VAERS Reports GJ6738

VAERS 2728608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 29.12.2023
Impfdatum: 30.11.2022
Beginn: 29.11.2023
Tage bis Beginn: 364,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Atrial fibrillation Atrial pressure increased Blood magnesium normal Blood potassium decreased Cough Diastolic dysfunction Dyspnoea Echocardiogram abnormal Ejection fraction COVID-19 Cardiac failure Chest X-ray normal Chills Condition aggravated Electrocardiogram normal End stage renal disease Glycosylated haemoglobin normal

Symptomtext

Patient is a 78 y.o. female patient of MD with history of history of CAD, HFFpEF, Atrial Fibrillation on coumadin, hypertension, hyperlipidemia, type 2 diabetes mellitus, ESRD in HD MWF schedule, chronic anemia presented to Hospital with worsening shortness of breath with hypoxia associated with dry cough, chills, generalized body ache. Reports she could not able finish dialysis due to worsening shortness of breath. Acute hypoxemic resp failure - Resolved COVID-19 infection Volume overload 2/2 ESRD with partial HD session HFpEF, mild decompensation P/w worsening shortness of breath associated with dry cough, chills, generalized body ache. Required 2L NC on admission, baseline room air Afebrile, no leukocytosis, HDS CXR no pneumothorax, pleural effusion or focal airspace consolidation. Started on oral decadron 6 mg for 10 days Volume mgmt via HD Albuterol inhaler, mucinex scheduled, PRN robitussin-DM Pulm toilet Now stable on RA Hypokalemia K 3.2, Mg wnl Likely 2.2 poor PO intake Hold off on PO replacement given ESRD on HD Recommend repeat BMP in 1 week Elevated troponin Chronic HFpEF A Fib S/p WATCHMAN device Denied chest pain Troponin elevated but adynamic, likely type II in setting of ESRD EKG no acute ischemic changes noted CXR Non acute S/p successful placement of WATCHMAN device 11/17/23 2/2023 ECHO with LVEF>70%, G2DD with elevated LAP. Mild pulmonary HTN; RVSP 55 Continue home aspirin and coreg pharmacy to dose coumadin Hypertension Continue home amlodipine, coreg and hydralazine ESRD on HD MWF Anemia of chronic kidney disease Consult nephrology for maintenance HD. Stable hemoglobin 8.4 (baseline 8-10) No active bleeding noted Monitor Labs T2DM Well controlled A1c 4.7 Patient reports common AM hypoglycemic episodes Decreased home lantus SSI, DM diet Recommend BG log and follow up with PCP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2726894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 22.12.2023
Impfdatum: 14.11.2022
Beginn: 22.10.2023
Tage bis Beginn: 342,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Bundle branch block right COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Electrocardiogram ST segment abnormal Respiratory failure Rhinovirus infection Sinus rhythm Supraventricular extrasystoles Troponin increased Ventricular extrasystoles

Symptomtext

Patient is a 73 y.o. male patient of DO with history of COPD, atrial fibrillation, who presented to Hospital with shortness of breath. COPD exacerbation: - resolving Acute on chronic hypoxemic respiratory failure: baseline of 2 liters CXR consistent with COPD DuoNebs scheduled Albuterol PRN Patient is back to his baseline of 2 liters, will discharge with close otupatient follow up Rhinovirus COVID 19 Pulmonary following - added remdesvir and dexaethadone. Patient is back to his baseline of 2 liters, will discharge with close otupatient follow up Elevated troponin: down tredning Due to COPD exacerbation EKG sinus rhythm with occasional PVCs and PACs with RBBB and marked ST abnormality; possible inferior subendocardial injury Atrial fibrillation: CAD: HTN: HLD: Eliquis and sotalol, losartan, Toprol, statin Plavix

Weitere VAERSDATA-Felder

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

VAERS 2722226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 08.12.2023
Impfdatum: 14.11.2022
Beginn: 02.12.2023
Tage bis Beginn: 383,0
Dosis: 4
Route/Site: IM / UN

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

Acute respiratory failure Anxiety Blood creatinine increased Blood sodium decreased COVID-19 Cardiomegaly Chest X-ray abnormal Chills Cough Diarrhoea Dyspnoea Hypertension Lung disorder Pleural effusion Positive airway pressure therapy Pulmonary congestion Pyrexia Respiratory tract congestion

Symptomtext

Admit date: 12/2/2023 Discharge date: 12/05/2023 Admitting Physician: DO Attending Physician at the Time of Discharge: DO Primary Care Physician: MD, Reason for Admission: Acute hypoxic respiratory failure secondary to covid infection Brief Summary of Hospital Stay: As per H&P Patient is a 80 YO female with a past medical history of PPM, COPD, T2DM, HTN, Atrial fibrillation on Xarelto, HLD, asthma and obesity that presents to the emergency department with complaints of worsening dyspnea and shortness of breath over the past 2 days. Patient's husband is COVID positive and is currently admitted to the hospital. Patient notes that she has had increased coughing with congestion that was worse today than previous days. She has felt some chills and fever though did not check temperature. She called EMS today because she could not catch her breath and became very anxious. She had 2 episodes of diarrhea prior to arrival. EMS noted that patient's SpO2 was 85% on RA. Patient was also given 125 mg of Solu-medrol and a Duoneb treatment. They placed her on non-rebreathing Patient denies any diaphoresis, numbness, tingling, unilateral muscle weakness, headache, dizziness, dysphagia, chest pain, sputum production, hemoptysis, nausea, vomiting, abdominal pain, dysuria, change in bowel regimen, hematochezia or melena. In the ED, patient presented hypertensive with BP 187/91. Was placed on BiPap momentarily for 88% and was weaned to 2L nasal canula. Labs notable for Na 128, serum creatinine 1.4. COVID PCR positive. CXR showing cardiomegaly and pulmonary vascular congestion with small bilateral pleural effusions and bibasilar airspace disease could be due to atelectasis/scarring. Patient is being admitted under general medicine service for further work-up and management Hospital Course: Patient was started on steroids, Remdesivir was not given, as patient declined. She continued her home medication, as well as prn duonebs. Symptoms improved. She was weaned off O2. PT recommends home independently. Upon exam this morning, patient feeling overall better. Cough persists but has improved since admission. Patient was medically optimized. Vital signs were stable for discharge. Discharged to Home Health Care.

Weitere VAERSDATA-Felder

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

VAERS 2692103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 92,0
Geschlecht: F
Eingang: 06.10.2023
Impfdatum: 01.12.2022
Beginn: 08.09.2023
Tage bis Beginn: 281,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Anaemia Angiogram Angiogram pulmonary normal Anticoagulant therapy Atrial fibrillation Back pain Bacterial test positive Bacteriuria Blood culture positive CHA2DS2-VASc-score COVID-19 Chest pain Condition aggravated Cough Culture urine positive Dysuria Escherichia test positive

Symptomtext

Patient is a 93 y.o. female with a history of a fib, T1DM, CML, chronic thrombocytopenia who presented to ED 9/8/2023 for chest and back pain with cough and fevers. In ED, she was found to be in a fib with RVR, COVID 19 positive and with bacteruria. CTA TAP nonacute. She was transferred to Facility 9/8/2023 for ongoing management. 1. Atrial fibrillation with RVR: known history of A fib. CHADS2Vasc 5. Follows with Dr. (cardio). S/p cardizem drip on admit. Improved on arrival to Facility. BB and eliquis continued. 2. COVID-19 Infection: presented with sore throat, fevers, cough on 9/7/23. Vaccinated. Positive test 9/8/23. CTPA nonacute on admit. Started on decadron on admit due to hypoxia, continued on discharge; pt requested paxlovid. Isolation per protocol. 3. Acute Respiratory Failure with Hypoxia: in setting of COVID. Required 2LPM per NC in ED. CTPA on admit nonacute; no PE. Weaned off O2 9/9/23. 4. Bacteruria: with increased frequency and mild dysuria as well as occasional right flank pain PTA. UA with bacteria on admit; Cx 9/8/23 grew >10K EColi. 1 of 2 blood cx 9/8/23 grew strep mitis; suspect contaminant. IV Rocephin completed 9/10/23. 5. T1DM: per history. Follows with Dr. (endo). A1c 6.1 on 8/30/23. Continued home dose of Lantus on admit, dose reduced her carb coverage on admit as she reported not being exact at home. 6. CML: per history, follows with Dr. (heme/onc). Previously on hydroxyurea, stopped in 7/2023 due to minimal improvement in labs. Continued outpatient follow up 7. Chronic Thrombocytopenia: in setting of CML. Plt on admit 44, baseline around 50-80. 8. Anemia: in setting of CML. Hbg on admit at baseline at 10.7. 9. Code status: full code, confirmed on admit 10. DVT Prophylaxis: Eliquis

Weitere VAERSDATA-Felder

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

VAERS 2667065

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 07.08.2023
Impfdatum: 07.12.2022
Beginn: 13.07.2023
Tage bis Beginn: 218,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19 Chronic obstructive pulmonary disease Computerised tomogram liver abnormal Computerised tomogram normal Computerised tomogram thorax normal Condition aggravated Confusional state Cough Electrocardiogram normal Haemorrhoids Hepatic lesion Hypoxia Imaging procedure abnormal Mental status changes Metabolic encephalopathy Proctalgia Rectal haemorrhage

Symptomtext

Patient is a 86 y.o. female patient of, MD with history of CAD, hypertension, hyperlipidemia, former smoker, breast cancer presented to Hospital from nursing facility with hypoxia and confusion. Acute metabolic encephalopathy resolved Etiology not clear, CT is negative Urine analysis was normal, per family history of frequent UTIs As per daughter mental status back to baseline Acute respiratory failure with hypoxia Probable COPD 2/2 COVID-19 infection? Has about a 30-pack-year history of smoking but quit about 30 years ago per patient and daughter. CT PE study negative for acute abnormality Auscultation revealed clear lung sounds, without wheezes. No indication for Auscultation revealed clear lung sounds, without wheezes. No indication for albuterol at this time. Patient denies shortness of breath. Has slight cough. Required 2 L but able to wean off to room air, encourage incentive spirometer Covid-19 Virus Infection Date of onset of symptoms: Unsure Symptoms present on admission: Confusion Date of covid positive test: 7/13/2023 Vaccination status: Unknown Imaging: CT without evidence of PE or pneumonia Oxygen requirements on admission: 2L Current oxygen requirements: On room air Medical therapy: steroids, cont on decadron for 6 more days at dc Consultants following: N/A Anticipated special isolation end date: 7/23/2023 Rectal bleeding with pain History of internal and external hemorrhoids, on rectal exam noted to have multiple external hemorrhoids with pain Frank BRBPR noted, started on sitz bath with Anusol HC Surgery consulted, recd rectal MRI given abnormal finding on rectal exam Daughter was unsure if they want to proceed with rectal MRI. Continue maximum medical treatment and follow-up with surgery in 2 weeks as an outpatient for possible anoscopy and then discuss with family whether or not to pursue additional testing Coronary artery disease No history of chest pain EKG nonacute, troponin 19, recheck is pending Continue cardioprotective medications Abnormal liver imaging H/o breast ca CT showed right hepatic lobe ill-defined low-density heterogeneous lesion With history of breast cancer malignancy is on differential Discussed with son-in-low, family not considering aggressive measures Possible liver mets Outpatient MRI if family will reconsider Vascular dementia Continue ASA/statin Essential hypertension Continue home medications As needed hydralazine for limited BPs above 170 systolic RLE edema Chronic. Right lower extremity venous Doppler-interval resolution of common femoral vein and right great saphenous vein noted Daughter notes that patient might not be able to take blood thinners if needed though since she has had bleeding complications in the past. History of breast cancer Continue on Femara

Weitere VAERSDATA-Felder

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

VAERS 2657672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 18.07.2023
Impfdatum: 12.12.2022
Beginn: 23.03.2023
Tage bis Beginn: 101,0
Dosis: 4
Route/Site: IM / RA

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

Acute myocardial infarction Diabetic nephropathy

Symptomtext

I21.4 ACUTE NON ST ELEVATION MI 3/27/2023 ACUTE NON ST ELEVATION MI I21.4 ACUTE NON ST ELEVATION MI 3/27/2023 ACUTE NON ST ELEVATION MI I21.4 ACUTE NON ST ELEVATION MI 3/27/2023 DM 2 W RENAL MANIFESTATION

Weitere VAERSDATA-Felder

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

VAERS 2653139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 91,0
Geschlecht: F
Eingang: 06.07.2023
Impfdatum: 21.11.2022
Beginn: 10.01.2023
Tage bis Beginn: 50,0
Dosis: 5
Route/Site: IM / LA

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

Cerebrovascular accident

Symptomtext

ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2652813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 05.07.2023
Impfdatum: 25.11.2022
Beginn: 15.01.2023
Tage bis Beginn: 51,0
Dosis: 5
Route/Site: IM / LA

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

Acute respiratory failure Pulmonary embolism

Symptomtext

ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE ACUTE PULMONARY EMBOLISM

Weitere VAERSDATA-Felder

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

VAERS 2652368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 04.07.2023
Impfdatum: 29.11.2022
Beginn: 31.03.2023
Tage bis Beginn: 122,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure COVID-19 Chest X-ray abnormal Dyspnoea Lung opacity Pleural effusion Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

He is a 68 y.o. male patient of MD with history of COPD/Emphysema, Amyloidosis, Asthma, Beta Thalassemia, PAF s/p PPM and Watchman device, DM2, HFpEF, HTN, OAB, Prostate Cancer presented to the Medical Center with shortness of breath found to have COVID-19 . Acute Respiratory Failure with hypoxia, resolved Presented with shortness of breath Sat > 90% on room air in ER but increased work of breathing Secondary to COVID-19 Weaned to room air (3/31) Pulm followed Covid-19 Virus Infection Date of onset of symptoms: 3/30 Symptoms present on admission: Shortness of breath Date of covid positive test: 3/31 Vaccination status: vaccinated and boosted Imaging: CXR (3/30) with mild perihilar opacities, interstitial thickening, small R pleural effusion Oxygen requirements on admission: BIPAP, for increased work of breathing, no hypoxia Current oxygen requirements: Room air Medical therapy: steroids, will discharge on 6mg dexamethasone to complete 10 day course Consultants following: Pulm Anticipated special isolation end date: 4/10/23 COPD/Emphysema Asthma No acute exacerbation Continue home Atrovent, Albuterol, Breo Ellipta, Spiriva DM2, not on long term insulin A1C pending Holding home jardiance, linagliptan SSI Resume home meds at discharge HTN Continue home aldactone and torsemide Chronic HFpEF EF 60-65% per history Euvolemic on exam Continue home aldactone and torsemide PAF S/P PPM and Watchman Continue home amiodarone Continue home eliquis Gout Continue home allopurinol Pt states not taking colchicine BPH Continue home flomax

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2651994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 03.07.2023
Impfdatum: 02.12.2022
Beginn: 01.01.2023
Tage bis Beginn: 30,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Chronic respiratory failure Hypoxia Respiratory failure Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPOXIA 1/17/2023 -- 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: -

VAERS 2651432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 30.06.2023
Impfdatum: 08.12.2022
Beginn: 18.01.2023
Tage bis Beginn: 41,0
Dosis: 5
Route/Site: IM / LA

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

Acute myocardial infarction

Symptomtext

ACUTE NON ST ELEVATION MI ACUTE NON ST ELEVATION MI (NSTEMI), TYPE 2 MI (SUPPLY/DEMAND)

Weitere VAERSDATA-Felder

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

VAERS 2651289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 30.06.2023
Impfdatum: 19.12.2022
Beginn: 09.02.2023
Tage bis Beginn: 52,0
Dosis: 5
Route/Site: IM / RA

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

Acute myocardial infarction Acute respiratory failure

Symptomtext

ACUTE NON ST ELEVATION MI ACUTE HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2651254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 30.06.2023
Impfdatum: 23.12.2022
Beginn: 26.12.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / RA

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

Acute respiratory failure Chronic respiratory failure Obstructive sleep apnoea syndrome Respiratory failure Symptom recurrence

Symptomtext

OBSTRUCTIVE SLEEP APNEA ACUTE HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 3/20/2023 -- 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: -

VAERS 2650897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 29.06.2023
Impfdatum: 04.01.2023
Beginn: 12.01.2023
Tage bis Beginn: 8,0
Dosis: 5
Route/Site: IM / RA

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

Acute myocardial infarction

Symptomtext

ACUTE NON ST ELEVATION MI

Weitere VAERSDATA-Felder

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

VAERS 2650442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 28.06.2023
Impfdatum: 29.12.2022
Beginn: 17.02.2023
Tage bis Beginn: 50,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Chronic respiratory failure Respiratory failure Sepsis

Symptomtext

J96.00 ACUTE RESPIRATORY FAILURE 2/26/2023 SEPSIS UNSPECIFIED ORGANISM J96.12 CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 4/25/2023 SEPSIS UNSPECIFIED ORGANISM J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/22/2023 SEPSIS UNSPECIFIED ORGANISM J96.22 ACUTE ON CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 2/22/2023 SEPSIS UNSPECIFIED ORGANISM

Weitere VAERSDATA-Felder

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

VAERS 2650441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 28.06.2023
Impfdatum: 08.02.2023
Beginn: 16.03.2023
Tage bis Beginn: 36,0
Dosis: 4
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2650338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 28.06.2023
Impfdatum: 09.12.2022
Beginn: 23.12.2022
Tage bis Beginn: 14,0
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 HYPOXEMIC RESPIRATORY FAILURE 1/2/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

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

VAERS 2648309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 30.12.2022
Beginn: 23.01.2023
Tage bis Beginn: 24,0
Dosis: 5
Route/Site: IM / LA

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

Acute respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE

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

VAERS 2644716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 89,0
Geschlecht: F
Eingang: 13.06.2023
Impfdatum: 21.11.2022
Beginn: 11.04.2023
Tage bis Beginn: 141,0
Dosis: 4
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

J96.00 ACUTE RESPIRATORY FAILURE 4/11/2023 ACUTE RESPIRATORY FAILURE

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

VAERS 2643559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 09.06.2023
Impfdatum: 12.12.2022
Beginn: 23.03.2023
Tage bis Beginn: 101,0
Dosis: 5
Route/Site: IM / LA

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

Acute myocardial infarction Angina pectoris Troponin I increased

Symptomtext

STABLE ANGINA 2/6/2023 ELEVATED TROPONIN I ACUTE NON ST ELEVATION MI 3/22/2023 ELEVATED TROPONIN I

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

VAERS 2642274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 07.06.2023
Impfdatum: 08.12.2022
Beginn: 23.12.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: IM / LA

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

Deep vein thrombosis Pulmonary embolism

Symptomtext

ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN ACUTE PULMONARY EMBOLISM

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

VAERS 2641114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 05.06.2023
Impfdatum: 15.11.2022
Beginn: 14.05.2023
Tage bis Beginn: 180,0
Dosis: 5
Route/Site: - / -

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

Angiogram pulmonary abnormal Anticoagulant therapy Anxiety Asthenia COVID-19 Cardiac failure congestive Cardiomyopathy Condition aggravated Discomfort Ejection fraction abnormal Epistaxis Humerus fracture Hypoxia Left ventricular failure Muscular weakness Pneumonia Procalcitonin normal Pulmonary embolism

Symptomtext

5/14/2023 - 5/21/2023 (7 days) HEART CENTER DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute pulmonary embolism, unspecified pulmonary embolism type, unspecified whether acute cor pulmonale present HOSPITAL COURSE: Patient is a 91 y.o. male with medical history of asthma, HFreF 45-50%, HTN, hx of complete heart block s/p pacemaker, hx of duodenal ulcer and upper GI bleed, frequent falls, vitamin-D deficiency, CKD with unknown baseline and recent medical hx of hospitalization for left humerus fracture 5 months ago who presented to the ER 5/13/23 after syncopal episode at Rehabilitation Center, was found to be hypoxic and covid 19 positive with acute b/l multifocal occlusive and nonocclusive emboli also involving the distal left main pulmonary artery without evidence of heart strain on CTA chest. ? Patient was seen by the team however conservative management was recommended. He received IV heparin and was transitioned to oral Eliquis ? In regards to COVID-19 infection and hypoxic respiratory failure and tracheobronchitis patient treated with steroids (Decadron 6mg, on D#6 of 10 on discharge day) and antibiotic ( completed azithromycin inpatient), with significant improvement in respiratory status noted as of 5/16 and current on room air on discharge day. ? In regards to cardiomyopathy with systolic heart failure and worsening ejection fraction cardiology was consulted to evaluate and give further recommendations at this time patient has been treated with IV Lasix for CHF exacerbation, then transition to home oral Lasix doses. ? In regards to generalized debility He states he was discharged to rehab but has been unable to return to independent living due to significant generalized weakness in his legs. He states he is mainly ambulating with a wheelchair. ? On 5/19/2023 patient had an episode or right epistaxis, ENT consulted and found a nasal cavity evaluated, large blood clots removed, light oozing with removal of blood clots, hemostatic powder to right nare, and placed of dissolvable hemopore packing to right nare. Suggest starting aggressive local nasal hydration with saline sprays (2 sprays to each nostril TID for 2 weeks), and apply a small dab of bacitracin ointment to front of each nostril, just inside the vestibule, and genitally pinch the nostril closed to spread the ointment against the nasal septum. Also recommended may use Afrin nasal spray for any minor bleeds , followed by external pressure to the nose. and small amount of oozing is anticipated, however is epistaxis is uncontrolled would recommend Rhinorocket placement ? Patient also found to have a new left lung pneumonia on 5/19/2023 and was started on IV abx, however procalcitonin was negative and IV abx discontinued the following day. ? Patient was very anxious and was started on hydroxyzine 25 mg TID Patient medically stable to discharge to Rehabilitation Center on 5/21/23.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Wheelchair dependent Asthma Complete heart block s/p pacemaker HFrEF 45-50% Frequent falls hx of duodenal ulcer and upper GI bleed Vitamin D deficiency Chronic kidney disease-unknown baseline Acute pulmonary embolism, unspecified pulmonary embolism type, unspecified whether acute cor pulmonale present COVID-19 virus infection Acute b/l femoral vein DVT
Andere Medikamente: acetaminophen (TYLENOL) 325 MG CAPS albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 mg tablet bisacodyl (DULCOLAX)
Allergien: Celebrex [Celecoxib] Propoxyphene Tramadol
Vorherige Impfungen: -

VAERS 2640375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 02.06.2023
Impfdatum: 16.08.2022
Beginn: 09.10.2022
Tage bis Beginn: 54,0
Dosis: 5
Route/Site: UN / UN

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

Acute myocardial infarction Facial paresis Hemiparesis Ischaemic stroke Neuropathy peripheral Rectal haemorrhage

Symptomtext

NEUROPATHY 12/22/2022 BRIGHT RED BLOOD PER RECTUM ACUTE NON ST ELEVATION MI 10/8/2022 BRIGHT RED BLOOD PER RECTUM ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 10/9/2022 BRIGHT RED BLOOD PER RECTUM LEFT FACIAL MUSCLE WEAKNESS 10/8/2022 BRIGHT RED BLOOD PER RECTUM NEUROPATHY 12/22/2022 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY ACUTE NON ST ELEVATION MI 10/8/2022 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 10/9/2022 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY LEFT FACIAL MUSCLE WEAKNESS 10/8/2022 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2639676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 01.06.2023
Impfdatum: 21.11.2022
Beginn: 19.12.2022
Tage bis Beginn: 28,0
Dosis: 5
Route/Site: IM / RA

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

Acute myocardial infarction Acute respiratory failure Glaucoma Hypoxia

Symptomtext

ACUTE NON ST ELEVATION MI (NSTEMI), TYPE 2 MI (SUPPLY/DEMAND) 12/18/2022 BILAT GLAUCOMA SUSPECT ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/18/2022 BILAT GLAUCOMA SUSPECT HYPOXIA 1/3/2023 BILAT GLAUCOMA SUSPECT

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

VAERS 2617643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: MN
Alter: 70,0
Geschlecht: F
Eingang: 19.04.2023
Impfdatum: 26.12.2022
Beginn: 05.01.2023
Tage bis Beginn: 10,0
Dosis: N/A
Route/Site: IM / LA

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

Acute respiratory failure Bronchoalveolar lavage abnormal Bronchoscopy COVID-19 COVID-19 pneumonia Cough Dyspnoea Pneumonia Respiratory pathogen panel SARS-CoV-2 test positive Sepsis

Symptomtext

Patient with history of breast cancer and lymphoma. She was seen in the ED on 1/5/23 for a breathing problem - she reported she had been coughing a lot and could barely catch her breath. This had been going on for about a month, and her symptoms had been progressively worsening. A COVID PCR test done in the ED resulted negative. Initially she was admitted 1/5/23 for sepsis due to multifocal community-acquired pneumonia and acute respiratory failure with hypoxia. On room air, SPO2 was 88%, and improved to 90% after being placed on 1-2L nasal cannula. Severe sepsis, acute hypoxemic respiratory failure eventually resolved after patient completed antibiotic treatment. On 1/17, a bronchoscopy was performed, and a right lower lobe BAL specimen was sent for respiratory panel, PCR. This returned positive for SARS-CoV-2. Patient was discharged 1/23/23 with discharge diagnoses including severe sepsis due to multifocal community-acquired pneumonia and acute respiratory failure with hypoxia, as well as moderate to severe COVID-19 and COVID pneumonia, among other diagnoses. Patient has received the primary COVID vaccine series and two boosters.

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

VAERS 2585548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj6738

kritisch

Staat: IN
Alter: 75,0
Geschlecht: M
Eingang: 22.02.2023
Impfdatum: 04.11.2022
Beginn: 19.02.2023
Tage bis Beginn: 107,0
Dosis: 4
Route/Site: SYR / -

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

Activated partial thromboplastin time normal Activated partial thromboplastin time shortened Acute respiratory failure Anion gap Asthenia Atypical pneumonia Base excess Basophil count normal Basophil percentage decreased Benign prostatic hyperplasia Blood bicarbonate increased Blood calcium normal Blood chloride normal Blood creatinine normal Blood culture Blood gases abnormal Blood glucose increased Blood lactic acid

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on February 19, 2023 18:30 Verified By: MD on February 19, 2023 18:30 Encounter Info: Hospital, Emergency, 02/19/23 - 02/19/23 * Final Report * History of Present Illness/Subjective Patient is 75-year-old male with past history significant for chronic obstructive lung disease, type 2 diabetes mellitus and hypertension presented emergency room with increasing symptoms of shortness of breath and dyspnea on exertion. Patient states that he was in the ER on the 14th with increased right lower extremity edema and erythema. At that time he was very short of breath and was unable to lay flat on his back and therefore was unable to get an ultrasound of his leg. His D-dimer was relatively low at that time as well. He also had symptoms of cough and congestion but these were secondary to what he was complaining about with regards to leg erythema.Chest x-ray at that time showed multifocal interstitial airspace disease suspicious for atypical pneumonia with small bilateral pleural effusions. He was discharged from the ER with oral antibiotic therapy. Since that time he states the erythema in his leg have improved slowly and to some degree but his shortness of breath cough and congestion have persisted. He still is unable to lay on his back because of shortness of breath and has had several episodes of paroxysmal nocturnal dyspnea. His peripheral edema is partially dependent. He has had low-grade fever at times but no chills. No symptoms of nausea, vomiting, or diarrhea. He presented back to the emergency room today having failed outpatient therapy. Patient does continue to smoke and reportedly up to 4 packs/day. He had been smoking up into the last ER visit. Of note the x-ray of his right foot did show a very small foreign body in his right heel that was to be evaluated as an outpatient by podiatry. O2 sat at home was found be 77% on room air he was placed on 6 L/min and given a nebulizer treatment by EMS prior to coming to the emergency room where his saturations were 95 to 97%. In the emergency room his blood pressure was 156/127, heart rate 112, temperature 36.5, respiratory rate 30, O2 sat 97% on 6 L per nasal cannula. Serology: White count 9100 over differential hemoglobin 13.1 hematocrit 40.3 and a platelet count of 205,000. Sed rate was found to be 45. INR 1.18 with a PTT of 33.4. Sodium 139 potassium 3.6 chloride of 98 bicarb 30 BUN 8 creatinine 0.89 and a blood sugar of 277. Magnesium 1.6 troponin I of 19 BNP 917 serum lactate 1.3. Venous blood gas pH 7.40 PCO2 55 PO2 of 40 CRP was 2.7. COVID PCR negative. Chest x-ray showed increasing multifocal bilateral airspace disease with small bilateral pleural effusions. Past medical history: Type 2 diabetes mellitus, hypertension, COPD, chronic pain syndrome, hyperlipidemia, osteoarthritis, low back pain, tobacco use 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) 36.5 (36.5-36.5) Temp (FAHR) 97.7 (97.7-97.7), BP 118/90 (118-179)/(86-127), HR 98 (98-135), RR 20 (16-38), O2Sat 99 (77-99) Neurologic (most recent and range for last 24 hours) GCS 15(15-15) Patient Weight Current Daily Weight: 104.5 kg 02/19/23 Patient Height Current Height: 177 cm 02/19/23 General: Alert and oriented, moderate respiratory distress sitting upright and leaning forward to catch his breath Eye: Extraocular movements are intact, Vision unchanged HEENT: Normocephalic, Normal hearing Neck: Supple, Non-tender, elevated jugular venous pressure Respiratory: Bibasilar crackles with accessory muscle use for breathing, diffuse scattered wheezing as well, Respirations are non-labored, Breath sounds are equal, No chest wall tenderness. Cardiovascular: Regular rate, Normal rhythm, No murmur, No gallop, Normal peripheral perfusion, Good pulses equal in all extremities, 2+ right lower extremity edema 1+ left lower extremity edema. Gastrointestinal: Soft, nontender, nondistended, normal bowel sounds, no evidence of hepatosplenomegaly. Lymphatics: No lymphadenopathy neck Musculoskeletal: Normal range of motion, generalized weakness Integumentary: Warm, Dry, No rash. Diffuse erythema extending from the distal foot up to just below the knee with associated warmth and edema of the right lower extremity Feet: Diffusely edematous right greater than left, diminished pulses and sensation bilaterally. Neurologic: Alert, Oriented, Normal motor function Psychiatric: Cooperative, Appropriate mood & affect, Normal judgment. Assessment/Plan 1. Acute respiratory failure with hypoxia Patient has acute on chronic respiratory failure. He has been placed on BiPAP at this time. It appears to be combination of CHF exacerbation with COPD exacerbation and underlying pneumonia. Unclear how much of the infiltrate is infection versus pulmonary edema. Will start on IV diuretic therapy in conjunction with frequent nebulizer treatments, RT protocol, IV Solu-Medrol and treatment of underlying infection. He will place in the intensive care setting and wean BiPAP accordingly. Continue ongoing RT protocol. We will check cardiac echo to evaluate LV systolic function continue to monitor renal function and electrolyte status closely. 2. Sepsis Patient does meet sepsis criteria although many of the symptoms may be associated with CHF and pulmonary edema. That being said sepsis protocol has been instituted. Given his findings of heart failure we will not bolus or start him on IV fluids at this time. Broad-spectrum IV antibiotic therapy has been started. Source of combination of cellulitis of the right lower extremity and pneumonia. 3. COPD exacerbation As above. Ongoing RT protocol. We stressed the need for him to stop smoking. Frequent nebulizer treatments in conjunction with IV Solu-Medrol and treatment of underlying infection ongoing. BiPAP therapy as needed and wean to O2 as best and quickly as possible. 4. CHF exacerbation This appears to be new onset. He has elevated jugular venous pressure, elevated BNP, what appears to be pulmonary edema on chest x-ray and significant peripheral edema. We will continue cardiac echo to evaluate LV systolic function. We will start him on ACE inhibitor and beta-blocker therapy once he is more stable hemodynamically. IV Lasix over the next 24 to 48 hours and monitor urine output as well as peripheral edema. Consider placing him on a Lasix drip at some point the near future. May consider also adding an nitrate and/or nitroglycerin for symptoms persist. 5. Cellulitis of right leg It appears he likely developed significant peripheral edema from either CHF or right-sided heart failure. Cardiac echo pending. Ill he placed on broad-spectrum IV antibiotic therapy. Wound and blood cultures pending. Continue close monitoring. 6. Multifocal pneumonia There appears to multifocal pneumonia on chest x-ray although it may represent pulmonary edema. Blood cultures x2 have been sent. Urine for Legionella and strep antigens both pending. Procalcitonin level pending as well. Continue treatment of underlying respiratory compromise. Broad-spectrum IV antibiotic therapy has been started. 7. Hypertension Blood pressure was elevated in the emergency room but now improving. We will titrate in his home medication as indicated. 8. Hyperlipidemia Noted. Restart home statin therapy 9. BPH (benign prostatic hyperplasia) Clinically stable at this time. We will start his Flomax therapy as well. 10. Tobacco use Noted. We will give him education regarding his need to stop smoking. And offer him treatment options to aid with this. GI and DVT prophylaxis have been addressed. Home medications were reviewed and appropriate medications ordered at this time. Total critical care time: Approximately 50 minutes?acute respiratory failure/CHF exacerbation/COPD exacerbation/sepsis/pneumonia/cellulitis Due to a high probability of clinically significant, life threatening deterioration, the patient required my highest level of preparedness to intervene emergently and I personally spent this critical care time directly and personally managing the patient. This critical care time included obtaining a history; examining the patient; pulse oximetry; ordering and review of studies; arranging urgent treatment with development of a management plan; evaluation of patient's response to treatment; frequent reassessment; and, discussions with other providers. This critical care time was performed to assess and manage the high probability of imminent, life-threatening deterioration that could result in multi-organ failure. It was exclusive of separately billable procedures and treating other patients and teaching time. Code Status None Recorded Chronic Problem List Anxiety BPH (benign prostatic hyperplasia) CHF exacerbation Chronic pain syndrome Chronic use of opiate for therapeutic purpose Chronic, continuous use of opioids Depression Emphysema/COPD Headache, migraine Hyperlipidemia Hypertension Insomnia Joint pain Low back pain Low vitamin D level Pain in joint involving multiple sites Pulmonary nodule Right carotid bruit Sepsis Tobacco use Type 2 diabetes mellitus Vitamin D deficiency Wrist joint pain Procedure/Surgical History ?Diabetic retinal eye exam (02/05/2019) ?Gallbladder (2012) ?Tonsillectomy Medications Home Medications (18) Active albuterol-ipratropium inh soln 2.5 mg-0.5 mg/3 mL See Instructions, INHALE 3ML BY MOUTH 4 TIMES DAILY Amaryl 4 mg oral tablet 4 mg = 1 Tablet, Orally, BID aspirin 81 mg oral tablet 81 mg = 1 Tablet, Orally, Daily atorvastatin 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily Augmentin 875 mg-125 mg oral tablet 1 Tablet, Orally, Q12H buDESOnide-formoterol 80 mCg-4.5 mCg/inh inhalation aerosol 2 Puff, Inhalation, BID cloNIDine 0.1 mg oral tablet 0.1 mg = 1 Tablet, Orally, TID, to take prn if blood pressure over 160/90 doxycycline monohydrate 100 mg oral tablet 100 mg = 1 Tablet, Orally, BID EpiPen 2-Pak 0.3 mg injectable solution 0.3 mg, PRN, IM, ONCE Glucophage XR 500 mg oral tablet, extended release 1,000 mg = 2 Tablet, Orally, BID, for sugar losartan 100 mg oral tablet 100 mg = 1 Tablet, Orally, Daily mirtazapine 30 mg oral tablet See Instructions, TAKE 1 TABLET BY MOUTH EVERY NIGHT AT BEDTIME Norvasc 10 mg oral tablet 10 mg = 1 Tablet, Orally, Daily pantoprazole 40 mg oral delayed release tablet 40 mg = 1 Tablet, Orally, Daily ProAir HFA 90 mCg/inh inhalation aerosol 2 Puff, PRN, Inhalation, Q6H Singulair 10 mg oral tablet 10 mg = 1 Tablet, Orally, QPM, for cough / allergies tamsulosin 0.4 mg oral capsule See Instructions, TAKE ONE CAPSULE BY MOUTH DAILY AT BEDTIME FOR PROSTATE AND BLOOD PRESSURE Vitamin D3 1000 intl units oral capsule 1,000 IntlUnits = 1 Capsule, Orally, Daily Active Scheduled Inpatient Medications None Reported One-Time Medications Given 02/18/23 00:00:00 TO 02/19/23 18:29:31 albuterol (albuterol 2.5 mg/0.5mL (0.5%) inhalation solution), Inhalation SOLN, 10 mg, Neb Inhal, ONCE, (1 DOSE 02/19/23 06:09:00) albuterol (albuterol 2.5 mg/0.5mL (0.5%) inhalation solution), Inhalation SOLN, 5 mg, Neb Inhal, ONCE, (1 DOSE 02/19/23 07:42:00) albuterol (albuterol 2.5 mg/0.5mL (0.5%) inhalation solution), Inhalation SOLN, 5 mg, Neb Inhal, ONCE, (1 DOSE 02/19/23 17:21:00) cefePIME, Injection, 1 GM, IV Push, ONCE, (1 DOSE 02/19/23 07:25:00) doxycycline, Injection, 100 mg, IVPB, ONCE, (1 DOSE 02/19/23 07:29:00) Lactated Ringers (Lactated Ringers - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 02/19/23 07:00:00) magnesium sulfate, Infusion, 2 GM, IVPB, ONCE, (1 DOSE 02/19/23 07:29:00) magnesium sulfate, Infusion, 2 GM, IVPB, ONCE, (1 DOSE 02/19/23 07:51:00) Vancocin, Injection, 2 GM, IVPB, ONCE, (1 DOSE 02/19/23 08:38:00) PRN Medications (0600 - 0559) from 02/18 - 02/19 None Reported Allergies Bee Stings (critical) Cymbalta (critical) sulfa drugs (critical) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment Married, 2 children Substance Abuse Denies Tobacco Tobacco Use: 10 or more cigarettes (1/2 pack or more)/day in last 30 days. Family History Lung cancer..: Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 9.1 k/cumm (02/19/23 06:44:00) RBC: 4.53 million/cumm (02/19/23 06:44:00) Hgb: 13.1 GM/dL Low (02/19/23 06:44:00) Hct: 40.3 % (02/19/23 06:44:00) MCV: 89 fL (02/19/23 06:44:00) MCH: 28.8 pg (02/19/23 06:44:00) MCHC: 32.4 GM/dL (02/19/23 06:44:00) RDW: 14.5 % (02/19/23 06:44:00) Platelet: 285 k/cumm (02/19/23 06:44:00) MPV: 9.7 fL (02/19/23 06:44:00) Neutrophils %: 68 % (02/19/23 06:44:00) Lymphocytes %: 13 % (02/19/23 06:44:00) Monocytes %: 8 % (02/19/23 06:44:00) Eosinophils %: 10 % (02/19/23 06:44:00) Basophils %: 0 % (02/19/23 06:44:00) Absolute Neutrophil: 6.2 k/cumm (02/19/23 06:44:00) Absolute Lymphocyte: 1.2 k/cumm (02/19/23 06:44:00) Absolute Monocyte: 0.7 k/cumm (02/19/23 06:44:00) Absolute Eosinophil: 0.9 k/cumm High (02/19/23 06:44:00) Absolute Basophil: 0.1 k/cumm (02/19/23 06:44:00) Sed Rate: 45 mm/hr High (02/19/23 06:44:00) Chemistry: Sodium SerPl QN: 139 mmol/L (02/19/23 06:44:00) Potassium SerPl QN: 3.6 mmol/L (02/19/23 06:44:00) Chloride SerPl QN: 98 mmol/L (02/19/23 06:44:00) Carbon Dioxide SerPl QN: 30 mmol/L High (02/19/23 06:44:00) Anion Gap: 11 mmol/L (02/19/23 06:44:00) BUN SerPl QN: 8 mg/dL (02/19/23 06:44:00) Creatinine SerPl QN: 0.89 mg/dL (02/19/23 06:44:00) Estimated GFR (CKD-EPI, no race): 89 mL/min/1.73m2 (02/19/23 06:44:00) Estimated CRCL (CG): 86 mL/min (02/19/23 06:44:00) Glucose SerPl QN: 277 mg/dL High (02/19/23 06:44:00) Calcium Total SerPl QN: 9.1 mg/dL (02/19/23 06:44:00) Magnesium SerPl QN: 1.6 mg/dL (02/19/23 06:44:00) Troponin-I High Sensitivity: 19 ng/L (02/19/23 08:37:00) BNP Pl QN: 917 pg/mL High (02/19/23 06:44:00) Lactate Venous Pl QN: 1.3 mmol/L (02/19/23 06:44:00) pH Bld Venous QN: 7.4 (02/19/23 06:44:00) PCO2 Bld Venous QN: 55 mmHg (02/19/23 06:44:00) PO2 Bld Venous QN: 40 mmHg (02/19/23 06:44:00) Base Excess Bld Venous: 8 mmol/L High (02/19/23 06:44:00) Bicarb Bld Venous Calc: 34 mmol/L High (02/19/23 06:44:00) O2 Sat Bld Venous Calc: 75 % (02/19/23 06:44:00) C-Reactive Prot SerPl QN: 2.7 mg/dL High (02/19/23 06:44:00) Coagulation: PT: 13.5 seconds (02/19/23 06:44:00) INR: 1.18 (02/19/23 06:44:00) aPTT: 33.4 seconds (02/19/23 06:44:00) All Other Labs: COVID 19 Specimen Source: Nasal (02/19/23 06:48:00) Coronavirus SARS-CoV2 Rapid: Not Detected (02/19/23 06:48:00) Diagnostics Radiology Results - Last 24 hours Across Visits 02/19/2023 08:48 - XR Chest PA or AP Portable IMPRESSION:1. Increasing multifocal bilateral airspace disease.2. Small bilateral pleural effusions.Thank you for consulting our team of subspecialty radiologists at Physicians Radiology. Please contact us with any questions. Signature Line Electronically Signed on 02/19/23 18:30 ________________________________________________________ MD

Weitere VAERSDATA-Felder

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

VAERS 2570582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: IL
Alter: 86,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 09.12.2022
Beginn: 20.12.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: IM / RA

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

Angiogram cerebral abnormal Cerebral atrophy Cerebral infarction Cerebrovascular accident

Symptomtext

May be completely unrelated but wanted to note that patient did have CVA on 12/20/2023 then readmitted 1/29/2023 again for CVA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: IMPRESSION: Motion artifact. 1. Multiple scattered bilateral punctate acute infarcts in the supratentorial brain as detailed above, likely embolic. No mass effect or midline shift 2. Age-appropriate parenchymal volume loss, extensive chronic microvascular ischemic changes and likely small chronic right cerebellar hemisphere infarct. 12/21/2022 7:41 AM IMPRESSION: 1. Subcentimeter acute infarct in the right frontal periventricular white matter. Additional few punctate high DWI signal along the bilateral centrum semiovale, right greater than left, suggesting recent infarcts. The infarcts are predominately in the watershed zones. Chronic microvascular ischemic changes and age-related parenchymal volume loss. 2. No significant interval change when compared to prior CT angiogram head. Redemonstrated advanced multifocal narrowing involving bilateral intracranial ICA pronounced at the skull base, right greater than left. Otherwise anterior and posterior cerebral circulation are patent. Significant decreased/absent flow related signal along the right distal vertebral artery, better assessed on prior CT angiogram. Rest as above. 01/29/2023 3:41 PM
Aktuelle Erkrankungen: Controlled type 2 diabetes mellitus with diabetic nephropathy, with long-term current use of insulin Hypothyroidism due to Hashimoto's thyroiditis Mixed hyperlipidemia Obesity (BMI 30-39.9) Primary hypertension Polyneuropathy Coronary artery disease involving native coronary artery of native heart without angina pectoris Urinary retention Stress incontinence in female Osteoarthritis Chronic kidney disease, stage 4 (severe) Anemia of chronic disease Gout Obstructive uropathy Osteomyelitis Critical lower limb ischemia PAD (peripheral artery disease) Compartment syndrome Normocytic anemia Transaminitis Chronic heart failure with preserved ejection fraction S/P BKA (below knee amputation) unilateral, right Complex renal cyst Bilateral arm weakness Embolic stroke Acute cystitis without hematuria
Vorgeschichte: as above
Andere Medikamente: allopurinoL (ZYLOPRIM) 100 mg, Oral, DAILY ? amLODIPine (NORVASC) 10 mg, Oral, DAILY ? aspirin chewable 81 mg PO Chew chewable tablet Oral, DAILY ? atorvastatin (LIPITOR) 20 mg PO tablet TAKE 1 TABLET BY MOUTH EVERY NIGHT AT BEDTIME ? bloo
Allergien: NKA
Vorherige Impfungen: -

VAERS 2563478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: WV
Alter: 85,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 07.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 21,0
Dosis: UNK
Route/Site: IM / LA

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

Cerebrovascular accident Myocardial infarction

Symptomtext

Patient had a stroke on 11-28-22 and was taken to a hospital. While at the hospital patient had a second heart attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Finasteride 5mg, Ferrous sulfate 325mg, Flomax 0.4mg, Metoprolol ER 25mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2560095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: VA
Alter: 79,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 02.12.2022
Beginn: 04.12.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / -

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

Cerebrovascular accident

Symptomtext

CVA 12/04-2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: ER and IP care ER,
Aktuelle Erkrankungen: -
Vorgeschichte: MAC, CAD, migraines, asthma, bronchietasis, osteoarthritis, hypertension, pre-diabetes, peripheral neuropathy, GERD, Osteopenia
Andere Medikamente: ASA 81 mg, Plavix, Azithromycin, Ethambutol, Rifampin, Colcrys, Isosorbide, Valsartin, Bystolic, Amlodipinec, Neurontin, Omeprazole, Singulair, Symbicort, Glucosamine, Vitamin D, Repatha, Duoneb.
Allergien: Atenolol, Chlorhexidine, Dilaudid, Codiene,Doxycycline, Erythromycin,Cipro, Sulfa, Cleocin, Bextra,Trimethoprim,Biaxin, Levaquin,Trazadone,Lunesta,Prednisone,Avelox,Furesemide, Clonidine,Clonazepam,SimvastatinZetia,Pravacol,Niacin,Zocor,Lipitor,Mevacor,Gentamycin.
Vorherige Impfungen: -

VAERS 2559513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: MN
Alter: 94,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 11.01.2023
Beginn: 12.01.2023
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Death

Symptomtext

Patient was reported to be deceased the morning after vaccination on 1/12/23. Unknown exact time of death during the night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Glaucoma, IBS, Chronic Congestive Heart failure, Atrial fibrillation, prostate carcinoma, malignant melanoma, pulmonary hypertension
Andere Medikamente: apixaban, brimonidine tartrate ophthalmic drops, carboxymethylcellulose ophthalmic drops, dorzolamide HCL ophthalmic drops, furosemide, latanoprost ophthalmic drops, biotin, gelatin capsule, multivitamin/mineral/antioxidant tab, oxycodone a
Allergien: felodipine
Vorherige Impfungen: -

VAERS 2552857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: WA
Alter: 76,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 11.11.2022
Beginn: 02.01.2023
Tage bis Beginn: 52,0
Dosis: 4
Route/Site: IM / -

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

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

Symptomtext

Patient received Pfizer COVID vaccine on 3/2/21 (lot # EN6198), 3/30/21 (lot # ER8732), 10/23/21 (lot # GG3527), and Pfizer Bivalent COVID booster vaccine on 11/11/22 (lot # GJ6738). On 12/29/22, patient tested positive for COVID. On 1/2/23, patient admitted to our inpatient facility (med/surg unit) with acute hypoxic respiratory failure, COVID-19 pneumonia, and hypoglycemia. Patient discharged home on 1/5/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: COVID status positive 12/29/22.
Aktuelle Erkrankungen: -
Vorgeschichte: history of prior V. fib cardiac arrest status post AICD, type 2 diabetes, B-cell lymphoma, rheumatoid arthritis, and hypertension
Andere Medikamente: atorvastatin, carvedilol, glipizide, losartan, metformin er, pioglitazone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2548981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: ID
Alter: 74,0
Geschlecht: M
Eingang: 03.01.2023
Impfdatum: 29.12.2022
Beginn: 29.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cerebrovascular accident Death

Symptomtext

Patient had a stroke within 24 hours of the vaccination and passed away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COPD, Hypertension, MDD, insomnia, anxiety, hyperlipidemia, dementia, edema, GERD, anemia, gout, BPH, neuropathy
Vorgeschichte: history of TBI, History of TIA, alcohol abuse
Andere Medikamente: Aspirin, Ferrous Sulfate, Flomax, Furosemide, Losartan, Potassium, Senna, Rosuvastatin, Atropine, Clonazepam, Citalopram, Olanzapine, Norco, Melatonin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2537907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: NY
Alter: 71,0
Geschlecht: M
Eingang: 20.12.2022
Impfdatum: 17.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dyspnoea Myocardial infarction Myocardial necrosis marker increased

Symptomtext

Pt received Pfizer bivalent and fluad quad on 12/17/22. Pt called on 12/20/22 stating on 12/18/22 pt awoke feeling dizzy and shortness of breath. Pt went to urgent care oxygen levels were normal but cardiac enzyme were "off" and thus told he may have suffered a heart attack. the urgent care suggested doing a cat scan but did not conduct it because pt has stage 3 kidney disease. Pt proceeded to visit hospital, also cat scan not conducted due to stage 3 kidney disease and diabetic. Upon reassessing enzyme levels were normal and after 6 hours of observation pt was released from hospital. On 12/20/22 pt states he feels better today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Pt received Pfizer bivalent and fluad quad on 12/17/22. Pt called on 12/20/22 stating on 12/18/22 pt awoke feeling dizzy and shortness of breath. Pt went to urgent care oxygen levels were normal but cardiac enzyme were "off" and thus told he may have suffered a heart attack. the urgent care suggested doing a cat scan but did not conduct it because pt has stage 3 kidney disease. Pt procEeded to visit hospital, also cat scan not conducted due to stage 3 kidney disease and diabetic. Upon reassessing enzyme levels were normal and after 6 hours of observation pt was released from hospital. On 12/20/22 pt states he feels better today.
Aktuelle Erkrankungen: DIABETES
Vorgeschichte: DIABETES KIDNEY DISEASE
Andere Medikamente: OZEMPIC 4MG/3ML 1MG/DOSE PEN, CHLORHEX GLU 0.12% SOL, NITROFURANTOIN MONO 100MG CAP, PREGABALIN 300MG CAP, FARXIGA 10MG TAB, TESTOST CYP 200MG/ML INJ, GLUCOSAMINE 500MG CAP, AMMONIUM LAC 12% LOT, CELECOXIB 200MG CAP, SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2521986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: WA
Alter: 78,0
Geschlecht: M
Eingang: 02.12.2022
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Acute myocardial infarction Asthenia Atrioventricular block second degree Cardiac pacemaker insertion Dyspnoea Dysuria Electrocardiogram normal Intensive care Malaise Troponin increased

Symptomtext

Presented to ER that evening with malaise, general weakness, and dysuria. Work up in the ER showed Tropinins trending up and patient admitted with a NSTEMI. Later patient was transferred to the ICU with significantly dyspnea and Mobitz type II second degree heart block with a heart rate in the 20's. He responded well to an epinephrine drip. He was transferred to a higher acuity hospital via transport on 11/23/2022 where he received placement of a permanent pacemaker which resolved his issues. He was discharged the following day much improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 7,0
Labordaten: initial HS Troponin in ER was 21 ng/L. No ST changes on EKG. Troponin peaked at 31 ng/L.
Aktuelle Erkrankungen: nothing acute.
Vorgeschichte: Hypertension, hyperlipidemia, hypothyroid, obesity, type 2 diabetes mellitus, benign prostate hypertrophy, mantle cell lymphoma, peripheral neuropathy, first degree heart block, bi-fascicular block with right bundle branch block and left anterior fascicular block.
Andere Medikamente: Amitriptyline, Ibrutinib, Levothyroxine, liothyronine, Losartan, Metformin, Nifedipine, Potassium Chloride, Simvastatin, Tamsulosin.
Allergien: N/A
Vorherige Impfungen: -

VAERS 2517409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

kritisch

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 26.11.2022
Impfdatum: 09.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Back pain Computerised tomogram Electrocardiogram Embolism arterial Full blood count Pain Pulmonary embolism

Symptomtext

Pain in upper torso right side and back, CT Scan, EKG, CBC Radio;ogist report: right-sided pulmonary artery emboli

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT scan, EKG, CBC on 11/10/22
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension
Andere Medikamente: Propranolol ER, Eplerenone,
Allergien: Penicillin,
Vorherige Impfungen: -

VAERS 2509200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

kritisch

Staat: NE
Alter: 85,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 02.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Pulmonary embolism

Symptomtext

Pulmonary embolism; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. An 85-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 02Nov2022 as dose 4 (booster), single (Lot number: GJ6738) at the age of 85 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, NDC, LOT, EXP of previous dose: unknown), administration date: 05Feb2021, when the patient was 83-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, NDC, LOT, EXP of previous dose: unknown), administration date: 25Feb2021, when the patient was 83-year-old, for COVID-19 immunization; BNT162b2 (Dose 3, NDC, LOT, EXP of previous dose: unknown), administration date: 29Sep2021, when the patient was 84-year-old, for COVID-19 immunization. The following information was reported: PULMONARY EMBOLISM (medically significant) with onset Nov2022, outcome "unknown". The event "pulmonary embolism" required emergency room visit. Clinical Course: There was a correlation between the Bivalent Pfizer COVID 19 vaccine (does not know specific cap color) and blood clots. Caller says and clarifies the patient did not get the vaccine here, the patient's wife was calling in, he got his 4th dose of COVID vaccine on 02Nov2022 and it was the bivalent and then 07Nov2022 he went to the ER and had a pulmonary embolism so the wife was calling today asking if there is a correlation between the two. Doctor wanted to check on giving this patient the COVID vaccine. Patient got the COVID vaccine 02Nov2022. Went to the emergency room 07Nov2022, with pulmonary embolis. Patient's wife was calling to see if there was a correlation between the COVID vaccine and the pulmonary embolism. Unable to clarify which formulation of the COVID vaccine caller was referring to, stating she only knows it was the Pfizer COVID vaccine. Clarified that patient went to the emergency room 07Nov2022 but unknown if patient was admitted to hospital. Clarified that this COVID vaccine patient received 02Nov2022 was the Bivalent COVID vaccine. When caller looked up patient's vaccine in their system, states that under manufacturer, it states it is unknown but, patient's wife states that it was the Pfizer Bivalent vaccine the patient received. Prior Vaccinations within 4 weeks nothing noted in chart, unless they got it somewhere else. Does not know for sure.; Sender's Comments: Based on the limited information, the serious event Pulmonary embolism cannot be excluded fully for the suspect product BNT162B2, BNT162B2 OMI BA.4-5. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 2714069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: -
Alter: 13,0
Geschlecht: F
Eingang: 15.11.2023
Impfdatum: 01.08.2023
Beginn: 01.08.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Echocardiogram Electrocardiogram Laboratory test Nausea Postural orthostatic tachycardia syndrome Syncope Tremor Tunnel vision

Symptomtext

12 hours after injection, fainted, had nausea, tunnel vision, shaking. Now has likely dx of POTS. Continues to have nausea and increased anxiety.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Echo, lab work, EKG
Aktuelle Erkrankungen: Keratosis pilaris
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2651577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 30.06.2023
Impfdatum: 06.12.2022
Beginn: 18.02.2023
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / RA

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

Deep vein thrombosis Symptom recurrence

Symptomtext

ACUTE DVT OF LEFT POPLITEAL VEIN 3/1/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2651309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 30.06.2023
Impfdatum: 13.12.2022
Beginn: 03.01.2023
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: IM / LA

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

Deep vein thrombosis Hypoxia

Symptomtext

ACUTE DVT, UNSPECIFIED VEIN HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2643491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

schwer

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 09.06.2023
Impfdatum: 05.12.2022
Beginn: 29.03.2023
Tage bis Beginn: 114,0
Dosis: 4
Route/Site: IM / LA

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

Frontal lobe epilepsy Syncope

Symptomtext

G40.009 FRONTAL LOBE EPILEPSY 3/29/2023 SYNCOPE AND COLLAPSE

Weitere VAERSDATA-Felder

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

VAERS 2603860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: VA
Alter: 16,0
Geschlecht: F
Eingang: 26.03.2023
Impfdatum: 04.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / RA

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

Blood test normal Electroencephalogram abnormal Magnetic resonance imaging head normal Seizure Tremor Urine analysis normal

Symptomtext

About two weeks after 2nd booster, my daughter started tremors in her hands and legs. Unrollable small shakes in both arms and legs. The termers got stronger, and we visited hospital ER at the end of November. All blood and urine test were normal, but she kept shaking in the morning. On January 1st, 2023 she had a seizure and we ended up in another hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Nov 30, 2022 (Hospital ER) ---blood and urine test---all normal Jan 2, 2023 (Hospital ER) ----blood and urine test---all normal Jan 3, 2023 (Hospital Neurology Department) ---EEG test showed some unknown spikes in front lobe of brain. Late Jan, 2023 (Hospital) ---Brain MRI---all normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Gummy vitamins.
Allergien: None
Vorherige Impfungen: -

VAERS 2593937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: WI
Alter: 82,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 04.11.2022
Beginn: 14.12.2022
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: UN / UN

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

Asthenia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram thorax normal Cough Fatigue Hypoxia Illness Lung opacity Malaise Pyrexia Respiratory distress Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On 12/14/2022, patient presented to the emergency department from facility with chief complaint of weakness. She had a 3-day history of illness with cough, congestion, intermittent fevers, malaise/fatigue. Upon arrival in the ED, she was hypoxic and required oxygen, and had a positive COVID-19 NAA test; No shortness of breath; Chest X-ray showed mild left basilar opacity may represent atelectasis or pneumonia. CT of Chest was negative for pulmonary embolism and there were no acute findings. Diagnoses: Pneumonia due to COVID-19 virus, Hypoxia, Respiratory distress. Patient was treated with Decadron along with albuterol and Atrovent. She was admitted to the hospital for further treatment. Submitter does not have access to further medical information on this case. If more information is needed, please contact the admitting hospital:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 2,0
Labordaten: 12/14/2022 - positive COVID-19 NAA test; Chest X-ray showed mild left basilar opacity may represent atelectasis or pneumonia; CT of Chest was negative for pulmonary embolism and there were no acute findings.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Dementia, Chronic Kidney Disease Stage 3, Spinal stenosis in cervical region, Degenerative Joint Disease of knee, Essential hypertension, benign, Hypothyroidism, Pure hypercholesterolemia, Diverticulosis of colon.
Andere Medikamente: Unknown
Allergien: Allergies: Food-Shrimp Rash all around mouth and on face, Aspirin Shortness Of Breath, Tree Nuts Hives Not specific on nut type.
Vorherige Impfungen: -

VAERS 2588461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 10.12.2022
Beginn: 11.01.2023
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy Aphasia Atrial septal defect Contrast echocardiogram Embolic stroke Facial paralysis Magnetic resonance imaging head abnormal Middle insomnia Sensory disturbance

Symptomtext

On January 11th, I woke up in the middle of the night and felt strange sensations in my face. Had trouble speaking and had right side face droop. Next day went to heath care provider. I was given an exam. Vitals were all within range. PA gave me baby aspirin and suggested a hospital visit. I checked into hospital and got an MRI and CAT scan. MRI showed I had had recent embolic stroke activity. Tests showed I had a Patent Foramen Oval, which was previously unknown. My test showed good health otherwise. Doctors treated me with Lipitor Plavix and baby aspirin. I?ve had no symptoms since.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolic stroke
Hospital-Tage: 2,0
Labordaten: Jan 11 MRI showed recent stroke activity. Jan 11 Cardiac ultrasound bubble test showed patent foramen oval
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: -

VAERS 2584246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: OH
Alter: 58,0
Geschlecht: M
Eingang: 20.02.2023
Impfdatum: 15.11.2022
Beginn: 12.02.2023
Tage bis Beginn: 89,0
Dosis: 5
Route/Site: IM / LA

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

Anticoagulant therapy Computerised tomogram thorax abnormal Deep vein thrombosis Peripheral swelling Pulmonary thrombosis Surgery Ultrasound Doppler abnormal

Symptomtext

Fortunately, I was not having chest pains. I went into the emergency for right leg, it was very swollen. They did a CAT scan of my lungs and found that I had blood clots in my lungs. They ordered an ultrasound for my right leg and found that I had DVT. I was then admitted to the hospital. A cardiovascular surgeon was brought in, I did have surgery and was released on Tuesday. I am now giving myself shots of Lovenox twice a day for a while and taking Clopidogrel to help thin my blood to help keep me from getting another blood clot as well as dissolve the ones in my lungs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 3,0
Labordaten: CAT; Ultrasound
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure
Andere Medikamente: Norvasc; Benicar
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2583519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: -
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Computerised tomogram normal Contusion Electrocardiogram normal Loss of consciousness Magnetic resonance imaging normal Memory impairment Mobility decreased Pain

Symptomtext

In October I went to bathroom early in the morning. I looked at the looked clock it was 2am in the morning the next thing I know it is 4am in the morning. I don't remember anything. I went to the hospital, I had bruises on my stomach, under my chin, under my arm. It was very hard for me to get up. I had to pray and ask God to help me to get up. After three days in the hospital, I was released, my test came back showing nothing caused me to pass out. I have been to the chiropractor, pain specialist and primary care doctor. No one has been able to help me. I cannot turn my head to the right without it causing me a lot of pain. I can barely lift my hand halfway up my body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: MRI; CAT scan; bloodwork; EKG; negative for all test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Lisinopril/hctz; Omeprazole, Alprazolam; Lipitor; Melatonin; Multivitamins; Magnesium
Allergien: Sensitivity to latex or dental anesthetic
Vorherige Impfungen: -

VAERS 2579541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: PA
Alter: 80,0
Geschlecht: M
Eingang: 07.02.2023
Impfdatum: 01.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 18,0
Dosis: UNK
Route/Site: IM / AR

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

Haemorrhagic stroke Subdural haemorrhage

Symptomtext

Hemorrhagic stroke versus subdural bleed Nov 19 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Haemorrhagic stroke
Hospital-Tage: -
Labordaten: HOSPITALIZED
Aktuelle Erkrankungen: chronic Balance, A Fib
Vorgeschichte: A Fib.
Andere Medikamente: Flecainide, propranolol, Xarelto
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2576510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: MI
Alter: 95,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 11.11.2022
Beginn: 06.12.2022
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: - / -

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

Atrial fibrillation Cardiac failure congestive Chronic left ventricular failure Coronary artery disease Essential hypertension Gastrooesophageal reflux disease Orthostatic hypotension Syncope

Symptomtext

All Hospital Problems (Other Diagnoses): Active Hospital Problems Diagnosis o Principal Problem: Syncope o Orthostatic hypotension o Chronic combined systolic and diastolic congestive heart failure (CMS/HCC) o Atrial fibrillation (CMS/HCC) o History of prostate cancer o History of lung cancer o Gastroesophageal reflux disease without esophagitis o Hx of CABG o CAD (coronary artery disease) o Primary hypertension

Weitere VAERSDATA-Felder

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

VAERS 2565128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: IL
Alter: 56,0
Geschlecht: F
Eingang: 21.01.2023
Impfdatum: 02.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Dizziness Dyspnoea Echocardiogram abnormal Electrocardiogram abnormal Electrocardiogram ambulatory normal Fatigue Heart rate abnormal Laboratory test normal Loss of personal independence in daily activities Pericarditis Scan with contrast abnormal Ventricular extrasystoles

Symptomtext

Wednesday Nov. 2, 2022 vaccinated, Friday Nov. 4, 2022, chest pain, shortness of breath, constant PVCs, thought I was being dramatic or having panic attacks, so I waited. Went to Urgent Care on November 14, 2022 for continued abnormal heartbeats, chest pain, exhaustion. Was referred to Hospital ER after EKG showed multiple PVCs. All labs normal at ER, referred to Heart Center for Holter monitor to track abnormal heart activity, findings showed nothing. Follow up with PCP where he referred to cardiologist with Clinic. Upon exam pericardial "rub" was evident when listening to heart. Referred to Medicine for echo on 1-6-2023, finding of pericarditis, already waning. Have had no follow up from this doctor, info I have is from accessing the patient portal. Continuing to have abnormal heart beats. I can feel them throughout chest and am breathless and dizzy to the point of incapacitation. During PCP follow up blood work was ordered, found to have severe iron deficiency.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: EKG November 14 2022 Urgent Care Blood and urine labs November 14 2022 Hospital Holter Monitor November 2022 Institute Echocardiogram with contrast January 2023
Aktuelle Erkrankungen: none
Vorgeschichte: fibromyalgia, iron deficient anemia
Andere Medikamente: none
Allergien: codeine
Vorherige Impfungen: -

VAERS 2564584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: WI
Alter: 57,0
Geschlecht: M
Eingang: 20.01.2023
Impfdatum: 27.10.2022
Beginn: 13.11.2022
Tage bis Beginn: 17,0
Dosis: 4
Route/Site: IM / RA

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

Blood test Carotid artery occlusion Computerised tomogram head abnormal Eyelid ptosis Intensive care Ischaemic stroke Laboratory test Magnetic resonance imaging Mobility decreased Neurological symptom Speech disorder Thrombectomy Visual impairment

Symptomtext

On 11-13-2022 we were shopping at a store when my left eye became dark. The problem cleared in a few minutes. After we checked out of the store and started driving home I started to lose function on the right side of my body and lost the ability to speak. My wife was able to stop the car while going 79 mph and safely get us to the side of the interstate, switch spots with me so she could drive, and get me to the nearest hospital where I was admitted to the emergency room with signs of a stroke. My stroke score was 21 of 36. I was given a CT scan where it was determined I was having an ischemic stroke. I was taken to the operating room where a clot was removed from my brain that had blocked the left hemisphere of my brain. My left inner carotid artery had somehow become blocked, which had supposedly released what was referred to as a tandem clot, causing the stroke. We were at the hospital around 1:30 pm, and I was out of surgery by a little after 4pm that day. I spent 3 days in the ICU and was then released to go home. Other than a blind spot in my left eye, and a droopy left upper eyelid, I have come out of this near-death experience without the need for any type of therapy. I got lucky because when the event happened, we just happened to be near one of the three hospitals in the state that could fix my adverse event. I have never had anything like this happen to me before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: Various CT scans, blood/labs, and an MRI, with follow-up with an ophthalmologist. Future CT scan is scheduled to see how the left inner carotid artery is healing (or not).
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2564284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: NE
Alter: 64,0
Geschlecht: F
Eingang: 20.01.2023
Impfdatum: 06.12.2022
Beginn: 24.12.2022
Tage bis Beginn: 18,0
Dosis: UNK
Route/Site: IM / -

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

Blood disorder Blood test abnormal Blood thyroid stimulating hormone normal Blood urea increased C-reactive protein normal Differential white blood cell count normal Diplopia Full blood count normal Magnetic resonance imaging head normal Metabolic function test normal Monocyte percentage increased Muscle disorder Red blood cell sedimentation rate normal Scan with contrast normal Thyroxine free normal Urine analysis normal VIth nerve paralysis

Symptomtext

On 12-6-22 I received the Pfizer-BioNTech bivalent COVID-19 vaccine. On 12-24-22 I suddenly had diplopia (double vision). The image from my left eye is not lining up with the image from the right eye. I am a healthy 64 year old female with no risk factors for stroke On 12-26-22 I had an MRI and multiple blood and urine tests. My BUN and %Monocytes were slightly elevated. All other results were normal. The MRI showed no sign of ischemia. On 12-27-22 my optometrist performed tests and found no problem within the eyeballs. She referred me to an ophthalmologist, who I saw on 12-30-22. She said I have Sixth Nerve Palsy, which she described as a micro-stroke, too small to be seen on an MRI. The blood vessel which feeds the nerve controlling the left lateral rectus muscle had been interrupted. She said the blood should find another pathway and my vision should return to normal or near-normal in 3-6 months. I did not report this on my latest V-Safe check-in from the CDC because it did not occur to me that it could be related to the vaccine. But, as I stated, I have no other risk factors for the occurrence of stroke. I have pages of reports from the blood work which I can provide if needed. As I stated, all values were normal except the BUN and %Monocytes, which were only slightly high. Tests done were: CRP, Urinalysis, T-4 Assay Free, ESR, TSH-Thyroid Stimulating Hormone, Comprehensive Metabolic Panel and CBC/Auto Diff.

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: 12/26/2022 MRI OF BRAIN WITH AND WITHOUT IV CONTRAST DYE Negative 12/26/2022 CRP <0.5 Test Unit MILLIGRAMS PER DECILITRE Low Test Range 0.50 High Test Range 1.00 12/26/2022 T-4 ASSAY FREE 0.91 ng/dL Test Unit NANOGRAMS Low Test Range 0.7 ng/dL High Test Range 1.70 ng/dL 12/26/2022 9 mm/hr MILLIMETERS Low Test Range 0 mm/hr High Test Range 20 mm/hr 12/26/2022 2 mlU/L Test Unit MILLI INTERNATIONAL UNITS Low Test Range 0.49 mlU/L Hight Test Range 4.67 mlU/L 12/26/2022 COMPREHENSIVE METABOLIC PANEL see comments above 12/26/2022 CBC/AUTO DIFF see comments above 12/26/2022 URINALYSIS see comments above
Aktuelle Erkrankungen: non-smoker; no pregnancies; moderate alcohol use (0-4 drinks/week)
Vorgeschichte: Sixth Nerve Palsy, Left; Ductal Carcinoma of Left Brest (2007); Allergic Rhinitis, mild; Degenerative disc disease, L5-S1; osteopenia; osteoarthritis, mild; OBSTRUCTIVE SLEEP APNEA, mild.
Andere Medikamente: Tramadol 50 mg with Acetaminophen 1000 mg daily; CPAP daily; Fluticasone Propionate Nasal Spray USP 50 mcg, Seasonally as needed; Cromolyn Sodium Ophthalmic Solution, USP 4%, Weekly as needed; Decadrone/DepoMedrol 8mg/80 mg injections, Semi
Allergien: pollen, house dust, mold, adhesive tape
Vorherige Impfungen: -

VAERS 2560231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

schwer

Staat: MN
Alter: 58,0
Geschlecht: F
Eingang: 15.01.2023
Impfdatum: 06.01.2023
Beginn: 07.01.2023
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Electrocardiogram normal Influenza like illness Syncope

Symptomtext

Within 24 hours of booster feeling flu like a d syncope episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: ER visit 4 days later with normal ekg result
Aktuelle Erkrankungen: None
Vorgeschichte: Narrow angle glaucoma
Andere Medikamente: None
Allergien: Meclazine
Vorherige Impfungen: -

VAERS 2559621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: WA
Alter: 56,0
Geschlecht: F
Eingang: 13.01.2023
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

Dyspnoea Heart rate irregular Syncope

Symptomtext

-Fainting - Heavy breathing - Irregular heartbeat - Fever These symptoms lasted about 24 hours and were similar the one she experienced with previous pfizer covid-19 vaccination in 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sumatriptan succinate 50mg tablet
Allergien: None
Vorherige Impfungen: Pfizer covid-19; 54 years old; Administered on 09/10/2021;

VAERS 2550477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: NM
Alter: 69,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 08.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / RA

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

Deep vein thrombosis Fibrin D dimer Ultrasound Doppler abnormal

Symptomtext

Patient called reported that had vaccine on 12/08/2022 and 2 days later went to ER was diagnosed with DVT in right upper leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: D. Dimer Quantatative 7650> Ultrasound of BLE -+ in right leg.
Aktuelle Erkrankungen: None
Vorgeschichte: None listed by patient in chart.
Andere Medikamente: None listed in chart by patient.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2543609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: ME
Alter: 36,0
Geschlecht: F
Eingang: 27.12.2022
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: ja Erholt: nein

Anaphylactic reaction Anxiety Blood test normal Borrelia test negative Cardiac disorder Cardiac monitoring Chest pain Chills Confusional state Dizziness Ear pain Echocardiogram Electrocardiogram normal Feeling abnormal Gastrointestinal disorder Inflammatory marker test Injection site pain Nervousness

Symptomtext

She got her vaccine, about 15-30 minutes later she was having what she would describe as an anaphylactic reaction of tingling and pain up from her jaw to her inner ear, and feeling dizzy like she was going to pass out. Kind of out of it, and having heart palpitations due to anxiety and nervousness and was also driving. She had a similar reaction the previous year from the booster and it went away and felt that she was going to be fine. She took her daughter to basketball practice, went home and went to bed. The next day she had the normal body aches and chills, but nothing out of the ordinary of any of the other vaccines. Those resolved by probably Sunday. Then the next Monday on 11/14/22 that she went to work, was feeling very brain fog, still the pain through her upper jaw/inner ear, feeling very confused, dizzy. She is a teacher so she told the school nurse how she was feeling and felt that she needed to go to the ER. They did blood work, tested for POTS, Lyme disease, did an EKG and everything came back normal. They gave her a heart monitor to make sure it was not the case and sent her home. She dealt with brain fog/dizziness/pain in the jaw for 2 more weeks until holiday break. She spent the week at home, and the next Monday night she was still having the brain fog so she went to the ER once again, blood work and EKG came back normal once again. The doctor said that he did not see any trauma, nothing wrong with her heart and that she could go home. She told him that she needed help and asked some questions about the shot, and asked if it could be inflammation and had seen her PCP that it could inflammation from the vaccine. He gave her a prescription for Celebrex 200 mg twice daily for 7 days. She took that and it did alleviate the brain fog and the injection site pain. The PCP felt it was common of what they were seeing for vaccine reactions that it caused inflammation and to continue on the Celebrex if it was working. She asked if it didn't work after the 7 days they told her that they could give her 7 more days worth. The ER doctor had also given her Meclizine for dizziness, but did not take it. The Celebrex was prescribed on 11/29/22. When she came off of it she was still having the pain from her jaw to inner ear and her sinuses. She called doctor to get another 7 day supply and it took about 4 days to get it, and was probably on and off of it for a course of 20 days. She went back to her doctor on 12/16/22 and she did another EKG and inflammation markers blood work. The inflammation markers came back negative, and stopped the Celebrex and started her on Prednisone and Doxycycline thinking it might be a lingering sinus infection from prior to the vaccine. On Saturday morning about mid-day she had a heart event, palpitations and pulse rate above 160 and could not get it down to 120 through the entire day. She went to the ER at 8:30 that evening, they did blood work and that she was not going to die, did blood work and EKG and told her to stop taking the prednisone and Doxycycline. She called her PCP's office and told them what happened in the ER and they told you stop taking the Prednisone but continue the Doxycycline. She took the Doxycycline from 12/19/22 to 12/22/22, was having constant heart palpitations and stomach issues and on 12/22/22 she told her doctor that she could not take it any more and she stopped the Doxycycline and made her an APT for 12/29/22. She did have an echocardiogram on 12/23/22 to check for myocarditis and has not gotten the results for that yet. She is still having injection site pain, traveling up to her shoulder, and the pain in the back of her jaw and through to her sinuses is still present. Her heart has stopped palpitating. She had really bad chest pain yesterday, but thinking it was mostly from having so many palpitations in a week that it was really sore. She did have COVID last May, mild case of it. Also had flu vaccines and no AE from those. First two vaccines no reaction other than typical symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: EKG, blood work and echo.
Aktuelle Erkrankungen: Sinus infection.
Vorgeschichte: SVT since age 16, herpes simplex.
Andere Medikamente: None.
Allergien: Benadryl, Surgical glue, Prednisone.
Vorherige Impfungen: The booster on 11/13/21 gave her similar symptoms, but as an EMT she took the newest booster.

VAERS 2542207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: KY
Alter: 18,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 20.12.2022
Beginn: 20.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Dizziness Fall Loss of consciousness Nausea Pallor

Symptomtext

patient came in for her covid booster (pfizer bivalent) and flu shot. after administration pt was sitting on the blood pressure machine; a few minutes later the patient fell to the floor. Grandma threw her purse under her head to soften her fall. I ran out to the patient and she was already coming to. She was very pale, nauseous and light headed. we got her a coke, water and some chocolate. pt sat for 15-20 minutes on the ground. then we helped her to a wheelchair. She sat for a while longer until she felt better

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: flu 11/18
Vorgeschichte: none
Andere Medikamente: lamotrigine 200mg 1 QDay buspirone 10mg 2 Qday Quetiapine 25mg 1 QDay Nore/Eth/Fer 1/20 cap 1 QDay Venlafaxine ER 75mg & 150mg (225mg total) 1 QDay
Allergien: no know
Vorherige Impfungen: -

VAERS 2539260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 10.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Magnetic resonance imaging head normal Magnetic resonance imaging normal VIth nerve paralysis

Symptomtext

Abducens (sixth cranial) nerve palsy. Left eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: MRI Brain and neck area eliminating brain event. at hospital emergency Nov 15th. Ophthalmologist complete test at institute, Nov 15th.
Aktuelle Erkrankungen: mild cold
Vorgeschichte: diabetes kidney transplant recipient
Andere Medikamente: Humalog Amlodipin Lisinopril Atrovastatin Envarsys Synthroi Plavix
Allergien: none
Vorherige Impfungen: -

VAERS 2536828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: WI
Alter: 37,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 19.12.2022
Beginn: 19.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Loss of consciousness Malaise Syncope

Symptomtext

Patient received both the flu vaccine and COVID booster at 0915 and sat in the lobby for the 15 minute waiting period. At 0930, the patient came to the counter of the pharmacy and stated she did not feel well. The pharmacist and myself (pharmacy intern) approached the patient, grabbed both arms and gently lowered her to the ground as she had fainted. The pharmacy is within a healthcare facility and urgent care staff were alerted and attended to the patient. The patient was unconscious for less than a minute and recovered quickly. Urgent care staff included two RNs and one MD. Patient was evaluated in the lobby without a office visit and given snack and juice and recovered quickly. After she woke up, she stated she was anxious and didn't eat much prior to her vaccine appointment. She left the health care facility feeling well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Anxiety, seasonal allergies, GERD
Andere Medikamente: Escitalopram
Allergien: Alba-derm, penicillins
Vorherige Impfungen: -

VAERS 2535348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 16.12.2022
Beginn: 16.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Syncope

Symptomtext

Pt fainted after the vaccine was administered while pt is sitting down .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Denies
Vorgeschichte: None
Andere Medikamente: Sprintec 1 tablet daily (birth control)
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2529493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: AZ
Alter: 44,0
Geschlecht: M
Eingang: 12.12.2022
Impfdatum: 12.12.2022
Beginn: 12.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysstasia Syncope

Symptomtext

PATIENT RECEIVED VACCINE AROUND 3:43PM. HE LEFT FOR HIS DOCTOR APPOINTMENT NEXT DOOR. HE CAME BACK TO PICK UP HIS MEDICATION AROUND 4:55PM. PATIENT COLLAPSED ON THE FLOOR. HE HAD DIFFICULT STANDING BUT HE WAS FULLY CONCIOUS AND ABLE TO COMMUNICATE. WE CALLED 911 AND HAD DR. FROM VILLAGE MEDICAL TO CHECK ON HIM WHILE WAITING FOR EMS. PATIENT TRIED TO LEAVE AND COLLAPSED ON THE FLOOR AGAIN. EMS ARRIVED A FEW MINUTES LATER. VITAL ARE NORMAL. PATIENT MENTIONED HE HAD A FEAR FOR VACCINATION AND HE HAD NOT HAD ANY MEAL. PATIENT REFUSED TO GO TO HOSPITAL. EMS CONTACTED A DOCTOR, AND CONFIRMED PATIENT IS STABLE, HE JUST NEEDS TO REST FOR 20-30 MINUTES. PHARMACY STAFF CHECKED ON PATIENT EVERY 5 MINUTES FOR ABOUT 20 MINUTES. PATINET WAS ABLE TO WALK TO THE PARKING LOT. PATIENT 'S MOTHER CAME TO PICK UP HIM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO KNOWN ILLNESS
Vorgeschichte: NO KNOWN MEDICAL CONDITION. PATIENT HAS FEAR AGAINST IMMUNIZATION
Andere Medikamente: CLOTRIMAZOLE 1% CREAM
Allergien: NO
Vorherige Impfungen: PATIENT MENTIONED HE HAD SIMILAR REACTION WITH PREVIOUS VACCINE

VAERS 2528514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: PA
Alter: 17,0
Geschlecht: F
Eingang: 11.12.2022
Impfdatum: 11.12.2022
Beginn: 11.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient experienced vasovagal syncope after receiving both vaccinations lasting less than 1 minute.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: Unknown
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2526816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: IA
Alter: 75,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 11.11.2022
Beginn: 26.11.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: SYR / LA

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

Cough Hypoglycaemia Influenza virus test negative Loss of consciousness Pyrexia Respiratory syncytial virus test positive Rhinorrhoea SARS-CoV-2 test negative Syncope

Symptomtext

My adverse event started on 11/26/2022 at night around 8:00AM. I started coughing, yellow drainage in my nose. On Saturday morning I had fever and cough. I went to the urgent care on Sunday morning. I passed out in the bathroom. They diagnosed me with Syncope Hypoglycemia. I tested negative for flu and COVID-19. I was positive for RSV. In the urgent care they gave me IV with fluids to hydrate me. They also prescribed me with benzoate 10 mg 3 times per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 08DEC2022 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; Osteoporosis
Andere Medikamente: TYLENOL arthritis; atenolol; vitamin D; gabapentin; hydrocortisone; fish oil; triamterene
Allergien: CT contrasts
Vorherige Impfungen: -

VAERS 2525844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

schwer

Staat: PA
Alter: 14,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 03.12.2022
Beginn: 03.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

About 1 minute administering the Pfizer Bivalent Vaccine and the season Influenza Immunization the patient started to faint. The patient was unconscious for approximately 2 minutes. We laid the patient on the ground and the patient regained conscious at this time.

Weitere VAERSDATA-Felder

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

VAERS 2522595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

schwer

Staat: CO
Alter: 25,0
Geschlecht: M
Eingang: 04.12.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 2518384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: UT
Alter: 67,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 05.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 17,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal X-ray Asthenia Central venous catheterisation Chest X-ray Computerised tomogram head Hypoaesthesia Hypoaesthesia oral Mobility decreased Sensory loss Electrocardiogram Endotracheal intubation Fall Immunoglobulin therapy Intensive care Laboratory test Lumbar puncture Magnetic resonance imaging spinal Muscular weakness

Symptomtext

Covid, Influenza and Zoster vaccines were all administered at Pharmacy on 11/5/2022. On 11/22/2022 patient came into the ER. Patient claimed she felt weak the day after the vaccines. with lost of all sensation and control over her legs. Patient was admitted in the ER and sent to the medical floor for observation. Numbness also spreads to her hands and the tip of her tongue. Patient received Neurology Consult and possible Guillain Barre Syndrome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: UT
Alter: 67,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 05.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: IM / LA

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

Abdominal X-ray Asthenia Central venous catheterisation Chest X-ray Computerised tomogram head Hypoaesthesia Hypoaesthesia oral Mobility decreased Sensory loss Electrocardiogram Endotracheal intubation Fall Immunoglobulin therapy Intensive care Laboratory test Lumbar puncture Magnetic resonance imaging spinal Muscular weakness

Symptomtext

Covid, Influenza and Zoster vaccines were all administered at Pharmacy on 11/5/2022. On 11/22/2022 patient came into the ER. Patient claimed she felt weak the day after the vaccines. with lost of all sensation and control over her legs. Patient was admitted in the ER and sent to the medical floor for observation. Numbness also spreads to her hands and the tip of her tongue. Patient received Neurology Consult and possible Guillain Barre Syndrome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2517450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

schwer

Staat: MA
Alter: 38,0
Geschlecht: M
Eingang: 27.11.2022
Impfdatum: 27.11.2022
Beginn: 27.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Immediate post-injection reaction Syncope

Symptomtext

Patient had a known history of syncope after vaccination. As soon as the vaccine was injected, patient stated "it's going to happen". Pt immediately knew he was about to faint. He closed his eyes, then the pharmacist and patients wife got patient safely to the floor, raised his legs, and provided patient an ice pack. After about 5 or 10 minutes patient felt fine again. He stayed another 30 minutes, then left facility with his family.

Weitere VAERSDATA-Felder

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

VAERS 2514159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

Syncopal episode with LOC of approximately 10 seconds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: asthma
Andere Medikamente: Albuterol PRN
Allergien: peanuts
Vorherige Impfungen: -

VAERS 2512639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

schwer

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Lethargy Seizure

Symptomtext

Systemic: Exhaustion / Lethargy-Severe, Systemic: Seizure-Severe

Weitere VAERSDATA-Felder

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

VAERS 2512431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 19.11.2022
Impfdatum: 29.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Anticoagulant therapy Deep vein thrombosis Joint swelling Laboratory test abnormal Limb discomfort Pain Pain in extremity Peripheral swelling Thrombectomy

Symptomtext

Patients husband came in over a week after vaccines were administered and notified us of DVT that patient had experienced with symptoms starting 2 days after receiving her vaccine . Started as pain in toes and pressure and traveling up the leg. Strong burning pain and swollen ankle and calf. Patient's son took her to the hospital a week after her symptoms began fearing it was a clot. Hospital ran tests/exams and diagnosed that she had a clot in her inguinal area and started patient on blood thinners and surgical removal. Patient believes it was the Pfizer Bivalent Vaccine or possible combination of the 3 vaccines (Pfizer bivalent, Fluad, Pnuemovax 23). Patient was released from hospital 4 days after she entered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: not indicated
Vorgeschichte: not indicated
Andere Medikamente: Metformin ER 500 mg once daily ; unsure of other medications
Allergien: not known
Vorherige Impfungen: -

VAERS 2510650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

schwer

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 11.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Blood glucose normal Electrocardiogram normal Feeling hot Heart rate increased Hyperhidrosis Presyncope Vision blurred

Symptomtext

within 24 hours, increased heart rate 130-170s, symptomatic 11/14/22, within 72 hours, felt blurry vision, hot, sweating and near syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: ECG normal 11/14/22 glucose normal, 104 11/14/22
Aktuelle Erkrankungen: no
Vorgeschichte: hypothryoidism
Andere Medikamente: levothyroxine 137mcg daily
Allergien: none
Vorherige Impfungen: -

VAERS 2506833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: IA
Alter: 23,0
Geschlecht: F
Eingang: 13.11.2022
Impfdatum: 12.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Confusional state Fall Loss of consciousness Pallor

Symptomtext

Patient sat down after getting shot and after sitting a few minutes the person with her yelled help. When I arrived, she was slumped over on the bench leaning on the person with her. I called her name and she woke up but was a bit confused and her lips were pale. After resting for approximately 10 mintues, she felt completely fine and was able to walk away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2504024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: CO
Alter: 16,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 09.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Syncope

Symptomtext

Patient fainted, but came to in less than a minute. 2 BP readings were normal; gave patient water and a cold wet towel was placed on his forehead.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None Known
Vorgeschichte: none
Andere Medikamente: Received a flu shot at the same time
Allergien: NKA
Vorherige Impfungen: -

VAERS 2500708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

schwer

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 07.11.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Haematemesis Lethargy Syncope

Symptomtext

patient found having syncopal episode after Shingrix shot. patient helped to seat by staff, responsive @ 11:20am, this RN called MD stat @ 11:21. RN noted pt breathing with grunting breath sound with small coffee ground emesis around comer of mouth, VS 143/97 HR 68 on RA 100% @ 11:23. MD stat team arrived @ 11:24am. SBAR report given to MD and RN. Care handed over. Patient was lethargic after taken over and 911 was call, Engine arrived @ 11:31am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: patient sent to ED
Aktuelle Erkrankungen: unknown
Vorgeschichte: HTN Prediabetes, BPH hyperlipidemia
Andere Medikamente: Lopressor, lipitor, norvasc, vatamin C, ferrous sulfate
Allergien: no known
Vorherige Impfungen: -

VAERS 2500071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

schwer

Staat: IN
Alter: 18,0
Geschlecht: F
Eingang: 06.11.2022
Impfdatum: 06.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Loss of consciousness Nausea

Symptomtext

Patient passed out about 60 seconds after receiving the flu shot. Covid shot had been given about 15 mins prior to flu shot. Patient was sitting in a chair and slumped over onto the floor. Was checked by EMTs and refused to be taken to hospital, signed medical release forms to not go. Was unconscious for less than 60 seconds. Could hold a conversation immediately after passing out, stated that she could see me and that she felt ok other than a little nauseous and dizzy. Patient stayed on floor until EMT arrival about 5 mins later. Vitals were good other than slightly high HR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2499811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Syncope

Symptomtext

Pt felt light headed and fainted for few seconds then woke up. We called emergency services and then the paramedics came and assessed her and left Pt was free to go home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: None known to pharmacy
Andere Medikamente: None
Allergien: no known allergy to pharmacy
Vorherige Impfungen: -

VAERS 2726895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 22.12.2023
Impfdatum: 31.10.2022
Beginn: 22.10.2023
Tage bis Beginn: 356,0
Dosis: 1
Route/Site: - / -

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

Angiogram pulmonary normal Asthma Atrial fibrillation Blood thyroid stimulating hormone normal Brain natriuretic peptide normal Condition aggravated Dyspnoea Dyspnoea exertional Echocardiogram Echocardiogram abnormal COVID-19 Cardiac ablation Cardiac stress test normal Cardioversion Chest pain Ejection fraction Fatigue Laboratory test normal

Symptomtext

Patient is a 40 y.o. F with hx of anxiety/depression and ADHD. Recent admit (10/11-10/13/23) for new onset A fib with RVR. EP followed and pt was placed on Eliquis, Flecainide and Cardizem. Pt re-presented on 10/23/23 with CC of palpitations and episodes of A fib (noted on smart watch) with associated chest pain and SOB. Noted to be in A fib with RVR in ED but converted back to NSR and fluid bolus. Per ED, pt uncomfortable about returning home. As such admit to OBS for EP evaluation. S/p ablation 10/23/23. Hospital course complicated by dyspnea with unclear etiology, possibly related to OSA/OHS deconditioning in the setting COVID. Repeat ECHO unchanged, only trivial pericardial effusion, likley reactive to ablation. EP followed. Pulmonology followed, trial prednisone and breathing inhalers for possible asthma exacerbation. Stress test unremarkable. Sniff test negative. CTPA 10/23/23 unremarkable but suboptimal, Q scan with low probability of PE. RT performed NIF which was normal with VC 1950 ml. Pt notes continued shortness of breath on exertion, typically after 5 min. CM to order nurses aid, family called previous day to ensure coverage. 1. A fib: Noted last admit. TSH normal. CHADS2-VASC 1. TTE on 10/13/2023 normal LVEF, no WMA. EP followed and pt initiated Eliquis, Flecainide, and Cardizem. Now presented as above. S/p ablation 10/23/23. Continued home meds. In sinus during admission. EP followed 2. Dyspnea: ongoing with questionable worsening after ablation. Patient notes conversational and exertional dyspnea. No hypoxia. No wheezing; did not improve with prednisone/breathing tx. ECHO 10/13/23 as above. BNP 10/24/23 normal. Unclear etiology, possibly related to OSA/OHS deconditioning in the setting COVID. Repeat ECHO unchanged, only trivial pericardial effusion, likley reactive to ablation. EP followed. Pulmonology followed, trial prednisone and breathing inhalers for possible asthma exacerbation. Stress test unremarkable. Sniff test negative. CTPA 10/23/23 unremarkable but suboptimal, Q scan with low probability of PE. RT performed NIF which was normal with VC 1950 ml. Pt notes continued shortness of breath on exertion, typically after 5 min. CM to order nurses aid, family called previous day to ensure coverage. 3. COVID +: Not a candidate for paxlovid due to drug interaction. ID followed, remdesivir completed. 4. ADHD/Anxiety/Depression: Continued home Wellbutrin. Vyvanse discontinued on last admit. 5. Mild intermittent Asthma exacerbation: Xopenex scheduled as home med. Ipatroprium neb ordered. Prednisone thru 10/30/23. Ordered xopenex inhaler and neb, ipatropium neb for discharge. 6. Suspected OSA: Suspected on last admit. Often feel tired, fatigued, or sleepy during the daytime? + 1, Observed you stop breathing during sleep? + 1, BMI > 35 +1, Neck circumference > 40 cm + 1, and Patient's score is > 3 implying high risk for OSA. Referral was made for sleep study on last admit. 7. Morbid Obesity: BMI 46. Recommend lifestyle modification and weight loss.

Weitere VAERSDATA-Felder

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

VAERS 2719995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 01.12.2023
Impfdatum: 20.12.2022
Beginn: 27.11.2023
Tage bis Beginn: 342,0
Dosis: 4
Route/Site: IM / UN

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

Blood glucose increased COVID-19 Costovertebral angle tenderness Cough Dyspnoea Musculoskeletal chest pain Oral candidiasis Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

Admit date: 11/27/2023 Discharge date: 11/29/2023 Admitting Physician: DO Attending Physician at the Time of Discharge: DO Reason for Admission: cough, shortness of breath, bilateral rib pain Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) 82 YO-year-old female with h/o hypertension, hyperlipidemia, CKD 4, type 2 diabetes, peripheral vascular disease, AAA status post aortoiliac stent placement, vestibular neuronitis, and chronic rhinitis presents for evaluation of dry cough and shortness of breath. My admission, patient found to be COVID positive. She was started on Decadron 6 mg daily on remdesivir IV. Initially placed on 1-2 L nasal cannula O2, was then weaned off today. Patient is now saturating well on room air and walking around independently without any shortness a breath. She NS associated bilateral costovertebral angle tenderness, worse with coughing, and improved with cough drops. Her blood glucose has been elevated into the 200s to 300s range while on Decadron. We will plan to resume her home glipizide 5 mg daily along with insulin 40 units long-acting and Ozempic when she goes home. Plan for total 7 day Decadron 6 mg daily. PT/OT evaluated patient and recommended home on discharge. Patient found to have some oral candidiasis on examination, started on nystatin swish and spit with improvement of throat pain. Also given Robitussin for cough with improvement. No other active concerns. Discharged to home.

Weitere VAERSDATA-Felder

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

VAERS 2718168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: MO
Alter: 79,0
Geschlecht: F
Eingang: 27.11.2023
Impfdatum: 02.12.2022
Beginn: 03.12.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test Computerised tomogram Dyspnoea Echocardiogram Giant cell arteritis Headache Hypoacusis Magnetic resonance imaging head abnormal Tinnitus Visual impairment

Symptomtext

Hearing is terrible, eyesight is foggy, breathing is worse, headaches and had mri done a month after symptoms and diagnosed inflammation of temporal artery

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: MRI CT Scan Ultrasound of heart Numerous blood tests Buzzing in right ear
Aktuelle Erkrankungen: None
Vorgeschichte: COPD High blood pressure
Andere Medikamente: Lisinopril 40 mg, nifedipine 60mg Xanax Sertraline Breztri Albuterol Sulfate HFA Oxygen 2 liters
Allergien: None
Vorherige Impfungen: Flu shot

VAERS 2712009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 09.11.2023
Impfdatum: 17.11.2022
Beginn: 02.08.2023
Tage bis Beginn: 258,0
Dosis: 5
Route/Site: - / -

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

Aspartate aminotransferase increased Asthenia Bile duct stent insertion Bile duct stent removal Blood bilirubin increased Blood culture negative Blood prolactin increased COVID-19 Chest X-ray abnormal Chills Hepatic enzyme increased Leukocytosis Lung opacity Pyrexia SARS-CoV-2 test positive Tachycardia

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 8/2/2023 Discharge Date: 8/5/2023 Discharge Disposition: Home with services - Occupational therapy and Physical therapy DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is a 94 y.o. female who presented to Hospital with generalized weakness fever, chills. In the emergency department she had a temperature 39.4?, with leukocytosis and tachycardia. She is found to be COVID-19 positive. X-rays showed left opacity, suspicious for infection. Prolactin levels were increased, blood cultures are negative since discharge. Throughout the hospital course patient was on room air and did not complain of any SOB. She did note to have generalized weakness. PT and OT recommended home with healthcare, patient is agreeable and understands the plan. Patient also had elevated liver enzymes with AST in the 70-60 range. Was noted in the past patient had a biliary stent placed and removed sometime this year. Since then is noted that her bilirubin and liver enzymes have been elevated. Her bilirubin levels were increasing, however patient was asymptomatic and will be seeing PCP on 8/8. Will need further workup outpatient. She was discharged on stable condition and was to complete her antibiotic course.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Cognitive communication deficit Diaphragmatic hernia without obstruction or gangrene Dysphagia, unspecified Essential (primary) hypertension Fibromyalgia Nutritional anemia, unspecified Acidosis, unspecified Other abnormalities of gait and mobility Restless legs syndrome Supraventricular tachycardia Unspecified osteoarthritis, unspecified site Sepsis due to COVID-19 Transaminitis
Andere Medikamente: acetaminophen (TYLENOL) 650 MG suppository bisacodyl (DULCOLAX) 10 MG suppository haloperidol (HALDOL) 2 MG/ML solution hyoscyamine (ANASPAZ,LEVSIN) 0.125 MG tablet LORazepam (ATIVAN) 0.5 mg tablet nystatin (MYCOSTATIN) 100000 UNIT/ML suspe
Allergien: Amoxicillin AspirinUnknown Calcium Calcium Carbonate Doxycycline Hydromorphone Levofloxacin MeperidineUnknown Methocarbamol MetronidazoleUnknown MorphineUnknown Promethazine Raloxifene Sulfa DrugsUnknown Sulfamethoxazole-trimethoprim Systane Preservative FreeUnknown TrimethoprimUnknown
Vorherige Impfungen: -

VAERS 2685228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 22.09.2023
Impfdatum: 17.11.2022
Beginn: 02.09.2023
Tage bis Beginn: 289,0
Dosis: 4
Route/Site: IM / -

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

Chemotherapy Dyspnoea Fatigue Palpitations

Symptomtext

8/28/2023 - 9/11/2023 (14 days) Discharge Disposition: Home with Home Health Services PMH: -right breast cancer-ductal carcinoma; most recent chemotherapy on 08/24/2023 -immunocompromised -anxiety; depression -hyperlipidemia -macular degeneration -atrial fibrillation -HFrEF; echocardiogram showing LVEF: 30-35%; Presents emergency department with shortness of breath, palpitations and fatigue. 11/17/2022 Pfizer, Inc GJ6738 9/28/2021 Pfizer, Inc FC3184 3/4/2021 Pfizer, Inc EN6198 2/10/2021 Pfizer, Inc EL9269

Weitere VAERSDATA-Felder

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

VAERS 2520043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: CO
Alter: 40,0
Geschlecht: F
Eingang: 21.09.2023
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: ja

Brain fog Burning sensation Culture urine negative Dizziness Eye pain Hypoaesthesia Lacrimation increased Full blood count normal Heart rate increased Influenza virus test negative Muscle spasms Oedema peripheral Paraesthesia Respiratory syncytial virus test negative SARS-CoV-2 test negative Tachycardia Tongue discomfort Urine analysis

Symptomtext

Symptoms started at night the day off vaccination and include: burning to bilateral soles of feet excluding toes, right calf cramping at rest and while walking, burning of the tip of tongue, burning sensation after urination, tingling and loss of sensation to clitoral area during sexual intercourse. All these symptoms lasted for 3-4months. I also developed dizziness, brain fog and intermittent blurry and painful vision. Blurry vision was noted when looking at near objects, e.g. while reading, these symptoms resolved weeks later. The morning after vaccination I developed increased heart rate at rest ranging at 100-110s bpm which is normally in the 60s and elevated heart rate while walking or standing at 130-140s bpm. Tachycardia resolved 2 days later. Edema to right axilla resolved several days later. 11/25/2022 I was seen in Hospital ED for ongoing symptoms. Snellen eyes test was applied and normal, vital signs, CBC, urinalysis and Covid19/flu/rsv rapid test were normal. Received 1 dose of Ketorolac for eye pain, no change after intervention noted. Was told I probably had some viral illness and was told to take Ibuprofen around the clock for 2 weeks which I did and no improvement noted. 12/23/2022 I was seen by PA at Medical Center as a follow up. Urinalysis and urine culture test and neurological exam were normal. I was prescribed Gabapentin which I didn?t take.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: See above
Aktuelle Erkrankungen: -
Vorgeschichte: Dupuytren's contracture, motion sickness
Andere Medikamente: None
Allergien: Allergy to metal-skin rash
Vorherige Impfungen: Burning to the soles of feet as 2nd dose of Moderna vaccine in January 2021

VAERS 2658274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: -
Alter: 89,0
Geschlecht: F
Eingang: 19.07.2023
Impfdatum: 14.11.2022
Beginn: 17.07.2023
Tage bis Beginn: 245,0
Dosis: 5
Route/Site: - / -

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

Acute kidney injury COVID-19 Dehydration Hypophagia Orthostatic hypotension SARS-CoV-2 test positive Viral infection

Symptomtext

Patient admitted to hospital with COVID detected PCR. Provider discharge note "Patient is a 90 YO F with history of HTN, HLD, anxiety/depression, who presented with symptoms of orthostasis in setting of poor PO intake and viral syndrome. She was found to have COVID-19 infection and AKI due to dehydration. She was treated with IV fluids and supportive care. Symptoms and AKI resolved overnight and patient reported she felt back to her baseline. Sh was able to eat and drink a regular diet prior to discharge. Will continue holding indapamide and lisinopril on discharge and recommend PCP follow-up in 1 week for repeat BP check and labs. Consider resumption of one or both HTN medications at that time. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 2,0
Labordaten: COVID detected PCR on 7/17/23
Aktuelle Erkrankungen: -
Vorgeschichte: Dyslipidemia Class 1 obesity due to excess calories with serious comorbidity and body mass index (BMI) of 31.0 to 31.9 in adult Anxiety and depression History of colon cancer History of colon resection History of vitamin D deficiency Essential hypertension Osteoarthritis Prediabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2657107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 17.07.2023
Impfdatum: 05.12.2022
Beginn: 12.04.2023
Tage bis Beginn: 128,0
Dosis: 4
Route/Site: IM / LA

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

Cholecystitis acute Hypotension

Symptomtext

I95.9 HYPOTENSION 4/12/2023 ACUTE CHOLECYSTITIS

Weitere VAERSDATA-Felder

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

VAERS 2651277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 30.06.2023
Impfdatum: 29.12.2022
Beginn: 29.04.2023
Tage bis Beginn: 121,0
Dosis: 4
Route/Site: IM / LA

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

Hypotension Lumbar spinal stenosis Spinal fusion surgery Urethral stenosis

Symptomtext

HYPOTENSION 4/28/2023 FEMALE URETHRAL STRICTURE HYPOTENSION 4/28/2023 SPINAL STENOSIS OF LUMBAR SPINE HYPOTENSION 4/28/2023 FUSION OF LUMBOSACRAL SPINE

Weitere VAERSDATA-Felder

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

VAERS 2645868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 15.06.2023
Impfdatum: 21.11.2022
Beginn: 14.03.2023
Tage bis Beginn: 113,0
Dosis: 4
Route/Site: IM / RA

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

Gastrointestinal haemorrhage Hypotension

Symptomtext

HYPOTENSION 3/14/2023 GI HEMORRHAGE

Weitere VAERSDATA-Felder

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

VAERS 2642806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 08.06.2023
Impfdatum: 02.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: SYR / RA

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

Arthralgia Arthritis Autoimmune disorder Condition aggravated X-ray

Symptomtext

I was tested positive for COVID 19 last year in January the vaccine flared up my autoimmune disease and I was diagnosed severe joint pain Arthritis, the joint pain is unbearable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: X-ray
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Potacl Micros; Furosemide;
Allergien: Allergic to insects
Vorherige Impfungen: -

VAERS 2642251

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GJ6738

moderat

Staat: WI
Alter: 62,0
Geschlecht: M
Eingang: 07.06.2023
Impfdatum: 04.01.2023
Beginn: 26.01.2023
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: SYR / AR

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

Abdominal pain upper Blood test Bronchoscopy Chest X-ray Computerised tomogram Cough Decreased appetite Dyspnoea Electrocardiogram Fatigue Impaired driving ability Laboratory test abnormal Oxygen saturation decreased Sleep disorder Ultrasound scan Urine analysis Weight decreased

Symptomtext

Coughing, stomach pains, low oxygen levels, fatique, weight loss, loss of appetite. This all started between 2 and 3 weeks after this shot. Allergist prescribed Z-Pak, after that did not resolve the problem, he ordered another one. On 3/5/23 I went to urgent care, my oxygen level was so low they sent me straight to the R. They did EKG and Chest X-Ray after labs showed possible blood clots. No blood clots. I was given Prednisone. On 3/30/23 my breathing got bad enough that I went to my regular doctor who prescribed me a higher dose of Advair and sent me to see my allergist the following day with a cough so bad I could barely drive to get there. He prescribed me a nebulizer, which gave minimal results. On April 26th I went bac to the Hospital and got more x-rays and a CT scan. I was referred to a pulmonologist. Next I had a bronchoscopy there on 5/12/23. On 5/18/23 I had an ultrasound . On 5/23/23 I had more blood labs and a urine lab run. I still don't know the results of these tests. I am scheduled for 2 MRIs on June 22nd. Somewhere in the middle of all that (5/14/23) I went to the ER for the terrible stomach pains that have been keeping me up each night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Advair - Lossartan - Claritin - Omeprozole
Allergien: None
Vorherige Impfungen: -

VAERS 2641674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 06.06.2023
Impfdatum: 05.12.2022
Beginn: 11.02.2023
Tage bis Beginn: 68,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chest pain Fatigue Headache Inflammation Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

I didn't feel good in general after receiving the vaccine for about a day. I tested positive for COVID-19 on 02/11/2023. I felt tired, headache, chest pain and a low-grade fever. I contacted my doctor, but I did not receive a prescription. I took over the counter medication to help with my symptoms. As of today, I continue to have fatigue and in general not feeling good. The chest pain was the result of inflammation from a previous respiratory illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11FEB2023 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2639597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 95,0
Geschlecht: F
Eingang: 01.06.2023
Impfdatum: 19.12.2022
Beginn: 25.05.2023
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: IM / -

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

Cardiac failure congestive Condition aggravated

Symptomtext

CHF exacerbation

Weitere VAERSDATA-Felder

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

VAERS 2634793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: WI
Alter: 72,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 17.11.2022
Beginn: 03.05.2023
Tage bis Beginn: 167,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal X-ray Blood test abnormal Cholelithiasis Computerised tomogram abdomen abnormal Fall Infection Mobility decreased Ultrasound abdomen abnormal Urine analysis abnormal

Symptomtext

I had a hard time early in the morning getting out of bed. I had to have my husband help me. I went to the bathroom on the way back I fell, He could not get me up off the floor and I could not help enough to get myself up. He called help assist to get me up, they took me to the hospital, to find out what was going on with me. Once I arrived at the hospital, they started running test. I had bloodwork that came showing I had an infection, x-ray and CT scan that showed I had gallstones. An ultrasound was ordered to find out how big they were, the ultrasound revealed some of the stones are .7mm in size. I stayed in the hospital for three days until they felt the infection was cleared up enough for me to leave. I will be having the gallstones removed as soon as I am able to get back into the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 3,0
Labordaten: 03MAY2023 Ultrasound, gallstones ranging in various sizes; 03MAY2023 Bloodwork positive for infection; 03MAY2023 X-ray, positive for gallstones; 03MAY2023 CT scan confirmed multiple gallstones; 03MAY2023 Urinalysis, positive for infection
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; COPD
Andere Medikamente: Cyclobenzaprine; LUNESTA; oxybutynin; CRESTOR; NEXIUM; gabapentin; fluoxetine; metoprolol succinate; diltiazem ER; iron; sumatriptan; TYLENOL arthritis as needed; albuterol inhaler; STIOLTO RESPIMAT inhalation spray; ipratropium bromide and
Allergien: CHLORAPREP ONE STEP; ZESTORETIC; atorvastatin; chlorhexidine topical; lisinopril/hydrochlorothiazide; metronidazole; nitrofurantoin; tramadol
Vorherige Impfungen: -

VAERS 2632512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 16.05.2023
Impfdatum: 12.11.2022
Beginn: 01.03.2023
Tage bis Beginn: 109,0
Dosis: 5
Route/Site: IM / RA

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

Arthralgia Arthritis Dysgraphia Mobility decreased Pain in extremity Trigger finger X-ray limb abnormal

Symptomtext

In early March 2023 my right thumb became difficult to bend. It was sore near the joint and was awkward to write. My doctor referred me to a specialist. I was diagnosed with trigger finger and I received an injection. I visited the specialist on April 26, 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-Ray on my right hand, arthritis, 04/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: No Thyroid
Andere Medikamente: ARMOUR THYROID; multivitamin; calcium; vitamin D3
Allergien: N/A
Vorherige Impfungen: -

VAERS 2632425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: PA
Alter: 54,0
Geschlecht: F
Eingang: 16.05.2023
Impfdatum: 14.11.2022
Beginn: 04.04.2023
Tage bis Beginn: 141,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Chest pain Cough Fatigue Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

4/4/23 I had fatigue, pain in my chest, a cough and body aches. Overnight, I began running a fever that ranged over three days between 101 and 103. I was sick for three days. I took an at home COVID test and it was positive. I had a telehealth visit on 4/5/23 and was started on Paxlovid. I took the Paxlovid for the five days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 5APR23-At Home COVID Test-Positive
Aktuelle Erkrankungen: Does not remember
Vorgeschichte: High Blood Pressure, High Cholesterol, GERD, Hypothyroidism, Peripheral Neuropathy, Anxiety
Andere Medikamente: Pregabalin, Synthroid, Losartan, Atorvastatin, Pantoprazole, Sertraline, Xiidra Eye Drops
Allergien: Penicillin, Erythromycin, Sulfa
Vorherige Impfungen: Flu like symptoms with all tetnus vaccines

VAERS 2613013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 14.11.2022
Beginn: 14.12.2022
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: SC / UN

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

Condition aggravated Haptoglobin decreased Laboratory test Platelet count decreased Thrombotic thrombocytopenic purpura

Symptomtext

Patient received 4 previous Moderna COVID 19 vaccinations on 6/22/22, 12/6/21, 3/25/21, and 2/25/21. She received above Pfizer booster COVID vaccine exactly 30 days before a recurrence of her Thrombotic, thrombocytopenic purpura. She was hospitalized on 12/14/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 16,0
Labordaten: 12/14 Platelet count 35, shistocytes 2plus 12/15 platelet count 13 12/14 ADAMTS13 less than 5 12/14 Haptoglobin less than 10
Aktuelle Erkrankungen: None known
Vorgeschichte: Hx of Thrombotic Thrombocytopenic Purpura in 1998 Type 2 DM, atrial fibrillation, hyperlipidemia, remote hx of DVT
Andere Medikamente: Allopurinol 100mg Digoxin 0.125mg Famotidine Metformin Metoprolol 25mg Pravastatin warfarin
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2610176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 29.11.2022
Beginn: 23.01.2023
Tage bis Beginn: 55,0
Dosis: 4
Route/Site: IM / LA

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

Blood creatinine normal Blood glucose increased Blood test abnormal Cardiac stress test abnormal Chest X-ray normal Chest pain Echocardiogram abnormal Electrocardiogram normal Extrasystoles Flushing Full blood count normal Glomerular filtration rate normal Headache Heart rate irregular Hypertension Hypoaesthesia Laboratory test normal Left ventricular hypertrophy

Symptomtext

On 01/23/2023, I woke up around 02:00AM and I was flushed, and I had chest pain and my left arm was numb. I could feel my heart beating really hard. That's what led me to the emergency room. When I was at the emergency room, my blood pressure was 221 over 109 and my pulse was 65. I also had a bad headache and left calf pain. They gave me an x-ray to make sure my lungs were clear, and they were. I had a lot of blood work done that did not indicate a cardiac event. They discharged me without any other testing and told me to follow up with a cardiologist. I followed up and I had an echocardiogram, a stress test, and an ultrasound of my left calf. I have subsequently had high blood pressure. I have been placed on losartan. I started at 25 milligrams, and I am now up to 100 milligrams and my blood pressure is not yet controlled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 23JAN2023 Lung X-Ray, nothing abnormal found; Basic Metabolic Panel, nothing abnormal found; Globular Filtration Test, nothing abnormal found; Troponin Test, nothing abnormal found; POCT ABL Panel, Low PC02 And Low P02; ISTAT8, high glucose; ISTAT Creatinine, nothing abnormal found; POC Hepatic Panel, nothing abnormal; SECO Draw QBC, nothing abnormal found; CBC with platelets no differential, nothing abnormal found; EKG, nothing abnormal found; 08FEB2023 Echocardiogram, Moderate Asymmetric Left Ventricular Hypertrophy; Stress Test, more occasional PVC's with increased Stress including a four beat run and couplet; Ultrasound of calf, nothing abnormal found
Aktuelle Erkrankungen: None
Vorgeschichte: Reactive Airway Disease
Andere Medikamente: RESTASIS; multivitamin; fish oil; vitamin B12; vitamin D; estradiol; flaxseed; PRESERVISION AREDS 2
Allergien: OMNICEF
Vorherige Impfungen: -

VAERS 2600139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: KY
Alter: 58,0
Geschlecht: M
Eingang: 21.03.2023
Impfdatum: 13.02.2023
Beginn: 17.03.2023
Tage bis Beginn: 32,0
Dosis: 5
Route/Site: SYR / LA

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

Chest X-ray abnormal Dyspnoea Pneumonia Respiratory tract congestion

Symptomtext

I had pneumonia, I was short of breath, and they did a chest X-ray and said I had pneumonia. They gave me shots and some medication. After taking the medication I feel a bit better, but I still feel congested. I feel stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 17MAR2023 X-ray
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic obstructive pulmonary disease; Asthma; Kidney disease; Degenerative disc disease
Andere Medikamente: CoQ10; autophagy renew; vitamin E; metabolic activator; acetylcysteine; MEG FRT; VECTOMEGA; vitamin B12; SNEECURE
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2594665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 28.10.2022
Beginn: 04.03.2023
Tage bis Beginn: 127,0
Dosis: 4
Route/Site: - / -

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

Asthenia COVID-19 Chest X-ray normal Computerised tomogram abdomen abnormal Condition aggravated Constipation Gait disturbance Mobility decreased SARS-CoV-2 test positive

Symptomtext

Discharge Provider: DO Primary Care Provider, MD Admission Date: 3/4/2023 Discharge Date: 3/6/2023 PRESENTING PROBLEM: Generalized weakness [R53.1] COVID-19 virus infection [U07.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 6-year-old male who presented to the ER on 03/04/2023 with chief complaint of weakness. At home patient was having increased weakness with inability to get off the toilet by himself. He was helped back to bed however continued to have difficulty ambulating and was brought to the ER by EMS. In the emergency department he was positive for COVID-19. Chest x-ray is negative. CT scan of the abdomen done in the emergency department is consistent with constipation. He was admitted to the hospitalist service for further management of generalized weakness and COVID-19. He was started on remdesivir and completed 2 doses PT and OT were consulted during hospitalization who recommend outpatient therapy services. The patient remained on room air throughout hospitalization. On day of discharge patient states that he has been feeling well and agrees with plan to discharge home with additional outpatient resources. All questions and concerns were addressed to patient's satisfaction and he was discharged in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: PAC (premature atrial contraction) LAFB (left anterior fascicular block) Frequent PVCs CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) Shortness of breath Chest heaviness Constipation Nephrolithiasis COVID Weakness COVID-19
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Ascorbic Acid 500 MG CAPS aspirin 81 MG tablet dilTIAZem (CARDIZEM CD) 120 MG 24 hr capsule Magnesium 250 MG TABS metoprolol succinate-XL (TOPROL-XL) 50
Allergien: None
Vorherige Impfungen: -

VAERS 2591818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 02.12.2022
Beginn: 19.12.2022
Tage bis Beginn: 17,0
Dosis: 5
Route/Site: IM / RA

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

Blood pressure increased COVID-19 Cardiac stress test abnormal Chest pain Echocardiogram abnormal Fatigue Hypokinesia Left ventricular end-diastolic pressure increased Pain in extremity SARS-CoV-2 test positive

Symptomtext

I had little soreness in my arm and fatigue after receiving the vaccine. I contracted COVID-19 while on vacation and tested positive for COVID-19 on 09/17/2022. I took PAXLOVID starting on 09/18/2022 and tolerated the medication very well. I developed random chest pains and got worse. I went for a stress and echocardiogram on 01/11/2023 it showed an abnormal atypical hypokinesis and stress portion was normal and elevated blood pressure. I saw a cardiologist on 01/17/2023 and showed a left ventricle elevated diastolic pressure. I was prescribed amlodipine and my symptoms got better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 17SEPT2022 COVID-19 test positive; 11JAN2023 STRESS/ECHO positive
Aktuelle Erkrankungen: Chest Discomfort
Vorgeschichte: High Cholesterol; Atypical Migraines; Depression; Osteoporosis
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Moderna vaccine, no fevers, muscle aches, fatigue and headaches.

VAERS 2577263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

moderat

Staat: TX
Alter: 76,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 30.01.2023
Beginn: 01.02.2023
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / AR

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

Arrhythmia

Symptomtext

Patient received the Pfizer bivalent vaccine on Monday 1/30/2023 and had no reactions that day or the next day (01/31/2023). On Wednesday (02/01/2023), she started experiencing arrhythmias, which still are occurring. She contacted her doctor, who advised her to contact us to report it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: unknown
Vorgeschichte: a.fib
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2574263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MD
Alter: 65,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 31.10.2022
Beginn: 23.12.2022
Tage bis Beginn: 53,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Migraine Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sinus congestion

Symptomtext

The week before I had a terrible migraine. I got sore throat and runny nose and sinus congestion with a cough. I tested at home, and I was COVID-19 positive. I called urgent care they prescribed PAXLOVID, because I have asthma and they thought it would be best. I started feeling better at least 24 hours after starting the PAXLOVID. I was tired for maybe a week or more. It was more tired than normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 23DEC2022 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism
Andere Medikamente: Magnesium glycinate; vitamin D3 K2-7; DIVIGEL; progesterone; SYNTHROID; CYTOMEL
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2573285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: NE
Alter: 77,0
Geschlecht: M
Eingang: 01.02.2023
Impfdatum: 27.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: 6
Route/Site: IM / LA

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

Aphasia Brain neoplasm Computerised tomogram head Craniotomy Echocardiogram Electrocardiogram Headache Laboratory test Magnetic resonance imaging head abnormal Paraesthesia

Symptomtext

Onset of intermittent headaches and tingling of the right hand began in mid December. The 2nd week of January, I had a transient episode of expressive aphasia that lasted about 1 minute. A week after that, a 2nd episode of expressive aphasia happened that was much longer which resulted in an ER visit and hospital admission. The subsequent work up showed a brain tumor in the left parietal lobe on an MRI scan. On 01/17/2023 I had a craniotomy which removed most of the tumor. Now I'm waiting for an oncology evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: 1,0
Labordaten: Carotid Studies; EKG; CT Scan of the Head; Echocardiogram; 09JAN 2023 Brain MRI - Indicated Left Parietal Lobe Tumor; Lab Work
Aktuelle Erkrankungen: None
Vorgeschichte: Myasthenia Gravis; Chronic Kidney Disease; Essential Hypertension (Controlled); Degenerative Joint Disease; Vitamin B12 Deficiency; Vitamin D Deficiency; Hypothyroidism; Gout
Andere Medikamente: Acetaminophen; Allopurinol; Low Dose Aspirin; Calcium Carbonate; Vitamin B12 Injection; Dapagliflozin; Denosumab Injection Every 6 Months; Eculizumab Infusion Every 2 Weeks; Vitamin D2 Once a Month; Ferrous Sulfate XR; Folic Acid; Levothyro
Allergien: Azathioprine; Immune Human Globulin; Mycophenolate; Bactrim; Nonsteroidal Anti-inflammatories
Vorherige Impfungen: -

VAERS 2570544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

moderat

Staat: GA
Alter: 74,0
Geschlecht: M
Eingang: 30.01.2023
Impfdatum: 01.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 19,0
Dosis: UNK
Route/Site: - / -

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

Asthenia Blood test Cardiac stress test Dizziness Magnetic resonance imaging heart Palpitations

Symptomtext

Weakness, dizziness, heart racing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 2,0
Labordaten: MRI of heart, stress test. Blood tests. Cat scan not yet done.
Aktuelle Erkrankungen: hypertension
Vorgeschichte: hypertension
Andere Medikamente: allopurinol, amlodapine, lisinopril/hctz, sertaline, divalproex
Allergien: none
Vorherige Impfungen: -

VAERS 2563263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 14.11.2022
Beginn: 15.01.2023
Tage bis Beginn: 62,0
Dosis: 5
Route/Site: IM / LA

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

C-reactive protein increased COVID-19 Condition aggravated Hyperglycaemia Influenza Influenza A virus test positive Insulin-requiring type 2 diabetes mellitus SARS-CoV-2 test positive

Symptomtext

COVID+ 1/15/2023. Vaccination status - Pfizer x4 + Pfizer BIVALENT x1 PRIOR VAERS SUBMISSION - VAERS 929214 BRIEF OVERVIEW: Discharge Provider: M* Primary Care Provider: DO Admission Date: 1/15/2023 Discharge Date: 01/18/2023 Presenting Problem: COVID Active Hospital Problems Diagnosis Date Noted POA ? CRP elevated 01/17/2023 Unknown ? COVID 01/15/2023 Unknown ? Influenza 01/15/2023 Unknown ? Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin 02/23/2022 Yes ? Status post heart transplant DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: This patient is a 59 yo M with PMH of heart transplant 5/9/19, DM2, HTN, dyslipidemia and paralyzed vocal cord who was admitted to the heart transplant team on 1/15/23 after testing positive for COVID and Influenza A. He was started on Tamiflu and Remdesivir (for total of 4 doses). ID was consulted. He did not require antibiotics. He was not hypoxemic. He was seen by medical services for management of his diabetes His immunosuppression goals were not changed, but his doses were adjusted to keep him toward the lower end of goal. He was medically ready for discharge on 1/18/23. Consults: Infectious disease Medical Services

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Vocal cord paralysis Unspecified hearing loss Hypertriglyceridemia Chronic bilateral low back pain without sciatica Anemia Status post heart transplant Immunosuppressed status Seasonal allergies Other osteoporosis without current pathological fracture Stage 3a chronic kidney disease Thoracic aortic aneurysm, without rupture Gastro-esophageal reflux disease without esophagitis Emphysema, unspecified Dyskinesia of esophagus COVID-19 Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin
Andere Medikamente: Acetaminophen 500-1,000 mg Oral Every 8 hours PRN Alendronate Sodium 70 mg Oral Weekly, Taking on Sunday amLODIPine Besylate 2.5 mg Oral Daily Amoxicillin 2,000 mg Oral As Instructed, Take one hour prior any dental visit Ascorbic Acid 500 m
Allergien: NSAIDS - other
Vorherige Impfungen: -

VAERS 2561389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: IL
Alter: 18,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 06.01.2023
Beginn: 08.01.2023
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

2 days after shot developed numbness and tingling in left wrist and hand, this did not resolve. Client saw her provider and was given Prednisone. Symptoms have since resolved

Weitere VAERSDATA-Felder

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

VAERS 2554817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: AR
Alter: 30,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 13.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Back pain Condition aggravated Hypoaesthesia Paraesthesia

Symptomtext

I was having issues with lower back pain, and it got worse after being vaccinated. I am having numbness, tingling, and pain in my legs that extends to my ankles at times. I contacted my doctor and was prescribed meloxicam and Physical Therapy. I am still dealing with these symptoms at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: XYZAL; omeprazole; multivitamin
Allergien: Perfume
Vorherige Impfungen: -

VAERS 2552579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 09.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Chest pain Cough Diarrhoea Ear infection Headache Influenza like illness Nasal congestion Nausea Pain Pyrexia SARS-CoV-2 test negative Throat irritation

Symptomtext

My flu like symptoms started on 12/10/2022 in the morning at 08:00AM. I woke up with a stuffy nose, itchy throat, headache, dry cough, body aches, nausea, diarrhea, fever, ear infection on the right, and chest pains. I did a telehealth with my doctor on 12/29/2022. He prescribed me with methylprednisolone 4mg for 6 days. I took DAYQUIL and NYQUIL from 12/10/2022-12/29/2022.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 06JAN2023 COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia 7 years ago June 2015
Andere Medikamente: Omeprazole
Allergien: None
Vorherige Impfungen: Flu shot 2008 I got pneumonia

VAERS 2552456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: IL
Alter: 68,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 08.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 6,0
Dosis: 5
Route/Site: SYR / AR

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

Anticoagulant therapy Atrial fibrillation Blood pressure abnormal Cardiac monitoring Condition aggravated Echocardiogram Electrocardiogram Fatigue Haemoptysis Heart rate abnormal Laboratory test Renal impairment Surgery

Symptomtext

The vaccine was on 11/08/2022. I had a scheduled surgical procedure on 11/14/2022 and at that time, I was on the operating table and I was going to have a vein procedure. Apparently, I began to cough off blood and they stopped the procedure. We were going to try again on the 12/14/2022. The EMT came before I was released from the hospital after this incident and they looked through all my sinuses to make sure there was no apparent reason for this happening and they noted it could have just been a nose bleed. In December, during pre-op, they noted my blood pressure was 198/105 and my heart rate was 198. I was hospitalized to determine why I was in stroke range and called off the procedure. They told me I needed to be seen by a cardiologist and a nephrologist. My kidney had showed reduced function. I have a sleep study coming up in February. I am not symptomatic of heart palpitations or irregularity. What I feel is complete exhaustion. I can't tell when I'm getting episodes of possible a-fib. None of this was apparent back in April and August boosters. We're trying to figure out what the causes are. I am not aware when I'm in a-fib, but I just feel total exhaustion. I've assumed since this diagnosis that it could be structural. I am now taking metoprolol and ELIQUIS until this is controllable. Everything is uncertain at this time. I've taken my blood pressure on and off during this time, and I've never seen anything abnormal. I also had a bad COVID-19 infection back in April and events throughout this time have gotten worse. I've spent 9 months since April experiencing symptoms heart related, both blood pressure and heart rate. Nothing has been caught until these recent surgical dates. Heart related events began to stack up. The sleep study can confirm if there is a-fib. I am currently wearing a heart monitor for 30 days for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: EKG; Echocardiogram; Numerous tests
Aktuelle Erkrankungen: None
Vorgeschichte: Inflammatory Aggressive Erosive to the Joint Osteoarthritis; Varicose vein in leg
Andere Medikamente: Vitamin D3; fish oil; coQ10; vitamin C; calcium; fiber gummy; low dose aspirin; VOLTAREN gel; CRESTOR
Allergien: NEXIUM; PRILOSEC; codeine; ATIVAN; AMBIEN; NSAIDs; duloxetine; adhesives
Vorherige Impfungen: -

VAERS 2550324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 28.10.2022
Beginn: 30.12.2022
Tage bis Beginn: 63,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chest X-ray normal Cough Dyspnoea Hypoxia Nasal congestion Oxygen saturation decreased SARS-CoV-2 test positive

Symptomtext

COVID+ 12/28/2022. Vaccination status - pfizer x3 _ Pfizer BIVALENT BRIEF OVERVIEW: Discharge Provider: PRIVATE MD Primary Care Provider: PRIVATE MD Admission Date: 12/30/2022 Discharge Date: 01/02/2023 Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypoxia [R09.02] COVID-19 [U07.1] HOSPITAL COURSE: The patient is a 73-year-old male with history of Pompe disease, ischemic CMP, CAD, systolic heart failure, Afib on Eliquis, COPD, HTN, and anemia who presented with nasal congestion, cough, and shortness of breath. His symptoms started 12/26 and he tested positive for COVID 12/28. In the emergency department his oxygen dropped to 84% with ambulation. Chest x-ray was without an acute process. He received 1 dose of IV steroids and albuterol. He was admitted to the hospitalist service. Steroids were continued on admission. His symptoms improved and he was evaluated for home oxygen, but did not qualify as his oxygen saturation remained stable at rest and with activity.He had clinically improved on the day of discharge and was discharged home in stable condition. Decadron was stopped as he was on room air and he felt it was not allowing him to sleep at night. He was advised to follow up with his PCP within 5 days of discharge. He also will need to reschedule his infusion of Nexviazyme which he missed this am while hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: ED visit on 10/25/2022: CHIEF COMPLAINT: BACK PAIN and SHORTNESS OF BREATH Assessment/Plan DIAGNOSIS at time of disposition: 1. Chronic low back pain without sciatica, unspecified back pain laterality 2. Dyspnea, unspecified type 3. Peripheral edema 4. COVID-19 ruled out
Vorgeschichte: Colon polyps Environmental allergies HTN (hypertension), benign Impaired fasting glucose Vitamin D deficiency Paroxysmal atrial fibrillation (HCC) Coronary artery disease involving native coronary artery of native heart Alcohol abuse Dyslipidemia S/P coronary artery stent placement NSTEMI (non-ST elevated myocardial infarction) (HCC) Ischemic cardiomyopathy OSA (obstructive sleep apnea) Typical atrial flutter (HCC) Restrictive airway disease 3-vessel CAD H/O heart artery stent Proximal muscle weakness Pompe disease (HCC
Andere Medikamente: Acetaminophen 1,300 mg Oral 3 times daily PRN Apixaban 5 MG TAKE 1 TABLET BY MOUTH TWO TIMES A DAY for blood thinner Patient taking differently: Take 5 mg by mouth 2 times daily. Ascorbic Acid 500 mg Oral Daily Aspirin 81 mg Oral Daily Ca
Allergien: environmental
Vorherige Impfungen: -

VAERS 2548950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 03.01.2023
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: ja

Mobility decreased Pain in extremity

Symptomtext

My arm was in so much pain. I could not move my arm. The treatment was putting a cold towel on it. The pain lasted a couple of days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Sinus infection
Vorgeschichte: Mild Asthma; Takotsubo
Andere Medikamente: Vitamin D3; acidophilus; magnesium oxide; B12; MCG; calcium; NEURIVA; multivitamin; alendronate; levocetirizine; atorvastatin; montelukast; losartan; levothyroxine; nadolol; hydrochlorothiazide; albuterol
Allergien: Environmental allergies; pineapple; off spice; fresh tomatoes; fresh plums; fresh peaches
Vorherige Impfungen: Flu, 5 years ago. I was in the hospital for 10 days

VAERS 2547582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: NC
Alter: 82,0
Geschlecht: F
Eingang: 31.12.2022
Impfdatum: 13.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

Blood pressure increased Blood pressure measurement Burning sensation Chills Paraesthesia

Symptomtext

high blood pressure (mentioned 173/93 but was not able to confirm); burning and tingling sensation in the leg/Burning in her legs, and at times it goes further up into the her body; burning and tingling sensation in the leg/ tingling go to her head at times/ tingling went up further in her body; chills; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. An 82-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Dec2022 as dose 5 (booster), single (Lot number: GJ6738) at the age of 82 years for covid-19 immunisation. The patient's relevant medical history included: "blood clot in her leg", start date: 2013 (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, LOT: Unknown), administration date: 13Jan2021, when the patient was 80-year-old, for COVID-19 immunization, reaction(s): "COVID-19"; BNT162b2 (Dose 2, LOT: Unknown), administration date: 04Feb2021, when the patient was 80-year-old, for COVID-19 immunization, reaction(s): "COVID-19"; BNT162b2 (Dose 3, LOT: Unknown), administration date: 04Oct2021, when the patient was 81-year-old, for COVID-19 immunization, reaction(s): "COVID-19"; BNT162b2 (Dose 4, Unknown arm, LOT: Unknown), administration date: 20Jul2022, when the patient was 82-year-old, for COVID-19 immunization, reaction(s): "COVID-19". The following information was reported: BLOOD PRESSURE INCREASED (non-serious), outcome "unknown", described as "high blood pressure (mentioned 173/93 but was not able to confirm)"; BURNING SENSATION (non-serious), outcome "unknown", described as "burning and tingling sensation in the leg/Burning in her legs, and at times it goes further up into the her body"; PARAESTHESIA (non-serious), outcome "unknown", described as "burning and tingling sensation in the leg/ tingling go to her head at times/ tingling went up further in her body"; CHILLS (non-serious), outcome "unknown". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller was asking regarding Pfizer COVID vaccine. When asked, she mentioned all three were "Pfizer shot". Caller was not able to verify if that was the bivalent shot. Had a blood clot in her leg in 2013 that never did dissolve, but this seems to be a lot worse than after she had the clot. This burning and tingling went up further in her body. Tingling and burning is in both legs. As per caller it was her booster shot or third dose and she want to know if burning ang tingling sensation in the leg was a side effect of the vaccine. She also added that she was experiencing chills and high blood pressure (mentioned 173/93 but was not able to confirm). Caller also expressed that she did not have problem with the other vaccine. No Investigations: No, Other Products: No. Have been having some problems with her legs. Burning in her legs, and at times it goes further up into the her body. Wondering if this has anything to do with the Pfizer shots. Legs get very hot and tingling. Has had the burning and tingling go to her head at times. She has shrunk as she has aged. Has been going on for at least 3 weeks. Had vaccine on 13Dec2022. Burning and tingling started around that time. Guessing about the time. Can't remember exactly when it started. It was worse at night. Adverse event does not required visit to: Emergency room or Physician's office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:High, mentioned 173/93 but was not able to confirm
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Thrombosis of leg superficial venous
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: PA
Alter: 73,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 26.12.2022
Beginn: 26.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Cold sweat Diarrhoea Disturbance in attention Dyspnoea Headache Insomnia Night sweats Pain Pyrexia

Symptomtext

I experienced body aches, short of breath, cold sweats, fever, headaches, severe diarrhea, lack of concentration, lack of sleep, and night sweats.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Spinal stenosis, High cholesterol
Andere Medikamente: Metformin; Atorvastatin; Lyrica; Valsartan; Aspirin; Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2540686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: WI
Alter: 29,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 23.11.2022
Beginn: 13.12.2022
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Dyspnoea Headache Respiratory tract congestion SARS-CoV-2 test positive Vomiting

Symptomtext

I tested positive for COVID-19 on 12/13/22. I had congestion, vomiting, shortness of breath and headache. I contacted my doctor and was prescribed 5 days' worth of PAXLOVID. I still have some congestion and shortness of breath, but I am feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 13DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anxiety; Depression; Autism
Andere Medikamente: Sertraline; WELLBUTRIN; TYLENOL; ibuprofen; vitamin D; vitamin C; ZYRTEC
Allergien: N/A
Vorherige Impfungen: -

VAERS 2540117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 01.12.2022
Beginn: 02.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / RA

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

Chills Cough Decreased appetite Headache Illness Investigation Pain Pyrexia SARS-CoV-2 test Tremor Weight Weight decreased White blood cell analysis

Symptomtext

never been this sick in her life; shaking; Weight started at 196, but when she weighed herself 2 days ago , it was 190; Cough; chills; Fever; Loss of appetite; Body aches; Headache; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 49-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Dec2022 at 18:00 as dose 4 (booster), single (Lot number: GJ6738) at the age of 49 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: BNT162b2 (1st dose 14Jan2021 , Lot EH9999, expiration 14Jan2021. Says 16:00 but she got in the morning, thinks that is the time it expired), administration date: 14Jan2021, when the patient was 47-year-old, for Covid-19 immunization; BNT162b2 (2nd dose 03Feb2021, Lot EL9262, expiration is 03Feb2021 at 14:00 but she got it at 10:25, so it was not expired. Injected in right arm), administration date: 03Feb2021, when the patient was 47-year-old, for Covid-19 Immunization; BNT162b2 (3rd (Booster) dose, 01Dec2021, Lot FJ1620, expiration unknown, injected in right arm.), administration date: 01Dec2021, when the patient was 48-year-old, for COVID-19 Immunization; Flu vaccine (She had flu vaccine, but that was in Sep 2022, which was more than 4 weeks prior to this.), administration date: Sep2022, when the patient was 49 years old, for immunisation. The following information was reported: PAIN (medically significant) with onset 02Dec2022, outcome "not recovered", described as "Body aches"; PYREXIA (disability) with onset 02Dec2022, outcome "not recovered", described as "Fever"; HEADACHE (disability) with onset 02Dec2022, outcome "not recovered"; DECREASED APPETITE (medically significant) with onset 02Dec2022, outcome "not recovered", described as "Loss of appetite"; CHILLS (disability) with onset 02Dec2022, outcome "not recovered"; COUGH (disability) with onset 14Dec2022, outcome "not recovered"; ILLNESS (disability), 12 days 6 hrs after the suspect product(s) administration, outcome "unknown", described as "never been this sick in her life"; TREMOR (disability), outcome "unknown", described as "shaking"; WEIGHT DECREASED (medically significant), outcome "unknown", described as "Weight started at 196, but when she weighed herself 2 days ago , it was 190". The patient underwent the following laboratory tests and procedures: annual physical: (Nov2022) All good and labs good, notes: 3 weeks ago; SARS-CoV-2 test: (13Dec2022) Negative, notes: she had a COVID-19 test and was negative; Weight: (unspecified date) 196, notes: Weight started at 196, but when she weighed herself 2 days ago , it was 190; (13Dec2022) 190, notes: Weight started at 196, but when she weighed herself 2 days ago , it was 190; White blood cell analysis: (Nov2022): No indication that white blood cell showed any infection, notes: 3 weeks ago. Therapeutic measures were taken as a result of headache, cough, chills, pyrexia, decreased appetite, pain, illness, tremor, weight decreased. Clinical course: Received call from patient regarding the Pfizer Bivalent COVID vaccine booster. She is having an overreaction. She received it on 01Dec2022. Starting on 02Dec2022, she began having headache, body aches, chills, fever, loss of appetite and this has been daily since that day until today. She is supposed to be at work now and cannot. It is all through night. This has been going on since 02Dec2022. Monday, she tried to go to work and by 11am, she could not handle it anymore. She took Tylenol. Was shaking all over the place. She is concerned because last night, began with dry cough and never been this sick in her life. 3 weeks ago, did annual physical and it was all good and labs good. No indication that white blood cell showed any infection. She wants to know why after 2 weeks, she is still having this. She is the bread winner for her children. If she cannot work, she cannot earn any money. She needs some help and explanation. She contacted the (place name withheld) and they told her it was an over reaction to the vaccine. Weight started at 196, but when she weighed herself 2 days ago, it was 190. Had loss of appetite and not eating. She scheduled an appointment today to see a coworker (name withheld) because her primary is not there today. As she coughs it pounds in her head. That is getting worse. All started 02Dec2022, except cough, it started last night. Headache not constant. Mostly when she coughs. Fever, chills are constant. Has them in mid morning and late evening. Preceded by chills and Body Ache. Headache it felt like it was the same, but now it is worsening because her head pounds when she coughs. Body aches when wakes up in the morning, wakes up the same and is not changing, and so is the loss of appetite. It is the same not worsening or better. If she had an adult to stay with her daughter, she would have gone to the ER last night. Loss of appetite, not complaining because she has ben wanting to lose weight but not wanting to do it that way. She wanted to fortify herself because she was seeing a lot of patients with viral symptoms. Had a coworker that had it last month. She only had soreness in arm and nothing this month. She did have a few days of soreness in arm and then it is better. She did not wish to complete report for her and unable to confirm which vaccine she received. Previous Pfizer COVID vaccine products: 1st dose 14Jan2021 got in (state name withheld), Lot EH9999, expiration 14Jan2021. Says 16:00 but she got in the morning, thinks that is the time it expired. Needed to get glasses to see it and confirmed she needed prescription glasses prior to getting the Pfizer COVID vaccines. Injected in Unknown arm. She thinks it is the right arm and thinks she got all of them in the right arm. 2nd dose 03Feb2021, Lot EL9262, expiration is 03Feb2021 at 14:00 but she got it at 10:25, so it was not expired. Injected in right arm. Of all 4 vaccines, besides this one that she received on 01Dec2022, this is only other one she had reaction to. She has a picture of the reaction she got on this 2nd one. This 2nd dose is what gave her red wheel on arm. Itchy and tender and lingered for a few days and went away. The first and third one had zero symptoms. Pfizer COVID vaccine Booster for last year was 3rd dose: 01Dec2021, Lot FJ1620, expiration unknown, injected in right arm. She takes no other medications except Vit D, C, Zinc and does not take them regularly. No prescription medications.She does not have any medical conditions. She did COVID test and she does not have result, but they showed it to her on Tuesday and it was negative. Confirmed it was this past Tuesday on 13Dec2022. Tylenol and Advil have been her friend since then. She takes it everywhere she goes. Feels insecure without it. Pfizer/BioNTech COVID-19 Vaccine Follow-up Questionnaire. Time: 18:00. 4.Vaccination Facility Type: Pharmacy. Vaccine Administered at Military Facility? No. 5. Prior Vaccinations (within 4 weeks): none. She had flu vaccine, but that was in Sep2022, which was more than 4 weeks prior to this. 8. Family Medical History Relevant to Adverse Events (AEs): none. 11. Adverse Events: No medical treatment other than Tylenol and Advil. The caller refers she got the gray cap Pfizer BioNTech COVID-19 bivalent on 01Dec2022 and on 02Dec2022 she started with headache, cough, fever, chills, loss of appetite and body aches. After two weeks of having this, on 13Dec2022 she had a COVID-19 test and was negative. I cannot work. I cannot think of my family. It is so bothersome. When I cough there is a pound in my head. It makes my headache worse. What can I do?.I am the breadwinner for my family and I am not able to work. Is there any program.; Sender's Comments: Based on the available information in the case, the causal association between the events headache, cough, chills, pyrexia, decreased appetite, pain, illness, tremor, weight decreased and the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 202211; Test Name: annual physical; Result Unstructured Data: Test Result:All good and labs good; Comments: 3 weeks ago; Test Date: 20221213; Test Name: Covid-19 Test; Test Result: Negative ; Comments: she had a COVID-19 test and was negative; Test Name: weight; Result Unstructured Data: Test Result:196; Comments: Weight started at 196, but when she weighed herself 2 days ago , it was 190; Test Date: 20221213; Test Name: weight; Result Unstructured Data: Test Result:190; Comments: Weight started at 196, but when she weighed herself 2 days ago , it was 190; Test Date: 202211; Test Name: white blood cell; Result Unstructured Data: Test Result:No indication that white blood cell showed any inf; Comments: 3weeks ago.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2531192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 03.12.2022
Beginn: 11.12.2022
Tage bis Beginn: 8,0
Dosis: 6
Route/Site: IM / LA

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

COVID-19 Chest discomfort Decreased appetite Dyspnoea Fatigue Influenza virus test negative SARS-CoV-2 test positive

Symptomtext

On Sunday evening late began having shortness of breath and heaviness in chest. Also experienced loss of appetite and fatigue. Monday morning called PCP and made an appointment. Went into clinic and tested negative for COVID-19. PCP instructed me to retest in 24-48 hours. Retested on Tuesday 12/13/2022, and tested positive. Reached out to PCP's office and waiting for them to return my message. PCP said they would prescribe PAXLOVID. Symptoms have remained about the same. I have increased my cortisone dose per my doctors instructions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 x2 1 positive & 1 negative; flu negative
Aktuelle Erkrankungen: Mild cough due asthma
Vorgeschichte: Asthma; Secondary adrenaline insufficiency; IBS; general anxiety, ADHD, GERD, Oral thrush; Chronic allergies; gluten intolerant; type 2 diabetes; Hypothyroid; sleep apnea; history of SVT corrected by surgery in 2020;
Andere Medikamente: BENADRYL; hydrocortisone; multivitamin; vitamin D3; ca; fe; vitamin B12; SYMBICORT 160; pantoprazole; GAVISCON; ALEVE; TRULICITY
Allergien: Prednisone; azithromycin; hydrocodone; doxycycline; metformin; empagliflozin; amoxicillin; JARDIANCE; soy; tree nuts; beans; egg; elderberry; pollen; strawberry; banana; blueberry; lactose; nuts; gluten; garlic; apples; fragrances; dyes in laundry detergent
Vorherige Impfungen: COVID-19 minor itching, took BENADRYL as preventative medication.

VAERS 2530667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Mobility decreased Pain Pain in extremity

Symptomtext

Patient stated presently having left arm pain/discomfort with limited range of motion which has continued since vaccine administration. Pt has taken both Tylenol 500mg & Ibuprofen 800mg at different times w/c would give her temporary relief. Hot/cold compresses have not been effective.

Weitere VAERSDATA-Felder

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

VAERS 2529434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 23.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Hypoaesthesia Injection site pain Musculoskeletal stiffness Pain in extremity Paraesthesia

Symptomtext

Tingling in her pinky and ring finger, as well as the side of her hand; Fingers stiffness; Left arm was sore; Injection soreness in that muscle; Can't feel that finger; 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 56-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Nov2022 at 18:00 as dose number unknown (booster), single (Lot number: GJ6738, Expiration Date: 31Jul2023) at the age of 56 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Past drug history included: Simvastatin for high on cholesterol, notes: Just due to her family line runs kind of high on cholesterol. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; Unknown manufacturer), for COVID-19 Immunization. The following information was reported: HYPOAESTHESIA (non-serious) with onset 23Nov2022, outcome "unknown", described as "Can't feel that finger"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 23Nov2022, outcome "unknown", described as "Fingers stiffness"; INJECTION SITE PAIN (non-serious) with onset 23Nov2022, outcome "unknown", described as "Injection soreness in that muscle"; PAIN IN EXTREMITY (non-serious) with onset 23Nov2022, outcome "recovering", described as "Left arm was sore"; PARAESTHESIA (non-serious) with onset 23Nov2022, outcome "not recovered", described as "Tingling in her pinky and ring finger, as well as the side of her hand". The events "tingling in her pinky and ring finger, as well as the side of her hand" required physician office visit. Additional information: She reported left arm was sore; tingling in her pinky and ring finger and side of hand where pinky finger was on left hand; She called for information on if this was a side effect and expected duration to last. She had been waiting to see if the tingling event would go away and had seen multiple doctors and nurse practitioners about this. She noticed tingling event a little, but she did not directly notice the tingling event at that time due to left arm was sore event overshadowing the gravity of the tingling event. The tingling event was overshadowed more by the injection soreness in that muscle; so she did notice, but did not really think it was much of anything due to the fact that upper part of her left arm was so sore. Every doctor and nurse practitioner she spoke with and had seen all said to wait and see if it goes away. 2 weeks have gone by and event had not changed and not gone away, still have thickness and tingling feel and sometimes can't feel that finger that much when she picks things up so she starts to drop them because she thinks she has a grip. Also she called the pharmacy at which she received this product within the week she was experiencing the tingling event; they recommended she see a doctor for it on 29Nov2022. This tingling event with her finger was really weird, she hopes it goes away. Left arm was sore: biggest soreness was the night of the injection, on 23Nov2022; the second day was slightly sore, but by the second day she was already noticing the tingling event. She thought it was from the shot. Initially reported event as 'gone' but clarified as still had some tenderness so improved but not recovered completely. The doctor she saw put a note that if this persists she could follow-up with a hand specialist, they would provide referral. She verified there were no concomitant products to report. She was supposed to be taking Simvastatin, but had been out of Simvastatin for quite some times so there wouldn't have even been any Simvastatin in the bloodstream at the time of onset of events. She had since then gotten the Simvastatin refilled, dispensed Simvastatin. Unknown, product dispensed in pharmacy vial. Indication: Just due to her family line runs kind of high on cholesterol, she was not overweight so it was not that. Just a control factor that elevates a little high enough they feel she should be on low dose. She verified there has been no relevant test results to provide. They said right now they would watch it because they did try a strength test and she's still maintaining strength in the arms, including that left arm. They were hoping would to see this tingling event disappear within a week, some said a week, some said 2 weeks, some said 3 weeks. By the third week she will probably be at the hand specialist. It will take another week to get to see them probably because everyone at end. of December trying to be seen, but she begged and pleaded on this one. When she does go into the hand specialist they're gonna ask her all kind of questions so she wants to be as prepared as possible. She verified there have been no relative treatments or medical interventions. She mentioned her husband also was administered a dose of Pfizer COVID Bival 12 y up, booster on 23Nov2022 like she did, in his right arm.

Weitere VAERSDATA-Felder

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

VAERS 2529497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: VA
Alter: 31,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 09.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Hypoaesthesia Lymphadenopathy Mobility decreased

Symptomtext

Patient arm became numb on Saturday, and her lymph nodes became swollen. She could hardly move her arm. She went to her PCP on 12/12/2022 and was given Medrol dose pack and Doxycycline 100 mg BID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: NOT aware
Aktuelle Erkrankungen: NONE ON FILE
Vorgeschichte: UNKNOWN
Andere Medikamente: SPRINTEC
Allergien: NONE ON FILE
Vorherige Impfungen: -

VAERS 2524364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: NV
Alter: 38,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 19.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Asthma Erythema Injection site erythema Injection site exfoliation Injection site pruritus Migraine New daily persistent headache Peripheral swelling Pyrexia

Symptomtext

After the injection, My arm swelled up and had a fever, was bright red. After that my injection site started to lose skin. I covered the site with a band aid with antibiotic ointment. The skin loss grew to the size of the bandage which actually contained it to that size. The top dermas came off. The under dermas was bright red and itchy. I had a asthma attack which lasted for 3.5 days. I have had daily migraines/headaches since I received the shot. I have been taking Ibuprofen along with Benadryl daily since trying to lessen the effects. I took albuterol for the asthma attack and turned on my humidifiers to put moisture in the air. My arm is fine, no scarring. Still itches. no outward sign I received the shot. Migraines/Headaches are still continuing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Haven't been to a Dr. Don't have 1. Just letting you know the effects of the shot.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Ibprophen
Allergien: Fresh Pineapple Amoxicillin
Vorherige Impfungen: Swelling, Itchy, Fever, Redness in arm from Flu shot. Get the flu for 5 days from the shot.

VAERS 2523725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: TX
Alter: 58,0
Geschlecht: M
Eingang: 05.12.2022
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Chills Decreased appetite Dizziness Gait disturbance Hypotension Somnolence Tremor

Symptomtext

This happens every time I get the Covid vaccine. About 4-5 hours after injection I get the chills and shake slightly. I then go to sleep. When I wake the next morning my blood pressure is very low. So low that it is hard to walk because of dizziness. So much so that I will crawl to go to the restroom or to get water. I have very little appetite and just want to sleep. This will last an entire day. On the second morning after the injection my blood pressure will not be as low as the first day afterwards, and good enough to carefully walk around the house (and sometimes forced to sit on the floor or hold onto an object to regain control) to get water, a bit of food, and go to the bathroom, and this slowly improves throughout the day, and by the second night i'm much better, but not 100% yet and have an appetite back. On the third day after the injection, I'm back to normal. I never feel nauseous nor have a fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Non-Hodgkin's lymphoma, CLL/SLL
Vorgeschichte: Non-Hodgkin's lymphoma, CLL/SLL
Andere Medikamente: Calquence Allopurinol Prednisone Entresto Metoprolol amlodipine omeprazole tamsulosin
Allergien: -
Vorherige Impfungen: Same adverse events after each Covid vaccine

VAERS 2523114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: KS
Alter: 57,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 30.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site erythema Mobility decreased Peripheral swelling

Symptomtext

pt states she had swelling in the arm that radiated into the fingertips to the point she couldn't move her fingers. She experienced some redness at the site. pt stated the swelling receded by Saturday when she reported the reaction, but was still present. The redness had resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2520078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 03.12.2022
Impfdatum: 29.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / RA

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

Arthralgia Chest pain Chills Fatigue Feeling hot Asthenia Headache Pain Injection site pain Malaise Myalgia Pain in extremity Vaccination site pain

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). 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 29Nov2022 as dose 4 (booster), single (Lot number: GJ6738) at the age of 55 years intramuscular, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Single, Time: unknown, Anatomical Site of injection: right arm, Route of Administration: Intramuscular;, Batch/Lot number: EL9261, Expiration: May2021), administration date: 03Feb2021, when the patient was 53-year-old, for COVID-19 Immunization; BNT162b2 (Dose 2, Single, Time: unknown, Anatomical Site of injection: Upper right arm, Route of Administration: Intramuscular, Batch/Lot number: EN6201), administration date: 24Feb2021, when the patient was 53-year-old, for COVID-19 Immunization; BNT162b2 (Dose 3, Single, Time: unknown, Anatomical Site of injection: Upper right arm, Route of Administration: Intramuscular;, Batch/Lot number: FF2593), administration date: 28Oct2021, when the patient was 54-year-old, for COVID-19 Immunization. Additional information: Patient got vaccine booster yesterday. Patient experienced events when she woke up this morning. Booster dose due to high risk or frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications): states she is a home aid; works with elderly patients. No prior vaccination (within 4 weeks).

Weitere VAERSDATA-Felder

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

VAERS 2520078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 03.12.2022
Impfdatum: 29.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Chest pain Chills Fatigue Feeling hot Asthenia Headache Pain Injection site pain Malaise Myalgia Pain in extremity Vaccination site pain

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). 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 29Nov2022 as dose 4 (booster), single (Lot number: GJ6738) at the age of 55 years intramuscular, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Single, Time: unknown, Anatomical Site of injection: right arm, Route of Administration: Intramuscular;, Batch/Lot number: EL9261, Expiration: May2021), administration date: 03Feb2021, when the patient was 53-year-old, for COVID-19 Immunization; BNT162b2 (Dose 2, Single, Time: unknown, Anatomical Site of injection: Upper right arm, Route of Administration: Intramuscular, Batch/Lot number: EN6201), administration date: 24Feb2021, when the patient was 53-year-old, for COVID-19 Immunization; BNT162b2 (Dose 3, Single, Time: unknown, Anatomical Site of injection: Upper right arm, Route of Administration: Intramuscular;, Batch/Lot number: FF2593), administration date: 28Oct2021, when the patient was 54-year-old, for COVID-19 Immunization. Additional information: Patient got vaccine booster yesterday. Patient experienced events when she woke up this morning. Booster dose due to high risk or frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications): states she is a home aid; works with elderly patients. No prior vaccination (within 4 weeks).

Weitere VAERSDATA-Felder

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

VAERS 2518790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: NY
Alter: 68,0
Geschlecht: M
Eingang: 29.11.2022
Impfdatum: 08.11.2022
Beginn: 18.11.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Acupuncture Blood test Burning sensation Computerised tomogram head Electrocardiogram Hypoaesthesia Neurological examination Paraesthesia Sensory disturbance

Symptomtext

I was fine when I woke up the morning of 11/18. At 8:30 I got out of the car to go shoppling and the feedback from my left leg was strange. It felt dead. I did my shopping, then drove to another store at 9:30. While driving, my left thigh became very numb. I called my GP, and while I had no other signs of stroke or heart attack, she suggested that I go to the ER. The left thigh continued to be numb but varied in intensity and location of the numbness. My left arm and left side of my face also felt tingley or numb. Today, 11/29, I am still feeling numbness on the left side, but it varies in location and intensity throughout the day. On the 19th I reviewed the health records that I keep on my computer. It turns that I had burning or numbness on the left side (thigh, arm, face) in 1997. My neurologist prescibed amytriptylene, but it made my muscles twitch/spasm so I stopped it. I began acupuncture treatments in 1997 and the symptoms gradually dissappeared. I still get acupuncture treatments monthly. I sometimes have minor numbness if I am tired, stressed, or sick, but nothing as severe as what I experienced on the 18th. My current level of symptoms is better than on the 18th but worse than I had had in the past 25 years.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EKG, head CT, blood work, and neurological tests did not suggest a cause of the symptoms. Given my history of GBS, they suggested that it appeared something upset my nervous system.
Aktuelle Erkrankungen: None
Vorgeschichte: Had Guillain-Bare Syndrome (GBS) in 1957. Severe nerve damage. No voluntary muscle movement below either knee. Left with chronic peripheral neuropathy.
Andere Medikamente: MultiVitamin, Calcium 600mg, Magnesium 250mg, Vitamin C 1000mg, Turmeric 500mg, Citrucel, Chlorpheneramine maleate 4mg.
Allergien: Penicillan, Ampicyline. Intolerance to orange juice (Eosinophile Esophagitis) and grapes, strawberries, and eggs (diarrhea)
Vorherige Impfungen: -

VAERS 2510903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: IN
Alter: 55,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Discomfort Hypoaesthesia Limb discomfort Muscle tightness Paraesthesia Injection site discomfort Injection site paraesthesia

Symptomtext

tightness; numbness; discomfort; arm started hurting most immediately; tingling/tingling in neck and cheek; 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 55-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 as dose 4 (booster), 0.3 ml single (Lot number: GH6738, Expiration Date: 17Nov2023) at the age of 55 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Hyperthyroid" (unspecified if ongoing). Concomitant medication(s) included: METHIMAZOLE taken for thyroid disorder. Vaccination history included: BNT162b2 (Dose: 2, Route of Administration: Intramuscular), administration date: 15Jul2021, when the patient was 53-year-old, for COVID-19 Immunization, reaction(s): "nerve pain and couldn't move her arm", "1st dose Pfizer COVID-19 Vaccine: Date Received: Apr2021/2nd dose Pfizer COVID-19 Vaccine: Date Received: 15Jul2021"; coviD-19 vaccine moderna (Dose: 3, Route of Administration: Intramuscular , Batch/Lot number: unknown), administration date: 01Nov2021, when the patient was 53-year-old, for COVID-19 Immunization, reaction(s): "drug ineffective", "Suspected COVID-19"; Bnt162b2 (Dose: 1, Route of Administration: Intramuscular), administration date: Apr2021, when the patient was 53 years old, for COVID-19 Immunization, reaction(s): "nerve pain and couldn't move her arm". The following information was reported: LIMB DISCOMFORT (non-serious) with onset 17Nov2022, outcome "unknown", described as "arm started hurting most immediately"; PARAESTHESIA (non-serious) with onset 17Nov2022, outcome "unknown", described as "tingling/tingling in neck and cheek"; MUSCLE TIGHTNESS (non-serious), outcome "unknown", described as "tightness"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "numbness"; DISCOMFORT (non-serious), outcome "unknown". The events "arm started hurting most immediately", "tingling/tingling in neck and cheek", "tightness", "numbness" and "discomfort" required physician office visit. Additional information: NDC number of Bivalent Booster: 59267-0304-2. The patient just had about 48 minutes ago the Bivalent Booster. She states that her arm started hurting most immediately. States that it felt like the vaccine went from her arm and was crawling up her neck and side of her face. Relays that she is now having tingling, tightness, numbness, strange/odd feeling on the side of her face and neck. She just started experiencing right away and wonders if the person put the booster low enough in her shoulder. She has tingling in her neck and cheek and this is concerning to her. She is moving her face and is moving through her body. She had the vaccine around noon and her dad and her had just left and was ready to leave. She noticed in the car and noticed right at stop sign, that she had a funny feeling in her neck and face. Her cheek felt tightness and discomfort. She doesn't know if this is the chemical moving through her body. The tingling heat and nerve sensation today is in her right arm. She got COVID in Jan and states she presumes this wouldn't have happened had she got the Pfizer booster instead of the Moderna.She went to lie down since she was told if she had tingling or numbness to lie down. This is such a bizarre feeling. Treatment: She is trying to stay warm to help move the medication through quickly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hyperthyroidism
Andere Medikamente: METHIMAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2513107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: MD
Alter: 47,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 19.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Back pain Chest pain Pain in extremity

Symptomtext

Had pain on the Left arm Sunday morning and wake up Monday with pain on my chest and sharp pain on my back.

Weitere VAERSDATA-Felder

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

VAERS 2512904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: -
Alter: 28,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 19.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Chest pain Chills

Symptomtext

Chest pain, sharp continuous: Lasted from post dose hour 12 to post dose hour 36. No shortness of breath. Chills: Lasted from post dose hour 12 to post dose hour 24

Weitere VAERSDATA-Felder

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

VAERS 2512538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: VA
Alter: 39,0
Geschlecht: F
Eingang: 20.11.2022
Impfdatum: 11.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SC / LA

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

Condition aggravated Impaired work ability Migraine Pain Photosensitivity reaction

Symptomtext

I have had severe migraine events for over a week with little to no relief from tylenol, advil, sumatriptan, lidocaine patches, icing painful area. All of my regular ways to abort a migraine have failed for the last week and I have been in severe and unrelenting pain This has disrupted my ability to work. Also I have had photosensitivity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None
Vorgeschichte: Ehlers Danlos/ History of Migraines but hadn't had one in a month
Andere Medikamente: Topamax, Welbutrin XL, Naproxen, Tylenol, Flexeril
Allergien: Celiacs/ Gluten Free
Vorherige Impfungen: -

VAERS 2512367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: WI
Alter: 57,0
Geschlecht: F
Eingang: 19.11.2022
Impfdatum: 18.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / LA

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

Fatigue Feeling hot Feeling of body temperature change Generalised oedema Injection site pain Insomnia Mobility decreased Pain

Symptomtext

Received injection at 2:30ish. By 4pm I was cold and couldn't warm up. Then I got very tired and had to rest. By 7pm I was getting very hot, like I was on fire, alternating with cold. I also developed a sore arm near the injection site. By 7pm I also very painful all over. By the next morning my body was swollen which made it difficult to sleep and move.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none at this time.
Aktuelle Erkrankungen: Normal, chronic illnesses
Vorgeschichte: autoimmune hepatitis, Mast Cell Activation, ankylosing spondylitis, and more
Andere Medikamente: lots, but normal for me
Allergien: lots, but no newer ones. Listed at PCP office
Vorherige Impfungen: -

VAERS 2506630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: OK
Alter: 74,0
Geschlecht: F
Eingang: 12.11.2022
Impfdatum: 29.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Arrhythmia Diarrhoea Heart rate decreased Mobility decreased Muscular weakness

Symptomtext

Patient reports diarrhea, muscle weakness, low pulse, arrhythmias starting the day after her vaccines. Says she could barely move enough to get out of bed. Patient went to the Emergency room because of her low pulse and arrhythmias. She was put on Metoprolol to control her arrhythmia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Unknown, Patient went to Medical Center Emergency Room
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Eplerenone, Potassium, Montelukast, Lisinopril, Hydrochlorothiazide
Allergien: None
Vorherige Impfungen: -

VAERS 2504498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 09.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Paraesthesia oral Throat irritation

Symptomtext

Patient started to have lip tingling and itching throat 5 minutes after vaccination. Patient was given benadryl and famotidine. Patient's husband took her to the emergency room to be monitored.

Weitere VAERSDATA-Felder

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

VAERS 2503187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

moderat

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Inflammation Mobility decreased Pain in extremity

Symptomtext

pain and imflammation in right hand so bad cant move my fingers treating it with cold and hot packs and ibpofin

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: just virtual dr visit
Aktuelle Erkrankungen: nine
Vorgeschichte: diabetes
Andere Medikamente: metflorin,atorvastatin,lisopril apple cider gummies tumeric capsules collagen drink vitamins
Allergien: lactose intolerant
Vorherige Impfungen: -

VAERS 2495187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

moderat

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 29.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Lethargy Malaise Mobility decreased

Symptomtext

Patient states that about 8 hours after getting vaccine, she was extremely sick and could not get out of bed for 4 days afterward. She stated she felt lethargic, "sick", and overall ill. She was not specific about what types of symptoms she had or anything else.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None that were stated
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes
Andere Medikamente: Lantus injection, Metformin 500, Fenofibrate 160, Lisinopril 2.5, Trazodone 100, Venlafaxine 75, Simvastatin 20, ASA/Tylenol
Allergien: Stellazine, Codeine, Compazine, milk products
Vorherige Impfungen: -

VAERS 2714680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: MA
Alter: -
Geschlecht: M
Eingang: 16.11.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

Vaccination site pain

Symptomtext

Soreness in the arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose 5 (booster), single (Lot number: GJ6738) for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, lot number: EK4176), for COVID-19 immunisation, reaction(s): "soreness in the arm"; Bnt162b2 (DOSE 2, SINGLE, lot number: EL9261), for COVID-19 immunisation, reaction(s): "soreness in the arm"; Bnt162b2 (DOSE 3, SINGLE, lot number: 3055BA or 30155BA, the writing is not very clear.), for COVID-19 immunisation, reaction(s): "soreness in the arm"; Bnt162b2 (DOSE 4, SINGLE, lot number: FJ4895 or 85), for COVID-19 immunisation, reaction(s): "soreness in the arm". The following information was reported: VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "Soreness in the arm". Additional information: When probed to clarify consumer did not experienced side effect after previous Pfizer COVID-19 Vaccines, consumer stated, "The previous, no, just soreness in the arm. I guess the usual common side effects but nothing unusual.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300367340 same patient, different vaccine dose number/different event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2713054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

mild

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 12.11.2023
Impfdatum: 07.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 14,0
Dosis: N/A
Route/Site: IM / LA

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

Pain in extremity

Symptomtext

Patient complains that she has pain in the left arm. She described the pain as transient and at times flaring up really bad. This issue started after two weeks since she had gotten the previous covid booster last year. She did not feel like it was a big deal and thought the pain would go away on its own; therefore she never notified the pharmacy or her provider about it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none listed
Vorgeschichte: Diabetes
Andere Medikamente: none listed
Allergien: non listed
Vorherige Impfungen: -

VAERS 2547660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TN
Alter: -
Geschlecht: F
Eingang: 28.06.2023
Impfdatum: 20.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / LA

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

Biopsy Blood test Cataract Dermatitis Dizziness Nausea Pruritus Vomiting Dysgeusia Dyspepsia Hypersensitivity Lethargy Pain Pain in extremity Rash Rash papular Superficial inflammatory dermatosis

Symptomtext

cataract surgery; body aching; dizzy; Bilateral Rash on arms and legs/ breaking out; Throwing up/Vomiting; itching; Lethargic; soreness in her left arm; sour stomach; Things didn't taste right/ horrible taste/ bad taste/ terrible taste in her mouth; Sometimes they're raised and filled with fluid; Allergic to unspecified product; Paravascular dermatitis; Interstitial dermatitis; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. A female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Dec2022 as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "allergic to medicine" (unspecified if ongoing). Concomitant medication(s) included: LORATADINE. Vaccination history included: Covid-19 vaccine (DOSE 1, MANUFACTURER UNKNOWN), for COVID-19 immunisation, reaction(s): "No issues"; Covid-19 vaccine (DOSE 2, MANUFACTURER UNKNOWN), for COVID-19 immunisation, reaction(s): "No issues"; Covid-19 vaccine (DOSE 3 (BOOSTER), MANUFACTURER UNKNOWN), for COVID-19 immunisation, reaction(s): "No issues". The following information was reported: HYPERSENSITIVITY (non-serious) with onset Dec2022, outcome "unknown", described as "Allergic to unspecified product"; RASH (non-serious) with onset Dec2022, outcome "unknown", described as "Bilateral Rash on arms and legs/ breaking out"; DERMATITIS (non-serious) with onset Dec2022, outcome "unknown", described as "Interstitial dermatitis"; LETHARGY (non-serious) with onset Dec2022, outcome "unknown", described as "Lethargic"; SUPERFICIAL INFLAMMATORY DERMATOSIS (non-serious) with onset Dec2022, outcome "unknown", described as "Paravascular dermatitis"; RASH PAPULAR (non-serious) with onset Dec2022, outcome "unknown", described as "Sometimes they're raised and filled with fluid"; DYSGEUSIA (non-serious) with onset Dec2022, outcome "not recovered", described as "Things didn't taste right/ horrible taste/ bad taste/ terrible taste in her mouth"; VOMITING (non-serious) with onset Dec2022, outcome "unknown", described as "Throwing up/Vomiting"; PAIN (non-serious) with onset Dec2022, outcome "unknown", described as "body aching"; DIZZINESS (non-serious) with onset Dec2022, outcome "unknown", described as "dizzy"; PRURITUS (non-serious) with onset Dec2022, outcome "not recovered", described as "itching"; PAIN IN EXTREMITY (non-serious) with onset Dec2022, outcome "not recovered", described as "soreness in her left arm"; DYSPEPSIA (non-serious) with onset Dec2022, outcome "unknown", described as "sour stomach"; CATARACT (medically significant) with onset 03Mar2023, outcome "unknown", described as "cataract surgery". The events "bilateral rash on arms and legs/ breaking out", "itching", "sometimes they're raised and filled with fluid", "paravascular dermatitis" and "interstitial dermatitis" required physician office visit. The patient underwent the following laboratory tests and procedures: Biopsy: (unspecified date) subtle, superficial dermatitis, notes: She saw her dermatologist and got biopsy done. Her results read "paravascular and interstitial dermatitis, with rare eosinophils."; Blood test: (2020) she was immune to the virus.. Therapeutic measures were taken as a result of cataract, pain, dizziness, rash, vomiting, pruritus, lethargy, pain in extremity, dyspepsia, dysgeusia, rash papular, hypersensitivity, superficial inflammatory dermatosis, dermatitis. Clinical course: The first thing she got was vomiting and vomiting; for quite a while until it got down to having nothing left and a sour stomach. She had body aches the first day of the shot, she felt dizzy. However the main thing was breaking out. The rash started the same day she got the bivalent shot. She got it on her legs and arms, and she was really upset and didn't have reactions to the other one. The itching has never gone away. It first started on her legs, then moved to her ankles. Then it went to her arms, her forearm. They look like little moles, and all kinds of little bumps, it looks terrible from all the breakouts. Sometimes the splotches were big and sometimes they were small. Prior to the bivalent shot, she was already taking loratadine. They increased the dose of loratadine/Claritin. She saw her doctor and they told her to start taking Benadryl. The Benadryl didn't really help so she stopped it. So she was on Loratadine and Benadryl. It would calm down for a few hours during the day. Then her doctor gave her triamcinolone ointment 0.1%. She put it on the rash, and then she will develop a rash somewhere else on the body. She could not put it on her entire body everyday. The doctor told her to use that for 2 weeks so that's what she did. When she applied the ointment topically it gave her a horrible taste her mouth. She did clarify that she did not put any ointment in her mouth but she did develop a bad taste after applying the ointment topically. The places where she put the triamcinolone, it would help and then she'd break out somewhere else. The last thing they had her try was Zyrtec, but after 3-4 day she stopped. It made her very lethargic and it gave her a terrible taste in her mouth. They also told her to take Pepcid, but she was not sure that was what causes the sour taste in her mouth and stomach. The last time she took Zyrtec, she had the rash from waist to under the bust, real fine watery blisters, so the Zyrtec didn't seem to help any. Now it was on her back, middle of her back, lower legs, upper thighs buttocks, close to vaginal area. Under her eyes is extremely dry, and she's stayed off of deodorant. When she got it on her bust and nipples it itched, they told her they could put the triamcinolone on it but not to use it too long. The only thing that had helped. had tried taking some detox tea and detox foot pads. Everything she had tried did not seem to work. What was odd was that if she started getting a rash on one side of her body, it would show up in the exact same place on the other side of her body. Sometimes they were raised and filled with fluid. They had got this viscous liquid inside of them. There will be one blister then an inch from that one and an inch from that another one. Now it went down to her wrist, the wrist wasn't included at first but now it is. Yesterday her wrist broke out on the other side in the same place. On 03Mar2023 she had cataract surgery. She had to go back a couple time, because pressure in her eyeball increased. The pressure was so great they had to puncture it to release pressure. They also gave her prednisolone eye drops. That put a bad taste in her mouth too. She thought they were done but last month, her eye started hurting again with pressure like before and it was the weekend. So she called and asked if there was anything to recommend and they told her to take the prednisolone eye drops and that helped. The eye doctor wants her to get the other eye done, but wont do it again the eye pressure. She did not take much medicine, only levothyroxine and hydrochlorothiazide. Her doctor suggested maybe stopping one of those to see if it's the problem. The dermatologist is recommending another biopsy, deplete herself, allergy test, maybe stop taking some of the medicine and see if that will help. They also told her to get Sarno. She wanted to reach out to an herbalist and see if they could help her. On 20Dec had number four shot, the Bivalent Covid Shot, received at about a quarter till 12. Wait for a while before leaving and waited 15 to 20 minutes then left and went home. About 5 o'clock started throwing up, was dizzy, had sour taste in stomach and was itching and breaking out. So tried to do relaxing and do whatever could do. Sour stomach was bad. Finally stopped throwing up because nothing there. Had been itching ever since, for 6 months. She took some flesh and checked it out and said was allergic to a medicine. 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.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300232282 same patient, different drug/events;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Name: Biopsy; Result Unstructured Data: Test Result:subtle, superficial dermatitis; Comments: She saw her dermatologist and got biopsy done. Her results read "paravascular and interstitial dermatitis, with rare eosinophils."; Test Date: 2020; Test Name: Blood test; Result Unstructured Data: Test Result:she was immune to the virus.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy
Andere Medikamente: LORATADINE
Allergien: -
Vorherige Impfungen: -

VAERS 2648845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: OH
Alter: 36,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 15.12.2022
Beginn: 26.04.2023
Tage bis Beginn: 132,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia No adverse event Rheumatoid arthritis

Symptomtext

I did not have an adverse reaction to the vaccine. I have had full body joint pain since the fall of 2022. The symptoms just got worse, and I had an appointment with my doctor who referred me to a rheumatologist. I was diagnosed with rheumatoid arthritis on 04/26/2023. I am currently in treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Aleve
Allergien: N/A
Vorherige Impfungen: -

VAERS 2645301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 14.06.2023
Impfdatum: 19.11.2022
Beginn: 18.12.2022
Tage bis Beginn: 29,0
Dosis: 5
Route/Site: IM / RA

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

Ageusia COVID-19 Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Tinnitus

Symptomtext

12/18/2022 I had a runny nose all day, then towards the end of the day I got a sore throat, and 99-degree fever that evening for maybe an hour. 12/21/2022 I went out to eat and couldn?t taste the food. Took and At Home COVID-19 Test, positive. Loss of taste lasted about 3 days. Reached out to doctor by email and didn?t hear back. 12/23/2022 I had a little bit of a sore throat in the evening. I stated home for the next 2 weeks and didn?t notice symptoms. Late January of 2023 I noticed a ringing in my ears. I got into see an audiologist on March 7. That doctor advised hearing is fine, ringing not related to hearing loss. Ringing in ears continues to time of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 21/Dec2022 At Home COVID-19 Test, positive
Aktuelle Erkrankungen: NA
Vorgeschichte: Thyroid Disorder; High Cholesterol; Obesity; Depression; Asthma
Andere Medikamente: Levothyroxine; Rosuvastatin; Escitalopram; Bupropion; Vitamin C; Zinc; Melatonin; Elderberry
Allergien: Seasonal Allergies
Vorherige Impfungen: -

VAERS 2643882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 09.06.2023
Impfdatum: 12.12.2022
Beginn: 12.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Inflammation Myalgia

Symptomtext

Inflamation & muscle pain that continues 6 months after Injection on (L) UE.

Weitere VAERSDATA-Felder

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

VAERS 2639645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: AR
Alter: 69,0
Geschlecht: F
Eingang: 01.06.2023
Impfdatum: 14.12.2022
Beginn: 01.01.2023
Tage bis Beginn: 18,0
Dosis: 5
Route/Site: IM / AR

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

Pain in extremity

Symptomtext

In January I started having some leg pain, I went to my primary care physician who said that it may be venous insufficient, and he would keep an eye on it. They pain kept getting worse, so I took it upon myself to make an appointment with a vein specialist in April. He did a general exam and had me start wearing compression stockings. I will be going back to see him on June 27 to have an ultrasound done on my legs to see if they can find what is causing the pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; Pre-Diabetic
Andere Medikamente: Metformin; Hydrochlorothiazide; Losartan; Low Dose Aspirin; Vitamin D; Zyrtec; Potassium; Magnesium; Women's Multivitamin
Allergien: Augmentin
Vorherige Impfungen: -

VAERS 2624413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TX
Alter: 64,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 15.11.2022
Beginn: 24.02.2023
Tage bis Beginn: 101,0
Dosis: 5
Route/Site: SYR / AR

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

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

Covid February 2/24/23 mild symptoms treated w/ paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: self test positive antigen 2/24/23
Aktuelle Erkrankungen: -
Vorgeschichte: CAD, hypertension, hyperlipidity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2624398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NH
Alter: 70,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 03.11.2022
Beginn: 04.04.2023
Tage bis Beginn: 152,0
Dosis: 5
Route/Site: IM / RA

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

Pain Stomatitis

Symptomtext

4/4/23 I had a lesion on the roof of my mouth that would not go away. It was very painful. I could not eat or drink anything hot. I went to the dentist about a week later. He could not figure out what it was. He said to gargle with salt water and be careful with what you are eating. I stopped taking all dietary supplements. The lesion is still there. It has gotten better but has not gone away. I saw the dentist today. He said it has not gotten any smaller. I go see an oral surgeon next week for a biopsy to see what is going on.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Fistula Migraines
Andere Medikamente: Topiramate; metoprolol succinate; magnesium; vitamin B2; fish oil; naproxen; CENTRUM SILVER women's multivitamin
Allergien: Tomato leaves; tetracycline; erythromycin
Vorherige Impfungen: -

VAERS 2624034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: PA
Alter: 64,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 17.11.2022
Beginn: 02.04.2023
Tage bis Beginn: 136,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia Anosmia Fatigue Feeling abnormal Headache Infection SARS-CoV-2 test negative

Symptomtext

No reaction to the vaccine. I had general fatigue, headache, tested twice for COVID-19 and it was negative, I called the doctor because I did not feel good, and he prescribed methylprednisolone on 4/06/2023. Then, a week went by wasn't feeling good, I called the doctor again and he gave me another prescription, an antibiotic for infection. 10 days' supply which I have finished now. During this period, I lose my sense of smell and taste, but I still tested negative for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 04APRIL2023 COVID-19 test, negative; 05APRIL2023 COVID-19 test, negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Simvastatin; olmesartan
Allergien: SINUPROL
Vorherige Impfungen: -

VAERS 2623962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 14.12.2022
Beginn: 23.04.2023
Tage bis Beginn: 130,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury COVID-19 Cough Laboratory test abnormal Malaise SARS-CoV-2 test positive

Symptomtext

discharge summary "Patient is a 72 YO female history of liver cirrhosis from NASH, hypertension presented with cough and malaise. Labs reveal AKI and COVID 19 +. She was admitted for COVID 19 and AKI management. During her stay, she received IVF that resolved her AKI. She was also placed on decadron for her COVID 19 infection. Social worker has given extra resources to help with her financial stress at home. She was discharged in stable condition. Strict return precautions given".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: 4,0
Labordaten: positive COVID PCR testing 4/23/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2623678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: WI
Alter: 69,0
Geschlecht: F
Eingang: 30.04.2023
Impfdatum: 30.04.2023
Beginn: 30.04.2023
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Dizziness Flushing Hyperhidrosis

Symptomtext

vaccine was administered without issues; several minutes after administration, pt was sweating, flushed, light headed and said her chest felt heavy. pt remained seating and was instructed to rest, water was offered, pt took 50mg benadryl and still wasn't feeling good, 911 was called; pt did not lose consciousness, EMT evaluated pt (didn't notice any hives but pt may have been hyperventilating) and ended up transporting pt to hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: Keflex, Sulfa
Vorherige Impfungen: -

VAERS 2619085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: IN
Alter: 68,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 26.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I started to develop a very bad headache. I took one of my medications and it did not help my headache. I started to develop a sore throat. My headache did not go away so I took a COVID-19 test and it came back negative. A couple days later my symptoms did not improve so I took another COVID-19 test and it came back positive. My headache was so bad that I went to urgent care. They prescribed me Paxlovid. After the first dose I got relief from my headache. Two days later my symptoms were gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 30 NOV-COVID-19 Test- Negative; 2 DEC- COVID-19 Test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine Headaches; Depression; Diabetes; Thyroid
Andere Medikamente: Trintellix; Lamotrigine; Levothyroxine; Topiramate; Tizanidine; Candesartan; Nebivolol; Atorvastatin; Colace; Aimovig; Victoza
Allergien: Tylenol
Vorherige Impfungen: -

VAERS 2617620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: IL
Alter: 56,0
Geschlecht: F
Eingang: 19.04.2023
Impfdatum: 20.12.2022
Beginn: 06.04.2023
Tage bis Beginn: 107,0
Dosis: 5
Route/Site: IM / LA

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

Bloody discharge Ear congestion Headache Infection Nasal discharge discolouration Nasopharyngitis Otorrhoea Paranasal sinus discomfort Parosmia Productive cough Taste disorder

Symptomtext

On April 6, 2023, I started having a cold, cough that had a little congestion, no fever, my ear felt a little congested. Four days later, I started noticing I was getting that rotten taste and smell that you get when you get an infection, I had sinus pressure that made my head hurt, some bloody discharge when I blew my nose and some that came out of my ear. I called to have a telehealth visit with my doctor, we discussed my symptoms, I was prescribed an antibiotic and prednisone. I am currently taking the medications, the infection in clearing up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Trazadone; Lipitor; Propranolol; Atomoxetine; Bupropion XL; Pantoprazole; Multivitamin; Magnesium; Calcium; Probiotic
Allergien: No
Vorherige Impfungen: -

VAERS 2610783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MS
Alter: 80,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Pain in extremity

Symptomtext

Patient approached pharmacy on 4/6/23 around 11:15 am stating that ever since she had her updated booster shot in November that her arm has been sore, almost feeling like it was bruised, but that there was nothing visible there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None mentioned at the time of reporting to us
Aktuelle Erkrankungen: None mentioned or listed at time of vaccination
Vorgeschichte: None mentioned or listed at time of vaccination
Andere Medikamente: None mentioned - does not fill prescriptions here
Allergien: None mentioned or listed at time of vaccination
Vorherige Impfungen: -

VAERS 2604388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: NV
Alter: -
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 19.12.2022
Beginn: 21.12.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / LA

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

Deafness Dizziness Ear disorder Motion sickness SARS-CoV-2 test Vertigo

Symptomtext

Sudden and severe hearing loss in left ear.; full ear feeling; vertigo; dizziness; motion sickness; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Dec2022 at 15:30 as dose 4 (booster), single (Lot number: GJ6738), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Arnold Chiari Malformation" (unspecified if ongoing); "Known allergies: Latex" (unspecified if ongoing); "Known allergies: Avocado" (unspecified if ongoing). Concomitant medication(s) included: PROPRANOLOL. The patient had no other vaccine in four weeks. Vaccination history included: Covid-19 vaccine (Dose 1, unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose 2, unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose 3 (Booster), unknown manufacturer), for COVID-19 immunization. The patient had no covid prior vaccination. The following information was reported: DEAFNESS (disability, medically significant) with onset 21Dec2022 at 03:30, outcome "not recovered", described as "Sudden and severe hearing loss in left ear."; DIZZINESS (disability) with onset 21Dec2022 at 03:30, outcome "not recovered"; EAR DISORDER (disability) with onset 21Dec2022 at 03:30, outcome "not recovered", described as "full ear feeling"; MOTION SICKNESS (disability) with onset 21Dec2022 at 03:30, outcome "not recovered"; VERTIGO (disability) with onset 21Dec2022 at 03:30, outcome "not recovered". The events "sudden and severe hearing loss in left ear.", "full ear feeling", "vertigo", "dizziness" and "motion sickness" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (26Dec2022) Negative. Therapeutic measures were taken as a result of deafness, ear disorder, vertigo, dizziness, motion sickness including steroid injection x3 into the ear and oral medicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 20221226; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chiari malformation; Fruit allergy; Latex allergy
Andere Medikamente: PROPRANOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2603403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: PA
Alter: 60,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 20.12.2022
Beginn: 08.02.2023
Tage bis Beginn: 50,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Malaise Nasopharyngitis Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I started having symptoms on Feb 8th, bad head cold, low grade fever and body aches. It was about two weeks before I got help because I started to improve and then it got worse. I was starting to cough more so I saw a doctor. I did a home test which was positive, and I was told to treat the symptoms with over-the-counter medication. I was improving and then two days ago (03/22/2023) I started to feel sick again. I plan on testing myself again to see if I am positive for COVID-19 again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Lisinopril; multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2602457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: OR
Alter: 38,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 07.04.2021
Beginn: 18.02.2023
Tage bis Beginn: 682,0
Dosis: 4
Route/Site: IM / RA

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

Chest X-ray Chills Cough Diarrhoea Headache Influenza virus test Nasal congestion Nausea Pyrexia SARS-CoV-2 test Sputum discoloured

Symptomtext

Diarrhea starting 02/17/2023 headache and nausea, after a few days I felt better than reoccurred 02/21/2023. Continues until 02/23/2023. Starting coughing and high fever diarrhea and chills came back, coughing and diarrhea continued until 02/27/2023. Started having green flehm with stuffy nose, reached out to telemedicine 03/01/2023, went to see doctor after telemedicine suggested I might have pneumonia, chest x-ray was needed. Tested for influenza and COVID 03/01/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Chest X-Ray - 01MAR2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: metformin 500mg; levothyroxine; daily multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2543657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 16.12.2022
Beginn: 19.12.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / LA

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

Injection site pain Vertigo

Symptomtext

vertigo (it has been persistent); This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Dec2022 at 15:00 as dose 4 (booster), single (Lot number: GJ6738) at the age of 22 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Autism" (ongoing), notes: other medical history: Autism; "ADHD" (ongoing), notes: other medical history: ADHD; "Depression" (unspecified if ongoing), notes: other medical history: Depression; "Anxiety" (unspecified if ongoing), notes: other medical history: Anxiety; "Migraine Disorder" (unspecified if ongoing), notes: other medical history: Migraine Disorder. Concomitant medication(s) included: DULOXETINE; METHYLPHENIDATE; RESTASIS. Past drug history included: Amoxicillin, reaction(s): "known allergies: Amoxicillin", notes: known allergies: Amoxicillin; Codeine, reaction(s): "known allergies: Codeine", notes: known allergies: Codeine. 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; MANUFACTURER UNKNOWN), for Covid-19 immunization. The following information was reported: VERTIGO (non-serious) with onset 19Dec2022 at 08:00, outcome "not recovered", described as "vertigo (it has been persistent)". The event "vertigo (it has been persistent)" required physician office visit. Therapeutic measures were taken as a result of vertigo. Additional information: Treatment for the adverse event was reported as Meclizine. It was reported that there was no vaccination prior covid vaccine and covid was not tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: ADHD (other medical history: ADHD); Autism (other medical history: Autism)
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety (other medical history: Anxiety); Depression (other medical history: Depression); Migraine (other medical history: Migraine Disorder)
Andere Medikamente: DULOXETINE; METHYLPHENIDATE; RESTASIS
Allergien: -
Vorherige Impfungen: -

VAERS 2543657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 16.12.2022
Beginn: 19.12.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

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

Injection site pain Vertigo

Symptomtext

vertigo (it has been persistent); This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Dec2022 at 15:00 as dose 4 (booster), single (Lot number: GJ6738) at the age of 22 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Autism" (ongoing), notes: other medical history: Autism; "ADHD" (ongoing), notes: other medical history: ADHD; "Depression" (unspecified if ongoing), notes: other medical history: Depression; "Anxiety" (unspecified if ongoing), notes: other medical history: Anxiety; "Migraine Disorder" (unspecified if ongoing), notes: other medical history: Migraine Disorder. Concomitant medication(s) included: DULOXETINE; METHYLPHENIDATE; RESTASIS. Past drug history included: Amoxicillin, reaction(s): "known allergies: Amoxicillin", notes: known allergies: Amoxicillin; Codeine, reaction(s): "known allergies: Codeine", notes: known allergies: Codeine. 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; MANUFACTURER UNKNOWN), for Covid-19 immunization. The following information was reported: VERTIGO (non-serious) with onset 19Dec2022 at 08:00, outcome "not recovered", described as "vertigo (it has been persistent)". The event "vertigo (it has been persistent)" required physician office visit. Therapeutic measures were taken as a result of vertigo. Additional information: Treatment for the adverse event was reported as Meclizine. It was reported that there was no vaccination prior covid vaccine and covid was not tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: ADHD (other medical history: ADHD); Autism (other medical history: Autism)
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety (other medical history: Anxiety); Depression (other medical history: Depression); Migraine (other medical history: Migraine Disorder)
Andere Medikamente: DULOXETINE; METHYLPHENIDATE; RESTASIS
Allergien: -
Vorherige Impfungen: -

VAERS 2591956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 02.12.2022
Beginn: 29.01.2023
Tage bis Beginn: 58,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Feeling abnormal SARS-CoV-2 test positive

Symptomtext

I was feeling really run down and tired which is not like me. I started cough and feeling like I do when I need a breathing treatment. My wife suggested that I use a home COVID-19 test, I did, and it came back positive immediately. I called and had a telehealth visit. I was prescribed PAXLOVID that I started taking as soon I got it from the pharmacy. I took me two weeks before I felt like was back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 positive
Aktuelle Erkrankungen: No
Vorgeschichte: GERD; High Blood Pressure: High Cholesterol
Andere Medikamente: FLOMAX; CRESTOR; amlodipine; irbesartan/HCTZ; pantoprazole; trazadone; multivitamin; vitamin D; baby aspirin; fish oil
Allergien: No
Vorherige Impfungen: -

VAERS 2584241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 03.01.2023
Beginn: 17.01.2023
Tage bis Beginn: 14,0
Dosis: 5
Route/Site: SYR / LA

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

Cough Influenza virus test negative Nasal congestion Pyrexia Respiratory tract congestion SARS-CoV-2 test negative Sinus congestion

Symptomtext

I had extreme sinus congestion and slight cough, which started on the 17th of January. I used over the counter medicine as directed by doctor until January 29th when I called the doctor and she said it was time for antibiotics. So I went to the Urgent Care and they gave me a z-pack. I took that as prescribed and kept contact with my doctor via system. The infection improved but it was not all gone because I was still stuffy and it came back pretty strong. When I went to bed on the 7th, I was up all night because the congestion was so bad and started having a low grade fever for a few days. On the 8th she prescribed Augmentin and by day 8 of 10 of the medication I felt better. My blood pressure is still a little high, but don't know if it is related. I'm keeping an eye on it and reporting to my doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 2023Jan29- COVID-19 (negative); 2023Jan29-Influenza (negative)
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure; Hypothyroidism
Andere Medikamente: Lisinopril hydrochlorothiazide; Synthroid; Probiotic
Allergien: N/A
Vorherige Impfungen: -

VAERS 2583389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: DC
Alter: 39,0
Geschlecht: M
Eingang: 17.02.2023
Impfdatum: 05.01.2023
Beginn: 08.02.2023
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: IM / RA

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

Headache Pruritus Rash Varicella zoster virus infection

Symptomtext

I had a rash on the left side of my torso that kept growing. I went into the doctor; they called in a dermatologist who immediately identified it as the zoster virus. I had very mild itching, slight headache. I was given a prescription that helped to clear it up and feel that I am doing much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: Flu like symptoms
Vorgeschichte: Asthma
Andere Medikamente: SINGULAIR
Allergien: No
Vorherige Impfungen: -

VAERS 2583377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: FL
Alter: 61,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: 05.01.2023
Beginn: 09.02.2023
Tage bis Beginn: 35,0
Dosis: 4
Route/Site: IM / LA

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

Bronchiolitis Cough Pyrexia Sinusitis

Symptomtext

I had a fever that went away in a couple of days. I developed a cough that just would not go away. Normally when I take over the counter medication a cough will go away, this time it did not. I made an appointment with my doctor and discovered I had a sinus infection and bronchiolitis. I was prescribed an albuterol inhaler and doxycycline. I haven't totally recovered but I am starting to feel better,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2580419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: NC
Alter: 58,0
Geschlecht: F
Eingang: 13.02.2023
Impfdatum: 06.01.2023
Beginn: 06.02.2023
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / AR

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

Chest discomfort Cough Fatigue Headache Influenza virus test negative Malaise Myalgia Nausea Pain in extremity Pyrexia Respiratory tract congestion SARS-CoV-2 test negative Vertigo

Symptomtext

I had a sore arm for a couple of days but that was it. I started not feeling well on 02/06/2023 with vertigo, headache, cough, congestion, chest tightness, nausea, fatigue and muscle aches. I did see my doctor and was tested for COVID-19 and the flu on 02/09/2023 but both were negative. I was put on ZITHROMAX and a cough medicine. I have had these symptoms for seven days. Today is the first day without a fever. As of today, I continue to be tired but have not tested again for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09FEB2023 COVID-19 test negative; 09FEB2023 FLU test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2579697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NV
Alter: 56,0
Geschlecht: F
Eingang: 10.02.2023
Impfdatum: 10.11.2022
Beginn: 11.01.2023
Tage bis Beginn: 62,0
Dosis: 4
Route/Site: IM / LA

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

Cough Fatigue Feeling abnormal Headache Paranasal sinus hypersecretion Pyrexia Respiratory tract congestion Sinusitis

Symptomtext

Congestion in head, Fever over 100.3 for over 3 days Cough, headache Fatigue brain fog nasal sinus congestion, lingering sinusitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: allergic Asthma
Andere Medikamente: Qvsar: Dayquil
Allergien: Percocet
Vorherige Impfungen: Shingles soreness at injection site, Covid dose 3 was sick for about a day

VAERS 2577286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 26.12.2022
Beginn: 26.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Pain of skin Sensitive skin Skin burning sensation Skin irritation

Symptomtext

About an hour after being vaccinated, I noticed that my skin was very irritated on my chest. It got worse and worse. It was burning and very painful. I was using Cortisone, and then my doctor prescribed a stronger Cortisone cream. I was also using Benadryl. It started to get better in about 2 weeks. It was about ninety percent better in a months' time. It is still very sensitive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain of skin
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; Calcium
Allergien: Sulfa; Ergots
Vorherige Impfungen: -

VAERS 2576415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MO
Alter: 67,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 05.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Adverse food reaction Urticaria

Symptomtext

I had not complications after receiving the vaccine. A couple of weeks later, I developed hives on my left calf. They started spreading all over my body. I noticed they come up more so when I have sugar. I can't eat much bread, potatoes or kind of sugar and the hives return. I use CORTIZONE 10 to relieve my symptoms. At this time, I know what to do to prevent the outbreak so I have to be careful.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Pre-Diabetic
Andere Medikamente: SYNTHROID; metformin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2573084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: PA
Alter: 49,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 01.12.2022
Beginn: 01.01.2023
Tage bis Beginn: 31,0
Dosis: N/A
Route/Site: - / -

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

Cough Fatigue Flank pain Herpes zoster Impaired work ability Rash

Symptomtext

A few days after the booster started with cough then stated to get pain in flank. The cough went away in about 2 weeks but the pain remined intermittent. Thought it was a pulled muscle from coughing. Then stating around Jan 3rd 2023 the pain became more consistent, Mid January I was more fatigued to the point didn't want to drive and by Jan 26th pain was worse. On Jan 29th broke out in a rash where the pain was. Saw Dr and was diagnosed with shingles.

Weitere VAERSDATA-Felder

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

VAERS 2572154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 26.01.2023
Beginn: 26.01.2023
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Extra dose administered Pain Pain in extremity

Symptomtext

The LVN did not see that the patient had already received their COVID-19 bivalent booster since the information was documented at the back of the COVID-19 vaccine card and inadvertently administered the vaccine to the patient. The patient was observed for 5-10 mins post-vaccination. They were stable and did not exhibit any concerning s/sx that would have warranted additional medical attention. A follow-up call was conducted on 1/31 to check in on the patient and they said they were "fine" and aside from the arm soreness and body aches, no other concerning symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: COVID-19 vaccination was administered at SNF/long-term care facility. Medical tests/lab were not available.
Aktuelle Erkrankungen: No concerning medical illness up to one month prior to and at time of vaccination.
Vorgeschichte: No history of concerning chronic or long-standing health conditions (i.e., GBS, myocarditis/pericarditis, HIT, TTS).
Andere Medikamente: The individual was not taking immunosuppressant or chemotherapy treatment, blood thinners, or any other medications that would deem them ineligible for the COVID-19 vaccination.
Allergien: No history of allergies to medications, food, or other products.
Vorherige Impfungen: -

VAERS 2569105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: -
Alter: 15,0
Geschlecht: F
Eingang: 27.01.2023
Impfdatum: 25.01.2023
Beginn: 25.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Chills Headache Nausea Pyrexia

Symptomtext

My 15 yr old child received the bivalent Covid booster by Pfizer around 6:30 pm yesterday. Overnight developed chills, fever (101), headache, nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: N/A
Andere Medikamente: Supralin Implant One A Day Teen Multi Gummies
Allergien: -
Vorherige Impfungen: -

VAERS 2561940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 28.12.2022
Beginn: 04.01.2023
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Exercise tolerance decreased Fatigue Muscle spasms

Symptomtext

I am a healthy, very active (bicycle ride 1 hour daily) adult male. I have no serious health conditions. However, for the past few weeks I've been more fatigued than usual and have had lowered muscle strength and cramps in my arms and leg muscles.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No testing was completed. I can see my cycling data and I feel I need to work harder to go the same distance. My lap times are slower.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2558539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 12.01.2023
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: ja

Lymph node pain Lymphadenopathy

Symptomtext

I felt ok the day after receiving the vaccine. On 12/29/2022 my lymph nodes under my left armpit began to swell and hurt. I used only hot compress to relieve the pain. I had these symptoms for two days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: N/A
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2557943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: WI
Alter: 73,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 14.12.2022
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

Myalgia Pain

Symptomtext

Muscle in arm still sore after 4 weeks. She reported not sore all the time, but more so when she lays on that side or when using it.

Weitere VAERSDATA-Felder

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

VAERS 2557764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: FL
Alter: 82,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 11.01.2023
Beginn: 11.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Atrial fibrillation Dizziness Fall Unresponsive to stimuli

Symptomtext

Patient waited 15 minutes after receiving the vaccine. He proceded to walk to our drop off area and got dizzy and fell on the floor. It took him about 3 minutes to recuperate from the fall and I helped him to sit on a chair. Patient started being unresponsive so I decided to call the ambulance. I put ice behind his neck and continue trying to communicate with him. Patient says he was just diagnosed with Afib and that his doctor has been swiching his medications . Patient says he has fallen twice at home . Furthermore, this spell might not be caused by the vaccine but by the patient present condition and medications taken at the time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: not known.
Aktuelle Erkrankungen: HIgjh blood pressure, Afib and diabetes
Vorgeschichte: High blood pressure, Afib and diabetes
Andere Medikamente: I do not have this information
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2557462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: SC
Alter: 57,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 01.12.2022
Beginn: 03.01.2023
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Myalgia Oropharyngeal pain Paranasal sinus hypersecretion Productive cough Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had muscle aches at night, I woke up the next day with bronchitis symptoms a sore throat, sinus drainage, and a runny nose including sneezing, and coughing up mucous. It became worse throughout the day. On 01/04/2023 my COVID-19 test was negative and by 01/05/2023 I had a positive test. I went to urgent care on 01/05/2023 and my COVID-19 test their was positive there as well, PAXLOVID was prescribed and I reported in VSAFE the same day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: COVID-19 test positive result.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Asthma; Diabetes; High Cholesterol
Andere Medikamente: Amlodipine; simvastatin; metformin; hydrochlorothiazide; albuterol
Allergien: ADVAIR
Vorherige Impfungen: -

VAERS 2555874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: VA
Alter: 58,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 06.01.2023
Beginn: 06.01.2023
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Headache Lymph node pain Lymphadenopathy Pain Vaccine positive rechallenge

Symptomtext

Swelling/pain of lymph node under arm (armpit area). Symptoms began later in the day and is still slightly swollen to date of this report (1/10/2023). I understand this is a common side effect, but I felt it should be reported as this is my third booster 11/20/21 with the same reaction (swollen and painful lymph node under arm (armpit) that linger for about 10 days to 2 weeks. Other less bothersome/shorter symptoms are extreme headache and body aches for about 1 day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: osteoarthritis in knees; high blood pressure
Andere Medikamente: amlodipine besylate 5mg
Allergien: sulfa
Vorherige Impfungen: Pfizer boosters 11/20/21 (LOT #FH8030) and on 6/9/22 (LOT FM9992)

VAERS 2554246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 07.01.2023
Impfdatum: 19.12.2022
Beginn: 19.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Headache Pyrexia Swelling

Symptomtext

Headache, Fever, FATIGUE SWELLING Narrative: Seen on 12/23/22 at facility EH

Weitere VAERSDATA-Felder

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

VAERS 2551530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 05.11.2022
Beginn: 02.01.2023
Tage bis Beginn: 58,0
Dosis: 5
Route/Site: SYR / -

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

Pain Pyrexia

Symptomtext

I received my Covid 19 vaccine on 11/5/2022. On the morning of 01/02/2023 I was feeling achy and had a fever. I went to the doctor and was prescribed LAGEVRIO and benzonatate. Symptoms are still ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypermobile Ehlers Danlos syndrome; Mast cell Activation syndrome; Postural ortho spadix; Fibromyalgia; Asthma;
Andere Medikamente: TROKENDI XR; tramadol; leflunomide; tizanidine; montelukast; sertraline; eszopiclone cetirizine; famotidine; vitamin D ; albuterol
Allergien: Statin; fluoroquinolones; pork; mint; LYSOL
Vorherige Impfungen: -

VAERS 2551282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MO
Alter: 28,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 30.12.2022
Beginn: 31.12.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Chills Fatigue Headache Lethargy Pain Pyrexia

Symptomtext

Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: paint in the armpit of same arm that was injected-Medium, Systemic: Headache-Medium

Weitere VAERSDATA-Felder

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

VAERS 2550352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: TN
Alter: 56,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 20.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

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

Dizziness Ear infection Ear pain Impaired driving ability Impaired work ability Influenza virus test negative SARS-CoV-2 test negative Sinusitis

Symptomtext

No symptoms, no problems after the vaccine. In November I started having feel very dizzy, I couldn't drive, I couldn't work, my ear hurt, no fever. I went to the doctor twice and they gave me steroid shot, antibodies and steroids pills. I had ear and sinus infection. I went back last Friday, and I had an ear infection again, left ear hurt but no dizziness this time, they gave me prescriptions to take for 10 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: NOV2022 -COVID-19 TEST - Negative; NOV2022 - Flu Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril; Flonase; Effexor; Aspelin; Topiramate; Relizen
Allergien: Benzonatate
Vorherige Impfungen: -

VAERS 2550220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TX
Alter: 47,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 22.11.2022
Beginn: 27.12.2022
Tage bis Beginn: 35,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Cough Fatigue Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

On 12/27 started having congestion and irritated sore throat. Then fatigue set in. On 12/28 tested positive on at home test. Took NYQUIL and DAYQUIL provided minor relief. Developed persistent cough. Ran fever of 100.9 with TYLENOL. Took SUDAFED for congestion. 12/29 had telehealth visit with PCP. Was prescribed PAXLOVID but didn't take it. Was prescribed TESSALON PEARLS for cough and they really helped. Symptoms began resolving the 12/30 no fever. 12/31 worst of the symptoms resolved but lost entire sense of smell and most of taste. 01/02/2023 smell began to return. 01/03/2023 smell and taste mostly returned 01/04/2023 still having congestion and occasional cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home COVID-19 X4, all positive
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative Colitis; Allergies
Andere Medikamente: Methylamine; montelukast; olopatadine; FLONASE; XYZAL; allergy injections; multivitamin; vitamin D3
Allergien: MEDROL steroids
Vorherige Impfungen: -

VAERS 2546485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: IL
Alter: 17,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 18.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Off label use Peripheral swelling Product use issue Rash

Symptomtext

Swelling of fingers; Rash on knee and elbows; Patient received BNT162B2 and FLU VACCINE VII on 18Nov2022; Patient received BNT162B2 and FLU VACCINE VII on 18Nov2022; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 17-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Dec2022 at 10:30 as dose 3 (booster), single (Lot number: GJ6738) at the age of 17 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Peanut" (unspecified if ongoing), notes: Name of Drug as Reported: Peanut, tree nuts and shellfish , Reaction: Allergy; "Shellfish" (unspecified if ongoing), notes: Name of Drug as Reported: Peanut, tree nuts and shellfish , Reaction: Allergy; "Tree nuts" (unspecified if ongoing), notes: Name of Drug as Reported: Peanut, tree nuts and shellfish , Reaction: Allergy; "if covid prior vaccination: Yes" (unspecified if ongoing), notes: if covid prior vaccination: Yes. Concomitant medication(s) included: FLU VACCINE VII, on 18Nov2022 as dose 1, single; DOXYCYCLINE. Vaccination history included: comirnaty (DOSE 2, SINGLE; Lot number: FL3198), administration date: 27Dec2021, when the patient was 16-year-old, for COVID-19 immunization; comirnaty (DOSE 1, SINGLE; Lot number: EW0186), administration date: 09Jun2021, when the patient was 15-year-old, for COVID-19 immunization. The following information was reported: PRODUCT USE ISSUE (non-serious), OFF LABEL USE (non-serious) all with onset 18Dec2022 at 10:30, outcome "unknown" and all described as "Patient received BNT162B2 and FLU VACCINE VII on 18Nov2022"; RASH (non-serious) with onset 20Dec2022, outcome "not recovered", described as "Rash on knee and elbows"; PERIPHERAL SWELLING (non-serious) with onset 20Dec2022, outcome "not recovered", described as "Swelling of fingers". Therapeutic measures were taken as a result of peripheral swelling, rash. Additional information: Prior to vaccination, patient was diagnosed with COVID-19. Since the vaccination, patient was not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts (Name of Drug as Reported: Peanut, tree nuts and shellfish Reaction: Allergy); COVID-19 (if covid prior vaccination: Yes); Peanut allergy (Name of Drug as Reported: Peanut, tree nuts and shellfish Reaction: Allergy); Shellfish allergy (Name of Drug as Reported: Peanut, tree nuts and shellfish Reaction: Allergy)
Andere Medikamente: DOXYCYCLINE
Allergien: -
Vorherige Impfungen: -

VAERS 2546472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: PA
Alter: 12,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 20.12.2022
Beginn: 20.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / LA

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

Pain in extremity

Symptomtext

Sore arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 12-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Dec2022 as dose 4 (booster), single (Lot number: GJ6738) at the age of 12 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Is bivalent=False, Prev dose lot number=FJ4985, Prev dose lot unknown=False, Prev dose administrator route=Intramuscular, Prev dose administration date=21May2022, Prev dose dose number=3), administration date: 21May2022, when the patient was 11-year-old, for COVID-19 immunization; BNT162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Is bivalent=False, Prev dose lot number=FK5127, Prev dose lot unknown=False, Prev dose administrator route=Intramuscular,, Prev dose administration date=26Nov2021, Prev dose dose number=2), administration date: 26Nov2021, when the patient was 10-year-old, for COVID-19 immunization; BNT162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Is bivalent=False, Prev dose lot number=FK5127, Prev dose lot unknown=False, Prev dose administrator route=Intramuscular, Prev dose administration date=05Nov2021, Prev dose dose number=1), administration date: 05Nov2021, when the patient was 10-year-old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 20Dec2022, outcome "recovering", described as "Sore arm". Therapeutic measures were not taken as a result of pain in extremity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MD
Alter: 39,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 27.11.2022
Beginn: 02.12.2022
Tage bis Beginn: 5,0
Dosis: 5
Route/Site: IM / LA

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

Cough Cough variant asthma Feeling abnormal SARS-CoV-2 test negative Vomiting

Symptomtext

I did not feel good 12/02/22, by 12/07/22 and 12/08/22 I was feeling even worse. I used two at home COVID-19 test from on 12/16/22 that came back negative. Work requested that I take another on 12/17/22 that also came back negative. I went to a clinic and saw the saw doctor that I had seen back in September when I had tested positive for COVID-19. He felt that I may have a cough variant of asthma and I needed to be using my albuterol inhaler more. I cough so hard that I have been throwing up. I started taking OZEMPIC. The coughing seems to come on at night, in the cold air. I have been taking TUMS to help keep my stomach calm, so I do not want to throw up. I will be following up with the doctor in January.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: Home COVID-19 test negative
Aktuelle Erkrankungen: No
Vorgeschichte: Type I Diabetes; Anemia
Andere Medikamente: TRESIBA; FIASP; albuterol inhaler as needed; SINGULAIR
Allergien: Diflucan; clindamycin; seasonal allergies
Vorherige Impfungen: -

VAERS 2543659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: PA
Alter: 36,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 08.11.2022
Beginn: 04.12.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chills Cough Malaise Oropharyngeal pain Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sinusitis Streptococcus test Throat clearing Throat irritation

Symptomtext

My husband had tested positive for COVID-19 on November 30th and I was having symptoms on the 4th. I was having a slightest sore and scratchy throat, but it was not enough to think I was sick. On the 5th my daughter and I went in and I also tested positive for COVID-19. From there the sore throat got worse, I had a dry cough, Wednesday I had a fever and chills and was out until about Friday the fever did not go away with medication either, I had body aches and chills that would not go away. I had a runny nose that turned into a sinus infection as well. I am still recovering in the mornings I have to clear my throat and its like I cant get it clear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 rapid test; Strep test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Essential Tremor; Anxiety; Depression
Andere Medikamente: Vitamin C; vitamin D3; biotin; multivitamin; vitex berry
Allergien: Sulfa drugs; amoxicillin
Vorherige Impfungen: COVID-19 Pfizer first dose, swollen lymph nodes 4/10/2021

VAERS 2543138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 26.12.2022
Impfdatum: 23.12.2022
Beginn: 24.12.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pruritus Injection site swelling Injection site warmth

Symptomtext

Patient is experiencing hot, swollen, and itching at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Patient had similar reaction to Moderna covid vaccine. Patient reports swelling, hot, and itching at injection site.

VAERS 2543134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 26.12.2022
Impfdatum: 20.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / RA

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

Lymphadenopathy Rash pruritic

Symptomtext

Swollen left occipital lymph node accompanied by small itchy bumps that come and go.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: None at this time.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin 10mg 1x daily, OTC multivitamin 1x daily
Allergien: None
Vorherige Impfungen: -

VAERS 2543116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 26.12.2022
Impfdatum: 20.12.2022
Beginn: 21.12.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Injection site erythema

Symptomtext

Site: Redness at Injection Site-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2543078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TN
Alter: 62,0
Geschlecht: M
Eingang: 26.12.2022
Impfdatum: 13.12.2022
Beginn: 13.12.2022
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 bruising Injection site nodule Injection site pain Neck pain

Symptomtext

Pt experienced pain in right arm from elbow to neck, bruising from elbow to injection site and a knot at injection site,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Pt wife called to let us know that patient had "excruciating" pain from his right elbow to his neck. He was also bruised from the site to the elbow and had a knot at the site of injection. Stated she thought the site was too far to the righ
Allergien: NKA
Vorherige Impfungen: -

VAERS 2542865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: WI
Alter: 56,0
Geschlecht: F
Eingang: 25.12.2022
Impfdatum: 21.12.2022
Beginn: 23.12.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Abdominal pain Arthralgia Back pain Bladder pain Bone pain Discomfort Dysuria Pain

Symptomtext

Public Health gave me the shot. Mid section soreness, different feeling urination like slower,with soreness. Very much uncomfortable all day. Took some AZO maximum strength to relieve pain, kinda helped. Sore right lower back wrapping around to front hip bone. Bladder is sore and does not like pressure on it. Drinking plenty of water. I begin urination and feel plugged at the end. Very much irritated even with AZO. I know what a uti feels like and haven?t had one for many years.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Haven?t gone anywhere trying to work through it. My primary knew I was getting the Covid shot at public health on the 12/21/2022. I just had my physical with her on 12/15/2022
Aktuelle Erkrankungen: None
Vorgeschichte: After Moderna shots became weak in muscles, balance, stuttered, motion sickness, weight loss
Andere Medikamente: Levothyroxine 0.05mg Ibuprofen 200 mg clear lax polyethylene glycol 3350
Allergien: Lidocaine, sulfa meds, amoxicillin, afrin nasal spray
Vorherige Impfungen: Moderna 4/7&5/4&11/29 2021 5/16/2022

VAERS 2542047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 06.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

On 12/06/2022 client presented to the vaccination site and was vaccinated with a Covid Pfizer Bivalent Booster Lot# GJ6738 on left arm by vaccinator. At approximately 1728 while sitting in the observation area, client notified nurse that she was feeling ?Dizzy?. Nurse proceeded to take her vital signs; BP:122/78, HR:67, O2:98%, RR:13. Client was able to move to the gravity chair without assistance. Client denied itchiness on any part of the body, denied difficulty breathing, and denied pain. Client reported a history of high blood pressure (medication unknown) and no known allergies. Client stated she experienced dizziness about six months ago due to being stressed. She also denied dizziness or any adverse reaction with the previous Covid Vaccines; Janssen primary series (04/10/2021) and Janssen booster (11/23/2021). Client reported she ate lunch around 1500, ?Sandwich and french-fries with coffee and soda.? At approximately 1741 PHN offered client to have EMS activated for a follow up assessment, client declined. Client reported dizziness had subsided. Client was offered a water bottle. 1740 vital signs; BP: 122/68, HR:68, O2:98%, RR:14. Client rested for a few minutes. 1750 vital signs; BP: 118/76, HR:68, O2:98%, RR:16. Client denied itchiness, difficulty breathing and dizziness. Husband reported he would be driving back home. PHN educated on possible side effects after vaccine, to seek emergency care if symptoms worsened and to follow up with her primary care provider. Client verbalized understanding. 1756 vital signs: BP:120/78, HR:73, O2:99%. Client denied dizziness and that she was feeling ?Fine.? Client was able to stand up without assistance from gravity chair. Client left the facility accompanied by husband with a steady gait at 1759.

Weitere VAERSDATA-Felder

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

VAERS 2541980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: IN
Alter: 75,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Decreased appetite Dizziness Fatigue Hypersomnia Myalgia Rhinorrhoea

Symptomtext

Dizzy and severe runny nose first within a few hours after injection. Next by early evening fatigue and weakness and loss of appetite and muscle aches. No fever! Slept many hours that night and the next morning but by evening of the 12th of November started feeling better! Slowly better each day! Lasting about 3-4 days total. Notified Medical Center and nurse contacted me and took details! Since essentially back to normal the weekend no studies done

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No acute!
Vorgeschichte: Hypothyroidism and hypercholesterolemia and trigeminal neuralgia of left face
Andere Medikamente: Levothyroxin 125, Simvastatin 40 mg , Vitamin D3 2000 mg daily and zinc 50 mg daily and lyrica 75 mg daily and Vitamin B12 2500 mcg daily! ASA 81 mg weekly
Allergien: Sulfa and tegretol, myalgia with lipitor
Vorherige Impfungen: -

VAERS 2537777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: IA
Alter: 76,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 04.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / -

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

Pruritus

Symptomtext

Patient had severe itching over body for 3 days after vaccination but did not break out in hives. She took Zyrtec and the itching went away.

Weitere VAERSDATA-Felder

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

VAERS 2537308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 18.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Pain Pyrexia Vomiting

Symptomtext

63 year old patient had 3 vaccines administered, Fluzone Quad, Prevnar-20 and Pfizer Bivalent. About 2 hours later patient started with aches and fever. About 12 hours later patient started Vomiting. Patients daughter is bringing her to provider, or emergency Dept

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: not known
Aktuelle Erkrankungen: none
Vorgeschichte: Heart, diabetes, hypertension,
Andere Medikamente: Jardiance, Trulicity, Lisinopril, Atorvastatin, Zetia, clopidogrel, aricept, basaglar, isosorbide mono ER, metformin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2536786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 08.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 1,0
Dosis: 6
Route/Site: IM / LA

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

Headache Inflammation Noninfective gingivitis Orthosis user Pain Pain in extremity Sinus disorder

Symptomtext

Inflammation in just about every system in my body. I have no insurance or doctor, so I used braces for my hands and elbows, hot compresses and saline for my sinuses, and after a week, aspirin for headache. I took extra Vitamin C and used my waterpik 3x per day to reduce gum inflammation. I removed all piercings as they also became painful. Ten days later, my hands and feet are still inflamed and painful, and I still have a headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: NONE: I have no health insurance and no doctor.
Aktuelle Erkrankungen: NONE
Vorgeschichte: Hepatitis C
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: All of the Pfizer COVID vaccines and boosters--same side effects reported here.

VAERS 2536077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 17.12.2022
Impfdatum: 17.12.2022
Beginn: 17.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Headache

Symptomtext

patient developed severe headache within 10 minutes of following the administration of the vaccine. pt applied ice pack to back of neck and was good after 30 minutes of being seated and monitored

Weitere VAERSDATA-Felder

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

VAERS 2536028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: PA
Alter: 31,0
Geschlecht: F
Eingang: 17.12.2022
Impfdatum: 22.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal distension Abdominal pain Decreased appetite Pain

Symptomtext

PT STATES THAT THE FOLLOWING DAY SHE STARTED TO EXPERIENCE ABDOMINAL PAIN, DECREASED APPETITE, BLOATING, ACHES, AND SEVERE PAIN. STATED THAT SHE HAD RECEIVED INJECTION FOR XOLAIR 1 TO 2 WEEKS PRIOR TO VACCINE AND HAD A HISTORY OF MODERNA COVID VACCINES. SHE WENT TO HER DOCTORS OFFICE ON THAT FRIDAY FOLLOWED BY A HOSPITAL VISIT THAT SUNDAY. CURRENTLY WORKING WITH PCP AND GI RE SYMPTOMS AND HAS BLOOD WORK AND A SCOPE SCHEDULED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: NO DATES GIVEN BUT STATES THAT SHE IS SCHEDULED FOR BLOODWORK AND A SCOPE.
Aktuelle Erkrankungen: N/A
Vorgeschichte: ASTHMA
Andere Medikamente: XOLAIR, EURYNG
Allergien: N/A
Vorherige Impfungen: -

VAERS 2533849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: KS
Alter: 52,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 13.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Induration Injection site reaction Injection site warmth Joint range of motion decreased Pain in extremity Rash Rash macular Tenderness

Symptomtext

On 12/14/2022 at 2pm, patient noticed three red blotches on left arm below deltoid that was warm to the touch. Her arm was hurting and was unable to lift past shoulder height. On the evening of 12/15/2022, patient came to pharmacy and rash was tender and about a 5 inch circle with a hard knot in the middle. Patient went to medical clinic and was prescribed antibiotics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site reaction
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2533270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 15.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Abdominal pain upper Dizziness Nausea

Symptomtext

pt became very nauseous and sharp pain in stomach, dizzy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2531247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: WI
Alter: 67,0
Geschlecht: F
Eingang: 14.12.2022
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: nein

Erythema Headache Pain of skin Pruritus Scab Skin lesion Vaccination site pain

Symptomtext

Headache soreness at vaccination site Left arm on inside of elbow a sore that developed 2 days after vaccination in that arm which was very red, angry, sore, itchy, painful. It had bubbles that eventually turned to scab. It still exists & will probably scar.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lisinopril 5mg; Multi-vitamin; Fish oil; Calcium, magnesium & zinc (bone & muscle health)
Allergien: none
Vorherige Impfungen: -

VAERS 2531063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: WI
Alter: 49,0
Geschlecht: M
Eingang: 14.12.2022
Impfdatum: 13.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chills Fatigue Influenza like illness Injection site pain Myalgia Pain in extremity Thirst

Symptomtext

patient reported to public health nurse that he started to have "a reaction to my booster vaccine" that he received yesterday (vaccine administered on 12/13/22 around 4:30 p.m.); onset of symptoms was today, 12/14/22, at 10:25 AM; side effects reported to public health nurse from patient included sudden onset of muscle aches, flu like symptoms, chills, feeling very thirsty, tiredness, and a sore arm at site of injection.. At 12:10 PM patient reports that all side effects have subsided, with the exception of the sore arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GERD
Andere Medikamente: Magnesium 500 mg daily Statin - drug 15 mg daily OTC CoQ10 daily MVI daily
Allergien: PCN, Amoxicillin, oxycodone Peanuts & tree nuts Fresh fruits, especially citrus
Vorherige Impfungen: -

VAERS 2530044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: WI
Alter: 37,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 12.12.2022
Beginn: 13.12.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Cold sweat Coordination abnormal Dysstasia Heart rate increased Myalgia Pain Pyrexia SARS-CoV-2 test negative Urinary incontinence

Symptomtext

Fever of 102 degrees, heart rate was elevated to 118 bpm, patient was clammy, unable to physically stand up due to loss of coordination, experienced urinary incontinence, experienced pain and muscle aches. Patient was given ibuprofen and told to go home and rest. As of today, 12 hours later, patient reports feeling better and fever has resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: COVID test was administered at ER, came back negative. Bloodwork was done and came back normal.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Duloxetine, Gabapentin, Amantadine, Vitamin D
Allergien: No known drug allergies
Vorherige Impfungen: Previous COVID vaccine

VAERS 2528471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 10.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Injection site bruising Injection site swelling

Symptomtext

When I delivered the vaccine, a small bump appeared on the patient's left arm around the injection site. Patient didn't feel any pain at that time. I advised the patient what signs to watch out. I followed up with the patient the next day (December 10 2022), and she said the bump disappeared but there were bruises around the injection site. Patient confirmed that she didn't have any fever or pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2528413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MN
Alter: 46,0
Geschlecht: M
Eingang: 10.12.2022
Impfdatum: 06.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Gastrooesophageal reflux disease Headache Influenza like illness Pyrexia

Symptomtext

Acid reflux, flu-like aches & pains, headache, slight fever for 4 days (so far)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Dermatographism
Andere Medikamente: Zertek, multi-vitamin, Relaxium Sleep
Allergien: -
Vorherige Impfungen: Same symptoms after Covid booster in Dec. 2021

VAERS 2528197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: KS
Alter: 66,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 02.12.2022
Beginn: 02.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia

Symptomtext

Patient complained of pain in her knees following covid booster vaccine. Reported that pain started soon after vaccine and was still there (although much reduced) 1 week later at time of this report. Just pain, no inflammation or swelling present. Patient also states that she does have arthritic pain for which she undergoes physical therapy for, but had not had pain like this before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Arthritis pain.
Vorgeschichte: Osteoarthritis
Andere Medikamente: -
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2527789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TX
Alter: 25,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 05.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Hypersomnia Immunisation reaction Injection site erythema Injection site pain Injection site pruritus Injection site swelling Injection site warmth Pain

Symptomtext

24 hours after presented normal side effects (redness and swelling the size of a quarter near the injection site). 48 hour after, the injection site swelled 4x the size so it was the size of my palm, was itchy, bright red, raised about 1/2? off my arm, tender to the touch, incredibly hot, and I slept for nearly 24 hours. 72 hours after, the swelling and redness spread slightly, my arm stung, ibuprofen, Tylenol and cold packs were not making a difference on my site. This was when I contacted my doctor and she informed me it was ?Covid arm?, which was normal. Now, 96 hours after, the swelling has increased to the size of my hand, the redness has decreased and the soreness and heat of my sore has decreased. I was advised to take Benadryl, so that may have helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: 12/08/2022 images were sent to my doctor via the patient portal for my doctor to examine. She advised that it was Covid arm and if it does not improve, to visit her
Aktuelle Erkrankungen: 1 week prior had levocetirizine withdrawals that caused hives and itchy skin for 3 days
Vorgeschichte: Iron deficiency anemia, high BMI
Andere Medikamente: 35mg iron daily, 10mg Lexapro daily, 5mg buspirone 2x daily, Zyrtec, multivitamin for women
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2526184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: OH
Alter: 33,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 06.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Peripheral coldness Poor peripheral circulation Pruritus Rash Skin discolouration

Symptomtext

Event 1: Poor circulation in hands and feet (they turned white and cold after washing hands in mildly cold water). Treatment and Outcome 1: This is abnormal for me, and I simply manage it by not using cold water. Monitoring if this becomes more severe and will seek treatment if necessary. Event 2: after 36-37 hours I developed a rash all over my body (30-40%) similar to Poison Ivy/Oak in terms of itchiness, and focused in areas where there is higher warmth or rubbing (e.g. elbows, arms, backs of knees, fronts of thighs, chest). lesser degree on my back and backs of legs) Treatment and Outcome 2: Tried Calamine lotion and provided some relief, but only marginally successful. Monitoring and will try lotion and re-application of Calamine to provide relief. Will seek treatment if it becomes more severe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: nothing yet.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2525846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: PA
Alter: 48,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 06.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Epistaxis Pain Pyrexia

Symptomtext

Patient stated that besides pain and fever he also had a nosebleed the following morning after receiving the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Symbicort inhaler
Allergien: nka
Vorherige Impfungen: -

VAERS 2525174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 16.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Rash

Symptomtext

SkinRash numbness hands and feet

Weitere VAERSDATA-Felder

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

VAERS 2524862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Gj6738

mild

Staat: TX
Alter: 32,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 06.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Pain in extremity

Symptomtext

Administered flu shot and Pfizer in the same left arm and they are separated by 1/2 in ch Vs 1 in on the same arm little pain felt but nothing happened

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No e
Vorherige Impfungen: -

VAERS 2524263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 28.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Abdominal discomfort Balance disorder Vertigo Vomiting

Symptomtext

"Received flu and Covid booster Monday 11am. Wednesday about noon experienced really weird vertigo. My balance was way off and the spinning sensation upset my stomach and I vomited many times between 1 and 5 pm. Recovered by 11 pm and was back to 90% Thursday am. I have never experienced vertigo before"

Weitere VAERSDATA-Felder

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

VAERS 2522578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: ME
Alter: 35,0
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

Urticaria

Symptomtext

Hives/Welts on bottom and upper back of thighs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Propranolol
Allergien: Penicillin & Sulfa
Vorherige Impfungen: -

VAERS 2520857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: AZ
Alter: 55,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 30.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Memory impairment Renal pain

Symptomtext

I am experiencing kidney pain post vaccination. It is bilateral and rates a 2-3/10. I am remembering now that I had this after other COVID vaccinations, but memory fails on the details. I had written it off to other causes but felt today when I made the connection, that I should report it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Renal pain
Hospital-Tage: -
Labordaten: I am not seeking medical care unless it worsens. I am making sure to stay hydrated today and tracking symptoms myself.
Aktuelle Erkrankungen: I was in good health at time of vaccination, although I am a retail pharmacist and have been exposed to a host of viruses this season all of which had resolved at time of vaccination. I was not going to report this but I remembered that I have had kidney pain after each Pfizer COVID booster and just thought it may warrant reporting. I had written it off to other things before.
Vorgeschichte: hypothyroidism, managed with levoxyl
Andere Medikamente: Levoxyl 88mcg qd Flonase nasal spray
Allergien: adhesive in bandages
Vorherige Impfungen: kidney pain with other covid vaccinations

VAERS 2520130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 14.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cyst Injection site pain Injection site swelling Muscle swelling Myalgia Ultrasound scan abnormal

Symptomtext

Within 24 hours of receiving left deltoid COVID by Valent vaccine, developed tenderness and swelling around left deltoid but also posterior scapular area, subaxillary, teres minor, and pectoralis minor area. On exam tender and swollen, no discrete lesion and no lymph nodes, left breast within normal limits. Referred for ultrasound, which was performed on 11/17/2022, 48 hours after onset of symptoms. This showed "nonspecific 2.8X 1.8 cm partially solid and 2.2 x 2.2 x 1.1 cm cystic and anechoic structure is noted in the area of clinical concern in the left axilla. No typical lymph nodes are seen." On telephone follow-up with patient on 11/28/2022, patient says that symptoms completely resolved and feels back to normal with no tenderness or swelling, with resolution a few days ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: See ultrasound report above.
Aktuelle Erkrankungen: None
Vorgeschichte: HIV infection generally well controlled, no history of AIDS or related conditions. Arthralgia in several joints. Presumed peripheral neuropathy in lower extremities. Possible seizure disorder (only 1 seizure several years ago). History of major depression and urinary incontinence.
Andere Medikamente: TDF/FTC (Truvada), nelfinavir 1250 mgtwice daily. Also has prescriptions for Keppra Exar 500 daily, potassium chloride, diclofenac 1% topical gel, albuterol MDI and nebulizers, naproxen 500 mg p.o. twice daily, acetaminophen, as needed onda
Allergien: Listed allergies and adverse drug reactions: Trimethoprim?sulfamethoxazole (rash/hives) Lamotrigine (rash) Pregabalin (swelling)
Vorherige Impfungen: -

VAERS 2518265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 23.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / RA

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

Erythema Pruritus

Symptomtext

Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time; Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time; peri-orbital redness; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Nov2022 at 10:00 as dose 5 (booster), single (Lot number: GJ6738) at the age of 55 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ESTROGEN. Past drug history included: Neomycin, reaction(s): "Allergy". Vaccination history included: BNT162b2 (prev dose product=COVID 19,, prev dose brand=Pfizer,, prev dose brand unknown=False, is bivalent=False,, prev dose lot number=FJ4989,, prev dose lot unknown=False,, prev dose administration date=04May2022,, prev dose administration time=06:00 PM,, prev dose dose number=4,, prev dose vaccine location=Right arm,), administration date: 04May2022, when the patient was 54-year-old, for COVID-19 immunization, reaction(s): "peri-orbital redness", "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time", "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time"; BNT162b2 (prev dose product=COVID 19,, prev dose brand=Pfizer,, prev dose brand unknown=False, is bivalent=False,, prev dose lot number=FF2587,, prev dose lot unknown=False,, prev dose administration date=08Oct2021,, prev dose administration time=12:00 PM,, prev dose dose number=3,, prev dose vaccine location=Right arm), administration date: 08Oct2021, when the patient was 53-year-old, for COVID-19 immunization, reaction(s): "peri-orbital redness", "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time", "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time"; Covid-19 vaccine (DOSE 1 , UNKNOWN MANUFACTURER), for COVID-19 immunization, reaction(s): "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time", "peri-orbital redness", "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time"; Covid-19 vaccine (DOSE 2, UNKNOWN MANUFACTURER), for COVID-19 immunization, reaction(s): "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time", "peri-orbital redness", "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time". The following information was reported: PRURITUS (non-serious), PRURITUS (non-serious), outcome "unknown" and all described as "Each time I was extremely itchy on my scalp and in all joint areas. itching last for several hours. Also had peri-orbital redness each time"; ERYTHEMA (non-serious), outcome "unknown", described as "peri-orbital redness". Therapeutic measures were not taken as a result of pruritus, pruritus, erythema. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient had been tested positive for COVID-19 reported unknown. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201325402 same reporter/patient/event, different vaccine dose;US-PFIZER INC-202201325408 same reporter/patient/event, different vaccine dose;

Weitere VAERSDATA-Felder

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

VAERS 2518015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: VA
Alter: 69,0
Geschlecht: F
Eingang: 28.11.2022
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: nein

Fatigue Headache Injection site pain Pruritus

Symptomtext

Injection day (headache and tiredness). Since then, headache; injection site soreness; random itching (behind ears, head, shoulders, upper back, legs, arms - not constant nor all of the time no redness nor rash) - taking Tylenol for headache and Benadryl and Aveeno shower gel for itching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: Zyrtec; Losartan; Singular; Synthroid, multi-vitamin
Allergien: Penicillin, sulfa, local anesthetics, mycins; codeine; cyclines, others
Vorherige Impfungen: -

VAERS 2517412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 73,0
Geschlecht: M
Eingang: 27.11.2022
Impfdatum: 15.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Diarrhoea Flatulence Gastrooesophageal reflux disease Hypersensitivity Immunisation reaction Pain Urticaria

Symptomtext

Adverse allergic reaction to Pfizer Booster shot was noted on the evening of Nov. 17, 2022, with Hives appearing on neckline and armpit areas. Then had pain on poke area for two days. By Nov. 18, have experienced loose stools and sometimes watery discharge. Color was normal but consistency was soft. Hives disappeared by Nov. 19. Also Gastric Reflux experienced from Nov. 17 until today, Nov. 26 2022. Too much gas being emitted via mouth and anus areas during the day and nighttime. Diarrhea also occurs sometimes but only once per day. Have taken Diphenhydramamine for Hives and Imodium for Diarrhea and watery stools.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes, Hypertension, High Triglycerides, High Cholesterol, Glaucoma
Andere Medikamente: Diphenhydramamine (Benadryl) 25 mg for Allergy. Atenolol, 50 mg/ daily; Lisinopril 20 mg/daily; Metformin 1000 mgs/daily; Rosuvastatin 10mg/daily; Centrum Silver; Vitamin C 500mg; Vitamin D3; Zinc 50mg.; Imodium for Diarrhea
Allergien: Penicillin Injection and Moderna CoVid19 Vaccination /Booster Shots.
Vorherige Impfungen: Moderna Vaccines 1 & 2; Moderna Boosters 1 & 2

VAERS 2515730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MD
Alter: 41,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Fatigue Rash

Symptomtext

I had Pfzer for both my two primary doses and two boosters, however, this is the first time I had skin rash reaction to the vaccine. About 5 hours after taking the bivalent booster, I had mild rashes around my waist and shoulder; then on the next day, my legs also started to have rashes. Other than that, just feeling a bit more tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None, the rashes slowly went away by themselves
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Was allergy to Tylenol when I was a teenager, had not taken that again; allergic to crab (skin rash)
Vorherige Impfungen: -

VAERS 2515313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ 6738

mild

Staat: OH
Alter: 70,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 23.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / -

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

Flushing Immediate post-injection reaction Nasal pruritus Tongue pruritus

Symptomtext

On 11/23/22 - Patient told RN that she always gets some "type of reaction" when she get her COVID vaccine and that her doctor told her to make sure she goes to a facility that is close to a hospital. Nurse gave the patient the vaccine on the gurney at 12:08. She stated that she had an Immediate flush reaction. She said she states she gets this when she has an anxiety attack. She states that she has over a 100 allergies to medication. Also allergic to lobster and eggs? No other illness at time of vaccination. Medications include: Aldactone 50mg and Chlorthalidone 25mg for Hypertension She stated that she took a Benadryl 25 mg prior to coming to covid center. Patient drove herself to COVID center. 12:12 173/98 Pulse 92 and Sat 97% "Immediate flush" 12:20 142/106 P 89 Sat 98%- nose feels itchy and tongue feels itchy. Encouraged her to drink her Gatorade that she brought. 12:30 148/88 Pulse 85 Sat 93% "tongue itchy". " I feel much better than I have in the past once given the vaccine. 12:40 Up to wheel chair with minimal assistance/ VS in w/c 167/97 p 86 Sat 99%. Still states tongue is a bit itchy. Very talkative and appears in no distress. States again how much better she feels than last time. Instructed to call 911 if symptoms increase (SOB, tongue swelling, difficulty breathing or swallowing. Nurse escorted patient from facility - no difficulty walking, no dizziness, no SOB or issues when leaving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nasal pruritus
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: denies
Vorgeschichte: HTN, Fibromyalgia, Neck issues,
Andere Medikamente: Aldactone 50mg chlorthalidone 25 mg Zofran
Allergien: She states "over 100 medications that she is allergic and lobster and eggs as far as food ALLERGIES Contrast Dye, Amlodipine Besylate, Desipramine Hcl, Sulfamethoxazole-Trimethoprim, Tegretol [Carbamazepine], Ace Inhibitor [Other], Ace Inhibitors, Adhesive Tape (Rosins), Amrix [Cyclobenzaprine], Atenolol, Augmentin [Amoxicillin-Pot Clavulanate], Baclofen, Bee Sting, Bee Stings [Other], Betablocker [Other], Buspirone, Buspirone Hcl, Carvedilol, Celebrex [Other], Celecoxib, Cephalexin, Cephalosporins, Chlorine, Cipro [Other], Ciprofloxacin, Clindamycin Hcl, Clindamycin [Other], Cliniril [Other], Clonidine, Codeine, Codeine [Other], Coumadin [Warfarin Sodium], Darvocet-N 100 [Other], Darvon [Other], Desipramine, Dicyclomine, Diflucan [Fluconazole], Diovan [Valsartan], Doxycycline, Doxycycline Hyclate, Elavil [Other], Enalapril, Estrogens, Fluoxetine Hcl, Gabapentin, Gadolinium-Containing Contrast Media, Hydralazine, Ibuprofen, Iodine, Keflex [Other], Ketorolac Tromethamine, Levaquin [Levofloxacin], Lidocaine, Lisinopril, Meclizine, Meclizine [Other], Metoclopramide, Metoprolol Tartrate, Morphine Sulfate, Morphine Sulfate [Other], Naltrexone, Neurontin [Other], Nitrofuran Analogues, Nitrofurantoin, Non-Ionic Contrast [Other], Nortriptyline Hcl, Nucynta [Tapentadol], Opioids - Morphine Analogues, Oxycodone, Pamelar [Other], Pantoprazole Sodium, Pcn [Other], Penicillins, Pool Chemicals [Other], Prempro [Other], Prilosec [Omeprazole], Prozac [Other], Sulfamethoxazole, Sulindac, Tekturna [Aliskiren], Telmisartan, Tolmetin, Tramadol, Tramadol Hcl, Trazadone [Other], Trazodone, Ultram [Other], Vancomycin, Vancomycin Hcl [Other], Voltaren-Xr [Other], Cardizem [Diltiazem Hcl], Nisoldipine, and Sucralfate
Vorherige Impfungen: pfizer

VAERS 2513909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: GA
Alter: 49,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 17.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Cough Insomnia Malaise Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I woke up mid morning and I started feeling congested with a sore throat and as the day wore on my symptoms became worse with a dry cough. The next morning symptoms were worse yet no fever I was unable to sleep that night and an at home COVID-19 test showed positive. The next morning I wen to the Doctor and a rapid antigen COVID-19 showed positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Rapid antigen COVID-19 result positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Gabapentin; Diazepam; Promethazine; Progesterone; Melatonin; Nutrafol
Allergien: Sulfa;
Vorherige Impfungen: -

VAERS 2512499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NJ
Alter: 44,0
Geschlecht: F
Eingang: 20.11.2022
Impfdatum: 16.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site vesicles Pyrexia

Symptomtext

PATIENT CALLED ON 11/19/22 STATING SHE HAD 104.1 FEVER AND INJECTION SITE REACTION AREA BLISTERED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site vesicles
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2512480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NY
Alter: 24,0
Geschlecht: M
Eingang: 20.11.2022
Impfdatum: 18.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain lower Micturition urgency Penile pain

Symptomtext

11/19/2022 6:00 am, intermittent RLQ abdominal pain. Treatment of 1 gallon water intake, 1 cup fenugreek tea. Problem resolved. 11/19/2022 2:30 am, urinary urgency with intermittent penile pain. Treatment of 1 gallon water intake, 1 tbsp of honey, problem lessened but on going.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ashwagandha, escitalopram
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2512281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 18.11.2022
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

Diarrhoea Swelling Swelling face

Symptomtext

Patient said the evening of the vaccines that her face started to swell including the bottom eye and her neck and she had diarrhea. No trouble breathing. She said it lasted for 3 days and it went away

Weitere VAERSDATA-Felder

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

VAERS 2511324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Gj6738

mild

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 11.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / RA

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

Urticaria

Symptomtext

Severe whole body hives; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 67-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Nov2022 at 08:45 as dose 1, single (Lot number: Gj6738) at the age of 67 years, in right arm for covid-19 immunisation; influenza vaccine inact split 3v (FLUZONE HIGH DOSE), on 11Nov2022 as dose 1, single (Lot number: Uj934aa), in left arm for immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The patient has no known allergies and no covid prior vaccination or other vaccine in four weeks. The following information was reported: URTICARIA (medically significant) with onset 13Nov2022 at 20:00, outcome "not recovered", described as "Severe whole body hives". The event "severe whole body hives" required physician office visit. Therapeutic measures were taken as a result of urticaria including Prednisone 40 mg per day. The patient was not tested for covid-19 post vaccination.; Sender's Comments: As per the available information the causality of the event urticaria with the suspect BNT162b2, BNT162b2 omi ba.4-5 can not be ruled out completely. 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, Ethics committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2509648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: SC
Alter: 63,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 16.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Injection site erythema Injection site swelling

Symptomtext

patient had swelling and redness at site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: -
Andere Medikamente: Montelukast
Allergien: aspirin, penicillin, vancomycin, clindamycin
Vorherige Impfungen: -

VAERS 2509621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

mild

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 16.11.2022
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: ja

Injection site pain Pain

Symptomtext

Site: Pain at Injection Site-Mild, Additional Details: I selected wrong reasoning on previous report as route but it was an event of she felt radiating pain day after shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2509465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: KS
Alter: 37,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 15.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Chills Headache Night sweats Pain Pyrexia

Symptomtext

Slight fever, chills, excessive night sweats, headache, achy all over body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Buspirone, vit D, atenolol, xyzal, vyvanse
Allergien: Propranolol, morphine, keflex
Vorherige Impfungen: -

VAERS 2509463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: PA
Alter: 41,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 11.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Injection site erythema Injection site swelling Injection site warmth Lymph node pain Lymphadenopathy Pyrexia Tenderness

Symptomtext

Pain and swelling in lymph nodes under right arm were the issue of concern. Patient did also run a fever (100-102) for 3+ days after receiving injection. Note that injection site swelled, turned red, and radiated heat in about a 5-8" circle around the injection. Patient called primary care doctor due to concern when lymph nodes' swelling and pain did not improve 36 hours after onset. PCP advised ibuprofen, application of heat (patient was already doing this), and to visit the ER if symptoms did not improve within 2 more days. After 30 more hours (from talking to PCP), swelling and tenderness lessened (though still present). This was approx. 90 hours after injection. Patient agreed to report adverse reaction and follow-up with PCP if needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma Abdominal Hernia
Andere Medikamente: Claritin tablet, 10mg, 1 daily LoLoestrin FE 1-10, tablet, 1 daily
Allergien: Sulfa Bromfed
Vorherige Impfungen: -

VAERS 2509235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

mild

Staat: IL
Alter: 54,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Malaise Off label use Product use issue

Symptomtext

just didn't feel good; Pfizer COVID-19 Bivalent Booster last Friday and also had flu shot as well; Pfizer COVID-19 Bivalent Booster last Friday and also had flu shot as well; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 54-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 as dose number unknown (booster), single (Lot number: GJ6738, Expiration Date: 30Jun2023) at the age of 54 years, in right deltoid for COVID-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 04Nov2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: COVID-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 04Nov2022, outcome "unknown" and all described as "Pfizer COVID-19 Bivalent Booster last Friday and also had flu shot as well"; MALAISE (non-serious) with onset 05Nov2022, outcome "not recovered", described as "just didn't feel good".; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201296261 Same reporter/patient/drug, different event/dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2508927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 15.11.2022
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: unbekannt

Pain Wrong product administered

Symptomtext

Pt came in asking for the flu shot and covid vaccine, but only wanted flu shot that day. He received covid 19 booster instead-- per pt he experienced body aches that evening

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: pfizer covid 19 with all 3 doses before this one

VAERS 2508314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 13.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

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

Immunisation reaction Injection site erythema Injection site swelling Pain in extremity Pruritus

Symptomtext

COVID Arm - Left arm has just developed a large, swollen, red ring has around the injection site less than 2 days later. Arm is sore and a little itchy. I elected to have both Flu Shot and Bivalent administered in same arm. I did this for booster in 2021 and had no issues, but am now experiencing this side effect for the first time after the Bivalent booster. Monitoring condition and have not sought treatment at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Cough
Vorgeschichte: -
Andere Medikamente: Junel FE
Allergien: None known
Vorherige Impfungen: -

VAERS 2507279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 11.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Immunisation reaction Nodule Pain Rash Rash pruritic

Symptomtext

COVID arm - lump, 1 & 1/2 -2 inch itchy rash on arm, pain. Instructed patient to use Ibuprofen or Acetaminophen and cold compresses as needed for pain and itchiness.

Weitere VAERSDATA-Felder

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

VAERS 2507186

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ6738

mild

Staat: MN
Alter: 58,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 10.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / RA

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

Pruritus Urticaria

Symptomtext

Hives appeared on day 3 after vaccine. Inner ears started itching one day after vaccine. Hives were very itchy and covered trunk and lower arms. No hive reaction at injection site. Hives are still present on Day 4 and do not seem to be improved by showering or allergy relief medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine, Lipoflavanoid
Allergien: Sulpha
Vorherige Impfungen: -

VAERS 2507156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: PA
Alter: 84,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Chills Pyrexia

Symptomtext

Patient experienced fever and chills lasting about 6 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: unknown
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 2506884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: -
Alter: 13,0
Geschlecht: F
Eingang: 13.11.2022
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: unbekannt

Dizziness

Symptomtext

pt felt light headed after administeratoin. felt better by lying down and drinking cold water

Weitere VAERSDATA-Felder

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

VAERS 2506642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: WA
Alter: 42,0
Geschlecht: F
Eingang: 12.11.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Arthralgia Bone pain Chills Dyspepsia Pyrexia

Symptomtext

Severe bone, joint (all joints) pain, chills, fever, for over 12 jours, slight indigestion. Has gappened with all covid shots (moderna included) so far. I had not reported before. Pain severe alleviatted slightly with 500mg tylenol. Pain is ongoing as of now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish oil; Vitamin D; Probiotics.
Allergien: Omeprazole; Iodine; Shirmp; Lactose intolerant; Sulfa antibiotics.
Vorherige Impfungen: Covid Moderna, same symptoms. Not with other vaccines for other pathogens

VAERS 2504102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: MA
Alter: 38,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 08.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Cough Headache Myalgia Oropharyngeal pain Rhinorrhoea

Symptomtext

Chills (no fever), sore throat, runny nose, cough, headache, muscle aches. All symptoms started shortly after 8 am and continued throughout the day until bedtime. Took DayQuil, Ibuprofen, Tylenol, slept, and increased fluids. Symptom management helped, especially extra sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety, Major Depression, OCD, ADHD, Chronic Motor Tic Disorder, Infertility (2 MMC's and no live births)
Andere Medikamente: Sertraline, Bupropion, Lamotrigine, Guanfacine, Claritin-D, Vitron-C (65 mg elemental iron - Rx.), Probiotic, CoQ10, Vitamin D, Prenatal vitamin, B-Complex 100, Melatonin (OTC)
Allergien: Sulfa antibiotics
Vorherige Impfungen: -

VAERS 2503967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: IN
Alter: 58,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 07.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Body temperature increased Chills

Symptomtext

Patient had horrible chills, and a temperature of 104.

Weitere VAERSDATA-Felder

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

VAERS 2503274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: MI
Alter: 15,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blindness Dizziness Pallor

Symptomtext

PATIENT RECIEVED 2 VACCINES FIRST THE PFIZER BIVALENT 30MCG/0.3ML FOLLOWED BY A FLUARIX FLU SHOT. Less than 2 minutes later the patient felt faint and lost vision. the patient appeared to very pale and I had her immediately put her head between her legs. After a few seconds color returned to her ears and face. She stated she felt much better after doing that. I had her maintain the position until she felt comfortable. She was provided drinking water. About 15 minutes later i checked her blood pressure (109/70) and hr (65) pt stated they felt much better and were okay to leave.

Weitere VAERSDATA-Felder

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

VAERS 2501940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: TX
Alter: 79,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Balance disorder COVID-19 Chills Fatigue Pain Vomiting

Symptomtext

10:pm Strong Chills, 1:00 Chills then vomiting, no fever until 9:30 am, says he aches all over. I have been giving him liquids and tylenol. In Feb. 2021 he had Covid 19 and was in the hospital for close to a month. He still has re-percussions from that, his balance and gets tired easily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None so far
Aktuelle Erkrankungen: No
Vorgeschichte: Had Heart By-Pass Surgery in 2013
Andere Medikamente: Low dose Aspirin, Bupropion, Omeprazole, Metoprolol, Atorvastin, Saw Palmetto, Vitamin D3, Colace, Mucinex, Zyrtec, Potassium, Iron, Zinc, Magnesium, Fibercon
Allergien: None
Vorherige Impfungen: -

VAERS 2501063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: CA
Alter: 9,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered Pain Pyrexia

Symptomtext

Patient was given adult dose (0.3 mL) as opposed to pediatric dose recommended for age (0.1 mL). Followed up with mother over span of 3 days (11/4, 11/5, 11/7) - no serious side effects. Per mother, patient experienced "normal side effects" associated with vaccinations and previous doses (slight fever, achiness, etc. )

Weitere VAERSDATA-Felder

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

VAERS 2500590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

mild

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 05.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Pyrexia

Symptomtext

Patient started to have fever after about 24 hours later on 11/6/2022. fever has not resolved as of 11/7/2022. Patient is taking Tylenol OTC three times daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: non
Vorgeschichte: N/A
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2495133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: FL
Alter: 36,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Dizziness

Symptomtext

Systemic: Dizziness / Lightheadness-Mild

Weitere VAERSDATA-Felder

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

VAERS 2494737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

mild

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 29.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Immunisation reaction Injection site erythema Injection site rash Injection site swelling Peripheral swelling

Symptomtext

Patient reports on 10/31/22 to pharmacist that had reaction in arm after receiving Pfizer bivalent booster. Right arm swollen around injection spot and little bumps and red spots. Patient reported no issues with previous doses of Pfizer Covid-19 vaccines. Patient reported arm swelling has gone done and pharmacist counseled patient to take oral benadryl and put cold compress over area of injection and report to primary care doctor to make determination if true allergic reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2718792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 29.11.2023
Impfdatum: 17.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 as dose number unknown (booster), single (Lot number: GJ6738) at the age of 61 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 24May2022 as dose number unknown, single (Lot number: FM9992), in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, Covid-19 with Paxlovid from 11Nov2023 to 15Nov2023. Clinical course: The patient had no known allergies. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300392303 same reporter/patient, different drug/AE;

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
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2713435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 68,0
Geschlecht: F
Eingang: 13.11.2023
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Blister Contusion Phantom limb syndrome Swelling

Symptomtext

Patient also received Flu shot at same time in left arm. 11/3/2022. Reaction in just a few hours - bruising, 2nd degree blistering and swelling the size of an orange. Took over a month for swelling to subside. Continues now a year later with phantom pain in that arm. Patient wanted another Covid shot 11/13/2023, given Moderna not Pfizer. She will report back to office if there is any reaction this time. RN BSN

Weitere VAERSDATA-Felder

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

VAERS 2709081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 03.11.2023
Impfdatum: 14.11.2022
Beginn: 01.10.2023
Tage bis Beginn: 321,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

Interchange of vaccine products; Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Nov2022 as dose 5 (booster), single (Lot number: GJ6738) at the age of 61 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 18Sep2023 at 13:15 as dose 6 (booster), single (Lot number: 3030368), 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: "Asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Codeine, reaction(s): "Allergies". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Oct2023, outcome "unknown" and all described as "Treatment of COVID-19"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown". Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid from 12Oct2023 to 16Oct2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2708206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 01.11.2023
Impfdatum: 09.03.2023
Beginn: 01.03.2023
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Staff was not aware that Pfizer vaccine was administered after the bud.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2692258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 06.10.2023
Impfdatum: 16.11.2022
Beginn: 01.09.2023
Tage bis Beginn: 289,0
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

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 60-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Nov2022 at 10:00 as dose 5 (booster), single (Lot number: GJ6738) at the age of 59 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 had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2023, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Covid-19 treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19 which includes Paxlovid treatment from 16Sep2023 to 20Sep2023. Clinical course: No known allergies.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300317526 same reporter/patient, different drug/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19/Covid-19 virus test; Test Result: Positive ; Comments: Covid-19 treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2683747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: CA
Alter: -
Geschlecht: F
Eingang: 19.09.2023
Impfdatum: 18.11.2022
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

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An adult female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Nov2022 as dose 5 (booster), single (Lot number: GJ6738), 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: "hypothyroid" (unspecified if ongoing). The patient's concomitant medications were not reported. The patient had no known allergy. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 including Paxlovid from 04Sep2023 to 08Sep2023. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Home Test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2683742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 19.09.2023
Impfdatum: 10.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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 a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 as dose 5 (booster), single (Lot number: GJ6738) at the age of 68 years for covid-19 immunisation; bnt162b2 (BNT162B2), on 16Feb2021 as dose 1, single (Lot number: EN6201), on 09Mar2021 as dose 2, single (Lot number: EN6199), on 07Oct2021 as dose 3 (booster), single (Lot number: FF2589) and on 13Apr2022 as dose 4 (booster), single (Lot number: FK9729) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient received Paxlovid from 01Sep2023 to 05Sep2023 as COVID 19 Treatment. Patient had no Known allergies. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300302452 same 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: -
Allergien: -
Vorherige Impfungen: -

VAERS 2681417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: MA
Alter: 44,0
Geschlecht: F
Eingang: 12.09.2023
Impfdatum: 14.11.2022
Beginn: 02.09.2023
Tage bis Beginn: 292,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Nov2022 as dose 4 (booster), single (Lot number: GJ6738) at the age of 44 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 22Mar2021 as dose 1, single (Lot number: ER2613), in left arm, on 14Apr2021 as dose 2, single (Lot number: ER8731), in right arm and on 07Dec2021 as dose 3 (booster), single (Lot number: FG3527), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hashimoto disease" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE, start date: 01Jan1992. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 02Sep2023, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (02Sep2023) positive, notes: Tested positive on 02Sep2023; (05Sep2023) negative, notes: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep; (06Sep2023) negative, notes: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep; (07Sep2023) negative, notes: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep; (08Sep2023) negative, notes: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep; (09Sep2023) positive, notes: Symptoms returned on 09Sep and tested positive again. Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230902; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested positive on 02Sep2023.; Test Date: 20230905; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep.; Test Date: 20230906; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep.; Test Date: 20230907; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep.; Test Date: 20230908; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Symptoms subsided quickly and tested negative for 4 days 05Sep-08Sep.; Test Date: 20230909; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Symptoms returned on 09Sep and tested positive again.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2679721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 06.09.2023
Impfdatum: 22.12.2022
Beginn: 01.08.2023
Tage bis Beginn: 222,0
Dosis: UNK
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 62-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Dec2022 as dose number unknown (booster), single (Lot number: GJ6738) at the age of 62 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Thyroid" (unspecified if ongoing); "high bp" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2023, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 including Paxlovid from 22Aug2023 to 26Aug2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300291372 Same reporter/ drug/ event for different patients.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Sulfonamide allergy; Thyroid disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2678191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 31.08.2023
Impfdatum: 09.12.2022
Beginn: 14.04.2023
Tage bis Beginn: 126,0
Dosis: 3
Route/Site: IM / RA

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

Facial paresis

Symptomtext

R29.810 LEFT FACIAL MUSCLE WEAKNESS 4/14/2023 LEFT FACIAL MUSCLE WEAKNESS

Weitere VAERSDATA-Felder

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

VAERS 2671407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 15.08.2023
Impfdatum: 06.01.2023
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 69-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Jan2023 at 13:30 as dose 4 (booster), single (Lot number: GJ6738) at the age of 68 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) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "CAD s/9 6 vessel CABG" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Hyperlipidemia" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Treatment was Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: CABG; Hyperlipidemia; Hypertension; Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2662982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MD
Alter: 61,0
Geschlecht: F
Eingang: 28.07.2023
Impfdatum: 09.01.2023
Beginn: 10.01.2023
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Deafness Hearing aid user Hyperacusis Impaired work ability Tinnitus

Symptomtext

A documented mild hearing loss of 12+ years ago left me with hyperacusis, mild intermittent tinnitus (bacon sizzling sounds), and intermittent flares of hearing loss (treated with steroids). These symptoms have been replaced with more frequent intermittent loss, constant tinnitus and moderate/severe hyperacusis since the third COVID booster in January 2023. My hearing condition changed within a day of the booster and is listed on my VSAFE account (which I no longer have a chance to access). I tried a 2-week trial of Widex Hearing Aids to see if the sounds could be adjusted. The hearing aids rendered no benefit. I cannot access VSAFE information to list specific dates and times. This was my 5th COVID shot (3rd booster) COVID test positive 12/9/2020 COVID Vaccine - 1/14/2021 Moderna COVID Vaccine - 2/17/2021 Moderna COVID Booster #1 - 11/1/2021 Moderna COVID Booster #2 - 4/20/2022 Moderna COVID test positive - 7/25/2022 COVID Booster #3 - 1/9/2023 Pfizer Bivalent The constant tinnitus is now in a form of white noise/summer insect sounding noise. The hyperacusis has dramatically increased to the point where I am forced to step back as a pharmacist at the end of July 2023 . I have suffered increased hyperacusis issues at church listening to certain pitches of voices. At home, when my family members are talking or eating, I often leave the room to avoid listening to the crunching issues that are now almost deafening. Telephone reception sometimes sounds "metallic" in my ears. I currently have custom-made ear plugs on order from my audiologist. (I received a telephone call in April 2023 from a CDC representative who encouraged me to file a VAERS report. I waited to file the report until I could provide updated information on symptoms and treatment.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deafness
Hospital-Tage: -
Labordaten: My ENT physician, who was treating me for hoarseness/vocal cord issues, recommended hearing testing by my current audiologist. Hearing tests were conducted in March 2023. At that time, the audiologist recommended a trial of hearing aids to possibly assist with the constant tinnitus and moderate/severe hyperacusis. The 2-week trial starting on April 18, 2023, did not offer any benefits.
Aktuelle Erkrankungen: Hoarseness from vocal cord scarring
Vorgeschichte: PAI-1 4G clotting variant, mild hearing loss from 12+ years ago, hypertension controlled by medications, mild arthritis in hands and neck, exercise-induced asthma, breast cancer survivor almost 12 years
Andere Medikamente: Breo Ellipta 200/25 , Verapamil SR 240 qd, Losartan 100mg qd, Spironolactone 37.5mg qd, Vitamin D 4000IU qd, Zinc 50mg qd, Biotin qd
Allergien: Cinnamon oil used for baking
Vorherige Impfungen: Just the usual soreness/lethargy from the first two COVID vaccines. All documented in VSAFE app.

VAERS 2657357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: WA
Alter: 64,0
Geschlecht: F
Eingang: 18.07.2023
Impfdatum: 21.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; 4th dose is Moderna vaccine, 5th dose is pfizer vaccine; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Nov2022 as dose 5 (booster), single (Lot number: GJ6738) at the age of 64 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 06Apr2022 as dose 4 (booster), single (Lot number: 033K2124), 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: "Known allergies: wheat gluten" (unspecified if ongoing); "Known allergies: sulfa antibiotics" (unspecified if ongoing); "Known allergies: Opiates" (unspecified if ongoing); "Recent severe weight loss from GI" (unspecified if ongoing); "Recent severe weight loss" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 21Nov2022, outcome "not recovered", described as "4th dose is Moderna vaccine, 5th dose is pfizer vaccine"; 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 using Paxlovid from 04Jul2023 to 08Jul2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300250591 same reporter/patient ,different drug/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to analgesics; Gastro-intestinal disorder NOS; Gluten intolerance; Sulfonamide allergy; Weight loss
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 40,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 18.01.2023
Beginn: 18.01.2023
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 No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 20.03.2023
Beginn: 20.03.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 18.01.2023
Beginn: 18.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 42,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 16.05.2023
Beginn: 16.05.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 01.02.2023
Beginn: 01.02.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 23.01.2023
Beginn: 23.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: ID / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 18.01.2023
Beginn: 18.01.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None- Vaccine given beyond use date. Patient had no adverse events.

Weitere VAERSDATA-Felder

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

VAERS 2655706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 23.01.2023
Beginn: 23.01.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 09.03.2023
Beginn: 09.03.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 09.03.2023
Beginn: 09.03.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 01.05.2023
Beginn: 01.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date. Pt had no adverse events.

Weitere VAERSDATA-Felder

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

VAERS 2655700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 01.05.2023
Beginn: 01.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 02.05.2023
Beginn: 02.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 03.05.2023
Beginn: 03.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 08.05.2023
Beginn: 08.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 08.05.2023
Beginn: 08.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 08.05.2023
Beginn: 08.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 11.05.2023
Beginn: 11.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 11.05.2023
Beginn: 11.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 08.03.2023
Beginn: 08.03.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 12.05.2023
Beginn: 12.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Product use issue

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product use issue
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 01.05.2023
Beginn: 01.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date Pt had no adverse events

Weitere VAERSDATA-Felder

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

VAERS 2655689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 25.01.2023
Beginn: 25.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 11.05.2023
Beginn: 11.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 15.05.2023
Beginn: 15.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 16.05.2023
Beginn: 16.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 01.05.2023
Beginn: 01.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 16.05.2023
Beginn: 16.05.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 17.05.2023
Beginn: 17.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 18.05.2023
Beginn: 18.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine give beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 15.05.2023
Beginn: 15.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date Pt had no adverse events

Weitere VAERSDATA-Felder

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

VAERS 2655678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 15.05.2023
Beginn: 15.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date Pt had no adverse events

Weitere VAERSDATA-Felder

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

VAERS 2655677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 13.02.2023
Beginn: 13.02.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date Pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 22.05.2023
Beginn: 22.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date Pt had no adverse events

Weitere VAERSDATA-Felder

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

VAERS 2655675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 08.05.2023
Beginn: 08.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date Pt had no adverse events

Weitere VAERSDATA-Felder

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

VAERS 2655674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 17.05.2023
Beginn: 17.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 19,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 16.05.2023
Beginn: 16.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 26,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 18.05.2023
Beginn: 18.05.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given Beyond use date Pt had no adverse events

Weitere VAERSDATA-Felder

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

VAERS 2655671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 02.05.2023
Beginn: 02.05.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 18.05.2023
Beginn: 18.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 11.05.2023
Beginn: 11.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 22.05.2023
Beginn: 22.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 01.05.2023
Beginn: 01.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 12.07.2023
Impfdatum: 18.05.2023
Beginn: 18.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

No adverse event Product use issue

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655664

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 16.05.2023
Beginn: 16.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2654061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 10.07.2023
Impfdatum: 22.05.2023
Beginn: 22.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

NONE - Vaccine given beyond use date pt had no adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2654060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 10.07.2023
Impfdatum: 18.05.2023
Beginn: 18.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered

Symptomtext

None. Vaccine given beyond use date. Patient had no adverse events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2654057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 10.07.2023
Impfdatum: 22.05.2023
Beginn: 22.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None - Vaccine given beyond use date. Patient had no adverse events.

Weitere VAERSDATA-Felder

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

VAERS 2654056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 10.07.2023
Impfdatum: 18.05.2023
Beginn: 18.05.2023
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

None- Vaccine given beyond use date. Patient had no adverse events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2652809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 05.07.2023
Impfdatum: 25.11.2022
Beginn: 13.01.2023
Tage bis Beginn: 49,0
Dosis: 5
Route/Site: IM / LA

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

Hypoxia

Symptomtext

HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2650870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 29.06.2023
Impfdatum: 06.01.2023
Beginn: 18.01.2023
Tage bis Beginn: 12,0
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, MILD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2650831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 29.06.2023
Impfdatum: 20.01.2023
Beginn: 15.04.2023
Tage bis Beginn: 85,0
Dosis: 3
Route/Site: IM / RA

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

Alcohol use disorder Alcohol withdrawal syndrome Obstructive sleep apnoea syndrome Rectal haemorrhage

Symptomtext

G47.33 ADULT OBSTRUCTIVE SLEEP APNEA, MILD 4/15/2023 BRIGHT RED BLOOD PER RECTUM G47.33 ADULT OBSTRUCTIVE SLEEP APNEA, MILD 4/15/2023 SEVERE ALCOHOL USE DISORDER W ALCOHOL WITHDRAWAL, UNCOMPLICATED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alcohol use disorder
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2649014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 14.12.2022
Beginn: 14.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2649013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 13.12.2022
Beginn: 13.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 12.12.2022
Beginn: 12.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 12.12.2022
Beginn: 12.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 10.12.2022
Beginn: 10.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 10.12.2022
Beginn: 10.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 09.12.2022
Beginn: 09.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 17,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 09.12.2022
Beginn: 09.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 13,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 09.12.2022
Beginn: 09.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 08.12.2022
Beginn: 08.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 08.12.2022
Beginn: 08.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 08.12.2022
Beginn: 08.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 07.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 07.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 05.12.2022
Beginn: 05.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 12,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 05.12.2022
Beginn: 05.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 03.12.2022
Beginn: 03.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 13,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 03.12.2022
Beginn: 03.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 03.12.2022
Beginn: 03.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 03.12.2022
Beginn: 03.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 17,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 03.12.2022
Beginn: 03.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 02.12.2022
Beginn: 02.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that theDepartment of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 28,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 02.12.2022
Beginn: 02.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 12,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 01.12.2022
Beginn: 01.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 13,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 01.12.2022
Beginn: 01.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 01.12.2022
Beginn: 01.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 01.12.2022
Beginn: 01.12.2022
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

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Product storage error

Symptomtext

The patient received a vaccine that had not been stored properly. Rather than storing under refrigeration upon receipt from the manufacturer, the vaccine was placed into a freezer that maintained temperatures between -4- and 5-degrees Fahrenheit. Guidance from the manufacturer states that while administration of a vaccine having undergone this temperature excursion would not cause harm to the patient, the effectiveness of the vaccine cannot be verified. No harm has been reported by this patient and they have been notified that the Department of Health recommends being revaccinated at their earliest convenience.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 10.01.2023
Beginn: 19.03.2023
Tage bis Beginn: 68,0
Dosis: 4
Route/Site: IM / RA

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

Chronic respiratory failure Respiratory failure Symptom recurrence

Symptomtext

CHRONIC HYPOXEMIC RESPIRATORY FAILURE 2/1/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2647198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 20.06.2023
Impfdatum: 01.12.2022
Beginn: 20.12.2022
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / RA

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

Epilepsy Obstructive sleep apnoea syndrome

Symptomtext

EPILEPSY, UNSPECIFIED OBSTRUCTIVE SLEEP APNEA

Weitere VAERSDATA-Felder

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

VAERS 2644143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 12.06.2023
Impfdatum: 11.11.2022
Beginn: 13.12.2022
Tage bis Beginn: 32,0
Dosis: 5
Route/Site: IM / LA

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

Transient ischaemic attack

Symptomtext

TRANSIENT CEREBRAL ISCHEMIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Transient ischaemic attack
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2641108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 05.06.2023
Impfdatum: 11.12.2022
Beginn: 26.04.2023
Tage bis Beginn: 136,0
Dosis: 5
Route/Site: IM / AR

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

Bronchitis Chest X-ray abnormal Cough Upper-airway cough syndrome Wheezing

Symptomtext

4/26/23 I had a dry, nonproductive cough and it would not stop. I also had a lot of wheezing. I went into coughing episodes. On 4/30/23, I went to the urgent care. I was diagnosed with bronchitis. I had a chest x-ray which they did not see pneumonia. I was prescribed AUGMENTIN and steroids. I began taking the medications that night. The symptoms continued. I had no fever. I developed a horrible postnasal drip which made the cough much worse. I went to my primary doctor who prescribed albuterol nebulizer. Gradually, the symptoms abated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bronchitis
Hospital-Tage: -
Labordaten: 30APR23 Chest X-Ray, Bronchitis
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Type II; Asthma; Sleep Apnea; High Cholesterol; Survivor of Endometrial Cancer; Pulmonary Hypertension; Proneness to Cellulitis; Venal Insufficiency; Acid Reflux; Proneness to Sinus Infections; Lymphedema; Anxiety; Hyperlipidemia; Coronary Artery Disease; Proximal RCA; Osteoarthritis; Acquired Keratoderma; Plantar Fascia; Fibromyalgia; Obese; Enlarged liver; Vertigo; Diverticulitis
Andere Medikamente: Clonazepam; glipizide; albuterol; OZEMPIC; TRESIBA; LIPITOR; losartan with hydrochlorothiazide; baby aspirin.
Allergien: Pollen; cat dander; horsehair; pine trees; weeds; flower; grass; pollen; sap; bee stings
Vorherige Impfungen: Pneumo vax, twice. Ages 41 and in 2010. I had trouble breathing the first time. I had chest pains which gradually went away. The

VAERS 2639186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 07.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 6,0
Dosis: 5
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 5 vaccines Pfizer 1/20/21 lot# EL3249; Pfizer 2/10/21 lot# EL9267; Pfizer 10/15/21 lot# FE3590; Pfizer 5/16/22 Lot# FK9894; Pfizer 11/7/22 Lot# GJ6738

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2635197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: NM
Alter: -
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 05.11.2022
Beginn: 02.04.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

Covid-19 treatment; Covid-19 treatment; Moderna Dose1, Dose 2, Dose 3, Dose 4/Pfizer Dose 5; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Nov2022 at 12:30 as dose 5 (booster), single (Lot number: GJ6738), in left arm for covid-19 immunisation; elasomeran (COVID-19 VACCINE MODERNA), on 19Mar2021 at 13:45 as dose 1, single (Lot number: 045A21A), in left arm, on 19Apr2021 at 14:30 as dose 2, single (Lot number: 044B21A), in left arm, on 05Nov2021 at 14:30 as dose 3 (booster), single (Lot number: 058F21A), in left arm and on 02Apr2022 at 13:45 as dose 4 (booster), single (Lot number: 048L21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Thalassemia minor" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 02Apr2022, outcome "unknown", described as "Moderna Dose1, Dose 2, Dose 3, Dose 4/Pfizer Dose 5"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Covid-19 treatment". 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: Thalassemia minor
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 27.04.2023
Beginn: 05.05.2023
Tage bis Beginn: 8,0
Dosis: 6
Route/Site: SYR / RA

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

Anxiety Blood test normal Diplopia Eye movement disorder Impaired quality of life Magnetic resonance imaging normal

Symptomtext

I had my vaccination on 04/27/2023. On 05/05/2023 I started to have double vision. It started to have intermittent double vision and it made my anxiety very high. I put in message to my optometrist as my eye was tracking inward and it was affecting my daily life. It has not resolved on 05/22/2023. I was referred to urgent care and had blood panel performed with an MRI. The results have not found any abnormalities. They think its 6th cranial nerve palsy. No course of treatment has been provided at this time except alternative eye patching. I have follow up appointment with ophthalmologist in 06/2023 and possible neurologist referral.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anxiety
Hospital-Tage: -
Labordaten: 05/2023 Blood panel MRI and 2 eye medical exams.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteoarthritis; Post Surgical Neurotic Issues; Hypertension; Hypothyroidism
Andere Medikamente: Hydrocodone; lisinopril; levothyroxine; baclofen; hydroxyzine; vitamin D; calcium; magnesium; naproxen; vitamin B complex; vitamin C
Allergien: NEURONTIN; hydrochlorothiazide
Vorherige Impfungen: -

VAERS 2634613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 56,0
Geschlecht: F
Eingang: 21.05.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED VACCINE PAST BUD, CONSIDERED AS AN INVALID DOSE AND WILL COME BY NEXT WEEK FOR RE-VACCINATING NOT EXPERIENCING ANY ADVERSE EVENTS FROM THAT DOSE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 81,0
Geschlecht: F
Eingang: 21.05.2023
Impfdatum: 28.01.2023
Beginn: 28.01.2023
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED VACCINE PAST BUD, CONSIDERED AS AN INVALID DOSE. PATIENT CAME BY 05/20/2023 FOR RE-VACCINATING NOT EXPERIENCING ANY ADVERSE EVENTS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 56,0
Geschlecht: M
Eingang: 21.05.2023
Impfdatum: 25.01.2023
Beginn: 25.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED VACCINE PAST BUD, CONSIDERED AS AN INVALID DOSE . PATIENT STATED NOT EXPERIENCING ANY ADVERSE EVENTS AND WILL COME BY WHEN HAVE TIME FOR RE-VACCINATING

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 58,0
Geschlecht: M
Eingang: 21.05.2023
Impfdatum: 26.01.2023
Beginn: 26.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

PATIENT RECEIVED VACCINE PAST BUD, CONSIDERED AS AN INVALID DOSE AND WILL COME BY NEXT WEEK FOR RE-VACCINATING

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 55,0
Geschlecht: M
Eingang: 21.05.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BOOSTER PAST BUD. SPOKE TO HIS SON, PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS AND AWARE TO SCHEDULE TO GET RE-VACCINATED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 69,0
Geschlecht: F
Eingang: 21.05.2023
Impfdatum: 08.02.2023
Beginn: 08.02.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER PAST BUD, SPOKE TO PATIENT AND SHE IS AWARE TO SCHEDULE TO GET RE-VACCINATED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 53,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 25.01.2023
Beginn: 25.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 90,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO DAUGHTER AND STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS. WILL CONSIDER TO SCHEDULE TO BE RE-VACCINATED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 67,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO PATIENT AND SHE STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 55,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO HUSBAND AND HE STATED THAT HIS WIFE HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 21,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO DAD AND HE STATED THAT PATIENT HAS NOT EXPERIENCING ANY ADVERSE EVENTS. WHOLE FAMILY WILL SCHEDULE TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 47,0
Geschlecht: M
Eingang: 20.05.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO PATIENT AND HE STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 57,0
Geschlecht: M
Eingang: 20.05.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO PATIENT AND HE STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 97,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 17.01.2023
Beginn: 17.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO DAUGHTER AND STATED THAT HER MOM HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE FOR HER MOM TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 45,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 17.01.2023
Beginn: 17.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO PATIENT AND SHE STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 47,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 16.01.2023
Beginn: 16.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO PATIENT AND SHE STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE TO BE RE-VACCINATED NEXT WEEK (AT LEAST 8 WEEKS APART PER CDC GUIDELINES)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 38,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 16.01.2023
Beginn: 16.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO PATIENT AND SHE STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS. PATIENT WILL SCHEDULE TO BE RE-VACCINATED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 77,0
Geschlecht: F
Eingang: 20.05.2023
Impfdatum: 12.02.2023
Beginn: 12.02.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

PATIENT RECEIVED A DOSE OF PFIZER BIVALENT BOOSTER DOSE WAS PAST BUD, SPOKE TO PATIENT AND SHE STATED HAS NOT EXPERIENCING ANY ADVERSE EVENTS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2627782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: CA
Alter: 38,0
Geschlecht: M
Eingang: 06.05.2023
Impfdatum: 16.12.2022
Beginn: 13.02.2023
Tage bis Beginn: 59,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 38-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: GJ6738) at the age of 38 years for covid-19 immunisation; BNT162b2 (BNT162B2), on 19Dec2021 as dose number unknown, single (Lot number: FJ8760) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 13Feb2023, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13Feb2023) Positive, notes: on day 1 of testing positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 which includes: Paxlovid from 14Feb2023 to 18Feb2023. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230213; Test Name: Covid-19 Test; Test Result: Positive ; Comments: on day 1 of testing positive.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2621564

GLAXOSMITHKLINE BIOLOGICALS · TDAP (BOOSTRIX) · Charge GJ6738

gering

Staat: VA
Alter: 20,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 25.04.2023
Beginn: 25.04.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Inappropriate schedule of product administration Wrong product administered

Symptomtext

Pt. was supposed to get an MMR vaccine. A previous T-Dap given 4/19/2023

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2614499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: NC
Alter: 80,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 14.11.2022
Beginn: 12.03.2023
Tage bis Beginn: 118,0
Dosis: 5
Route/Site: IM / AR

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

Fall Splint application Surgery Upper limb fracture

Symptomtext

I fell. I tripped over my friends' feet. I broke my elbow. I was getting on a cruise ship and had decided not to go to the hospital there. I returned home and went to the doctor the next day. I had surgery on 03/20/2023. I am now in a splint. I'm feeling okay. I had no side effects from my vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fall
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: CRESTOR; calcium; vitamin D; TYLENOL
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2610410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: IN
Alter: 39,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 02.12.2022
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

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 39-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 02Dec2022 as dose 5 (booster), single (Lot number: GJ6738) at the age of 39 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 had no relevant medical history. No known allergies . There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2609121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: IL
Alter: 28,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 14.02.2023
Beginn: 14.02.2023
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

Patient was supposed to receive the pfizer monovalent vaccine as ordered but received the pfizer bivalent vaccine as the first dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2608455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 40,0
Geschlecht: M
Eingang: 03.04.2023
Impfdatum: 25.01.2023
Beginn: 03.04.2023
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

- Patient was given Covid-19 Bivalent (grey top) Vaccine which was beyond the usage date of 01/11/2023, lot #GJ6738. Patient has been notified. No adverse effects reported. Reports filed. - ?Pulled a report of all administered vaccines by lot number and verified those that were administered past the BUD. - Pulled all vaccines in fridge and placed a ?Do Not Use? sign on them while we completed investigation - Sat with each MA within the clinic going over the following: o Training on administration workflows to include ? entering vaccine information into System prior to administering vaccine, always having a team check which includes verification of vaccine, verification of patients age, timeframe between vaccines, BUD, dosage o BUD versus expiration date versus puncture expiration o Dosage of maroon top, orange top and gray top for monovalent and bivalent o The difference between monovalent and bivalent o Storage instructions o Workflow associated with what to do when clinic receives the vaccine o Training on lot manager and immunization system reconciliation o Training on how to enter information into System when a provider places an order versus immunization clinic - Reached out to Pfizer who is recommending all patients who received an expired vaccine get re-vaccinated due to unknown efficacy - Clinic will reach out to all patients letting them know about the situation and offer to have them come into the clinic free of charge for re-vaccination or to a sister clinic if they prefer?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: ADHD, Depression, PTSD, TBI
Andere Medikamente: Lipitor, Krill Oil, Metoprolol
Allergien: Steroids
Vorherige Impfungen: -

VAERS 2608450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 29,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 24.03.2023
Beginn: 03.04.2023
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

- Patient was given Covid-19 Bivalent (grey top) Vaccine which was beyond the usage date of 01/11/2023, lot #GJ6738. Patient has been notified. No adverse effects reported. Reports filed. - ?Pulled a report of all administered vaccines by lot number and verified those that were administered past the BUD. - Pulled all vaccines in fridge and placed a ?Do Not Use? sign on them while we completed investigation - Sat with each MA within the clinic going over the following: o Training on administration workflows to include ? entering vaccine information into tracking system prior to administering vaccine, always having a team check which includes verification of vaccine, verification of patients age, timeframe between vaccines, BUD, dosage o BUD versus expiration date versus puncture expiration o Dosage of maroon top, orange top and gray top for monovalent and bivalent o The difference between monovalent and bivalent o Storage instructions o Workflow associated with what to do when clinic receives the vaccine o Training on lot manager and data collection reconciliation o Training on how to enter information into data tracking when a provider places an order versus immunization clinic - Reached out to Pfizer who is recommending all patients who received an expired vaccine get re-vaccinated due to unknown efficacy - Clinic will reach out to all patients letting them know about the situation and offer to have them come into the clinic free of charge for re-vaccination or to a sister clinic if they prefer?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: Seasonal Allergies
Andere Medikamente: Buspirone, Qvar, Zoloft, Albuterol, Paraguard
Allergien: Acyclovir, Loratadine
Vorherige Impfungen: -

VAERS 2608446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 73,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 01.03.2023
Beginn: 03.04.2023
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

- Patient was given Covid-19 Bivalent (grey top) Vaccine which was beyond the usage date of 01/11/2023, lot #GJ6738. Patient has been notified. No adverse effects reported. Reports filed. - ?Pulled a report of all administered vaccines by lot number and verified those that were administered past the BUD. - Pulled all vaccines in fridge and placed a ?Do Not Use? sign on them while we completed investigation - Sat with each MA within the clinic going over the following: o Training on administration workflows to include ? entering vaccine information into system prior to administering vaccine, always having a team check which includes verification of vaccine, verification of patients age, timeframe between vaccines, BUD, dosage o BUD versus expiration date versus puncture expiration o Dosage of maroon top, orange top and gray top for monovalent and bivalent o The difference between monovalent and bivalent o Storage instructions o Workflow associated with what to do when clinic receives the vaccine o Training on lot manager and immunization system reconciliation o Training on how to enter information into system when a provider places an order versus immunization clinic - Reached out to Pfizer who is recommending all patients who received an expired vaccine get re-vaccinated due to unknown efficacy - Clinic will reach out to all patients letting them know about the situation and offer to have them come into the clinic free of charge for re-vaccination or to a sister clinic if they prefer?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: Arthritis, Breast Cancer, Gout, Hyponatremia, RA, HTN
Andere Medikamente: Timolol, Plavix, Lipitor, Xalantan, Restatsis, ASA 81mg, Methotrexate
Allergien: PCN, Cortisone, Guiafed, Benadryl
Vorherige Impfungen: -

VAERS 2608409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 29,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 20.02.2023
Beginn: 03.04.2023
Tage bis Beginn: 42,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

- Patient was given Covid-19 Bivalent (grey top) Vaccine which was beyond the usage date of 01/11/2023, lot #GJ6738. Patient has been notified. No adverse effects reported. Reports filed. - ?Pulled a report of all administered vaccines by lot number and verified those that were administered past the BUD. - Pulled all vaccines in fridge and placed a ?Do Not Use? sign on them while we completed investigation - Sat with each MA within the clinic going over the following: o Training on administration workflows to include ? entering vaccine information into data tracking prior to administering vaccine, always having a team check which includes verification of vaccine, verification of patients age, timeframe between vaccines, BUD, dosage o BUD versus expiration date versus puncture expiration o Dosage of maroon top, orange top and gray top for monovalent and bivalent o The difference between monovalent and bivalent o Storage instructions o Workflow associated with what to do when clinic receives the vaccine o Training on lot manager and lot tracking reconciliation o Training on how to enter information into data tracker when a provider places an order versus immunization clinic - Reached out to Pfizer who is recommending all patients who received an expired vaccine get re-vaccinated due to unknown efficacy - Clinic will reach out to all patients letting them know about the situation and offer to have them come into the clinic free of charge for re-vaccination or to a sister clinic if they prefer?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: Depression, Fibromyalgia
Andere Medikamente: Zyrtec, Mirena
Allergien: NKA
Vorherige Impfungen: -

VAERS 2608265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 26.11.2022
Beginn: 01.04.2023
Tage bis Beginn: 126,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

PT CAME IN LOOKING FOR PRIMARY SERIES SHOT (PFIZER COVID) AND DUE TO MISUNDERSTANDING AND LANGUAGE BARRIER RECEIVED BIVALENT COVID 19 BOOSTER--ON 11/26/22---PT CAME IN FOR 2ND SHOT ON 4/2/23 WHEN THIS WAS DISCOVERED---AFTER TALKING WITH HEALTH CARE COORDINATOR PHARMACIST GAVE MONOCLONAL (PRIMARY) SHOT AS SECOND SHOT AND SUGGESTED SHE COME AND GET BOOSTED IN 2 MONTHS

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: -

VAERS 2605643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 29.03.2023
Impfdatum: 30.12.2022
Beginn: 01.03.2023
Tage bis Beginn: 61,0
Dosis: 5
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 (Consumer or other non HCP) from product quality group. The reporter is the patient. A 57-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 30Dec2022 at 19:00 as dose 5 (booster), single (Lot number: GJ6738) at the age of 56 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), 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 was not reported. Concomitant medication(s) included: ATORVASTATIN, start date: 15Dec2011. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Mar2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received treatment with Paxlovid from 04Mar2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2604990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 45,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 17.01.2023
Beginn: 28.03.2023
Tage bis Beginn: 70,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given Covid-19 Bivalent (grey top) Vaccine which was beyond the usage date of 01/11/2023, lot #GJ6738 on 01/17/2023. Attempted to reach patient by phone today, 03/28/2023, and had to leave a voicemail for patient to call back. Reports filed with local registrar and Pfizer. Awaiting response from Pfizer on efficacy of vaccination. Staff has been reeducated on 7 rights and Covid Vaccine Safety Workflow. The remaining doses of BUD vaccines have been discarded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2604872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 71,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 27.03.2023
Beginn: 28.03.2023
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Patient was given Covid-19 Bivalent (grey top) vaccine on 03/27/2023 which was beyond the usage date of 01/11/2023. Patient has been notified. No adverse side effects. Report also filed with Pfizer and Agency. Awaiting response on efficacy from Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: BPH, Hypertension, High Cholesterol, Sleep Apnea
Andere Medikamente: Atorvastatin, Lisinopril, Flomax, Finasteride
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2604109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 27.03.2023
Impfdatum: 23.11.2022
Beginn: 26.03.2023
Tage bis Beginn: 123,0
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; Moderna 3/6/21 Lot# 027L20A; Moderna 4/2/21 Lot# 032H20A; Moderna 5/20/22 Lot# 056M21A; Pfizer 11/23/22 Lot# GJ6738

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2602662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: KY
Alter: 71,0
Geschlecht: F
Eingang: 23.03.2023
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: ja

Incorrect dose administered Product quality issue

Symptomtext

Pharmacist discovered vial did not have enough serum to draw a sixth and final dose. Another pharmacist had done two prior vaccines. Pharmacist has made patient aware there is a possibility (however unlikely) that she may have received a larger dose than intended (0.3 ml). Pharmacist was waiting to try and confirm through camera footage but not able to be done. It is also not known if different calibrated syringes were used thus making easier to waste product. Product could also have been a quality issue as well. Pharmacist is brain storming all possibilities even if an error has not occurred but treating as such due to nature of vaccine and EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: SCALP ISSUES, DERMATITIS.
Vorgeschichte: DERMATOLOGICAL RELATED ISSUES. LESIONS.
Andere Medikamente: PRISTIQ, TRAZODONE, SINGULAIR , FLONASE NASAL, VENTOLIN HFA IHALER.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2600270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 50,0
Geschlecht: M
Eingang: 21.03.2023
Impfdatum: 26.01.2023
Beginn: 01.03.2023
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

no adverse event reported by patient, no symptoms or signs. reporting that dose was given after 11 days after beyond use date and was stored in the refrigerator with average temperature of 38 degrees.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2600261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 21.03.2023
Impfdatum: 30.01.2023
Beginn: 21.03.2023
Tage bis Beginn: 50,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

no adverse event reported by patient, no symptoms or signs. reporting that dose was given after 16 days after beyond use date and was stored in the refrigerator with average temperature of 38 degrees.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: -
Vorherige Impfungen: -

VAERS 2600255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 21.03.2023
Impfdatum: 20.01.2023
Beginn: 01.03.2023
Tage bis Beginn: 40,0
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

no adverse event reported by patient, no symptoms or signs. reporting that dose was given after 6 days after beyond use date and was stored in the refrigerator with average temperature of 38 degrees.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2597783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 25.11.2022
Beginn: 25.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

Patient received a second Pfizer COVID-19 bivalent vaccination on 11/25/2023. Her first Pfizer COVID-19 Bivalent vaccination was received on 10/04/2023. No adverse symptoms reported. This adverse event was incidentally discovered during review of staff time related to COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI, Vertigo, hypertension, chronic allergic rhinitis
Vorgeschichte: hypertension, hyperlipidemia, seasonal allergies, vertigo, pelvic mass, SUI, Situational depression, mild cognitive impairment, dizziness
Andere Medikamente: Atorvastatin, azelastine, tolterodine, meclizine, zolpidem, metoprolol, duloxetine, losartan
Allergien: -
Vorherige Impfungen: -

VAERS 2596992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 01.12.2022
Beginn: 01.01.2023
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / RA

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

Magnetic resonance imaging head Vision blurred Visual impairment

Symptomtext

Vision change--blurry vision, decreased vision

Weitere VAERSDATA-Felder

Praegender Schweregrund: Magnetic resonance imaging head
Hospital-Tage: -
Labordaten: Referral to ophthalmology, workup by ophthalmology, MRI brain.
Aktuelle Erkrankungen: hypothyroidism
Vorgeschichte: hypothyroidsm
Andere Medikamente: Synthroid
Allergien: none
Vorherige Impfungen: -

VAERS 2595764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WA
Alter: 19,0
Geschlecht: M
Eingang: 13.03.2023
Impfdatum: 03.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

No reported symptoms from patient or unknown at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2594848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: TN
Alter: 70,0
Geschlecht: F
Eingang: 10.03.2023
Impfdatum: 02.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 9,0
Dosis: 5
Route/Site: IM / LA

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

Blood pressure fluctuation Blood pressure increased Blood test Confusional state Fear Feeling abnormal Head discomfort Hemiparesis Magnetic resonance imaging head normal Memory impairment Muscular weakness Transient ischaemic attack Visual impairment

Symptomtext

She got her vaccine, 9 days later on 11/11/22 she had crazy vision, eyes like they were going back into her head This did not last long and was scary. She was told to go sit down at work and went away. A week later she had this again and that time she got confused and did not remember what day it was. She went to the doctor about it, did not see anything wrong with her. On 1/7/23 she was feeling weird and listing at home, having problems with her face and her left side and her head felt weird. She had a virus in December, and her eyes were acting crazy at that time. Then in January she went to the ER on 1/7/23, and they thought that she was having TIA's. She was kept and had an MRI of her brain and then said that everything looked fine, all vessels and arteries were fine, but had symptoms of stroke like. She is scheduled to have a brain wave study on 3/20/23. She did have an MRI on her cervical neck, not related to the vaccine. Her blood pressure has increased, and has some pressure in her head since starting BP medicine, started in February of 2023. She feels really bad with the BP. She went to her PCP the next day and it was normal, and she continues to have fluctuations of her blood pressure, weakness in her left arm, strange feelings in her face. She has had about 6 episodes of the cray vision and have gone and is hoping that these other symptoms will be going away, but none of the doctors have any idea what is going on. She has been to the hospital 2 times due to BP issues. Her heart was checked on the 2nd visit to the ER, all of her values were OK, and right now it is 160/83. She is now taking Carvedilol 3.125 twice a day. She just does not feel good and feels sometimes like she is not going to make it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure fluctuation
Hospital-Tage: 1,0
Labordaten: MRI and blood work.
Aktuelle Erkrankungen: None.
Vorgeschichte: Thyroid disease, neck problems, osteoarthritis, Sjogren's syndrome, spinal stenosis in neck, myelopathy.
Andere Medikamente: Armour thyroid 75 mg, Garden of Life over 50, magnesium, vitamin B, multiple vitamin, calcium, Melatonin, sialic garlic, multi-green supplement, vitamin C, Bromalin, fish oil.
Allergien: Sulfa.
Vorherige Impfungen: -

VAERS 2592471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 07.03.2023
Impfdatum: 10.11.2022
Beginn: 10.01.2023
Tage bis Beginn: 61,0
Dosis: 5
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 5 vaccines Moderna 2/16/21 Lot# 004M20A; Moderna 3/16/21 Lot# 031L20A; Moderna 12/10/21 Lot# 045J21A; Moderna 5/11/2 Lot# 057M21A; Pfizer 11/10/22 Lot#GJ6738

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2590263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: PA
Alter: 15,0
Geschlecht: F
Eingang: 02.03.2023
Impfdatum: 06.12.2022
Beginn: 27.12.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: IM / LA

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

Computerised tomogram normal Dyskinesia Magnetic resonance imaging normal Tic

Symptomtext

Precisely 3 weeks post-administration of vaccines a TIC disorder developed. An uncontrollable head movement developed. Continues as of March 2, 2023, but with varying degrees of frequency and unsuccessful medical management.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Computerised tomogram normal
Hospital-Tage: -
Labordaten: CT Scan - December 27th - negative MRI - January 5th - negative
Aktuelle Erkrankungen: possibly a cold in December
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2589740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CT
Alter: 60,0
Geschlecht: M
Eingang: 01.03.2023
Impfdatum: 02.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: SYR / LA

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

Interstitial lung disease

Symptomtext

Acute Interstitial Pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interstitial lung disease
Hospital-Tage: 17,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: sleep apnea,obesityatrial fibrillation
Andere Medikamente: levothyroxine,pravastatin,xarelto,carvedilol,lisinopril
Allergien: -
Vorherige Impfungen: -

VAERS 2589394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 19.12.2022
Beginn: 19.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Pt was on the schedule or a covid vaccine--she wanted the Pfizer vaccine. When she came in she was actually given the bivalent vaccine and she had not received and previous vaccines for covid before. Was later determined that patient should receive primary series as well, and received primary dose on 2/13/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2589343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: MO
Alter: 66,0
Geschlecht: F
Eingang: 01.03.2023
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

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: -

VAERS 2588968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 35,0
Geschlecht: M
Eingang: 01.03.2023
Impfdatum: 28.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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 35-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Nov2022 at 15:30 as dose 4 (booster), single (Lot number: GJ6738) at the age of 35 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 08Apr2021 at 13:30 as dose 1, single (Lot number: ER8737), in left arm, on 29Apr2021 at 13:30 as dose 2, single (Lot number: ER8736), in left arm and on 17Dec2021 at 13:30 as dose 3 (booster), single (Lot number: FE3594), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ZOLPIDEM TARTRATE. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ZOLPIDEM TARTRATE
Allergien: -
Vorherige Impfungen: -

VAERS 2587791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 20,0
Geschlecht: M
Eingang: 27.02.2023
Impfdatum: 24.02.2023
Beginn: 24.02.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Inappropriate schedule of product administration No adverse event Product administration error

Symptomtext

No adverse event reported. I am reporting a vaccine administration error. The minimum interval had not been met between completion of the primary series and the administration of the bivalent booster dose. Last dose of primary series was 1/30/23. The bivalent booster was administered 2/24/23. Contacted Pfizer to report and find out if dose needs to be repeated. Recommendation was to wait 8 weeks after invalid dose and repeat the bivalent booster. Patient will be contacted regarding this information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2587327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

gering

Staat: KY
Alter: 84,0
Geschlecht: M
Eingang: 25.02.2023
Impfdatum: 06.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

Tinnitus

Symptomtext

Tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lisinopril Gabapentin Paroxetine Zorcor Januvia
Allergien: None
Vorherige Impfungen: -

VAERS 2586987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WI
Alter: 16,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 21.11.2022
Beginn: 21.11.2022
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 No adverse event

Symptomtext

Patient was given a bivalent booster for 1st vaccination in series instead of the monovalent as indicated. No symptoms reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2585315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: VA
Alter: 71,0
Geschlecht: F
Eingang: 22.02.2023
Impfdatum: 15.11.2022
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 contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Nov2022 at 10:00 as dose 5 (booster), single (Lot number: GJ6738) at the age of 71 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: "Diabetes" (unspecified if ongoing); "Cancer" (unspecified if ongoing); "Penicillin" (unspecified if ongoing); "Known allergies: Latex" (unspecified if ongoing); "Known allergies: Procaine" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Metformin, start date: 15Jun1998; Januvia, start date: 01Jun2016. 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: I was tested positive for Covid-19 first time. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received other medication in 2 weeks was reported as yes. The patient was tested positive for Covid-19 first time and received Anti-viral COVID 19 Treatment with Paxlovid from 09Feb2023 to 13Feb2023 with Lot number # 660050.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: tested positive for Covid-19; Test Result: Positive ; Comments: I was tested positive for Covid-19 first time
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to chemicals; Cancer; Diabetes; Latex allergy; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: WY
Alter: 54,0
Geschlecht: F
Eingang: 21.02.2023
Impfdatum: 30.01.2023
Beginn: 30.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Per CDC guidelines, patient continued series with primary series shot. only adverse reaction was the patient being concerned of not being fully vaccinated to take a cruise trip

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: N/a
Vorherige Impfungen: -

VAERS 2584839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: WY
Alter: 46,0
Geschlecht: M
Eingang: 21.02.2023
Impfdatum: 30.01.2023
Beginn: 30.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

No adverse event Wrong product administered

Symptomtext

Patient came in to receive their first pfizer covid shot. They instead received the new pfizer updated bivalent booster. patewint reported no adverse reactions. They only needed to verify they would be able to get fully vaccinated before they leave on a cruise trip

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: N/a
Allergien: N/a
Vorherige Impfungen: -

VAERS 2584364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MO
Alter: 66,0
Geschlecht: M
Eingang: 20.02.2023
Impfdatum: 02.12.2022
Beginn: 20.01.2023
Tage bis Beginn: 49,0
Dosis: 4
Route/Site: - / -

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

Cerebellar haemorrhage Computerised tomogram Laboratory test Posterior fossa decompression

Symptomtext

Patient admitted to hospital on 1/20/2023 and diagnosed with a cerebellar hemorrhage requiring posterior fossa decompression.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebellar haemorrhage
Hospital-Tage: 26,0
Labordaten: Numerous labs, CT, etc. 01/20/2023 through 02/15/2023.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: ASA 325MG DAILY
Allergien: NKA
Vorherige Impfungen: -

VAERS 2582734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 63,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 16.01.2023
Beginn: 16.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

no adverse effects--72 day temperature was 1/12/23 so vaccine was expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 58,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 16.01.2023
Beginn: 16.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

No adverse effects--72 day temperature was 1/12/23 so vaccine was expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: vancomycin
Vorherige Impfungen: -

VAERS 2582729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 74,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

no adverse effects--72 day temperature was 1/12/23 so vaccine was expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 72,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

no adverse effects--72 day temperature was 1/12/23 so vaccine was expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 70,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

no adverse effects--72 day temperature was 1/12/23 so vaccine was expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: latex
Vorherige Impfungen: -

VAERS 2582718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 13,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

no adverse effects--72 day temperature was 1/12/23 so vaccine was expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2582715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 76,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

no adverse effects--72 day temperature was 1/12/23 so vaccine was expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: heart attack 10 years ago
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2581519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 14.02.2023
Impfdatum: 14.11.2022
Beginn: 21.12.2022
Tage bis Beginn: 37,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Feeling abnormal SARS-CoV-2 test positive Sinus disorder Throat irritation

Symptomtext

I started having sinus problems, scratchy throat, things did not feel right, my body felt weird. I decided to take home COVID-19 test that came back positive. After a couple of days when the symptoms did not resolve I called my doctor who advised me that I had just missed the window of getting the medication to help. It did take three weeks for me to get over what I was going through, I finally tested negative on 01/09/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; High Blood Pressure; High Cholesterol; Sleep Apnea; Carpal Tunnel
Andere Medikamente: Metformin; LANTUS; JARDIANCE; lisinopril; atorvastatin; fludrocortisone; vitamin D
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2580408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 48,0
Geschlecht: M
Eingang: 13.02.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

No adverse event, Vaccine administered was past BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2579743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

gering

Staat: MO
Alter: 70,0
Geschlecht: F
Eingang: 10.02.2023
Impfdatum: 04.01.2023
Beginn: 01.01.2023
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

vaccine administration error, pt had stem cell transplant she was getting covid series re-vaccinated had pfizer monovalent 12/5/22, she couldn't find monovalent so her Dr told her to get the bivalent. CDC told us to count this as 1 of her primary series and to continue with series

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: had stem cell transplant and this is re-vaccination
Vorgeschichte: na
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 2579620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NJ
Alter: 78,0
Geschlecht: U
Eingang: 10.02.2023
Impfdatum: 13.01.2023
Beginn: 09.02.2023
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

temp exlcusioni

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2579618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NJ
Alter: 77,0
Geschlecht: U
Eingang: 10.02.2023
Impfdatum: 20.01.2023
Beginn: 09.02.2023
Tage bis Beginn: 20,0
Dosis: 4
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2579614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NJ
Alter: 68,0
Geschlecht: U
Eingang: 10.02.2023
Impfdatum: 14.01.2023
Beginn: 09.02.2023
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

temp exclusion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2579611

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge gj6738

gering

Staat: NJ
Alter: 50,0
Geschlecht: M
Eingang: 10.02.2023
Impfdatum: 18.01.2023
Beginn: 09.02.2023
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

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

VAERS 2579609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NJ
Alter: 74,0
Geschlecht: U
Eingang: 10.02.2023
Impfdatum: 19.01.2023
Beginn: 09.02.2023
Tage bis Beginn: 21,0
Dosis: 5
Route/Site: IM / RA

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

Product storage error

Symptomtext

temp exlusion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: na
Allergien: na
Vorherige Impfungen: -

VAERS 2579607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NJ
Alter: 78,0
Geschlecht: M
Eingang: 10.02.2023
Impfdatum: 19.01.2023
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2578968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NJ
Alter: 76,0
Geschlecht: M
Eingang: 09.02.2023
Impfdatum: 09.02.2023
Beginn: 09.02.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

temp exclusion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: -
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2578964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NJ
Alter: 75,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 09.02.2023
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

temp excursion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: -
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2578957

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge gj6738

gering

Staat: NJ
Alter: 82,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 24.01.2023
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / RA

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

Product storage error

Symptomtext

temperature excursion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2578952

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge gj6738

gering

Staat: NJ
Alter: 30,0
Geschlecht: M
Eingang: 09.02.2023
Impfdatum: 09.02.2023
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / LA

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

Product storage error

Symptomtext

temperature excursion of vial

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2578950

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge gj6738

gering

Staat: NJ
Alter: 88,0
Geschlecht: M
Eingang: 09.02.2023
Impfdatum: -
Beginn: 28.01.2023
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

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

Product storage error

Symptomtext

temperature exclusion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n0
Vorgeschichte: -
Andere Medikamente: nk\0
Allergien: n0
Vorherige Impfungen: -

VAERS 2578947

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge gj6738

gering

Staat: NJ
Alter: 87,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 28.01.2023
Beginn: 09.02.2023
Tage bis Beginn: 12,0
Dosis: UNK
Route/Site: - / LA

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

Product storage error

Symptomtext

temperature exclusion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2576496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 88,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 03.02.2023
Beginn: 03.02.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 02/03/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 62,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 01.02.2023
Beginn: 01.02.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 02/01/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 56,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 27.01.2023
Beginn: 27.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/27/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 47,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 26.01.2023
Beginn: 26.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/26/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 73,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 25.01.2023
Beginn: 25.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/25/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 64,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/21/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 64,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 21.01.2023
Beginn: 21.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/21/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

gering

Staat: WY
Alter: 83,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 17.01.2023
Beginn: 17.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/17/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 89,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 17.01.2023
Beginn: 17.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/17/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 81,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 17.01.2023
Beginn: 17.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/17/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 84,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 17.01.2023
Beginn: 17.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/17/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WY
Alter: 73,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 16.01.2023
Beginn: 16.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/16/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: FL
Alter: 55,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given the COVID 19 Bivalent Booster past the Beyond Use Date. The BUD date was 01/13/2023. The patient received the vaccine on 01/13/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2541486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: PA
Alter: 61,0
Geschlecht: M
Eingang: 03.02.2023
Impfdatum: 14.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / AR

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

Dysgeusia Off label use Product use issue Oral discharge

Symptomtext

Sour/Salty/Bitter taste and/or drainage in right side of mouth. It is constant over 24 hours never leaves. Note received Flu shot on same day at same location but they were approx. 1 hour apart.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysgeusia
Hospital-Tage: -
Labordaten: Went to Primary care as well as ENT doctors. They tried 2 different antibiotics as well as a steroid count down pact - no improvement.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2573538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 10.01.2023
Beginn: 10.01.2023
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

Patient came in for a scheduled appointment for their first dose of the primary series (monovalent) COVID vaccine. The technician who took in the patient failed to check what the appointment was for in the appointment scheduler and failed to verify which vaccine the patient was expecting to receive. She then entered the Bivalent booster instead of the monovalent and administered it. Patient came back 21 days later for their second dose and a different technician noticed and investigated the error. The CDC was contacted and upon their guidance the patient was given the monovalent as a completion to the initial series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2573533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: FL
Alter: 26,0
Geschlecht: M
Eingang: 01.02.2023
Impfdatum: 10.01.2023
Beginn: 10.01.2023
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

Patient came in for a scheduled appointment for their first dose of the primary series (monovalent) COVID vaccine. The technician who took in the patient failed to check what the appointment was for in the appointment scheduler and failed to verify which vaccine the patient was expecting to receive. She then entered the Bivalent booster instead of the monovalent and administered it. Patient came back 21 days later for their second dose and a different technician noticed and investigated the error. The CDC was contacted and upon their guidance the patient was given the monovalent as a completion to the initial series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2571754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 05.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 41-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Dec2022 as dose 4 (booster), single (Lot number: GJ6738) at the age of 41 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) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing); "sulfa drugs" (unspecified if ongoing). Concomitant medication(s) included: NORTRIPTYLINE; ZOLMITRIPTAN. Past drug history included: Keflex, reaction(s): "Drug Allergy: Keflex". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 (Paxlovid taken from 16Jan2023 to 21Jan2023, lot number: GF4000).

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine; Sulfonamide allergy
Andere Medikamente: NORTRIPTYLINE; ZOLMITRIPTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2570612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6738

gering

Staat: GA
Alter: 30,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 30.01.2023
Beginn: 30.01.2023
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

The LPN inadvertently gave a bivalent (booster dose) instead of the monovalent (primary) dose. This was supposed to be the second does in the primary series. No adverse effects noted .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2568921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: CT
Alter: 56,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 08.11.2022
Beginn: 13.01.2023
Tage bis Beginn: 66,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Nov2022 at 13:00 as dose 5 (booster), single (Lot number: GJ6738) at the age of 56 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 18Mar2021 as dose 1, single (Lot number: EN6208), in left arm, on 08Apr2021 as dose 2, single (Lot number: EW0150), in left arm, on 28Oct2021 as dose 3 (booster), single (Lot number: FF2593), in left arm and on 19Jul2022 as dose 4 (booster), single (Lot number: FP7139), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Salmon" (unspecified if ongoing), notes: known allergies: Salmon; "Osteoarthritis" (unspecified if ongoing); "Cutaneous Lupus" (unspecified if ongoing); "Obstruct Sleep Apnea" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "HBP" (unspecified if ongoing); "Mild asthma" (unspecified if ongoing); "Overweight" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Nsaids, reaction(s): "lichen planus". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 13Jan2023 at 08:00, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13Jan2023) Positive, notes: I tested positive 13Jan2023 took the 5 days medication; (21Jan2023) Negative, notes: Retest on Saturday 21Jan2023 w 2 tests negative; (22Jan2023) Positive, notes: Then 22Jan2023 Sunday got positive test and negative test with one kit; (22Jan2023) Negative, notes: Then 22Jan2023 Sunday got positive test and negative test with one kit; (22Jan2023) Positive, notes: Follow up same day 6 hrs later and got 2 positive tests. Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230113; Test Name: Covid test; Test Result: Positive ; Comments: I tested positive 13Jan2023 took the 5 days medication.; Test Date: 20230121; Test Name: Covid test; Test Result: Negative ; Comments: Retest on Saturday 21Jan2023 w 2 tests negative.; Test Date: 20230122; Test Name: Covid test; Test Result: Positive ; Comments: Then 22Jan2023 Sunday got positive test and negative test with one kit.; Test Date: 20230122; Test Name: Covid test; Test Result: Negative ; Comments: Then 22Jan2023 Sunday got positive test and negative test with one kit.; Test Date: 20230122; Test Name: Covid test; Test Result: Positive ; Comments: Follow up same day 6 hrs later and got 2 positive tests.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Blood pressure high; Cutaneous lupus erythematosus; Fibromyalgia; Fish allergy (known allergies: Salmon); Obstructive sleep apnea syndrome; Osteoarthritis; Overweight
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 01.01.2023
Beginn: 01.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Administered after vaccine Beyond Use Date, the Beyond Use Date was 01/13/2023 and immunization was given 01/16/2023. No adverse reaction reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: IN
Alter: 66,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 01.01.2023
Beginn: 16.01.2023
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Administered after vaccine Beyond Use Date, the Beyond Use Date was 01/13/2023 and immunization was given 01/16/2023. No adverse reaction reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 19.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

No adverse event. Was discovered that vaccine was administered past the BUD expiration. BUD was 1/13/2023, was given to patient on 1/19/2023. Patient is 30 weeks pregnant but no complications/adverse events reported thus far.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 14.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

No adverse side effects but was given past the BUD and product was considered "expired". Per BUD expired on 1/13/2023, given on 1/14/2023. Per Pfizer they do have additional stability info that did say it was still a stable product and the CDC states the dose does not need to be repeated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: VA
Alter: 29,0
Geschlecht: M
Eingang: 24.01.2023
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: ja

Incorrect product formulation administered No adverse event

Symptomtext

Bivalent booster given without primary series No adverse reactions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Skin infection on Daptomycin
Vorgeschichte: Type II Diabetes
Andere Medikamente: Received flulaval, Prevnar 20 on same day. Daptomycin, Lantus 20 units daily, Regular Insulin 8 units 3 times a day, and Lamisil topical
Allergien: No known
Vorherige Impfungen: -

VAERS 2564575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NH
Alter: 84,0
Geschlecht: M
Eingang: 20.01.2023
Impfdatum: 14.12.2022
Beginn: 04.01.2023
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / LA

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

Transient ischaemic attack

Symptomtext

Systemic: TIA per emergency room md-Severe, Additional Details: Patient went to ER on 1/4, stayed overnight in hospital. Was told he had a TIA. Patient felt this should be reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Transient ischaemic attack
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2563512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: OR
Alter: 68,0
Geschlecht: F
Eingang: 19.01.2023
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 was to begin series after bone marrow transplant but patient was administered the bivalent vaccine as the primary vaccine in the series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Multiple myeloma with bone marrow transplant
Vorgeschichte: -
Andere Medikamente: -
Allergien: nkda
Vorherige Impfungen: -

VAERS 2563345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: AZ
Alter: 58,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 22.12.2022
Beginn: 22.12.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Extra dose administered No adverse event

Symptomtext

Patient received an additional Pfizer Bivalent booster on 12/22/2022. She originally received the bivalent booster on 9/22/2022. Patient has no adverse effects so far.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2563334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: AZ
Alter: 56,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 22.12.2022
Beginn: 22.12.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / RA

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

Inappropriate schedule of product administration No adverse event

Symptomtext

Patient received an additional dose of the Pfizer Bivalent Booster on 12/22/2022. His first booster dose of Pfizer Bivalent was administered on 09/22/2022. Patient does not have any adverse effects so far.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2561952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 28,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 15.01.2023
Beginn: 15.01.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

no outcomes

Weitere VAERSDATA-Felder

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

VAERS 2561063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 31.10.2022
Beginn: 29.10.2021
Tage bis Beginn: -
Dosis: 5
Route/Site: - / RA

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; Vaccine brand=Pfizer / BioNTech, Vaccine administration date=29Oct2021, Vaccine dose number=3 / Vaccine brand Other=Moderna, Vaccine administration date=09Mar2021, Vaccine dose number=2; This is a spontaneous report received from a non-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 31Oct2022 at 10:00 as dose 5 (booster), single (Lot number: GJ6738) at the age of 67 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 29Oct2021 as dose 3 (booster), single (Lot number: FF2590), in right arm and on 14Jul2022 as dose 4 (booster), single (Lot number: FJ4989), in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 08Feb2021 as dose 1, single (Lot number: 007M20A), in right arm and on 09Mar2021 as dose 2, single (Lot number: 029A21A), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Other medical history: Cholesterol" (unspecified if ongoing), notes: Other medical history: Cholesterol. The patient's concomitant medications were not reported. Past drug history included: Codeine, reaction(s): "Known allergies: Codeine", notes: Known allergies: Codeine. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 29Oct2021, outcome "unknown", described as "Vaccine brand=Pfizer / BioNTech, Vaccine administration date=29Oct2021, Vaccine dose number=3 / Vaccine brand Other=Moderna, Vaccine administration date=09Mar2021, Vaccine dose number=2"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood cholesterol abnormal (Other medical history: Cholesterol)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CO
Alter: 86,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 28.12.2022
Beginn: 28.12.2022
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

Symptomtext

PATIENT RECIEVED 2 BIVALENT BOOSTERS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: HTN, HYPERCHOLESTEROLEMIA
Andere Medikamente: LOSARTAN POTASSIUM 50MG, DOXAZOSIN 4MG, SIMVASTATIN 20MG
Allergien: LABETALOL AND SULFA
Vorherige Impfungen: -

VAERS 2559700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 28.11.2022
Beginn: 27.12.2022
Tage bis Beginn: 29,0
Dosis: 5
Route/Site: IM / LA

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

Influenza A virus test negative SARS-CoV-2 test negative Sinusitis

Symptomtext

Sinus infection treated with Augmentin for 8 days. From start to finish, infection lasted 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Influenza A virus test negative
Hospital-Tage: -
Labordaten: 1-1-23 covid and flu tests negative.
Aktuelle Erkrankungen: -
Vorgeschichte: mild chronic gastritis, GERD
Andere Medikamente: Prilosec, Premarin Vaginal cream, MVI, B complex, Vitamin D, Biotin, Tumeric, AREDS preservision, Calcium
Allergien: celebrex, voltarenmild
Vorherige Impfungen: -

VAERS 2559610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NY
Alter: 63,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 10.01.2023
Beginn: 10.01.2023
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: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: MI
Alter: 32,0
Geschlecht: F
Eingang: 08.01.2023
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: unbekannt Erholt: ja

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: -

VAERS 2552836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: MA
Alter: 70,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 04.01.2023
Beginn: 04.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Neck injury Periarthritis

Symptomtext

frozen shoulder, lt side of neck issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck injury
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: cad native artery, qt prologa, abdominal aneurysm, hashimoto, disc disease, cyst, diverticulosis, mycosis fungoids, asthma, fibromyalgia
Andere Medikamente: levothyroxine
Allergien: citalopram, cymbalta, diflucan, doxycycline, efexor, immitrex, osmoprep, quetiapine, trazadone, dilotid, phenytoin, myacin drugs, augmentin
Vorherige Impfungen: -

VAERS 2552576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: SC
Alter: 45,0
Geschlecht: M
Eingang: 06.01.2023
Impfdatum: 28.12.2022
Beginn: 28.12.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Gave the bivalent vaccine as second Covid vaccine dose for this patient. No adverse response reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2551496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 29.11.2022
Beginn: 03.01.2023
Tage bis Beginn: 35,0
Dosis: 5
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 5 vaccines Pfizer 2/16/21 Lot# EN6200; Pfizer 3/9/21 Lot# EN6207; Pfizer 9/24/21 Lot# FE3592; Pfizer 3/31/22 Lot# FM0698; Pfizer 11/29/22 Lot# GJ6738

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2549024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 18.11.2022
Beginn: 19.12.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / LA

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

Herpes zoster

Symptomtext

Developed shingles 12/19/2022; took antiviral medication started to improve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; probiotics; mushroom extract
Allergien: No
Vorherige Impfungen: -

VAERS 2548247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 02.01.2023
Impfdatum: 19.12.2022
Beginn: 19.12.2022
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

no symptoms, pt received bivalent booster shot vs receiving primary series pfizer. pt has no symptoms of any ILL effect. pt just notified primary doctor that they received bivalent vs primary series.

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: -

VAERS 2548162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: -
Alter: 12,0
Geschlecht: F
Eingang: 02.01.2023
Impfdatum: 23.12.2022
Beginn: 23.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Incorrect product formulation administered No adverse event

Symptomtext

Pt was given bivalent covid for first covid immunization. No adverse events known at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2546497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: FL
Alter: 45,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 26.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: - / RA

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

Disease recurrence Drug ineffective Suspected COVID-19

Symptomtext

Rebound COVID-19 infection 6 days post completion of the complete course of Paxlovid; COVID-19; COVID-19; This is a spontaneous report received from contactable reporter (Consumer). The reporter is the patient. A 45-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 26Nov2022 as dose 4 (booster), single (Lot number: GJ6738) at the age of 45 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 07Mar2021 as dose 1, single (Batch/Lot number: unknown), in left arm, on 28Mar2021 as dose 2, single (Lot number: EP7534), in right arm and on 01Oct2021 as dose 3 (booster), single (Lot number: FC3181), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing); "Anemia" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Aspirin, reaction: "known allergies: Aspirin"; Ibuprofen, reaction: "known allergies: ibuprofen", notes: known allergies: ibuprofen; Naproxen sodium, reaction: "known allergies: Naproxen Sodium". The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant) all with onset Dec2022, outcome "recovered" and all described as "COVID-19"; DISEASE RECURRENCE (medically significant) with onset 21Dec2022, outcome "recovering", described as "Rebound COVID-19 infection 6 days post completion of the complete course of Paxlovid". Therapeutic measures were taken as a result of drug ineffective, suspected covid-19. Therapeutic measures were not taken as a result of disease recurrence. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Disease recurrence
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anemia; Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MN
Alter: 33,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 29.12.2022
Beginn: 29.12.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Bivalent booster given when he was supposed to get regular Pfizer dose. Patient had 1 Pfizer dose prior to today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Kidney stone
Vorgeschichte: -
Andere Medikamente: Tamsulosin, Ibuprofen
Allergien: NKA
Vorherige Impfungen: -

VAERS 2545681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WA
Alter: 62,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 07.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was given the bivalent when she was to get the monovalent. Pt had no symptoms or side effect

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: n/a
Vorgeschichte: Acid Reflux/heartburn Arthritis, Knee(s) Arthropathy NOS, unspecified ASCUS of cervix with negative high risk HPV Back pain Behcets syndrome Chronic pain, not elsewhere classified Cough Degenerative arthritis of knee ENCOUNTER FOR LONG-TERM (CURRENT) USE OF OTHER MEDICATIONS Endometrial cells on cervical Pap smear inconsistent w/LMP Epigastric pain Fibromyalgia Hearing loss High blood pressure History of breast lump removal Hormone replacement therapy Hyperpathia Idiopathic hypersomnia with long sleep time Immunosuppression due to drug therapy LBP [Low back pain] Long term current use of opiate analgesic Mass of left chest wall Myalgia and myositis, unspecified Neuropathic pain NONSPECIFIC REACTION TO TUBERCULIN SKIN TEST WITHOUT ACTIVE TUBERCULOSIS Obstructive sleep apnea syndrome Comments: Per addition of OSA or related diagnosis. Osteoarthritis Pain in right knee Postoperative stiffness of total knee replacement Removal of ovary (Right) Restless leg syndrome RHEUMATOID ARTHRITIS S/p knee replacement Seasonal Allergies UNSPECIFIED INFLAMMATORY POLYARTHROPATHY
Andere Medikamente: Yes
Allergien: dust, fish, latex, methadone
Vorherige Impfungen: -

VAERS 2545620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: AR
Alter: 12,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 28.12.2022
Beginn: 28.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine was given after it had exceeded it's stability time outside of refrigeration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2544300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: OH
Alter: 44,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 27.11.2022
Beginn: 22.12.2022
Tage bis Beginn: 25,0
Dosis: 5
Route/Site: SYR / LA

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

Galactorrhoea

Symptomtext

patient stated she started lactating after receiving vaccine

Weitere VAERSDATA-Felder

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

VAERS 2543699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 03.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Herpes zoster

Symptomtext

Shingles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis
Andere Medikamente: Calcium, Vitamins A, C, D, and E, Lutein
Allergien: Biaxin
Vorherige Impfungen: -

VAERS 2542860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: TX
Alter: 10,0
Geschlecht: M
Eingang: 25.12.2022
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: 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: -

VAERS 2540553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: IN
Alter: 20,0
Geschlecht: M
Eingang: 22.12.2022
Impfdatum: 23.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient went in for First Monovalent Pfizer Vaccine. Pharmacy ensured that they were administering Monovalent First Dose, Pharmacist administering dose knowingly gave patient Bivalent Pfizer Booster instead on the Monovalent First Dose. Patient did NOT have adverse reaction to Bivalent dose that was given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: NO
Allergien: NO
Vorherige Impfungen: -

VAERS 2536749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 05.11.2022
Beginn: 11.12.2022
Tage bis Beginn: 36,0
Dosis: 5
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

covid +

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2536559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 12.12.2022
Beginn: 12.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

No adverse event Product storage error

Symptomtext

It was discovered at teh end of the day on 12/12/2022 that the pfizer bivalent vaccine that was given was taken out of the fridge on 12/8/2022 at 8:55 AM. Vaccine was given on 12/12/2022 at 12:40PM. This was beyond the 12 hours that the vaccine was good for. Patient did not have a reaction at the time vaccine was given or 15 minutes following administration and has not reported reaction to the vaccine that was given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, leukocytosis, osteopenia
Andere Medikamente: alendronate, amlodipine, vitamin D, losartan
Allergien: lisinopril
Vorherige Impfungen: -

VAERS 2536117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: GA
Alter: 42,0
Geschlecht: F
Eingang: 18.12.2022
Impfdatum: 14.12.2022
Beginn: 14.12.2022
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: -

VAERS 2536048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: KS
Alter: 79,0
Geschlecht: F
Eingang: 17.12.2022
Impfdatum: 15.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Extra dose administered

Symptomtext

Patient came into pharmacy asking about new covid vaccine, stating her last dose was over 6 months ago. She did not have her card on her but was on break (Employee) and stated she would bring card in from car after her shift. Clinical services had host error, RPh did not re-try. STC was not checked due to busniess/help ratio at time of request. Verbal account is considered "acceptable" as current health information from patient, so proceeded with vaccination as patient did not appear confused or hesitant in answering last injeciton date. When patient brought back card; she had her last dose 09/23/2022 and was the bivalent pfizer; currently CDC guidelines only indicate 1 bivalent booster dose at this time. Educated patient that she received TWO doses of bivalent pfizer; and she is only indicated to have one bivalent at this time. Educated her on reporting adverse effects to us following vaccine administration. Was not upset, actually stated she was 79 and diabetic so happy to have an additional dose. Re-educated it was still not indicated for her to have two bivalent doses regardless of age or comorbidities. Will recheck profile not just clin services file folder to avoid this in the future

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: DIABETES MELLITUS TYPE 2
Andere Medikamente: NONE LISTED AT THIS FACILITY OR REPORTED BY PATIENT
Allergien: NONE
Vorherige Impfungen: -

VAERS 2536011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 17.12.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2536009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 17.12.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

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: -

VAERS 2536008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 17.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / AR

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: -

VAERS 2536006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NY
Alter: 74,0
Geschlecht: M
Eingang: 17.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / AR

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: -

VAERS 2533852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 35,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 15.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient stated he did not have his vaccination record, but when screened, answered questions that would make him eligible for booster. After vaccine was administered, found out patient had already received the bivalent booster on November 1st. This was a gift card incentive event. Patient wanted gift cards

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2533848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 46,0
Geschlecht: M
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: ja

Extra dose administered

Symptomtext

Clinic was serving patients and their was a gift card incentive. Patient was screened and he stated that he was eligible based on the last date of his covid vaccination. After patient received vaccine, found out patient received a bivalent booster on 11/1.

Weitere VAERSDATA-Felder

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

VAERS 2533819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 15.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient stated he did not have his vaccine record but was determined to be eligible based on the information he gave about his previous vaccinations. This was a incentive vaccination event and the patient just wanted gift cards. We found out he was given his bivalent booster a month earlier when we were at the same site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: Patient was fine. Just upset when his plan for more gift cards was foiled.
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2533211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WI
Alter: 63,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 01.12.2022
Beginn: 13.12.2022
Tage bis Beginn: 12,0
Dosis: UNK
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Patient received bivalent booster from local Healthcare on 11/30/22. Pharmacy was unaware of this and administered a bivalent booster on 12/13/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: senna docusate 8.6-50mg one po qhs APAP 325mg 2 tablets po tid lisinopril 5mg po qhs spironolactone 25mg qd paliperidone ER 6mg qd Eliquis 5mg bid calcium antacid 1000mg qd magnesium oxide 500mg tid carvedilol 6.25mg one po bid gabapentin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2530621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 14.12.2022
Impfdatum: 07.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Therapeutic response unexpected

Symptomtext

neuropathy tingling sensation and aches in both feet had almost gone away; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from License Party. The reporter is the patient. Other Case identifier(s): INT-20600 (BioNTech SE). A 78-year-old patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Nov2022 as dose 4 (booster), 0.3 ml single (Lot number: GJ6738, Expiration Date: 31Jul2023) for covid-19 immunisation. The patient's relevant medical history included: "Diabetes II", start date: 1997 (unspecified if ongoing); "Neuropathy" (unspecified if ongoing). Concomitant medication(s) included: ROSUVASTATIN; HYDROCHLOROTHIAZIDE; LOSARTAN; AMLODIPINE; METFORMIN; CARVEDILOL. Vaccination history included: BNT162b2 (dose 3 (booster), Lot number: unknown), administration date: 20Dec2021, for COVID-19 immunization, reaction(s): "neuropathy tingling sensation and aches in both feet had almost gone away"; Covid-19 janssen (dose 1, Lot number: 202A21A), for COVID-19 Immunization; Covid-19 janssen (dose 2 (booster), Lot number: 202A21A), for COVID-19 Immunization. The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious) with onset Nov2022, outcome "unknown", described as "neuropathy tingling sensation and aches in both feet had almost gone away". Additional information: Patient has been diagnosed with diabetes II for the past twenty-five years. The neuropathy has become more and more pronounced over the years. It was a constant tingling along with aches and sometimes constriction in the toes. The soles of feet were where the tingling and aches occurred every day and continued to a lesser degree throughout the day. The patient noticed that after two-three days after the Pfizer covid vaccine booster injections that the neuropathy tingling sensation and aches in both feet had almost gone away. This cessation had also occurred after the previous Pfizer COVID booster on 20Dec2021. The previous cessation gradually diminished after six months and the neuropathy symptoms returned. The patient has other health issues (not further specified). NDC: 59267-0304-02. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : PFIZER INC-202201362450 same patient/event, different drug;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Therapeutic response unexpected
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Neuropathy; Type II diabetes mellitus
Andere Medikamente: ROSUVASTATIN; HYDROCHLOROTHIAZIDE; LOSARTAN; AMLODIPINE; METFORMIN; CARVEDILOL
Allergien: -
Vorherige Impfungen: -

VAERS 2530607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6738

gering

Staat: MI
Alter: 13,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 04.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / LA

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

Blood test Lymphadenopathy Vulval ulceration

Symptomtext

vulvar aphthous ulcer in adolescent; swollen lymph nodes in left armpit; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 13-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Dec2022 at 16:00 as dose 4 (booster), single (Lot number: GJ6738) at the age of 13 years intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: SLOW FE; ALLEGRA 24 HOUR. Vaccination history included: BNT162b2 (dose 3 (booster), administered intramuscularly in the left arm at 18:15, Batch/Lot no: unknown), administration date: 06Jan2022, when the patient was 12-year-old, for COVID-19 immunization; Covid-19 vaccine (primary immunization series complete, manufacturer unknown), for COVID-19 immunization. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 05Dec2022 at 18:00, outcome "recovering", described as "swollen lymph nodes in left armpit"; VULVAL ULCERATION (non-serious) with onset 05Dec2022 at 18:00, outcome "recovering", described as "vulvar aphthous ulcer in adolescent". The events "vulvar aphthous ulcer in adolescent" and "swollen lymph nodes in left armpit" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of vulval ulceration, lymphadenopathy. Additional information: Patient had no other vaccine in four weeks. Doctor confirmed the events on 07Dec2022. Bloodwork was ordered and it was confirmed that no other virus present such as mono, flu, or pneumonia. Therapeutic measures were taken as a result of vulval ulceration, lymphadenopathy which included topical cortisone, topical lidocaine, and ibuprofen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Test Name: Bloodwork; Result Unstructured Data: Test Result:no other virus present such as mono, flu; Comments: or pneumonia
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: SLOW FE; ALLEGRA 24 HOUR
Allergien: -
Vorherige Impfungen: -

VAERS 2530129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 12.12.2022
Beginn: 12.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient received an additional bivalent booster dose when one was not needed. She received the bivalent booster in September 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Osteoporosis Hypothyroidism
Andere Medikamente: Amlodipine, Albuterol, Levothyroxine, Losartan, Meloxicam.
Allergien: Hazelnut Meperidine Tree nut
Vorherige Impfungen: -

VAERS 2530061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: NH
Alter: 55,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 05.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Tinnitus

Symptomtext

Tinnitus, I've never had it but it started within a day or 2 of getting the booster

Weitere VAERSDATA-Felder

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

VAERS 2529502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: VA
Alter: 69,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 09.11.2022
Beginn: 12.12.2022
Tage bis Beginn: 33,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

The patient received an additional dose of the bivalent booster after reporting she had not had it yet. She reported no bad reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: parkinsons
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2529085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 59,0
Geschlecht: M
Eingang: 12.12.2022
Impfdatum: 07.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Tinnitus

Symptomtext

onset of bilateral tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: na
Vorgeschichte: diabetes high cholesterol
Andere Medikamente: metformin Jardiance glipizide atorvastatin
Allergien: nka
Vorherige Impfungen: -

VAERS 2528646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: GA
Alter: 71,0
Geschlecht: M
Eingang: 12.12.2022
Impfdatum: 06.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 0,0
Dosis: 6
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: -

VAERS 2528488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 11.12.2022
Impfdatum: 07.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

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: -

VAERS 2528416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj6738

gering

Staat: OH
Alter: 63,0
Geschlecht: M
Eingang: 10.12.2022
Impfdatum: 07.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

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: -

VAERS 2528400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

gering

Staat: OR
Alter: 14,0
Geschlecht: M
Eingang: 10.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

dad asked for wrong drug , meant flu but said covid , and i gave covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2528326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: CA
Alter: 10,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Administered Pfizer Bivalent 12 and up for a 10 year old patient. Pharmacist consulted father that patient does not need extra booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2527858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: WI
Alter: 52,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Covid19 Pfizer Bivalent vaccine given after beyond use date and time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: No Medications
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2527758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

gering

Staat: MA
Alter: 77,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 08.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

No adverse event

Symptomtext

no adverse events,

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No other illnesses at the time of vaccination
Vorgeschichte: Personality D/O Major Depressive Disorder DM PTSD
Andere Medikamente: -
Allergien: Bacitracin, Ciprofloxacin, Heparin, Morphine, Salmeterol, Vitamin K, Lovenox, Sulfa Abx, melon
Vorherige Impfungen: -

VAERS 2527571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

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Staat: MN
Alter: 53,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

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: -

VAERS 2527449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

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Staat: CA
Alter: 11,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 08.12.2022
Beginn: 08.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Patient was given regular adult dose of Pfizer Bivalent Booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2526747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

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Staat: OH
Alter: 60,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 08.12.2022
Beginn: 08.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Patient was given the bivalent booster dose as his first dose of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: Neuropathy, Hypertension, Vitamin D deficiency, Mixed Hyperlipidemia, AIDS
Andere Medikamente: Ibuprofen 800mg, Gabapentin 600, Biktarvy, Amlodipine 10, Klor-con
Allergien: NKA
Vorherige Impfungen: -

VAERS 2526740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

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Staat: GA
Alter: 63,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 06.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

Patient received 0.5ml instead of the normal 0.3ml dose. Two days post injection, he had not had any adverse reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none known
Andere Medikamente: None known
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2521965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

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Staat: GA
Alter: 27,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 01.12.2022
Beginn: 01.12.2022
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 No adverse event

Symptomtext

patient was given pfizer bivalent as first time dose, never had covid vaccine before

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2524230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

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Staat: IL
Alter: 24,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 03.12.2022
Beginn: 03.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

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: -

VAERS 2524229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6738

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Staat: IL
Alter: 43,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 03.12.2022
Beginn: 03.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

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: -

VAERS 2524153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

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Staat: KY
Alter: 62,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 17.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

Pfizer vaccine was placed in Freezer instead of Refrigerator for storage. Was thawed and administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes Hypertension Hyperlipidemia
Andere Medikamente: Metformin Levostatin
Allergien: NONE
Vorherige Impfungen: -

VAERS 2523713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

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Staat: CO
Alter: 39,0
Geschlecht: M
Eingang: 05.12.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Shoulder injury related to vaccine administration

Symptomtext

Patient says he thinks he has SIRVA from injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shoulder injury related to vaccine administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2521874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6738

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Staat: WI
Alter: 73,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 16.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was inadvertently administered Pfizer bivalent COVID-19 vaccine that was beyond the best use date. Vial was left at room temperature for ~9hrs past the 12hr best use timeframe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HLD, CAD, osteopenia
Andere Medikamente: pitavastatin, estradiol cream
Allergien: atorvastatin, lovastatin, pravastatin, rosuvastatin, simvastatin
Vorherige Impfungen: -