VAERS Reports 330 25 BD

VAERS 2644062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 12.06.2023
Impfdatum: 27.01.2022
Beginn: 25.04.2023
Tage bis Beginn: 453,0
Dosis: 1
Route/Site: UN / UN

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

Acute respiratory failure Asthma-chronic obstructive pulmonary disease overlap syndrome Condition aggravated Hypoxia

Symptomtext

J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/25/2023 ACUTE EXACERBATION OF ASTHMA COPD OVERLAP SYNDROME (ASTHMA W COPD) R09.02 HYPOXIA 4/25/2023 ACUTE EXACERBATION OF ASTHMA COPD OVERLAP SYNDROME (ASTHMA W COPD)

Weitere VAERSDATA-Felder

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

VAERS 2637412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 26.05.2023
Impfdatum: 18.12.2021
Beginn: 03.06.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: UN / UN

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

Acute respiratory failure Adult T-cell lymphoma/leukaemia Febrile neutropenia Hypertension

Symptomtext

J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/20/2022 HTN (HYPERTENSION) J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/20/2022 NEUTROPENIC FEVER, UNSPECIFIED J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/20/2022 ADULT T-CELL LEUKEMIA W LYMPHOMA J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/20/2022 NEUTROPENIC FEVER, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2627394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 05.05.2023
Impfdatum: 21.12.2021
Beginn: 24.08.2022
Tage bis Beginn: 246,0
Dosis: 3
Route/Site: - / -

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

Acute myocardial infarction Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI 10/29/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2626696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 04.01.2022
Beginn: 05.07.2022
Tage bis Beginn: 182,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Atrial fibrillation Respiratory failure

Symptomtext

J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 7/5/2022 ATRIAL FIBRILLATION, UNSPECIFIED J96.21 ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 7/5/2022 ATRIAL FIBRILLATION, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2579737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 10.02.2023
Impfdatum: 26.01.2022
Beginn: 03.11.2022
Tage bis Beginn: 281,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

Patient had a breakthrough infection and expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: Positive COVID test on 9/27/22 and 10/14/22.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2604566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: -
Alter: 87,0
Geschlecht: M
Eingang: 10.01.2023
Impfdatum: 28.12.2021
Beginn: 08.06.2022
Tage bis Beginn: 162,0
Dosis: 3
Route/Site: IM / RA

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

Adrenal neoplasm Asthenia Atrial fibrillation Benign prostatic hyperplasia COVID-19 Chest X-ray normal Condition aggravated Confusional state Cough Glaucoma Hypertension Hypokalaemia Nasal congestion Pyrexia Residual urine volume increased Rhinitis allergic SARS-CoV-2 test positive Sickle cell trait

Symptomtext

Narrative: 85 y/o male w/ PMH of essential hypertension, dementia with cognitive impairment, recently diagnosed adrenal incidentaloma, BPH, sickle cell trait, and glaucoma. Pt presented to ED on 06/08/22 w/ increased confusion after he has his allergy shot from community clinic that morning and noted generally weak upon going back home. Pt w/ afib RVR, nasal congestion, cough, fever and positive for COVID 19 and admitted to hospital. Chest X-ray negative for infiltrates. Pt treated with remdesivir (06/08-06/10). Pt also treated for chronic hypertension, chronic BPH , PVRs x 1 high now normal on Tamsulosin, chronic vitamin D deficiency, chronic unspecified glaucoma both eyes, chronic allergic rhinitis, acute hypokalemia and mild Thrombocytopenia due to COVID syndrome most likely. Pt improved and discharged to home on 06/14.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Glaucoma
Hospital-Tage: -
Labordaten: 06/08/2022- COVID 19 Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2604554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 10.01.2023
Impfdatum: 10.01.2022
Beginn: 04.06.2022
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Anaemia of chronic disease COVID-19 Cardiac failure Chronic kidney disease Condition aggravated Dyspnoea Hypertensive urgency Intensive care Pulmonary hypertension SARS-CoV-2 test positive

Symptomtext

Narrative: 71 y/o male w/ PMH for HTN, Asthma, HLD, Lumbago, CKD, and HF. Pt presented to the ED on 06/04/22 with SOB worsening over 5 days. Pt admitted to hospital ICU w/ acute hypoxic respiratory failure secondary to heart failure with reduced ejection fraction exacerbation. Pt also treated for Acute kidney injury on CKD 4, pulmonary hypertension, hypertensive urgency, anemia secondary to chronic disease and COVID-19 infection. Pt treated with dexamethasone (06/4-06/05) and supportive treatment during hospital stay for COVID. Pt improved and discharged to home on 06/14.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 06/04/2022- COVID 19 Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2547649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: WA
Alter: 49,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 30.12.2021
Beginn: 26.12.2022
Tage bis Beginn: 361,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Ascites Atelectasis COVID-19 Hepatic cirrhosis Hypervolaemia Pleural effusion Portal hypertension SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 4/2/21 (lot # ER8732), 5/2/21 (lot # EW0171), and 12/30/21 (lot # 33025BD). On 12/26/22, patient admitted to our inpatient facility (med/surg unit) with acute hypoxic respiratory failure secondary to COVID-19 infection and hypervolemia /pleural effusion with atelectasis, prominent ascites, cirrhosis with portal hypertension related to alcohol use, symptomatic ascites, and alcohol use disorder with history of delirium tremens/hospitalization. Patient was discharged home on 12/29/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: COVID status positive 12/26/22.
Aktuelle Erkrankungen: -
Vorgeschichte: history of alcohol use disorder and HTN
Andere Medikamente: albuterol inh, lisinopril
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2542146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 22.12.2021
Beginn: 24.11.2022
Tage bis Beginn: 337,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Asthenia Blood bicarbonate normal Blood creatinine increased Blood gases Blood glucose decreased Blood pH normal COVID-19 Cardiac telemetry Cardiomegaly Cerebral small vessel ischaemic disease Chest X-ray abnormal Chronic obstructive pulmonary disease Computerised tomogram head abnormal Condition aggravated Cough Diastolic dysfunction

Symptomtext

Patient is a 83 y.o. female patient of DO with history of COPD, hypertension, DM type 2, CAD, CKD presented to Hospital with AMS . AMS Likely multifactorial with COVID, hypoglycemia Slurred speech and slow to respond reported by family, glucose by medics 101 Febrile T max 100.8 CT head negative for acute intracranial abnormality, moderate large amount of chronic microvascular ischemic change in supratentorial white matter UDS - negative S/b Neurology AMS likely from covid and hypoglycemia No indication for MRI Brain Acute Hypoxic Respiratory Failure No home o2 at baseline RA 88% 2L NC on admission Supportive care as below Now on room air. Covid-19 Virus Infection Date of onset of symptoms: 11/24/2022 Symptoms present on admission: fever, cough Date of covid positive test: 11/24/2022 Vaccination status: vaccinated Imaging: CXR cardiomegaly, pulmonary vascular congestion Oxygen requirements on admission: 2L Current oxygen requirements: 2L Medical therapy: steroids and remdesivir Consultants following: ID Anticipated special isolation end date: 12/4/2022 Completed 5-day course of remdesivir. Switch to oral dexamethasone to 6 mg daily for 4 more days to complete a 10-day course. COPD Exacerbation In setting of COVID and tobacco abuse Diffuse wheezing on exam VBG 7.41 co2 45 po2 102 Hco3 28 Requiring 2L nc on admission Completed Zithromax dose. DM type 2 Episode Hypoglycemia Glucose in ED 41 treated with dextrose repeat 500 likely inaccurate Repeat chem 128 Resume home regimen. Elevated Troponin CAD HFpEF Echo 1/2020 EF 60%, mild diastolic dysfunction Trop 27 ECG non ischemic CXR pulm vascular congestion, bilateral lower extremity edema Was on 40 mg IV lasix daily, now on hold due to elevated creatinine Repeat 2D echocardiogram on 1128 showed EF of 50 to 60% and grade 2 diastolic dysfunction. Continue to monitor on tele, delta essentially flat Continue Lipitor AKI on CKD stage 3 Creatine 1.26 on admission Slightly better then baseline (2.23-1.52) Avoid nephrotoxic medications Cr 1.6 - monitor Creatinine back to baseline Tobacco Abuse Continues to smoke NRT Debility. PT and OT recommended home with home health. She will be discharged home today.

Weitere VAERSDATA-Felder

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

VAERS 2362628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: IL
Alter: 66,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 25.01.2022
Beginn: 01.02.2022
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure Anticoagulant therapy Anxiety Arrhythmia Atrial fibrillation Blood culture negative COVID-19 Cardiac arrest Computerised tomogram thorax abnormal Coronary arterial stent insertion Culture urine negative Death Deep vein thrombosis Device intolerance Device placement issue Dyspnoea Endotracheal intubation Fatigue

Symptomtext

Pfizer Dose 1 1/25/22 (33025BD) COVID Positive 2/10/2022 2/10/22: Patient is a 66-year-old male with past medical history significant for hypertension, COPD, hyperlipidemia, rheumatoid arthritis, history of pneumococcal pneumonia status post lung surgery at outside hospitals has come to the emergency room with complaints of worsening shortness of breath for 10 days. He apparently was not vaccinated for COVID-19 till 10 days ago. He thinks that soon after vaccination he started having symptoms which gradually progressed. He had associated cough with occasional yellow sputum. He denied any sore throat or loss of sense of smell or taste. He denies any nasal congestion. He denies any vomiting but had nausea. He denies any diarrhea. He had mild headache. He denies any fever or chills. He finally presented to the emergency room where he was needing BiPAP support to maintain the oxygenation. He was weaned to 5 L OxyMask at my exam. Patient's COVID test was pending initially, but came back positive at the time of my exam. He had the highly elevated D-dimer for which he underwent a CT chest which was negative for PE but did show fibrotic chronic interstitial lung disease. There was also possible pneumonitis with chronic changes. Patient is being admitted for further management. Patient denies any chest pain, he denies any abdominal pain or any other concerns except for shortness of breath and cough during my exam in the emergency. He has no other acute health concerns. 3/22/22: Course during Hospitalization: 2/10: 66-year-old male patient with history of hypertension, dyslipidemia, rheumatoid arthritis, COPD was admitted to the hospital on 02/10. Patient was vaccinated on 02/01 for the SARS-CoV-2 virus. Patient was started on remdesivir and dexamethasone and given dose of Actemra. 2/13: Pulmonology consultation was obtained for acute hypoxic respiratory failure. Patient was maintained on BiPAP. 2/17: Patient was transition to OptiFlow to maintain pulse ox above 90%. Possibility of rheumatoid arthritis affecting the lungs was considered. Antitussives and Xanax were given for relief due to cough and anxiety respectively. 2/21: Patient was started on Solu-Medrol per pulmonology as patient also has history of COPD to see if he could get some relief. Patient also had a brief run of SVTs. Minimal movement even in bed was causing significant hypoxia. 2/28: Patient expresses his significant fatigue with OptiFlow and wants to be intubated. Intubation performed per anesthesia. 3/1: Patient started on low-dose of Levophed for hypotension. Solu-Medrol. Started on a Zosyn. 3/3: Patient's urine, sputum, blood cultures from 3/1 are NGTD 3/4: Sedation vacation was tried. Pt able to follow commands and coughing. 3/7: Tube feeld held due to significant amount of copious secretions. Dietitian consulted. 3/8: Checked Abdominal series for constipation-normal X-ray 3/9: Slow introduction of Tube feeds. 3/11: s/p trach and PEG placement. Pt had significant arrhythmias from SVT, atrial fibrillation and V-tach overnight 3/12: 1 DES to the RCA placed, Levophed and dopamine started. Significant oral and G-tube secretions present. 3/13: Patient off of dopamine. Tube feeding held. 3/17: Pt not tolerating the tube feeds, unable to get the tip of the tube into the jejunum. Currently tip present between 2nd and 3rd part of duodenum. 3/18 : LUE Cephalic vein thrombosis+, on BID dosing of Lovenox. 3/20: Patient tolerating tube feeds better. Tracheal secretions present. 3/21: Patient's FiO2 increased from 80-100% today. Tracheostomy area erythematous. Patient made DNR/DNI. 3/22: Patient on 100% FiO2. Started on Levophed at 30 mcg/minute Patient went into PEA at around 18:10 and asystole at 18:13 and passed away on 3/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 40,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN CoPD HLD RA h/o pneumococcal pneumonia s/p lung surgery
Andere Medikamente: vitamin D 500 mg PO QD benxonatate 100 mg PO TID cetirizine 10 mg PO HS cholecalciferol 250 mcg PO QD folic acid 2 mg PO QD furosemide 20 mg PO QD gabapentin 200 mg PO TID losartan 100 mg PO QD methotrexate 15 mg PO QSaturday multivit 1 tab
Allergien: codeine - unknown lactose - unkown
Vorherige Impfungen: -

VAERS 2082183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: WI
Alter: 30,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 06.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / RA

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

Atrioventricular block complete Chest pain Echocardiogram abnormal Electrocardiogram Myocardial infarction Stent placement

Symptomtext

I woke started having chest pain I went by ambulance to the hospital, I was having heart attack. I had a 100% blockage and they put a stent in. The doctors could not find any reason, my BP has been normal and cholesterol always been amazing and no precursors, my A1C always been good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: EKG; ultrasound of my heart to find the blockage
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Nothing
Allergien: None
Vorherige Impfungen: -

VAERS 2073315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: KS
Alter: 88,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 22.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / RA

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

Body temperature increased Chest X-ray abnormal Death Decreased appetite Dyspnoea Lung infiltration Oxygen saturation decreased Respiratory tract congestion Resuscitation Unresponsive to stimuli Use of accessory respiratory muscles

Symptomtext

Upon reviewing skilled nursing facility's chart, it appears his temperature was normal the day of vaccination, and the day after vaccination. On 12/24/21, however, his temperature increased to 100.9 degrees. It came down later that day and started between 97.1 and 99.8 in the days following. Nursing notes state that patient was noted to have reduced appetite and difficulty breathing. On 12/28/21, an XRay was ordered due to difficulty breathing and loratadine 10mg daily was started "for congestion". The XRay findings report that there was a slight right lower lobe infiltrate. Left side appeared clear and heart unremarkable. Doxycycline 100mg BID started in response. On 12/31/21, at approximately 7pm, patient called nursing and asked for the doctor to be contacted because he was having an extremely difficult time breathing. Nursing noted he was using his accessory muscles to breath and his oxygen sats were 70-73% on room air. Nurse applied oxygen 3L and it did not increase O2 sats. Breathing treatment administered and MD contacted. Orders to go to ER were given. EMS arrived and upon repositioning / transferring patient, the patient became unresponsive. CPR was initiated but patient was never able to regain a sustained heartbeat. Per facility staff, family denies having given authorization for COVID booster to be given and believes that booster was cause of death.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: XRay as noted conducted 12/28/21 and showed infiltrate.
Aktuelle Erkrankungen: Temperatures began to increase, including values >100, within 72 hours of vaccination. Chest XRay performed 12/28/21 in response to difficulty breathing. Right lower lobe infiltrate identified and doxycycline 100mg BID started. Patient had extremely labored breathing and below normal oxygen saturations the evening of 12/31/21 for which EMS was called and patient passed in the process of EMS staff moving/transferring patient.
Vorgeschichte: Cellulitis of left lower limb, non-pressure chronic ulcer of left calf with fat layer exposed, lymphedema, chronic diastolic heart failure, hx bacteremia 6/2021, hx COVID 10/2020, localized edema, BMI 40-45, facial cellulitis, delusional disorders, dementia, hyperlipidemia, hypertension, paranoid personality disorder, lack of coordination, dysphagia, dementia, vitamin D deficiency.
Andere Medikamente: Furosemide 40mg BID, Divalproex ER 250mg TID, Pentoxifylline 400mg TID, Doxycycline 100mg BID (started 12/28/21), Loratadine 10mg daily x 7 days (started 12/28/21 for congestion), Potassium ER 20mEq daily, Hydrocodone/APAP 5/325mg BID, PRN
Allergien: No allergies noted
Vorherige Impfungen: -

VAERS 1967509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

kritisch

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Brain death Cardiac arrest Computerised tomogram head abnormal Deafness unilateral Headache Resuscitation Screaming Seizure Subarachnoid haemorrhage

Symptomtext

Yesterday in the evening, some hours after receiving the booster for the Pfizer Covid vaccine, family heard the patient scream and complained of sudden and severe onset headache and hearing loss in the right ear, followed by a seizure and cardiac arrest. She was brought to hospital where she was resuscitated and found to have a large subarachnoid hemorrhage. She was transferred to hospital, a stroke center but it was determined that that she was already brain-dead. Family denied any family history of brain aneurysm or subarachnoid hemorrhage and also denied the patient have any history of high blood pressure or any other significant medical problems.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain death
Hospital-Tage: -
Labordaten: CT brain
Aktuelle Erkrankungen: -
Vorgeschichte: None significant per family
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2462771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: GA
Alter: 65,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 10.04.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Cardiac operation Dyspnoea Pain Pericarditis Pleural effusion Pyrexia

Symptomtext

Pericarditis; Heart surgery; Experienced shortness of breath which turned out to be fluid around the lining of her heart/I was almost died and it was hard for me to breath; Experienced shortness of breath which turned out to be fluid around the lining of her heart/fluid around her heart which was pericarditis and did have heart surgery; I did get extreme pain and fever; I did get extreme pain and fever; 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 65-year-old female patient received BNT162b2 (BNT162B2), on 10Apr2022 as dose 3 (booster), single (Lot number: 33025BD) at the age of 65 years for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure high" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE taken for hypertension. Vaccination history included: pfizer coviD-19 vaccine (Dose: 02, Lot no.: ER8733), administration date: 29Mar2021, when the patient was 64-year-old, for COVID-19 immunization; pfizer coviD-19 vaccine (Dose: 01, Lot no.: EN6205), administration date: 04Mar2021, when the patient was 64-year-old, for COVID-19 immunization. The following information was reported: PERICARDITIS (medically significant), outcome "unknown"; CARDIAC OPERATION (medically significant), outcome "unknown", described as "Heart surgery"; DYSPNOEA (non-serious), outcome "unknown", described as "Experienced shortness of breath which turned out to be fluid around the lining of her heart/I was almost died and it was hard for me to breath"; PLEURAL EFFUSION (non-serious), outcome "unknown", described as "Experienced shortness of breath which turned out to be fluid around the lining of her heart/fluid around her heart which was pericarditis and did have heart surgery"; PYREXIA (non-serious), PAIN (non-serious), outcome "unknown" and all described as "I did get extreme pain and fever". The events "pericarditis", "experienced shortness of breath which turned out to be fluid around the lining of her heart/i was almost died and it was hard for me to breath" and "experienced shortness of breath which turned out to be fluid around the lining of her heart/fluid around her heart which was pericarditis and did have heart surgery" required emergency room visit. Therapeutic measures were taken as a result of pericarditis, cardiac operation, dyspnoea. Clinical course: The patient reported that when she took the vaccine she did get extreme pain and fever and then after some time she felt shortness of breath, and pericarditis. She do not know what was wrong with her when she was having shortness of breath she went to the hospital and they keep telling her they do not know. They gave her asthma medicine and then she went to emergency in the month of January. She was almost died and then they did test and said there was fluid in her heart that was pericarditis. She did not know what was wrong. What she knew she was having shortness of breath and it was hard for her to breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high
Andere Medikamente: AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2377288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: MO
Alter: 52,0
Geschlecht: M
Eingang: 21.07.2022
Impfdatum: 05.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / UN

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

Abdominal discomfort Basal ganglia haemorrhage Blood test Bradycardia Cerebral mass effect Computerised tomogram head abnormal Craniotomy Decompressive craniectomy Disability Fatigue Haemorrhage intracranial Headache Hypertension Hypotonia Intensive care Intracerebral haematoma evacuation Laboratory test Oropharyngeal pain

Symptomtext

Shortly afterwards, complained of headache, sore throat and general tiredness. Symptoms continued along with upset stomach and unrest throughout the night and next night. At 5 am on the 3rd day afterwards, In the ED, he was noted to be flaccid on the right side and with a poor exam. Head CT demonstrated a large left BG IPH with 6 mm midline shift, no IVH. BP 189/88, pulse 46. He was given keppra 1 g load for prophylaxis, and mannitol 100g given concern for herniation (midline shift, hypertension, bradycardia); he was started on propofol and nicardipine and transferred to hospital. On 1/10/22 had craniotomy decompression and evacuation. He was in NICU until 1/24/22 and was then transferred to Rehabilitation hospital. On 3/9/22 was transferred to Rehabilitation. Was discharged to home 7/6/22 and is currently attending outpatient therapy for PT, OT, ST. He was deemed completely disabled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 180,0
Labordaten: Ct scan, bloodwork, and labs galore throughout this time listed above.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma GERD Anxiety
Andere Medikamente: Albuterol HFA Alprazolam Citalopram fluticasone-salmetero hydrOXYzine pamoate medical marijuana
Allergien: Hay fever
Vorherige Impfungen: -

VAERS 2273685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: VT
Alter: 51,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Acoustic stimulation tests Dizziness Head injury Impaired work ability Loss of consciousness Magnetic resonance imaging head Vertigo Vestibular neuronitis Vomiting

Symptomtext

Within a day or so of receiving my 3rd Covid vaccine , I developed severe dizziness. This increased to vomiting with movement. I also had vertigo so severe one day that I passed out and hit my head. These symptoms took 4 months to improve. I missed a lot of work, attended PT and am now just getting back to my job as a nurse. I still have occasional dizziness. I was worked up by my PCP, Neurologist and ENT. They all agreed it Vestibular Nephritis from the Covid vaccines

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Brain MRI Physical Therapy Hearing Test Lots of doctor appointments
Aktuelle Erkrankungen: none
Vorgeschichte: Post Covid Syndrome_fatigue/body aches
Andere Medikamente: HRT Tylenol
Allergien: EMycin Sulfa Levoquin Sulfa
Vorherige Impfungen: -

VAERS 2245974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 29.01.2022
Beginn: 10.04.2022
Tage bis Beginn: 71,0
Dosis: 3
Route/Site: IM / LA

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

Syncope Urinary incontinence

Symptomtext

Syncope: passed-out in for a few seconds and bladder incontinence. I am suspecting either neurogenic syncope vs. cardiogenic syncope.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: We worked her up today.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec
Allergien: No known food or drug allergies
Vorherige Impfungen: -

VAERS 2194469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 24.01.2022
Beginn: 06.02.2022
Tage bis Beginn: 13,0
Dosis: UNK
Route/Site: - / -

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

Fatigue Guillain-Barre syndrome Headache Infectious mononucleosis Mononucleosis heterophile test positive Oropharyngeal discomfort Productive cough Pyrexia Stomatitis

Symptomtext

Headache, fatigue progression of symptoms to severe fatigue, throat discomfort, low grade fever, oral sores, croup like coughing. Diagnosed with Guillane Barre and active mono.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Positive Guillane Barre and diagnosis of mono
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2140098

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33025BD

schwer

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Herpes virus infection Hospitalisation Influenza Urinary tract infection

Symptomtext

Felt like getting flu and had a herpes type 2 outbreak, then had another and had several more. Acyclovir and started taking lysine and had to change diet. Increased allergy problems, was hospitalized for 1 day with a UTI 11/25/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hospitalisation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OAS
Andere Medikamente: Lysine, Vitamin C, Probiotics and Prebiotics, Digestive Enzyme, Turmeric, Omega 3, Vitamin D with K, Magnesium, Adrenals, Spirulina, Olive leaf, Trace minerals, Zinc
Allergien: Sulfa, Environmental allergies to different foods, hay fever, mold and dust
Vorherige Impfungen: -

VAERS 2124204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: KS
Alter: 14,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 18.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness Malaise Nausea Pallor Syncope

Symptomtext

14 year female in Clinic to receive Covid 19 Vaccine Booster dose. After received dose in L deltoid stood up to go to observation area and she told her mother she didn't feel very well and fainted. Mother was behind her and caught her as she fainted and helped her to floor, she did loose consciousness for les than 1 minute. Patient re gain consciousness and denies any pain or discomfort she was helped to wheelchair and take to Special Care Room to access. Helped to cot and complains of nausea. 14:40 pm , Given water to sip and vitals as follows: Sat 98, BP 101/56, P 86. color pale. 15:00 , states feeling better, color improving, no complaints of pain or discomfort stated and no dizziness stated Sat 97, BP 102/62, P72. Taken to car per wheelchair with mother waiting .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: pine nuts
Vorherige Impfungen: -

VAERS 2116423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: KS
Alter: 50,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Immediate post-injection reaction Loss of consciousness Respiratory rate increased Tremor

Symptomtext

Vaccine administered with pt. lying down on exam table at HCF with Dr. present and as well as office nurse. and pt. spouse. Dr and nurse familiar with pt. previous reactions to vaccines. Pt lost consciousness immediately with visible shaking and rapid breathing. Dr. and staff nurse provided verbal and physical support. Pt regained consciousness after approx. 2-3 minutes. Patient stated she took 3 Ativan prior to appointment. Pt. observed for 30 minutes and return to baseline. Pt verbalized well being.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: severe needle phobia
Andere Medikamente: Ativan
Allergien: PCN Sulfa Prednisone Ipatropium
Vorherige Impfungen: stated needle phobia and previous issues w vaccines. This was done in her Drs office with physician and office nurse in room wh

VAERS 2109416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: KS
Alter: 16,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 12.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Cold sweat Disorientation Erythema Fall Head injury Headache Pallor Syncope

Symptomtext

16 year old male at table 4 received booster dose of Pfizer Covid vaccine to left deltoid. Patient started to rise to go to observation and immediately fainted and fell out of chair onto the floor landing on his left side rolling to rest on back, his back was pressed against the bottom bar of privacy screen. Patient did hit his head on floor w fall. Patient woke immediately slightly disoriented, pale in color and clammy. No blood or open injuries noted no contusion noted to back of head. Patient answered questions and stated back of head was a little sore, ice pack applied to area. No dizziness stated and pupils equal. Help to wheelchair taken to Care Room, BP 124/82, P64, R 20, o2 97% Given water, snack and stated feeling better, color returning to face. ice continues to back of head. States no pain or discomfort . RN inspected back and a 2 inch red mark noted mid line no bleeding or laceration noted . Back of head inspected no contusion or bleeding noted. !4:15 pm BP 117/58, P 70, R 18, o2 99%, pupils Equal reactive to light. Denies any pain or discomfort, Father declined EMS to be notified to evaluate patient. Father and Patient educated to monitor for disorientation, dizziness, headache, nausea, vomiting, and if needed to contact physician or if needed go to a ER. Left w father at 14:20 pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: as a child would pass out w vaccines

VAERS 2087733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 29.01.2022
Beginn: 03.02.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Arterial catheterisation C-reactive protein increased Chest X-ray normal Chest discomfort Chest pain Decreased activity Differential white blood cell count Dizziness Dyspnoea Dyspnoea at rest Dyspnoea exertional Echocardiogram abnormal Ejection fraction Electrocardiogram repolarisation abnormality Fibrin D dimer Influenza virus test Intensive care Laboratory test normal

Symptomtext

Patient is a 17 year old female admitted from the ED for midsternal to left-sided chest pain. She reports that her pain sarted yesterday morning and it woke her up. She describes the pain as a 4/10 pain. She took tylenol and it got a little bit better. Her pain was worse this morning to 6/10. She said pain was also worse with lying down and better when sitting up. She was also experiencing SOB, dizziness, pre-syncope. +palpitations and chest tightness which was mostly on the left with pressure and squeezing feeling, radiating to the right occasionally. Mom brought her to ED this morning. In the ED she had an elevated troponin and slightly elevated Nt pro BNP. She received Covid booster 5 days ago. Only recent illness noted is from a double AOM on 1/9. Pertinent results: Elevated troponin Medication given: None Recent history of travel: No Contact with sick person: No Recent immunizations: Covid booster 1/30/22 REVIEW OF SYSTEMS GENERAL: Positive for: decreased activity Negative for: change in appetitite, fever, chills, diaphoresis, fatigue, irritability, excessive weight loss, excessive weight gain PSYCH/BEHAVIOR: Positive for: none Negative for: agitation, behavioral problems, confusion, hallucinations NEURO: Positive for: dizziness, presyncopal Negative for: head injury, seizures, change in gait EYES: Positive for: none Negative for: photophobia, pain, discharge, redness ENT: Positive for: none Negative for: congestion, ear discharge, hoarseness, sore throat RESPIRATORY: Positive for: chest tightness, shortness of breath Negative for: cough, wheezing CARDIOVASCULAR: Positive for: chest pain, palpitations, dyspnea on exertion Negative for: cyanosis, swelling of feet GASTRO: Positive for: none Negative for: abdominal pain, nausea, vomiting, diarrhea GU: Positive for: none Negative for: decreased urine output, frequency, urgency ENDOCRINE: Positive for: none Negative for: cold intolerance, heat intolerance MUSCULOSKELETAL: Positive for: none Negative for: joint pain, joint swelling, limitiation of movement, muscle pain, back pain SKIN: Positive for: pallor Negative for: rash HEME: Positive for: pallor Negative for: easy bruising, excessive bleeding Problem List Troponin level elevated POA: Yes Active Problems: Troponin level elevated POA: Yes Patient is a previously healthy 17 year old healthy female with 2 days of acute chest pain and elevated troponin. BNP mildly elevated. Otherwise reassuring clinical exam. EKG showing early repolarization. Differential is most concerning for for Acute Myocarditis, pericarditis of unknown etiology, likely related to viral illness or possible recent Covid booster administration. Plan to trend troponin with ECG Q 6 hours and follow up ECHO. Further plan detailed below. PLAN CNS -Neurochecks q4h and prn changes -Resume home Concerta 72 mg and OCP (mom will bring in from home) RESP - Maintain POX >93%, continuous pox - Send RVP (Rapid flu, RSV and COVID negative) CVS - Continuous cardiorespiratory monitor, q1h VS per PICU routine - Consult to peds cardiology - ECHO today - Trend troponin Q 6 hours with ECG - If further increasing troponins, may need cardiac MRI FEN/GI - NPO until results of echo to evaluate for pericardial effusion - IVF NS at 80% at 60 ml/hr RENAL - Strict I&Os ID - monitor fever curve, follow up RVP LINES/TUBES/RESTRAINTS - PIV Plan of care discussed with Provider, RN, Patient, Family/Significant Other: mother and Consultants: cardiology Cardiology Note: History of Present Illness: Patient is a 17 year old female with history of ADHD who presents with left sided chest pain. Her chest pain first started yesterday AM, waking he reform sleep. The pain is described as pressure, and is worse when laying down and better when leaning forward. She took a tylenol and got a bit better, but developed shortness of breath with activity and with rest, dizziness, and feeling like she will pass out. Admits to heart pounding with chest pain. Brought to ED by mother, where she was foun to have an elevated troponin, mildly elevated NTproBNP, and otherwise normal labs. ECG showed early repolarization. Of note, patient received her third COVID booster this past weekend, and had a bilateral ear infection early January. ACTIVE PROBLEM LIST: Active Hospital Problems Diagnosis Date Noted ? Troponin level elevated 02/03/2022 REVIEW OF SYSTEMS: All other systems were reviewed and found to be negative unless otherwise stated above. CXR: Lines, tubes, and devices: None. Lungs and pleura: No focal consolidation.. No pleural effusion. No pneumothorax. Cardiomediastinal silhouette: Normal cardiomediastinal silhouette. Bones and soft tissues: No osseous abnormality. ECG: NSR with early repolarization ECHO: 1. No structural abnormalities. 2. Trivial tricuspid regurgitation. 3. Normal left ventricular size and wall thickness with qualitatively normal systolic and diastolic function. LVEF 2D 60%. Average global strain -19%. 4. Normal right ventricular size with qualitatively normal systolic function. 5. No arch obstruction. 6. 3/4 pulmonary veins seen. 7. No pericardial effusion. Cardiac Diagnosis: Perimyocarditis Impression: Patient is a 17 year old female with history of ADHD admitted with chest pain associated with shortness of breath and elevated troponin concerning for perimyocarditis. BNP and CRP mildly elevated, and active troponin leak suggests acute inflammatory process. Echocardiogram demonstrated normal cardiac structure and function. Unclear etiology, potentially viral or related to recent immunization. RVP in process. Overall plan to control pain, trend troponins, monitor hemodynamics. Troponin leak still trending up, if continues to increase overnight will plan for cardiac MRI in the morning to assess for scar burden and consideration of IVIG and steroids. Plan/ Recommendations: CNS - Ibuprofen q6h - Tylenol PRN CV - RVP pending PULM - CRM, monitor hemodynamics - Trend troponin T q6h with ECG - If uptrending overnight, will order cMRI in the AM FEN/GI - Regular diet - Strict I/O HEM/ID - Monitor fever curve Lines, Drains, and Airways Line Peripheral 02/03/22 0849 Right Antecubital 20 Gauge <1 day Please page pediatric cardiology fellow on call with concerns.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: Troponin: 2/3 1430: 0.334 2/3 2100: 0.327 2/4 0300: 0.371 2/4 0830: 0.349 D Dimer - 2/3 0847: 320 Chest X Ray - 2/3 - normal chest radiograph Echo 2/3 1411: Ht: 165.00 cm MRN: Age: 17 years Wt: 60.80 kg Study Date: 2/3/2022 11:31:52 AM Gender: F BSA: 1.67 m2 Requested By: doctor BP: 127/82 mmHg Diagnosing Physician: doctor Study Location: IP Indications: evaluate cardiac anatomy, function History: chest pain, elevated troponin Diagnosis: Chest Pain, unspecified Procedure Transthoracic, complete (w/Doppler and color) Image Quality: The images were of adequate diagnostic quality. Imaging Limitations: Prominent Lung Artifact. INTERPRETATION SUMMARY 1. No structural abnormalities. 2. Trivial tricuspid regurgitation. 3. Normal left ventricular size and wall thickness with qualitatively normal systolic and diastolic function. LVEF 2D 60%. Average global strain -19%. 4. Normal right ventricular size with qualitatively normal systolic function. 5. No arch obstruction. 6. 3/4 pulmonary veins seen. 7. No pericardial effusion. POSITION/CONNECTION: Situs: Abdominal visceral situs solitus. Levocardia. Atrial situs solitus. Normal atrioventricular alignment. Normally related great arteries. VEINS: Systemic Veins: Normal systemic venous return. The right superior vena cava drains normally to the right atrium. The inferior vena cava right-sided, entering the atrium. Pulmonary Veins: At least 3 pulmonary veins are seen returning to the left atrium. ATRIA/SEPTUM: Atria: The left atrium is normal size. The right atrium is normal in size. No hemodynamically significant atrial septal defect. AV VALVES/CANAL: Mitral Valve: The mitral valve leaflets are normal in appearance. There is no mitral valve prolapse. Trivial mitral regurgitation is present. Tricuspid Valve: The tricuspid valve is normal in appearance. Trivial tricuspid regurgitation is present. Tricuspid regurgitation jet was not quantifiable to estimate right ventricular systolic pressure. VENTRICLES: Left Ventricle: The left ventricle is normal in size. There is normal wall thickness. Left ventricular systolic function is normal. The LV global average strain is -19.0 %. Right Ventricle: The right ventricular chamber is of normal size. The right ventricular function appears qualitatively normal. Right ventricular diastolic Doppler filling patterns are normal. VSD: There is an intact ventricular septum. OUTFLOW TRACTS: LVOT: There is no left ventricular outflow tract obstruction. Aortic Valve: The aortic valve is normal and trileaflet. There is no aortic stenosis. Aortic valve velocity is 1.19 m/s. Aortic valve mean gradient is 3.5 mmHg. No aortic regurgitation is present. RVOT: There is no right ventricular outflow tract obstruction. Pulmonic Valve: The pulmonary valve is normal in appearance. There is no pulmonary valve stenosis. GREAT ARTERIES: Aorta: There is a left aortic arch with normal branching. The aortic root appears normal in size. Ascending aorta is normal. No evidence of coarctation of the aorta. The descending aortic Doppler pattern is nonobstructive. Pulmonary Arteries: The main, right and left pulmonary arteries appear normal. The right pulmonary artery is of normal size and origin. Suboptimal visulization of branch PAs. No obstruction noted. PDA: No evidence of a patent ductus arteriosis. OTHER: Coronary Arteries: The coronary artery anatomy appears to be normal. The left main coronary artery contains antegrade flow. LAD contains antegrade flow. The right coronary artery contains antegrade flow. Pericardium: There is no pericardial effusion. MEASUREMENTS: Ventricle IVS d, Mmode: 0.88 cm Zscore: -0.32 LV d, Mmode: 4.55 cm Zscore: -0.91 LV s, Mmode: 2.80 cm Zscore: -1.02 LV Vol d, Mmode: 94.8 ml Zscore: -1.88 LV Vol s, Mmode: 29.7 ml Zscore: -2.11 LVPW d, Mmode: 0.59 cm Zscore: -2.39 LV FS Mmode: 38.4 % LV vol d, MOD A4C: 107.9 ml LV vol s, MOD A4C: 47.2 ml LV Vol Index d, A4C: 64.68 ml/m? LV Stroke Vol: 36.4 ml/m? LV EF (A4C): 56.3 % LV Mass M-Mode 103.5 g LV Mass M-mode index (BSA) 62.0 g/m? LV Mass M-mode index g/(m^2.7) LV EF A/L A4C 59.7 % Pulmonary Valve PV Peak Velocity: 0.88 m/s PV Peak Grad: 3.1 mmHg Tricuspid Valve TR Vmax: 2.03 m/s TR Peak Grad: 16.4 mmHg Aorta Ao Root s, 2D: 2.95 cm Z score: 0.94 Asc Aorta: 2.92 cm Z score: 1.69 Ao Annulus: 1.91 cm Z score: -0.61 Aortic valve Ao V Vmax: 1.19 m/s Ao V Peak Grad: 5.7 mmHg Ao V Mean Velocity: 0.880 m/s Ao V Mean Grad: 3.5 mmHg Ao V VTI: 0.265 m Ao V Ejection Time: 301 msec
Aktuelle Erkrankungen: Viral illness (negative for COVID-19/Influenza/RSV) Acute otitis media treated with Amoxicillin x 10 days
Vorgeschichte: ADHD, Acne Vulgaris
Andere Medikamente: Methylphenidate ER 36 mg tablet - take 2 tablets by mouth every day with breakfast Levonorgestrel-ethinyl edtradiol 0.15-0.03 mg tablet - take 1 tablet by mouth once daily Clonidine 0.1 mg tablet - take 1-2 tablets by mouth at bed time as n
Allergien: Dextroamphetamine-amphetamine (Adderall) - nightmares/hallucinations
Vorherige Impfungen: -

VAERS 2069361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Abdominal pain Chest pain Condition aggravated Dizziness Electrocardiogram normal Headache Hypertension Musculoskeletal chest pain Myalgia Syncope Troponin normal Vision blurred X-ray normal

Symptomtext

Pt had a syncopal episode. Pt was caught and lowered to the ground. Pt reported a HA, dizziness, and left anterior chest pain Vitals: 175/122, 78, 17, 100%RA -- > 12:41 164/115. Emergency number was called @ 12:32 and pt taken to ED. IN ED: Pt had blurry vision, chest pain, and abdominal pain. Symptoms resolved by 18:05 and pt discharged after labs WNL, Trop negative x2, negative EKG, and negative X Ray. Vitals: 144/100, 69, 18 -- > 171/115, 61, 17 -- > 169/108, 65, 18 Pt given ibuprofen, Norco, and Hydromorphone. Pt went to another ED because she felt her care was not adequate. Pt had reproducible chest and trapezius tenderness to palpation. Recommended pt f/u w/ PCP for HTN. MD indicated it was unlikely hypertensive urgency/emerge

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Had syncope and was admitted for HTN urg after 2nd covid vax. dvt and lupus per chart, no longer on anticoag
Andere Medikamente: Medications: NORF-EE 0.18-0.215-0.25/0.035
Allergien: Allergies: Morphine (hives, hydromorphone ok), sulfa (rash), Fentanyl (hives)
Vorherige Impfungen: -

VAERS 2062893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 13,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 03.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Bell's palsy on left, happened around 1/15/,22, sought care 1/22/22, started on steroids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: Epilepsy
Andere Medikamente: -
Allergien: None known
Vorherige Impfungen: -

VAERS 2058059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 23.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Chest discomfort Dyspnoea Flushing Throat tightness

Symptomtext

Anaphylaxis to include difficulty breathing, throat closing, chest tightness and flushing of the face and upper body. Treatment consisted of Epinephrine (IM), Atrovent, Xopenex, Benadryl, Pepcid, Prednisone. She was admitted to ER for 4 hours for treatment observation and discharged on prednisone, pepcid, epi pen and benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Influenza, Tetanus, Anthrax vaccines

VAERS 2057517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: KS
Alter: 15,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Patient in vaccine clinic to receive 1st dose Pfizer Covid-19 vaccine, patient with her mother, stated she sometimes gets lightheaded with vaccines but has never fainted. After paperwork completed staff suggested that a quiet room and ability to lay down with vaccine would be best , staff, patient and mother walked to EMS room half way to EMS room tp get vaccine patient fainted and staff able to catch her with chair. Transported to EMS room per w/c. Able to lie down on cot and given ice packs and water when feeling better received Vaccine dose of Pfizer in L deltoid no issues. Remained in EMS room until 5:15 then ambulated w/o assist with mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: lightheaded w vaccines but never fainted

VAERS 2057218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: MD
Alter: 14,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 09.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Dizziness Electrocardiogram Headache Immunisation Incoherent Loss of consciousness Nausea Pyrexia Right atrial enlargement SARS-CoV-2 test

Symptomtext

lost consciousness; incoherent; dizzy; Right Atrial Enlargement; fever; nausea; headache; Booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 14-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) administered in arm right, administration date 09Jan2022 13:30 (Lot number: 33025BD) at the age of 14 years as dose 3 (booster), single for covid-19 immunisation. The facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. Relevant medical history included: "Asthma" (unspecified if ongoing); "Allergies" (unspecified if ongoing); "Known allergies: Latex" (unspecified if ongoing). Concomitant medications included: levocetirizine dihydrochloride (XYZAL); fluoxetine hydrochloride (PROZAC) 20 mg; VITAMIN D NOS. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0196, Location of injection: Arm Right), administration date: 12Jun2021, when the patient was 13 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0187, Location of injection: Arm Right), administration date: 22May2021, when the patient was 13 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (medically significant) with onset 09Jan2022 13:30, outcome "unknown", described as "Booster"; LOSS OF CONSCIOUSNESS (medically significant) with onset 10Jan2022 09:00, outcome "not recovered", described as "lost consciousness"; INCOHERENT (medically significant) with onset 10Jan2022 09:00, outcome "not recovered", described as "incoherent"; DIZZINESS (medically significant) with onset 10Jan2022 09:00, outcome "not recovered", described as "dizzy"; RIGHT ATRIAL ENLARGEMENT (medically significant) with onset 10Jan2022 09:00, outcome "not recovered", described as "Right Atrial Enlargement"; PYREXIA (non-serious) with onset 10Jan2022 09:00, outcome "not recovered", described as "fever"; NAUSEA (non-serious) with onset 10Jan2022 09:00, outcome "not recovered", described as "nausea"; HEADACHE (non-serious) with onset 10Jan2022 09:00, outcome "not recovered", described as "headache". The events "lost consciousness", "incoherent", "dizzy", "right atrial enlargement", "fever", "nausea" and "headache" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: electrocardiogram (EKG): (10Jan2022) was indicative of right atrial enlargement; COVID Nasal Swab: (10Jan2022) negative. Therapeutic measures were not taken as a result of loss of consciousness, incoherent, dizziness, right atrial enlargement, fever, nausea and headache. Prior to the vaccination, the patient was not diagnosed with COVID-19. It was also reported that since the vaccination, the patient had been tested for COVID-19. Clinical course: Patient was at school and lost consciousness, was incoherent, dizzy and needed to be wheeled to the nurse for dismissal. Urgent Care diagnosis from EKG was indicative of Right Atrial Enlargement. Scheduled a Cardiology Appointment for this Thursday at 3PM. Has accompanying fever, dizziness, and nausea and headache as well

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20220110; Test Name: EKG; Result Unstructured Data: Test Result:was indicative of Right Atrial Enlargement; Test Date: 20220110; Test Name: COVID Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma; Latex allergy
Andere Medikamente: XYZAL; PROZAC; VITAMIN D NOS
Allergien: -
Vorherige Impfungen: -

VAERS 2048385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

syncope- did not fall she was seated. vitals were stable. regained consciousness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: sleep apnea, resp failure, neck pain, degeneration of lumbar disc, diverticulitis
Vorgeschichte: see above
Andere Medikamente: Gabapentin, Duloxetine, Albuterol, Alvesco, Aspirin, Montelukast, Hydrochlorothiazide, amlodipine, Zanaflex, diclofenac gel 1%
Allergien: Ceftriaxone, Cephalexin, Mastisol Adhesive (gum Mastic storax-msal-alcohol), Acyclovir, Adhesive tape, Kepra, macrodantin, Zostavax, Contrast Dye (iodine).
Vorherige Impfungen: 02/25/2021 covid vaccine Pfizer

VAERS 2038227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: WI
Alter: 16,0
Geschlecht: M
Eingang: 16.01.2022
Impfdatum: 16.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blindness transient Eye movement disorder Heart rate increased Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

vasovagal syncope for 30 seconds, sweating, rapid pulse pale skin. gave patient juice and he felt better and walked out on his own after 15 minutes

Weitere VAERSDATA-Felder

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

VAERS 2038227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

schwer

Staat: WI
Alter: 16,0
Geschlecht: M
Eingang: 16.01.2022
Impfdatum: 16.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blindness transient Eye movement disorder Heart rate increased Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

vasovagal syncope for 30 seconds, sweating, rapid pulse pale skin. gave patient juice and he felt better and walked out on his own after 15 minutes

Weitere VAERSDATA-Felder

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

VAERS 2031997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: KS
Alter: 36,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Anaphylactic reaction Intensive care

Symptomtext

Anaphylactic after 15 minutes. Oral Benadryl-no relief, two epi pens 5 minutes apart, and one injection for solu-cortef. Pharmacy located inside hospital so patient was taken to ER. Pulse Ox and BP was monitored the whole time. Patient was admitted to ICU and on an EPI drip for 36 hours.

Weitere VAERSDATA-Felder

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

VAERS 2028864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: PA
Alter: 29,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fall Haemorrhage Head injury Loss of consciousness

Symptomtext

Patient received his booster dose at the pharmacy. Following administration he was instructed to wait the 15 minutes post vaccine to monitor for side effects. Within a couple minutes he felt faint and passed out. He was sitting on a chair and went to put his head between his legs and just kept going forward and fell on the ground. He hit his head on an end cap display in the store and started bleeding. EMTs were called to the scene and patient was transported to local hospital for additional care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Unknown at this time
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2026104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

Patient experienced syncope. Smelling salts utilized. Patient recovered and removed to lie on floor with feet elevated. He chatted calmly during a 30-minute recuperation before departing.

Weitere VAERSDATA-Felder

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

VAERS 2019625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: IL
Alter: 13,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Fall Head injury Hypotension Nausea Syncope Vision blurred

Symptomtext

About between 2 and 3 minutes after vaccination patient felt nausea, blurred vision followed by fall. Patient was in standing position at the vaccination table and just finished taking a picture of the vaccination record with the phone. Nausea, blurred vision and loss of consciousness happened quickly in a 3 seconds interval so patient did not get time to react or inform the parent and medical personnel which was sitting within 2 feet. Patient lost consciousness and fall hitting the head on concrete.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EMS personnel performed vitals monitoring and patient was diagnosed with syncope. EMS reported patient had low blood pressure. Fluid were administered and patient was kept in bed for about 20 minutes until blood pressure increased and stabilized. Patient was released home and no additional tests performed.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: No prescriptions or over-the-counter medications
Allergien: None
Vorherige Impfungen: -

VAERS 2019336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: NY
Alter: 24,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Patient received vaccine at 1:51 p.m. At 1:55 p.m. while in observation area, patient stated she felt dizzy and faint. Feet elevated, RRT called, patient remained alert and verbal. VS 87/56-97.9-50-16-99%RA. At 2:00 p.m. RRT responded, patient states she is feeling better. Patient remained in clinic for further observation. Patient given water and crackers. VS at 2:00 p.m. 106/65-97.9-86-18-100%RA. RRT exited clinic at 2:03 p.m. Patient states she ate today and that this happens when she gets blood drawn and with her previous vaccine. At 2:30 p.m. VS retaken in sitting position 102/59-97.9-60-18-100%RA. At 2:32 p.m. Vs taken in standing position 112/61-97.9-74-18-100%RA. patient with no c/o at this time. patient educated if any adverse reaction occurs to go to ER. Patient left clinic at 2:33 p.m. with no c/o.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: Penicillin G Benzathine
Vorherige Impfungen: Patient states with previous vaccine on 5/21/21

VAERS 2014145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

Vaccinated: 18:05 Reaction: 18:08 Patient was taken to medical bay for vaccine booster injection for history of syncope after 1st vaccine. He was released from medical bay to observation. While sitting, patient reported he "zoned out, started to shake and flipped out of chair" onto floor. He denied pain anywhere. Vitals: @18:09: 96/57, 89, O2 100% -> @18:14: 110/65 He was given water and within minutes was released to observation. Patient was stable and released from vaccination site @18:21 walking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known PMH
Vorgeschichte: No known PMH
Andere Medikamente: No known medications
Allergien: NKA
Vorherige Impfungen: -

VAERS 2010317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 26,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Dizziness Fall Flushing Hyperhidrosis Hyperventilation Presyncope

Symptomtext

5 minutes after 1st dose Pfizer, patient experienced high anxiety leading to vasovagal episode. Patient reported flushing/sweating and dizziness that led to patient falling forward from his chair, face first into the ground. Patient was transported to bay on wheelchair. Vitals: @16:41: 129/83, 75, 30 -> @16:44: 111/75, 78, 24 -> 17:12: 119/74, 84, 20 Vitals stable. Patient slowly regained consciousness, diaphoretic oriented with full motor control. Hyperventilation subsided. O2 stable. Patient given juice and crackers and continued resting. Patient was released from vaccination site once stable at 17:25.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known PMH
Vorgeschichte: No known PMH
Andere Medikamente: No known medications
Allergien: NKA
Vorherige Impfungen: -

VAERS 2000728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: IL
Alter: 24,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling cold Syncope Tachycardia Tremor Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Pt stated he was cold. Mild, Systemic: Shakiness-Mild, Systemic: Tachycardia-Mild, Additional Details: Pt fainted and woke up and sat back on the bench. We ran out to him and called 911 (per Pts request). He stated that he had not eaten or drank any water today. We gave him water, orange juice, and chips. By the time the ambulance got here his BP and blood glucose were stabilized. We had him sit for an additional 30 minutes before letting him leave. Everything was normalized by the time he left.

Weitere VAERSDATA-Felder

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

VAERS 1999877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain upper Nausea Syncope

Symptomtext

Vaccinated: 12:43PM Reaction: 12:45PM Patient reported syncope, nausea, stomach pain 2 minutes after vaccination Vitals: 126/73, 72, 20 Patient was given water and stated ""feels better"" @1300. Patient stable and released from vaccination site at 13:05 "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known illnesses at time of vaccination and up to one month prior
Vorgeschichte: Fibromyalgia
Andere Medikamente: No Known Medications
Allergien: No Known Allergies
Vorherige Impfungen: Pt reported dizziness, anxiety, severe headache, with improvement after observation and vitals wnl after 2nd Pfizer covid vaccin

VAERS 1996047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 31.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Feeling abnormal Syncope Vomiting

Symptomtext

13yr old female who were with her parents. Patient got her first shot of Pfizer Vaccine and fainted. Patient's eyes rolled upwards and was in a daze for about a minute. Patient then returned to her normal self and vomited about 100ml of clear emesis. Patient denied any chest pain or SOB. Said that she felt fine after she threw up. No distress noted after that. Patients mother said that the patient has a history of passing out with any needle work being done to her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Patient has a history of fainting and dizzy spell with any Lab Blood Draws or Care Involving Needles.
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1992826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: NC
Alter: 17,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness Tremor

Symptomtext

Patient's father reported that patient passed out and "violent shaking" (possibly chills) approximately 24 hours after receiving Pfizer booster on 12/28/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: no known drug allergies
Vorherige Impfungen: -

VAERS 1992278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Interchange of vaccine products Paraesthesia Presyncope Rash

Symptomtext

Janssen Primary Dose and Pfizer Booster 9mins post vaccination pt had a near syncopal event. Pt also developed dizziness, tingling in extremities, and a rash on her chest and neck. VITALS: 1900: 99% SPO2 78 HR 17 RESPIRATION BP 138/80 1925: 99% SPO2 66 HR 14 RESPIRATION BP 130/78 Pt was given 50mg PO benadryl @19:05 Pt stable and released from the vaccination site. Pt reported reaction to PCP immediately after leaving vaccination site . No further action taken at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Hx of abnormal pap smear, umbilical hernia and epigastric hernia.
Andere Medikamente: Medications: Paragard IUD
Allergien: NKA
Vorherige Impfungen: -

VAERS 1991915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: IL
Alter: 16,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Disorientation Eye movement disorder Fall Musculoskeletal stiffness Posture abnormal Seizure

Symptomtext

Patient & mom were discussing history of fainting with HPV vaccine prior to vaccination. COVID-19 (Pfizer (2)) dose 2 was administered to patient-seconds (~20-30) later patients head fell back. Mo thought he was joking. Patient then arched back, tensed up and fell out of his chair. Mom was closest to him and tried to protect his head from the wall/floor. Patients eyes were rolled back. Mom was blocking view, but appeared patient was mildly convulsing. Mom said she felt it. Patient was slightly disoriented but smiled one he was off floor. Whole event was less than 1 minute. Advised patient to stay for at least 20 minutes near pharmacy. They soon appeared fine after event. Patient had "hardly" eaten all day and ate cookies & chocolate milk after event. Mom was advised to call peidiatician in AM & ''seek emergent help if event occurred again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: Patient has history of fainting after HPV vaccine in 8th grade per mom. She does not have date or specifics of vaccine, other th

VAERS 1984903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 19,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fall Head injury Syncope Tenderness

Symptomtext

2mins post vaccination pt had a syncopal event and hit her head on the floor Vitals: 19:40 104/47, 69, 18, 100% -- > 19:50 101/49, 78, 18, 100 -- > 100/64, 83, 18, 100% No medications given, cold pack to head. Pt c/o tenderness to the back of head on palpation. No Visitble redness or bump on palpation of area. 20:00 pt sitting upright. 20:10 Pt VSS but still c/o pain/tenderness to affected area. NO dizziness or nausea while standing. Pt talking smiling, conversational w/ mom. 20:30 Pt stable and released from the vaccination site w/ parents. Recommended ER check to patient secondary to fall/tenderness on back of head

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH - Fainting w/ blood draws
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1982251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Paraesthesia oral Pruritus Stomatitis Throat irritation Throat tightness Tongue disorder

Symptomtext

1505: Pt walked to AR monitoring area after reporting that following 1st Pfizer (33025BD) pt started experiencing "symptoms like my allergy to shellfish, I am itching all over, theres tingling to my lips, my mouth feels funny and my throat is scratchy". Pt ambulated with very steady gait to gurney and placed on monitors. He is AxO x4, speaking in full and very clear sentences, RR even and unlabored. Pt denies any difficulty swallowing his own saliva. He also denies any chest pain, palpitations, dizziness, headache or SOB. LSCTA, -wheezing/stridor. Pt reports that in October 2021, pt developed a shellfish allergy where he experienced anaphylaxis which required him to seek medical care in the ER in which he experienced "my throat closed up" and he was treated and recovered. Pt denies any more episodes of those symptoms up until today. He denies having any throat closing and is very calm and cooperative. Call out to on call ER MD and verbal orders obtained for Cetirizine ODT now and pt tolerated very well. Will continue to monitor very closely. T 96.8 BP 139/87 HR 88 RR 20 SPO2 100 on Room Air 1512: Pt tolerated po Cetirizine odt and drinking water without incident. Continue to monitor. 1520: Pt reports that he feels his tongue becoming "thicker" and rated it 2/10 however he is still speaking in full and clear sentences. He continues to deny any respiratory symptoms or drooling and he is drinking the water at bedside without incident. Pt's tongue has no rash, lips do not feel swollen as per pt and he also denies any throat closing. Pt also indicates that he feels "very relaxed" and monitoring his HR. Pt continues to deny any chest pain or palpitations. States his overall symptoms he believes is not worsening but the itching is "getting better". Will continue to monitor closely for any worsening. 152/91 55 20 100 on RA 1528: Repeat VS as charted below. Pt states his "thick" tongue is now a "1.5/10" and the generalized itching has "gotten better". Pt reports that he remains with no new other symptoms. Still calm and cooperative, no acute respiratory distress. 153/94 61 20 100 on RA 1542: Pt reports that his overall symptoms are "back to normal" and the generalized itching is "minimal". Pt continues to deny any respiratory or cardiovascular symptoms. Remains free of any rash/hives or swelling and continues to speak in full and clear sentences. -stridor or wheeze. Call out to ER MD and report given. Advised pt to seek medical attention in the ED should his symptoms return, changes, worsens or becomes life threatening. EUA, VIS and educational tools reviewed with pt who verbalizes understanding. Pt road tested and ambulated with very steady gait. He remains in no acute respiratory distress, VSS. Pt released from vaccine clinic to drive himself back to work. Ambulated with very steady gait and in no acute distress. 149/97 63 18 100 on RA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sleep apnea HTN
Vorgeschichte: as above
Andere Medikamente: Amilodipine Lisinopril-hydroclorothiazide
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 1980196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: NH
Alter: 26,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Cold sweat Dizziness Hypotension Loss of consciousness Pallor Syncope

Symptomtext

History of syncope after receiving 1st dose of Pfizer but not second. Vaccine administered at 1259. Several minutes later, patient reported feeling 'woozy', and had LOC for approximately 5 seconds. He awoke without further symptoms. Skin was pale and clammy. BP 80/40, HR 52. He recovered to baseline within 15 minutes. No chest pain, shortness of breath, hives. BP returned to 100/55, HR 55. He was advised to follow up with his PCP regarding above.

Weitere VAERSDATA-Felder

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

VAERS 1975535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 31.12.1983
Beginn: 23.12.2021
Tage bis Beginn: 13.872,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Presyncope

Symptomtext

Patient had a vasovagal episode post vaccination @ 15:16. Patient appeared lightheaded, dizzy, Sweating. Patient was by herself Patient was instructed to lay down and elevate her legs patient was given Water Outcome:Recovered at 15:35 patient educated about ER precaution, signs of vasovagal reactions and what to do if exhibit symptoms again . Patient acknowledged understanding. Patient left after being observed for extra 15 minutes. Vital Signs: @ 15:16 Blood Pressure: 122/79 Pulse: 69 O2: 98% room air Vital Signs: @ 15:25 Blood Pressure: 125/85 Pulse: 66 O2: 98% Vital Signs: @ 15:30 Blood Pressure: 121/81 Pulse: 68 O2: 98%

Weitere VAERSDATA-Felder

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

VAERS 1975426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 17,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Presyncope

Symptomtext

Patient had a vasovagal episode post vaccination. Patient appeared light headed, sweating. Patient was accompanied by his mother, who consented for care. Patient was instructed to lay down and elevate his legs, but refused, instead sat on a chair. Patient was given Water, juice. Outcome: recovered fully, no sweating, no lightheadedness. Patient and his mother educated about ER precaution, to drink fluids lay down and elevate his legs if similar symptoms appeared. Patient and his mother acknowledged understanding. Patient has recovered @ 14:42. Patient left observation after being watched for another 15 minutes. Vital Signs: @ 14:20 Blood Pressure: 110/80 97 Pulse: 97 O2: 99% room air. Vital Signs: @ 14:28 Blood Pressure: 112/80 Pulse: 86 O2: 97 Vital Signs: @ 14:32 Blood Pressure: 112/80 Pulse: 82 O2: 98%

Weitere VAERSDATA-Felder

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

VAERS 1974648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

schwer

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Medium, Systemic: Hypotension-Severe, Additional Details: pt passed out in observation chair bp was low 11:47a 101/56 pilse 48, 11:52a 98/59 pulse 74, pt was put on back with feet elevated bp was unstable and continued to stay low even while on back, called emergency at 12:05pm arrived at 12:15pm and parmedics took patient outside to monitor

Weitere VAERSDATA-Felder

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

VAERS 1971499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 44,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Presyncope

Symptomtext

Patient had a vasovagal episode post vaccination. Patient appeared with feeling of dizziness, no paleness, alert and oriented. Patient was by himself Patient was instructed to lie down and elevate his leg. Patient was given Water, crackers. Outcome: Patient recovered without difficulties Patient educated about ER precaution. Patient acknowledged understanding. Patient has recovered and was observed for additional 15 minuttes. Patient left observation. Vital Signs: @ 8:40 Blood Pressure: 100/ Pulse: 54 O2: 98% room air Vital Signs: @ 8:43 Blood Pressure: 120/78 Pulse: 60 O2: 100% room air Vital Signs: @ 8:45 Blood Pressure: 121/80 Pulse: 62 O2: 98% room air

Weitere VAERSDATA-Felder

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

VAERS 1970989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: WA
Alter: 18,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Face injury Haemorrhage Head injury Pulse abnormal Skin laceration Syncope Unresponsive to stimuli Visual impairment

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient received 3rd dose of Pfizer Covid vaccine. Upon walking away from the vacccination area, patient fainted. Patient hit head and chin on base of the Target end cap. Immunizer RN, responded immediately. Assessed the patient, 1 inch laceration on lower left chin, bleeding, weak pulse. Patient said she was seeing black dots, so activated the EMS and called 911. Paramedics arrived and took over care. Called patient tonight to check on her, and her dad said she was in the ER.

Weitere VAERSDATA-Felder

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

VAERS 1967909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fall Presyncope

Symptomtext

Pt had a vasovagal episode post vaccination leaves without observation, then fell on carpet as walking outside, patient insisted on getting outside to get some fresh air. Found by poice officer, Nurse was called to assist outside, Patient brought in via wheelchair for observation. Pt denied any injury to head or body from fall, no swelling no bleeding no loss of consciousness . Patient was alert and oriented was able to communicate, no pallor, no Shortness of breath. Patient was by herself, then patient called her mother who came to assist. Pt declined vital signs to be taken. We were able to take O2 sat and pulse rate. Vital Signs: @10:30 Blood Pressure : Patient refused Pulse: 74 O2: 98% room temprature Patient and parent educated about vasovagal symptoms, signs and symptoms of when to seek medical care or when to seek emergency care. Pt was given water, crackers. Patient was observed for another 15 min. Patient acknowledged understanding. Outcome: Patient recovered and left without assistance with her mother.

Weitere VAERSDATA-Felder

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

VAERS 1963607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 14,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction Syncope

Symptomtext

Immediately after vaccination @16:47 pt reported that he was light headed and had "fainting like symptoms". Vitals: 109/69, 77, 18, 100%, 98.7F Pt stable and released from the vaccination site @17:27

Weitere VAERSDATA-Felder

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

VAERS 1963525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Syncope

Symptomtext

Pt received Janssen Primary and Pfizer booster. 5 mins post vaccination pt had a syncopal episode w/ associated flushing/sweating and dizziness. Vitals: 133/81, 78, 12 -- > 124/81, 78, 12 Pt given water and advised the patient that the pt's friend should drive home. Pt observed for and additional 10 mins. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Palpitations, Fibroids, Iron Def Anemia, hx of colonic polyps, Hx of laparoscopic cholecystectomy, Low TSH level, Menorrhagia, Tobacco dependency, Mild benzo use disorder, neuralgia and neuritis, Lumbago, hereditary and idiopathic peripheral neuropathy, and allergic rhinitis, GERD, Fibromyalgia, Graves Disease, Asthma.
Andere Medikamente: Ferrous Sulfate (IRON) 325 (65 Fe) MG TABS Take by mouth twice daily pantoprazole (PROTONIX) 40mg EC Tab Indications: Gastroesophageal reflux disease, unspecified whether esophagitis present Take one Tab by mouth daily 30 minutes before
Allergien: Allergies: PCN (Rash), Amoxicillin (Rash), shrimp (Rash), Ibuprofen (Rash), Other unknown medication (swelling)
Vorherige Impfungen: -

VAERS 1959117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: CA
Alter: 76,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Eyelid ptosis Facial paralysis Facial paresis Hypoaesthesia

Symptomtext

Patient brought into Covid Observation Area after reporting Left facial/jaw weakness and numbness, 15 minutes after receiving Pfizer Booster. Noted Left eye and Left facial droop. Daughter states patient has history of TIA 2004, with residual Left sided weakness. No deficits noted to Left arm, left leg, strong grips to both hands, positive push pull to both feet. Patient alert and oriented x 4, speech clear. Denies any chest pain or shortness of breath. 10:40am: VS: Temp 96.9, BP 130/71, HR 59. RR 18, 100%. 10:45: Patient reports improving numbness to left side of face, but reports left arm feeling numb. Noted strong grips bilaterally. Blood pressure cuff removed from left arm and placed on right arm. VS: BP 152/70, HR 57, RR18, 02 sats 100% RA. 10:46am- Call placed to on call ED physician, Dr. Informed of patient symptoms above. Per Dr, have patient evaluated in ER via family transport or 911. Daughter states she is able to drive patient to ED for further evaluation. Explained importance of early intervention due to patient history and symptoms she is experiencing. 10:50am: VS: BP 159/66, HR 57, RR 20, 02 sats 100% RA. 10:51am- Patient discharged. Family to transport patient to ED via via private vehicle for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: See below
Vorgeschichte: Angina, h/o TIA 2004, Hyperlipidemia, Hypothyroidism, Depression, Osteoarthritis of both knees, Prediabetes
Andere Medikamente: Levothyroxine, Atorvastatin, Nabumatone, Gabapentin, Trazadone, Prednisone, Vitamin D3
Allergien: Clindamycin, Naproxen
Vorherige Impfungen: -

VAERS 1955950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

schwer

Staat: MA
Alter: 54,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anaphylactic reaction

Symptomtext

Patient started experiencing signs and symptoms of an anaphylactic reaction and received an Epi-Pen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Patient was transported to the hospital for further evaluation
Aktuelle Erkrankungen: Unknown
Vorgeschichte: unknown
Andere Medikamente: None
Allergien: Allergies to medications and food. No previous reaction to CoViD19 Vaccine
Vorherige Impfungen: -

VAERS 2675318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: PR
Alter: 40,0
Geschlecht: F
Eingang: 22.08.2023
Impfdatum: 21.03.2021
Beginn: 11.04.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: IM / LA

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

Blood cholesterol increased Chest pain Computerised tomogram abdomen abnormal Diarrhoea Hepatic cyst Lipids Magnetic resonance imaging Pancreatic cyst

Symptomtext

For Chest pain, high colesterol, prescription for Creator 10 mg at the beginning of 2023, on july the colesterol level was decreased to normal range. Diarreas symptoms, MTI and CT were performed with finding in liver and pancreas in 2022 and 2023, ( cysts of 1 cm) . The cysts is in monitoring every year since 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Lipid panel test, MRI & CT
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chest pain, high colesterol LDL, cyst in pancreas and liver
Andere Medikamente: N/A
Allergien: Salmon
Vorherige Impfungen: -

VAERS 2573496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: HI
Alter: 35,0
Geschlecht: M
Eingang: 01.02.2023
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SC / LA

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

Blood cholesterol increased Blood test abnormal Blood triglycerides increased Electrocardiogram normal Limb discomfort Paraesthesia Tenderness

Symptomtext

The very next I started having tingling in my left leg and then it gave me the feeling like I slept on it. These feeling continued and then in March I started having issues feeling like my heart was tender. The feeling in my left leg continued along with the tender feeling in my heart and then I started having discomfort and tingling in my arm. The next day I went to the doctor, and I was told I should've gone to the ER until I saw a doctor because it could've been a stroke. He did an EKG and it was fine and then he did bloodwork. The doctor said he found high cholesterol and high triglycerides range was off. The doctor told me I was too young for medication, so he gave me a nutrition's to try and fix the issue naturally. I changed my diet over 5 months and exercise on paper it looked like it fixed everything but tested me again the numbers were even high 150 and now its 173. The doctor suggested 6 more months of a strict diet and more exercise to see if it would improve. I am set to go back to the doctor next week so I will call back to give an update.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EKG & Bloodwork
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2551325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: NJ
Alter: 68,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 13.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

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

Hypoaesthesia Laboratory test normal Paraesthesia

Symptomtext

Tingling in right leg and numbness in right foot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: tested for blood clot - negative
Aktuelle Erkrankungen: No
Vorgeschichte: Tingling in right leg and numbness in right foot.
Andere Medikamente: Telmisartan & Hydrochlorothiazide 80mg/25mg Amlodipine Besylate 10mg Rosuvastin Calcium 5mg Low Dose Aspirin 81mg Vitamin D3 50mcg (2000 IU) Centrum Silver Women PreserVision AREDS 2 Ester-C Loratadine 10mg/Antihistamine
Allergien: None
Vorherige Impfungen: -

VAERS 2550237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: AZ
Alter: 21,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Amenorrhoea Autoimmune thyroiditis Colonoscopy normal Fatigue Hepatic enzyme abnormal Influenza Palpitations SARS-CoV-2 test negative Weight increased

Symptomtext

The day after the vaccine started feeling severe flu symptoms; Was worse than previous COVID-19 vaccine reactions; Took a COVID-19 test and it was negative; Reaction lasted for 2 weeks; Over the next couple of months started having heart palpitation's with extreme fatigue and weight gain, GI problems and stopped getting period; Went to doctor to rule out Pregnancy; Doctor ran blood testing and it was determined that Thyroid levels were off; Was sent to Endocrinologist and was diagnosed with Hashimoto's Syndrome; Was prescribed levothyroxine, propranolol and started taking magnesium; Was given a Colonoscopy because of new Gastro problems.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: COVID-19 test negative; Blood testing determined elevated Liver enzymes; Colonoscopy normal.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: CLARITIN D
Allergien: NEOSPORIN
Vorherige Impfungen: -

VAERS 2548858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 03.01.2023
Impfdatum: 30.12.2021
Beginn: 08.12.2022
Tage bis Beginn: 343,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Chills Cough Fatigue Feeling abnormal Headache Hypersomnia Illness Influenza Mobility decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

I received my Pfizer COVID-19 booster on 12/30/2021. On 12/08/2022, I began to feel like I had a sickness coming on. On 12/9/2022, I started to feel bad at around noon and went home at 3 PM. I had chills, headache, and fever. I took some ibuprofen for the headache and some OTC cold/flu medicine, because I thought I just had the flu. On 12/10/2022, I didn't get out of bed until 11 AM. The symptoms I had were pretty much the same as they had been on 12/9/2022, and I spent most of the time in bed. I would get occasionally get up and move around, but I usually wasn't up long. On 12/11/2022, I took a home antigen test and got a positive result. I slept for the rest of the day. On 12/12/2022, my chills were gone, and my symptoms began to subside, though I still had a headache and fever. My symptoms continually got better for the rest of the week, though the weakness persisted. On 12/13/2022, I had a telehealth visit with my doctor, who prescribed PAXLOVID, which I began taking on 12/14/2022. On 12/13/2022 and 12/15/2022 I took the test again and got positive results. I took another test on 12/17/2022, and the result was negative. By the time I tested negative on 12/17/2022, all of my symptoms were gone, though I still had fatigue and weakness. At the time of this writing, the weakness is pretty much gone, but I still get an occasional headache and an intermittent cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 12/11/2022, 12/13/2022, 12/15/2022 home antigen tests positive results; 12/17/2022 home antigen test negative result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma.
Andere Medikamente: DULERA inhaler; levalbuterol inhaler; rosuvastatin; multivitamins; vitamin C; glucosamine; vitamin D; vitamin B; iron.
Allergien: None.
Vorherige Impfungen: -

VAERS 2540847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: VA
Alter: 37,0
Geschlecht: M
Eingang: 22.12.2022
Impfdatum: 17.12.2021
Beginn: 31.07.2022
Tage bis Beginn: 226,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Cough Discomfort Fatigue Headache Illness Mobility decreased Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On 07/31/2022 I was or felt heavy and tired on 08/01/2022 I had a headache and started coughing on 08/02/2022 I took a COVID19 test which resulted in positive. I had a severe illness, fever, body pain, coughing and remained at home in bed for a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 test result was positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2533258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 17.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Alopecia Anxiety Chest discomfort Dizziness Dyspnoea Fatigue Feeling abnormal Headache Laboratory test Nausea Neuropathy peripheral Pyrexia Rash

Symptomtext

Fever- normal fever for several days after booster, then on 12/24 the fever was 104? and developed facial rash and rash on leg. 12/29- dr visit prescribed cephalexin. 1/2/22- ED visit and admitted to hospital. Fever, facial rash, headache, lightheaded.. Discharged 1/4/22. 1/12/22 ED- admitted to hospital. Chest pressure, SOB, nausea, lightheaded, headache, extreme fatigue facial rash. Released 1/13/22. Follow up with PCP weekly, ophthalmology, rheumatology, dermatology, endocrinology I still suffer from brain fog, LE neuropathy, extreme fatigue, anxiety, hair loss, nausea, dizziness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: Too many to write. Willing to send chart
Aktuelle Erkrankungen: Not an illness, but had laser facial the day before Covid booster
Vorgeschichte: Asthma
Andere Medikamente: Protonix, prevastatin, famodidine, albuterol
Allergien: Codeine, iv iodine, phenobarbital, sulfa, morphine, hydrocodone, ondansetron, cipro, metronidazole, hydroxizine, avocado, banana, shrimp
Vorherige Impfungen: -

VAERS 2499575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: ID
Alter: 51,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 04.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Amnesia Blood test COVID-19 Condition aggravated Depression Electroencephalogram Feeling abnormal Magnetic resonance imaging Suicidal ideation Urine analysis

Symptomtext

I had already been diagnosed with depression in 2021 after my COVID-19 infection. But in early 2022 after my first booster, I began experiencing suicidal ideation. After my infection in December 2020, I was subsequently diagnosed with depression anxiety. As the months continued and I received the vaccines and the booster, my depression worsened. I have experienced a memory loss that began after dose 3. I have seen the neurologist regarding my memory, and I was scheduled to have a memory test. But I no longer live in that city. I have also experienced a severe case of COVID-19 fog.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MRI, June2022; EEG, June2022; blood panels, January2022; Urinalysis, January2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Depression; Epilepsy; Anxiety
Andere Medikamente: TEGRETOL; KEPPRA; naproxen; LEXAPRO; calcium
Allergien: N/A
Vorherige Impfungen: -

VAERS 2491764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 20.04.2022
Beginn: 01.09.2022
Tage bis Beginn: 134,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Dyspnoea Electrocardiogram

Symptomtext

In September of 2022, no changes in my medications have been done. I was given an EKG and the doctors did not give me any definite diagnosis. I had some shortness of breath, I had some problems with my knees, and I also had received a different vaccination as well nothing to do with COVID-19. My symptoms have not really improved and unfortunately it is very sudden when it comes on and then it will go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 21SEPT2022 EKG Test - No Diagnosis Given
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes;
Andere Medikamente: Metformin; Lipitor; Lisinopril
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2439759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: VT
Alter: 52,0
Geschlecht: M
Eingang: 10.09.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain upper Ageusia Anosmia Arthralgia Chest pain General physical health deterioration Inappropriate schedule of product administration Irritability Lymphadenopathy

Symptomtext

swollen lymph nodes; stomach pain; irritability; my sense of taste and smell is gone after the 2nd shot; my sense of taste and smell is gone after the 2nd shot; Overall declined in health; joint pain; chest pain; Inappropriate schedule of vaccine administered; 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 52-year-old male patient received BNT162b2 (BNT162B2), on 30Dec2021 as dose 2, single (Lot number: 33025BD) at the age of 52 years, in left deltoid for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), in 2021 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Had COVID 6 weeks before being forced into getting first shot. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; LOT: 32030BD; NDC, EXP: Unknown; Anatomical site of vaccination: right deltoid), administration date: 23Oct2021, when the patient was 52-year-old, for COVID-19 Immunization, reaction(s): "Overall declined in health since he was forced to get these shots". The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 30Dec2021, outcome "unknown", described as "Inappropriate schedule of vaccine administered"; CHEST PAIN (non-serious) with onset 31Dec2021, outcome "not recovered"; ARTHRALGIA (non-serious) with onset 31Dec2021, outcome "not recovered", described as "joint pain"; LYMPHADENOPATHY (non-serious), outcome "not recovered", described as "swollen lymph nodes"; ABDOMINAL PAIN UPPER (non-serious), outcome "not recovered", described as "stomach pain"; IRRITABILITY (non-serious), outcome "not recovered"; AGEUSIA (non-serious), ANOSMIA (non-serious), outcome "not recovered" and all described as "my sense of taste and smell is gone after the 2nd shot"; GENERAL PHYSICAL HEALTH DETERIORATION (non-serious), outcome "unknown", described as "Overall declined in health". Therapeutic measures were taken as a result of arthralgia. Therapeutic measures were not taken as a result of chest pain. Additional information: The patient was treated with 300 mg Acetamenophen for arthralgia, which he takes when he aches so bad he can't stand anymore. The patient wants to know how long the side effects will last. He states he "was pretty much experiencing all of them". 9 months and he was getting joint pain chest pain, swollen lymph nodes, stomach pain, irritability, its all still there. Overall declined in health since he was forced to get these shots. He had tried to follow up with them (HCP) they just dont want to know nothing about it, they cant tell him anything, they said he would be all right. They keep telling him the shot was safe". Caller stated that he was wondering the longevity of the side effects. He also noted that he really truly wish he had never been poked. Caller also reported having lost his sense of taste and smell after the 2nd shot. Sense of taste and smell is pretty much gone: Started right after he got the shot. Sense of taste and smell came back after that and was pretty good and everything was normal. Everything was pretty good after being forced to take first shot. Pretty much as soon as he got second shot, sense of taste and smell were completely gone again. Patient was still experiencing chest pain now, all day long, every day. Sometimes are a little worse than others. Joint pain was still the same. Has arthritis, which has excelled since he has gotten that shot. Has been real bad since then. Caller stated that these side effects have been ongoing for 9 months. No visits of emergency room and physician office. No prior vaccinations within 4 weeks. No AEs prior vaccinations. No Family medical history relevant to AEs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Had COVID 6 weeks before being forced into getting first shot)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: MI
Alter: 18,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 21.12.2021
Beginn: 30.07.2022
Tage bis Beginn: 221,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest X-ray normal Cough Dyspnoea Electrocardiogram normal Oropharyngeal pain Pain SARS-CoV-2 test positive Tachycardia Tachypnoea

Symptomtext

Discharge Provider: Private, DO Primary Care Provider at Discharge: Private, MD Admission Date: 7/30/2022 Discharge Date: 8/1/2022 HOSPITAL COURSE: Patient is a 19 y.o. woman with a history significant for chronic lung disease of infancy, Moebius syndrome, Pierre Robin sequence, and adrenal insufficiency who presented to ED on 7/30/22 with 1 day history of sore throat, nonproductive cough, body aches, SOB and a positive home COVID test. In the ED, she was tachycardiac with HR 120, tachypnea > 30 and afebrile. EKG was insignificant and chest X-ray showed no acute cardiopulmonary abnormalities. She was given fluids, one dose of remdesivir in the ED, and started on hydrocortisone 15 mg q6h as part of her stress dosing regimen for adrenal insufficiency. She was admitted and management was continued on the medicine floors. Admission remained uncomplicated and patient's respiratory status improved. Two doses of remdesivir were administered during admission. Patient and mother were informed that the course of monoclonal antibodies could be completed in outpatient infusion clinics if needed. On 8/1/22, patient was medically and vitally stable for discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Pierre Robin syndrome Syndactyly of fingers Talipes equinovarus Syrinx, persistent central canal (HCC) GERD (gastroesophageal reflux disease) MRSA (methicillin resistant Staphylococcus aureus) colonization Allergic rhinitis, cause unspecified CLD (chronic lung disease) Adrenal insufficiency (HCC) Short stature (child) Hx of neurological testing - DO NOT EDIT Dependence on enabling machine Feeding by G-tube (HCC) Severe OSA on CPAP Other speech disturbance Sensorineural hearing loss (SNHL) of both ears Constipation, unspecified constipation type Vomiting, intractability of vomiting not specified, presence of nausea not specified, unspecified vomiting type Mobius syndrome Multiple cranial nerve palsies Micrognathia Hypernasality Generalized anxiety disorder Cleft palate Articulation disorder Arterial hypotension Dysphagia, oropharyngeal phase Pneumonia due to COVID-19 virus Adjustment disorder with depressed mood
Andere Medikamente: acetaminophen (TYLENOL) 32 MG/ML suspension albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization budesonide (PULMICORT) 0.5 MG/2ML nebulizer solution Enteral Nutrition Supplies (COMPAT ENTERAL FEEDING PUMP) MISC Feeding Tubes - Tubing
Allergien: VancomycinRash
Vorherige Impfungen: -

VAERS 2388253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: GA
Alter: 46,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 12.01.2022
Beginn: 05.07.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: SYR / LA

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

Balance disorder Condition aggravated Headache Impaired work ability Migraine Vision blurred

Symptomtext

Starting 07/05/2022, I got this massive headache that is like a migraine. It spanned from the back of the head to the front. I had to take off work for it. Also, I experienced blurred vision and imbalance issues. After I took a nap, the headache subsided. Unsure if its related to heat or not.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GOUT; tension headaches
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2370546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Bedridden Illness Impaired work ability Migraine Myalgia Vertigo

Symptomtext

Vertigo, Migraine, Myalgias and bedridden for 24 hrs began at time indicated above resulting in work loss and illness lasting for 3-5 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Raynauds, Hyperhidrosis
Andere Medikamente: Vit.D; MVI
Allergien: NKA
Vorherige Impfungen: Pfizer Covid-19 dose #2

VAERS 2360956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: MD
Alter: 61,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 04.01.2022
Beginn: 16.05.2022
Tage bis Beginn: 132,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Headache Impaired work ability Influenza like illness Influenza virus test negative Malaise Mobility decreased Oropharyngeal pain Pain Productive cough Pyrexia SARS-CoV-2 test positive Streptococcus test negative Tachycardia

Symptomtext

COVID-19 symptoms started around 1:30/2 AM 05/16/22; tested positive on 05/17/22. I felt achy, had fever, sore throat, headache, flu-like symptoms, strep-like symptoms, and COVID-19 symptoms. I called my PCP and they said I needed to come in and be tested for all 3 (Covid, strep, flu) and all came back negative except COVID-19. I had a fever that went up to 103 and didn't break until that Thursday 05/19/22. It started at 101 and the highest was 103. They put me on medication PAXLOVID for twice a day and I started that on 05/17/22 and I was on it the whole time but fever still went up. I had a cough and the cough was a wet cough and that lingered for another week and I had coughing fits. I had no difficulty breathing, and I was checking pulse ox and that was OK but I became tachycardic. Pulse was in the 90s and usually it's in the 60s or 70s and it was very rapid. I had fever, chills, and cough, but the cough took the longest to go away. I was bed ridden and couldn't go to work like that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 (positive), Flu (negative), Strep (negative) 05/17/22.
Aktuelle Erkrankungen: None
Vorgeschichte: Graves Disease; Hyperthyroidism
Andere Medikamente: Vitamin D; vitamin C; methimazole; metoprolol
Allergien: Penicillin; sulfa
Vorherige Impfungen: -

VAERS 2263137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 20.12.2021
Beginn: 06.04.2022
Tage bis Beginn: 107,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Dizziness Endodontic procedure Fatigue Feeling abnormal Impaired work ability Influenza like illness Mobility decreased Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had got COVID-19 started feeling bad 4/6/22 but I also had a root canal, so I thought that's why I felt bad. By Saturday and Sunday, I couldn't get out of bed, really bad congestion, sore throat, tired, achy. It felt like a really bad flu I was in bed from Saturday through Monday and wasn't able to work until Tuesday. I had dizzy spells but didn't lose my sense of smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: At home COVID-19 test on Monday - positive PCR COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Slight Nut Allergy Shellfish Digestive Intolerance for mushrooms and mushroom products Lactose Intolerant
Vorherige Impfungen: Body aches after my 2nd Pfizer shot

VAERS 2261630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: NY
Alter: 25,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 28.12.2021
Beginn: 25.04.2022
Tage bis Beginn: 118,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective Dyspnoea Facial pain Lethargy Rhinorrhoea

Symptomtext

Rebound COVID; Rebound COVID; lethargy; Shortness of breath; Post-nasal drip; Facial pain; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 25-year-old male patient received BNT162b2 (BNT162B2), on 28Dec2021 at 09:00 as dose 3 (booster), single (Lot number: 33025BD) at the age of 25 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "WPW" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series, unknown manufacturer), for Covid-19 immunization. The following information was reported: FACIAL PAIN (non-serious) with onset 25Apr2022 at 20:00, outcome "recovering"; RHINORRHOEA (non-serious) with onset 25Apr2022 at 20:00, outcome "recovering", described as "Post-nasal drip"; COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant) all with onset 25Apr2022 at 20:00, outcome "recovering" and all described as "Rebound COVID"; DYSPNOEA (non-serious) with onset 25Apr2022 at 20:00, outcome "recovering", described as "Shortness of breath"; LETHARGY (non-serious) with onset 25Apr2022 at 20:00, outcome "recovering". Therapeutic measures were not taken as a result of covid-19, drug ineffective, lethargy, dyspnoea, rhinorrhoea, facial pain. Clinical Course:Adverse event: "Rebound COVID". Redevelopment of symptoms (lethargy, shortness of breath, post-nasal drip, facial pain) 5 days following completion of treatment course; Sender's Comments: Based on available information a contributory role of BNT162B2 to the reported events Covid-19 and Drug ineffective cannot be totally excluded as efficacy of a drug varies from individual to individual depending upon the immune status. As with any vaccine, vaccination with BNT162B2 may not protect all vaccine recipients, so the expectedness of covid-19 and drug ineffective is : expected. The case will be reassessed further upon receipt of additional information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: WPW syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: IL
Alter: 60,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Confusional state Dyspnoea Dysstasia Fatigue

Symptomtext

Very fatigue, shortness of breath, and confusion. I could not stand up very long for about 5 to 7 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: COPD Asthma; Cardio Valve Replacement; Artificial Vertebrae; Stomach Ulcers; Severe Acidic Disease; Severe Bone Degeneration Disease; CPAP; Gastritis
Andere Medikamente: Allegra Melatonin 10mg Famotidine 20mg Nexium Generic Warfarin Orphenadrine Citrate 100mg Nebulizer Budesonide Lonsulucast Cough Suppressant Trelegy Inhaler for COPD Metoprolol Tranter tine Potassium Chloride 10nlq Magnesium Oxide 400mg H
Allergien: Avocado; Bandaids; Cefaclor Capsules; Azferol; Cephalexin; Erythromycin; Gentamicin; Metronidazole; Oxycodone; Pravastatin; Prednisone; Simvastatin; Sulfa drugs; ZPack
Vorherige Impfungen: -

VAERS 2220992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Chest pain Electrocardiogram normal Hypoaesthesia Paraesthesia Paraesthesia oral

Symptomtext

Before I got my vaccine, they asked if I had an adverse events prior to any other vaccines. I did tell them about my experiences with my first and second dose. They tried to talk me out of getting the vaccine and tried to get me to switch vaccine manufacturer. I denied changing the vaccine. Within 5-10 mins my face and mouth started to tingle. After about an hour I started to have the severe chest pain on left side which is the same side as the vaccination. The chest pain started to increase so I made an appointment to see my doctor. They did an EKG but I wasn't having the chest pain at that moment so they could not confirm anything was wrong. They told me I was having an anxiety attack and sent me home. I tried to explain that the chest pains would come on at random times. For example I went to the grocery store to buy chicken then the severe chest pain would come on. The chest pain lasted about 1.5 weeks. I am still experiencing the numbness and it comes at sporadic times and lasts for about 5-45 mins.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 01/10/2022: Normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, Zyrtec
Allergien: Seasonal Allergies; Peanuts
Vorherige Impfungen: Pfizer First Dose 04/24/2021; Second Dose 05/15/2021; Completed VAERS report for both.

VAERS 2198341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: TX
Alter: 59,0
Geschlecht: M
Eingang: 25.03.2022
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Mobility decreased Pain

Symptomtext

I am not able to move my arm stretching back.; has intermittent pain down to his elbow and wrist in his left arm; It has been several months & I have moderate to severe pain in the shoulder that radiates to the elbow/has intermittent pain down to his elbow and wrist in his left arm; It has been several months & I have moderate to severe pain in the shoulder that radiates to the elbow/whenever he reaches behind him it causes him pain in his left shoulder; It has been several months & I have moderate to severe pain in the shoulder that radiates to the elbow/whenever he reaches behind him it causes him pain in his left shoulder; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 59 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Dec2021 (Lot number: 33025BD) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Lot: EIV6207, Expiry: Unknown, Site of administration: Left Arm), administration date: 17Mar2021, when the patient was 58 years old, for Covid-19 Immunization; Bnt162b2 (Lot: 33025BD, Expiry: Unknown, Site of administration: right arm), administration date: 07Apr2021, when the patient was 59 years old, for Covid-19 Immunization. The following information was reported: ARTHRALGIA (non-serious), PAIN (non-serious) all with onset 29Dec2021, outcome "not recovered" and all described as "It has been several months & I have moderate to severe pain in the shoulder that radiates to the elbow/whenever he reaches behind him it causes him pain in his left shoulder"; ARTHRALGIA (non-serious) with onset 07Mar2022, outcome "not recovered", described as "It has been several months & I have moderate to severe pain in the shoulder that radiates to the elbow/has intermittent pain down to his elbow and wrist in his left arm"; MOBILITY DECREASED (non-serious), outcome "unknown", described as "I am not able to move my arm stretching back."; ARTHRALGIA (non-serious) with onset 07Mar2022, outcome "not recovered", described as "has intermittent pain down to his elbow and wrist in his left arm". Additional information: Patient reported whenever he reaches behind him it causes him pain, and he also has been having intermittent pain down to his elbow and wrist in his left arm. Caller clarifies that the pain in his left shoulder whenever he reaches behind him started the morning after he got the booster Covid vaccine. The pain stayed the same for a long time, then just recently he started getting intermittent pain going down to his elbow and wrist in his left arm as well. Pfizer Covid 19 Vaccine 1st dose received on 17Mar2021 in right arm. He had a surgery scheduled for 13Jan2022 and he wasn't sure if they were going to make him get the booster in order to do the surgery, so he went ahead and got the booster just in case. States the pain in his left shoulder was there the next day when he woke up, he just attributed in to the shot. No prior Vaccinations (within 4 weeks), prior to the first administration date of the suspect vaccine(s). Patient made the statement that he tries to avoid moving too much because he had a 3rd back surgery since last June, on 13Jan2022. Time the vaccination was given early afternoon. Vaccination facility type was pharmacy. Additional Vaccines Administered on Same Date of the Pfizer Suspect was none. AE(s) following prior vaccinations was none. Relevant Tests were none. AE(s) did not require a visit to Emergency Room or Physician Office. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History:Patient Other Relevant History 1: None.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: WA
Alter: 39,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 12.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site reaction Mobility decreased

Symptomtext

Muscle that injection was given near is extremely limited in mobility. Arm is not sore as it is at the needle site typically, it's a range of motion issue. I cannot move my arm certain ways since the booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Sertraline
Allergien: Amoxicillin, Penicillin
Vorherige Impfungen: -

VAERS 2193871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: VA
Alter: 52,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 22.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / RA

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

Condition aggravated Frustration tolerance decreased Investigation Joint swelling Peripheral swelling

Symptomtext

Swelling in hands are still there and it is frustrating; Joints swollen in wrist, hands, fingers, ankles and pretty much all joints, except elbow and shoulders was reported as worsened; swelling in every joint in her body/ Joints swollen in wrist, hands, fingers, ankles and pretty much all joints, except elbow and shoulders; Swelling in hands are still there and it is frustrating; began experiencing swelling in her bilateral knees; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 52 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 22Dec2021 (Lot number: 33025BD) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Gestational Diabetes" (unspecified if ongoing), notes: Gestational Diabetes 10 years ago and it has resolved.; "She has allergy, slight, to garlic", start date: 2020 (unspecified if ongoing); "diagnosed allergies" (unspecified if ongoing); "obesity" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, Lot EW0158, expiration is unknown, Anatomical Location: Injected into left arm), administration date: 15Apr2021, when the patient was 51 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, Lot EW0173, expiration is unknown, Anatomical Location: Injected into left arm), administration date: 10May2021, when the patient was 51 years old, for COVID-19 immunization; Flu (Manufacturer: Unknown, Lot Number: Unknown Route, Anatomical Location: Injected in left arm. , No. of Previous Doses: not provided (with in four week).), administration date: 30Nov2021, when the patient was 52 years old, for Immunization. The following information was reported: JOINT SWELLING (non-serious) with onset 26Dec2021, outcome "recovering", described as "began experiencing swelling in her bilateral knees"; JOINT SWELLING (non-serious) with onset 11Jan2022, outcome "not recovered", described as "swelling in every joint in her body/ Joints swollen in wrist, hands, fingers, ankles and pretty much all joints, except elbow and shoulders"; PERIPHERAL SWELLING (non-serious) with onset 11Jan2022, outcome "not recovered", FRUSTRATION TOLERANCE DECREASED (non-serious), outcome "unknown" and all described as "Swelling in hands are still there and it is frustrating"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "Joints swollen in wrist, hands, fingers, ankles and pretty much all joints, except elbow and shoulders was reported as worsened". The events "began experiencing swelling in her bilateral knees", "swelling in every joint in her body/ joints swollen in wrist, hands, fingers, ankles and pretty much all joints, except elbow and shoulders", "swelling in hands are still there and it is frustrating" and "joints swollen in wrist, hands, fingers, ankles and pretty much all joints, except elbow and shoulders was reported as worsened" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of joint swelling, joint swelling, peripheral swelling, condition aggravated. Additional information: She had Knee swelling on both knees and went to an orthopedist because she thought she had been skiing and the swelling might have something to do with that. She saw him on 06Jan2022, and he told her to take ibuprofen and rest and don't exercise, then follow up in 2 weeks. Then, she went for follow-up and then between time she saw and follow up, wrist, hands, fingers, ankles, and pretty much all of the joints except elbow and shoulders all were swollen. Knee swelling improved after 3 weeks of steroids. This started 2 weeks after her knee, probably. It was very subtle on 11Jan2022, and then it got really bad on 16Jan2022 and could not see her bones in her hands. It has been 8 weeks later. She said she would have rather had COVID. She has not had COVID and had friends that did not have swelling 8 weeks later. She went to the Orthopedist twice and had an initial and follow up to which he said to go to a Rheumatologist and she made an appointment with one. It is really hard because maybe a lot of people are having adverse reactions. She gave her a week of Steroids of a taper dose, 6,5,4,3,2,1. The rheumatologist said it was too high of a dosage and too drastic of change. The very next day, they swelled up again. Even though it was a high dose, she felt completely normal. On 11Feb2022, she started her back on steroids and she is still swollen and going for another follow up. The one she is taking now is Prednisone. She was taking 10mg a day and now she increased to 20 and it is still not doing it. It is in a pharmacy vial with no lot or expiration. She just thinks it is not a high enough dose. Initially she wanted her to take 2 of the 5mg and does not know what she will do now, since she is still swollen. She was supposed to take 10mg, and she said email her if swelling is not going down, so she wrote her back and said to increase to 20mg, or 4 tablets. The initial steroid from her Primary Care was Methylprednisolone, 4mg, 21 of those. First day, she was to take 6, and then taper down from there. It was a blister pack. She threw it away and no longer has the lot or expiration or a sample to send. It was sealed and intact. She gave her the 60 count, because she knew she would be tapering her. List other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebro-spinal fluid culture, pleural fluid culture, urine culture, diagnostic imaging, (e.g., chest X-ray, MRI)Test: Date: Result: Units: Normal Range: Low: High: Patient was on Prednisone 10mg daily and she was still having swelling, so the doctor had to increase the dose to 20mg daily. She said it was not that it wasn't working, but just that the dose was not high enough. She is still swelling even after taking 20mg daily. They are all the 5mg dose from the bottle. It was in a pharmacy vial with no lot or expiration. She gave her the 60 count, because she knew she would be tapering her. Product strength and count size dispensed: 5mg, 60 count. The initial steroid from her Primary Care was Methylprednisolone, 4mg, 21 of those. She said she felt completely normal while taking, but as soon as she stopped, the swelling returned. She had to go back to a Rheumatologist and he prescribed Prednisone. First day, she was to take 6, and then taper down from there. It was a blister pack. She threw it away and no longer has the lot or expiration or a sample to send. Product strength and count size dispensed: 4mg, 21 count. Yes the packaging sealed and intact. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: tested her for 13 things, such as Rheumatoid Arthritis, Lupus, Lyme Disease, Scleroderma; Result Unstructured Data: Test Result:Everything was normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Food allergy; Gestational diabetes (Gestational Diabetes 10 years ago and it has resolved.); Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: MN
Alter: 64,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 05.01.2022
Beginn: 21.03.2022
Tage bis Beginn: 75,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Hypoxia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Transferred with respiratory failure to a higher level of care with hypoxia, COVID 19 pneumonia. Covid 19 Positive 3/10/2022 hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Immunodeficiency due to medication for Heart Transplant 1995 and Kidney transplant 2008 Initial dose of Pfizer 10/15/2021 lot number FF2587
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: NH
Alter: 41,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 21.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Chest pain Lymphadenopathy

Symptomtext

After two days I started to get a huge lymph node by my left collar bone. It went away after 10 days but I have had a bad pain my left shoulder and upper left chest area since then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Woman?s multivitamin
Allergien: N-a
Vorherige Impfungen: -

VAERS 2181896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 04.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: - / RA

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

Chest discomfort Dyspnoea Heart rate increased

Symptomtext

chest tightness; shortness of breath; rapid heartbeat; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 04Jan2022 18:30 (Lot number: 33025BD) at the age of 39 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Colitis ulcerative" (unspecified if ongoing), notes: other medical history: Ulcerative Colitis, known allergies: Note that I am aware of; "COVID-19" (unspecified if ongoing), notes: if covid prior vaccination: Yes. Concomitant medication(s) included: LIALDA; VYVANSE. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FH8020, Location of injection: Arm Right, Vaccine Administration Time: 05:30 PM), administration date: 02Nov2021, when the patient was 39 years old, for COVID-19 Immunization, reaction(s): "numbness and tingling in both arms n hands, entire arms fall asleep", "numbness and tingling in both arms n hands, entire arms fall asleep". The following information was reported: CHEST DISCOMFORT (non-serious) with onset 10Jan2022, outcome "not recovered", described as "chest tightness"; DYSPNOEA (non-serious) with onset 10Jan2022, outcome "not recovered", described as "shortness of breath"; HEART RATE INCREASED (non-serious) with onset 10Jan2022, outcome "not recovered", described as "rapid heartbeat". The events "chest tightness", "shortness of breath" and "rapid heartbeat" were evaluated at the physician office visit and emergency room visit. Additional information: The patient did not receive any other vaccines within 4 weeks. Other medications in two weeks were Prescribed Lialda & Vyvanse. The patient was waiting to see a doctor today (11Jan2022). Post vaccination, the patient had not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes); Ulcerative colitis (other medical history: Ulcerative Colitis known allergies: Note that I am aware of)
Andere Medikamente: LIALDA; VYVANSE
Allergien: -
Vorherige Impfungen: -

VAERS 2181870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 07.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Pain in extremity Tremor

Symptomtext

she had soreness in her arm; Strong shaking for probably like 30 minutes; 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. Other Case identifier(s): US-PFIZER INC-202200035131 (Pfizer). A 31 year-old female patient received bnt162b2 (BNT162B2), administration date 07Jan2022 (Lot number: 33025BD) at the age of 31 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: TREMOR (non-serious) with onset Jan2022, outcome "recovered" (Jan2022), described as "Strong shaking for probably like 30 minutes"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "she had soreness in her arm". Therapeutic measures were not taken as a result of tremor. Additional information: Patient had no other products, had no patient history and had no investigation assessment, consumer stated, she was calling because she received the first dose of the Pfizer vaccine yesterday and last night, she started having just like some really strong, like shaking, it wasn't chills but it was like really strong shaking for probably like 30 minutes. Had been seeing before, side effect to that something serious enough she should not get the next one, had no treatment. Had no prior vaccination (within 4 weeks), she reported feeling fine at first, then about 12 hours later, her body started shaking, and she couldn't stop. It lasted for about 30 minutes. When asked if it was similar to chills, she stated that she would compare it to something similar she experienced after giving birth. She also stated she had soreness in her arm. Also informed about timing as Monday to Friday, 08:00 to 21:00, est. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2177008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain Back pain Blood pressure measurement Chest pain Cough Headache Heart rate Heart rate increased Hypertension Insomnia Palpitations

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 20-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Jan2022 12:00 (Lot number: 33025BD) at the age of 20 years as dose 2 (booster), single for Covid-19 immunisation. Relevant medical history included: "Johnson & Johnson Dose Number: 1", start date: 20Jan2022 (unspecified if ongoing), notes: Verbatim: Johnson & Johnson Dose Number: 1. The patient's concomitant medications were not reported. Vaccination history included: Johnson & Johnson (Dose Number: 1, Batch/Lot No: 201A21A, Location of injection: Arm Left, Vaccine Administration Time: 03:45 PM), administration date: 09Apr2021, when the patient was 20 years old, for COVID-19 immunization. The following information was reported: COUGH (medically significant) with onset 20Jan2022 18:30, outcome "not recovered", described as "Coughing"; ABDOMINAL PAIN (medically significant) with onset 20Jan2022 18:30, outcome "not recovered", described as "Abdominal Pain"; CHEST PAIN (medically significant) with onset 20Jan2022 18:30, outcome "not recovered", described as "Chest pain"; HYPERTENSION (medically significant), HEART RATE INCREASED (medically significant) all with onset 20Jan2022 18:30, outcome "not recovered" and all described as "High BP and HR"; HEADACHE (medically significant) with onset 20Jan2022 18:30, outcome "not recovered", described as "Headache"; BACK PAIN (medically significant) with onset 20Jan2022 18:30, outcome "not recovered", described as "Back pain"; PALPITATIONS (medically significant) with onset 20Jan2022 18:30, outcome "not recovered", described as "Palpitations"; INSOMNIA (medically significant) with onset 20Jan2022 18:30, outcome "not recovered", described as "Insomnia because of the pain". The events "coughing", "abdominal pain", "chest pain", "high BP and HR", "high BP and HR", "headache", "back pain", "palpitations" and "insomnia because of the pain" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (20Jan2022) high; heart rate: (20Jan2022) high. Therapeutic measures were taken as a result of cough, abdominal pain, chest pain, hypertension, heart rate increased, headache, back pain, palpitations, insomnia. Clinical Course: The patient experienced coughing, Abdominal Pain, Chest pain, high BP and HR, headache, back pain, palpitations, and insomnia because of the pain. AE treatment included Tylenol and Ibuprofen. No other vaccine in four weeks. No Covid prior vaccination and no Covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220120; Test Name: BP; Result Unstructured Data: Test Result: High; Test Date: 20220120; Test Name: HR; Result Unstructured Data: Test Result: High.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Interchange of vaccine products (Verbatim: Johnson & Johnson Dose Number: 1).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2155024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 29.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Impaired work ability

Symptomtext

I had a lump above my right clavicle that lasted for a few months after the second dose. I got Moderna for the first two doses and Pfizer for the third. I experienced extreme headaches after the first dose which subsided after the second dose. It is still a little noticeable a year later. After getting my third dose of the vaccine I experienced chest pain. When I got up two days later I started to get the chest pain and it got progressively worse over the course of four days. The first time I noticed the pain was when I stood up in the morning. The pain got so severe that I ended up going to the Emergency Room. I was prescribed Prilosec. I took it for two days and the pain started to subside. The chest pain was mostly in the middle of my chest. It felt a little better when I put pressure on it. It moved around a little but it was in my upper chest. The pain came and went during the four days until it escalated and then I was unable to work. Each bout of pain lasted for 20 minutes and it was hard to get any relief and then it would disappear. I have not had any more chest pain since that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ER Visit 01/05/2022-Heart testing. Dose 1: 01/31/2021 007M20A. Dose 2: 03/02/2021 023M20A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2109648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 27.02.2022
Impfdatum: 22.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Pain assessment Renal pain SARS-CoV-2 test Tremor Pain

Symptomtext

1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.; 1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.; 1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Jan2022 (Lot number: 33025BD) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Polycystic kidney disease" (unspecified if ongoing); "Type II diabetes" (unspecified if ongoing). Patient had an underlying disease. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 2, single, Batch/Lot No: EN6206, Location of injection: Arm Left), administration date: 13Mar2021, when the patient was 40 years old, for Covid-19 immunization, reaction(s): "my kidneys went from being in no pain to a 10/10 on the pain scale 1 week after receiving the vaccine."; Bnt162b2 (Dose1, single, Batch/Lot No: EN6200), administration date: 20Feb2021, when the patient was 40 years old, for Covid-19 immunization, reaction(s): ". I did not have an adverse reaction to the first vaccine". The following information was reported: RENAL PAIN (disability), TREMOR (disability), CONDITION AGGRAVATED (disability) all with onset 23Jan2022, outcome "not recovered" and all described as "1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.". The patient underwent the following laboratory tests and procedures: pain assessment: (23Jan2022) 10+; sars-cov-2 test: (unspecified date) negative. Therapeutic measures were taken as a result of renal pain, tremor, condition aggravated. Clinical course: One week after receiving second dose of the vaccine his kidneys went from being in no pain to a 10/10 on the pain scale 1 week after receiving the vaccine. This pain dissipated down to a 8/10 after 3 months but never resolved. He was required to get the booster to continue attending school. 1 day after receiving the vaccine his pain was back to a 10+ to the point he was shaking from the pain. This has still not resolved 3 weeks later. Nephrologist stated no treatment available. Patient had no known allergies. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine (prior vaccination was none). Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20220123; Test Name: Pain; Result Unstructured Data: Test Result:10+; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Polycystic kidney; Type II diabetes mellitus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2109648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 27.02.2022
Impfdatum: 22.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Pain assessment Renal pain SARS-CoV-2 test Tremor Pain

Symptomtext

1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.; 1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.; 1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Jan2022 (Lot number: 33025BD) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Polycystic kidney disease" (unspecified if ongoing); "Type II diabetes" (unspecified if ongoing). Patient had an underlying disease. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 2, single, Batch/Lot No: EN6206, Location of injection: Arm Left), administration date: 13Mar2021, when the patient was 40 years old, for Covid-19 immunization, reaction(s): "my kidneys went from being in no pain to a 10/10 on the pain scale 1 week after receiving the vaccine."; Bnt162b2 (Dose1, single, Batch/Lot No: EN6200), administration date: 20Feb2021, when the patient was 40 years old, for Covid-19 immunization, reaction(s): ". I did not have an adverse reaction to the first vaccine". The following information was reported: RENAL PAIN (disability), TREMOR (disability), CONDITION AGGRAVATED (disability) all with onset 23Jan2022, outcome "not recovered" and all described as "1 day after receiving the vaccine my pain was back to a 10+ to the point I was shaking from the pain.". The patient underwent the following laboratory tests and procedures: pain assessment: (23Jan2022) 10+; sars-cov-2 test: (unspecified date) negative. Therapeutic measures were taken as a result of renal pain, tremor, condition aggravated. Clinical course: One week after receiving second dose of the vaccine his kidneys went from being in no pain to a 10/10 on the pain scale 1 week after receiving the vaccine. This pain dissipated down to a 8/10 after 3 months but never resolved. He was required to get the booster to continue attending school. 1 day after receiving the vaccine his pain was back to a 10+ to the point he was shaking from the pain. This has still not resolved 3 weeks later. Nephrologist stated no treatment available. Patient had no known allergies. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine (prior vaccination was none). Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20220123; Test Name: Pain; Result Unstructured Data: Test Result:10+; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Polycystic kidney; Type II diabetes mellitus
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2134605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: KS
Alter: 34,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 19.02.2022
Beginn: 19.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Anxiety Palpitations

Symptomtext

Patient in for booster dose 2/19/2022, patient received booster dose Pfizer dose 33025BD in observation area and stated she felt like heart was racing and high anxiety noted. Vitals taken P87, O2 100%, BP 120/82, R 20 patient given sips of H20 and visited w patient. States increased anxiety was because days after 1st dose Pfizer her right eye became irritated and red, Went to eye dr. and he stated she has had a reaction to something. No treatment needed. After 20 minutes she was calmer and states feeling better. 4:50 pm vitals were BP 116/60 , R 18, P 84, 02 98% Recommended if any issues contact physician or go to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: 1st dose, Pfizer Covid 19 vaccine 4/6/2021

VAERS 2110409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Cough Epistaxis Fatigue Feeling abnormal Headache Hyperhidrosis Illness Mobility decreased Nasal congestion Oropharyngeal pain Pain Pain in extremity Pyrexia Rhinorrhoea SARS-CoV-2 test negative Throat irritation Tremor

Symptomtext

The same night, I got a scratchy/sore throat and didn't think much of it. The next day, I was really feeling off like I was coming up with something. I also got a pain in my leg that wouldn't go away like a charlie horse. But the time I hit the next night, 36 hours later, I knew I had a fever and my sore throat was very painful. Going on to day 2, the sore throat continued, and got worse. The fever, headache, body aches. Hard to move. Basically stayed in bed all day. Moving on to night 2, 60 hours in, fever had worsened, aches had worsened. This is when I felt that I needed to go to the doctor. The fever was so bad, I was having the shakes and I could not get warm and I was shivering. We called the doctor and they said if my fever reached 104 or more to go to the ER. It never did reach that point so I endured through it. The next day I spoke with a doctor in detail about what was going on. Day 3, that's when I developed a cough. Up until that point, I didn't have a cough just the sore throat. Mucus started in my nose and it was bloody. The headaches and body aches continued and basically stayed in bed for a 2nd day. That's when I spoke with the doctor in depth. I called in and we had a virtual appointment and they said if it gets any worse to come into ER but I did endure through it. Night 3- after drifting in and out of sleep all day, I woke up drenched where I sweat 64 oz of sweat into the bed. I changed the sheets and the mattress was still wet. After I sweat that amount, I did start to feel better. The first time in 3 days where I felt better and it seemed to take a turn towards my recovery. Day 4 felt even more better. Still had a sore throat and stuffed up nose. It wasn't as nearly as bad and the fever had gone away. I knew I was on the mend, but I didn't know how quickly I would recover. Night 4 it turned around again and that's when my sore throat got worse. My stuffed up nose got worse. Just seemed like after I thought I was getting better, I was getting worse again. For the rest of the days, I would feel bad in the morning, feel better by midday, and feel worse again by night time. That's been going on for over a month now. It's been one month and 11 days since this. I still have a sore throat and a runny nose on a regular basis. I'm always tired and this was the exact opposite of how I was the day before the vaccine. On the 2nd day of me being sick my wife got the at home COVID test and it came up negative. It was not COVID, or at least the test said that. The doctor asked if there was anything that could have made this easier for me that would be if I could have had a pain reliever, the pain during the 1st four days was nearly unbearable. Doctor's visits were telehealth visits.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: AMPK metabolic activator; burn evolved metabolic boost; Prima Surge testosterone booster; L-carnitine extra strength; conjugated linoleic acid; biotin; fish oil; vitamin E; amino acid; Lysine amino acid; L-ornithine; probiotic
Allergien: None
Vorherige Impfungen: 1st COVID Pfizer vaccine (01/17/2021) left arm as I was driving home after the vaccine, numb for about 20 minutes and that was t

VAERS 2079291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: KS
Alter: 81,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 31.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Dizziness Dyspnoea

Symptomtext

ON 1/31/22 PATIENT STATED TO THE LADIES AT CHECK IN THAT SHE WAS SHORT OF BREATH AFTER THE LONG WALK IN & WANTED TO SIT DOWN FOR A MINUTE. THEY OFFERED HER A WHEELCHAIR ASSIST TO THE TABLE, BUT SHE SAID NO, THIS IS NORMAL FOR HER LATELY & SHE NEEDS TO WALK. SHE WAS WALKED TO TABLE WITH THE FLAGGER. RIGHT BEFORE GETTING THE VACCINE PATIENT RECEIVED A CALL FROM HER NEPHROLOGIST STATING HER HEMOGLOBIN WAS CRITICAL AT 5.8 & HE WAS REQUESTING HER TO GO TO THE HOSPITAL. SHE THEN STATED SHE CAME IN FOR HER BOOSTER & SHE WASN?T LEVING WITHOUT GETTING THE VACCINE. FOLLOWING WAS ASSISTED TO A SEAT IN OBSERVATION. THE SITUATION WAS DISCUSSED WITH OBSERVATION RNS & FLOOR LEAD. FLOOR LEAD SPOKE WITH PATIENT ABOUT HOW UNSAFE IT WOULD BE FOR HER TO DRIVE HERSELF & SHE SAID SHE WANTED FAMILY TO TAKE HER THE HOSPITAL NOT EMS. SHE GOT ON HER PHONE & LEAD CONTACTED VACCINE BRANCH MANAGER. WHILE IN OBSERVATION SHE REPORTED SLIGHT SHORTNESS OF AIR & A LITTLE DIZZINESS & THAT SHE WAS A DIABETIC. SpO2 WAS 92%, SHE WAS GIVEN A SODA & SOME PEANUTS, WHICH SHE SAID HELPED. BOTH MANAGER & LEAD DISCUSSED WITH PATIENT THE UNSAFE SITUATION. DAUGHTER WAS CONTACTED & ARRIVED AT 1745, MANAGER & LEAD ESCORTED TO DAUGHTER?S CAR VIA WHEELCHAIR & DAUGHTER WAS UPDATED ABOUT SITUATION. SHE STATED SHE WOULD IMMEDIATELY TAKE HER TO HOSPITAL. LEAD DISCUSSED WITH PATIENT & DAUGHTER THAT IF HER SHORTNESS OF AIR SYMPTOMS GET WORSE OR ANY OTHER PROBLEMS TO CALL EMERGENCY IMMEDIATELY. THEY LEFT FOR THE HOSPITAL AT 1749

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: CRITICAL HEMOGLOBIN 5.8 - RECEIVED CALL WHILE AT VACCINATION TABLE
Vorgeschichte: DIABETES
Andere Medikamente: ASPIRIN 81MG
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2076645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 04.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac disorder Cardiac monitoring Chest X-ray Computerised tomogram head Computerised tomogram thorax Dizziness Electrocardiogram Heart rate increased Hypotension

Symptomtext

Having cardiac complication that is new condition and Faint feeling while at work, low blood pressure and high heart rate. 1st time was 01/10/2022, 01/11/2022 workplace at hospital called code 01/23/2022 taken to er to check for blood clots and heart monitoring and was admitted for two days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 2,0
Labordaten: Check for blood clots and heart monitoring, Chest ex-ray CG of head and chest, ECG
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Trilosprintet 453 (1) tablet daily, Vyvanse 50mg 1once daily
Allergien: No
Vorherige Impfungen: -

VAERS 2075674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: WI
Alter: 51,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 22.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Mobility decreased Pain Pain in extremity

Symptomtext

Pain to left arm. Unable to lift left arm due to pain after receiving vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2073080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 17.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Chest pain Condition aggravated Contusion Dizziness Dyspnoea exertional Extrasystoles Fatigue Feeling abnormal Inflammation Loss of personal independence in daily activities Musculoskeletal chest pain Pain in extremity Painful respiration Palpitations Pyrexia Tenderness

Symptomtext

After the expected fever, I started to develop heart palpitations the next day. I had ongoing, random bouts of heavy palpitations over the next week. Out of breath when even walking up stairs. Pounding heart especially when laying down. 1 week after first shot developed chest pain/rib pain. Extremely sore to breath in and also to the touch. Feels like inflammation on ribs/sternum. This lasted 2 days. Started feeling normal again after 9 days but when I try to do activities I am quickly out of breath and my heart pounds more than usual. I had a previous covid infection in March 2020 with similar out of breath feeling with no lung issues. Still have some continuing arm pain & bruising 11 days after first shot but is manageable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I went back to the doctor office 2 days after 1st shot and told them about my reaction. I was told I was just having anxiety and no tests were performed, they only spoke with me. I don't feel it is anxiety as I've never had this type of heart response and quick fatigue. I also don't feel particularly stressed except when it starts to pound or skip over and over. I feel better than the previous week but cannot resume normal activities yet as I am quickly fatigued and dizzy.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Had an unexpected and fast "black-out" after the Hepatitis B vaccine. Was told not to take a second shot at the time. I was arou

VAERS 2072046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: OR
Alter: 53,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 21.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

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

Dizziness Fatigue Pain Palpitations

Symptomtext

Felt woozy after the shot, that passed. Felt mostly okay except for heart palpitations several times a day. And on 1/28, my body "crashed". I suddenly became very fatigued. And following morning I had body aches. This delayed fatigue reaction also occurred after my first PFIZER shot last spring. I can't remember if I had palpitations though.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None, treated at home with lorazepam.
Aktuelle Erkrankungen: Mild cold
Vorgeschichte: High blood pressure, High cholesterol
Andere Medikamente: Estradiol patch (.25mg lowest dose), Progesterone 100mg, B12 shots, Vitamin D pills 50,000 dose, Dandelion root, Niacin, Folic acid
Allergien: Erythromycin, Gala apples
Vorherige Impfungen: Delayed fatigue after first shot 53, 4/24/21, Pfizer.

VAERS 2071729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: WI
Alter: 35,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 17.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Blood test Cardiac monitoring Chest X-ray Chest pain Electrocardiogram Hypoaesthesia

Symptomtext

Chest pain on left-side with numbness in arm started less than week after 4th shot. Went to emergency room; told no heart issues and sent home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: X-rays of chest, blood work, EKG and heart monitor.
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: Humira, Methotrexate, Folic acid, D3, A, C, Fiber, Biotin
Allergien: Topamax and Nickel
Vorherige Impfungen: -

VAERS 2057077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: PA
Alter: 80,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Heart rate Heart rate increased Immunisation Influenza like illness Interchange of vaccine products Lethargy Off label use Pain Palpitations

Symptomtext

Flu-like symptoms; achy; Lethargic; pounding sensation when moving around; booster; Her first shot was J&J and she opted for a Pfizer booster; Her first shot was J&J and she opted for a Pfizer booster; pulse is 50% faster than normal; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 80 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 05Jan2022 15:30 (Lot number: 33025BD) at the age of 80 years as dose 2 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Johnson and johnson vaccine (First Dose, Lot: 206A21A), administration date: 03Aug2021, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022, outcome "unknown", described as "booster"; OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 05Jan2022, outcome "unknown" and all described as "Her first shot was J&J and she opted for a Pfizer booster"; HEART RATE INCREASED (non-serious) with onset 05Jan2022, outcome "unknown", described as "pulse is 50% faster than normal"; INFLUENZA LIKE ILLNESS (non-serious) with onset 06Jan2022, outcome "unknown", described as "Flu-like symptoms"; PAIN (non-serious) with onset 06Jan2022, outcome "unknown", described as "achy"; LETHARGY (non-serious) with onset 06Jan2022, outcome "unknown", described as "Lethargic"; PALPITATIONS (non-serious) with onset 06Jan2022, outcome "unknown", described as "pounding sensation when moving around". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient stated that she had a booster shot yesterday. Her first shot was J&J and she opted for a Pfizer booster, that was the only thing being offered. The patient stated that everything was fine. It was totally painless, however last night she noticed her pulse was fast. The patient tested and took her pulse and it was like 50% faster than normal. Her pulse was around 88-90, but normally her pulse was very slow pulse like around 60. The patient stated she took her pulse again this morning and it was a little bit slower. Later in the morning, her pulse was like 80. She was feeling sort of like flu-like symptoms. She was achy, not severely achy, but just enough to be noticeable. She was feeling lethargic. The patient also stated that when she first got up she noticed when she was moving around, exercising a little bit, like walking around, she did had a pounding sensation. She stated she noticed this sensation today, but it was subsided. The patient did not administered any additional vaccines on same date of Pfizer vaccine. The patient not received any other vaccine within four weeks prior to the first administration date of the suspect vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20220105; Test Name: Pulse rate; Result Unstructured Data: Test Result:88-90; Test Date: 20220106; Test Name: Pulse rate; Result Unstructured Data: Test Result:80
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: IA
Alter: 43,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain

Symptomtext

Mild pain around left chest, feeling like finger-pushing around heart.

Weitere VAERSDATA-Felder

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

VAERS 2048582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Dyspnoea Rash Vomiting

Symptomtext

Patient started to experience dizziness and shortness of breath within 10 minutes after the vaccine. Some rash was observed on her arm and neck area. She then stated that she couldn't breathe, and started to vomit. Epipen 0.3 mg was given to her on her right thigh. Paramedics was called. They arrived and took her away. Patient did not loose consciousness during the entire event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: allergic to Covid vaccine per pt
Vorherige Impfungen: Patient stated she had "anaphylactic" reaction to her first dose of Pfizer.

VAERS 2045883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 18.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Dyspnoea Muscle contracture Paraesthesia

Symptomtext

Tingling/contraction like pains in chest, shortness of breath.

Weitere VAERSDATA-Felder

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

VAERS 2044616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Arrhythmia Blood creatinine normal Blood test Chest X-ray normal Chest discomfort Chills Condition aggravated Culture urine Electrocardiogram Electrocardiogram T wave abnormal Headache Influenza like illness Laboratory test normal Menstruation irregular Pain Palpitations Polymerase chain reaction Pregnancy test negative

Symptomtext

Went to bed at 10pm a little flu-like symptoms (aches, headache, chills). By middle of night could not find a comfortable position to sleep due to exaggerated symptoms noted above. Woke up 1:30pm following day throbbing headache, racing heart rate 155bpm, chest heaviness, no fever. Heart rate reduced over the next day to 113/112 (my resting normal is 60-75 sitting upright)- still with some chest heaviness.no headache... went to ER took bloodwork troponin and creatine normal, PCR negative, neg pregnancy, chest X-ray normal , neg for pneumonia, EKG t-wave flattening mild arrthmia- sent home with 92-89 resting HR and to follow up with cardiology echo-stress test and holter. Following day heart rate lower to 94-92 resting HR, mild chest heaviness have a little nagging tickle in my chest that I need to cough/clear- rapid test neg?now I?m spotting (no pain) today (very strange since I did not have a period for quite some time-months).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: ECG, bloodworkup, chest X-ray, urine culture, vitals telemetry,
Aktuelle Erkrankungen: None, 1 year post menopause
Vorgeschichte: Borderline mild thrombocytopenia
Andere Medikamente: Multivitamin , vit D
Allergien: None.
Vorherige Impfungen: Same but not heart symptoms and no Er visit

VAERS 2043553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: ME
Alter: 44,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Palpitations

Symptomtext

Heart was racing, blood pressure spiked, lasted about 3 or more hours. Fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Bladder infection
Vorgeschichte: None
Andere Medikamente: None
Allergien: Codeine, Lamictal
Vorherige Impfungen: -

VAERS 2037953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: VA
Alter: 40,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Breast pain COVID-19 Fatigue Flank pain Headache Injected limb mobility decreased Lymph node pain Lymphadenopathy Musculoskeletal stiffness Nausea Pain Productive cough Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Vomiting

Symptomtext

Vaccines received at 1:15PM. Felt slightly feverish and worn out at bedtime. Woke up next morning to a fever of 102.4 - and achy, exhausted, and stiff, presenting with headache, slight productive cough, and mild congestion. Lymph nodes under armpit (on arm that was injected) so inflamed that cannot raise arm above head without sending shooting pains down side and into breast. Proceeded to treat fever with a lukewarm bath as needed, and alternating tylenol and advil along keeping hydrated. All day, fever never went away or below 100. The following night, it went up to 103. Same symptoms, treated same way. The next day, at 6pm, temp dipped below 100 for the first time ever, and began to feel a little hopeful. The next morning, however, nausea and vomiting set it. Fever has remained low grade, but nausea, headache, body aches, congestion, coughing, and exhaustion as well as excruciatingly painful lymph nodes remain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Took one at home rapid covid test (unfortunately, it was expired) and it resulted in a positive. I tested negative on monday from an official testing facility, and was vaccinated on wednesday. I have been nowhere.
Aktuelle Erkrankungen: Had chest cold in December, with low-grade fever that lasted two weeks Dec 16-30th. Tested negative for Covid and Flu.
Vorgeschichte: None
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Similar but much milder reaction to the 2nd Covid vaccine. Report was filed.

VAERS 2033062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 07.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Breast pain Mobility decreased Pain Pain in extremity Peripheral swelling

Symptomtext

Feeling of extreme swelling and soreness of left arm radiating to left breast area and back. Could not lift arm. Referred to urgent care.

Weitere VAERSDATA-Felder

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

VAERS 2029392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Erythema Interchange of vaccine products

Symptomtext

at 6pm pt complain of redness on her neck , denies any SOB. Pt stated " she has the same reaction from the past from Covid vaccine MRNA( moderna)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None
Vorgeschichte: Female rectocele, history of total hysterectomy ,Vitamin D deficiency, urinary frequency
Andere Medikamente: None
Allergien: Amoxicillin, penicillin, septra, covid vaccine MRNA ( moderna)
Vorherige Impfungen: Covid vaccine MRNA ( Moderna)

VAERS 2029241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Asthenia Balance disorder Flushing Nausea Tremor Unresponsive to stimuli Vomiting

Symptomtext

Pt. felt nauseated about 4 minutes after her vaccination and ran out to the bathroom where staff followed and witnessed emesis. The pt. also felt weak and was unsteady on her feet, her brother and staff accompanied her back to the observation area where she appeared flushed and tremulous, with ongoing nausea but no further vomiting, could not answer questions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Pulse was 125, O2 sat did not give a good reading, patient was transferred to the Emergency Room for ongoing assessment and care.
Aktuelle Erkrankungen: Reaction to previous Covid vaccine requiring E.R. visit.
Vorgeschichte: Obesity; Other unknown.
Andere Medikamente: unknown.
Allergien: unknown.
Vorherige Impfungen: Pfizer vaccine # 2 required E.R. eval, pt.'s brother shared at time of this reaction. Med record not available at time of submis

VAERS 2028014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: WI
Alter: 46,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Dyspnoea

Symptomtext

dizziness and shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none known
Vorgeschichte: Obstructive Sleep apnew Obesity Ex Smoker Anxiety Acute systolic heart failure cardiomyopathy circumscribed scleroderma depression
Andere Medikamente: Multivitamin-mineral biotin
Allergien: aspirin penicillins metronidazole bee sting cat dander
Vorherige Impfungen: -

VAERS 2027895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: MD
Alter: 52,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Back pain Chest pain Cough Myalgia Neck pain Pain Pain in extremity Rhinorrhoea

Symptomtext

I have been experiencing neck and back pain, I am currently in physical therapy and seeing an orthopedic surgeon. I also have been having chest pains that radiates to the left arm and causes muscle pains, runny nose, and coughing.

Weitere VAERSDATA-Felder

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

VAERS 2027305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Dental discomfort Mouth ulceration Noninfective gingivitis Oral pain Toothache

Symptomtext

Approximately 30 minutes after receiving my 3rd vaccination (booster dose), I began to experience strong pain in my two upper rear molars on the left side of my mouth. Inflammation of my gums was slightly noticeable. A few days later, I developed mouth ulcers across the roof of my mouth for no reason. The ulcers lasted about 10 days and were very painful. Salt rinses were done daily to keep them from becoming infected. The tooth pain has continued daily since my booster. I am currently taking Advil's and Tylenol daily to manage the discomfort. The pain varies and the gums do not seem infected. Teeth are not loose. I am seeking medical attention from my dentist this week. Within an hour of my 3rd vaccination (booster dose) I experienced the same strong, sharp chest pain as I noticed in my 2nd dose. It only lasted about an hour at the time, but since that event I have experienced the chest pain several times a week with no warning or discernible reason. I will be reaching out to a doctor for assistance this week. I am no longer with this facility for health care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: none
Vorgeschichte: Narcolepsy, Endometriosis
Andere Medikamente: none
Allergien: Percocet
Vorherige Impfungen: -

VAERS 2019362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: OH
Alter: 67,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 31.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chest pain Chills Fatigue Injection site pain Joint stiffness Musculoskeletal pain Neck pain Pain in jaw Painful respiration Pyrexia Tremor

Symptomtext

The shot to my upper left arm, at the time of administration, caused no pain. Immediately afterward I went home and rested. By early evening, a sensation of tightness and pain began in my upper left shoulder and quickly spread across the top of my shoulder into my neck, left chest, around to my left shoulder blade, and even briefly into my left jaw. This progressed, and I found I was unable to take a deep breath without pain in my chest. Other symptoms I had were chills, fever to 99.5, fatigue, and weakness to the point of tremor. After 3 days I remembered I had Ativan 1 mg tablets originally prescribed by my cardiologist, so I tried taking 0.25 mg Ativan (which is all I ever need), and this did help my breathing for the next 24 hours or so. A couple nights after that I tried one Tylenol 500 mg capsule instead of the Ativan, and it also helped the pain, so I presumed it was not heart related. However, the pain was scary and quite debilitating, and I am wondering if it is some sort of brachial neuritis. I also tried my chiropractor yesterday, 1/7/22, but the pain has returned today, milder, but persistent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None. I plan to follow up with my PCP.
Aktuelle Erkrankungen: Tooth infection on 11/29/21 - tooth was pulled on 11/30/21 and antibiotics given (Clindamycin 300 mg 3x/daily for 7 days).
Vorgeschichte: Mild COPD. CHF with preserved EF. Permanent colostomy. History of Stage 3 anorectal cancer (5 years ago) treated with chemo and radiation, with NED.
Andere Medikamente: B complex 50 mg daily. Hair, Skin and Nails 1 tablet daily. Vitamin D3, 2000 mcg daily.
Allergien: Penicillin and sulfa - rash. Prednisone - palpitations. Dairy insensitivity. Mold and dust.
Vorherige Impfungen: -

VAERS 2019168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: KY
Alter: 45,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Body temperature increased Feeling cold Heart rate Heart rate increased Immunisation Interchange of vaccine products Off label use Pain Pyrexia Swelling Tremor

Symptomtext

My fever continued to increase up to 102.3 at 8:40 am; Shaking really bad; Freezing; Neck swollen; Body aches; 101.4 fever; Heart rate 120; Dose 1: Janssen COVID-19 vaccine and Dose 2 (Booster): Pfizer COVID-19 vaccine; Dose 1: Janssen COVID-19 vaccine and Dose 2 (Booster): Pfizer COVID-19 vaccine; Dose number 2 (Booster); This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 45-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 30Dec2021 at 14:00 (Lot number: 33025BD) at the age of 45 years as dose 2 (booster), single for COVID-19 immunisation. Relevant medical history included: "Rheumatoid arthritis" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "Gastroparesis" (unspecified if ongoing), "Thyroid function decreased" (unspecified if ongoing), notes: Under active thyroid and "Lupus erythematosus" (unspecified if ongoing), notes: Lupus. Concomitant medications were not reported. Past drug history included: Effexor, reaction: "Drug allergy", notes: Known allergies: Effexor and Reglan, reaction: "Drug allergy", notes: Known allergies: Reglan. Vaccination history included: Janssen covid-19 vaccine (johnson &Johnson) (DOSE 1, SINGLE; Lot Number: 1808980; Anatomical site: Right arm), administration date: 21May2021, when the patient was 45 years old, for COVID-19 immunisation. The following information was reported: OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 30Dec2021 at 14:00, outcome "unknown", and all described as "Dose 1: Janssen COVID-19 vaccine and Dose 2 (Booster): Pfizer COVID-19 vaccine"; IMMUNISATION (non-serious) with onset 30Dec2021 at 14:00, outcome "unknown", described as "Dose number 2 (Booster)"; TREMOR (non-serious) with onset 31Dec2021 at 06:30, outcome "recovering", described as "Shaking really bad"; FEELING COLD (non-serious) with onset 31Dec2021 at 06:30, outcome "recovering", described as "Freezing"; SWELLING (non-serious) with onset 31Dec2021 at 06:30, outcome "recovering", described as "Neck swollen"; PAIN (non-serious) with onset 31Dec2021 at 06:30, outcome "recovering", described as "Body aches"; PYREXIA (non-serious) with onset 31Dec2021 at 06:30, outcome "recovering", described as "101.4 fever"; HEART RATE INCREASED (non-serious) with onset 31Dec2021 at 06:30, outcome "recovering", described as "Heart rate 120"; BODY TEMPERATURE INCREASED (non-serious) with onset 31Dec2021 at 08:40, outcome "recovering", described as "My fever continued to increase up to 102.3 at 8:40 am". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of tremor, feeling cold, swelling, pain, pyrexia, heart rate increased and body temperature increased. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient had vaccine on 30Dec2021 at 14:00. Woke up on 31Dec2021 at 06:30 due to shaking really bad, freezing, neck swollen, body aches, and 101.4 fever and heart rate 120. Patient fever continued to increase up to 102.3 at 08:40. Fever started to break around 14:40. Body aches were still present at 17:00 (at the time of this report). Patient did not go to emergency room and if her fever had not broken, she would have gone. Currently temperature was staying around 100. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20211231; Test Name: Heart rate; Result Unstructured Data: Test Result:120; Comments: at 06:30; Test Date: 20211231; Test Name: Body temperature; Result Unstructured Data: Test Result:100; Test Date: 20211231; Test Name: Body temperature; Result Unstructured Data: Test Result:102.3; Comments: at 08:40; Test Date: 20211231; Test Name: Body temperature; Result Unstructured Data: Test Result:101.4; Comments: at 06:30
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fibromyalgia; Gastroparesis; Lupus erythematosus (Lupus); Rheumatoid arthritis; Thyroid function decreased (Under active thyroid)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: IL
Alter: 41,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 29.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Joint noise Muscular weakness

Symptomtext

Weakening of rotator cuffs and cracking of shoulders. Occurs identically in both shoulders. This occurred one week after Dose 2 as well, and persisted for several months, including a shoulder injury that occurred during non-strenuous activity (throwing frisbee), but was unreported. I was unable to do work above my shoulders without tremendous pain for about 2 months. I could not do pushups or military press without risking injury. The condition improved after 3 months, and I was back to normal prior to getting boosted. One day after getting boosted, the same weakness and joint cracking returned and has not abated. This is not due to the physical administration of the vaccine because the pain/weakening is identical in both shoulders. The pharmacy staff who administered the vaccine did an outstanding job.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None. Self care. I have not reported these events to my doctor because online research indicated that rest of the associated muscles was the best course of treatment for minor rotator cuff injuries.
Aktuelle Erkrankungen: Headache, possibly influenza 3 weeks prior
Vorgeschichte: none
Andere Medikamente: Vitamin D, Zinc
Allergien: Pen
Vorherige Impfungen: COVID dose 2, as described previously

VAERS 2015109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 16,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction Tremor

Symptomtext

Patient brought into Covid Observation area after becoming light-headed immediately after receiving 2nd dose Pfizer vaccine. Patient was assisted to floor by her dad and staff, with legs elevated on chair. Per staff, patient did not hit her head or loose consciousness. Remained alert and oriented x 3, speaking in complete sentences. Denied any difficulty breathing or throat tightness. No swelling noted to face lips or tongue. No rash or hives noted. Patient assisted up to wheelchair and to then to gurney. Placed in trendelenburg position. Reports feeling better lying down. Per dad, patient did not experience any of the above symptoms with 1st dose Pfizer. Patient states she had an egg sandwich and iced coffee this morning and bag of veggie chips this afternoon. States she has not had any water to drink today. 3:33 pm- VS: BP 134/64, HR 65, RR 18, 02 SATs 100% RA 3:41 pm- VS-BP 112/50, HR 63, RR 18, 02 SATs 100% RA- Patient reports feeling better. Provided bottle of water to drink. Will continue to monitor 3:48 pm- Call placed to on call ED physician, informed of patient symptoms above. Per Dr, continue to monitor patient for additional 30 minutes and if vital signs remain stable, ok to be discharged home and no need to be evaluated in Emergency Department. 3:54 pm- VS:BP 123/74, HR 68, RR 18, 02 SATs 100% RA. States she still feels a little shaky, but not as much as initially. 4:09 pm-VS: BP 123/76, HR 73, RR 20, 02 SATs 100% RA. Reports feeling better and less shaky. 4:27 pm-VS: BP 125/74, HR 64, RR 20, 02 SATs 100% RA. Assisted patient to sitting position and standing. Denies dizziness with position changes. States shakiness resolved and she feels back to normal. 4:31pm- Discharged home in stable condition, accompanied by dad. Informed dad to seek emergent care for any returning or worsening symptoms. Also advised ok to give OTC Tylenol or Ibuprofen as directed for sore arm or body aches. Dad verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: No know allergies
Vorherige Impfungen: -

VAERS 2007417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: WA
Alter: 48,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Chest pain Discomfort Headache Swelling

Symptomtext

Patient reported adverse reactions: painful and large swollen area in his armpit and on the side of chest area. Headache and discomfort.

Weitere VAERSDATA-Felder

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

VAERS 1999444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Cough Lip swelling Productive cough Throat clearing Throat tightness

Symptomtext

0928 Patient received Pfizer booster after consulted Dr. because of previous reaction of lips/tongue swelling, rash on face with 1st vaccine and second vaccine tingling of tongue and lips while resolved without treatment. Patient premedicated at home with Zyrtec 10mg at 0830 1/3/22. Patient alert oriented x4 talking in full sentences able to swallow. Lungs clear, no stridor, intra oral swelling, wheezing, chest pain or tightness , 0930 Patient reports feels lips puffy and looks mildly swollen but denies intraoral swelling,drooling, difficulty breathing, wheezing, chest pain/tightness. Talking in full sentences. Consulted Dr. regarding symptoms and advised may give Benadryl 25mg orally if necessary and continue to monitor symptoms for another 45 minutes. 0935 Vitals BP 123/76 Temporal Temp. 98.8 Pulse 63 SPO2 98% on room air RR 12 0940 Patient states lips swelling resolved, 0958 Patient reports mucus in throat and feels need to clear with cough, but no difficulty breathing/throat tightness/ lungs clear with no wheezing no stridor or intra oral swelling, swelling of face/lips. 1001 Patient given Benadryl 25mg tab orally with water and tolerated well. 1007 Patient states feels mild throat tightness with mild cough, but able to swallow and not drooling, no stridor, lungs clear.Patient sitting up in bed talking in full sentences, and laughing. Has called dad to come to observation area. Bp 112/72 Spo2 98 % on room air Pulse 75 RR 18 1014 states throat tightness resolved but feels mild cough not related to clearing throat/mucus but clearing chest. Rechecked Lungs and clear to ascultation, no wheezing, stridor, drooling or difficulty breathing/chest tightness or pain 1020 Consulted Dr. regarding new symptoms and advised may observe until 1030.and if patient symptoms not worse may discharge home with driver. Patient may observe symptoms at home and may call 911/Ed if necessary and should follow up with primary care Md regarding symptoms. 1030 Vitals Bp 117/70 SPO2 99% on room air Pulse 69 Patient states she feels fine to go home with her dad sitting next to her. Denies throat tightness/facial swelling/wheezing and hasn't coughed in last 5 minutes. Patient states she fine, has vaccine info sheet and verbalized understand regarding 911/Ed precautions.Patient passed the walk test with Rn and father at side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Covid
Vorgeschichte: INTERMITTENT ASTHMA EXERCISE INDUCED ASTHMA SCOLIOSIS ALLERGIC RHINITIS IUD SURVEILLANCE
Andere Medikamente: Albuterol (PROAIR/PROVENTIL/VENTOLIN) 90 mcg/actuation Inhl HFAA Ciclesonide (Alvesco) 80 mcg/actuation Inhl HFAA Zyrtec 10 mg
Allergien: Cefuroxime Clarithromycin Walnuts
Vorherige Impfungen: 12/22/20 Patient received first dose of Pfizer and had swelling of lips/tongue, rash to face which resolved. Second Pfizer 1/12

VAERS 1997926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: NC
Alter: 40,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 29.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Burning sensation Discomfort Hypoaesthesia Nerve compression Paraesthesia Peripheral coldness Peripheral swelling Poor peripheral circulation Vasodilatation

Symptomtext

Burning/ Cold sensation starting in my left hand and lasted about 10 min. Strange pinching/nerve, tingling and dull sensations in left leg on second and third day after injection. The evening of the third day I experienced numbness in right arm and puffy right hand as well as vein enlarging. The strange sensations in my right arm continued into the 4th day and the hand abnormalities appeared again into the evening. The discomfort in my right hand feels like poor or irregular circulation similar the cold feeling of your limb falling asleep. During the course of these experiences, I have taken low dose aspirin, a generic allergy pill, and ibuprofen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Bromelain, Women's multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1997496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: -
Alter: 37,0
Geschlecht: M
Eingang: 01.01.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Agitation Anxiety Dyspnoea Eye pain Fatigue Headache Nausea

Symptomtext

The following side effects occurred after receiving a booster of the COVID 19 vaccine, but not during the first two shots. Approximately 12 hours after the injection, there was nausea. Fatigue, headache, and eye soreness were experienced the second day after the injection. In the afternoon of that day, shortness of breath occurred. Intense anxiety and agitation were experience on the third day after injection.

Weitere VAERSDATA-Felder

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

VAERS 1992772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: AZ
Alter: 23,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Paraesthesia Urticaria

Symptomtext

Patient later disclosed she had hives with last Pfizer shot, and also hand tingling. Observation time switched to 30 minutes. She had hand tingling "like it's falling asleep" in the right hand about 20 minutes after the vaccine, but it went away. Her left hand was still tingling. 50mg diphenhydramine PO administered. About 20 minutes later, still tingling but less so. Patient did not wish to proceed to urgent care and left observation. No difficulty breathing or facial swelling. Followed-up with patient via phone 2 hours later. She stated immediately after leaving, her face broke out in hives but since resolved. Never any throat or lip swelling or difficulty breathing. Tingling in hand has not resolved. Recommended follow-up if symptoms do not abate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Minor hives with 1st Pfizer; disclosed after.

VAERS 1992634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: MO
Alter: 42,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Chest pain Electrocardiogram Heart rate increased Laboratory test

Symptomtext

Heart rate of 110 to 125 while at rest and chest pain. It started at about 6pm the day of the vaccine. I hoped it would pass by morning but it had not ceased. I was monitoring my pulse via fitbit. I went to the Hospital ER at about 9am the next morning, 12/29/21. They did an EKG, ran labs and gave me fluids then sent me home and said to rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: On 12/29/2021: EKG, labs at Hospital.
Aktuelle Erkrankungen: Ear infection
Vorgeschichte: Asthma, allergies, psoriasis, autoimmune progesterone dermatitis, autism spectrum disorder level 1, anxiety, OCD, depression, arthritis, chronic pain, migraines, venous reflux (had venous ablation to greater saphenous in both legs).
Andere Medikamente: Multi vitamin, Zyrtec
Allergien: Sulfa drugs, Valium, kiwi fruit, pollen, dander, dust mites, mold
Vorherige Impfungen: Pfizer lot EW0162 - 1st dose, shortness of breath and high pulse, 4/15/2021 age 42.

VAERS 1989350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Condition aggravated Diarrhoea Fatigue Myalgia Pyrexia Vomiting

Symptomtext

Vomiting, diarrhea, chills, fever, muscle aches, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Fibromyalgia
Andere Medikamente: sertraline
Allergien: sulpha drugs, ivp dye
Vorherige Impfungen: 2/5/21 - Chills, body aches, fatigue - Pfizer, Age 71 2/28/21 - body aches, fatigue, chills, all reported via the app previously

VAERS 1984802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: GA
Alter: 36,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Limb discomfort Paraesthesia oral

Symptomtext

TINGLING OF THE LIPS AND A HEAVINESS IN LEGS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1979266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: AZ
Alter: 38,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Altered state of consciousness Anxiety Hyperhidrosis Pain in extremity Pallor Paraesthesia

Symptomtext

Patient was administered Booster dose of Pfizer vaccine. He moved out to the waiting area and during his period of observation, suddenly became very pale, began coming in and out of consciousness, started sweating heavily, and reported tingling in his hands and feet. Patient reported no issue with either of the first 2 doses of the vaccine. Pharmacy contacted EMS and monitored patient until arrival. EMS assessed and continued monitoring patient until he was able to stand up and walk out on his own. Pharmacy contacted patient the following day. He reported EMS had suspected some kind of anxiety attack and had not administered any medication. Patient stated he had not sought out any further medical care and was no longer experiencing any symptoms except for a sore arm.

Weitere VAERSDATA-Felder

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

VAERS 1974920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Muscular weakness Peripheral coldness Tremor

Symptomtext

11mins post vaccination pt reported dizziness. Pt was taken to med bay via ambulation, layed down on cot Vitals: @16:44 125/69, 96, 22, 100% -- > 17:05 120/77, 96, 22, 100% -- > 17:19 113/77, 95, 100% 16:47 Hands feel weak/cold. Pt stated she can breath but feels shaky. NO clamminess, no palpeness. Pt appears to be in NAD. Resting back in cot. 16:50 Blanket, juice, water given 17:05 pt reports improvement in symptomsw but hands still weak. 17:11 Hands warm, adverse side effects improving but hands still feel a little weak. no dizziness. no SOB or respiratory issues 17:19 All adverse side effects resolved except hand still feel a litttle weak but pt feels well and wants to leave 17:25 Pt ambulated independently and w/ steady gait accompanied by staff. NAD to women's restroom and then out of facility. Pt was educated to rest and take it easy @home tonight. Also informed pt that for any future vaccination of this incident and stay well hydrated. Dizziness and feeling cold/shaky resolved. Pt stable and released from the vaccination site. NAD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Inappropriate sinus tachycardia, Allergic Rhinitis
Andere Medikamente: Medications: Fluvoxamine 50mg PO daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 1974877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Feeling cold Palpitations

Symptomtext

Patient c/o of heart palpitations to observation RN. Patient escorted into triage area with observation RN. Charge RN and on-site provider notified. @1130AM BP 135/90 HR 69 RR 16 O2sat 100% AOx4. Assess by observation RN- Patient denies chest pain N/V, headache. SOB. Patient reported having an anxiety to needles and feeling cold, was provided jacket by husband. Pt reported consuming 2 cups of coffee prior to time of vaccination and has not had any other drinks. On site provider recommended extended observation. Patient given 1 water bottle. @1204PM BP 119/88 HR 67 RR 16 O2sat 100% AOx4, VSS. Patient fully drank 1 water bottle. Patient denies chest pain N/V, headache, and no longer feels palpitations, and SOB. On site provider recommended pt follow up with PCP. Patient educated to call 911/ER services for any worsening symptoms. Patient verbalized understanding. Pt d/c @1204PM to home with husband.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: PCOS, hx of hysterectomy, hx of Radiofrequency ablation of 9cm myoma
Andere Medikamente: Medications: omega-3 fatty acids (FISH OIL) 1000mg Cap Cholecalciferol (VITAMIN D) 2,000 units CAPS metFORMIN 24Hr-XR (GLUCOPHAGE XR) 500mg Tab Indications: PCOS (polycystic ovarian syndrome) Take two Tabs by mouth twice daily wi
Allergien: Allergies: Cherry
Vorherige Impfungen: -

VAERS 1971796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

moderat

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Condition aggravated

Symptomtext

Janssen Primary, Pfizer booster 12mins post vaccination pt c/o anxiety. Vitals: 11:18 126/58, 84, 99% -- > 11:30 120/64, 84, 99% Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Vertigo Syncope without other cardiovascular symptoms Onychomycosis Globus sensation Anxiety Unexplained weight loss
Andere Medikamente: None significant
Allergien: Allergies: mild seasonal allergies, PCNs, Ibuprofen, unknown allergy w swollen tongue
Vorherige Impfungen: -

VAERS 2635150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: ID
Alter: 64,0
Geschlecht: M
Eingang: 22.05.2023
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Injection site pain Mental impairment Pain in extremity

Symptomtext

Still experiencing bouts of very sore upper arm and was particularly acute today to the point that i called my doctor to figure out therapy. Right arm where i had the 2nd booster (3rd shot) is very sore and is making it difficult to think clearly today and is as sore today or even more sore than the day after receiving the jab back in December 2021. Left arm has bouts of soreness that come and go. That shot was 2 years ago on May 21, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: over the counter vitamins
Allergien: allergic to mango
Vorherige Impfungen: -

VAERS 2633814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: HI
Alter: 43,0
Geschlecht: M
Eingang: 18.05.2023
Impfdatum: 01.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Diarrhoea Irritable bowel syndrome

Symptomtext

Stomach upset, diarrhea, irritable bowels, loose stool

Weitere VAERSDATA-Felder

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

VAERS 2555840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 07.01.2022
Beginn: 25.12.2022
Tage bis Beginn: 352,0
Dosis: 3
Route/Site: SYR / LA

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

Bone pain COVID-19 Exposure to SARS-CoV-2 Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I was exposed on 12/25/2022 and symptoms started @ 12/26/2022 with upper body and skeletal aches, my fever started around 8PM the same day and it reached a high of 103 degrees. I tested positive for COVID-19 with a home rapid test. I contacted my doctor through my portal and due tome being high risk from Diabetes I was prescribed PAXLOVID, I took a five day course. Fever remained through day six. I tested negative on January 3 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: COVID-19 test result was positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Hypothyroidism; Hypoparathyroidism; Hypocalcemia; High Cholesterol
Andere Medikamente: LEVOXYL; calcitriol; CALTRATE; NOVOLOG insulin
Allergien: None
Vorherige Impfungen: -

VAERS 2549107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 31.12.2022
Beginn: 25.12.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Chills Cough Ear pain Feeling abnormal Oropharyngeal pain Pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had a 102 fever, loss taste and smell, coughing, chills, body aches, running nose, earache, sore throat, foggy in the head, and still getting fevers at night but not as high. I tested positive for COVID-19 at home. My doctor put me on the Z-pack and steroids. I am feeling better. I still have no taste or smell and coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 Test, 12/25/2022, Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bipolar
Andere Medikamente: Famotidine; Lipitor; Lisinopril; Seroquel; Trileptal; Prilosec; Multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2548943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: DE
Alter: 73,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 30.12.2021
Beginn: 18.08.2022
Tage bis Beginn: 231,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Feeling hot Headache Influenza Nasopharyngitis Oropharyngeal pain Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I was exposed on 08/18/22, I started feeling achy, sore throat, hot but no fever, cough, runny nose, stuffy head, headache. I would describe it as the worse flu or cold I ever had. On 08/25/22, I used a home COVID-19 test that came back positive. I called my doctor's office we discussed my symptoms and decided not to prescribe medication. The symptoms were gone within two to three weeks with the exception of the cough and fatigue. They lasted for six weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: SYNTHROID
Allergien: AVELOX
Vorherige Impfungen: Shingles vaccine

VAERS 2544988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 27.12.2021
Beginn: 25.11.2022
Tage bis Beginn: 333,0
Dosis: 3
Route/Site: IM / LA

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

Eye pain Eye swelling Headache Herpes zoster Rash

Symptomtext

I was having a bad headache like something was stabbing and pinching on the left side of my brain. About four days later I was having more pain around my left eye near my eyebrow. Then a rash appeared on the left side of my forehead near my hairline. That moved down toward my eye, and this led me to go to the ER. After looking at the rash they also called an eye doctor to take a look at me as well. They then told me that it was Shingles, and I was given some pain medication and then and medication for the shingles and an ointment for my eye. I had a follow up with the eye doctor to check my eye and at that time it was painful and swollen. The swelling is better along with the rash but I still have the pain in my head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Visual exam
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2542110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge 33025BD

mild

Staat: LA
Alter: 70,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 22.12.2021
Beginn: 21.12.2022
Tage bis Beginn: 364,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Middle ear effusion Pharyngeal erythema SARS-CoV-2 test positive Sinus headache Sinusitis Vertigo

Symptomtext

I had a slight sinus headache and a small bout of Vertigo. I went to the doctor, and she checked my ears, and my throat was red. She said that my ears had fluid in them. I was prescribed some mediation for Sinusitis. The next night my grandson was having some stomach issues and I took him to the doctor at his primary care office. They tested both of us and we both tested positive for COVID-19 on 12/21/22. I was prescribed 5 days' worth of Paxlovid. I am feeling better, but still dealing with most of the symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus headache
Hospital-Tage: -
Labordaten: 21DEC2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Type 2 Diabetic
Andere Medikamente: Biotin; Zinc; Vitamin C; Iron; Vitamin D3; Nifedipine ER; Metoprolol; Metformin; Rosuvastatin; Valsartan; Pantoprazole
Allergien: N/A
Vorherige Impfungen: -

VAERS 2439963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 330 25 BD

mild

Staat: IN
Alter: 80,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 11.01.2022
Beginn: 21.02.2022
Tage bis Beginn: 41,0
Dosis: UNK
Route/Site: SYR / LA

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

Loss of personal independence in daily activities Sleep disorder Urticaria

Symptomtext

Patient initially used J&J vaccine with no adverse effects. She developed hives about 6 weeks after mRNA booster. After three months working with her internist, she was referred to an allergist. She was told that the allergist has seen similar cases "almost every day" related to the mRNA covid boosters and recommended Xolair shots but could not say if or when they would be effective. Patient conferred with her internist and decided that the possible positive outcome did not overcome the potential for no relief or adverse response. Patient now on regimen of 2 Zyrtec twice a day plus refrigerated Sarna Sensistive, unable to wear clothes or sleep more than three hours at a time.

Weitere VAERSDATA-Felder

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

VAERS 2401350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 03.01.2022
Beginn: 02.08.2022
Tage bis Beginn: 211,0
Dosis: 3
Route/Site: - / -

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

Cough Pyrexia Respiratory tract congestion

Symptomtext

Fever, congestion and cough.

Weitere VAERSDATA-Felder

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

VAERS 2323264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 16.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia Asthenia COVID-19 Dizziness Feeling abnormal Nasopharyngitis Nausea Paranasal sinus discomfort Productive cough Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sick relative

Symptomtext

Thursday the 28th in the morning my head felt a little off so I took some Tylenol. I went to work that day, my sinus felt like sinus pressure from my allergies and around noon I picked up some Sudafed. And around 3 pm I got out of my car and stood up and I felt so woozy like I was gonna fall down. I was at my doctor to pick up some med and I also grabbed some COVID-19 test. When I got home I took and test and it was positive. By the next day I had no energy, nauseous, congestion and my nose was running more then it was with a cold. I had a fever it was about 102. I was nauseous but nothing throwing up with a little dihedral. It was really hard to stay awake. I called to get a hold of my doctor they set me up with a telehealth. The prescribed paxalif. I had a very strong cough in my chest, but i was progress cough and a lot flehm would come out. My husband picked up my meds for me. By Saturday i lost taste of smell and everything else was still going. Those symptoms kept going until 05/05/2022. I was not sleepy as much and was still draining a lot of flehm. I realized on the 05/05/2022 that i was not taking the meds correctly. I called my doctor to get the right dosage. By that time my husband also tested positive for COVID-19. I think it around 05/07 where i was testing negative. I was feeling more energy but still had a lingering cough and congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: COVID-19- positive
Aktuelle Erkrankungen: Stomach Pain - Treated for Ulcer
Vorgeschichte: Pre Diabetic, High Cholesterol
Andere Medikamente: Daily Women's Vitamin, Fish Oil, Cerebral Fibrate, Zyrtec, Tylenol as needed
Allergien: outdoor allergies
Vorherige Impfungen: -

VAERS 2292616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: DC
Alter: 63,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 01.05.2022
Beginn: 22.05.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: SYR / LA

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

Pruritus Skin reaction Urticaria

Symptomtext

three days following vaccination I began having itchy, red hives all over my body, bilaterally including knees, ears, fingers, thighs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sinus infection
Vorgeschichte: sinus infections
Andere Medikamente: Vitamin B, Calcium, Vitamin D antibiotic-Cefdinir 300 mg
Allergien: Sulfa allergy
Vorherige Impfungen: -

VAERS 2256908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 18.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Pain Pyrexia

Symptomtext

Starting the following day after receiving the vaccine, I woke up fatigued and was having body aches. I felt a little feverish/chills which didn't last all day. The fatigue persisted and I ended up sleeping the rest of the day. By the next day, I was totally fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C and Vitamin D
Allergien: Doxycycline
Vorherige Impfungen: 2nd dose of Moderna: Slight woozy for an hour then it was gone.

VAERS 2223134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 05.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Agitation Injection site erythema Injection site oedema Injection site warmth Insomnia

Symptomtext

agitation and insomnia 2 days after vaccines along with erythema, edema, warmth at injection sites

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: asthma, HTN, depression, anxiety, difficulty concentrating, trouble sleeping
Andere Medikamente: albuterol inhaler prn; alprazolam prm, amlodipine-benzapril, symbicort, flonase nasal spray, loratadine, metoprolol, sertraline, ambien
Allergien: latex, amitriptyline
Vorherige Impfungen: -

VAERS 2222920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MD
Alter: 33,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Pruritus Skin irritation Urticaria

Symptomtext

Patient vaccinated approx. 5pm. Patient reported itching following her vaccination period and 15 minutes of observation time. Patient presented with redden welts from scratching on the upper extremities and abdomen. Patient placed in triage room and assessed by provider on site. Benadryl 50mg given at 1730. Patient progresses in irritation to upper torso, thighs, and lower extremities. 911 contacted at 1742, 1mg Epi administered. EMS arrives at 1751. Patient left with EMS to ED at 1803 after assessment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Denies
Vorgeschichte: Denies
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2216410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 04.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Pain Tenosynovitis stenosans

Symptomtext

Patient describes pain in left radial part of wrist over area associated with deQuervain's tenosynovitis and has had pain with lifting things.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None known
Vorgeschichte: Prediabetes, NASH, Obesity, Vitamin D deficiency
Andere Medikamente: None known
Allergien: None
Vorherige Impfungen: Pfizer COVID lot EW0162 on 4/15/21- IM in left arm, had right forearm pain starting 2 days later and unable to hold a cup of wat

VAERS 2214922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: DC
Alter: 55,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 01.03.2022
Beginn: 01.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Immediate post-injection reaction Injection site pain Pain in extremity

Symptomtext

The area where I received the booster still hurts a month later. It hurts to the bone and stings to the touch. Immediately after the shot, the left arm, which didn't receive the shot, hurt more than the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: high cholesterol, Carpal Tunnel
Andere Medikamente: none
Allergien: aspirin, cucumbers, limes, gluten
Vorherige Impfungen: Soreness after Pfizer shots 1 and 2 that lasted for a day.

VAERS 2196921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 30.04.2021
Beginn: 16.01.2022
Tage bis Beginn: 261,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dizziness Hypophagia Myalgia Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

01/16/22 presents to EC ED for "nausea, vomiting, myalgias, decreased PO intake, and lightheadedness". PMHx of "lupus nephritis s/p renal transplant 3/2020, bipolar disorder requiring hospitalization, GERD, ADHD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 01/16/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2194629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: AL
Alter: 46,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 05.01.2021
Beginn: 19.01.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal pain upper Chest X-ray Chills Feeling cold Full blood count Impaired work ability Lipase Metabolic function test Muscle spasms Nausea Pain Pyrexia SARS-CoV-2 test negative Vomiting

Symptomtext

It starts with light stomach ache and nausea, as time progresses (avg 30-90) mins the ache become cramps and spasms, some mild but about half have developed to severe needed to bee seen in ER. Most spike fevers from 99.6 to 102.3. vomiting usually happens around 90 min mark but not always. After vomiting, then I continue to have Aches and spasms but begin to have the chills, even being wrapped in blankets I just cant seam to stay warm. ER visit dates over last year: @local Hospital ER - 1/19/21; 3/7/21; 6/9/21; 7/14/21 (PCM visit); 8/18/21; 12/15/21(covid clinic) ER Visits to regional Hospital ER - 9/28/21; 1/14/22; 1/22/22. I have had many more just not as painful that i did not go to ER. If needed I can submit Leave days taken from work due to this that I did not go to ER. Since this first event i have continued to have them even up to last week (3/17) small event and (3/18) ER visit event. With all my conditions, I have never had this very specific problem, which continues to happen in recent weeks, before receiving the vaccine in Jan '21, and I hesitated submission of this as the professionals I have seen are not sure its vaccine related but after all the ER visits, PCM visits, Gastrointestinal Providers i see for Transplant and other issues they have no other explanation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: COVID test-Neg Lipase Hemogram+Differential Auto Comprehensive Metabolic Panel Chest Xray
Aktuelle Erkrankungen: none
Vorgeschichte: Primary Sclerosing Cholangitis(liver transplant candidate), Ulcerative Colitis, GERD, Ulcers, Sleep Apnea
Andere Medikamente: Mercaptipurine 150mg 3xDay Colazal 750mg 3xDay Prilosec 40 MG 2xDay Ursadiol 500mg 2xDay Carafate 15Ml 4xDay Sucralose 10ML 2xDay
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2191505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: -
Alter: 36,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 08.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Chills Fatigue Nausea

Symptomtext

Chills; nausea; fatigue; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Feb2022 (Lot number: 33025bd) at the age of 36 years as dose 3 (booster), single for covid-19 immunization. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Eic 1283), for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Eic 5730), for COVID-19 Immunization. The following information was reported: CHILLS (non-serious) with onset 09Feb2022, outcome "unknown", described as "Chills"; NAUSEA (non-serious) with onset 09Feb2022, outcome "unknown", described as "nausea"; FATIGUE (non-serious) with onset 09Feb2022, outcome "unknown", described as "fatigue". Therapeutic measures were taken as a result of chills, nausea, fatigue. Additional information: The patient received Tylenol treatment for an AE. No covid prior vaccination. No covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: None other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Headache

Symptomtext

Headache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (159558). The reporter is the patient. A 67 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 30Dec2021 (Lot number: 33025BD) at the age of 67 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: HEADACHE (non-serious) with onset 30Dec2021, outcome "not recovered", described as "Headache". Therapeutic measures were taken as a result of headache. Additional information: Reporter stated she was a healthy 67-year-old with no problems, no diabetes and no cancer and no high blood pressure and had nothing of that nature and stated she had bronchitis which was diagnosed twenty years ago prior to her getting the Pfizer Covid vaccine and the spelling of bronchistis was captured as stated by the reporter as she was unsure of the spelling of that. Reporter stated she was not a sick person and was very well and had been on the job for 35 years. Stated she can't get an appointment with the people at the hospital where she took the Pfizer Covid vaccine and stated her headache began when she took the vaccine on 30Dec2021, and it was ongoing and the same and she had never had headaches. Stated she began no new medication and was taking the same medications she always took and her headache was strange and she had the headache all last week until now and takes Tylenol enough and the dosage of that was 600mg and she took it when she came home on 30Dec2021 and had the headache and took the Tylenol and the only thing was that when she took the Pfizer Covid vaccine she had not eaten all day long and never gets headaches if she did not eat; stated she had no lot, expiry date to provide for the Tylenol. No other products and investigation assessment reported. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchitis (diagnosed twenty years ago); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2177716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MI
Alter: 29,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 09.01.2022
Beginn: 07.02.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: UN / UN

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

Anaemia of pregnancy COVID-19 Constipation Delivery Epidural injection Episiotomy Exposure during pregnancy Glucose tolerance test abnormal Hypothyroidism Influenza A virus test negative Influenza B virus test Pain Postpartum state Respiratory syncytial virus test negative Rhesus antigen positive Rubella antibody test SARS-CoV-2 test positive Vacuum extractor delivery

Symptomtext

Diagnosis ? Anemia affecting pregnancy in third trimester ? Status post vacuum-assisted vaginal delivery ? Hypothyroidism ? Blood type, Rh positive ? Rubella immune ? Abnormal glucose tolerance test (GTT) Please see the prenatal record and admission history and physical for details. Labor Analgesics: Epidural;Local OB Complications: Cervical Ripening Type: None Cervical Ripening Comment: Induction: None Induction Indications: Augmentation: Oxytocin Delivery Date: (Privacy) Delivery Time: (Privacy) Gestational Age(weeks days/7): 39 1/7 Method of Delivery: Vaginal, Vacuum (Extractor) Birth Weight: 3.58 kg (7 lb 14.3 oz) Sex: male Apgar Score (1 min): 9 Apgar Score (5 min): 9 Laceration Episiotomy: Midline Laceration Type: 2nd Perineal Laceration: Quantified Blood Loss (ml): Est Blood Loss For further details of the delivery see the delivery summary. Her post partum course was complicated by: None Patient with uncomplicated post-partum recovery. On the day of discharge pain was well controlled with oral pain meds, she was ambulating and voiding without difficulty, and was tolerating diet without nausea/vomiting. Patient reports constipation and a Rx for a stool softener was sent to her pharmacy. Patient was requesting discharge home. Following complete examination and review of recovery course, patient was deemed stable for discharge. Patient will need 2hr GTT at her 6 week post partum visit. Procedures performed: VA-VD w/ RML episiotomy Discharge All Hospital Problems (Other diagnoses): Active Hospital Problems Diagnosis ? Principal Problem: Status post vacuum-assisted vaginal delivery [Z87.59] ? Hypothyroidism [E03.9] ? Blood type, Rh positive [Z67.90] ? Rubella immune [Z78.9] ? Abnormal glucose tolerance test (GTT) [R73.09] ? Anemia affecting pregnancy in third trimester [O99.013] Resolved Hospital Problems No resolved problems to display.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: 3,0
Labordaten: <NOCOVER> 1 (Privacy) HEALTH SYSTEM (Privacy) LABORATORY Chart Review Copy Patient name: HAR: (Privacy) DOB: (Privacy) (29 yrs) PT CLASS: Inpatient CSN: (Privacy) DEPT: (Privacy) PATIENT STATUS: Discharged GENDER: female BED: (Privacy) ORD DR: (Privacy) AUTH DR: (Privacy) Results Covid-19, Flu, RSV by NAA (Order (Privacy)) Contains abnormal data Covid-19, Flu, RSV by NAA Order: (Privacy) Status: Final result Visible to patient: Yes (seen) Next appt: 03/23/2022 at 03:00 PM in Obstetrics and Gynecology ((Privacy), DO) Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR)
Aktuelle Erkrankungen: ? Anemia affecting pregnancy in first trimester 8/3/2021 ? Hypothyroidism ? Varicella
Vorgeschichte: -
Andere Medikamente: Current Outpatient Medications Medication Instructions ? docusate (COLACE) 100 mg, Oral, DAILY ? ferrous sulfate 325 mg, Oral, THREE TIMES DAILY ? levothyroxine (SYNTHROID, LEVOTHROID) 75 mcg, Oral, BEFORE BREAKFAST, THYRORICH 75MCG. EQUIVA
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2147364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: FL
Alter: 35,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Abdominal discomfort Abdominal distension Constipation Diarrhoea Flatulence Muscle spasms Nausea

Symptomtext

Severe stomach trouble; Nausea; Constipation; Diarrhea; cramping; Bloating; gassy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 12Jan2022 17:45 (Lot number: 33025BD) at the age of 35 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfa" (unspecified if ongoing); "Known allergies: latex" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: ABDOMINAL DISCOMFORT (non-serious) with onset 13Jan2022 12:00, outcome "not recovered", described as "Severe stomach trouble"; NAUSEA (non-serious) with onset 13Jan2022 12:00, outcome "not recovered", described as "Nausea"; CONSTIPATION (non-serious) with onset 13Jan2022 12:00, outcome "not recovered", described as "Constipation"; DIARRHOEA (non-serious) with onset 13Jan2022 12:00, outcome "not recovered", described as "Diarrhea"; MUSCLE SPASMS (non-serious) with onset 13Jan2022 12:00, outcome "not recovered", described as "cramping"; ABDOMINAL DISTENSION (non-serious) with onset 13Jan2022 12:00, outcome "not recovered", described as "Bloating"; FLATULENCE (non-serious) with onset 13Jan2022 12:00, outcome "not recovered", described as "gassy". Therapeutic measures were not taken as a result of abdominal discomfort, nausea, constipation, diarrhoea, muscle spasms, abdominal distension, flatulence. Additional information: The patient did not receive other Vaccine in four weeks. The patient had not covid prior vaccination. The patient has not covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Latex allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2134608

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 33025BD

mild

Staat: NJ
Alter: 22,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Flushing Immediate post-injection reaction Rash macular Urticaria

Symptomtext

Instantly within seconds of shot became drastically flushed in face and neck with some hive/blotching. Lasted for about 45 mins-1hr. O2 was fine, no breathing issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: Was taken by employees in private room, laid down, monitored and vitals checked for about 45 mins. Was given dose of liquid benedryl. In hind sight I am confused why they never took an official report or followed up with me, especially that it's a hospital and the serious chronic health conditions I have.
Aktuelle Erkrankungen: -
Vorgeschichte: Cystic fibrosis, Bicuspid aortic valve, Ehlers-Danlos, hypermobile type, Gastroparesis, Pancreatic insufficiency, GERD, POTS, Hypersomnia, major depressive disorder, Irritable bowel syndrome with constipation, Impaired glucose tolerance,
Andere Medikamente: modafiniL 200 mg tablet 2-3 a day, ondansetron 8 mg disintegrating tablet prn, cyclobenzaprine 10 mg tablet prn, DULoxetine DR 30 mg capsule, TRIKAFTA 100-50-75 mg(d) /150 mg (n) tablets, sequential, dicyclomine 10 mg capsule, buPROPion ER
Allergien: Spirulina, Honeydew melon, latex sensitivity
Vorherige Impfungen: Mild reaction low grade fever, injection site pain, and felt under weather with the first two vaccines for Covid-19

VAERS 2127667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: WI
Alter: 53,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Alopecia Anxiety Biopsy skin Fatigue Feeling abnormal Full blood count Headache Pain Pyrexia

Symptomtext

High Fever, body aches, fatigue, headache. extreme hair loss, mental fog, anxiety

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: biopsy of scalp, CBC on one occasion
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: citalopram 10 mg daily Alprozalam .25 prn
Allergien: Cipro Mprophine
Vorherige Impfungen: -

VAERS 2119690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Injection site induration Injection site mass

Symptomtext

Patient reported a large, hard lump near bicep of vaccination arm that occurred the day following vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site induration
Hospital-Tage: -
Labordaten: Patient had dr examine, dr said he may refer patient to a surgeon
Aktuelle Erkrankungen: None reported
Vorgeschichte: Hypertension, Hypercholestermia
Andere Medikamente: -
Allergien: None reported
Vorherige Impfungen: -

VAERS 2119361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 9,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Incorrect dose administered Pain

Symptomtext

Patient received 12 years and older dose of Pfizer COVID-19 vaccine as the first dose. Mother stated patient had headache and body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: obesity
Andere Medikamente: none
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2113341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: MO
Alter: 57,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 07.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Pain Pain in extremity Spinal pain

Symptomtext

lumbar and spine throbbing, leg pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: fibro myalgia, spinal stenosis, blood pressure, cholesterol,
Andere Medikamente: vit d
Allergien: nuerotin, plavix, ace inhibitors
Vorherige Impfungen: -

VAERS 2109651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: TX
Alter: 57,0
Geschlecht: F
Eingang: 13.02.2022
Impfdatum: 27.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain upper Decreased appetite Headache Injection site pain Pain Pyrexia

Symptomtext

after 24 hours . i experienced a low grade fever of 99.2. .severe headache that has lasted 2 weeks, pain at the injection site, body aches, moderate stomach pain for 2 weeks., lack of appetite for 2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: nonr
Vorgeschichte: none
Andere Medikamente: tylenol
Allergien: none
Vorherige Impfungen: pfizer covid first dose-moderate reaction 2nd dose of pfiser-moderate reaction with vision changes. seeing red auras age 57

VAERS 2099518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NJ
Alter: 62,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 30.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Ascites Headache

Symptomtext

Customer shared that she is experiencing excess fluid in stomach, Stomach Aches and Headaches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Rhinitis
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2099502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: VA
Alter: 37,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 18.12.2021
Beginn: 10.01.2022
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: SYR / RA

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

Dry skin Rash Rash erythematous Rash pruritic Skin discolouration

Symptomtext

In early January (approximately 01/10/2022) I developed the same rash as I developed after the second dose. It was red, itchy, rough in texture, darker in color and extended from mid forearm to shoulder area on both arms. I went to the dermatologist and they gave me a cream (Clobetasol) which alleviated the symptoms in about 3-4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Breast lumps
Andere Medikamente: Birth control pill; vitamin D3; BENADRYL
Allergien: None
Vorherige Impfungen: Fatigue, body aches, joint pain, nausea and headaches, along with the same rash after the 2nd Pfizer dose.

VAERS 2091873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: OR
Alter: 54,0
Geschlecht: M
Eingang: 06.02.2022
Impfdatum: 03.02.2022
Beginn: 03.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Headache Injection site pain

Symptomtext

Within 6 hours, a moderate headache manifested that progressed into a severe headache by 12 hours. Patient has had a history of migraines. The was also pain at the injection site that peaked approximately 24 hours later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2082530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Exposure during pregnancy Pain Pain in extremity

Symptomtext

30 minutes after the vaccine I experienced painful stinging sensation in both hands and feet. I have had this symptoms everyday since the vaccine up to this current day. Symptoms are affecting my ability to function as it is very painful. Pregnant when I took the vaccine- EDD 05/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None done as to date. I have been waiting to see if the symptoms would go ago before going to a doctor because of insurance high deductible. However I will now go as symptoms are persistent.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2082164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: WI
Alter: 23,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 01.02.2022
Beginn: 02.02.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chest discomfort Dizziness Fatigue Joint stiffness Nausea Vomiting

Symptomtext

- Stiffness in all joints - Tightness in chest - Nausea and vomiting - Feeling faint - Fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: - COVID-19 21 days prior to 2nd dose of vaccine
Vorgeschichte: Asthma
Andere Medikamente: N/A
Allergien: - Lactose and gluten intolerant - Allergic to latex
Vorherige Impfungen: -

VAERS 2080536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 18,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 21.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Gingival pain

Symptomtext

Pain in gums

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gingival pain
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2079565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: WI
Alter: 22,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pruritus Swelling Urticaria

Symptomtext

Patient experienced prolonged itching, swelling, and hives post Pfizer COVID vaccination. Please see next page for detail.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sprintec Birth Control, CBD
Allergien: PCN, Amoxicillin: hives, intense itching, facial swelling
Vorherige Impfungen: -

VAERS 2074368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NC
Alter: 42,0
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Pyrexia

Symptomtext

Fever 12 hours after vaccine; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 42 year-old male patient received bnt162b2 (BNT162B2), administration date 12Jan2022 (Lot number: 33025BD) at the age of 42 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FISH OIL. Past drug history included: Keflex, reaction(s): "known allergies: keflex", notes: known allergies: keflex. Vaccination history included: Bnt162b2 (Dose Number: 1, Lot No: ER9727), administration date: 24Mar2021, when the patient was 41 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 2, Lot No: ER8737), administration date: 14Apr2021, when the patient was 41 years old, for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 13Jan2022, outcome "recovered" (Jan2022), described as "Fever 12 hours after vaccine". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine The patient received other medications within 2 weeks of vaccination are fish oil, mutli vitamin The patient did not diagnosed with COVID-19 Prior to vaccination. The patient had not been tested for COVID-19 Since the vaccination. Follow-Up (19Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20220113; Test Name: fever; Result Unstructured Data: Test Result:unknown; Comments: Fever 12 hours after vaccine
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: FISH OIL.
Allergien: -
Vorherige Impfungen: -

VAERS 2074340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 62,0
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Fatigue Tinnitus

Symptomtext

Had strong ringing in my ears; Very tired; This is a spontaneous report received from a contactable reporter(s) (other healthcare professional). The reporter is the patient. A 62-year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 06Jan2022 08:15 (Lot number: 33025BD) at the age of 62 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Being treated from a bad fall which had several surgeries as a result from falls." (Unspecified if ongoing), "Being treated from a bad fall which had several surgeries as a result from falls." (Unspecified if ongoing). Concomitant medication(s) included: GABAPENTIN, CARISOPRODOL, HYDROCODONE/IBUPROFEN, ATORVASTATIN, TRAZODONE, DICLOFENAC SODIUM. Vaccination history included: Bnt162b2 (Dose number: 1, Lot number: EH9899, Route: Intramuscular, Vaccine location: Right arm) administration date: 29Dec2020 for COVID-19 immunisation, Bnt162b2 (Dose number: 2, Lot number: EL1284, Route: Intramuscular, Vaccine location: Right arm) administration date: 19Jan2021 for COVID-19 immunisation. The following information was reported: TINNITUS (non-serious) with onset 06Jan2022 12:30, outcome "recovering", described as "Had strong ringing in my ears", FATIGUE (non-serious) with onset 06Jan2022 12:30, outcome "recovering", described as "Very tired". Therapeutic measures were not taken as a result of tinnitus, fatigue. Additional information: Prior to vaccination, was the patient did not diagnosed with COVID-19. Since the vaccination, patient has been tested for COVID-19 was unknown. Patient not had known allergies. Patient adverse event started with in four and half hours after the third dose patient became very tired, had strong ringing in my ears. Had to go home from work. Follow-Up (18Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fall; Surgery
Andere Medikamente: GABAPENTIN; CARISOPRODOL; HYDROCODONE/IBUPROFEN; ATORVASTATIN; TRAZODONE; DICLOFENAC SODIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2069244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MD
Alter: 25,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Feeling hot Hypersensitivity Rash erythematous Tongue eruption

Symptomtext

Prior to vaccination of booster, patient indicated that she had an "allergic reaction" to first dose Pfizer vaccine where she indicated that she was tachycardic, sweating, flushing, and had raised bumps on tongue. Patient said that clinic staff had administered 25mg PO benadryl after the reaction, and symptoms completely resolved. Patient reported no reaction after 2nd dose of Pfizer vaccine. Today, clinic staff decided to go ahead with Pfizer booster and monitor patient closely. Baseline vitals at 4:41pm: BP 135/89, HR 96, SpO2 99%. IM booster of Pfizer administered via IM injection to R arm at 4:44pm. Vitals at 4:44pm: BP 140/77, HR 106, SpO2 99%. Patient's fiance noticed raised bumps on patient's tongue at 4:58pm during observation period post-vaccination. This RN confirmed raised red bumps on back of tongue near pharynx. Patient felt "warm" but was afebrile (temp 97.9F). 25mg PO liquid benadryl administered. Vitals at 4:58pm: BP 125/77, HR 88, SpO2 99%. Vitals at 5:06: BP 137/85, HR 87, SpO2 100%. Emergency assistance called at 5:08pm after no resolution of bumps on tongue. EMS arrived at 5:18pm. EMS transferred patient via stretcher to Medical Center at 5:35pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: food allergies (eggs, nuts, shellfish)
Andere Medikamente: unknown
Allergien: eggs, nuts, shellfish
Vorherige Impfungen: Covid vaccine, Pfizer, 1st dose, patient age 24, tachycardia/sweating/flushing/red bumps on tongue

VAERS 2068541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: WI
Alter: 64,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Burning sensation Erythema Limb mass Madarosis Pain in extremity Pruritus Skin exfoliation

Symptomtext

One week of sore arm with lump and red. from the 2nd day for four weeks extreme itching and burning from top of forehead down through the chest, skin peeled, no redness. Then loss of all my eyelashes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Depression.
Andere Medikamente: Bupropion; Vitamins.
Allergien: Iodine; Shellfish; Morphine.
Vorherige Impfungen: -

VAERS 2066160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Head discomfort Headache Hyperhidrosis Immediate post-injection reaction Musculoskeletal stiffness Neck pain

Symptomtext

Pt reported flushing/sweating, dizziness and stiffness of neck/neck pain. Vitals: 136/71, 82, 18, 100%, 98.1F Pt transported to ED. In ED: Received 3rd COVID vaccine today, immediately started feeling like her head is "heavy" with mild neck pain and posterior headache. Feels flushed,. Denies fever, n/v/d, cough, sob, swelling, sore throat, vision changes, numbness/weakness. Steady Gait A&Ox4. Vitals: 140/84, 70,20, 100%, 97.7F, Pain Score = 8 Pt discharged 18:53

Weitere VAERSDATA-Felder

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

VAERS 2062173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Pruritus

Symptomtext

Patient states she is itchy and requests IM Benadryl injection, patient is visibly itchy and lagging. Patient given therapy then monitored for 30 minutes prior to release from observation.

Weitere VAERSDATA-Felder

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

VAERS 2058975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IL
Alter: 55,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site bruising Injection site pain Injection site swelling

Symptomtext

Pt. states that after receiving the 3rd dose of Phizer 01/22/2022, started experiencing symptoms that evening of swelling at and around the injection site and sharp "stabbing" pain in the Left arm through the shoulder area with Minor bruising. No noted Primary visit/communications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: GURD, Epilepsy
Andere Medikamente: N/A
Allergien: Neomycin, Peanut Shells, Protein Powder
Vorherige Impfungen: Shingrix & Influenza 2020 (fever, chills)

VAERS 2054782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal discomfort Dizziness Flatulence Headache

Symptomtext

Began feeling like I had a gas bubble/burb in my upper abdomen that wouldn?t come up. Then I developed a very mild headache. In the late evening around 9pm on 7-Jan, I was standing up at my desk and began to feel faint. That resolved by 8-Jan, but the pressure in my upper abdomen, mild headache, and light headedness didn?t resolve until 10-Jan. Since then I?ve felt fine. If the symptoms hadn?t started to lessen on 9-Jan, I would have called my doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis in left knee
Andere Medikamente: Spirolactone
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2050568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: IN
Alter: 15,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Headache Vomiting

Symptomtext

Vomiting 3:30 pm followed by headache and tiredness through 1/18/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: uti
Vorgeschichte: Asthma, epilepsy
Andere Medikamente: Vestura
Allergien: Hydrocodone, Norco
Vorherige Impfungen: -

VAERS 2050328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 22.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Immunisation Rash pruritic

Symptomtext

husband got the third dose of Pfizer yesterday for COVID; rash in his whole body is really itchy is starting on the leg on the upper part of leg up to all the neck; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received bnt162b2 (BNT162B2), administration date 22Dec2021 (Lot number: 33025BD) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (Dose 2, MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021, outcome "unknown", described as "husband got the third dose of Pfizer yesterday for COVID"; RASH PRURITIC (non-serious) with onset Dec2021, outcome "unknown", described as "rash in his whole body is really itchy is starting on the leg on the upper part of leg up to all the neck". Additional information: Reporter stated that reporter's husband (patient) received the third dose of Pfizer vaccine for covid on the morning of 22Dec2021. Patient experienced rash in his whole body, and was really itchy, started on the leg, on the upper part of the leg up to all the neck. Reported stated that it was pretty bad and enquired if any medication was available for the itchiness. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2046244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MO
Alter: 36,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 03.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Herpes zoster Rash

Symptomtext

Systemic: Allergic: Rash Generalized-Medium, Additional Details: Rash/Shingles

Weitere VAERSDATA-Felder

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

VAERS 2045418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IL
Alter: 23,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 10.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Pruritus Vaccine positive rechallenge

Symptomtext

red, itchy patch on back of neck. This also happened after my second vaccine + went away after 2-3 months

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: migraines
Andere Medikamente: hormonal birth control
Allergien: Doxycycline
Vorherige Impfungen: red, itchy patch on back of neck following 2nd covid shot

VAERS 2043953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea

Symptomtext

Patient expressed that after the vaccine and during the 15 minute observation period that she was feeling nauseous and dizzy. Patient explained previously that she had tested positive for COVID recently and was still experiencing lingering effects since. Patient was advised to remain in the lobby for observation for an additional 15 minutes for any worsening or new symptom development. Patient eventually left without additional reportings.

Weitere VAERSDATA-Felder

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

VAERS 2042316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Immunisation Injection site erythema Pain Swelling Vaccination site pain

Symptomtext

it seems a little red; swelled; booster; got a little sore; hurting; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54 year-old female patient received bnt162b2 (Pfizer COVID 19 Vaccine- Solution for injection), administered in arm right, administration date 22Dec2021 (Lot number: 33025BD) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (1st dose, LOT# of first shot: EW0158), administration date: 02Apr2021, when the patient was 53 years old, for COVID-19 Immunization; Bnt162b2 (2nd dose, LOT# of second shot: EW0164), administration date: 03May2021, when the patient was 53 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021, outcome "unknown", described as "booster"; VACCINATION SITE PAIN (non-serious) with onset 22Dec2021, outcome "not recovered", described as "got a little sore"; PAIN (non-serious) with onset 22Dec2021, outcome "not recovered", described as "hurting"; INJECTION SITE ERYTHEMA (non-serious) with onset 23Dec2021, outcome "not recovered", described as "it seems a little red"; SWELLING (non-serious) with onset 23Dec2021, outcome "not recovered", described as "swelled". Therapeutic measures were not taken as a result of vaccination site pain, pain, injection site erythema, swelling. Additional information: she got a little sore (Further clarification unknown hence event captured as per verbatim) after came back to apartment and it was been hurting and today (date not specified) it seems a little red and it was swelled and that was still hurting." No follow-up attempts are possible. Information about batch number cannot be obtained.Vaccination facility: Consumer stated, "The first two was done at the withheld. Done by Regulatory authority." Prior to the vaccination, the patient was not diagnosed with COVID-19.

Weitere VAERSDATA-Felder

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

VAERS 2038301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IN
Alter: 32,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 14.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Ear swelling Throat irritation Urticaria

Symptomtext

On the second morning (Jan-16-2022) after receiving the booster vaccination, I woke up with hives over my entire body, swelling of my ears, and a slightly scratchy throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: mild mitral and tricuspid regurgitation
Vorgeschichte: Allergies Superior canal dehiscence syndrome
Andere Medikamente: Xyzal, prenatal vitamin
Allergien: Red dye, sulfa, azithromyacin
Vorherige Impfungen: After the second Pfizer vaccine, I had a few hives on the morning after I received the vaccine that quickly went away.

VAERS 2037790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: PR
Alter: 65,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 15.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Hyperhidrosis Pallor

Symptomtext

Patient sweaty, pale and dizzy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Dextrose 63; Blood pressure 110/60
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes; High blood pressure; Heart failure
Andere Medikamente: Insulin
Allergien: None
Vorherige Impfungen: -

VAERS 2037660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Immunisation Swelling

Symptomtext

Swelling and pain in left armpit; Swelling and pain in left armpit; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 34-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 10Jan2022 (Lot number: 33025BD) at the age of 34 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. The patient had received unspecified concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EW0158, Anatomical Location: Left arm), administration date: 15Apr2021, when the patient was 33 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0172, Anatomical Location: Left arm), administration date: 06May2021, when the patient was 33 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 10Jan2022, outcome "unknown", described as "Dose received: 3"; SWELLING (non-serious), AXILLARY PAIN (non-serious) all with onset 11Jan2022, outcome "unknown", and all described as "Swelling and pain in left armpit". Therapeutic measures were not taken as a result of swelling and axillary pain. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2036040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: WA
Alter: 56,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Oedema peripheral Skin warm

Symptomtext

swelling/heat/soreness left underarm that is still ongoing despite taking regular ibuprofen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: NONE
Andere Medikamente: UNKNOWN
Allergien: MIRTAZAPINE, APAP
Vorherige Impfungen: -

VAERS 2034506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NJ
Alter: 45,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Headache Immunisation SARS-CoV-2 test Sinusitis Vaccination failure

Symptomtext

Pfizer COVID vaccine #1 09Apr2021 & #2 30Apr2021. I had my booster 30Dec2021 then tested positive for COVID 31Dec2021; she thought it went right to her head, her head was going to explode and when that happens it is usually a sinus infection; she thought it went right to her head, her head was going to explode and when that happens it is usually a sinus infection; Pfizer COVID vaccine #1 09Apr2021 & #2 30Apr2021. I had my booster 30Dec2021 then tested positive for COVID 31Dec2021; Pfizer COVID vaccine #1 09Apr2021 & #2 30Apr2021. I had my booster 30Dec2021 then tested positive for COVID 31Dec2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 45-year-old female patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE), administered in arm left, administration date 30Dec2021 11:15 (Lot number: 33025BD) at the age of 45 years as dose 3 (booster), single, administered in arm left, administration date 30Apr2021 (Lot number: EW0170) as dose 2, single and administered in arm left, administration date 09Apr2021 10:00 (Lot number: EP7533) as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Flu shot, administration date: Sep2021, for immunisation. The following information was reported: IMMUNISATION (medically significant) with onset 30Dec2021 11:15, outcome "unknown", VACCINATION FAILURE (medically significant), outcome "unknown" and all described as "Pfizer COVID vaccine #1 09Apr2021 & #2 30Apr2021. I had my booster 30Dec2021 then tested positive for COVID 31Dec2021"; COVID-19 (medically significant) with onset 31Dec2021, outcome "unknown", described as "Pfizer COVID vaccine #1 09Apr2021 & #2 30Apr2021. I had my booster 30Dec2021 then tested positive for COVID 31Dec2021"; HEADACHE (non-serious), SINUSITIS (non-serious), outcome "unknown" and all described as "she thought it went right to her head, her head was going to explode and when that happens it is usually a sinus infection". The events "pfizer covid vaccine #1 09apr2021 & #2 30apr2021. i had my booster 30dec2021 then tested positive for covid 31dec2021", "pfizer covid vaccine #1 09apr2021 & #2 30apr2021. i had my booster 30dec2021 then tested positive for covid 31dec2021", "pfizer covid vaccine #1 09apr2021 & #2 30apr2021. i had my booster 30dec2021 then tested positive for covid 31dec2021", "she thought it went right to her head, her head was going to explode and when that happens it is usually a sinus infection" and "she thought it went right to her head, her head was going to explode and when that happens it is usually a sinus infection" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (unspecified date) negative, notes: tested negative for 5 days straight at the rehab center; (30Dec2021) negative, notes: tested negative the day before; (31Dec2021) positive. Clinical course: The patient who had her Covid vaccine on 09Apr2021 and 30Apr2021 and just had her booster on 30Dec2021 tested positive for Covid on 31Dec2021. Patient tested negative for 5 days straight at the rehab center her mom was in and was wondering if it would affect her booster dose. The patient went back and forth from the hospital to rehab so she knows she got it in there, she touched one of it and she has a feeling that was where she got it. States she went to pick up her cell phone and it was full of people with Covid. The patient went in to (institute name withheld) on 31Dec2021 because she thought it went right to her head, her head was going to explode and when that happens it is usually a sinus infection. States they gave her a prescription and tested her for Covid and sent her home and called her 2 hours later and said she tested positive for Covid and she has just tested negative the day before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Name: Covid Test; Test Result: Negative ; Comments: tested negative for 5 days straight at the rehab center; Test Date: 20211230; Test Name: Covid Test; Test Result: Negative ; Comments: tested negative the day before; Test Date: 20211231; Test Name: Covid Test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2033067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 07.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Breast pain Lymphadenopathy Tenderness

Symptomtext

Severe mid underarm pain and swelling radiating to left breast area and tender feeling

Weitere VAERSDATA-Felder

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

VAERS 2033057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IN
Alter: 41,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Headache Pain

Symptomtext

I woke up Saturday at 7 AM felt a little achy laid back down and by 10 AM was unable to get out of bed I had severe aches and pains on a scale of 1 to 10 was a 9, unable to sit up or stand. Very bad fatigue. A very bad throbbing headache from Saturday until Monday that Tylenol would not help.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: Genital herpes, arthritis
Andere Medikamente: Morning- 200mg venlafaxine, 10mg adderall, 50mg spironolactone Before bed- 300mg gabapentin, 400mg acyclovir, 2mg prazosin , 0.5mg klonopin, 2mg melatonin
Allergien: Doxycycline
Vorherige Impfungen: Pfizer Covid vaccine 1 and 2, shots in May, 4 weeks apart, 41 years old, had severe aches and pains, fatigue, unable to sit or

VAERS 2032094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 08.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Nausea SARS-CoV-2 test

Symptomtext

Patient woke early the next morning (approx 2-3 am) with a severe headache with nausea. Went to Urgent Care facility the next morning because HA wouldn't go away & was continuing to have nausea. Prescribed zofran prn nausea-last dose on 1/11/2022. Last HA 1/12/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID test
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Amox, Augmentin
Vorherige Impfungen: -

VAERS 2028759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: WA
Alter: 21,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Gingival pain Pain Vision blurred

Symptomtext

blurry vision, lightheadedness, gums throbbing/painful

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: epilepsy/seizures
Andere Medikamente: Unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2025499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: KS
Alter: 35,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injection site reaction Lip swelling Rash macular Urticaria

Symptomtext

PATIENT STARTED HAVING A BLOTCHY RASH ON LEFT SIDE OF BODY WITH WELTS AROUND THE INJECTION SITE ABOUT 2 HOURS AFTER INJECTION. TOOK BENADRYL 50MG, NO RELIEF. RECEIVED A STERIOD PRESCRIPTION FROM HER PROVIDER BUT STILL NO RELIEF. THEN ENDED UP RECEIVING AN EPINEPHRINE SHOT ABOUT 3 1/2 HOURS AFTER VACCINATION DUE TO NO RELIEF AND LIPS STARTING TO SWELL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: BIATRIAL ENLARGEMENT WITH 1ST COVID VACCINE.
Vorherige Impfungen: DURING HER 1ST DOSE, SHE EXPERIENCED BI-ATRIAL ENLARGMENT ABOUT 3 DAYS AFTER VACCINATION.

VAERS 2025353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 10.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Pain of skin Rash macular Skin warm Urticaria

Symptomtext

pt called at 10am to report that when she woke up at 6am that she had red hot welts on her face and red hot blochy patches all over her body. they hurt to touch., she took benadryl at 6am but it still looked the same and felt the same at 10am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain of skin
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: NOTHING
Allergien: NONE
Vorherige Impfungen: -

VAERS 2019830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: GA
Alter: 39,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Pyrexia

Symptomtext

Almost passed out while driving. Extremely dizzy with any movement or anything visual moving. Had to be picked up. Dizzy for 3 days. Low grade fever and chills for 1 night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Negative dix-hallpike maneuver Normal blood pressure 122/68 Heart rate 89 Oxygen 99 On 1/7/21 1pm
Aktuelle Erkrankungen: No. Test weekly for work and have been covid negative
Vorgeschichte: Pcos
Andere Medikamente: Prozac Metformin
Allergien: None
Vorherige Impfungen: -

VAERS 2019253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 05.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Periorbital swelling Rash pruritic

Symptomtext

When she woke up two mornings after date of shot, she had painless, puffy swelling under her left eye and slightly itchy mild rash on both hands (slightly worse on right hand than on left hand). These symptoms decreased over the course of the day, but when she woke up this morning (3rd morning after shot) the symptoms reappeared.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: epilepsy
Andere Medikamente: Lamotrigine, 100 mg two times per day
Allergien: penicillin, topical benzoyl peroxide, chemical sunscreen all cause skin rash
Vorherige Impfungen: -

VAERS 2019164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 44,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Arthralgia Headache Lymphadenopathy Myalgia Nausea Vaccination site pain

Symptomtext

Swollen lymph nodes; Nausea; Injection site pain; Headache; Muscle and joint pain; Muscle and joint pain; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 44-year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 30Dec2021 at 09:00 (Lot number: 33025BD) at the age of 44 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "None". There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: 33026BD; Anatomical location: Right arm), administration date: 09Dec2021 at 09:00, when the patient was 44 years old, for COVID-19 immunisation. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 31Dec2021 at 00:00, outcome "not recovered", described as "Swollen lymph nodes"; NAUSEA (non-serious) with onset 31Dec2021 at 00:00, outcome "not recovered", described as "Nausea"; VACCINATION SITE PAIN (non-serious) with onset 31Dec2021 at 00:00, outcome "not recovered", described as "Injection site pain"; HEADACHE (non-serious) with onset 31Dec2021 at 00:00, outcome "not recovered", described as "Headache"; MYALGIA (non-serious), ARTHRALGIA (non-serious) all with onset 31Dec2021 at 00:00, outcome "not recovered", and all described as "Muscle and joint pain". The events "Swollen lymph nodes", "Nausea", "Injection site pain", "Headache" and "Muscle and joint pain" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of lymphadenopathy, nausea, vaccination site pain, headache, myalgia and arthralgia. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
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 2014185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 21,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Hyperventilation Vomiting

Symptomtext

Reaction: 9:30AM Patient reported flushing/sweating, dizziness, and vomiting. Vitals: 123/70, 81, 18 Patient was given water and had deep breathing. Patient later became stable and was released from vaccination site @9:50AM

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known PMH
Vorgeschichte: No known PMH
Andere Medikamente: No known medications
Allergien: NKA
Vorherige Impfungen: -

VAERS 2014063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: WI
Alter: 61,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: ID / -

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

Dizziness Inappropriate schedule of product administration

Symptomtext

Patient was scheduled for a vaccine at clinic today. Patient came and employee checked system. Employee couldn?t find patient in system and sent her over to get her 2nd vaccine. Patient didn?t have her CDC card. Patient was vaccinated after having 1st dose on 12/29/2021. Patient c/o dizziness, water was given and cold compress applied. Patient stated that she had HTN and Diabetes and haven?t had any medications since 2/2021. Patient was observed for 40 min and stated that she felt better. COVID clinic manager made aware. Patient felt better and left the clinic asymptomatic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes and Hypertension
Andere Medikamente: NONE
Allergien: NKA
Vorherige Impfungen: -

VAERS 2010861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: HI
Alter: 16,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Muscle tightness Pyrexia

Symptomtext

Back tightened within 2-3 hours of receiving the booster shot vaccination. Fever and chills within 24 hours of receiving the booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: 6/7/2021 Pfizer EW0217.

VAERS 2010363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: WI
Alter: 47,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Erythema Injection site erythema Injection site swelling Tenderness

Symptomtext

Where I received the injection is still swollen (red circle) but I also have a similar large spot on the same side of my body on my lower neck that is red and slightly painful to the touch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: I had Covid-19 in November - December. I tested positive on 11-24-21 & 11-29-21 but I did test negative on Friday December 3rd.
Vorgeschichte: none
Andere Medikamente: Adderall, Celexa, vitamin D, Lexapro
Allergien: no
Vorherige Impfungen: -

VAERS 2010047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NJ
Alter: 42,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Hypoaesthesia Injection site erythema Injection site pruritus Injection site swelling Injection site warmth

Symptomtext

The next day my injection site swelled up like a bee sting. It was huge. My arm also felt number. Next day it was less swollen but the whole area was a huge bloch of red and hot to the touch for about 3 days. The last two days it was itchy. Now I'm fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: cancer survivor, epileptic, autoimmune
Andere Medikamente: Lamicatal for epilepsy
Allergien: none
Vorherige Impfungen: -

VAERS 2005510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 23,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure decreased Dizziness Vomiting

Symptomtext

Vaccinated: 13:36 Reaction: 13:38 2 minutes after vaccination, patient reported vomiting and dizziness Vitals: 97/60, 71, 18 No medications were administered and patient became stable and was released from vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known PMH
Vorgeschichte: No known PMH
Andere Medikamente: No known medications
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2001352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Cold sweat Dizziness Feeling cold Hyperhidrosis

Symptomtext

Vaccinated: 13:00 Reaction: 13:05 Pt reported dizziness, sweating, cold clammy skin, and felt like fainting Vitals: 101/53, 51, 16, O2 100% -> @13:18: 116/74, 62, 18, O2 100% Patient later denied unusual symptoms and skin was warm/dry and later stable and released from vaccination site at 13:22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known PMH
Vorgeschichte: -
Andere Medikamente: No Known Medications
Allergien: NKA
Vorherige Impfungen: -

VAERS 2001139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NJ
Alter: 16,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

patient complained dizziness. she was alert and calm. vital signs stable with blood pressure 110/20 heart rate 72, pulse ox 98%. patient was lying down for 20 minutes. 1:16 pm patient said she felt better and she drank apple juice. she denied any dizziness, vital sign stable. she was alert and calm and sent home with their father.

Weitere VAERSDATA-Felder

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

VAERS 1999250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 16,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness

Symptomtext

5mins post vaccination pt reported dizziness. Vitals: 123/89, 16, 96% -- > 130/91, 100, 16, 96% -- > 147/90, 110 Pt hydrated w/ water and given crackers. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Atrial septal defect s/p repair w/ MV repair; Non-rheumatic mitral regurg, cleft leaflet mitral valve
Andere Medikamente: No known
Allergien: NKA
Vorherige Impfungen: -

VAERS 1997884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: HI
Alter: 68,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 30.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Abdominal discomfort Chills Nausea Pain in extremity Pyrexia

Symptomtext

Chills and fever started at 2:30 AM I also had pain in my left arm and my legs it took like 14 hours before I got the symptoms. Then on January 1 I woke up I still had a fever and I was nauseated. Today January 2 I still have a slight fever and my stomach still bothers me but I can?t tell if that's from my problem I already have which I probably do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Stomach issues from stress and certain food; I had chills and fever nauseous 2 nd day.
Vorgeschichte: Chronic.
Andere Medikamente: Famotidine; Pravastatin; Lisinopril-HCTZ; Rabeprazole DR; Levothyroxine; vitamin D3 1000 IU.
Allergien: Cipro; Bactrim; Zofran; Predizone; Shrimp; Tomatoes
Vorherige Impfungen: -

VAERS 1997786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IN
Alter: 52,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 29.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary mass Pain Tenderness

Symptomtext

Woke Friday morning with large mass left armpit. About the size of a tennis ball. Sore to touch. It is now Sunday afternoon and size has started to decrease slightly. Soreness has went away. Have taken ibuprofen and staying hydrated.

Weitere VAERSDATA-Felder

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

VAERS 1979378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NJ
Alter: 16,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain upper Appendicectomy Appendicitis Nausea Ultrasound abdomen abnormal Pyrexia Vomiting

Symptomtext

Within 7 hours of my son receiving the Pfizer booster shot on December 22, 2021, he started to get a bad stomachache and 3 hours later he experienced severe vomiting and nausea. This lasted into the following day. By 10pm December 23, 2021 we took him to the emergency room where they preformed an ultra-sound and determined he had appendicitis. They performed an emergency appendectomy on December 24th, 2021 at 9:30am. There were no complications and he is recovering well. Prior to this incident, he was a very healthy 16 year old athlete.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: 1,0
Labordaten: Ultra sound December 23, 2021 determined appendicitis.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergic to penicillin
Vorherige Impfungen: -

VAERS 1979378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NJ
Alter: 16,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal pain upper Appendicectomy Appendicitis Nausea Ultrasound abdomen abnormal Pyrexia Vomiting

Symptomtext

Within 7 hours of my son receiving the Pfizer booster shot on December 22, 2021, he started to get a bad stomachache and 3 hours later he experienced severe vomiting and nausea. This lasted into the following day. By 10pm December 23, 2021 we took him to the emergency room where they preformed an ultra-sound and determined he had appendicitis. They performed an emergency appendectomy on December 24th, 2021 at 9:30am. There were no complications and he is recovering well. Prior to this incident, he was a very healthy 16 year old athlete.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: 1,0
Labordaten: Ultra sound December 23, 2021 determined appendicitis.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergic to penicillin
Vorherige Impfungen: -

VAERS 1995907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: VA
Alter: 32,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 29.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Headache Injection site pain Nausea Pain Pyrexia

Symptomtext

Nausea, Fever, Chills, Headache, body aches, injection site tenderness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Upper respiratory Infection
Vorgeschichte: N/A
Andere Medikamente: -
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1995635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 30.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Chills Headache Myalgia Pyrexia

Symptomtext

Fever, chills , muscles ache,headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pfizer covid 19 vaccine, pain, fever, chills. Muscle weakness

VAERS 1993254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MI
Alter: 43,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymph node pain Lymphadenopathy

Symptomtext

Ipsilateral supraclavicular lymphadenopathy. Very painful

Weitere VAERSDATA-Felder

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

VAERS 1989261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Hypoaesthesia Immediate post-injection reaction Lip pruritus Sensation of foreign body Skin tightness Tongue pruritus

Symptomtext

Patient brought into Covid Observation Area stating that immediately after receiving Booster dose Pfizer vaccination, she noticed itchy prickly feeling in tongue, lump on left side of her throat and itchiness to lips. Patient also reports that after her 2nd dose Moderna vaccine she experienced numbness to tongue, tight itchy lips and numbness to right side of her face. Patient states that after her 2nd dose Moderna she was observed for 30 minutes without any medications, her symptoms resolved and she was discharged home. 10:15 am- VS Temp 97.8, BP 159/80, HR 77, RR 20, 97% RA 10:34 am- VS- BP 139/83, HR 72, RR 20, 99% RA. Patient reporting that right side of her face/upper cheek area feels numb and tight. States Right side of face feels tight when she smiles. No swelling noted to right side of faces, eyes, lips or tongue. Face is symmetrical when patient smiles and no drooping noted. Patient denies any weakness or numbness to right side of body and able to move extremities normally. Patient speaking in complete sentences. Denies any difficulty breathing. Able to swallow saliva and water without difficulty. 10:38 am- Call placed to on call ED physician, , informed of patient symptoms above. Verbal order given from Dr. to give Benadryl 50 mg orally x 1, continue to observe patient for additional 30 minutes and if symptoms improved, ok to discharge patient home. Verbal order repeated and confirmed. 10:40 am- Benadryl 50 mg orally x 1 given to patient as ordered. 10:47 am- VS- Temp- 97.8, BP 142/83, HR 68, RR 18, 02 SATs 98% RA. Provided patient with an Ice pack to apply to right side of face. 11:05 am- Patient reports lips feel normal, prickly sensation to tongue improving, and tight feeling to right side of face improving. States ice/cold is helpful. 11:07 am- VS- BP 140/78, HR 68, RR 20, 02 SATs 100% RA. Will continue to monitor. 11:24 am- VS- Temp 97.9, BP 137/76, HR 69, RR 20, 02 SATs 97% RA. Patient reports feeling much better. States itchiness to lips resolved, prickly feeling to tongue resolved, lump in throat has improved. Denies any difficulty swallowing or breathing. Also reports that tight feeling to right side of face has improved. 11:25 am- Patient discharged home in stable condition, husband awaiting in car and will drive patient home. Advised to continue to apply ice/cold compress to right side of face, rest, drink plenty of fluids. Also advised to go to ED or call 911 if worsening symptoms return. Patient verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lip pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sleep Apnea, Hypertension, Chronic Ulcerative Pancolitis, Abnormal Liver Enzymes
Vorgeschichte: Sleep Apnea, Hypertension, Chronic Ulcerative Pancolitis, Abnormal Liver Enzymes
Andere Medikamente: EPINEPHrine (ADRENACLICK/EPIPEN) 0.3 mg/0.3 mL Inj AutoInjector Labetalol (NORMODYNE/TRANDATE) 100 mg Oral Tab Chlorthalidone (HYGROTON) 25 mg Oral Tab Ergocalciferol, Vit D2, (DRISDOL) 1,250 mcg (50,000 unit) Oral Cap Cetirizine (ZyrTEC) 1
Allergien: Clindamycin-Diarrhea Co-trimoxazole-Diarrhea Ibuprofen-Diarrhea Lobster-Angioedema Penicillins Class
Vorherige Impfungen: Patient experienced similar symptoms, itchy lips and tongue after 2nd dose Moderna

VAERS 1988837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IN
Alter: 40,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary mass Injection site erythema Injection site pain

Symptomtext

Shot site redness, sore to touch, and lump in armpit area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2524988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

mild

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pain Pyrexia

Symptomtext

Patient IS TAKING TYLENOL FOR PAIN AND FEVER

Weitere VAERSDATA-Felder

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

VAERS 1985073

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge 33025BD

mild

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Pruritus

Symptomtext

itching, no- other symptoms. no rash, swelling,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Tremfya, Cymbalta, abilify, trimtillix,
Allergien: co-trimoxazole, erythromycin base, penicillins
Vorherige Impfungen: -

VAERS 1981862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IL
Alter: 60,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Pruritus

Symptomtext

Itching to left arm/ hand and possible rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Chronic obstructive asthma Atopic dermatitis Papular urticaria Prurigo nodularis
Andere Medikamente: triamcinolone (KENALOG) 0.5 % ointment atorvastatin (LIPITOR) 20 MG tablet albuterol 108 (90 Base) MCG/ACT inhaler chlorhexidine gluconate (PERIDEX) 0.12 % solution amLODIPine (NORVASC) 10 MG tablet Advair Diskus 100-50 MCG/DOSE inhale
Allergien: Egg-products Penicillins
Vorherige Impfungen: -

VAERS 1981298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: MI
Alter: 30,0
Geschlecht: M
Eingang: 26.12.2021
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Inflammation Pain Peripheral swelling

Symptomtext

Large swelling in Left armpit caused by inflammation and is very painful.

Weitere VAERSDATA-Felder

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

VAERS 1978807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CO
Alter: 45,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Immunisation Swelling

Symptomtext

My armpit is swollen to the site of a softball causing some pain.; My armpit is swollen to the site of a softball causing some pain.; Dose received 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 45-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 16Dec2021 at 11:15 (Lot number: 33025BD) at the age of 45 years as dose 3 (booster), single for COVID-19 immunisation. The patient had no relevant medical history. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: FN6207,Route of Administration: Unspecified, Anatomical Location: Left arm, Time of Administration: 18:30), administration date: 05Apr2021, when the patient was 44 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0151,Route of Administration: Unspecified, Anatomical Location: Left arm, Time of Administration: 18:30), administration date: 26Apr2021, when the patient was 44 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 at 11:15, outcome "unknown", described as "Dose received 3"; SWELLING (non-serious), AXILLARY PAIN (non-serious) all with onset 18Dec2021 at 12:00, outcome "not recovered", and all described as "My armpit is swollen to the site of a softball causing some pain". Therapeutic measures were not taken as a result of swelling and axillary pain. Additional information: The patient had no known allergies. The patient did not receive any other vaccine within four weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 11,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered Injection site pain

Symptomtext

11 year old female received a adult Pfizer vaccine. Follow-up telephone call to parent, she reported that she was fine except for a sore arm at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 1971824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SC / LA

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

Pruritus Urticaria

Symptomtext

10 minutes into 15 minute observation period patient complained of generalized itching and hives noted across his back; administered 10mg of cetirizine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Ibuprofen; Probiotic
Allergien: Clindamycin
Vorherige Impfungen: -

VAERS 1971491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Fatigue Injection site pain Myalgia

Symptomtext

Fatigue, muscle aches, joint pain, injection site pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Multivitamin, claritin, osteobiflex
Allergien: -
Vorherige Impfungen: -

VAERS 1967584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Feeling hot Pruritus

Symptomtext

1149 Patient walked up to Rn and reported itching/warmth of top Left ear/nose/side of nose and back of head. Patient received Pfizer booster at 1136 12/20/21. Patient walked to observation area and sat on gurney. Patient alert oriented x4, talking in full sentences and denies chest pain/tightness, intra oral swelling, rash. Lungs clear to ausculation, no stridor. Vitals BP 120/79 Pulse 69 SPO2 99% on room air Temporal Temp. 98.8 RR18 1152 Consulted SCC ED Dr. regarding symptoms and advised Certirizine 10mg orally now And monitor for 20-30 minutes. If symptoms resolve may discharge home or call back if not improving. 1154 Administered Certirizine 10 orally with water. 1205 States ear and nose itching/warmth resolved. Vitals BP110/74 Pulse 70 SPO2 100 % on room air 1222 Vitals BP114/80 Pulse 64 SPO2 100% on room air 1229 Patient reports symptoms resolved and ready to leave. Advised to call 911/Ed if appropriate for new or returning symptoms and has vaccine information. Patient passed the walk test Vtials BP118/73 Pulse 69 SPO2 98% on room air

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: POSTTRAUMATIC STRESS DISORDER OBSESSIVE COMPULSIVE PERSONALITY DISORDER BIPOLAR 1 DISORDER, DEPRESSED EPISODE
Andere Medikamente: Tegretol
Allergien: Allergies ClonazepamAnaphylaxis Diazepam Valproic Acid Clonazepam CodeineNausea/Vomiting Diazepam Seroquel [Quetiapine Fumarate]Other. Valproic Acid
Vorherige Impfungen: -

VAERS 1963840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 14.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / LA

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

Erythema Injection site erythema Pain Pruritus Rash Skin warm

Symptomtext

rash, redness, hot to the touch, itchiness, pain, large red spot about 5in x 4in upper left arm. vaccine on the 14th issues started around the 17th and still continue as of 12/20/2021. after the second shot same arm as first. I did not go to a doctor and filled this out myself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: none called pharmacist they said I can take benadryl.
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure prediabetes thyroiditis
Andere Medikamente: Cozaar Atenanol Indepamide
Allergien: ?
Vorherige Impfungen: -

VAERS 1963763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction

Symptomtext

Immediately after vaccination @14:25 pt reported dizziness. Vitals: 109/72, 70, 16 Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Iron deficiency, Vegetarian diet, Vasovagal syncope
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1963723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

10mins post vaccination pt reported dizziness. Vitals: 133/91, 69, 18 -- > 120/75, 66 Pt stable and released from the vaccination site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Fibroid uterus Lumbar degenerative disc disease Mixed hyperlipidemia Pain due to neuropathy of facial nerve Facial neuralgia (trigeminal) Facial pain Right trigeminal neuralgia Encounter for surveillance of contraceptives, unspecified Heart murmur Major depressive disorder, recurrent episode Migraine
Andere Medikamente: Medications: DULoxetine (CYMBALTA) 60 MG capsule Take 60 mg by mouth 2 (two) times a day. 60 mg in morning, 30mg in evening therapeutic multivitamin (THERAGRAN) tablet Take 1 tablet by mouth daily. lamoTRIgine (LaMICtal) 100 MG tablet
Allergien: Allergies: Baclofen (fatigue, depression), Oxcarbazepine (rash), Carbamazepine (rash), Rizatriptan (felt like face was on fire)
Vorherige Impfungen: -

VAERS 1963575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Immediate post-injection reaction Vision blurred

Symptomtext

Immediately after vaccination @11: 14, pt reported flushing/sweating, dizziness, blurry vision and lightheadedness. Vitals: 123/75, 71, 20 Pt stable and released form the vaccination site @12:00.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: No Significant PMH
Andere Medikamente: Medications: Ibuprofen 200mg Q 6hrs PRN
Allergien: Allergies: APAP (Hives/urticaria)
Vorherige Impfungen: -

VAERS 1962319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

mild

Staat: IN
Alter: 58,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Feeling hot Flushing Headache Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Hot, flushed within 20 minutes, body aches, fever, headache, cough and all Covid symptoms by following day. Sick for 5 consecutive days before taking Covid Test. Tested positive. Starting antibiotics and steroids also going for infusion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Covid test 12-19-21
Aktuelle Erkrankungen: no
Vorgeschichte: arthritis high blood pressure Diabetes
Andere Medikamente: Cymbalta etodolac Breo gabapentin Tramadol Mucinex DM Jardiance Lasartin Metformin atorvastatin zyrtec Albuterol
Allergien: Penicillan
Vorherige Impfungen: Covid- 2nd shot 24 hr illness

VAERS 2655620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: VA
Alter: 56,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 14.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Eye irritation

Symptomtext

eye lids burned after each shot. Pretty badly.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Jan2022 as dose 3 (booster), single (Lot number: 33025BD) at the age of 56 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: latex" (unspecified if ongoing), notes: Known allergies: latex. There were no concomitant medications. Past drug history included: Albuterol, reaction(s): "Known allergies: Albuterol", notes: Known allergies: Albuterol. Vaccination history included: BNT162b2 (Dose 2; lot number: EW0173; dose vaccine location: Right arm), administration date: 07May2021, when the patient was 55-year-old, for COVID-19 immunization, reaction(s): "My eye lids burned after each shot. Pretty badly."; BNT162b2 (Dose 1; lot number: EW0164; dose vaccine location: Left arm), administration date: 16Apr2021, when the patient was 55-year-old, for COVID-19 Immunization, reaction(s): "My eye lids burned after each shot. Pretty badly.". The following information was reported: EYE IRRITATION (non-serious), outcome "not recovered", described as "eye lids burned after each shot. Pretty badly.". Additional information: Patient's eye lids burned after each shot. Pretty badly. 1st occurrence, they made her sit with the paramedics for a bit. After each subsequent shot, the patient knew it would pass so did not report. Now, all this time later, every single time she cry or her eyes get watery, her tears still burn her eyelids. Pretty significantly, to the point that she have to wipe them away or it's unbearable.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300247349 Same patient, same event, same product, different dose (Dose 1);US-PFIZER INC-202300247350 Same patient, same event, same product, different dose (Dose 2);

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye irritation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Latex allergy (Known allergies: latex)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2629465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: WA
Alter: 26,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; Interchange of vaccine products; This is a spontaneous report received from a contactable consumer. The reporter is the patient. A 27-year-old male patient received BNT162b2 (BNT162B2), on 07Jan2022 as dose 3 (booster), single (Lot number: 33025BD) at the age of 26 years, in left arm for COVID-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 06Apr2021 as dose 1, single (Lot number: 027B21A), in left arm and on 04May2021 as dose 2, single (Lot number: 017C21A), in left arm for COVID-19 immunisation. The patient's relevant medical history included: "ADHD" (unspecified if ongoing). Concomitant medication(s) included: DEXTROAMPHETAMINE [DEXAMFETAMINE], start date: Sep2022, stop date: May2023; TRAZODONE, start date: Sep2022, stop date: May2023. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 07Jan2022, outcome "recovered with sequelae"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "recovered with sequelae" (May2023) and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (May2023) Negative. Therapeutic measures were taken as a result of drug ineffective, COVID-19 which included nirmatrelvir/ ritonavir (PAXLOVID) from 28Apr2023 to 02May2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202305; Test Name: COVID-19 test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD
Andere Medikamente: DEXTROAMPHETAMINE [DEXAMFETAMINE]; TRAZODONE
Allergien: -
Vorherige Impfungen: -

VAERS 2628535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 08.05.2023
Impfdatum: 04.01.2022
Beginn: 16.07.2022
Tage bis Beginn: 193,0
Dosis: 3
Route/Site: IM / LA

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

Hypoxia

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2561152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 34,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 27.04.2021
Beginn: 01.10.2021
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: IM / LA

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

Echocardiogram Electromyogram Hypoaesthesia Magnetic resonance imaging Metabolic function test Muscular weakness Ventricular extrasystoles

Symptomtext

Right arm weakness, PVCs, numbness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Echocardiogram
Hospital-Tage: -
Labordaten: MRI, EMG, CMP, Echocardiogram,
Aktuelle Erkrankungen: -
Vorgeschichte: Seasonal allergies
Andere Medikamente: -
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2561092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 13.01.2022
Beginn: 29.11.2022
Tage bis Beginn: 320,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Ear infection Impaired work ability Laboratory test

Symptomtext

Got Covid 11/29/2022 after the November holiday, off from work 10 days. 12/13/2022 went to a clinic, diagnosed with ear infection. Developing problem in both ears, prescribed steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Ear test
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: -

VAERS 2550794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 46,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 02.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Balance disorder SARS-CoV-2 antibody test Vertigo

Symptomtext

Developed extreme vertigo lasted 3 months. Vertigo would be off/on started using vertigo wrist support bracelets for balance. Was prescribed medication but didn't take.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Balance disorder
Hospital-Tage: -
Labordaten: Covid antibody test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: ALLEGRA; vitamin D3 zinc
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2543047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: GA
Alter: 56,0
Geschlecht: F
Eingang: 26.12.2022
Impfdatum: 20.03.2021
Beginn: 09.06.2022
Tage bis Beginn: 446,0
Dosis: 3
Route/Site: - / -

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

COVID-19 immunisation SARS-CoV-2 test Suspected COVID-19

Symptomtext

SUSPECTED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient through other manufacturer (Pfizer) concerned a 58 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy (Cleocin), and other pre-existing medical conditions included: The patient was not pregnant at the time of reporting and the patient stated that she was taking other medication or products within 2 weeks of starting covid-19 treatment (Paxlovid). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805031 expiry: unknown) dose was not reported, 1 in total was administered on 20-MAR-2021 to left arm for covid-19 prophylaxis. Age at time of vaccination 56 years old. Concomitant medications included ibuprofen/pseudoephedrine hydrochloride (Advil cold and sinus) The patient additionally received non-company suspect vaccine Pfizer Biontech Covid-19 vaccine (tozinameran) (dose number in series 2) (form of admin, route of admin, and were not reported, batch number: FH80Z8 expiry: unknown) dose was not reported, administered on 29-NOV-2021 to left arm for covid-19 prophylaxis. The patient received non-company suspect vaccine Pfizer Biontech Covid-19 vaccine (tozinameran) (dose number in series 3) ( form of admin, route of admin, and were not reported, batch number: 33025BD expiry: unknown) dose was not reported, administered on 09-JUN-2022 to left arm for covid-19 prophylaxis which was an revaccination with different covid-19 vaccine (dose number in series 3). On NOV-2022, the patient experienced COVID-19 (suspected covid-19 infection) (dose number in series 3). On 29-NOV-2022, the patient was treated with non-company suspect drug Paxlovid (route of administration, batch number and expiry were not reported) dose and frequency were not reported for covid-19 treatment and last administered on 3-DEC-2022. The patient had reoccurrence of symptoms 3 days after symptoms ended. On 09-DEC-2022, six days after non company suspect drug paxlovid treatment (for covid) laboratory data included: COVID-19 rapid POC test Negative (dose number in series 3). The action taken with covid-19 vaccine ad26.cov2.s, and tozinameran was not applicable. The patient was recovering from suspected covid-19 infection, and the outcome of revaccination with different covid-19 vaccine was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 immunisation
Hospital-Tage: -
Labordaten: Test Date: 20221209; Test Name: COVID-19 RAPID TEST; Test Result: Negative
Aktuelle Erkrankungen: Drug allergy (Cleocin)
Vorgeschichte: Comments: The patient was not pregnant at the time of reporting and the patient stated that she was taking other medication or products within 2 weeks of starting covid-19 treatment (Paxlovid).
Andere Medikamente: ADVIL COLD & SINUS
Allergien: -
Vorherige Impfungen: -

VAERS 2538699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: GA
Alter: 58,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 09.06.2022
Beginn: 29.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Interchange of vaccine products; 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 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Nov2021 as dose 2 (booster), single (Lot number: FH8028), in left arm and on 09Jun2022 as dose 3 (booster), single (Lot number: 33025BD) at the age of 58 years, in left arm for covid-19 immunisation; coviD-19 vaccine nrvv ad26 (jnj 78436735) (JANSSEN COVID-19 VACCINE), on 20Mar2021 as dose 1, single (Lot number: 1805031), in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Cleocin, reaction(s): "known allergies: Cleocin". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 29Nov2021, outcome "unknown"; 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: Negative, notes: after negative rapid test. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received other medication in 2weeks. Patient received Anti viral product Paxlovid on 29Nov2022 to 03Dec2022 for the Treatment of COVID-19. Reoccurrence of symptoms 3 days after symptoms ended and after negative rapid test. No medical history. Conclusion of Previously Completed Investigation of Lot FH8028: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot FH8028 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FH8028, fill lot FH4341 and the formulated drug product lot FH4347. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Conclusion of Previously Completed Investigation of Lot 33025BD: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE was investigated. The investigation included reviewing incoming quality and manufacturing batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type and final release assay testing. This product is received as preformulated bulk, and is manufactured, labeled and packaged by Pfizer (withheld). The final scope was determined to be lot 33025BD. No quality issues were identified during the investigation. There is no impact on product quality. An was not issued for the complaint. No regulatory notification were held because of this complaint. The complaint condition of lack of effect was not confirmed, therefore the root cause cannot be attributed to manufacture or vendor processes as incoming quality component testing and all analytical tests performed at the time of lot release confirmed that the batch met potency specifications. No corrective or preventative actions are required as the complaint condition was not determined to be manufacture or vendor related and there are quality systems in place to detect defects prior any lot being released to the market.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Negative ; Comments: after negative rapid test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2513894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: VA
Alter: 31,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 22.12.2021
Beginn: 26.10.2022
Tage bis Beginn: 308,0
Dosis: 3
Route/Site: SYR / RA

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

Bandaemia COVID-19 Incisional drainage Infective myositis Lymphadenectomy Lymphadenitis bacterial Lymphadenopathy Myositis Sepsis Septic arthritis streptococcal Streptococcal infection Subcutaneous abscess

Symptomtext

Axillary lymphadenopathy caused axillary abscess with suppurative lymphadenopathy pectoralis and latissimus myositis, which led to: Sepsis without acute organ dysfunction, due to unspecified organism (HCC) - Primary Infective myositis of right shoulder Streptococcal arthritis of right shoulder (HCC) Abscess of axillary region Bandemia Severe sepsis (HCC) Streptococcal infection COVID-19 virus infection Septic arthritis of shoulder, right (HCC)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bandaemia
Hospital-Tage: 9,0
Labordaten: Excision of deep right axilla lymph nodes and washout of axilla. Incision and drainage right chest, right flank. Findings of Right axillary abscess with suppurative lymphadenopathy pectoralis and latissimus myositis. Procedure Laterality Date HX CYST INCISION AND DRAINAGE Right 11/1/2022 INCISION AND DRAINAGE RIGHT AXILLA, CHEST, AND RIGHT BACK performed by MD at local OR
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Sertraline, 50mg once daily
Allergien: -
Vorherige Impfungen: -

VAERS 2483163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: WI
Alter: 21,0
Geschlecht: U
Eingang: 19.10.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Inappropriate schedule of product administration

Symptomtext

Patient had 2nd dose too soon.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2469337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 20.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Tinnitus

Symptomtext

Tinnuitis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: Had doctor check on eardrum in early March.
Aktuelle Erkrankungen: Had a pretty bad flu, and did blow out eardrums. Have a messed up jaw as well.
Vorgeschichte: Overweight?
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2450314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 36,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 18.01.2022
Beginn: 24.08.2022
Tage bis Beginn: 218,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; 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 36-year-old male patient received BNT162b2 (BNT162B2), on 18Jan2022 at 13:00 as dose 3 (booster), single (Lot number: 33025BD) at the age of 36 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The patient had not received any other medication within 2 weeks of vaccination. The following information was reported: COVID-19 (medically significant) with onset 24Aug2022, outcome "not recovered", DRUG INEFFECTIVE (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (30Aug2022) Negative, notes: Tested Negative on Day 7. Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient had received Paxlovid from 24Aug2022 to 29Aug2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20220830; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Tested Negative on Day 7
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: No, known allergies No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: -
Alter: 25,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 08.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

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 25-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Jan2022 as dose 3 (booster), single (Lot number: 33025BD) at the age of 25 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "bandage adhesive" (unspecified if ongoing), notes: Known allergies: bandage adhesive; "Pain" (unspecified if ongoing), notes: Other medication in 2weeks product=for pain,. Concomitant medication(s) included: LEVOTHYROXINE, start date: 11Jul2012; IBUPROFEN taken for pain, start date: 08Sep2022; TYLENOL taken for pain, start date: 08Sep2022; VITAMIN D NOS, start date: 09Sep2022; ZINC [ZINC SULFATE], start date: 09Sep2022. Past drug history included: Vienva for Known allergies: vienva, notes: Known allergies: vienva. 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. Clinical course: The patient started COVID 19 treatment, brand: Paxlovid from 10Sep2022 till 11Sep2022, Lot number:GC8123. 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
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy (Known allergies: bandage adhesive); Hypothyroidism; Pain (Other medication in 2weeks product=for pain,)
Andere Medikamente: LEVOTHYROXINE; IBUPROFEN; TYLENOL; VITAMIN D NOS; ZINC [ZINC SULFATE]
Allergien: -
Vorherige Impfungen: -

VAERS 2413233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 17.08.2022
Impfdatum: 28.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment/ Had COVID rebound; COVID 19 Treatment/ Had COVID rebound; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Dec2021 as dose number unknown, single (Lot number: 33025bd) at the age of 49 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Thyroid disorder" (unspecified if ongoing); "food allergies" (unspecified if ongoing); "Known allergies: amoxicillin families" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; PROGESTERONE; MELOXICAM. Past drug history included: Keflex, reaction(s): "Known allergies: Keflex". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment/ Had COVID rebound". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive; Positive, notes: COVID rebound. Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid (treatment start date: 01Aug2022; treatment stop date: 06Aug2022).

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Had COVID rebound; Test Result: Positive ; Test Name: Had COVID rebound; Test Result: Positive ; Comments: COVID rebound
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy; Food allergy; Thyroid disorder
Andere Medikamente: LEVOTHYROXINE; PROGESTERONE; MELOXICAM
Allergien: -
Vorherige Impfungen: -

VAERS 2399155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 24.12.2021
Beginn: 27.07.2022
Tage bis Beginn: 215,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after three vaccines: Pfizer 3/9/2021 batch/lot# EN6199; Pfizer 3/30/2021 batch/lot# EW8733; Pfizer 12/24/2021 batch/lot# 33025BD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19+.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2327030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Biopsy lymph gland Blood test normal Lymphadenopathy Mammogram abnormal Ultrasound scan abnormal

Symptomtext

Extremely reactive/swollen lymph nodes in both armpits and behind ear (possibly in other lymph nodes in body) that have not subsided in 6 months. Bloodwork, ultrasounds, mammogram, and biopsy. No other known symptoms. Still waiting on results of biopsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy lymph gland
Hospital-Tage: -
Labordaten: Bloodwork = normal Ultrasound = Many reactive lymph nodes Biopsy = Waiting results
Aktuelle Erkrankungen: None
Vorgeschichte: Reactive/Swollen lymph nodes throughout body (mammogram and ultrasounds show at least in both armpits and behind one ear) that have not subsided in 6 months. No other known symptoms. Biopsy was done. Waiting on results.
Andere Medikamente: Motrin
Allergien: Sulfa Allergy Onions, garlic Wool
Vorherige Impfungen: -

VAERS 2325209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MO
Alter: 64,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 21.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; 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 64-year-old male patient received BNT162b2 (BNT162B2), on 16Feb2021 as dose 1, single (Lot number: EN6200), in right arm, on 08Mar2021 as dose 2, single (Lot number: EN6205), in left arm and on 21Dec2021 as dose 3 (booster), single (Lot number: 33025BD) at the age of 64 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Yes, sulfa based antibiotics give me a rash" (unspecified if ongoing); "known allergies: Yes, sulfa based antibiotics give me a rash" (unspecified if ongoing). There were no concomitant medications. 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: Unknown Result. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient had not other medication in 2 weeks. The patient had received covid 19 treatment, paxlovid, from 01Jun2022 (Lot number: FY4445) to 04Jun2022 for COVID-19 treatment. 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; Result Unstructured Data: Test Result:Unknown Result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Rash; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2305083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 51,0
Geschlecht: M
Eingang: 01.06.2022
Impfdatum: 03.02.2022
Beginn: 21.05.2022
Tage bis Beginn: 107,0
Dosis: 2
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 2298895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 15.04.2022
Beginn: 07.05.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Hypoaesthesia Muscle spasms

Symptomtext

A couple weeks after my fourth vaccine I started developing acute muscle spasms in my leg, which persist. Two days ago I started having numbness and lost of strength and muscle use in right arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Sicca syndrome, fibromyalgia, non-hereditary hypoimmunoglobulinemia
Andere Medikamente: Gabapentin, hydrocodone, leflunomide, cymbalta, hydroxycloroquine, cevimeline
Allergien: Penicillin and all other "cillins"
Vorherige Impfungen: -

VAERS 2286693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 19.12.2021
Beginn: -
Tage bis Beginn: -
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

COVID 19 Treatment; COVID 19 Treatment; 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 32-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Dec2021 as dose number unknown, single (Lot number: 33025BD) at the age of 32 years for covid-19 immunisation. The patient's relevant medical history included: "Multiple sclerosis" (unspecified if ongoing), notes: other medical history: Multiple Sclerosis; "Crawfish" (unspecified if ongoing), notes: known allergies: Crawfish. Concomitant medication(s) included: VITAMIN D [VITAMIN D NOS]; IBUPROFEN; TYLENOL. 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: (unspecified date) Positive; (13May2022) Positive, notes: COVID came back. Therapeutic measures were taken as a result of drug ineffective, covid-19 with paxlovid from 03May2022 to 08May2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Positive ; Test Date: 20220513; Test Name: Covid-19 Test; Test Result: Positive ; Comments: COVID came back
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fish allergy (known allergies: Crawfish); Multiple sclerosis (other medical history: Multiple Sclerosis)
Andere Medikamente: VITAMIN D [VITAMIN D NOS]; IBUPROFEN; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 2281411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 21.12.2021
Beginn: 21.01.2022
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: IM / LA

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

Hyposmia

Symptomtext

Decreased sense of smell for only some types of smells

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hyposmia
Hospital-Tage: -
Labordaten: None so far
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, impaired fasting glucose, obstructive sleep apnea
Andere Medikamente: Lisinopril, Hydrochlorothiazide, Atenolol, vitamin B12
Allergien: none
Vorherige Impfungen: -

VAERS 2260158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 12,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 21.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

Vaccine was given after being at room temperature for 6 hours and 25 minutes after dilution.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 22.02.2022
Beginn: 22.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

No adverse event Product storage error

Symptomtext

None--pt was given vaccine that had been stored in conventional freezer for more than 2 weeks. Pt offered additional dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 23,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 09.03.2022
Beginn: 09.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in conventional freezer for more than 2 weeks. Pt offered additional dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257487

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 17,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 07.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in conventional freezer for more than 2 weeks. Pt offered additional dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 87,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in conventional freezer for more than 2 weeks. Pt offered additional dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 15,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 08.03.2022
Beginn: 08.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in conventional freezer for more than 2 weeks. Pt offered additional dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 07.02.2022
Beginn: 07.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in conventional freezer for more than 2 weeks. Pt offered additional dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 18,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 08.03.2022
Beginn: 08.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in conventional freezer for more than 2 weeks. Pt offered additional dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 34,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Product storage error

Symptomtext

None--pt was given two doses of vaccine that had been stored in a conventional freezer for > 2 weeks. Second dose administered 3/9/22. Error was not caught until after 2nd dose given. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 02.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 28.02.2022
Beginn: 28.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 30,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 28.02.2022
Beginn: 28.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 22.02.2022
Beginn: 22.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 19.02.2022
Beginn: 19.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 14.02.2022
Beginn: 14.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2257043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 33,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 07.02.2022
Beginn: 07.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose. Pt's 2nd dose was from same group that had been stored in freezer for more than 2 weeks (administered 2/28/22).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2256882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 14,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 07.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

None--pt was given vaccine that had been stored in a conventional freezer for > 2 weeks. Pt offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2254683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 27.04.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Muscular weakness

Symptomtext

Patient states he developed muscle weakness in the region where the buttocks and thighs meet. It still has not resolved and patient states he saw his pcp. He was prescribed anti-inflammatory/pain relief medications.

Weitere VAERSDATA-Felder

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

VAERS 2248200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 87,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 08.03.2022
Beginn: 08.03.2022
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

Symptomtext

None. Pt received vaccine that had been stored in conventional freezer since 1/5/22 (expired 1/19/22). Pt was offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2248183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 36,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 07.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

None. Pt received vaccine that had been stored in conventional freezer since 1/5/22 (expired 1/19/22). Pt was offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2248178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 07.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered Product storage error

Symptomtext

None. Patient received vaccine stored in conventional freezer since 1/5/2022 (expired 1/19/2022). Patient offered another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2248172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: TX
Alter: 48,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 07.03.2022
Beginn: 07.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

None. Pt was given vaccine that had been stored in conventional freezer since 1/5/22 (expired since 1/19/22).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KY
Alter: 74,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 18.01.2022
Beginn: 14.04.2022
Tage bis Beginn: 86,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19

Symptomtext

covid-19 hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2226418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

No adverse event Product preparation issue

Symptomtext

Patient was administered .3 mL of vaccination via intramuscular with no adverse reactions. However, I forgot to dilute the vial with 1.8mL of saline, so the patient received the equivalent of 6 doses of vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2223159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: OH
Alter: 68,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 26.03.2021
Beginn: 23.09.2021
Tage bis Beginn: 181,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Rhabdomyolysis SARS-CoV-2 test positive

Symptomtext

Received Pfizer COVID vaccines on 3/5/2021 and 3/26/2021 Hospitalized on 9/23/2021 with positive COVID 19 and Rhabdomyolitis Booster Pfizer vaccine received on 1/8/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2215893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 58,0
Geschlecht: M
Eingang: 05.04.2022
Impfdatum: 02.04.2022
Beginn: 02.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

BOOSTER GIVEN EARLY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2215893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 58,0
Geschlecht: M
Eingang: 05.04.2022
Impfdatum: 02.04.2022
Beginn: 02.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

BOOSTER GIVEN EARLY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2196320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NV
Alter: 79,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 25.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Immunisation reaction

Symptomtext

Spoke with son and power of attorney on 3/21/22 to schedule his mother's second dose of the covid-19 vaccine, and he stated that she was not the same since the vaccination on 1/25/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Immunisation reaction
Hospital-Tage: -
Labordaten: unknown if any
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2194426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MT
Alter: 17,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 06.04.2021
Beginn: 03.02.2022
Tage bis Beginn: 303,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19

Symptomtext

Patient was hospitalized with COVID after receiving COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2187294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 40,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 06.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: - / LA

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

Heavy menstrual bleeding Polymenorrhoea

Symptomtext

Started my menstrual cycle 3 weeks early. I am normally very regular in my cycle. It also lasted 4 days longer than normal.; Started my menstrual cycle 3 weeks early. I am normally very regular in my cycle. It also lasted 4 days longer than normal.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Jan2022 11:30 (Lot number: 33025BD) at the age of 40 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: MCT OIL [MEDIUM-CHAIN TRIGLYCERIDES]; MELATONIN; COLLAGEN. Vaccination history included: Bnt162b2 (lot number: EP7534, time: 04:45 PM, dose number:2 vaccine location:Right arm), administration date: 30Mar2021, when the patient was 40 years old, for covid-19 immunisation; Bnt162b2 (lot number: EP7534, administration time: 04:45 PM, dose number: 1, vaccine location: Right arm), administration date: 20Apr2021, when the patient was 40 years old, for covid-19 immunisation. The following information was reported: POLYMENORRHOEA (non-serious), HEAVY MENSTRUAL BLEEDING (non-serious) all with onset 20Jan2022, outcome "recovered" and all described as "Started my menstrual cycle 3 weeks early. I am normally very regular in my cycle. It also lasted 4 days longer than normal.". Therapeutic measures were not taken as a result of polymenorrhoea, heavy menstrual bleeding. Adverse event: Facility type vaccine at facility Patient did not received other vaccine in four weeks. Started my menstrual cycle 3 weeks early. I am normally very regular in my cycle. It also lasted 4 days longer than normal. Ae resulted in: [None of the above] Patient did had covid prior to vaccination and not tested covid post vaccination. The patient had known allergies. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Heavy menstrual bleeding
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: MCT OIL [MEDIUM-CHAIN TRIGLYCERIDES]; MELATONIN; COLLAGEN
Allergien: -
Vorherige Impfungen: -

VAERS 2166007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 10,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect dose administered No adverse event

Symptomtext

The adverse event was that the patient was given a Covid 30 mcg dose for 12+ yrs but was only 10 yrs of age at time of administration. Patient should have received the recommended the recommended Covid 10 mcg dose for 5-11 yr olds. Follow up with the family was done on 1/3/2022 by speaking to mom on phone. No adverse events regarding symptoms were noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2157850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 01.03.2022
Beginn: 01.03.2022
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 Product storage error

Symptomtext

Patient given COVID-19 vaccination on 3/1/2022 at 8:45 am. When medical assistant input the vaccination, it was discovered the expiration date on the vial was 2/28/2022 and the BUD date on the bag: 2/28/2022. It was brought to the manager, and she called Pfizer regarding the vaccination error. The expiration date on the vial had been extended by Pfizer to 5/2022, thus making it still viable vaccination. As for the BUD date, Pfizer representative stated per the viability studies on vaccination excursions, the vaccination was good for 45 excursion days. March 1, 2022, would only count as 1 excursion day. Patient was notified about the incident by the provider, and reassured she received a viable vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: None known
Allergien: Ceclor; Septra
Vorherige Impfungen: -

VAERS 2140346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 11,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect dose administered

Symptomtext

Eleven year old patient given Pfizer (Purple, 12+)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2137165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MO
Alter: 5,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 24.02.2022
Beginn: 24.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

Patient was administered BioNtech Covid-19 vaccine>12 years formulation. Should have received BioNtech Covid-19 vaccine 50-11 years. Administration error disclosed to patients mother and counseling was provided on what to expect in relation to increased side effects and systemic symptoms such as fatiques and fever noted with the higher doses. Patient was monitored in the clinic for 25 minutes after administration. No side effects noted during that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Certirazine, Multi-Vitamin, flonase
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2134525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 26,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 23.02.2022
Beginn: 23.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

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

Inappropriate schedule of product administration Interchange of vaccine products

Symptomtext

Patient received 1st dose Janssen 02/18/2022 Lot # 211D21A Patient received a 2nd Dose Pfizer 02/23/2022 Lot # 33025BD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2131505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: OR
Alter: 29,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Underdose

Symptomtext

Patient was mistakenly given a lesser dose of Pfizer Covid-19 booster. Instead of the correct dose of 0.3ml, she was given the child dose of 0.2ml. We are in the process of informing the patient that a lower dose was given.

Weitere VAERSDATA-Felder

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

VAERS 2105296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 12,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
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 a vaccines 2 hours after viable time from the dilution and being drawn into a syringe. It was past the 6 hours of viable time when administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
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

Patient was given a vaccines 2 hours after viable time from the dilution and being drawn into a syringe. It was past the 6 hours of viable time when administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Product preparation issue

Symptomtext

Patient was given a vaccines 2 hours after viable time from the dilution and being drawn into a syringe. It was past the 6 hours of viable time when administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product preparation issue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 17,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
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

Patient was given a vaccines 2 hours after viable time from the dilution and being drawn into a syringe. It was past the 6 hours of viable time when administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 19,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Mild persistent asthma; allergic rhinitis; deviated nasal septum; scoliosis
Andere Medikamente: Astelin (azelastine) 137mcg (0.1 %) nasal aero spray; Nizoral (ketoconazole) 2% topical shampoo
Allergien: Peanuts
Vorherige Impfungen: -

VAERS 2105090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 13,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Prediabetes/obesity PEDS (BMI 95-99 percentile)
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2105084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: AZ
Alter: 36,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 05.02.2022
Beginn: 05.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Patient received booster early (less than 5 months).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 58,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HTN (HYPERTENSION) DM 2 RENAL CALCULUS LICHEN SIMPLEX CHRONICUS
Andere Medikamente: Glimepiride (AMARYL) amlodipine (NORVASC) Lisinopril-hydrochlorothiazide (PRINZIDE/ZESTORETIC) Atorvastatin (LIPITOR) metformin (GLUCOPHAGE) Simethicone (MYLICON)
Allergien: Aspirin
Vorherige Impfungen: -

VAERS 2105043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 15,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
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

Symptomtext

Vaccine administered 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 2104954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 55,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (HYPERTENSION) PREDIABETES MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE MIGRAINE SEVERE OBESITY EQUIVALENT (BMI 35-39.9 W CO-MORBIDITY) FUNCTIONAL DISORDER OF GI TRACT RENAL MASS CHEST PAIN INSOMNIA
Andere Medikamente: Nortriptyline (AVENTYL/PAMELOR) Lorazepam (ATIVAN) Lisinopril-hydrochlorothiazide (PRINZIDE/ZESTORETIC) Diclofenac Sodium (VOLTAREN) Simethicone (MYLICON) ASPIRIN 81 MG OMEGA 3-DHA-EPA-FISH OIL
Allergien: Tetanus, diphtheria, toxoid
Vorherige Impfungen: -

VAERS 2104939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 12,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: MODERATE PERSISTENT ASTHMA ECZEMA ALLERGIC RHINITIS
Andere Medikamente: SYMBICORT Triamcinolone Acetonide (ARISTOCORT/KENALOG)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2104922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 50,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (HYPERTENSION) HYPOTHYROIDISM ANXIETY DISORDER GERD (GASTROESOPHAGEAL REFLUX DISEASE) PREDIABETES TERATOGENIC MEDICATION MONITORING ACUTE DVT OF LEFT ARM HYPOKALEMIA OBESITY, BMI 30-34.9, ADULT ALLERGIC RHINITIS DERMOID CYST, OVARY. ENDOMETRIAL THICKENING MICROCYTOSIS RIGHT SHOULDER JOINT PAIN HEADACHE
Andere Medikamente: Potassium Chloride (K-TAB/KLOR-CON) Levothyroxine (LEVOTHROID/SYNTHROID) Triamterene-Hydrochlorothiazide Betamethasone Dipropionate Aug Omeprazole (PRILOSEC) Famotidine (PEPCID) hydrochlorothiazide (ESIDRIX/HYDRODIURIL) Cetirizine (Z
Allergien: Pcn Class
Vorherige Impfungen: -

VAERS 2104878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 81,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: OSTEOPOROSIS ADVANCE DIRECTIVE ON FILE LONG TERM NON WARFARIN ORAL ANTICOAGULANT THERAPY HX OF RIGHT TOTAL SHOULDER ARTHROPLASTY HX OF BREAST CANCER HYPOCALCEMIA HX OF COLONIC POLYP OSTEOARTHRITIS OF LEFT SHOULDER
Andere Medikamente: PRADAXA Ketoconazole (NIZORAL) VITAMIN B-12 1000 MCG ORAL TAB CHOLECALCIFEROL (VITAMIN D3) CALCIUM CARBONATE MAGNESIUM OXIDE VITAMIN C OMEGA 3-DHA-EPA-FISH OIL MULTIVITAMIN WITH MINERALS
Allergien: Allergies Pcn Class [Penicillins Class] Ceftin Penicillin V Potassium
Vorherige Impfungen: -

VAERS 2104856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 29,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine administered BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HTN (Hypertension), DM 2, Supraventricular Tachycardia, Paroxysmal, Prediabetes, Obesity, BMI 35-39.9, Adult HX Of Cardiac Arrhythmia Radiofrequency Ablation, HX Of Paroxysmal Supraventricular Tachycardia
Andere Medikamente: Metoprolol Tartrate (LOPRESSOR). metronidazole (FLAGYL)< DESCOVY, metformin (GLUCOPHAGE XR), Emtricitabine-Tenofovir Disoproxil Fumarate (TRUVADA), Lisinopril (PRINIVIL/ZESTRIL)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2102115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 41,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: MAJOR DEPRESSIVE DISORDER, SINGLE EPISODE INTERMITTENT ASTHMA
Andere Medikamente: PROAIR HFA
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2102086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 54,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: HYPERLIPIDEMIA ASTHMA, UNSPECIFIED HYPOTHYROIDISM MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE MOOD DISORDER, UNSPECIFIED TYPE ADHD LIVER CYST HX OF COLONIC POLYP HX OF DEPRESSION ANXIETY RECTAL PROLAPSE PULMONARY NODULE
Andere Medikamente: Levothyroxine (LEVOTHROID/SYNTHROID) Desvenlafaxine (PRISTIQ) Dextroamphetamine-Amphetamine LIDOCARE IBUPROFEN MULTIVITAMIN WITH MINERALS OMEGA 3 FISH OIL
Allergien: Fluconazole Pcn Class [Penicillins Class
Vorherige Impfungen: -

VAERS 2102057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 24,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Moderate Persistent Asthma
Andere Medikamente: Albuterol (PROAIR/PROVENTIL/VENTOLIN) ALVESCO Albuterol (PROVENTIL/VENTOLIN)
Allergien: Penicillin v Potassium
Vorherige Impfungen: -

VAERS 2102004

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 53,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HYPERLIPIDEMIA MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE RESTLESS LEGS SYNDROME LONG TERM OPIOID THERAPY TOBACCO SMOKER
Andere Medikamente: Methadone (DOLOPHINE) 5 mg Oral Tab buPROPion (WELLBUTRIN XL) 150 mg Oral 24hr XL Tab Paroxetine (PAXIL) PEG 3350 - Electrolytes (GAVILYTE-C) Bisacodyl (DULCOLAX) Simethicone (MYLICON) Rosuvastatin (CRESTOR)
Allergien: PCN Class
Vorherige Impfungen: -

VAERS 2101973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 48,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE, IN PARTIAL REMISSION CEREBRAL VENOUS SINUS THROMBOSIS HEADACHE DIVERTICULOSIS OF COLON
Andere Medikamente: Phentermine (ADIPEX-P) Escitalopram (LEXAPRO)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2101948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 19,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: DM 1 ELEVATED ALKALINE PHOSPHATASE OBESITY, BMI 30-34.9, ADULT
Andere Medikamente: Cyclobenzaprine (FLEXERIL) hydroxyzine HCL (ATARAX) Nortriptyline (AVENTYL/PAMELOR) Insulin NPH Human (HUMULIN N NPH U-100 INSULIN)
Allergien: Cat dander
Vorherige Impfungen: -

VAERS 2101919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 41,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: SEVERE OBESITY, BMI 45-49.9, ADULT MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE DYSLIPIDEMIA PREDIABETES LONG TERM ANTICOAGULANT THERAPY HX OF EMBOLIC STROKE W UNSPECIFIED RESIDUAL DEFICITS POSTCONCUSSION SYNDROME MIXED SLEEP APNEA LUMBAR DISC HERNIATION HUMAN PAPILLOMA VIRUS INFECTION UTERINE FIBROIDS GENITAL HERPES SIMPLEX ANXIETY LONG TERM ASPIRIN THERAPY
Andere Medikamente: Warfarin (COUMADIN) Propranolol (INDERAL) Duloxetine (CYMBALTA) bupropion (WELLBUTRIN XL) VITAMIN B-12
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2101878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 61,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: INTERMITTENT ASTHMA;HYPERLIPIDEMIA;HYPOTHYROIDISM; HYPERTRIGLYCERIDEMIA; PREDIABETES; CHRONIC PAIN SYNDROME LONG TERM OPIOID THERAPY;INTERVERTEBRAL DISC DEGENERATION OBESITY, BMI 30-34.9, ADULT; MENOPAUSAL HOT FLASHES; OSTEOARTHRITIS OF BILAT KNEES.
Andere Medikamente: Levothyroxine (LEVOTHROID/SYNTHROID);Ibuprofen (MOTRIN);Fluoxetine (PROZAC); Gabapentin (NEURONTIN); tramadol (ULTRAM) ;FLOVENT HFA PROAIR HFA ;Simvastatin (ZOCOR).
Allergien: Penicillins Class ; Sulfa Class [Sulfa (Sulfonamide Antibiotics.)
Vorherige Impfungen: -

VAERS 2101853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 36,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: EXERCISE INDUCED ASTHMA SEVERE OBESITY (BMI >= 40) PREDIABETES MIXED SLEEP APNEA SLEEP RELATED HYPOVENTILATION OR HYPOXEMIA POLYCYSTIC OVARIES LUMBAR SPONDYLOSIS HIDRADENITIS SUPPURATIVA LUMBAR DISC HERNIATION W RADICULOPATHY PRESENCE OF IMPLANTABLE SUBDERMAL CONTRACEPTIVE
Andere Medikamente: Nystatin (MYCOSTATIN) Chlorhexidine Gluconate (HIBICLENS) IBUPROFEN
Allergien: Chocolate Sulfa Percocet
Vorherige Impfungen: -

VAERS 2101812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 65,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: HIV POSITIVE HYPERLIPIDEMIA PREDIABETES HX OF PULMONARY EMBOLUS ALLERGIC RHINITIS NONALLERGIC RHINITIS HYPERTROPHY OF NASAL TURBINATES COUGH, UNSPECIFIED CHORIORETINAL SCAR. IMMUNITY TO HEPATITIS A, POSITIVE SEROLOGY
Andere Medikamente: BIKTARVY Rosuvastatin (CRESTOR) SUPER DHA CHOLECALCIFEROL (VITAMIN D3)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2101776

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33025BD

gering

Staat: CO
Alter: 52,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Bipolar 2 Disorder, Unspecified Episode, Premenstrual Dysphoric Disorder, Single Seizure, Unspecified Type, Urge Incontinence, Obesity (BMI 30-39.9), Allergic Rhinitis, Female Cystocele
Andere Medikamente: Ondansetron (ONDANSETRON), bupropion (WELLBUTRIN XL), Levetiracetam (KEPPRA), Lithium Carbonate (ESKALITH), Trazodone (DESYREL)
Allergien: Augmentin
Vorherige Impfungen: -

VAERS 2101749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 14,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Eczema
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2099361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 16,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2099168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 14,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Urticaria
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2099142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 14,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: CAFE AU LAIT SPOTS OBESITY PEDS, BMI >=95 PERCENTILE
Andere Medikamente: None
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2099112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 39,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered Beyond Use Date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: MIGRAINE W AURA BILAT BREAST LUMPS FIBROCYSTIC CHANGE OF BREAST.
Andere Medikamente: Ergocalciferol, Vit D2, (DRISDOL) Sodium Bicarbonate-Sodium Chloride (NEILMED SINUS RINSE COMPLETE) Fluticasone (FLONASE ALLERGY RELIEF)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2099077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 13,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: SEVERE OBESITY PEDS, BMI >99 PERCENTILE OSGOOD SCHLATTERS DISEASE OF RIGHT KNEE
Andere Medikamente: Flonase
Allergien: Omnicef, Amoxicillin
Vorherige Impfungen: -

VAERS 2099049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 14,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered Beyond Use Date.

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 2098995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HYPOTHYROIDISM PREDIABETES REFLUX ESOPHAGITIS GERD (GASTROESOPHAGEAL REFLUX DISEASE) SEAFOOD ALLERGY DERMATOGRAPHIC URTICARIA DYSHIDROTIC ECZEMA RIGHT SENSORINEURAL HEARING LOSS W LEFT SIDE UNRESTRICTED HEARING RIGHT SUBJECTIVE TINNITUS URTICARIA MENOPAUSAL HOT FLASHES
Andere Medikamente: Levothyroxine (LEVOTHROID/SYNTHROID) Venlafaxine (EFFEXOR XR) Omeprazole (PRILOSEC)
Allergien: Cod, shrimp
Vorherige Impfungen: -

VAERS 2098974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 13,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: SEVERE OBESITY PEDS, BMI >99 PERCENTILE DERMATITIS
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2098930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 62,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HX OF DIVERTICULITIS BPH W URINARY FREQUENCY
Andere Medikamente: Aspirin, Tamsulosin
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2098880

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 42,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE W ASSOCIATED FEATURES FEMALE INFERTILITY IUD INSERTION PERIORAL DERMATITIS
Andere Medikamente: Sertraline (ZOLOFT) Doxycycline Monohydrate (AVIDOXY) Diclofenac Sodium (VOLTAREN) Levonorgestrel (MIRENA)
Allergien: Ceclor
Vorherige Impfungen: -

VAERS 2098866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 62,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: BIPOLAR DISORDER, UNSPECIFIED TYPE ANXIETY DISORDER POSTTRAUMATIC STRESS DISORDER HYPERLIPIDEMIA GERD (GASTROESOPHAGEAL REFLUX DISEASE) DM 2 W CKD STAGE 3 (GFR 30-59) HTN (HYPERTENSION) MODERATE TOBACCO USE DISORDER LEUKOCYTOSIS HX OF HEPATITIS C INSOMNIA RIGHT SHOULDER JOINT PAIN HX OF ALCOHOL ABUSE. HX OF H PYLORI INFECTION HX OF ABNL PAP SMEAR
Andere Medikamente: Erythromycin Ophth Oint Omeprazole (PRILOSEC) Lisinopril (PRINIVIL/ZESTRIL) LANTUS U-100 INSULIN glipizide (GLUCOTROL) Lorazepam (ATIVAN) metformin (GLUCOPHAGE XR) Atorvastatin (LIPITOR) Buspirone (BUSPAR)
Allergien: Lamotrigine
Vorherige Impfungen: -

VAERS 2098833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 21,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GENERALIZED ANXIETY DISORDER DEPRESSIVE DISORDER. PREDIABETES ADHD, PREDOMINANTLY INATTENTIVE PRESENTATION INSOMNIA BINGE EATING DISORDER UNHEALTHY SUBSTANCE USE BEHAVIOR HX OF TRAUMATIC BRAIN INJURY OBESITY, BMI 30-34.9, ADULT
Andere Medikamente: None
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2098821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 60,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GERD (GASTROESOPHAGEAL REFLUX DISEASE) HTN (HYPERTENSION) HYPERLIPIDEMIA PREDIABETES POLYCYSTIC OVARIAN SYNDROME UTERINE FIBROIDS MENOPAUSE HX OF COLONIC POLYP
Andere Medikamente: Simvastatin (ZOCOR) Estradiol (ESTRACE) Lisinopril (PRINIVIL/ZESTRIL) Ergocalciferol, Vit D2, (VITAMIN D2) BLACK COHOSH ROOT EXTRACT
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2098794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 29,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: SUPERVISION NORMAL MULTIGRAVIDA PREGNANCY RH NEGATIVE ADJUSTMENT DISORDER W DEPRESSED MOOD FETAL PYELECTASIS IN PREGNANCY
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2098781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered 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 2096283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IN
Alter: 13,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 10.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Respiratory symptom Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

1/16/22 13-year-old male with history of asthma presenting to the emergency department with upper respiratory symptoms for the past 3 days. There has been cough, congestion and rhinorrhea. There has been no wheezing or stridor noted at home. There has been no labored breathing or increased work of breathing. There has been no vomiting or diarrhea. Appetite and activity levels have been normal. Urine output has been normal. No home treatment has been initiated. ROS positive for cough, congestion and rhinorrhea, negative for vomiting or diarrhea, rash, labored breathing, change in mental status, sore throat, eye or ear discharge; ROS o/w negative HEENT: TMs normal, oropharynx normal, mucus membranes moist. 1/16/22 Discharge: 13-year-old male presenting to the emergency department with chief complaint of upper respiratory symptoms for the last few days. Exam reveals a healthy young man with occasional bronchospastic cough, rhinorrhea and congestion. Dexamethasone x1 was given p.o. mother was advised to continue asthma regimen at home. Benadryl to be taken at night. Mother to allow rest and to push p.o. fluids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 1/16/22 COVID-19 Result Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: ADHD (attention deficit hyperactivity disorder) Aggression, Anxiety, Asthma, Constipation, Current ab, Current abuse involving hitting, punching, kicking, or slapping 11/16/2020, Depression, DMDD (disruptive mood dysregulation disorder), Henoch-Schonlein purpura (CMS/HCC) 2/19/14 Hypothyroidism, ITP (idiopathic thrombocytopenic purpura), Obesity, Oppositional defiant behavior, Reflux, Seasonal allergies, HEENT: TMs normal, oropharynx normal, mucus membranes moist. Nasal congestion/rhinorrhea present. Neck: supple/non-tender, full range of motion without pain, Chest: clear, no grunting, flaring, or retracting, CV: no, murmurs/gallops/rubs, 2+ pulses, GI: no hepatosplenomegaly, Skin: no rash, cap refill normal, Neuro: alert.
Andere Medikamente: Albuterol HFA, BENADRYL, FLONASE, FLOVENT, GuanFACINE HCl, NIZORAL, ZADITOR, LAMICTAL, SYNTHROID, CLARITIN, CONCERTA ER, SINGULAIR, FLINTSTONES W/IRON, GLYCOLAX, SENOKOT, ZOLOFT, TOPAMAX, KENALOG
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2095895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 47,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: DM 2 CHRONIC HYPOXEMIC RESPIRATORY FAILURE HTN (HYPERTENSION) HYPERLIPIDEMIA SEVERE OBESITY (BMI >=50) OBSTRUCTIVE SLEEP APNEA SUBCLINICAL HYPOTHYROIDISM OXYGEN SATURATION REMOTE MONITORING HX OF ATRIAL FIBRILLATION HX OF CORONAVIRUS COVID-19 DISEASE
Andere Medikamente: Lisinopril-hydrochlorothiazide (PRINZIDE/ZESTORETIC) Duloxetine (CYMBALTA) Doxazosin (CARDURA) Carvedilol (COREG) Lovastatin (MEVACOR) metformin (GLUCOPHAGE) hydrochlorothiazide (ESIDRIX/HYDRODIURIL) Ondansetron (ZOFRAN ODT)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2095729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 59,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE, IN FULL REMISSION HYPERLIPIDEMIA HTN (HYPERTENSION) LONG TERM OPIOID THERAPY TOBACCO SMOKER CHRONIC LOW BACK PAIN > 3 MONTHS POSTMENOPAUSAL HORMONE REPLACEMENT THERAPY UNHEALTHY SUBSTANCE USE BEHAVIOR OSTEOARTHRITIS OF RIGHT HIP OSTEOARTHRITIS OF RIGHT KNEE LEFT CORNEAL ULCER ABNL CHEST CT SCAN LUNG MASS
Andere Medikamente: Estradiol (ESTRACE) Cyclobenzaprine (FLEXERIL) Fluoxetine (PROZAC) Ascorbic Acid (VITAMIN C)
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 2092821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 53,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GERD (GASTROESOPHAGEAL REFLUX DISEASE) HYPERLIPIDEMIA HYPERTRIGLYCERIDEMIA PREDIABETES GALLBLADDER POLYPS DYSPHAGIA INGUINODYNIA OVERWEIGHT (BMI 25-29.9) METABOLIC SYNDROME X VITAMIN D DEFICIENCY PARESTHESIA VITAMIN B12 DEFICIENCY
Andere Medikamente: Cyanocobalamin (VITAMIN B-12) Duloxetine (CYMBALTA) Omeprazole (PRILOSEC) Cholecalciferol, Vitamin D3, (VITAMIN D3) Hydrocortisone Acetate (ANUSOL-HC/ANUCORT-HC)
Allergien: Venlafaxine Hcl
Vorherige Impfungen: -

VAERS 2092773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 67,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: DM 2 W DYSLIPIDEMIA HTN (HYPERTENSION) ADULT OBSTRUCTIVE SLEEP APNEA DM 2 W PERIPHERAL NEUROPATHY OCCULT BLOOD IN STOOL
Andere Medikamente: Metformin (GLUCOPHAGE) Lisinopril (PRINIVIL/ZESTRIL) ASPIRIN
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2092757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 49,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GERD LOW BACK PAIN, UNSPECIFIED RIGHT CARPAL TUNNEL SYNDROME RIGHT ARM PAIN
Andere Medikamente: Omeprazole (PRILOSEC) Fluticasone (FLONASE ALLERGY RELIEF) Loratadine (CLARITIN)
Allergien: Keflex Oxycodone. Pcn Class Percocet
Vorherige Impfungen: -

VAERS 2092711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 15,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 17.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HYPERLIPIDEMIA NUMMULAR ECZEMA NEWBORN AFFECTED BY MATERNAL EXPOSURE TO UNSPECIFIED SUBSTANCE
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2091814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 13,0
Geschlecht: F
Eingang: 06.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: ATYPICAL MIGRAINE COUGH VARIANT ASTHMA NONALLERGIC RHINITIS LEFT HIGH FREQUENCY SENSORINEURAL HEARING LOSS W RIGHT SIDE UNRESTRICTED HEARING
Andere Medikamente: RETIN-A PANOXYL Clindamycin Phosphate (CLEOCIN) Sumatriptan (IMITREX) Ondansetron (ONDANSETRON)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2091807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 15,0
Geschlecht: M
Eingang: 06.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Cephalexin
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2091804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 17,0
Geschlecht: F
Eingang: 06.02.2022
Impfdatum: 17.01.2021
Beginn: 17.01.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety Disorder
Andere Medikamente: Nexplanon
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2091495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 26,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HYPOTHYROIDISM GERD (GASTROESOPHAGEAL REFLUX DISEASE)
Andere Medikamente: Levothyroxine (LEVOTHROID/SYNTHROID) Omeprazole (PRILOSEC)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2091473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 80,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HTN (HYPERTENSION) HYPERLIPIDEMIA PULMONARY EMBOLISM, UNSPECIFIED. ATRIAL FIBRILLATION, PAROXYSMAL DEMENTIA ERECTILE DYSFUNCTION BILAT TINNITUS SEVERE ALCOHOL USE DISORDER ASYMMETRIC BILAT SENSORINEURAL HEARING LOSS OSTEOARTHRITIS OF RIGHT KNEE
Andere Medikamente: Rosuvastatin (CRESTOR) diltiazem (DILT-XR)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2091470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 20,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: MIGRAINE ANXIETY DISORDER DEPRESSIVE DISORDER, OTHER SPECIFIED
Andere Medikamente: Doxycycline Monohydrate (AVIDOXY) predniSONE (ORASONE) Albuterol (PROAIR/PROVENTIL/VENTOLIN) Sumatriptan (IMITREX)
Allergien: Augmentin [Amoxicillin With Clavulanate Potassium] Claritin [Loratadine] Depacon [Valproate Sodium]
Vorherige Impfungen: -

VAERS 2091463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 69,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
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

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: COPD (CHRONIC OBSTRUCTIVE PULMONARY DISEASE) MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE DM 2 W DYSLIPIDEMIA HYPOTHYROIDISM CHRONIC HYPOXEMIC RESPIRATORY FAILURE GERD (GASTROESOPHAGEAL REFLUX DISEASE) IRRITABLE BOWEL SYNDROME CKD STAGE 3B (GFR 30-44) URGE INCONTINENCE HX OF LUNG CANCER INTERNAL HEMORRHOID TMJ PAIN DYSFUNCTION SYNDROME. HX OF H PYLORI INFECTION FEMALE RECTOCELE FEMALE CYSTOCELE HX OF TOBACCO USE CONVERGENCE INSUFFICIENCY Sensorineural hearing loss. HX OF UTERINE CANCER
Andere Medikamente: Fluoxetine (PROZAC) glipizide (GLUCOTROL) metformin (GLUCOPHAGE) amlodipine (NORVASC) Atorvastatin (LIPITOR) Levothyroxine (LEVOTHROID/SYNTHROID) Lisinopril (PRINIVIL/ZESTRIL) SPIRIVA RESPIMAT Trospium (SANCTURA) SENNA LAX OXYGEN
Allergien: Adhesive Tape Aspirin Penicillins Class Sulfa
Vorherige Impfungen: -

VAERS 2088011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 17,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HYPERTRIGLYCERIDEMIA MAJOR DEPRESSIVE DISORDER, SINGLE EPISODE ACANTHOSIS NIGRICANS OVERWEIGHT
Andere Medikamente: Ventolin
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2087986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 73,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GENERALIZED ANXIETY DISORDER FRAILTY HTN (HYPERTENSION) MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE HYPERLIPIDEMIA PREDIABETES OSTEOPENIA OSTEOARTHRITIS OF BILAT KNEES GASTRITIS BRADYCARDIA FATTY LIVER
Andere Medikamente: Simvastatin (ZOCOR) Lisinopril-hydrochlorothiazide Sertraline (ZOLOFT)
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2087822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 26,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2085970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 21,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine administered BUD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: VENTRICULAR SEPTAL DEFECT AUTOSOMAL DOMINANT ADULT POLYCYSTIC KIDNEY DISEASE
Andere Medikamente: Ketoconazole topical shampoo
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2079547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 19,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

COVID vaccine, removed from freezer 12-17-21 at 930am, administered to patient on 1-17-2022 after 930am.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Intermittent asthma, Major depressive disorder, Generalized anxiety disorder, PTSD, Panic Disorder, Abnormal weight loss, Cerebral venous sinus thrombosis, allergic rhinitis, Scoliosis, Irregular menstrual cycle
Andere Medikamente: Prilosec, Ondansetron, Dicyclomine, Effexor, Remeron, Atarax
Allergien: Amoxicillin, Levofloxacin, Vancomycin, Peanut, Beans Lima, Curry Powder, Ceftriaxone, Metronidazole
Vorherige Impfungen: -

VAERS 2079500

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33025BD

gering

Staat: CO
Alter: 24,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was given one day past BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prozac
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2079438

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33025BD

gering

Staat: CO
Alter: 82,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was given one day past BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Shortness of breath since COVID diagnosis
Vorgeschichte: Hypothyroidism, Coronary artery disease w/o angina, Hypercholesterolemia, COPD, Atrial Fibrillation unspecified, Coronavirus COVID-19 disease, Long term non warfarin oral anticoagulant therapy, BPH
Andere Medikamente: Wixela inhub, Cardizem, Lipitor, Levothyroxine, Pradaxa
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2079343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 63,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was given one day past BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Major Depressive disorder, Idiopathic Parkinsons disease, Polyneuropathy, Mild cognitive impairment, Fatigue, Vitamin D Deficiency, Bilateral subjective tinnitus, Right inguinal hernia, Ganglion cyst
Andere Medikamente: Sinemet, Zoloft, Cholecalciferol Vitamin D-3
Allergien: PCN Class
Vorherige Impfungen: -

VAERS 2079334

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 33025BD

gering

Staat: CO
Alter: 62,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

When COVID vaccine was received from state on 12/17/21 an incorrect Beyond Use Date was assigned to the vaccine by the receiving pharmacist. The date assigned was 1/18/22 when it should have been 1/17/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Prediabetes, Intermittent asthma
Andere Medikamente: Albuterol
Allergien: Epinephrine
Vorherige Impfungen: -

VAERS 2075757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 71,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

No adverse event Product storage error

Symptomtext

COVID vaccine Lot 33025BD, removed by CDPHE from freezer 12-17-21 at 930am, administered to patient on 1-17-2022 after 930am, NO adv rx from pt

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: HX of Prostate Cancer, Prediabetes, long term use of warfarin
Andere Medikamente: Pradaxa
Allergien: KNDA
Vorherige Impfungen: -

VAERS 2075738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 65,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

COVID vaccine Lot 33025BD, removed from freezer 12-17-21 at 930am, administered to patient on 1-17-2022 after 930am. NO adv rx from pt

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, DME, Hyperlipidemia, lumbar radiculopathy
Andere Medikamente: Actos, Cozaar, Glucophage. Zocor
Allergien: Glimepiride, Lisinopril
Vorherige Impfungen: -

VAERS 2075660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 12,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

COVID vaccine Lot 33025BD, removed by Agency from freezer 12-17-21 at 930am, administered to patient at Baseline Primary Care on 1-17-2022 after 930am. NO adv rx from pt

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety, migraines
Andere Medikamente: Temovate
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2075603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IL
Alter: 30,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Pfizer Covid Vaccine was expired, vaccine was left out over 12 hours prior to patient receiving the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Attention Deficit Hyperactivity Disorder (ADHD)
Vorgeschichte: -
Andere Medikamente: Amphetamine-dextroamphetamine 15mg
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2074768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: OR
Alter: 11,0
Geschlecht: M
Eingang: 29.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

11 yo male was given Pfizer Covid-19 vaccine dose 0.3 ml instead of 0.2 ml. There have been no adverse effects per patient's father.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 21.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Adverse reaction Vision blurred

Symptomtext

On Sunday morning, upon waking up at 8 am, 01/23/2022, patient reported "haziness and blurry vision" started. She was afraid for her sudden loss of vision. She went to ER. She said they ran all kinds of test and did not find anything. She also visited her optometrist to check her eyesight. He said everything was ok. She still has problems with her vision as of today 01/29/2022. She wanted to report this possible adverse reaction after booster vaccine dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse reaction
Hospital-Tage: -
Labordaten: Not available.
Aktuelle Erkrankungen: Not reported
Vorgeschichte: Hypertension
Andere Medikamente: Tylenol
Allergien: Not reported
Vorherige Impfungen: -

VAERS 2072468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 11,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 27.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

The patient's mother falsified her daughter's birthday so she could receive the adult dose of Pfizer vaccine. The patient received her first and second dose from a pharmacy where the mother indicated she was born in 2009 which made her appear 12 at the time. The pharmacy vaccinated the child and issue a CDC card with the DOB of 2009. The child was actually born in 2010 so she received her first dose of Pfizer for age 12+ on 7/26/2021 at age 11 and her second dose for Pfizer 12+ on 8/16/2021 at age 11. The mother registered her child under the DOB of 2009 at a county vaccine clinic for her booster. Clinic staff and the vaccinator confirmed the DOB with both the mother and child and they both falsely stated she was born in 2009. Once the vaccine had been given and the child was in the monitoring area, the mother confided to the nurse that the child was actually age 11 and born in 2010. She received her booster of Pfizer 12+ vaccine 5 months after her primary series at the age of 11 meaning that she received 3 full adult doses of Pfizer vaccine at age 11 in a span of 6 months total.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: Nursing staff monitored the pt.'s vital signs immediately after vaccination for 30 minutes and there was no obvious distress, BP 98/70 and HR 82.
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2072091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 30,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 26.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient received 1st dose Covid 19 vaccine Moderna 3/5/2021 lot # 042L20A at facility Patient received 2nd dose Covid 19 vaccine Moderna 4/2/2021 lot # 042L20A at facility Patient received 3rd dose Covid 19 vaccine Pfizer 4/26/2021 lot # EW0169 at facility Patient received 4th dose Covid 19 vaccine Pfizer 1/8/2022 lot #33025BD at facility

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2071734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IL
Alter: 10,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

Patient's mom received COVID-19 vaccination. She asked if her child could also be vaccinated. Adult dose of Pfizer given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2069385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Patient signed up and checked in for Janssen first dose. Vaccinator card has Janssen documented, with Janssen alert card. Vaccinatore gave Pfizer dose after speaking with patient. Incident explained to patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2067906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NJ
Alter: 60,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Dysuria Immunisation Urine flow decreased

Symptomtext

Urine flow/slowed to a painful drip. Urination became incredibly difficult; Urine flow/slowed to a painful drip. Urination became incredibly difficult; Dose number=3; This is a spontaneous report received from a contactable Other HCP. The reporter is the patient. A 60 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 20Dec2021 15:00 (Lot number: 33025BD) at the age of 60 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Possible prostate hypertrophy" (unspecified if ongoing). Concomitant medication(s) included: TAMSULOSIN; CEFUROXIME. Vaccination history included: Bnt162b2 (dose number=2, product=COVID 19, brand=Pfizer, lot number=EW0151, administration date=14Apr2021, administration time=05:15 PM, vaccine location=Right arm), administration date: 14Apr2021, when the patient was 59 years old, for Covid-19 Immunization; Bnt162b2 (product=COVID 19, brand=Pfizer , lot number=EN6207, administration date=22Mar2021, administration time=06:00 PM, dose number=1, vaccine location=Right arm), administration date: 22Mar2021, when the patient was 59 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Dec2021 15:00, outcome "unknown", described as "Dose number=3"; URINE FLOW DECREASED (non-serious), DYSURIA (non-serious) all with onset 20Dec2021 19:00, outcome "recovered" (Dec2021) and all described as "Urine flow/slowed to a painful drip. Urination became incredibly difficult". The event "urine flow/slowed to a painful drip. urination became incredibly difficult" and "urine flow/slowed to a painful drip. urination became incredibly difficult" was evaluated at the physician office visit. Therapeutic measures were not taken as a result of urine flow decreased, dysuria. Additional information: The patient did not receive any other vaccine in four weeks. The patient did not had COVID prior vaccination and post vaccination, patient had not tested with COVID-19. Within 4-6 hours post vaccine, urine flow, which had been improving slowed to a painful drip. Urination became incredibly difficult over the next 36hrs and then it began to improve. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysuria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Prostatic hypertrophy
Andere Medikamente: TAMSULOSIN; CEFUROXIME
Allergien: -
Vorherige Impfungen: -

VAERS 2067875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: WA
Alter: 75,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 23.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Erythema Mass Swelling

Symptomtext

Pt developed a lump in her arm which then became more raised, red & swollen.

Weitere VAERSDATA-Felder

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

VAERS 2065421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IN
Alter: 12,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

booster dose given too early

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2065415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IN
Alter: 12,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

Booster dose given too early.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: unknown
Vorgeschichte: Unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2063797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 11,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 24.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Incorrect dose administered

Symptomtext

RN gave patient an adult dose on 1/3/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2063062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 37,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

none

Weitere VAERSDATA-Felder

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

VAERS 2063028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 12,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

none

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2062994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 46,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

4TH DOSE OF PFIZER GIVEN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2062183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient received a 4th dose of vaccine 2 months after 3rd dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2061944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: AZ
Alter: 46,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 10.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: - / LA

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

Alopecia

Symptomtext

Significant hair loss on day 9 since receiving vaccine; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 46-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 10Jan2022 at 09:15 (Lot number: 33025BD) at the age of 46 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19: Yes. Concomitant medication included: VIT D. The following information was reported: ALOPECIA (non-serious) with onset 19Jan2022 at 08:00, outcome "unknown", described as "Significant hair loss on day 9 since receiving vaccine". Therapeutic measures were not taken as a result of alopecia. Additional information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. The event did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19: Yes)
Andere Medikamente: VIT D [VITAMIN D NOS.]
Allergien: -
Vorherige Impfungen: -

VAERS 2058761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 64,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 22.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Booster dose given early

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: N/A
Allergien: n/a
Vorherige Impfungen: -

VAERS 2057883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 23.01.2022
Impfdatum: 08.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Facial paresis Hypoaesthesia

Symptomtext

11 days after Covid dose #3, patient developed left sided facial weakness and numbness. Presented for evaluation 1/21 and prednisone prescribed. F/U scheduled in 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paresis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: no
Allergien: none
Vorherige Impfungen: -

VAERS 2057380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NJ
Alter: 17,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Axillary mass

Symptomtext

Lump in left armpit; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 17-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 27Dec2021 at 01:45 (Lot number: 33025BD) at the age of 17 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19? Yes. Patient did not receive any concomitant medications. The following information was reported: AXILLARY MASS (non-serious) with onset 28Dec2021 at 09:00, outcome "recovered", described as "Lump in left armpit". Therapeutic measures were not taken as a result of axillary mass. Additional Information: The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: CA
Alter: 34,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation SARS-CoV-2 test Tinnitus

Symptomtext

Significant tinnitus in both ears; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 23Dec2021 18:00 (Lot number: 33025bd) at the age of 34 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergy: Sulfa" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Ew0150, Location of injection: Arm Left, Vaccine Administration Time: 03:00 PM), administration date: 03May2021, when the patient was 34 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Ew0164, Location of injection: Arm Left, Vaccine Administration Time: 03:00 PM), administration date: 12Apr2021, when the patient was 34 years old, for Covid-19 immunization. The following information was reported: TINNITUS (disability) with onset 29Dec2021 15:00, outcome "not recovered", described as "Significant tinnitus in both ears"; IMMUNISATION (non-serious) with onset 23Dec2021 18:00, outcome "unknown", described as "Booster". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: negative. Therapeutic measures were not taken as a result of tinnitus. No follow-up attempts are possible. No further information is expected. Dose received: 3 Most recent dose details: Product=COVID 19 Brand= Pfizer Brand unknown=False Lot number= 33025bd Lot unknown=False Administration date= 23Dec2021 Administration time=06:00 PM Dose number=3 Vaccine location= Left arm Previous dose details: Prev dose product=COVID 19 Prev dose brand=Pfizer Prev dose brand unknown=False Prev dose lot number= Ew0150 Prev dose lot unknown= False Prev dose administration date= 03May2021 Prev dose administration time=03:00 PM Prev dose dose number=2 Prev dose vaccine location=Left arm Prev dose product=COVID 19 Prev dose brand=Pfizer Prev dose brand unknown=False Prev dose lot number= Ew0164 Prev dose lot unknown= False Prev dose administration date= 12Apr2021 Prev dose administration time= 03:00 PM Prev dose dose number=1 Prev dose vaccine location=Left arm Facility type Vaccine: Hospital If other vaccine in four weeks : No Other medications in two weeks: No Adverse event: Significant tinnitus in both ears Adverse event start date: 29Dec2021 Adverse event start time: 03:00 PM Adverse event country: AE resulted in: Disability or permanent damage If patient recovered: Not recovered If treatment ae: No If Covid prior vaccination: No If Covid tested post vaccination: Yes Covid test post vaccination Covid test type post vaccination=Nasal Swab Covid test result=Negative Known allergies: Sulfa drug Follow-Up (12Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Immunisation
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IN
Alter: 15,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered Syringe issue

Symptomtext

Patient was receiving covid Pfizer booster when near the end of injection of vaccine, fluid (vaccine noted to be going down patient's arm. Pt received some vaccine but provider unsure of exact amount. Offered to provide another booster at time of incident. Mother wishes to not have another vaccine given at this time due to being unsure of received amount

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: No
Vorherige Impfungen: -

VAERS 2047850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: AZ
Alter: 82,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Heart rate increased

Symptomtext

Increased heartrate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Heart rate increased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Penicillin, Tetracycline
Vorherige Impfungen: -

VAERS 2043434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cough Throat irritation

Symptomtext

Pt started to cough and complained her throat was itchy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: BP and pulse taken afterwards
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Benadryl 25 mg PO
Allergien: no
Vorherige Impfungen: -

VAERS 2038361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KS
Alter: 10,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 16.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Pt was given 2nd dose Pfizer vaccine 0.3ml dose approved for 12 yrs and up instead of the pediatric pfizer 0.2ml dose approved for ages 5-11. Mistake not noticed until reporter went to document vaccine, which was not in real time. Once mistake was noticed, reported and incident report completed as well. Advised pt parent would be contacted in regards to error.d

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2033072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MN
Alter: 33,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Thrombophlebitis Ultrasound scan X-ray

Symptomtext

Thrombophlebitis, 45 day prescription of Xaralto, outcome not yet applicable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombophlebitis
Hospital-Tage: -
Labordaten: Ultrasound, Xray 01/12/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism, HS
Andere Medikamente: Humira, Seroquel, Levothyroxine, Cymbalta
Allergien: N/A
Vorherige Impfungen: -

VAERS 2032106

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge 33025BD

gering

Staat: IN
Alter: 75,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Incorrect dose administered Product preparation issue

Symptomtext

The pfizer product was not diluted as intended at the time of vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety, Depression, Coagulopathy, Migraines, GERD, IBS, HX of DVT,
Andere Medikamente: Abilify 5 mg, Cymbalta 90 mg, Levbid 0.375 mg, Prilosec 40 mg, Coumadin 4mg
Allergien: Prednisone
Vorherige Impfungen: -

VAERS 2030763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 10.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Haematuria

Symptomtext

Hematuria (blood in urine)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Haematuria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: History of recurrent pancreatitis
Andere Medikamente: Vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 2027858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: VT
Alter: 32,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 21.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / LA

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

C-reactive protein increased Peripheral swelling

Symptomtext

swelling of several toes L foot, pain and swelling of pad of R foot CRP elevated @ 26.5 CRP repeated 1/10/22 @ 7.8

Weitere VAERSDATA-Felder

Praegender Schweregrund: C-reactive protein increased
Hospital-Tage: -
Labordaten: ER visit, labs - elevated CRP 1/2/2022
Aktuelle Erkrankungen: none
Vorgeschichte: congenital heart defect
Andere Medikamente: Mirena IUD
Allergien: opiates
Vorherige Impfungen: -

VAERS 2020649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 13,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 06.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Epistaxis

Symptomtext

Child with no history of nosebleeds is now having spontaneous nose bleeds post booster vaccine on 6 January 2021.

Weitere VAERSDATA-Felder

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

VAERS 2019987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: PR
Alter: 37,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Muscle spasms Swelling

Symptomtext

swelling and spasm on the left side of the neck, near the collarbone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Muscle spasms
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2019515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 11,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

11 year old came in for 2nd dose of Pfizer vaccine. Patient was given 0.3 ml (30 mcg) of Pfizer vaccine instead of 0.2 ml (10 mcg)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Aphasia Lethargy

Symptomtext

While checking on the patient I noticed she was lathergic and unable to use her words to communicate with me. I proceeded to ask her name and she was unable to give me an answer. During this time she placed her hands on her head several times as if she was thinking of things to say. Her manners at this time were totally different from our initial conversation. Upon her arrival to the clinic she was able to answer all questions and make small talk before she received her booster. We communicated a several times during her monitoring time and before s/s were presented before discharge from the vaccination clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Aphasia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cardiac and Vasculature Benign hypertension with CKD (chronic kidney disease) stage III Hyperlipidemia Endocrine and Metabolic Prediabetes Genitourinary and Reproductive Postmenopausal bleeding Endometrial polyp Hematology and Neoplasia Benign tumor of meningioma (cerebral) Cerebral meningioma Musculoskeletal and Injuries Pain of right lower extremity Neuro VP (ventriculoperitoneal) shunt status Skin Idiopathic urticaria
Vorgeschichte: -
Andere Medikamente: levETIRAcetam (KepPRA) 500 MG tablet (Expired) acetaminophen (TYLENOL) 325 MG tablet docusate sodium 100 MG Cap polyethylene glycol (MIRALAX) 17 g packet HYDROcodone-acetaminophen (NORCO) 5-325 MG per tablet fexofenadine (ALLEGRA) 180 MG ta
Allergien: Dilantin
Vorherige Impfungen: -

VAERS 2014766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Pt was administered with higher concentrated Pfizer vaccine by accident

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: cervical polyp
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2014539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 79,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Product preparation issue

Symptomtext

The Pfizer vaccine was not properly diluted and resulting in more concentrated vaccine was administered to patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: Iron Deficiency and Osteopenia
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2006445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Eye swelling Swelling face

Symptomtext

Patient called today stating she experienced an allergic reaction to the Pfizer BioNtech vaccine which she received on 1/4/22 at 9:18am. Patient went home, and around 10:40am when she got home. She began to have facial swelling. The patient called me today 1/5/22 at 2:15pm to report that her eyes and face were still swollen since yesterday. The patient was instructed to go to emergency room as this is where her primary care physician is located. The patient agreed to go to the ER immediately. Medical Provider who was on site was notified of incident.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye swelling
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient stated she had cardiac surgery one month ago when she came to receive vaccine.
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2005553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NJ
Alter: 38,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Anxiety Erythema

Symptomtext

Had booster while under observation developed mild erythema (not rash) on both arms appears was likely due to anxiety- Resolved after a few minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anxiety
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: na
Allergien: vancomycin
Vorherige Impfungen: -

VAERS 2005483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NJ
Alter: 48,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia Feeling abnormal Feeling hot

Symptomtext

Had 1st dose of pfizer "felt bad" . He said he feels weak & hot. got him in medical tent placed in supine position spoke to his wife regarding him allergies. "Horse Serum" After few minutes he felt better. Refused OJ & water. Hx. of covid 19 seven months ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: na
Allergien: horse serum
Vorherige Impfungen: -

VAERS 2004265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MI
Alter: 13,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

No adverse event occurred today; patient received Pfizer 0.3ml BOOSTER at age 13 today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2004219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: WA
Alter: 11,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was given the 12+ dose (30mcg/0.3ml) dose of Pfizer 01/04/2022 at 12:30pm. He is currently only 11 years old and does not turn 12 until 02/01/2022. Mother was notifed at 7pm 1/04/22 when discovered. No known current adverse events

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2001566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: MI
Alter: 56,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

No adverse event Wrong product administered

Symptomtext

Patient was mistakenly administered a Fluad vaccine which is only indicated for patients 65+ and he is 56. It was intended to administer a standard quadrivalent flu vaccine. Patient was informed of the error and potential side effects to be aware of. No immediate adverse reactions occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2001169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IL
Alter: 15,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Patient was given Pfizer booster shot. Boosters approved for only 16+ at time. Mistake was not caught at registration before vaccine administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None Known
Vorgeschichte: None Known
Andere Medikamente: None
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2000242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: GA
Alter: 9,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect dose administered No adverse event

Symptomtext

.2 ml of an adult Pfizer dose given to a 9 year old female, no immediate adverse events occurred after the vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: None at this time
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: None
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1999277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IL
Alter: 30,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Inappropriate schedule of product administration No adverse event

Symptomtext

Patient was given the second dose of vaccine prior to the 21 days and prior to the 4 day grace period. Patient has had no side effects. She was notified of need for another dose per CDC guidelines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1999220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Interchange of vaccine products Pharyngeal swelling

Symptomtext

Moderna Primary; Pfizer Booster 12mins post vaccination pt reported that she was feeling like her throat is swelling. No Wheezing, pt is able to talk. Pt given 50mg PO Benadryl @ 10:59. Vitals: @11:05 152/97, 74, 20, 100% --? 130/90, 63 Pt stable and released from the vaccination site. Recommended pt f/u w/ PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Allergies: PCN, Motrin
Vorherige Impfungen: -

VAERS 1996553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: WA
Alter: 31,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 31.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Device connection issue Incorrect dose administered

Symptomtext

technician was administering pfizer covid shot and as she was injecting the imz, the syringe disengaged from the needle and as a result pt got lower dose than recommended (unknown exactly how much dose got into patient.) i apologized to patient. per cdc recommendation, I repeated the dose with a full amount (done in her other arm.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Device connection issue
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1996133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: WI
Alter: 15,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Patient is only 15 years old, but was given a Booster shot (3rd shot)on 12/29/21. First shot given 3/22/21 second shot given 4/19/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1996092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 14,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 31.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

PATIENT WAS GIVEN A PFIZER BOOSTER AT AGE 14.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1993222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: KY
Alter: 28,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 26.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

12/30/21 Patient is a server at a restaurant. Last week general manager was positive and the restaurant closed for 1 week. He had a test done on December 23 that was negative for Covid. Had one a couple weeks prior to that that was also negative. However on his own he went to Pharmacy and had a rapid test done there on Tuesday the 28th. That test was positive. He had a little bit of a scratchy sore throat otherwise per review of systems below negative. He wanted to be tested again to see if he really has it or not. Feels fine today. Review of Systems Constitutional: Negative for chills and fever. HENT: Negative for rhinorrhea, sore throat and voice change. Respiratory: Negative for cough. 12/30/21 Musculoskeletal: Negative for myalgias. Neurological: Negative for headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 12/30/21- COVID Result IPOC PCR Detected Abnormal.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, GERD, Scoliosis
Andere Medikamente: Epinephrine 0.3mg/0.3ml sol A-IJ as needed.
Allergien: Nuts, all
Vorherige Impfungen: -

VAERS 1992990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MN
Alter: 15,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age Product administration error

Symptomtext

Child came in today for their booster dose of Pfizer (12 years+/purple cap) today. After they were vaccinated and left it was noted that the child was only 15 years old and current CDC/FDA recommendations are for booster doses starting at 16 years and older. Parent was contacted and notified of the vaccine administration error. "normal" mild to moderate side effects were reviewed. Procedure for reviewing Covid-19 vaccination appointments was addressed and staff notified to be aware of the age of the child and ensuring that a booster dose is appropriate for their age before vaccinating.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1992975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NY
Alter: 31,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Throat tightness

Symptomtext

Patient given vaccine at 3:46 p.m., while in observation area patient stated his throat felt tight, patient states this happened with his previous two doses of covid vaccine. RRT called immediately at 4:13 p.m. B/P 128/80 P 72 RR 18 O2 sats 98%RA. Patient denies feeling shortness of breath. RRT arrived at 4:15 p.m. and patient left with RRT team to go to ER at 4:16 p.m.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Throat tightness
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: Patient states had similar reaction to first two doses of covid vaccine.
Vorherige Impfungen: Patient states had similar reaction to previous doses of covid vaccine.

VAERS 1992967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MN
Alter: 15,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient came in for the Pfizer (age 12+ purple cap) booster dose of vaccine today. After they left, it was noted the patient was 15 years 7 months old. Pfizer booster doses are currently only recommended down to age 16. Parent contacted and informed of the administration error. No out of the ordinary side effects noted at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1992757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: IN
Alter: 62,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Speech disorder Visual impairment

Symptomtext

This was the booster shot I had visuals and my speech was affected for about 10 min while I was at work it took about 4 hours after the shot to show symptoms!

Weitere VAERSDATA-Felder

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

VAERS 1992744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

pt received regeneron on 12/14, should not have received 1st dose Pfizer until 90 days post mab infusion. Will delay 2nd dose until after 90 days per current CDC guidance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: AZ
Alter: 14,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Pt received Regeneron mab on 12/17 and presented for vaccination on 12/29, it was mistakenly administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Moderna Primary Series , Pfizer Booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: ? Abnormal Pap smear ? Anemia ? Anxiety state ? Gall bladder disease ? GERD (gastroesophageal reflux disease) ? Hypothyroid ? Obesity ? OSA (obstructive sleep apnea)
Andere Medikamente: Medications: Mirena IUD
Allergien: Allergies: Morphine (anaphylaxis), PCN (Rash), Iopamidol (hives)
Vorherige Impfungen: -

VAERS 1988728

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge 33025BD

gering

Staat: TX
Alter: 7,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

Adult dose of COVID 19 vaccine accidentally given to a 7 year old patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1985216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: MA
Alter: 58,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Received booster early. Patient received second dose of initial primary series on August 8, 2021. Patient should not have received booster until February 8, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: na
Allergien: nka
Vorherige Impfungen: -

VAERS 1985209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Oropharyngeal discomfort

Symptomtext

1300 Pt received vaccine. At 1305, Pt c/o throat feeling like moss was growing, described as something thick inside. Pt rated sensation between mild and moderate. Pt denied SOB, pain, swelling in throat and itching. Pt had previous reaction to the first and second Pfizer vaccines, swelling of throat and itching. Was given Benadryl with last vaccine. At 1310 MD called. Dr. called and made aware of previous reaction and intervention, SBAR given. Per MD, since Pt able to swallow water and saliva, speaking in full sentences and has no other s&s, can monitor for an additional15 more mins and DC Pt to home if no new or worsening symptoms occur, if worsens send Pt to ED. After Pt was being monitored for appx 20 more mins reported symptoms subsiding and felt good to go home. Verbal discharge instructions given, 911 for emergencies. Pt verbalized understanding and ambulated independent. DC home at 1335.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal discomfort
Hospital-Tage: -
Labordaten: VS done 1300 temp 97.6, 119/85, hr 90, 98% on room air, rr 18, denied pain 1310: 132/77, hr 76, 99% on room air. rr 16, denied pain 1320: 126/80, hr 78, 97% on room air, rr 16 1330: temp 97.2, 114/76, hr 86, 99% on room air, rr 16, denied pain
Aktuelle Erkrankungen: see below
Vorgeschichte: HTN, Pre DM, Anxiety
Andere Medikamente: Lisinopril-hydroCHLOROthiazide (PRINZIDE/ZESTORETIC) 10-12.5 mg Oral Tab, Fluticasone (FLONASE ALLERGY RELIEF) 50 mcg/actuation Nasl SpSn, norethindrone (NORA-BE) 0.35 mg Oral Tab
Allergien: Erythromycin Base, Penicillins Class, Sulfa (Sulfonamide Antibiotics)
Vorherige Impfungen: 4/8/21, 4/29/21 Pt reported throat swelling & itching after Pfizer vaccines

VAERS 1985177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 9,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Patient was given adult Pfizer dose. No side effects when patient was informed of event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1981094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: WI
Alter: 41,0
Geschlecht: F
Eingang: 26.12.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Lymphadenopathy

Symptomtext

Extremely swollen lymph nodes especially in left armpit, swollen the size of a grapefruit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymphadenopathy
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Fibromyalgia, interstitial cystitis
Vorgeschichte: Fibromyalgia, interstitial cystitis
Andere Medikamente: Low dose naltrexone, magnesium supplements, potassium supplements, womens one a day vitamin, 550mg naproxen sodium, 10mg nortriptyline, 150mg trazadone, Zyrtec,
Allergien: Sulfa, tramadol
Vorherige Impfungen: -

VAERS 1980963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CT
Alter: 46,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 22.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Tinnitus Visual impairment

Symptomtext

I have developed an uncomfortable ringing in my left ear . I received my Pfizer Covid booster vaccine. It is hard to read the lot # " 33025bd" or "3302SB0".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: No current health conditions.
Andere Medikamente: Thyroid medication-stable for 20+ years with no side effects, Zolpidem (only used while traveling, so not used in the last 2 weeks).
Allergien: Pennicilin
Vorherige Impfungen: -

VAERS 1978978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too Low-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1977016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025bd

gering

Staat: CA
Alter: 14,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

She got a booster when it is not approved for her age

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: not sure
Allergien: none
Vorherige Impfungen: -

VAERS 1975513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Head discomfort Musculoskeletal discomfort

Symptomtext

Patient received vaccine. Proceeded to observation area and 10 minutes into wait period of 15 she started complaining of pressure in her neck and head and in middle of her chest. Vital signs taken, pt states normal blood pressure is 120/70, current B/P 166/82, O2 sat 100 HR 66, 10 minutes later B/P 181/79, Team Alert called and patient taken to the Emergency Deparment via gurney, alert and oriented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest discomfort
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Problem List Moderate SLEEP APNEA Other ASYMMETRY OF BREASTS ATHEROSCLEROSIS OF AORTA BASAL GANGLIA CALCIFICATION DM 2 DM 2 W MIXED HYPERLIPIDEMIA HX OF INVASIVE BREAST CANCER LEFT PTOTIC BREAST OSTEOPENIA PROBLEM RELATED TO PSYCHOSOCIAL CIRCUMSTANCES
Andere Medikamente: Outpatient Medications blood sugar diagnostic (OneTouch Verio test strips) Misc Strips glipiZIDE (GLUCOTROL XL) 2.5 mg Oral TR24 SR TAB Atorvastatin (LIPITOR) 40 mg Oral Tab blood-glucose meter (OneTouch Verio Flex Start) Misc Kit lancets (
Allergien: Allergies Tylenol W Codeine [Acetaminophen-codeine]Other. Asa [Aspirin]Itching Hydrocodone Metformin Sulfa (Sulfonamide Antibiotics)Rash
Vorherige Impfungen: -

VAERS 1968107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Limb mass

Symptomtext

A hard lump on the skin, left forearm. Very similar to a swollen lymph node, but not in an area where clusters of lymph nodes are located.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Limb mass
Hospital-Tage: -
Labordaten: None to date. Will follow-up in one week of knot hasn't gone away.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Effexor; Adderall XR
Allergien: Sulfa drug allergy
Vorherige Impfungen: -

VAERS 1967708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: GA
Alter: 18,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration No adverse event

Symptomtext

Patient received booster dose of Pfizer, Covid-19 vaccine, before the 6 month guidelines placed by the CDC. His second dose of Pfizer being 07/06/2021, it had only been 5 and a half months. Patient received appropriate medication for age and had no adverse reaction to the dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1967137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: LA
Alter: 21,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1964232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: NY
Alter: 15,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

PFIZER BOOSTER GIVEN TO 15 YEAR OLD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1963392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: GA
Alter: 11,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

Patient received 0.3ml dose of Pfizer. No adverse outcome. No signs or symptoms. no treatment needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: NONE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1962448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: IN
Alter: 34,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 16.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Oedema peripheral

Symptomtext

Swelling under left armpit which began 48 hours after booster shot and has not gone away as of 72 hours post shot. Swelling is very fluid like

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oedema peripheral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lipitor (10 mg), Zyrtec D
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1962006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CO
Alter: 45,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Vision blurred

Symptomtext

Patient arrived to observation area. Observation team noticed redness on left ear, left neck, and left flank. Patient denied itching, pain, nausea, vomiting, and chest pain, but did say he had "slurred vision" explained as delayed tunnel vision. Patient refused to have vital signs taken but agreed to 25mg of PO Benadryl. Observation staff asked patient if he would like to get out of the car to be more closely monitored--patient refused. Patient refused observation time and stated "I just want to go walk in a department store." Patient was educated to call 911/go to emergency room if condition worsened or new symptoms developed. Patient and family communicated understanding and left the site in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unkown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: No
Vorherige Impfungen: -

VAERS 1955256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was 15 years today and was given a booster. The age group has not been approved for boosters. Patient did not have any adverse reactions to the vaccination. Child's parent was notified of the mistake.

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 1951491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 33025BD

gering

Staat: CA
Alter: 11,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

11 y/o patient (who was turning 12 y/o in 4 days on 12/18.) was given adult dose of pfizer for dose 1. No SEs reported following observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -