- Staat
- -
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 21.11.2023
- Impfdatum
- 21.10.2022
- Beginn
- 26.09.2023
- Tage bis Beginn
- 340,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Acute respiratory failure
Arthropod bite
Asthenia
Biopsy skin
Borrelia test
COVID-19
Chest X-ray normal
Chronic obstructive pulmonary disease
Condition aggravated
Cough
Dyspnoea
Mobility decreased
Physical deconditioning
Rash
Respiratory failure
SARS-CoV-2 test positive
Symptomtext
Patientis a 82 y.o. female with a history of COPD, RA, TIA who was admitted to first hospital 9/19-9/26/23 for COPD exacerbation (discharged on 3L NC), hospital stay complicated by possible Lyme's disease. She was discharged to SNF but family eloped the pt within six hours due to reported suboptimal care. She represented to second hospital 9/26/2023 with persistent dyspnea and abdominal pain. Found to have COPD exacerbation and COVID-19 +. Discharged to SNF 10/4/23 in stable condition. 1. COPD Exacerbation: Patient reports COPD normally stable on home regimen but very severe cough/dyspnea PTA. CXR 9/26/23 negative for focal consolidation. Completed doxycycline course. Continued steroid, pulmonary toilet, acapella, scheduled duonebs. 2. COVID Infection: Prior Vaccinations, (+) testing 9/27/23, completed 9 days of Decadron. 3. Acute on Chronic Hypoxic Respiratory Failure: discharged from first hospital to SNF on 9/26/23 on 3L NC. Required up to 4-5 L in p.m. on 10/4/2023 but with the goal O2 sat of greater than 88% patient was able to be weaned down to 3.5 L on discharge. 4. Indeterminate Lyme Serology: Patient with atypical rash on LEs and noted tick contact. Rash has resolved. Lyme serologies and skin biopsy at first hospital were inconclusive, ID at first hospital recommended empiric course of 10 days of doxycycline (completed). 5. Rheumatoid Arthritis: Held home methotrexate. Resume when ok with pts Rheumatology. 6. TIA: Continued home ASA/statin 7. Generalized Weakness: with deconditioning and reduced mobility POA. Patient reports she normally ambulates w/ walker, complains of significant weakness. Therapy recs for SNF. 8. Code Status: DNR-CCA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 13.12.2022
- Beginn
- 05.09.2023
- Tage bis Beginn
- 266,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Anticoagulant therapy
Atelectasis
Atrial fibrillation
COVID-19
COVID-19 pneumonia
Cardiomegaly
Chest X-ray abnormal
Cough
Dyspnoea
Major depression
Parkinson's disease
Physical deconditioning
SARS-CoV-2 test positive
Symptomtext
Patient is a 84 y.o. male who presented from home on 9/5/2023 with SOB, positive COVID with acute respiratory failure. Was treated with Decadron with improvement. Patient was weaned down to room air. Was asymptomatic on the day of discharge. Discharged to skilled nursing facility for physical deconditioning Assessment and Plan Acute respiratory failure with hypoxia COVID pneumonia - Presented with: SOB, cough - Symptom onset: 9/5/23 - Positive COVID-19: at PCP office - Vaccination status: Vaccinated and boosted - CXR on admission showed mild cardiomegaly, minimal fluid/atelectasis in the left lung - Oxygen status: started on 15L HFNC on admit, now on room air - Decadron: Yes. Expected end date 9/15/23. Patient is currently on room air. Per discussion with wife at the bedside discontinued Decadron - Remdesivir: Completed 5 day course -Discussed with nursing staff importance of pulmonary hygiene - DVT prophylaxis:Currently on full anticoagulation - Serial COVID labs ordered: Yes - Case Management/Social Services consulted: Yes Chronic atrial fibrillation - Has previous CV/ablation and pacemaker. -Rate is stable -Continue with Eliquis Parkinson's disease Dementia without agitation - Follows with neurology. -Lives at home with wife w HH and PT -Progressive deconditioning in setting of acute illness. Patient and wife agreed to skilled nursing facility. -Continue with home Sinemet, Aricept, and Seroquel nightly Major depression in remission -Continue with BuSpar BID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 07.08.2023
- Impfdatum
- 16.12.2022
- Beginn
- 08.07.2023
- Tage bis Beginn
- 204,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary abnormal
COVID-19
COVID-19 pneumonia
Intensive care
Laboratory test normal
Lung infiltration
Pneumonia
Positive airway pressure therapy
Respiratory failure
Sepsis
White blood cell count normal
Symptomtext
Patient is a 72 y.o. male patient of a MD with history of asthma presented on 7/8/2023 with acute respiratory failure with hypoxia 2/2 pneumonia and COVID. HCP consulted by HCF, for continued post ICU medical care. Acute respiratory failure with hypoxia and hypercapnia Sepsis POA due to Covid 19 multifocal PNA AF, WBC normal, CTPA without PE, with R>L infiltrates on exam, PCT normal Needed bipap on admission, now on RA ID and Pulm following; completed dexamethasone and remdesivir Asthma, not in exacerbation Follows with Dr. last seen 5/2023. Denies home oxygen use. Patient denies hx of OSA but states pulmonologist has previously recommended sleep s
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 10,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 07.08.2023
- Impfdatum
- 10.01.2023
- Beginn
- 18.04.2023
- Tage bis Beginn
- 98,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Acute respiratory failure
Angina pectoris
Symptomtext
I20.9 ANGINA, UNSPECIFIED 1/19/2023 ABDOMINAL PAIN J96.20 ACUTE ON CHRONIC RESPIRATORY FAILURE 4/18/2023 ABDOMINAL PAIN I20.9 ANGINA, UNSPECIFIED 1/19/2023 ACUTE ON CHRONIC RESPIRATORY FAILURE J96.20 ACUTE ON CHRONIC RESPIRATORY FAILURE 4/18/2023 ACUTE ON CHRONIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 26.07.2023
- Impfdatum
- 10.12.2022
- Beginn
- 13.06.2023
- Tage bis Beginn
- 185,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Angiogram pulmonary normal
Aphasia
Blood creatinine
Blood folate
Blood thyroid stimulating hormone
COVID-19
Cerebrovascular accident
Chills
Cough
Diabetic diet
Dyspnoea
Echocardiogram normal
Encephalopathy
Glycosylated haemoglobin increased
Hypoxia
Lacunar stroke
Symptomtext
Patient is a 84 y.o. female patient of, MD with history of Diabetes, hypertension, hyperlipidemia presented to Hospital with altered mental status. Patient was found to be hypoxic and COVID-positive and was treated initially with steroids and remdesivir. Due to CTPA being unremarkable pulmonology recommended cessation of steroids and continuation of remdesivir while inpatient. She was weaned to room air and did not require any oxygen on home O2 evaluation. Due to some word finding difficulty patient obtained an MRI brain which showed an acute CVA. Neurology recommended medication change meds and close outpatient follow-up with stroke neurology or Center. Patient is otherwise back to baseline and doing well with no acute complaints. She is otherwise stable this time for discharge home and outpatient follow-up as above. All questions and concerns answered at bedside. Acute Respiratory Failure with Hypoxia Covid-19 Virus Infection Date of onset of symptoms: 6/13/23 Symptoms present on admission: fever, chills, cough, SOB Date of covid positive test: 06/14/23 Vaccination status: unable to verify at this time Imaging: Hypoinflation of lungs Oxygen requirements on admission: 3 L Current oxygen requirements: RA, no oxygen needs on home O2 evaluation Medical therapy: remdesivir and steroids initially but now stop steroids Consultants following: Pulmonology Anticipated special isolation end date: 6/24/2023 Acute stroke Acute Encephalopathy, resolved Thought to be secondary to COVID and hypoxia The patient does have an accent, though she states that she speaks language, and is able to answer some of her questions Neuro consulted, MRI brain with small right parietal lacunar stroke Echo with no PFO MR cow carotid brain with no extracranial carotid stenosis, slightly hypoplastic vertebral artery and short segment significant irregularity in the M1 segment of the left cerebral artery but flow is preserved Obtain MRA head neck and obtain echo Placed on aspirin and Plavix for 21 days then aspirin alone. Continue atorvastatin Outpatient stroke neurology follow-up Center referral placed B12/Folate, TSH not low AKI Serum creatinine of 1.32, appears baseline is between 1 and 1.1 but no previous labs for definitive. SCr down to 1.18 Give gentle IV fluid hydration Stop home losartan?HCTZ, continue losartan on discharge Hypertension Continue Lopressor, nifedipine Stop home losartan?HCTZ, continue losartan on discharge Hyperlipidemia Continue statin therapy Lipid panel pending Diabetes Type 2 Holding Metformin, Amaryl 2 mg BID, Steglatro 15 mg daily, Januvia 25 mg daily and Ozempic 0.5 mg weekly therapy at this time A1c of 8.5 We will continue with sliding scale insulin coverage and lantus increased to 18 units. Glucose control should be improving since steroids have been discontinued Continue Januvia Diabetic diet Continue to monitor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 28.12.2022
- Beginn
- 21.02.2023
- Tage bis Beginn
- 55,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Acute respiratory failure
Respiratory failure
Symptomtext
ACUTE NON ST ELEVATION MI ACUTE NON ST ELEVATION MI (NSTEMI), TYPE 2 MI (SUPPLY/DEMAND) ACUTE HYPOXEMIC RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 30.12.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Hypoxia
Symptomtext
ACUTE NON ST ELEVATION MI HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 30.12.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 80,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptom recurrence
Symptomtext
ACUTE RESPIRATORY FAILURE 2/24/2023 & 1/10/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 12.01.2023
- Beginn
- 13.02.2023
- Tage bis Beginn
- 32,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Hypotension
Symptomtext
ACUTE NON ST ELEVATION MI HYPOTENSION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 29.06.2023
- Impfdatum
- 17.01.2023
- Beginn
- 23.01.2023
- Tage bis Beginn
- 6,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE ON CHRONIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 26.05.2023
- Impfdatum
- 19.12.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Cardiac failure acute
Chronic respiratory failure
Dyspnoea
Left ventricular failure
Respiratory failure
Symptomtext
J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/11/2023 COMBINED SYSTOLIC AND DIASTOLIC HEART FAILURE, ACUTE ON CHRONIC J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/18/2023 COMBINED SYSTOLIC AND DIASTOLIC HEART FAILURE, ACUTE ON CHRONIC J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/11/2023 SHORTNESS OF BREATH J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/18/2023 SHORTNESS OF BREATH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 30.11.2022
- Beginn
- 19.04.2023
- Tage bis Beginn
- 140,0
- Dosis
- 4
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Angiogram pulmonary abnormal
Anticoagulant therapy
Atrial flutter
COVID-19
Condition aggravated
Culture negative
Death
Dyspnoea
Electrocardiogram abnormal
Fatigue
General physical health deterioration
Hypotension
Hypoxia
Intensive care
Lung adenocarcinoma
Lung consolidation
Lung neoplasm malignant
Symptomtext
Discharge Provider: Primary Care Physician at Discharge: Admission Date: 4/19/2023 PRESENTING PROBLEM: Acute respiratory failure with hypoxemia [J96.01] COVID-19 virus infection [U07.1] Acute on chronic respiratory failure with hypoxia [J96.21] HOSPITAL COURSE: Patient is a 65 yr old M with PMHx of recently diagnosed metastatic right lung adenocarcinoma (3/2023), CAD s/p CABG in 2021 with post-operative atrial fibrillation (no longer on anticoagulation), HTN, 40 pack year smoking hx, chronic right shoulder pain 2/2 rotator cuff tear and cancer pain who presented to the ED in respiratory distress. At baseline, he is on 3L nasal cannula at home and dyspneic on exertion but noticed worsening shortness of breath and profound fatigue Visiting palliative care home nurse found the patient to be hypoxic to 70% on room air and hypotensive, thus EMS was called. On admission he was placed on a non-rebreather mask then BIPAP. He was found to be tachycardic in the 130s to 140s with EKG showing atrial flutter. CT angiogram thorax with contrast was negative for PE but showed extensive mixed consolidation and ground-glass opacities of bilateral lungs as well as interval enlargement of the metastatic disease. In the intensive care unit, he was found to have COVID 19 and treated with tocilizumab, remdemisvir, steroids, and broad-spectrum antibiotics. His work of breathing improved and was subsequently moved off of BiPAP and transitioned to high-flow nasal cannula. He remained on high-flow nasal cannula with slow titration. Pulmonology consulted and he completed 10 days of remdesivir and 10 days of Decadron. A tapering dose of prednisone was planned after. He was started on IV Lasix to facility the negative fluid balance. SLP consulted recommended general nectar thick liquids. He was initially placed on Rocephin and azithromycin then cefepime. With negative cultures, antibiotics were discontinued. Regarding his atrial flutter and RVR he was placed on amiodarone metoprolol increased to 50 mg 2 times a day and Cardizem. Heparin drip transition to oral Eliquis. Seen by pulmonology, concern for lymphangitic spread of lung cancer, recommended hospice. Continued to require 100% FiO2 via high-flow nasal cannula, due to overall poor prognosis, patient and family agreed for hospice. Patient continued to decline and was made comfort care before passing on 5/10/23. Date of Death: 5/10/23 Time of Death: 1:17 AM Preliminary Cause of Death: Hypoxia Discharge Disposition: Deceased
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 21,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mixed hyperlipidemia Former smoker NSTEMI, initial episode of care CAD s/p CABG x 2 Sciatica, right BMI 29.0-29.9,adult Elevated PSA of 4.4 ng/ml on 7/12/19 Lesion of skin of scalp Stress hyperglycemia Acute on chronic anemia Acute respiratory failure Atrial flutter Primary lung adenocarcinoma Right lower lobe lung mass Degenerative tear of acetabular labrum Bilateral shoulder pain Drug-induced constipation Cancer related pain Goals of care, counseling/discussion COVID-19 with associated ARDS and acute on chronic hypoxic respiratory failure Hyponatremia Elevated LFTs Elevated alkaline phosphatase level Primary hypertension Lung cancer metastatic to bone Multiple comorbid conditions Anxiety End of life care
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet aspirin 81 MG chewable tablet Coenzyme Q10 (COQ10) 100 MG CAPS ezetimibe (ZETIA) 10 mg tablet fentaNYL (DURAGESIC) 12 MCG/HR patch fentaNYL (DURAGESIC) 25 MCG/HR patch fentaNYL (DURAGESIC) 37.5 MCG/HR p
- Allergien
- PenicillinsNausea and Vomiting StatinsJoint Pain
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 26.03.2023
- Impfdatum
- 20.12.2022
- Beginn
- 02.01.2023
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Malaise
Symptomtext
Given with flu shot, resulting in death within 13 days. Patient complained not feeling well after receiving vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- hospitalized 1/2/23
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- blood pressure and a nebulizer
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 08.02.2023
- Impfdatum
- 21.11.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 24,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Brain scan abnormal
Cerebral thrombosis
Cerebrovascular accident
Gait inability
Laboratory test
Speech disorder
Surgery
Symptomtext
Severe stroke caused by blood clot. She is still in onsite rehab and not able to speak or walk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 45,0
- Labordaten
- hospital performed initial scans and surgery. hospital provided inpatient rehab. Subacute rehab ongoing. Many documented tests showing cause and effect.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 07.02.2023
- Impfdatum
- 07.12.2022
- Beginn
- 20.01.2023
- Tage bis Beginn
- 44,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
Hospital Principal Problem (Discharge Diagnoses): Acute respiratory failure with hypoxia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 07.01.2023
- Impfdatum
- 23.12.2022
- Beginn
- 24.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Body temperature
Chest pain
Myocardial infarction
Myocarditis
Pyrexia
SARS-CoV-2 test
Symptomtext
high temperature/fever; severe chest pain; heart attack; myocarditis; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Dec2022 as dose 3 (booster), single (Lot number: GJ3274) at the age of 42 years for covid-19 immunisation. The patient's relevant medical history was not reported (no other medical history). Concomitant medication(s) included: FLU [INFLUENZA VACCINE] taken for immunisation, on 13Dec2022 as dose number unknown, single. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: FF2590), administration date: 31Oct2021, when the patient was 41-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: FF2587), administration date: 15Nov2021, when the patient was 41-year-old, for COVID-19 immunization. There was no other medications in two weeks, no covid prior vaccination, no known allergies. The following information was reported: MYOCARDIAL INFARCTION (hospitalization, medically significant, life threatening) with onset 24Dec2022, outcome "not recovered", described as "heart attack"; PYREXIA (hospitalization, life threatening) with onset 24Dec2022, outcome "not recovered", described as "high temperature/fever"; MYOCARDITIS (hospitalization, medically significant, life threatening) with onset 24Dec2022, outcome "not recovered"; CHEST PAIN (hospitalization, life threatening) with onset 24Dec2022, outcome "not recovered", described as "severe chest pain". The patient was hospitalized for pyrexia, chest pain, myocardial infarction, myocarditis (hospitalization duration: 3 day(s)). The events "high temperature/fever", "severe chest pain", "heart attack" and "myocarditis" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Body temperature: (unspecified date) high; SARS-CoV-2 test: (26Dec2022) Negative, notes: Nasal Swab. It was unknown if therapeutic measures were taken as a result of pyrexia, chest pain, myocardial infarction, myocarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 3,0
- Labordaten
- Test Name: temperature/fever; Result Unstructured Data: Test Result:high; Test Date: 20221226; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac arrest
Death
Resuscitation
Ventricular fibrillation
Symptomtext
One day after Pfizer COVID bivalent booster, patient experienced a sudden, fatal cardiac arrest while exercising at the gym. Resuscitation efforts were unsuccessful. His 3 prior COVID vaccines were Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- V-fib arrest per paramedic documentation.
- Aktuelle Erkrankungen
- CAD native artery without angina; high cholesterol
- Vorgeschichte
- CAD native artery without angina
- Andere Medikamente
- metoprolol, atorvastatin, aspirin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 20.12.2022
- Impfdatum
- 19.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
The resident died several hours after receiving the bivalent COVID-19 booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Other malaise, dementia, hyperlipidemia, hypertension, atherosclerosis, hypokalemia, hypothyroidism, anxiety disorder, macular degeneration, type 2 diabetes, peripheral vascular disease, benign prostatic hyperplasia, iron deficiency anemia, dysphagia, vitamin d deficiency, and edema
- Andere Medikamente
- Gabapentin 100mg, Omeprazole 40mg, Levothyroxine 88mcg, Tamsulosin 0.4mg, Acidophilus cap, Sertraline 100mg, Amlodipine besylate 10mg, Melatonin 3mg, trazadone 100mg, Carvedilol 3.125mg, Finasteride 5mg, Ocusoft pads, Lorazepam 0.5mg, Morph
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breath sounds abnormal
Chest X-ray
Chills
Cough
Death
Dyspnoea
Influenza virus test positive
Productive cough
Respiratory disorder
Respiratory distress
Stridor
Symptomtext
Resident expired on 12/1/2022 at 1405. . Resident began having respiratory issues on the morning of 12/01/2022. Oxygen was applied. Breathing treatment's given. Chest x-ray performed and flu swab also performed. Resident was a DNR, 12/1/2022 05:00 Called to resident's room. Resident coughing and having difficulty breathing. O2 sats 88% Inhaler administered. O2 started at 2 liters. Breathing treatment administered. O2 sats up to 95% Temp- 100.2 P- 98 B/P- 100/60. R- 20. 12/1/2022 09:58 Resident resting in bed at this time. No s/s of adverse reaction to covid booster. Resident denies pain/discomfort to the site. Resident remains afebrile at this time. 12/1/2022 12:02 Signee called to resident's room by CNA stating family wanted to see the nurse. Signee entered room and family states "He just sounds gunky." Resident noted to have a productive cough. Stridor noted to BIL lungs. O2 94% via nasal cannula. T 99.1. Resident noted to have chills. Breathing treatment administered. Dr. notified. New order received to obtain CXR and swab resident for the flu. Resident aware and agreeable. 12/1/2022 16:05 Entered residents' room to check on him and noted resident to be in respiratory distress. . Resident suction by staff related to resident has coughed up secretions/phlegm. No visible signs of life noted. Resident is a DNR. Time of death is 4:05 pm. Family remains at bedside and Dr. notified of residents passing and gave order to release body to funeral home of choice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- flu swab-12/01/2022 chest xray-12/01/2022
- Aktuelle Erkrankungen
- He received the vaccine on 11/30/2022. No issues noted. No temp before vaccine given. The morning of 12/01/2022 started having respiratory issues. Oxygen applied. Started running a temp and was tested for the flu. He tested positive.
- Vorgeschichte
- PARKINSON'S DISEASE ATHEROSCLEROTIC HEART DISEASE OF NATIVE CORONARY ARTERY WITHOUT ANGINA PECTORIS OTHER DISEASES OF SPLEEN OTHER SPECIFIED DISEASES OF LIVER DIFFICULTY IN WALKING, NOT ELSEWHERE CLASSIFIED NEED FOR ASSISTANCE WITH PERSONAL CARE DEPRESSION, UNSPECIFIED CHANGES IN RETINAL VASCULAR APPEARANCE, BILATERAL PRESENCE OF INTRAOCULAR LENS ONYCHOGRYPHOSIS OTHER SPECIFIED PERIPHERAL VASCULAR DISEASES ALLERGIC RHINITIS, UNSPECIFIED DIVERTICULOSIS OF LARGE INTESTINE WITHOUT PERFORATION OR ABSCESS WITHOUT BLEEDING UNSPECIFIED INJURY OF URETHRA, SEQUELA PRESENCE OF AORTOCORONARY BYPASS GRAFT TUBULO-INTERSTITIAL NEPHRITIS, NOT SPECIFIED AS ACUTE OR CHRONIC HYPERLIPIDEMIA, UNSPECIFIED GASTRO-ESOPHAGEAL REFLUX DISEASE WITHOUT ESOPHAGITI UNSPECIFIED ATRIAL FIBRILLATION CHRONIC IDIOPATHIC CONSTIPATION S HYPO-OSMOLALITY AND HYPONATREMIA DYSPHAGIA, PHARYNGEAL PHASE GOUT, UNSPECIFIED ESSENTIAL (PRIMARY) HYPERTENSION
- Andere Medikamente
- 1. Albuterol Sulfate Aerosol Powder Breath Activated 108 (90 Base) MCG/ACT 2 puff inhale orally every 4 hours as needed for Wheezing rinse mouth after using. 2. Albuterol Sulfate Nebulization Solution (2.5 MG/3ML) 0.083% 3 mg inhale orally
- Allergien
- Flomax
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 13.11.2023
- Impfdatum
- 25.11.2022
- Beginn
- 04.09.2023
- Tage bis Beginn
- 283,0
- Dosis
- 5
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood sodium decreased
COVID-19
Chest X-ray normal
Cognitive disorder
Computerised tomogram head abnormal
Condition aggravated
Culture urine positive
Device related infection
Encephalomalacia
Enterococcus test positive
Fall
Head injury
Hyponatraemia
Mental status changes
Productive cough
SARS-CoV-2 test positive
Seizure
Symptomtext
Discharge Provider: DO Primary Care Provider at Discharge: MD Admission Date: 9/4/2023 Discharge Date: 9/06/2023 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hyponatremia [E87.1] Generalized weakness [R53.1] Urinary tract infection associated with indwelling urethral catheter, subsequent encounter [T83.511D, N39.0] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a an 83-year-old male with a history of hypothyroidism, dyslipidemia, hypertension, seizures, CVA and urinary retention with chronic indwelling catheter who presented to Emergency Department for a fall. Patient fell out of bed the night prior and hit his head on the nightstand. He denies LOC and is not anticoagulated. This was an unwitnessed fall. Patient lives at a memory care center and when his family came to visit him the day of arrival they noticed he was not interacting as his normal self. Patient was alert and oriented upon exam x4 and very pleasant. Patient was seen in ED on 8/29 and diagnosed with urinary tract infection and sent home on cefuroxime. UC with Enterococcus faecalis. He was admitted and discharged on 8/19 for seizure and Neurology recommended that his Depakote dose be increased. He denies fever, chills, nausea, or vomiting. He does complain of productive cough for the past few days. On arrival to the ED, his vital signs were stable. Labs significant for hyponatremia. Sodium 122. Viral PCR panel positive for COVID-19. UA with infection. CXR negative. head CT negative for acute findings, there is encephalomalacia from prior infarct. Patient received a L of IV normal saline and a dose of fosfomycin. Patient accepted to Hospital Service for management of hyponatremia. Patient is admitted and slowly improved over the next 2 days. He had persistent cognitive deficits which are likely his baseline. He tolerated antibiotic therapy. His sodium stabilized. Arrangements were made for him to return to the memory care center given his worsening cognitive function. He was seen on day of discharge stable and discharged back follow-up outpatient with primary care provider and urologist. 35 minutes were spent discharging this patient over 50% was in coordination of care and face-to-face counseling with family
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 10/30/2022 - 11/16/2022 (17 days) Hospital PRESENTING PROBLEM: left sided weakness, suspected CVA 10/23/2022 - 10/30/2022 (7 days) Hospital PRESENTING PROBLEM: Left-sided weakness [R53.1]
- Vorgeschichte
- chronic Peripheral neuropathy Primary hypertension Acquired hypothyroidism Dyslipidemia AAA (abdominal aortic aneurysm) (HCC) Thoracic ascending aortic aneurysm (HCC) History of right MCA stroke Seizures (HCC) Urinary retention Platelets decreased (HCC) Left-sided weakness Lower extremity edema Hemiplegia and hemiparesis following cerebral infarction affecting left non-dominant side (HCC) Acute kidney injury (nontraumatic) (HCC) History of non-Hodgkin's lymphoma Constipation COVID Urinary tract infection associated with indwelling urethral catheter NSTEMI (non-ST elevated myocardial infarction) (HCC)
- Andere Medikamente
- acetaminophen (TYLENOL) 650 MG suppository compounded oral medication misc diazePAM (DIASTAT ACUDIAL) 10 MG diazePAM 10 mg (adult) suppository (COMPOUNDED) Divalproex Sodium POWD Divalproex Sodium POWD hyoscyamine (LEVSIN/SL) 0.125 MG SL ta
- Allergien
- Ativan [Lorazepam]Agitation Tape AdhesiveRash
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.11.2023
- Impfdatum
- 03.02.2023
- Beginn
- 08.09.2023
- Tage bis Beginn
- 217,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
COVID-19 pneumonia
Electroencephalogram normal
Facial paralysis
Fall
Fluid intake restriction
Fraction of inspired oxygen
Hemiparesis
Hyponatraemia
Magnetic resonance imaging normal
Respiratory distress
SARS-CoV-2 test positive
Symptomtext
BRIEF OVERVIEW: Admission Date: 9/8/2023 Discharge Date: 9/15/2023 Discharge Disposition: home health care svc DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hyponatremia [E87.1] Weakness [R53.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 67 year old female with history of bipolar on ECT who presented on 9/8 with left sided weakness and facial droop and a fall at home. She was admitted for a stroke work up. EEG and MRI were unremarkable and thus stroke was ruled out. Shortly after admission, she had declining respiratory status and was found to be positive for COVID. Oxygen requirements escalated to 60% FiO2 on 40 L high flow oxygen so she was started on Decadron and Remdesivir. Over the ensuing days, patient was slowly weaned off of oxygen and was back to room air by 9/11. She completed 5 days of Remdesivir and was scheduled for a 10 day course of Decadron which was converted to oral for outpatient completion. Patient also had an acute on chronic hyponatremia that was attributed to her ECT and this resolved during her stay with fluid restrictions. Patient was evaluated by PT and OT and originally recommended inpatient rehab though with continued treatment of her COVID, she progressed to the point of recommending home health care. Patient was discharged home in stable condition on 9/15.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bipolar affective disorder (HCC) Essential hypertension Acquired hypothyroidism Menopause Anxiety Senile nuclear cataract, bilateral Insomnia Sleep walking Memory impairment Chronic sore throat Acne rosacea Leg length discrepancy Weakness Chronic hyponatremia Elevated LFTs
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet ALPRAZolam (XANAX) 0.25 MG tablet Calcium Carb-Cholecalciferol (CALCIUM 600 + D PO) cyanocobalamin (VITAMIN B-12) 1000 MCG tablet estradiol (ESTRACE) 2 mg tablet levothyroxine (SYNTHROID) 50 mcg tablet
- Allergien
- Nsaids Terazol 3 Alc-terconazole Terconazole
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 30.06.2023
- Impfdatum
- 08.12.2022
- Beginn
- 09.03.2023
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Symptomtext
ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN ACUTE DVT, UNSPECIFIED VEIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 29.06.2023
- Impfdatum
- 03.01.2023
- Beginn
- 23.03.2023
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Ischaemic stroke
Obstructive sleep apnoea syndrome
Symptom recurrence
Symptomtext
OBSTRUCTIVE SLEEP APNEA ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 3/6/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 28.06.2023
- Impfdatum
- 07.02.2023
- Beginn
- 17.03.2023
- Tage bis Beginn
- 38,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Ischaemic stroke
Symptomtext
ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.06.2023
- Impfdatum
- 03.12.2022
- Beginn
- 28.04.2023
- Tage bis Beginn
- 146,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deep vein thrombosis
Partial seizures
Symptomtext
G40.109 PARTIAL EPILEPSY 2/2/2023 ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN I82.402 ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN 5/2/2023 ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN I82.409 ACUTE DVT, UNSPECIFIED VEIN 4/21/2023 ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 19.06.2023
- Impfdatum
- 21.12.2022
- Beginn
- 30.03.2023
- Tage bis Beginn
- 99,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deep vein thrombosis
Dementia with Lewy bodies
Hypotension
Symptomtext
ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN 3/29/2023 LEWY BODY DEMENTIA, UNSPECIFIED SEVERITY, WO BEHAVIORAL DISTURBANCE. HYPOTENSION 4/12/2023 LEWY BODY DEMENTIA, UNSPECIFIED SEVERITY, WO BEHAVIORAL DISTURBANCE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 15.11.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
COVID-19
Cough
Loss of consciousness
Nasopharyngitis
Pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
X-ray
Symptomtext
I had a general feeling of a cold, sneezing and little cough and achy. I started to run allow grade fever and then I was at the hospital with my husband while he was having a procedure done, I passed out. I was then taken down to the locale ER and they discovered I was positive for COVID-19. The medication did work, and I fully recovered within two weeks and I isolated during this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 test, bloodwork; X-rays.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Immune Disorder; Hypogammaglobulinemia
- Andere Medikamente
- Gabapentin; bupropion XL; atorvastatin; montelukast; losartan; isosorbide; XYLO; ZOFRAN; prescription calcium; TYLENOL; MOTRIN
- Allergien
- Walnuts; pecans; penicillin; codeine mint; SIALOR; EFFEXOR; poppy seeds; NEXIUM; erythromycin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 10.03.2023
- Impfdatum
- 21.12.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antibody test negative
Antinuclear antibody increased
Back pain
Bacterial test negative
Borrelia test negative
C-reactive protein increased
Dyspnoea
Epstein-Barr virus test negative
Pericardial effusion
Pericarditis
Pyrexia
Red blood cell sedimentation rate increased
Respiratory viral panel
Viral pericarditis
Viral test negative
Symptomtext
Patient admitted to hospital on 3/2/23 with moderate pericardial effusion after 2 months of gradual back pain, SOB, intermittent fevers. Exudative on pericardial fluid analysis. Peds Infectious Diseases consulted and believed postviral pericarditis or pericarditis secondary to mRNA vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- 5,0
- Labordaten
- ANA 1:1280 CRP 8.2 mg/dL ESR 50 Resp Path Panel negative for viral targets Pericardial fluid culture negative Lyme Ab negative, Quantiferon Gold Negative, EBV serologies negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Pectus excavatum, being evaluated for repair
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 08.03.2023
- Impfdatum
- 03.12.2022
- Beginn
- 24.01.2023
- Tage bis Beginn
- 52,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood test
Cardiac monitoring
Electrocardiogram
Syncope
Therapy change
Symptomtext
I had syncopal episodes and was very weak, administered IV fluids received 3 hours of heart monitoring, blood pressure and blood sugar. Went to cardiologist 12 lead EKG, 2 week heart monitor Zio-patch. Decreases blood pressure medication, blood work drawn, one week later had blood work repeated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- EKG 24Jan2023, Zio-Patch removal 07Feb2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Amlodipine; atenolol; vitamin D3; baby aspirin; LIPITOR; PROTONIX
- Allergien
- DEMEROL
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 14.01.2023
- Impfdatum
- 13.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
15 Y/O PATIENT PASSED OUT AFTER RECEIVING TWO VACCINES ( FLUCEVAX AND COVID 19 BIVALENT PFIZER-BIONTECH). PHARMACIST ASK HER FATHER FOR HELP, SHE REGAINED CONSCIOSNESS AND APROXIMATLY 60 SECONDS SHE PASSES OUT AGAIN. PHARMACIST HAD A TECH TO CALL 911 AND ALSO A PHARMACY TECH THAT IS ALSO EMT. AFTER 911 LISTENED TO THE SITUATION AND ASSESSED THEY ELECT NOT TO COME. PATIENT FATHER EXPLAINED THAT THIS IS SOMETHING THAT HAPPENED EVERYTIME THAT PATIENT IS ON PAIN SINCE SHE WAS 3 YERAS OLD. PATIENT REGAINED CONSCIOUSNESS AND ENDED UP LEAVING WITH THE FATER AFTER WAIT AROUND 20 MINUTES SIT DOWN IN THE WAITING AREA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOW
- Allergien
- NKNA
- Vorherige Impfungen
- MOST OF VACCINE SINCE 2010
- Staat
- MO
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 07.01.2023
- Impfdatum
- 03.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fatigue
Feeling hot
Immediate post-injection reaction
Lethargy
Nausea
Syncope
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Nausea-Mild, Systemic: Vomiting-Mild, Additional Details: Patient was receiving 2 vaccines (flu+covid). She fainted immediately after receiving 2nd vaccine. Patient was seating during administration and vaccinator caught her as she was slumping forward. Patient was extremely fatigued and hot after episode. It was 10:30am and patient had not eaten anything yet all day. Patient was given orange juice and crackers. Blood pressure 97/50. Continued to monitor for 15-20 mins. She was able to correctly answer what her name is, where she was, and what happened
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Blood pressure decreased
Blood test normal
Chills
Contusion
Dehydration
Dry mouth
Electrocardiogram normal
Fall
Headache
Immunisation reaction
Loss of consciousness
Nausea
Symptomtext
Severe chilling on and off in the night. My mouth was so dry and never remember it being so dry. In the morning, I started feeling weak, nauseous and headache. I started asking for help. I passed out on the floor for 3-4 mins. My husband helped me out. I was all bruised. He called 911 and they took my blood pressure and it would drop. They took me to the Emergency room. IV fluid, I started feeling better. They did EKG and blood work and everything came out normal. The doctor at the ER said it was orthostasis vaccination reaction. I believe I was dehydrated and doctor also thought as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- high cholesterol thyroid problems high blood pressure
- Andere Medikamente
- no not that morning but I did take before medication for my thyroid.
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 01.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Dizziness
Flushing
Hyperhidrosis
Hypotension
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Systemic: Chills-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Severe, Systemic: Shakiness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 01.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Confusional state
Dysarthria
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Confusion-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: slurred speech-Mild, Systemic: Weakness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 27.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
Dizziness, fainting overnight
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Metformin Farxica Humalog
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 23.12.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Additional Details: paramedics check patients vitals and transported to hospital for further evaluation - patient was alert and talking when transported to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 6,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cerebral thrombosis
Computerised tomogram head abnormal
Confusional state
Dizziness postural
Dyspnoea
Magnetic resonance imaging head abnormal
X-ray
Symptomtext
On 12.21.2022 patient had acute onset of confusion, dizziness upon standing, and shortness of breath at a restaurant. EMS was called and patient was brought to the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral thrombosis
- Hospital-Tage
- -
- Labordaten
- Blood work, xray, CT scans and MRI on 12.21.2022. Patient has an acute left parietal clot.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- BENIGN MENINGIOMA, ANXIETY, COPD, HYPERTENSION
- Andere Medikamente
- ALBUTEROL, DUONEB, ALLOPURINOL, AMLODIPINE/VALSARTAN, ASPIRIN, CARVEDILOL, CLORAZEPATE, COLCHICINE, DICLOFENAC, FLUTICASONE, ADVAIR, HYDROCHLOROTHIAZIDE, KETOCONAZOLE, OMEPRAZOLE, SIMVASTATIN
- Allergien
- DOXYCYCLINE, IBUPROFEN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 8,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Deep vein thrombosis
Ultrasound Doppler abnormal
Symptomtext
Blood clot in left calf. (Previous COVID19 vaccines in April 2021 and booster in December 2021 were Moderna.)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Vascular left venous duplex LE on 12/16/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Fiber capsules & vitamin D3
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 17.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient fainted after pfizer vaccine administration. per patient he did not eat before coming in the morning, he has a history of fainting and fear of needles. called 911, vitals and blood glucose normal. patient felt better and left
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Loss of consciousness
Mydriasis
Symptomtext
Patient presented to clinic with her family for flu and Covid Bivalent booster vaccine. Vaccines were administered without incident, patient was walking from exam room to lobby and mentioned to her mother that she felt like she was "blacking out" at this time mom was hugging patient and I inquired if everything was ok. At this time, the patient was lowered to the ground by mom, she sustained no injury from the fall. The patients pupils were enlarged but she was responsive within 5 seconds. Her blood pressure, pulse oxygen saturation and HR were all evaluated and were normal. After about 5 minutes she was moved to a chair in the lobby were she was monitored for an additional 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- Blood pressure, pulse oximeter and HR.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 04.12.2022
- Beginn
- 04.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Confusional state
Dizziness
Flushing
Headache
Hyperhidrosis
Nausea
Syncope
Unresponsive to stimuli
Visual impairment
Symptomtext
Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Nausea-Medium, Systemic: Visual Changes/Disturbances-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 02.12.2022
- Impfdatum
- 29.11.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Head injury
Injury
Syncope
Symptomtext
Fainting with injury-- After patient received her vaccines, she remained seated while her mother received vaccines. She did not report any dizziness. When she approached the door to leave she fainted falling forward hitting the front of her head on the door, then backwards hitting the back of her head on the floor. She quickly regained consciousness, but 911 was called to check her over. EMT cleared and released her. She had no signs of concussion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood pressure systolic decreased
Confusional state
Dizziness
Fatigue
Hypotension
Lethargy
Loss of consciousness
Nausea
Syncope
Unresponsive to stimuli
Visual impairment
Symptomtext
Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Hypotension-Mild, Systemic: Visual Changes/Disturbances-Mild, Systemic: Weakness-Mild, Additional Details: patient was seated, fainted/passed out, regained conciousness, systolic bp low, HR normal. monitored it and it came back up, he stated vision changes and nausea, notified parent we were going to call the ambulance due to low bp and as precaution, parent did not want that, told parent take him to ER to be monitored. patient did recover after seating and gained normal function and was able to walk out with parent (Dad)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 19.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- 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
- VA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 11.11.2022
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Fatigue
Pallor
Syncope
Symptomtext
Patient was in the pharmacy around 11:30AM for Flublok, Boostrix, and Pfizer bivalent. After the vaccines, pharmacist advised patient to stay in the store for 15 minutes. A moment later, patient fainted at the shelf-checkout in the front near customer service. Manager on duty heard the fall and came over. Patient regained consciousness right away. A customer nearby claimed to be a nurse advised patient to be seated. Manager gave the patient some water and the patient claimed to feel fine. Pharmacist came to offer additional assistance, but patient refused and claimed to be okay. The patient looked very tired and pale, few minutes later patient left store and refused further assistance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- na
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 11.11.2022
- Impfdatum
- 06.11.2022
- Beginn
- 06.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Visual impairment
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Systemic: Visual Changes/Disturbances-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 22.12.2023
- Impfdatum
- 28.11.2022
- Beginn
- 15.10.2023
- Tage bis Beginn
- 321,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Blood magnesium normal
Blood potassium decreased
COVID-19
Chest X-ray normal
Computerised tomogram head normal
Confusional state
Cough
Dehydration
Encephalopathy
Hypokalaemia
Hypophagia
Mental status changes
Nausea
Oropharyngeal pain
SARS-CoV-2 test positive
Urine analysis normal
Vomiting
Symptomtext
Patient is an 81 y.o. female who presented from home on 10/15/2023 with generalized weakness, altered mental status. Recently diagnosed with COVID-19 and started on Paxlovid on 10/11.She completed Paxlovid while inpatient and did well throughout her course, though remains generally weak so discharged to SNF for continued therapy. Assessment and Plan Generalized weakness Acute encephalopathy Presents with increased generalized weakness and confusion over the last day or so prior to admit. Recently diagnosed with COVID-19, started on Paxlovid on 10/11/23. +Nausea and vomiting, decreased oral intake - CT head on admission negative for acute intracranial abnormality. - Urinalysis unremarkable - Symptoms likely due to COVID-19 infection and mild dehydration - Slowly improving but remains generally weak. PT/OT/CM following- discharged to SNF COVID-19 infection Diagnosed week prior to admit, prescribed Paxlovid on 10/11/23 - Presented with: Generalized weakness, confusion - Symptom onset: ~10/10/23 (cough, sore throat) - Positive COVID-19: 10/11/23; home test - Vaccination status: Vaccinated with Pfizer with last dose 11/28/22 - CXR on admission showed no acute cardiopulmonary abnormalities. Lungs are clear. - Oxygen status: > 92% on room air - Continued Paxlovid for the last dose while inpatient, now complete. - Isolation discontinued 10/20 after discussion with infection prevention. Hypokalemia K 2.8 on admission. Likely due to poor oral intake - Replaced in the ED and has since been stable for the most part. Mg normal. Appetite improved. Parkinsonism Follows with neurology, Dr. - Continue Sinemet as per home regimen Alzheimer's dementia - Continue home Aricept and Namenda Large granular lymphocytic leukemia Follows with hematology/oncology at facility. On weekly methotrexate - Hold methotrexate in the setting of acute infection- discussed with husband will hold this weeks's dose (usually takes Thursday) and resume 10/26 if continues to improve. - Follow-up with hematology/oncology as outpatient Hypothyroidism - Continue Synthroid at home dose Overactive bladder - Resume Myrbetriq on discharge Recurrent major depression - Continue sertraline 100 mg daily as per home regimen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 08.11.2023
- Impfdatum
- 24.01.2023
- Beginn
- 20.07.2023
- Tage bis Beginn
- 177,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial flutter
Back pain
Balance disorder
Benign prostatic hyperplasia
Blood pressure increased
Computerised tomogram spine
Condition aggravated
Coronary artery disease
Cough
Depression
COVID-19
Cardiac failure congestive
Chronic left ventricular failure
Chronic obstructive pulmonary disease
Computerised tomogram abnormal
Dyslipidaemia
Essential hypertension
Fall
Symptomtext
BRIEF OVERVIEW: Discharge Provider: , MD Primary Care Provider at Discharge: DO Admission Date: 7/20/2023 Discharge Date: 7/22/203 DISCHARGE DIAGNOSES 1. COVID 2. L1 compression fracture 3. Mild hyponatremia 4. Chronic obstructive pulmonary disease 5. BPH 6. Chronic atrial flutter 7. Chronic diastolic congestive heart failure 8. Obstructive sleep apnea 9. Depression 10. Dyslipidemia 11. Essential hypertension 12. Sick sinus syndrome 13. Coronary artery disease DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is a 63 y.o. male who presented on 7/20 with cough, congestion and fatigue for 3 days, initially hypoxic to 88% with ambulation, found to be COVID+. Admitted for treatment. Patient also had a recent fall, and CT showed acute compression fracture at L1. Back pain controlled with tylenol and motrin. Patient's COVID symptoms improved with decadron for 3 doses, satting well on room air. Upon discharge patient's back pain is improved. Of note patient's blood pressure was elevated in the hospital. Should be monitored by PCP and Cardiology outpatient. Discharge with out-patient PT referral due to recent falls and balance deficits. Prescribed 3 day course Decadron 6 mg on discharge, start taking 7/23, total steroid treatment will be 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- 01/09/2023 Bacterial Conjunctivitis
- Vorgeschichte
- COPD, group D, by GOLD 2017 classification (HCC) Essential hypertension, benign Dyslipidemia Depression ETOH abuse CAD (coronary artery disease), s/p CABG 8/13/19 Atrial fibrillation (HCC), now NSR S/P CABG x 4 Traumatic tear of supraspinatus tendon, left, initial encounter Rotator cuff arthropathy of left shoulder Opacity of lung on imaging study OSA (obstructive sleep apnea) History of smoking Macrocytic anemia Elevated serum immunoglobulin free light chain level Lower leg edema Dyspnea on exertion Coordination of complex care Shortness of breath Right knee pain CHF (congestive heart failure), NYHA class I, acute on chronic, diastolic (HCC) Atherosclerosis of native arteries of extremities with rest pain, bilateral legs (HCC) Chronic idiopathic constipation Cardiac pacemaker in situ COVID-19 BPH (benign prostatic hyperplasia) Compression fracture of L1 lumbar vertebra (HCC) Bilateral carotid artery stenosis
- Andere Medikamente
- albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 mg tablet buPROPion (WELLBUTRIN XL) 300 MG 24 hr tablet clopidogrel (PLAVIX)
- Allergien
- HydrochlorothiazideOther
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 17.08.2023
- Impfdatum
- 16.08.2023
- Beginn
- 17.08.2023
- Tage bis Beginn
- 1,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Confusional state
Hypertension
Pyrexia
Symptomtext
Fever, hypertension and confusion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 8/17/23- ordered Flu/Covid/RSV test and CBC with diff
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Parkinsons, HTN, depression, CAD, Thoracic aortic aneurysm, hyperlipidema, aortic valve sclerosis
- Andere Medikamente
- Lansoprazole, carbidopa, metamucil, rosuvastin, acetaminophen, ipratoropium nasal spray, colace, eucerin, senna, pramipexole, lasix, eliquis, tramadol
- Allergien
- Kiwi
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 30.06.2023
- Impfdatum
- 22.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Symptom recurrence
Symptomtext
HYPOTENSION 2/20/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 26.01.2023
- Beginn
- 25.02.2023
- Tage bis Beginn
- 30,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 26.06.2023
- Impfdatum
- 09.12.2022
- Beginn
- 31.03.2023
- Tage bis Beginn
- 112,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aortic valve incompetence
Cardiac failure congestive
Condition aggravated
Hypoxia
Symptomtext
HYPOXIA 3/31/2023 CHF EXACERBATION, UNSPECIFIED HYPOXIA 3/31/2023 AORTIC VALVE REGURGITATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 23.06.2023
- Impfdatum
- 16.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Tremor
Symptomtext
I had a sore arm for about a day after receiving the vaccine. In 12/2022, I began to have tremors in both hands. The morning time is the worst and by the end of day it calms down. The symptoms got worse, and I recently went to the doctor. I have started taking medication which is helping. At this time, we are waiting on how the medication works.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Crohn's Disease
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 20.12.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Computerised tomogram thorax normal
Erythema
Headache
Hypertension
Middle insomnia
Pruritus
Scan myocardial perfusion normal
Tinnitus
Symptomtext
12/21/2022 ? I got up in the night and noticed my face was red and itchy and it was spreading. I took Benadryl and it continued to get worse. I went to a walk-in clinic. I was told to take more Benadryl and Pepcid Complete which resolved the issue. The doctor told me to report this to the pharmacy, which I did. On 12/24/2022, my blood pressure went up high. I had never had issues with my blood pressure before. My ears began ringing and I had a headache. I could not get the blood pressure down. I went to the Emergency Room and was kept overnight. I was started on Amlodipine which did not help and I had side effects, so I stopped taking the medication. I then started taking 7.5mg ? 12.5mg of Hydrochlorothiazide and my blood pressure is now coming down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- 2,0
- Labordaten
- 24DEC22- Nuclear Stress Test-Normal; 24DEC22 -CT of Chest-Normal;24DEC22-Bloodwork-Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Oxybutynin, Premarin, Levothyroxine, Amour Thyroid, Bayer Aspirin, Vitamin B Complex
- Allergien
- Penicillin, Sulfa , Morphine, Being tested for possible allergy to Lidocaine and Epinephrine, Prednisone , Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.06.2023
- Impfdatum
- 03.12.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 60,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy to chemicals
COVID-19
Chest X-ray normal
Condition aggravated
Cough
Dyspnoea
Feeling abnormal
Headache
Hypersensitivity
Influenza like illness
Malaise
Mobility decreased
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
2/1/23 I woke up with a sore throat. I tested positive with an at home COVID test. As the day went on, I started to not feel overall good and had a severe headache which lasted 3-4 days. I had a fever later that afternoon. The next day, I could not get out of bed. I had flu like symptoms and felt horrible which lasted about 2-3 days. Then I began coughing and had a little bit of a runny nose. I was sick for a good 10-12 days. I tested positive for 14 days. During that time, around day 5 or 6, I was having trouble breathing and had a telehealth appointment. I was prescribed a Z-PAK and albuterol inhaler. I still did not feel good after finishing the Z-PAK. I had a chest x-ray which came back negative. It was three to four weeks, before I felt better. At times, I would have trouble getting my breath. My allergies are now magnified. I can't touch anything with the chemical in it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 1FEB23 at home COVID test positive; 2FEB23-15FEB23 at home COVID tests every day, positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Paraphenylenediamine
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 16.03.2023
- Impfdatum
- 13.12.2022
- Beginn
- 19.01.2023
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacterial test positive
Culture positive
Cystitis
Diverticulitis
Enterococcus test positive
Pneumonia klebsiella
Urine analysis
Symptomtext
On January 19, I went to the doctor and was told I had Diverticulitis and a Bladder infection. I was given Flagel which is an antibiotic and Ceftin. The culture came back within four day later and was told it was Klebsiella Pneumoniae. I went back on 1/30 and was told I had a bladder infection again. I was given Bactrian and sent the sample to be cultured. The sample showed no growth, and I was told to stop the medication because it was affecting my pulse blood pressure. I still had symptoms so I went back on Feb 23, I was told I had a bladder infection, and they sent the sample to see if they could find growth. It came back as Klebsiella Pneumoniae. I was called in some Doxycycline, and this didn't help it caused issues with blood pressure and my pulse. I called the clinic and spoke with a nurse and the doctor on duty didn't feel comfortable calling in medication and he wanted me to come back in. I did return on March 2 and was told for the fourth time I was having a bladder infection. The doctor I have seen through most of this I was put back on Ceftin 250 and the sample was sent out to measure growth. It came back different with a bacteria called Enterococcus Faecalis I was put back on Macrobid for 6 days and I have recently be refereed to see a Urologist on April 4th. Although I don't think its related....
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia klebsiella
- Hospital-Tage
- -
- Labordaten
- Urinalysis
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Athirst; High Blood Pressure; Migraines; Panic Disorder; Depression
- Andere Medikamente
- Lisinopril HCTZ; Nexium; Multivitamin; Vitamin D; Zoloft Sucralfate; Tylenol; Fioricet; Sudafed; Zetia
- Allergien
- Sulfa Drugs; Amoxicillin; Bacterin; Keflex; Cipro; Pravastatin; Doxycycline; Steroids; Nsaids; Retinol; Differin
- Vorherige Impfungen
- 2019 Tdap- I had a small lymph and my arm was very sore. The lymph knots swell and some discharge at the injection site.
- Staat
- MA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 15.02.2023
- Impfdatum
- 17.01.2023
- Beginn
- 22.01.2023
- Tage bis Beginn
- 5,0
- Dosis
- 5
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Symptomtext
Left sided chest pain over heart
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Head cold; chest congestion
- Vorgeschichte
- Coronary artery disease
- Andere Medikamente
- Linsinopril 20 mg twice daily; amlodipine bestylate 5 mg. Once daily; Ezetimibe 20 mg once daily; duoxetine dr30 once daily; mirtazapine 15 mg once at bedtime; Praluent 150 mg/ml subcutaneous inj. Once every 14 days; lorazepam 0.5 mg o
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 02.11.2022
- Beginn
- 03.02.2023
- Tage bis Beginn
- 93,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain lower
Acute kidney injury
Alanine aminotransferase normal
Anion gap
Anticoagulant therapy
Aspartate aminotransferase normal
Auscultation
Back pain
Bacterial test positive
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin increased
Blood calcium normal
Blood chloride normal
Blood creatinine increased
Blood glucose normal
Blood potassium normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By, NP on February 03, 2023 17:48 Verified By: NP on February 03, 2023 17:48 Encounter Info: Hospital, Emergency, 02/03/23 - 02/03/23 * Final Report * Document Contains Addenda History of Present Illness/Subjective Patient is a 77-year-old female with past medical history of myeloproliferative disorder, myelodysplastic syndrome, splenomegaly, anemia, arthritis, CKD, COPD, recurrent UTIs who presented to the emergency room with chief complaint of lower abdominal and back pain for the last several days at home additionally she has had fevers and chills. Upon ER evaluation her temperature was 97.7, heart rate was 104, respiratory rate was 17 and room air sat was 95%. Blood pressure was 103/66. Lab work revealed a white blood cell count of 8.7, hemoglobin was 8.2, sodium was 134, GFR was 22, creatinine was 2.21. Her baseline creatinine is around 1.1. Troponin initially was 35 with repeat being 33 and her BNP was 101. UA revealed evidence of UTI. CT abdomen pelvis was completed showed continued splenomegaly, inflammation in the right renal pelvis may be artifact however can be seen in the setting of an a sending urinary tract infection. No hydronephrosis. Patient was started on IV antibiotics, ampicillin, gentamicin IV fluids and Tylenol. She will be admitted for further evaluation management UTI, sepsis, pyelonephritis. Patient is a full CODE STATUS. Review of Systems All 13 point review of systems were reviewed with the patient and are negative except as specified in the HPI Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 37.6 (36.9-38.2) Temp (FAHR) 99.7 (98.4-100.8), BP 115/52 (100-126)/(49-62), HR 83 (83-95), RR 19 (16-25), O2Sat 99 (86-99) Patient Weight Current Daily Weight: 63.6 kg 02/03/23 Patient Height Current Height: 160 cm 02/03/23 Constitutional: No acute distress , well-nourished Eyes: PEERL, EOMI, normal conjunctiva , no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs CTAB Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, mildly tender bilateral lower quadrant, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment , no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Sepsis A41.9 Sepsis order set initiated We will continue with IV Zosyn as patient is allergic to Ceftin. Previous micro on urine grew out E. coli pansensitive. Blood cultures are pending 2. Pyelonephritis N12 Urine culture pending, IV antibiotics given in the ER we will continue with Zosyn 3. Urinary tract infection N39.0 As above 4. Elevated troponin R77.8 Chronic problems Myelodysplastic syndrome/ Myeloproliferative disorder -Under treatment per Dr. splenomegaly As above this appears to be related to mixed bone marrow disorder both the dysplastic syndrome along with the myeloproliferative neoplasm. Splenomegaly is more associated with myeloproliferative disorder. HLD Resume home meds anxiety Resume home meds ???????Patient is full CODE STATUS. DVT prophylaxis with Lovenox. 5. Acute kidney injury N17.9 CKD stage III, give IV fluids normal saline at 100 mL an hour Code Status None Recorded Chronic Problem List Acute bronchitis Anemia Anxiety Arthritis Axillary lymphadenopathy Body aches Chronic back pain CMC arthritis CRF (chronic renal failure) Diffuse cutaneous mastocytosis Dysuria Emphysema/COPD Encounter for long-term (current) use of medications Fatigue Ganglion cyst of finger of left hand H/O bone density study Health care maintenance Herniated disc, cervical Hyperlipidemia Hypertrophy of both inferior nasal turbinates Hypoxemia Insomnia Left upper quadrant pain Leg cramps Leukocytosis MDS (myelodysplastic syndrome) Medicare annual wellness visit, subsequent MGUS (monoclonal gammopathy of unknown significance) Mucous cyst of finger Needs flu shot Nocturnal hypoxia Osteoarthritis Osteoarthritis of CMC joint of thumb Osteoarthritis of finger of left hand Osteoarthritis of finger of left hand Osteoarthritis of right knee Pain of right thumb Pulmonary nodule seen on imaging study Pyelonephritis Refractory obstruction of nasal airway Right knee pain S/P total knee replacement Sepsis Situational depression Skin rash Spleen enlarged Stomatitis Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease Trigger finger of right hand Trigger finger, right middle finger Trigger finger, right ring finger Urinary tract infection UTI (urinary tract infection) Procedure/Surgical History melanoma removed from neck (12/05/2021) Knee replacement (04/01/2021) BACK SURGERY (01/10/2019) colonoscopy (12/13/2017) Rt LF- DIPJ Fusion, HWR OWW 6/6/2017 (No pkg) (06/06/2017) Rt Thumb CMCA w/FCR Tendon Trans, LF- DIPJ Fusion, Cyst Exc OWW 4/24/17 (04/24/2017) egd (03/13/2009) Appendectomy Cataract Cesarean section left nipple reconstruction Nasal surgery right breast biopsy Tonsillectomy and adenoidectomy Tubal ligation Varicose vein stripping Surgical History Internal 04/01/2021 Knee Arthroplasty (Right) MD 01/10/2019 Spine Fusion Posterior Lumbar MD 12/13/2017 Colonscpy Diagnostic/Screen MD Medications Home Medications (19) Active amoxicillin 500 mg oral tablet 2,000 mg = 4 Tablet, Orally, ONCE, 1 hour before dental procedure Calcium 600+D oral tablet 1 Tablet, Orally, QHS Colace 100 mg oral capsule 100 mg = 1 Capsule, Orally, QHS CoQ10 300 mg oral capsule 300 mg = 1 Capsule, Orally, BID cranberry oral capsule 1 Capsule, Orally, QAM doxepin 25 mg oral capsule 50 mg = 2 Capsule, Orally, At Bedtime EpiPen Auto Injector 0.3 mg, PRN, IM, ONCE famotidine 20 mg oral tablet 20 mg = 1 Tablet, Orally, BID fluocinolone 0.025% topical cream 1 App, Topical, BID GaviLyte-G oral powder for reconstitution See Instructions, as directed. hydroxyurea 500 mg oral capsule See Instructions, 1 Capsule Orally Daily Mon-Fri, 2 capsules on Sat & Sun hydrOXYzine pamoate 25 mg oral capsule 25 mg = 1 Capsule, PRN, Orally, 4 Times Daily levocetirizine 5 mg oral tablet 5 mg = 1 Tablet, Orally, BID Lidocaine Viscous 2% mucous membrane solution See Instructions, PRN, Apply directly to mouth sore with cotton swab Q3-4H prn pain Mobic 15 mg oral tablet 15 mg = 1 Tablet, Orally, Daily montelukast 10 mg oral tablet 10 mg = 1 Tablet, Orally, Daily Requip 0.25 mg oral tablet 0.25 mg = 1 Tablet, Orally, At Bedtime tiZANidine 4 mg oral tablet 4 mg = 1 Tablet, Orally, Q8H Tylenol Extra Strength 500 mg oral tablet 1,000 mg = 2 Tablet, PRN, Orally, Q6H Active Scheduled Inpatient Medications None Reported One-Time Medications Given 02/02/23 00:00:00 TO 02/03/23 17:48:03 acetaminophen, Tablet, 1,000 mg, Orally, ONCE, (1 DOSE 02/03/23 13:18:00) ampicillin, Injection, 2 GM, IVPB, ONCE, (1 DOSE 02/03/23 14:29:00) gentamicin, Injection, 280 mg, IVPB, ONCE, (1 DOSE 02/03/23 15:26:00) ketoROLAC, Injection, 15 mg, IV Push, ONCE, (1 DOSE 02/03/23 11:49:00) Lactated Ringers (LR - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 02/03/23 11:49:00) ondansetron, Injection, 4 mg, IV Push, ONCE, (1 DOSE 02/03/23 11:49:00) PRN Medications (0600 - 0559) from 02/02 - 02/03 None Reported Allergies Ceftin (Rash) sulfa drugs (Rash) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Retired Home/Environment married, 2 children - retired, Lives with Spouse. Nutrition/Health Diet: Regular. Caffeine intake amount: 2-3 cups coffee/day. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Arthritis: Mother. CAD - Coronary artery disease: Father. Coronary artery bypass graft: Father. Depression: Mother. Diabetes..: Mother. Heart disease: Mother and Father. Heart murmur: Mother. Kidney stones: Son. Liver cancer..: Father. Osteoporosis...: Mother. Stroke..: Mother. Uterine cancer: Mother. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 8.7 k/cumm (02/03/23 11:48:00) RBC: 2.86 million/cumm Low (02/03/23 11:48:00) Hgb: 8.2 GM/dL Low (02/03/23 11:48:00) Hct: 25.1 % Low (02/03/23 11:48:00) MCV: 88 fL (02/03/23 11:48:00) MCH: 28.6 pg (02/03/23 11:48:00) MCHC: 32.6 GM/dL (02/03/23 11:48:00) RDW: 33.4 % High (02/03/23 11:48:00) Platelet: 50 k/cumm Low (02/03/23 11:48:00) MPV: 10.3 fL (02/03/23 11:48:00) # WBC Counted in Diff: 100 (02/03/23 11:48:00) Band: 12 % (02/03/23 11:48:00) Neutrophil: 68 % (02/03/23 11:48:00) Lymphocyte: 17 % (02/03/23 11:48:00) Monocyte: 3 % (02/03/23 11:48:00) Number of Nucleated RBCs: 1 /100 WBC High (02/03/23 11:48:00) Absolute Band: 1 k/cumm High (02/03/23 11:48:00) Absolute Neutrophil: 5.9 k/cumm (02/03/23 11:48:00) Abs Lymphocyte: 1.5 k/cumm (02/03/23 11:48:00) Absolute Monocyte: 0.3 k/cumm (02/03/23 11:48:00) RBC Morphology: See description UC (02/03/23 11:48:00) Dacryocyte: Moderate (2+), (02/03/23 11:48:00) Hypochromasia: Moderate (2+), (02/03/23 11:48:00) Macrocyte: Moderate (2+), (02/03/23 11:48:00) Microcyte: Moderate (2+), (02/03/23 11:48:00) Ovalocyte: Moderate (2+), (02/03/23 11:48:00) Platelet Estimate: Decreased. (02/03/23 11:48:00) Platelet Morphology: Normal, (02/03/23 11:48:00) Chemistry: Sodium SerPl QN: 134 mmol/L Low (02/03/23 11:48:00) Potassium SerPl QN: 4.5 mmol/L (02/03/23 11:48:00) Chloride SerPl QN: 100 mmol/L (02/03/23 11:48:00) Carbon Dioxide SerPl QN: 25 mmol/L (02/03/23 11:48:00) Anion Gap: 9 mmol/L (02/03/23 11:48:00) BUN SerPl QN: 48 mg/dL High (02/03/23 11:48:00) Creatinine SerPl QN: 2.21 mg/dL High (02/03/23 11:48:00) Estimated GFR (CKD-EPI, no race): 22 mL/min/1.73m2 Low (02/03/23 11:48:00) Estimated CRCL (CG): 19 mL/min Low (02/03/23 11:48:00) Glucose SerPl QN: 90 mg/dL (02/03/23 11:48:00) Calcium Total SerPl QN: 9.4 mg/dL (02/03/23 11:48:00) Alkaline Phos SerPl QN: 101 Units/L (02/03/23 11:48:00) ALT SerPl QN: 25 Units/L (02/03/23 11:48:00) AST SerPl QN: 31 Units/L (02/03/23 11:48:00) Bilirubin Total SerPl QN: 1.9 mg/dL High (02/03/23 11:48:00) Total Protein SerPl QN: 6.5 GM/dL (02/03/23 11:48:00) Albumin SerPl QN: 3.8 GM/dL (02/03/23 11:48:00) Troponin-I High Sensitivity: 33 ng/L High (02/03/23 13:00:00) BNP Pl QN: 101 pg/mL High (02/03/23 11:48:00) Urine Studies: Color: Yellow (02/03/23 13:18:00) Clarity: Clear (02/03/23 13:18:00) Specific Gravity: 1.020 (02/03/23 13:18:00) pH: 6.0 (02/03/23 13:18:00) Protein: 100 Abnormal (02/03/23 13:18:00) Glucose: NEGATIVE (02/03/23 13:18:00) Ketones: NEGATIVE (02/03/23 13:18:00) Bilirubin: SC Small Abnormal (02/03/23 13:18:00) Hgb Ur: SMALL. Abnormal (02/03/23 13:18:00) Nitrite: NEGATIVE (02/03/23 13:18:00) Urobilinogen: NormalUro (02/03/23 13:18:00) Leukocyte Esterase Ur: MODERATE. Abnormal (02/03/23 13:18:00) WBC: 11-20 Abnormal (02/03/23 13:18:00) RBC: 3-5 Abnormal (02/03/23 13:18:00) Bacteria: Moderate Abnormal (02/03/23 13:18:00) Squamous Epithelial: NONE (02/03/23 13:18:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (02/02/23 15:02:00) Rapid Influenza A PCR: Not Detected (02/02/23 15:02:00) Rapid Influenza B PCR: Not Detected (02/02/23 15:02:00) Diagnostics Radiology Results - Last 24 hours Across Visits 02/03/2023 12:07 - XR Chest PA or AP Portable IMPRESSION: Mediastinal contour and heart size are stable and within normallimits. No focal consolidation, pulmonary edema, pneumothorax, orpleural effusion. No new acute cardiopulmonary abnormalities sincethe previous examination. Thank you for consulting with Radiology. Healthcare providerswishing to discuss this case further can contact the Emergency Radiology reading room at. 02/03/2023 14:26 - CT Abd/Pelvis W/O IV Contrast IMPRESSION:1. Negative for acute findings to explain the patient's left lowerquadrant pain. Persistent significant splenomegaly measuring up to4.2 cm and extending into the left pelvis which may contribute to thepatient's pain.2. Inflammation in the right renal pelvis which may be artifacthowever can be seen in the setting of an ascending urinary tractinfection. Recommend correlation with urinalysis. Negative forhydronephrosis.3. Chronic massive effect from the enlarged spleen appears to becausing mild atrophy of the left kidney. 4. Additional chronic findings as described above. Thank you for consulting our team of subspecialty radiologists at Physicians Radiology. Please contact us with any questions. Signature Line Electronically Signed on 02/03/23 17:48 ________________________________________________________ NP Addendum by MD on February 03, 2023 18:05:57 (Verified) General: Alert and oriented Eye: Pupils are equal, round and reactive to light HEENT: Normocephalic Neck: Supple, normal range of motion Oropharynx: No erythema or drainage. Respiratory: Lungs are clear to auscultation. Cardiovascular: Normal rate, Regular rhythm. Gastrointestinal: Soft, Non-tender. Musculoskeletal: Normal range of motion, No focal tenderness Integumentary: Warm, Dry, No rash Neurologic: No focal weakness. Sensation intact. Normal mood and affect I saw and evaluated the patient in addition to the APP. I provided a substantive portion of the care for this patient. I personally performed in its entirety examfor this encounter. I have reviewed and verified this documentation and it accurately reflects our care. MD Hospital Medicine Signature Line Electronically Signed on 02/03/23 18:06 ________________________________________________________ MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 29.12.2022
- Beginn
- 07.01.2023
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Bronchitis
Cardiomegaly
Chest X-ray abnormal
Chest pain
Condition aggravated
Cough
Echocardiogram abnormal
Full blood count abnormal
Influenza A virus test negative
Influenza B virus test
Influenza like illness
Pain in extremity
Pancytopenia
Pericardial effusion
SARS-CoV-2 test negative
Troponin
Symptomtext
Received vaccine on 12/29/2022, reports weakness, chest pain and left arm pain when coughing on 1/7/2023, she was diagnosed with bronchitis and influenza-like illness on 1/10/2023, but Influenza A&B were negative and rapid COVID was negative on this date. She was prescribed a Z-pak on 1/10/2023. On 1/17/23, she still complained of cough and weakness and was seen by her PCP. A chest Xray and CBC was ordered on this date. Chest Xray (1/20/23) showed cardiomegaly and CBC (1/20/23) showed pancytopenia which is a known chronic condition for this patient. She started experiencing chest pain, weakness, right arm pain on 1/27/2023 and went to the ER. Patient was admitted to hospital on 1/27/2023. Echocardiogram on 1/28/2023 shows moderate pericardial effusion. Patient was started on prednisone and colchicine. She is still hospitalized at time of this submission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 4,0
- Labordaten
- Troponin, high sensitivity = 266 on 1/28/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CKD stage 3, thrombocytopenia, DM, PVD
- Andere Medikamente
- ASA, atorvastatin, Questran, Plavis, Bentyl, glipizide, Tradjenta, loratadine, MVI, olmesartan, Protonix
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 27.01.2023
- Beginn
- 27.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Formication
No reaction on previous exposure to drug
Paraesthesia
Pruritus
Symptomtext
Patient received covid-19 pfizer bivalent booster today around 8:46 am in the left arm. A couple minutes later, patient developed a tingling sensation on left side of body. It feels as though there are ants crawling underneath her skin. It started by left underarm and has spread throughout left side of body. The sensation level as remained the same. Patient is also experiencing itchiness of the left side. Denies pain, shortness of breath, tongue swelling, rash, chest pain, feeling warm, and change in vision. Patient stated for previous covid injections, she did not have any reactions. RN spoke with DO who prescribed patient benadryl and prednisone for 3 days. Patient to take and monitor symptoms. Dr. advised patient to wait in lobby until symptoms resolve. RN informed patient scripts were sent to pharmacy next door and to wait in lobby until symptoms resolve. Patient stated she was called in to work (which is from home) and cannot stay. RN walked with patient to pharmacy, waited for prescriptions to be filled, and walked patient out. RN advised patient with any change in symptoms, to call office or seek medical attention. Patient verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 13.12.2022
- Beginn
- 13.01.2023
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19 pneumonia
Chest X-ray abnormal
Pleural effusion
Ultrasound scan abnormal
Symptomtext
Clinical Narrative: Patient was treated for COVID-19 pneumonia, of which she was started on breathing treatments, steroids with Decadron, guaifenesin, and she completed 5 days of remdesivir this morning. She is presently afebrile, no shortness of breaths she is on room air saturating 95% and she is anxious to be discharged back home she was started on empirical antibiotics with ceftriaxone and Zithromax for possible superimposed bacterial pneumonia, completed 45 days of antibiotic Chest x-ray has shown blunting of the costophrenic angle on the right, consent for pleural effusion and ultrasound was done this morning which shows very small right pleural effusion Patient will be discharged to follow closely with her family physician
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Respiratory Seasonal allergic rhinitis due to pollen COPD exacerbation Allergic rhinitis due to other allergen Deviated nasal septum Epistaxis Asthma Hypertrophy of nasal turbinates Other seasonal allergic rhinitis Pneumonia due to COVID-19 virus Pleural effusion, right Digestive Vitamin D deficiency disease Endocrine/Metabolic Mixed hyperlipidemia Pure hypercholesterolemia Other Tobacco use disorder Osteopenia DVT prophylaxis
- Andere Medikamente
- albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler alendronate (FOSAMAX) 70 MG tablet aspirin 81 MG EC tablet atorvastatin (LIPITOR) 20 MG tablet dexa
- Allergien
- Sulfacetamide Sodium Soy Aspergillus Fumigatus Black Willow Cat Hair Extract Dogs English Plantain Environmental Mite Red Cedar Rough Pigweed Russian Thistle Tree Extract Ulmus Fulva Weeds White Ash White Oak
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 19.12.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 16,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Canalith repositioning procedure
Condition aggravated
Ear discomfort
Ear infection
Eczema
Vertigo
Symptomtext
01/04/2023 eczema in left ear canal few days later began to feel pressure in left ear, suspected ear infection in left ear. 01/08/2023 went to workout and experienced vertigo. Episodes of vertigo continued. 01/11/2023 saw nurse practitioner. Prescribed antibiotics for ear pressure. Elevated blood pressure, ask to record blood pressure and report after a week. Epley was performed to reduce vertigo symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma; eczema
- Andere Medikamente
- PULMICORT; epinephrine; CLARITIN; famotidine; acetaminophen
- Allergien
- Amoxicillin; bacitracin; latex; nuts; shellfish; fruits; vegetable; dust; pollen; animal dander
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 22.01.2023
- Impfdatum
- 16.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Injection site erythema
Injection site pain
Injection site swelling
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Severe, Systemic: numbness-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Additional Details: fingers tingling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site pain
Injection site swelling
Limb injury
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Joint Pain-Severe, 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
- 17,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure increased
Dyspnoea
Symptomtext
patient was administered covid pfizer bivalent booster vaccine and within minutes she had trouble breathing and holding her throat. pharmacist administered epinephrine and 911 was contacted. patient immediately improved after administration, her throat felt better and breathing improved. local county sheriff was in close proximity to pharmacy and came in while awaiting local ems and police to arrive. pt was stable and was assessed by local ems. she had elevated blood pressure due to epinephrine. mother opted not to transport to ER by ems. Patient and mother left the pharmacy about 7pm. Pharmacist followed up with parent next day 1/6 about 930am and mother stated she did take daughter local ER for further evaluation where she was given rx for benadryl, prednisone, and epinephrine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- apples
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 05.01.2023
- Impfdatum
- 04.01.2023
- Beginn
- 04.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Chest discomfort
Dyspnoea
Electrocardiogram
Lip swelling
Swelling face
Symptomtext
Patient reported lip swelling, facial swelling, shortness of breath, chest tightness approximately 30 minutes after administration of vaccine. Patient was given one dose of Epi-pen 0.3 mg intramuscular injection and sent to ED via ambulance for observation. Patient was seen in ED and discharged home after 6 hour observation (pt given another dose of Epi-pen, steroids, Benadryl, Pepcid in the ED).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- EKG and blood work done at ED.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Morbid Obesity; Obstructive Sleep Apnea; Type 2 Diabetes Mellitus; Hypertension; Pacemaker; Complete Heart Block; Major Depressive Disorder; Mild Persistent Asthma Osteoarthritis of Knee; PTSD; Dyspnea; Syncope.
- Andere Medikamente
- -
- Allergien
- Contrast Dye; Metrizamide; Ace Inhibitor; Avocado; Banana; Potassium Chloride; Kiwi; Tree Nut Latex.
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 02.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Palpitations
Symptomtext
PER PATINET, AWOKE OVERNIGHT WITH HEART PALPITATIONS/MILD CHEST PAIN THAT HAS CONTINUED TO PRESENT TIME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- cough reported 12/19 per medication history; visit to urgent care
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- thyroid np/levothyroxine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 31.12.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Symptomtext
Systemic: Allergic: Difficulty Breathing-Medium, Additional Details: PATIENT WAS HAVING TROUBLE BREATHING. GAVE PATIENT 20 ML BENADRYL. PATIENT BREATHING IMPROVED QUICKLY. PARAMEDICS WERE CALLED. REPORTED PATIENT VITALS NORMAL. PATIENT DID NOT GO TO HOSPITAL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Hyperhidrosis
Hypotension
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Additional Details: 6:05pm - BP 92/60 hr 71 patient reports feeling dizzy and flused, alert and oriented X4 6:20pm - BP 95/64 hr 81 - no longer reports feeling dizzy - alert and oriented x4 laughing with father and drinking water, walks out to waiting room and sits with dad 6:30pm BP 99/64 hr 81 - denies dizziness and all symptoms. Alert and oriented x 4
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.12.2022
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscle twitching
Ophthalmic migraine
Symptomtext
Ocular Migraines Muscle twitching buttock
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ophthalmic migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Estrodial Progesterone
- Allergien
- None
- Vorherige Impfungen
- Ocular migraine
- Staat
- NJ
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 26.12.2022
- Impfdatum
- 22.12.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Hyperventilation
Tremor
Symptomtext
Systemic: Hyperventilation-Severe, Systemic: Shakiness-Medium, Additional Details: Patient left after receiving the vaccine then the patient's son came back and she was having trouble breathing, the store manager called 911, the patient was given a blanket to keep warm and she drink some water while waiting in the car. The ambulance came, EMT techs took a vitals and transported her to the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 16.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 11,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Cough
Discomfort
Dyspnoea
Exposure to SARS-CoV-2
Headache
Nasal congestion
Nausea
Pain
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I received the Pfizer Bivalent booster on 11/17/2022. On 11/28/2022, I had a severe headache and a little bit of nausea. I took some hydrocodone and promethazine. They didn't get rid of the headache, but the promethazine did take away the nausea. After I took the medicines, I just slept, because there was nothing else to do. During the week of 11/28/2022 to 12/2/2022, the symptoms got progressively worse. On 11/30/2022, I had persistent chest pains. On that day, I had a telehealth visit with a PA who works with my pulmonologist. She agreed to ask my pulmonologist to prescribe me some prednisone. At this point, I had taken a home antigen test every day between 11/27/2022 and 11/30/2022 and had gotten a negative result each time. However, my wife had tested positive, so the PA felt pretty confident that I also had it, despite the results of the tests. On 12/1/2022, I took another home antigen test and got a positive result. The symptoms I was dealing with during this time included difficulty breathing, body aches, severe cough, chest pains, nasal congestion, and nausea. I had to use my rescue inhaler when I had difficulty breathing; the inhaler helped somewhat, but not completely. On 12/1/2022, I finally got a prescription for prednisone, Z-PAK, and promethazine, and I began taking the prednisone and the Z-PAK on 12/2/2022. On the night of 12/2/2022, the chest pains had diminished somewhat, so I had less discomfort. At the time of this writing, I continue to have chest pains, which are now somewhat intermittent and are much milder than they were at the beginning of my illness. I also continue to have a persistent (but milder) headache, a mild cough, and intermittent nausea. Of all those, I would say that nausea is the worst symptom, but it now seems to be diminishing. On 12/13/2022, I took another home antigen test and got a positive result. When I took another antigen test on 12/15/2022, I finally got a negative result for the first time since the beginning of my illness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 11/27/2022 11/30/2022 home antigen tests negative results; 12/1/2022, 12/13/2022 home antigen test positive results; 12/15/2022 home antigen test negative result.
- Aktuelle Erkrankungen
- Possible sinus infection.
- Vorgeschichte
- Type II Diabetes; Severe Persistent Asthma; Gastroesophageal Reflux Disease; Neuropathy (Feet and Lower Legs); Muscle Spasms (Back, Neck, and Legs); Chronic Pain; Post-Traumatic Stress Disorder; Enlarged Prostate; History of Atrial Septal Defect (Surgically Corrected); Presence of One Kidney (Congenital); History of Injury to Right Rotator Cuff.
- Andere Medikamente
- Turmeric; multivitamin; ginkgo biloba; stool softener; baby aspirin; omeprazole; pregabalin; lisinopril; tizanidine; hydrocodone; famotidine; amitriptyline; montelukast; rosuvastatin; silodosin; trazodone; BREO ELLIPTA; TOUJEO; TRULICITY.
- Allergien
- Sulfa drugs; bee stings; some antibiotics.
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 05.11.2022
- Beginn
- 04.12.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Confusional state
Cough
Fatigue
Headache
Influenza A virus test positive
Influenza B virus test
Mobility decreased
Nasal congestion
Pain
Panic reaction
Pyrexia
SARS-CoV-2 test negative
Symptomtext
12/4/22 I woke up with just a small cough. Went through most of the day. Around 4:00, the cough began getting stronger. Between 4:00 and 6:00 I went to chills, body ache and headache. I went to bed and stayed in bed until I had to go to the doctor on 12/5/22. My COVID test was negative, Flu A was positive. I was prescribed TAMIFLU and started taking it that evening, 12/5/22. I was in bed on the 5th and 6th. My fever broke on the night of 12/6/22. I got up mid-morning 12/7/22 and worked from home the rest of the week. On 12/8/22 early in the morning, I woke up with a very bad panic and confusion feeling. I ended up video calling my wife to calm me down. My family doctor suggested that unless I still need the TAMIFLU, I should stop it, this could have caused those symptoms. I still have a cough and nasal congestion and have been tired since then. I have not completely recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- COVID, negative; Flu B negative; Flu A positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Prediabetes
- Andere Medikamente
- Metformin HCL; probenecid; men's multivitamin; acetaminophen
- Allergien
- VICODIN; alopurinol
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Paraesthesia oral
Symptomtext
Employee began to c/o strange feeling on the R side of her tongue. She continued to report the feeling was spreading to the back of her tongue. Employee was immediately taken to ER by Employee Health Nurse
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- Employee was treated with medication as per protocol
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 29.11.2022
- Impfdatum
- 24.03.2021
- Beginn
- 31.03.2022
- Tage bis Beginn
- 372,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood testosterone decreased
Chest pain
Musculoskeletal pain
Symptomtext
When I received my first two covid shots in 2021, my testosterone levels dropped. After my testosterone dropped, I had to visit a urologist to receive medication to increase my natural levels of testosterone back to normal. The decreased levels of testosterone lasted me for around six months. I later developed a musculoskeletal soreness within my pictorial muscles. This pictorial injury has lasted me almost a year and I have gone to a general practitioner to receive anti-inflammatory medicine and muscle relaxers to heal my chest. But my chest pain still lingers almost a year later. This chest pain has been Amplified after I received my booster shot, which was the third covid shot in 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- My doctors have not been able to trace the effects of the covid shot oh, back to the shot themselves but, I did not develop these symptoms until I received the shots. These symptoms of dropped testosterone and pictorial chest pain developed Within three to four weeks after The first two shots (Mar & Apr 2021) and the third/last shot (Nov 2022).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 21.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain
Arthralgia
Back pain
Blood test
Chest X-ray
Chest pain
Chills
Dizziness
Headache
Palpitations
Phantom limb syndrome
Urine analysis
Symptomtext
Got vaccine on 11/21/2022 around 5:15pm woke the next morning with chest pain and random joint pain all over body, heart palpitations experienced chills; abdominal pain and lower back pain. Felt as though I was going to faint. Random phantom pain all over body and severe headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Blood test, urinalyses and chest x-ray
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- ortheocorralitis
- Andere Medikamente
- Multivitamin
- Allergien
- Gluten and ciproflaxin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 22.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Migraine
Myalgia
Symptomtext
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 female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Nov2022 at 17:30 as dose 4 (booster), single (Lot number: GJ3274) at the age of 49 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "migraines" (unspecified if ongoing), notes: 25 plus year history of migraine; "hypothyroidism" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "obesity" (unspecified if ongoing); "If covid prior vaccination: Yes" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE; LEVOTHYROXINE; RIZATRIPTAN; NURTEC ODT; IBUPROFEN; BOTOX. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 3 (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: FATIGUE (non-serious) with onset 16Nov2022 at 02:30, outcome "recovering"; MIGRAINE (non-serious) with onset 16Nov2022 at 02:30, outcome "recovering"; MYALGIA (non-serious) with onset 16Nov2022 at 02:30, outcome "recovering", described as "muscular pain at injection site". Therapeutic measures were taken as a result of migraine. Therapeutic measures were not taken as a result of myalgia, fatigue. Additional information: Patient had not received any vaccines within four weeks. Patient received the treatment with rizatriptan and neurotic for migraine nothing for fatigue or muscle pain. Patient had COVID-19 prior to vaccination. Patient had not been tested for COVID-19 post vaccination. The patient had no known allergies. Did does not result in physician office visit or emergency room visit.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Hypertension; Hypothyroidism; Migraine (25 plus year history of migraine); Obesity
- Andere Medikamente
- AMLODIPINE; LEVOTHYROXINE; RIZATRIPTAN; NURTEC ODT; IBUPROFEN; BOTOX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood urine present
Diarrhoea
Headache
Pyrexia
Tremor
Urine analysis abnormal
Vaginal discharge
Vaginal haemorrhage
Vomiting
Symptomtext
bad headache,fever 101.3, vomiting & diarrhea along with bodyshakes. But two days later my daughter wiped & something that she said looked like a grape skin & blood came from vagina.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Went to primary doctor on Nov.10th 2022. They did a urine test, said there was blood in her urine but not to worry.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Tylenol, birth control
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 10.11.2023
- Impfdatum
- 19.12.2022
- Beginn
- 24.08.2023
- Tage bis Beginn
- 248,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Echocardiogram abnormal
Fatigue
Hypokinesia
Magnetic resonance imaging heart
Troponin increased
Symptomtext
Discharge Provider: MD Primary Care Provider : DO Admission Date: 8/24/2023 Discharge Date: 8/27/2023 CONDITION ON DISCHARGE: Stable and improved. Admitted as an Inpatient HOSPITAL COURSE: Came with fatigue and was found to have covid. He did not have any oxygen requirement, but improved with nebs and steroids. He was found to have a troponin elevation to > 1000 and septal hypokinesis on echo. Cardiology recommended heparin drip for 48 hours, stabilization of covid, then transfer for Cardiac MRI. He was transferred on Sunday for MRI Monday. A further discharge summary will follow that admission. He Has DM2, CKD, BPH, HTN ,HLD, chronic back and neck pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 diabetes mellitus with stage 3a chronic kidney disease, without long-term current use of insulin BPH without obstruction/lower urinary tract symptoms Psoriasis Peripheral vascular disease Recurrent major depressive disorder, in full remission Iron deficiency anemia due to chronic blood loss LBBB (left bundle branch block) Coronary artery disease of native artery of native heart with stable angina pectoris Chronic bilateral low back pain without sciatica Hypertension associated with diabetes Dyslipidemia associated with type 2 diabetes mellitus Neck pain COVID Chronic kidney disease Carotid stenosis Postoperative hypotension Postoperative atrial fibrillation Respiratory failure, post-operative Ischemic cardiomyopathy Chronic combined systolic and diastolic heart failure
- Andere Medikamente
- acetaminophen (TYLENOL) 500 mg tablet amiodarone (PACERONE) 200 mg tablet aspirin 81 MG tablet blood glucose test strips cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet furosemide (LASIX) 20 mg tablet gabapentin (NEURONTIN) 300 mg caps
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 22.12.2022
- Beginn
- 24.03.2023
- Tage bis Beginn
- 92,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Angiogram
Asthenia
Body temperature
Computerised tomogram abdomen
COVID-19
Nasopharyngeal swab
SARS-CoV-2 test
Vaccination failure
Fatigue
Flank pain
Hydronephrosis
Ovarian cyst
Pyelonephritis
Pyrexia
Renal atrophy
Renal impairment
Renal scan
Symptomtext
test positive; test positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Dec2022 as dose 4 (booster), 0.3 ml single (Lot number: GJ3274) at the age of 36 years intramuscular, in left deltoid for covid-19 immunisation; bnt162b2 (BNT162B2), on 19Mar2021 as dose 1, 0.3 ml single (Lot number: ER2613), in left arm, on 09Apr2021 as dose 2, 0.3 ml single (Lot number: EW0158), in left deltoid and on 10Dec2021 as dose 3 (booster), 0.3 ml single (Lot number: FJ8757), in left deltoid, all intramuscular 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 24Mar2023, outcome "unknown" and all described as "test positive". The patient underwent the following laboratory tests and procedures: Nasopharyngeal swab: (24Mar2023) positive; SARS-CoV-2 test: (21Feb2022) Detected; (24Mar2023) positive.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202300135086 same patient/vaccine, different dose and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230324; Test Name: Cov19/COVID/NasopharyngealSwab (Swab); Test Result: Positive ; Test Date: 20220221; Test Name: Cov-19; Result Unstructured Data: Test Result:Detected; Test Date: 20230324; Test Name: Cov19/COVID/NasopharyngealSwab (Swab); Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 18.10.2023
- Impfdatum
- 14.10.2023
- Beginn
- 16.10.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Pyrexia
Symptomtext
Low grade fever continues five days after injection; skin is red in a rectangular shape diagonally from the injection site (site was upper left arm near the shoulder and the shape is down and on the inner arm towards the body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HIV+ (undetectable for 13 years)
- Andere Medikamente
- Biktarvy, valacyclovir, allopurinol, atorvastatin
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 29.09.2023
- Impfdatum
- 06.02.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Pain in extremity
Symptomtext
Interchange of vaccine products; Little soreness in upper arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Feb2023 as dose 4 (booster), single (Lot number: GJ3274) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure abnormal" (unspecified if ongoing), notes: Takes blood pressure medicine, takes a statin, has been taking now for a year, or 9 months. The patient took concomitant medications. Vaccination history included: janssen covid-19 vaccine (DOSE 1, SINGLE, Anatomical location: Left arm), administration date: 12May2021, for COVID-19 immunisation; janssen covid-19 vaccine (DOSE 2, SINGLE, Anatomical location: Left arm), administration date: 22Dec2021, for COVID-19 immunisation; bnt162b2 (DOSE 3 (BOOSTER), SINGLE, Batch/lot number: FP7138, Anatomical location: Left arm), administration date: 24Aug2022, for COVID-19 immunisation, reaction(s): "Interchange of vaccine products", "On 10Dec2022 she had an ischemic stroke that she described as mild and deep in the brain". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2023, outcome "recovered" (2023), described as "Little soreness in upper arm"; INTERCHANGE OF VACCINE PRODUCTS (non-serious), outcome "recovered". Additional information: This report was not related to a study or programme. Previously had one of the boosters, did not have much as much reaction, had a little soreness, nothing to speak of. Just had a little soreness in upper arm, which was fine. Had that before, did not think much of it. All COVID vaccines given in left arm. Is right-handed, would have likely had in left arm. Nothing changed before she took this, was all same stuff she had always been taking and supplements, stuff like that. Never had COVID, thank God. There was no Family Medical History Relevant to Adverse Events (AEs).; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300312069 same patient/vaccine, different dose and event;US-PFIZER INC-202300312075 different patient/vaccine, different dose and event;US-PFIZER INC-202300024576 same patient/vaccine, different dose and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure abnormal (Takes blood pressure medicine, takes a statin, has been taking now for a year, or 9 months.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.07.2023
- Impfdatum
- 28.06.2023
- Beginn
- 03.07.2023
- Tage bis Beginn
- 5,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Symptomtext
Circular area of induration and erythema surrounding injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No acute illnesses
- Vorgeschichte
- Chronic kidney disease, heart failure, anemia, DM II, gout, hypertension, and hyperlipidemia.
- Andere Medikamente
- Allopurinol, Aspirin, Biofreeze Gel, Coreg, Cranberry Tablet, Cyanocobalamin, Colace, Eliquis, Ferrous Sulfate, Gabapentin, Glipizide, Lactulose, Lodicaine Patch, Lasix, Lipitor, Magnesium Oxide, Metformin, Omeprazole, Potassium Chloride, R
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 13.12.2022
- Beginn
- 04.03.2023
- Tage bis Beginn
- 81,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Dizziness
Extra dose administered
Headache
SARS-CoV-2 test positive
Symptomtext
The patient was brought to the ED by EMS on 3/5/23 for evaluation of dizziness, generalized weakness, and a headache. A COVID-19 PCR test performed in the ED resulted positive. Ultimately he was admitted 3/4/23 - 3/7/23. Discharge diagnoses included COVID-19 infection. Of note, the patient has received the primary COVID vaccine series and three boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 30.05.2023
- Impfdatum
- 27.11.2022
- Beginn
- 16.05.2023
- Tage bis Beginn
- 170,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaemia
Blood test abnormal
Dizziness
Symptomtext
She started feeling lightheaded and dizzy, we were at the doctor's office already for a visit. They did bloodwork at that time; it did come back showing that she was anemic. She was prescribed liquid iron that we are giving her and tracking for six weeks, since she has absorption issues. If her body has not absorbed the iron as needed we will go forward with the transfusion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 16MAY2023 Bloodwork - positive for anemia
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Thyroid Disorder; Epilepsy; Factor 5 Leiden; Wolf Parkinson White
- Andere Medikamente
- Levothyroxine; Nature thyroid; Keppra; Pantoprazole; Xarelto; Vitamin D3; Vitamin B-12; Probiotic; Miralax
- Allergien
- Gluten Intolerance; Dairy Intolerance
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 26.05.2023
- Impfdatum
- 24.05.2023
- Beginn
- 25.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Erythema
Neck pain
Pain
Skin warm
Symptomtext
Resident began experiencing T100.2, decreased to 98.8 after tylenol, chills, body aches, increasing pain in both shoulder/nek and warm/red face.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Physician notified and orders received to provide comfort measures.
- Aktuelle Erkrankungen
- Pyelonephritis
- Vorgeschichte
- chronic kidney disease, macular degeneration, edema, hemiplegia, hypertension, retention of urine, obstructive sleep apnea, GERD, hyperlipidemia, cerebral infarction, incontinence, opioid dependence, depression, anxiety, BPH, polyneuropathy, dysphagia.
- Andere Medikamente
- Gabapentin, finasteride, floraster, simethicone, naloxone, ferrous sulfate, amlodipine, doxazosin, guaifenesin, omeprazole, clopidogrel, losartan, duloxetine, lipitor, docusate sodium, oxycodone, diazepam, sennosides, loperamide, tizanidine
- Allergien
- Tetanus toxoids
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 25.05.2023
- Impfdatum
- 29.11.2022
- Beginn
- 14.03.2023
- Tage bis Beginn
- 105,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy bone marrow
Blood test abnormal
Computerised tomogram
Contusion
Immune thrombocytopenia
Immunoglobulin therapy
Platelet count decreased
Platelet transfusion
Pyrexia
Transfusion
X-ray
Symptomtext
On March 14, 2023 after a doctor's visit about his bruising, blood lab test shows very low platelets. Advised to go to ER and from there got admitted to hospital and was diagnosed with Immune thrombocytopenia (ITP). Prior to this, he had several big bruising on his leg and body that might have span 3-5 weeks. This led to the visit to doctor and blood test on March 14, 2023. While at hospital, he did some testing including scans, xray, and bone marrow biopsy and received infusion of IVIG and Platelets as well as steroids. The steroids medication continued as out patient for the next 2 weeks or so where his platelets did not show increase count. He then went to next treatment of Rituximab infusion for the next 4 weeks and he recently completed this also not showing a good increase in his platelets. During above treatment, he did blood transfusion a couple of times and another round of platelets transfusion. Most recently, he got admitted to ER again then in hospital due to fever and possible infection where he received another blood transfusion and infusion of IVIG and platelets. This week, he started on the next viable treatment of Promacta medication
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- 6,0
- Labordaten
- March 14, 2023 - Blood tests March 15-16, 2023 - CT scan, xray, bone marrow biopsy + more blood tests More and continuous blood tests until present
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Before (none) After (ITP)
- Andere Medikamente
- Nature?s Way Sambucus Elderberry Gummies, Immune Support Gummies*, Black Elderberry with Vitamin C, Vitamin D and Zinc Kirkland Signature Calcium 500 mg with D3 & Zinc
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 25.05.2023
- Impfdatum
- 02.11.2022
- Beginn
- 09.05.2023
- Tage bis Beginn
- 188,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
COVID-19
Chills
Cough
SARS-CoV-2 test positive
Symptomtext
On 08MAY2023 I had chills and a minor cough. My temperatre was one hundres point four. The next morning 09MAY2023 I tested positive for the COVID-19 virus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 09MAY2023 COVID-19 Test-Positve.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prooxitane; Atorvastatin; Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 19.05.2023
- Impfdatum
- 12.11.2022
- Beginn
- 18.05.2023
- Tage bis Beginn
- 187,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
No adverse event
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 on 05/18/2023. I have a runny nose, cough and fatigue. I contacted my doctor and got a prescription for Paxlovid. I have taken two doses and so far, I am tolerating the medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 18MAY2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 10.11.2022
- Beginn
- 24.04.2023
- Tage bis Beginn
- 165,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Fatigue
Headache
Loss of personal independence in daily activities
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
4/24/23 I woke up with a sore throat and fatigue. Throughout the day it progressed to congestion, cough and a headache. I took an at home COVID test which was positive. The next night I began to have a fever of up to 100.4. I had chills, fatigue, body aches and cough. I messaged my doctor and he prescribed PAXLOVID which I began taking the next day. I took the PAXLOVID for the full five days. After the second day I began feeling better and the symptoms were better. I have continued to have persistent fatigue. I am unable to do most of my daily activities, including running which is what I do.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 24APR23 at home COVID test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- Multivitamin with calcium and vitamin D; vitamin B2; magnesium; coQ10; baby aspirin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 28.04.2023
- Impfdatum
- 15.12.2022
- Beginn
- 03.01.2023
- Tage bis Beginn
- 19,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye swelling
Nasopharyngitis
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test negative
Visual impairment
Symptomtext
Approximately 2-3 weeks after receiving the vaccine, I developed cold like symptoms (sore throat & congestion). I also developed some swelling around my right eye which was affecting my vision (this was the primary reason for going to the doctor). I performed an at-home COVID test which was negative prior to visiting the doctor. At the doctors office the doctor checked for Bell's Palsy (negative) and then prescribed an injection (Dexmethoson Sodim Phoshate 1 Mg) and antibiotics. All symptoms cleared up within a few days of the visit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cold symptoms - Sore throat/coughing/congestion (negative at COVID test) - approximately 2 weeks prior to vaccination
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 28.04.2023
- Impfdatum
- 27.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear discomfort
Ear pruritus
Nasal congestion
Otorrhoea
Symptomtext
I woke up the day after getting the vaccine noticing that my sinuses were a little stuffy. I was thinking it may be the unseasonable weather, so I didn't pay much attention to it. The next day when I got up my sinuses were not only stuffy, but my ears were also stuffy, itchy, running. I made an appointment to go to the doctor. She felt that it may just be allergies, she gave me a prescription for Singulair. I also made an appointment with an ENT to ensure that I did not have anything blocking my ear canal. He did not see anything in my ear and gave me steroid ear drops. Both the Singulair and steroid ear drops have helped to remedy the my stuffiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pruritus
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Rheumatoid Arthritis; GERD; Dry Eye
- Andere Medikamente
- Methotrexate; Metoprolol: Losartan; Caltrate: Restasis; Nexium; Folic Acid; Gabapentin; Tramadol; Xanax as needed; Low Dose Aspirin as needed
- Allergien
- Macrobid; Lipitor
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 30.11.2022
- Beginn
- 25.02.2023
- Tage bis Beginn
- 87,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Bronchitis
COVID-19
Chest X-ray abnormal
Cough
Eye discharge
Eye swelling
Feeling abnormal
Foreign travel
Gait inability
Hypersomnia
Impaired work ability
Lacrimation increased
Lethargy
Lip swelling
Oropharyngeal pain
SARS-CoV-2 test positive
Sinusitis
Symptomtext
The evening 02/25/2023, I was having lethargy, my throat hurt and I was coughing. I took a COVID-19 Home Test, and the result was positive immediately. I went to the clinic, and they tested me again and the result was positive. I quarantined from 02/25/2023 - 03/02/2023, the day we finished the trip. The night of 02/28/2023, my eyes were like tearing, I got Kleenex to wipe my right eye and there was a pale green of gunk on it and on the other eye there were yellow gunk coming out of my eyes. It was thick gunk. All of a sudden my eyes started draining and at the same time the lower part of my face, underneath my nose, my lips was swollen and it swelled up like a balloon right in front of my eyes. I went to the clinic and the doctor prescribed me an antibiotics and 2 IV's. IV Cetirizine and IV Loratadine. The doctor told me it was a reaction to COVID-19. The next day my eyes were no longer swollen and there wasn't more green and yellow gunk coming out. I recovered. I see well now. My eyes don't bother me. When I returned back to from the trip, I was so weak and could not walk. My doctor, on 03/09/2023, diagnosed me with bronchitis and sinusitis and she prescribed antibiotics, and an inhaler, Albuterol. I lost 10 pounds and was wiped out for the whole month of March 2023 and mostly slept, I had a cough. I laid low most of April and returned to work for the first time on 04/24/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 25FEB2023 - COVID-19 - Positive; 25FEB2023 - COVID-19 Nasal Swab - Detected; 08MAR2023 - Lung X-rays - Bronchitis
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Low Thyroid
- Andere Medikamente
- Estradiol; Amlodipine; Lisinopril Hydrochlorothiazide; Lisinopril; Venlafaxine; Calcium D3; Centrum Silver for Women Over 50; Biotin
- Allergien
- IV Scopolamine
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 24.04.2023
- Impfdatum
- 20.01.2023
- Beginn
- 22.01.2023
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Decreased appetite
Headache
Impaired work ability
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I got a severe headache and began to ache all over my body. I just wanted to be in bed. The next day still had headaches, chills, aching all over. I had no appetite. I developed a fever on 01/22/2023 in the evening. I tested myself on 01/23/2023. My O2 stats never got below 92. I could not think while I was at work. I have recovered from my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 23JAN COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Amlodipine; vitamin D
- Allergien
- Prednisone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 10.04.2023
- Impfdatum
- 12.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Headache
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
On December 16, 2022, I had a sore throat and fever. It developed into severe body aches and headache. I called the doctor and had a video chat. He listened to my symptoms and prescribed Paxlovid. I did not take it because by Sunday I began to feel better. By the following Tuesday the body aches were mostly gone, and my sore throat was better. The rest of the week I was feeling mostly weak and had low energy. I continued to test positive until December 23, 2022. By that following weekend I was feeling normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 home, positive,12162022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes Type 2
- Andere Medikamente
- Atorvastatin; Gradience; Metformin; Valsartan; Metoprolol
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 07.04.2023
- Impfdatum
- 14.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Inflammation
Pain in extremity
Symptomtext
PATIENT STATED TODAY THAT SHE WANTED TO REPORT ADVERSE EVENT TO PHARMACY THAT HER COVID SHOT IN THE LEFT ARM WAS RED PAINFUL AND INFLAMMED AND HER RIGHT ARE WAS SAME REACTION JUST NOT AS SEVERE AS THE LEFT ARM. PT DID NOT CALL THE PHARMACY AND OR CALL HER DOCTOR AND THAT IT FINALLY HEALED UP AFTER ABOUT 3 WEEKS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 03.01.2023
- Beginn
- 29.03.2023
- Tage bis Beginn
- 85,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Dysphagia
Neck pain
Oropharyngeal pain
Platelet count decreased
Throat tightness
Thyroid mass
Ultrasound thyroid abnormal
Symptomtext
3/29/23 I noticed difficulty swallowing and a pain in my neck and throat. I was seen yesterday in the Emergency Room because I am having more trouble swallowing. I have pain in neck and tightness in my throat. I had an ultra sound on 4/4/23 and nodules on my thyroid were found. I have a follow up, uncertain of date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- 4APR23-Bloodwork-Platelets low, everything else was normal; 4APR23-Ultrasound- Nodules on Thyroid
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Factor 5 Leiden
- Andere Medikamente
- Prenatal Vitamin, Iron
- Allergien
- Demerol, Fentanyl, Cefprozil, Benadryl
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.03.2023
- Impfdatum
- 06.12.2022
- Beginn
- 22.02.2023
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysphagia
Fluid intake reduced
Hypophagia
Oropharyngeal pain
Symptomtext
I had difficulty swallowing with significant pain in my throat so I really could not eat or drink. I was already taking ibuprofen 800 and gargling. I went to the doctor on February 27th and was prescribed antibiotic AUGMENTIN 875 for a week. Once I started the medication it has taken the full 7 days to feel better. I am still recovering as it still does not feel normal yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Acetaminophen; azithromycin; beef; chicken; wheat; milk; eggs; soy; nuts; fish; seafood
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.03.2023
- Impfdatum
- 01.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Injection site pain
Pyrexia
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fever-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Limb injury
Symptomtext
Site: Pain at Injection Site-Medium, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 12.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Arthritis
Blood test normal
Joint stiffness
Joint swelling
Pain in extremity
Scan normal
X-ray limb normal
Symptomtext
Development of Arthritic Conditions: Bilateral pain in both heels beginning 1/17/23 (no injury prior to pain). Pain worsened 1/20/23 and continued to worsen every day and moved to ankles/feet. Extreme swelling occurred in both ankles. Saw a podiatrist on 1/24/2023 - had xrays and bone scans of both feet/ankles - both negative. Saw podiatrist again on 1/31/2023 - ordered blood work to check for arthritic conditions/rheumatoid arthritis. Pain/joint stiffness developed in knees, wrists, and elbows beginning 2/2/2023. Started Medrol Dosepak treatment on Friday 2/3/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 1/24/2023 - X-Ray - Negative 1/30/2023 - Dexascan - Negative 2/1/2023 - Blood work - Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tri-Sprintec (Birth Control)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 04.02.2023
- Impfdatum
- 25.01.2023
- Beginn
- 01.01.2023
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast pain
Discomfort
Pain
Symptomtext
She has pain under her arm pit into her breast area/it was a sharp pain, extremely painful/from where the lymph nodes are into the side of the breast; She has pain under her arm pit into her breast area/it was a sharp pain, extremely painful/from where the lymph nodes are into the side of the breast; It is very uncomfortable; it was a sharp pain, extremely 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 55-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 25Jan2023 as dose 3 (booster), single (Lot number: GJ3274) at the age of 55 years for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure high" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE taken for hypertension. Vaccination history included: Covid-19 vaccine (Dose 1, Manufacturer: Unknown), for COVID-19 immunization; Covid-19 vaccine (Dose 2, Manufacturer: Unknown), for COVID-19 immunization. The following information was reported: DISCOMFORT (non-serious) with onset Jan2023, outcome "not recovered", described as "It is very uncomfortable"; AXILLARY PAIN (non-serious), BREAST PAIN (non-serious) all with onset Jan2023, outcome "not recovered" and all described as "She has pain under her arm pit into her breast area/it was a sharp pain, extremely painful/from where the lymph nodes are into the side of the breast"; PAIN (non-serious) with onset Jan2023, outcome "not recovered", described as "it was a sharp pain, extremely painful". Therapeutic measures were taken as a result of axillary pain, breast pain, discomfort, pain. Additional Information: Patient did not take any medication Prior vaccination (Within 4 weeks). Caller stated she received her 3rd booster of the Pfizer covid 19 vaccine on Wednesday. she received the bivalent vaccine. she had pain under her arm pit into her breast area. It was a sharp pain, extremely painful. It was very uncomfortable. It was from where the lymph nodes are into the side of the breast. The area was sore and the pain was on the same side as the shot. She cannot lift her arm. Caller asked why it is going into the breast area. she took Tylenol, Motrin 800 mg and applied ice. The iced soothed it. When she removed the ice, the pain goes back to the pain level. she did not have any side effects with the other vaccines. Caller asked should she go to the ER. Caller wanted to know what she can do. Caller said it has lasted for two days. Caller asked what does reporting to Safety do. When paraphrased the concern: Consumer stated, "No, what I told her was that underneath my arm and all the way into the side of my breast was extremely painful I was taking Tylenol doesn't help, and the next I was taking Motrin 800 and I have to keep ice on it when I remove the ice, it just I can't lower the ice on my breast but you know I like I told the lady is just a you know how like when you get the mammogram and they squeeze your breast that's the that pain I am experiencing constantly and the first day it was like on a scale 1-10 it was like a 8 and today it was 10 and I called the pharmacy and the Pharmacist said I need to report it."Vaccine name: Consumer stated, "Its the bivalent, the third booster, Tylenol and Motrin is not helping me, I can't lift my arm."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high
- Andere Medikamente
- AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 26.01.2023
- Beginn
- 31.01.2023
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Nausea
Pain
Rash
Symptomtext
1/31/23 started with headache, nausea, body aches 2/1 full body rash took benadryl 2/1 rash still present will continue antihistamine treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure asthma
- Andere Medikamente
- olmesartan
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 28.01.2023
- Impfdatum
- 05.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- 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
- NC
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immunisation reaction
Periorbital swelling
Urticaria
Symptomtext
Pt reported that approximately 2 days after receiving dose, she experience periorbital swelling and hives. She reports that she consulted with her PCP and Dermatologist who diagnosed her with a post vaccination reaction and started oral prednisone and topical cream. Pt reports that her symptoms are almost resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 10.01.2023
- Beginn
- 10.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Rash macular
Visual field defect
Symptomtext
Left side peripheral vision become wavy and spotted over with light blotches. Happened the night of the injection so far. Lost sense of taste in eating food for 5 days after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic Bronchiecstasis; Hospitalized for unknown COPD exacerbations , then given vaccine upon discharge.
- Vorgeschichte
- Skin allergy/ rash when very young.
- Andere Medikamente
- Escitalopram, Amlodipine Besylate, Folic Acid, Atorvastatin Calcium, Vitamin D, Azithromycin, Albuterol Sulfate, Anoro Ellipta, Combivent, Docusate sod, Simethicone Chew, Tamsulosin.
- Allergien
- Bananas, Walnuts, peanuts, chocolate.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 14.01.2023
- Impfdatum
- 11.01.2023
- Beginn
- 11.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Chills
Gait disturbance
Insomnia
Myalgia
Symptomtext
Patient described chills, back aches, muscle aches, and shoulder pain that caused a lack of sleep and trouble walking. These effects started at 8:00PM the night of receiving the vaccination (1/11/23). She took Tylenol, which helped all side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Eliquis 2.5mg, Hydrocortisone 5mg tablet, Metropolol Tartrate 50 mg Tablet
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 03.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Symptomtext
Severe fatigue starting 6 pm and lasting 48 hours Headache moderate, took 400 mg ibuprofen lasted 36 hrs, started 6 pm Chills started 6 pm, lasted 36 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Arthroscopy right knee on 12-23-2022
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Triameterene, HCTZ, Singulair, X-Hance, glucosamine, calcium, 320 mg ASA, Tylenol/codeine
- Allergien
- Dilaudid - urticaria
- Vorherige Impfungen
- Fatigue
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 02.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Pain
Pyrexia
Symptomtext
Between 1-2 days after receiving the vaccination, the patient experienced fever, aches, headaches, and fatigue. Tylenol was taken to relieve symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 02.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Fatigue
Headache
Pain
Pyrexia
Symptomtext
Pt called on 1/6/23 around 10am saying he experienced fever,aches,headache,cough,fatigue 1-2 days after getting the shots. Side effects ressolved but he still have fatugue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.01.2023
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain lower
COVID-19
Nitrite urine absent
Pollakiuria
Urine leukocyte esterase positive
Symptomtext
Frequent urination with lower abdominal pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- Over the counter UTI test is positive for leukocytes, negative for nitrites.
- Aktuelle Erkrankungen
- COVID-19 - 12/06/2022
- Vorgeschichte
- Irritable Bowel Syndrome with Diarrhea Depression Anxiety Endometriosis
- Andere Medikamente
- Fluvoxamine 100mg, Buspirone 10mg, Colestid 1G, Vitamin B12, Vitamin D3, Uquora Probiotic, Turmeric
- Allergien
- Artificial sweeteners
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 08.01.2023
- Impfdatum
- 12.12.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Injection site pain
Pain
Pain in extremity
Symptomtext
Site: Pain at Injection Site-Severe, Systemic: Joint Pain-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Additional Details: radiating pain/numbness in arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 05.12.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 21,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Headache
Myalgia
Nausea
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Congestion, fever, chills, muscle/body aches, headaches, severe nausea, cough, runny nose, sore throat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- POSITIVE Covid test 12/27/22
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Psoriasis, Migraines, Depression, Generalized anxiety, S/P laparoscopic sleeve gastrectomy, anemia, immunodeficiency due to drugs, GERD
- Andere Medikamente
- Humira 40 mg/0.4 mL (every two weeks), Junel Fe (birth control - daily), Vyepti 300 mg (IV infusion every 3 months), Magnesium 100 mg (twice daily), Topamax 50 mg (twice daily), Nadolol 20 mg (daily), Amitriptyline 10 mg at bedtime (as need
- Allergien
- Sulfa, Omnicef, Lamictal, Prednisone, Amoxicillin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 06.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Site: Pain at Injection Site-Severe, Additional Details: Came in and explained that his arm was sore and he was in severe pain, He was going to visit his doctor to seek treatment for the pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 04.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site pain
Limb injury
Nausea
Pain
Pain in extremity
Symptomtext
patient stated had pain immediately upon injection (not abnormal amount, similar to other vaccines), arm started out sore like after other vaccines, but later that night pain continued to spread down to the elbow. since that day has had pain in the muscle from shoulder to elbow. also reported at one point in the last month he hit his hand and felt intense pain shoot up his arm so painful he felt sick to his stomach. has an appointment with his PCP january 10 for follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 22.12.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Fatigue
Musculoskeletal stiffness
Nausea
Neck pain
Pain
Pyrexia
Symptomtext
About 20-22 hrs after booster, neck and shoulder of the same side as shot became so stiff and sore I could not straighten my head without excruciating pain accompanied by severe nausea. This lasted until the following afternoon of 12/23. Ran fever and had chills as well as very fatigued through 12/25.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- MC/CFS, ADHD, hidradenitis suppurativa, eczema, migraines
- Andere Medikamente
- Adderall, minocycline, aleve, elderberry, vitamin C, vitamin D/K2 , calcium, cranberry, magnesium/potassium, Zyrtec, Benadryl, turmeric/ginger
- Allergien
- Sulfa drugs, wheat, coconut, beef, apples, pollen, mold
- Vorherige Impfungen
- Severe joint pain with Moderna 3rd dose given in 11/2021. Age37.
- Staat
- VA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 24.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Panic reaction
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Additional Details: pt felt lightheaded after vaccinations, then panicked, emergency personnel checked her out, all was normal, pt felt better and left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 20.11.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 25,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Headache
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Toothache
Symptomtext
I woke up with a fever of over 100. I had a cough, very sore throat, really bad headache and chills during the day. My teeth were also hurting. When I called the nurse, she asked me if I had any chronic conditions or anything. I don't have anything so she said I wouldn't qualify for any oral treatments. I used ibuprofen and TYLENOL at home. I'm still testing positive today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 12/16/2022 at home COVID-19 test positive; 12/17/2022 at home COVID-19 test positive; 12/21/2022 at home COVID-19 test positive; 12/22/2022 at home COVID-19 test positive; 12/23/2022 at home COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression; Seasonal allergies
- Andere Medikamente
- Estradiol patch; progesterone capsule; trazadone; PROZAC; hair supplements
- Allergien
- Penicillin; ZITHROMAX
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Neck pain
Off label use
Pain in extremity
Product use issue
Rash erythematous
Vaccination site pain
Symptomtext
Patient got a rash on the injection point of his arm which moved down his arm with painful red bumps./He noticed the rash after pain started in his arm; Swollen lymphnodes; sore neck; Patient got a rash on the injection point of his arm which moved down his arm with painful red bumps; Patient got a rash on the injection point of his arm which moved down his arm with painful red bumps.; Location of injection for vaccine received same date: Flu shot - left arm; Location of injection for vaccine received same date: Flu shot - left arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 16-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Nov2022 as dose 4 (booster), single (Lot number: GJ3274) at the age of 16 years, in left arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 21Nov2022 as dose 1, single (Batch/Lot number: unknown), in left arm. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: FL3209, Location of injection: Arm Left), administration date: 10Jan2022, when the patient was 15-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EW0178, Location of injection: Arm Left), administration date: 03Jun2021, when the patient was 15-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EW0168, Location of injection: Arm Left), administration date: 13May2021, when the patient was 14-year-old, for COVID-19 immunization. The following information was reported: PRODUCT USE ISSUE (non-serious), OFF LABEL USE (non-serious) all with onset 21Nov2022, outcome "unknown" and all described as "Location of injection for vaccine received same date: Flu shot - left arm"; VACCINATION SITE PAIN (non-serious) with onset 05Dec2022, outcome "recovering", described as "Patient got a rash on the injection point of his arm which moved down his arm with painful red bumps"; RASH ERYTHEMATOUS (non-serious) with onset 05Dec2022, outcome "recovering", described as "Patient got a rash on the injection point of his arm which moved down his arm with painful red bumps."; PAIN IN EXTREMITY (non-serious) with onset 05Dec2022, outcome "recovering", described as "Patient got a rash on the injection point of his arm which moved down his arm with painful red bumps./He noticed the rash after pain started in his arm"; LYMPHADENOPATHY (non-serious) with onset 05Dec2022, outcome "recovering", described as "Swollen lymphnodes"; NECK PAIN (non-serious) with onset 05Dec2022, outcome "recovering", described as "sore neck". The events "patient got a rash on the injection point of his arm which moved down his arm with painful red bumps./he noticed the rash after pain started in his arm", "swollen lymphnodes", "sore neck", "patient got a rash on the injection point of his arm which moved down his arm with painful red bumps" and "patient got a rash on the injection point of his arm which moved down his arm with painful red bumps." required physician office visit. Therapeutic measures were taken as a result of pain in extremity, lymphadenopathy, neck pain, vaccination site pain, rash erythematous. Additional information: Patient got a rash on the injection point of his arm which moved down his arm with painful red bumps. He also had swollen nymphonids which is creating a sore neck. He noticed the rash after pain started in his arm and is not sure how long the rash existed before the pain. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not receive any other medications within 2 weeks of vaccination. Treatment received for the adverse event: Steroid cream. 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
- Neck 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
- NY
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 22.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Eye movement disorder
Symptomtext
Nurse entered room to vaccinate patient with COVID Pfizer Bivalent Booster, Menquadfi, and Fluzone. Patient stated that last year after receiving her flu vaccine she passed out. Nurse asked patient if she had anything to eat/drink prior to visit and patient stated she had. Nurse gave patient flu and menquadfi in left arm. Patient was feeling ok and nurse then gave COVID into the right arm, as needle was being capped patient stated "I am feeling woozy". Patient's eyes rolled in back of head, nurse laid bed down and raised her legs. Patient was given apple juice and a snack. Patient left office 20 minutes after event occured.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none.
- Aktuelle Erkrankungen
- idiopathic arthritis, asthma, gerd, migraine
- Vorgeschichte
- -
- Andere Medikamente
- methotrexate, folic acid, vitamin d3
- Allergien
- amoxil, cefzil
- Vorherige Impfungen
- Patient has previously passed out after receiving a flu vaccination.
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Dyspepsia
Headache
Heart rate irregular
Pain
Product administered to patient of inappropriate age
Pyrexia
Product preparation issue
Symptomtext
body aches; Diarrhea; Heartburn; Chills; Fever; Headache; received the Pfizer bivalent vaccine orange top, supposed to be for 5 to 11 year old's and was not diluted; heart was beating weird; 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 61-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Dec2022 as dose 5 (orange cap; booster), 30 ug single (Lot number: GJ3274) at the age of 61 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (1st dose:, Regular Pfizer vaccine, caller not sure what specific name for the vaccine., Date: 30Jun2021, NDC number, lot number, expiration date: EN6205), administration date: 30Jun2021, when the patient was 60-year-old, for COVID-19 immunization; BNT162b2 (2nd dose:, Regular Pfizer vaccine, caller not sure what specific name for the vaccine., Date: 31Jul2021, NDC number, lot number, expiration date: EW0150), administration date: 31Jul2021, when the patient was 60-year-old, for COVID-19 immunization; BNT162b2 (3rd dose:, Regular Pfizer vaccine, caller not sure what specific name for the vaccine., Date: 02Dec2021, NDC number, lot number, expiration date: FG3527), administration date: 02Dec2021, when the patient was 60-year-old, for COVID-19 immunization; BNT162b2 (4th dose:, Regular Pfizer vaccine, caller not sure what specific name for the vaccine., Date: 09Jun2022, NDC number, lot number, expiration date: FM9992), administration date: 09Jun2022, when the patient was 61-year-old, for COVID-19 immunization. The following information was reported: HEART RATE IRREGULAR (non-serious) with onset 10Dec2022, outcome "unknown", described as "heart was beating weird"; PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 10Dec2022, outcome "unknown", described as "received the Pfizer bivalent vaccine orange top, supposed to be for 5 to 11 year old's and was not diluted"; CHILLS (non-serious) with onset 11Dec2022 at 02:45, outcome "recovered" (12Dec2022); PYREXIA (non-serious) with onset 11Dec2022 at 02:45, outcome "recovering", described as "Fever"; HEADACHE (non-serious) with onset 11Dec2022 at 02:45, outcome "recovering"; DYSPEPSIA (non-serious) with onset 11Dec2022 at 02:45, outcome "unknown", described as "Heartburn"; DIARRHOEA (non-serious) with onset 12Dec2022, outcome "unknown", described as "Diarrhea"; PAIN (non-serious), outcome "unknown", described as "body aches". Therapeutic measures were taken as a result of headache. Additional information: Calling about the Pfizer bivalent vaccine, caller got the vaccine on Saturday and after caller got the vaccine, which was caller's 5th one in the series, the last one, heart was beating weird, has a fitness tracker, didn't feel anything, but had a FitBit on and heart was going up and down. Then had heartburn and then went to sleep and woke up around 2 in the morning with chills, 100 degree fever, and headache Saturday. Had no adverse reactions to any of the other doses. Fever is down, still has headache but headache is a little better. What happened was the pharmacist who gave the shot called and told caller that pharmacist made a mistake and gave caller the vaccine from the orange top vial, that is supposed to be for children and is supposed to be diluted but pharmacist didn't dilute the vaccine, gave caller the full strength and did not dilute, gave caller 30mcg which was the proper amount. Never got a reaction from the prior vaccines. Received the Pfizer bivalent vaccine orange top on 10Dec2022, about 12 noon got the shot. Supposed to be for 5 to 11 year old's and was not diluted and is supposed to be diluted. Did have some diarrhea also. On 10Dec2022, immediately after came home from getting vaccine noticed heart rate going up and down. Stop date of adverse event: Unknown, has not noticed if ongoing, has not noticed, was making caller nervous and caller was not feeling anything. Then at 2:45AM in morning on 11Dec2022, got chills, fever, headache, and heartburn. Still has fever and headache. Chills: Stop date of adverse event: 12Dec2022, as of now does not have chills, has not had again. Fever: Stop date of adverse event: Seems to be gone right now, seems to have been gone. Headache: Has lingering headache still. Outcome of event: Thinks improved, on and off and has been taking Tylenol but took Tylenol last at 11 o'clock in morning so Tylenol ran out because last time caller took the Tylenol was at 11 o'clock, if shakes head feels like has headache. Diarrhea: Start date of adverse event: Just got today, does not remember if occurred before. Stop date of adverse event: Was really 1 loose movement a couple of hours ago. Not that hungry, was not eating much because of fever. Products: Confirmed this, Pfizer bivalent vaccine orange top, was caller's 5th total dose. Confirmed all 4 prior doses caller had were the regular Pfizer vaccine, caller not sure what specific name for the vaccine for 4 prior doses, isn't there just one? Hard to read vaccination card. 5th dose: Pfizer bivalent vaccine orange top, Date: 10Dec2022, Dose amount, route: Thinks 30mcg. Indication: Just wanted to take the vaccine. Consumer stated, "I had called before because, I start from the end then I will go back I got my Pfizer Bivalent vaccine (Clarified as Pfizer COVID-19 vaccine) this Saturday and I just got a call from the pharmacist and the pharmacist said to me he made mistake he gave me the vaccine from the orange cap vial instead of the grey cap vial and he gave it to me undiluted 30 micrograms or something like that and he claims that is the same as he has given it to me from the grey vial the adult Vial I just want to say that this is the Fifth vaccine I had first four had no side effects at all this one as soon as I got the vaccine (Pfizer COVID-19 vaccine) I do not know my heart was jumping up and down my question is this if the two vials are the same the orange and the grey but you have to dilute the grey one I mean the orange one why because it come into two colored Vials if they both exactly the same thing but you have to dilute one of them why is it two colors caps if they are exactly the same?" Consumer was informed about the role of Pfizer drug safety. Caller stated she called yesterday but she's been thinking about something else, so she wanted to follow up. She went in to get a dose of the Pfizer Bivalent vaccine and her pharmacist called and said "he accidentally gave me, took the orange cap vial, which is the kids vial, and he gave me that dose, but he did not dilute it. And he claims that he's pretty sure that it's the same dose as the adult dose because the adult dose does not have to be diluted and the kids' dose has to be diluted. So, I was just thinking about that. I was just thinking about the concentration of the solution and why would there be an orange vial and a gray vial if they're both exactly the same thing except one has to be diluted? Like I'm just wondering the concentrations are exactly the same prior to dilution." "I know one technically would have to be diluted because kids are supposed to get less but what I'm saying is why can't they just take the gray vial and dilute it for kids If its the same exact thing? Why do they need two colored vials? I just want to make sure I got the right amount. That I didn't get too much or too little." Caller confirmed she received the orange top bivalent as her booster instead of the gray cap bivalent."And I had a lot of side effects this time that I did not have the last time or any of the other times." "Because I just thought it was weird that I've had 4 prior vaccines and I had absolutely no side effects and this time I had very bad side effects. I had it Saturday and I still have a headache. And I had fever and chills so I thought that was odd. And body aches." Caller and her husband received the bivalent orange cap COVID-19 vaccine undiluted by mistake instead of receiving the gray cap vaccine on Saturday. They received 0.3 (didn't specify if this was in mL or mcg), their pharmacist indicated that this administration is equivalent (receiving the orange cap dose undiluted vs receiving the gray cap dose diluted). No additional details were asked since near the end of the call she mentioned to be an attorney and said that she "didn't want to have to sue Pfizer". Her husband was also on the line with her.
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: Other Conditions: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 17.12.2022
- Impfdatum
- 14.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Injection site erythema
Injection site mass
Injection site pain
Injection site swelling
Lymphadenopathy
Malaise
Peripheral swelling
Skin tightness
Symptomtext
General feeling of tiredness / sickness / weakness for 3 days. Swelling in the left arm , swelling in left lymph node under the armpit, multiple red raised lumps on left arm from injection site down to the elbow with significant swelling and tightness with pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- Lupus, Rheumatoid Arthritis, Connective Tissue Disease
- Andere Medikamente
- none reported
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 17.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Additional Details: patient was lightheaded after receiving both vaccines. she said she has history of this happening to her, also afraid of vaccines. called 911, she was assessed and all was normal. patient felt better and left.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 16.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Vaccination site pain
Symptomtext
Injection site soreness; Body aches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Dec2022 at 17:30 as dose 4 (booster), single (Lot number: GJ3274) at the age of 39 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "congenital heart disease" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Aspirin, reaction(s): "Known allergies: aspirin"; Ibuprofen, reaction(s): "Known allergies: ibuprofen". Vaccination history included: Covid-19 vaccine (DOSE 1, SINGLE), for Covid-19 immunization; Covid-19 vaccine (DOSE 2, SINGLE), for Covid-19 immunization; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE), for Covid-19 immunization. The following information was reported: PAIN (non-serious) with onset 07Dec2022 at 09:00, outcome "recovered", described as "Body aches"; VACCINATION SITE PAIN (non-serious) with onset 07Dec2022 at 09:00, outcome "recovered", described as "Injection site soreness". Therapeutic measures were taken as a result of vaccination site pain, pain which included Tylenol. Additional information: The patient did not receive other vaccine in four weeks and other medications in two weeks. The patient did not had covid prior vaccination and not tested covid post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Heart disease congenital
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Skin warm
Swelling
Tenderness
Urticaria
Symptomtext
Patient received Prevnar 20 vaccination in left deltoid. Reported to pharmacy staff on 12/14/22 that on 12/13/22 he began experience a "red welt" on skin under arm near the axillary area that was tender, swollen and warm to the touch. Patients states that he has not taken anything or sought medical care for the adverse event, and that is has been stable over the last 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mood disorder, anxiety, seasonal allergies, arthritis, hypertension, hypothyroidism
- Andere Medikamente
- Xanax, Mobic, Norvasc, Singulair, mirtazapine, quetiapine, levothyroxine
- Allergien
- Keflex
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 14.12.2022
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Injection site erythema
Injection site mass
Injection site pruritus
Injection site swelling
Injection site warmth
Pyrexia
Symptomtext
The evening after receiving my fourth dose of Pfizer, I noticed that I was having some itching in my left deltoid at the injection site. I also noticed a lump around the size of a quarter. I went to bed and when I woke up the next morning, the area had doubled in size, was red, hot, and itchy. I was also running a low-grade fever of around 100.6. I was having headaches and tiredness as well. I stayed in bed taking 600 milligrams of ibuprofen every six hours as needed. I also applied ice packs to the injection site. The next day, the area continued to grow. I had outlined the area with a marker to monitor the size. I sought treatment that evening after work. I was prescribed 40 milligrams of prednisone for 7 days and clindamycin. The doctor advised that I only take the clindamycin if things got worse. As a nurse, I did not take the clindamycin because it is more of a site reaction than an infection. I continue to take the prednisone. The sight is only slightly warm now and the redness has gone down. It does still itch, however. I continue to apply ice to the sight and have switched to TYLENOL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Narcolepsy; Asthma; Obesity; Dermographism
- Andere Medikamente
- VYVANSE; multivitamin
- Allergien
- Sulfa; cefdinir; vancomycin; meloxicam; tramadol; COMPAZINE; succinylcholine
- Vorherige Impfungen
- 12/28/2021 Pfizer, rotating pain throughout body and in joints.
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 13.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Dizziness
Headache
Neuralgia
Symptomtext
On the second day of vaccination, I felt minor dizzy on the morning with a little bit headache, but the symptom disappeared in the afternoon. On the third and forth days after vaccination, I felt sore on both of my shoulders, especially on the right side, I can feel a nerve pulling from my shoulder to my rare side of my head causing headache occasionally, but the symptom disappeared after two and three days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 10.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pain in extremity
Symptomtext
Patient's Dad scheduled appointments on our app for Pfizer Covid Bivalent booster and Flu shots for both himself and patient. He chose the dropdown item indicating the adult (over 12 y/o) Pfizer Covid vac , ndc 59267-0304-02 which was really not intended for children under 12 y/o. The Pharmacist Rph did not notice the date of birth and administered the full adult 0.3ml dose to patient. We did not realize the error was made until we were catching up on the billing of the shots late Friday evening., I was informed by my RPH of the error at closing time around 7:00 PM Friday 12/9/2022. I notified my manager Saturday morning when I arrived at the pharmacy. I was directed to inform the patients dad and follow procedures. The Dad , returned my call on Saturday morning around 11:00 Am and informed me that patient was doing fine. His only complaint was of a sore arm. I explained to him the error and asked if he had any questions or concerns. I informed him of the potential for a greater chance of adverse reactions such as fatigue, aches, fever or flu-like symptoms. I asked the dad if he wanted me to contact his family physician to inform them of the event and he stated he would let them know instead. I plan to follow up with the Dad on Monday to check on patient's condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None at this time
- Aktuelle Erkrankungen
- No Known
- Vorgeschichte
- No Known
- Andere Medikamente
- No Known
- Allergien
- No Known
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 10.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Joint range of motion decreased
Pain in extremity
Symptomtext
UPPER ARM PAIN DEVELOPED IN THE MID-AFTERNOON, A FEW HOURS AFTER THE INJECTION, GOT WORSE OVER THE NEXT SEVERAL HOURS AND IS NOW STABLE/UNCHANGING. PATIENT STATES PAIN IS AT SITE OF INJECTION AND IS CURRENTLY LIMITING RANGE OF MOTION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ANXIETY
- Andere Medikamente
- IBUPROFEN 400 MG TO TREAT PAIN AT INJECTION SITE
- Allergien
- SULFAALAZINE
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 06.12.2022
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Dizziness
Fall
Fatigue
Headache
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Taste disorder
Symptomtext
In the same evening as the Pfizer booster, he starting feeling chills and slight headache, felt dizzy and fell down, was not injured by the fall. Symptom severity worsened the next day. Other symptoms reported include cough, sore throat, runny nose, impaired sense of taste, and fatigue. Went to urgent care on 12/1/2022 and tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- RT-PCR was positive for SARS-CoV2 with test performed 12/1/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Fatigue
Nausea
Vomiting
Symptomtext
I have had 3 moderna shots before this, last one 12/2/21. So I was not sure how to answer the dose questions. I started to feel nauseous around 5:30 pm on Saturday. I started throwing up around 8:30 pm and it continued until about 4:00 am. I threw up about 10 times, then diarrhea started and I was doing both at the same time. It really felt like food poisoning. But everything that I had eaten that day, was something that I had already had. (Opened box of hot pockets, etc.) Fever got up to 100. I was exhausted. Sunday throughout the day, I just stayed in bed, but I didn't throw up or poop anymore. I went to work Monday and felt great.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- No tests were taken.
- Aktuelle Erkrankungen
- Runny nose on the 18th.
- Vorgeschichte
- no
- Andere Medikamente
- buPROPion HCl ER (XL) 150mg x 3, , Excedrin migraine x 2,
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 29.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Breath sounds normal
Chest discomfort
Dizziness
Heart sounds normal
Symptomtext
Patient received both vaccines on 11/29/22. She reported feeling dizzy and feeling a funny sensation in chest within one minute of administration. Vital signs were checked and HR 96 RR 20 BP 162/90, Sp02 99%. Blood sugar was 147. Heart and lungs sounds were normal. After a few minutes patient felt chest symptoms were gone. Reported dizziness persisted, repeat BP were all about the same at 20-30 minutes after. Patient stated did not take her HTN medication that morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Patient chose not to go to urgent care or call physician office
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- T2DM Hypothyroid HTN Hyperlipidemia
- Andere Medikamente
- Trulicity Levothyroxine Atorvastatin Glipizide Losartan
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 04.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Inflammation
Influenza like illness
Injection site pain
Injection site pruritus
Swelling
Symptomtext
Flu like symptoms, large, inflamed red raised swelling. Itching and pain at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 20.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray normal
Cough
Malaise
Productive cough
Symptomtext
I had a cold weeks before my vaccination then I got better. A day after my vaccination I started to get sick again. I got the same phlegm in my throat and cough that got worst. I went into the doctor, and she sent me to get a chest X-ray which was clear. She prescribed me prednisone and FLONASE. It has been up and down I still have the cough today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Chest X-ray, clear, 11/22/2022
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Asthma; Hyperthyroid; Obesity
- Andere Medikamente
- PULMICORT Inhaler; XYZAL; propylthiouracil; vitamin D; calcium
- Allergien
- Azithromycin; TAPAZOLE; CEFTIN
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Additional Details: Pt felt lightheadness, fell slightly on ground (did not injury head).pt did not pass out/loss consciousness. pt rested with legs ups on chair for 15 mins. Ambulance came just in case to check on pt. vital signs were checked. Pt given ok from ambulance - pt stable.pt provided water and chocolate for energy. Pt started to feel better was monitored for 20 mins more then pt went home. follow up call was made later that day around 7p. Pt stated was feeling much better. No further issues. Pt healthy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Expired product administered
Feeling cold
Pain
Pyrexia
Symptomtext
Pt received expired dose of bivalent vaccine. Pt reports having cold chills, body aches, and a low grade fever for 24 hours post vaccine dose. Reports no vaccine site reaction. Pt also received flublok vaccine at the same visit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 26.11.2022
- Impfdatum
- 17.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 5,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Cardiac function test normal
Contusion
Haemorrhage subcutaneous
Injection site erythema
Injection site pain
Injection site warmth
Joint swelling
Peripheral swelling
Renal function test normal
Vein disorder
Symptomtext
Both feet, ankles & lower legs to the knee swelled, then within 5 days kept swelling more & more, to the point of blood spots on my shins, veins appearing & bruising on lower legs. Went to Immediate care on 11/25, all doctors' offices closed. They gave me an IV of 40 mg of Lasix, did blood work to check heart & kidney functions, all ok, the swelling is still just as bad, just slightly less swollen after 24 hours, everything else I could think of that could possibly cause this has been eliminated. There are no other reactions I have had to any meds or food, and nothing different has been done, eaten or had exposure to, for I am home most of the time. I have not had a cold since January 2005. Then I remembered I had the last booster for Covid, therefore I considered the possibility of a reaction to this booster, (had more than normal redness, heat & pain in my arm, area of injection, until the swelling of my feet & legs started. I have not had any reaction to the other vaccines & boosters. I cannot find anything relating to my symptoms, other than mostly respiratory, but it could be an issue with me!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- bloodwork on 11/25, results were good for functioning, no coreelation to swelling, no definitive answer other than "maybe" veins in legs getting weak! IV 40 mg Lasix administered 11/25, swelling not gone, but slightly deminished. Legs elevated. messaged, icing to help reduce swelling, but it has not....
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- AFIB, HIGH BLOOD PRESSURE, FIBROUS DISPLAYSIA, OSTEO ARTHRITIS (CHONDROCALCINOSIS), OVERWEIGHT 31 BPM,
- Andere Medikamente
- RX DOSAGE TREATMENT FOR DILTIAZIUM 1/ 60 MG/DAILY RAPID PULSE LOSARTAN 1/100 MG BLOOD PRESSURE ELI
- Allergien
- ALLERGIES TO PRESCRIPTION DRUGS & MISCELANEOUS ALLERGIES ANY DRUGS CONTAINING SULFA; AMOXICILLIN; ALLOPURINOL ALL LATEX RUBBER PRODUCTS; CAUSE RASHES/HIVES MY SKIN HAS BEEN DIAGNOSED AS ULTRA SENSITIVE
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 26.11.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain
Vaccination site inflammation
Symptomtext
greatly fatigued, sore entire leftside of body; greatly fatigued, sore entire leftside of body; 4 inch round circle of inflammation around injection; 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 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Nov2022 at 10:00 as dose 4 (booster), single (Lot number: GJ3274) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Osteopenia" (unspecified if ongoing); "Elevated BP" (unspecified if ongoing); "Some dehydration issues" (unspecified if ongoing); "known allergies: latex" (unspecified if ongoing), notes: known allergies: latex, hay fever, tramadol - that's IT. Concomitant medication(s) included: FLU VACCINE VII, in Oct2022 as dose number unknown, single; LEVOTHYROXINE; AMLODIPINE BESYLATE. Vaccination history included: Covid-19 vaccine (Primary immunization series completed unknown manufacturer), for COVID-19 immunization; Bnt162b2 (Dose Number: 3, Batch/Lot No: FJ4989, Location of injection: Arm Right, Vaccine Administration Time: 12:00 AM), administration date: Jun2022, for COVID-19 immunization. The following information was reported: VACCINATION SITE INFLAMMATION (non-serious) with onset 16Nov2022, outcome "recovered" (18Nov2022), described as "4 inch round circle of inflammation around injection"; FATIGUE (non-serious), PAIN (non-serious) all with onset 16Nov2022, outcome "recovered" (18Nov2022) and all described as "greatly fatigued, sore entire leftside of body". Therapeutic measures were not taken as a result of fatigue, pain, vaccination site inflammation. Additional information: It was reported, the patient took other medications in two weeks include Levothyroxine/Amlodipine Besylate/several supplmts. The patient did well on initial Covid shot and follow up booster. Did fine on 3rd booster in June of 2022. This last one in Nov of 2022 - greatly fatigued, sore entire left side of body - 4 inch round circle of inflammation around injection. Duration of "reaction" a full 48 hours on 16Nov2022 12:00 AM. The patient was recovered. No treatment was given. Covid was not tested prior to or post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Dehydration; Elevated BP; Hypothyroidism; Latex allergy (known allergies: latex, hay fever, tramadol - that's IT.); Osteopenia
- Andere Medikamente
- LEVOTHYROXINE; AMLODIPINE BESYLATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Headache
Nausea
Symptomtext
2-3 hours after the injection I developed a slightly elevated temperature, a headache and severe nausea which resolved approximately 4 hours later. There was no vomiting. 12 hours later there was still a slight headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pre-diabetic
- Andere Medikamente
- Sertraline 50 mg
- Allergien
- Lactose intolerance Seasonal allergic rhinitis
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.11.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Neck pain
No adverse event
Pain in extremity
Product preparation issue
Wrong product administered
Symptomtext
THE PATIENT WAS IN FOR A MMR VACCINE. I PULLED OUT THE DILUENT AND THE VACCINE. WHEN I RECONSTITUTED THE VACCINE I ACCIDENTALLY USED THE PFIZER BIVALENT INSTEAD OF THE DILUENT AND MIXED THEM TOGETHER. I THEN INJECTED THE PATIENT SUB-Q . WHEN I GOT BACK TO THE VACCINE TABLE I NOTICED THE DILUENT WAS STILL CAPPED. THEREFORE I MUST HAVE MIXED THE PFIZER BIVALENT WITH THE MMR VACCINE INSTEAD OF THE DILUENT. PATIENT COMPLAINS OF SORE ARM UP TO NECK AREA. NO OTHER ADVERSE EFFECTS SO FAR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- PATIENT IS GOING TO HOSPITAL TO BE CHECKED OUT
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Herpes zoster
Musculoskeletal pain
Pain
Rash
Urticaria
Symptomtext
Pain on the left side of my body from my buttocks to my ankle began the evening the same day of getting the booster shot. Two welts/rashes appeared on left leg 4 days after booster. Called doctor next day as rash spread. Doctor looked at rash and diagnosed shingles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- ZYRTEC
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 14.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Erythema
Interchange of vaccine products
Peripheral swelling
Skin warm
Symptomtext
Patient right arm is swollen, red, and hot. Swelling is 5cmX10cm. Localized shoulder pain. Has only had moderna covid19 vaccine X4. This was first Pfizer vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Fatigue
Headache
Pain
Pyrexia
Symptomtext
Woke up next morning with low-grade fever, headache, upset stomach, body ache all over. Seemed to get worse as the day progressed. Took sleeping aid Sunday night and was able to sleep through the night. Monday morning, felt much better, but symptoms began to return around noon and by night fall they were worse than ever. Took sleeping aid again and was able to sleep through the night. Tuesday morning, felt much better and continued to feel much better, except very fatigued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cold two weeks prior
- Vorgeschichte
- Enlarged Prostate
- Andere Medikamente
- Acetaminophen PM, Allopurinol 300 mg, Finasteride 5 mg, Triamterene/hctz 37.5-25 mg, Vitamin D3 2000 IU, One-A-Day Men's 50+
- Allergien
- Penicillin, Sulfa, Cipro, Cedar
- Vorherige Impfungen
- Penicillin in 1958, severe swelling and respiratory issues.
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Malaise
Pain in extremity
Pyrexia
Rash
Rash papular
Symptomtext
About 6 hours after receiving vaccine, I had a rash on my face. It started out about 2 inches long and about 1/4 inch wide next to my nose on my left cheek. Sunday morning, rash had spread to my entire left cheek. By that night, my nose was covered in rash. The rash was now swollen and hurt. Monday morning the rash had spread over my nose. I could not wear my glasses due to the swelling. Monday night the rash had spread to my hair line on my left side. Tuesday morning the rash has spread to cover half of my right cheek. Monday afternoon I saw my doctor. She gave me a six day prednisone prescription. I started taking the pills this morning (Tuesday). She told me to see my dermatologist if the prednisone didn't take care of the rash. I also had a low-grade fever, was drained of energy, and still don't feel well. With the other 3 vaccines, I had very little reactions (mostly a sore arm). This time my arm still hurts and was very sore.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Flu two weeks prior
- Vorgeschichte
- Congestive Heart Failure, Chronic Kidney Disease (stage 3), Rheumatoid Arthritis
- Andere Medikamente
- Calcium Citrate Magnesium and Zinc with Vitamin D3, Fish Oil 1000 mg, Vitamin E 180 mg, Aspirin 81 mg, Vitamin D3 1000 IU, L-5-MTHF 1700 mcg DFE, Atorvastatin 20 mg, Levothyroxine Tab 75 mcg, Losartan Tab 25 mg, Potassium CL SR MC TB 20 meq
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Rash
Symptomtext
RASH ON TORSO , HEADACHE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- COLLAGEN, VITAMIN C AND BIOTIN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.11.2022
- Impfdatum
- 31.10.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal discomfort
Diarrhoea
Erythema
Pain
Pruritus
Swelling
Symptomtext
Patient developed big red bump/spot on arm which itches and diarrhea which started within a few hours along with achiness. The spot was still big and red several days later as well as upset stomach.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 17.10.2023
- Impfdatum
- -
- Beginn
- 01.08.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Angiogram
Cardiac disorder
Echocardiogram
Electrocardiogram
Myocardial fibrosis
SARS-CoV-2 test
Ventricular remodelling
Symptomtext
heart changes; left ventricular remodeling with fibrosis of the left ventricle; left ventricular remodeling with fibrosis of the left ventricle; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose 4 (booster), single (batch/lot number: GJ3274) at the age of 60 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "type II diabetes" (unspecified if ongoing); "emphysema" (unspecified if ongoing). Concomitant medication(s) included: MELOXICAM; EDARBI; FARXIGA; ASPIRIN [ACETYLSALICYLIC ACID]. Past drug history included: Oxycodone, reaction: "drug allergy". Vaccination history included: Bnt162b2 (dose 1, batch/lot number EP6955, anatomical location arm left), for COVID-19 immunization; Bnt162b2 (dose 2, batch/lot number ER8729, anatomical location arm left), for COVID-19 immunization; Bnt162b2 (dose 3, batch/lot number 301358A, anatomical location arm left), for COVID-19 immunization. The following information was reported: VENTRICULAR REMODELLING (disability), MYOCARDIAL FIBROSIS (disability) all with onset Aug2022, outcome "recovered with sequelae" and all described as "left ventricular remodeling with fibrosis of the left ventricle"; CARDIAC DISORDER (disability) with onset Oct2023, outcome "unknown", described as "heart changes". The events "left ventricular remodeling with fibrosis of the left ventricle" and "heart changes" required physician office visit. The patient underwent the following laboratory tests and procedures: angiogram: (unspecified date) unremarkable, notes: with any stenosis seen under 25%; echocardiogram: (Oct2023) heart changes; EKG: (Aug2021) normal; (Aug2022) unknown results; (Aug2022) left ventricular remodeling, notes: with fibrosis of the left ventricle; nasal swab (covid-19 test): (Jun2023) negative. Therapeutic measures were not taken as a result of ventricular remodelling, myocardial fibrosis, cardiac disorder. Clinical course: The patient had no covid prior vaccination. The vaccination facility type was pharmacy/drug store. The left ventricular remodeling with fibrosis of the left ventricle, first detected by EKG changes in Aug2022, confirmed in Aug2023. The patient recovered with lasting effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angiogram
- Hospital-Tage
- -
- Labordaten
- Test Name: angiogram; Result Unstructured Data: Test Result:unremarkable; Comments: with any stenosis seen under 25%; Test Date: 202310; Test Name: echocardiogram; Result Unstructured Data: Test Result:heart changes; Test Date: 202108; Test Name: EKG; Result Unstructured Data: Test Result:normal; Test Date: 202208; Test Name: EKG; Result Unstructured Data: Test Result:unknown results; Test Date: 202208; Test Name: EKG; Result Unstructured Data: Test Result:left ventricular remodeling; Comments: with fibrosis of the left ventricle; Test Date: 202306; Test Name: nasal swab (covid-19 test); Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Emphysema; Type II diabetes mellitus
- Andere Medikamente
- MELOXICAM; EDARBI; FARXIGA; ASPIRIN [ACETYLSALICYLIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 12.10.2023
- Impfdatum
- 25.09.2023
- Beginn
- 05.10.2023
- Tage bis Beginn
- 10,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pityriasis rosea
Symptomtext
I have developed pityriasis rosea. It started on 10/04/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pityriasis rosea
- Hospital-Tage
- -
- Labordaten
- I saw my doctor 10/6/23 , he gave me an itching cream.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Just mental health, no physical ailments
- Andere Medikamente
- Lamictal, Celexa, Unisom, Omeprizole, Magnesium, calcium and zinc, Valtrex, Incassia
- Allergien
- Keflex
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.09.2023
- Impfdatum
- 23.11.2022
- Beginn
- 19.09.2023
- Tage bis Beginn
- 300,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
SARS-CoV-2 test positive
Symptomtext
COVID vaccine breakthrough case. Pfizer 4/2/21 ER8730, 4/23/21 EW0162, 12/17/21 33130BA, 5/25/22 FN2908, and 11/23/22 bivalent GJ3274
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive COVID test 9/19/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 28.08.2023
- Impfdatum
- 05.12.2022
- Beginn
- 15.03.2023
- Tage bis Beginn
- 100,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Obstructive sleep apnoea syndrome
Renal mass
Symptomtext
OBSTRUCTIVE SLEEP APNEA 3/17/2023 RENAL MASS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 16.08.2023
- Impfdatum
- 30.12.2022
- Beginn
- 03.04.2023
- Tage bis Beginn
- 94,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chronic obstructive pulmonary disease
Insomnia
Obstructive sleep apnoea syndrome
Sleep apnoea syndrome
Symptomtext
INSOMNIA W SLEEP APNEA 5/2/2023 COPD (CHRONIC OBSTRUCTIVE PULMONARY DISEASE) OBSTRUCTIVE SLEEP APNEA 5/2/2023 COPD (CHRONIC OBSTRUCTIVE PULMONARY DISEASE)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic obstructive pulmonary disease
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 15.08.2023
- Impfdatum
- 11.07.2023
- Beginn
- 11.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
Vaccine stored outside of manufacturer guidelines, product stability is unknown. Potential expired product used for immunization. No adverse events reported after vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 15.08.2023
- Impfdatum
- 12.07.2023
- Beginn
- 12.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Vaccine stored outside of manufacturer guidelines, product stability is unknown. Potential expired product used for immunization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 31.07.2023
- Impfdatum
- 29.11.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 20,0
- Dosis
- 5
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccine breakthrough infection
Symptomtext
Covid Breakthrough Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypertension, Dyslipidemia, DM type II, CAD, PVD, GERD, Hypothyroidism, AFIB
- Andere Medikamente
- Atorvastatin, Bupropion, Menthol/Zinc Oxide, MiraLAX, Lactulose, HCTZ, APAP, Insulin, Levothyroxine, Omeprazole, Oxybutynin, pregabalin,
- Allergien
- Sulfonamide antibiotics, Macrobid
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 24.07.2023
- Impfdatum
- 22.12.2022
- Beginn
- 19.07.2023
- Tage bis Beginn
- 209,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Insomnia
SARS-CoV-2 test
Symptomtext
Tested positive for COVID with a home test kit; Tested positive for COVID with a home test kit/runny nose for 24 hours; had difficulty sleeping last night; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. A 47-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Dec2022 as dose 4 (booster), single (Lot number: GJ3274) intramuscular for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "low thyroid" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID taken for hypothyroidism. The following information was reported: INSOMNIA (non-serious) with onset 19Jul2023, outcome "not recovered", described as "had difficulty sleeping last night"; DRUG INEFFECTIVE (medically significant) with onset 20Jul2023, outcome "not recovered", described as "Tested positive for COVID with a home test kit"; COVID-19 (medically significant) with onset 20Jul2023, outcome "not recovered", described as "Tested positive for COVID with a home test kit/runny nose for 24 hours". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Tested positive for COVID with a home test kit; (20Jul2023) Positive, notes: Nasal Swab. Clinical course: Patient complained of runny nose for 24 hours, had difficulty sleeping last night. Tested positive for COVID with a home test kit. No Covid prior vaccination and Covid was tested post vaccination. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information in the case report, a possible causal relationship between the events drug ineffective, covid-19 and suspect drug BNT162B2 cannot be excluded.,Linked Report(s) : US-PFIZER INC-202300255944 same patient, different vaccine dose number, different event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 antigen Rapid Test; Test Result: Positive ; Comments: Tested positive for COVID with a home test kit.; Test Date: 20230720; Test Name: COVID-19 antigen Rapid Test; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 30.06.2023
- Impfdatum
- 12.12.2022
- Beginn
- 10.02.2023
- Tage bis Beginn
- 60,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Obstructive sleep apnoea syndrome
Symptomtext
OBSTRUCTIVE SLEEP APNEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 30.06.2023
- Impfdatum
- 12.12.2022
- Beginn
- 28.01.2023
- Tage bis Beginn
- 47,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypersensitivity
Symptomtext
ALLERGIC REACTION, INIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 30.06.2023
- Impfdatum
- 22.12.2022
- Beginn
- 04.03.2023
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypoxia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoxia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 05.01.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Obstructive sleep apnoea syndrome
Symptomtext
ADULT OBSTRUCTIVE SLEEP APNEA, SEVERE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 17.01.2023
- Beginn
- 07.02.2023
- Tage bis Beginn
- 21,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Coagulopathy
Symptomtext
COAGULOPATHY, UNSPECIFIED TYPE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coagulopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 01.06.2023
- Impfdatum
- 09.01.2023
- Beginn
- 28.02.2023
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Obstructive sleep apnoea syndrome
Symptomtext
OBSTRUCTIVE SLEEP APNEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Obstructive sleep apnoea syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 31.05.2023
- Impfdatum
- 22.12.2022
- Beginn
- 01.05.2023
- Tage bis Beginn
- 130,0
- Dosis
- 5
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; 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 71-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Dec2022 at 15:00 as dose 5 (booster), single (Lot number: GJ3274) at the age of 71 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 06Mar2021 at 11:00 as dose 1, single (Lot number: EN6298), in left arm, on 27Mar2021 at 11:00 as dose 2, single (Lot number: ER8732), in right arm, on 13Oct2021 at 12:00 as dose 3 (booster), single (Lot number: 30130BA), in left arm and on 13Jul2022 at 15:00 as dose 4 (booster), single (Lot number: FP7135), in right arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: SIMVASTATIN, start date: 01Jan2017, stop date: 18May2023. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset May2023, outcome "not recovered" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300204080 same reporter/patient, different drug/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: No
- Andere Medikamente
- SIMVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 18.05.2023
- Impfdatum
- 23.03.2023
- Beginn
- 12.05.2023
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
No adverse event; Patient administered the 2nd bivalent dose to a patient 6 weeks after the 1st one instead of 8 weeks; This spontaneous case was reported by an other health care professional and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient administered the 2nd bivalent dose to a patient 6 weeks after the 1st one instead of 8 weeks) and NO ADVERSE EVENT (No adverse event) in a 74-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. GJ3274) for COVID-19 prophylaxis. No Medical History information was reported. On 23-Mar-2023, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On 12-May-2023, received fifth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to 1 dosage form. On 12-May-2023, after starting mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient administered the 2nd bivalent dose to a patient 6 weeks after the 1st one instead of 8 weeks). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient administered the 2nd bivalent dose to a patient 6 weeks after the 1st one instead of 8 weeks) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient administered the 2nd bivalent dose to a patient 6 weeks after the 1st one instead of 8 weeks). No concomitant medications were reported. The patient did not receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2023-724230 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-724230:(Monovalent Case)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 10.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 21,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy skin abnormal
Cancer surgery
Skin cancer
Symptomtext
On December 5, 2022, I went in to have a biopsy of an area on my shin, that came back to reveal that I had skin cancer. I scheduled a time to come in to have the areas removed. It did take time to get in for that, I was able to get back in on April 11, 2023, where the dermatologist was able to remove all of the skin cancer cells. The area on my leg is still healing, but all cancer cells are gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy skin abnormal
- Hospital-Tage
- -
- Labordaten
- 05DEC2022 Biopsy, skin cancer
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Vitamin D; vitamin B-12
- Allergien
- Codeine; glucosamine; chondroitin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 12.05.2023
- Impfdatum
- 20.12.2022
- Beginn
- 10.05.2023
- Tage bis Beginn
- 141,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
No adverse event
SARS-CoV-2 test positive
Symptomtext
No adverse effect from the vaccine. Please update this form. All I wanted to do was report that I contacted covid-19 on 5/10/2023. I signed up for V-safe checkins when I received my first covid vaccine shot and have been responding to the email check ins. They said to report new symptoms can be reported to VAERS. There's nothing in this form to enter this information. or that I started taking Paxlovid on 5/11/2023 that my doctor called in to the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Atoravastatin, Lisinopril
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 16.12.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 16,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Peripheral swelling
SARS-CoV-2 test negative
Symptomtext
On 01/2023 'I've noticed that both of my legs swelled up. I also lost balance so I started seeing a physical therapist from 03/02/2023. They prescribed Bumex for 60 days. It helped for awhile. The swelling of the legs went away eventually. I also took a Pneumonia vaccine on the same day so may be it could be from there am not sure. Am also taking my regular medication Lasix for swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- 02MAY2023 COVID-19 Test- Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Spondylitis ; Diabetes; Sjogren's Syndromes; Venous Stasis Dermatitis
- Andere Medikamente
- Lasix; Levothyroxine; Zoloft; Prednisone; Humalog; Gabapentin; Potassium; Flax Seed Oil; Artificial Tears; Vitamin D3
- Allergien
- Ultram
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 27.04.2023
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Symptomtext
Suspect patient received the correct vaccine (5-11 years COVID PFR BIV) but the vaccine was ordered wrong and therefore documented wrong. This may be the case because every vaccine is double verified by other staff members before administering to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Klinefelter's syndrome
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 25.04.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; Interchange of vaccine products; 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 44-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Jan2023 as dose 4 (booster), single (Lot number: GJ3274) at the age of 44 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 30Jan2021 as dose 1, single (Lot number: 010M20A), in left arm, on 27Feb2021 as dose 2, single (Lot number: 030M20A) and on 01Feb2022 as dose 3 (booster), single (Lot number: 037F21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 05Jan2023, outcome "unknown"; 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: (17Apr2023) Negative, notes: Tested negative for 2 days after treatment course ended; (19Apr2023) Positive, notes: Tested positive on day 4 after treatment course ended. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received Paxlovid as COVID-19 treatment from 10Apr2023 to 15Apr2023. Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the Pfizer-Biontech Covid-19 Vaccine lot GJ3274 was investigated. The investigation included a review of manufacturing and packaging records, deviations, and the complaint history for in scope lots. The final scope was determined to be the finished goods lot GJ3274, bulk and fill lots GJ2419, and GJ2425. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300163470 Same reporter/patient, different drug, different event.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230417; Test Name: Tested; Test Result: Negative ; Comments: Tested negative for 2 days after treatment course ended.; Test Date: 20230419; Test Name: Tested; Test Result: Positive ; Comments: Tested positive on day 4 after treatment course ended.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 21.04.2023
- Impfdatum
- 17.03.2023
- Beginn
- 07.04.2023
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Menstruation irregular
Wrong product administered
Symptomtext
I specifically told the pharmacist that this was my first ever Covid vaccine and that i will not take the Johnson and Johnson, but i preferred Pfizer. After being administered the shot, he was like your all done. I said i have to come back for the second dose and specified that i dont need the second dose. I made him aware that my job wants me to have both shots. He stated if thats the case come back in 3 weeks (April 7th, 2023) and he will give me another one. i come back three weeks later, and was told i was given the wrong shot, which i already figured out as soon i walked it and they told me they did not have the shot. Then i started putting the puzzle pieces together myself and figured out i was administered the wrong shot all in all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation irregular
- Hospital-Tage
- -
- Labordaten
- no one can tell me anything due to this. Have i had any symptoms? no, except two menstrual cycles in one month.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 06.04.2023
- Impfdatum
- 01.04.2023
- Beginn
- 01.04.2023
- 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
Product use issue
Vaccination error
Symptomtext
pt was given Pfizer bivalent. as a booster and she is 9 y.o. not indicated for that age group.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- non known
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 21.03.2023
- Beginn
- 21.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vial was punctured on 3/17/2023, but administered to the patient on 3/21/2023. The vial was expired when given to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Arthralgia, Chronic Pain, Carpal Tunnel, Chronic fatigue Syndrome, Obesity
- Vorgeschichte
- Chronic Fatigue Syndrome, Arthralgia
- Andere Medikamente
- Buspirone Wegovy Duloxetine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 07.11.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 114,0
- Dosis
- 5
- 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 a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 49-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Nov2022 at 17:30 as dose 5 (booster), single (Lot number: GJ3274) at the age of 49 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), as dose 1, single (Lot number: EM9810), as dose 2, single (Lot number: EN6204), as dose 3 (booster), single (Lot number: FC3181) and on 08Jul2022 as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation. The patient's relevant medical history included: "Rheumatoid arthritis" (unspecified if ongoing); "Migraines" (unspecified if ongoing), notes: Migraines; "Epilepsy" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing), notes: known allergies: Penicillin. The patient's concomitant medications were not reported. Past drug history included: Tegretol, reaction(s): "Allergy_Tegretol"; Cephalasporin, reaction(s): "Allergy_Cephalasporin". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Mar2023, outcome "unknown" and all described as "COVID 19". Therapeutic measures 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: Epilepsy; Migraine (Migraines); Penicillin allergy (known allergies: Penicillin); Rheumatoid arthritis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 30.03.2023
- Beginn
- 01.03.2023
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Product administration error
Product packaging confusion
Symptomtext
Employee received Pfizer booster instead of first dose of Pfizer primary series. New hire came to Employee Health to receive COVID vaccine (Pfizer primary series). Injection administered by RN. The next day when discarding opened vial RN noticed that vial opened was Pfizer Bivalent Booster. Pharmacy notified. Pharmacy instructed EH to follow instructions from the CDC which states: "If a Bivalent vaccine is administered in error for a primary series dose: do not repeat the dose. The primary and booster dosages are the same; the bivalent dose can be counted as primary series dose. Continue with the recommended vaccination schedule." Employee who received vaccine notified of error. Employee Health nurse explained situation. Employee denies questions at this time employee instructed to call Employee Health with any questions or concerns. Primary series had been ordered from pharmacy. Booster vial dispensed from pharmacy in bag that did not indicate that it was a bivalent booster on label. EH RN spoke with pharmacy asked for form of vaccine to be indicated on label. Clinical Pharmacy Utilization Specialist agrees to label bag with form of vaccine moving forward. Booster and primary series vials are the same size, shape and color. the only difference is the name on the label. Pharmacy and EH agree that this is increases potential for wrong dose to be administered. Employee who administered vaccine will be notified and educated on verifying correct dose prior to administration.?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None needed
- Aktuelle Erkrankungen
- no known
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 13.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 35-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Jan2023 as dose 4 (booster), single (Lot number: GJ3274) at the age of 34 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) 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 "not recovered" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient received Paxlovid from 18Mar2023 to 23Mar2023 as Treatment of COVID-19.; Sender's Comments: Considering a plausible drug-event temporal association, a reasonable possibility that the events drug ineffective and COvid-19 are related to BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5) cannot be excluded. This case will be reassessed should additional information become available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 29.03.2023
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Body mass index
Body temperature
Coronary artery bypass
Heart rate
Hepatic enzyme increased
Laboratory test
Liver function test
Oestrogen receptor assay
Oxygen saturation
Poor quality product administered
Product administration error
Product use issue
Respiratory rate
Symptomtext
coronary artery bypass graft; A multi-dose vial of this vaccine was opened (punctured) yesterday at 2:30 PM and a dose was administered today at 8:44 AM; A multi-dose vial of this vaccine was opened (punctured) yesterday at 2:30 PM and a dose was administered today at 8:44 AM; Pneumococcal (Pneumovax 23) 14Dec2022; This is a spontaneous report received from a contactable reporter (Other HCP) from medical information team. A 67-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Dec2022 at 11:09 as dose 5 (booster), single (Lot number: GJ3274, Expiration Date: 07Feb2023) at the age of 67 years intramuscular, in right deltoid for COVID-19 immunisation; pneumococcal vaccine (PNEUMOVAX 23 [PNEUMOCOCCAL VACCINE]), on 14Dec2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history included: "Smoking Never" (unspecified if ongoing), notes: Smoking Never , Smokeless Tobacco Never , Vaping Never used; "Alcohol No" (unspecified if ongoing); "Breast cancer" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Laparoscopic ovarian cystectomy" (unspecified if ongoing), notes: laparoscopic ovarian cystectomyX2; "Knee surgery" (unspecified if ongoing); "mastectomy right" (unspecified if ongoing); "Breast reconstruction right" (unspecified if ongoing); "Essential hypertension" (unspecified if ongoing); "Hyperlipidaemia" (unspecified if ongoing); "Precordial pain" (unspecified if ongoing); "Dyspnea on exertion" (unspecified if ongoing); "Coronary artery disease" (unspecified if ongoing); "Hx of CABG" (unspecified if ongoing); "neuropathy" (unspecified if ongoing); "Skin eruption" (unspecified if ongoing); "Physical deconditioning" (unspecified if ongoing); "Bone disorder" (unspecified if ongoing); "Current tear of medial cartilage or meniscus of knee" (unspecified if ongoing); "Knee pain" (unspecified if ongoing); "Pain in limb" (unspecified if ongoing); "Sprain of ankle" (unspecified if ongoing). Concomitant medications included: ASPIRIN 81 chewable tablet; EXEMESTANE 25 mg tablet; ZETIA 10 mg tablet; FLUOCINOLONE ACETONIDE ACETATE 0.01 %; HYDRODIURIL 25 MG tablet; HYDROCORTISONE 2.5 % cream; LOPRESSOR 100 MG tablet; NITROSTAT sublingual 0.4 MG SL tablet; CRESTOR 40 MG tablet; KENALOG [TRIAMCINOLONE ACETONIDE] 0.1 % cream; CALCIUM CARBONATE;COLECALCIFEROL;MINERALS NOS 600-400 MG-UNIT Tab. Past drug history included: Clotrimazole, reaction: "Rash". Vaccination history included: moderna (Dose: 01), administration date: 11Feb2021, when the patient was 65-year-old, for COVID-19 immunization; moderna (Dose: 02), administration date: 23Mar2021, when the patient was 65-year-old, for COVID-19 immunization; moderna (Dose: 03), administration date: 16Nov2021, when the patient was 65-year-old, for COVID-19 immunization; moderna coviD-19 (red cap booster), mrna (Dose: 04), administration date: 11Jul2022, when the patient was 66-year-old, for COVID-19 immunization; afluria (Dose: Unknown), administration date: 02Oct2019, when the patient was 63-year-old, for Immunisation; fluzone (0.5 ml Prefilled Syringe, Dose: Unknown), administration date: 13Oct2020, when the patient was 64-year-old, for Immunisation; fluzone (High dose > Age 65 (Prefilled Syringe), Dose: Unknown), administration date: 19Oct2022, when the patient was 66-year-old, for Immunisation; fluzone (High dose > Age 65 (Prefilled Syringe), Dose: Unknown), administration date: 22Oct2021, when the patient was 65-year-old, for Immunisation; influenza (Dose: Unknown, Manufacturer: Unknown), administration date: 16Oct2013, when the patient was 57-year-old, for Immunisation; influenza (Dose: Unknown, Manufacturer: Unknown), administration date: 12Nov2014, when the patient was 58-year-old, for Immunisation; influenza (Dose: Unknown, Manufacturer: Unknown), administration date: 31Oct2017, when the patient was 61-year-old, for Immunisation; influenza adult (Dose: Unknown, Manufacturer: Unknown), administration date: 02Oct2019, when the patient was 63-year-old, for Immunisation; influenza adult (Dose: Unknown, Manufacturer: Unknown), administration date: 01Jan2017, when the patient was 61-year-old, for Immunisation; influenza adult (Dose: Unknown, Manufacturer: Unknown), administration date: 01Nov2016, when the patient was 60-year-old, for Immunisation; prevnar 13 (Dose: Unknown), administration date: 15Sep2021, when the patient was 65-year-old, for Immunisation; shingrix (Dose: Unknown), administration date: 07Jun2022, when the patient was 66-year-old, for Immunisation; shingrix (Dose: Unknown), administration date: 25Mar2022, when the patient was 66-year-old, for Immunisation; zostavax (Dose: Unknown), administration date: 12Jan2017, when the patient was 61-year-old, for Immunisation; Influenza adult (Dose: Unknown, Manufacturer: Unknown, (2 more)), for Immunisation. The following information was reported: PRODUCT USE ISSUE (non-serious) with onset 14Dec2022, outcome "unknown", described as "Pneumococcal (Pneumovax 23) 14Dec2022"; POOR QUALITY PRODUCT ADMINISTERED (non-serious), PRODUCT ADMINISTRATION ERROR (non-serious) all with onset 14Dec2022 at 11:09, outcome "unknown" and all described as "A multi-dose vial of this vaccine was opened (punctured) yesterday at 2:30 PM and a dose was administered today at 8:44 AM"; CORONARY ARTERY BYPASS (medically significant) with onset 21Dec2022, outcome "unknown", described as "coronary artery bypass graft". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (17Feb2023) 128/79; Body mass index: (unspecified date) 33.0-33.9 adult; Body temperature: (17Feb2023) 97.6 Fahrenheit, notes: 36.4 degree Celsius; Heart rate: (17Feb2023) 70; Hepatic enzyme increased: (unspecified date) Increased; Temp src: (17Feb2023) Temporal; Liver function test: (unspecified date) Elevated; Oestrogen receptor assay: (unspecified date) Positive, notes: Estrogen receptor positive status (ER+); (unspecified date) Positive, notes: Malignant neoplasm of upper-outer quadrant of right breast in female, estrogen receptor positive; Oxygen saturation: (17Feb2023) 99 %; Respiratory rate: (17Feb2023) 16. Therapeutic measures were taken as a result of coronary artery bypass. Additional information: It was reported for Pfizer-BioNTech COVID-19 Vaccine, bivalent gray cap that multi-dose vial of the vaccine was opened (punctured) on 13Dec2022 (reported as yesterday) at 2:30 PM (also reported as 2:13 PM) and a dose was administered on 14Dec2022 (reported as today) at 8:44 AM. Reporter wanted to know stability of the vaccine. The case was reported as non-serious. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received. Follow-up (17Mar2023): This is a spontaneous follow up report received from a contactable Other HCP in response to HCP letter. Updated information included: Historical vaccine details, medical history, lab data, past drug, co-suspect drug (added Pneumovax 23), suspect drug details (dose number, lot number, and expiration date), concomitant medications, new events (Coronary artery bypass graft and product use for unapproved combination), and clinical course of events. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Reported event coronary artery bypass graft is considered an intercurrent medical condition and is therefore not related to the suspect drug. Case to be re-assessed upon receipt of new information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure measurement
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230217; Test Name: Blood pressure; Result Unstructured Data: Test Result:128/79; Test Name: BMI; Result Unstructured Data: Test Result:33.0-33.9 adult; Test Date: 20230217; Test Name: Temp; Result Unstructured Data: Test Result:97.6 Fahrenheit; Comments: 36.4 degree Celsius; Test Date: 20230217; Test Name: Pulse; Result Unstructured Data: Test Result:70; Test Name: Liver enzymes; Result Unstructured Data: Test Result:Increased; Test Date: 20230217; Test Name: Temp src; Result Unstructured Data: Test Result:Temporal; Test Name: Liver function tests; Result Unstructured Data: Test Result:Elevated; Test Name: Estrogen receptor; Test Result: Positive ; Comments: Estrogen receptor positive status (ER+); Test Name: Estrogen receptor; Test Result: Positive ; Comments: Malignant neoplasm of upper-outer quadrant of right breast in female, estrogen receptor positive; Test Date: 20230217; Test Name: SpO2; Test Result: 99 %; Test Date: 20230217; Test Name: Resp; Result Unstructured Data: Test Result:16
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Abstains from alcohol; Ankle sprain; Bone disorder; Breast cancer female; Breast reconstruction; CABG; Coronary artery disease; Dyspnoea exertional; Essential hypertension; Hyperlipidaemia; Hypertension; Knee pain; Knee surgery NOS; Mastectomy; Neuropathy; Non-smoker (Smoking Never Smokeless Tobacco Never Vaping Never used); Ovarian cystectomy (laparoscopic ovarian cystectomyX2); Pain in limb; Physical deconditioning; Precordial pain; Skin eruption; Tear of medial cartilage or meniscus of knee, current
- Andere Medikamente
- ASPIRIN 81; EXEMESTANE; ZETIA; FLUOCINOLONE ACETONIDE ACETATE; HYDRODIURIL; HYDROCORTISONE; LOPRESSOR; NITROSTAT; CRESTOR; KENALOG [TRIAMCINOLONE ACETONIDE]; CALCIUM CARBONATE;COLECALCIFEROL;MINERALS NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 27.03.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient did not exemplify any adverse reaction to the vaccine after administration of incorrect vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccine Administration Error. Patient administered bivalent during first series of doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccine administration error. Patient was administered bivalent for first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccination Administration Error. Patient given bivalent during first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccine Administration Error. Patient administered Bivalent during first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccine Administration Error. Patient administered bivalent for first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccine Administration Error. Patient was given bivalent for first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccine administration Error. Patient administered bivalent for first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccine administration error. Patient was administered bivalent on first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccination administration error. Patient was administered bivalent booster for first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Vaccination administration error. Patient given bivalent for first series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 21.03.2023
- Impfdatum
- 09.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersomnia
Memory impairment
Neurological examination normal
Symptomtext
Patient received vaccine on 12/9 and from 12/10 - 12/19 the patient slept alot, watched re-runs on TV and could not remember basic things about her life. The patient does not remember those days at all. She "woke up" on 12/19 and feels she's piecing her life back together since then.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersomnia
- Hospital-Tage
- -
- Labordaten
- Neurologic Exam - Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension, hyperlipidemia, xistory of pulmonary embolism, peripheral neuropathy, post covid cognitive impairment,
- Andere Medikamente
- Eliquis, Lisinopril, Metoprolol, Synapsim, Multi-vitamin
- Allergien
- Clam Shell, Aprepitant
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.03.2023
- Impfdatum
- 10.12.2022
- Beginn
- 26.01.2023
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Electrocardiogram abnormal
Tricuspid valve incompetence
Symptomtext
In January, diagnosed with increased right tricuspid valve regurgitation during a routine scan. It was previously minimal leakage, in January it was described as moderate. No treatment needed, no symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram abnormal
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- Sertraline 50mg, multivitamin, ashwaghanda, valerian
- Allergien
- Sulfa antibiotics/meds
- Vorherige Impfungen
- One time ocular migraine a couple months after the third Pfizer covid vaccine
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.03.2023
- Impfdatum
- 05.01.2023
- Beginn
- 02.03.2023
- Tage bis Beginn
- 56,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cellulitis
Symptomtext
Cellulitis of right ankle 03/02/2023 took cephalexin 500mg 4 x times a day for 7 days, then resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Aspirin; B12; biotin; calcium carbonate; vitamin D3; vitamin E; multivitamin without iron
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 12.03.2023
- Impfdatum
- 26.02.2023
- Beginn
- 26.02.2023
- 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
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 12.03.2023
- Impfdatum
- 07.02.2023
- Beginn
- 07.02.2023
- 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
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 12.03.2023
- Impfdatum
- 18.02.2023
- Beginn
- 18.02.2023
- 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
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 12.03.2023
- Impfdatum
- 28.02.2023
- Beginn
- 28.02.2023
- 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
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- U
- Eingang
- 12.03.2023
- Impfdatum
- 08.02.2023
- Beginn
- 08.02.2023
- 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
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 08.03.2023
- Impfdatum
- 08.03.2023
- Beginn
- 08.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
pt received unknown vaccine. by error bivalent was given instead of monovalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 08.03.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
Patient was administered a Bivalent vaccine as their second dose of COVID vaccine when they should have been administered a monovalent COVID vaccine to complete the primary series. There were no adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 13.01.2023
- Beginn
- 13.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 27.02.2023
- Beginn
- 27.02.2023
- 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
given after bud date. date on box was written as 7/31/23 but was incorrect and should have been 1/18/23 10 weeks after receiving on 11/10/22. no adverse reaqction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- 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
vaccine given after bud date of 1/18/23 bud date on box was written as 7/31/23 was not correct. no adverse reactions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- 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
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- 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
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 25.11.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
No adverse event
Symptomtext
Booster gave too soon. we gave bivalent booster on 4/1/2023, pharmacy 9/7/2022 then clinic again on 11/25/2022. Patient did not have reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Vaers being submitted per work policy due to getting booster too early. we gave bivalent booster on 4/1/2023, pharmacy 9/7/2022 then we did again on 11/23/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 18.02.2023
- Impfdatum
- 17.02.2023
- Beginn
- 17.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Fall
Symptomtext
Patient lost her balance and fell, in the waiting room after receiving vaccines. Patient states that she was not injured and thinks that she did not fall as a result of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Balance disorder
- Hospital-Tage
- -
- Labordaten
- Paramedics performed blood pressure, heart rate and blood oxygen saturation test. All results came back normal.
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- 1. Diabetes 2. Hypertension 3. Thyroid Disease
- Andere Medikamente
- none kown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 14,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Central nervous system inflammation
Eye haemorrhage
Visual field defect
Visual impairment
Vitreous floaters
Symptomtext
I did not have a reaction to the vaccine. Around Christmas time, I noticed vision changes in my right eye. I noticed more floaters moving in my right eye, it was not floaters but a hemorrhage. The nerve was very inflamed. I did see my primary care doctor and my eye doctor. They stated they are seeing cases like this more often. I was put on steroids which helped but I continue to have blind spot(s). I have been told that in time these symptoms will improve.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Central nervous system inflammation
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Melatonin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 14.11.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Anal incontinence
Clostridium difficile infection
Clostridium test positive
Frequent bowel movements
Symptomtext
On 12/06/22 I started having symptoms of excessive bowel movements, no pain just urgency, no control, I went to my doctor and had a stool sample and tested positive for C-diff, I was given medication an antibiotic, vancomycin to help get rid of the bacteria that was causing the C-diff. I took the antibiotic for 10 days, everything cleared within 3 to 4 days after I started taking the medication. My stomach is sensitive even now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal discomfort
- Hospital-Tage
- -
- Labordaten
- Stool sample
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Multivitamins
- Allergien
- Cephalosporin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.02.2023
- Impfdatum
- 10.01.2023
- Beginn
- 10.02.2023
- Tage bis Beginn
- 31,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no illnesses
- Vorgeschichte
- none
- Andere Medikamente
- The patient received bivalent Pfizer-BioNTech vaccine as a the first primary series dose instead of monovalent Pfizer-BioNTech vaccine. Error noted today when member came back in for second dose of primary series
- Allergien
- no reaction noted
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 07.02.2023
- Impfdatum
- 11.01.2023
- Beginn
- 23.01.2023
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram
Lower urinary tract symptoms
Tinnitus
Urinary retention
Symptomtext
Tinnitis Luts (severe urinary tract symptoms ) urinary retention, had to visit patient first then had to visit emergency department
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Computerised tomogram
- Hospital-Tage
- -
- Labordaten
- CT scan have appointment with urologist
- Aktuelle Erkrankungen
- hypertension
- Vorgeschichte
- hypertension
- Andere Medikamente
- Norvasc
- Allergien
- nkda
- Vorherige Impfungen
- tinnitis; 49yo,;12/23/21 covid vaccine pfizer
- Staat
- OH
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 05.02.2023
- Impfdatum
- 05.02.2023
- Beginn
- 05.02.2023
- 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
patient was supposed to get dose 2 monovalent, gave bivalent in error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
received flu at another clinic, No reactions. Mother had forgotten she already gotten a flu vaccine elsewhere.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 02.02.2023
- Impfdatum
- 16.12.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
headquarters contacted me by voice mail and said to call the local pharmacy about the vaccine. I called and was told there was a refrigeration issue and to see a doctor. pharmacy refused to provide any more details nor would they give me any written information. My doctor asked what he supposed to do since it's been nearly 7 weeks since the vaccine was administered and pharmacy will not provide guidance. They said a pharmacist would call me and talk to me but it has not happened (they have not called me).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- None - seeking guidance on what to do. I do not know what I should be looking for.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Losartan Potassium 50mg Pravastatin Sodium 10mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 31.01.2023
- Beginn
- 31.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Pt was given wrong dose of Pfizer Bivalent, given 0.3ml. Should have been given 0.2ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 27.01.2023
- Beginn
- 27.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series 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
- MI
- Alter
- 97,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 23.01.2023
- Tage bis Beginn
- 16,0
- Dosis
- 4
- 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 4 vaccines Pfizer 2/11/21 Lot# EM9810; Pfizer 3/48/21 Lot# EN6201; Pfizer 10/9/21 Lot# FF2590; Pfizer 1/7/23 Lot# GJ3274
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 26.01.2023
- Beginn
- 26.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received bivalent Pfizer dose for second dose in primary series, instead of receiving monovalent Pfizer dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 26.01.2023
- Beginn
- 26.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient was administered Pfizer bivalent dose for second dose within primary series, instead of Pfizer monovalent dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient should have been given a standard (original formulation) Pfizer Covid vaccine, but was given a Bivalent vaccine instead. No harm to patient reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- migraine without aura
- Andere Medikamente
- magnesium, sumatriptan
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 26.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The patient received a vaccine that was drawn up 18 hours prior which would have made it expire.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- N/A
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The patient was given a vaccine after being drawn up 18 hours prior. Which would be consider expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 26.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received Vaccine that was drawn up 18 hours prior
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
The patient received a vaccine that was expired due to being drawn up 24 hours earlier
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- ALFALFA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 08.01.2023
- Beginn
- 08.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 08.01.2023
- Beginn
- 08.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 08.01.2023
- Beginn
- 08.01.2023
- 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 (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 08.01.2023
- Beginn
- 08.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 08.01.2023
- Beginn
- 08.01.2023
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 11.11.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 21,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Symptomtext
Blood pressure, which is normally low, rose to the point of needing medication for 4 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Tendency for delayed and prolonged bleeding after surgery and procedures. Pre-diabetes, allergy induced asthma
- Andere Medikamente
- Flonase, Calcium, vitamin D3
- Allergien
- Penicillin, Sudafed, azithromycin, dairy intolerance
- Vorherige Impfungen
- Jansen Covid vaccine
- Staat
- NJ
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 08.01.2023
- Beginn
- 08.01.2023
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- 19.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 10.01.2023
- Beginn
- 10.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Patient had received a Pfizer bivalent covid vaccine 9/10/2022. Patient then erroneously received a second Pfizer bivalent booster on 1/10/2023. No adverse reactions were reported by the patient, but this second bivalent booster does not follow CDC guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, hypercholesterolemia, type 2 diabetes, dysphagia
- Andere Medikamente
- Flonase, albuterol, omeprazole (20 mg), simvastatin (20 mg), amlodipine besylate (5 mg), celecoxib (100 mg), ezetimibe (10 mg), losartan potassium (50 mg), metformin (500 mg), vitamin D (50 mcg), calcium carbonate 1250 mg)
- Allergien
- Atorvastatin, codeine, sulfur, lisinopril, tuberculin tests
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 22.01.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series 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
- UT
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 20.01.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
After giving vaccination, upon further review of record, client had received Bivalent Pfizer previously on 09/30/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 19.01.2023
- Impfdatum
- 12.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymphadenopathy
Tenderness
Symptomtext
Left axillary adenopathy. Pt noticing tenderness of the area. Selling easily palpated with large olive sized node). Watchful waiting. Self resolved within 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Primary hypertension Severe obesity due to excess calories with serious comorbidity and body mass index (BMI) in 99th percentile for age in pediatric patient Prediabetes
- Andere Medikamente
- losartan (COZAAR) 50 mg tablet: one PO QHS metFORMIN (GLUCOPHAGE-XR) 500 mg 24 hr tablet: Four (2000mg) PO with dinner Melatonin 1 mg PO QHS PRN
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 19.01.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
Patient came to see PCP on 12/15 for annual checke up. PCP reviewed immunization record, last dose of covid vaccine was given on 04/15/2022 which was monovalent, pt denied any other covid vaccine received afterwards. Then PCP offerred Pfizer Bivalent booster, pt agreed and received on same day, left office w/o any complaint after 15 min observation. Later afternoon, patient called PCP office that he found vaccine record at home which showed he had Moderna Bivalent booster on 10/18/2022 by Pharmacy already. Pt denied any discomfort at that time. Nurse called pt on 12/16 for f/u. Pt reported doing well, denied fever, body aches/chills or any discomfort. No erythema or swelling noted at injection site. Reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 19.01.2023
- Impfdatum
- 11.01.2023
- Beginn
- 11.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase
Aspartate aminotransferase
Blood alkaline phosphatase
Blood glucose
Blood triglycerides
Glycosylated haemoglobin
Laboratory test abnormal
Poor quality product administered
Product administration error
Symptomtext
patient was given the product "out of the window" for the bivalent. The product was previously punctured for greater than 12 hours. Total hours post puncture was 5-6 hours beyond the 12 hours; patient was given the product "out of the window" for the bivalent. The product was previously punctured for greater than 12 hours. Total hours post puncture was 5-6 hours beyond the 12 hours; Labs were drawn yesterday and three came in abnormal 30 minutes after the visit yesterday,; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team, Program ID. A 35-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Jan2023 at 11:30 as dose 5 (booster), 0.3 ml single (Lot number: GJ3274, Expiration Date: 31Jul2023) at the age of 35 years, in right deltoid for covid-19 immunisation. The patient's relevant medical history included: "Diabetes type 2", start date: 2018 (ongoing); "Hypertension", start date: 2018 (ongoing). The patient's family history included: "Liver disease", start date: 2005 (ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1 Monovalent Manufacturer: Pfizer, Lot & Exp Unknown), administration date: 01Jan2021, when the patient was 33-year-old, for Covid-19 immunization; BNT162b2 (Dose 2 Monovalent Manufacturer, LOT: EL9267, EXP: Unknown Dose and Route: 0.3ml injected into right deltoid Time: 09:36), administration date: 20Feb2021, when the patient was 33-year-old, for Covid-19 immunization; BNT162b2 (Dose 3 Monovalent LOT: EN6202 EXP: Unknown, Dose and Route: 0.3ml and intramuscular injection, injection site is unknown Time: 09:36), administration date: 13Mar2021, when the patient was 33-year-old, for Covid-19 immunization; BNT162b2 (Dose 4 Monovalent, LOT: FH8028, 0.3ml intramuscular on right deltoid, Time: 09:36), administration date: 16Nov2021, when the patient was 34-year-old, for Covid-19 immunization; flu shot (Dose/Route: 0.5ml injected into left deltoid Lot Number/ Expiry Date: UJ893AA / Expiry date is unknown), administration date: 06Nov2022, for Immunization. The following information was reported: LABORATORY TEST ABNORMAL (non-serious) with onset 11Jan2023, outcome "unknown", described as "Labs were drawn yesterday and three came in abnormal 30 minutes after the visit yesterday,"; POOR QUALITY PRODUCT ADMINISTERED (non-serious), PRODUCT ADMINISTRATION ERROR (non-serious) all with onset 11Jan2023 at 11:30, outcome "unknown" and all described as "patient was given the product "out of the window" for the bivalent. The product was previously punctured for greater than 12 hours. Total hours post puncture was 5-6 hours beyond the 12 hours". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: As per COVAX: "One was given outside of the time frame and she wants to know if they need to be revaccinated." Caller states a patient yesterday was given the product "out of the window" for the bivalent. The product expired 11:30 PM and was inadvertently given the following AM. The product was previously punctured for greater than 12 hours. Total hours post puncture was 5-6 hours beyond the 12 hours. Max 18 hours of puncture time. Total cumulative time post-puncture: Up to 24 hours at 2 degree Centigrade and 30 degree Centigrade (35 degree Fahrenheit to 86 degree Fahrenheit), depending on storage container Total cumulative time post-puncture cannot exceed 24 hours, regardless of container. Upon follow-up on 12Jan2023, calling from a primary care and wants to give us a call regarding the Pfizer Covid 19 bivalent injection. They had one given outside the timeframe and wanted to see if they needed to revaccinate or what steps they needed to do. Upon follow-up on 12Jan2023 it was reported that a shot of the Covid-19 vaccine Bivalent was administered outside the time frame and the caller wanted to see if they needed to revaccinate the patient or what were the next steps to take. Concomitant Products: All medications were current. They did send in three new medications yesterday for the patient. Labs were drawn yesterday (at the time of report) and three came in abnormal 30 minutes after the visit yesterday, 11Jan2023. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received. Follow-up (12Jan2023): This is a spontaneous follow-up report received from a HCP. This contactable HCP reported for a patient that: Updated information included: Reporter info (Institution). New Reporter (slider#2). Patient details (DOB, age, unit, weight, height, race, gender). Historical vaccine (Dose#1, dose#2, dose#3, dose#4). Relevant Med History (Diabetes type 2, Hypertension and Liver disease). Lab test. Dosage regimen (Start Date/Time, dose no., lot# and Anatomical Location). Vaccine Facility Information. Event onset date. Historical vaccine (Flu shot). New event added (Labs were drawn yesterday and three came in abnormal 30 minutes after the visit yesterday). Concomitant Therapy and additional information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alanine aminotransferase
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230111; Test Name: ALT; Result Unstructured Data: Test Result:126; Comments: Result: 126; Unit: Not Provided; Test Date: 20230111; Test Name: AST; Result Unstructured Data: Test Result:75; Comments: Result: 75; Unit: Not Provided; Test Date: 20230111; Test Name: Alkaline phosphatase; Result Unstructured Data: Test Result:158; Comments: Result: 158; Unit: Not Provided; Test Date: 20230111; Test Name: Glucose; Result Unstructured Data: Test Result:129; Comments: Result: 129; Unit: Not Provided; Test Date: 20230111; Test Name: Triglycerides; Result Unstructured Data: Test Result:162; Comments: Result: 162; Unit: Not Provided; Test Date: 20230111; Test Name: Hemoglobin A1C; Result Unstructured Data: Test Result:7.6; Comments: Result: 7.6; Unit: Not Provided
- Aktuelle Erkrankungen
- Hypertension; Liver disorder; Type II diabetes mellitus
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 6
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
COVID-19
Drug ineffective
Symptomtext
Covid; Covid; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Sep2022 as dose 5 (booster), single (Lot number: PGJ2524), in right arm and on 27Dec2022 at 15:00 as dose 6 (booster), single (Lot number: GJ3274) at the age of 67 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "asthma" (unspecified if ongoing); "acid reflux" (unspecified if ongoing); "menopause" (unspecified if ongoing); "Known allergies: Yes" (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 "not recovered" and all described as "Covid". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: High. Therapeutic measures were taken as a result of drug ineffective, covid-19. Treatment drug included Paxlovid from 01Jan2023 to 06Jan2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure measurement
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood pressure; Result Unstructured Data: Test Result:High
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Acid reflux (esophageal); Allergy; Asthma; Blood pressure high; Menopause
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 14.01.2023
- Impfdatum
- 01.01.2023
- Beginn
- 01.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Patient received a second dose of the bivalent covid booster .no adverse event reported .previous dose was back in November
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- No adverse event reported
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 12.01.2023
- Beginn
- 12.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient received Covid booster 1 day passed beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Low vitamin D
- Vorgeschichte
- Prediabetes, Hypertension, Chronic Left shoulder pain
- Andere Medikamente
- Dicyclomine 10 mg capsule Ergocaliciferol 1.250 mcg ibuprofen 800mg tablet lisinopril 20mg tablet metformin 500 mg tablet Revatio 20 mg tablet sulfacetamide sodium 10% eye drops tamsulosin 0.4 mg capsule testosterone cypionate 200 mg/ml in
- Allergien
- No known medical allergies/. food allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 17.11.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 52,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Asymptomatic COVID infection/Nasal swab positive; Asymptomatic COVID infection/Nasal swab positive; This is a spontaneous report received from a contactable reporter (Physician). A 61-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 as dose 4 (booster), single (Lot number: GJ3274) at the age of 61 years intramuscular for covid-19 immunisation; BNT162b2 (BNT162B2), on 22Mar2021 as dose 1, single (Lot number: EP6955), on 12Apr2022 as dose 2, single (Lot number: EP6955) and on 09Jun2022 as dose 3 (booster), single (Lot number: FF2589), all intramuscular for covid-19 immunisation. The patient had no relevant medical history. The patient has no known allergies. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 08Jan2023, outcome "recovering" and all described as "Asymptomatic COVID infection/Nasal swab positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08Jan2023) Positive, notes: Nasal swab. Therapeutic measures were not taken as a result of drug ineffective, covid-19. Additional information: the reporter considered the events as non-serious. The patient did not receive other vaccines in the four weeks.; Sender's Comments: Based on available information, a lack of efficacy with the suspect vaccine BNT162B2 in this patient cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230108; Test Name: Siemens Clinitest; Test Result: Positive ; Comments: Nasal swab
- 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
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 12.01.2023
- Impfdatum
- 05.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- 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 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 67-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Dec2022 at 14:30 as dose 5 (booster), single (Lot number: GJ3274) at the age of 67 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 01Aug2022 at 14:30 as dose 4 (booster), single (Lot number: FP7139), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "hypothyroid" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; LIOTHYRONINE. Past drug history included: Cipro, reaction(s): "Known allergies: Cipro". 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, notes: antigen tested positive on day 13 prior antigen negative tests on day 9 and day 11; Negative, notes: antigen tested positive on day 13 prior antigen negative tests on day 9 and day 11; Negative, notes: antigen tested positive on day 13 prior antigen negative tests on day 9 and day 11. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information: Adverse event: new symptoms on day 12; only sinus congestion and fatigue antigen tested positive on day 13 prior antigen negative tests on day 9 and day 11.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: antigen tested; Test Result: Positive ; Comments: antigen tested positive on day 13 prior antigen negative tests on day 9 and day 11; Test Name: antigen tested; Test Result: Negative ; Comments: antigen tested positive on day 13 prior antigen negative tests on day 9 and day 11; Test Name: antigen tested; Test Result: Negative ; Comments: antigen tested positive on day 13 prior antigen negative tests on day 9 and day 11
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism
- Andere Medikamente
- LEVOTHYROXINE; LIOTHYRONINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- 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
Symptomtext
dose drawn up on 12.27.22 @ 2:30pm but given on 12.28.22 @ 5:39pm, outside the 12 hr expiration and 24 hr pfizer stability data, will need to be repeated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Overweight (BMI 25.0-29.9) ? Diabetes mellitus treated with oral medication ? Hyperlipidemia, unspecified hyperlipidemia type ? Diabetes mellitus type 2 without retinopathy ? Dermatochalasis of both upper eyelids ? Hyperopia of both eyes ? Hyperlipidemia associated with type 2 diabetes mellitus
- Andere Medikamente
- atorvastatin (LIPITOR) 20 MG tablet Take 1 tablet by mouth daily. ? fluticasone (FLONASE) 50 MCG/ACT nasal spray 2 sprays in each nostril daily ? glipiZIDE CR (GLUCOTROL) 5 MG 24 hr tablet TAKE 1 TABLET BY MOUTH EVERY DAY ? metFORMIN (GLUC
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Poor quality product administered
Symptomtext
Dose drawn up on 12.27.22 @ 2:30pm but given on 12/28/22 @ 4:57pm therefore outside the 12 hr expiration and 24 hr stability data from Pfizer. Dose will need to be repeated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Class 1 obesity due to excess calories with serious comorbidity and body mass index (BMI) of 34.0 to 34.9 in adult 06/02/2021 ? Prediabetes 05/28/2020 ? Decreased hearing of both ears 05/28/2020 ? Gastroesophageal reflux disease, esophagitis presence not specified 05/27/2020 ? Benign prostatic hyperplasia, presence of lower urinary tract symptoms unspecified, unspecified morphology 05/18/2017 Updated by Regulatory 2019 R2 ? Adenomatous polyp of colon, unspecified part of colon 05/18/2017 ? Nocturia 04/14/2016 ? Ingrown left big toenail 04/14/2016 ? Insulin resistance 04/14/2016 ? Tremor of left hand 04/14/2016 ? ED (erectile dysfunction) Levitra has been helpful. ? Environmental allergies flonase had been helpful but seems to be losing efficacy. claritin as needed. ? Hypogonadism male Ha been using androgel regularly but has stopped and has not noticed any difference. His energy levels seem to be OK. Libido is OK. Some ED issues but levitra helps. ? Essential hypertension Is on propranol and lisinopril. Tolerates them well with no SE. BP generally about 120/80. No sx of high or low BP. ? Familial tremor Both hands, esp the left. Propranolol seems to help some. It continues to be a little bit of an issue but does not interfere with his life. ? Hyperlipidemia Had been on simvastatin and trilipix. Switched to lipitor because of cost and it has worked well. He tolerates it well with no SE. Stopped trilipix because of cost - was going to replace with fenofibrate but did not and trigs have been close to 250. He is working on diet and exercise and trying to lose weight.
- Andere Medikamente
- atorvastatin (LIPITOR) 20 MG tablet TAKE 1 TABLET DAILY ? fluticasone (FLONASE) 50 MCG/ACT nasal spray USE 2 SPRAYS IN EACH NOSTRIL ONCE DAILY ? lisinopril (PRINIVIL,ZESTRIL) 10 MG tablet TAKE 1 TABLET DAILY ? metFORMIN-XR (GLUCOPHAGE-XR) 5
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product administration error
Symptomtext
administered after 12hr expiration period, vaccine was drawn up on 12/27/22 @ 2:30pm. Pfizer stability data supports dose being valid as it was given within 24 hrs. No need to repeat dose. Reporting as administration error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hyperlipidemia associated with type 2 diabetes mellitus 09/29/2021 ? Chronic low back pain 05/03/2019 ? Insomnia, unspecified type 10/05/2018 Has tried trazodone. Not sure that it helped so stopped it. Nyquil seems to work fairly well. ? Depression with anxiety 10/05/2018 Is on zoloft and tolerates it well with no SE. Seems to be effective. ? Personal history of kidney stones 10/05/2018 Had one episode. Thinks it was about 2005. ? Right hip pain 07/12/2018 OA of the hip per xray 10/2017. Also degenerative spine disease. Is on daily meloxicam. Not sure how helpful it is. ? Class 3 severe obesity due to excess calories with serious comorbidity and body mass index (BMI) of 40.0 to 44.9 in adult 06/22/2017 ? Neuropathy 03/16/2017 Pain in legs. Right more than left. Is on gabapentin. Tolerates it well with no SE. Finds it somewhat helpful. Decreased sensation bottom 1st and 2nd toes right foot. Otherwise normal. Normal sensation on the top of the toes both feet. ? Hyperlipidemia, unspecified hyperlipidemia type 08/31/2016 Is on lipitor. Tolerates it well with no SE. ? Smoker 05/28/2015 Not ready to quit. ? Hepatitis C 02/04/2015 Managed by Dr. Genotype 3a. Biopsy in September 2012 by Dr. showed grade 1 stage 1 and 2. AFP elevated (21), RUQ US pending. Drinks quite a bit, advised total alcohol cessation. ? Diabetes mellitus treated with oral medication 02/04/2015 New diagnosis in early 2015. Has one touch Verio meter. Victoza made him nauseated. Is on metformin XR 1000 BID. ? Hypertension associated with type 2 diabetes mellitus 02/04/2015 amlodipine and lisinopril. Tolerates both meds well with no SE Past Medical History: Diagnosis Date ? Arthritis back and knees especially ? Depression with anxiety 10/5/2018 ? Diabetes mellitus type 2 in obese ? Hepatitis C treated a long time ago in a clinical trial. ? Hypertension ? Insomnia, unspecified type 10/5/2018 ? Personal history of kidney stones 10/5/2018 ? Right hip pain 7/12/2018 ? Smoker unmotivated to quit
- Andere Medikamente
- amLODIPine (NORVASC) 10 MG tablet TAKE 1 TABLET BY MOUTH EVERY DAY ? aspirin 81 MG tablet take 1 Tab by mouth Daily. ? atorvastatin (LIPITOR) 20 MG tablet Take 1 tablet by mouth daily. ? Blood Glucose Monitoring Suppl (FREESTYLE LITE) DEVI
- Allergien
- Victoza
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 07.01.2023
- Impfdatum
- 07.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
no adverse event reported, but after completion of the vaccine, patient reported she never received primary doses yet on the consent form she said she completed the primary doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 07.01.2023
- Impfdatum
- 04.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect route of product administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- seasonal allergies cough
- Vorgeschichte
- hypertension type 2 diabetes long covid DOE from covid pneumonia 1/2021
- Andere Medikamente
- losartan 100mg amiloride 5mn amlodipine 5mg levothyroxine 75mg metformin 5oomg atorvastatin 40mg aspirin 81mg azelastine nose spray robitussin DM cough syrup
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 06.01.2023
- Impfdatum
- 24.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
COVID 19 /Sore throat, Weakness; This is a spontaneous report received from a non-contactable reporter(s) (Pharmacist). The reporter is the patient. A 43-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Dec2022 at 17:00 as dose 4 (booster), single (Lot number: GJ3274) at the age of 43 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 3 (booster), single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: COVID-19 (non-serious) with onset 29Dec2022, outcome "unknown", described as "COVID 19 /Sore throat, Weakness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of covid-19. Additional information: The patient had no known allergies. Patient started COVID symptoms on 29Dec2022 late night with very bad sore throat. The next day on 30Dec2022 patient started feeling weak and tested positive for COVID on 31Dec2022 morning. Patient started taking paxlovid. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221231; Test Name: covid test; Test Result: Positive ; Comments: tested positive for Covid on 31Dec2022 morning
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 03.01.2023
- Beginn
- 03.01.2023
- 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
No adverse event
Symptomtext
Patient did not have any adverse reactions to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Not known
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 23.12.2022
- Beginn
- 23.12.2022
- 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
Gave Pfizer Bivalent 12 and older given to pt. No side effects reported by parents to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 03.01.2023
- Impfdatum
- 03.01.2023
- Beginn
- 04.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
NO APPARENT ADVERSE REACTION, BIVALENT VACCINE ADMINISTERED FOR DOSE 1 INSTEAD OF MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 03.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- 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: Wrong Age for Vaccine Given-
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
- 49,0
- Geschlecht
- F
- Eingang
- 02.01.2023
- Impfdatum
- 29.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
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
- CT
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 02.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series 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
- KS
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 31.12.2022
- Impfdatum
- 27.12.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus left ear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Allergy shots, daily multi vitamin
- Allergien
- Mold
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 31.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 31.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 30.12.2022
- Impfdatum
- 29.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Bivalent booster given erroneously as Primary series. Patient's and his caregiver notified. Primary care Provider notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Gave patient a 12 year + bivalent booster. Should have received a 5-11 booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- down syndrome, GERD
- Andere Medikamente
- omeprazole, ondansetron, loratadine, hydrocortisone cream
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 30.10.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 58,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Patient received a second dose of the pfizer bivalent vaccine which is not within guidelines. Patient has reported no adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 26.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 7,0
- Dosis
- N/A
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Herpes ophthalmic
Herpes zoster
Symptomtext
Developed Shingles symptoms one week after the booster vaccine. Shingles outbreak was to the left side of the face and eye.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes ophthalmic
- Hospital-Tage
- -
- Labordaten
- Dr. visit (urgent care/ Teledoc) on 12-24-2022. Prescribed Valacyclovir HCL 1 gram tablet three times per day. Symptoms worsened on 12-25-2022 and I went to the Emergency Room. Prescribed Oxycodone, and eye drops, and erythromycin 5 mg ointment 4 times a day. Have follow up with eye doctor to check the retina of the left eye.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prednisone Breo Elipta Fluticisone
- Allergien
- Sulfa Gluten
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 25.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- 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
Error: Dose in Series 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
- CO
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 19.12.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Pt received a bivalent Pfizer dose when the patient should have received 2nd Monovalent Pfizer dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 23.12.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Both the patient and the Mom were sent to the LPN's station for a Pfizer Booster and Flu vaccine. In error, the pediatric patient was administered the Adult Pfizer Bivalent booster. The parent was informed of this error. Follow up for assessment of any symptoms will be performed by an RN with the parent on 12/24/2022 and 12/25/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Non
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 21.12.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Patient was given a second bivalent vaccination. Patient showed no symptoms or signs of distress at time of discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, Prediabetes
- Andere Medikamente
- MetFormin HCI ER 500 mg, Losartan Potassium 100 mg, Wellbutrin XL 150 mg, Atorvastatin Calcium 40 mg
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- 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: Wrong Age for Vaccine Given-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product leakage
Underdose
Symptomtext
when giving vaccine it leaked out of the syringe; when giving vaccine it leaked out of the syringe; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 68-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Dec2022 as dose number unknown (booster), single (Lot number: GJ3274, Expiration Date: 31Jan2023) at the age of 68 years, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "High cholesterol" (unspecified if ongoing), notes: High cholesterol takes medication for this. There were no concomitant medications. Vaccination history included: flu shot (had a flu shot 25Sep2022), administration date: 25Sep2022, when the patient was 68-year-old; Pfizer covid-19 vaccine (Dose number unknown), administration date: Oct2021, when the patient was 67 years old, for COVID-19 immunization; Pfizer covid-19 vaccine (Dose number unknown , lot FK9895), administration date: Apr2022, when the patient was 67 years old, for COVID-19 immunization. The following information was reported: UNDERDOSE (non-serious), PRODUCT LEAKAGE (non-serious) all with onset 16Dec2022, outcome "unknown" and all described as "when giving vaccine it leaked out of the syringe". Additional information: This hasn't happened before, and they have used these needles and syringes before with no issues. It leaked out where the needle meets the syringe at the luer-lock junction. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product leakage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: High cholesterol (High cholesterol takes medication for this)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series 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
- OH
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
NO adverse event. pt would like to have 1st dose of shingle. I gave Varivax.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- -
- Andere Medikamente
- n/a
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syringe issue
Symptomtext
Error: Leaking from Syringe-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 19.12.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient presented to the clinic with her husband. They both came in to receive their flu and covid vaccinations. Patient requested the high-dose flu vaccine because of her medical history. She received the high-dose flu vaccine even though she is under the age of 65. Patient was monitored for 10 minutes after the vaccine administration and had no adverse reaction. She then left the clinic with her husband after he received his vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- patient stated she was immunocompromised and required the high dose flu vaccine
- Andere Medikamente
- unknown
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 16.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient given bivalent booster dose for 1st covid vaccine series dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 16.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient has not received any doses of primary series previously. Patient received bivalent booster as 1st dose today (should have been monovalent). Per CDC guidance on clinical considerations site, will continue with schedule of dose 2 (monovalent) in 3 weeks, dose 3 (monovalent) 4 weeks after dose 2, and 4th dose (bivalent) 2 months after dose 3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESRD on HD Hx kidney transplant on immunosuppresive therapy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
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
- Common Cold
- Vorgeschichte
- -
- Andere Medikamente
- Sertraline Vitamin D3 ashwagandha Biotin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bradycardia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bradycardia
- Hospital-Tage
- -
- Labordaten
- sent to hospital
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ashd, sick - sinus syndrome
- Andere Medikamente
- vitamin D3
- Allergien
- atorvastatin , dabigatran
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Poor quality product administered
Symptomtext
MA administered the Pfizer COVID-19 Vac Bivalent 16 hours after the vial was punctured. Vial was stored appropriately and was never out of temperature range. No issues reported from patient at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- MALIGNANT NEOPLASM OF UPPER-OUTER QUADRANT OF RIGHT BREAST, HYPERTENSION, HYPERLIPIDEMIA, CORONARY ARTERY DISEASE
- Andere Medikamente
- METROPROLOL, EZETIMIBE
- Allergien
- NONE PROVIDED
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
This was a duplicate bivalent dose. Patient previously received bivalent booster dose on 10/10/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESRD on HD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Bivalent COVID vaccine given instead of monovalent for primary dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 20.11.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Patient given COVID Bivalent vaccination instead of requested Influenza vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- Nasocort 1 spray daily-seasonal allergies and Ibuprofen 600mg as needed daily.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Interchange of vaccine products
Symptomtext
Patient was receiving Pfizer Bivalent vax during his in-clinic appointment at clinic instead of Moderna 2nd dose to complete his series. Pfizer Bivalent vaccine incorrectly administered for the primary series. Patient is aware and feels good, no symptoms. Per CDC guideline: Do not repeat dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
Instead of the patient receiving the monovalent primary dose, the patient was given the bivalent as her first vaccine. No adverse reaction noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- vaginal delivery/ postpartum, preeclampsia
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- keflex- tachycardia, nausea
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- 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 (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- 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 (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 11.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series 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
- MA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 11.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series 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
- NV
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series 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
- AR
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 13.11.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 13.11.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 13.11.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- -
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient has never had a pfizer vaccine and came for pfizer vaccine dose 1, instead given pfizer bivalent by provider on duty instead in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorgeschichte
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Andere Medikamente
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Allergien
- N/A. NO ADVERSE EVENT TO VACCINE. VACCINE OUTSIDE OF STORAGE REQUIREMENTS. REVACCINATION RECOMMENDED.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 06.12.2022
- Impfdatum
- 07.11.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Paranasal sinus hypersecretion
Respiratory syncytial virus test positive
SARS-CoV-2 test negative
Sleep disorder
Symptomtext
On 11/27/2022 in the morning around 8:00AM. I woke up with a Sinus drainage and cough. I couldn't sleep because of the cough. So on 11/30/2022 I called my doctor and she prescribed me with cough medication which didn't help. On 12/05/2022 I called my doctor again since the cough medication wasn't helping at all. She then prescribed me an antibiotics called amoxicillin. I just started taking it from yesterday. I have to take it for at least 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- 06DEC2022 COVID-19 test negative; RSV test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Sertraline; benazepril
- Allergien
- None
- Vorherige Impfungen
- COVID-19 vaccines usual symptoms for a day.
- Staat
- AR
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 05.12.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
N/A. NO ADVERSE EVENT. PATIENT WAS GIVEN VACCINATION THAT WAS STORED OUTSIDE OF REQUIRED TEMPERATURE FOR STORAGE. REVACCINATION REQUIRED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A. NO ADVERSE EVENT. PATIENT WAS GIVEN VACCINATION THAT WAS STORED OUTSIDE OF REQUIRED TEMPERATURE FOR STORAGE. REVACCINATION REQUIRED.
- Aktuelle Erkrankungen
- N/A. NO ADVERSE EFFECT. PATIENT WAS GIVEN VACCINE THAT WAS OUTSIDE OF RECOMMENDED TEMPERATURE STORAGE.
- Vorgeschichte
- N/A. NO ADVERSE EFFECT. PATIENT WAS GIVEN VACCINE THAT WAS OUTSIDE OF RECOMMENDED TEMPERATURE STORAGE.
- Andere Medikamente
- N/A. NO ADVERSE EFFECT. PATIENT WAS GIVEN VACCINE THAT WAS OUTSIDE OF RECOMMENDED TEMPERATURE STORAGE.
- Allergien
- N/A. NO ADVERSE EFFECT. PATIENT WAS GIVEN VACCINE THAT WAS OUTSIDE OF RECOMMENDED TEMPERATURE STORAGE.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 05.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Covid vaccine given after 24hr expiration, patient had no adverse reaction at that time. Nurse manager notified along with calling Pfizer for next step regarding if patient will need to be revaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 03.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
Dad was contacted by the pharmacy stave and given counseling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 03.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
The parents were contacted and made aware of the incorrect dosage. At the time there were no reported symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 03.12.2022
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received this vaccine by accident. When I checked in with the patients mom on 11/27 she reported that her daughter was feeling fine and was not experiencing fever, headaches, chills or body aches. She was acting as her usual self
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 02.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Postmenopausal haemorrhage
Symptomtext
Post menopausal bleeding second time after getting the Pfizer booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postmenopausal haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Valsertan
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Aphonia
Dysphonia
Endoscopy abnormal
Hyperkeratosis
Speech disorder
Symptomtext
Patient had to travel after the Vaccination. She travelled and by the time she landed there her voice became very hoarse. She visited the Physician and found to have Keratotic Patch on her vocal chord (Bilateral). Patient is a non-smoker and has no known allergies. This started on 17th Nov, 2022 and within a week she lost the voice almost completely. the voice back. Physicians/Specialists are treating her with medications and have advised if situation remains same may need surgery. She still have the symptom and cannot talk. She doesn't have any other symptoms - no fever, no runny nose, no allergic conditions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aphonia
- Hospital-Tage
- -
- Labordaten
- On 11/24/2022 - An Endoscopy was performed and patient was found to have Bilateral Keratotic Patch on Vocal Chords 0n 11/28/2022 - An Endoscopy was performed as a follow-up as the complaint persisted with similar results as previous.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None other than thyroid condition
- Andere Medikamente
- Levothroxine 88mcg - once daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 29.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient received 12+ bivalent at age 11years
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ADHD, anxiety
- Andere Medikamente
- celexa, guanfacine, vyvanse
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 20.11.2022
- Beginn
- 20.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Received the Bivalent and has never had a Pfizer vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Interchange of vaccine products
Symptomtext
Received Bivalent instead of the Mono. Never had a Pfizer before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 29.11.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Flushing
Oxygen saturation decreased
Respiratory tract congestion
Symptomtext
patient had pressure in her chest, face and chest became flushed. Had trouble clearing her throat. Oxygen saturation dropped to low 90's but returned to normal in a short time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multivitamin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Pt received bivalent booster instead of pfizer monovalent dose 1. The bivalent booster was expired by 12 hours. Pt reported no known side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 29.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Pt received expired bivalent booster. Pt reports no side effects after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- 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
this vaccine is for ages 12 and up, pt is 9.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- fluoride 2.2 mg tablet
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 26.11.2022
- Impfdatum
- 17.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Uveitis
Symptomtext
anterior, non-granulomatous uveitis of the left eye
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Uveitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- emtricitabine/tenofovir disoproxil fumarate, bupropion, duloxetine
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 25.11.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Symptomtext
Error: Diluent Administered Instead of Vaccine-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 43,0
- Geschlecht
- U
- Eingang
- 21.11.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- 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
No adverse event
Product storage error
Symptomtext
No adverse event; Expired Covid vaccine given. Vial opened Friday, November 18, 2022 and should have been tossed at the end of business day. Medical assistant came in Monday morning and gave a dose of the covid vaccine that was left over from Friday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 17.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
Patient received a bivalent booster at age 11, no adverse reactions occured
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 17.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Did not have prior series. No symptoms or negative outcome.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.11.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
None - vaccine error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Augmentin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Inadvertently gave bivalent booster dose instead of monovalent 2nd dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Patient was administered vaccine that had experienced temperature excursion during shipment and should have been quarantined. Quality report was not seen/received by provider prior to administering dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Patient was administered vaccine that had experienced temperature excursion during shipment and should have been quarantined. Quality report was not seen/received by provider prior to administering dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Patient was administered vaccine that had experienced temperature excursion during shipment and should have been quarantined. Quality report was not seen/received by provider prior to administering dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 31.10.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient was incorrectly administered Pfizer COVID19 bivalent booster instead of the first monovalent dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin, steroids
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 30.10.2022
- Impfdatum
- 30.10.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Throat irritation
Symptomtext
Pt reported scratchy throat after receiving the vaccinations (Pfizer Bivalent booster dose)- previously had Pfizer vaccine series, and the Flublok vaccination- occurred on 10/30/22 at 3:30pm, Provider administered Benadryl 12.5mg IM and continued to monitor the patient for 20 minutes, pt was stable and no acute distress when leaving the clinic- O2 sat was 98% and patient was calm with normal respirations, no complaints of difficulty swallowing or breathing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Throat irritation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -