- Staat
- IL
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 19.05.2023
- Impfdatum
- 07.01.2021
- Beginn
- 07.05.2023
- Tage bis Beginn
- 850,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Coagulopathy
Death
Embolism
Respiratory distress
Respiratory failure
Tachycardia
Thrombosis
Symptomtext
She had sudden onset respiratory distress/tachycardia on two occasions: 05/05/2023 and 05/07/2023. She expired on 05/09/2023. Her death certificate was completed as respiratory failure, but it was told by the mortician and that had marked, excessive blood clots within her vascular system at the time of embalming. It is now highly suspected that death was due to thromboembolism secondary to blood coagulopathy - due to the COVID vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- It was told by the mortician and that had marked, excessive blood clots within her vascular system at the time of embalming.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Dementia anxiety chronic back pain
- Andere Medikamente
- Cymbalta Buspirone Tramadol levothyroxine Vitamin D
- Allergien
- Penicillin hydrocodone
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 12.05.2023
- Impfdatum
- 14.12.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 34,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebrovascular accident
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 04.12.2021
- Beginn
- 01.03.2023
- Tage bis Beginn
- 452,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Respiratory failure
Sleep apnoea syndrome
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE SLEEP APNEA ACUTE HYPERCAPNIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 05.05.2023
- Impfdatum
- 15.12.2021
- Beginn
- 02.05.2022
- Tage bis Beginn
- 138,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 20.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Pulmonary embolism
Shock
Symptomtext
ACUTE RESPIRATORY FAILURE 1/25/2022 PULMONARY EMBOLISM, UNSPECIFIED. ACUTE HYPOXEMIC RESPIRATORY FAILURE 1/25/2022 PULMONARY EMBOLISM, UNSPECIFIED. SHOCK, UNSPECIFIED 1/25/2022 PULMONARY EMBOLISM, UNSPECIFIED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 17.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: ja
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Dyspnoea
Laboratory test
Life support
Unresponsive to stimuli
Symptomtext
Patient had trouble breathing. Ambulance was called immediately & she became unresponsive just as they arrived. She was taken to Hospital & we were told right away that her condition was probably fatal. She was put on life support & died on 11/21/21 a few hours after she was taken off of it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 4,0
- Labordaten
- Tests were done on her lungs & heart for several days from 11/18/23 through 11/21/23
- Aktuelle Erkrankungen
- Diabetes, had heart valve replacement around 2019
- Vorgeschichte
- Same as in item 11
- Andere Medikamente
- Insulin, metoprolol, depression /anxiety medication & several other medications which need to be verified by her family doctor
- Allergien
- Allergic to most scented products
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 10.10.2022
- Beginn
- 24.01.2023
- Tage bis Beginn
- 106,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acidosis
Acute respiratory failure
Anticoagulant therapy
Apnoea
Blood gases abnormal
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Chest pain
Dialysis
Dyspnoea
Echocardiogram abnormal
Ejection fraction normal
Electrocardiogram normal
Encephalopathy
Interstitial lung disease
Mental status changes
Metabolic encephalopathy
Symptomtext
Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: "52-year-old female with a past medical history of ESRD on HD, hydronephrosis with urostomy in place, and schizophrenia who presented to the emergency department with dyspnea and chest pain, symptom onset 1/19, tested positive for COVID 1/20. CXR showed central interstitial prominence. EKG showed no ST or T-wave ischemic morphologies, troponin was elevated at 326, no clear established baseline in the setting of ESRD, delta was negative. Cardiology was consulted and patient was started on a heparin drip given concern for NSTEMI. Echo was obtained which showed EF 70-75%, small posterior pericardial effusion, otherwise unremarkable. Given these findings and her symptoms, there was low suspicion for ACS, and heparin gtt was discontinued. Suspect her presenting symptoms were attributable to COVID pneumonia. During her hospitalization, the patient developed acute encephalopathy, with reported apneic episodes overnight her nursing. STAT ABG was obtained which showed acidosis with acute hypercapnic respiratory failure. The patient was subsequently put on BiPAP and she underwent urgent dialysis with Nephrology consultation. After these measures, the patient had resolution of her acute metabolic encephalopathy and hypercapnic respiratory failure with return to baseline mentation and maintained stable respiratory status and was weaned back to room air. She was started on 5 day course of Decadron 6 mg daily to treat COVID, she will complete her course on discharge. Given her apnea and hypercapnic respiratory failure, there was concern for underlying lung disease, for which referral for sleep study was placed and PFT was ordered. Patient was evaluated for and recommended home therapies, for which RN/PT/OT home services were arranged. She was discharged in stable condition. "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- Covid PCR detected on 01/20/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Depression Autistic spectrum disorder Atrophy of left kidney Hydronephrosis, right Acquired hypothyroidism Allergic rhinitis GERD (530.11) Obstructive sleep apnea Essential hypertension, benign Intellectual disability Hyperlipidemia Asthma Chronic diastolic heart failure (HCC) Encounter for long-term (current) use of medications Constipation Schizophrenia (HCC) Migraine without aura and without status migrainosus, not intractable COVID Macrocytic anemia Increased ammonia level Fatty liver Anemia in ESRD (end-stage renal disease) (HCC) History of ileal conduit Pyuria At risk for malnutrition History of chronic constipation Blood loss anemia Secondary hyperparathyroidism of renal origin (HCC) ESRD (end stage renal disease) (HCC) Bipolar disorder (HCC) Hypothyroidism Altered mental status Hyperammonemia (HCC)
- Andere Medikamente
- acetaminophen (TYLENOL) 500 mg tablet Take 1 tablet by mouth every 6 (six) hours as needed for Pain. levothyroxine (SYNTHROID,LEVOTHROID) 150 mcg tablet Take 1 tablet by mouth every morning before breakfast for 30 days Take on an empty stom
- Allergien
- Abilify [Aripiprazole]Confusion Erythromycin BaseUnknown Morphine TramadolOther (See Comments
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 15.02.2023
- Impfdatum
- 07.12.2021
- Beginn
- 09.02.2023
- Tage bis Beginn
- 429,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Emphysematous cystitis
Leukocytosis
SARS-CoV-2 test positive
Symptomtext
Patient received Moderna COVID vaccine on 4/3/21 (lot # 026B21A), 5/1/21 (lot # 021C21A), and Pfizer COVID vaccine on 12/7/21 (lot # 33030BD). On 2/9/23, patient admitted to our inpatient facility (med/surg unit) with acute hypoxic respiratory failure secondary to COVID-19 pneumonia, leukocytosis and emphysematous cystitis related to her Crohn's disease, and AKI on CKD. Patient discharged home on 2/13/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- COVID status positive 2/9/23.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- medical history significant for Crohn's disease not on controller medication, IDDM type II, GERD, HLD, HTN, CAD
- Andere Medikamente
- acetaminophen, ascorbic acid, aspirin, carvedilol, clopidogrel, diphenhydramine, duloxetine, ezetimibe, ferrous sulfate, furosemide, glipizide, isosorbide mononitrate, losartan, melatonin, nitroglycerin sl, pantoprazole, tramadol
- Allergien
- statins, lisinopril
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 03.12.2021
- Beginn
- 31.01.2023
- Tage bis Beginn
- 424,0
- Dosis
- 3
- 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
Death on 01/31/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Positive Covid-19 test on 01/10/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COVID-19, CHF, COPD, CAD, AFIB, DM2, PAD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 30.11.2021
- Beginn
- 19.11.2022
- Tage bis Beginn
- 354,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Cough
Hypoxia
SARS-CoV-2 test positive
Symptomtext
Patient with history of CKD, diabetes, and lung adenocarcinoma with metastasis to bone. She was seen in the ED on 11/19/22 for evaluation of a cough for the past several months, however the day prior, her cough began to worsen. COVID-19 PCR test was done that day which was positive. To note, the patient also recently had COVID-19 in September 2022. Ultimately, patient was admitted 11/19/22 - 11/25/22. Discharge diagnosis included acute hypoxic respiratory failure secondary to COVID-19 pneumonia and COVID-19 pneumonia with superimposed pneumonia. During admission, she developed hypoxia and required supplemental oxygen, however her respiratory status improved. At discharge, she was on room air.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 22.11.2022
- Impfdatum
- 02.12.2021
- Beginn
- 01.11.2022
- Tage bis Beginn
- 334,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram pulmonary abnormal
Anxiety
Death
Dyspnoea
Dyspnoea exertional
Hypoxia
Pneumonia bacterial
Positive airway pressure therapy
Symptomtext
Patient had a prolonged stay at select specialty hospital with a goal of titrating down his oxygen requirements and increasing his strength and conditioning so that he may be able to be discharged to a skilled nursing facility. Patient was able to be titrated down as low as 7 L/min via high flow nasal cannula. His prednisone dosage was titrated down to 15 mg daily. He was doing well but still had issues with exertion requiring nonrebreather mask on top of his high flow nasal cannula. Patient got to a point he was not progressing and further work-up was completed on 11/18 to rule out reversible causes of acute on chronic hypoxia. He had a CT chest angiogram which showed no acute pulmonary emboli but worsening bilateral bacterial pneumonia. Patient had steroids increased to IV Solu-Medrol 40 mg every 8 and restarted on IV cefepime and vancomycin. 24 hours later, patient had significant oxygen requirements and was placed on continuous BiPAP with Precedex drip for anxiety. Despite this, patient had increased work of breathing and decision was made with together with his family to transition to comfort measures. Patient was placed back on nonrebreather and heated high flow nasal cannula and started on intermittent morphine and Ativan pushes. Patient died peacefully at 2:32 AM on 11/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 2 diabetes mellitus htn GERD colonic diverticulosis Idiopathic pulmonary fibrosis Grade 2 diastolic dysfunction Trivial PFO
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.08.2022
- Tage bis Beginn
- 243,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
Acute respiratory failure
Blood creatinine increased
Blood lactic acid
COVID-19
COVID-19 pneumonia
Death
Fatigue
General physical health deterioration
Hypotension
Positive airway pressure therapy
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Pfizer BIO-NTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Received Pfizer BIO-NTech vaccine on 2/13/21, 3/06/21 and 12/03/21. Presented to ED 7/30 c/o fatigue x3days. In ED, fever of 100.4, spO2 91% on R and RR 26 and hypotensive. Admitted for Covid PNA w/acute resp failure and AKI. Cr was 1.41, lactic 0.7. Required High Flow oxygen as well as bipap to maintain oxygenation. He had an acute decline overnight on 8/3 and was transitioned to DNR/DNI. Expired on 8/3/22. Treated w/azithromycin, ceftriaxone, vancyomycin, aztreonam, levofloxacin, remdesivir, tocilizumab, and decadron.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- Covid + 7/30/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalen.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD, CABGx4 in 2008, HTN, HLD, Ventricular tachycardia, compete heart block, PPM
- Andere Medikamente
- aspirin, atorvastatin, calcium/vitamin D3, docusate, doxazosin, metoprolol, multivitamin, omeprazole, vitamin b-12, vitamin c, vitamin e
- Allergien
- PCNs
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 17.12.2021
- Beginn
- 18.02.2022
- Tage bis Beginn
- 63,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Amnesia
Anaphylactic shock
Blood culture
Blood test
Colonoscopy
Computerised tomogram
Headache
Heart rate decreased
Hypotension
X-ray
Symptomtext
On 02/18/2022 I went into an anaphylactic shock. The ambulance took me to the hospital where I stayed to days because of low blood pressure and low heart rate. I was taken off all blood pressure medications. I can't be on anything with ace inhibitor or R inhibitor. I had memory lost and terrible headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic shock
- Hospital-Tage
- 2,0
- Labordaten
- Blood work; Blood culture; CT scan; X-ray; Colonoscopy
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Metformin, Lisinopril, Vitamin D3, Vitamin B12, Nexium, Gostatin, Jardence, Triaperene HCTZ
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 22.12.2021
- Beginn
- 16.03.2022
- Tage bis Beginn
- 84,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Acute respiratory failure
Alanine aminotransferase normal
Anion gap
Anticoagulant therapy
Anxiety
Aspartate aminotransferase normal
Asthma
Blood albumin decreased
Blood alkaline phosphatase normal
Blood bicarbonate
Blood bilirubin increased
Blood bilirubin normal
Blood calcium decreased
Blood chloride decreased
Blood creatinine normal
Blood glucose decreased
Blood glucose increased
Blood lactic acid
Symptomtext
Hospitalized (3.16.22 - 3.22.22); COVID-19 positive (3.16.22); fully vaccinated PLUS Booster pfizer x3 D/c Summary:Discharge Summary MD (Physician) ? ? General Medicine BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 3/16/2022 Discharge Date: Mar 22, 2022 Active Hospital Problems Diagnosis Date Noted POA ? Hyperlipidemia associated with type 2 diabetes mellitus 06/24/2009 Yes ? COVID-19 03/17/2022 Yes ? Pneumonia due to COVID-19 virus 03/16/2022 Yes ? Chronic diastolic heart failure 03/16/2022 Yes ? Right heart failure due to pulmonary hypertension 08/09/2021 Yes ? Pulmonary hypertension 11/19/2020 Yes ? Bradycardia 08/15/2016 Yes ? Type 2 diabetes mellitus without complication, with long-term current use of insulin 02/24/2016 Yes ? Hypertension associated with diabetes 09/30/2015 Yes ? Restrictive lung disease 10/17/2014 Yes ? Diabetic gastroparesis Yes ? GERD (gastroesophageal reflux disease) Yes ? OSA treated with BiPAP Yes ? Morbid obesity 05/03/2011 Yes ? Severe persistent asthma without complication 10/07/2010 Yes ? Depression Yes ? CAD (coronary artery disease) 04/11/2009 Yes ? Sarcoidosis 04/11/2009 Yes ? Urge urinary incontinence 04/11/2009 Yes Discharge Disposition: home health care svc Active Issues Requiring Follow-up: Follow up CXR in 2 weeks Have increased home norvacs to 10 mg daily and hydralazine 25 mg 3 times a day was added. DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Community acquired pneumonia, unspecified laterality [J18.9] Pneumonia due to COVID-19 virus [U07.1, J12.82] COVID-19 [U07.1] Acute on chronic hypoxemic respiratory failure (3 L NC base)--improving Severe COVID-19 pneumonia Leukocytosis, likely steroid induced Hx mild COVID 11/2021 Mod-severe pulmonary hypertension, 5/2021 Restrictive lung disease 2/2 obesity Severe persistent asthma, not exacerbated Pulmonary sarcoidosis OSA on BIPAP HOSPITAL COURSE: The patient is a 73 yo woman with a PMH of chronic hypoxic respiratory failure requiring 3 L O2 secondary to restrictive lung disease attributed to obesity, pulmonary hypertension, pulmonary sarcoidosis, moderate persistent asthma, chronic diastolic heart failure, coronary artery disease s/p multiple DES, insulin-dependent type 2 diabetes, squamous cell carcinoma and GERD who presents to the emergency department with 8 days of gradual worsening of her chronic dyspnea accompanied by nonproductive cough and fatigue. She was prescribed prednisone 40 mg x 5 days by her pulmonology office which initially improved her dyspnea but then worsened after completing steroids on 3/13. The patient was admitted for COVID-19 Pneumonia. She is fully vaccinated and boosted and has had prior mild COVID infection in 11/2021. She was placed on Decadron and trial of IV lasix due to findings of mild pulmonary vascular congestion on CXR. She quickly improved with Decadron and completed 10 day course. Patient was subsequent transition back to home Lasix 80 mg daily. Patient was discharged in stable condition on 3 L of oxygen at rest and 5 L with activity. Due to uncontrolled hypertension, her home norvacs was increased to 10 mg daily, and hydralazine 25 mg 3 times a day was added. Patient has been intolerant to higher dose of Coreg so she was kept at 3.25 mg 2 times a day. CONSULTS / RECOMMENDATION: Consult Orders (From admission, onward) IP CONSULT TO DIABETES & ENDOCRINOLOGY Provider: MD INPATIENT PROCEDURES: BP 159/75 | Pulse 52 | Temp 36.3 ?C (Oral) | Resp 18 | Ht 1.575 m | Wt 114.8 kg | SpO2 95% | BMI 46.29 kg/m? Physical Exam General: Alert and oriented. Obese body habitus Respiratory: Lungs are coarse to auscultation, Respirations are non-labored. Cardiovascular: Normal rate, Regular rhythm. Trace 1+ pitting edema- resolved Gastrointestinal: Soft, Non-distended Musculoskeletal: B/L LEs swelling. Integumentary: Warm, No pallor. Psychiatric: Cooperative but anxious 3/16/22 H&P: Admission History and Physical CHIEF COMPLAINT dyspnea ASSESSMENT Principal Problem : Pneumonia due to COVID-19 virus Active Problems: Hyperlipidemia associated with type 2 diabetes mellitus CAD (coronary artery disease) Sarcoidosis Urge urinary incontinence Depression Severe persistent asthma without complication Morbid obesity GERD (gastroesophageal reflux disease) Diabetic gastroparesis OSA treated with BiPAP Restrictive lung disease Hypertension associated with diabetes Diabetes mellitus type 2 without retinopathy Bradycardia Pulmonary hypertension Right heart failure due to pulmonary hypertension Chronic diastolic heart failure PLAN Acute on chronic hypoxemic respiratory failure (3 L NC base, 4 L currently)\ COVID-19 pneumonia Leukocytosis, likely steroid induced Hx mild COVID 11/2021 Primary symptoms: cough, worsening dyspnea, malaise, decreased appetite Symptom onset 3/9 (8 days PTA), fully vaccinated and boosted (1/2022) Chest x-ray: moderate alveolar opacification in the left mid and lower lung zone most consistent with left-sided pneumonia and mild pulmonary vascular congestion A&P -Tenuous baseline respiratory status due pulm HTN, pCHF, asthma, obesity -Received outpatient Prednisone 40 mg x 5 days (end 3/13) w/ subsequent symptom relapse -Low concern for bacterial superinfection w/ indeterminate procal but monitor closely w/ leukocytosis (likely steroid induced) and predominately left sided infiltrates -Decadron 6 mg daily started 3/17 -Qualifies for Remdesivir (and amenable) but hold off w/ concern for volume overload -Trial IV lasix 80 mg x 1 on 3/17 for congestion on imaging but appears clinically dry -Transition back to baseline PO lasix 80 mg pending response -Consider limited echo if not improving (5/2021 w/ nml EF) -Trend daily CMP, d dimer, CRP -Follow blood cultures Chest pressure, resolved -Associated w/ movement, improved after decadron? -EKG without acute changes and troponin x 2 normal -D dimer pending with AM labs -Further work-up pending recurrence Mod-severe pulmonary hypertension, 5/2021 Restrictive lung disease 2/2 obesity Severe persistent asthma, not exacerbated Pulmonary sarcoidosis OSA on BIPAP On 3 L nasal cannula O2 at baseline Follows a pulmonary hypertension clinic with Dr. -No wheezing on exam to suggest exacerbation. Treating with steroids for COVID regardless -Continue home inhaler regimen: Symbicort (in lieu of Wixela due to formulary), Spiriva, albuterol p.r.n., Flonase and montelukast -continue nightly BiPAP -Maintain O2 sats 88-92% to prevent hypercarbia Coronary artery disease s/p DES (2004, 2005, 2006, 2018) Chronic diastolic heart failure 2/2 pulmonary hypertension Hypertension Hyperlipidemia Right heart catheterization/Echo 05/2021: Preserved EF, moderate right ventricular dilation, mild MR, unable to quantify tricuspid regurgitation -Chest x-ray suggest vascular congestion but clinically euvolemic/hypovolemic with decreasing weight and decreased PO intake -Trial of Lasix 80 mg x 1 on AM of 3/17 (home regimen lasix 80 mg PO daily) -Continue losartan, Imdur, Coreg, ASA and statin -Hold norvasc to allow for diuresis -Daily weights, strict I&O Hyperglycemia, with reported hypoglycemia Insulin-dependent type 2 diabetes Pseudohyponatremia, secondary to hyperglycemia -A1c 5.9 on 2/22 -Recently decreased home regimen Novolog 70/30 44 units BID -- > 40 units q AM, 35 q PM due to BG in 50s attributed to very poor PO intake (despite steroid burst) -Quite hyperglycemic on admission (due to recent steroids?) -Novolog converted to Lantus 40 units q AM with high-dose corrective -low threshold for involvement Squamous cell carcinoma Noted GERD History of esophageal stricture Continue PPI Overactive bladder Oxybutynin Depression Celexa DVT ppx: Lovenox 40 mg BID Diet: diabetic liberal, heart healthy, 2 g Na 2 L fluid restrict Code status: DNR/DNI with aggressive measures per discussion with patient on admission HISTORY OF PRESENT ILLNESS Patient is a 73 y.o. female with past medical history significant for chronic hypoxic respiratory failure requiring 3 L O2 secondary to restrictive lung disease attributed to obesity, pulmonary hypertension, pulmonary sarcoidosis, moderate persistent asthma, chronic diastolic heart failure, coronary artery disease s/p multiple DES, insulin-dependent type 2 diabetes, squamous cell carcinoma and GERD who presents to the emergency department with 8 days of gradual worsening of her chronic dyspnea accompanied by nonproductive cough and fatigue. She was prescribed prednisone 40 mg x 5 days by her pulmonology office which initially improved her dyspnea but then worsened after completing steroids on 3/13. She sought ED evaluation after developing, non pleuritic, nonpalpable central chest pressure on day prior to admission occurring with any exertion and resolving after a few minutes of rest. Has only experienced similar discomfort 6 months ago when treated for COPD flare. Currently pain free after receiving decadron in ED. a day prior to admission, she desaturated to 86% on her 3 L and temporarily had to bump her oxygen to 4 L, but is now back to baseline O2 needs. She is typically able to walk several steps before feeling dyspneic but now short of breath with any small movement and at rest. Has been using albuterol 5-6 times per day (typically once a day) with mild symptomatic improvement. She feels better when propped up and has increased from 2 pillows to 3 pillows but has no lower extremity edema, decreased urine output or Lasix noncompliance. Overall she has had poor oral intake past week due to feeling ill and actually lost a documented 28 lb since last month which has been partially intentional. She lives with her children who are feeling well and denies any recent COVID exposures, sick contacts, fevers, chills, loss of smell, loss of taste, rhinorrhea, sore throat, abdominal pain, nausea, vomiting, diarrhea, dysphagia, choking, dysuria, leg pain or history of VTE. Fully vaccinated and was treated for COVID-19 with last dose 01/2022. She previously COVID 11/2021 which is very mild in the not require any specific treatment. No tobacco or EtOH use. Compliant with inhalers and nightly BiPAP. Arrival to the emergency department, she was afebrile, respiration rate 20, mildly hypertensive, heart rate 60s and SpO2 92% on 3 L nasal cannula. Labs remarkable for sodium of 138, glucose 355, T bili 1.8, NT proBNP 972, troponin 11 with repeat at 10p, leukocytosis of 24,000 but lactic acid of 1.5. COVID-19 positive but RSV/influenza negative. Chest x-ray showed moderate alveolar opacification in the left mid and lower lung zone most consistent with left-sided pneumonia and mild pulmonary vascular congestion. Independent review of EKG shows normal sinus rhythm with left anterior fascicular block, LVH which appears similar to prior EKG. She was given decadron in ED. Admitted to hospital medicine for dyspnea and fluctuating oxygen requirement in the setting of likely COVID-19 pneumonia. REVIEW OF SYSTEMS Constitutional: Positive for appetite change and fatigue. Negative for chills, fever and unexpected weight change. HENT: Negative for congestion, rhinorrhea, sore throat and trouble swallowing. Respiratory: Positive for cough, shortness of breath and wheezing. Negative for chest tightness. Cardiovascular: Positive for chest pain. Negative for leg swelling. Gastrointestinal: Negative for abdominal pain, diarrhea, nausea and vomiting. Genitourinary: Negative for dysuria. Musculoskeletal: Negative for back pain. Skin: Negative for rash. Neurological: Positive for light-headedness. Negative for dizziness and headaches. Hematological: Does not bruise/bleed easily. OBJECTIVE BP 170/73 | Pulse 68 | Temp 36.5 ?C (Oral) | Resp 20 | Ht 1.575 m | Wt 114.4 kg | SpO2 91% | BMI 46.13 kg/m? Physical ExamVitals and nursing note reviewed. Constitutional: Appearance: She is not ill-appearing. Comments: Resting comfortably, mild conversational dyspnea HENT: Mouth/Throat: Mouth: Mucous membranes are dry. Pharynx: Oropharynx is clear. Eyes: Extraocular Movements: Extraocular movements intact. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: Normal heart sounds. No murmur heard. Pulmonary: Effort: Pulmonary effort is normal. Breath sounds: Rhonchi (E bilateral rhonchi) present. No wheezing or rales. Comments: Audible rhonchi, mildly tachypneic with mild conversationally dyspneic Abdominal: General: Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: General: No tenderness. Right lower leg: No edema. Left lower leg: No edema. Skin: General: Skin is warm and dry. Neurological: Mental Status: She is alert and oriented to person, place, and time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- Comprehensive Metabolic Panel (CMP) (Abnormal) Collected: 03/22/22 0724 Order Status: Completed Specimen: Blood, Venous Updated: 03/22/22 0754 Sodium Level 135 134 - 146 mmol/L Potassium Level 3.4 3.4 - 5.0 mmol/L Chloride 94 Low 98 - 112 mmol/L HCO3 31 High 21 - 29 mmol/L Anion Gap 10 9 - 18 mmol/L Glucose Level 110 High 70 - 99 mg/dL Blood Urea Nitrogen 29 High 8 - 20 mg/dL Creatinine 0.72 0.50 - 1.10 mg/dL MDRD eGFR >60 >=60 mL/min/1.73 CG eCrCl 55 mL/min/1.73 m2 Calcium Level Total 8.8 8.6 - 10.4 mg/dL Protein Total 7.0 6.0 - 8.0 g/dL Albumin Level 2.4 Low 3.5 - 5.0 g/dL Bilirubin Total 0.7 0.2 - 1.0 mg/dL Alkaline Phosphatase 96 35 - 104 IU/L ALT w/ P5P 12 0 - 35 IU/ AST w/ P5P 13 0 - 35 IU/L
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Severe persistent asthma with exacerbation 09/30/2021 Unknown ? Dry eyes, bilateral 01/07/2021 Unknown ? Cough 10/02/2020 Unknown ? SOB (shortness of breath) 05/04/2018 Unknown ? Abnormal stress test 05/04/2018 Unknown ? Chest pain, unspecified type 05/04/2018 Unknown ? Precordial pain 04/27/2018 Unknown ? Hypoxemia 11/08/2017 Unknown ? Osteoporosis, unspecified osteoporosis type, unspecified pathological fracture presence 04/18/2017 Unknown ? Regular astigmatism of both eyes 09/01/2016 Unknown ? Rhinosinusitis 04/02/2013 Unknown ? Arthritis Unknown ? Colitis Unknown ? Diverticulosis Unknown ? OA (osteoarthritis) of knee 10/07/2010 Unknown ? CHF (congestive heart failure) 04/11/2009 Unknown
- Andere Medikamente
- Acetaminophen 650 mg Oral 2 times daily PRN Albuterol Sulfate 2.5 mg Nebulization Every 6 hours PRN 108 (90 Base) MCG/ACT Aers, INHALE 2 PUFFS BY MOUTH EVERY 6 HOURS AS NEEDED FOR WHEEZING OR SHORTNESS OF BREATH Patient taking differently:
- Allergien
- No Known allergies
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Cough
Dyspnoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID Vaccine Breakthrough Case Pfizer Dose 1 3/5/21 (EN6206) Pfizer Dose 2 3/25/21 (ER8732) Pfizer Dose 3 12/10/21 (33030BD) COVID Positive 12/10/21 12/10/21: Patient was sent to the emergency department after getting his COVID-19 booster shot. Patient is a poor historian. Patient told the clinic at the booster shot initially that he has been feeling well. After shot checked on him and he reported that he felt short of breath. He he then let them know that he felt short of breath for a few days and has been coughing. They checked his pulse oximetry and found it to be 84% on room air and sent him here for further evaluation. Patient arrived to the emergency department with a pulse oximetry of 84% on room air. 12/14/21: Patient was admitted for acute hypoxemic respiratory failure secondary to COVID-19 and COVID pneumonia. Patient was treated primarily with dexamethasone and remdesivir with supplemental oxygen and nebulizer treatments. Patient has progressed well. Patient was provided antibiotic regimen to prevent secondary bacterial infection. Patient progressed well in the hospital and completed his course of remdesivir. He is afebrile and breathing easy. His oxygen saturations are 94-95% on room air. Patient feels well for home disposition. Patient will be discharged home on dexamethasone and continued antibiotics and nebulizer treatments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- obesity
- Vorgeschichte
- obesity
- Andere Medikamente
- acetaminophen 650 mg PO Q4h PRN amlodipine 5 mg PO QD asprin 81 mg PO QD atorvastatin 80 mg PO QD HCTZ-triametere 25-37.5 mg PO QD lisinopril 20 mg PO QD metoprolol tartrate 100 mg PO BID
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 18.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Cough
Dizziness
Dyspnoea
Intensive care
Pulmonary embolism
Pulmonary thrombosis
Thrombectomy
Symptomtext
Suffered an acute massive pulmonary embolism. Two-weeks prior to returning to campus, I immediately start with symptoms of shortage of breathe, dry coughing, and dizziness. Hospitalized for six(6) days of which, I spent three days in ICU. Dr. had to perform an emergency caterization to remove the massive blood clot from my lungs. Additionally, they found other smallers clots that they used Heparin and other blood thinners to resolve the clots. Currently I am on Eliquis twice a day and plan to be seen as a follow up with Hemologist. Lot number - First Vaccination was EW0186 Second Vaccination lot number is EW0191
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 6,0
- Labordaten
- PE with massive blood clots
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vestura 3 mg (to control acne) Spironolazton - E 50 mg
- Allergien
- Fruit allergies
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Activated protein C resistance test
Angiogram cerebral
Anticoagulant therapy
Antinuclear antibody negative
Atrial septal defect
Beta-2 glycoprotein antibody negative
Blood fibrinogen
Blood homocysteine
Cardiolipin antibody
Computerised tomogram abdomen
Computerised tomogram thorax
Echocardiogram
Embolic stroke
Gene mutation identification test
Hemiparesis
Intensive care
International normalised ratio normal
Laboratory test normal
Symptomtext
Initial presentation was to the Hospital on 1/6/22 with right sided weakness and paresthesias, emergently transferred for specialized intervention to larger Health System - Hospital. Patient had pulmonary embolism (left lower lobe segmental branch) and acute embolic stroke (mid distal left P2 segment) requiring mechanical thrombectomy and anticoagulation. Later found to have patent foramen ovale, no evidence of deep venous thrombosis on lower extremity doppler ultrasound. Has progressive strength and sensory recovery but still with deficit at time of discharge. Treated by interventional neurology, neurology critical care, and hematology. Suspected etiology pro-thrombotic/provoked from oral contraceptive with embolism but did receive vaccine within 28 days of acute illness presentation. Discharge planning to home with outpatient therapies and oral anticoagulation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 6,0
- Labordaten
- CT angiogram head: 1/6/22, MRI brain without contrast: 1/6/22 CT chest/abd/pelvis: 1/9/22 Doppler ultrasound legs: 1/7/22 PT/INR/PTT/Thrombin Time/Fibrinogen/Cardiolipin IgG, IgM/Beta 2 glycoprotein IgG/Antithrombin activity/Activated Protein C/S: 1/7/22 (within normal limits) ANA/ENA Jo 1/La/RNP/Ro/Scl70/Sm Ab IgG/RF: 1/8/22 (negative) Lipoprotein a, Homocysteine: 1/8/22 (pending) SARS-CoV-2 PCR nasopharyngeal swab: 1/9/22 (negative) Factor V/II mutation: 1/8/22 (pending) SARS-CoV-2 nucleocapsid antibody: 1/11/22 (pending) Transesophageal Echocardiogram: 1/10/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ethinyl estradiol-norelgestromin patch
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 07.01.2022
- Impfdatum
- 29.11.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 25,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Arterial disorder
Blood fibrinogen normal
Blood immunoglobulin G increased
Blood lactate dehydrogenase increased
Computerised tomogram thorax abnormal
Fibrin D dimer
Gingival bleeding
Heparin-induced thrombocytopenia
Hypoxia
Influenza A virus test negative
Influenza B virus test
Influenza virus test negative
Mouth haemorrhage
Platelet count decreased
Platelet factor 4
Pulmonary embolism
Respiratory syncytial virus test negative
Symptomtext
Presented to Hospital with acute hypoxia - Acute Pulmonary embolism, with Thrombocytopenia with no clear cause and no previous heparin 25 days post Covid Vaccine. Heparin was administered to treat PE with further drop in platlet count within 12 hours. VITT reaction considered (PLT 161 11/29 to 55 12/24 ) heparin stopped immediately switched to argatroban infusion with increase in platelets within 24 hours . Hep-Ind Thrombocytopenia PF4 Ab, IgG lab test sent for evaluation, returned positive see section 19 and continuation page for detail. Transitioned to rivaroxaban (Xarelto) once stable and discharged from the hospital. Mouth/gums were bleeding during the hospital admission PE is being treated - he continues to take anticoagulation medication and will get further follow up . Platelet count was recovered at time of discharge
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 6,0
- Labordaten
- Plt count 161 x10(9)/L 11/29/2021 day of vaccine ; Plt count 55 x10(9)/L 12/24 presentation to hospital- heparin started PLT 43 x10(9)/L 12/25 heparin stopped argatroban started 12/25/2021; PLT count 62 x10(9)/L 12/26/2021; PLT 88 x10(9)/L 12/27/2021; PLT Count 150x10(9)/L 12/28/2021 CTE PE 12/24/2021 shows " Filling defects in a subsegmental pulmonary artery of the anterior left lower lobe- IMPRESSION: 1. Subsegmental anterior left lower lobe pulmonary embolus. No other pulmonary emboli identified.2. No focal airspace consolidation. No pneumothorax." 4 extremity dopplers 12/25 show no evidence for DVT 12/24/2021 D-Dimer 1.22; 12/24/2021 COVID/Influenza A&B/RSV not detected for all ; 12/25/2021 Hep-Ind Thrombocytopenia PF4 Ab, IgG lab test is POSITIVE : Screen = 0.46 OD units (likely muted by some heparin contamination from the initial infusion. The presence of heparin may falsely lower the result ); Confirm = 0.13 OD units ; % inhibition 98%. If the patient was not exposed to heparin in the weeks prior to the ELISA test, this may represent a rare example of vaccine induced thrombotic thrombocytopenia. 12/25/2021 Lactate dehydrogenase blood 316 U/L 12/25/2021 Fibrinogen Quant 222 mg/dL
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Nonintractable epilepsy without status epilepticus; Achondroplasia; Hydrocephalus with VP shunt; Migraine
- Andere Medikamente
- Divalproex - pre2012; Ipratropium Nasal spray; Levetiracetam (8/2021); prochloperazine; propranolol; sumatriptan nasal solution; triamcinolone topical cream; Pfizer Bion Tech given as a booster - Prior vaccinbes were Covid 19 Moderna Spike
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 30.01.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 264,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Neurological symptom
Symptomtext
patient presents from home with stroke like symptoms on 10/22/2021. admitted for 14 days (10/22/2021 - 11/5/2021). discharged to rehab facility with diagnosis of pontine stroke.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 14,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Essential hypertension Stroke Type 2 diabetes, HbA1C goal < 8% (*) (HCC) Hyperlipidemia Depression RSD (reflex sympathetic dystrophy) Vascular dementia (HCC) Glaucoma - Both Eyes OSA (obstructive sleep apnea) Sensorineural hearing loss (SNHL), bilateral Constipation Multinodular goiter (nontoxic) CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) Microalbuminuria due to type 2 diabetes mellitus (*) (HCC) Gastroesophageal reflux disease Esophagitis Diabetic retinopathy (*) (HCC) Vision loss of right eye Polyp of large intestine Diverticulosis Hemorrhoids Uterine leiomyoma Major neurocognitive disorder, due to vascular disease, without behavioral disturbance, mild (*) (HCC) Bee sting allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Fatigue
Malaise
Pyrexia
Resuscitation
Unresponsive to stimuli
Symptomtext
PATIENT AND MOTHER CAME IN WEDNESDAY 11.24.21 AFTERNOON FOR COVID BOOSTER. MOTHER REPORTED TO PHARMACY ON FRIDAY 11.26.21 (DEPARTMENT CLOSED THURSDAY 11.25.21) THAT PATIENT HAD STARTED FEELING "UNWELL" (FEVER/TIREDNESS) LATE 11.24.21 / EARLY 11.25.21. MOTHER REPORTED DIDNT THINK MUCH OF IT BUT THAT HER SON (PATIENT) WAS GOING TO REST. MOTHER REPORTED THAT LATER IN THE DAY SON WENT INTO THE BATHROOM AND WAS IN THERE FOR SOME TIME, WHEN SHE WENT TO CHECK ON HIM, SHE COULD NOT GET THE DOOR OPEN. UPON OPENING THE DOOR, SON WAS FOUND UNRESPONSIVE. ATTEMPTS TO REVIVE SON BY MEDICAL PERSONEL WERE UNSUCCESSFUL. PER MOTHER AN AUTOPSY IS SCHEDULED BUT AS OF REPORTING NO CAUSE OF DEATH HAS BEEN LISTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PATIENT USES local PHARMACY - PRESCRIPTION HISTORY UNKNOWN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 09.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antibody test
Antinuclear antibody
Blood copper
Blood test
Burning sensation
Contusion
Electric shock sensation
Electromyogram
Electrophoresis protein
Feeling abnormal
Feeling cold
Formication
Glycosylated haemoglobin
Heavy metal test
Hypoaesthesia
Limb discomfort
Magnetic resonance imaging spinal
Muscle spasms
Symptomtext
Feet/Ankles: ? extreme coldness sensation, ? pins/needles, ? tingling, ? stinging, ? burning, ? parts of feet feel numb (top of left foot, left and right big toes, ball of right foot), ? electric shocks in toes, at times top of feet and ankles, ? sensation of feet vibrating, ? pain, ? blueish/purpleish blotches/spots on tops of both feet Legs: ? feel as if they are vibrating mostly lower legs but starting to feel it up into my thighs, ? electric shocks in left and right shins and calves, ? stinging, pricks, pins/needles ? burning in calves and shins, ? cold spots that move around my leg (from side of knee to back of leg), ? feels like a sock has been pulled up over my left calf/shin, ? muscles feel tight and sometimes sore, ? sometimes legs feel heavy but not all the time, ? pins/needles and/or crawling sensation, ? calf feels like small cramps/squeezing Hands/Forearms: ? extreme coldness intermittently in hands, ? stinging in fingertips and palm intermittently, ? burning/pins/needles in fingertips/palm and forearms and wrist, ? Left thumb twitching (started Sunday, Sept. 11), ? Electric zaps at times in fingertips, ? Cold spots on elbows that come and go, ? Icey/burning sensation mainly left wrist, forearm, and upper arm Treatments tried gabapentin, supplements, naproxen over the last 11 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- EMG of lower extremities - July 2022 EMG of upper extremities - October 2022 MRI of neck and thoracic - August 2022 Physical Therapy - February 2022 and October 2022 Blood work completed August 2022 ? Serum Protein Electrophoresis Reflex to Immunofixation (For Initial Diagnosis Only) ? Rheumatoid Factor, Quant-Blood (normal) ? Sjogrens Ab SSA-Blood ? Sjogrens Ab SSB-Blood ? Assay Vitamin E-Blood ? Glycohemoglobin, Total-Blood ? Heavy Metals, BLD ? WBC Antibody Identification-Blood ? ANA Screen Blood work completed September 2022: - CBC WITH DIFFERENTIAL; Future - CMP (BAMP,TP,ALB,TBIL,ALK,AST,ALT); Future - LIPID PANEL (CHOL, TRIG, HDL, LDL); Future - TSH WITH REFLEX TO FREE T4; Future - VITAMIN D (25 OH); Future - C-REACTIVE PROTEIN; Future Blood work completed November 2022: ? B1 ? Copper ? B6
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- endometriosis, high blood pressure
- Andere Medikamente
- Naproxen Sertraline Metoprolol
- Allergien
- Allergy to penicillin, amoxicillin, and tetracycline
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 03.12.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 41,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of consciousness
Road traffic accident
Seizure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- black out seizure causing car accident on 3-18-2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 07.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Blood test
Dizziness
Dyspnoea
Fall
Headache
Heavy menstrual bleeding
Imaging procedure
Pain in extremity
Palpitations
Pulmonary thrombosis
Syncope
Thrombectomy
Vena cava filter insertion
Symptomtext
On Christmas Day 2021 I was out shopping and started getting pain in my left calf area in my leg. It felt like a pulling sensation. I went to urgent care. Then I went to the hospital to get a DVT Scan on my left leg. The doctor said I need to get on a blood thinner. They gave me a blood thinner shot. Then I was prescribed Xarelto. The pain was subsidizing and then things were getting better so I stopped taking Xarelto because I was having a heavy menstrual cycle. One day in February 2022 I started getting out of bed one morning, and I was feeling pain in the right leg It felt like tugging in my lower right calf. I went to urgent care again. They did another DVT scan. I was sitting in urgent care for a while so I went to get something to eat. I walked a couple feet and then I started to get palpitations in my chest. I collapsed on the floor. I felt dizzy. People tried to wake me up. My head hurt because of the fall. I felt like I couldn't breathe. The ambulance was called and I was in the hospital. They told me I have blood clot in my lungs. I was told I need to get the blood clot taken out so they did the procedure. There were a lot of blood clots. They put a filter in my chest somewhere so I don't get any more blood clots in my lungs. They said it should be taken out after 6 months. I was given IV blood thinner. They checked my blood and said that Xarelto isn't the best for me so they changed my medication to Eliquis. My menstrual cycle is better and more manageable now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- 4,0
- Labordaten
- (2) DVT Scans, blood work.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 27.11.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 49,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Cough
Dyspnoea
Headache
Oropharyngeal pain
Pain
Pulmonary fibrosis
Pulmonary oedema
Pyrexia
SARS-CoV-2 test positive
X-ray abnormal
Symptomtext
I had a reaction from the shot. I had chest pain and I could not breath that lasted for about 24 hours. I had fever and a headache that lasted for about 3 days. Then on Jan 15th, I tested positive for COVID-19. I had a fever, body aches, sore throat, difficulty breathing, and coughing that lasted for about 3 weeks. I have long hall COVID-19 test. I am having difficulty breathing, chest pain and coughing. I went the doctor about this. They did x-ray and medicine. The x-rays show that my lungs are scars and my lungs a full of fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, x-ray
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 28.02.2022
- Impfdatum
- 10.12.2021
- Beginn
- 13.02.2022
- Tage bis Beginn
- 65,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Compression garment application
Deep vein thrombosis
Discomfort
Joint swelling
Superficial vein thrombosis
Ultrasound scan abnormal
Venous thrombosis limb
Symptomtext
Patient was referred to me after his chiropractor noted that he had swelling to the inner left ankle. The swelling started about 02/13/2022. He had negligible discomfort and swelling to the medial posterior left ankle. No pretibial edema was found in either leg. Calf and ankle circumferences were the same on both legs. Normal pedal pulses. No skin changes. An upright venous Doppler done by me revealed an occlusive DVT from the left proximal femoral vein to the popliteal area into the upper calf. The left small saphenous vein was thrombosed from the popliteal area to the distal calf. A DVT ultrasound done the next day confirmed these findings. He was prescribed Eliquis 5 mg, 2 tabs 2x/day for 7 days then 1 tab 2x/day. He was fitted with 20-30 mmHg graduated compression hose, knee high, which are to be worn daily during the day. He has been limited to normal light activity and will follow up on 3-11-2022. He is contacted by phone every 1-2 days. He will follow up 3-11-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound exams noted above.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ulcerative colitis well controlled with Balazide
- Andere Medikamente
- Balazide, Vitamin D, Multivitamin
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 27.02.2022
- Impfdatum
- 02.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest discomfort
Cyst
Investigation
Presyncope
Swelling
X-ray
Symptomtext
felt like he was fainting; felt like his heart was coming out of his chest; a cyst in his neck on the left side; The caller received the vaccine in his left shoulder and there are 2 bumps that show up in the x-ray; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (005570). The reporter is the patient. A 53 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Dec2021 (Lot number: 33030BD) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "gets sick from pollen" (unspecified if ongoing), notes: gets sick from pollen. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose: 1, Manufacturer unknown), for COVID-19 immunization. The following information was reported: SYNCOPE (medically significant), outcome "unknown", described as "felt like he was fainting"; CARDIAC DISORDER (non-serious), outcome "unknown", described as "felt like his heart was coming out of his chest"; CYST (non-serious), outcome "unknown", described as "a cyst in his neck on the left side"; SWELLING (non-serious), outcome "unknown", described as "The caller received the vaccine in his left shoulder and there are 2 bumps that show up in the x-ray". The events "felt like he was fainting", "felt like his heart was coming out of his chest" and "a cyst in his neck on the left side" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: unknown results; investigation: unknown results; x-ray: there are 2 bumps/ 2 small cysts. Clinical course: Clinical course: On Dec the patient had the second vaccine and can't really remember the day but it was in Dec. The patient had a really bad side effect, it didn't do that with the first one but the second one had him on the bed and felt like his heart was coming out of his chest and had to be taken to the hospital and the doctor said it was a side effect of the Covid 19 vaccine. The caller had to go to the emergency room. The patient had the vaccine in his left shoulder and it created a cyst in his neck on the left side. They did an x-ray and it showed 2 small cysts, the said cysts but its called something else. Anytime the caller touches that part it was like he was going to faint. There was an artery on that side of the neck and the caller felt like he was fainting and it was really bad and he had to go to the hospital. They did an x-ray to his neck and blood work and a lot of tests. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Test Name: blood work; Result Unstructured Data: Test Result:unknown results; Test Name: lot of tests; Result Unstructured Data: Test Result:unknown results; Test Name: x-ray to his neck; Result Unstructured Data: Test Result:there are 2 bumps/ 2 small cysts
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Pollen allergy (gets sick from pollen)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 26.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Body temperature fluctuation
Bone pain
Chest discomfort
Chest pain
Body temperature
Chills
Confusional state
Cold sweat
Delirium
Dizziness
Electrocardiogram normal
Hyperhidrosis
Immunisation
Night sweats
Oropharyngeal pain
Dysgeusia
Feeling hot
Symptomtext
bad metallic taste; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 36 year-old female patient received BNT162b2 (BNT162B2), administered in arm right, administration date 26Mar2021 14:00 (Lot number: EP6955) at the age of 36 years as dose 1, single and administered in arm right, administration date 16Apr2021 (Lot number: 6W0161) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Hashimoto's disease" (unspecified if ongoing); "Overactive bladder" (unspecified if ongoing); "permanent nerve damage" (unspecified if ongoing); "C5C6 plates and screws" (unspecified if ongoing); "concussion", start date: 2015 (unspecified if ongoing); "hurt at work with a concussion", start date: 2015 (unspecified if ongoing), notes: hurt at work with a concussion; "post concussion syndrome", start date: 2015 (unspecified if ongoing), notes: for 16 months; "permanent damage with the right arm", start date: 2015 (unspecified if ongoing), notes: This injury was in 2015; "Muscle spasms" (unspecified if ongoing); "migraines" (unspecified if ongoing); "chronic pain" (unspecified if ongoing); "swine flu" (unspecified if ongoing). Concomitant medication(s) included: LAMICTAL; SYNTHROID; LYRICA taken for nerve injury; TRAMADOL; VALIUM taken for muscle spasms. Past drug history included: Bupivacaine, notes: having the bupivacaine injections for years and has never had a problem with them; Reglan, reaction(s): "Known allergies: reglan"; Compazine, reaction(s): "Known allergies: compazine". The following information was reported: DYSGEUSIA (non-serious), outcome "unknown", described as "bad metallic taste". Additional information: The patient had a bad metallic taste after the first two doses of the Pfizer covid vaccine but other than that she was fine. The lot number of dose 2 was also reported as EW0161. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arm injury (This injury was in 2015); Bone operation; Chronic pain; Concussion; Hashimoto's disease; Hypothyroidism; Injury at work (hurt at work with a concussion); Migraine; Muscle spasms; Nerve damage; Overactive bladder; Post concussion syndrome (for 16 months); Swine influenza
- Andere Medikamente
- LAMICTAL; SYNTHROID; LYRICA; TRAMADOL; VALIUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 26.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Body temperature fluctuation
Bone pain
Chest discomfort
Chest pain
Body temperature
Chills
Confusional state
Cold sweat
Delirium
Dizziness
Electrocardiogram normal
Hyperhidrosis
Immunisation
Night sweats
Oropharyngeal pain
Dysgeusia
Feeling hot
Symptomtext
bad metallic taste; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 36 year-old female patient received BNT162b2 (BNT162B2), administered in arm right, administration date 26Mar2021 14:00 (Lot number: EP6955) at the age of 36 years as dose 1, single and administered in arm right, administration date 16Apr2021 (Lot number: 6W0161) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Hashimoto's disease" (unspecified if ongoing); "Overactive bladder" (unspecified if ongoing); "permanent nerve damage" (unspecified if ongoing); "C5C6 plates and screws" (unspecified if ongoing); "concussion", start date: 2015 (unspecified if ongoing); "hurt at work with a concussion", start date: 2015 (unspecified if ongoing), notes: hurt at work with a concussion; "post concussion syndrome", start date: 2015 (unspecified if ongoing), notes: for 16 months; "permanent damage with the right arm", start date: 2015 (unspecified if ongoing), notes: This injury was in 2015; "Muscle spasms" (unspecified if ongoing); "migraines" (unspecified if ongoing); "chronic pain" (unspecified if ongoing); "swine flu" (unspecified if ongoing). Concomitant medication(s) included: LAMICTAL; SYNTHROID; LYRICA taken for nerve injury; TRAMADOL; VALIUM taken for muscle spasms. Past drug history included: Bupivacaine, notes: having the bupivacaine injections for years and has never had a problem with them; Reglan, reaction(s): "Known allergies: reglan"; Compazine, reaction(s): "Known allergies: compazine". The following information was reported: DYSGEUSIA (non-serious), outcome "unknown", described as "bad metallic taste". Additional information: The patient had a bad metallic taste after the first two doses of the Pfizer covid vaccine but other than that she was fine. The lot number of dose 2 was also reported as EW0161. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arm injury (This injury was in 2015); Bone operation; Chronic pain; Concussion; Hashimoto's disease; Hypothyroidism; Injury at work (hurt at work with a concussion); Migraine; Muscle spasms; Nerve damage; Overactive bladder; Post concussion syndrome (for 16 months); Swine influenza
- Andere Medikamente
- LAMICTAL; SYNTHROID; LYRICA; TRAMADOL; VALIUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Blood thyroid stimulating hormone normal
Burning sensation
C-reactive protein normal
Chest pain
Cold sweat
Differential white blood cell count normal
Electric shock sensation
Full blood count normal
Glycosylated haemoglobin normal
Hypoaesthesia oral
Injection site pain
Limb discomfort
Metabolic function test normal
Neck pain
Pain
Palpitations
Paraesthesia
Symptomtext
Day 1: Intense arm pain at and around injection site (left arm);Day 1 - current: feeling of heart racing.Day 3 - 25: chest and upper back pain, radiates up to neck; Day 3- 9: feeling of walking on a marble under right foot. Left foot affected days 8-9 but w/ less intensity. Day 5: Right foot, inner side, felt wet and cold for a day.Day 3 current: increased tinnitus in both ears, continues on and off all day, 30-40 times/day. Day 10: Paresthesia/ pins and needles with sharp, painful zaps in both hands, feet and lower legs. More intense after exercise.Day 17: electric zaps now felt in face and head.Day 17 - current: strange sensation on front 1/3 of tongue that progressed to numbness. Day 21 - 25: Both arms and top of hands have a burning sensation.Day 10 current: Body vibrations in core when at rest, more intense at bedtime. Feet feel like they are vibrating.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- - Consult to Neurology Clinic (pending);11/12/2021 Completed;Comprehensive Metabolic Panel Glycosylated Hgb(A1C), Blood Lavender;CBC w/ Diff; TSH w/Reflex to FT4;Vitamin D, 25-OH Total Vitamin B12, Blood Green Plasma Separator Tube;Sedimentation Rate (ESR), Blood Lavender; C-Reactive Protein, Blood Green Plasma Separator Tube; All Normal w/ Vitamin D Status 25-OH Vitamin D: 25 ng/mL; Deficiency: <20 ng/mL; Insufficiency: 20 - 29 ng/mL; Optimal: > or = 30 ng/mL.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines with aura and mild tinnitus with migraine.
- Andere Medikamente
- Multi vitamin; Ibuprofen
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Hyperhidrosis
Hypopnoea
Pallor
Peripheral coldness
Pulse abnormal
Seizure like phenomena
Syncope
Symptomtext
client received 3rd dose of Pfizer BIONTech COVID19 vaccine at 1450. At 1455 father/mother report syncopal episode with "seizure like" movement. Client noted to be pale, diaphoretic, shallow and even respirations, conscious with c/o SOB, unable to obtain BP with manual cuff, unable to obtain SpO2 R/T coldness of hands, lungs CTAB, pulse weak and regular. Administered Epi-Pen 0.3mg IM to LVL x 1 and Benadryl 50mg IM to RVL x 1, patient transported to ER for evaluation, report to ER staff at 1500.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- Follow up call to ER at 1625, RN reports client still in ER for observation, no additional treatment administered, improved status, cardiac workup in progress and awaiting results at that time.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 04.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site erythema
Paralysis
Symptomtext
Paralysis easy and redness of the left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 04.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anaphylactic reaction
Dyspnoea
Symptomtext
Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Breathing-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac disorder
Myocarditis
Chest pain
Dyspnoea
Echocardiogram
Ejection fraction abnormal
Electrocardiogram normal
Troponin increased
Symptomtext
Systemic: Cardiac Disorder (diagnosed by MD)-Severe, Additional Details: myocarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 08.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
COVID-19 pneumonia
Respiratory distress
SARS-CoV-2 test positive
Symptomtext
Received Pfizer vaccines on 2/25, 3/18, 12/8/21 COVID-19 positive by PCR on 12/12/21. Hospitalized 12/12-12/26/21 d/t COVID 19 pneumonia readmitted on 1/10/22 d/t respiratory distress in setting of COVID 19. underlying COPD, HTN, h/o stroke, pulmonary fibrosis, AAA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 24.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Loss of consciousness
Nausea
Retching
Syncope
Symptomtext
Patient developed chills, nausea and was dry heaving, which resulted in a syncopal episode with LOC for 10-15 seconds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- peanut allergy
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 12.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 20,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Dehydration
Dizziness
Dyspnoea
Syncope
Symptomtext
49-year-old male presents for chest pain dizziness and a syncopal episode. Patient states he had a ostomy placed in November for bowel obstruction. He has noticed significant increase in the output from his ostomy. He believes he is getting dehydrated. He's having dizziness and feels like he is going to pass out when he stands up quickly. He did actually have one episode of syncope an hour ago after standing up quickly. He also admits that he said some intermittent tightness since midnight on the left side of his chest. He said some mild shortness of breath. Denies any black or bloody stools. Denies cough cold or covid symptoms. No other aggravating or alleviating factors. No other complaints
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 2,0
- Labordaten
- 49-year-old male presents for chest pain dizziness and a syncopal episode. Patient states he had a ostomy placed in November for bowel obstruction. He has noticed significant increase in the output from his ostomy. He believes he is getting dehydrated. He's having dizziness and feels like he is going to pass out when he stands up quickly. He did actually have one episode of syncope an hour ago after standing up quickly. He also admits that he said some intermittent tightness since midnight on the left side of his chest. He said some mild shortness of breath. Denies any black or bloody stools. Denies cough cold or covid symptoms. No other aggravating or alleviating factors. No other complaints
- Aktuelle Erkrankungen
- CHOLECYSTECTOMY ? HERNIA REPAIR ? LAPAROTOMY, EXPLORATORY 11/02/2021 With small bowel resection, creation of end proximal ileostomy, abdominal closure. ? LAPAROTOMY, EXPLORATORY 10/27/2021 Small bowel resection x2, Abthera placement. ? OHS CHOLECYSTECTOMY ? OHS COLON SURGERY colon resection 2007 ,2009
- Vorgeschichte
- Dentition fine per pt ? Diverticulosis ? Leisure activity mets 5-6 ? Spinal headache
- Andere Medikamente
- Medication Administration Record reviewed. collagenase, , Topical, DAILY heparin injection, 5,000 Units, Subcutaneous, Q 8 H loperamide, 2 mg, Oral, 4 TIMES DAILY magnesium gluconate, 500 mg, Oral, DAILY opium, 6 mg, Oral, BID piperacillin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deep vein thrombosis
Pain
Pain in extremity
Peripheral swelling
Thrombosis
Ultrasound scan
Symptomtext
Lower left leg painful to walk on was swollen down to the ankle tight, throbbing. Blood clots, DVT. Placed on blood thinners for 6 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes; IBF
- Andere Medikamente
- Kemolog Zoloft Estradiol Lisinipril
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 30.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 26.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Diarrhoea
Fatigue
Nausea
Palpitations
Presyncope
Pyrexia
Vomiting
Symptomtext
First day: high fever, shivers, diarrhea, nausea, felt like vomiting, near syncope episodes for hours (when trying to get out of bed and walk and when lying down in bed), heart palpitations. Second and third day: high fever, tiredness, exhaustion After the third day developed a consistent dry cough that still exists but not intensive anymore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- sulfa, MSG
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure decreased
Blood test
Deafness
Electrocardiogram
Loss of consciousness
Palpitations
Visual impairment
Symptomtext
Daughter woke up and stated she cant see or hear 3 days after taking the booster, then she passed out. Her blood pressure dropped real low and her heart was racing. Mom took her to the ER. They did EKG and blood work and started her on an IV.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- yes EKG, blood work
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Head injury
Headache
Loss of consciousness
Syncope
Symptomtext
Systemic: Fainting/Unresponsive-Medium, Additional Details: Patient was checking blood pressure directly after the vaccine with a self-use upper arm blood pressure kiosk. Lost consciousness when cuff tightened and fell backward hitting head on a metal chair arm. Patient unconscious for about 10 seconds. Lay on floor with feet elevated for about 30 minutes and then went to ER for head pain. This was a Pfizer booster dose. He had no reactions to previous 2 Pfizer doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immunisation
Interchange of vaccine products
Off label use
Presyncope
Tachycardia
Symptomtext
Felt like was going to pass out; Dizziness; Extended tachycardia; Moderna Covid-19 Vaccine First Dose: 25Feb2021/Second dose: 26Mar2021/Pfizer Cornavirus booster : 10Dec2021; Moderna Covid-19 Vaccine First Dose: 25Feb2021/Second dose: 26Mar2021/Pfizer Cornavirus booster : 10Dec2021; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 80 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 10Dec2021 (Lot number: 33030BD) at the age of 80 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Had double mastectomy for cancer", start date: 2018, stop date: 2018; "cancer" (unspecified if ongoing). Concomitant medication(s) included: ANASTROZOLE; AMLODIPINE; HYDROCHLOROTHIAZIDE. Vaccination history included: Moderna covid-19 vaccine (First Dose: 25Feb2021, Lot: 010M20A, Exp: 19Jul2021 , Administered in left arm), administration date: 25Feb2021, when the patient was 79 years old, for Covid-19 immunisation, reaction(s): "The patient did not have AE following vaccination"; Moderna covid-19 vaccine (Second Dose: 26Mar2021, Lot: 010M20A, Exp: 19Jul2021, Administered in left arm), administration date: 26Mar2021, when the patient was 79 years old, for Covid-19 immunisation, reaction(s): "The patient did not have AE following vaccination". The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 10Dec2021, outcome "unknown" and all described as "Moderna Covid-19 Vaccine First Dose: 25Feb2021/Second dose: 26Mar2021/Pfizer Cornavirus booster : 10Dec2021"; IMMUNISATION (non-serious) with onset 10Dec2021, outcome "unknown", described as "Booster"; DIZZINESS (non-serious) with onset 15Dec2021, outcome "recovered" (15Dec2021), described as "Dizziness"; TACHYCARDIA (non-serious) with onset 15Dec2021, outcome "recovered" (15Dec2021), described as "Extended tachycardia"; PRESYNCOPE (non-serious) with onset 16Dec2021, outcome "unknown", described as "Felt like was going to pass out". Additional Information: The patient stated that she had dizziness and tachycardia on 15Dec2021 and it lasted about 30min to an hour. She dismissed it, put out of head and relaxed, and looked to see what do for tachycardia. About an hour before on 16Dec2021 she was in the grocery store and all of a sudden she got to the point where had to call for assistance, felt like was going to pass out. She was at the store and one of associates in store came to help. The associate assisted to a place to sit, asked if she had eaten. The associate got her some Pita chips and water. The patient sat, ate chips, drank water, went to restroom, then went to register for purchases and went to car. After she left the grocery store she was going to go to Emergency, but home was closer. The patient did not visit emergency room and not visit physician office for adverse event.There was no history of all previous immunization with the Pfizer vaccine considered as suspect. There was no additional vaccines administered on same date of the Pfizer suspect. The patient did not have prior vaccination within 4 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cancer; Mastectomy
- Andere Medikamente
- ANASTROZOLE; AMLODIPINE; HYDROCHLOROTHIAZIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Flushing
Hyperhidrosis
Hypotension
Loss of consciousness
Syncope
Unresponsive to stimuli
Visual impairment
Symptomtext
Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild, Additional Details: Patient received 3rd Covid shot about 3-5 minutes later patient lost consciousness and fell out of chair he was sitting in. Patient was face down laying on the ground when rph got to his. He regained consciousness when rph went over to check on patient. He states he felt it coming his vision started to go and it went black when he came back to rph was next to him. Rph had patient remain on the ground and went on to check on patient. Paramedics arrived and check out patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Hypertension
Myocarditis
Symptomtext
Chest Pain, high blood pressure, shortness of breath, potential myocarditis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Computerised tomogram head
Facial paralysis
Pyrexia
Symptomtext
Fever Loss of taste Facial paralysis left side
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- CT Scan of the head on 12/16/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arithmia
- Andere Medikamente
- Propafenone 300 mg - twice a day Enalapril 10 mg - twice a day Metoprolol 12.5 - once a day
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Syncope
Symptomtext
Patient fainted after receiving his first vaccine during his mandatory monitoring period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Blood test
Facial paralysis
Hypoaesthesia
Symptomtext
Left face numb/ paralyzed starting 7am on 7/15/2021 7/16/2021 Lost of muscle control on left face, can?t close left eye, half smile, can?t raise left eyebrow 1pm went to hospital Bells Palsy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Blood drawn 3pm
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Flushing
Loss of consciousness
Symptomtext
pt was given vaccine at approximately 6:26pm and he was monitored based on his previous history of fainting after a vaccine. He sat in his chair and after about 4 to 5 minutes, he began to pass out. His father caught him and held him up, and he quickly came back to. He was flushed and felt warm. His temp was within normal range. A cold pack was applied to his neck and he was given water. He felt better shortly after. He was observed for 20 more minutes and looked well. He left with his parent/family.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No- per registration form
- Vorgeschichte
- No -per registration form
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- He said he has reacted about 3 times prior like this to vaccines.
- Staat
- PA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Muscle spasms
Symptomtext
Patient woke up in the middle of the night after getting her shot and reports having severe foot and leg cramping. She got up to stretch and passed out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Loss of consciousness
Syncope
Symptomtext
Patient came in for a Pfizer covid vaccine booster today and also received Flucelvax vaccine. The order was reviewed by precepting pharmacist, and vaccines were administered by intern. The patient was then sitting in the observation area when she started feeling weak and then started to lose consciousness. The mother quickly alerted the pharmacy staff and we rushed to assist patient. We paged code white over the intercom to alert management of the situation. We placed an ice pack behind patient's neck and the patient immediately regained consciousness. We also provided them with some snacks and cold water in case the patient was feeling low on sugar. We took a blood pressure reading and the patient had a BP of 84/48 which could explain the syncopy. Market manager was immediately. Reassessed patient after 30 minutes and the blood pressure is now 97/84. The patient is alert and oriented to everything happening. The mother will drive patient home and will alert the pharmacy if anything else occurs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Concussion
Electrocardiogram
Head injury
Heart rate decreased
Impaired driving ability
Impaired work ability
Skin laceration
Syncope
Vaccination complication
Symptomtext
Fainting within less than 5 minutes of vaccination, very low heart rate, head injury, ambulance arrival and transport to Hospital where Patient received care. Laceration on head, low heart rate and concussion required Patient to be out of work, unable to drive and required PCP immediate follow-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Discharged paperwork noted monitored heart rate stayed low @ Hospital 12/7/21 Discharged paperwork noted Laceration care @ Hospital 12/7/21 CAT scan, EKG, Blood work noted on discharge paperwork @ Hospital 12/7/21 Diagnosed with concussion and vaccine reaction on 12/8/21 By PCP.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Amnesia
Aphasia
Dizziness
Dyspnoea
Fall
Hyperhidrosis
Impaired driving ability
Insomnia
Loss of consciousness
Seizure
Sensory disturbance
Urinary incontinence
Symptomtext
I was sitting at my computer with my partner. It was time to go to bed. on the third floor. As I turned in my chair I was dizzy and fell over into my partners lap. I sat up and thought it was the end. As I stood up to go to the third floor to go to bed, I felt like my brain and forehead moved back and forth in my head. That's all I remember. I went to wash my hands I was falling into to sink. My partner got me to bed and noticed I was unconscious. My partner called 911. I somehow ended up on the floor. And my spouse said he had to yell for me to breathe. The EMT came, the took my vitals and said that everything was normal. They did not want to take me to the hospital because the hospital was not accepting patients. They stood me up and noticed that I was drenched in sweat. I had peed all over myself while I was still upright. I have no memory of this. It has never happened before. The EMT left, I did not sleep at night. The next day I was afraid to drive. I was afraid it would happen again. ALL that day and into the next day., It was hard for me to find words. It was very strange. It has so far been okay, but I now still get dizzy spells. The EMT mentioned during the call and assessment that I seemed as if I had a seizure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- I had my vitals taken by the EMT and he stated that it was apparent that I might have had a seizure.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Lorazepam 0.5 mg once a day
- Allergien
- None
- Vorherige Impfungen
- The 2nd shot of Pfizer experienced tingling, they hit a nerve.
- Staat
- -
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Syncope
Symptomtext
Fainting, diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Reynods syndrome
- Andere Medikamente
- Zyrtec, Depo shot, Flovent Inhailer
- Allergien
- Soy, tree nuts, sesame seeds, codine, penicillin, chicken pox shot, HPV shot
- Vorherige Impfungen
- Chicken pox shot, local reaction, 16
- Staat
- PA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Lymphadenopathy
Symptomtext
Systemic: Bell's Palsy-Mild, Systemic: Lymph Node Swelling-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Immediate post-injection reaction
Syncope
Symptomtext
Immediately after the vaccine was given , the patient fell down and collapsed. We called 911 , paramedic came and attended to him for a while before taking him to the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Not to my knowledge
- Allergien
- NKA
- Vorherige Impfungen
- confirmed by the wife
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose normal
Loss of consciousness
Somnolence
Symptomtext
Patient reported ?falling asleep?/losing consciousness. Received pfizer at 10:05, reported symptom at 12:20. Bp 219/135 temp 97.4 oxygen 99% pulse 63 blood sugar 105. Patient currently admitted at a local rehab center. Teceived clonidine and lisinopril scheduled in the morning. Patient reported feeling better after applying wet cloth over eyes. Notified facility staff nurse. Facility staff contacting facility MD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Vital signs taken results above
- Aktuelle Erkrankungen
- Patient vaccinated at a rehab center facility
- Vorgeschichte
- Hypertension, Diabetes
- Andere Medikamente
- Clonidine 0.3 Lisinopril
- Allergien
- Denied
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Loss of consciousness
Presyncope
Symptomtext
Patient received vaccine fine. I told mom to have all her children sit, and 3-4 minutes later she came to me and said one of her sons were passing out. She brought him to sit, and we gave him wet paper towels and ice packs. Then Dad brought this patient around because he was light headed too. We gave him the wet paper towels and ice packs too. He passed in and out of consciensness. Dad was working with him and kept wiping his face and kept him upright. Finally after several minutes he was responding and staying awake. They sat for several minutes more until they both felt ready to go.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- none reported
- Vorherige Impfungen
- mom reported fainting after vaccines AFTER he passed out, but they marked no on the consent form to reaction of vaccines.
- Staat
- KY
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of consciousness
Presyncope
Symptomtext
Patient received injection fine. We asked them to sit and about 3 or 4 minutes later the patient's mom came back to ask for help, Patient was passing out. She sat him in chair and then asked for wet rags. I got the wet paper towels and an ice pack. Patient did pass out and had a vasovagal reaction. He came in and out of consciousness. Patients twin brother had the same reaction at the same time. We used the ice pack on his neck, wrists and forehead. He then seemed to come back together and we used the wet paper towels on him. Then his color returned and we had him sit longer while his brother recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- None known
- Allergien
- none reported
- Vorherige Impfungen
- unknown reaction but reported by parents AFTER reaction
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Loss of consciousness
Muscular weakness
Palpitations
Vomiting
Symptomtext
Cold Sweat and racing heart followed by momentary loss of consciousness which was then followed with total loss of muscle control for 3.5 hours while laying immobilzed on bathroom floor. Could only turn head which resulted in vomiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Benadryl
- Allergien
- rondamycin
- Vorherige Impfungen
- After 2nd Pfizer shot, fainted approximately 18 hours later
- Staat
- PA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Confusional state
Dizziness
Fatigue
Headache
Lethargy
Syncope
Tinnitus
Unresponsive to stimuli
Symptomtext
Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Medium, Systemic: Headache-Mild, Systemic: Tinnitus-Mild, Additional Details: Patient briefly passed out 6-7 minutes after receiving vaccine. She appeared to have a 20 to 30 second seizure(later confirmed from emt that it is possible for that to happen with syncope. Patient was walked out of pharmacy by EMTs and taken to hospital for evaluation. There are no further up details at this point. I will follow up with parents and pateint tomorrow as this vaccine was given late at night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 23.12.2023
- Impfdatum
- 26.02.2021
- Beginn
- 28.02.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Chest pain
Computerised tomogram head
Computerised tomogram neck
Full blood count
Headache
Immunology test
Magnetic resonance imaging head
Magnetic resonance imaging neck
Muscle fatigue
Muscular weakness
Nausea
Scan with contrast
Symptomtext
CHRONIC AND CONSTANT HEAD PAIN, MUSCLE FATIGUE AND WEAKNESS, SEVERE JOINT PAIN, NAUSEA, CHEST PAIN; ALL SYMPTOMS/EVENTS HAVE BEEN ONGOING AND INCREASED WITH EACH VACCINATION TO THE POINT OF DEBILITATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 2021; DURING THE COURSE OF 2021 VARIOUS TESTS; MRI W/W/OUT CONTRAST OF HEAD AND NECK, CT SCANS OF HEAD AND NECK, CBC TESTS, AUTO-IMMUNE TESTING
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.06.2023
- Impfdatum
- 15.12.2021
- Beginn
- 03.04.2023
- Tage bis Beginn
- 474,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Dyspnoea
Headache
Hypoxia
Pain
Pyrexia
SARS-CoV-2 test positive
Tachycardia
Symptomtext
The patient presented to the ED on 4/3/23 with fever, cough, shortness of breath, body aches, and headaches. She tested positive for COVID-19 at home the morning of her visit to the ED. Notably, she was found to be tachycardic and mildly hypoxic in the ED. Repeat COVID-19 PCR test performed in the ED also resulted positive. Ultimately she was admitted 4/3/23 - 4/4/23 for observation. Discharge diagnosis included COVID. Of note, she has received the primary COVID vaccine series and one booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 06.01.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 159,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Neuropathy peripheral
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE NEUROPATHY HYPOTENSION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 18.05.2023
- Impfdatum
- 01.12.2021
- Beginn
- 30.01.2022
- Tage bis Beginn
- 60,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
COVID-19
Exposure to SARS-CoV-2
Fatigue
Head titubation
Headache
Hyperacusis
Impaired work ability
Loss of personal independence in daily activities
Magnetic resonance imaging head
Muscle twitching
Neuropathy peripheral
Ocular discomfort
Ocular hyperaemia
Palpitations
Photophobia
SARS-CoV-2 test positive
Sensory disturbance
Symptomtext
Jan 2022: Headaches and pressure behind eyes March 2022: Inner vibrations and head tremor (head twitches), pulsating sensations, red eyes, July 2022: (First infection with Covid 19, positive for 12 days), intensified tremors and vibrations, onset of neuropathy in hands and feet Oct 2022: (Exposure to Covid 19), Neuropathy spread to legs and arms, racing heart, palpitations and pounding heart, fatigue, Nov 2022: Symptoms above intensified, neuropathy started in face, intolerance to sound and light started, headaches (had to give up my job), wasn't able to look into screens or socialize anymore. Best place was a dark and quiet room. Dec 2022: Neuropathy was getting intenser in my face, nose, ears and cheeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- MRI head
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Multi Vitamins
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 07.12.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 84,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Adrenal mass
Gastrointestinal disorder
Hypothyroidism
Impaired work ability
Laboratory test abnormal
Migraine
Neoplasm
Pain
Symptomtext
Originally, I went to my primary doctor, and I had abdominal issues. He sent me to the ER and they ran some test and labs. They found a mass on my adrenal gland. They gave me some medications for the pain I was experiencing. I thought it was Appendicitis. Which it did not end of being that. About a few days of rest, the abdominal issues subsided. That was the end of that. I did go back to my primary to follow-up on the mass. He sent me to the endocrinologist about the mass. They are monitoring my labs and my hypothyroidism. So far it has not changed or worsen. They have prescribed weight loss medication. They have also prescribed me Topamax for the migraines that I always have. Around September I started having more migraines that I have had to miss work more. I have been seeing a neurologist. They have changed medications. I have stopped the Topamax. I have also done recent labs which show increased levels of cortisol. I am unsure if it has anything to do with tumor they found. Then on October 16th I got my 4th COVID shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Labs
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraines; IBS; Hypothyroidism
- Andere Medikamente
- Levothryroxine; Migraine Medication; Flonase; Zyrtec; Omeprazole; Singular; Albuterol
- Allergien
- Kevlex.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 07.02.2023
- Impfdatum
- 15.09.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 79,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Impaired self-care
Pneumonia
SARS-CoV-2 test positive
Symptomtext
Patient with history of Parkinson's and COPD. He was brought to the ED by EMS on 12/3/22 for evaluation of weakness. Patient reportedly has been feeling weak since being diagnosed with pneumonia on 11/9/22. He was hospitalized until 11/23/22 and was sent to a rehab center after discharge, and left the rehab center on 12/2/22 (day prior to presenting to the ED). Since leaving the rehab center, he has been feeling weak and does not believe he could take care of himself at home. COVID PCR test performed in the ED resulted as positive. Ultimately he was admitted 12/3/22 - 12/10/22 for what the provider notes as weakness due to mild COVID illness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 01.12.2021
- Beginn
- 04.01.2023
- Tage bis Beginn
- 399,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
01/04/23 presents to the ED for "shortness of breath". PMHx of "COPD on 2 L, CAD, hyperlipidemia"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 01/04/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 30.12.2022
- Impfdatum
- 12.04.2021
- Beginn
- 13.11.2022
- Tage bis Beginn
- 580,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
11/13/22 presents to ED for "shortness of breath". PMHx of "COPD"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 11/13/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 20.12.2021
- Beginn
- 28.11.2022
- Tage bis Beginn
- 343,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthma
COVID-19
Condition aggravated
Cough
Malaise
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I was sick for about 7-8 days. I had cough, runny nose, fever, body aches, asthma exacerbation. Doctor prescribed a different inhaler which was helpful. Highest fever that I took on thermometer was 101.6.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- PROZAC; ZYRTEC; SINGULAIR; PEPCID; FLONASE; azelastine; BREO ELLIPTA
- Allergien
- Penicillin; sulfa; BACTRIM; ROBAXIN; CEFTIN
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 10.12.2021
- Beginn
- 03.12.2022
- Tage bis Beginn
- 358,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphonia
COVID-19
Cough
Dyspnoea
Feeling abnormal
Headache
Hyperhidrosis
Hypersomnia
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Throat irritation
Symptomtext
My symptoms began on 12/03/2022 with a tickle in my throat and then a cough and then my throat was sore. I then had sniffles and runny nose. I went to bed and when I woke up, I had a nasty headache and my whole body hurt. I was coughing and sweaty. I tested positive for COVID-19 on 12/04/2022. I lost my voice. I had a fever of 103. I took TYLENOL and then ibuprofen. I called the doctor and had telehealth visit the next day. My fever had not decreased. I slept a lot. I had a severe shortness of breath. I truly felt like I was dying. I received an inhaler, and I got a humidifier for my room. My symptoms began getting better after about 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Home COVID-19, positive, 12/04/2022; Home, COVID-19 test, negative, 12/13/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Endometriosis; PCOS; Anxiety; Depression; Borderline Mood Disorder; PTSD; Scoliosis; Reynard's Syndrome; Heart Palpitations
- Andere Medikamente
- Topiramate; hydrocodone
- Allergien
- Kiwi; tramadol; fruit punch flavoring
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 26.11.2021
- Beginn
- 01.09.2022
- Tage bis Beginn
- 279,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Blister
Blood iron
Blood iron decreased
Chest discomfort
Chest pain
Condition aggravated
Cough
Electrocardiogram
Fatigue
Limb discomfort
Malaise
Menstrual disorder
Nasopharyngitis
Palpitations
Serum ferritin
Serum ferritin decreased
Symptomtext
the Pfizer Covid 19 vaccine has been affecting her cycle; Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots; Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots/affecting her cycle/significant iron drop; last April she was at a 5 for her ferritin prior to the shots and now is a 5.7.; fatigued; needed to take naps and not feeling really well; chest pain, left discomfort; back pain; left arm discomfort; chest pain, left discomfort; palpitations; significant iron drop; strange phlegmy cold; Cough/throat clearing cough thing but nothing like it was; 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 51-year-old female patient received BNT162b2 (BNT162B2), on 26Nov2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 50 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: progesterone" (unspecified if ongoing); "fibroids" (unspecified if ongoing), notes: Later clarified that she was diagnosed with fibroids 12 years ago. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE:2, Lot: EW0162), administration date: 21Apr2021, when the patient was 49-year-old, for Covid-19 immunization, reaction(s): "Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots", "Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots", "April's cycle was 4 -5 days late after the shot and extremely heavy/Had more bleeding in the month of September getting three periods a month and losing an excessive amount of iron", "Had more bleeding in the month of September getting three periods a month and losing an excessive amount of iron", "?last April she was at a 5 for her ferritin prior to the shots and now is a 5.7"; BNT162b2 (dose:1, Batch/lot number : ER87:33 , intramuscular left arm), administration date: 26Mar2021, when the patient was 49-year-old, for COVID-19 Immunization, reaction(s): "the Pfizer Covid 19 vaccine has been affecting her cycle", "Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots", "Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots", "unsure if her fibroids increased in size or not", "last April she was at a 5 for her ferritin prior to the shots and now is a 5.7". The following information was reported: COUGH (non-serious) with onset Sep2022, outcome "recovering", described as "Cough/throat clearing cough thing but nothing like it was"; NASOPHARYNGITIS (non-serious) with onset Sep2022, outcome "unknown", described as "strange phlegmy cold"; CHEST PAIN (non-serious) with onset 07Oct2022, outcome "recovered" (17Oct2022), CHEST DISCOMFORT (non-serious), outcome "unknown" and all described as "chest pain, left discomfort"; LIMB DISCOMFORT (non-serious) with onset 07Oct2022, outcome "recovered" (17Oct2022), described as "left arm discomfort"; PALPITATIONS (non-serious) with onset 07Oct2022, outcome "recovered" (17Oct2022); BACK PAIN (non-serious) with onset 13Oct2022, outcome "recovered" (15Oct2022); BLOOD IRON DECREASED (non-serious) with onset Oct2022, outcome "unknown", described as "significant iron drop"; MENSTRUAL DISORDER (non-serious), outcome "unknown", described as "the Pfizer Covid 19 vaccine has been affecting her cycle"; BLISTER (non-serious), outcome "not recovered", described as "Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots"; CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots/affecting her cycle/significant iron drop"; SERUM FERRITIN DECREASED (non-serious), outcome "unknown", described as "last April she was at a 5 for her ferritin prior to the shots and now is a 5.7."; FATIGUE (non-serious), outcome "not recovered", described as "fatigued"; MALAISE (non-serious), outcome "unknown", described as "needed to take naps and not feeling really well". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of menstrual disorder, blister, blood iron decreased, condition aggravated, serum ferritin decreased, nasopharyngitis, fatigue, malaise, cough, chest pain, chest discomfort, palpitations, back pain, limb discomfort. Clinical course: Caller stated that she has two questions. Wanted to know if her iron is 32 and her ferritin is 5.7 is due for the Pfizer Omicron shot on Wednesday do advise build up iron and wait or the shot should not effect her iron levels. Since its been affecting her cycle; she had the three shots and did not get a fourth booster she wanted to know when would be best time to get it. Is starting her cycle next week. With the other shots she got those during her period. What would be the best time for it. Knows the iron question is kind of tricky. Clarified that she had all three Pfizer shots. Clarified again that she had the Pfizer Covid shots. Has a progesterone allergy where she would break out in blisters on her neck way is worst after the Pfizer Covid shots. Noticed it was worst 26Mar2021. Is unsure if the Pfizer Covid shot affected her progesterone or estrogen and increased side effects or if her age is making everything come into effect. Clarified that she had the progesterone allergy before Pfizer Covid shots. Clarified that she had fibroids along with shot. Later clarified that she was diagnosed with fibroids 12 years ago. Mentioned that she is unsure if her fibroids increased in size or not that her doctor would have that information. Had first Pfizer Covid shot while cycling. April's cycle was 4 -5 days late after the shot and extremely heavy. Is at the age of peri-menopause and it is very difficult to determine if perimenopause if her hormones affected her cycle or the Pfizer Covid shot affected her cycle. Had more bleeding in the month of September getting three periods a month and losing an excessive amount of iron. Clarified that her iron was normal up until just this last blood draw. Two draws after the three Pfizer Covid shot series everything stayed the same and she had no inconsistencies at all until Sep2022. Just got her labs drawn last week. Was significant iron drop and her ferritin has been relatively low all along. Later clarified that last April she was at a 5 for her ferritin prior to the shots and now is a 5.7. Caller rambling on despite multiple attempts to redirect. Unable to clarify details. Noticed that her progesterone allergy was worst after the first shot. Last booster was the day after Thanksgiving last year. Will be a year of having no shots in November of this year. Her chest pain irregularities last week led her to get her iron drawn. Had a strange phlegmy cold early September and tested negative for Covid. Clarified it as she was very fatigued, needed to take naps and not feeling really well for at least a week ago. Was not hungry and all those things. Cough and chest pain went away and she showed up with back pain. Clarified that the cough started the first week in Sep. Now she has a throat clearing cough thing but nothing like it was. Fatigued was the first week of Sep2022. Had chest pain, left discomfort, palpitations and the EKG came back normal. Chest pain started around 07Oct. For 12 hours her lower back was killing her. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: iron; Result Unstructured Data: Test Result:32; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Name: Ferritin; Result Unstructured Data: Test Result:5.7; Test Date: 202104; Test Name: Ferritin; Result Unstructured Data: Test Result:5
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Fibroids (Later clarified that she was diagnosed with fibroids 12 years ago.); Progesterone
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 13.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Computerised tomogram
Gait disturbance
Movement disorder
Tremor
Symptomtext
whole body shaking; limping; his right arm doesn't swing anymore though it works good; This is a spontaneous report received from contactable reporter (Consumer or other non HCP) from medical information team. The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 13Dec2021 as dose 2 (booster), single (Lot number: 33030BD) at the age of 68 years, in the right arm for COVID-19 immunisation. The patient's relevant medical history included: "heart surgery", start date: 2001 (unspecified if ongoing), notes: He had been busted open and they fixed his heart for a while which he had for 22 years. The patient took concomitant medications. Vaccination history included: Janssen COVID-19 vaccine (dose 1, single), administration date: 17Mar2021, when the patient was 67-year-old, for COVID-19 immunisation. The following information was reported: TREMOR (hospitalization) with onset 26Dec2021, outcome "recovered", described as "whole body shaking"; GAIT DISTURBANCE (non-serious), outcome "unknown", described as "limping"; MOVEMENT DISORDER (non-serious), outcome "unknown", described as "his right arm doesn't swing anymore though it works good". The patient was hospitalized for tremor (start date: 26Dec2021, discharge date: 29Dec2021, hospitalization duration: 3 day(s)). The patient underwent the following laboratory tests and procedures: brain CT scan: Unknown results. Clinical course details: Consumer said he got one before and the day after it put him in the hospital with his whole body shaking. He was in the hospital three days then they finally started pulling stuff out of him. Caller doesn't clarify this statement. They haven't helped anymore, he is not shaking, he is limping and his right arm doesn't swing anymore though it works good, it doesn't swing anymore when he walks. It was his second one, he had one almost a year ago, with one given as two shots at one time, which he was fine after that. Then he got this thing here, the Pfizer vaccine. He wants to know what to do, his doctor even done a check on his brain right side. His shaking is gone and he can hold his right hand out and it will shake and rock back and forth. His right leg limps a lot when he walks. He limps and has to go up steps one at a time, he can't put one down then one on the next, he has to pull himself up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 3,0
- Labordaten
- Test Name: brain CT scan; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cardiac operation (He had been busted open and they fixed his heart for a while which he had for 22 years)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 14.12.2021
- Beginn
- 06.09.2022
- Tage bis Beginn
- 266,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Tested COVID positive, symptoms include shortness of breath and chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Swab collected 9/05/2022 detected detected 2019 Coronavirus RNA on 9/06/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic lung disease, hypertension, current smoker, Hepatitis C, and severe obesity.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 13.12.2021
- Beginn
- 28.04.2022
- Tage bis Beginn
- 136,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Computerised tomogram head normal
Confusional state
Lung disorder
Mental status changes
Pleural effusion
SARS-CoV-2 test positive
Symptomtext
4/26/2022-Covid + on 4/14 treated with Decadron, presents with AMS and increased confusion. CT head- no acute intracranial abnormality. CXR: small to moderate left pleural effusion with left lower airspace disease. Admit Covid-19 pneumonia with possible concomitant steroid confusion. Start ceftriaxone and azithromycin. 4/30/2022- Improvement in AMS since d/c decadron and continues on RA, VSS. 5/2/2022-Improved, D/C to home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD s/p angioplasty, Alcoholic liver cirrhosis with esophageal varices, HTN and hyperlipidemia
- Andere Medikamente
- -
- Allergien
- Dexamethasone
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 23.11.2021
- Beginn
- 14.04.2022
- Tage bis Beginn
- 142,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Condition aggravated
Impaired gastric emptying
Prostate cancer
Symptomtext
onset of gastroparesis and aggressive prostate cancer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Osteoporosis, Essential Hypertension, Pure Hypercholesterolemia (disorder) Insomnia with Sleep Apnea Lumbosacral Spond Aortic Incompetence, Non-Rheumatic Mitral Regurgitation Alcoholic Fatty Liver Carcinoma Of Prostate Peptic Reflux Disease
- Andere Medikamente
- desmopressin; Azo Men; Methyl B Complex; amlodipine; losartan; oxycodone-acetaminophen; tamsulosin; Prolia; Marinol; Aleve; amitriptyline; protodophilus; Atorvastatin; CoQ10; EPA/DHA; SPM active; cal apatite magnesium; B12; clonidine HCl; D
- Allergien
- sulfonamides
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 27.04.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 70,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abscess drainage
COVID-19
Chest X-ray
Dyspnoea
Electrocardiogram
General physical condition abnormal
Inflammation
Laboratory test
Lung infiltration
Necrosis
Pathology test
Productive cough
Pseudomonas test positive
SARS-CoV-2 test positive
Sputum culture positive
Sputum discoloured
Squamous cell carcinoma of lung
Tachycardia
Symptomtext
Patient presented to Hospital ED on 7/6/2022 with shortness of breath, which had been present but worsened over past several days. Patient was chronically on 4 L of oxygen but for EMS on 4 L he was 85%. He did receive breathing treatments in the ambulance prior to arrival. Patient had been coughing up yellow phlegm, No fever. no chest pains. Patient appeared chronically ill. Heart rate was regular and tachycardic. Lung sounds were fairly clear anteriorly. Patient had been recently admitted to the hospital on June 15, 2022 and discharged on the 30th. The patient was hospitalized for shortness of breath, persistent right lower lobe infiltrate, suspected relapsed stage IV right lung cancer. He had been on chronic Augmentin therapy since September 2021. His sputum culture on May 9, 2022 grew sensitive Pseudomonas. He was initially treated with Zosyn. Patient was not a candidate for lobectomy according to CT surgery. Patient did have IR drainage of abscess/mass on June 21, the culture was negative and the pathology showed necroinflammatory debris. The chart indicated admitting differential diagnoses included but not limited to pneumonia, COPD, other viral URI and positive for COVID-19 per PCR. Public Health Department has no further information on this client. Please contact provider for any additional information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Labs EKG Chest XR
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- ? Arrhythmia ? Atrial fibrillation ? Atrial flutter ? COPD (chronic obstructive pulmonary disease) ? Depression ? Heart failure ? Lung cancer ? Squamous cell carcinoma 08/2020 right lung
- Andere Medikamente
- unknown
- Allergien
- Albuterol
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 26.01.2022
- Beginn
- 27.03.2022
- Tage bis Beginn
- 60,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Inappropriate schedule of product administration
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Pfizer Dose 1 2/19/21 9EN6200) Pfizer Dose 2 3/13/21 (EN6204) Pfizer Does 3 1/26/22 (33030BD) COVID Positive 3/27/22 3/27/22: Patient has significant history of cognitive deficits multiple medical problems and tested positive for COVID in the ER. Patient has an oxygen demand and is a good candidate at this time from the severe protocol. Patient is not short of breath and is not in any respiratory distress. 3/29/22: Patient was admitted with Covid 19. She had been found on the floor at her home by family, and had a low grade fever and complained of dyspnea at that time. She was admitted for IV Remdesivir treatment. Patient has not required oxygen at all since admission, she has no respiratory symptoms, has been afebrile, is eating well, and wants to be released today. She has been fully immunized against Covid prior to this illness, and her symptoms seem to have completely resolved at this point, so she will be discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- adrenal adenoma asthma thyroid cancer HLD HTN obesity OCD osteopenia OSA CKD III
- Andere Medikamente
- amlodipine 10 mg PO QD aspirin 81 mg PO QD bisoprolol 10 mg PO QD calcitriol 0.25 mcg PO BID fluoxetine 40 mg PO QD levothyroxine 88 mcg PO QD melatonin 10 mg PO QD montelukast 10 mg Po QD multivitamin 1 tab PO QD KCl 20 mEq PO QD simvastat
- Allergien
- ciprofloxacin - unknown macrobid - hallucination penicillin - vomiting
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 24.11.2021
- Beginn
- 11.06.2022
- Tage bis Beginn
- 199,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdomen scan
Abdominal pain
Asthenia
Back pain
Bedridden
Change of bowel habit
Chest X-ray
Condition aggravated
Dyspepsia
Dysstasia
COVID-19
Oxygen saturation
SARS-CoV-2 test
Vaccination failure
Eating disorder
Hypersomnia
Investigation
Muscle disorder
Symptomtext
Caller tested positive for COVID and with her breathing difficulties; Caller tested positive for COVID and with her breathing difficulties; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group, Program ID: (172086). The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 26May2021 as dose 1, single (Lot number: EWO177), in right arm, on 16Jun2021 as dose 2, single (Lot number: EWO181) and on 24Nov2021 at 09:00 as dose 3 (booster), single (Lot number: 33030BD) at the age of 71 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "COPD" (ongoing), notes: COPD, He lung function was 40% when last tested. The diagnosis was years ago.; "Mastectomy" (unspecified if ongoing), notes: She had a mastectomy, they did a deep flap reconstruction, what it does is they cut you hip to hip and take the muscle from the lower abdomen and some of the fat tissue and essentially move it up and form a breast. They are removing muscle tissue from lower abdomen. She does have scar tissue; "Leiomyoma sarcoma" (unspecified if ongoing), notes: Leiomyoma sarcoma Started 4-5 years ago from radiation treatments. She has stage-IV cancer. Leiomyoma sarcoma is a cancer of soft tissue and it travels and it's hard to explain and ended up in lung. It started with radiation for breast surgery.; "gall bladder removed" (unspecified if ongoing), notes: gall bladder removed; "depression" (unspecified if ongoing), notes: Her depression has been ongoing since her diagnosis of cancer. The patient took concomitant medications. Vaccination history included: Flu (Vaccine/Brand Name: Flu, Vaccination Date: unknown), for Immunization, reaction(s): "sick". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 11Jun2022, outcome "unknown" and all described as "Caller tested positive for COVID and with her breathing difficulties". The patient underwent the following laboratory tests and procedures: Chest X-ray: (unspecified date) Unknown result; Oxygen saturation: (unspecified date) 96-95%, notes: oxygen levels had been dropping and staying around 96-95%; SARS-CoV-2 test: (11Jun2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Yes report is related to a study or programme. Yes Other Conditions. Yes COVID-19 BioNTech booster a Pfizer product. Additional Context: Warm transfer from #, Paxlovid Call Center IVR, CEP 172086, with consumer already taking Paxlovid, that is concerned because she has underlying issue with her digestive system for a month. She is asking if there is an adverse event while taking Paxlovid with her underlying issue? The caller confirmed the details provided by the transfer agent. She has been having an issue since last Nov and they haven't been able to diagnose it as yet. She has a lot of severe pain in lower abdomen and trouble with digestion. It may mean nothing but she got the booster shot for COVID the day before the holidays and that evening she started getting the severe pain and nausea and whatever. States she ended up spending the holidays and the next two days she was in bed. Whether that has to do with shot, she has no idea. She started taking Paxlovid one full day and night dose so far. She got concerned with her digestive system and she has stage IV cancer and COPD. With her medical history, is there a chance the Paxlovid can be more harmful than helpful? Her severe pain and abdomen with digestive system started before taking Paxlovid, and after receiving the COVID booster. She received her COVID booster on 24Nov2021. If she wants to retest for COVID to see if it's gotten any better, does Paxlovid effect the results of her home test? Patient Details: She weighs #withheld, which has dropped. She's lost weight. Last time she went to the doctor it was #withheld. She's dropped 20 lbs, when she has these bouts she cannot eat since the COVID booster. It is spasmodic. If she eats normal food, she will get the bout it in day or two, lasting 3-4 days where she spends the day in the bathroom and also while going to the bathroom she is vomiting. If there is nothing there to vomit it is usually mucus and water. States she is not vomiting any bile whatsoever, she doesn't think her body is producing bile at this point. She sleeps most of the time when she has it because she has no energy to do anything else regardless other than to deal with the severe pain. Nobody can tell her what is going on. HCP details: Caller does not have a primary care doctor. The Paxlovid was prescribed by her pulmonologist, at # and Critical Care Medicine. HCP email unknown. Event Details: She didn't report at the time because she didn't think the shot did it. Severe pain in lower abdomen: States she had the shot on the 24th and it started late that day and she had it in the morning and it continued for 3-4 days. States it stops and it restarts if she tries to eat normally. If she lives on water, crackers, and soup it doesn't happen. When it does happen it's very severe. It comes and goes. If she starts feeling normal and eats a little bit of food, about a cup of vegetables, mashes potatoes and drinks plenty of water sometimes that works. States but if she goes along 2-3 days she is back in the same thing for another 3-4 days and she has been dealing with it since then. She was in bed all day Thanksgiving and next few days. Spends time in bathroom and vomiting: At the beginning of the bout she gets the very severe pain where she can't sit or stand or anything with pain. With the severe pain she tries to have bowel movements the vomiting begins, so she is doing both. Sometimes it brings up nothing, sometimes fluid. It comes from, the exertion is from her toes and she has a lot of back pain from the muscles. It is so hard to explain. It is hard to say when the back pain began because it's not top priority. She attributes it to when she started straining to vomit, she thinks her back muscles got effected. She has issues with her lower back anyway, any kind of straining or pressure is going to make it worse. It was taken care of when she had shots and basically eliminated it until this started it again. She believes it's the stress on her muscles. It is ongoing, she is at the end of a bout of it right now that has lessoned because she stopped eating. Overall it has worsened. Products: COVID-19 vaccines: First dose COVID-19 vaccine received 26May2021: Lot number: EWO177; NDC and Expiry unknown. Received at # Injected in Arm. Second dose of Pfizer COVID-19 vaccine received 16Jun2021: Lot number EWO181; NDC and Expiry unknown. Received at Injected in Arm. Pfizer COVID-19 BioNTech booster: Dose: unknown, it is not listed on her vaccine card. Formulation: All three vaccines were injections. Products: Paxlovid Caller has to see if she can see it, what it is it's printed in the, on the foil imprinted on the bottom. Caller is looking at the individual packs and not the box. She thinks the lot number says 9914, but is not sure. Indication: Caller tested positive for COVID and with her breathing difficulties and all that goes with it, she called her pulmonologist because she doesn't have a primary care physician, and asked if she should be on something.as her oxygen levels had been dropping and staying around 96-95% and not seeming to come up too much, and she didn't know if COVID was affecting her lung. Concomitant Medications: Caller states just her regular medications. Other medical conditions: Will it be pertinent to what Pfizer finds or what they need to see? States she doesn't know what is pertinent other than all of her surgery history and all that bull. Caller states she doesn't think they need to know what her cancer was caused by or anything else. States if they do want to know they can call her. She wants to be able to test herself for having COVID because she has an upcoming doctor's appointment. Investigations: She's had 3-4 tests done on her abdomen and no one is getting anywhere. She is a little but depressed over this. Her depression has been ongoing since her diagnosis of cancer. States they upped the dose of her medication after she was diagnosed with cancer. Treatment: They've done testing but nobody has been able to find anything. She had a mastectomy, they did a deep flap reconstruction, what it does is they cut you hip to hip and take the muscle from the lower abdomen and some of the fat tissue and essentially move it up and form a breast. They are removing muscle tissue from lower abdomen. She does have scar tissue. Leiomyoma sarcoma Started 4-5 years ago from radiation treatments. She has stage-IV cancer. Leiomyoma sarcoma is a cancer of soft tissue and it travels and it's hard to explain and ended up in lung. It started with radiation for breast surgery. VACCINE SUPPLEMENTAL FORM 1. Patient Details is available 2. Patient Age at Time of Vaccination in Months: or Years: 71-years 3. Pfizer Suspect Vaccine and Vaccination Details Vaccine Lot Number: 33030BD, Vaccine Lot Expire Date: unknown Time the Vaccination Was Given: early in the morning, around 0900. Anatomical Location of Administration of Pfizer vaccine considered as suspect: It would have been in Right arm. She doesn't have anything done in her left arm due to lymph nodes and the stuff they took out of her. 4. For Only: Vaccination Facility Type: Pharmacy: First two in # the booster in 5. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): First dose COVID-19 vaccine received 26May2021: Second dose of Pfizer COVID-19 vaccine received 16Jun2021: 6. Additional Vaccines Administered on Same Date of the Pfizer Suspect: None 7. Adverse Event (AE) Details: Provide the time of onset of AE(s): Adverse Event: severe abdominal pain Time of Onset: (24-hour clock): toward late afternoon, didn't feel anything after but late afternoon is when it started Adverse Event: vomiting. Time of Onset: (24-hour clock): either through the night or early the next morning 8. Additional Information Did any AE(s) require a visit to: Emergency Room? No; Physician Office? Yes; She went to gastrology doctor and they did a number of different scopes. They didn't seem to find anything. She is scheduled for gastro emptying test on the 29Jun2022. ER: When it continued she went to walk-in care and they sent her to the hospital where she sat for 9 hours. They did a report, did not admit her or have a doctor look at her. She took out her IV and said she was leaving. They did write a nice report about a doctor seeing her which was bullshit. Aware this is discrepant, but details were confirmed and documented as provided by the caller. 9. 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 10. AE(s) following prior vaccinations: None or Unknown Adverse Event: was not good, and have not taken them sense, that was years, she got real sick; Onset Age: cannot remember, Vaccine/Brand Name: Flu, Vaccination Date: unknown 11. Patient's Medical History (including any illness at time of vaccination)? COPD, partial bottom quarter of lung removed due to cancer. Dates unknown, it was a while ago. 12. Family Medical History Relevant to AE(s): She had a mastectomy, they did a deep flap reconstruction, what it does is they cut you hip to hip and take the muscle from the lower abdomen and some of the fat tissue and essentially move it up and form a breast. They are removing muscle tissue from lower abdomen. She does have scar tissue. She questioned whether that would be a factor. She had gall bladder removed as well. 13. Relevant Tests: None or Unknown She's had tons of those, results unknown. If Pfizer wants to call they can and she will dig it out. Her chest X-ray, her doctor at # can speak to Pfizer about it. 14. For Lack of Efficacy, request the following information if not included in the initial report What is the primary infection site? not applicable 15. Please specify any secondary site(s) (e.g. empyema): not applicable 16. Are there predisposing factors? Unknown/No/ Yes (e.g. immunosuppression, contact with other infected persons) The first time she contracted COVID and it was her grandson she's pretty sure because he tested positive Thursday, and she tested positive Saturday, which is when she took the test. 17. Was a culture performed? Unknown/No/Yes. She just did a home test. 18. If Yes, was the culture positive? not applicable 19. If Yes, was serotyping done? No 20. If Yes, please specify organism(s) (and serotype if available): not applicable 21. Please specify the culture source (e.g. blood): not applicable 22. Please specify Antipyretic Use (around the date(s) of Vaccination): Product Name / Strength: Not to her knowledge. What does antipyretic mean? Is there a product complaint to report? Yes, Description of Product Complaint: Description of complaint: LOE for Pfizer COVID-19 vaccine, caller tested positive for COVID. Is a sample of the product available to be returned, if requested (Y/N): not applicable Packaging sealed and intact? not applicable. Description of complaint: Caller taking Paxlovid. She is looking at the individual packs and not the box. Caller has to see if she can see it, what it is it's printed in the, on the foil imprinted on the bottom. She thinks the lot number says #, but is not sure. Product strength and count size dispensed: not provided. Additional lot numbers: not provided. Is a sample of the product available to be returned, if requested (Y/N): not provided Packaging sealed and intact? not provided. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Name: Chest X-ray; Result Unstructured Data: Test Result:Unknown result; Test Name: oxygen levels; Result Unstructured Data: Test Result:96-95%; Comments: oxygen levels had been dropping and staying around 96-95%; Test Date: 20220611; Test Name: COVID test; Test Result: Positive
- Aktuelle Erkrankungen
- COPD (COPD He lung function was 40% when last tested. The diagnosis was years ago.)
- Vorgeschichte
- Medical History/Concurrent Conditions: Depression (Her depression has been ongoing since her diagnosis of cancer.); Gallbladder removal (gall bladder removed); Leiomyoma; Mastectomy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 12.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Injection site pain
Pain
Pain in extremity
Symptomtext
Site: Pain at Injection Site-Severe, Additional Details: Patient still experiences pain at the injection site and throughout her left arm. She has limited mobility and cannot lift her arm to the same extent as prior to the vaccination. She also experiences pain with any movement involving her left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 05.12.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
COVID-19
Cough
Dyspnoea
Fatigue
Mobility decreased
Oxygen saturation decreased
SARS-CoV-2 test positive
Symptomtext
I woke up with a cough and having difficulty breathing and very tired. I waited 6 hours and did an at home covid test and it was positive. It was bad, the severe symptoms lasted 4-5 days and at one point oxygen level was down to 85. I just stayed in bed for the whole time, it was too hard to get up and have been extremely tired since then. I went to my regulary scheduled doctors appointment in march and she did bloodwork.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- bloodwork - came back fine
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- copd
- Andere Medikamente
- Gabapentin, Levothyroxine, Lamictal
- Allergien
- mushroom
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 29.12.2020
- Beginn
- 10.02.2022
- Tage bis Beginn
- 408,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Maternal exposure before pregnancy
Tachycardia foetal
Symptomtext
02/10/22 presents to Triage for "Fetal Tachycardia in the setting of a known COVID-19 infection" "38w2d". "No past medical history on file"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia foetal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 03.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Amnesia
Cognitive disorder
Confusional state
Fatigue
Headache
Arthralgia
Back pain
Condition aggravated
Dizziness
Injection site pain
Lethargy
Lymph node pain
Lymphadenopathy
Myalgia
Muscular weakness
Pain in extremity
SARS-CoV-2 test
Nausea
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 62 years, in left arm for Covid-19 immunisation. The patient's relevant medical history included: "Stage 1 Hypertension" (unspecified if ongoing), notes: Stage 1 Hypertension; "Mild sleep apnea" (unspecified if ongoing), notes: Mild sleep apnea. Concomitant medication(s) included: COZAAR. Past drug history included: Keflex, reaction(s): "Known allergies: Keflex", notes: Known allergies: Keflex. Vaccination history included: BNT162b2 (Dose Number: 1; Batch/Lot No: EL9265; Location of injection: Arm Left), administration date: 12Feb2021, when the patient was 61-year-old, for COVID-19 immunization, reaction(s): "Mild headache", "Moderate fatigue exacerbated with activity"; BNT162b2 (Dose Number: 2; Batch/Lot No: EN6199; Location of injection: Arm Left; Unresolved memory loss), administration date: 09Mar2021, when the patient was 61-year-old, for COVID-19 immunization, reaction(s): "Unresolved memory loss", "Confusion", "Cognitive delay", "Mild headache", "Moderate fatigue exacerbated with activity". The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, was the patient was not diagnosed with COVID-19. The following information was reported: HEADACHE (disability), outcome "not recovered", described as "Mild headache"; FATIGUE (disability), outcome "not recovered", described as "Moderate fatigue exacerbated with activity"; AMNESIA (disability), outcome "not recovered", described as "Unresolved memory loss"; CONFUSIONAL STATE (disability), outcome "not recovered", described as "Confusion"; COGNITIVE DISORDER (disability), outcome "not recovered", described as "Cognitive delay"; PAIN IN EXTREMITY (disability), MUSCULAR WEAKNESS (disability), outcome "not recovered" and all described as "Unresolved pain and weakness in both arms". The events "mild headache", "moderate fatigue exacerbated with activity", "unresolved memory loss", "confusion", "cognitive delay" and "unresolved pain and weakness in both arms" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (21Feb2021) Negative, notes: Covid test type post vaccination=Nasal Swab; (22Feb2021) Negative, notes: Covid test type post vaccination=Nasal Swab. Therapeutic measures were not taken as a result of headache, fatigue, amnesia, confusional state, cognitive disorder, pain in extremity, muscular weakness. Reported Events for 1st dose: Unresolved mild headache and moderate fatigue exacerbated with activity; 2nd dose: In addition to unresolved side effects from the 1st dose, unresolved memory loss, confusion, and cognitive delay. 3rd dose: In addition to unresolved side effects from 1st and 2nd doses, unresolved pain and weakness in both arms. As a result of these unresolved side effects, initially worked a modified schedule of 4 hours/day beginning 20Apr2021 and now no longer able to work at all effective 16Aug2021 as a public health nurse. No hospitalization prolonged. The adverse event resulted in doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient has been tested for COVID-19. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Sender's Comments: As there is limited information in the case provided, the causal association between the event Headache, Fatigue, Amnesia, confusion, cognitive function abnormal, pain in arm and Weakness of arm and the suspect drug cannot be excluded. The case will be reassessed once new information is available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210221; Test Name: Nasal Swab; Test Result: Negative; Comments: Covid test type post vaccination=Nasal Swab; Test Date: 20210222; Test Name: Nasal Swab; Test Result: Negative; Comments: Covid test type post vaccination=Nasal Swab.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension (Stage 1 Hypertension); Sleep apnea (Mild sleep apnea).
- Andere Medikamente
- Cozaar
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 03.12.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
COVID-19
Condition aggravated
Emotional distress
Exposure to SARS-CoV-2
Fatigue
Feeling abnormal
Headache
Memory impairment
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
01/04/2022, I had a headache, not like my regular headaches, it was an echoing headache. My daughter had COVID 5 days earlier. My headache lingered for about 3 days. My throat hurt for a little bit. The 3rd day, my body started hurting and I just shut down. My joints, back and everything was hurting. It was more like the mental toll, it was exhausting. I have anxiety and depression previously. The 3rd day was the worst day. The physical recovery was pretty fast. After COVID, I started noticing brain fog and forgetfulness. Brain fog and forgetfulness remains today. I have an appointment on Friday with my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- COVID Test, abnormal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- One a day Prenatal Vitamins; Sertraline
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 24.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Epstein-Barr virus infection
Fatigue
Headache
Hot flush
Illness
Myalgia
Pain
Symptomtext
viral sickness, headache, muscle ache, exhaustion, hot flashes, lasting several months, exacerbated all existing conditions including my inflammatory disease creating chronic pain, and epstein barr,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Factor V Leiden, Endometriosis, Epstein Barr Virus, Enondroma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- yellow fever
- Staat
- PA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 14.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Feeling abnormal
Hypoaesthesia
Inappropriate schedule of product administration
Insomnia
Limb discomfort
Mobility decreased
Paraesthesia
Vaccination site pain
Symptomtext
cannot even sleep; got the first dose on 25Apr2021/received the second dose of the Pfizer COVID vaccine on 14Nov2021; It does not let her raise her arm; It was so numb or tingly in her hands; It was so numb or tingly in her hands; Left arm pain at injection site/ When she touches that area, it hurts; It is weird; After 2nd shot, it hurt more.; It felt like something was in her arm.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 23 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 14Nov2021 (Lot number: 33030BD) at the age of 23 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, Lot number: EW0176, Anatomical location: left arm, Time the Vaccination Was Given: In the daytime around 12:00 for both.), administration date: 25Apr2021, when the patient was 22 years old, for COVID-19 Immunization, reaction(s): "Left arm pain at injection site", "it really hurt like something was in her arm/ Feels heavy", "her arm tingles". The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 14Nov2021, outcome "unknown", described as "got the first dose on 25Apr2021/received the second dose of the Pfizer COVID vaccine on 14Nov2021"; MOBILITY DECREASED (non-serious) with onset 2021, outcome "unknown", described as "It does not let her raise her arm"; INSOMNIA (non-serious) with onset 27Dec2021, outcome "unknown", described as "cannot even sleep"; HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 2021, outcome "unknown" and all described as "It was so numb or tingly in her hands"; VACCINATION SITE PAIN (non-serious) with onset 2021, outcome "not recovered", described as "Left arm pain at injection site/ When she touches that area, it hurts"; FEELING ABNORMAL (non-serious) with onset 2021, outcome "unknown", described as "It is weird"; CONDITION AGGRAVATED (non-serious) with onset 2021, outcome "unknown", described as "After 2nd shot, it hurt more."; LIMB DISCOMFORT (non-serious) with onset 2021, outcome "unknown", described as "It felt like something was in her arm." Additional information: Reporter stated she was a dietary aide before. She got the first dose on 25Apr2021. She went in and got shot and a day after, it really hurt like something was in her arm. Ever since then, her arm tingles and feel heavy. After 2nd shot, it hurt more. It felt like something was in her arm. It does not let her raise her arm. It was weird. It was given in her left arm. When she touches that area, it hurts. She does not know what was in there. It never happened before. Yesterday, she cannot even sleep. It was so numb or tingly in her hands. She has previous health problems and she got it to prevent herself from getting sick. Time of the vaccination was given in the daytime around 12:00 for both. Anatomical location of administration of pfizer vaccine considered as suspect was injected in left arm. Unable to confirm if given in the muscle. Vaccination facility type was pharmacy. Events does not require visit to emergency room and physician office. Patient had not taken prior vaccinations within four weeks prior to the first administration date of the suspect vaccine. Patient's medical history (including any illness at time of vaccination) are none or unknown. Family medical history relevant to AE was none. Relevant tests were reported 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
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 30.11.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Back pain
Muscle twitching
Paraesthesia
SARS-CoV-2 test negative
Symptomtext
felt tingling in left side of head; developed muscle twitch in left palm below thumb; developed sudden onset lower back, abdominal pain; abdominal pain; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 30Nov2021 (Lot number: 33030BD) at the age of 40 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Covid-19" (unspecified if ongoing), notes: If COVID prior vaccination: Yes. Concomitant medication(s) included: LEVOTHYROXINE. Past drug history included: No, reaction(s): "Allergy". The following information was reported: PARAESTHESIA (non-serious) with onset 02Dec2021 12:00, outcome "unknown", described as "felt tingling in left side of head"; MUSCLE TWITCHING (non-serious) with onset 02Dec2021 12:00, outcome "unknown", described as "developed muscle twitch in left palm below thumb"; BACK PAIN (non-serious) with onset 02Dec2021 12:00, outcome "unknown", described as "developed sudden onset lower back, abdominal pain"; ABDOMINAL PAIN (non-serious) with onset 02Dec2021 12:00, outcome "recovered" (2021), described as "abdominal pain". The events "felt tingling in left side of head", "developed muscle twitch in left palm below thumb", "developed sudden onset lower back, abdominal pain" and "abdominal pain" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of paraesthesia, muscle twitching, back pain, abdominal pain. Additional information: 2 days after vaccine, 02Dec2021, felt tingling in left side of head, periodically, lasting 1-2 days. 4 days after vaccine, 04Dec2021, developed muscle twitch in left palm below thumb. 7 days after vaccine, 08Dec2021, developed sudden onset lower back, abdominal pain which improved after 2-3 days. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had covid prior to vaccination. Patient was tested Covid post vaccination. Patient had no known allergies. Follow-Up: Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211212; Test Name: Abbot binax now; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (If COVID prior vaccination: Yes); Hypothyroidism
- Andere Medikamente
- LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 09.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dyspnoea
Pulmonary function test
Symptomtext
Towards the end of Dec I developed a severe cough to the point where I couldn't really catch my breath. I visited a Dr. who gave me medication that didn't really help so he referred me to an allergist who gave me a another medication which helped. I then went to a lung Dr. who prescribed another medication which helped clear up the cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Lung test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure and blood sugar
- Andere Medikamente
- Nebivolol, Hydrochlorothiazide, Bugupacide, Metformin, amlodipine, Atorvastatin, Aspirin
- Allergien
- Codeine
- Vorherige Impfungen
- After 1st COVID-19 vaccine I developed a large lump in my elbow which had to be drained.
- Staat
- MO
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 04.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray abnormal
Chest pain
Dyspnoea
Hypertension
Pulmonary mass
Symptomtext
Approximately the next day after my booster shot I experienced the following symptoms: Difficulty breathing (cannot breathe), Chest pain, High blood pressure. I went to the ER and they took my blood pressure and did some blood work, IV line (Blood vials), Chest X-Ray (showed spots on both lungs - especially the right side). After doing all those tests I got discharged eventually - I started to feel better. It took a few days for the chest pain to subside and the breathing difficulty took 1 week to subside and the blood pressure took a month - until I got my normal pressure back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood work, Chest X-Ray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ovarian Cancer
- Andere Medikamente
- Probiotic, Aspirin
- Allergien
- Bee stings, Adhesive, Volcumizine
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Cough
Hypertensive crisis
Sinus congestion
Symptomtext
Stroke range hypertension, increased sinus congestion, cough. Antibiotic for sinus and cough. Cardiologist is monitoring blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- hypertension, hyperlipidemia, diabetes
- Vorgeschichte
- hypertension (well controlled with medication)
- Andere Medikamente
- Atorvastatin, lisinopril, metoprolol, brilinta, metformin, 81mg ASA,
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 20.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein increased
Dyspnoea
Dyspnoea exertional
Echocardiogram
Exercise tolerance decreased
Laboratory test
Red blood cell sedimentation rate normal
Troponin increased
Symptomtext
On November 20, 2021, patient received his first COVID-19 Pfizer vaccine (batch/lot#33030BD). He reported no symptoms initially but one to two weeks later noted more dyspnea, notable with exertion and some labored breathing. He reported no wheezing, cough or chest pain. He was able to perform aerobic activity to include running, but felt this was more difficult compared to the past. He received his 2nd COVID-19 vaccine on December 12, 2021 with no reported change regarding immediate symptoms. Labored breathing continued. He thought it was slowly improving over the past few weeks. He was evaluated by cardiology (labs and echocardiogram). He reported being told cardiac workup normal. There is no planned follow-up appointment pending.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Troponin: 19.8ng/L; C-reactive protein: <30mg/dL; ESR: 6mm/hr.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergic rhinitis
- Andere Medikamente
- Zyrtec 10mg daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 12.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood pressure measurement
C-reactive protein
C-reactive protein increased
Chills
Chromaturia
Fatigue
Hypertension
Nausea
Protein urine
Protein urine present
Pyrexia
Red blood cells urine
Red blood cells urine positive
SARS-CoV-2 test
Urine albumin/creatinine ratio
Urine albumin/creatinine ratio increased
Vomiting
Symptomtext
Rust colored urine; Fever; chills; Aching joints; Nausea; vomiting; fatigue; Elevated c-reactive protein; Elevated urine RBC/HPF; Elevated urine albumin/creatinine ratio; Elevated urine total protein; High blood pressure on exam; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administration date 08Dec2021 (Lot number: 33030BD) at the age of 31 Years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was reported as none. Concomitant medications were not reported. Past drug history included: Cephalexin, reactions: "Drug allergy". Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Lot number: E13249.), administration date: 28Jan2021, when the patient was 30 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 1, SINGLE, Lot number: E13246.), administration date: 07Jan2021, when the patient was 30 years old, for COVID-19 immunisation. The following information was reported: CHROMATURIA (non-serious) with onset 09Dec2021, outcome "not recovered", described as "Rust colored urine"; PYREXIA (non-serious) with onset 09Dec2021, outcome "not recovered", described as "fever"; CHILLS (non-serious) with onset 09Dec2021, outcome "not recovered", described as "chills"; ARTHRALGIA (non-serious) with onset 09Dec2021, outcome "not recovered", described as "aching joints"; NAUSEA (non-serious) with onset 09Dec2021, outcome "not recovered", described as "nausea"; VOMITING (non-serious) with onset 09Dec2021, outcome "not recovered", described as "vomiting"; FATIGUE (non-serious) with onset 09Dec2021, outcome "not recovered", described as "fatigue"; C-REACTIVE PROTEIN INCREASED (non-serious) with onset 09Dec2021, outcome "not recovered", described as "elevated c-reactive protein"; RED BLOOD CELLS URINE POSITIVE (non-serious) with onset 09Dec2021, outcome "not recovered", described as "Elevated urine RBC/HPF"; URINE ALBUMIN/CREATININE RATIO INCREASED (non-serious) with onset 09Dec2021, outcome "not recovered", described as "Elevated urine albumin/creatinine ratio"; PROTEIN URINE PRESENT (non-serious) with onset 09Dec2021, outcome "not recovered", described as "Elevated urine total protein"; HYPERTENSION (non-serious) with onset 09Dec2021, outcome "not recovered", described as "High blood pressure on exam". The events "Rust colored urine", "fever", "chills", "aching joints", "nausea", "vomiting", "fatigue", "elevated c-reactive protein", "Elevated urine RBC/HPF", "Elevated urine albumin/creatinine ratio", "Elevated urine total protein" and "High blood pressure on exam" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of chromaturia, pyrexia, chills, arthralgia, nausea, vomiting, fatigue, c-reactive protein increased, red blood cells urine positive, urine albumin/creatinine ratio increased, protein urine present and hypertension. Additional Information: Prior to vaccination, the patient was not diagnosed with COVID -19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Since the vaccination, the patient had been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211209; Test Name: Blood pressure; Result Unstructured Data: Test Result:High; Comments: High blood pressure; Test Date: 20211209; Test Name: Urine total protein; Result Unstructured Data: Test Result:Elevated; Comments: Elevated urine total protein; Test Date: 20211209; Test Name: urine albumin/creatinine ratio; Result Unstructured Data: Test Result:Elevated; Comments: Elevated urine albumin/creatinine ratio; Test Date: 20211209; Test Name: urine RBC/HPF; Result Unstructured Data: Test Result:Elevated; Comments: Elevated urine RBC/HPF; Test Date: 20211209; Test Name: C-reactive protein; Result Unstructured Data: Test Result:Elevated; Comments: Elevated C-reactive protein; Test Date: 20220105; Test Name: SARS-CoV-2 test; Test Result: Negative ; Comments: Corona SARS-CoV-2 by nucleic acid amplification
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dizziness
Feeling hot
Pain
Symptomtext
Client c/o "generalized pain and lightheadedness and hot, was assisted to floor onto yoga mat, with feet elevated. VS taken 153/88 Pulse 109 SP02 100%, cold compresses applied. Verbal support provided, with no improvement and client c/o of "chest pain emergency called client remained alert and conscious was transported to local hospital via ambulance, departing VS @ 3:22pm 142/82 Pulse 109 SP02 100%, mother at side.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Bipolar, Anxiety, heart condition reported by mother after reaction
- Vorgeschichte
- anxiety, bipolar
- Andere Medikamente
- Wellbutrin, Claritin, Seroquel,
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Electrocardiogram normal
Symptomtext
Quick immune response. Heart rate went up- per FitBit. Chest pain, pressure going to back. Heart rate got better only when resting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG- normal.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- multivitamin, probiotics
- Allergien
- rash from amoxicillin, sulfa sensitivity
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 22.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Arthralgia
Bone disorder
Condition aggravated
Hypokinesia
Joint swelling
Magnetic resonance imaging
SARS-CoV-2 test
X-ray
Symptomtext
elbow started aching; elbow started aching and swelling for no reason, worse than ever; Lost 10 degrees of motion; attack my bone transplant and its bond; elbow started aching and swelling; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Dec2021 (Lot number: 33030BD) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "L shoulder repair", start date: 1985 (unspecified if ongoing); "R shoulder repair", start date: 1998 (unspecified if ongoing); "tumor removed", start date: 1985 (unspecified if ongoing), notes: In 1985 I had synovial sarcoma soft tissue tumor removed from right elbow followed by radiation.; "radiation", start date: 1985 (unspecified if ongoing), notes: In 1985 I had synovial sarcoma soft tissue tumor removed from right elbow followed by radiation.; "synovial sarcoma soft tissue tumor", start date: 1985 (unspecified if ongoing), notes: In 1985 I had synovial sarcoma soft tissue tumor removed from right elbow followed by radiation.; "right medial epicondyle", start date: Mar2017 (unspecified if ongoing), notes: Mar2017, I had a second tumor removed from right medial epicondyle; "tumor removed", start date: Mar2017 (unspecified if ongoing), notes: Mar2017,a second tumor removed from right medial epicondyle bone and soft tissue; "my elbow allograft fractured", start date: Jul2021 (unspecified if ongoing), notes: In mid-Jul2021 my elbow allograft fractured using a bicycle pump. Concomitant medication(s) included: AMLODIPINE BESYLATE; FAMOTIDINE. Vaccination history included: Bnt162b2 (Dose 2 Product: COVID Vaccine, Brand: Pfizer, lot no: en6208, date: 19Mar2021, vaccine location: Left arm), administration date: 19Mar2021, when the patient was 62 years old, for Covid-19 immunization, reaction(s): "shoulders were very sore", "elbow allograft fractured", "aching and swelling for no", "aching and swelling for no"; Bnt162b2 (Dose 1Product: COVID Vaccine, Brand: Pfizer, lot no: en6208, date: 26Feb2021, vaccine location: Left arm), administration date: 26Feb2021, when the patient was 62 years old, for Covid-19 immunization. The following information was reported: ARTHRALGIA (disability), outcome "not recovered", described as "elbow started aching"; JOINT SWELLING (disability), outcome "not recovered", described as "elbow started aching and swelling"; CONDITION AGGRAVATED (disability), outcome "not recovered", described as "elbow started aching and swelling for no reason, worse than ever"; HYPOKINESIA (disability), outcome "not recovered", described as "Lost 10 degrees of motion"; BONE DISORDER (disability), outcome "not recovered", described as "attack my bone transplant and its bond". The events "elbow started aching", "elbow started aching and swelling", "lost 10 degrees of motion" and "attack my bone transplant and its bond" were evaluated at the physician office visit and emergency room visit. The event "elbow started aching and swelling for no reason, worse than ever" was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: magnetic resonance imaging: (unspecified date) unknown results; sars-cov-2 test: (17Jan2022) negative, notes: Nasal swab; x-ray: (unspecified date) unknown results. Therapeutic measures were taken as a result of arthralgia, joint swelling, condition aggravated, hypokinesia, bone disorder. Vaccination facility type is pharmacy or drug store. No other vaccine in four weeks. Other medications in two weeks: Amlodipine Besylate, Famotadine. Background-In 1985 he had synovial sarcoma soft tissue tumor removed from right elbow followed by radiation. Mar2017, he had a second tumor removed from right medial epicondyle bone and soft tissue caused by radiation. Repair included allograft bone and tendon with plate and screws. Results were very good with little issue and problems for 4+ years. After 2nd Pfizer shot shoulders were very sore for a week. In mid-Jul2021 my elbow allograft fractured using a bicycle pump. Since then, he was elbow gets better and worse but has not mended. He was very limited to 5 lbs lifting. He was hestitant to get the booster but did. 7 days after he was elbow started aching and swelling for no reason, worse than ever. The swelling lasted 5 days. Lost 10 degrees of motion that has not recovered. He had no proof, but he was suspicious that the vaccine may attack his bone transplant and its bond. He was very hesitant of future vaccines. AE resulted in doctor or other healthcare professional office/clinic visit, Disability or permanent damage. AE treatment received X-Rays, MRIs, bracing and continued monitoring. No covid prior vaccinations. Covid tested post vaccination. No Known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220117; Test Name: Nasal swab; Test Result: Negative ; Comments: Nasal swab; Test Name: X-Ray; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Elbow fracture (In mid-Jul2021 my elbow allograft fractured using a bicycle pump.); Ostectomy (Mar2017, I had a second tumor removed from right medial epicondyle); Radiation therapy (In 1985 I had synovial sarcoma soft tissue tumor removed from right elbow followed by radiation.); Shoulder arthroplasty; Synovial sarcoma (In 1985 I had synovial sarcoma soft tissue tumor removed from right elbow followed by radiation.); Tumor excision (Mar2017,a second tumor removed from right medial epicondyle bone and soft tissue); Tumour excision (In 1985 I had synovial sarcoma soft tissue tumor removed from right elbow followed by radiation.)
- Andere Medikamente
- AMLODIPINE BESYLATE; FAMOTIDINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 04.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Discomfort
Headache
Malaise
Paraesthesia
Vaccination complication
Symptomtext
Nerve tingling after shot felt in lower left-back. Ill with a headache for a day or two. The week after the shot felt uncomfortable but better until the following week started. A sharp pain was felt under the underarm area. The pain increased. I tried Motrin to help, but it still persisted. Used ice pack to help decrease irritation but only helped a little. Made an appointment in Jan to be seen. After being checked, I was told to continue with a higher dose of ibuprofen and to have an ultrasound with my breast specialist. The area was felt for swollen lymph nodes. None was found at the time. The doctor felt it was an adverse result from the booster and most likely need time to heal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Ultrasound ordered (recommended a follow-up with breast specialist later that month), Jan 31, 2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid removal
- Andere Medikamente
- Synthroid 175 mg, Vitamin E & D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 30.11.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
Onset of chest pain a couple of days after receiving Pfizer Covid-19 vaccine. Sharp pain over left chest - some days it is persistent and other days it is intermittent. No meds taken, pain eventually subsides. Vaccine was given at local discount store.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- migraine, mild mitral valve prolapse
- Andere Medikamente
- none
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 28.12.2021
- Beginn
- 23.01.2022
- Tage bis Beginn
- 26,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
Pain in the right side of my chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 07.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Cardiac stress test
Chest X-ray normal
Echocardiogram
Electrocardiogram ambulatory abnormal
Electrocardiogram normal
Palpitations
Supraventricular extrasystoles
Supraventricular tachycardia
Symptomtext
I started having heart palpitations about a week after receiving the booster shot. I'm not sure of the exact date and time but there were several episodes the week of December 13, 2021. I called my primary care doctor on December 20, 2021 and the office told me to go to the Emergency Room which I did. They did an EKG, chest x-ray and blood work which was all normal. I saw a cardiologist on December 22, 2021. He did another EKG, and ordered a stress test, an echo-cardiogram, and an external mobile cardiovascular telemetry unit which showed supraventricular tachycardia (SVTs) and Premature Atrial Contractions (PACs)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 12/20/21 ER, KG, chest x-ray and blood work, 12/22/21 EKG, 12/27/21 stress test, 1/11/22 echo-cardiogram, 12/22/21 to 1/2/22 external mobile cardiovascular telemetry unit
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Daily multi-vitamin (no iron), B-12 (1000 mcg taken weekly)
- Allergien
- Codeine/Percocet/Demerol and Cefdinir (severe vomiting)
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Lymphadenopathy
Migraine
Pain in extremity
Symptomtext
Left arm pain for the past days and now swollen/enlarged (central) armpit lymph node Migraine (left side but had similar symptoms - headaches/migraines on and off before)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic allergies to something (may be dust, mold etc) causing inferior turbinate hypertrophy accompanied with migraine (chronic - sinisitis)
- Vorgeschichte
- IBS, allergies to something (may be dust, mold etc) causing inferior turbinate hypertrophy accompanied with migraine (chronic - sinisitis), Migraines, Fibroids, dysmenorrhea with pms or its worst version,
- Andere Medikamente
- Vitamin D high dose over the counter gummies, iron supplement, multivitamins, ginger tea, cumin drink, turmeric in food, Flonase, Claritin D, vicks humidifier with Vick steamed vapors
- Allergien
- Allergies to food (ibs), allergies to something (may be dust, mold etc) causing inferior turbinate hypertrophy accompanied with migraine (chronic - sinisitis)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 05.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Asthenia
Back pain
Discomfort
Hypoaesthesia
Magnetic resonance imaging
Pain
Paraesthesia
Pelvic pain
Tenderness
Symptomtext
On Dec 22, 2021 (two weeks after Covid booster), I started with pain in my lower back (left side). Pain went along left hip, left pelvis, left thigh. Numbness, tingling in left hip, pelvis and left thigh. I do not feel my pelvis area (left ingle) and left thigh. Left thigh is sensitive to touch, even my clothes sometimes hurt me. Sometimes I feel like sharp objects or coldness. Weakness in left thigh. Heavy sensation in my lower left back and left side of pelvis. Walking and sitting is painful. I have to be most of the time in bed. Doctor prescribed Prednisone 20mg, during 9 days, Tylenol, Cyclobenzaprine, Oneoprazole. After taking the medication, pain continues, as well as numbness and tingling. Doctor recommended Norco for pain. I continued with Tylenol. MRI spine lumbar wo contrast was done, with no evidence of cord compression and normal results. Even though, pain and numbness continues. Today is January 13. Appointment with Neurologist is suggested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- 1. Unremarkable MRI of the lumbar spine. Narrative MRI LUMBAR SPINE WITHOUT CONTRAST CLINICAL HISTORY: Low back pain. COMPARISON: None TECHNIQUE: Multiplanar multisequence imaging was performed through the lumbar spine without intravenous contrast using a 3T MRI scanner. _________________________________________________ FINDINGS: Spinal Canal: No evidence of cord compression. No epidural fluid collection or mass. Conus and Cauda Equina: The conus is normally positioned, terminating above the L2 level. Cauda equina nerve roots normal in morphology. Vertebrae: Vertebral body heights within normal limits. Alignment: Normal alignment. Marrow signal: Unremarkable. Discs: See level by level analysis below. Soft Tissues: Paravertebral soft tissues within normal limits. T12-L1: Unremarkable. L1-2: Unremarkable. L2-3: Unremarkable. L3-4: Unremarkable. L4-5: Unremarkable. L5-S1: Unremarkable.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- N/A
- Andere Medikamente
- The Perfect Womens Multi Vitamins
- Allergien
- Methroclopramide, Iodine, penicilline
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ciliary body disorder
Condition aggravated
Eye pain
Eye pruritus
Iridocyclitis
Ocular hyperaemia
Vision blurred
Symptomtext
left anterior uveitis developed approximately 1 week after vaccination. This is the third time I have had it. (The first time was in 2019, and the second time was last year). Currently have eye redness/ciliary flush, minimal pain/pruritis, blurred vision. Started smoldering a couple of weeks ago, became much more pronounced about 5 days ago.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Exam by ophthalmologist
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- ehlers danlos syndrome (hypermobility type) POTS depression idiopathic hypersomnia GERD asthma 2 previous episodes of uveitis (anterior -> panuveitis Jul 2019, anterior Jun 2020)
- Andere Medikamente
- zyrtec, singulair, celebrex, nuvigil, lexapro, wellbutrin, pepcid magnesium oxide, b12 1000mcg BIW, vit d 5000 IUs weekly
- Allergien
- acetaminophen, amoxicillin (?), IV contrast (for CT scan), latex, peanuts and nuts
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dyspnoea
Symptomtext
Patient reported that he felt dizziness and shortness of breath in addition to itching all over the skin. An oxygen cannula was placed and his vials were taken. Doctor was called, he ordered the administration of .50ml of BENADRYL. The patient was oriented on the medical order and refused the treatment of .50 ml of BENADRYL intramuscularly. Patient reports having BENADRYL PO and that he would wait for the symptoms to pass. The patient was observed for a further 30 min.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Thyroid
- Andere Medikamente
- Synthroid 25mg
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 11.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Burning sensation
Chest pain
Inflammation
Musculoskeletal chest pain
Symptomtext
On 12/13/2021 about 3 after the shot I had severe inflammation in my back, pain in my ribcage, it was worse in my left side. It continued for about 10 days. Mostly burning in my back around the top front of my chest. I tried resting but it came back. I didn't go initially but I called my doctor this week and had to go to my urgent care where they prescribed prednisone. I am going to schedule a follow-up with my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- I had labs between my 1st and 2nd shot in beginning of December and they were normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- I had Covid in August and had some issues since then but that's it.
- Andere Medikamente
- Tylenol 500 MG
- Allergien
- None
- Vorherige Impfungen
- I used to not react well to Flu vaccine but nothing serious. Just felt a little sick
- Staat
- WI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Injection site swelling
Mobility decreased
Skin tightness
Symptomtext
Swelling at injection site approx. 8-10 hours after injection with skin tightness, feeling "hot" and inability to bend arm. S/s lasted for approx. 4 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pulmonary sarcoidosis, back pain, chronic cough, bipolar, Diabetes Type II, Hypertension, Esophageal reflux, obesity, chronic knee and hip pain
- Andere Medikamente
- Albuterol, Abilify, Cogentin, Valium, Advair, Flonase, Neurontin, Microzide, Lidoderm, Lisinopril, Claritin, Metformin, Prednisolone acetate, Promethazine, Zocor
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 05.01.2022
- Impfdatum
- 28.11.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 38,0
- Dosis
- 1
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angina pectoris
Anxiety
Cardiac discomfort
Chest pain
Dizziness
Exercise tolerance decreased
Metabolic function test
Symptomtext
My symptoms began on 12/1/2022 a few short days after receiving my booster shot. I had left class after my final on 12/1/22 and became lightheaded with pain in my chest where my heart is located. I spoke with my PCP and she believed it was anxiety. The symptoms have only gotten worse and I often feel pain in my heart area. I am not under any stress or anxiety but have continued to have complications since. This week has been challenging and my heart feel very unconfutable. I am also having trouble exercising and cannot run as long as I use to.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- CMP was all in range. I have set up an annual wellness appointment on 01/08/2022 and will ask for a referral to the cardiologist.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dyspnoea
Fatigue
Influenza virus test negative
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I had low-grade fever, SOB, body aches, severe fatigue, and congestive. These symptoms are still ongoing. I went to my primary care on Dec. 30th for a Covid-19 test, positive result. They also did a flu test, negative result on those.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Covid-19 test; Flu test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic FC- lumbar; Chronic Lyme Disease
- Andere Medikamente
- Vitamin C; Zinc
- Allergien
- Diary; Milk
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 13.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 18,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Asthenia
B-cell lymphoma
Dysstasia
Loss of personal independence in daily activities
Mobility decreased
Skin infection
Symptomtext
CHIEF COMPLAINT: Pt states, "I got up too fast out of bed and slid. I had a hard time getting up myself. My son helped me." Denies hitting head or LOC. Denies blood thinners. HISTORY OF PRESENT ILLNESS: 63-year-old gentleman who was recently diagnosed with B-cell lymphoma involving his sigmoid colon, right ureter, lung presenting for the evaluation of generalized weakness. Patient reports 1 week of progressively worsening weakness and states tonight he was unable to get out of bed which prompted his evaluation in the ED. He denies falls or head trauma. Patient does note that he was recently diagnosed with lymphoma and was seen by his oncologist today where he was started on several medications including an antibiotic for a gluteal skin infection. He is denying fevers or chills. He reports abdominal pain. Denies chest pain or shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- COPD, Hypertension, Type 2 Diabetes mellitus
- Andere Medikamente
- Unknown
- Allergien
- Ceftin, Pollen,
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 30.11.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysphagia
Pharyngeal swelling
Pyrexia
Rash
Swelling
Heart rate increased
Hypertension
Swollen tongue
Throat tightness
Symptomtext
Swelling in left shoulder/collarbone area, neck and throat, right shoulder/collarbone area. Rash on both shoulders, back, neck, face, ears, was quickly spreading. Tightness in throat that impaired talking (breathing okay), swelling on back of tongue. Extremely high BP and HR. Urgent care on 12/2/21, given 50 ml Benadryl and rash went away, swelling went down (not gone completely). Emergency room on 12/3/21 because all swelling and rash and tight throat came back. Given IV meds of Benadryl, pepcin and epinephrine. All symptoms went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 28.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary pain
Blood test
Injection site pain
Lymphadenopathy
Mobility decreased
Neck pain
Pain in extremity
X-ray
Symptomtext
Swollen lymph node in arm pit for 3-4 days and mild pain at injection site. After the pain from the arm pit mostly stopped pain got worse in the arm at injection site went down the side of my body and up into my neck. The pain gradually got worse and was only in my arm and neck. The pain was in my neck and all up and down my arm to the point I could not use my arm. By day 5 the pain got so bad I had to go and see my doctor whom prescribed steroids and a strong muscle relaxer. The medication made the pain manageable but it did not go away. the next week the pain increased and my doctor sent me for X-rays and blood work to rule out injury, which they found n o sign of injury. The pain was deep in the muscle and would move from my neck to my lower arm and my bicep. All of this went on for 3 weeks after the vaccination and it went away just as quickly as it started. The pain I experienced is some of the worse I have ever felt in my life. If another booster is needed at some time in the future this will only be done at the advisement of my doctor and much apprehension on my part.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- X-rays & blood work. 12/3/21
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Benzapril
- Allergien
- Pennisulin Sulfa IBuophren
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood electrolytes
Blood thyroid stimulating hormone
Cardiac flutter
Chest discomfort
Electrocardiogram
Palpitations
Supraventricular extrasystoles
Symptomtext
Heart palpitations, heart flutter, and anxiety after about 3 days after first dose. Heart flutters continued on and off for one week. Heart flutters and palpation 3 hours after second dose. Chest felt very heavy. Went in to see primary care Dr. who stated that a brief PAC was heard. EKG performed. No structural issues noted. Sources of magnesium has improved issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG. TSH and electrolyte panel.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate increased
Palpitations
Tachycardia
Symptomtext
Systemic: palpitations and rapid heart rate/rythm-Medium, Systemic: Tachycardia-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Joint swelling
Non-cardiac chest pain
Paraesthesia
Symptomtext
Pt stated shortly after receiving the vaccination : 1) His right knee swelled and the swelling was still an issue one month later 2) He has been left with an uncomfortable feeling below his left clavicle that is still troubling him, esp when coughing 3) for 6 days following the vaccination he had "vibrations" in his left facial and head areas
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Non-cardiac chest pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unsure
- Vorgeschichte
- psoriasis rheumatoid arthritis
- Andere Medikamente
- Adderall XR 30mg
- Allergien
- steroids
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Myalgia
Pain in extremity
Paraesthesia
Symptomtext
The patient has experienced lingering arm and muscle pain in the vaccinated arm. There is also numbness/tingling in three fingers of the same hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 24.12.2021
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Diarrhoea
Dyspnoea
Nausea
Pyrexia
Vomiting
Symptomtext
CHIEF COMPLAINT: Pt c/o SOB, cough, fever, N&V x 5 days. Pt received covid booster 2 wks ago. On arrival EMS states spo2 85% RA, on15L Non rebreather to 96% spo2. HISTORY OF PRESENT ILLNESS: 52-year-old male with a history of type 2 diabetes, obesity presenting for the evaluation of shortness of breath. Patient reports 5 days of progressively worsening shortness of breath. He reports a dry cough. He reports fever. Denies chest pain or palpitations. Denies cardiac history. No known COVID-19 exposures. Additionally reporting several episodes of watery diarrhea over the past 2 days. He is fully vaccinated and boosted against COVID-19. No leg swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Diabetes,
- Andere Medikamente
- Unknown
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Condition aggravated
Fatigue
Headache
Nausea
Pain in extremity
Symptomtext
- soreness of arm & tiredness ~6:30pm 12/23/21 -chills ~9:00pm -11pm ish (fell asleep) 12/23/21 ; 11:00 am -11:45 am 12/24/21 -headache & nausea 11:20am 12/24/21 - 5:00am 12/25/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- arm soreness and tiredness, age 24, 5/1/21, COVID-19 Pfizer
- Staat
- MD
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Fatigue
Impaired work ability
Influenza virus test negative
Nausea
Pain
Rhinorrhoea
SARS-CoV-2 test negative
Symptomtext
Still experiencing: (12/21 - 8 days post booster) - EXTREME fatigue - EXTREME body aches - Nausea - Chest pain - Runny nose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Thought I had covid or flu. Tested negative twice. I have taken time off from this and my first dose.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Celiac, VST
- Andere Medikamente
- Buspar - 15 mg
- Allergien
- -
- Vorherige Impfungen
- 1st dose of Pfizer vaccine on 3/24/21. Almost 2 weeks.
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hypertension
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Hypertension-Medium, Additional Details: patient felt lightheaded after around 10-15 min of the vaccination , blood pressure checked was 150/90 then 148/87 after 10 min , offered water , lifted legs , offered to call 911 or the doctor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Eructation
Symptomtext
within 15 mins, started burping weirdly, about 6 hours later, could hardly breathe, both symptoms were taking turns recurring
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes
- Andere Medikamente
- metphormin, victoza
- Allergien
- adhesive, artificial sweeteners
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Ear, nose and throat examination
Pain in extremity
Paraesthesia
Tension headache
Symptomtext
Patient comes in 12/18/21 and reports to me that after her booster shot on 11/29/2021, days later, she experienced tingling in the fingers, arm pain and a tightness in the back of the head. She consulted with her PCP and her ENT, whose care she was under. The ENT cleared her and her PCP told her to take 2 Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Fatigue
Hypoaesthesia
Tremor
Symptomtext
Wed 12/15, 9am: Experienced weakness, chills, exhaustion. Wed 12/15, noon: Started experiencing numbness in both feet - not much at first but grew. Wed 12/15, 4pm: Chills so severe, I was literally shaking. Thu 12/16, chills subsided through the day, though some exhaustion remained. Feet/lower leg numbness grew more extensive, estimate about 80% numb. Fri 12/17, by about 2pm, all symptoms had subsided except for numbness which has continued to this moment (9:45pm).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- none so far
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- No chronic conditions. Rods in my back from surgery one year ago but no existing back conditions.
- Andere Medikamente
- Vitamin C, glucosamine, Vitamin D
- Allergien
- erythromycin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Confusional state
Dizziness
Flushing
Headache
Hyperhidrosis
Hypotension
Symptomtext
Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Hypotension-Severe, Additional Details: flucelvax and pfizer were given on the same day 12-16-2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood electrolytes
Chest discomfort
Chest pain
Computerised tomogram neck
Computerised tomogram normal
Computerised tomogram thorax
Dyspnoea
Electrocardiogram
Fibrin D dimer increased
Full blood count
Paraesthesia
Sensory loss
Troponin
Symptomtext
12/2 Sharp tingling, decreased sensation in right hand 1 hour post injection, tingling and decreased sensation migrated to my right arm and right leg/foot which lasted until the next day around mid-afternoon. 12/9 I was awoken at 5am with sharp chest pain on the left lateral side, under my left breast. This lasted about 10 minutes and then developed into a heaviness in my chest with a feeling of shortness of breath. 12/10 I woke up and both arms were completely asleep (never had this happened before). My arms continued to feel tingly and my chest still felt heavy/SOB so I went to the Emergency Department for evaluation. 12/17 still having some intermittent chest pain with exertion. I am a healthy individual with no prior comorbidities or risk factors other than having the factor V gene.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 12/10: EKG, CBC, electrolytes, troponin, D-dimer (positive), CT scan of chest (negative)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Factor V
- Andere Medikamente
- Vitamin D, Vitamin B complex
- Allergien
- Gluten intolerance, dairy intolerance
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Cough
Dysphagia
Dysphonia
Feeling abnormal
Hypoaesthesia
Hypoaesthesia oral
Injection site pruritus
Pharyngeal hypoaesthesia
Pruritus
Throat clearing
Throat irritation
Tongue disorder
Symptomtext
Within minutes of getting the vaccine I developed itching at the injection site on left arm ...the itching went to my right arm...then developed numbness to left elbow that went down to my fingers on left hand...had chest pressure and a pain that shot up to right side of my head.......had an overwhelming feeling that something wasn't right. I could taste the medicine /vaccine at the back of my throat, and I started to develop itching to back of throat and was clearing my throat and starting to cough....no difficulty breathing, but my voice was getting hoarse Pharmacist was watching me closely and kept me about 45 minutes.......I was given water and that helped a little and I was able to swallow at that time Symptoms didn't seem to get worse at the store so I was able to leave, but when I was driving home, I developed numbness around my mouth, my cheeks, and into my throat and down into my chest.... felt like my muscles were paralyzed and I could not swallow....my tongue felt thick and heavy, and my throat was tight by the time I got home.... I took more Benadryl as we were getting ready to call EMS....the symptoms gradually subsided and the numbness to chin and throat stayed through the next day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid Arthritis, Graves Disease, Hypothyroidism, Vitamin D and B 12 Deficiency
- Andere Medikamente
- Synthroid 112 mcg daily Pepcid 20 mg bid Was instructed by Primary MD to take Aspirin 80 mg x 5 days before taking vaccine and also to take Tylenol and Benadryl 25 mg before Injection
- Allergien
- Sulfa Severe Allergic Reaction to Flu Vaccine
- Vorherige Impfungen
- flu vaccine
- Staat
- FL
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Heart rate increased
Symptomtext
I started on Sunday evening experiencing rapid heart beat had trouble catching my breath lasted to Tuesday afternoon. I called my sister in law she is NP advised me to call my doctor. My doctor informed me that was common side effects to continue to monitor if symptoms worsened to go to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- 112 Micro Levothyroxine: 10 mg Lexapro
- Allergien
- Cipro, Environmental Allergies (tree, grass, mold), Citrus, Eggs, Nuts, Corn, Soy, Wheat, Carrot, Green Peas
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Decreased appetite
Diarrhoea
Fatigue
Migraine
Symptomtext
Upset stomach, poor appetite (eating only crackers & jello for 3 days), watery diarrhea, fatigue, migraine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD, hypertension
- Andere Medikamente
- Adderrall XR hydroCHLOROthiazide Zoloft Xyzal Junel FE nortriptyline zonisamide
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Symptomtext
Systemic: Chest Tightness / Heaviness / Pain-Severe, Additional Details: pt called back on dec 11th complaining about severe chest pain. pt counseled to go see primary care md/emergency room/cardiologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Hypoaesthesia
Symptomtext
Dose 1 received on 12/6/21. Patient's mother called pharmacy on 12/14 to report that on 12/13 patient experienced left facial numbness and shortness of breath lasting around 10 minutes. It resolved on its own and he did not seek medical attention. I advised mother to have patient seek medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Fatigue
Hypoaesthesia
Malaise
Oedema peripheral
Paraesthesia
Symptomtext
Bilateral upper extremity numbness/tingling. Unusual fatigue and malaise. Axillary swelling bilaterally with pain to left axillae.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Fatigue
Hypoaesthesia
Malaise
Oedema peripheral
Paraesthesia
Symptomtext
Bilateral upper extremity numbness/tingling. Unusual fatigue and malaise. Axillary swelling bilaterally with pain to left axillae.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Dyspnoea
Extra dose administered
White blood cell count decreased
Symptomtext
Pt. states that after receiving the 3rd dose of Phizer 12/03/2021, started experiencing symptoms 12/09/2021 of shortness of breath and fluttering in the heart. Still experiencing symptoms, No noted Primary visit/communications. (Previous 1st dose of Phizer 04/05/2021. 04/21/2021 Blood Work = White Blood Cell count Low)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multi-Vitamins
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Hypoaesthesia
Joint swelling
Pain in extremity
Paraesthesia
Swelling
Swollen tongue
Symptomtext
right side of tongue started to swell; right side of my face became tingling; right side of my face became tingling and a numb feeling.; Next day sore arm; tired; left back and hip swelling; left back and hip swelling; This is a spontaneous report from a contactable reporter (consumer or other non hcp). The reporter is the patient. A 45-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 28Nov2021 at 14:30 (Lot number: 33030BD) at the age of 45 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Allergy" (unspecified if ongoing), notes: Known allergy: Zinc. The patient did not receive any medications within two weeks of vaccination. Past drug history included: Erythromycin, reaction: "Drug allergy", notes: Known allergies: Erythromycin. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 29Nov2021, outcome "recovered with sequelae" (30Nov2021), described as "Next day sore arm"; FATIGUE (non-serious) with onset 29Nov2021, outcome "recovered with sequelae" (30Nov2021), described as "tired"; SWELLING (non-serious), JOINT SWELLING (non-serious) all with onset 01Dec2021 at 10:00, outcome "recovered with sequelae" (an unknown date in Dec2021), and all described as "left back and hip swelling"; SWOLLEN TONGUE (non-serious) with onset 01Dec2021 at 10:00, outcome "recovered with sequelae" (an unknown date in Dec2021), described as "right side of tongue started to swell"; PARAESTHESIA (non-serious) with onset 01Dec2021 at 10:00, outcome "recovered with sequelae" (an unknown date in Dec2021), described as "right side of my face became tingling"; HYPOAESTHESIA (non-serious) with onset 01Dec2021 at 10:00, outcome "recovered with sequelae" (an unknown date in Dec2021), described as "right side of my face became tingling and a numb feeling". The events "Next day sore arm", "tired", "left back and hip swelling", "right side of tongue started to swell", "right side of my face became tingling" and "right side of my face became tingling and a numb feeling." were evaluated at the physician office visit. Therapeutic measures were taken as a result of pain in extremity, fatigue, swelling, joint swelling, swollen tongue, paraesthesia and hypoaesthesia which included treatment with BENADRYL every 4 hours. Additional Information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy (Known allergy: Zinc)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Blood pressure measurement
Chest pain
Headache
Hypertension
Hypoaesthesia
Immunisation
Pain
Tinnitus
Ulcer
Vomiting
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 70-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Nov2021 17:00 (Lot number: 33030BD) at the age of 70 years as dose 3 (booster), single for covid-19 immunization. Patients' medical history included rheumatoid arthritis, fibromyalgia, shrogen's syndrome, hypertension, heart murmur, ulcer, known allergies: Penicillin from an unknown date and unknown if ongoing. Concomitant medication(s) included: lisinopril; multivitamins, Nyquil, Tylenol, magnesium. past drug history included: morphine, reaction(s) include known allergies: morphine, Demerol, reaction(s): known allergies: Demerol, tramadol, reaction(s): known allergies: tramadol, stadol, reaction(s): known allergies: stadol. Patient previously received Bnt162b2 (COVID 19, Pfizer, lot number=EW0167, location=Left arm), on 21Mar2021, at 12:00 am, when the patient was 74 years old, as DOSE 1 SINGLE, for COVID-19 immunization and Bnt162b2 (COVID 19 immunization, Pfizer, lot number=EW0167, location=Left arm) as DOSE 2, SINGLE, on 29Apr2021 at 12:00 am, when the patient was 70 years old, for Covid-19 immunization. On 20Nov2021patient experienced dose number: 3, On 20Nov2021 12:00 Persistent hypertension even with Lisinopril. Was taking 15mg OD (had weaned down over past year from 30mg BID) Had to go back to 30mg BID. Still ranging from 180/110 to 140/90, PVC's chest pain, left arm numbness with tinnitus, left arm numbness with tinnitus, headache, Aggravated ulcer with abdominal pain, vomiting, Multiple joints and muscles painful, Aggravated ulcer with abdominal pain. Patient underwent lab tests and procedures which include blood pressure measurement 180/110 to 140/90 on an unspecified date. Therapeutic measures were not taken as a result of hypertension, chest pain, hypoesthesia, tinnitus, headache, abdominal pain, vomiting, pain. The outcome of events was not recovered. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood pressure; Result Unstructured Data: Test Result:180/110 to 140/90
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Fibromyalgia; Heart murmur; Hypertension; Penicillin allergy; Rheumatoid arthritis; Syndrome Sjogren's; Ulcer
- Andere Medikamente
- LISINOPRIL; MULTIVITAMINS [VITAMINS NOS]; NYQUIL; TYLENOL; MAGNESIUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Immunisation
Vaccination site bruising
Vaccination site discomfort
Vaccination site erythema
Vaccination site pain
Vaccination site pruritus
Symptomtext
bruise about injection site and red spot underneath; bruise about injection site and red spot underneath; bruise right about injection site which she is not comfortable about; she got the booster; it is about 5 inches by 1 inch and is just getting bigger, wants to know if this is norma/bruise that is slightly above the injection site and a red spot that is getting worse; itchy/itches below the injection site that is painful; itchy/itches below the injection site that is painful; 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 71 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 19Nov2021 (Lot number: 33030BD) as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Second dose, LOT-ER8731), administration date: 22Apr2021, for Covid-19 immunization, reaction(s): "tired", "sore arm"; Bnt162b2 (First dose, LOT-ER8735), administration date: 01Apr2021, for Covid-19 immunization. The following information was reported: VACCINATION SITE BRUISING (non-serious), VACCINATION SITE ERYTHEMA (non-serious) all with onset 20Nov2021, outcome "not recovered" and all described as "bruise about injection site and red spot underneath"; VACCINATION SITE PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "itchy/itches below the injection site that is painful"; VACCINATION SITE PRURITUS (non-serious) with onset Nov2021, outcome "unknown", described as "itchy/itches below the injection site that is painful "; VACCINATION SITE DISCOMFORT (non-serious) with onset 20Nov2021, outcome "not recovered", described as "bruise right about injection site which she is not comfortable about"; CONDITION AGGRAVATED (non-serious) with onset Nov2021, outcome "not recovered", described as "it is about 5 inches by 1 inch and is just getting bigger, wants to know if this is norma/bruise that is slightly above the injection site and a red spot that is getting worse"; IMMUNISATION (non-serious) with onset 19Nov2021, outcome "unknown", described as "she got the booster". Follow-up attempts are completed. 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, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Pain in extremity
Paraesthesia
Peripheral swelling
Symptomtext
woke up morning after vaccine c/o parasthesias in bilateral lower legs came in to office for full neurologic exam which was normal. full sensation, no weakness also had the normal arm pain and swelling of left upper extremity
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Full neurologic exam, EKG, no laboratory test 12/4/2021
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- pistachio cashew
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Tremor
Symptomtext
Shortness of breath, sharp pains in chest area, quivers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Sulfa.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Limb injury
Pain
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Mobility decreased
Pain
Skin discolouration
Symptomtext
Large white circle on skin on the underneath side of injection site just below the tricep muscle; swollen lymph node in armpit with extreme pain and restricting movement
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- No tests - consulted with physician 12/6/2021 who confirmed it is a swollen lymph node protruding from my left armpit with other deeper nodes also likely swelling contributing to the pain and restriction of movement
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec allergy medication
- Allergien
- Flonase Augmentin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Migraine
Vomiting
Symptomtext
Light fewer and in case of that (I guess) a strong migraine attack with vomit. In case of pain relief 200mg ibuprofen has been taken.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Chest discomfort
Chest pain
Dizziness
Dyspnoea
Headache
Hypertension
Injection site pain
Tachycardia
Symptomtext
Site: Pain at Injection Site-Severe, Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Abdominal Pain-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Headache-Medium, Systemic: Hypertension-Medium, Systemic: Tachycardia-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 05.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Chest pain
Disorientation
Dizziness
Dyspnoea
Fatigue
Headache
Hyperhidrosis
Lip discolouration
Myalgia
Pain in extremity
Pruritus
Pyrexia
Vomiting
Symptomtext
1st dose: could not lift left arm after vxn for 2 days due to pain in arm and had sinus issues. 2nd dose: Had arm pain for 3 days past having vaccine, have sweats, trouble breathing, chest pain, white lips, headache, subcutaneous itching under skin, felt feverish, fatigue, muscle pain, weakness, dizziness, vomiting, and disorientation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chesapeake Regional Health Center- ER
- Aktuelle Erkrankungen
- Hashimoto's Thyroiditis (Hypothyroidism) Asthma History of Pericarditis Endometriosis
- Vorgeschichte
- Hashimoto's Thyroiditis (Hypothyroidism) Asthma History of Pericarditis Endometriosis
- Andere Medikamente
- Effexor Levoxyl Montelukast
- Allergien
- Penicillin Doxycycline Lactose intolerant Rosemary
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal dreams
Chills
Dyspnoea
Fatigue
Heart rate increased
Hyperhidrosis
Impaired work ability
Migraine
Pulse abnormal
Pyrexia
Symptomtext
high heart rate at rest (approx 150; Chills; fatigue; migraine; pulse ox; shortness of breath; very vivid dreams; sweats like a fever; sweats like a fever; could not function; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An adult female patient received bnt162b2 (BNT162B2), administration date 19Nov2021 (Lot number: 33030BD) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Er8735), administration date: 07May2021, for COVID-19 immunisation; Bnt162b2 (Dose Number: 1, Batch/Lot No: Ew0150), administration date: 16Apr2021, for COVID-19 immunisation. The following information was reported: HEART RATE INCREASED (non-serious) with onset 20Nov2021, outcome "recovering", described as "high heart rate at rest (approx 150"; CHILLS (non-serious) with onset 20Nov2021, outcome "recovering", described as "Chills"; FATIGUE (non-serious) with onset 20Nov2021, outcome "recovering", described as "fatigue"; MIGRAINE (non-serious) with onset 20Nov2021, outcome "recovering", described as "migraine"; PULSE ABNORMAL (non-serious) with onset 20Nov2021, outcome "recovering", described as "pulse ox"; DYSPNOEA (non-serious) with onset 20Nov2021, outcome "recovering", described as "shortness of breath"; ABNORMAL DREAMS (non-serious) with onset 20Nov2021, outcome "recovering", described as "very vivid dreams"; HYPERHIDROSIS (non-serious), PYREXIA (non-serious) all with onset 20Nov2021, outcome "recovering" and all described as "sweats like a fever"; IMPAIRED WORK ABILITY (non-serious) with onset 20Nov2021, outcome "recovering", described as "could not function". Therapeutic measures were not taken as a result of heart rate increased, chills, fatigue, migraine, pulse abnormal, dyspnoea, abnormal dreams, hyperhidrosis, pyrexia, impaired work ability. Additional Information: It was reported that name of drug as reported was no with reaction: allergy. Seriousness criteria was reported as no for death, life threatening, caused/prolonged hospitalization, disabling/Incapacitating, congenital anomaly/birth defect. Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. Reporter stated that I had only minimal reactions with the first two shots. I won't be getting a fourth shot! Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. 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
- FLU
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Injection site pruritus
Injection site rash
Symptomtext
rash and itchiness appeared at the injection site 4 days later, on Tuesday night patient begin to experience sharp pinching pain around the heart area, patient called the pharmacy on 12/02/2021 around 7 pm and was advised to have the chest pain check up, rash is normal and she can take benadryl but chest pain need to be check out. patient then went to urgent care and is awaiting examination, follow up with patient at 8:30pm but she has not been seen by the doctor yet, only put in the room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- no information
- Aktuelle Erkrankungen
- 2 weeks ago patient was seen be her doctor for sharp pain in the right chest area and md ruled as possible viral infection, she was in quarantine because her coworker was positive for covid 19. all of her tests come back negative
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- latex allergy
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Tachycardia
Symptomtext
Patient went to observation area, after receiving third dose of Pfizer vaccine and reports feeling tachycardia. Head nurse is notified at 1:00pm and called Dr. who indicated to reposition patient on Trendelenburg position and to keep patient in observation for 30 minutes and then reevaluated. At 1:48pm patient is reevaluated and head nurse notified Dr. and discharged patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- high pressure
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Pain in extremity
Paraesthesia
Symptomtext
Skin on my left arm and upper back feels prickly when touched. It's like someone has replaced the hair on my left arm and upper back with needles. The slightest touch to my skin or hair feels like needles are being inserted and wiggled around. The sensation only lasts as along as touch is being applied. I also have arm pain at (and 3 inches around) the injection site, but that has been reported by others and is listed as a currently known side effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- I have not had any additional testing for this adverse event.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity, Degenerative Joint Diesase, Gastritis
- Andere Medikamente
- Pregabalin, Methocarbamol, Tramadol, Omeprazole
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 18.08.2023
- Impfdatum
- 08.12.2021
- Beginn
- 24.06.2023
- Tage bis Beginn
- 563,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
COVID-19
Fall
SARS-CoV-2 test positive
Symptomtext
6/21/2023 - 6/24/2023 (3 days) evaluation of left hip pain post mechanical fall at the ALF patient tested positive on a transfer screen, and then on the same day tested negative on a transfer screen. no treatment was required. EN6198 3/1/2021 ER8727 3/22/2021 33030BD 12/8/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 05.02.2023
- Impfdatum
- 01.09.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 181,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Arthralgia
Blood test
Fatigue
Feeling abnormal
Myalgia
Symptomtext
Extreme fatigue 3 to 4 times a week, must lay down for several hours and rest Brain fog, short-term memory loss Muscle and joint pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Doctors can not explain any of these issues via blood work tests Doctors have not been much help
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high bp - low thyroid
- Andere Medikamente
- bp med - thyroid med
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 16.01.2023
- Impfdatum
- 26.11.2021
- Beginn
- 30.04.2022
- Tage bis Beginn
- 155,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Impaired work ability
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Sinus congestion
Throat irritation
Symptomtext
I received my first Pfizer COVID-19 booster on 11/26/2021. On 4/30/2022, I woke up with a sore throat. I found out that some people I had socialized with recently had tested positive for COVID-19, so I decided to test myself. I took a home antigen test, and it was positive. I was out of work for a week, and by the time 5/4/2022 rolled around, I was pretty much back to normal. For the most part, my illness was very mild. I started off with a scratchy throat, which went away. I then had sinus congestion and runny nose, but I don't remember sneezing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 4/30/2022 home antigen test positive result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension.
- Andere Medikamente
- Losartan; CENTRUM for men 50+.
- Allergien
- Aspirin sensitivity.
- Vorherige Impfungen
- After I got the second dose of the Shingrix shot, I had a really sore arm and a fever that lasted for a couple of hours.
- Staat
- SC
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 17.12.2021
- Beginn
- 23.10.2022
- Tage bis Beginn
- 310,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Respiratory symptom
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 around 10 months after receiving the COVID-19 vaccine I had breathing issues and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Rapid COVID-19 test was positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin; furaneol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 18.12.2022
- Impfdatum
- 11.01.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 202,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood immunoglobulin A
Blood immunoglobulin M
Blood test
Dry eye
Dry throat
Eye pain
Facial pain
Laboratory test
Lacrimation decreased
Loss of personal independence in daily activities
Neck pain
Oropharyngeal pain
Schirmer's test abnormal
Sjogren's syndrome
Strabismus
Throat irritation
Symptomtext
Dry eyes and throat got painful in August 2022 after being dry and itchy and light pain for a few months. Went to rheumatology and ophthalmologist for eyes and blood work up. Sjogrens diagnosed Corneas painful very dry eyes not producing tears . On Xiidra twice a day from Sept 8, 2022 and artificial tears 10 times a day at least. Starting Vital Tears biological on Tuesday. Squinting eyes tightly which has caused facial and neck pain from tightening so much with no moisture . Eyes are bone dry on tear test, (schirmers test) corneas very dry painful . Outdoor activities are zero as this affects my eyes greatly causing much corneal pain with facial contortions due to the lack of tears and pain in eyes. Affecting glands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- Salivary Protein. 1. IGM. Carbonic Anhydrase VI IGA Parotid Specific Protein IGA
- Aktuelle Erkrankungen
- No illness
- Vorgeschichte
- Asthma since childhood no episodes for the last 10 years
- Andere Medikamente
- Bioflavonoids 1000 mg 3 times a week. Magnesium 250 mg 2 tablets per day. Vitamin D 3 2000 IU per day Vagifem 10 mcg. 3 times a week. Pepcid 10-20 mg per day split dose. Fiorocet as needed only head/neck pain.
- Allergien
- Neomycin. Iodine Contrast. Sunflower seeds/Pineapple/Shellfish/Pistachios/ Cashews/Sesame Seeds/Peaches
- Vorherige Impfungen
- Shringvrix
- Staat
- IL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 11.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Computerised tomogram head abnormal
Head discomfort
Headache
Hyperacusis
Muscle twitching
Photophobia
Sleep disorder
Symptomtext
After getting vaccine on the day of 11/11/21 about hour or so later I felt my lip twitch or tremor like. About a week less later, 11/16/1021 about 3;00 am in the morning. I had a SEVERE EXTREME Headache woke me out of my sleep, I layed on my floor, pain was EXTREME hurt terribly. light and sound was unbearable and went away after laying there for two or three hours. 12/15/2021 SEVERE Headache, painful not as severe as previous headache. Went to emergency room. ABNORMAL CT Scan. headaches has been ongoing since vaccination. Headache pain, and pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- abnormal CT Scan Brain
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- pre-hypertension controlled
- Andere Medikamente
- none
- Allergien
- Allergic to (black) hair Dye
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 03.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Bacterial test
Computerised tomogram
Depression
Dizziness
Fall
Gait disturbance
Investigation
Laboratory test
Muscular weakness
Symptomtext
Depression/Severe depression; Body weakness; Dizziness; Falling; severe weakness in my arms and legs; she can barely walk; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. A 65-year-old female patient received BNT162b2 (BNT162B2), on 03Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 65 years for covid-19 immunisation. The patient's relevant medical history included: "Thyroid issues" (unspecified if ongoing); "Defibrillator/pacemaker insertion" (unspecified if ongoing); "muscular dystrophy" (unspecified if ongoing), notes: she had muscular dystrophy; "Parkinson's" (unspecified if ongoing), notes: Parkinson's. Concomitant medication(s) included: CLONAZEPAM; ALPRAZOLAM. Vaccination history included: BNT162b2 (First Dose, Lot EN6199), administration date: 05Mar2021, when the patient was 65-year-old, for COVID-19 immunization, reaction(s): "Severe depression", "Body is weak in the leg, arms, hands/ weakness", "She can barely walk", "Falling several times", "Dizziness"; BNT162b2 (Second Dose, Lot ER8733), administration date: 26Mar2021, when the patient was 65-year-old, for COVID-19 immunization, reaction(s): "Dizziness", "Falling several times", "Severe depression", "She can barely walk", "Body is weak in the leg, arms, hands/ weakness". The following information was reported: DEPRESSION (non-serious), outcome "not recovered", described as "Depression/Severe depression"; ASTHENIA (non-serious), outcome "not recovered", described as "Body weakness"; DIZZINESS (non-serious), outcome "not recovered"; FALL (non-serious), outcome "not recovered", described as "Falling"; MUSCULAR WEAKNESS (non-serious), outcome "unknown", described as "severe weakness in my arms and legs"; GAIT DISTURBANCE (non-serious), outcome "not recovered", described as "she can barely walk". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: Daughter which is the caregiver for her mom wanted to know if the onset of depression, body weakness, dizziness and falling were related to the vaccine. Reporter then stated being interested in knowing if there was anything to do to reverse the side effects and how long the vaccine stays in the system. Ever since she has gotten it or actually every time she has gotten each dose, she experiences severe depression, her body is weak in the leg, arms, hands to the point she can barely walk and is falling several times. She also experiences dizziness each time, between the dizziness and weakness she has fallen a few times because of it. Caller is wondering if there is anything she can do to reverse the side effects or help. Caller states that her mom has had 5 doses of the COVID vaccine and all of them are Pfizer. Third Dose: Date 03Dec2021 Lot is either 33030BD or 33030DD. The reporter clarified that only the Fifth dose was the Pfizer COVID Bivalent Vaccine. The Fifth dose was the worst for her as of side effects. Doses One to Four were the Monovalent COVID Vaccine. Caller also clarified that each time with each dose, with the last dose being the worst, but each time her mom would experience Depression, Body weakness, and dizziness. She was 65 when she got her first dose, she is 66 at the moment. During the call, caller's mom withheld says she thought she had muscular dystrophy or something like that. The Dizziness is on and off, it is not constant. The side effects happen with each vaccination, however the start of the side effects typically started a few days after getting the vaccine and gets worse. Investigation: She recently had a brain scan clarifying it was actually a CT scan of the brain, back and neck. She also had labs done since she is suppose to be having her hip replaced next Friday. The CT scans results had nothing, when it came back, besides showing that she has some deterioration in the hips. For the labs, she recalls is was Blood work and they did a bacterial swab, she cant remember what bacteria she was positive for but she had an infection, The CT scans and lab work was back in Sep2022 she is guessing since the doctor appointment was in early Oct2022. The patient had no allergies. Reporter states that her mom asked the doctor if she had muscular dystrophy, the doctor ruled that out, the doctor also said Parkinson's is ruled out, He ruled out all of that and said its not what it is, they don't know what it was, but just noticed it comes on every time she gets the covid vaccines. Furthermore, it was reported that Since patient started the vaccine, she overcome with depression, dizziness, and severe weakness in her arms and legs. She have fallen many times due to the weakness and dizziness. She received her last dose of the Pfizer vaccine on Wednesday 26Oct. The next day her depression was out of control and she could hardly walk. She came to realize it was the vaccine causing her problems.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201296028 Same patient, different dose and event.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Test Name: Bacterial swab; Result Unstructured Data: Test Result:had an infection.; Comments: she cant remember what bacteria she was positive for but she had an infection.; Test Name: CT scan; Result Unstructured Data: Test Result:Not Provided; Comments: Had a brain scan clarifying it was actually a CT scan of the brain, back and neck. The CT scans results had nothing, when it came back,; Test Name: CT Scan Hip; Result Unstructured Data: Test Result:some deterioration in the hips; Comments: besides showing that she has some deterioration in the hips.; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown result; Test Name: Lab Work; Result Unstructured Data: Test Result:Unknown Result; Comments: She also had labs done
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Defibrillator/pacemaker insertion; Muscular dystrophy (she had muscular dystrophy); Parkinson's disease (Parkinson's); Thyroid disorder
- Andere Medikamente
- CLONAZEPAM; ALPRAZOLAM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 11.11.2022
- Impfdatum
- 06.04.2021
- Beginn
- 16.09.2022
- Tage bis Beginn
- 528,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
COVID-19
SARS-CoV-2 test positive
Symptomtext
09/16/22 presents to ED for "abdominal pain". PMHx of "enteritis"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 09/17/22 SARS-CoV-2 (COVID-19) detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 23.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Erythema
Inflammation
Pain in extremity
Peripheral swelling
Pruritus
Rheumatoid arthritis
Symptomtext
all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day; all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day; all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day; all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day; all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day; all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Nov2021 at 19:00 as dose 3 (booster), single (Lot number: 33030BD) at the age of 48 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (prev dose lot number=EW0175,, prev dose administration time=05:00 PM,, prev dose dose number=2,, prev dose vaccine location=Left arm), administration date: 23Apr2021, when the patient was 48-year-old, for COVID-19 immunization; BNT162b2 (prev dose lot number=Er8730,, prev dose administration time=12:00 PM,, prev dose dose number=1,, prev dose vaccine location=Left arm), administration date: 01Apr2021, when the patient was 48-year-old, for COVID-19 immunization. The following information was reported: RHEUMATOID ARTHRITIS (medically significant), PERIPHERAL SWELLING (non-serious), INFLAMMATION (non-serious), PAIN IN EXTREMITY (non-serious), PRURITUS (non-serious), ERYTHEMA (non-serious) all with onset 24Nov2021, outcome "recovered with sequelae" and all described as "all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day". The events "all my fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood test: Unknown results. Therapeutic measures were taken as a result of rheumatoid arthritis, peripheral swelling, inflammation, pain in extremity, pruritus, erythema. Clinical course: On 24Nov, all of patient fingers were swelling, it started swelling on one hand each fingers, it red inflammation sore hurt and itchy all fingers all day, patient was treated with steroids medication and symptoms was referred to a Rheumatologist. Patient has been tested with many types of blood test to find out what caused the illness. Patient was treated with RA medication (Simponi) for 6 months from Mar2022, Sep2022 then had switched to Methotrexate on 22Oct2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Name: blood test; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Hallucination
Headache
Hordeolum
Pain
Vomiting
Symptomtext
Severe body aches, headache, vomiting. Hallucination, chills eye styes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Wellbutrin Losartin, Omeprozal
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 18.06.2022
- Impfdatum
- 09.12.2021
- Beginn
- 15.06.2022
- Tage bis Beginn
- 188,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Back pain
Chills
Cough
Headache
Lethargy
Loss of personal independence in daily activities
Vaccination site pain
Symptomtext
Sore arm at injection site; aching across my back (from waist to neck); chills; headache; no energy to get up out of bed; no energy to get up out of bed; some coughing; lethargic; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Dec2021 at 10:00 as dose 3 (booster), single (Lot number: 33030BD) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High Cholestrol" (unspecified if ongoing), notes: other medical history: High Cholestrol; "low thkyroid" (unspecified if ongoing), notes: other medical history: low thkyroid; "acidic stomach" (unspecified if ongoing), notes: other medical history: acidic stomach. Concomitant medication(s) included: LEVOTHYROXINE; ATORVASTATIN; PROTONIX [OMEPRAZOLE]. Past drug history included: Pseudoephedine for loss of breath, reaction(s): "Known Allergies: pseudoephedine", notes: known allergies: pseudoephedine-loss of breath. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EN6206, Location of injection: Arm Left, Vaccine Administration Time: 10:15 AM), administration date: 09Mar2021, for Covid-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: not listed, Location of injection: Arm Left, Vaccine Administration Time: 01:30 PM), administration date: 11Feb2021, for Covid-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 15Jun2022 at 01:00, outcome "recovering", described as "Sore arm at injection site"; BACK PAIN (non-serious) with onset 15Jun2022 at 01:00, outcome "recovering", described as "aching across my back (from waist to neck)"; CHILLS (non-serious) with onset 15Jun2022 at 01:00, outcome "recovering"; HEADACHE (non-serious) with onset 15Jun2022 at 01:00, outcome "recovering"; LETHARGY (non-serious) with onset 15Jun2022 at 01:00, outcome "recovering", described as "lethargic"; ASTHENIA (non-serious), LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) all with onset 15Jun2022 at 01:00, outcome "recovering" and all described as "no energy to get up out of bed"; COUGH (non-serious) with onset 15Jun2022 at 01:00, outcome "recovering", described as "some coughing". Therapeutic measures were taken as a result of vaccination site pain, back pain, chills, headache, asthenia, loss of personal independence in daily activities, cough, lethargy. Reported Event: Sore arm at injection site, aching across her back (from waist to neck), chills, headache, no energy to get up out of bed, some coughing and lethargic. Consumer did not have any of these effects when she got other Booster Shots. Consumer took withheld Brand Pain Relief pill before bed. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Device Date: 15Jun2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Acid reflux (oesophageal) (other medical history: acidic stomach); High cholesterol (other medical history: High Cholestrol); Thyroid hormones decreased (other medical history: low thkyroid)
- Andere Medikamente
- LEVOTHYROXINE; ATORVASTATIN; PROTONIX [OMEPRAZOLE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 16.12.2021
- Beginn
- 07.06.2022
- Tage bis Beginn
- 173,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Exposure during pregnancy
Lacrimation increased
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID-19 case: I had a sore throat and a cough. I took a rapid test and it came back negative. The next day it morphed into what I would describe was allergies. Runny nose, congestion, watering eyes. I would feel like I needed to sneeze, but couldn't and my eyes would water. I took TYLENOL. It did help a bit and I was able to go back to sleep. I tested again on 06/10/2022 and it came back positive. I contacted my OBGYN because I'm pregnant. I ended up getting monoclonal antibodies. I tested again on 06/15/2022 and it came back with a slight positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 06/07/2022: rapid test: negative. 06/10/2022: rapid test: positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D3; RITUAL prenatal
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 22.03.2021
- Beginn
- 01.06.2022
- Tage bis Beginn
- 436,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Injection site pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
No major adverse effects - mild pain at injection site for 2 days, overall mild fatigue for maybe 2 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- This form is not going to convey the information correctly. It doesn't even ask the dates of the vaccinations nor let me clarify the Pfizer shot was a booster more than 6 months after my original vaccinations. Nor is this form letting me clarify that the whole reason I was asked to report was because on 6/1/2022, the day I'm reporting issues, was because I was diagnosed positive with Covid. But the person who called me said to use this form for "breakthrough" covid cases. But it seems to only be for reporting adverse effects to the vaccinations. Again with question #20, the adverse event is Covid and as of 6/10 I'm still working through it.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 07.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
COVID-19
Eye disorder
Fatigue
Influenza
Loss of personal independence in daily activities
Pain
Pain in extremity
SARS-CoV-2 test positive
Somnolence
Visual impairment
Symptomtext
After getting the vaccine I had soreness in my arm. Then I had caught Covid 2 days later. I had body aches, was super tired, and I felt like I had the flu. It took about 3 or 4 days before I got over it. I had slept for 3 days. Right after Covid symptoms went away I have been really fatigued. My body is just tired all the time. My left eye is always in a fog. My joints hurt. I think I may have a little arthritis, but my joints hurt in places they never hurt before. Sometimes I took some TYLENOL. I think I have a high tolerance for medication so if I get something it has to be kind of strong to work. I feel like I can't get as much done as I used to. I'm still having issues with my joints and vision that is ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Covid test positive (12/9/2021).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; Bladder Cancer
- Andere Medikamente
- Gabapentin; amlodipine; lisinopril; tamsulosin
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 03.12.2021
- Beginn
- 20.04.2022
- Tage bis Beginn
- 138,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Headache
Lower respiratory tract infection
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had a headache and sore throat, my temperature moved to a second degree above normal (99), chest cold. I email my doctor and tell me to take TYLENOL for the fever and MUCINEX for the chest cold. I took it for 7-10 days. I was fever but I still have cough for 3 weeks. I still have flame. I have allergy season. I took the home test, and it was positive. I have COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Levothyroxine 50mcg daily; alendronate 70mg once a week
- Allergien
- Penicillin; Seasonal Allergy
- Vorherige Impfungen
- After a flu vaccine I was 54 yrs old and I had a temperature one week later.
- Staat
- GA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 03.06.2022
- Impfdatum
- 28.11.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 154,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Burning sensation
Herpes zoster
Rash
Stress
Symptomtext
Starting 05/01/2022, I started getting a rash on my leg. I thought it was an allergic reaction to something outside because I was working outside. It started spreading to the left side of my body and was burning. So, I decided to go to the clinic and they diagnosed me with Shingles. I was given an antiviral, valacyclovir, which I took for 7 days and it subsided. They said it was most likely a stress reaction due to my father passing away. The pain and the rash remained on my left side and never spread to the other side of my body during this event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Sertraline HCL 100mg QD; Adderall XR 25mg QD; testosterone injections 2x weekly
- Allergien
- Cefzil
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 09.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pain in extremity
SARS-CoV-2 test
Symptomtext
The pain in legs and muscles started in Dec2021 or Jan2022; The pain in legs and muscles started in Dec2021 or Jan2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 62-year-old male patient received BNT162b2 (BNT162B2), on 09Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 61 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: high blood pressure diagnosed about twenty years ago; "Immunization" (unspecified if ongoing). Concomitant medication(s) included: RAMIPRIL oral taken for hypertension, taking for 20 years; METOPROLOL TARTRATE oral taken for hypertension, taking for 20 years; SHINGRIX taken for immunisation; FLU VACCINE VII. Vaccination history included: BNT162b2 (First dose Pfizer covid 19 vaccine: 17Apr2021, Lot: EW0162, Expiration: 31Jul2021, NDC: unknown), administration date: 17Apr2021, for COVID-19 immunization; BNT162b2 (Second dose Pfizer covid 19 vaccine: 22May2021, Lot: EW0177 (populated lot number), Expiration: 31Aug2021), administration date: 22May2021, for COVID-19 immunization, reaction(s): "mental brain fog"; BNT162b2 (Second dose Pfizer covid 19 vaccine: 22May2021, Lot: EW0177 (populated lot number), Expiration: 31Aug2021), administration date: 22May2022, for COVID-19 immunization, reaction(s): "having electric shock in the feet / sharp pain pain and very brief sensation", "cognitive disorder/disassociated disorder", "pain in the joints and muscles", "pain in the joints and muscles", "mental issues". The following information was reported: PAIN IN EXTREMITY (non-serious), MYALGIA (non-serious), outcome "not recovered" and all described as "The pain in legs and muscles started in Dec2021 or Jan2022". The events "the pain in legs and muscles started in dec2021 or jan2022" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity, myalgia. Additional information: The report was not related to a study or programme. The event was ongoing, he took a pain tablet a week ago and the pain tablet lasts a week, so his pain was not severe. He tried to avoid taking medication. No family medical history relevant to AE(s). He tested multiple times and haven't had covid.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200750480 similar report from same reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- Test Name: covid-19 test; Result Unstructured Data: Test Result:haven't had covid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (high blood pressure diagnosed about twenty years ago); Immunization
- Andere Medikamente
- RAMIPRIL; METOPROLOL TARTRATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 27.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Blood pressure abnormal
Fatigue
Headache
Influenza like illness
Pain in extremity
SARS-CoV-2 test negative
Symptomtext
So at the time I was having fatigue and basically all flu like symptoms with joint pain and headache. It last 24 hrs. and fatigue for 2 days. It went away and I also had arm soreness. I went and saw the doctor within a week, but I don't have the exact dates. I did get a COVID-19 test but it was negative. I am having blood pressure issues now kinda out of nowhere and the doctor says that is worth looking at since the COVID-19 is known to increase blood pressure but no one knows for sure. No medication has been prescribed but was referred to a nephrologist in case it has something to do with a kidney infection. That appointment has not happened yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 test negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Lessina birth control; Claritin
- Allergien
- Penicillin; doxycycline
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 05.01.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 140,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Nausea
Vomiting
Symptomtext
Nausea, Vomiting, chills started on 5/25/22. Treatment includes: ST/PT consult, IV zosyn and monitoring in hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 24.11.2021
- Beginn
- 10.05.2022
- Tage bis Beginn
- 167,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bronchitis
COVID-19
Chills
Cough
Dysstasia
Fatigue
Feeling abnormal
Head discomfort
Headache
Malaise
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID on 05/12/2022. At first I thought I was having bad allergies, because where I live is know for having bad allergy season. I was doing a lot of coughing and blowing my nose. I went to go to bed and I ache all over and I thought that was weird because I hadn't did anything to be sore. An I didn't think anything about it and then I went to work and I usually stand at my desk and work but I couldn't. By 9AM I got a call from one of my co-workers and she said that she had COVID. So I left work and went to the doctor. My symptoms were severe for the first 3 days. An now I would said that they are mild. I have a cough, head congestion, headache, body aches, fever, fatigue and chills. It has been 16 since days and am still feeling bad. I went back to the doctor on 05/25/2022 and they said that they believe it had turn into bronchitis. They didn't do a COVID test at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- PCR
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Progesterone 250mg, Estradiol 1mg, C-Testosterone SRC 2.5mg, Allegra, Ondatra, Muti Vitamin, Vitamin C, and Activated You Morning Complete.
- Allergien
- Dust mites
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 30.11.2021
- Beginn
- 24.04.2022
- Tage bis Beginn
- 145,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Loss of personal independence in daily activities
Muscle spasms
Symptomtext
I began having lower back pain and then severe, excruciating muscle spasms in my lower back on 4/24/2022 that caused me to be unable to perform normal functions. I took Flexeril for several days, then began a Medrol pak prescription as prescribed by my PCP, which resolved the worst of it. It was 5 months after my last vaccination, and I have had back pain in the past (though never this severe), so I would expect that it was unrelated to the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Claritin
- Allergien
- Ciprofloxacin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 22.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal distension
Abdominal pain upper
Biopsy pharynx
Gastrointestinal disorder
Laboratory test
Oesophagogastroduodenoscopy
Pain
Vomiting
Symptomtext
The day following the vaccine I began to feel stomach pain and my stomach was upset after eating. I vomited that night. The same thing the next day. I could only eat a very small amount of food and felt very very full. I vomited again then next day. Stomach pain and upset stomach pain continued for three weeks. I felt pain and digestive issues at each meal. It would come in waves. I saw the doctor after week 3. I was prescribed Pepcid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- nuclear medicine gastric solid food test - normal; EGD; upper endoscopy - mild non specific inflammation; biopsy from throat
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sjogren's Syndrome
- Andere Medikamente
- Multivitamin; Fish Oil; Flaxseed Oil; Vitamin C; Calcium; Metamucil
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 09.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Head discomfort
Headache
Symptomtext
Slight headache; Pressure headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 40-years-old female patient received bnt162b2 (BNT162B2), administered in deltoid left, administration date 09Dec2021 11:00 (Lot number: 33030BD) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1), for COVID-19 Immunization; Covid-19 vaccine (Dose 2), for Covid-19 Immunization. The following information was reported: HEADACHE (non-serious) with onset 09Dec2021, outcome "not recovered", described as "Slight headache"; HEAD DISCOMFORT (non-serious) with onset Dec2021, outcome "not recovered", described as "Pressure headache". Therapeutic measures were taken as a result of headache, head discomfort. Additional Information: It was reported that consumer went yesterday morning at 11:00 to get her PFIZER BOOSTER shot and everything was fine and then later on that night, she started getting a slight headache but then it went away and she went to bed and woke up with slight headache again. So, she took some IBUPROFEN and went back to bed and when woke up had a pressure headache and it was been like this all day long. When probed if consumer wanted to report this or have some medical query too, she stated that need to know if there was something she needs to do or was she supposed to be worried about it or mean if it was going to go away. About weight she stated her weight, she did not know how much she weighed. About anatomical site and route of administration, she stated, "You mean where I went in to get my PFIZER shot. Oh, it was kind of difficult to understand you, it was on my left shoulder. When probed for prior family medical history of same adverse event, she stated does anybody in my family have problem with like high blood pressure, yes actually her fianc?, he had his shot yesterday and he had the same symptoms as me. About treatment she stated that she used some Ibuprofen, dose used was 600mg. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.03.2022
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Site: Pain at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspepsia
Rash papular
SARS-CoV-2 test
Urticaria
Symptomtext
15 hrs later, woke with horrible itchy bumps all over my legs, hips and back. Then went away; 8 days later they came back - huge welts across my legs (depending on the day, front and back) buttocks, hips, thighs, stomach, arms, face, LIPS! - large welts; Horrible breath taking heartburn; This is a spontaneous report from a contactable reporter (consumer or other non-hcp). The reporter is the patient. A 59-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 25Jan2022 at 10:00 (Lot number: 33030BD) at the age of 59 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: PCN and "Sulfonamide allergy" (unspecified if ongoing), notes: Known allergies: Sulfa. Concomitant medications included: TYLENOL; VIT D3; VITAMIN K2 and B COMPLEX. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: UNKNOWN; Anatomical Location: Left arm; Administration time: 10:00), administration date: 07Aug2021, when the patient was 59 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: FD8448; Anatomical Location: Left arm; Administration time: 10:00), administration date: 28Aug2021, when the patient was 59 years old, for COVID-19 immunisation. The following information was reported: RASH PAPULAR (non-serious) with onset 26Jan2022 at 04:00, outcome "not recovered", described as "15 hrs later, woke with horrible itchy bumps all over my legs, hips and back. Then went away"; URTICARIA (non-serious) with onset 26Jan2022 at 04:00, outcome "not recovered", described as "8 days later they came back - huge welts across my legs (depending on the day, front and back) buttocks, hips, thighs, stomach, arms, face, LIPS! - large welts"; DYSPEPSIA (non-serious) with onset 26Jan2022 at 04:00, outcome "not recovered", described as "Horrible breath taking heartburn". The events "15 hrs later, woke with horrible itchy bumps all over my legs, hips and back. Then went away", "8 days later they came back - huge welts across my legs (depending on the day, front and back) buttocks, hips, thighs, stomach, arms, face, LIPS! - large welts" and "Horrible breath taking heartburn" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash papular, urticaria and dyspepsia. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Treatment for the reported events included Xyzal, Benadryl, Steroids, Pepcid, Singular, Hydroxyzine. Since the vaccination, the patient had been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash papular
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220217; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: PCN); Sulfonamide allergy (Known allergies: Sulfa)
- Andere Medikamente
- TYLENOL; VIT D3; VITAMIN K2 [MENAQUINONE-7]; B COMPLEX [VITAMIN B COMPLEX]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Illness
Nausea
Pain
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
For three days I became more I?ll than when I actually had Covid. Fever 102, nausea/vomiting, body aches with terrible headache. My headaches and fatigue have continued to this day. I later tested positive for covid 19 on 1/4/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Was prescribed phenergan and OTC medications to take.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Chronic back pain
- Andere Medikamente
- Only PRN meds
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Prior to vaccination Patient reported being light-headed following previous vaccination. After discussing with Patient and Mother, it was decided to vaccinate Patient in a recumbent position. Patient was placed on yoga mat on the floor, supine. Feet were elevated on a chair. Patient was vaccinated. Patient returned to a sitting position within five minutes but then reported feeling light-headed. He was returned to a supine position, and a cold compress was applied to his forehead. VS at 1910: HR-68, B/P-120/68, O2 Sat-97%, Room Air. Patient was observed for 20 minutes at which time he reported feeling better. VS at 1925: HR-102, B/P-106/56, O2 Sat-99% Room Air. HR was regular. Mother declined EMS. Instructions given to go to the ER if any further problems arise. Mother verbalized understanding. Patient exited site with Mother. Follow-up phone call made and spoke with Mother who stated Patient is feeling fine, ate a good supper, and has had no further problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Light-headed and nauseated following first vaccination
- Staat
- AZ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Influenza like illness
Pain
Pain in extremity
Tinnitus
Symptomtext
Stared with headache, body aches (flu like symptoms). After a couple of days I started hearing a high pitch sound in both ears. It was not loud at the time. The ringing in my ears has gotten worse over the past couple of weeks to the point where I felt I needed to contact my doctor. The doctor feels this is related to the booster shot so I am preparing this report per his request. I also have pain in my arms and legs (where they bend). I don't know how to describe this in text. I have had no treatment, but it's getting worse!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Levothyroxine; Finasteride.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Symptomtext
Patient stated he felt tired and needed to lay down, so he was assisted to a floor mat per RN. He remained oriented x3, then started feeling better. He sat up, drank water and ate a protein bar.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- BP: 110/78; HR: 84; R:16 and 02: 99%.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Lingering arm pain at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Dilaudid
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 22.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
The patient has had severe itching since soon after the vaccinations. Patient is being treated with first triancinolone 0.1% ointment starting on 12-10-2021 then fluocinonide 0.05% ointment starting on 1-28-2022 with no relief yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown. appeared in generally good health
- Vorgeschichte
- unknown. none reported on vaccine consent form
- Andere Medikamente
- Unknown, patient visited our pharmacy for immunizations only
- Allergien
- no known allergy reported
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 01.12.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 45,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eating disorder
Herpes zoster
Oral pain
Stomatitis
Symptomtext
The roof of my mouth became very painful. It was difficult to eat. Two days after initial symptoms I went to a dentist to find out what was going on. The Dentist indicated that I had chicken pox sores in my mouth,. She took photos and showed them to me. I had chicken pox as a child but had the full series of Shingrix vaccine about 2 years ago, The Dentist prescribed Acyclovir 400 MG 3 x a day for 10 days and a gargle with Dexamethasone 0.5mg/5ML 4 x a day for for 2 min each. Symptoms resolved in about 8 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- mild asthma
- Andere Medikamente
- Citalopram 10mg once a day
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Blood thyroid stimulating hormone
Blood uric acid
C-reactive protein
Laboratory test
Metabolic function test
Pain
Symptomtext
Next day (Dec. 1st, 2021) body aches, day after (Dec. 2nd, 2021) not as bad but still debilitating and has not improve to this day (Jan. 27th, 2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- On January 19th, 2022, these tests were done and the results do not explain my symptoms. COMPLETE BLOOD COUNT WITH DIFFERENTIAL TSH REFLEX COMPREHENSIVE METABOLIC PANEL URIC ACID CYCLIC CITRULLINATED PEPTIDE ANTIBODY RHEUMATOID FACTOR, QUANTITATIVE ANTI NUCLEAR ANTIBODY SCREEN WITH REFLEX ESR C-REACTIVE PROTEIN (INFLAMMATION)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroidism, vaso vagal sincope, asthma
- Andere Medikamente
- Armour Thyroid, fludrocortisone, acyclovir, aspirin, cod liver oil, collagen, COQ10, DHEA, ESTER C, glucosamine sulfate, mag64, slo-niacin, pregnenolone, SAM-e, Vitamin D3, VITAMIN-B COMPLEX, ZINC
- Allergien
- sulpha drugs, ceclor, penicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Dizziness
Symptomtext
Pt felt dizzy and light headed after receiving Pfizer booster. Pt vitals: BP 90/70, P56, 98% on room air, Glucose 90. Pt given water, ice pack, laid down with feet up. Approximately 10 minutes later patient reported feeling better and with assistance was moved from floor to chair. Vitals at 16:02 were 120/82, P59, 99% on room air. Pt remained in vaccination clinic until her mother arrived to pick her up. This nurse walked with patient to car. Pt reported feeling much better and mother assured this nurse that she would remain with patient all night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 18.11.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 25,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Blood test
Cardiac monitoring
Chills
Dizziness
Echocardiogram
Epistaxis
Fatigue
Feeling abnormal
Insomnia
Magnetic resonance imaging head
Throat irritation
Visual impairment
Vitamin B12 deficiency
Symptomtext
After getting the first dose it was about a day later i started with loss of taste all my liquids has a sort of gas taste and a slight burn sensation when i swallow, my fatigue which i already had from when I had covid back in April has gotten worse, after the second dose i started having bloody noses a few times a day could be coincidence with weather so I did try to keep the humidity in home but the bleeds were bad i have also been experiencing dizzy spells which I have had since having covid back in April but now have got worse to the point I started passing out. my vision has got worse after second dose, I find it hard to sleep yet my exhaustion is extremely bad to the point when i get home from work i do not eat I pretty much go strait to bed until next day , i am also experiencing cold chills not a normal cold but cold to the point that when a person says chilled to the bone I understand the term , to say i am miserable is an understatement. i have been working with dr they did echo heart monitor and standard blood work all they found is vitamin B12 deficiency so far , i have also had an MRI of the brain everything comes back fine, but i don't get what has changed? has anyone else had trouble like this?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- blood work done several times all good except B12 Deficincy brain MRI good echo Good heart monitor good
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PROZAC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 12.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Axillary mass
Axillary pain
Pyrexia
Symptomtext
Fever 102.9 for 8 hours, nothing would bring it down! Felt like I got hot by a speeding train for 5 days... had huge (softball size) hard, very painful mass in left armpit to side boob
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cyclic Vomiting Syndrome
- Vorgeschichte
- Cyclic vomiting syndrome, bipolar
- Andere Medikamente
- Phenergan 25mg daily
- Allergien
- Allergic to Sulfa
- Vorherige Impfungen
- Moderna
- Staat
- PR
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Mass
Pain in extremity
Peripheral swelling
Symptomtext
Big Lump under left arm. Swollen and painful; Big Lump under left arm. Swollen and painful; Big Lump under left arm. Swollen and painful; Booster; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 (Lot number: 33030bd) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Previous dose product: COVID 19, Previous dose brand: Pfizer , Previous dose brand unknown: False, Previous dose lot unknown: True, Previous dose lot unknown reason: Misplaced/discarded, Previous dose dose number: 2, Previous dose vaccine location: Left arm), for Covid-19 Immunization; Bnt162b2 (Previous dose product: COVID 19, Previous dose brand: Pfizer, Previous dose brand unknown: False, Previous dose lot number: 33030BD, Previous dose lot unknown: False, Previous dose dose number: 1, Previous dose vaccine location=Left arm), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 29Dec2021, outcome "unknown", described as "Booster"; MASS (non-serious), PERIPHERAL SWELLING (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 02Jan2022, outcome "not recovered" and all described as "Big Lump under left arm. Swollen and painful". Therapeutic measures were not taken as a result of mass, peripheral swelling, pain in extremity. Additional Information: other vaccine in four weeks reported as no. Ae resulted in reported as none of the above. covid prior vaccination and covid tested post vaccination reported as no. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 09.03.2021
- Beginn
- 09.03.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Today is Tuesday, January 18th, 2022. For the last 9 months, ever since my first COVID shot, my left arm has been stinging. Nearly each day, I am grabbing my left arm, at the injection site, in pain. The only treatments that I do are that I self-massage the injection site, multiple times each day. I stretch my arm out each day as well. Since I have gotten my booster shot, the pain has gotten worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Developed a rash on both arms, legs, hands, and feet. Denies itching or pain. Denies any other symptoms. Went to her PCP 1 week after vaccination. No treatment given. She has not taken any medication for the rash. The rash continues to this day, 01/14/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure abnormal
Dizziness
Immediate post-injection reaction
Nausea
Symptomtext
Patient reported feeling faint and nauseous immediately after receiving the Pfizer booster. Patient was escorted to the nurse clinic where he was assessed. Vitals were taken with soft BPs noted. Patient reported having a history of fainting and history of vasovagal after receiving vaccines. Patient was repositioned to a trendelenburg position and closely monitored. Patient reported feeling better and back to normal after a few minutes of rest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Optic neuritis
- Andere Medikamente
- Lexapro and flonase
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 28.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Grip strength decreased
Injection site pain
Joint stiffness
Musculoskeletal stiffness
Pain
X-ray normal
Symptomtext
soreness in body, right arm at injection site, joint stiffness in body, long lasting joint stiffness in both hands, right hand is worse in right thumb, index finger, ring finger and pinky. decreased grip strength in hands and achy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- X-ray on 12/14/21 and arthritis blood work. Xray came back normal and so did blood work.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes mellitus, hypothyroidism, hyperlipidemia
- Andere Medikamente
- levothyroxine, metformin, atorvastatin, novolog, lantus
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Muscular weakness
Symptomtext
Patient claims to have previous neurological conditions indicates he does not feel strength in the lower extremities and feels dizzy. It is taken s/v and it is instructed to remain seated resting initial patient who has no strength and is taken in a wheelchair to the vehicle of his mother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- Neurological conditions
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Headache
Hyperhidrosis
Hyperthermia
Symptomtext
69 year old patient orientated x3 states dizziness, sweating, headache and sensation of heat, 15 minutes after being vaccinated 180/90 BP 76P Dext is re-evaluated 140/70 BP, 16 R, 72 P, 36.8 Temp. 3608 again repeated. Patient is taking PANADOL form he's own belongings.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Metoprolol; Losartan; Simvastatin; Synthroid
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 18.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Patient has a rash on the back of her neck. She went to her doctor who prescribed a steroid cream which has improved the rash but it is still there. Her doctor ok'd the 2nd dose of the vaccine which she got today and waiting 30 minutes in case of severe reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 31.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Pain
Symptomtext
Mild body aches; Dose number 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). A 20-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in right arm, administration date 31Dec2021 (Lot number: 33030BD) at the age of 20 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EP6955; Route of administration: Unspecified), administration date: 27Mar2021, when the patient was 20 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot Number: EP6955; Route of administration: Unspecified), administration date: 17Apr2021, when the patient was 20 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 31Dec2021, outcome "unknown", described as "Dose number 3"; PAIN (non-serious) with onset 01Jan2022, outcome "recovering", described as "Mild body aches". Therapeutic measures were not taken as a result of pain. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- 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
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 05.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Lymph node pain
Lymphadenopathy
Vaccination site pain
Symptomtext
slight soreness on Left bicep at injection site; Third Shot - Swollen and tender lymph nodes on the Left axillary area began 24-30 hours after injection. (same side as injection arm) slight soreness on Left bicep at injection site; Swollen and tender lymph nodes on the Left axillary area began 24-30 hours after injection. (same side as injection arm); Third Shot; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Dec2021 21:30 (Lot number: 33030bd) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included ACCUTANE. No Past drug history included. Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot Number: EM9009, Location of injection: Arm Left, Vaccine Administration Time: 10:00, Left arm completely numb, sore, and unable to move for 24 hours, pain diminished after 72 hours.), administration date: 11Feb2021, for Covid-19 immunization, reaction(s): Left arm completely numb; Bnt162b2 (Dose 1, Batch/Lot Number: el8982, Location of injection: Arm Left, Vaccine Administration Time: 08:00, only slight bruise pain at injection site), administration date: 21Jan2021, for Covid-19 Immunization, reaction(s) pain at injection site. The following information was reported IMMUNISATION (non-serious) with onset 05Dec2021 21:30, outcome unknown, described as Third Shot; VACCINATION SITE PAIN (non-serious) with onset 07Dec2021 06:00, outcome not recovered; LYMPHADENOPATHY (non-serious) with onset 07Dec2021 06:00, outcome not recovered, described as same side as injection arm; LYMPH NODE PAIN (non-serious) with onset 07Dec2021 06:00, outcome not recovered. Therapeutic measures were not taken as a result of vaccination site pain, lymphadenopathy, and lymph node pain. The patient did not receive any other vaccines within four weeks prior to the vaccination. Patient reported had not diagnosed with COVID-19 prior to the vaccination. Since the vaccination, the patient had not tested for COVID-19. Patient had no other symptoms with the dose 3 vaccine. Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected. Linked Report(s) US-PFIZER INC-202101796151 similar report from same reporter; US-PFIZER INC-202101796133 similar report from same reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- ACCUTANE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- -
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Pain in extremity
Symptomtext
who received the booster dose of the Pfizer covid vaccine on "09Sep2021 around 5:00pm, within the 24 hours after receiving the vaccine, I started to intense pain under my left arm; who received the booster dose of the Pfizer covid vaccine on "09Sep2021 around 5:00pm, within the 24 hours after receiving the vaccine, I started to intense pain under my left arm; 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 32 year-old male patient received bnt162b2 (BNT162B2), administration date 09Dec2021 17:00 (Lot number: 33030BD) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, Single), for COVID-19 Immunization; Bnt162b2 (DOSE 2, Single), for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 09Dec2021 17:00, outcome "unknown", PAIN IN EXTREMITY (non-serious) with onset Dec2021, outcome "not recovered" and all described as "who received the booster dose of the Pfizer covid vaccine on "09Sep2021 around 5:00pm, within the 24 hours after receiving the vaccine, I started to intense pain under my left arm". Additional information: The patient was a 32-year-old patient who received the booster dose of the Pfizer covid vaccine on 09Dec2021 (discrepant information: also reported as 09Sep2021) around 17:00, within the 24 hours after receiving the vaccine, he started to intense pain under his left arm, the same he received the shot. It has mostly resolved, the intensity was not as bad, but he still feel it. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Chills
Cough
Diarrhoea
Headache
Immunisation
Nasal congestion
Pyrexia
SARS-CoV-2 test
Taste disorder
Respiratory tract congestion
SARS-CoV-2 test negative
Symptomtext
lost my sense of smell; Developed a cough; Congestion; Headache; Chills; Fever; I can taste some food but it must be strong in flavor; Booster; 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), administered in arm left, administration date 09Dec2021 12:15 (Lot number: 33030BD) at the age of 70 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Heart Disease" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL; PANTOPRAZOLE; ASPIRINE; COQ10 [ASCORBIC ACID;BETACAROTENE;CUPRIC OXIDE;MANGANESE SULFATE;SELENIUM;TOCOPHERYL ACETATE;UBIDECARENONE;ZINC OXIDE]; RAM. Past drug history included: Lipitor, reaction(s): "Known Allergy: Lipitor". Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EL9266, Location: Arm Right, Time: 01:00 PM), administration date: 25Feb2021, when the patient was 69 years old, for Covid-19 Immunization, reaction(s): "No adverse effect"; Bnt162b2 (DOSE 2, SINGLE, Lot Number: EN6199, Location: Arm Right Vaccine Administration, Time: 02:00 PM), administration date: 18Mar2021, when the patient was 69 years old, for Covid-19 Immunization, reaction(s): "No adverse effect". The following information was reported: IMMUNISATION (non-serious) with onset 09Dec2021, outcome "unknown", described as "Booster"; HEADACHE (non-serious) with onset 09Dec2021 17:00, outcome "not recovered", described as "Headache"; CHILLS (non-serious) with onset 09Dec2021 17:00, outcome "not recovered", described as "Chills"; PYREXIA (non-serious) with onset 09Dec2021 17:00, outcome "not recovered", described as "Fever"; COUGH (non-serious) with onset 10Dec2021, outcome "recovered" (13Dec2021), described as "Developed a cough"; NASAL CONGESTION (non-serious) with onset 10Dec2021, outcome "recovered" (13Dec2021), described as "Congestion"; ANOSMIA (non-serious) with onset 12Dec2021, outcome "not recovered", described as "lost my sense of smell"; TASTE DISORDER (non-serious) with onset 09Dec2021 17:00, outcome "not recovered", described as "I can taste some food but it must be strong in flavor". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of immunisation, headache, chills, pyrexia, cough, nasal congestion, anosmia, taste disorder. Additional information: The patient took no other vaccine in four weeks of Pfizer vaccine. On 09Dec2021 around 17:00 hours, the patient got a headache, chills, and a fever, which lessened in severity by 23:00 hours. On 10Dec2021, the patient developed a cough and congestion which diminished by 13Dec2021. On 12Dec21, when the patient awoke in the morning, lost sense of smell, which has not returned at this time 14Dec2021 13:00 hours. The patient can taste some food, but it must be strong in flavor. The patient had no adverse reactions to the first and second shots. The patient had a Covid 19 test on 12Dec2021 which was Negative. In the review, there was no date or time for the 3rd shot, which was 09Dec2021 12:15 hours. The patient did not have covid-19 prior vaccination. Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211212; Test Name: Nasal Swab; Test Result: Negative ; Comments: Covid test result- Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Heart disorder
- Andere Medikamente
- METOPROLOL; PANTOPRAZOLE; ASPIRINE; COQ10 [ASCORBIC ACID;BETACAROTENE;CUPRIC OXIDE;MANGANESE SULFATE;SELENIUM;TOCOPHERYL ACETATE;UBIDECA; RAM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 29.01.2021
- Beginn
- 01.02.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Discharge
Headache
Menstrual disorder
Pelvic pain
Premenstrual syndrome
Symptomtext
Longer and intermittent menstruation Change in discharge blood color PMS intense headaches pain in breasts and pelvic area
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Fibromyalgia
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- None
- Allergien
- Lobster
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Patient called me today on 1/6/2022 at the pharmacy stating she has pain in the arm at the injection site from the day she received the vaccine on 12/22/21 til now. She contacted the doctor who will see her in a week but her doctor said takes ibuprofen to help with pain or inflammation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Unknown
- Andere Medikamente
- NA
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 08.04.2021
- Beginn
- 02.01.2022
- Tage bis Beginn
- 269,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Nasal congestion
Oropharyngeal pain
Respiratory tract congestion
Symptomtext
sore throat, cough, stuffy nose, congestion. starting 1/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Tremor. History of first and second degree burn, right arm. History of frostbite- right great toe. Gout. Dyslipidemia.
- Andere Medikamente
- ?Atorvastatin Calcium 20 MG Tablet 1 tablet Orally Once a day ?Allopurinol 300 MG Tablet TAKE ONE TABLET BY MOUTH ONE TIME DAILY , Notes: Due for annual exam Nov 2021 Not-Taking ?Indomethacin 50 MG Capsule 1 capsule with food Orally t
- Allergien
- Amoxicillin: rash - Allergy
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 20.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ear pain
Tinnitus
Symptomtext
It eventually was an earache on right ear and it was outside the ear, not deep inside. Used hydrogen peroxide and used homeopathic Earache drops. That relieved it a little bit. 01/01/2022 it hurt unbearably bad. Went to Urgent care and he said that I packed it all in with the stuff I was using and he prescribed me an antibiotic and steroid. Neomycin and polymyxin B sulfate and hydrocortisone optic solution, USP. To this day, still have an earache, pain is not as bad. It wasn't just an earache, there was also tinnitus. ringing and pulsing in ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Synthroid; NuvaRing
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 03.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Parosmia
Taste disorder
Vomiting
Symptomtext
Weird smell and taste, vomiting. After receiving 2nd dose weird taste and smell disappeared.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Decreased appetite
Fatigue
Headache
Lymph node pain
Lymphadenopathy
Myalgia
Nausea
Neck pain
Pain in extremity
Peripheral swelling
Photophobia
Somnolence
Symptomtext
Chills, muscle aches, joint pain, severe headache, neck pain, nausea, arm swelling and soreness, severe fatigue began gradually that night. Next day, I had increased need to sleep, no appetite, headache and photophobia intensified. Axilla lymph node was swollen on side of injection, later, left neck lymph node became tender as well as the one on groin area. Back pain started. Side effects continued for 3 days. At the time of this writing (6 days after booster), muscle aches, joint pain have improved. All other symptoms continue. Most prominent are lymph node enlargement on axilla, groin, and neck, fatigue, headaches, and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None. Just treating with Tylenol and hydration.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Migraines, Osteoporosis
- Andere Medikamente
- Alendronate Sodium 70 mg tabs, Montelukast 10 mg tabs, Olopatadine Ophthalmic Drops, Topiramate 25 mg tabs, Zonisamide 100 mg tabs, Citracal, and Vitamin D 3.
- Allergien
- Peanuts, Penicillin, and Sumatriptan
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 07.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Lymph node pain
Lymphadenopathy
Symptomtext
Enlarged lymph nodes in the left are of the neck - still present a month later. Area is tender to the touch with noticeable erythema
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 31.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Fatigue
Symptomtext
low grade temp, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- blod clots
- Andere Medikamente
- xarelto
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 02.01.2022
- Impfdatum
- 10.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Heart rate increased
Mental fatigue
Night sweats
Pain
Pyrexia
Respiratory rate increased
Symptomtext
Fever, achiness, high mental and physical fatigue, night sweats, elevated respiratory and resting heart rate lasting approximately 10 days after Pfizer booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin, doxycycline
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 31.12.2021
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Injection site erythema
Injection site swelling
Symptomtext
patient says at injection site its swollen and red for now on 3rd day. he had no other "immune response" or side effects but is concerned about that the injection went in sub-q and not IM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental overdose
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
received a 30 mcg dose of the Pfizer COVID-19 vaccine (adult formulation-purple cap) instead of the recommended dose of 10 mcg from the orange cap; They had a vaccination error, instead of administering Pfizer kids for 11 year old they have administered Pfizer vaccines for 12; has a slight fever; This is a spontaneous report received from a contactable reporter (Pharmacist) from medical information team for a Pfizer sponsored program. A 10-year-old female patient received bnt162b2 (BNT162B2, solution for injection), intramuscular, administered in deltoid left, administration date 13Dec2021 (Lot number: 33030BD, Expiration Date: 30Dec2021) at the age of 10 years as dose number unknown, 30 ug single for covid-19 immunization. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PYREXIA (non-serious) with onset Dec2021, outcome "unknown", described as "has a slight fever"; ACCIDENTAL OVERDOSE (non-serious) with onset 13Dec2021, outcome "unknown", described as "received a 30 mcg dose of the Pfizer COVID-19 vaccine (adult formulation-purple cap) instead of the recommended dose of 10 mcg from the orange cap"; PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 13Dec2021, outcome "unknown", described as "They had a vaccination error, instead of administering Pfizer kids for 11 year old they have administered Pfizer vaccines for 12". Additional information: A 10-year-old female patient inadvertently received a 30-mcg dose of the Pfizer COVID-19 vaccine (adult formulation-purple cap) on 13Dec2021 between like 3:15 and 3:20 like around that time in afternoon instead of the recommended dose of 10 mcg from the orange cap. NDC number of COVID-19 Vaccine: 59267-1000-01. The patient did not receive any prior vaccinations within 4 weeks of covid vaccine. Follow-up attempts are completed. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenitis
Lymphadenopathy
Symptomtext
Very large inflammed lymph nodes in armpit with visible swelling and soreness to the touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Migraines, HSV, Depression, Seasonal Allergies
- Andere Medikamente
- Valtrex, Desvenlafaxine, Mucinex, Amoxycillin - Clav
- Allergien
- None
- Vorherige Impfungen
- 12 hrs of severe exhaustion resulting in bedrest, Age 44, 4/9/21, Pfizer SARCOV2 VAC Dose #2
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cough
Fatigue
Headache
Influenza virus test negative
SARS-CoV-2 test negative
Symptomtext
I had fatigue, headache, and cough. These symptoms lasted for about a week. I went to medical facility about. They checked me for the flu and exam me. I did a at home Covid-19 test, negative results.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Flu test, Covid-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Musculoskeletal stiffness
Myalgia
Pyrexia
Symptomtext
The patient received the Pfizer booster on Sunday 12/26/21. She woke up on Monday 12/27/21 with a severe headache that was not alleviated with Ibuprofen. She also has had fever, chills, muscle aches, and a stiff neck. These symptoms have persisted since Monday morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- oral contraceptive, multivitamin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash Generalized-Medium, Additional Details: Patient self reported to pharmacy on 12/29/21 - patient has been treating it with benadryl and triamcinolone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hyperhidrosis
Illness
Pyrexia
Sluggishness
Symptomtext
Sluggish, mild sick symptoms starting at 3pm the day after. Around 8pm fever up to 102 degrees, chills, sweating, etc fever broke after 24 hours. Roughly 1 week later felt completely better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Adderall, melatonin
- Allergien
- -
- Vorherige Impfungen
- Fever etc after 2nd covid shot (Pfizer)
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Additional Details: Patinet inidcated feeling a little light headed/dizzy, helped patient lay down and proved OJ, no allergic reaction was observed or reported by patient, per patient has history of feeling dizzy post vaccination, after OJ patient was oberseved for 30min and was without any symptoms or complicatoins, patient said he felt back to normal after OJ.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain upper
Back pain
Blood test
Computerised tomogram
Myalgia
Pain
Renal pain
Symptomtext
48 hours after being vaccinated, my muscles in my arm were really painful and sore abnormally. I couldn't pick up my newborn and then, I got a sharp pain by my kidney, and I felt like I was having labor contractions. I was in crippling pain, and nothing would relieve the pain. The pain radiated from my stomach to my back. Went to the ER the same day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Blood work 12-19-21 CT Scan with Contrast 12-19-21
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
COVID-19
Cough
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I had running nose, lower back pain, and cough. It has been mild in general. These are still ongoing. It has been 5 days now. I took the home COVID-19 test on Dec 24th, positive results. I also have a low-grade fever of 101.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Sleep Apnea, High Cholesterol
- Andere Medikamente
- Benaquir
- Allergien
- N/A
- Vorherige Impfungen
- flu
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Headache
Inappropriate schedule of product administration
Incorrect product formulation administered
Interchange of vaccine products
Symptomtext
Systemic: Fatigue-Medium, Systemic: Headache-Medium, Systemic: Weakness-Medium, Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-, Additional Details: Patient received first Moderna dose on 10/28/21 and received Pfizer dose 12/13/2021. Did not receive the same manufacturer for the first 2 dose series of the mRNA vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 26.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Nausea
Pain in extremity
Rash
Tinnitus
Vertigo
Symptomtext
Vertigo, tinnitus, nausea, rash on left-side of face, swollen left eye and pain in left underarm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Benign paroxysmal positional vertigo (BPPV); irritable bowel syndrome; psoriasis
- Andere Medikamente
- Enskyce birth control (once daily); Tylenol (3-4 hours after vaccine)
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- -
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Immunisation
Myalgia
Pyrexia
Symptomtext
Symptoms following booster shot; fever; headache; joint and muscle ache for >24hr; joint and muscle ache for >24hr; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51 year-old female patient received bnt162b2 (BNT162B2) (Lot number: 33030BD) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose number unknown, Unknown manufacturer), for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "Symptoms following booster shot"; PYREXIA (non-serious), outcome "unknown", described as "fever"; HEADACHE (non-serious), outcome "unknown", described as "headache"; ARTHRALGIA (non-serious), MYALGIA (non-serious), outcome "unknown" and all described as "joint and muscle ache for >24hr". No follow-up attempts are possible. No further information is expected. Follow-Up (14Dec2021): Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fatigue
Pain
Pyrexia
Tenderness
Symptomtext
A day after the booster shot, around late afternoon, armpit near the breast side became tender and needle like pain, increasing pain as it approached night time. Fever 99.9F started around 5:00pm. Toss and turn during bedtime due to fever. Body feel week and tired. I woke up at 5:30am on 12/24 and did not feel cold but temperature is still at 99.9F. Armpit is still tender but less painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- neck, shoulder, and back pain
- Andere Medikamente
- none
- Allergien
- peanuts, zithromax, fabric tape adhesive
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 24.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Illness
Immunisation
Lymphadenopathy
Symptomtext
booster; sick; chills; Under my armpit my lymph nodes are swollen as the size of tennis ball; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 26-year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 07Dec2021 17:30 (Lot number: 33030BD) at the age of 26 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 01), for Covid-19 Immunization; Bnt162b2 (Dose Number: 02), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 07Dec2021 17:30, outcome "unknown", described as "booster"; ILLNESS (non-serious) with onset Dec2021, outcome "unknown", described as "sick"; CHILLS (non-serious) with onset Dec2021, outcome "unknown", described as "chills"; LYMPHADENOPATHY (non-serious) with onset Dec2021, outcome "unknown", described as "Under my armpit my lymph nodes are swollen as the size of tennis ball". Therapeutic measures were taken as a result of illness, chills. Additional information: clinical course: Patient reporting an adverse effect to the vaccine, for the Pfizer booster shot. So, this part is normal the whole getting sick, having chills and all of that, that is not his biggest concern. (Further clarification unknown. Hence, captured as event conservatively). The biggest concern is that effect that he was really concerned about was under his armpit his lymph nodes were swollen as the size of tennis ball. Patient asking that have you heard this happening because 1st two shots he did not feel anything he was totally fine. Have you heard of this happening with swollen lymph node before from the booster shot? He never had a reaction; this was the first time it happened to him 2 days after the vaccine. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Headache
Immunisation
Pain
Pain in extremity
Symptomtext
Got struck twice with the needle during vaccination; Arm hurts bad/ her left arm hurt; It did not hurt this bad with the two primary doses/her left arm hurt was reported as worsened; Headache; Two pin pricks; Booster; 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 55 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Dec2021 17:00 (Lot number: 33030BD) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (1st Dose), administration date: 2021, for COVID-19 Immunization, reaction(s): "It did not hurt this bad with the two primary doses"; Bnt162b2 (2nd Dose), administration date: 2021, for COVID-19 Immunization, reaction(s): "It did not hurt this bad with the two primary doses". The following information was reported: IMMUNISATION (non-serious) with onset 07Dec2021, outcome "unknown", described as "Booster"; CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (non-serious) with onset 07Dec2021 17:00, outcome "unknown", described as "Got struck twice with the needle during vaccination"; PAIN IN EXTREMITY (non-serious) with onset 07Dec2021, outcome "not recovered", described as "Arm hurts bad/ her left arm hurt"; PAIN (non-serious) with onset 07Dec2021, outcome "not recovered", described as "It did not hurt this bad with the two primary doses/her left arm hurt was reported as worsened"; HEADACHE (non-serious) with onset 07Dec2021, outcome "not recovered", described as "Headache"; PAIN (non-serious) with onset 07Dec2021, outcome "unknown", described as "Two pin pricks". Therapeutic measures were taken as a result of pain in extremity, pain, headache, pain. Additional information: Patient received the booster dose of the Pfizer BioNTech Covid-19 vaccine and got struck twice with the needle during vaccination. Patient would like to know if this was okay and if she should receive another shot. Patient stated her arm hurts bad, it did not hurt this bad with the two primary doses of the Covid-19 vaccine. Patient stated when she got home she looked under the band-aid and she could see two pin pricks just above one another. Patient stated she got struck with the needle twice and it happened so fast. Stated that she had lasting effects from being stuck with the need twice of her left arm hurting. Stated that her left arm started hurting on 07Dec2021 at 5pm when she had the shot. Stated that Ibuprofen does not help. Stated that she took one dose but is going to take another dose in 6 hours. Ibuprofen strength: 200 mg. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Hyperhidrosis
Pyrexia
Symptomtext
fevers, chills, sweats, headache, low-grade fever with T-max at 100.4?. continues to have symptoms at clinic visit 13 days post 3rd dose/booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Antibiotics
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 20.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Abdominal pain upper
Peripheral swelling
Pyrexia
Swelling
Symptomtext
swollen left arm, swollen left armpit, fever, stomach pain, tummy ache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- not known
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Fatigue
Feeling abnormal
Lethargy
Pain
Psychiatric symptom
Symptomtext
Systemic: Body Aches Generalized-Severe, Systemic: Confusion-Medium, Systemic: Exhaustion / Lethargy-Medium, Additional Details: Patient reported psychiatric type side effects. She felt like her "biceps were going through her skin" as stated verbatim by her. She has never had a side effect like this and she wants it reported. Her daughter also reported having an out of body feeling after covid booster and her husband felt like he was high.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Pruritus
Rash
Skin irritation
Symptomtext
Patient experienced delayed reaction from vaccine; a red, itchy, irritated rash developed approximately 2 days after receiving her booster dose of Pfizer. This reaction was about 4 to 6 inches long on patient's arm. Resolved approximately 5 days after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Arthralgia
Blood glucose increased
Body temperature
Chills
Diarrhoea
Fatigue
Flatulence
Head discomfort
Heart rate
Heart rate increased
Immunisation
Laboratory test
Muscle tightness
Myalgia
Pain
Pyrexia
SARS-CoV-2 test
Symptomtext
booster dose; Injection site tenderness and swelling; Injection site tenderness and swelling; he can feel the typical virus body aches.; Chills; checked his temperature it was 100.5 degrees. His temperature dipped down to 99.8 degrees after 9am, and at 11:47am it was 100.3 degrees.; blood sugar was slightly elevated, about 7-8 points above what he normally tracks in the morning; heart rate was a bit higher this morning than what he is used to seeing; was 115; GI distress; gas and diarrhea; General fatigue; muscle tension at the base of his head; generalized muscle and joint pain; muscle tension at the base of his head; generalized muscle and joint pain; GI distress; gas and diarrhea; GI distress; gas and diarrhea; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 02Dec2021 (Lot number: 33030BD, Expiration Date: 31May2022) at the age of 57 years as dose 3 (booster), 0.3ml single for covid-19 immunisation. Relevant medical history included: "Blood pressure high", start date: Mar2021 (unspecified if ongoing); "Type 2 diabetes mellitus", start date: Mar2021 (unspecified if ongoing); "Abscess", start date: Mar2021 (unspecified if ongoing); "States that he had Covid in Mar2020", start date: Mar2020 (unspecified if ongoing); "hospitalized" (unspecified if ongoing). Concomitant medication(s) included: OZEMPIC taken for diabetes mellitus; METFORMIN ER taken for diabetes mellitus, start date: 08Mar2021 (ongoing); LISINOPRIL taken for hypertension, start date: 08Mar2021 (ongoing); PREVNAR 13 taken for immunisation, administration date 12Nov2021; INSULIN. Vaccination history included: Bnt162b2 (1st dose received on 11Mar2021., Lot: EN6204, Expiry: Unknown), administration date: 11Mar2021, when the patient was 57 years old, for Covid-19 immunization, reaction(s): "Injection site tenderness and swelling", "Injection site tenderness and swelling", "General fatigue", "muscle tension at the base of his head", "muscle tension at the base of his head", "generalized muscle and joint pain", "generalized muscle and joint pain", "Chills", "Fever", "GI distress; gas and diarrhea", "GI distress; gas and diarrhea", "GI distress; gas and diarrhea", "blood sugar was slightly elevated, about 7-8 points above what he normally tracks in the morning", "His heart rate was a bit higher this morning than what he is used to seeing", "he can feel the typical virus body aches/body aches"; Bnt162b2 (2nd dose received on 01Apr2021., Lot: ER8737, Expiry: Unknown), administration date: 01Apr2021, when the patient was 57 years old, for Covid-19 immunization, reaction(s): "Injection site tenderness and swelling", "Injection site tenderness and swelling", "General fatigue", "muscle tension at the base of his head", "muscle tension at the base of his head", "generalized muscle and joint pain", "generalized muscle and joint pain", "Chills", "Fever", "GI distress; gas and diarrhea", "GI distress; gas and diarrhea", "GI distress; gas and diarrhea", "blood sugar was slightly elevated, about 7-8 points above what he normally tracks in the morning", "His heart rate was a bit higher this morning than what he is used to seeing", "he can feel the typical virus body aches/body aches"; Shingrix vaccines (1st dose on 20Apr2019, Lot:MX2LT, Expiry:21May2021), administration date: 20Apr2019, reaction(s): "adverse reaction"; Shingrix vaccines (2nd dose on 15Jun2019, Lot:23JKS, Expiry:13Apr2020.), administration date: 15Jun2019, reaction(s): "adverse reaction". The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "booster dose"; VACCINATION SITE SWELLING (non-serious), VACCINATION SITE PAIN (non-serious), outcome "unknown" and all described as "Injection site tenderness and swelling"; FATIGUE (non-serious) with onset 02Dec2021, outcome "unknown", described as "General fatigue"; HEAD DISCOMFORT (non-serious), MUSCLE TIGHTNESS (non-serious) all with onset 02Dec2021, outcome "recovered" (02Dec2021) and all described as "muscle tension at the base of his head"; ARTHRALGIA (non-serious), MYALGIA (non-serious) all with onset 02Dec2021, outcome "recovering" and all described as "generalized muscle and joint pain"; CHILLS (non-serious) with onset 03Dec2021, outcome "unknown", described as "Chills"; PYREXIA (non-serious) with onset 03Dec2021, outcome "unknown", described as "checked his temperature it was 100.5 degrees. His temperature dipped down to 99.8 degrees after 9am, and at 11:47am it was 100.3 degrees."; DIARRHOEA (non-serious), ABDOMINAL DISCOMFORT (non-serious), FLATULENCE (non-serious) all with onset 02Dec2021, outcome "unknown" and all described as "GI distress; gas and diarrhea"; BLOOD GLUCOSE INCREASED (non-serious) with onset 03Dec2021, outcome "unknown", described as "blood sugar was slightly elevated, about 7-8 points above what he normally tracks in the morning"; HEART RATE INCREASED (non-serious) with onset 03Dec2021, outcome "unknown", described as "heart rate was a bit higher this morning than what he is used to seeing; was 115"; PAIN (non-serious), outcome "unknown", described as "he can feel the typical virus body aches." The patient underwent the following laboratory tests and procedures: blood glucose increased: (03Dec2021) blood sugar increased, notes: blood sugar was slightly elevated, about 7-8 points above what he normally tracks in the morning; body temperature: (unspecified date) 100.5, notes: when he got up at 7am and checked his temperature it was 100.5 degrees; (unspecified date) 99.8, notes: temperature dipped down to 99.8 degrees after 9am; (unspecified date) 100.3, notes: and at 11:47am it was 100.3 degrees; heart rate: (unspecified date) normally his heart rate is in the mid 60s-low 80s, notes: Normally his heart rate is in the mid 60s-low 80s; (unspecified date) but this morning it was 115, notes: but this morning it was 115; (03Dec2021) heart rate high, notes: His heart rate was a bit higher this morning than what he is used to seeing; laboratory test: (unspecified date) he was diagnosed with type 2 diabetes, notes: he was diagnosed with type 2 diabetes and high blood pressure; (unspecified date) he was diagnosed with type 2 diabetes and high blo, notes: he was diagnosed with type 2 diabetes and high blood pressure; (Mar2021) life threatening septic infection., notes: Caller explains that in March2021 he was diagnosed with a potentially life threatening septic infection; sars-cov-2 test: (Mar2020) states that he had covid in mar2020, notes: States that he had Covid in Mar2020; (Jul2020) positive, notes: He wasn't able to get tested in Mar2020, but he had an antibody test in Jul2020 that confirmed he had it. Additional information: His side effects had running consistent with what had been publicly recorded and had been consistent with all 3 doses. Stated that he also had many of the same side effects with the Shingrix vaccines. Stated he had a noticeably stronger immune response with the Covid and Shingrix vaccines than with any other vaccine. Injection site tenderness and swelling. Stated he does want to say that having had a full on natural exposure of Covid, the side effects were better than having the illness itself. General fatigue began around 3pm the afternoon he got the injection, but that was typical for him after receiving any injection. He noticed muscle tension at the base of his head that afternoon, it lasted from 3 to 4:30pm. Stated he does not typically get headaches. He had generalized muscle and joint pain, it was a little less now, but if he moves around he can feel the typical virus body aches. Chills started around midnight and when he got up at 7am and checked his temperature it was 100.5 degrees. His temperature dipped down to 99.8 degrees after 9am, and at 11:47am it was 100.3 degrees. He had some GI distress since late yesterday evening; he had some gas and diarrhea, but that stopped. Stated that he was a type 2 diabetic. His blood sugar was slightly elevated, about 7-8 points above what he normally tracks in the morning. Caller explains that in Mar2021 he was diagnosed with a potentially life threatening septic infection. He had an abscess on his side with cellulitis. He was hospitalized, the abscess was drained and while in the hospital he was diagnosed with type 2 diabetes and high blood pressure. He was discharged on 08Mar2021. Caller verifies that all this occurred prior to getting his 1st dose of the Covid 19 Vaccine. His heart rate was a bit higher this morning than what he was used to seeing. Normally his heart rate was in the mid 60s to low 80s, but this morning it was 115. He told his family that his body was just reacting to the foreign substance. Stated he had taken no treatment for the side effects. His instinct was to not take anything unless it was really unpleasant because he didn't want to reduce the effectiveness of the vaccine. By 12:30pm today he was feeling better. Stated that with the 1st dose of the Covid 19 vaccine, he started to feel fever and body aches within 6 hours after getting the dose. Stated that he went to bed early that night. He had noticeable side effects for 12 to 18 hours after they started at 6 pm that night. Metformin ER, dosage changed over the course of managing the disease and Lisinopril, dosage may have started a little lower. It was stated that he was on long acting and short insulin, but he just got off the short acting insulin as of Sept2021. Patient had not attended any Emergency Room and Physician Office for the reported events. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101725303 same reporter/patient/product, different dose/event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211203; Test Name: Blood sugar; Result Unstructured Data: Test Result:Blood sugar increased; Comments: blood sugar was slightly elevated, about 7-8 points above what he normally tracks in the morning.; Test Name: Body temperature; Result Unstructured Data: Test Result:100.5; Comments: when he got up at 7am and checked his temperature it was 100.5 degrees; Test Name: Body temperature; Result Unstructured Data: Test Result:99.8; Comments: temperature dipped down to 99.8 degrees after 9am.; Test Name: Body temperature; Result Unstructured Data: Test Result:100.3; Comments: and at 11:47am it was 100.3 degrees.; Test Name: heart rate; Result Unstructured Data: Test Result:Normally his heart rate is in the mid 60s-low 80s; Comments: Normally his heart rate is in the mid 60s-low 80s.; Test Name: heart rate; Result Unstructured Data: Test Result:but this morning it was 115; Comments: but this morning it was 115.; Test Date: 20211203; Test Name: heart rate; Result Unstructured Data: Test Result:Heart rate high; Comments: His heart rate was a bit higher this morning than what he is used to seeing.; Test Name: Lab test; Result Unstructured Data: Test Result:he was diagnosed with type 2 diabetes; Comments: he was diagnosed with type 2 diabetes and high blood pressure; Test Name: Lab Test; Result Unstructured Data: Test Result:he was diagnosed with type 2 diabetes and high blo; Comments: he was diagnosed with type 2 diabetes and high blood pressure; Test Date: 202103; Test Name: Lab Test; Result Unstructured Data: Test Result:life threatening septic infection.; Comments: Caller explains that in March2021 he was diagnosed with a potentially life threatening septic infection.; Test Date: 202003; Test Name: Covid-19; Result Unstructured Data: Test Result:States that he had Covid in Mar2020; Comments: States that he had Covid in Mar2020.; Test Date: 202007; Test Name: Covid-19; Test Result: Positive ; Comments: He wasn't able to get tested in Mar2020, but he had an antibody test in Jul2020 that confirmed he had it.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Abscess; Blood pressure high; COVID-19; Hospitalization; Type 2 diabetes mellitus
- Andere Medikamente
- OZEMPIC; METFORMIN ER; LISINOPRIL; INSULIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Immunisation
Lymph node pain
Lymphadenopathy
Symptomtext
48 hours - lymph node swelling; 48 hours - lymph node swelling and pain in armpit area (left side) same side as injection site. Currently swelling still present and slight pain; chills; fatigue; booster; This is a spontaneous report received from a contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 56-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 30Nov2021 10:00 (Lot number: 33030BD) at the age of 56 years as dose 3 (booster), single for covid-19 immunization. The patient's relevant medical history was not reported. Concomitant medication(s) included ATORVASTATIN; VITAMIN D 2000. Vaccination history included Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6203, Location of injection: Arm Left, Vaccine Administration Time: 02:15 PM), administration date: 27Feb2021, when the patient was 56 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8727, Location of injection: Arm Left, Vaccine Administration Time: 01:15 PM), administration date: 21Mar2021, when the patient was 56 years old, for COVID-19 immunization, reaction(s) chills; Bnt162b2 (2nd dose), when the patient was 56 years old, for COVID-19 immunization, reaction(s) fatigue. The following information was reported IMMUNISATION (non-serious) with onset 30Nov2021 10:00, outcome unknown; LYMPHADENOPATHY (non-serious) with onset 02Dec2021 09:00, outcome recovering; LYMPH NODE PAIN (non-serious) with onset 02Dec2021 09:00, outcome recovering. Currently swelling still present and slight pain; CHILLS (non-serious) with onset 02Dec2021 09:00, outcome recovering; FATIGUE (non-serious) with onset 02Dec2021 09:00, outcome recovering. Therapeutic measures were not taken as a result of lymphadenopathy, lymph node pain, chills, fatigue. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was neither diagnosed with COVID-19 Prior to vaccination nor been tested for COVID-19 since the vaccination. 48 hours - lymph node swelling and pain in armpit area (left side) same side as injection site. Currently, swelling still present and slight pain. The lymph node adverse event was new, after her 2nd dose & 3rd dose, the patient had chills, and fatigue that lasted less than 24 hours. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ATORVASTATIN; VITAMIN D 2000
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 27.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Lymphadenopathy
Urticaria
Symptomtext
Left lymph nods swollen; Breaking out in hives on stomach and back; Dose number: 3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2, solution for injection), administered in arm left, administration date 27Nov2021 14:45 (Lot number: 33030BD) at the age of 45 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Thyroid" (unspecified if ongoing), notes: Other medical history: Thyroid; "Hoshimoto" (unspecified if ongoing), notes: Other medical history: hoshimoto. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Lot number: EW973, Administration time: 01:15 PM, Vaccine location: Left arm, Dose number: 2), administration date: 05May2021, when the patient was 44 years old, for COVID-19 Immunization; Bnt162b2 (Lot number: EW0153, Administration time: 03:00 PM, Vaccine location: Left arm, Dose number: 1), administration date: 07Apr2021, when the patient was 44 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 27Nov2021 14:45, outcome "unknown", described as "Dose number: 3"; LYMPHADENOPATHY (non-serious) with onset 29Nov2021 05:45, outcome "not recovered", described as "Left lymph nods swollen"; URTICARIA (non-serious) with onset 29Nov2021 05:45, outcome "not recovered", described as "Breaking out in hives on stomach and back". Therapeutic measures were not taken as a result of lymphadenopathy, urticaria. Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hashimoto's disease; Thyroid disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Diarrhoea
Dizziness
Fatigue
Headache
Injection site swelling
Nausea
Oedema peripheral
Vomiting
Symptomtext
Nausea, vomiting, headache, diarrhea, swelling under arm of the right arm (injection site), headache, joint pain, extreme exhaustion, chills and dizziness - lasted approximately 5 days (except for vomiting and diarrhea that only happened once at 2 - 4 am), the day after the shot was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Had a cold 3 weeks prior to the booster shot
- Vorgeschichte
- GERD
- Andere Medikamente
- Pepcid 40mg BID, Lexapro 5mg QD, Ativan 0.5mg QHS
- Allergien
- Penicillin and most antibiotics, Ventolin, Macrodantin, Codeine, Sulfa meds
- Vorherige Impfungen
- Mild pain under arm at site of injection; chills that lasted 24 hours after the injection of 2nd dose of Pfizer COVID-19 vaccine
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Myalgia
Pruritus
Pyrexia
Rash
Symptomtext
RASH, ITCHEY, HEADACHE, A LBIT FEVER, JOINT PAIN, MUSCLE PAIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- RASH, ITCHEY, HEADACHE, MUSCLES PAINS, JOIN PAINS, A BIT FEVER
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 19.12.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymphadenopathy
Symptomtext
Swollen lymph node in left arm pit close to breast. A lot of pain even without applied pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Genital ulceration
Headache
Influenza like illness
Pyrexia
Vaginal ulceration
Vulvovaginal pain
Symptomtext
Systemic: pt had lipschutz ulcer-Severe, Additional Details: patient got flu shot not covid. Had a headache and fever(flu-like symptoms) for 2 days. Then had extreme pain and ulcer on vagina. Patient went to the doctor and was told she had lipschutz ulcer and was screened for cancer. Unknown if the vaccine triggered the response at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Hyperhidrosis
Nausea
Symptomtext
Systemic: Flushed/Sweating-Medium, Systemic: Nausea-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Peripheral swelling
Rash
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: swelling of right arm and armpit-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Immunisation
Muscle spasms
Symptomtext
Had extreme pain in back, hips, knees; Had extreme pain in back, hips, knees; Extreme muscle spasms also at these sites; Dose number: 3; This is a spontaneous report from a contactable reporter (consumer or other non hcp). The reporter is the patient. A 50-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 11Dec2021 at 12:30 (Lot number: 33030BD) at the age of 50 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Fibromyalgia"; "Spondylitis", notes: Arthritis of the back; "Knee arthritis", notes: Arthritis of the back, knees, and hips,; "Coxarthritis", notes: Arthritis of the back, knees, and hips and "Latex allergy", notes: Known allergies: Latex; all (unspecified if ongoing). The patient received unspecified concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: EN6206; administration time: 14:00, vaccine location: left arm), administration date: 03Mar2021, when the patient was 49 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; lot Number: EP7534, administration time: 13:30, vaccine location: right arm), administration date: 24Mar2021, when the patient was 49 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 11Dec2021 at 12:30, outcome "unknown", described as "Dose number: 3"; BACK PAIN (non-serious), ARTHRALGIA (non-serious); with onset 12Dec2021 at 03:00, outcome "recovering" both described as "Had extreme pain in back, hips, knees" and MUSCLE SPASMS (non-serious) with onset 12Dec2021 at 03:00, outcome "recovering" described as "Extreme muscle spasms also at these sites". Therapeutic measures were not taken as a result of back pain, arthralgia and muscle spasms. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. It was reported that pain was near unbearable. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Coxarthritis (Arthritis of the back, knees, and hips,); Fibromyalgia; Knee arthritis (Arthritis of the back, knees, and hips,); Latex allergy (Known allergies: Latex); Spondylitis (Arthritis of the back)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Axillary pain
Blood test
Dizziness
Electrocardiogram
Fatigue
Headache
Lymphadenopathy
Nausea
Pain
Sensitive skin
Symptomtext
Swelling of lymph nodes in armpit on left side, Intense pain within the armpit, headache, dizziness, lightheaded, nausea, fatigue, body aches, sensitive skin all symptoms showed within 12 hours of the shot being administered. Emergency Room: treated with IV fluids, zofran, and IV Tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- full panel blood work performed, results came back normal EKG- normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth Control Pill
- Allergien
- Penn. Ammox. Septra
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Arthralgia
Decreased appetite
Fatigue
Peripheral swelling
Symptomtext
Fingers swollen and joint pain, Fatigue, no desire to eat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Vascular Disease which is stable at this time
- Andere Medikamente
- HZT 12.5 mg daily
- Allergien
- Bactrim DS and Fish
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site pain
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Exposure during pregnancy
Symptomtext
3mins post vaccination pt c/o dizziness Vitals: 117/83, 81, 18, 97% RA -- > 113/77, 77, 18, 96% RA -- > 112/75, 75, 16, 97% RA Pt was hydrated. No further c/o dizziness. Pt stable and released from the vaccination site @12:45pm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Pt is currently pregnant (Due 2/7/22), depression in pregnancy, scoliosis
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Feeling hot
Oedema peripheral
Symptomtext
I have slight swelling and pain in the armpit of my left arm started the next day of Pfizer booster dose and continuing on the Day 2 as well. I took 2 capsules of Tylenol on 14Dec as well as 15Dec but not much effect. I am also feeling a bit hot but no fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None. Not visited the primary care Physician yet. If symptoms persists, then I will go to the PCP or urgent care tomorrow (16Dec)
- Aktuelle Erkrankungen
- GERD LPRD (Laryngopharyngeal Reflux Disease)
- Vorgeschichte
- GERD LPRD (Laryngopharyngeal Reflux Disease)
- Andere Medikamente
- Nexium 20 mg (2 times, 2 capsules daily)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Tunnel vision
Symptomtext
Patient was feeling dizzy and tunnel vision at 11:18 am
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Neyomycin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Injection site mass
Injection site pain
Limb discomfort
Symptomtext
Bruising, lump, and pain around shot area around 2.5 inches in diameter. Legs feel heavy. Still present after a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Elevated hematocrit since 2nd Pfizer vaccine SVT
- Andere Medikamente
- D3 B12 vitamins
- Allergien
- Cipro Levaquin
- Vorherige Impfungen
- Pfizer 2nd shot
- Staat
- IL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Crying
Illness
Malaise
Myalgia
Parosmia
Pyrexia
Sensory disturbance
Somnolence
Vomiting
Symptomtext
Vomiting, fever, muscle aches. 5 days later still sick taking Zofran now. Not acting himself at all, crying frequently, sleeping all the time, heightened sensory issues smells, sounds making him feel sick. He's really out of it. He's not acting like himself at all since the day after the covid vaccine. Younger son had one too and he's fine just a headache for a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Took him to urgent care last night. Covid, rsv, flu and strep all negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chairi
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Developed a rash on face and neck from the Pfizer booster shot within 15 hours of the vaccination. The rash started out on the right side of my face and neck, and moved to the left side throughout the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- Penicillin, Dilaudid
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 12.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site inflammation
Injection site swelling
Lymphadenopathy
Symptomtext
swollen and inflamed injection site. swollen lymph nodes arm pits.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site inflammation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- escitalopram; toprimax
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pruritus
Injection site swelling
Lymphadenopathy
Rash
Symptomtext
Site: Itching at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: Lymph Node Swelling-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- -
- Beginn
- 04.12.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Oropharyngeal pain
Pyrexia
Vaccination site erythema
Vaccination site hypersensitivity
Vaccination site mass
Vaccination site pain
Vaccination site pruritus
Vaccination site swelling
Vaccination site warmth
Symptomtext
Dose number 3; Redness and slight itching sensation / at the injection site; Redness and slight itching sensation / at the injection site; mild fever; sore throat; injection sight became very sensitive to the touch, a slight bump of the spot would hurt; injection sight became very sensitive to the touch, a slight bump of the spot would hurt; injection sight became very sensitive to the touch, a slight bump of the spot would hurt; the spot was hotter to the touch; has been roughly 4 days of it being itchy bed and swollen; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left (Lot number: 33030BD) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Allergies: some types of bandage adhesive" (unspecified if ongoing), notes: Known allergies: some types of bandage adhesive. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Location of injection: Arm Left), administration date: 26Apr2021, when the patient was 21 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Location of injection: Arm Left), administration date: 05Apr2021, when the patient was 21 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "Dose number 3"; VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE PRURITUS (non-serious) all with onset 04Dec2021, outcome "not recovered" and all described as "Redness and slight itching sensation / at the injection site"; PYREXIA (non-serious) with onset 04Dec2021, outcome "not recovered", described as "mild fever"; OROPHARYNGEAL PAIN (non-serious) with onset 04Dec2021, outcome "not recovered", described as "sore throat"; VACCINATION SITE HYPERSENSITIVITY (non-serious), VACCINATION SITE MASS (non-serious), VACCINATION SITE PAIN (non-serious) all with onset 04Dec2021, outcome "not recovered" and all described as "injection sight became very sensitive to the touch, a slight bump of the spot would hurt"; VACCINATION SITE WARMTH (non-serious) with onset 04Dec2021, outcome "not recovered", described as "the spot was hotter to the touch"; VACCINATION SITE SWELLING (non-serious) with onset 04Dec2021, outcome "not recovered", described as "has been roughly 4 days of it being itchy bed and swollen". Therapeutic measures were not taken as a result of vaccination site erythema, vaccination site pruritus, pyrexia, oropharyngeal pain, vaccination site hypersensitivity, vaccination site mass, vaccination site pain, vaccination site warmth, vaccination site swelling. No follow-up attempts are possible. No further information is expected. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Adhesive tape allergy (Known allergies: some types of bandage adhesive)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mass
Pain in extremity
Symptomtext
the first 2 days , my arm was very sore, then I took some IBprofin and the pain subsided. On the 2nd day I noticed a lump, located on my clavicle, between my bra strap & the base of my neck. It will roll around when pressed with my fingers. after 5 days, it has gotten smaller.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- metoprolo
- Allergien
- penicilin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site inflammation
Injection site warmth
Rash macular
Symptomtext
Patient states face was red where her mush was on the evening of these 2 vaccines. The next day chest and arms were red and blotch. No itchiness, not raised, not hot. No breathing problems - injection sites not red, warmer inflamed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site inflammation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Axillary pain
Lymphadenopathy
Swelling
Symptomtext
PT came stating she got adverse reaction of booster pfizer she got yesterday, swelling and soreness at left armpit. consulted pt to use warm compression and advil , and directed to report to v-safe. and will do scrt .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 27.11.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Rash papular
Tinnitus
Urticaria
Symptomtext
Tinnitus; Hives; raised red rash left chest, sporadic over body; raised red rash left chest, sporadic over body; This is a spontaneous report from a contactable reporter (nurse). The reporter is the patient. A 66-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 27Nov2021 at 10:15 (Lot number: 33030BD) at the age of 66 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Hypertension (HTN)" (unspecified if ongoing); "Asthma" (unspecified if ongoing) and "COVID-19" (unspecified if ongoing). Concomitant medications included: VALSARTAN; ATENOLOL; NORVASC; PROTONIX; ASPIRIN and HTZ. Past drug history included: Naproxen, reaction: "Drug allergy", notes: known allergies: Naproxen and Codeine, reaction: "Drug allergy", notes: known allergies: codeine. The following information was reported: TINNITUS (non-serious) with onset 03Dec2021, outcome "recovering", described as "Tinnitus"; URTICARIA (non-serious) with onset 03Dec2021, outcome "recovering", described as "Hives"; RASH ERYTHEMATOUS (non-serious), RASH PAPULAR (non-serious) both with onset 03Dec2021, outcome "recovering", and both described as "raised red rash left chest, sporadic over body". Therapeutic measures were not taken as a result of tinnitus, urticaria, rash erythematous and rash papular. Additional Information: Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes); Hypertension (HTN)
- Andere Medikamente
- VALSARTAN; ATENOLOL; NORVASC; PROTONIX [PANTOPRAZOLE SODIUM SESQUIHYDRATE]; ASPIRIN [ACETYLSALICYLIC ACID]; HTZ
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pyrexia
Symptomtext
This 9 year old patient was given the adult dosage of COVID vaccine #2 instead of the dosage for 5-11 year old children. Developed fever to 103 the same evening he got the incorrect dose of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Swollen lymph node in armpit. Painful to touch. Tender. Size of testicle. In my armpit! Gross.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Injection dye
- Vorherige Impfungen
- Pfizer
- Staat
- MD
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Injection site pain
Lymphadenopathy
Myalgia
Nausea
Pyrexia
Symptomtext
chills, fever, fatigue, muscle aches, nausea, pain at injection site, swollen lymph nodes;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- levothyroxine, Junel
- Allergien
- none
- Vorherige Impfungen
- Pfizer COVID
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Immunisation
Pain in extremity
Symptomtext
Fatigue; Headache; Chills; Left arm sore; Dose received: 3; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 27-year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Dec2021 at 18:30 (Lot number: 33030BD) at the age of 27 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EP6955; Anatomical site: left arm; Route of administration: unspecified), administration date: 18Mar2021, when the patient was 27 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EP6955; Anatomical site: left arm; Route of administration: unspecified), administration date: 08Apr2021, when the patient was 27 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 02Dec2021 at 18:30, outcome "unknown", described as "Dose received: 3"; FATIGUE (non-serious) with onset 03Dec2021 at 07:00, outcome "recovering", described as "Fatigue"; HEADACHE (non-serious) with onset 03Dec2021 at 07:00, outcome "recovering", described as "Headache"; CHILLS (non-serious) with onset 03Dec2021 at 07:00, outcome "recovering", described as "Chills"; PAIN IN EXTREMITY (non-serious) with onset 03Dec2021 at 07:00, outcome "recovering", described as "Left arm sore". Therapeutic measures were not taken as a result of fatigue, headache, chills and pain in extremity. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Chills
Confusional state
Lymphadenopathy
Pyrexia
Symptomtext
Swollen lymph nodes, anxiety, confusion, fever and chills for 2 days and still has symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Additional Details: After the patient's 15 minutes observation time was up, the patient complained of dizziness. We asked her to sit down for longer and got her water. Her blood pressure was taken, reading: 146/97. She stated she only had soup to eat before her evening vaccine appointment. She did not have any reaction/problems with her first 2 doses (this was her booster). The patient did not have any relatives or friends call. She insisted to leave after I asked she stay longer or I call her a ride.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Immunisation
Symptomtext
Significant pain in armpit; Dose received 3/ dose number=3; This is a spontaneous report received from a non-contactable reporter (consumer or other non HCP). The reporter is the patient. A 41-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in left arm, administration date 30Nov2021 at 11:15 (Lot number: 33030BD) at the age of 41 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: ER8730, Anatomical site: left arm), administration date: 23Mar2021, when the patient was 41 years old, for COVID-19 immunisation and BNT162b2 (DOSE 2, SINGLE, Lot number: EW0162, Anatomical site: left arm), administration date: 13Apr2021, when the patient was 41 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 30Nov2021 at 11:15, outcome "unknown", described as "Dose received 3/ dose number=3"; AXILLARY PAIN (non-serious) with onset 01Dec2021 at 08:00, outcome "not recovered", described as "Significant pain in armpit". Therapeutic measures were not taken as a result of axillary pain. Additional information: The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 01.03.2021
- Beginn
- 01.03.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
Severe hip pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- Seroquel, Celexa, Topamax, Xanax,
- Allergien
- Morphine, Lamictal
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Symptomtext
Patient felt light headed and nauseous
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Tremfya
- Allergien
- Griseofulvin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Immunisation
Lymphadenopathy
Nausea
Pain
Symptomtext
Swollen lymph nodes in left arm; Nausea; Headache; Body aches; Dose number:3; This is a spontaneous report received from a non-contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 23-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 28Nov2021 (Lot number: 33030BD) at the age of 23 years as dose 3, single for COVID-19 immunisation. Relevant medical history included: "None". Concomitant medications were not reported. Vaccination history included: bnt162b2 (BNT162B2, DOSE 1, SINGLE, Lot Number: EN6207, Route of administration: Unspecified, Anatomical site: left arm), administration date: 01Apr2021 when the patient was 23 years old and bnt162b2 (BNT162B2, DOSE 2, SINGLE, Lot Number: EW0164, Route of administration: Unspecified, Anatomical site: left arm), administration date: 20Apr2021, when the patient was 23 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 28Nov2021, outcome "unknown", described as "Dose received: 3"; LYMPHADENOPATHY (non-serious), NAUSEA (non-serious), HEADACHE (non-serious) and PAIN (non-serious) all with onset 29Nov2021, outcome "recovering" and all described as "Swollen lymph nodes in left arm, nausea, headache and body aches". Therapeutic measures were not taken as a result of lymphadenopathy, headache, nausea and pain. Additional Information: The patient's known allergies were reported as not applicable. The patient did not receive any other vaccines within four weeks prior to COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- 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
- -
- Staat
- IA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Symptomtext
DIZZINESS, NAUSEA REPORTED HAD PT LAY ON GROUND AND ELEVATE FEET, PLACED COLD PACK ON FOREHEAD AND INSIDES OF WRISTS. MONITORED BP SHE ENDED UP NOT STAYING FOR THE END OF HER SHIFT- A FAMILY MEMBER PICKED HER UP AND WAS SENT HOME TO REST, IF SX GET WORSE SHE WAS TOLD TO SEEK MEDICAL ATTN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Injection site reaction
Keloid scar
Symptomtext
Day after vaccination patient presents with bullae and keloid formation around the vaccine administration site in his right arm. The patient is currently treating it with topical cortisone and was recommended to visit his primary physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- V/S WNL
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- DMTII, HTN
- Andere Medikamente
- Lantus, Januvet, Losartan, Metoprolol, Lipitor, Plavix, Cilostazol
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Bone pain
Pain
Symptomtext
Sunday morning patient woke up with body aches and bone pain it lasted from about 6am-8pm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 05.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Photopsia
Tunnel vision
Symptomtext
On Saturday - 2 days after dose, patient started complaining about feeling very dizzy. He was nauseous and was experiencing tunnel vision with 'bursts' of light on his vision periphery. He did not want to go the emergency room. He spent most of the remaining part of the day resting in bed. The next morning, Sunday 12/5, patient said he felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety, Depression
- Andere Medikamente
- ADDERALL 30 mg, LEXAPRO 20 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Symptomtext
Patient received pfizer booster (3rd dose) felt faint and fell off her chair. Patient has no recollection of falling off the chair. Patient was lowered and placed in supine position feet where then elevated. Patient was given water and crackers. Patient stated "she did not eat anything today". 911 was called EMT took blood glucose was 97 after crackers were eaten. Heart rate was 79, Pulses 3+ equal and bilateral, O2 99%. Patient was responsive and orientated. Patient resumed seated position with in 10 minutes and refused additional care by EMT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No illnesses
- Vorgeschichte
- No chronic conditions
- Andere Medikamente
- No
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
PT. RETURN 1 HOUR AFTER IMMUNIZED REFERRING ITCHING AND RUNCHES ALL OVER THE BODY. PT. I REPORT THAT THIS HAPPENED EVERY TIME THAT HAS BEEN IMMUNIZED BUT THIS TIME THE REACTION TAKEN LONGER. ESTIMATED VITALS BP 130/90, P 120, SAT. 98%. ANTIISTAMINE (BENADRYL) WAS ADMINISTERED BY MOUTH. DR. WHO RECOMMEND TRANSFER TO THE EMERGENCY ROOM. PT. HE REFUSED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- RHUMATOID, ARTHRITIS, OSTEOPOROSIS, HYPERTENSION
- Vorgeschichte
- Arthritis, RHUMATOID, HYPERTENSION
- Andere Medikamente
- Methotrexate, Humira, Lisinopril
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 28.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Injection site swelling
Lymphadenopathy
Oedema peripheral
Pruritus
Symptomtext
This was the Pfizer Covid19 Booster. Started with bad chills approx 24 hrs after vaccine. Within 24 hrs I had swollen lymph nodes in my underarm area and swelling at injection site. Appox 2-3 days after, swelling underarm, next to injection site and breast which became itchy. (I assume all lymph node areas). It is now 5 days later and still have the swelling and itching. I did have swollen lymph nodes after 2nd Pfizer Covid19 vaccine, but just underarm and no itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Multiple Sclerosis, High Blood Pressure
- Andere Medikamente
- Modifinal 200 mg 2 per day, Metoprolol ER Succ 50 mg 1 per day, Amlodipine 5 mg 1 per day, Aubagio 7 mg 1 per day, Diazepam 2 mg as needed, Levocehrizine 5 mg 1 per day, Estrace cream 0.01 2 times a week, Clobetasol Propionate 0.05 as neede
- Allergien
- sulfa, lisinipril, losarton, amoxicillin, high doses of Motrin, Hydrochlorot, seasonal allergies and thimerosol
- Vorherige Impfungen
- Covid19 Phizer 2nd dose LotER8733 on 3/27/21 swollen lymph nodes
- Staat
- MA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Lymph node pain
Lymphadenopathy
Nasopharyngitis
Symptomtext
No issues at the time of vaccination. The day after the vaccine I experienced mild typical symptoms associated with vaccination (chills, cold-like); that night I noticed moderate lymphedema to the left axilla only which is painful. It hasn't resolved yet. Note- I'm not concerned about the symptoms but for statistical purposes wanted to report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- loratadine, birth control
- Allergien
- misoprostol
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 17.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cystitis
Fatigue
Pain in extremity
Productive cough
Urine analysis abnormal
Symptomtext
I was tired and I had coughing with phlegm. I felt weak and I had a little sore arm. I had a bladder infection as well. I went to the doctors on 11/22/2021 and I got antibiotics for that.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Urine test- found infection (11/22/2021)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma Allergies Migraines IBS Anxiety Depression
- Andere Medikamente
- Zyrtec
- Allergien
- Dust Dust Mites Bactrim Augmentin Keflex Doxycycline
- Vorherige Impfungen
- COVID (1st and 2nd)- headache, coughing, sleepy, sore arm. (January 2021)
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Vaccination site erythema
Vaccination site pain
Symptomtext
Pink spot on arm close to injection site about 2 inches wide; Pink spot on arm close to injection site about 2 inches wide only slightly tender; Received 3rd dose of BNT162B2 Pfizer vaccine; This is a spontaneous report received from a contactable reporter (consumer). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in arm left, administration date 26Nov2021 at 11:15 (Batch/Lot number: 33030BD) at the age of 42 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: VENLAFAXINE and ADDERALL. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot Number: ER8730, Anatomical location: Left arm, Route of administration: Unspecified), administration date: 31Mar2021, when the patient was 41 year(s) old, for COVID-19 immunisation and BNT162b2 (DOSE 2, SINGLE, Lot Number: EW0153, Anatomical location: Left arm, Route of administration: Unspecified), administration date: 21Apr2021, when the patient was 41 year(s) old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 26Nov2021 at 11:15, outcome "unknown", described as "Received 3rd dose of BNT162B2 Pfizer vaccine"; VACCINATION SITE ERYTHEMA (non-serious) and VACCINATION SITE PAIN (non-serious), both described as "Pink spot on arm close to injection site about 2 inches wide only slightly tender", with onset 28Nov2021, outcome "not recovered". Therapeutic measures were not taken as a result of the events vaccination site erythema and vaccination site pain. Additional Information: The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. It was reported that the pink spot on arm which was slightly tender might have been there earlier, but the patient didn't look; had been wearing long sleeves. The patient reported that this wasn't a problem but figured it was worth reporting just for the information; the patient realized it wasn't dangerous or harmful (as reported). Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- VENLAFAXINE; ADDERALL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site swelling
Lymphadenopathy
Oedema peripheral
Symptomtext
Headache was relieved after taking Tylenol. Injection site Swelling lasted three days. Lymph node swelling under left arm continues after three days (as of 7 p.m. of Dec. 2); Would like to know what to do to reduce swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram neck
Dizziness
Full blood count normal
Hypoaesthesia
Magnetic resonance imaging head normal
Metabolic function test
Tinnitus
Symptomtext
Sudden onset right ear tinnitus, right facial numbness, dizziness Had episode of tinnitus after 2nd Pfizer COVID19 vaccine. Dx possible Meniere's disease No treatment; observation; follow up with neurology if persistent symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Neck CT angio, normal MRI brain, normal CBC, CMP, normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Headache
Myalgia
Symptomtext
Extreme headache, muscle aches, heavy fatigue, joint pain including ankles, back shoulders elbows wrists
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Arthritis and high blood pressure
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 27.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Laboratory test
Nausea
Symptomtext
Stomach pain 2 days post vaccination. When eating, feels nauseous and may vomit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Labs were drawn 11/30/21 unknown results at this time. Assessing for pancreatitis
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LOSARTAN
- Allergien
- PAROXETINE, LATEX
- Vorherige Impfungen
- tongue swelling with 1st dose of pfizer on 11/05/2021
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Hyperhidrosis
Injection site pain
Injection site swelling
Lymph node pain
Lymphadenopathy
Myalgia
Nausea
Pyrexia
Symptomtext
Injection site pain and swelling started 6 hours after booster. 25 hours (2 pm) after receiving the booster I started having severe muscle aches, fatigue (the "I got hit by a large truck" feeling). By 6 pm the aches were worsening, by 8 pm I started having nausea & chills and couldn't warm up. By 11 pm I had a fever of 100.5. The chills turned into sweating. The fever abated by 6 am and Lymph nodes in left arm pit are now swollen and painful. The sweating /chills continued into the next day (day2 after Booster). Today is day 2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- HSV 1 outbreak
- Vorgeschichte
- none
- Andere Medikamente
- Lisinopril, Levothyroxine, buproprion, sertraline, Vit B supp
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Fall
Symptomtext
The patient was purchasing items at the register when she reported feeling dizzy. She then fell down and paramedics were called.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Vertigo
- Vorgeschichte
- History of Vertigo, Diabetes
- Andere Medikamente
- Unknown
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 27.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site pruritus
Injection site swelling
Pyrexia
Symptomtext
FEVER (USED NAPROXEN AND IS FELLS BETTER). HOWEVER, REDNESS, ITHING, SWELLING AT INJECTION SITE PERISTS. PATIENT CURRENTLY USING COOL COMPRESS. ADVISED TO USE BENADRYL ORALLY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Vomiting
Symptomtext
Dizziness and then pt threw up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 28.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 28.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pyrexia
Rash
Urticaria
Symptomtext
Patient reported high fever on the night of receiving vaccine and the following day. Then 3 days after vaccination patient reported rash and hives all over body. Patient went to an urgent care and treatment from urgent care is not known.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 27.11.2021
- Impfdatum
- 27.11.2021
- Beginn
- 27.11.2021
- 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 glucose decreased
Dizziness
Emotional distress
Hyperhidrosis
Pallor
Peripheral coldness
Visual impairment
Symptomtext
Patient became dizzy, weak, light headed, sweaty, with coldness of extremities, pale and had visual disturbances due to low blood sugar at time of vaccination and emotional response to "needle" / shot. After caring for patient in post-immunization waiting area with her mother and father giving her drink and food to bring up her blood sugar to normal range, patient felt better and went home with her mother and father. No signs of allergic reaction were noted by pharmacist. Patient never lost consciousness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no known illnesses
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Vaccine positive rechallenge
Symptomtext
She had lots of dizziness for 20 + minutes after getting her shot. The paramedics came and checked her out. The dizziness was worsened by her new glasses. She took them off and had someone come pick her up to take her home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- addison's disease, trigeminal neuralgia
- Andere Medikamente
- budesonide oral taper
- Allergien
- -
- Vorherige Impfungen
- dizziness
- Staat
- NC
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 17.11.2023
- Impfdatum
- 09.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
the patient did end up getting covid virus in 2022; the patient did end up getting covid virus in 2022; The initial case was missing the following minimum criteria: adverse event and suspect drug (unspecified). Upon receipt of follow-up information on 13Nov2023, this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter(s) (Consumer) from product quality group, Program ID:. The reporter is the parent. A 23-year-old male patient received bnt162b2 (BNT162B2), on 09Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 21 years for covid-19 immunization. The patient's relevant medical history included: "dialysis" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: PFIZER covid vaccine (Dose 1, Lot: EN9581), administration date: 24Feb2021, when the patient was 21-year-old, for COVID-19 immunization; PFIZER covid vaccine (Dose 2, Lot: EP7534), administration date: 17Mar2021, when the patient was 21-year-old, for COVID-19 immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "the patient did end up getting covid virus in 2022".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Dialysis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 08.11.2023
- Impfdatum
- 19.03.2021
- Beginn
- 07.11.2023
- Tage bis Beginn
- 963,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
ADMITTED WITH COVID ON 11/7/23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 07.10.2023
- Impfdatum
- 16.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cardiac disorder
Exercise tolerance decreased
Heart rate abnormal
Symptomtext
Difficulty with exercise, heart felt weak and remains a long term concern. Now includes galloping heart occasionally during sleep. Not entirely feel like I did before this one booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Difficulty hiking at the same pace as prior to the vaccine, my heart felt oddly weak and was a concern and remains a concern. I have to monitor my heart rate now more carefully when exercising. Besides feeling the need to be careful, now I experience a galloping heart at night, say 6 times a month. Something new, thought I'd share it as it may relate to my heart weirdness after this 3rd Vaccine (the booster).
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 01.12.2021
- Beginn
- 22.04.2022
- Tage bis Beginn
- 142,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
Symptomtext
Covid-19; Covid-19; Pfizer Dose 1,2,3; Moderna Dose: 4; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 22Mar2021 as dose 1, single (Lot number: ER8730), in left arm, on 12Apr2021 as dose 2, single (Lot number: EW0158), in left arm and on 01Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 64 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 22Apr2022 as dose 4 (booster), single (Lot number: 033K21-2A), in left arm for covid-19 immunisation; davesomeran, elasomeran (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), on 23Sep2022 as dose 5 (booster), single (Lot number: AS7146B), in left arm and on 05May2023 as dose 6 (booster), single (Lot number: AS7173B), in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 22Apr2022, outcome "unknown", described as "Pfizer Dose 1,2,3; Moderna Dose: 4"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "Covid-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received COVID 19 Treatment (Paxlovid). Treatment stop date 28Sep2023. Known allergies: No.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300316477 Same patient, different drug and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- 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
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 23.09.2022
- Beginn
- 30.05.2023
- Tage bis Beginn
- 249,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fall
SARS-CoV-2 test positive
Symptomtext
Date of Admission: 5/29/2023 Discharge Date: June 7, 2023 Discharge Disposition: Inpatient Rehab Facility or Unit Presented to the hospital after a fall. 5/30 COVID+ Does not have any respiratory symptoms. Afebrile, no leukocytosis, no respiratory distress or hypoxia. No need for respiratory medications, antivirals or steroids. EN5318 2/3/2021 EN6201 2/25/2021 33030BD 12/6/2021 GJ2524 9/23/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of personal independence in daily activities
Urinary incontinence
Symptomtext
Urinary incontinence. Pt wears a panty liner and cannot leave the house.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of personal independence in daily activities
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Urinary incontinence
- Andere Medikamente
- Aspirin Schiff glucosamine and hyaluronic acid with MSM Nature's Bounty curcumin Zinc Vitamin D
- Allergien
- Penicillin Codeine
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 12.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. The reporter is the patient. An elderly female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Mar2021 as dose 1, single (Lot number: EP7534), on 13Apr2021 as dose 2, single (Lot number: EW0162) and on 12Jan2022 as dose 3 (booster), single (Lot number: 33030BD) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: penicillins" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Amoxicillin, reaction(s): "Known allergies: Amoxicillin"; Clozapine, reaction(s): "Known allergies: clozapine"; Ibuprofen, reaction(s): "Known allergies: ibuprofen"; Cipro, reaction(s): "Known allergies: cipro"; Loxapine, reaction(s): "Known allergies: loxapine". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19 which includes Oral Paxlovid from 05Apr2023 to 08Apr2023. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information currently available, there is a reasonable possibility of a causal association between the reported adverse events vaccination failure, Covid-19 and the suspect product BNT162b2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 06.01.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 82,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 16.03.2023
- Impfdatum
- 22.03.2021
- Beginn
- 04.03.2023
- Tage bis Beginn
- 712,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 3/4/2023 - 3/7/2023 (3 days) Presentation to the ED: increasing weakness over the past 1 week prior to arrival. COVID + date: 3/4/2023 Treatment: supportive care, no specific medications. Discharge to: SNF 33030BD 12/18/2021 013M20A 2/18/2021 047A21A 3/22/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes mellitus type 2, peripheral vascular disease, liver transplant on tacrolimus, BPH, anxiety, depression, AAA
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 07.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test abnormal
Lymphadenopathy
Mammogram normal
Symptomtext
I received the Covid 19 booster shot (my first and only booster) on 12/7/21 and on 12/9/21 my lymph nodes were swollen in my armpit. After a couple weeks I went to see my PCP and she suggested warm compresses and Advil or something similar. My lymph nodes were not sticking out, but it is what we called "full" basically just swollen. A few weeks and nothing worked so she sent me for tests.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test abnormal
- Hospital-Tage
- -
- Labordaten
- Blood work done in January 2022 only revealed inflammation, she then sent me for another mammogram off cycle and those results were fine, next I was sent to a breast surgeon who ordered additional films to be taken 6 months later which also revealed nothing so no further treatment was needed. This is very alarming because today is 2/23/23 and it's still swollen and no one has any answers for me.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure (I got this at 41 years old, my father also has it. Mine is under control).
- Andere Medikamente
- Amlodipine 2.5 mg, Vitamin D 5,000 units, Norethindrone 0.35 mg (Birth control), Clindamycin Phosphate topical lotion 1% (used for my Rosacea).
- Allergien
- Epinephrine (makes my heart race), HZT (my potassium dropped slightly)
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 21.02.2023
- Impfdatum
- 18.11.2021
- Beginn
- 31.01.2022
- Tage bis Beginn
- 74,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Pfizer 1/22/21 Lot# El9261; Pfizer 3/3/21 Lot# EL9267; Pfizer 11/18/21 Lot# 33030BD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVDI +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 20.02.2023
- Impfdatum
- 02.12.2021
- Beginn
- 17.02.2023
- Tage bis Beginn
- 442,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 2/14/23 COVID PCR positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 16.11.2021
- Beginn
- 08.04.2022
- Tage bis Beginn
- 143,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body mass index
COVID-19
Interchange of vaccine products
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; Pfizer / BioNTech, Dose Number: 3 ; Moderna, Dose Number: 4; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient received BNT162b2 (BNT162B2), on 09Apr2021 as dose 1, single (Lot number: EW0150), in left arm, on 30Apr2021 as dose 2, single (Lot number: EW0167), in left arm and on 16Nov2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 61 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 08Apr2022 as dose 4 (booster), single (Lot number: 066K21A), in left arm and on 06Sep2022 as dose 5 (booster), single (Lot number: AS7143C), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Slightly overweight (BMI of 26-27)" (unspecified if ongoing), notes: Slightly overweight (BMI of 26-27); "History of TIA (1 event in 1992)", start date: 1992 (unspecified if ongoing), notes: History of TIA (1 event in 1992); "high blood sugar due to gestational diabetes" (unspecified if ongoing), notes: high blood sugar due to gestational diabetes; "high blood sugar due to gestational diabetes" (unspecified if ongoing), notes: high blood sugar due to gestational diabetes; "Hepatitis A", start date: 1989 (unspecified if ongoing); "Thyroid nodules" (unspecified if ongoing); "squamous and basal cell skin cancers (resolved)" (not ongoing), notes: squamous and basal cell skin cancers (resolved); "squamous and basal cell skin cancers (resolved)" (not ongoing), notes: squamous and basal cell skin cancers (resolved). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 08Apr2022, outcome "unknown", described as "Pfizer / BioNTech, Dose Number: 3 ; Moderna, Dose Number: 4"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: Body mass index: 26-27. Therapeutic measures were taken as a result of vaccination failure, covid-19 including Paxlovid from 31Jan2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body mass index
- Hospital-Tage
- -
- Labordaten
- Test Name: BMI; Result Unstructured Data: Test Result:26-27
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Basal cell carcinoma (squamous and basal cell skin cancers (resolved)); Blood glucose increased (high blood sugar due to gestational diabetes); Gestational diabetes (high blood sugar due to gestational diabetes); Hepatitis A; Overweight (Slightly overweight (BMI of 26-27)); Squamous cell carcinoma of skin (squamous and basal cell skin cancers (resolved)); Thyroid nodule; TIA (History of TIA (1 event in 1992))
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 02.02.2023
- Impfdatum
- 31.12.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 32,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Menstruation irregular
Symptomtext
Irregular menstrual cycle - extremely heavy periods, and now have 2 periods per menstrual cycle (period every two weeks).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 08.12.2021
- Beginn
- 22.01.2023
- Tage bis Beginn
- 410,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Covid test positive.; Covid test positive.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 44-year-old male patient received BNT162b2 (BNT162B2), on 12Feb2021 as dose 1, single (Lot number: EL9265), in left arm, on 04Mar2021 as dose 2, single (Lot number: EN6200), in left arm and on 08Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 43 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 22Jan2023, outcome "unknown" and all described as "Covid test positive.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Jan2023) Positive. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and any Other medications in two weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since vaccination, patient had tested for COVID-19.Patient did not have any known allergies and no other medical history. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230122; Test Name: BinaxNow; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Incorrect vaccine administered. Should have been age 5-11 dose and was given 12+ dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 30.12.2022
- Impfdatum
- 08.12.2021
- Beginn
- 22.08.2022
- Tage bis Beginn
- 257,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
Diagnosed and hospitalized with COVID 19 while vaccinated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 30,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 11.12.2021
- Beginn
- 12.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abnormal behaviour
Anger
Decreased appetite
Gait disturbance
Mental status changes
Hand fracture
Laboratory test
Loss of personal independence in daily activities
Mental impairment
Slow response to stimuli
Staring
Symptomtext
Within 24 hours his mind deteriorated and could not function very well. He would just stand in oncoming traffic, hit street signs, walk barefoot and no coat in the cold, walk sideways or backward and could no longer play piano. His boss asked us to pick him up because she feared he was going to run over by a car and this was the day after his shot. Things just got worse by the day. He hit a sign and broke his hand. He tried to jump out of a moving car. He was a danger to himself and others. The first hospital was the Hospital, The second one was the hospital again, the 3rd hospital was hospital, the 4th hospital was hospital again . The 5th hospital was Mental hospital, The 6th place was the facility for 3 months!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abnormal behaviour
- Hospital-Tage
- 140,0
- Labordaten
- Numerous test at the hospitals
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- U
- Eingang
- 22.12.2022
- Impfdatum
- 20.12.2021
- Beginn
- 12.12.2022
- Tage bis Beginn
- 357,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
HOSPITALIZED WITH COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 20.12.2021
- Beginn
- 20.11.2022
- Tage bis Beginn
- 335,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Productive cough
SARS-CoV-2 test negative
Sputum discoloured
Symptomtext
I started developing a chronic cough that was bringing up phlegm that was from light green to opaque white in color. I took a COVID test that was negative. I was given a nasal spray, azithromycin, montelukast. The cough went away but still persists a little bit till this day. It's intermittent and cold air seems to trigger it and then it lingers for a few hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- COVID-19 test negative
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.12.2022
- Impfdatum
- 01.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Deafness
Tinnitus
Symptomtext
Tinnitus approximately week or so after the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- Hearing test- saw ENT Loss of hearing and tinnitus
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteopenia
- Andere Medikamente
- Lipitor, Flonase, Zyrtec, calcium, multivitamin, fish oil
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 19.10.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 45,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated. COVID infection breakthrough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 30.11.2021
- Beginn
- 23.11.2022
- Tage bis Beginn
- 358,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Herpes zoster
Symptomtext
Shingles : onset 11/23/22, diagnosis 11/28/22, Rx: Valacyclovir 1 GM Tab, lidocaine patch, and 600mg ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pirmella 1-35 28 Tab, Olly women's multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.11.2022
- Impfdatum
- 21.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Apr2021 as dose 1, single (Lot number: ER8732), in left arm, on 04May2021 as dose 2, single (Lot number: EW0167), in left arm and on 21Nov2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 61 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 01Jun2022 as dose 4 (booster), single (Lot number: 054A22A), in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Neomycin, reaction(s): "Allergy". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (2022) Positive, notes: Treatment of COVID-19; (08Nov2022) Negative; (09Nov2022) Negative; (12Nov2022) Positive; (12Nov2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Paxlovid was used for treatment of COVID-19 from 03Nov2022 to 07Nov2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: home rapid antigen test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20221108; Test Name: home rapid antigen test; Test Result: Negative ; Test Date: 20221109; Test Name: home rapid antigen test; Test Result: Negative ; Test Date: 20221112; Test Name: home rapid antigen test; Test Result: Positive ; Test Date: 20221112; Test Name: home rapid antigen test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 30.11.2021
- Beginn
- 23.10.2022
- Tage bis Beginn
- 327,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Systemic inflammatory response syndrome
Symptomtext
Hospitalization for SIRS due to COVID-19 on dates 10/23/22- 10/30/22. Treated with dexamethasone, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 06.12.2021
- Beginn
- 12.07.2022
- Tage bis Beginn
- 218,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Tinnitus
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Nasal Swab Positive; Nasal Swab Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 18Mar2021 at 13:00 as dose 1, single (Lot number: EN6208), in right arm, on 09Sep2021 at 13:00 as dose 2, single (Lot number: ER8732), in right arm and on 06Dec2021 at 16:00 as dose 3 (booster), single (Lot number: 33030BD) at the age of 61 years, in right arm for covid-19 immunization. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 12Jul2022, outcome "unknown" and all described as "Nasal Swab Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (12Jul2022) Positive.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201269702 same patient/drug, different dose/event;US-PFIZER INC-202201269523 same patient/drug, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220712; Test Name: Nasal Swab; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies No; other medical history None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 06.12.2021
- Beginn
- 12.07.2022
- Tage bis Beginn
- 218,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Tinnitus
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Nasal Swab Positive; Nasal Swab Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 18Mar2021 at 13:00 as dose 1, single (Lot number: EN6208), in right arm, on 09Sep2021 at 13:00 as dose 2, single (Lot number: ER8732), in right arm and on 06Dec2021 at 16:00 as dose 3 (booster), single (Lot number: 33030BD) at the age of 61 years, in right arm for covid-19 immunization. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 12Jul2022, outcome "unknown" and all described as "Nasal Swab Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (12Jul2022) Positive.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201269702 same patient/drug, different dose/event;US-PFIZER INC-202201269523 same patient/drug, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220712; Test Name: Nasal Swab; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies No; other medical history None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 05.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19; COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Apr2021 at 14:00 as dose 1, single (Lot number: EW0153), in right arm, on 27Apr2021 at 14:00 as dose 2, single (Batch/Lot number: unknown), in right arm and on 05Dec2021 at 14:00 as dose 3 (booster), single (Lot number: 33030BD) at the age of 47 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Thyroid disorder" (unspecified if ongoing); "long QT syndrome" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "depression" (unspecified if ongoing); "ADD" (unspecified if ongoing); "restless leg syndrome" (unspecified if ongoing); "overweight" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: MOBIC, start date: 01Jan2016; SYNTHROID, start date: 01Jan2016; CYTOMEL, start date: 01Jan2016; TRAZODONE, start date: 01Jan2016; LAMICTAL, start date: 01Jan2016; PROPRANOLOL, start date: 01Jan2016; BUSPAR, start date: 01Jan2016; ADDERALL, start date: 01Jan2016. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: COVID 19 Treatment; (23Oct2022) positive, notes: I took 2 antigen self tests, and both came back positive; (23Oct2022) Positive, notes: I took 2 antigen self tests, and both came back positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received other medications in 2 weeks started in 01Jan2016. Patient received treatment for covid-19 which was Paxlovid from 14oct2022 to 19oct2022. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 20221023; Test Name: Covid-19 test; Test Result: Positive ; Comments: I took 2 antigen self tests, and both came back positive.; Test Date: 20221023; Test Name: Covid-19 test; Test Result: Positive ; Comments: I took 2 antigen self tests, and both came back positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ADD; Anxiety; Depression; Hypertension; Long QT syndrome; Overweight; Penicillin allergy; Restless leg syndrome; Thyroid disorder
- Andere Medikamente
- MOBIC; SYNTHROID; CYTOMEL; TRAZODONE; LAMICTAL; PROPRANOLOL; BUSPAR; ADDERALL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 02.12.2021
- Beginn
- 25.09.2022
- Tage bis Beginn
- 297,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), on 08Mar2021 as dose 1, single (Lot number: EN6201), in left arm, on 29Mar2021 as dose 2, single (Lot number: EP6955), in left arm and on 02Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 59 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. No allergies were reported. The following information was reported: COVID-19 (medically significant), VACCINATION FAILURE (medically significant) all with onset 25Sep2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (25Sep2022) Positive; (03Oct2022) Negative. Therapeutic measures were taken as a result of covid-19, vaccination failure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220925; Test Name: COVID; Test Result: Positive ; Test Date: 20221003; Test Name: COVID; 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
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 02.12.2021
- Beginn
- 22.07.2022
- Tage bis Beginn
- 232,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal operation
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 7/22/22 - 8/14/22 (23 DAYS) Presentation to the ED: PATIENT WAS HOSPITALIZED D/T ABDOMINAL SURGERY. COVID-19 + date: 7/22/22; PATIENT STATES SHE TESTED POSITIVE INITALLY 3 WEEKS PRIOR TO THE CONFIRMED TEST WHILE HOSPITALIZED. Treatment: NONE. Discharge to: HOME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal operation
- Hospital-Tage
- 23,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHF, DM, DEPRESSION, GERD, TIA.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 14.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old male patient received BNT162b2 (BNT162B2), on 01Mar2021 as dose 1, sigle (Lot number: EL3248), in right arm, on 22Mar2021 as dose 2, single (Lot number: EL3248), in right arm and on 14Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 44 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: no
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 02.12.2021
- Beginn
- 10.09.2022
- Tage bis Beginn
- 282,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
patient hospitalized
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 15.12.2021
- Beginn
- 23.08.2022
- Tage bis Beginn
- 251,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Tested positive for Covid 19 after receiving 3 doses of the Pfizer Covid 19 Vaccine; Tested positive for Covid 19 after receiving 3 doses of the Pfizer Covid 19 Vaccine; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the patient. A 66-year-old female patient received BNT162b2 (BNT162B2), on 17Feb2021 as dose 1, single (Lot number: EL9266), on 10Mar2021 as dose 2, single (Lot number: EN6206) and on 15Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 66 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 23Aug2022, outcome "unknown" and all described as "Tested positive for Covid 19 after receiving 3 doses of the Pfizer Covid 19 Vaccine". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (23Aug2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient use Paxlovid for the treatment of covid 19. Reporter stated that she originally tested positive for Covid 19 on Tuesday 23Aug2022, and she did not know if she was still testing positive or not, she had not retested. Caller also corrects that she started Paxlovid on Wednesday 24Aug2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220823; Test Name: Covid-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 18.12.2021
- Beginn
- 01.08.2022
- Tage bis Beginn
- 226,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33-year-old male patient received BNT162b2 (BNT162B2), on 07Apr2021 as dose 2, single (Lot number: EW0150), in left arm and on 18Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 33 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Lactose, reaction(s): "Known allergies: Lactose". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: COVID rebound 4 days after completing Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
INDIVIDUAL RESTARTED PRIMARY SERIES OVER BECAUSE THEY DID NOT RECEIVE THE 2ND DOSE WITHIN 21 DAYS. NOTIFIED FACILITY THAT 2ND DOSE IN SERIES CAN BE GIVEN AT ANY TIME AFTER 21 DAYS AND THAT YOU DO NOT NEED TO RESTART SERIES. NO ADVERSE EVENTS REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 03.12.2021
- Beginn
- 01.08.2022
- Tage bis Beginn
- 241,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Pfizer 3/19/21 Lot# ER8727; Pfizer 4/21/21 Lot# EW0164; Pfizer 12/3/21 Lot# 33030BD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- 30.07.2022
- Tage bis Beginn
- 220,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19 test in fully vaccinated and boosted patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 13.12.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 139,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Bladder spasm
Blood test normal
Breast mass
Menstruation irregular
Micturition urgency
Tenderness
Ultrasound breast normal
Symptomtext
Irregular Menstrual Cycle since February of 2022, test done that tested me for menopaused and it came back negative. I also developed a lump in my left breast with localized tenderness around spring time of 2022. I did an ultrasound in June of 2022, scan showed benign tissue however I was directed to follow-up in October. I am still having localized tenderness around left breast. My primary care doctor did have me see a breast specialist and to follow-up with a plan of care. My menstrual cycle has completely ceased. I did have to go to a urologist because it felt like I was having bladder spasms and thought that I had a UTI, urgent care and PCP stated that it was negative. I feel like I have to pee all the time. We are unclear of the cause as of now and this has been going on since April of 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amenorrhoea
- Hospital-Tage
- -
- Labordaten
- Ultrasound: Showing Benign Tissues in Left Breast Bloodwork for Menopause: Showing Negative Baseline Bloodwork: Created new Baseline for overall health
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Postural Orthostatic Hypertension Syndrome
- Andere Medikamente
- Fluoxetine; Women's Alive Multivitamin; Turmeric; Salt Tablets; Biotin; Iron; Magnesium; Midodrine; Vitamin D3; Maringa; Probiotic
- Allergien
- Gluten; Demurral
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 24.07.2022
- Impfdatum
- 12.01.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 170,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19; COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Apr2021 as dose 1, single (Lot number: EW0172), in left arm, on 14May2021 as dose 2, single (Lot number: EW0183), in right arm and on 12Jan2022 as dose 3 (booster), single (Lot number: 33030BD) at the age of 30 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Depression" (unspecified if ongoing); "adhd" (unspecified if ongoing); "asthma" (unspecified if ongoing); "arthritis" (unspecified if ongoing); "iron deficiency anemia" (unspecified if ongoing). Concomitant medication(s) included: VYVANSE, start date: 03Aug2016, stop date: 07Jul2022; BUPROPION, start date: 05Jan2022; IRON [FERROUS CITRATE], start date: 01Jan2018. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2022, outcome "unknown" and all described as "COVID 19". Therapeutic measures (Paxlovid) were taken as a result of drug ineffective, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ADHD; Arthritis; Asthma; Depression; Iron deficiency anemia
- Andere Medikamente
- VYVANSE; BUPROPION; IRON [FERROUS CITRATE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- F
- Eingang
- 24.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 1, single (Lot number: EW0161), in left arm, as dose 2, single (Lot number: EW0171), in left arm and as dose 3 (booster), single (Lot number: 33030BD), in left arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "depression" (unspecified if ongoing); "obesity" (unspecified if ongoing); "seasonal allergies" (unspecified if ongoing); "iron deficiency" (unspecified if ongoing); "acute asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset 2022, outcome "unknown", COVID-19 (medically significant) with onset 2022, outcome "recovered" (2022) and all described as "Treatment of COVID-19". The patient received paxlovid on 06Jul202 for treatment of COVID.The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative; Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID test/testing; Test Result: Negative ; Test Name: COVID test/testing; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; Asthma; Blood pressure high; Depression; Iron deficiency; Obesity; Seasonal allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 24.07.2022
- Impfdatum
- 03.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 28-year-old male patient received BNT162b2 (BNT162B2), on 07Apr2021 at 09:30 as dose 1, single (Lot number: EW0158), in left arm, on 28Apr2021 at 09:00 as dose 2, single (Lot number: ER8736), in left arm and on 03Dec2021 at 11:00 as dose 3 (booster), single (Lot number: 33030BD) at the age of 28 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Covid-19 treatment received of Paxlovid from 14Jul2022 to 17Jul2022 of lot number GC8236. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 17.12.2021
- Beginn
- 10.06.2022
- Tage bis Beginn
- 175,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive for COVID - 6/13/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Allergic to Tramadol
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 21.12.2021
- Beginn
- 27.05.2022
- Tage bis Beginn
- 157,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
covid-19; covid-19; This is a spontaneous report received from a contactable reporter (consumer). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (PFIZER BIONTECH COVID-19 VACCINE, solution for injection), on 21Dec2021 at 14:00 as dose 1, single (lot number: 33030BD) at the age of 61 years, in left arm for covid-19 immunization. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant) and COVID-19 (medically significant) with onset 27May2022, outcome "not recovered" and described as "covid-19". The patient underwent the following laboratory tests and procedures: covid-19 test: (27May2022) positive (first day of covid); (01Jun2022) negative; (06Jun2022) positive (woke up with symptoms, tested positive again). Therapeutic measures were taken as a result of drug ineffective and covid-19 which included Paxlovid. Clinical course: The patient started Paxlovid on first day of covid 27May2022. Took for 5 days. Tested negative on 01Jun2022. Woke up with symptoms on 06Jun2022 and tested positive again. No fever; head cold, cough and fatigue as of 09Jun2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220527; Test Name: Covid-19 Test; Test Result: Positive ; Comments: first day of covid; Test Date: 20220601; Test Name: Covid-19 Test; Test Result: Negative ; Test Date: 20220606; Test Name: Covid-19 Test; Test Result: Positive ; Comments: woke up with symptoms, tested positive again
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 13.12.2021
- Beginn
- 21.05.2022
- Tage bis Beginn
- 159,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Feb2021 at 18:00 as dose 1, single (Lot number: EM9810), in left arm, on 26Feb2021 at 10:45 as dose 2, single (Lot number: EN6202), in left arm and on 13Dec2021 at 18:30 as dose 3 (booster), single (Lot number: 33030BD) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Depression" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing), notes: known allergies: Penicillin. Concomitant medication(s) included: LEXAPRO, start date: 14Jun2010, stop date: 03Jun2022; IBUPROFEN, start date: 21May2022, stop date: 23May2022. The following information was reported: VACCINATION FAILURE (medically significant) with onset 21May2022, outcome "unknown", COVID-19 (medically significant) with onset 21May2022, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (21May2022) Positive, notes: Recent COVID test @ (institute name-withheld) on Sat 21May was Positive; (28May2022) Negative, notes: On 28May I tested and was Negative for COVID; (02Jun2022) Positive, notes: On Thursday, 02Jun while at work I felt the COVID symptoms again. Went home and tested positive for COVID; (03Jun2022) Positive, notes: Also had a test at booth Ive gone to many times today 03Jun and tested positive for COVID. Therapeutic measures were taken as a result of covid-19. Clinical course: The patient received treatment for COVID-19 included Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220521; Test Name: Covid-19; Test Result: Positive ; Comments: Recent COVID test @ (institute name-withheld) on Sat 21May was Positive; Test Date: 20220528; Test Name: Covid-19; Test Result: Negative ; Comments: On 28May I tested and was Negative for COVID; Test Date: 20220602; Test Name: Covid-19; Test Result: Positive ; Comments: On Thursday, 02Jun while at work I felt the COVID symptoms again. Went home and tested positive for COVID.; Test Date: 20220603; Test Name: Covid-19; Test Result: Positive ; Comments: Also had a test at booth Ive gone to many times today 03Jun and tested positive for COVID.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Depression; Penicillin allergy (known allergies: Penicillin)
- Andere Medikamente
- LEXAPRO; IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated and boosted twice. COVID breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 08.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Suspected COVID-19
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 37-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 24Mar2021 as dose 1, single (Lot number: EN6202), on 14Apr2021 as dose 2, single (Lot number: EN0169) and on 08Dec2021 as dose 3 (booster) single (Lot number: 33030BD) at the age of 37 years for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), SUSPECTED COVID-19 (medically significant), outcome "recovered" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, suspected covid-19. clinical course: Other medication in 2weeks: Yes, Known allergies: No.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Suspected COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 07.12.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 155,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19; COVID 19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 29-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 24Apr2021 as dose 1, single (Lot number: ER836), in right arm, on 22May2021 as dose 2, single (Lot number: EW0177), in right arm and on 07Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 28 years, in right arm for covid-19 immunisation. The patient was not pregnant at time of vaccination. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 11May2022, outcome "recovering" and all described as "COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (11May2022) Positive; (17May2022) Negative; (20May2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient did not receive other medication in 2weeks. The started taking Paxlovid on 11May (1 day after testing positive). Patient finished the dose on 15May and tested negative on 17May. On 20May, patient started feeling sick again and tested positive for Covid again. Patient wanted to report since these rebounds are rare and in case it is helpful. The patient received Treatment, Brand: Paxlovid, (Treatment start date: 11May2022, Treatment stop date: 15May2022). The patient known allergies was none. The patient other medical history was asthma. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220511; Test Name: Covid-19; Test Result: Positive ; Test Date: 20220517; Test Name: Covid-19; Test Result: Negative ; Test Date: 20220520; Test Name: Covid-19; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 03.12.2021
- Beginn
- 09.05.2022
- Tage bis Beginn
- 157,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received BNT162b2 (BNT162B2), on 17Mar2021 as dose 1, single (Lot number: EP7534), in left arm, on 05Apr2021 as dose 2, single (Lot number: ER8734), in right arm and on 03Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 49 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: LISINOPRIL; OMEPRAZOLE; BUPROPION; TURMERIC [CURCUMA LONGA]. The following information was reported: VACCINATION FAILURE (medically significant) with onset 09May2022, outcome "unknown", COVID-19 (medically significant) with onset 09May2022, outcome "not recovered" and all described as "COVID-19 Treatment". The event "covid-19 treatment" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06May2022) Negative; (09May2022) Positive; (13May2022) Positive; (15May2022) Negative; (20May2022) Positive. Therapeutic measures were taken as a result of vaccination failure. Therapeutic measures were not taken as a result of covid-19. Clinical course included patient started having symptoms Friday 06May2022. Rapid test resulted in a negative test. patient took another test Monday 09May2022 which came back positive. After consult with my Doctor Paxlovid was prescribed for me. Took first dose Monday 09May2022 evening. Last dose was taken Friday 13May2022, however patient still had a positive rapid test although I was feeling better. patient took another test Sunday 15May2022 and it came back negative. Mon thru most of Friday (16May2022 - 20May2022) patient felt fine. Friday 20May2022, patient started getting similar symptoms from the original onset (Stuffy / Runny nose, Sore throat, Random (infrequent) cough. Patient did another rapid test Friday 20May2022, and it showed a positive test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220506; Test Name: Rapid test; Test Result: Negative ; Test Date: 20220509; Test Name: Rapid test; Test Result: Positive ; Test Date: 20220513; Test Name: Rapid test; Test Result: Positive ; Test Date: 20220515; Test Name: Rapid test; Test Result: Negative ; Test Date: 20220520; Test Name: Rapid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LISINOPRIL; OMEPRAZOLE; BUPROPION; TURMERIC [CURCUMA LONGA]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 29.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) . The reporter is the patient. A 36-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Nov2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 36 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin; "Hypothyroid" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received anti-viral product for COVID 19 Treatment with Brand Paxlovid, treatment start date 13May2022, treatment stop date 17May2022. The patient experienced Itchy back and body 1 day after completing Paxlovid, taste is gone and vision is little blurry.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism; Penicillin allergy (Known allergies: Penicillin).
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 10.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19; COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 43 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: latex" (unspecified if ongoing), notes: Known allergies: latex; "Known allergies: Sulfa drugs" (unspecified if ongoing), notes: Known allergies: Sulfa drugs; "Mixed Connective Tissue Disease (auto-immune)" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset 2022, outcome "unknown", COVID-19 (medically significant) with onset 2022, outcome "not recovered" and all described as "COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (16May2022) Positive. Therapeutic measures were taken as a result of covid-19. Clinical course included: The patient received Paxlovid as COVID-19 treatment from 08May2022 to 12May2022. She completed Paxlovid treatment on 12May2022 and had a full relapse of symptoms and positive Rapid Test on 16May2022. The patient at the time of reporting was 3 days into fully symptoms, getting worse each day. The patient did not recover.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220516; Test Name: Rapid Test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Latex allergy (Known allergies: latex); Mixed connective tissue disease; Sulfonamide allergy (Known allergies: Sulfa drugs)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 01.12.2021
- Beginn
- 27.04.2022
- Tage bis Beginn
- 147,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
tested positive; tested positive; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 01Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 52 years, in left arm for covid-19 immunisation; COVID-19 Vaccine - Manufacturer Unknown, as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Overweight" (unspecified if ongoing). There were no concomitant medications. The following information was reported: COVID-19 (medically significant) with onset 27Apr2022, outcome "not recovered", DRUG INEFFECTIVE (medically significant) with onset 27Apr2022, outcome "unknown" and all described as "tested positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (27Apr2022) positive; (02May2022) negative, notes: a rapid in home test; (06May2022) negative, notes: a rapid in home test; (07May2022) positive. Therapeutic measures were taken as a result of covid-19. COVID 19 Treatment included Paxlovid from 27Apr2022 to 02May2022. Clinical course: No known allergies reported. The patient received no other medications in 2 weeks. Patient had tested positive on 27Apr and took the 5 days of Paxlovid and felt no symptoms upon completion. On his last day of taking Paxlovid 02May, he was tested negative with a rapid in home test. 3 days later on 05May he began experiencing minor symptoms (cough, runny nose). On 06May the symptoms worsened and he took a rapid in home test which was negative. On 07May the cough was much worse and he tested positive. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220427; Test Name: Covid test; Test Result: Positive ; Test Date: 20220502; Test Name: Covid test; Test Result: Negative ; Comments: a rapid in home test; Test Date: 20220506; Test Name: Covid test; Test Result: Negative ; Comments: a rapid in home test; Test Date: 20220507; Test Name: Covid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Overweight
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 19.11.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 47,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Alopecia areata
Symptomtext
Alopecia Areata, followed by hair loss from entire scalp. Currently I've lost about 50% of my hair, but it has started accelerating.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Eczema
- Andere Medikamente
- Zyrtec Iron supplements
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 07.12.2021
- Beginn
- 29.04.2022
- Tage bis Beginn
- 143,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Contracted covid - positive test 05/02/2022 (May ,2 2022)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Contracted covid - positive test 05/02/2022 (May ,2 2022)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.04.2022
- Impfdatum
- 06.12.2021
- Beginn
- 16.04.2022
- Tage bis Beginn
- 131,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
tested Covid positive/Caller states she is vaccinated and boosted and can't believe she got Covid; tested Covid positive/Caller states she is vaccinated and boosted and can't believe she got Covid; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 59-year-old female patient received BNT162b2 (BNT162B2), on 16Apr2021 as dose 1, single (Lot number: ER8733), in left arm, on 07May2021 as dose 2, single (Lot number: EW0158), in left arm and on 06Dec2021 as dose 3 (booster), single (Lot number: 33030BD) at the age of 59 years, in arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 16Apr2022, outcome "unknown" and all described as "tested Covid positive/Caller states she is vaccinated and boosted and can't believe she got Covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (16Apr2022) positive, notes: Unit: Not Provided. Clinical Course: Vaccination Facility Type: Pharmacy/Drug Store. Prior Vaccinations (within 4 weeks) was none. AE(s) following prior vaccinations: None, doesn't even get the flu shot. States as a matter of fact she had the least symptoms with Pfizer vaccine and wondered if it was effective, she barely had a sore arm.; Sender's Comments: Based on the information provided in the narrative, a causal association between the suspect drug and the events cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220416; Test Name: at home Covid test; Test Result: Positive ; Comments: Unit: Not Provided
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 22.03.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 224,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anti-thyroid antibody
Autoimmune thyroiditis
Blood thyroid stimulating hormone increased
Hypothyroidism
Thyroxine free normal
Symptomtext
Hypothyroidism, autoimmune hashimoto disease
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anti-thyroid antibody
- Hospital-Tage
- -
- Labordaten
- 12/7 Thyroglobulin antibody-2 Tsh -14.2 T4 free .94
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity , psoriasis
- Andere Medikamente
- Fiber pills and vitamins
- Allergien
- None
- Vorherige Impfungen
- Flu vaccine, increased blood pressure. Late 40s
- Staat
- MN
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 06.12.2021
- Beginn
- 09.04.2022
- Tage bis Beginn
- 124,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Gait disturbance
Joint swelling
X-ray limb normal
Symptomtext
I had swollen in my left knee for about 5 days. I contacted my doctor about this. They did x-ray, normal results. I was diagnosed with gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gait disturbance
- Hospital-Tage
- -
- Labordaten
- X-ray
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 30.11.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 15,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Amniorrhoea
Caesarean section
Exposure during pregnancy
Symptomtext
Patient G3P0202 at 31.3 weeks who presents with leaking fluid. She was given betamethasone and a magnesium bolus as well as her first dose of latency phase antibiotics and transferred to alternate facility for further care. Plan was for in-house monitoring until 34 weeks EGA or earlier date if medically indicated. The patient did reach 34 weeks EGA. The patient underwent a repeat cesarean delivery. Mother and baby did well with the procedure. The mother was sent to the floor in good condition, the baby was sent to the clinic. Birthweight (5 lb 9.2 oz). Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amniorrhoea
- Hospital-Tage
- 19,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 21.12.2021
- Beginn
- 16.01.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Unevaluable event
Symptomtext
Patient had an ED visit and/or hospitalization within 6 weeks of receiving COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 08.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Gastrointestinal tube insertion
Intestinal obstruction
Symptomtext
Partial small bowel obstruction - Patient symptoms rapidly resolved with NG tube. Her bowel function was restored. She is tolerating p.o. and she is having bowel movements. She will be discharged in stable condition. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gastrointestinal tube insertion
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 21.12.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Delivery
Exposure during pregnancy
Normal labour
Symptomtext
Normal labor and delivery. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Delivery
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 24.12.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 33,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Caesarean section
Exposure during pregnancy
Salpingectomy
Symptomtext
Bilateral - cesarean delivery with bilateral salpingectomy Primary Diagnosis: pregnancy at 39w0d. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Caesarean section
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 13.12.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 38,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Appendicectomy
Explorative laparotomy
Gastric lavage
Pneumoperitoneum
Symptomtext
Pneumoperitoneum of unknown etiology - Procedures performed: Exploratory laparotomy, abdominal lavage, appendectomy. Recovery in hospital and discharge home. Hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Appendicectomy
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 07.12.2021
- Beginn
- 31.03.2022
- Tage bis Beginn
- 114,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Fully vaccinated and boosted. COVID infection breakthrough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 02.12.2021
- Beginn
- 26.02.2022
- Tage bis Beginn
- 86,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Vaccination site extravasation
Vaccination site haemorrhage
Symptomtext
A vaccinator was vaccinating a client, and some fluid leaked out at injection site.; A vaccinator was vaccinating a client, and some fluid leaked out at injection site.; blood trickle down the arms; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. A 24 year-old male patient received bnt162b2 (COMIRNATY), administered in arm, administration date 08Feb2022 (Lot number: 33030BD, Expiration Date: 31May2022) at the age of 24 years as dose number unknown, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: INCORRECT DOSE ADMINISTERED (non-serious), VACCINATION SITE EXTRAVASATION (non-serious) all with onset 08Feb2022, outcome "unknown" and all described as "A vaccinator was vaccinating a client, and some fluid leaked out at injection site."; VACCINATION SITE HAEMORRHAGE (non-serious) with onset 08Feb2022, outcome "unknown", described as "blood trickle down the arms". Additional information: Reporter is a Physician Assistant, working at a vaccination site. A vaccinator was vaccinating a client, and some fluid leaked out at injection site. Unsure how much of the vaccine was actually administered. Asking that should we give another dose immediately. Patient was administered today (at the time of report, that is 08Feb2022). Physician assistant confirmed that not the entire dose of the purple cap Pfizer BioNTech covid-19 Vaccine has been administered to a patient. They estimate it to be about half or 3/4 of the dose only administered, after she pulled the needle out there is little bit of fluid and little bit of blood trickle down the arms. Reporter don't know how much actually got in but MA (further not clarified) told me after she pulled the needle out there is little bit of fluid and little bit of blood trickle down the arms. Reporter was thinking it was at least half the dose if not more actually got in, but just can't be sure and didn't see it. Follow-up attempts are completed. No further information is expected. Amendment: This follow-up report is being submitted to allow appropriate reporting to health authorities and updated event from injection site leaking to vaccination site extravasation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 21.03.2022
- Impfdatum
- 15.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Unevaluable event
Symptomtext
ED visit and hospitalization within 6 weeks of COVID vaccination. ED visit 11/27, hospitalization 12/2/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 17.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest tube insertion
Pneumothorax
Rib fracture
Symptomtext
Traumatic fracture of ribs of right side with pneumothorax - chest tube placement. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest tube insertion
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 10.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
-PFIZER COVID 12 plus VACCINE, HE IS 9 YEARS OLD. -PARENT NOTIFIED -NO REACTIONS/ NO ADVERSE EVENTS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Product preparation issue
Symptomtext
Pharmacist discovered vaccine product (Pfizer) had extra doses /solution then what he has normally come accustomed to into later part of working shift when recording/drawing a 6th and final dose to be administered of Pfizer vaccine. Pharmacist believes there were 1-2 more doses at least left worth remaining to able to be given from product. Pharmacist also discovered extra recording "tally" mark on vial on how pharmacy records vials per company standing operating procedure for Moderna opened product. Video footage has not been studied nor possibly will not be able to reviewed or confirm but am taking precautions in case vaccine product did not have "extra" doses and patient was inadvertently given wrong vaccine (Moderna) as booster and or overly diluted product.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- TAKING CONTRACEPTION DURING VACCINE ACCORDING TO MEDICAL HEALTH RECORD.
- Andere Medikamente
- NON KNOWN TO PHARMACY, DOES NOT FILL MEDICATIONS WITH THIS PHARMACY.
- Allergien
- NO KNOWN DRUG ALLERGIES.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Product preparation issue
Underdose
Symptomtext
Pharmacist discovered vaccine product (Pfizer) had extra doses /solution then what he has normally come accustomed to into later part of working shift when recording/drawing a 6th and final dose to be administered of Pfizer vaccine. Pharmacist believes there were 1-2 more doses at least left worth remaining to able to be given from product. Pharmacist also discovered extra recording "talley" mark on vial on how pharmacy records vials per company standing operating procedure. Video footage has not been studied nor possibly will not be able to reviewed or confirm but am taking precautions in case vaccine product did not have "extra" doses and patient was inadvertently given wrong vaccine (Moderna) as booster and or overly diluted product.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none at this time.
- Aktuelle Erkrankungen
- NOTHING THAT WAS PRESENTED TO PHARMACY.
- Vorgeschichte
- NOTHING THAT WAS PRESENTED TO PHARMACY.
- Andere Medikamente
- NOT KNOWN DOES NOT FILL MEDICATIONS AT THIS PHARMACY.
- Allergien
- NKDA.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Product preparation issue
Underdose
Symptomtext
Pharmacist discovered vaccine product (Pfizer) had extra doses /solution then what he has normally come accustomed to into later part of working shift when recording/drawing a 6th and final dose to be administered of Pfizer vaccine. Pharmacist believes there were 1-2 more doses at least left worth remaining to able to be given from product. Video footage has not been studied nor possibly will not be able to reviewed or confirm but am taking precautions in case vaccine product did not have "extra" doses and patient was inadvertently given wrong vaccine (Moderna) as booster and or overly diluted product. Incident reporting was delayed due to ideally wanting this all confirmed with visual footage however have decided to take extra over precaution.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- NONE AT THIS TIME.
- Aktuelle Erkrankungen
- None pharmacy is aware of.
- Vorgeschichte
- None pharmacy was made aware of.
- Andere Medikamente
- NOT KNOWN, DOES NOT FILL MEDICATIONS HERE.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 12.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Product preparation issue
Symptomtext
Pharmacist discovered vaccine product (Pfizer) had extra doses /solution then what he has normally come accustomed to into later part of working shift when recording/drawing a 6th and final dose to be administered of Pfizer vaccine. Pharmacist believes there were 1-2 more doses at least left worth remaining to able to be given from product. Video footage has not been studied nor possibly will not be able to reviewed or confirm but am taking precautions in case vaccine product did not have "extra" doses and patient was inadvertently given wrong vaccine (Moderna) as booster and or overly diluted product. Incident reporting was delayed due to ideally wanting this all confirmed with visual footage however have decided to take extra over precaution.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- HYPERTENSION, HEART HEALTH RELATED MEDICATIONS, HORMONAL IMABALANCE
- Andere Medikamente
- LEXAPRO, LOSARTAN, IBUPROFEN, ESTRADIOL, HYDROCHLOROTHIAZIDE, POTASSIUM CHLORIDE 10 MEQ ER, FLEXERIL (PRN)
- Allergien
- MORPHINE AND RELATED.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 12.03.2022
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Product preparation issue
Symptomtext
Pharmacist discovered vaccine product (Pfizer) had extra doses /solution then what he has normally come accustomed to into later part of working shift when recording/drawing a 6th and final dose to be administered of Pfizer vaccine. Pharmacist believes there were 1-2 more doses at least left worth remaining to able to be given from product. Video footage has not been studied nor possibly will not be able to reviewed or confirm but am taking precautions in case vaccine product did not have "extra" doses and patient was inadvertently given wrong vaccine (Moderna) as booster and or overly diluted product.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- thyroid condition
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Off label use
Product storage error
Symptomtext
INDIVIDUAL RECEIVED VACCINE STORED PAST THE BEYOND USE DATE (FOR REFRIGERATION) AND THE ADDITIONAL 14 DAY STABILITY DATE (OFF LABEL). INDIVIDUAL TO BE REVACCINATED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Off label use
Product storage error
Symptomtext
INDIVIDUAL RECEIVED VACCINE STORED PAST THE BEYOND USE DATE (FOR REFRIGERATION) AND THE ADDITIONAL 14 DAY STABILITY DATE (OFF LABEL). INDIVIDUAL TO BE REVACCINATED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Off label use
Product storage error
Symptomtext
INDIVIDUAL RECEIVED VACCINE STORED PAST THE BEYOND USE DATE (FOR REFRIGERATION) AND THE ADDITIONAL 14 DAY STABILITY DATE (OFF LABEL). INDIVIDUAL TO BE REVACCINATED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Off label use
Product storage error
Symptomtext
INDIVIDUAL RECEIVED VACCINE STORED PAST THE BEYOND USE DATE (FOR REFRIGERATION) AND THE ADDITIONAL 14 DAY STABILITY DATE (OFF LABEL). INDIVIDUAL TO BE REVACCINATED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Off label use
Product storage error
Symptomtext
INDIVIDUAL RECEIVED VACCINE STORED PAST THE BEYOND USE DATE (FOR REFRIGERATION) AND THE ADDITIONAL 14 DAY STABILITY DATE (OFF LABEL). INDIVIDUAL TO BE REVACCINATED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Off label use
Product storage error
Symptomtext
INDIVIDUAL RECEIVED VACCINE STORED PAST THE BEYOND USE DATE (FOR REFRIGERATION) AND THE ADDITIONAL 14 DAY STABILITY DATE (OFF LABEL). INDIVIDUAL TO BE REVACCINATED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Off label use
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 02.12.2021
- Beginn
- 18.02.2022
- Tage bis Beginn
- 78,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Adult dose given. Dr. was notified. I informed patient's mother after the shot was given. No Adverse reaction reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
The patient received a COVID-19 booster dose later found to be involved in a temperature excursion of 34 hours at max temp of 8.54 Celsius. The manufacturer was unable to provide additional stability information that applied to this excursion. The patient/parent notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Singulair
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
This patient received an adult dose of pfizer for his second shot, tolerated well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 01.04.2021
- Beginn
- 18.04.2021
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cervical cyst
Cyst removal
Heavy menstrual bleeding
Hypomenorrhoea
Ultrasound scan
Ultrasound uterus abnormal
Symptomtext
Periods became extremely heavy around the time of the vaccine. I didn't immediately make any connection but saw a few stories about women reporting similar symptoms. My periods have been consistently and extremely heavy since my shots. Previously they were sporadically heavy. This is extremely heavy bleeding that lasts for 2 or 3 day then stops. My periods used to last 5-7 days. Multiple times I have bled through clothing and had to drive home from work to change clothes. I've discussed this with my OB. They did a sonogram then a sonohysterogram (late 2021) and found no issues other than a Nabothian cyst. That cyst was removed, it was sent to pathology with no issue. My periods continue to be extremely heavy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cervical cyst
- Hospital-Tage
- -
- Labordaten
- 10/28/2021 - Sonogram - revealed possible polyp and recommended a follow up. 12/17/2021 - Sonohysterogram revealed no issues other than a Nabothian cyst. That cyst was removed, it was sent to pathology with no issue. My periods continue to be extremely heavy.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraine headaches lifelong although have tapered.
- Andere Medikamente
- Suboxone - 2 x 2 mg @ 2x / day, Famotidine - 20 mg @ 1x / day
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
11 year old female inadvertently administered a 12 year and older 1st dose of Pfizer Covid 19 Vaccine instead of 5-11 year old1st dose of Pfizer Covid 19 Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered a pfizer purple cap dose past the beyond use date. Patient was observed for the full 15 minute waiting period and didn't seem to have any type of adverse event occur. We wanted to document just in case something were to occur later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- n/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
Patient was administered a pfizer purple cap dose that was past the beyond use date. Patient was observed for the 15 minute period without any incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 11.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest X-ray
Chest discomfort
Fibrin D dimer
Fibrin D dimer increased
SARS-CoV-2 test negative
Ventilation/perfusion scan
Symptomtext
She even had an elevated D dimer test with no PE on VQ scan. She is slowly improving but continues to have some chest tightness with deep breaths.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest X-ray
- Hospital-Tage
- -
- Labordaten
- Chest X-Ray - Normal NM Profusion Lung Scan - Negative COVID-19 PCR - Negative
- Aktuelle Erkrankungen
- SOB
- Vorgeschichte
- Personal history of colon polyp, benign dyslipidemia
- Andere Medikamente
- N/A
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product preparation issue
Symptomtext
incorrect amount of dilutant was mixed with the pfizer bioNtech covid vaccine age group 12 yrs and up . 0.8 was mixed instead of the 1.8
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- cefdinir
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 10.02.2022
- Impfdatum
- 09.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus in both ears.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Peripheral neuropathy feet from lower back issues.
- Andere Medikamente
- Multivitamin, ibuprofen.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
During vaccination, MA withdrew and small amount of vaccine drained out of site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product preparation issue
Symptomtext
@ 0927 Patient received 0.3 undiluted dose of the pFizer vaccine on the left arm. This was the patients second dose of the pfizer vaccine. Patient was observed for 45 mins, no adverse reactions displayed. Patient mother at the side of patient, fully aware of the error. This was the vaccinators first time at the site, the vaccinators did not have the proper training at the time prior to incident error occurring. The mother of the patient work at the site where she is familiar with the policy and procedures. There was no on-site manager at the site at the time the incident occurred. Patient remained in stable condition throughout the duration of stay in observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product preparation issue
Symptomtext
At 09:27 patient received 0.3mL undiluted dose of the Pfizer vaccine in the left arm. This was the patient's second Pfizer vaccine dose. Patient observed for 45 minutes. No adverse reactions displayed. Patient's mother at his side, fully aware of the error. This was the vaccinator's first time at the site and did not have the proper training at the time prior to incident error occurring. The mother of the patient is familiar with the policy and procedures. There was no on-site manager at the site at the time the incident occurred. Patient remained in stable condition throughout the duration of stay in observation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 08.12.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 55,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Hypertensive crisis
Transient ischaemic attack
Symptomtext
TIA and urgent hypertensive crisis. Possible CVA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertensive crisis
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Eye movement disorder
Symptomtext
Patients head tilted back and eyes were rolled up, towards the top. She appeared clammy and remained conscious. Patient did not want to discuss past medical history but stated this has happened before when she received previous vaccines. Patient quickly returned to normal state. Vital signs were taken and she was offered water.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cold sweat
- Hospital-Tage
- -
- Labordaten
- Non medical tests or laboratory tests were ordered.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None
- Andere Medikamente
- Patient denies taking any prescriptions, OTC medications, dietary supplements or herbal remedies at the time of vaccination.
- Allergien
- None
- Vorherige Impfungen
- Patient did not want to elaborate any further about prior history besides that she has had similar reaction following prior vacc
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 25.01.2022
- Impfdatum
- 02.12.2021
- Beginn
- 21.01.2022
- Tage bis Beginn
- 50,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Possible breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID + on 1/21/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GU
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 29.11.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abortion spontaneous
Haemorrhage
Injury
Pregnancy test positive
Ultrasound scan abnormal
Symptomtext
LMP 10/06/2021 positive pregnancy test first week of December 2021 patient states bleeding from 12/7/2021-1/9/2022 consistent with miscarriage
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion spontaneous
- Hospital-Tage
- -
- Labordaten
- FIRST TRIMESTER MISCARRIAGE CONFIRMED POST VACCINE BY ULTRASOUND Patient is recovering from physical and emotional trauma. Will continue to follow.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- BIRTH CONTROL NORTEL 1/35
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Spoke with RN with Pfizer and staff regarding pfiizer vaccine that was adminstered to pt on 1/3/22 per immunizations due to vial was expired as of 12/31/21. Per RN there is a 32 day max on vials that are refrigerated. Staff Medical information told nurse to contact cdc to discuss 2nd step. Also contacted CDC and spoke with staff and recommended for pt to get re-vaccinated due to expired vaccine. Pt has no c/o adverse effects at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong vaccine formulation (ex. different manufacturer initial and booster).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
PATIENT RECEIVED COVID VACCINE FOR 12 AND UP INSTEAD OF 5-11 DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
PATIENT RECEIVED COVID 19 VACCINE FOR 12 AND UP INSTEAD OF 5-11 DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Computerised tomogram
Echocardiogram
Laboratory test
Magnetic resonance imaging
Musculoskeletal disorder
Neurological symptom
Sensory disturbance
Symptomtext
On 1/12/2022, I had a doctor appointment for an evaluation of my blood pressure. My appointment was at 2:00 pm. When I was leaving at 1:00, my left arm was feeling like I hit my funny bone from the shoulder to my finger tips. I took this as an effect of the shot in the arm. When I arrived for my appointment and was sitting in the waiting room, the same feeling started in my left leg, and I began to lose strength/use of my left foot. When I reported the situation to my doctor, she said it sounded like stroke symptoms and called for an ambulance. When I arrived a Hospital, they ran a few tests and CT scan as well as an MRI before admitting me. The next morning they did a echocardiogram. All of this happened within 48 hours of receiving to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 1,0
- Labordaten
- See Item 18
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Metoporol ER, Amlodapine, Losartan
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Ear, nose and throat examination
Tinnitus
Tympanometry
Symptomtext
Tinnitus - persistent ringing in both ears. Still occurring one month later. ENT could not find other causes for Tinnitus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear, nose and throat examination
- Hospital-Tage
- -
- Labordaten
- Exam performed by ENT doctor, Tympanometry and Audio Threshold Evaluation.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Ulcerative Colitis
- Andere Medikamente
- Mesalamine, Vitamin D suppement, Tylenol
- Allergien
- Pennicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive on 01/07/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine placed in freezer on 12/6/21 and removed from freezer on 1/3/22, outside the recommended freezer duration date. No adverse effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was placed in freezer on 12/6/21 and was pulled out of freezer on 1/3/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was placed in freezer on 12/6 and was not removed until 1/3/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine placed in freezer on 12/9/2021 and removed from freezer on 1/3/22, outside the recommended amount of time they are supposed to be in the freezer. No adverse effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was placed in freexer on 12/6 and pulled out of freezer on 1/3/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 03.01.2022
- Beginn
- 04.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Oedema
Symptomtext
significant edema to the left axilla
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oedema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperaesthesia
Immunisation
Joint swelling
Symptomtext
Left ankle swelled up with great deal of sensitivity, but no underlying injury. It went away suddenly after two days.; Left ankle swelled up with great deal of sensitivity, but no underlying injury. It went away suddenly after two days.; dose number=3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 51-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 26Dec2021 at 15:00 (Lot number: 33030BD)at the age of 51 year(s) as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE; Lot number: EW0177; Route of administration: Unspecified; Anatomical site: Left arm; Administration time: 12:00), administration date: 17May2021, when the patient was 51 year(s) old, for COVID-19 immunisation and Bnt162b2 (DOSE 1, SINGLE; Lot number: EW0171; Route of administration: Unspecified; Anatomical site: Left arm; Administration time: 11:30), administration date: 26Apr2021, when the patient was 51 year(s) old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 26Dec2021 at 15:00, outcome "unknown", described as "dose number=3"; JOINT SWELLING (non-serious), HYPERAESTHESIA (non-serious) all with onset 27Dec2021 at 22:00, outcome "recovered" (29Dec2021), and all described as "Left ankle swelled up with great deal of sensitivity, but no underlying injury. It went away suddenly after two days". Therapeutic measures were not taken as a result of joint swelling and hyperaesthesia. Additional Information: Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hyperaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient presented to clinic for Pfizer Booster. Her Pfizer #2 was administered on September 1, 2021. I administered her booster on January 10, 2021 ( 3 weeks early). Patient observed in clinic for 20 minutes and no complaints.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 13.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood smear test normal
Contusion
Differential white blood cell count
Fibrin D dimer normal
Full blood count
Hepatitis viral test negative
Immune thrombocytopenia
Immunoglobulin therapy
Metabolic function test
Oral blood blister
Petechiae
Platelet count decreased
Platelet transfusion
Symptomtext
About a week after my booster, I started noticing bruising on my body which worsened through the end of 2021. In early 2022, I noticed petechiae and mouth blood blisters (also on tongue). On Friday Jan 7 2022 I visited my primary provider who ran a full CBC and the platelet count was 2,000. She advised me to go to ER right away. In the ER they confirmed that my platelets were under 10,000 and consulted with the hematologist who started me on an aggressive dose of corto-steroid as the symptoms and timing corresponded to Immune-Mediated TCP due to Vaccine. That night after transferring to the regular hospital, I was also given IVIG and a platelet transfusion. I am still in the hospital and after a physical examination and review of my panels, the hematologist is even more confident that it's what was originally diagnosed. I do not know my long-term treatment plan is at this time but my platelet count is currently 38 after getting bumped to 50 on Sat Jan 8 and falling to 42 yesterday Sunday Jan 9. Hopefully stabilizing so I can be released but the doctor will make that call.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood smear test normal
- Hospital-Tage
- 4,0
- Labordaten
- Full CBC with differential daily since 1/7/22 (Primary, ER, in-hospital) Full metabolic panel daily since 1/7/22 (Primary, ER, in-hospital) Primary ran tests for thrombosis markers - all unremarkable - 1/7/22. Primary ran tests for hepititis infection - all unremarkable - 1/7/22. ER also ran blood smears for morphology - unremarkable - 1/7/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Paroxysmal Atrial Fibrillation High Lipoprotein A Occasional Iritis due to HLA-B27 Antigen Some osteo arthritis (minor) in toes and knees A bit of Rheumatoid Arthritis (suspected and minor) in one finger
- Andere Medikamente
- Flecainide 150 mg x 2 daily Atorvastin 40 mg daily Vitamin C 1000 mg x 2 daily Magnesium 250 mg x 2 daily Glucosomine 1500 mg x 2 daily Baby Aspirin 81 mg daily Flintstone's Multi Vitamin w/ Iron daily Vitamin D 2000 IU's every other day
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 29.11.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray normal
Symptomtext
After being vaccinated I started having an asthma exacerbation within a couple days of vaccination. My peak flow meter readings dropped almost 100 points. I started taking flovent 2x a day instead of one time daily and started using my nebulizer 3-4 times per day. I was waking nightly having to use my inhaler. I figured the asthma would settle down but it didn't. It continued to gradually get worse. I finally went to urgent care on January 4th. I've never had an asthma exacerbation last more than a day or two so this was getting scary after a month. At the clinic a lung x-ray was done and returned negative for disease. I was prescribed prednisone for 5 days and told to use my nebulizer every 4 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest X-ray normal
- Hospital-Tage
- -
- Labordaten
- Chest x-ray--negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Flovent one time daily. Albuterol Inhaler as needed or Albuterol in nebulizer as needed Calcium with D3 & K Benadryl as needed Aleve as needed
- Allergien
- Glycerin Chocolate Numerous antibiotics (sulfa, penicillin, tetracycline
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 27.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Intraocular pressure increased
Intraocular pressure test
Investigation
Toothache
Symptomtext
he got severe toothache in lower left jaw in molar; He got the booster dose; eye pressure/measured with gold standard was 32; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 70 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 27Nov2021 (Lot number: 33030BD) at the age of 70 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Chronic cough" (unspecified if ongoing), notes: Medical Conditions: he takes Flovent for chronic cough.; "Asthma" (unspecified if ongoing), notes: He has been tested for asthma he is called a slight asthmatic. Concomitant medication(s) included: FLOVENT taken for cough. Vaccination history included: Bnt162b2 (Dose 1 of Pfizer-BioNTech COVID-19 Vaccine, lot number: EN6203,, Anatomical location: Left arm shoulder, about a month after first one he developed a severe toothache), administration date: 09Mar2021, when the patient was 69 years old, for COVID-19 Immunization, reaction(s): "Severse toothache"; Bnt162b2 (Dose 2 of Pfizer-BioNTech COVID-19 Vaccine, lot number: EW0150, Anatomical location: Left arm shoulder), administration date: 06Apr2021, when the patient was 69 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 27Nov2021, outcome "unknown", described as "He got the booster dose"; INTRAOCULAR PRESSURE INCREASED (non-serious) with onset 2021, outcome "unknown", described as "eye pressure/measured with gold standard was 32"; TOOTHACHE (non-serious) with onset Dec2021, outcome "not recovered", described as "he got severe toothache in lower left jaw in molar". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of intraocular pressure increased. Therapeutic measures were taken as a result of toothache. Additional information: It was reported that after the booster dose, 2 days ago patient developed a severe toothache in lower left jaw in molar. He says that after he gets the vaccine he always had a tooth issue. He also had increase intraocular pressure in his right eye. Caller states the toothache in the left lower molar was ongoing. When patient went to the dentist, they said nothing except go to the endodontist which was the root canal people. The endodontist said they had seen more tooth issues. They didn't provide him with any more information than that. He chose this time not to take antibiotic and was managing the pain with Tylenol and Ibuprofen. Patient took Tylenol 500 milligram. Caller was taking it every 4 to 6 hours in that range. He has only been taking four per day now. Patitnt took Ibuprofen (strength was 200 milligram) with Tylenol because he was told that two of them together have better pain reliving. Caller clarified that he was taking two of the Ibuprofen and one of the Acetaminophen together. If it doesn't go away, he will go get antibiotics. He was thinking it will resolve itself. Patient's weight was 152 or 153 pounds. It was also reported that there may be a connection or not. He happened to go for his annual eye exam last Monday on 13Dec2021, and the doctor noted a concerning eye pressure, the intraocular pressure in right eye. The number the doctor measured with gold standard was 32. The doctor told caller that she likes to see the number below 20. The doctor was surprised because the previous year the eye pressure had been in the teens in the same eye. Caller has not received any treatment for the eye pressure. Caller is using Flovent and has been using it for about a year. There is a connection between steroids and Flovent has some steroid in it. He is going back in one month to have his eye pressure rechecked. No any additional vaccines administered on same date of the Pfizer Suspect. The patient had Shingles vaccine a good year or year and a half ago. It was a long time ago. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211213; Test Name: Eye pressure test; Result Unstructured Data: Test Result:32; Comments: the intraocular pressure in right eye. The number the doctor measured with gold standard was 32; Test Name: Tested for asthma; Result Unstructured Data: Test Result:slight asthmatic
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (He has been tested for asthma he is called a slight asthmatic.); Chronic cough (Medical Conditions: he takes Flovent for chronic cough.)
- Andere Medikamente
- FLOVENT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product preparation issue
Symptomtext
PFIZER BIONTECH COVID 19 VACCINE: ADMINISTRATION ERROR Vaccine vial was not diluted prior to giving dose resulting in error. Individual received 0.3ml of undiluted vaccine. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient mistakenly received Covid-19 booster before his age group was eligible
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 02.01.2022
- Impfdatum
- 30.12.2021
- Beginn
- 30.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Heart rate increased
Symptomtext
About 2 hours after booster was received on 12/30/2021 at 10:15am my heart rate rose to over 150+ bpm. Heart rate stayed above 150bpm until today 01/02/2022 in the am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes High blood pressure High chloresterol Thyroid Sleep apnea Obesity Osteoarthritis
- Andere Medikamente
- Metformin HCL ER 500mg Acarbose 25mg Enalapril-HCTZ10-25 mg Metoprolol SUCC ER 100mg Levothyroxine 75 mcg Atorvastatin 80 mg CoQ10 Low Dose aspirin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 01.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 29.12.2021
- Impfdatum
- 28.12.2021
- Beginn
- 28.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient is 14 years old and was administered a Pfizer Booster. Patient and mother were informed of the error. Both patient and mother were not concerned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 28.12.2021
- Impfdatum
- 26.12.2021
- Beginn
- 26.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (temperature)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 27.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint injury
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Joint injury
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Product administration error
Symptomtext
Pfizer COVID-19 vaccine EUA: Administration error. Booster dose given too soon. Received 3 doses of Pfizer COVID-19 vaccine on 08/11/2021, 09/01/2021 and 12/10/21 respectively. There was not 6 months between 2nd and booster (3rd dose). This appears to be an error. The dose was given before 03/01/2022. No adverse effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 24.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
PFIZER COVID-19 VACCINE EUA: ADMINISTRATION ERROR- BOOSTER DOSE GIVEN TOO SOON. RECEIVED 3 DOSES OF PFIZER COVID 19 VACCINE ON 06/15/21, 07/07/21, AND 12/10/21 RESPECTIVELY. THERE WAS NOT 6 MONTHS BETWEEN 2ND AND BOOSTER (3RD DOSE). THIS APPEARS TO BE AN ERROR THAT THE BOOSTER DOSE WAS GIVEN BEFORE 01/07/22. NO ADVERSE EFFECTS REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear discomfort
Symptomtext
Patient refers to feeling submerged in the ears. At 1:45 pm he is taken to the incident observation area and his vital signs were evaluated 100/70, 99% sat, 73P and 20R The case was consulted by Dr. and she refers to leaving him in the trender position and observing her for 30 min at 2:15 Dr. is called for re-evaluation of the patient 100/70, 99% sat 73p 20R. Patient reports feeling well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear discomfort
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Pharyngeal swelling
Symptomtext
Upper lip swollen, back of throat swollen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- Cold sore
- Vorgeschichte
- Ibs, anxiety,
- Andere Medikamente
- No
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
11yr. 11 month old received vaccine for the 12 years and up, 0.3ml , parent informed. Asked to monitor vaccination site. Nurse called next day, no issues identified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
10 year old received vaccine for the 12 years and up, dose 0.3mL, parent informed. Informed to monitor vaccination site. Nurse made phone call to parent next day, no issues identified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Gastrointestinal tube insertion
Hypophagia
Mental status changes
Somnolence
Symptomtext
more somnolent since vaccinations, decreased oral intake and unable to take medications, presented to ER on 12/9, admitted with altered mental status, weakness, and possible UTI, no improvement with antibiotic, hydration, and administering Parkinson's medications via NG tube, discharged on hospice care 12/8.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- possible UTI
- Vorgeschichte
- Symptomatic Parkinson disease Dementia Anxiety/Depression Constipation Hyperlipidemia IFG (impaired fasting glucose) Low serum vitamin B12 Low vitamin D level Osteoporosis urinary incontinence Weakness Malnutrition
- Andere Medikamente
- Aleve, 220 mg , By Mouth donepezil 5 mg oral tablet, 10 mg= 2 TAB per Dr at medical history, By Mouth, QHS folic acid , DAILY ibuprofen 200 mg oral tablet, 200 mg= 1 TAB , By Mouth, Q6H, PRN MegaKrill oral capsule, 1 CAP , By Mouth, DAILY m
- Allergien
- clindamycin and topical lidocaine
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given an adult dose of Pfizer-BioNtech COVID vaccine on 12/8/21. See note below: Of note, child dose of the COVID Pfizer vaccine was ordered, but we unfortunately do not have the child dose at our clinic yet, so she was inadvertently given the adult dose of the vaccine (30mcg instead of 10mcg). We explained to the mother what had happened and apologized extensively. We reassured her that this has happened elsewhere before, and no major adverse outcomes have occurred. Discussed that, if anything, she may have a stronger immune response, including increased redness and swelling in the area, as well as systemic symptoms such as fever, chills, fatigue. Counseled mother than she can use tylenol and ibuprofen as needed, and that if she has any further concerns, she should not hesitate to call or bring her back in for evaluation. Also discussed that she will need to get the booster dose at the pediatric clinic, as they currently have the child dose of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 18.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Symptomtext
Error: Wrong route (SC, IM, etc.).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness
Fear
Insomnia
Tinnitus
Symptomtext
I have noticed tinnitus in both ears, a constant high pitch ringing that is non stop and only exacerbated at night. Just a few days after my booster, this side effect began to keep me up at night. I fear hearing loss as a side effect of Covid-19 or its vaccines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression, treated and stable
- Andere Medikamente
- Fluoxetine 30mg, Wellbutrin 150 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 13,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaginal haemorrhage
Symptomtext
Abnormal vaginal bleeding
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaginal haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin, omega 3,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 16.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong vaccine formulation (ex. different manufacturer initial and booster).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Injury associated with device
Lymphadenopathy
Oedema peripheral
Symptomtext
Swollen lymph nodes/edema in armpit and underarm area for 3 days after injection. Patient commented they believe immunizer technique may be related to the adverse event, they believe the needle was inserted too aggressively.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Symptomtext
lump in right armpit
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary mass
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- none
- Andere Medikamente
- daily multivitamin
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Swelling face
Throat tightness
Symptomtext
REPORTS SWELLING OF THE FACE AND TIGHTENING OF THE THROAT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swelling face
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- AZYTHORMYCIN 1 GRAM PO ROCEPHIN 500 MG IM
- Allergien
- IBUPROFEN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 13.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Lymphadenopathy
Symptomtext
swollen lymph nodes under left arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Medical Assistant removed vaccine from RN table without RN knowledge and Medical Asssistant administered Pfizer Booster Vaccine to patient before eligible booster date of 6 months without RN knowledge. Instructions given at the start of site to not remove vaccines without RN knowledge. Medical assistant removed and administered vaccine without RN confirmation of dates and eligibility and knowledge. Patients second dose of Pfizer was administered 07/04/2021 and the Pfizer Booster was administered 12/14/2021. Patient was informed and date of Pfizer Booster dose documented on card for patient records and patient informed of early dose given. Patient observed for adequate amount of time and no adverse reactions observed by RN. Patient reported no adverse reactions or complaints to RN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Pt given a Pfizer booster at the age of 14, against CDC recommendations of 16 and older. No adverse reactions observed or reported during observation period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Pt given a Pfizer booster at the age of 15 by RN, against CDC recommendations of 16 and older. No adverse reactions observed or reported during observation period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Swollen tongue
Symptomtext
10 minutes after injection she complained of swollen tongue. She asked for bendadryl and had her own Epi-pen 0.3. emergency was called. She was given 50mg benadryl and 0.3mg epinephrine which seemed to help. A few minutes later the paramedics arrived and took over. She was conscious when taken by ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swollen tongue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- lamictal, ativan, trelegy, metformin ER,
- Allergien
- cephalexin, ciprofloxacin, nitrofurantoin, sulfa,
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Administration of Pfizer booster to a 16 y/o prior to authorization by FDA and CDC
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Incorrectly administered booster dose prior to authorization by FDA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 12.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Swelling
Symptomtext
Large swelling in lower armpit on right side. There is no pain or tenderness. I'm assuming it's related to the vaccine. I first noticed the swelling Saturday evening about 12 hours after receiving it. There is no change to the swelling on Sunday. will seek care if no improvement in a few days. I had no issues with the first two.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swelling
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 12.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
VERBALLY FATHER STATED PATIENT WAS 12 AND WHEN PROCESSING RX AT END OF SHIFT PHARMACIST REALIZED THAT PATIENT WAS 11 AND SHOULD HAVE RECIEVED PEDIATRIC PFIZER. PHARMACIST CALLED CELL PHONE LEFT MESSAGE AND HAS NOT HEARD BACK. IF PATIENT REPRESENTATIVE DOESN'T CALL BACK THEN PHARMACIST WILL TELL HER BROTHER WHEN HE COMES FOR HIS 2ND PFIZER SHOT ON 1-2-22. RPH HAS MADE ARRANGEMENTS FOR PATIENT TO RECIEVE PEDIATRIC PFIZER AT LATER DATE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 11.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Client received booster dose of pfizer at the age of 15, sooner than agency recommendation. No symptoms or adverse reactions observed or reported at this time. Pfizer notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 11.12.2021
- Beginn
- 11.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
Eight year old female pedatric patient was given a full 0.3mL adult pfizer dose instead of the 0.2mL pediatric dose in error. No adverse events to report at this time. Per call to the pfizer medical information line the dose is not to be repeated and patient will still be eligible for the 2nd pediatric dose in 21 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 09.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
PATIENT RECEIVED BOOSTER DOSE EARLIER THAN THE 6 MONTH RECOMMENDATION FROM DOSE #2; PATIENT IS AWARE AND STATES THAT HER LOCAL PHARMACIST (AT A PHARMACY) TOLD HER IT WAS OK TO GET THE BOOSTER DOSE SOONER. AT PUBLIC CLINIC THE CLOSE SPACING WAS MISSED DURING SCREENING.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
pt received vaccine 10 min post use by time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- elevated liver enzymes, HTN, prediabetes
- Andere Medikamente
- lisinopril
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Electrocardiogram normal
Symptomtext
29 mins post vaccine pt complained of chest pressure. Pt monitored by provider and EMS - stable referred to ED for further evaluation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- EKG - normal
- Aktuelle Erkrankungen
- covid-19 infection
- Vorgeschichte
- abnormal glucose, allergic rhinitis, apnea, carpal tunnel, obsesity, sleep apnea,
- Andere Medikamente
- flonase, hydrocodone,loratadine
- Allergien
- ibuprofen and aspirin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Severe pain under left arm/lymph node area - Lymphadenopathy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- Covid Booster Vaccine (Pfizer-BioNTech) taken the previous day
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol High Blood Pressure
- Andere Medikamente
- Valsartan and Hydrochlorothiazide 320mg/25mg Vitamin D 125 mcg Calcium 500mg Krill Oil 500mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient is 17 years old and received the Pfizer booster. Current CDC guidelines are for 18 years and over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immunisation
Tinnitus
Symptomtext
One day after the injection, experiencing tinnitus in left ear only; Dose received 3/ dose number=3; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), administered in left arm, administration date 29Nov2021 at 12:00 (Lot number: 33030BD) at the age of 40 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. Concomitant medications included: DAILY BIRTH CONTROL PILL, VITAMIN D3, VITAMIN C and M. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot Number: EW0150, Route of administration: Unspecified, Anatomical location: Left arm, Vaccine Administration Time: 12:00), administration date: 02Apr2021, when the patient was 40 years old, for COVID-19 immunisation and BNT162b2 (DOSE 2, SINGLE, Lot Number: EW0171,Route of administration: Unspecified, Anatomical location: Left arm, Vaccine Administration Time: 12:00), administration date: 23Apr2021, when the patient was 40 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 29Nov2021 at 12:00, outcome "unknown", described as "Dose received 3/ dose number=3"; TINNITUS (non-serious) with onset 30Nov2021 at 00:00, outcome "not recovered", described as "One day after the injection the patient experienced tinnitus in her left ear only". Therapeutic measures were not taken as a result of tinnitus. Additional Information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- VITAMIN D3; VITAMIN C [ASCORBIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
Counseled the patient about what had happened, and suggested watchful waiting. Patient is to report to the pharmacy and MD if anything outside of a natural immune response occurs (including fever, body aches and chills).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Topical Clindamycin Swabs
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Booster with Pfizer in a person younger than 18 y/o.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Patient was accidentally given booster shot. Patient has no adverse event and patient is doing okay
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 04.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Patient was accidentally given booster shot of pfizer. Patient has no adverse event. Patient is doing okay
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong patient
Symptomtext
Error: Wrong Patient (documentation in EMR)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong patient
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
This patient was given 0.2 ML of adult dose Pfizer instead of 0.2 of pediatric formulation. No reaction noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Muscle contracture
Pallor
Symptomtext
Patient locked his arms and became pale about 10 minutes after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle contracture
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Carrots, dogs, cats, dust
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Somnolence
Throat tightness
Symptomtext
Patient reported an anaphylactic reaction to her first vaccine (Janssen) on April 10, 2021. Patient went to the ED and was treated with Prednisone, Benadryl and Pepcid. Patient was given Benadryl and Pepcid at 4:08 PM, monitored for 30 minutes and given her Pfizer vaccine at 4:38PM and monitored again for 30 minutes. At the 25 minute mark she complained of throat tightness but not as bad as the first vaccine. Consulted with NP and additional Benadryl 25mg given. Patient was monitored for an additional 30 minutes. She denied shortness of breath and her vital signs remained stable. At 5:40 she said she was almost back to normal but felt a little drowsy from the medications. At 5:45 she left the clinic with her father.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Somnolence
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Benadryl 50mg Pepcid 20 mg
- Allergien
- N/A
- Vorherige Impfungen
- Janssen
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong vaccine formulation (ex. different manufact. initial and booster).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
17 year old male was given Pfizer vaccine booster shot. Waited 15 minutes in vehicle with mother. No untoward reactions noted. Left to go home after the required wait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None known.
- Vorgeschichte
- None known.
- Andere Medikamente
- None known.
- Allergien
- Gets rash with penicillin.
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 29.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
ADMINISTRATION ERROR. A 30 YEARS OLD FEMALE COMES TO THE CLINIC FOR HER BOSTER FOR PFIZER. AT THE MOMENT OF THE ADMINISTRATION THE NURSE DONT ESTIMATED THE TIME AND SHE IMMUNIZED THE PATIENT BEFORE THE 6 MONTHS AS THE HEALTH DEPARTMENT RECOMMENDS. PATIENT CALL TO THE CLINIC AT NOVEMBER 30,2021 BECAUSE SHE HAS HEADACHE AND TACHYCARDIA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
administered pediatric pfizer COVID to a patient that turned 12 years old 2 weeks previously instead of adult pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Electrocardiogram ST segment elevation
Fall
Symptomtext
Complains of right sided numbness/weakness for few "weeks/months" in clinic slumped in chair
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- BS 104 VS: pulse 83, resp 16. 122/68 99% VS: pulse 89 resp 16 116/70 94% EKG: MILD ST elevations
- Aktuelle Erkrankungen
- Diabetes Fell and since right sided numbness
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Administration Error: Patient received the Moderna COVID-19 vaccine for her primary series and came in for her booster appointment. She was okay with receiving any vaccine as a booster and was registered & sent to the Janssen lane for her booster. However, the vaccinator accidentally administered the Pfizer booster instead of Janssen. The vaccinator informed his lead of the error. Patient was informed by the pharmacist about the error and addressed all her questions and concerns. Patient mentioned that she was fine with the Pfizer booster vaccine. Her card and online record were accurately updated to reflect the Pfizer booster that was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 27.11.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 25.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 21.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
Patient was administered 0.3ml Covid 19 Immunization (pfizer) instead of 0.2ml peds Covid19 (pfizer) vaccination. We tried notifying mom as quickly as we could when the error was detected. Patient had no know reaction. We have attempted to reach family to f/u.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None, PCP made aware.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product label on wrong product
Symptomtext
The vaccine lot number B looks like an 8. This has resulted in charting incorrect lot occasionally by administering staff.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product label on wrong product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -