aspirin
Allergien: no
Vorherige Impfungen: -

VAERS 1458837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Chest discomfort Musculoskeletal discomfort Paraesthesia

Symptomtext

tightness in chest; upper back discomfort; tingling in right leg from calf to toes; This is a spontaneous report from a non-contactable consumer or other non hcp. A 71-years-old female patient received bnt162b2 (BNT162B2 Formulation: Solution for injection), via an unspecified route of administration, administered in Arm Right on 10Feb2021 12:00 (Batch/Lot Number: EL9267) as SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. Concomitant medication included alendronate sodium, calcium, colecalciferol (D3) taken for an and eicosapentaenoic acid ethyl ester (VASCEPA) taken for an unspecified indication, start and stop date were not reported. The patient previously took statins and experienced drug hypersensitivity, aspirin (acetylsalicylic acid) and experienced drug hypersensitivity. No vaccination to covid prior and not covid tested post vaccination. The patient experienced tingling in right leg from calf to toes on 10Feb2021, tightness in chest and upper back discomfort on 10Feb2021 19:00. No treatment received for events. The outcome of the events tightness in chest and upper back discomfort was resolved on 10Feb2021 21:00 and other event tingling in right leg from calf to toes resolved on an unspecified date. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ALENDRONATE; CALCIUM; D3; VASCEPA
Allergien: -
Vorherige Impfungen: -

VAERS 1458832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 35,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Chest pain Chills Fatigue Headache Nasopharyngitis Pain Pain in extremity Paraesthesia

Symptomtext

Hand tingled in the right arm that the vaccine was put in in under 5 minutes of getting it.; The next day, just my arm hurt; Within 20/25 minutes of waking up I began having a light chest pain; chills; cold; body aches; Head hurt; Very tired; This is a spontaneous report from a contactable consumer or other Non-health care professional. A 35-years-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number: EL9267), via an unspecified route of administration, in right arm (at the age of 35-year-old) on 11Feb2021 14:00 as dose 1, single for covid-19 immunization. Medical history included covid-19 from an unknown date and unknown if ongoing and was reported as none. The patient's concomitant medications were not reported. Patient had no known allergies. Prior to the vaccination, the patient was 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. The patient did not receive any other medications in two weeks prior to the vaccination. On 11Feb2021 14:15 the patient experienced hand tingled in the right arm that the vaccine was put in in under 5 minutes of getting it. Then, whole arm was tingling and later the whole arm hurt and tingled. Later that evening it was very cold. On the next day, just her arm hurt, and she felt great. Within 20/25 minutes of waking up she began having a light chest pain. It lingered all day. Later began with chills, cold and body aches. Just got worse throughout the day. Head hurt off and on all day for a few seconds and then would go away. Very tired. Arm hurt bad. The patient did not receive treatment. The outcome of events was recovered on an unspecified date in 2021. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1458828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: LA
Alter: 96,0
Geschlecht: F
Eingang: 09.07.2021
Impfdatum: 10.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Depressed mood Depression Tremor

Symptomtext

Uncontrollable shaking; Felt sadness; Very depressed; This is a spontaneous report from a contactable consumer (patient). A 96-year-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9267) via an unspecified route of administration, administered in right arm on 10Feb2021 at 10:45 (at the age of 96-year-old) as dose 2 single for covid-19 immunisation in doctor's office/urgent care. Medical history included congestive heart failure, 4 way bypass. The patient's concomitant medications were not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: unknown) via an unspecified route of administration, on an unknown date Jan2021 (four weeks prior to suspect vaccine), as dose 1 single for covid-19 immunisation. Prior to vaccination, the patient was not diagnosed with COVID-19. On 10Feb2021 at 17:30, the patient experienced uncontrollable shaking lasted for 3 hours, the patient felt well enough to go to bed. Patient took 2 tylenol and slept through the night until 9:00. Along with the shaking patient felt sadness and very depressed. The patient took 2 tylenol as treatment for the event uncontrollable shaking. No treatment medication was received for the events felt sadness and very depressed. Post vaccination, the patient had not tested for COVID-19. The outcome of the events was resolving. Follow-up attempts completed. No further information expected.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bypass surgery; Congestive heart failure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1454572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 54,0
Geschlecht: F
Eingang: 07.07.2021
Impfdatum: 21.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray Chest pain Electrocardiogram Magnetic resonance imaging heart Pain in extremity Pleurisy

Symptomtext

Right after the vaccine, I had a very mild sore arm. I started having symptoms in March around the 20th. My symptoms became more intense. I tried to avoid going to the ER . I couldn't find anybody that could fit me in. I ended up going to the ER. It hurt to breathe on the left side of my chest. They diagnosed Pleurisy. I took 4 days of Ibuprofen and that fixed it. I really don't think this had anything to do with the vaccine because it started a couple weeks after my first vaccine. I didn't have any symptoms from the 2nd vaccine.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG Chest X-Ray Chest MRI
Aktuelle Erkrankungen: -
Vorgeschichte: thyroid disease still person syndrome
Andere Medikamente: baclofen - 3xday/5mg - 1xday/10mg diazepam - 4xday/5mg IVIG - 1xday thyroid medication- thyroxin - 1xday/100micrograms Multivitamin - 1xday Vitamin D - 1xday Turmeric - 1xday
Allergien: Cephaclor
Vorherige Impfungen: -

VAERS 1443607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 65,0
Geschlecht: M
Eingang: 02.07.2021
Impfdatum: 02.03.2021
Beginn: 29.06.2021
Tage bis Beginn: 119,0
Dosis: 1
Route/Site: SYR / UN

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

Chest X-ray abnormal Chest pain Chills Condition aggravated Cough Diarrhoea Dyspnoea Odynophagia Oropharyngeal pain Pain Pneumonia Productive cough Pyrexia Sputum discoloured Tachycardia Vomiting

Symptomtext

Pt. is a 65 yrs. male with h/o renal transplant on immunosuppressive therapy, presenting with worsening productive cough of white sputum for the past couple of days. There is associated fever, chest pain while coughing, shortness of breath, sore throat, painful swallowing, chills, and generalized body aches. Had one episode of non-bloody emesis and watery stool. Denies change in urinary habits, no dysuria. He went to minute clinic at store pharmacy and an X-Ray showed RRL pneumonia per radiology report he is holding, got one dose of azithromycin, came her for worsening symptom. Portable X-Ray in ED was negative for infiltrate, he was febrile and tachycardiac. He is fully vaccinated for covid 19. Hospital medicine was asked to admit the patient for further evaluation and management.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHRONIC RENAL DISEASE HYPERTENSION FORMER SMOKER
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1041616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: -
Geschlecht: U
Eingang: 01.07.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Blood test Chest X-ray normal Computerised tomogram normal Electrocardiogram normal Blood pressure abnormal Hypertension Urine analysis

Symptomtext

My blood pressure was 210 over something; blood pressure reading that they recorded was 240 over something; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received bnt162b2 (BNT162B2), via an unspecified route of administration on an unspecified date at 11:30 (Batch/Lot number was not reported) as dose 1, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient reported at 3 o'clock the same day. When the patient went for examination it was discovered that patient's blood pressure was 210 over something. The patient had immediately sent me to the emergency clinic for further testing and when the patient got to the emergency clinic the blood pressure reading that they recorded was 240 over something. After 4-5 hours their patient had several tests done. The patient also reported that patient have got a second vaccine scheduled for 05Mar and patient was little concerned about it, even bothering to go because doctor tells patient that the blood pressure reading in 200 range was rather dangerous. The patient underwent lab tests and procedures which included blood pressure measurement was 240 (units not reported), blood pressure measurement: 210 (units not reported). The outcome of the events was reported as unknown. Information on the lot batch number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:240 over; Test Name: blood pressure; Result Unstructured Data: Test Result:210 over
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1426266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: IL
Alter: 52,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / RA

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

Blood glucose increased Blood test Dyspnoea Heart rate Heart rate increased Pyrexia

Symptomtext

Shortness of breath; racing heartbeat; feeling over heated; elevated blood sugar; This is a spontaneous report from a contactable other health care professional (patient). A 52-years-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EL9267), via an intramuscular route of administration, administered in arm right on 11Feb2021 13:30 (age at vaccination 52-years) as single doe for COVID-19 immunization. Medical history included a reaction to epinephrine, even a tiny amount results, causing feeling overheated, racing heart back, slight difficulty breathing, and elevated blood sugar. Concomitant medication included lispro insulin vial taken for an unspecified indication, start and stop date were not reported. The patient was not had COVID prior vaccination, and the test was not performed post vaccination. The patient did not receive any other vaccine within four weeks. On 11Feb2021 01:30, the patient experienced shortness of breath, racing heartbeat, feeling over heated, elevated blood sugar and it was lasted about 30-45 minutes. The treatment was received for the adverse events and reported that needed to take additional insulin. The patient underwent lab tests and procedures which included blood test: elevated, heart rate: racing on an unspecified date. The vaccination facility type was reported as hospital. The clinical outcome of the events was reported as recovered on an unspecified date in 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: elevated blood sugar; Result Unstructured Data: Test Result:Elevated; Test Name: racing heartbeat; Result Unstructured Data: Test Result:Racing
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy
Andere Medikamente: LISPRO INSULIN
Allergien: -
Vorherige Impfungen: -

VAERS 1406222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 17.06.2021
Impfdatum: 22.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Eczema

Symptomtext

Eczema outbreak on my arms and hands

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure, eczema
Andere Medikamente: Losartin, rosuvasatin calcium, amlodipine, meloxicam
Allergien: Nickel
Vorherige Impfungen: Headache & fatigue, 69, 2nd shingles shot

VAERS 1388097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 28.01.2021
Beginn: 05.05.2021
Tage bis Beginn: 97,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chest discomfort Chest pain Dyspnoea exertional Fatigue SARS-CoV-2 test positive

Symptomtext

Patient present to ED for chest pain and fatigue. Per patient, she was gardening last week and developed chest pressure/SOB when moving around some mulch this lasted on and off for 3 days and then was followed by intense fatigue which persisted today so she came into ED. She was placed in observation for chest pain, and to rule out ischemia. Upon admission, a COVID-19 test was run for screening, and was positive. Other than fatigue and chest pain, she was not endorsing other symptoms and did not have hypoxia or coughing at all. Although on admit, there was plan to get a stress test, given the COVID-19 diagnosis, this was deferred. She was discharged to home in stable condition on 5/5.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1378126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: CO
Alter: 60,0
Geschlecht: M
Eingang: 07.06.2021
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

Back pain Chest pain Dyspnoea Echocardiogram normal Electrocardiogram abnormal Hypertension

Symptomtext

Developed shortness of breath and high blood pressure within 48 hours. Chest pain and back pain. Shortness of breath when working out slightly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 5/10/2021. Showed AFIB. Echocardiogram 5/21/2021. Normal. Other signs had started dissipating.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Armour Thyroid, 60mg. Multi, calcium lactate, vitamin C, vitamin F, vitamin B
Allergien: None known.
Vorherige Impfungen: -

VAERS 1377679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 24.02.2021
Beginn: 27.05.2021
Tage bis Beginn: 92,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Chest X-ray abnormal Chest discomfort Cough Diarrhoea Dyspnoea Fatigue Hypoxia Lung infiltration Malaise Oxygen saturation decreased Refusal of treatment by patient Respiratory tract congestion Wheezing

Symptomtext

Patient is a 82 y.o. female with history of adenocardinoma left lower lobe lung s/p radiation, COPD, nocturnal use of 3 liters oxygen, dementia, eliquis for hx dvt, esophageal stricture who presents today from clinic secondary to hypoxia. History obtained from daughter bedside and chart review as patient has dementia. Patient began feeling ill one week ago. Complains of cough, congestion, wheezing, shortness of breath, mild wheezing, chest discomfort with coughing, fatigue, and decreased energy. She has had one episode of loose stool. Denies fevers, chills, loss of taste/smell. She was evaluated by pulmonology on 5/25 and noted to have oxygen desaturation. She was recommended to go to the ED for further evaluation however patient refused and preferred home treatment. She was prescribed Augmentin for possible aspiration pneumonia as well as prednisone taper. Patient reportedly felt some mild improvement since starting treatment however continued to require use of 3 liters of oxygen during day and night rather than just at night. She followed up with clinic today where she continued to have oxygen desaturation despite supplemental oxygen and chest xray noted new infiltrate. She was again recommended to go to the ED for further evaluation and management at which time patient agreed.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Elevated Cholesterol HTN Meningioma asthma Alzeimers Esophageal stricture
Andere Medikamente: Namenda albuterol Cozaar Norvasc Eliquis Symbicort Catapres Prilosec Oxygen therapy
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 1355207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

moderat

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 18.05.2021
Beginn: 22.05.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Chest pain Hypertension Paraesthesia Sleep disorder

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Hypertension-Medium, Systemic: Tingling (specify: facial area, extemities)-Mild, Systemic: Unable to Sleep-Medium, Additional Details: pt state went to ER twice will follow up with her dr

Weitere VAERSDATA-Felder

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

VAERS 1354294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 36,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 12.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: IM / LA

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

Electroencephalogram Full blood count Headache Hypoaesthesia Liver function test Magnetic resonance imaging head Metabolic function test Neuropathy peripheral Paraesthesia Rheumatoid factor

Symptomtext

Severe headache, tingling and numbness in hand and feet, neuropathy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI head - 4/19 & 5/25 EEG - 4/21 & 5/21 CBC, CMP, Rheumatoid factors, liver function, vitamin
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Rocephin
Vorherige Impfungen: -

VAERS 1354265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 05.03.2021
Beginn: 25.05.2021
Tage bis Beginn: 81,0
Dosis: 2
Route/Site: IM / -

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

Anaemia COVID-19 Condition aggravated Hypotension SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

Admitted to hospital on 5/21/21 for hypotension and anemia. During screen for discharge, was found to be COVID-19 positive. Is currently asymptomatic at time of writing. Patient remains admitted to hospital at this time, awaiting another COVID-19 test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: COVID-19 test negative on 5/21/21. COVID-19 test positive on 5/25/21. Awaiting an additional test.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Right pulmonary embolus Left pulmonary embolus Hypothyroidism, unspecified type Fatigue associated with anemia Anemia
Andere Medikamente: apixaban (ELIQUIS) 5 MG TABS tablet ferrous sulfate (FEOSOL, 65 FE,) 325 (65 FE) MG tablet FLUoxetine (PROZAC) 20 MG capsule furosemide (LASIX) 40 MG tablet levothyroxine (SYNTHROID) 200 MCG tablet midodrine (PROAMITINE) 5 MG tablet multivi
Allergien: Penicillin (hives), keflex (GI symptoms)
Vorherige Impfungen: -

VAERS 1353524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: CA
Alter: 90,0
Geschlecht: M
Eingang: 27.05.2021
Impfdatum: 16.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Arthralgia Back pain Body temperature Chills Computerised tomogram Dyspnoea Electrocardiogram Inappropriate schedule of product administration Lymphadenopathy Off label use Pain Pain in extremity Pain in jaw Pyrexia SARS-CoV-2 test negative X-ray

Symptomtext

The pain went down his left shoulder and back/he developed pain down his right side of his shoulder, and down in his hips/His left ankle, right side heel, and shoulders also hurt.; The pain went down his left shoulder and back; he was having problems breathing/difficulty breathing; possibly a swollen lymph node on his trachea; His left ankle, right side heel, and shoulders also hurt.; He has had pains in different parts of his body that last for 2-3 days and then some place else starts to hurt.; chills; His wife took his temperature and it was 100.3./He has weird fevers for one day with no other symptoms.; jaw pain; Dates for COVID vaccine: (Start: 5Feb2021 Stop: 16Feb2021), first dose on 5Feb2021 and second dose on 16Feb2021; Dates for COVID vaccine: (Start: 5Feb2021 Stop: 16Feb2021), first dose on 5Feb2021 and second dose on 16Feb2021; This is a spontaneous report from a contactable consumer (patient). A 90-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Right on 16Feb2021 (Lot Number: EL9267) (at age of 90-year-old) as 2ND DOSE SINGLE for covid-19 immunisation. Medical history included ongoing atrial fibrillation, stent placement from 19Jun2020 and ongoing (successful in the descending aorta), and ongoing Heart problems. The patient's concomitant medications were not reported. The patient received the first dose of BNT162B2, administered in Arm Right on 05Feb2021(Lot: EL9263) (at age of 89-year-old) for covid-19 immunisation. The patient would like to talk to an individual regarding his side effects he has been having since his two COVID vaccinations in Feb 2021. Ten days after the second inoculation on 26Feb2021, he woke in the middle of the night with jaw pain. He was in great pain. The pain went down his left shoulder and back . His wife said that morning that those were signs of heart problems. He does have Atrial Fibrillation, and he had a stent placed 19 Jun 2020. He went to the emergency room where they checked him out for heart problems. He had a clean bill of health. They sent him home, and told him to take Tylenol for the pain. The Tylenol certainly helps. It took whatever number of days for it to subside. It subsided for 2 weeks, but then he developed pain down his right side of his shoulder, and down in his hips. Once again they figured they better get back to the ER. They did EKG and a X-ray. There was absolutely nothing wrong with his stent. They told him just to continue with Tylenol to control the pain. He went a third time to the emergency room because he was having problems breathing. The emergency room put him through the COVID entry at Kaiser because of the difficulty breathing. They re did all the previous work, and did a scan of his lung to check for blood clots. He thinks they did that because 6 people died from blood clots from Johnsons and Johnson. They wanted to see if there were blood clots, but there were no blood clots. They told him he needed to make an appointment with his primary who then referred him to a Cardiologist. On 11May2021, he saw his primary doctor who ordered another scan because they found possibly a swollen lymph node on his trachea. The doctor measured that, and said to wait a month to do that again. To see any change in it. On the 26 May 2021, he has his next appointment to get that rechecked. He hasn't had a comfortable day since this started. He has had pains in different parts of his body that last for 2-3 days and then some place else starts to hurt. His left ankle, right side heel, and shoulders also hurt. The pain was under control if he takes ibuprofen, but his doctor advised him against too much of that because of his kidneys. It was very effective. The Tylenol works to some extent, but not like the Ibuprofen. He is just living with it day to day. He can play tennis some days. One day he played tennis and came home with chills. His wife took his temperature and it was 100.3. In the last week and half this has happened two times. After the second shot this has happened probably four times. He has weird fevers for one day with no other symptoms. Ever since 26Feb2021, it has been on a daily basis that some place else hurts. One subsides , but another pain starts up elsewhere. If that is not happening, then his whole demeaner is dead. He is just not comfortable and sitting around he feels like he was wasting what life he has left. He used to be a PE teacher. He has always been in good physical condition. He was 5k and walking 5ks every 4th of Jul. He would compete. He prepared for this 90 birthday/ His goal was to do a 5k in under 60 minutes. He worked out like always , and played tennis 3 days a week to prepare. He also played ball. He likes to walk run 2-3 miles most days. He did his 5k in 52minutes, and he was celebrating. Then ten days later this all started happening. The patient/caller has been tested for COVID, and it was negative. The aches and pains were moving around. He was still having breathing difficulties. Sometimes he can't talk because of the breathing. It just goes away. If it is something like the tumor or a node on the trachea wouldn't it be happening all the time? Sometimes he can't talk because the breathing is bad. It comes and goes. It is more often recently. It is like all the sudden he can't breath and can't talk. That started right at the beginning. It has gotten progressively worse. He took Tylenol to help the pain in his body. Nothing has helped his breathing. He tried antihistamines to see if maybe it was hay fever or something , but there was no difference. He didn't know where to go from here. He was feeling horrible. He was just waiting on 26 May2021, for the second scan without color of thorax to see those results. The patient said he didn't have questions. The outcome of events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: body temperature; Result Unstructured Data: Test Result:100.3; Test Name: scan; Result Unstructured Data: Test Result:Normal; Comments: did a scan of his lung to check for blood clots; Test Name: scan; Result Unstructured Data: Test Result:possibly a swollen lymph node on his trachea; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Comments: There was absolutely nothing wrong with his stent; Test Name: COVID test; Test Result: Negative ; Test Name: x-ray; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: Atrial fibrillation; Heart disorder; Stent placement
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1027958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NJ
Alter: 40,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 06.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Electrocardiogram abnormal Palpitations Paraesthesia Sinus arrhythmia Electrocardiogram SARS-CoV-2 test Tachycardia

Symptomtext

tachycardia; sinus arrhythmia; heart palpitations; This is a spontaneous report from a contactable healthcare professional (patient). A 40-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), intramuscular, administered in the right arm on 06Feb2021 16:00 (04:00 PM) (Batch/Lot Number: EL9267) at the age of 40-years-old as unknown, single dose for COVID-19 immunization at a workplace clinic. The patient had no other vaccine in four weeks. The patient had no COVID prior vaccination. The patient had no medical history and no known allergies. Concomitant medications included daily multi-vitamin and an iron supplement, both taken for unspecified indications, start and stop date were not reported (reported as other medications in two weeks). The patient had heart palpitations beginning 08Feb2021 at 08:00 AM, then had an ECG with a sinus arrhythmia present on 10Feb2021, and then went to emergency room (ER) on 19Feb2021 for severe tachycardia. The events resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient did not receive treatment for the events. The patient was tested for COVID post vaccination which was a nasal swab (PCR) with a negative result on 10Feb2021. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210210; Test Name: ECG; Result Unstructured Data: Test Result:sinus arrhythmia; Test Date: 20210210; Test Name: Nasal Swab (PCR); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: IRON
Allergien: -
Vorherige Impfungen: -

VAERS 1027958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NJ
Alter: 40,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 06.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: OT / RA

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

Electrocardiogram abnormal Palpitations Paraesthesia Sinus arrhythmia Electrocardiogram SARS-CoV-2 test Tachycardia

Symptomtext

tachycardia; sinus arrhythmia; heart palpitations; This is a spontaneous report from a contactable healthcare professional (patient). A 40-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), intramuscular, administered in the right arm on 06Feb2021 16:00 (04:00 PM) (Batch/Lot Number: EL9267) at the age of 40-years-old as unknown, single dose for COVID-19 immunization at a workplace clinic. The patient had no other vaccine in four weeks. The patient had no COVID prior vaccination. The patient had no medical history and no known allergies. Concomitant medications included daily multi-vitamin and an iron supplement, both taken for unspecified indications, start and stop date were not reported (reported as other medications in two weeks). The patient had heart palpitations beginning 08Feb2021 at 08:00 AM, then had an ECG with a sinus arrhythmia present on 10Feb2021, and then went to emergency room (ER) on 19Feb2021 for severe tachycardia. The events resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. The patient did not receive treatment for the events. The patient was tested for COVID post vaccination which was a nasal swab (PCR) with a negative result on 10Feb2021. The outcome of the events was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210210; Test Name: ECG; Result Unstructured Data: Test Result:sinus arrhythmia; Test Date: 20210210; Test Name: Nasal Swab (PCR); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: IRON
Allergien: -
Vorherige Impfungen: -

VAERS 1342426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 16.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test normal Dry skin Dysuria Erythema Paraesthesia Rash erythematous Skin exfoliation Swelling Urethral pain Vaginal discharge Vestibular disorder

Symptomtext

rash on face, back, shoulders, and stomach (dry, red, peeling skin--not itchy) extreme burning and stinging of urethra and vestibular tissues prickling of external vulvar tissues (labia majora and minora, perineum) swelling and redness of mans pubis and labia majora burning and stinging when urinating and deficating excoriated vulvar and vestibular tissues white, nonodorous vaginal discharge that comes back negative for every infection and virus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: every type of blood test, swab, and DNA test known to modern medicine pretty much was taken of my blood and the vaginal discharge. everything comes up normal and negative. I am having my hormones checked (via blood) this week, so we will see what those results are
Aktuelle Erkrankungen: -
Vorgeschichte: i have had 9 years of vestibular pain and atrophy due to hormone deficiency caused by birth control pills, but this was being treated successfully with the hormone gel listed above because I finally found speciality doctors who gave me accurate dx on 3/2020, and this condition had actually finally stopped causing me pain just a week prior to taking the second dose of the vaccine on 2/16 (improvement of condition was after 1 year of the hormone gel)
Andere Medikamente: estrogen testosterone compounded gel 1.0%/.10% Allegra once a day multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1328731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 64,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 06.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Flushing Paraesthesia Pruritus Urticaria

Symptomtext

Tingling in hands , flush in face, itching on skin and hives all over face and body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Going to have an allergy text on 5/20/2021 to find out if I?m allergic to the ingredients that the vaccine has.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Allegra Azestaline eyes Drops Flonaze
Allergien: Dust, trees, grass cats and several mores
Vorherige Impfungen: -

VAERS 1208180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 18.05.2021
Impfdatum: 30.01.2021
Beginn: 07.04.2021
Tage bis Beginn: 67,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain upper COVID-19 Chest discomfort Chills Cough COVID-19 pneumonia Influenza virus test Respiratory syncytial virus test SARS-CoV-2 test positive Dizziness Dyspnoea Nausea Nucleic acid test Pyrexia

Symptomtext

Pt tested positive for COVID and developed COVID pneumonia post vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19, flu, RSV by NAA positive for COVID-19 on 4/7/21
Aktuelle Erkrankungen: -
Vorgeschichte: Peripheral arterial disease
Andere Medikamente: Eliquis, Mucinex, Cardizem, Vitamin D, Mag-oxide
Allergien: none
Vorherige Impfungen: -

VAERS 1033953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

moderat

Staat: MD
Alter: 68,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 13.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

nose and upper lip got numb, it spread through her face, her cheeks and kind of her eyes and forehead; hands are tingling a little; arm was very painful; This is a spontaneous report from a contactable pharmacist (patient). A 68-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: el9267, expiry date: 31May2021) via unknown route of administration on 13Feb2021 at 17:00 as single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Caller reported that she received her first Pfizer COVID vaccine dose on Friday at 5pm. She reported that right away she got a numb nose, numb top lip then it spread to her chin and her cheeks and to her forehead. Saturday and Sunday her face was still numb, and she also had tingling in her hands. Caller explained that the feeling was like when your leg fell asleep and was waking back up. Caller also reported that her arm hurt. Caller stated her face still was not feel correct, still numb or tingling. During this call the caller mentioned that her husband's co-worker got a swollen face and needed a shot of Benadryl after getting her vaccine. And another report from the News that showed a woman's whole face got swollen. She reported that she read that people should not take Benadryl prior to getting the vaccine because it might mask effects. She reported that she did not take anything prior to the first one and was asking whether it was ok to take Benadryl while getting the COVID vaccine. and whether there were the contraindications to taking Tylenol prior to getting the vaccine. Caller stated It did not take long to produce a vaccine, we need more, they keep saying there was a shortage, it took 3 weeks to make an appointment. Pfizer need to do something about encouraging a lot of people to get the vaccine, I did not see many minorities getting these shots, this was very concerning to me as a pharmacist. Also, they were gone come up with something better or not so hard to handle for pharmacists. This whole ultra-cold thing was too much. Caller reported of being upset at Pfizer and the CDC stating 'Pfizer and the CDC said it was ok to use the overflow as a 6th dose. It's a 5-dose vial, people were pulling from multiple vials to get that 6th dose'. That's just not right, she did not see them, but she heard that now Pfizer was charging for the 6th dose. Pfizer really should put out a statement to these facilities giving the shot that the nurses should be taking names and lot numbers and sending a list to Pfizer of people who have a problem. No one was taking down adverse events at these places. She inquired that why was Pfizer putting PEG in their vaccine. It should not be in there. Caller was asking about the Bell's palsy - How long can it before someone could potentially have it after getting the vaccine. Caller was asking where her vaccine was manufactured. Follow up (15Feb2021): This is a follow up spontaneous report from a contactable pharmacist. This pharmacist reported that: nose and upper lip got numb, it spread through her face, her cheeks and kind of her eyes and forehead. both hands were tingling a little. arm was very painful. She was calling about COVID vaccine, wanted to let Pfizer know, she had the shot on Friday at 5PM, the 13Feb2021 and shortly after, her nose and upper lip got numb, it spread through her face, her cheeks and kind of her eyes and forehead, and on Friday it was still numb, and today, on Sunday it was a little bit, and today, she was still slightly numb, it was kind of tingling, like if she was outside shoveling snow a few hours like that was how the face feels. She did not want to forget, both hands were tingling a little and her arm, at night, when she came home her arm was fine, she had full range of motion, she was ok, then at night it was very painful, she woke up in the morning, it was ok, but felt like an ACE bandage tied around too tight. But she was very concerned about numbing of the face and tingling. She was a pharmacist. No none knows anything about this, it was very sad, in fact, she was concerned about the fact she had 2 nurses come over, both stood and were chatting, and no one took her name, the lot number, or took down the adverse reaction she had to it, it was not right at all, and she went on Sunday, she went with her husband, as they wouldn't let then have it at the same time, which was a joke, and in inclement weather, and there was a nice nurse and he helped her, but no one knows anything, she waited for her husband, and she specifically asked, she said she was concerned about the second shot, she did not want a reaction with the second, as she was not near a hospital, they were having massive vaccine areas, and a nurse came over and she said she knew nothing about it, said it could be a reaction, it could be the doctor, but caller said it was not a reaction, it happened immediately after she got the shot. If this has something to do with this nurses and doctors should be reporting back. Height and weight declined. States she did not want to provide all that. Primary care doctor information declined, she did not have one, if she goes to her cardiologist, he will say ask the doctor or pharmacist, she is a pharmacist, and no one know anything, nurses know less, her concern was; she was already on the phone for a long time, and she was afraid with the second shot she would have a worse reaction, she did want a reaction where she cannot breathe. This was an experimental drug, no one knows anything about it, it was approved for emergency use, and not FDA approved. She was the patient and could not get a question answered. Stated she spoke to USMI already, stated one nurse said plenty of people were having the same thing, stated to just document that someone should be at least looking into the lot numbers, then caller abruptly disconnected the call. There was a Product Complaint. Caller reported side effect and said someone should be at least looking into the lot numbers, then caller abruptly disconnected the call. Full details unable to be obtained. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1033953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge el9267

moderat

Staat: MD
Alter: 68,0
Geschlecht: F
Eingang: 18.05.2021
Impfdatum: 13.02.2021
Beginn: 13.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

nose and upper lip got numb, it spread through her face, her cheeks and kind of her eyes and forehead; hands are tingling a little; arm was very painful; This is a spontaneous report from a contactable pharmacist (patient). A 68-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: el9267, expiry date: 31May2021) via unknown route of administration on 13Feb2021 at 17:00 as single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Caller reported that she received her first Pfizer COVID vaccine dose on Friday at 5pm. She reported that right away she got a numb nose, numb top lip then it spread to her chin and her cheeks and to her forehead. Saturday and Sunday her face was still numb, and she also had tingling in her hands. Caller explained that the feeling was like when your leg fell asleep and was waking back up. Caller also reported that her arm hurt. Caller stated her face still was not feel correct, still numb or tingling. During this call the caller mentioned that her husband's co-worker got a swollen face and needed a shot of Benadryl after getting her vaccine. And another report from the News that showed a woman's whole face got swollen. She reported that she read that people should not take Benadryl prior to getting the vaccine because it might mask effects. She reported that she did not take anything prior to the first one and was asking whether it was ok to take Benadryl while getting the COVID vaccine. and whether there were the contraindications to taking Tylenol prior to getting the vaccine. Caller stated It did not take long to produce a vaccine, we need more, they keep saying there was a shortage, it took 3 weeks to make an appointment. Pfizer need to do something about encouraging a lot of people to get the vaccine, I did not see many minorities getting these shots, this was very concerning to me as a pharmacist. Also, they were gone come up with something better or not so hard to handle for pharmacists. This whole ultra-cold thing was too much. Caller reported of being upset at Pfizer and the CDC stating 'Pfizer and the CDC said it was ok to use the overflow as a 6th dose. It's a 5-dose vial, people were pulling from multiple vials to get that 6th dose'. That's just not right, she did not see them, but she heard that now Pfizer was charging for the 6th dose. Pfizer really should put out a statement to these facilities giving the shot that the nurses should be taking names and lot numbers and sending a list to Pfizer of people who have a problem. No one was taking down adverse events at these places. She inquired that why was Pfizer putting PEG in their vaccine. It should not be in there. Caller was asking about the Bell's palsy - How long can it before someone could potentially have it after getting the vaccine. Caller was asking where her vaccine was manufactured. Follow up (15Feb2021): This is a follow up spontaneous report from a contactable pharmacist. This pharmacist reported that: nose and upper lip got numb, it spread through her face, her cheeks and kind of her eyes and forehead. both hands were tingling a little. arm was very painful. She was calling about COVID vaccine, wanted to let Pfizer know, she had the shot on Friday at 5PM, the 13Feb2021 and shortly after, her nose and upper lip got numb, it spread through her face, her cheeks and kind of her eyes and forehead, and on Friday it was still numb, and today, on Sunday it was a little bit, and today, she was still slightly numb, it was kind of tingling, like if she was outside shoveling snow a few hours like that was how the face feels. She did not want to forget, both hands were tingling a little and her arm, at night, when she came home her arm was fine, she had full range of motion, she was ok, then at night it was very painful, she woke up in the morning, it was ok, but felt like an ACE bandage tied around too tight. But she was very concerned about numbing of the face and tingling. She was a pharmacist. No none knows anything about this, it was very sad, in fact, she was concerned about the fact she had 2 nurses come over, both stood and were chatting, and no one took her name, the lot number, or took down the adverse reaction she had to it, it was not right at all, and she went on Sunday, she went with her husband, as they wouldn't let then have it at the same time, which was a joke, and in inclement weather, and there was a nice nurse and he helped her, but no one knows anything, she waited for her husband, and she specifically asked, she said she was concerned about the second shot, she did not want a reaction with the second, as she was not near a hospital, they were having massive vaccine areas, and a nurse came over and she said she knew nothing about it, said it could be a reaction, it could be the doctor, but caller said it was not a reaction, it happened immediately after she got the shot. If this has something to do with this nurses and doctors should be reporting back. Height and weight declined. States she did not want to provide all that. Primary care doctor information declined, she did not have one, if she goes to her cardiologist, he will say ask the doctor or pharmacist, she is a pharmacist, and no one know anything, nurses know less, her concern was; she was already on the phone for a long time, and she was afraid with the second shot she would have a worse reaction, she did want a reaction where she cannot breathe. This was an experimental drug, no one knows anything about it, it was approved for emergency use, and not FDA approved. She was the patient and could not get a question answered. Stated she spoke to USMI already, stated one nurse said plenty of people were having the same thing, stated to just document that someone should be at least looking into the lot numbers, then caller abruptly disconnected the call. There was a Product Complaint. Caller reported side effect and said someone should be at least looking into the lot numbers, then caller abruptly disconnected the call. Full details unable to be obtained. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

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

VAERS 1319890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: OH
Alter: 65,0
Geschlecht: M
Eingang: 15.05.2021
Impfdatum: 11.02.2021
Beginn: 11.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Headache Hypoaesthesia Paraesthesia Peripheral swelling Pyrexia Urticaria

Symptomtext

Left arm swelling with hive; Left arm swelling with hive; left hand fingers numb; Fever; headache; Right Arm tingling; This is a spontaneous report from a contactable consumer reporting for himself. A 65-years-old male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 11Feb2021 14:00 (Batch/Lot Number: EL9267) at the age of 65 years as 1ST DOSE, SINGLE for covid-19 immunisation. Medical history included colectomy Colon resection 14 years ago. The patient's concomitant medications were not reported. On 11Feb2021 22:00 the patient experienced left arm swelling with hive, left hand fingers numb, fever, headache, right arm tingling all with outcome of not recovered. Therapeutic treatment: Tylenol. No follow up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Colectomy (Colon resection 14 years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1314642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 13.02.2021
Beginn: 14.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Headache Mobility decreased Pain

Symptomtext

Per patient report / description: "The day after the shot I had a lot of arthritic type pain all over my body for two days then continuing pain until now 5/14/21. I cannot walk more than a block, cannot stand for more than 5-10 minutes, Lingering pain all the time." Called PCP with this report: " adverse reaction to my Pfizer 2nd shot. The next day after the shot it seemed like the vaccine searched out every part of my body that might/might not have arthritis and moving was very difficult for two days. Thereafter I have had a great difficulty getting up in the morning, some days better than others. I have seen (chiropractor) often, but results have not cleared up the discomfort. I cannot walk more than a block without discomfort, cannot sit unless my feet are up for great amounts of time then expect to be able to move. Is there something that you could prescribe that would give me comfort and be able to walk without pain. I am not interested in anything that would be considered an opioid, would rather go without. Currently I am taking Excedrin. Someone told me that Advil would be better for arthritis, but I had a bad headache on day two of taking that." Told to scheduled appointment with PCP for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: hypercholesterolemia, hypertension, history of cervical cancer
Andere Medikamente: atorvastatin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1310632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 19.02.2021
Beginn: 09.05.2021
Tage bis Beginn: 79,0
Dosis: 2
Route/Site: IM / -

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

Atrial fibrillation COVID-19 pneumonia Fall Hypothermia Rhabdomyolysis SARS-CoV-2 test positive

Symptomtext

DIAGNOSIS at time of disposition: 1. COVID-19 virus detected 2. Fall, initial encounter 3. Traumatic rhabdomyolysis, initial encounter (HCC) 4. Hypothermia, initial encounter 5. Atrial fibrillation with rapid ventricular response (HCC) 6. Pneumonia due to COVID-19 virus

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: none known
Vorgeschichte: Cataract ? Family history of Alzheimer's disease ? Hyperlipidemia 2002 ? Osteopenia ? Right foot pain ? Swelling 2003 ? Tuberculosis generalized (excluding R70) 1950's ? Vaginal cyst
Andere Medikamente: Vitamin C Calcium multivitamin
Allergien: Flu vaccine Pneumococcal vaccine Tb
Vorherige Impfungen: Flu and pneumococcal

VAERS 1306643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 67,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 17.02.2021
Beginn: 17.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Mobility decreased Nerve injury Nodule Pain Pain in extremity Sleep disorder X-ray normal

Symptomtext

Patient and I spoke on May 7th, 2021. Her contact information was referred to me by one of the Call Center staff members. Patient reported that she received her first COVID-19 vaccine (Pfizer) on 2/17/2021 at Health Department. She reports that she is typically "fine with shots, no problem", but when she received her first dose of the Pfizer vaccine "it immediately started hurting". She reported taking round the clock Advil/Motrin and "could feel a knot and radiating into crease of arm". She reported difficulty raising arm to put bra on and awaiting in the middle of the night due to pain. She stated she presented 21 days later for her 2nd dose (3/10/21- right arm) and still had persistent pain in left arm. She stated she has seen a surgeon due to the pain and that they x-ray was negative. She states the surgeon told her that a nerve was affected and gave her a shot of steroids. She reports this has not resolved the pain and that she is taking diclofenac 75 mg BID with pain unresolved. States she has a f/u appt with provider 5/27/21 and will keep appointment.

Weitere VAERSDATA-Felder

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

VAERS 1303390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 72,0
Geschlecht: M
Eingang: 10.05.2021
Impfdatum: 25.01.2021
Beginn: 31.03.2021
Tage bis Beginn: 65,0
Dosis: 2
Route/Site: SYR / UN

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

Chest X-ray Haemoptysis Pneumonia Productive cough

Symptomtext

Hospitalization Pt has been admitted, he has had several diagnostic/imaging tests including chest x-ray which revealed he has pneumonia in the left lung only. Pt. rep noted coughing up blood and phlegm prior to hospital admit date on 04/01/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD and Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1302384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: FL
Alter: 69,0
Geschlecht: M
Eingang: 10.05.2021
Impfdatum: 22.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Condition aggravated Fatigue Headache Influenza like illness Myalgia Night sweats

Symptomtext

Flu like symptoms: headache, fatigue, night sweats, muscle and joint pain. That is, a big increase in Chronic Fatigue Syndrome

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Chronic Fatigue Syndrome (CFS)
Vorgeschichte: CFS
Andere Medikamente: alfuzosin HCLER, modafinil
Allergien: penicillin
Vorherige Impfungen: Chronic Fatigue Syndrome, 62. 05/26/2014, shingles vaccine - not the new Shinglex but an earlier vaccine for Shingles

VAERS 1299012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 08.05.2021
Impfdatum: 12.02.2021
Beginn: 16.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / LA

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

Headache Palpitations Pyrexia

Symptomtext

Fever 100.4; Heart Palpitations; Headache; This is a spontaneous report from a contactable other healthcare professional (patient). A 55-year-old non-pregnant female patient first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL9267), via unspecified route of administration on left arm on 12Feb2021 12:00 PM (at the age of 55-year-old) as a single dose for COVID-19 immunization. The patient's medical history was not reported. Concomitant medications included quetiapine fumarate (SEROQUEL), alprazolam (XANAX) atorvastatin (LIPITOR [ATORVASTATIN]), acetylsalicylic acid (BABY ASPIRIN) and lamotrigine (LAMICTAL). On 16Feb2021 14:00, the patient experienced fever 100.4, heart palpitations and headache. No treatment medications were received for the adverse events. Outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: SEROQUEL; XANAX; LIPITOR [ATORVASTATIN]; BABY ASPIRIN; LAMICTAL
Allergien: -
Vorherige Impfungen: -

VAERS 1292835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: TX
Alter: 71,0
Geschlecht: F
Eingang: 06.05.2021
Impfdatum: 09.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: UN / UN

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

COVID-19 pneumonia Vaccine breakthrough infection

Symptomtext

Vaccine 2/9, 3/9. Admit 4/12. Admit for COVID PNA, treated w/antibiotics, steroids, Remdesivir. DC'd to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1289725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WY
Alter: 57,0
Geschlecht: M
Eingang: 05.05.2021
Impfdatum: 08.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / RA

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

Blood glucose decreased Blood pressure normal Blood test abnormal Chest discomfort Dizziness Electrocardiogram normal Heart rate normal Paraesthesia

Symptomtext

Pressure in chest, light-headedness, tingling in arms continuing for two weeks after initial symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EKG was normal. Heart rate, pulse and blood pressure within normal/healthy range. Blood tests showed no signs of heart disease but tested low for blood sugar.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Celery seed extract, melatonin, multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1258414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WY
Alter: 17,0
Geschlecht: M
Eingang: 29.04.2021
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: unbekannt ER: unbekannt Erholt: ja

Chest pain Dyspnoea Face oedema Localised oedema Nausea Headache Peripheral swelling Swelling face Urticaria Vomiting Oedema peripheral Pruritus Rash

Symptomtext

Systemic rash with hives and itching, chest pain and shortness of breath, neck and facial edema, edema to extremities, nausea and vomiting Benadryl 50mg PO every 4-6 hours for 4 days and then PRN for itching/rash. Medrol Dose pack as directed, Daily Pepcid PO, Zofran PO PRN

Weitere VAERSDATA-Felder

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

VAERS 1258414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: WY
Alter: 17,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 21.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Chest pain Dyspnoea Face oedema Localised oedema Nausea Headache Peripheral swelling Swelling face Urticaria Vomiting Oedema peripheral Pruritus Rash

Symptomtext

Systemic rash with hives and itching, chest pain and shortness of breath, neck and facial edema, edema to extremities, nausea and vomiting Benadryl 50mg PO every 4-6 hours for 4 days and then PRN for itching/rash. Medrol Dose pack as directed, Daily Pepcid PO, Zofran PO PRN

Weitere VAERSDATA-Felder

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

VAERS 1259590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 18.01.2021
Beginn: 17.04.2021
Tage bis Beginn: 89,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Myasthenia gravis SARS-CoV-2 test negative

Symptomtext

developed SOB with Negative work up of COVID 19, symptoms progressed, resulted in hospitalization. There diagnosis of Myasthenia gravis crisis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: SCC of unknown primary Thyroid Nodule
Vorgeschichte: DMII, Obesity, HTN, Asthma
Andere Medikamente: Albuterol sulfate, Clotrimazole, Lantus, Losartan, Metformin, Naproxen, Olopatadine, ozempic, Prednisone, Simvastatin, Symbicort, Ventolin, Xanax
Allergien: Sulfa, Ace Inhibitors, PCN
Vorherige Impfungen: -

VAERS 1031021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: 09.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Abdominal discomfort Chills Depressed mood Diarrhoea Dysphonia Asthenia Dizziness Fatigue Headache Hypersomnia Illness Muscle spasms Muscle twitching Pyrexia Tachycardia Suspected COVID-19 Tremor Vomiting

Symptomtext

her head was hurting also/headache; violently throwing up; diarrhea; muscle cramps/the muscles in legs she had crapping and shivering; muscle cramps/the muscles in legs she had crapping and shivering; felt a little tired; her voice is still raspy from the amount of acid; she was able to calm her stomach down after this; sickest; she thought she came down with a virus; she slept most of the next day after taking the Zofran; she had quivering in muscles of her legs; feels little run down but it was not too bad; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9267) via unspecified route of administration in left arm on 09Feb2021, at 14:45 (at the age of 70-year-old) as a single dose for COVID-19 immunisation. The patient medical history and family medical history relevant to adverse event was none. The patient concomitant medication was not reported. The patient relevant tests were none. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Additional vaccines administered on same date of the pfizer suspect was none. History of all previous immunization with the Pfizer vaccine considered as suspect was none. The patient reported that she had the first dose on 09Feb2021 at about 14: 45pm. The next day, on 10Feb2021, she went to work but felt a little tired. That night about 22:00 she started violently throwing up, had diarrhea and had in the muscles in legs she had crapping and shivering on 10Feb2021. The diarrhea ended about the same time the vomiting stopped. It was so bad there was several time she didn't make to the restroom. She had quivering in muscles of her legs on an unknown date in Feb2021. The caller remarks that her voice was still raspy from the amount of acid. It was so bad she thought she came down with a virus because she thought it was too long after the vaccine. It was severe enough she called the doctor who gave her Zofran for the vomiting, she was able to calm her stomach down after this on an unknown date in Feb2021. If she hadn't she would have gone to the emergency room. She caller stated that she slept most of the next day after taking the Zofran. She could take 3 a day and then remarks she took at least 3 during the day on Thursday. Her second dose was scheduled on 02Mar2021, but she was not 100% sure she want to put her body back through that, it was bad, even the doctor said she may need to go get fluids at the emergency room. She doesn't want the virus but that was pretty brutal, probably the sickest she has ever been and she was not a sickly person. She stated she will definitely take a couple days off after the second dose if she does take it. She stated she has had all of the vaccines and has never had a reaction to any of them and this was pretty scary. She stated she will consult her healthcare provider, they may give her something to take before the vaccine to alleviate the symptoms. The caller asked, are these normal symptoms or was this a fluke. She stated she has heard the symptoms are worse after the second and asked if that is true. Later in the report the caller notes her head was hurting also on 11Feb2021. She had tried to refrain from taking Advil but did finally take some, she couldn't take the headache anymore. The patient feels little run down but it was not too bad. The outcome of the event muscle cramps/the muscles in legs she had crapping and shivering, violently throwing up and diarrhea was recovered on 11Feb2021 at 08:00, her head was hurting also recovered on 11Feb2021; felt a little tired, she was able to calm her stomach down after this was recovering; her voice is still raspy from the amount of acid was not recovered; sickest, she thought she came down with a virus, she slept most of the next day after taking the Zofran, she had quivering in muscles of her legs and feels little run down but it was not too bad was unknown

Weitere VAERSDATA-Felder

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

VAERS 1031021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EL9267

moderat

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 24.04.2021
Impfdatum: 09.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / LA

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

Abdominal discomfort Chills Depressed mood Diarrhoea Dysphonia Asthenia Dizziness Fatigue Headache Hypersomnia Illness Muscle spasms Muscle twitching Pyrexia Tachycardia Suspected COVID-19 Tremor Vomiting

Symptomtext

her head was hurting also/headache; violently throwing up; diarrhea; muscle cramps/the muscles in legs she had crapping and shivering; muscle cramps/the muscles in legs she had crapping and shivering; felt a little tired; her voice is still raspy from the amount of acid; she was able to calm her stomach down after this; sickest; she thought she came down with a virus; she slept most of the next day after taking the Zofran; she had quivering in muscles of her legs; feels little run down but it was not too bad; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9267) via unspecified route of administration in left arm on 09Feb2021, at 14:45 (at the age of 70-year-old) as a single dose for COVID-19 immunisation. The patient medical history and family medical history relevant to adverse event was none. The patient concomitant medication was not reported. The patient relevant tests were none. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Additional vaccines administered on same date of the pfizer suspect was none. History of all previous immunization with the Pfizer vaccine considered as suspect was none. The patient reported that she had the first dose on 09Feb2021 at about 14: 45pm. The next day, on 10Feb2021, she went to work but felt a little tired. That night about 22:00 she started violently throwing up, had diarrhea and had in the muscles in legs she had crapping and shivering on 10Feb2021. The diarrhea ended about the same time the vomiting stopped. It was so bad there was several time she didn't make to the restroom. She had quivering in muscles of her legs on an unknown date in Feb2021. The caller remarks that her voice was still raspy from the amount of acid. It was so bad she thought she came down with a virus because she thought it was too long after the vaccine. It was severe enough she called the doctor who gave her Zofran for the vomiting, she was able to calm her stomach down after this on an unknown date in Feb2021. If she hadn't she would have gone to the emergency room. She caller stated that she slept most of the next day after taking the Zofran. She could take 3 a day and then remarks she took at least 3 during the day on Thursday. Her second dose was scheduled on 02Mar2021, but she was not 100% sure she want to put her body back through that, it was bad, even the doctor said she may need to go get fluids at the emergency room. She doesn't want the virus but that was pretty brutal, probably the sickest she has ever been and she was not a sickly person. She stated she will definitely take a couple days off after the second dose if she does take it. She stated she has had all of the vaccines and has never had a reaction to any of them and this was pretty scary. She stated she will consult her healthcare provider, they may give her something to take before the vaccine to alleviate the symptoms. The caller asked, are these normal symptoms or was this a fluke. She stated she has heard the symptoms are worse after the second and asked if that is true. Later in the report the caller notes her head was hurting also on 11Feb2021. She had tried to refrain from taking Advil but did finally take some, she couldn't take the headache anymore. The patient feels little run down but it was not too bad. The outcome of the event muscle cramps/the muscles in legs she had crapping and shivering, violently throwing up and diarrhea was recovered on 11Feb2021 at 08:00, her head was hurting also recovered on 11Feb2021; felt a little tired, she was able to calm her stomach down after this was recovering; her voice is still raspy from the amount of acid was not recovered; sickest, she thought she came down with a virus, she slept most of the next day after taking the Zofran, she had quivering in muscles of her legs and feels little run down but it was not too bad was unknown

Weitere VAERSDATA-Felder

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