VAERS Reports GH9697

VAERS 2696986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 91,0
Geschlecht: F
Eingang: 17.10.2023
Impfdatum: 15.12.2022
Beginn: 11.09.2023
Tage bis Beginn: 270,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram cerebral abnormal Angiogram pulmonary abnormal Anticoagulant therapy Asthenia Atrial fibrillation Bradycardia COVID-19 Carotid artery stenosis Computerised tomogram abdomen abnormal Condition aggravated Diuretic therapy Hepatic lesion Malaise N-terminal prohormone brain natriuretic peptide increased Pleural effusion Pulmonary oedema Pyrexia

Symptomtext

Patient is a 92 y.o. female with a history of permanent afib, HFpEF, Hypothyroidism who presented to hospital 9/11/2023 with weakness, fever and malaise. Covid-19 positive, troponin 48, ntpro 2821. Hospitalization complicated by Afib with RVR. CTPA on admission with bilateral pleural effusions, treated with IV diuresis. 1. Acute hypoxemic respiratory failure: required 2L NC on admit. Multifactorial due to cardiogenic pulmonary edema and covid-19. Weaned to RA at discharge. 2. COVID-19 infection: symptom onset 9/9/23. Positive on admit. Steroids, remdesivir in house, no indication for continuation at discharge. 3. Permanent Atrial fibrillation with RVR: per history, afib on admit. Continued home coumadin. Dilt drip transitioned to PO then d/ced with bradycardia. Titrated home BB, f/u with PCP. 4. Acute decompensated heart failure with preserved EF: known history. EF 55-60% 2019. Ntpro 2821 with pleural effusion as above. IV lasix for diuresis, PO transition 9/16/23. F/u with PCP for lab monitoring, further titration 5. Mitral valve regurgitation: per history, s/p bioprosthetic valve replacement. 6. Tricuspid regurgitation: per history. 7. Right ICA stenosis: noted on cta head on admit with 87% stenosis on right ICA. Continued coumadin. 8. Incidental findings: simple cyst in left kidney and stable low density lesions in liver that are stable on CT. 9. Code status: DNRCC, confirmed with daughter, HCPOA on admit.

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

VAERS 2696149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 14.10.2023
Impfdatum: 14.12.2022
Beginn: 22.09.2023
Tage bis Beginn: 282,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Aortic valve incompetence COVID-19 Cough Dizziness Echocardiogram Fall Glomerular filtration rate decreased Glycosylated haemoglobin normal Mitral valve incompetence Mobility decreased Renal impairment SARS-CoV-2 test positive

Symptomtext

Patient is a 81 y.o. male who presented from assisted living on 9/22/2023 with lightheadedness and dizziness and falling twice. Had been coughing several days, tested positive for COVID in the ER. During admission, ID and Cardiology evaluated. ID recommended remdesivir 5 days and Decadron daily until discharge. Cardiology recommended pushing Mitraclip procedure to 21 days after isolation. He tolerated COVID therapy without issue and returned to room air. Medically stable for discharge to his facility and to follow-up with already established PT as outpatient. Falls Reduced Mobility, POA -Patient states he has been falling over the last 8 to 9 months however he fell twice on day of hospitalization. recently moved into assisted living, and review of his outpatient records it also appears he is in the process of obtaining an electric wheelchair/scooter -continue PT as outpatient; does have his own DME equipment COVID-19 Acute Hypoxemic respiratory failure, resolved - Symptom onset: suspected ~ 9/19 - Positive COVID-19: 9/22 at health clinic - Vaccination status: Vaccinated with Pfizer with last dose 12/14/22 - Decadron: Yes. Expected end date today - Remdesivir: Remdesivir completed 5 day course today -Stop decadron upon discharge; ensure COVID vaccination in near future; no home oxygen needs HFrecEF -Ischemic Cardiomyopathy; Grade C, Class I; Follows with heart failure clinic; Home regimen includes Entresto 49-51 mg twice daily, Toprol 50 mg daily, eplerenone 50 mg daily, Farxiga 10 mg daily(held Farxiga during admission) -TTE 5/2023 45+/- 5%. -continue Entresto, Toprol, eplerenone, and farxiga on discharge; resume Lasix 30mg PO on discharge; management of valvular pathology as below; weight at discharge 206lb Severe mitral valve regurgitation Moderate aortic valve regurgitation -Followed by structural heart -Patient scheduled to undergo MitraClip on 9/28/2023 -Structural heart to call and reschedule Mitraclip procedure upon discharge, recommending 21 days after isolation ends (Last day isolation would be 9/28/23) CKD stage IIIa History of renal transplant -His renal function appears to be at baseline with GFR near 50 -We will continue his anti-rejection medications and TMP-SMX for PCP prophylaxis and discharge; check BMP in one week Diabetes mellitus type 2 -Hemoglobin A1c 5.1% on 2/24/2023 -Home regimen includes Tresiba 30 units under the skin every evening; patient also on Farxiga given his CHF -Resume home regimen on discharge CAD -Continue aspirin and atorvastatin History of Reiter's syndrome History of rheumatoid arthritis -Patient with arthritis of all toes, cannot move toes BPH -Continue Flomax Anxiety -Resume home PRNs on discharge

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

VAERS 2689421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 90,0
Geschlecht: M
Eingang: 02.10.2023
Impfdatum: 27.10.2022
Beginn: 05.09.2023
Tage bis Beginn: 313,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Amnesia Bladder hypertrophy Bladder obstruction Brain contusion Brain herniation Brain oedema COVID-19 Cerebral haemorrhage Cerebral mass effect Chest X-ray Computerised tomogram head abnormal Computerised tomogram thorax abnormal Cough Diverticulum Echocardiogram Electroencephalogram normal Fall

Symptomtext

Clinical Summary PATIENT is a 91 y.o. male with a history of HTN, recent diagnosis COVID-19 at urgent care visit who presented to RMH 9/5/2023 as a trauma s/p mechanical fall. Found to have acute SDH, SAH, and hemorrhagic contusion requiring further care. Additionally developed acute hypoxia respiratory failure. Agency was consulted for geriatric evaluation, assumed care as primary on 9/7/23. 1. Acute SDH/SAH/Hemorrhagic Contusion with Cerebral Edema: Traumatic due to fall. Admit 9/5/23 with acute left subdural and subarachnoid hemorrhages with 8 mm left-to-right midline shift; acute cerebral hemorrhagic contusion in the right inferior temporal lobe. Repeat CTHs stable except for slightly increased rightward subfalcine herniation. NSG recommended NOM, OP follow up in 3-4 weeks for repeat CTH. 2. Fall: Pt went down to the basement for COVID-19 isolation, fell down the stairs, amnestic to event. Hit head with LOC. Injuries as discussed. TTE 9/7/23 with EF 69%, no WMA. Evaluated with EEG for 48hrs which did not reveal any seizures. 3. COVID-19 Infection: Patient with cough and congestion, tested positive for COVID-19 at urgent care 9/5/23. S/p 4 doses of Moderna. Admit CT chest 9/5/23 with nonspecific mild mosaic ground-glass attenuation of the lung parenchyma bilaterally. Initially had no need for O2 but later required so Decadron and Remdesivir initiated. 4. Acute Hypoxic Respiratory Failure: In setting of COVID-19. VBG niot obtained. CXR as discussed. Required up to 4L NC on admit, stable on 2L NC 9/7/23. Weaned off o2 by time of discharge. 5. Thrombocytopenia: Baseline Plt unknown. Admit Plt 168, down-trended to 119 on 9/6/23. In setting of illness/trauma. 6. Incidental Findings: Per admit imaging 9/5/23: Diverticulosis, prostatic enlargement, diffuse urinary bladder wall thickening consistent with chronic urinary bladder outlet obstruction, small bilateral fat-containing inguinal hernias, bilateral renal cysts. Asymptomatic. Recommend OP follow up.

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

VAERS 2672255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

kritisch

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 16.08.2023
Impfdatum: 07.11.2022
Beginn: 09.04.2023
Tage bis Beginn: 153,0
Dosis: 4
Route/Site: IM / RA

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

Dyspnoea Hypoxia Pulmonary embolism

Symptomtext

ACUTE PULMONARY EMBOLISM 4/9/2023 DYSPNEA HYPOXIA 4/9/2023 DYSPNEA

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

VAERS 2660547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

kritisch

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 25.07.2023
Impfdatum: 26.10.2022
Beginn: 21.07.2023
Tage bis Beginn: 268,0
Dosis: 5
Route/Site: SYR / -

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

Alanine aminotransferase normal Anaemia Anion gap Anticoagulant therapy Aortic stenosis Aspartate aminotransferase normal Atrial fibrillation Back pain Basophil count decreased Basophil percentage Bilirubin urine Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatine phosphokinase normal Blood creatinine normal

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on July 21, 2023 10:01 EDT Verified By: MD on July 23, 2023 07:28 EDT Encounter Info: Hospital, Inpatient, 07/21/23 - * Final Report * History of Present Illness/Subjective Patient is an 82-year-old woman who presents to the hospital with complaints of chest pain that started suddenly. She has a history of hypertension, hyperlipidemia, atrial fibrillation on anticoagulation. The chest pain happened while she was having an ice cream and it was sudden sharp radiated to the back and was unbearable which prompted her to come to the hospital. There were no associated symptoms At the moment she does have some uncomfortable feeling on the chest but no chest pain or pressure Her blood pressures were soft initially but have improved somewhat. She does meet severe sepsis criteria as per SIRS so was admitted to the ICU. Lab values are as significant for anemia of 10.5 she had normal hemoglobin in May this year. CKD. There is some elevation of troponin from 10-14. Lactic acid is 2.4 urine analysis is negative for infection Review of Systems 18 point review of system is negative except what is mentioned above Physical Exam/Objective Vitals & Measurements most recent past 24 hours BP: 105/72 HR: 89 (Monitored) RR: 27 SpO2: 96% Hemodynamics Neurologic Glasgow Coma Score: 15 Patient Weight Patient Height Current Height: 162.6 cm Constitutional: No acute distress, Eyes: PERRLA, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs CTAB Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: Varicose veins Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Severe sepsis R65.20 she was in Afib, LIKLEY confounding the Sirs CRITERIA A bit, Nevertheless sepsis can trigger afib as well. - protocol in place, broad spectrum antibiotics. pro cal , lactate 2. Chest pain R07.9 Last EF from May this year is 35. I will trend the troponins patient also has aortic stenosis which was seen by cardiology in May. The plan was to do a TEE as an outpatient. -I will repeat an echocardiogram this visit. - Lexi SCAN - i dont see a stress test in the system, - Cardiology consult 3. Pulmonary edema J81.1 - afib to be the inciting event, - lasix dose controlled by her blood pressures, they are soft, s/p lasix 40 IV. 4. Afib I48.91 - noted resume home meds and anticoagulation 5. Benign essential hypertension I10 - noted, HOLD MEDS FOR NOW, soft bp 6. Chronic kidney disease, stage 3 N18.30 - avoid nephrotoxic meds 7. Anemia D64.9 - will send anemia workup 8. Lactic acid acidosis E87.20 - repeat levels Orders: magnesium oxide, 400 mg, Orally, Tablet, Daily, 07/22/23 9:00:00 nitroGLYCerin, 0.4 mg, Sublingually, Tablet, Q5min, PRN, Chest Pain, 07/21/23 9:46:00 pantoprazole, 20 mg, Orally, Tab, Delayed Rel, Daily, 07/22/23 9:00:00 PARoxetine, 20 mg, Orally, Tablet, At Bedtime, 07/21/23 21:00:00 warfarin, See Instructions, Maintenance, Take 1 tablet (5mg) orally on Sun, Tues, THurs, Sat. Take 0.5 tablet (2.5mg) on Mon, Wed, Fri., 03/30/23 10:36:00 warfarin, 5 mg, Orally, Tablet, Every Tue Thur Sat Sun, 07/22/23 21:00:00 warfarin, 2.5 mg, Orally, Tablet, Every Mon Wed Fri, 07/21/23 21:00:00 Electrocardiogram NM Myo Perf Rest/Stress W/Lexiscan Pharmacy Dosing Consult Treadmill Only Troponin-I High Sensitivity Due to a high probability of clinically significant, life threatening deterioration, the patient required my highest level of preparedness to intervene emergently and I personally spent 50 minutes of critical care time directly and personally managing the patient. This critical care time included obtaining a history, examining the patient, pulse oximetry, ordering and reviewing the studies, arranging urgent treatment with development of a management plan, evaluation of the patient?s response to treatment, frequent reassessment, and discussions with other clinicians. The critical care time was performed to assess and manage the high probability of imminent, life-threatening deterioration that could result in multi-organ failure. It was exclusive of separately billable procedures and treating other patients and teaching time. Please see the MDM section and the rest of this note for further information on patient assessment and treatment. Code Status None Recorded Chronic Problem List Abdominal pain Abnormal loss of weight Aching Acquired hypogammaglobulinemia Acute respiratory failure Anticoagulated on warfarin Aortic stenosis Arthritis Benign essential hypertension CAD in native artery Cardiomyopathy Chronic atrial fibrillation Chronic diarrhea Chronic hypoxemic respiratory failure Chronic kidney disease, stage 3 Colon, diverticulosis Congestive heart failure Depression Dyspnea Elevated antinuclear antibody (ANA) level Elevated INR Elevated lipase Elevated rheumatoid factor Esophageal stricture Falls frequently Frequent UTI History of diverticulitis Hyperlipidemia Hypothyroidism, acquired Inflammatory arthritis Low magnesium level On warfarin therapy Periorbital swelling Pneumonia Preventive measure Pulmonary edema Recurrent falls Shortness of breath Skin lesions Sleep apnea Subcutaneous nodule of both hands Subtherapeutic anticoagulation Synovitis Thrombocytopenia Weakness Procedure/Surgical History ?Bowel Resection (03/01/2020) ?Colonoscopy (12/01/2018) ?Upper GI endoscopy (2018) ?TEE and cardioversoin (12/16/2016) ?Esophagogastroduodenoscopy (12/09/2016) ?Colonoscopy (06/16/2014) ?Cardiac Stents (01/01/2008) ?hysterectomy (1995) ?Tubal ligation (1972) ?tonsillectomy (1946) ?Ankle fracture ?cataract repair ?heart cath ?heart cath ?hysterectomy ?right bimal ORIF Surgical History Internal 03/19/2020 EGD Gastric Tube Place Chg/Removal MD 03/05/2020 Laparotomy Exploratory MD 12/08/2018 EGD Diagnostic MD 12/09/2016 EGD Diagnostic MD 04/08/2016 Ankle Fracture Open Reduction (Right) MD Medications Home Medications (21) Active cyanocobalamin 100 mCg oral tablet 100 mCg = 1 Tablet, Orally, QAM diltiaZEM 120 mg/24 hours oral tablet, extended release 120 mg = 1 Tablet, Daily folic acid 1 mg oral tablet , TAKE 1 TABLET BY MOUTH ONCE DAILY furosemide 40 mg oral tablet 40 mg = 1 Tablet, Orally, BID Macrobid 100 mg oral capsule 100 mg = 1 Capsule, Orally, BID magnesium oxide 400 mg oral tablet 400 mg = 1 Tablet, Orally, Daily methotrexate 2.5 mg oral tablet 2.5 mg = 1 Tablet, Orally, Daily metoPROLOL tartrate 50 mg oral tablet 25 mg = 0.5 Tablet, Orally, BID mirtazapine 15 mg oral tablet 15 mg = 1 Tablet, Orally, At Bedtime nalOXone 4 mg / 0.1 mL nasal spray , ADMINISTER A SINGLE SPRAY IN ONE NOSTRIL UPON SIGNS OF OPIOID OVERDOSE. CALL 911. REPEAT AFTER 2-3 MINUTES IF NO RESPONSE. Nitrostat 0.4 mg sublingual tablet 0.4 mg = 1 Tablet, PRN, Sublingually, Q5min omeprazole 20 mg oral delayed release capsule 20 mg = 1 Capsule, Orally, QAM ondansetron 4 mg oral tablet, disintegrating , DISSOLVE 1 TABLET IN MOUTH THREE TIMES DAILY AS NEEDED FOR NAUSEA OXYcodone-acetaminophen 5 mg-325 mg oral tablet 1 Tablet, TAKE 1 TABLET BY MOUTH EVERY 6 HOURS AS NEEDED FOR PAIN FOR 5 DAYS PARoxetine 20 mg oral tablet 20 mg = 1 Tablet, Orally, At Bedtime Potassium Chloride (Eqv-Klor-Con M20) 20 mEq oral tablet, extended release 20 mEq = 1 Tablet, Orally, Daily predniSONE 10 mg oral tablet 10 mg = 1 Tablet, Orally, QPM Vitamin C 500 mg oral tablet 500 mg = 1 Tablet, Orally, QAM Vitamin D3 1,000 intl units (25 mCg) oral capsule 1,000 Units = 1 Capsule, Orally, QAM vitamin E 400 intl units oral capsule 400 Units = 1 Capsule, Orally, QAM warfarin 5 mg oral tablet See Instructions, Take 1 tablet (5mg) orally on Sun, Tues, THurs, Sat. Take 0.5 tablet (2.5mg) on Mon, Wed, Fri. Active Scheduled Inpatient Medications magnesium oxide, Tablet, 400 mg, Orally, Daily, Start: 07/22/23 09:00:00 pantoprazole, Tab, Delayed Rel, 20 mg, Orally, Daily, Start: 07/22/23 09:00:00 PARoxetine, Tablet, 20 mg, Orally, At Bedtime, Start: 07/21/23 21:00:00 warfarin, Tablet, 5 mg, Orally, Every Tue Thur Sat Sun, Start: 07/22/23 21:00:00 warfarin, Tablet, 5 mg, Orally, Every Tue Thur Sat Sun, Start: 07/22/23 21:00:00 warfarin, Tablet, 2.5 mg, Orally, Every Mon Wed Fri, Start: 07/21/23 21:00:00 warfarin, Tablet, 2.5 mg, Orally, Every Mon Wed Fri, Start: 07/21/23 21:00:00 One-Time Medications Given 07/20/23 00:00:00 TO 07/21/23 10:01:08 None Reported PRN Medications (0600 - 0559) from 07/20 - 07/21 nitroGLYCerin, 0.4 mg, Sublingually, Q5min, 0 Dose(s) Allergies Contrast Dye (Rash) glycopyrrolate Red Dye (rash) ZyrTEC Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Retired Home/Environment daughter lives with pt Nutrition/Health Diet: Regular. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Cancer: Father. Diabetes mellitus: Father and Brother. Heart disease: Father. Heart disease..: Mother. High blood pressure..: Mother. Leukemia: Father. Myocardial infarction: Mother. Stroke...: Mother. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 10.4 k/cumm (07/21/23 01:46:00) RBC: 3.48 million/cumm Low (07/21/23 01:46:00) Hgb: 10.5 GM/dL Low (07/21/23 01:46:00) Hct: 32.3 % Low (07/21/23 01:46:00) MCV: 93 fL (07/21/23 01:46:00) MCH: 30.1 pg (07/21/23 01:46:00) MCHC: 32.4 GM/dL (07/21/23 01:46:00) RDW: 21.4 % High (07/21/23 01:46:00) Platelet: 253 k/cumm (07/21/23 01:46:00) MPV: 6.9 fL Low (07/21/23 01:46:00) Neutrophils %: 66 % (07/21/23 01:46:00) Lymphocytes %: 23 % (07/21/23 01:46:00) Monocytes %: 10 % (07/21/23 01:46:00) Eosinophils %: 0 % (07/21/23 01:46:00) Basophils %: 1 % (07/21/23 01:46:00) Absolute Neutrophil: 6.9 k/cumm (07/21/23 01:46:00) Absolute Lymphocyte: 2.4 k/cumm (07/21/23 01:46:00) Absolute Monocyte: 1 k/cumm (07/21/23 01:46:00) Absolute Eosinophil: 0 k/cumm (07/21/23 01:46:00) Absolute Basophil: 0.1 k/cumm (07/21/23 01:46:00) Chemistry: Sodium SerPl QN: 138 mmol/L (07/21/23 01:46:00) Potassium SerPl QN: 4.4 mmol/L (07/21/23 01:46:00) Chloride SerPl QN: 100 mmol/L (07/21/23 01:46:00) Carbon Dioxide SerPl QN: 27 mmol/L (07/21/23 01:46:00) Anion Gap: 11 mmol/L (07/21/23 01:46:00) BUN SerPl QN: 17 mg/dL (07/21/23 01:46:00) Creatinine SerPl QN: 1.04 mg/dL (07/21/23 01:46:00) Estimated GFR (CKD-EPI, no race): 54 mL/min/1.73m2 Low (07/21/23 01:46:00) Estimated CRCL (CG): 41 mL/min Low (07/21/23 01:46:00) Glucose SerPl QN: 140 mg/dL High (07/21/23 01:46:00) Calcium Total SerPl QN: 8.7 mg/dL (07/21/23 01:46:00) Alkaline Phos SerPl QN: 68 Units/L (07/21/23 01:46:00) ALT SerPl QN: 9 Units/L (07/21/23 01:46:00) AST SerPl QN: 14 Units/L (07/21/23 01:46:00) Bilirubin Total SerPl QN: 0.4 mg/dL (07/21/23 01:46:00) Total Protein SerPl QN: 7.2 GM/dL (07/21/23 01:46:00) Albumin SerPl QN: 3.8 GM/dL (07/21/23 01:46:00) Lipase SerPl QN: 43 Units/L (07/21/23 01:46:00) CK SerPl QN: 47 Units/L (07/21/23 01:46:00) Troponin-I High Sensitivity: 14 ng/L High (07/21/23 01:46:00) Lactate Venous Pl QN: 2.4 mmol/L High (07/21/23 04:15:00) Coagulation: PT: 18.8 seconds High (07/21/23 01:46:00) INR: 1.64 High (07/21/23 01:46:00) Urine Studies: Color: Yellow (07/21/23 02:35:00) Clarity: Clear (07/21/23 02:35:00) Specific Gravity: 1.020 (07/21/23 02:35:00) pH: 6.5 (07/21/23 02:35:00) Protein: NEGATIVE (07/21/23 02:35:00) Glucose: NEGATIVE (07/21/23 02:35:00) Ketones: NEGATIVE (07/21/23 02:35:00) Bilirubin: NEGATIVE (07/21/23 02:35:00) Hgb Ur: NEGATIVE (07/21/23 02:35:00) Nitrite: NEGATIVE (07/21/23 02:35:00) Urobilinogen: NormalUro (07/21/23 02:35:00) Leukocyte Esterase Ur: NEGATIVE (07/21/23 02:35:00) Micro - Last 7 days Urine CX: NEG (07/17/23 15:23:00) Diagnostics Radiology Results - Last 24 hours Across Visits 07/21/2023 02:14 - XR Chest PA or AP Portable IMPRESSION: 1. Possible small bilateral pleural effusion.2. Pulmonary vascular and interstitial prominence may indicateCHF/pulmonary edema in the correct clinical setting.Template Version: Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us at XRAY with any questions. Signature Line Electronically Signed on 07/23/23 07:28 EDT ________________________________________________________ MD

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

VAERS 2657658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 18.07.2023
Impfdatum: 11.10.2022
Beginn: 08.01.2023
Tage bis Beginn: 89,0
Dosis: 4
Route/Site: IM / RA

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

Chronic respiratory failure Cor pulmonale acute Pulmonary embolism Respiratory failure

Symptomtext

ACUTE COR PULMONALE ACUTE PULMONARY EMBOLISM CHRONIC HYPOXEMIC RESPIRATORY FAILURE

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

VAERS 2657650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 18.07.2023
Impfdatum: 11.10.2022
Beginn: 29.01.2023
Tage bis Beginn: 110,0
Dosis: 5
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

ACUTE NON ST ELEVATION MI

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

VAERS 2655036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 11.07.2023
Impfdatum: 31.10.2022
Beginn: 07.03.2023
Tage bis Beginn: 127,0
Dosis: 5
Route/Site: IM / LA

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

Pulmonary embolism

Symptomtext

ACUTE PULMONARY EMBOLISM

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

VAERS 2652063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 48,0
Geschlecht: M
Eingang: 03.07.2023
Impfdatum: 02.12.2022
Beginn: 16.01.2023
Tage bis Beginn: 45,0
Dosis: 4
Route/Site: IM / LA

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

Acute myocardial infarction Symptom recurrence

Symptomtext

ACUTE NON ST ELEVATION MI 1/15/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2650973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 29.06.2023
Impfdatum: 27.12.2022
Beginn: 03.02.2023
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / LA

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

Cerebral artery occlusion Cerebrovascular accident

Symptomtext

ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2649391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 26.06.2023
Impfdatum: 13.10.2022
Beginn: 31.12.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI ACUTE RESPIRATORY FAILURE 12/17/2022 & 2/19/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2648821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 09.10.2022
Beginn: 15.11.2022
Tage bis Beginn: 37,0
Dosis: 4
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE ST ELEVATION MI, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2645971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

kritisch

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 15.06.2023
Impfdatum: 14.12.2021
Beginn: 03.03.2022
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Diabetic retinopathy End stage renal disease Glomerular filtration rate Nephrogenic anaemia Type 2 diabetes mellitus

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/5/2023 DM 2 W BILAT MODERATE NONPROLIFERATIVE RETINOPATHY ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/5/2023 CKD STAGE 5 (GFR <15) ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/5/2023 ANEMIA DUE TO CKD

Weitere VAERSDATA-Felder

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

VAERS 2645814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 15.06.2023
Impfdatum: 21.12.2022
Beginn: 10.04.2023
Tage bis Beginn: 110,0
Dosis: 5
Route/Site: IM / LA

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

Deep vein thrombosis Hypertension Pulmonary embolism

Symptomtext

ACUTE PULMONARY EMBOLISM 4/10/2023 HTN (HYPERTENSION) ACUTE DVT OF BILAT LEGS, UNSPECIFIED VEINS 4/10/2023 HTN (HYPERTENSION)

Weitere VAERSDATA-Felder

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

VAERS 2644615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

kritisch

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 13.06.2023
Impfdatum: 06.12.2022
Beginn: 25.03.2023
Tage bis Beginn: 109,0
Dosis: 5
Route/Site: IM / LA

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

Acute respiratory failure Chronic respiratory failure Respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/25/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE HYPERCAPNIC RESPIRATORY FAILURE 3/25/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 3/25/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/4/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPERCAPNIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 3/30/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/25/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE HYPERCAPNIC RESPIRATORY FAILURE 3/25/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 3/25/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/4/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPERCAPNIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 3/30/2023 CHRONIC HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2629918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: KY
Alter: 95,0
Geschlecht: F
Eingang: 10.05.2023
Impfdatum: 25.10.2022
Beginn: 23.02.2023
Tage bis Beginn: 121,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

Tested positive for COVID on 2/23/23 when hospitalized for a fall. She died in the hospital on 3-5-23

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: Tested positive for COVID on 2/23/23.
Aktuelle Erkrankungen: unknown
Vorgeschichte: atrial fibrillation
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2617681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: MN
Alter: 70,0
Geschlecht: M
Eingang: 19.04.2023
Impfdatum: 17.10.2022
Beginn: 04.03.2023
Tage bis Beginn: 138,0
Dosis: 4
Route/Site: SYR / LA

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

Blood pressure abnormal Cerebral haemorrhage Cerebrovascular accident Computerised tomogram head abnormal Eye haemorrhage Impaired driving ability Magnetic resonance imaging head abnormal Therapy change

Symptomtext

On March 4, 2023, I had a stroke. I went to an urgent care first. They sent me to the emergency room. They did some tests and confirmed a blood bleed in my right rear brain. It's mostly affecting my left eye. I was in the hospital for about 12 days. After that, I went to a rehab center for five days. Since being released from the rehab center, I've been going to outpatient therapy. I was told I can't drive. They adjusted my medications. My blood pressure is under better control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 12,0
Labordaten: 03/04/2023 Multiple CT Scans - Showed Bleed in Right Rear Brain; 03/07/2023 MRI - Confirmed Stroke
Aktuelle Erkrankungen: Stomach Bleed
Vorgeschichte: Hypertension; High Cholesterol
Andere Medikamente: Lisinopril; Atorvastatin; Metoprolol; Symbicort
Allergien: None
Vorherige Impfungen: -

VAERS 2613246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 28.10.2022
Beginn: 27.03.2023
Tage bis Beginn: 150,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Blood culture negative Blood lactic acid COVID-19 Cardiac failure Cardiac failure acute Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Cough Diet noncompliance Dyspnoea Echocardiogram normal Ejection fraction normal Glycosylated haemoglobin increased Hyperglycaemia Leukocytosis

Symptomtext

Patient is a 73 y.o. male patient of MD with history of CHF, chronic respiratory failure (3 L/min at baseline), COPD, DM 2, HTN, prostate cancer, paroxysmal A-fib, presented to Medical Center with shortness of breath found to have acute on chronic respiratory failure secondary to to COVID-19, COPD exacerbation and multifocal pneumonia Acute on chronic respiratory failure with hypoxia and hypercapnia Secondary to COVID, COPD exacerbation, PNA and pulmonary edema On 3L O2 NC at baseline, requiring BIPAP on admission Weaned to home 3L O2 NC BIPAP at bedtime Pulm following Sepsis due to PNA, POA Multifocal Pneumonia Secondary to COVID-19 and Multifocal Pneumonia Afebrile, leukocytosis to 14.04k, lactate 2.0 CTPA (2/27) shows multifocal opacities L>R, pulmonary edema versus multifocal pneumonia Urine antigens pending Blood cx NGTD Continue Rocephin/Azithro, transitioned to Levaquin to complete 7 day course Covid-19 Virus Infection Date of onset of symptoms: 1 week ago Symptoms present on admission: Cough, sputum production, shortness of breath Date of covid positive test: 2/27 Vaccination status: vaccinated Imaging: CT imaging shows multifocal opacities L>R, pulmonary edema versus multifocal pneumonia Oxygen requirements on admission: BiPAP Current oxygen requirements: 3L O2 NC (home requirement) Medical therapy: remdesivir, steroids, rocephin, and zithromax (changed to levaquin at discharge) Consultants following: Pulm Anticipated special isolation end date: 3/5 COPD exacerbation Secondary to COVID-19, multifocal PNA Requiring BIPAP on admission, now weaned to home 3L O2 NC S/P Decadron, transitioned to prednisone with taper at discharge Continue Symbicort and Duonebs Acute on chronic HFrEF exacerbation Medical noncompliance Likely due to dietary non compliance Echo (2019) with EF 40-45% CT with findings of pulmonary edema Repeat echo (2/28) with EF 57% S/P IV lasix, transitioned to po lasix 40mg BID Continue home coreg, losartan, aldactone Paroxysmal Atrial fibrillation Continue home Eliquis, carvedilol, sotalol Rate controlled DM2 with hyperglycemia A1C 8.6 Held home Glipizide Decreased home Lantus SSI Hyperlipidemia Continue home lipitor

Weitere VAERSDATA-Felder

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

VAERS 2607444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 27.10.2022
Beginn: 06.03.2023
Tage bis Beginn: 130,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Asthenia Bradycardia COVID-19 COVID-19 pneumonia Cardiac failure acute Cardiac telemetry Condition aggravated Constipation Dyspnoea Echocardiogram Ejection fraction Left ventricular failure Lung disorder N-terminal prohormone brain natriuretic peptide increased Prosthetic cardiac valve regurgitation SARS-CoV-2 test positive

Symptomtext

Patient is a 83 y.o. male with a history of HTN, CAD, hyperlipidemia, aortic stenosis, HFpEF who presented to a HCF 3/6/2023 with worsening shortness of breath and found to have covid with CTPA c/w covid with possible edema. NTBNP 1.8K up from 574 in 2020. Cardiology followed. Patient required oxygen and completed remdesivir and steroid ,when weaned off of oxygen and vitals were stable , ambulating without oxygen , was discharged home. 1. Acute hypoxic respiratory failure: In setting of covid. Continued on remdesivir and steroids. Last dose of remdesivir will be 3/11/2023. Weaned to room air on 3/10/2023. Continued supportive treatment, and spirometry. 2. Acute on chronic diastolic heart failure: No edmea but increase in bnp with some lung findings on CTPA. Dry lung strategy with covid. Repeat echo with EF of 50 to 55% with mild to moderate paravalvular aortic regurgitation without stenosis. IV lasix has been switched to p.o Lasix.. Cardiology followed. Not volume overloaded 3. COVID19 Pneumonia: Symptoms for 1 day. Positive 3/6/23, isolation through 3/17/23. Required oxygen on admission. Started on remdesivir and steroids , continued. Supportive treatment. 4. Bradycardia: Patient heart rate was in 40s on 3/9/2023. Heart rate between 50-60 after reduction of atenolol dose from 100 mg to 25 mg/day, will be continued as patient blood pressure is a stable and have clinically no symptoms at all. Per patient his baseline heart rate is in 50s. Telemetry and electrolyte. Was discharged on low dose of atenolol, and was instructed to follow PCP as an outpatient. 5. Constipation: Patient with no bowel movement for last 3 to 4 days. KUB on 3/11/23 with no obstruction. Had BM . Resolved. 6. Generalized weakness: Likely in setting of above. PT/OT followed. 7. CAD: DES to LAD 1994. No current chest pain, trop normal. 8. Aortic stenosis: S/p TAVR 11/2018. Repeat echo as above. 9. HTN: Home mds. Continued home medications. Cardiology following. 10. Hyperlipidemia: Statin continued. 11. HFpEF: Echo 2020 with ef 50% functional TAVR with mild regurg grade 1 diastolic dysfunction, unchanged from previous.

Weitere VAERSDATA-Felder

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

VAERS 2603383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 24.03.2023
Impfdatum: 26.10.2022
Beginn: 07.03.2023
Tage bis Beginn: 132,0
Dosis: 5
Route/Site: - / -

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

Acute respiratory failure Atelectasis Bradycardia Bronchial secretion retention COVID-19 Chest X-ray abnormal Computerised tomogram thorax abnormal Cough Decreased appetite Dyspnoea Haemoglobin decreased Lung consolidation Oropharyngeal pain Pneumonitis Procalcitonin normal SARS-CoV-2 test positive

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 3/7/2023 Discharge Date: Mar 10, 2023 PRESENTING PROBLEM: Hypoxia [R09.02] Acute respiratory failure with hypoxia COVID-19 HOSPITAL COURSE: Patient is a 73 y.o. male with a past medical history of essential tremor, chronic back pain with implanted morphine pump, non insulin-dependent type 2 diabetes and depression who presents today with cough, dyspnea and anorexia. Symptoms started on 02/27. The patient states that it started with a sore throat and cough. In the ER the patient was noted to be hypoxic on room air with an SpO2 of 87%. He remained hypoxic on nasal cannula and required non-rebreather with 15 L of oxygen. He did receive an albuterol inhaler and 6 mg of Decadron. He was able to be weaned down to 6 L by nasal cannula. His other vital signs were unremarkable. Labs significant for hemoglobin 12.7. Procalcitonin was negative. Viral PCR positive for COVID-19. Chest x-ray with new mild left basilar atelectasis or pneumonitis. CTA thorax showed mucous plugging w consolidation. Pt was started on remdsivir and decadron. 02 req improved and after 48 hrs was on 3L. On the 3rd day he was able to be weaned off 02. Labs and VS stable throughout stay. Did become bradycardic in the 30's, believe it was due to remdesivir and this was discontinued. Stable for discharge on 3/10. Discharged with decadron to finish 10 day course.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Non-toxic multinodular goiter Hashimoto's disease End of battery life of intrathecal infusion pump Chronic pain Diabetes mellitus Tobacco dependence Disabling essential tremor Depression COVID-19
Andere Medikamente: Calcium Carb-Cholecalciferol 600-200 MG-UNIT TABS Cholecalciferol 1000 units CAPS clonazepam (KLONOPIN) 1 MG tablet docusate (COLACE) 100 MG capsule EPINEPHrine (EPIPEN) 0.3 MG/0.3ML escitalopram (LEXAPRO) 20 MG tablet metFORMIN (GLUCOPHAGE
Allergien: Shellfish AllergyHives LatexItching Topamax [Topiramate]Hives TrazodoneHives
Vorherige Impfungen: -

VAERS 2574709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: WA
Alter: 39,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 19.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Anticoagulant therapy Cerebral venous sinus thrombosis Computerised tomogram head abnormal Headache Lung assist device therapy Magnetic resonance imaging head abnormal Neck pain Pulmonary embolism Thrombectomy

Symptomtext

2-3 days after shot developed progressive headache and neck pain. progressive and had imaging almost a month later. Dural venous sinus thrombosis. treated with anticoagulation. Despite anticoagulation, 6 weeks later had submassive PE that had an acute and chronic component. unresponsive to thrombolytics and thrombectomy attempt. Required. Still hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 10,0
Labordaten: MRI brain and CT showing venous sinus thrombosis. 11/17.
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2548828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 20.01.2023
Impfdatum: 28.10.2022
Beginn: 16.01.2023
Tage bis Beginn: 80,0
Dosis: 4
Route/Site: IM / -

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

Acute respiratory failure Agitation Aspiration Behaviour disorder Blood culture negative Asthenia COVID-19 Condition aggravated Cough Drug hypersensitivity Chest X-ray normal Confusional state Dementia Gastrointestinal tube insertion Hypervolaemia Hypoxia Lethargy Malnutrition

Symptomtext

Prior VAERS submitted #929214 COVID+ 1/16/23. Vaccination Status- pfizer x3 + Pfizer BIVALENT x1 Expand All Collapse All BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: DO Admission Date: 1/16/2023 Discharge Date: Jan 19, 2023 Active Hospital Problems Diagnosis Date Noted POA ? Unspecified severe protein-calorie malnutrition 01/17/2023 Unknown ? Community acquired pneumonia, unspecified laterality DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Community acquired pneumonia, unspecified laterality [J18.9] Sepsis with acute organ dysfunction without septic shock, due to unspecified organism, unspecified type [A41.9, R65.20] COVID-19 [U07.1] HOSPITAL COURSE: 85yom pmhx LBD with Parkinsonism, dysphagia s/p G tube placement, prostate cancer on oral chemotherapy who was admitted for management of sepsis secondary to community acquired pneumonia. Reportedly started on Robinul several days prior to presentation and noted to have become increasingly lethargic and weak, with inability to clear secretions. Notably Covid19+ but suspected viral shedding from previous infection one month prior. He was treated with ceftriaxone and azithromycin and symptoms did improve over time. He was mildly hypoxic on presentation, corrected with 2L NC, and tachycardic 140-150s sinus corrected with sepsis bolus. Through his course his oxygen requirements improved but continued to have difficulty mobilizing thick secretions. Also developed mild fluid overload from resuscitation. Improved significantly with several doses of IV lasix. By day 4 he was off oxygen and mentation, activity, and sputum output had improved significantly. Wife was looking into hospice facilities prior to admission. She, along with her son, met with social work and hospice to discuss options for home hospice. Home hospice was set up and patient was discharged 1/19/23 in stable condition, with completion of 5 day course of antibiotics, transitioned from ceftriaxone and azithro IV to oral Augmentin for 1 additional day. Robinul discontinued and listed as allergy given severe AMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Stage 3a chronic kidney disease Lewy body dementia without behavioral disturbance Prostate cancer Other dysphagia Moderate episode of recurrent major depressive disorder Primary osteoarthritis involving multiple joints Dementia with behavioral disturbance Advance care planning Multiple comorbid conditions Other constipation
Andere Medikamente: Aspirin 81 mg Oral Daily Donepezil HCl 10 mg Oral Nightly Pimavanserin Tartrate 34 MG 1 tablet Oral Daily QUEtiapine Fumarate 25 mg Oral Nightly Simvastatin 40 mg Oral Nightly
Allergien: GlycopyrrolateDiarrhea
Vorherige Impfungen: -

VAERS 2548828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 20.01.2023
Impfdatum: 28.10.2022
Beginn: 16.01.2023
Tage bis Beginn: 80,0
Dosis: 4
Route/Site: IM / UN

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

Acute respiratory failure Agitation Aspiration Behaviour disorder Blood culture negative Asthenia COVID-19 Condition aggravated Cough Drug hypersensitivity Chest X-ray normal Confusional state Dementia Gastrointestinal tube insertion Hypervolaemia Hypoxia Lethargy Malnutrition

Symptomtext

Prior VAERS submitted #929214 COVID+ 1/16/23. Vaccination Status- pfizer x3 + Pfizer BIVALENT x1 Expand All Collapse All BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: DO Admission Date: 1/16/2023 Discharge Date: Jan 19, 2023 Active Hospital Problems Diagnosis Date Noted POA ? Unspecified severe protein-calorie malnutrition 01/17/2023 Unknown ? Community acquired pneumonia, unspecified laterality DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Community acquired pneumonia, unspecified laterality [J18.9] Sepsis with acute organ dysfunction without septic shock, due to unspecified organism, unspecified type [A41.9, R65.20] COVID-19 [U07.1] HOSPITAL COURSE: 85yom pmhx LBD with Parkinsonism, dysphagia s/p G tube placement, prostate cancer on oral chemotherapy who was admitted for management of sepsis secondary to community acquired pneumonia. Reportedly started on Robinul several days prior to presentation and noted to have become increasingly lethargic and weak, with inability to clear secretions. Notably Covid19+ but suspected viral shedding from previous infection one month prior. He was treated with ceftriaxone and azithromycin and symptoms did improve over time. He was mildly hypoxic on presentation, corrected with 2L NC, and tachycardic 140-150s sinus corrected with sepsis bolus. Through his course his oxygen requirements improved but continued to have difficulty mobilizing thick secretions. Also developed mild fluid overload from resuscitation. Improved significantly with several doses of IV lasix. By day 4 he was off oxygen and mentation, activity, and sputum output had improved significantly. Wife was looking into hospice facilities prior to admission. She, along with her son, met with social work and hospice to discuss options for home hospice. Home hospice was set up and patient was discharged 1/19/23 in stable condition, with completion of 5 day course of antibiotics, transitioned from ceftriaxone and azithro IV to oral Augmentin for 1 additional day. Robinul discontinued and listed as allergy given severe AMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Stage 3a chronic kidney disease Lewy body dementia without behavioral disturbance Prostate cancer Other dysphagia Moderate episode of recurrent major depressive disorder Primary osteoarthritis involving multiple joints Dementia with behavioral disturbance Advance care planning Multiple comorbid conditions Other constipation
Andere Medikamente: Aspirin 81 mg Oral Daily Donepezil HCl 10 mg Oral Nightly Pimavanserin Tartrate 34 MG 1 tablet Oral Daily QUEtiapine Fumarate 25 mg Oral Nightly Simvastatin 40 mg Oral Nightly
Allergien: GlycopyrrolateDiarrhea
Vorherige Impfungen: -

VAERS 2560889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: TN
Alter: 72,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 19.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 43,0
Dosis: 4
Route/Site: IM / RA

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

Blood culture positive Cardiac arrest Catheter placement Chest X-ray abnormal Dysphagia Endotracheal intubation Hypotension Lung infiltration Pleural effusion Septic shock Staphylococcus test positive Tracheostomy Ultrasound kidney normal

Symptomtext

12/5 admission 12/6 picc removed midline placed 12/9 FEES mild oropharyngeal dysphagia- cleared for puree 12/10 Cardiac arrest, intubation, septic shock 12/10 CXR bilateral infiltrates small effusions 12/11 +BCX MRSE 1of2 probable contaminant 12/14 Renal US - no hydronephrosis 12/20 BCX + MRSE 1 of 2 12/22 B CX no growth to date 12/22 Tracheostomy 1/4 Recurrent hypotension, possible sepsis, resumed pressors, goals of care DNR 1/4 CXR worsened right pleural effusion 1/8 proceed with comfort care

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Acute hypoxemic respiratory failure COVID-19 pneumonia recovered Atrial fibrillation with RVR Hypercalcemia Possible multiple myeloma
Vorgeschichte: CHF ejection fraction 40% grade 1 diastolic dysfunction Hypertension Type 2 diabetes Chronic kidney disease GERD
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2506756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

kritisch

Staat: NJ
Alter: 61,0
Geschlecht: M
Eingang: 13.11.2022
Impfdatum: 08.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Pulmonary embolism

Symptomtext

unprovoked pulmonary embolism on 11/10/22

Weitere VAERSDATA-Felder

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

VAERS 2473539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

kritisch

Staat: MD
Alter: 80,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Asthenia Death Hyperhidrosis Pallor Pulse absent Respiratory arrest Retching

Symptomtext

Received vaccine at approx. 11am on 10-7-2022 at 9:45pm on 10-7-2022, resident was diaphoretic, B/P 118/84, HR 125, PSOX 98%, at 10:10pm, feeling better, at 10:45pm BP 90/50 diaphoretic , weak and pale, 911 was called, 11:29pm 911 arrived, talked to resident he was able to stand to transfer to stretcher and then became weak, dry heaves, and he stopped breathing, resident was a DNR, so breathing was assisted until pulse stopped, pronounced deceased by 911 at 11:45pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none ordered-reviewed by medical director
Aktuelle Erkrankungen: diarrhea 9/29/22, 10/2/22-covid negative increased edema 10/5/22
Vorgeschichte: venous insufficiency, COPD, a-fib, hyperlipidemia, hypothyroidism, anemia, vit D def, pulmonary hypertension, Morbid obesity, depression, edema, BPH
Andere Medikamente: metolazone 5mg, metoprolol 50mg, tylenol 325, Vit D, Lasix, anoro Ellipta, escitalopram, Tamsulosin, ProAir, Eliquis, Synthroid, digoxin,
Allergien: Phenergan, tetanus toxoids
Vorherige Impfungen: -

VAERS 2657694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 18.07.2023
Impfdatum: 11.10.2022
Beginn: 20.02.2023
Tage bis Beginn: 132,0
Dosis: 5
Route/Site: IM / LA

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

Embolic stroke Lacunar stroke

Symptomtext

ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2649966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

schwer

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 27.06.2023
Impfdatum: 24.10.2022
Beginn: 30.03.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: IM / LA

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

Deep vein thrombosis Hypersensitivity Hypertension

Symptomtext

I82.4Z1 ACUTE DVT OF RIGHT CALF, UNSPECIFIED VEIN 3/30/2023 HTN (HYPERTENSION) T78.40XA ALLERGIC REACTION, INIT 4/17/2023 HTN (HYPERTENSION)

Weitere VAERSDATA-Felder

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

VAERS 2648893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: OH
Alter: 64,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 13.12.2022
Beginn: 13.01.2023
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / AR

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

Computerised tomogram abdomen Computerised tomogram thorax Echocardiogram Fatigue Heart rate increased COVID-19 Cardiac tamponade Cardioversion Chest pain Chills Hypotension Intensive care Magnetic resonance imaging Pericardial drainage Pericarditis SARS-CoV-2 test positive

Symptomtext

On 1/13/2023, I experienced fatigue, a heartrate of 150, a BP of about 70/40, midsternal chest pains, and chills. I went to the emergency room and was admitted to the hospital. While I was at the ER, I underwent CT scans of my chest and abdomen, an echocardiogram, and cardioversion. I tested positive for COVID-19 and was diagnosed with pericarditis. I was given metoprolol intravenously twice. I was given a calcium channel blocker, after which I bottomed out and had to be given epinephrine. I was given about three liters of saline solution intravenously. I stayed in the hospital for 24 hours and was released on 1/14/2023. I was prescribed aspirin (650 mg). which I was to take three times a day, and colchicine (0.6 mg) to take twice a day. On 1/22/2023, I was admitted again to the hospital with rapid heartrate and low blood pressure. I was given metoprolol intravenously and was admitted to the ICU. I underwent a pericardiocentesis. I was in the ICU for three days. I underwent several echocardiograms while I was in the hospital. I was diagnosed with pericarditis with tamponade. I was given colchicine, prednisone, digoxin, PROTONIX, ANAKINRA, and metoprolol while I was in the hospital. I was taken off the aspirin I had previously been prescribed and was then instructed to take ibuprofen (800 mg) three times a day. After I was discharged on 1/27/2023, I was prescribed all the aforementioned medications, except the digoxin, to take daily. As my conditioned improved after my release, I was gradually weaned off of prednisone, ibuprofen, PROTONIX, and ANAKINRA. On 5/17/2023, I had chills. I went to the ER and was admitted to the hospital for 24 hours. I underwent one echocardiogram, plus an MRI on 5/18/2023. I was diagnosed with recurring pericarditis. I was then started back on the prednisone, ibuprofen, PROTONIX, and ANAKINRA. At the time of this writing, I am doing okay. I am currently taking metoprolol (25 mg) once a day, colchicine (0.6 mg) twice a day, ibuprofen (800 mg) three times a day, and rilonacept (220 mg) once a week. I am off the prednisone, the PROTONIX, and the ANAKINRA. I still have pericarditis, though I am now asymptomatic. I was told it would be at least six months before it resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Facioscapulohumeral Muscular Dystrophy
Andere Medikamente: Fluticasone nasal spray
Allergien: Walnuts
Vorherige Impfungen: -

VAERS 2641650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

schwer

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 06.06.2023
Impfdatum: 13.10.2022
Beginn: 11.04.2023
Tage bis Beginn: 180,0
Dosis: 5
Route/Site: IM / RA

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

Hypoglycaemia Hypovolaemic shock

Symptomtext

HYPOVOLEMIC SHOCK 4/11/2023 HYPOGLYCEMIA

Weitere VAERSDATA-Felder

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

VAERS 2599022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

schwer

Staat: NM
Alter: 66,0
Geschlecht: M
Eingang: 18.03.2023
Impfdatum: 17.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / -

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

Thrombosis

Symptomtext

Developed blood clot in our lower calves; his started in his calf worked with ways up the leg and his was worse, his actually went to his lungs; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 67-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 at 04:30 as dose 4 (booster), single (Lot number: GH9697) at the age of 66 years intramuscular for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose: 1, 1st Pfizer COVID Vaccine LOT# and Expiration date: The very 1st one was PAA165969, Time for the 1st vaccine: It was around 11 in the morning, they were in the morning, Route of administration for the 1st vaccine: Reporter stated, "They were all intramuscular, all 4), administration date: 01Apr2021, when the patient was 65-year-old, for COVID-19 Immunization; BNT162b2 (Dose: 2, 11:45 in the morning, Route of administration for the 1st vaccine: Reporter stated, "They were all intramuscular, all 4), administration date: 22Apr2021, when the patient was 65-year-old, for COVID-19 Immunization; BNT162b2 (Dose: 3 (1st booster), Route of administration for the 1st vaccine: Reporter stated, "They were all intramuscular, all 4, LOT# for the 3rd dose: Reporter stated, "Its EW0150), administration date: 22Nov2021, when the patient was 65-year-old, for COVID-19 Immunization. The following information was reported: THROMBOSIS (hospitalization, medically significant), outcome "unknown", described as "Developed blood clot in our lower calves; his started in his calf worked with ways up the leg and his was worse, his actually went to his lungs". Therapeutic measures were taken as a result of thrombosis (Heparin for two days in the ICU at the local hospital and Eliquis).

Weitere VAERSDATA-Felder

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

VAERS 2599011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

schwer

Staat: NM
Alter: 69,0
Geschlecht: F
Eingang: 18.03.2023
Impfdatum: 17.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / LA

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

Thrombosis

Symptomtext

Developed blood clot in lower calves; It was in deep inside lower left calf; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 as dose 4 (booster), single (Lot number: GH9697) at the age of 69 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Patient route of administration: Intramuscular, Anatomical location: Left arm, lot number: PAA165969), administration date: 01Apr2021, when the patient was 68-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE, Patient route of administration: Intramuscular, Anatomical location: Left arm, 11:45), administration date: 22Apr2021, when the patient was 68-year-old, for COVID-19 immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Patient route of administration: Intramuscular, Anatomical location: Left arm, lot number: EW0150), administration date: 22Nov2021, when the patient was 68-year-old, for COVID-19 immunization. The following information was reported: THROMBOSIS (medically significant), outcome "unknown", described as "Developed blood clot in lower calves; It was in deep inside lower left calf". Therapeutic measures were taken as a result of thrombosis. Clinical course: The patient reported that she does not know if this was coincidence or what, had developed blood clot in lower calves. The patient stated she was very-very active, she just bike, runs, and walks. She was just very shocked to see that she had developed blood clot. So, she was on Eliquis, which is the extremely expensive drug. The patient have been on Eliquis about 3 weeks. So, she just started was very unusual that, she got blood clot. She had never have this in her life. So, she just wanted to call and report it and see if any one else has been calling in and to say that they have developed any kind of blood clot. Patient reported they did not put the time down for the vaccines but it was for dose 1 and dose 3 around 16, 16:30 in the afternoon.

Weitere VAERSDATA-Felder

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

VAERS 2563305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: NC
Alter: 73,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 05.10.2022
Beginn: 12.11.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: SYR / -

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

Ischaemic stroke

Symptomtext

Ischemic Stroke

Weitere VAERSDATA-Felder

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

VAERS 2560172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 14.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 18,0
Dosis: 5
Route/Site: IM / LA

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

Anticoagulant therapy Blood test Coagulation factor VIII level increased Condition aggravated Deep vein thrombosis Protein S increased Ultrasound Doppler abnormal

Symptomtext

11-1-22 symptoms initially noted in left calf suspicious for DVT. 11-4-22 visit to primary care provider due to no improvement and continued suspicion of DVT. Same day referral for ultrasound diagnosed 2 clots in lower left leg. Immediately went to ER for consultation and was started on Eliquis 10mg 2xday for 1 week with reduction to 5 mg 2xday after the first week and discharged with instructions to follow up with primary care doctor and referral to cardiovascular specialist and to discontinue birth control pills. Cardiovascular specialist indicates need for lifelong blood thinner medication due to hx of previous DVT 22 years ago.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: 11-4-22 ultrasound - outpatient 11-4-22 blood work through ER 12-8-22 blood work through lab - elevated factor VIII and protein S - recheck in 2 months
Aktuelle Erkrankungen: None
Vorgeschichte: Left leg DVT resolved since 2000 due to major accident trauma/repaired patella fracture.
Andere Medikamente: Norethindrone Acetate and Ethinyl Estradiol Tablets and Ferrous Fumarate Tablets, 1mg/20 mcg Pantoprozole Sodium EC 40 mg Cetirizine Hydrochloride Fluticasone Propionate 50mg
Allergien: Ampicillin Trihydrate
Vorherige Impfungen: -

VAERS 2549623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

schwer

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 15.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: OT / LA

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

Chest pain Condition aggravated Dyspnoea Echocardiogram Interchange of vaccine products Myocarditis Somnolence Ventricular extrasystoles

Symptomtext

Interchange of vaccine products; Shortness of breath; Myocarditis/feeling was worse than what she normally has.; Myocarditis/feeling was worse than what she normally has.; chest pain; sleepiness; bunch of PVCs in a row; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 78-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Dec2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 78 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: moderna coviD-19 vaccine (dose 1, Lot Number: 206L20A), administration date: 15Jan2021, when the patient was 76-year-old, for COVID-19 immunization; moderna coviD-19 vaccine (dose 2, Lot Number: 015M20A. Myocarditis on apr2021), administration date: 12Feb2021, when the patient was 76-year-old, for COVID-19 immunization, reaction(s): "Myocarditis", "Shortness of breath"; moderna coviD-19 vaccine (dose 3, Lot Number: 034F21A), administration date: 11Nov2021, when the patient was 77-year-old, for COVID-19 immunization; BNT162b2 (dose 4 (booster); Lot Number: FJ4991), administration date: 23Jun2022, when the patient was 77-year-old, for COVID-19 immunization; Flu shot, for Immunization. The following information was reported: MYOCARDITIS (medically significant, life threatening), CONDITION AGGRAVATED (life threatening) all with onset 18Dec2022, outcome "unknown" and all described as "Myocarditis/feeling was worse than what she normally has."; VENTRICULAR EXTRASYSTOLES (non-serious) with onset 18Dec2022, outcome "unknown", described as "bunch of PVCs in a row"; CHEST PAIN (life threatening) with onset 18Dec2022, outcome "recovered" (2022); SOMNOLENCE (life threatening) with onset 18Dec2022, outcome "recovered" (2022), described as "sleepiness"; INTERCHANGE OF VACCINE PRODUCTS (medically significant, life threatening), outcome "unknown"; DYSPNOEA (non-serious), outcome "unknown", described as "Shortness of breath". The patient underwent the following laboratory tests and procedures: Echocardiogram: Unknown Results, notes: they will do an echo then. Clinical information: She stated she "had myocarditis from a previous Covid vaccine" 1st three vaccines she received were Moderna and the last 2 were Pfizer booster doses, last was on 15Dec2022. She stated that she didn't feel well for a bit but went on home. She was sitting down and reading the information that they had given her and realized that she had myocarditis in April, which would have been after her Mar dose of a Covid booster. She stated that she doesn't have exact dates for this Myocarditis. She stated that it was approximately in the middle of Apr2021. She stated that she had terrible shortness of breath when she had Myocarditis in Apr2021. When prompted for specific seriousness criteria related to these events the caller replies with yes after the call handler asks life-threatening, then stated no she was not hospitalized. Stated that she didn't put it together, the myocarditis and the vaccine, until after she read the paper. She denies any other medications, medical conditions, labs, testing, or treatments relevant to these events. She stated that she will go for a checkup related to her myocarditis in Mar and they will do an echo then. She got this most recent booster on the 15th. She stated sometimes she still feels the myocarditis, she will get a pain in her heart and gets sleepy. She stated that after this most recent booster, on about 18Dec2022, this feeling was worse than what she normally has. She stated that it felt like she had a bunch of PVCs in a row, she got sleepy like she was when she had myocarditis. She stated that when she left the room after the vaccine, she started to feel funny. They told her to wait 10-15 minutes. She stated she got myocarditis form the Moderna vaccines and had chest pain, sleepiness and shortness of breath with the most current Pfizer booster dose. She got the shot on 15Dec2022 and has never had any side effects from previous Flu shots or her 5 previous Covid shots. She stated that chest pain, sleepiness began for her on 18Dec2022. She doesn't know how long it lasted, a few days. She stated that she cannot say that it was completely gone, but it wasn't like it was the first time. She stated that the symptoms from the myocarditis in Apr2021 have never gone away completely for her. She stated that her symptoms that began on 18Dec2022 probably lasted about a week. She was so sleepy for at least 2 weeks she could not do much. Serious: No.; Sender's Comments: Based on limited information in the case, a possible causal association between all the reported events and the suspect drug cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Name: echo; Result Unstructured Data: Test Result:Unknown Results; Comments: they will do an echo then
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2541482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

schwer

Staat: WA
Alter: -
Geschlecht: M
Eingang: 31.12.2022
Impfdatum: 25.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Aortic disorder Condition aggravated Pericarditis Pruritus Drug ineffective Suspected COVID-19

Symptomtext

Probably had pericarditis; Horrendous itching; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from License Party. Other Case identifier(s): US-MYLANLABS-2022M1147717. This Serious Spontaneous report was received from business partner, PFIZER, (Ref No. 202201389362) originated on 19-Dec-2022 and received by Viatris on 21-Dec-2022. This initial case, received from consumer, non health professional, involved a 78-years-old male patient who reportedly experienced pericarditis and pruritus while receiving gabapentin capsules, USP (gabapentin). Medical history, current conditions and concomitant medications were not reported. Non-company suspect medication included COVID-19 vaccine. Unknown Date: The patient initiated gabapentin capsule at a unknown dose and frequency via unknown route for an unknown indication. The patient experienced horrendous itching and probably had pericarditis. The event pericarditis was considered medically significant. 21-Oct-2022: The patient initiated COVID-19 vaccine at a unknown dose and frequency via unknown route (batch/lot number GH9697, expiration date unknown) for an unknown indication. Action taken with gabapentin was not reported. The outcome of events pericarditis and pruritus was unknown. Company Comment: Serious: Pericarditis is unlisted event whereas pruritus (Non-serious) is listed event as per company RSI of gabapentin. Causality has been assessed as possible for the events pericarditis and pruritus as contributory role of suspect drug cannot be completely excluded based on available information. Viatris Comment: Serious: Pericarditis is unlisted event whereas pruritus (Non-serious) is listed event as per company RSI of gabapentin. Causality has been assessed as possible for the events pericarditis and pruritus as contributory role of suspect drug cannot be completely excluded based on available information. GABAPENTIN is under agreement with Viatris Causality assessment: GABAPENTIN Pericarditis, Itching Per reporter: Possible Per Viatris: Possible; Sender's Comments: Based on the available information the causality for the reported events pericarditis and pruritus cannot be excluded for the suspect products gabapentin and COVID-19 vaccine. The impact of this report on the benefit risk profile of the Pfizer product and is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review as well as any appropriate action in response will be promptly notified to regulatory authorities, Ethics committees and Investigators as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 2541482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

schwer

Staat: WA
Alter: -
Geschlecht: M
Eingang: 31.12.2022
Impfdatum: 25.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Aortic disorder Condition aggravated Pericarditis Pruritus Drug ineffective Suspected COVID-19

Symptomtext

Probably had pericarditis; Horrendous itching; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from License Party. Other Case identifier(s): US-MYLANLABS-2022M1147717. This Serious Spontaneous report was received from business partner, PFIZER, (Ref No. 202201389362) originated on 19-Dec-2022 and received by Viatris on 21-Dec-2022. This initial case, received from consumer, non health professional, involved a 78-years-old male patient who reportedly experienced pericarditis and pruritus while receiving gabapentin capsules, USP (gabapentin). Medical history, current conditions and concomitant medications were not reported. Non-company suspect medication included COVID-19 vaccine. Unknown Date: The patient initiated gabapentin capsule at a unknown dose and frequency via unknown route for an unknown indication. The patient experienced horrendous itching and probably had pericarditis. The event pericarditis was considered medically significant. 21-Oct-2022: The patient initiated COVID-19 vaccine at a unknown dose and frequency via unknown route (batch/lot number GH9697, expiration date unknown) for an unknown indication. Action taken with gabapentin was not reported. The outcome of events pericarditis and pruritus was unknown. Company Comment: Serious: Pericarditis is unlisted event whereas pruritus (Non-serious) is listed event as per company RSI of gabapentin. Causality has been assessed as possible for the events pericarditis and pruritus as contributory role of suspect drug cannot be completely excluded based on available information. Viatris Comment: Serious: Pericarditis is unlisted event whereas pruritus (Non-serious) is listed event as per company RSI of gabapentin. Causality has been assessed as possible for the events pericarditis and pruritus as contributory role of suspect drug cannot be completely excluded based on available information. GABAPENTIN is under agreement with Viatris Causality assessment: GABAPENTIN Pericarditis, Itching Per reporter: Possible Per Viatris: Possible; Sender's Comments: Based on the available information the causality for the reported events pericarditis and pruritus cannot be excluded for the suspect products gabapentin and COVID-19 vaccine. The impact of this report on the benefit risk profile of the Pfizer product and is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review as well as any appropriate action in response will be promptly notified to regulatory authorities, Ethics committees and Investigators as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 2530091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: SC
Alter: 16,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Cold sweat Dizziness Dyskinesia Loss of consciousness Syncope

Symptomtext

The COVID vaccine was given first and the Flu vaccine was given second. When the vaccines were administered, and the patient attempted to stand. She exhibited signs of weakness, dizziness, muscle jerks, clamminess and she fainted. She was placed on the floor and her blood pressure was checked. The value was 106/68 HR68. She passed out for approximately 2 minutes and then she began to urinate. She woke up and said she was fine. Her Mother stated that this happens all the time and did not want EMS Called. The patient was given some water and she stated that she felt better. She waited in the Pharmacy Lobby 45 minutes after being in the immunization room 25 minutes.

Weitere VAERSDATA-Felder

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

VAERS 2526718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: MO
Alter: 41,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 08.12.2022
Beginn: 08.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Hyperhidrosis Loss of consciousness Posture abnormal Syncope Tremor Unresponsive to stimuli

Symptomtext

Vasovagal syncope event within moments of 2nd vaccine being administered. Covid vaccine was administered first. Flu vaccine was administered second. Stood up and grabbed his coat off the counter then moved back to the chair and was in the process of sitting back down. He slumped over the left arm of the chair. I asked if he was okay. He was unresponsive. I yelled for help and for someone to call 911. (Note that 911 was called at 11:18am). He regained consciousness before anyone else got to the room. He asked what happened. I explained that he fainted. He started sweating and his hands were shaky. He was able to respond to questions. I suggested that he put his head between his knees. He stayed in the chair with his head between his knees. EMS arrived at 11:28am. BP was 122/46, HR was 84 and O2 saturation was 99%. He declined transport and signed off on EMS documents. He moved from the vaccination room to the waiting area. I offered him a bottle of water. He drank the water and sat there until 11:59am. I took his blood pressure before he left. It was 121/90, and pulse was 69.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: D-amphetamine salt; Lorazepam
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2523223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: NJ
Alter: 17,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 05.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient fainted after receiving shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 911 called and evaluated patient
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2522658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

schwer

Staat: WA
Alter: 21,0
Geschlecht: F
Eingang: 04.12.2022
Impfdatum: 04.12.2022
Beginn: 04.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Fatigue Gait inability Hypotension Immediate post-injection reaction Loss of consciousness

Symptomtext

Pt received flushot on left arm. status normal. then pt received covid vaccine in right arm. immediately after the injection, pt became unconscious for ~ 5 seconds, and became very hypotensive. pt awoke and stated she has spells of fainting before and seemed very tired and unable to walk. pt was giving water and a snack and after 30 mins was able to walk.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: anemic
Vorgeschichte: Major depressive disorder, anemia
Andere Medikamente: missed dose of sertraline
Allergien: unknown
Vorherige Impfungen: -

VAERS 2522489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: TX
Alter: 79,0
Geschlecht: M
Eingang: 03.12.2022
Impfdatum: 01.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: IM / RA

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

Asthenia Blood disorder Injection site pain Thrombosis

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Blood Disorder (diagnosed by MD)-Mild, Systemic: blood clot in left leg-Mild, Systemic: Weakness-Mild, Additional Details: pt went to er where they found a small blood clot in left leg and put pt on eliquis

Weitere VAERSDATA-Felder

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

VAERS 2516876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: NY
Alter: 20,0
Geschlecht: M
Eingang: 25.11.2022
Impfdatum: 25.11.2022
Beginn: 25.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Nausea Syncope

Symptomtext

Patient stated he felt nauseous. A minute later fainted briefly. Approximately 10 seconds and revived. Patient was seated at the time. Emergency Medical services were called. His vitals were checked and determined the patient could leave. Patient did not want to go to hospital.

Weitere VAERSDATA-Felder

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

VAERS 2514229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: CA
Alter: 80,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 15.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / AR

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

Antibody test positive Anticoagulant therapy Asthenia Computerised tomogram thorax abnormal Dyspnoea General physical health deterioration Pulmonary thrombosis Thrombosis Thrombosis with thrombocytopenia syndrome

Symptomtext

She had increased shortness of breath that day. She went to the emergency, and they completed a CT scan of her chest and found lots of clots. She was then hospitalized and placed on supportive care with anti-coagulants. She has had testing that shows vaccine-induced Thrombotic Thrombocytopenia. She is getting worse and worse. She has had increased weaknesses. They have given her IV ID therapy. That has not been effective. She remains hospitalized for this condition since. Her doctor referred her to the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 30,0
Labordaten: CT Scan October 24, 2022 multiple clots found. Antibody test positive October 24, 2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2514212

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: CO
Alter: 32,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 21.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Syncope

Symptomtext

Pt fainted, was out for 2 minutes then came to was able to verbally express how she felt. Then fainted 2 more times. Advised to seek medical attention

Weitere VAERSDATA-Felder

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

VAERS 2513012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: MN
Alter: 63,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 16.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / UN

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

Loss of consciousness

Symptomtext

Passed out approximately at midnight, day of vaccination

Weitere VAERSDATA-Felder

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

VAERS 2504176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 06.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Patient fainted immediately after vaccine and had a convulsion when coming to-Medium

Weitere VAERSDATA-Felder

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

VAERS 2497375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: PA
Alter: 18,0
Geschlecht: M
Eingang: 03.11.2022
Impfdatum: 29.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site haemorrhage Loss of consciousness Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient Bled with both shots. First the Fluzone had a long drop of blood running down his arm about 5 inches, with the Pfizer Bivalent COVID shot hes had drop of blood about a 1/2 inch. After receiving both shot the patient passout briefly and was unresponsive for brief period of time. We then had him lay on the floor with his feet up on a chair. we called 911, ems came and evaluated the patient. no further action was necessary. pt was given water and apple juice to drink and the left the pharmac

Weitere VAERSDATA-Felder

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

VAERS 2495026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: MO
Alter: 37,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 27.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Bell's palsy Ear pain Eyelid function disorder Facial paralysis

Symptomtext

Left side face paralysis, Bells Palsy, left ear pain, trouble closing left eye. Treatment: Prednisone and Valacyclovir

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: -
Allergien: Penicillin, Nickel, Sulfa
Vorherige Impfungen: -

VAERS 2495025

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge gh9697

schwer

Staat: PA
Alter: 16,0
Geschlecht: M
Eingang: 01.11.2022
Impfdatum: 28.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

patient passed out after receiving shot

Weitere VAERSDATA-Felder

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

VAERS 2494805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: IN
Alter: 27,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Flushing Heart rate decreased Hyperhidrosis Hypotension Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Severe, Systemic: Shakiness-Mild, Additional Details: Patient received 1 vaccine in each arm. After sitting for a minute, patient fainted and became unresponsive. Pulse was checked which was very low and patient was not responsive, Epinephrine was given and patient quickly came to. We called emergency services and stayed with patient until they arrived. Patient was able to sit up with emergency services and elected to go home with her family.

Weitere VAERSDATA-Felder

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

VAERS 2492263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: NH
Alter: 72,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Confusional state Dizziness Fatigue Flushing Hyperhidrosis Incontinence Lethargy Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Medium, Systemic: Weakness-Medium, Additional Details: Patient was shaking upon initial injection of the Pfizer bivalent (but vaccine was not pushed through yet). After the vaccine was given, patient said she felt light-headed and felt like she was going to faint. Patient later was disoriented and and passing in and out. Patient soiled herself as well. Firefighters reported that she most likely had low blood sugar levels. She ultimately came back and a checkup at the hospital. Her other vaccine was not given that day.

Weitere VAERSDATA-Felder

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

VAERS 2490331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: MI
Alter: 12,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Balance disorder Fall Syncope Visual impairment

Symptomtext

Apparent syncopal reaction. 2-3 minutes after receiving her dose, the patient was standing in the checkout line and began to lose her balance nearly striking her head on the checkout counter. This progressed to a gradual collapse, eased to the ground by her father. She was then carried to a nearby chair where she recovered over the next few minutes, first responding verbally and then opening her eyes. She commented her vision started to go black and didn't really remember anything that followed, including fainting. Patient was stable after about 5 minutes and back to baseline without further issues, able to ambulate steadily and independently. No further issues noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Persistent asthma (mild)
Andere Medikamente: Montelukast once daily, Flintstone vitamin once daily, fexofenadine once daily
Allergien: NKMA
Vorherige Impfungen: -

VAERS 2487215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: KS
Alter: 24,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Blood lactic acid increased Computerised tomogram head normal Full blood count normal Head injury Laboratory test normal Loss of consciousness Metabolic function test normal Seizure

Symptomtext

Seizure activity, loss of consciousness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: Head CT scan (hit head during seizure)-normal Lactic acid (venous) 2.4 mmol/L (critical value) Other lab results unremarkable included complete blood count and basic metabolic panel
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety and depression
Andere Medikamente: Prozac, Wellbutrin, buspar, mirtazapine Received flu shot at same time as Covid booster
Allergien: Hydrocodone
Vorherige Impfungen: -

VAERS 2487037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

schwer

Staat: KY
Alter: 72,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Cardiac stress test Chills Dyspnoea Electrocardiogram abnormal Feeling abnormal Heart rate decreased Hypersensitivity Influenza Injection site erythema Injection site nodule Injection site swelling Injection site warmth Laboratory test normal Malaise Mobility decreased Respiratory distress SARS-CoV-2 antibody test positive Tremor

Symptomtext

She got her vaccine, she was told to wait 15-20 minutes and she did and had no reaction. Everytime she gets a booster she gets flu symptoms and was expecting this reaction. With this booster after supper she felt unusually not well and took a Tylenol and went to bed early about 8:00 PM. She went to sleep and about 11:00 PM she felt strange, had shakes, chills and kind of flu symptoms and was not able to get out of bed and in respiratory distress. She called her NP/daughter-in-law who took her BP/respirations and was below 40 and they called an ambulance as her heart rate was dropping and was not able to get up and breath. She was rushed to the hospital, thought she had a pulmonary embolism, gave her aspirin, oxygen, IV's, and nitroglycerin. She requested a different hospital and they took her to the closest one. Her pulse ox was 38 when she left they left the house, they kept telling her to stay with them. It was in the 20s when she got to the hospital and checked her all evening and checked for the blood clot. She was there until about 4:30 AM and was then admitted to the hospital. Her VS's were stabilized enough that she was admitted. They wanted to do some more work ups to make sure there were no issues with her heart. She was in the hospital and had part of a stress test on Friday and finished it on Saturday and deemed that she had a severe allergic reaction due to taking the flu and COVID vaccine at the same time. She asked them at pharmacy if there was any problem with her taking both vaccines at the same time, and was told that no that the FDA/CDC said it was OK and that there would be no problem. She was not informed that this was not a different type of flu shot, thought it was her usual yearly flu shot. She then saw the TV commercial and checked and found out that she had the new vaccine. She thinks it was terrible reaction that affected her in a terrible way. The arm with COVID vaccine swollen, red, feverish until a week later when she still had a knot, fever, redness in the arm. The flu vaccine arm was perfectly OK, it was sore the day after but nothing unusual. She feels that the booster of the COVID vaccine was the worst reaction. She was in the hospital for a week back in 2020 with COVID and had pneumonia with that, and it took months to get completely over it, possibly 6 months after that. Her doctor kept telling her that she would not have the antibodies in her blood, but when she would check her blood she still showed that she didn't need a booster as her levels were still high. Her doctor said that she should not get a flu/COVID vaccine and she said that she would never take a COVID booster again due to her reaction. With every booster her symptoms would be a little worse than the previous one. She is still having some problems with taking a deep breath. The tests ruled out the pulmonary embolism. The EKG's showed multiple PVC's in-between her regular heart beat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 2,0
Labordaten: EKG's, stress test, and other testing in the hospital.
Aktuelle Erkrankungen: None.
Vorgeschichte: Acid reflux.
Andere Medikamente: Diclofenac 75 mg, Estradiol 1 mg, Pantoprazole 40 mg, Sucralfate 1 gram, ES Tylenol 650 mg.
Allergien: Codeine, Propofol.
Vorherige Impfungen: -

VAERS 2486724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

schwer

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Confusional state Seizure Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Mild, Systemic: Shakiness-Mild

Weitere VAERSDATA-Felder

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

VAERS 2486715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

schwer

Staat: WA
Alter: 16,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Fall Head injury Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient recieved vaccine was waiting for about 5 minutes while other family members were recieving. She walked out of pharmacy to go sit down and fainted and hit her head on the floor before she got to the chair. She got up right away after faiting and sat in the chair. She was responsive. 911 was called and she was evauluated and released to leave with her family.

Weitere VAERSDATA-Felder

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

VAERS 2725355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 19.12.2023
Impfdatum: 23.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Asthma Condition aggravated Cough

Symptomtext

Pt presented to PCP on 11/3/22 reporting cough that had started since 10/24/22. Pt also reported that she had an asthma attach after her booster on 10/23/22 and was using expired albuterol. Pt diagnosed w/ mild intermittent asthma with acute exacerbation. pt prescribed levalbuterol PRN and prednisone 40 mg daily x 5 days. PCP deemed trigger of asthma attach unclear.

Weitere VAERSDATA-Felder

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

VAERS 2708147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: WI
Alter: 70,0
Geschlecht: F
Eingang: 01.11.2023
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SC / LA

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

Arthralgia Atrial fibrillation Chills Condition aggravated Diarrhoea Fatigue Formication Headache Heart rate abnormal Heart rate increased Urticaria

Symptomtext

9-10pm on day of vaccine 10/31/22, I had significant chills and diarrhea, which resolved 6 hrs later. The next morning (11/1/22) I was extremely fatigued and took 3 naps. I also had these symptoms: Slight headache. Joints ached. Skin felt crawly. My pulse increased from usual 50?s per minute to 70-80s per minute. My heartbeat had double beats every 3rd, 4th, or 5th beat. The background heartbeat was regular, with additional double beats. I was not in afib, These side effects resolved by the next day, 11/2/23. However, the frequency of afib episodes increased significantly after the vaccine in October 2022 until June 2023. I also had two episodes of hives all over my body after the vaccine . First episode was Jan 16, 2023. Second was Jan 20, 2023. I have never had hives in my life. They have not reoccurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Afib, arthritis.
Andere Medikamente: Eliquis, metoprolol, glucosamine chondroitin, calcium, vitamin d.
Allergien: None
Vorherige Impfungen: -

VAERS 2653627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 07.07.2023
Impfdatum: 10.10.2022
Beginn: 01.07.2023
Tage bis Beginn: 264,0
Dosis: 5
Route/Site: SYR / UN

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

COVID-19 pneumonia

Symptomtext

Hospitalization for Pneumonia due to COVID-19 on dates 7/1/2023- 7/5/2023. Treated with dexamethasone, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: beta blockers, penicillins, mold, celecoxib, chlorhexidine, erthyromycin base, levofloxacin, antibiotic ointments, cloth tapes.
Vorherige Impfungen: -

VAERS 2646472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 16.06.2023
Impfdatum: 08.12.2022
Beginn: 10.02.2023
Tage bis Beginn: 64,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chills Cough Dizziness Dyspnoea Fatigue Headache Impaired work ability Migraine Nasal congestion Oropharyngeal pain Pain Photophobia Pyrexia SARS-CoV-2 test positive

Symptomtext

On 2/10/2023, I began to have symptoms of what I now know was COVID-19. I had a fever, chills, body aches, and slight difficulty breathing. I treated my breathing difficulties with a nebulizer. I took TYLENOL for my fever and body aches. I also had a cough and fatigue, sore throat, and nasal congestion (my most bothersome symptom). On about 2/12/2023, I took a PCR test and got a positive result. I also took a home antigen test on 2/11/2023 and got a positive result. On 2/13/2023, I had a telehealth appointment with a PA. She prescribed me prednisone and nirmatrelvir-ritonavir, plus, she refilled my albuterol inhaler. She advised me to keep an eye on my pulse oximeter, because it was averaging between 93 and 96. If it ever went below 90 and was persistent, I was to contact my doctor's office. I think that the antiviral stopped the symptoms in their tracks; it took a couple of days for the symptoms to subside, but the antiviral helped keep them from worsening. The steroids also helped my breathing, and I was able to overcome my breathing difficulty pretty quickly. I used my nebulizer maybe about two or three times a day for the first three days. After that, I switched to my albuterol inhaler, which I used every four to six hours. I spent much of the time napping, because I was so fatigued. I was out of work until 2/20/2023. I'm doing okay now. This is the third time I have had COVID-19, and I think I recovered more quickly this time than I did the two previous times. After this last bout of COVID-19, though, I began getting headaches one to two times a week. They were sometimes migraines that characterized by sensitivity to light. I have also had occasional lightheadedness. At the time of this writing, I still sometimes experience the headaches and the lightheadedness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11FEB2023 home antigen test, positive result; 12FEB2023 PCR test, positive result
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Type II; Hypertension; High Cholesterol; Obesity
Andere Medikamente: JARDIANCE; TRULICITY; albuterol inhaler; hydrochlorothiazide; atenolol; WELLBUTRIN XL; lisinopril; metformin; fenofibrate; SINGULAIR; PROTONIX; atorvastatin; multivitamin; vitamin D3
Allergien: Mushrooms; almonds; shellfish; cat dander; some bandage resins
Vorherige Impfungen: -

VAERS 2641034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: AZ
Alter: 76,0
Geschlecht: F
Eingang: 05.06.2023
Impfdatum: 02.12.2022
Beginn: 25.01.2023
Tage bis Beginn: 54,0
Dosis: 5
Route/Site: IM / LA

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

Asthma COVID-19 Condition aggravated Cough Decreased appetite Infection Knee operation Pain Productive cough Pyrexia SARS-CoV-2 test positive Urinary tract infection Urine analysis abnormal

Symptomtext

I was in the hospital for a knee surgery: a couple of days after my surgery my asthma flared, I started coughing a lot and producing a lot of phlegm. I did have to have breathing treatments while in the hospital. I also contracted an UTI infection right before I left the hospital, I was given medication to take home with me so that I could get rid of the infection. In March I got COVID-19, I had a high fever of 102F-103F, loss of appetite, aching. I took a home COVID-19 test and was positive. I was given the antiviral Paxlovid, but it did take a month before I started to feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 00JAN2023 Urinalysis - positive; 00MAR2023 Home COVID-19 test - positive; 00APR2023 Home COVID-19 test - negative
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Levothyroxine; Metformin; Losartan; Metoprolol; Lipitor: Gabapentin; Montelukast; Low dose Aspirin; Multivitamin 50 Plus Vitamin C; Magnesium; Super B Complex; Fish Oil; Vitamin D3; Calcium/Magnesium/Zinc; Garlic; Stool Softener; Albuterol
Allergien: Bactrim; Latex; Raw Banana; Avocado
Vorherige Impfungen: -

VAERS 2633098

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

moderat

Staat: ME
Alter: 66,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 25.10.2022
Beginn: 15.03.2023
Tage bis Beginn: 141,0
Dosis: 5
Route/Site: IM / LA

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

Blood pressure increased Cardiac disorder Cardiac stress test abnormal Chest discomfort Dyspnoea Electrocardiogram abnormal

Symptomtext

Although I had shortness of breath since my second or third shot on 11/128/21 and 7/12/22 I did not equate it to the vaccine. However it did interfere with my wok cleaning my property and generally grounds work and cleaning. I just thought I was getting old. On March 15, 2023 I was moving snow after a severe storm the day before when I got a sudden tightening in my chest. I stopped immediately and went in side. The very next day was my yearly physical. They did an EKG after I told them what had happened and there was signs of minor damage. They ordered a stress test and when I started the test on. a incline machine, within five minutes my blood pressure shot so high they said we had to stop the stress test so an to not have me "stroke out". I was unfamiliar with the term but got the gist of it and stopped and lay down. Since that time I have been prescribed Losartan (50 ml) and the chest pain is almost gone but after Physical therapy my bp shoots up after exercise like it did on the treadmill. My shortness of breath persists. I never took pharmaceuticals and prided myself on having a healthy lifestye and eating habits. I wore a mask throughout Covid until April of this year. Tested for covid before visiting family and generrally have been healthy although about 15 pounds overweight (175) up from my long standing 160lbs. since 50.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG shoewing mild damage. Stress test failed
Aktuelle Erkrankungen: None. Not even a cold.
Vorgeschichte: Had Lyme Disease 15 years ago, No chronic illnesses
Andere Medikamente: Vit. c, vit D3, Womans Multi vitamin, MCT Wellness (powdered polyphenals), mushroom tincture (reishe, liuons Mane and turkeytail) (half dropper once a day as antiviral/antibacterial)
Allergien: None known
Vorherige Impfungen: -

VAERS 2629507

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

moderat

Staat: MT
Alter: 51,0
Geschlecht: F
Eingang: 10.05.2023
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Mobility decreased Myalgia

Symptomtext

Site: Pain at Injection Site-Medium, Additional Details: patient said muscle soreness and still unable to move arm fully up or backwards

Weitere VAERSDATA-Felder

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

VAERS 2624864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: NY
Alter: 71,0
Geschlecht: M
Eingang: 02.05.2023
Impfdatum: 31.10.2022
Beginn: 01.03.2023
Tage bis Beginn: 121,0
Dosis: 5
Route/Site: IM / RA

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

Accident Dyspnoea Dyspnoea exertional Fatigue Pain Pulmonary congestion Pyrexia

Symptomtext

On 3/1/2023 I started feeling feverish, achy, and tired with some minor lung congestion. This condition persisted for approximately 3 weeks where the fever was 100.5 to 101.5 during week 1, 99.5 to 100.5 during week 2, and with a slight fever (less than 99.5 but above 98.6) continuing into early April. The aches and tiredness lessened each day eventually ending around 3/20/2023. Some shortness of breath was noticed during exertion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Abbott 3/2/2023 positive PCR 3/3/2023 positive Abbott 3/10/23 positive Abbott 3/15/23 negative Abbott 3/17/23 negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin 40 mg Valsartan-HCTZ 320-12.5 mg Folic Acid 1 mg Multi Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2621803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 23.10.2022
Beginn: 12.03.2023
Tage bis Beginn: 140,0
Dosis: 5
Route/Site: IM / LA

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

Abscess Appendicectomy Appendicitis Appendicitis perforated Bacterial test positive Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Drain removal Pneumonia Post procedural drainage Pseudomonal bacteraemia

Symptomtext

I had a perforated appendix follow an appendectomy follow by access on the side and pneumonia in both lungs at the same time. On March 15th, 2023. I had surgical drain implanted and April 7th I had the drainage removed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: 13MARCH2023 - CT Scan - Appendicitis; 13MARCH2023 - Lab Test - abnormal Pseudomonas Bacteria-; 15MARCH2023 - CT SCAN - Abscess & Pneumonia.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Latex
Vorherige Impfungen: -

VAERS 2620616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

moderat

Staat: GA
Alter: 71,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 24.10.2022
Beginn: 11.01.2023
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain Biopsy uterus Chemotherapy Computerised tomogram normal Condition aggravated Endocervical mucosal thickening Hysterectomy Metastatic neoplasm Neoplasm malignant Ultrasound uterus abnormal Urinary tract infection Vaginal haemorrhage

Symptomtext

On the date of vaccination, I experienced no symptoms but my symptoms started on January 10th I went to Urgent Care for a urinary track infection and got treated, January 11th I started experiencing abdominal pain and thought it was a side affect of the urinary track infection medicine, in addition I have been spotting for years and it usually can be controlled with a vaginal moisturizer and this time it could not. I went to see my PCP and did a CT scan and nothing showed up, things continued to get worse so I went to see my gynecologist because I had a suspicion this may be uterine cancer and they did a ultrasound and saw that the uterine lining was thickened so they did a Biopsy on Feb 9th, I had a hysterectomy on March 13th and after that it showed cancer had gotten into other parts of the body so now I am undergoing chemotherapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 30thJan2023 - CT Scan 9thFeb2023 - Biopsy
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic Knee Pain
Andere Medikamente: N/A
Allergien: Penicillin; Sulfa; Spinach
Vorherige Impfungen: -

VAERS 2619024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: UT
Alter: 43,0
Geschlecht: M
Eingang: 21.04.2023
Impfdatum: 20.10.2022
Beginn: 21.03.2023
Tage bis Beginn: 152,0
Dosis: 4
Route/Site: UN / UN

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

Dyspnoea Fatigue Nasopharyngitis Oropharyngeal pain Sinusitis Thyroid function test

Symptomtext

I experienced sore throat and cold and sinus infection that last 3-4 days then following that I started to experience fatigue and being tired as if I was out of shape, I would feel winded and very fatigued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 13April2023 Thyroid check
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lisinopril; ADDERALL; sertraline; trazodone
Allergien: N/A
Vorherige Impfungen: -

VAERS 2597589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: NY
Alter: 68,0
Geschlecht: M
Eingang: 16.03.2023
Impfdatum: 12.09.2022
Beginn: 08.01.2023
Tage bis Beginn: 118,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Oropharyngeal pain Pain Paraesthesia Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sciatica

Symptomtext

Initially, the symptoms were a sore throat and congestion that progressed into body aches and pains and a low-grade fever. I took an at-home COVID-19 on 01/09/2023 which came back positive. The next hour, I contacted my doctor via telehealth appointment with the nurse practitioner where I explained my symptoms. I was prescribed PAXLOVID and hydration. Within 3-5 days, I was feeling a lot better. However, I started tingling in my fingertips in my right hand right after that lasted until about 02/23/2023. I knew it was sciatica because I had suffered from it before. The sciatica dissipated on its own, but the tingling persisted until I went to my cardiologist appointment on 01/27/2023. He indicated that people were reporting abnormal symptoms after contracting COVID-19 and insisted to continue resting. After traveling for about a month, I came back and all of my pains sort of settled on their own. As of now, I still have tingling in my right hand periodically.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 09JAN2023 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Heart Disease; Hypertension
Andere Medikamente: Gabapentin; CENTRUM SILVER; aspirin; ezetimibe tabs; rosuvastatin calcium; losartan potassium; vitamin D3
Allergien: N/A
Vorherige Impfungen: -

VAERS 2597064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: WI
Alter: 97,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 13.10.2022
Beginn: 30.12.2022
Tage bis Beginn: 78,0
Dosis: 5
Route/Site: UN / UN

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

Asthenia Bronchospasm COVID-19 Chest X-ray normal Cough Dyspnoea Fall Gait inability Hypoxia Rhonchi SARS-CoV-2 test positive Sepsis Urinary tract infection

Symptomtext

Patient initially had a positive COVID-19 NAA test on 12/25/2022. He is a resident of a long-term care facility. On 12/30/2022, patient presented to the emergency department after a fall/found lying on floor at the LTC facility, and with COVID-19 symptoms - shortness of breath, cough and generalized weakness. Patient had significant rhonchi and some bronchospasm; pulse oximetry stable in the low 90s; no signs of respiratory failure; chest x-ray showed no pneumonia. Patient was diagnosed Weakness, Fall, Unable to ambulate, COVID-19, Shortness of breath, Hypoxia, Acute bronchospasm, Urinary tract infection without hematuria, and site unspecified Severe sepsis. He was treated with DuoNeb nebulizer, ceftriaxone, dexamethasone, and normal saline bolus in the emergency department. Patient was then admitted to the hospital for additional care and treatment. Submitter does not have access to further medical information on this case. If more information is needed, please contact the admitting hospital

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/25/2022 - positive COVID-19 NAA test 12/30/2022 - chest x-ray showed no pneumonia.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Congestive Heart Failure, Hypersensitivity Lung Disease, Atrial fibrillation, Coronary Artery Disease, Type 2 Diabetes Mellitus, Hypertension, Hyperlipidemia, Glaucoma.
Andere Medikamente: Unknown
Allergien: ALLERGIES: Metoprolol ? bronchospasm; Penicillins ? Rash; Lisinopril - elevated creatinine and hyperkalemia.
Vorherige Impfungen: -

VAERS 2591816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 27.10.2022
Beginn: 23.02.2023
Tage bis Beginn: 119,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Asthenia Blood creatinine increased COVID-19 Chronic kidney disease Condition aggravated Constipation Cough Fall Laboratory test normal Malaise Pain Pyrexia Renal impairment SARS-CoV-2 test positive Ultrasound kidney abnormal

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 2/21/2023 Discharge Date: 2/27/23 PRESENTING PROBLEM: Weakness Fall, initial encounter Chronic kidney disease, unspecified CKD stage COVID COVID-19 HOSPITAL COURSE: Patient is a 74-year-old male with a past medical history of ankylosing spondylitis, chronic pain, hypertension, prostate cancer, decubitus ulcer stage IV, diabetes mellitus type 2 and dyslipidemia who presented with a chief complaint of fever, recent falls with a positive COVID test at home. Patient was feeling ill 2 days prior to admission with a temperature up to 103?. He recently had been weaning off of gabapentin and on to Lyrica per his nephrologist an outpatient PCP. His pain had increased with these adjustments. He had been started on Norco. He also had been noting constipation. He already was taking tramadol and p.r.n. morphine, but had significant side effects of nausea from his morphine and only took it for breakthrough pain. He had fallen multiple times prior to admission. His daughter noted he was 88% on room air on a home monitor. He was afebrile. His creatinine was elevated from baseline with AKI on CKD stage IV. Labs were otherwise stable. He was admitted to the hospitalist service for COVID-19 infection and generalized weakness with AKI. He was initially treated with gentle fluids without improvement of his kidney function. Renal ultrasound showed no obstruction, but showed bilateral medical renal disease. He was continued on fluids with eventual improvement of his kidney function towards his baseline. Nephrology was consulted and recommended continuing fluids and adding sodium bicarb. In regards to COVID-19, he required up to 3 L nasal cannul and received 5 days of Decadron therapy while inpatient, discharged on room air with mild dry cough. Palliative care was consulted to help with adjustments in his pain medication, His gabapentin was weaned down with plans to completely replace with Lyrica by March 3rd with prescription given on discharge. Final pain plan includes intermittent norco with low dose oxycodone for severe pain available, due to kidney dysfunction morphine was discontinued along with tramadol. PT/OT recommended subacute rehab but patient improved enough during stay to qualify for HHC for PT/OT, and RN for wound care. DC in stable condition on 2/27.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: 09/30/20122- Pressure injury of sacral region, stage 4 - Primary
Vorgeschichte: AS (ankylosing spondylitis) Encounter for long-term (current) use of other medications Pressure injury of sacral region, stage 4 Osteomyelitis CKD III Wound infection Constipation Multifocal pneumonia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 300 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG enteric coated tablet azithromycin (ZITHROMAX) 500 MG tablet benzonatate (TESSALON) 100 MG capsule cefuroxime (CEFTIN)
Allergien: DemerolNausea Only
Vorherige Impfungen: -

VAERS 2590979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 03.03.2023
Impfdatum: 01.12.2022
Beginn: 22.12.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: IM / LA

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

Chest X-ray normal Dizziness Dyspnoea Headache Magnetic resonance imaging head abnormal Sinusitis Ultrasound Doppler normal

Symptomtext

I had headaches on the top of my head, shortness of breath, I was also dizzy at times. I made an appointment with my doctor, who had an MRI done and found that I had a sinus infection, a chest x-ray and discovered my lungs were clear. I was referred to my cardiologist who did an ultrasound on my carotid artery to determine if it was helping to cause my headache. I was given an antibiotic to get rid of the sinus infection. The headaches are now gone, the shortness of breath comes and goes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Ultrasound negative; MRI, sinus infection
Aktuelle Erkrankungen: Allergy early November
Vorgeschichte: Open heart surgery at 17 years old
Andere Medikamente: Lisinopril; metoprolol; PANEX; CRESTOR; magnesium; vitamin D; coQ10; baby aspirin
Allergien: Penicillin; PLAVIX
Vorherige Impfungen: -

VAERS 2581816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: TN
Alter: 39,0
Geschlecht: M
Eingang: 14.02.2023
Impfdatum: 13.11.2022
Beginn: 12.12.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: SYR / RA

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

Cardiac monitoring abnormal Chest discomfort Fatigue Headache Heart rate increased Influenza virus test negative Malaise Pain Palpitations Respiratory rate increased Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative Streptococcus test negative Upper-airway cough syndrome

Symptomtext

My adverse event started on 12/12/2022 in the morning. I had a headaches, runny nose, fatigue, body aches, chest congestions and post nasal drip. On 12/15/2022 I went to an urgent care where they tested me for COVID-19 Infection, Flu, and Strep. All the tests were negative. I've noticed something new was happening with me. All of a sudden I had a rising heart rate. My resting heart rate increased by 10 since I wear a heart monitor I noticed it. I get heart palpation which slowly would stop. I also experienced chest pressure. I would start to breath faster. It happens all of a sudden I feel the chest pressure and then increased heart rate afterwards. On 12/15/2022 I went to an urgent care for symptoms of COVID-19. They advised me to care ibuprofen since I tested negative for COVID-19 infection. On 02/09/2023 when I started feeling the chest pressure and increased heart rate. I messaged my doctor since she doesn't work that day she told me to go to the urgent care. I went to the urgent care on 02/09/2023. When I explained to them about the issue I was experiencing they again tested me for COVID-19 infection, Flu and Strep. I was negative again. So, they told me to go see a Cardiologist. I scheduled an appointment for tomorrow 02/15/2023 at 12:30PM.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 15DEC2022 COVID-19 test negative; 15DEC2022 FLU test negative; 15DEC2022 STREP test negative; 09FEB2023 COVID-19 test negative; 09FEB2023 FLU test negative; 09FEB2023 STREP test negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2576468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: IL
Alter: 62,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 24.10.2022
Beginn: 29.12.2022
Tage bis Beginn: 66,0
Dosis: 4
Route/Site: SYR / LA

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

Anti-thyroid antibody Asthenia Biopsy endometrium Blood pressure increased Blood thyroid stimulating hormone normal Brain hypoxia Chest X-ray abnormal Computerised tomogram abdomen abnormal Computerised tomogram abnormal Condition aggravated Confusional state Cystoscopy normal Dizziness Dysgeusia Endometrial thickening Fatigue Full blood count normal Head discomfort

Symptomtext

I've been experiencing headaches, nausea, increased urination, vomiting, dizziness, tiredness, weakness, feeling faint, increased blood pressure and heart rate, room spinning, vertigo (BPPV), nasty taste in my mouth, and sweating. I've also experienced confusion and forgetfulness. I've felt pressure in my forehead.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: 11/14/2022 Urinalysis - Normal; 10/24/2022 Comprehensive Metabolic Panel - Normal; 10/24/2022 TSH Free - Normal; 10/24/2022 Triiodothyronine - Normal; 10/24/2022 T4 - Normal; 12/29/2022 Chest X-Ray - No specific evidence of pneumonia or pulmonary edema. Small bilateral pleural effusions; 12/30/2022 CT Scan - Scar tissue evident indicating loss of oxygen to the brain, possibility of stroke; 01/17/2023 CT Scan Upper Abdomen and Pelvis - Endometrial Lining Thickening, Large Fibroids; 01/31/2023 Complete Blood Panel - Normal; 01/31/2023 ER Panel 1 - High; 02/01/2023 Urinalysis - Slightly cloudy; 02/01/2023 Urinalysis - Normal; 02/01/2023 Cystoscope - Normal; 02/01/2023 Endometrial Lining Biopsy - Results Pending
Aktuelle Erkrankungen: Dark Urine; Nausea; Frequent Urination
Vorgeschichte: Hypertension; Hyperthyroidism; Erythema; Fibroids
Andere Medikamente: Irbesartan; Abaloparatide; Metoprolol; Vitamin D3; Oxybutynin; Tylenol; Aleve; Atorvastatin
Allergien: None
Vorherige Impfungen: 01/31/2022 Pfizer COVID-19 Dose 3 - Age 61, Headache, nausea, dizziness, room spinning, possible vertigo, increase blood pressur

VAERS 2559669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: OK
Alter: 71,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 13.10.2022
Beginn: 10.01.2023
Tage bis Beginn: 89,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia COVID-19 Chills Cough Hypotension Insomnia Pain Pyrexia SARS-CoV-2 test positive Shift to the left

Symptomtext

COVID-19 symptoms: severe chills and shivering, fever 101.0, lack of energy, body aches. This lasted for a day and a half along with a moderate cough for 2 days. I have also have been unable to sleep post COVID-19 and have a lower than normal BP.

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Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: COVID-19 PCR test 01/10/2023 positive, COVID-19 home test 01/10/2023 positive
Aktuelle Erkrankungen: None
Vorgeschichte: Atrial fibrillation; Asthma
Andere Medikamente: Oxybutynin; flecainide; omeprazole; atorvastatin; XARELTO; gabapentin; inhaler; finasteride; minoxidil; PRN medications; milk of magnesia; vitamin B3; multivitamin; OCUVITE for eyes; calcium; vitamin D3; vital proteins
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2555894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 26.11.2022
Beginn: 12.12.2022
Tage bis Beginn: 16,0
Dosis: UNK
Route/Site: SYR / LA

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

Condition aggravated Trigger finger

Symptomtext

I have had trigger finger intermittently for about 9 years. Normally I get treated with a cortisone shot and then it is resolved until the next episode. Starting around 12/12/2022, it flared back up again. I have tried ice packs and bicycle gloves to help but without much relief. My real problem is with the left hand middle finger but I am also having trouble in the right hand with the pointer finger. I will be seeing the hand doctor on 01/18/2023 for treatment. I did not take ibuprofen for it due to the fact that it does not really help and it upsets my stomach.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown flu-like virus around 10/31
Vorgeschichte: None
Andere Medikamente: Niacin; fish oil; borage seed oil; multivitamin; vitamin C with quercetin; pancreatic enzymes; calcium; probiotic; atrantil; cortisol manager; vitamin D
Allergien: Fish sensitivity; some sensitivities to other foods
Vorherige Impfungen: After the 1st booster (3rd dose of Pfizer), I developed a wart but it went away completely shortly after

VAERS 2550144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: NC
Alter: 67,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 09.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 8,0
Dosis: 5
Route/Site: SYR / RA

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

Chest discomfort Dyspnoea Fatigue Fear Feeling hot Musculoskeletal chest pain Myalgia Pain Pain of skin Painful respiration Rhinorrhoea SARS-CoV-2 test negative Streptococcus test negative Symptom recurrence

Symptomtext

I had my flu shot a week prior then my COVID-19 booster. A week later, I started feeling very achy. My normal temperature is a bit lower, so when it hit 99, I was starting to feel hot. I would wake up with that. My skin was hurting, muscles were hurting as well. I started taking Singulair at that time because I was having trouble breathing because it felt like someone was sitting on my chest. I had a runny nose like crazy and that went on. I waited 10 days before making an appointment. They did a strep test, an at home COVID-19 test and both were negative. The doctor gave me a z-pack and I went home. I felt better in about 4 days, then 2 weeks after that, the symptoms came back. They gave me another z-pack. So far, it's been okay and I've been better. I'm still tired but I can't tell if it's the weather because the weather affects my arthritis pretty bad. It was scary when I couldn't breathe well because when I would take a breath, my ribs would hurt and my chest was heavy. My husband and I don't get really go out often and we have been careful. I had another COVID-19 test before my second z-pack and that was also negative. I don't know what this is. In January of 2020, I was also sick at that time and it was very bad. I went to the doctor and the doctor tells me I had a virus that would last a month or so. I was given cough syrup (heavy duty) and he couldn't tell me what it was. I may have had COVID-19 back then, and it took me 3 weeks to get over it and I could barely get out of bed. It was very strange.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: At-Home COVID-19 Test - Negative; At-Home COVID-19 Test - Negative; Strep Test - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Degenerative Disc Disease; Severe Arthritis; Osteopenia; Migraines; Lack of Cartilage in Knees; Insomnia
Andere Medikamente: Metformin; Omeprazole; Cetirizine; Magnesium Glycinate and Malate with Vitamin D3; Earth's Pearl Pro and Prebiotic; Tramadol; Meloxicam; Tommy Chong's CBD Good Vibes Gummies
Allergien: Soy; Trees; Grasses; Ragweed; Seasonal Allergies
Vorherige Impfungen: All COVID-19 Pfizer vaccines had made me sick. First one sick for a week. Second vaccine was less time. Third wasn't too bad (2-

VAERS 2547105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: OH
Alter: 62,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 19.10.2022
Beginn: 23.10.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / RA

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

Anticoagulant therapy Blood pressure increased Blood test Catheterisation cardiac normal Chest X-ray Chest pain Coagulation test Echocardiogram Electrocardiogram normal Myocardial necrosis marker increased Troponin increased

Symptomtext

On 10/23 in the eVening, I developed chest pain which became severe, had very elevated blood pressure. Called the squad. Was given aspirin to chew. They started an IV and game me nitroglycerin under my tongue and fentanyl in my IV. Chest pain improved after nitroglycerin. I did not have EKG changes. My troponin was 48 upon arrival and increased to 150, then 860. I was on a heparin drip. I was taken for a heart cath and possible stint placement. My heart cath showed no blockage, despite my presentation and elevated cardiac enzymes.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: EKG Troponin levels every three hours-48, 150, 860 Cardiac echo Chest x ray Blood coag tests Test for pulmonary embolism( D- dymer?)
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid, reflux, depression
Andere Medikamente: Synthroid, lexapro, wellbutrin, lipitor, reglan, omeprazole
Allergien: None
Vorherige Impfungen: -

VAERS 2545822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: WI
Alter: 87,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 19.10.2022
Beginn: 20.11.2022
Tage bis Beginn: 32,0
Dosis: 4
Route/Site: UN / UN

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

Agitation Atrial fibrillation Blood electrolytes normal Blood lactic acid Bundle branch block left COVID-19 Chills Condition aggravated Confusional state Electrocardiogram abnormal Laboratory test Mental status changes Pyrexia Renal function test normal SARS-CoV-2 test positive Skin warm Thyroid function test normal Tremor

Symptomtext

Adverse event information provided in this submission, is per a report received by a Public Health Department from a submitting facility. Covid-19 vaccination information is from Immunization Registry. Pfizer 3/15/2021 lot number not available; Pfizer 4/07/2021 lot number not available; Pfizer 12/21/21 Lot number FE3594; Pfizer 10/19/22 Pfizer BvlntBstr 12+ Lot number: GH9697 Per note submitted from the hospital admission date 11/20/2022. ?Multiple diagnoses were considered for this patient including but not limited to pneumonia, UTI, arrhythmia, sepsis. Clinical impression appears to be most consistent with fever secondary to COVID-19 with altered menta l status and atrial fibrillation. Patient presents with subjective fevers and chills per the wife at home. Increased confusion and agitation today. Does have a history of dementia and i s normally confused. Per the wife he is essentially at his baseline but was slightly more agitated today. She noted that he felt warm at home and was shaking as though he was having chills. No temperatures measured at home. Here his lungs are clear and his urine is clean. White blood cell count is normal. Lactic acid is 1.8 and so below 2. Does not meet criteria for severe sepsis. No evidence of hypotension to suggest septic shock. Oxygenating normally. EKG shows what appears to be rate controlled atrial fibrillation which I cannot find a history of. There are no ischemic changes although he does have a more noticeable left bundle branch block on today's EKG when compared to previous. His troponin is normal. Thyroid function is normal. Electrolyte's and renal function are normal. Patient's C OVID swab did come back positive for COVID. I think this is likely the source of his fever. Given his age and risk factors and potential new A. fib I think admission for further evaluation is warranted. He is admitted in stable condition on 11/20/2022.? No further information is known on the outcome of this patient. Please contact provider for any additional information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: lab work EKG
Aktuelle Erkrankungen: unknown
Vorgeschichte: ? coronary artery disease involving native coronary artery of native heart without angina pectoris ?Essential hypertension ? Other hyperlipidemia ? PAD (peripheral artery disease) ? S/P peripheral artery angioplasty with stent placement ?S/P coronary artery stent placement ? Gastroesophageal reflux disease without esophagitis ? Urinary incontinence due to benign prostatic hyperplasia ? Neuropathic pain of hand, left ? Neuropathic pain of hand, right ? Mass of chest wall, left ? Neoplasm of uncertain behavior ? Confusion ? Dementia
Andere Medikamente: unknown
Allergien: Seasonal allergies CT IV contrast Omnipaque
Vorherige Impfungen: -

VAERS 2543274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

moderat

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 26.12.2022
Impfdatum: 11.12.2022
Beginn: 12.12.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Injection site injury Mobility decreased Nerve injury Pain Pain in extremity Peripheral swelling

Symptomtext

Patient claims that she has not been able to move her arm above parallel and has been in a lot of pain since the day after her vaccine. She waited until today to obtain treatment (12/26/22) Patient doesn't have a primary doctor. She saw the urgent care doctor because she doesn't have full use of her arm without pain and does not have full movement. She claims no redness at the injection site, however her arm is a little swollen. Doctor at the urgent care told patient that there is not sign of cellulitis but his thought is that a nerve was hit when she received the injection. Will follow up with the patient to see if improves with steroids.

Weitere VAERSDATA-Felder

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

VAERS 2542085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

moderat

Staat: ME
Alter: 72,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 15.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Arthralgia Balance disorder Chest X-ray normal Chest pain Malaise Musculoskeletal chest pain Musculoskeletal pain SARS-CoV-2 test negative Vertigo

Symptomtext

Haven't felt well since I received 5th vaccine, balance was effected experience vertigo. The night of 12/14/2022 started feeling pain in my left chest the pain continued the next pain progressed across chest into both shoulder to scapula. The 11/16/2022 the pain traveled to rib on the left side of my body. Prescribed Tylenol

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Covid home test-negative Chest x-ray also negative
Aktuelle Erkrankungen: no
Vorgeschichte: Hypertension; Neimar's-disease; hypothyroid
Andere Medikamente: Droxia
Allergien: Hyper sensitive to aspirin; NCISAD, and most antibiotics
Vorherige Impfungen: -

VAERS 2533850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

moderat

Staat: OH
Alter: 43,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Mobility decreased Pain in extremity

Symptomtext

The patient is complaining of constant arm pain since the day of the immunization to the point where she is unable to raise it above her head. The adverse effects were reported 5 days after the immunizations were given and the patient stated the pain has not improved. There was no itching, redness or other physical symptom reported. The rph counseled on around the clock use of ibuprofen for 48 hours at which point she will check on the patient again via a phone call. The rph called the patient and left a message asking for a call back with an update. At the time this is written, pt has not called back yet.

Weitere VAERSDATA-Felder

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

VAERS 2528433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 10.12.2022
Impfdatum: 17.10.2022
Beginn: 04.12.2022
Tage bis Beginn: 48,0
Dosis: 5
Route/Site: SYR / -

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

Acute kidney injury Alanine aminotransferase increased Anion gap Arteriosclerosis coronary artery Aspartate aminotransferase increased Asthenia Base excess Basophil count decreased Basophil percentage decreased Blood albumin normal Blood alkaline phosphatase normal Blood bicarbonate decreased Blood bicarbonate normal Blood bilirubin normal Blood calcium decreased Blood chloride decreased Blood creatinine increased Blood gases

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: NP on December 04, 2022 18:57 Verified By: NP on December 04, 2022 18:57 Encounter Info: Hospital, Observation, 12/04/22 - 12/04/22 * Final Report * History of Present Illness/Subjective 18:50 December 04, 2022 18:50:59 67 year old with a History of diabetes, hyperlipidemia, hypertension presents with 6 days of fever, chills, vomiting, diarrhea, weakness. He fell yesterday and hit his head, he was out of a short while. on interview,pt endorsed having black water stool x 6 days. occult blood is positive in the ER. And hemoglobin has been stable. No hematemesis, hematuria, chest pain, headache, fever, nausea or vomiting. Patient appears severely dehydrated and very tired, on auscultation by the NP, upper lobe wheezing and lower lobe crackles noted. In the ER Vital signs-blood pressure 117/45, heart rate 77, SPO2 95% on room air Labs WBC 7.8, hemoglobin 11.6, neutrophils 85% platelet 183 D-dimer 628, sodium 130, chloride 95, bicarb 20, anion gap 15, BUN/creatinine 53/2.12, glucose 251, calcium 8.3, ALT 51, AST 87, T bili 0.6, troponin 44, ketones negative Lactate 2.0 Venous blood gas-pH 7.33, PCO2 39, bicarb 21, O2 sat 40 COVID-negative Flu a positive occult blood positive Imaging Chest x-ray-Bilateral interstitial opacities with a focal opacity in the left lower lung findings which may represent pneumonia and/or edema. CT PE-Bilateral patchy ground glass opacities, which may be seen in setting of multifocal pneumonia CT head-no acute intracranial process CT cervical spine-no acute fracture Review of Systems A complete, 13-system review was performed and was negative except for as noted in the HPI Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.9 (36.9-36.9) Temp (FAHR) 98.4 (98.4-98.4), BP 145/63 (117-154)/(34-71), HR 79 (74-90), RR 20 (2-23), O2Sat 97 (94-97) Patient Weight Current Daily Weight: 130.1 kg 12/04/22 Previous Daily Weight: 131.7 kg 12/04/22 Difference from Previous: -1.600000 kg BMI: 44.9 12/04/22 Morbid Obesity (BMI > = 40) Patient Height Current Height: 170.2 cm 12/04/22 Constitutional: + Mild distress, well-nourished Eyes: PERRLA, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs Bilateral bases with expiratory crackles and Bilteral upper lobes expiratory wheezing Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan Assessment/Plan 67 year old presents with 6 days of fever, chills, vomiting, diarrhea, weakness and a fall. admitted for multiple problems 1. Influenza A J10.1 Positive for flu a -We will give Tamiflu 75 mg twice daily for 5 days. Antibiotics to cover for possible bacterial superinfection. We will give ceftriaxone and doxycycline -Airborne precaution 2. GI bleeding Patient endorsed passing watery black stool for the past 6 days, Last episode this am. Also appears very dehydrated on exam. Vital signs have been stable, and hemoglobin is currently stable. baseline hemoglobin is between 10 and 11. Occult blood positive We will monitor patient's closely and if patiently acutely decompensates i.e tachycardic, hypotensive or has a large black bowel movement, will consult GI urgently overnight for urgent endoscopy -In the meantime, will start IV PPI twice daily -N.p.o. except medication -Hb Q4 hr and notify provider if downtrending -Ensure adequate IV access. ensure fluid hydration -Transfuse as needed to keep Hb >7g/dl -Will notify GI -Telemetry 2. Hyperglycemia R73.9 Elevated blood sugars noted -Insulin ISS -Monitor BGM's with ACH S -Get A1c 3. Elevated troponin R77.8 Troponin is 44, no current chest pain. Trend to peak -We will get EKG to rule out ST changes -Place patient on telemetry 4. Hyponatremia E87.1 Sodium of 130 and chloride of 95. Symptomatic Likely hypovolemic hyponatremia. We will send sodium labs and give IV hydration -Trend sodium daily AKI (acute kidney injury) N17.9 BUN/creatinine higher than baseline. Likely prerenal given dehydration. Will give IV fluid hydration and trend creatinine daily, if not downtrending will get renal ultrasound and consult nephrologist Closed head injury S09.90XA History of fall yesterday, with head CT negative for acute intracranial process resulting from fall. -We will continue to monitor mental status -Ensure pain control Fall at home W19.XXXA Pneumonia J18.9 Seen on chest imaging. Likely secondary to influenza A. We will treat as listed above Sinusitis J32.9 Orders: acetaminophen, 1,000 mg, Orally, Tablet, Q8H, PRN, Pain Mild PO (1-3 out of 10), 12/04/22 18:46:00 ceftRIAXone, 1 GM, IVPB, Injection, Q24H, 12/04/22 19:00:00, 100 mL/hr, Infuse Over 30 minutes, Total Volume (mL) = 50 Dextrose 10% in Water 500 mL, Total Volume (mL) = 500, IV, 12/04/22 18:46:00, PRN - See Comments, Clinical Weight doxycycline, 100 mg, IVPB, Injection, Q12H, 12/04/22 19:00:00, 100 mL/hr, Infuse Over 1 Hours, Total Volume (mL) = 100 glucagon, 1 mg, IM, Injection, Unscheduled, PRN, Hypoglycemia, 12/04/22 18:46:00 glucose, Per Glucose Level, IV Push, Injection, Unscheduled, PRN, Low Blood Sugar, 12/04/22 18:46:00 hydroCODONE-acetaminophen, 1 Tablet, Orally, Tablet, Q8H, PRN, Pain Moderate PO (4-6 out of 10), 12/04/22 18:46:00 insulin lispro, Sliding Scale, Subcutaneous, Injection, With Glucose Testing, PRN, Serum Glucose, 12/04/22 18:46:00 labetalol, 10 mg, IV Push, Injection, Q6H, PRN, Systolic Blood Pressure, 12/04/22 18:46:00 ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 12/04/22 18:46:00 oseltamivir, 75 mg, Orally, Capsule, BID, 12/04/22 21:00:00 pantoprazole, 40 mg, IV Push, Injection, BID, 12/04/22 21:00:00 Sodium Chloride 0.9% 1,000 mL, Total Volume (mL) = 1,000, IV, 12/04/22 18:46:00, 150 mL/hr, Clinical Weight Admit to Inpatient Call (Specify) Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Cardiac Monitor Care Management Consult CBC w/Differential Comp Metabolic Panel Electrocardiogram Fluid Intake Requirement Gluc-Strip POC Hgb A1C HPLC Bld QN Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Skin and Wound Care Protocol Level of Care Medical Service Medication Message to Nursing Message to Nursing Message to Nursing Nasal Cannula Notify Provider Notify Provider Notify Provider OT Evaluation and Treatment Peripheral IV Insertion PT Evaluation and Treatment Reason for Not Ordering Long-acting Insulin Reason for Not Ordering Medication Prophylaxis Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Vital Signs Weight Code Status Resuscitation Status - Ordered -- 12/04/22 18:46:00, Full Code Chronic Problem List AKI (acute kidney injury) Closed head injury Diabetes mellitus Fall at home Hyperlipidemia Hypertension Pneumonia Severe obesity Sinusitis Procedure/Surgical History ?None Medications Home Medications (11) Active alfuzosin 10 mg oral tablet, extended release 10 mg = 1 Tablet, Orally, Daily amitriptyline 25 mg, Orally, At Bedtime citalopram 20 mg, Orally, Daily finasteride 5 mg, Orally, Daily Lantus (insulin glargine) 100 units/mL subcutaneous solution See Instructions, 60 units in morning Lipitor 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily losartan 25 mg, Orally, TID metFORMIN 1,000 mg, Orally, Daily metoPROLOL tartrate , Orally, BID NovoLOG Mix 70/30 subcutaneous suspension See Instructions, 40 units BID Ozempic 2 mg/1.5 mL (0.25 mg or 0.5 mg dose) subcutaneous solution 2 mg, Subcutaneous, Every Saturday Active Scheduled Inpatient Medications ceftRIAXone, Injection, 1 GM, IVPB, Q24H, Start: 12/05/22 13:00:00 doxycycline, Injection, 100 mg, IVPB, Q12H, Start: 12/04/22 19:00:00 influenza virus vaccine, inactivated (influenza virus vaccine, inactivated preservative-free quadrivalent IM suspension), Injection, 0.5 mL, IM, ONCE, Start: 12/04/22 21:00:00 oseltamivir (Tamiflu), Capsule, 75 mg, Orally, BID, Start: 12/04/22 21:00:00 pantoprazole, Injection, 40 mg, IV Push, BID, Start: 12/04/22 21:00:00 Sodium Chloride 0.9% 1,000 mL IV 150 mL/hr Dextrose 10% in Water 500 mL IV PRN - See Comments One-Time Medications Given 12/03/22 00:00:00 TO 12/04/22 18:56:40 Zithromax, Injection, 500 mg, IVPB, ONCE, (1 DOSE 12/04/22 12:55:00) ceftRIAXone, Injection, 2 GM, IV Push, ONCE, (1 DOSE 12/04/22 12:55:00) pantoprazole, Injection, 40 mg, IV Push, ONCE, (1 DOSE 12/04/22 10:16:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 12/04/22 10:16:00) PRN Medications (0600 - 0559) from 12/03 - 12/04 acetaminophen, 1,000 mg, Orally, Q8H, 0 Dose(s) glucagon, 1 mg, IM, Unscheduled, 0 Dose(s) glucose, Per Glucose Level , IV Push, Unscheduled, 0 Dose(s) hydroCODONE-acetaminophen, 1 Tablet, Orally, Q8H, 0 Dose(s) insulin lispro, Sliding Scale , Subcutaneous, With Glucose Testing, 0 Dose(s) labetalol, 10 mg, IV Push, Q6H, 0 Dose(s) ondansetron, 4 mg, IV Push, Q6H, 0 Dose(s) Allergies NKA Social History Alcohol Past Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 7.8 k/cumm (12/04/22 09:44:00) RBC: 3.84 million/cumm Low (12/04/22 09:44:00) Hgb: 11.6 GM/dL Low (12/04/22 09:44:00) Hct: 33.2 % Low (12/04/22 09:44:00) MCV: 87 fL (12/04/22 09:44:00) MCH: 30.2 pg (12/04/22 09:44:00) MCHC: 34.9 GM/dL (12/04/22 09:44:00) RDW: 14.1 % (12/04/22 09:44:00) Platelet: 183 k/cumm (12/04/22 09:44:00) MPV: 7.2 fL (12/04/22 09:44:00) Neutrophils %: 85 % (12/04/22 09:44:00) Lymphocytes %: 10 % (12/04/22 09:44:00) Monocytes %: 5 % (12/04/22 09:44:00) Eosinophils %: 0 % (12/04/22 09:44:00) Basophils %: 0 % (12/04/22 09:44:00) Absolute Neutrophil: 6.6 k/cumm (12/04/22 09:44:00) Absolute Lymphocyte: 0.8 k/cumm Low (12/04/22 09:44:00) Absolute Monocyte: 0.4 k/cumm (12/04/22 09:44:00) Absolute Eosinophil: 0 k/cumm (12/04/22 09:44:00) Absolute Basophil: 0 k/cumm (12/04/22 09:44:00) Chemistry: Sodium SerPl QN: 130 mmol/L Low (12/04/22 09:44:00) Potassium SerPl QN: 4.1 mmol/L (12/04/22 09:44:00) Chloride SerPl QN: 95 mmol/L Low (12/04/22 09:44:00) Carbon Dioxide SerPl QN: 20 mmol/L Low (12/04/22 09:44:00) Anion Gap: 15 mmol/L High (12/04/22 09:44:00) BUN SerPl QN: 53 mg/dL High (12/04/22 09:44:00) Creatinine SerPl QN: 2.12 mg/dL High (12/04/22 09:44:00) Estimated GFR (CKD-EPI, no race): 33 mL/min/1.73m2 Low (12/04/22 09:44:00) Estimated CRCL (CG): 44 mL/min Low (12/04/22 09:44:00) Glucose SerPl QN: 251 mg/dL High (12/04/22 09:44:00) Calcium Total SerPl QN: 8.3 mg/dL Low (12/04/22 09:44:00) Alkaline Phos SerPl QN: 74 Units/L (12/04/22 09:44:00) ALT SerPl QN: 51 Units/L (12/04/22 09:44:00) AST SerPl QN: 87 Units/L High (12/04/22 09:44:00) Bilirubin Total SerPl QN: 0.6 mg/dL (12/04/22 09:44:00) Total Protein SerPl QN: 7.1 GM/dL (12/04/22 09:44:00) Albumin SerPl QN: 3.8 GM/dL (12/04/22 09:44:00) Troponin-I High Sensitivity: 44 ng/L High (12/04/22 09:44:00) Ketones SerPl QN: Negative (12/04/22 09:44:00) Lactate Venous Pl QN: 2 mmol/L (12/04/22 09:44:00) pH Bld Venous QN: 7.33 Low (12/04/22 09:44:00) PCO2 Bld Venous QN: 39 mmHg Low (12/04/22 09:44:00) PO2 Bld Venous QN: <35 Low (12/04/22 09:44:00) Base Excess Bld Venous: -5 mmol/L Low (12/04/22 09:44:00) Bicarb Bld Venous Calc: 21 mmol/L Low (12/04/22 09:44:00) O2 Sat Bld Venous Calc: 40 % (12/04/22 09:44:00) Patient Temperature: 37 DegC (12/04/22 09:44:00) Coagulation: D-Dimer Pl QN: 698 ng/mL DDU High (12/04/22 09:44:00) All Other Labs: Specimen Type Occult Blood: Stool (12/04/22 09:43:00) Occult Blood Stool: Positive Abnormal (12/04/22 09:43:00) COVID 19 Specimen Source: Nasopharyngeal (12/04/22 09:27:00) Coronavirus SARS-CoV2 Rapid: Not Detected (12/04/22 09:27:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (12/04/22 09:27:00) Rapid Influenza A PCR: Detected Abnormal (12/04/22 09:27:00) Rapid Influenza B PCR: Not Detected (12/04/22 09:27:00) Diagnostics Radiology Results - Last 24 hours Across Visits 12/04/2022 11:26 - CT Head W/o IV Contrast IMPRESSION: 1. No acute intracranial hemorrhage or midline shift.2. Mild cerebral and cerebellar atrophy.3. Intracranial atherosclerosis.4. Partial opacification of the paranasal sinuses findings whichrepresent sinusitis. 12/04/2022 11:26 - CT Cervical Spine W/o IV Contrast IMPRESSION:1. No acute fracture or malalignment.2. Mild degenerative changes as described above. 12/04/2022 11:27 - XR Chest PA or AP Portable IMPRESSION:1. Bilateral interstitial opacities with a focal opacity in the leftlower lung findings which may represent pneumonia and/or edema. 12/04/2022 15:21 - CTA Chest Pulm Embolism W/IV Contrast IMPRESSION:Limited evaluation demonstrating no lobar or definite segmentalpulmonary embolism. Bilateral patchy ground glass opacities, which may be seen in settingof multifocal pneumonia. Clinically correlate.Coronary calcifications. Signature Line Electronically Signed on 12/04/22 18:57 ________________________________________________________ NP Electronically Signed on 12/05/22 18:29 ________________________________________________________ MD

Weitere VAERSDATA-Felder

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

VAERS 2516852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: CO
Alter: 63,0
Geschlecht: M
Eingang: 25.11.2022
Impfdatum: 13.10.2022
Beginn: 09.11.2022
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Blood test Chest X-ray Computerised tomogram Dyspnoea Electrocardiogram Heart rate increased Myocardial necrosis marker Scan with contrast Sleep disorder

Symptomtext

About 3 weeks after receiving the bivalent Pfizer vaccine, I started to experience perceived shortness of breath, elevated pulse and an elevated blood pressure that wouldn't resolve. My BP was running 187/104 and that made me go to the ER. At the ER, they did a chest X-Ray, a CT scan with contrast, an EKG, full blood work-up and tested for the enzymes for when someone has a heart attack. I was there for about four hours and they weren't able to find any problems. I was told to follow-up with my PCP. I followed up the following day with my PCP and she did a medication change from lisinopril to metoprolol succinate. The episodes continued, feeling like I couldn't breathe and an elevated pulse. Sometimes it would last for minutes and sometimes it would last for hours. On 11/14, I had the feeling that I couldn't breathe, all night long, and I couldn't sleep. I emailed my doctor and she decided to change the metoprolol to amlodipine besylate. I am still experiencing the feeling of not being able to breathe. On 11/24, the episodes continued from early morning through the entire day. I had the feeling that I couldn't breathe and my pulse was elevated. Today, I am doing good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: X-Ray; CT scan with contrast; an EKG; full blood work-up; tested for the enzymes for when someone has a heart attack.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; High Blood Pressure
Andere Medikamente: Lisinopril; HCTZ; montelukast sodium; albuterol; saw palmetto; multivitamin over 50; vitamin B12; vitamin D3; fish oil; loratadine; melatonin
Allergien: None
Vorherige Impfungen: -

VAERS 2506883

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GH9697

moderat

Staat: PA
Alter: 23,0
Geschlecht: M
Eingang: 13.11.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Chest discomfort Chest pain Dizziness Electrocardiogram abnormal Fatigue Imaging procedure Laboratory test Nausea Troponin I

Symptomtext

- Chest Pain, Abnormal EKG Reading, Nausea, Dizziness, Persistent Chest Pressure, Tiredness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Lab Tests, Imaging of Tests, Troponin - I, Heme Profile, + Elect Diff - ER Chemistry Panel, Electrocardiogram done 3 times, Pump Integration Assesssment, Result is that the heart is fine, no allergic reaction to anything (got flu in the same day as vaccine); chest pain persists.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lexapro (10 mg/day), Fish Oil, Melatonin (for sleep)
Allergien: Eggs
Vorherige Impfungen: -

VAERS 2504458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: NJ
Alter: 67,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 09.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Bladder dysfunction Peripheral coldness Respiration abnormal Sleep disorder Tremor

Symptomtext

I woke up at 1:00 a.m. with severe shaking from head to toe. This caused loss of bladder function. Hands were ice cold. This went on for a 1/2 hour. It happened to me also with the prior booster 3:00 a.m., and the shaking lasted an hour. My husband also experienced this with his prior booster. Our family dr. told us to premedicate with Tylenol to avoid this. I took a Tylenol at 12:00 noon an hour after the booster, but still had this reaction. I also took a Tylenol at 1:15 a.m., which caused the shaking to subside and calm down. The shaking is severe and encompassed every fiber of my body. My breathing was shaky, too, because I tried to take deep breaths.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: acid reflux, anxiety, IBS
Andere Medikamente: Citracal with Vit D, prilosec, saline solution, 24 hr Claritin
Allergien: Allergic to many antibiotics
Vorherige Impfungen: -

VAERS 2498720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

moderat

Staat: NV
Alter: 73,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 26.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Ageusia Anosmia Dyspnoea Nasal congestion Nasal inflammation Respiratory tract congestion Upper respiratory tract congestion

Symptomtext

loss of taste and smell; loss of taste and smell; he has difficulty breathing through his nose; inflammation in his nose; congestion in his nose; he has congestion in his chest and head; he has congestion in his chest and head; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 26Oct2022 as dose 4 (booster), single (Lot number: GH9697) at the age of 73 years for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (ongoing). Concomitant medication(s) included: AMLODIPINE oral taken for hypertension (ongoing); LOSARTAN oral taken for hypertension (ongoing). Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Anatomical Site of injection: left arm , Route of Administration: Intramuscular, Batch/Lot number: EL9267), administration date: 11Feb2021, when the patient was 71-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE, Anatomical Site of injection: left arm, Route of Administration: Intramuscular, Batch/Lot number: EN6205), administration date: 04Mar2021, when the patient was 71-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Anatomical Site of injection: left arm , Route of Administration: Intramuscular, Batch/Lot number: F31611), administration date: 24Nov2021, when the patient was 72-year-old, for COVID-19 Immunization. The following information was reported: UPPER RESPIRATORY TRACT CONGESTION (non-serious), RESPIRATORY TRACT CONGESTION (non-serious) all with onset Oct2022, outcome "unknown" and all described as "he has congestion in his chest and head"; NASAL CONGESTION (non-serious) with onset 28Oct2022 at 20:00, outcome "not recovered", described as "congestion in his nose"; DYSPNOEA (non-serious) with onset 30Oct2022, outcome "not recovered", described as "he has difficulty breathing through his nose"; NASAL INFLAMMATION (non-serious) with onset 30Oct2022, outcome "not recovered", described as "inflammation in his nose"; AGEUSIA (non-serious), ANOSMIA (non-serious) all with onset 30Oct2022, outcome "not recovered" and all described as "loss of taste and smell". Therapeutic measures were not taken as a result of nasal congestion, ageusia, anosmia, dyspnoea, nasal inflammation, upper respiratory tract congestion, respiratory tract congestion. Additional information: The reporter stated that he had difficulty breathing through his nose. Clarified as congestion in his nose, inflammation in his nose from using a tissue. he had congestion in his chest and head and loss of taste and smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high
Vorgeschichte: -
Andere Medikamente: AMLODIPINE; LOSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2493829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: AZ
Alter: 75,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Decreased appetite Dehydration Injection site bruising Injection site pain Injection site swelling Vomiting

Symptomtext

Site: Bruising at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: DEHYDRATION. LOSS OF APPETITE-Severe, Systemic: Vomiting-Severe

Weitere VAERSDATA-Felder

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

VAERS 2491447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: SD
Alter: 75,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Muscle spasms Tremor

Symptomtext

Resident had call light on, writer went into room and noted resident had tremors/body shakes. Resident stated that it started at about 11pm. No fever, no complaints of pain or feeling short of breath. Did go to hospital for evaluation. Came back from hospital early AM on 10/26/22; Got new orders from Dr prednisone 20 mg po BID x 3 days; Valium 2.50 mg po every 8 hours as needed for muscle spasms; Utilize prn tylenol order; Continue Baclofen and scheduled clonazepam; follow up with PCP in 1-2 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: No labs, had 25mg Benadryl, 650mg Tylenol, 10mg Valium and 40 mg Solimedrol at hospital 10/26/2022
Aktuelle Erkrankungen: Heart failure
Vorgeschichte: MS multiple sclerosis
Andere Medikamente: Calcium gummies multi vitamins
Allergien: Cyclobenzaprine, Flagyl, Sulfa antibiotics
Vorherige Impfungen: -

VAERS 2488891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: WI
Alter: 82,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 20.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Cellulitis Condition aggravated Fibrin D dimer Full blood count Metabolic function test Peripheral swelling

Symptomtext

developed cellulitis in his left arm. Had some pre-existing swelling he reports, but worsened two days after the vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: d-dimer, CBC, BMP 10/24/22
Aktuelle Erkrankungen: bullous pemphigoid
Vorgeschichte: CAD, HF, AF, arthritis, GAD
Andere Medikamente: amiodarone, atorvastatin, CoQ10, Dupixent, Eliquis, Lasix, Xalatan, methylphenidate, metoprolol, fish oil, MVI
Allergien: horse products
Vorherige Impfungen: -

VAERS 2481870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

moderat

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 15.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Asthenia Bone pain Chest pain Chills Dyspnoea Facial pain Headache Hypoaesthesia Mobility decreased Myalgia Nausea Peripheral coldness Renal pain

Symptomtext

Second vaccine listed (left arm) was a flu shot but I have no information on the type or lot #. Severe HA; Severe Weakness-could not get up out of bed from 8pm Sat until 10am Monday. Very bad chest pain; extremely short of breath without moving; pain felt in bones in muscles, including cheek bones; severe numbness in face and bone cold in extremities with hyper chills. Wanted to call the rescue squad but was too weak to get help. Nausea, no vomiting, severe pain in kidneys.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none, still waiting for doctor appointment
Aktuelle Erkrankungen: not verified by physician: chills with low fever x 2 weeks prior to vaccine
Vorgeschichte: SLE; RA; Liver Disease; HTN; Sjogren's; Obesity; Osteoporosis; Duodenal Hernia; high triglycerides; high uric acid
Andere Medikamente: Losartan 50mg x 1 tab every morning; Multivitamin x 1 every morning Ibuprofen 800 mg x 1 tab prn every 8 hours
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2724957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MN
Alter: 63,0
Geschlecht: M
Eingang: 18.12.2023
Impfdatum: 23.11.2022
Beginn: 16.12.2023
Tage bis Beginn: 388,0
Dosis: 5
Route/Site: IM / LA

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

Cough Oropharyngeal pain SARS-CoV-2 test Sinus disorder

Symptomtext

Cough, sinus problem, sore throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: IDNOW
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, hyperlipidemia, DM II
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2722795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MN
Alter: 86,0
Geschlecht: F
Eingang: 11.12.2023
Impfdatum: 02.11.2022
Beginn: 10.12.2023
Tage bis Beginn: 403,0
Dosis: 4
Route/Site: IM / LA

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

Chills Cough Malaise Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test

Symptomtext

General malaise, fevers/chills, congestion, rhinorrhea, cough

Weitere VAERSDATA-Felder

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

VAERS 2718036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MN
Alter: 90,0
Geschlecht: F
Eingang: 27.11.2023
Impfdatum: 18.11.2022
Beginn: 26.11.2023
Tage bis Beginn: 373,0
Dosis: 4
Route/Site: IM / LA

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

Fatigue

Symptomtext

Tired

Weitere VAERSDATA-Felder

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

VAERS 2658537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: MI
Alter: 31,0
Geschlecht: F
Eingang: 20.07.2023
Impfdatum: 21.10.2022
Beginn: 29.06.2023
Tage bis Beginn: 251,0
Dosis: 4
Route/Site: - / RA

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

Body temperature Headache Nasal congestion Pyrexia COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Headache; stuffy nose; low fever (38 C); This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Oct2022 at 17:00 as dose 4 (booster), single (Lot number: GH9697) at the age of 31 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Anxiety" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXIN; BUPROPIONE. Vaccination history included: BNT162b2 (DOSE 1, SINGLE at 03:00 PM, Batch/lot number: ER8730, Anatomical location: Right Arm), administration date: 26Mar2021, for COVID-19 immunisation; BNT162b2 (DOSE 2, SINGLE at 03:00 PM, Batch/lot number: EW0164, Anatomical location: Right Arm), administration date: 16Apr2021, for COVID-19 immunisation; BNT162b2 (DOSE 3 (BOOSTER), SINGLE at 03:00 PM, Batch/lot number: FG3527, Anatomical location: Right Arm), administration date: 24Nov2021, for COVID-19 immunisation. The following information was reported: HEADACHE (non-serious) with onset 29Jun2023 at 07:00, outcome "recovered"; PYREXIA (non-serious) with onset 29Jun2023 at 07:00, outcome "recovered", described as "low fever (38 C)"; NASAL CONGESTION (non-serious) with onset 29Jun2023 at 07:00, outcome "recovered", described as "stuffy nose". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of headache, nasal congestion, pyrexia. Clinical course: Patient denied for any other vaccine in four weeks. Patient denied for having covid prior to vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300253711 Same Patient/Product, Different Dose/Event (LOE);

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20230629; Test Name: Body Temperature; Result Unstructured Data: Test Result:38 Centigrade; Comments: at 07:00; low fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Hypothyroidism
Andere Medikamente: LEVOTHYROXIN; BUPROPIONE
Allergien: -
Vorherige Impfungen: -

VAERS 2646333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WI
Alter: 65,0
Geschlecht: F
Eingang: 16.06.2023
Impfdatum: 08.11.2022
Beginn: 02.06.2023
Tage bis Beginn: 206,0
Dosis: 5
Route/Site: IM / RA

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

Eye pruritus Hypersensitivity SARS-CoV-2 test negative Sinus headache Throat irritation

Symptomtext

I had an extremely itchy throat and sinus headache. I took a home COVID-19 test that came back negative, so I went to my doctor's office. Upon examination my doctor said he felt that it may be my seasonal allergies, he did prescribe an antibiotic just in case I was getting an infection. I am feeling better, I am experiencing some itchy eyes, but I believe that may be allergy related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pruritus
Hospital-Tage: -
Labordaten: 4JUN2023 Home COVID-19 test - negative
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes Type 2; Hypertension; Hyperlipidemia; Seasonal Allergies
Andere Medikamente: Metoprolol; Lisinopril; Simvastatin; Ozempic; Metformin; Calcium; Vitamin D; Vitamin C
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2644109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OH
Alter: 67,0
Geschlecht: M
Eingang: 12.06.2023
Impfdatum: 11.12.2022
Beginn: 09.05.2023
Tage bis Beginn: 149,0
Dosis: 5
Route/Site: IM / AR

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

Nasal congestion Nasopharyngitis Oropharyngeal pain Productive cough SARS-CoV-2 test negative

Symptomtext

5/9/23 I had an ordinary cold, stuffy sinuses and cough. I had an intense sore throat that lingered longer than normal. I had a productive cough that lasted for 3-4 weeks which is not common for me. I had an appointment with my doctor and was prescribed an antibiotic and steroids. This went away after I completed the two medications and now all is good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 9MAY23-At Home COVID Test-Negative; 11May23-At Home COVID Test-Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Benign Prostate Hypoplasia; High Cholesterol; High Blood Pressure' Skin Cancer
Andere Medikamente: Losartan; Simvastatin; Finasteride; Tamsulosin; Calcium/Vitamin D3; Multi-Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2629495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 25.04.2023
Beginn: 26.04.2023
Tage bis Beginn: 1,0
Dosis: 6
Route/Site: IM / LA

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

Pruritus

Symptomtext

Patient complained of full body itching but no rash present

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: diabetes (new?), hypothyroid, GI of some sort (omeprazole)
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2628487

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MN
Alter: 41,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 02.11.2022
Beginn: 18.04.2023
Tage bis Beginn: 167,0
Dosis: 5
Route/Site: IM / LA

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

Fatigue Herpes zoster Injection site erythema Pain in extremity

Symptomtext

I had a sore arm with some redness at the injection site for about a day. I also felt very tired too. I developed Shingles on 04/18/2023. I was a seven-day course of antibiotics. I am still healing but I do feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Mast Cell Activation; Ehlers Danlos Syndrome; Fibromyalgia; Chronic Spontaneous Urticaria; Endometriosis
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2624921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 31.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Chills Diplopia Dizziness Pain Pyrexia

Symptomtext

I had a fever, body aches and chills for about three days. In 11/2022, I started having dizziness and lightheaded at random times. In 02/2023, I also started having double vision. I have noticed it happens when I look at something in the distance. I have seen my ophthalmologist who to my primary care physician. Next doctor to see is a neurologist. On days that the symptoms start I stay home and just try to adjust. I previously tested positive for COVID-19 on 07/28/2022. I contacted a provider and got a prescription for Paxlovid. I tolerated the medication without any complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 28JUL2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Arthritis
Andere Medikamente: N/A
Allergien: Naproxen
Vorherige Impfungen: -

VAERS 2624852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 13.12.2022
Beginn: 01.04.2023
Tage bis Beginn: 109,0
Dosis: 5
Route/Site: IM / LA

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

Lymphadenopathy Pain in extremity

Symptomtext

I had a sore arm for a couple of days after receiving the vaccine. In 04/2023, I went to see my doctor about swollen lymph nodes in my right-side armpit and breast. I see my gynecologist in a couple of weeks to discuss the issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Factor 5 Leiden; Venus Inefficiency; Asthma; Migraines; Stroke
Andere Medikamente: ELIQUIS; atorvastatin; vitamin B; omega 3; low dose aspirin; coQ10; ZYRTEC
Allergien: Penicillin; KEFLEX; wheat; dairy
Vorherige Impfungen: -

VAERS 2624637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: TX
Alter: 55,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 03.11.2022
Beginn: 24.04.2023
Tage bis Beginn: 172,0
Dosis: 5
Route/Site: IM / LA

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

Fatigue Feeling abnormal Headache Oropharyngeal pain Pain SARS-CoV-2 test negative

Symptomtext

I was achy, headache, sore throat, very fatigued, felt puny, I tested for COVID-19 twice once with a home test, and once at the local urgent care with a PCR Rapid COVID -19 test. Both times it came back negative. I was advised to take Tylenol, get rest and retest if the symptoms got worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 24APR2023 PCR Rapid COVID-19 test negative; 24APR2023 Home COVID-19 test negative
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Provitalize; Previtalize; Multivitamin for Women 50 plus; Zyrtec
Allergien: Penicillin; Keflex
Vorherige Impfungen: -

VAERS 2624427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 64,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 30.10.2022
Beginn: 07.11.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Dysstasia Middle insomnia Retching Tinnitus Vertigo

Symptomtext

Exactly 7 days later in the middle of the night I awoke to find the room spinning so severely I was unable to stand. It was the first time ever that I had experienced Vertigo. As soon as it was light I called my neighbor who managed with difficulty to get me into her car and take me to the nearest clinic. I was retching the whole way from dizziness. Three days later after the symptoms had subsided somewhat, I developed tinnitus that had not been there before. It's a constant high pitched hissing and ringing, and to this day of my reporting this reaction is still going strong 24/7.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: The doctor in attendance the day I contracted Vertigo gave me a motion sickness medication, which I took for 2 days and stayed in bed. Although it has returned every few weeks, it has not been anything severe, mostly experienced in early morning and when turning over in bed.
Aktuelle Erkrankungen: None
Vorgeschichte: None.
Andere Medikamente: Since 2004 I have taken 15 mg non-time release generic adderall in the morning. Also take Vitamin D3.
Allergien: None
Vorherige Impfungen: -

VAERS 2622365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: AZ
Alter: 77,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 26.10.2022
Beginn: 15.04.2023
Tage bis Beginn: 171,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Decreased appetite Fatigue Increased viscosity of upper respiratory secretion Pain Pyrexia SARS-CoV-2 test positive Sinus congestion Sputum discoloured

Symptomtext

I had a long drive on that Friday, and I was thinking I was just tired from that drive but the next week i was having a fever all week, but I had a doctor's appointment, so I took a COVID-19 Home Test, and it was positive. I was so tired and achy with no appetite. My sinus' have been clogged and full of junk that is yellow and chunky, and I feel as if I may have a sinus infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Home Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic
Andere Medikamente: Simvastatin; Amlodipine; Losartan; Biotin; Vitamin E; Vitamin D; Vitamin B12; Zinc; Fish Oil; Baby Aspirin
Allergien: Codeine; Nabumetone
Vorherige Impfungen: -

VAERS 2622329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: AZ
Alter: 75,0
Geschlecht: M
Eingang: 27.04.2023
Impfdatum: 26.10.2022
Beginn: 23.04.2023
Tage bis Beginn: 179,0
Dosis: 5
Route/Site: IM / UN

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

COVID-19 Diarrhoea Influenza Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

On 4/13, I started having diarrhea and vomiting that lasted until about 4/15. On 4/16, I started having a fever about 100.8 with flu symptoms that evening. On the 4/18, I did a COVID-19 test which was negative. On 4/20, my fever broke. on 4/23, I tested again and it was positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At home rapid COVID-19 test- negative 4/18/2023; at home rapid COVID-19 test- positive 4/23/2023
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes
Andere Medikamente: Vitamin B12; Aspirin; Folic acid; Lovastatin; Flonase; Pantoprazole; Tamsulosin
Allergien: Oseltamivir
Vorherige Impfungen: -

VAERS 2621659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 22.10.2022
Beginn: 01.04.2023
Tage bis Beginn: 161,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Cough Diarrhoea Influenza A virus test negative Influenza B virus test Laboratory test normal Laryngitis Oropharyngeal pain Pyrexia Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

I woke up with a sore throat, laryngitis, a fever that went up to 103F, a cough, diarrhea. I went to a Clinic to get tested for COVID-19, RSV, Pneumonia, Influenza A and B all tests were negative except COVID-19. I was given a prescription for the antiviral Lagevrio, within 8 hours my fever started coming down. I tested negative on April 23, 2023, but I was feeling good within a week, the cough lingered it has gone now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 03APR2023 PCR Rapid COVID-19 test - positive; 23APR2023 PCR Rapid COVID-19 test - negative;
Aktuelle Erkrankungen: No
Vorgeschichte: Mineers Disease; Irritatable Bowel Disease: Hypertension
Andere Medikamente: Levothyroxine; Amlodipine; Valsartan; Hydrochlorothiazide; Vitamin D; Areds II; Dicyclomine
Allergien: Levaquin; Neosporin; Opioid sensitivity
Vorherige Impfungen: -

VAERS 2621657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: CO
Alter: 61,0
Geschlecht: M
Eingang: 26.04.2023
Impfdatum: 25.10.2022
Beginn: 15.03.2023
Tage bis Beginn: 141,0
Dosis: 5
Route/Site: SYR / UN

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

COVID-19 Decreased appetite Fatigue Headache Pain Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

I tested positive for Covid-19 on 03/15/2023. I experienced productive cough, fever, headaches, body aches, tiredness, loss of appetite.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Tylenol; Aspirin; Atorvastatin calcium; Cholecalciferol; Cyanocobalamin; Famotidine; Fluticasone; Glycerin; Motrin; Ipratropium; Lactobacillus; montelukast;
Allergien: N/A
Vorherige Impfungen: -

VAERS 2620126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: KS
Alter: 78,0
Geschlecht: M
Eingang: 24.04.2023
Impfdatum: 19.10.2022
Beginn: 08.02.2023
Tage bis Beginn: 112,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Fatigue Myalgia SARS-CoV-2 test positive

Symptomtext

On 2/8/2023, I began to feel very tired and have muscle aches. The symptoms worsened throughout the day, so I decided to go to the doctor on 2/9/2023. I underwent a PCR test and got a positive result. The doctor prescribed me Paxlovid, which I began taking that afternoon. I began to feel better pretty quickly. I isolated for either ten days or two weeks. I never developed any other symptoms besides the muscle aches and fatigue, and I had those only maybe two or three days. After I recovered, I felt fine and didn't have any residual symptoms. In fact, after the first two or three days, I felt well enough to go outside and walk for exercise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09FEB2023 - PCR Test - Positive Result
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Allopurinol; Valsartan; Testosterone Gel; Multivitamin; Iron; Loratadine; Glucosamine Chondroitin; Fish Oil; Vitamin C; Tamsulosin; Finasteride
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2618970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OK
Alter: 36,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 20.10.2022
Beginn: 21.03.2023
Tage bis Beginn: 152,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chills Exposure during pregnancy Exposure to SARS-CoV-2 Fatigue Malaise Nasopharyngitis Pain Premature delivery Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

3/21/23 I had been exposed to COVID. I began having a scratchy throat and I took an at home COVID Test that was negative. I called my doctor, they said to let it run its course. On 3/22/23, I had full body aches, chills, general aches that hurt everywhere and a fever that I had trouble controlling. My rapid COVID test was positive. I called the doctor back and told me the parameters to go to the Emergency Room if my fever got too high. From 3/21/23 ? 3/28-23 I had general cold symptoms, congestion, fatigue and did not feel well. I also had a lingering positive COVID test. My delivery date was at 38 weeks. No complications. The baby?s birthweight was 7lb12oz.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 21MAR23-At Home COVID Test-Negative; 22MAR23-At Home COVID Test-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, Post donating a Kidney
Andere Medikamente: Prenatal Vitamins, Zyrtec, Chlorpheniramine, Vitamin B12, Calcium-Magnesium-Zinc, Flonase, Flovent, Low dose Aspirin
Allergien: Sulfa Drugs , Cats, Dogs, All trees , Pollen
Vorherige Impfungen: -

VAERS 2618510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: AZ
Alter: 79,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Pain in extremity Tenderness

Symptomtext

Left leg had 24 hours where it was tender, then 24 hours later it was the right leg the wed pain got worse

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Atriophibulation: Mild Asthma: Gerd: Mild High Blood pressure
Andere Medikamente: Levothyroxin: Omeprisole: Losartin HCTZ: Notroprolol: Atorvastatin: Warfrin: Potasium: Calcium: Colace: Famotidine
Allergien: Micostatin: Nut aleergy
Vorherige Impfungen: -

VAERS 2616881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: CO
Alter: 67,0
Geschlecht: M
Eingang: 18.04.2023
Impfdatum: 26.11.2022
Beginn: 01.03.2023
Tage bis Beginn: 95,0
Dosis: 5
Route/Site: IM / RL

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

COVID-19 Pain in extremity SARS-CoV-2 test positive

Symptomtext

I had minor soreness in my arm for about a day. I tested positive for COVID-19 in 03/2023. I contacted my doctor and got a prescription for Paxlovid. I tolerated the medication without any complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: 13OCT2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Prostate Cancer
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2616856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: AZ
Alter: 75,0
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 17.10.2022
Beginn: 19.01.2023
Tage bis Beginn: 94,0
Dosis: 5
Route/Site: IM / LA

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

Arthralgia COVID-19 Headache SARS-CoV-2 test positive

Symptomtext

Started having a headache, joint pain in pelvis and legs. Took a home COVID-19 test and was positive. Contacted doctor and was prescribed Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 19JAN2023 Home COVID-19 test - Positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure.
Andere Medikamente: Levothyroxine; Lisinopril; Folic Acid; Vitamin B12; Vitamin B6; Glucosamine Chondroitin; Primrose Oil; Bone Up Vitamin Enhancement; Fish Oil; Estrogen Ring.
Allergien: Gluten; Lactose Intolerance
Vorherige Impfungen: -

VAERS 2616736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VT
Alter: 62,0
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 17.10.2022
Beginn: 21.03.2023
Tage bis Beginn: 155,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Discomfort Fatigue Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing Vomiting

Symptomtext

Tested positive for Covid-19 at home. Treated with cough medicine occasionally. Symptoms: Fever first 5 days; vomiting first 2 days; coughing 3 weeks; fatigue: heavy first 5 days, gradually decreasing over next 2 weeks; mild sneezing/runny nose/congestion 5 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Tested positive at home on 3/22/2023, 3/27/2023. Tested negative at home on 3/29/2023.
Aktuelle Erkrankungen: none
Vorgeschichte: mild seasonal allergies
Andere Medikamente: Alendronate, multivitamins
Allergien: none
Vorherige Impfungen: -

VAERS 2616292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NY
Alter: 59,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 13.10.2022
Beginn: 31.01.2023
Tage bis Beginn: 110,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Headache Malaise Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 1/31/23. I had very mild symptoms. I had a headache, congestion, and some body aches. I contacted my doctor and was prescribed PAXLOVID. I felt better after taking PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 31JAN2023 COVID-19 test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Prediabetic; History of AFIB; High Blood Pressure; Asthma
Andere Medikamente: Metoprolol; metformin; fenofibrate; lovastatin; ELIQUIS; multivitamin; vitamin D
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2615330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: FL
Alter: 77,0
Geschlecht: M
Eingang: 14.04.2023
Impfdatum: 11.10.2022
Beginn: 07.01.2023
Tage bis Beginn: 88,0
Dosis: 5
Route/Site: SYR / LA

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

Bladder catheter removal Bladder catheter replacement Bladder catheterisation Bladder hypertrophy Bladder neoplasm Bladder polypectomy Chills Cholelithiasis Computerised tomogram abdomen abnormal Cystoscopy abnormal Discomfort Dysuria Transurethral bladder resection Urinary bladder polyp Urinary retention Urothelial papilloma

Symptomtext

Around 11:00PM, I went to urinate, but I had a blockage and couldn't urinate. I tried several times with no success. It became somewhat painful. I called 911, and they sent an ambulance. The ambulance took me to the emergency room. They put in a catheter and sent me home. Three days later, I went to my Urologist. He removed the catheter and performed a Cystoscopy. He found a polyp in my bladder. I had outpatient surgery to remove the polyp. At that point, I received a pathology report that diagnosed a bladder tumor. They put in another catheter after the surgery. I had some discomfort and chills. The doctor sent me to get at CT scan of the abdomen and pelvis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 01/04/2023 Cystoscopy - Bladder Polyp; 01/31/2023 Transurethral Resection of Bladder Tumor - Bladder Tumor and Left Trigone, Turbt: Atypical Urothelial Proliferation; 02/03/2023 CT Scan Abdomen and Pelvis - No evidence for Urolithiasis, Hydronephrosis, Mesenteric and Periaortic Adenopathy, Chronic Appearing Pre Referral Interstitial Thickening, and Uncomplicated Cholelithiasis
Aktuelle Erkrankungen: Prostate Radiation Discitis
Vorgeschichte: Sleep Apnea; Double Bypass Surgery (2012); Chronic Lymphocytic Leukemia
Andere Medikamente: Rosuvastatin; Mirtazapine; Oxybutynin; Metoprolol Tartrate; Rabeprazole; Flecainide Acetate; Tamsulosin; Sertraline; Vitamin D3; Vitamin C; CoQ10
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 2613972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 72,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 11.10.2022
Beginn: 31.01.2023
Tage bis Beginn: 112,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Chills Nasal congestion Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started having a sore throat and nasal congestion, runny nose on January 31. The sore throat was upon me waking up and on February 3 I started having a low-grade fever and chills. Prior to that I did a COVID-19 test and I was negative. On February 4, I tested again, and I was positive for COVID-19. The test I did at home was flow flex and then I was given PAXLOVID which did help. On February 11 I tested again, and I was negative. I feel like my COVID-19 case was very mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Low Thyroid; Hypertension Controlled under medication
Andere Medikamente: Loratadine; atorvastatin; cholecalciferol; estradiol vaginal tablet; estradiol cream; fluticasone propionate; levothyroxine; lisinopril; nitrofurantoin; omeprazole; potassium chloride; triamterene-hydrochlorothiazide; ADVOCARE
Allergien: CECLOR
Vorherige Impfungen: -

VAERS 2613026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OR
Alter: 64,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 08.10.2022
Beginn: 28.02.2023
Tage bis Beginn: 143,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

02/28/2023 I started having a fever, cough, headache, and sore throat. After reaching out to my doctor I was diagnosed with Covid-19. I was prescribed PAXLOVID. Symptoms lasted 10 days with ongoing cough and fatigue as results from Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD
Andere Medikamente: Levothyroxine; multivitamin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2612604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 28.10.2022
Beginn: 20.11.2022
Tage bis Beginn: 23,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Fatigue Oropharyngeal pain Pain Respiratory tract congestion SARS-CoV-2 test positive Sneezing

Symptomtext

I had a sore throat, sneezing, fatigue, body aches, and congestion. I tested positive for COVID-19 test, then I went to an urgent care. They prescribed me prednisone and nasal spray. The fatigue and body aches lasted for a couple of weeks. I still have a little fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 11/21/2022, COVID-19 test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: Losartan; low dose aspirin; fenofibrate; amlodipine; atorvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2612427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 63,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 18.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Acupuncture Arthralgia Massage

Symptomtext

10/25/22 I started having joint pain in both shoulders. I thought I had torn a rotator cuff. On my left arm, at my elbow, it felt like tendinitis. Over the following month, I had joint pain in both hips and knees. No medication, massage or acupuncture would resolve the pain. A couple of weeks ago, it finally lifted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure, High Cholesterol
Andere Medikamente: Liothyronine, Amlodipine, Atorvastatin, COQ10
Allergien: None
Vorherige Impfungen: -

VAERS 2612322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 12.10.2022
Beginn: 28.11.2022
Tage bis Beginn: 47,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Dysphonia Impaired work ability Malaise Nasal congestion Oropharyngeal pain Pyrexia Respiratory symptom SARS-CoV-2 test positive

Symptomtext

I developed upper respiratory symptoms (sore throat, nasal congestion, cough, fever, and hoarseness) on 11/28/2022. I took a home antigen test and got a positive result. I then called my doctor, who had me come in the next morning for a COVID-19 test, which was also positive. She then prescribed Paxlovid, which I took. Things went poorly, because I became sicker and sicker. I went to urgent care maybe a week later, and I was prescribed two inhalers (albuterol and Flovent), Tessalon Perles, and loratadine. I was also advised to take OTC Mucinex DM. I was too sick to go to work for two more weeks afterwards. I was finally able to return to work the week of 12/19/2022. I feel that I have recovered from the COVID-19 symptoms, but I still have intermittent hoarseness. I feel that I actually damaged my vocal cords, but the hoarseness continues to improve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 28NOV2022 - Home Antigen Test - Positive Result; 29NOV2022 - Clinical Rapid Antigen Test(?) - Positive Result
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Type II; Hypertension
Andere Medikamente: Regular Insulin; Lantus; Victoza; Anastrozole; Atenolol; Atorvastatin; Hydroxychloroquine; Losartan; Trazodone; Vitamin B12; Calcium; Vitamin D
Allergien: Ranitidine
Vorherige Impfungen: -

VAERS 2610851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: AZ
Alter: 75,0
Geschlecht: M
Eingang: 06.04.2023
Impfdatum: 04.11.2022
Beginn: 05.03.2023
Tage bis Beginn: 121,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I was positive for COVID-19 on 05MAR2023, I was having a terrible cough I couldn't get rid off. A little bit of sore throat, low grade fever. At that time I had available test kit and I tested and it was positive, after I took the test I called my doctor and she had me pick up Paxlovid. I started taking it right away, I started feeling better about 3 days after. I feel a lot better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 05MAR2023 COVID-19- Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2607457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NM
Alter: 52,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 18.10.2022
Beginn: 26.03.2023
Tage bis Beginn: 159,0
Dosis: 4
Route/Site: IM / -

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

Myalgia Urinary tract infection

Symptomtext

Muscle aches in left calf and urinary tract infections.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: VAGIFEM; meclizine; diclofenac
Allergien: Amoxicillin; mollusks not shellfish
Vorherige Impfungen: -

VAERS 2606064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: GA
Alter: 72,0
Geschlecht: M
Eingang: 29.03.2023
Impfdatum: 22.09.2022
Beginn: 02.02.2023
Tage bis Beginn: 133,0
Dosis: 5
Route/Site: IM / AR

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

Ageusia Body temperature increased COVID-19 Chills Dysgeusia Feeling abnormal Insomnia Oropharyngeal pain Productive cough SARS-CoV-2 test positive

Symptomtext

The first thing I felt was a bit of a sore throat. That night I got no sleep. The next day I felt awful most of the day. I thought it might be allergies. On Saturday I felt awful and test for COVID-19 and it was positive. I started shivering. My temperature was 102.5 degrees. I was coughing and coughing stuff up. I called my doctor office and he called in Molnupiravir and I began taking it the same day. I started with a weird taste and then I started to lose my taste. After taking the medication, I started to feel better within a couple days. After testing negative on the 9th, on the 15th I had a rebound and tested positive again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 04FEB2023 - COVID-19 At Home Test - Positive; 09FEB2023 - COVID-19 At Home Test - Negative; 15FEB2023 - COVID-19 At Home Test - Positive; 19FEB2023 - COVID-19 At Home Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; Type II Diabetes; Hypothyroid; High Blood Pressure
Andere Medikamente: Metformin; Atorvastatin; Synthroid; Pantoprazole; Spironolactone; Ezetimibe; Losartan; Metoprolol; Xarelto; Ozempic; Low Dose Aspirin; Multivitamin; Metamucil
Allergien: N/A
Vorherige Impfungen: Possibly to a Flu Vaccine several years ago that I got a rash but have not had any adverse events to Flu Vaccines since.

VAERS 2606005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: PA
Alter: 65,0
Geschlecht: F
Eingang: 29.03.2023
Impfdatum: 27.09.2022
Beginn: 06.02.2023
Tage bis Beginn: 132,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Malaise Pyrexia SARS-CoV-2 test positive Sluggishness

Symptomtext

For two days, I felt a little sluggish and sick. I had high fever for one day before testing positive for COVID-19 on February 7, 2023. It was around 101-degrees. I was fine the rest of the week. On day four of Paxlovid, I had a fever again. It was also around 101-degrees. Afterwards, I was fine. I stopped taking Colchicine on February 5, 2023. My husband tested positive for COVID-19, and I knew I would probably test positive, too.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 02/07/2023 At Home COVID-19 Test - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Familial Mediterranean Fever; Prediabetes; Hypertension
Andere Medikamente: Ilaris; Prolia; Colchicine; Losartan; Chlorthalidone; Vitamin D; Vitamin C
Allergien: Penicillin; Reclast
Vorherige Impfungen: -

VAERS 2599491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: MD
Alter: 66,0
Geschlecht: F
Eingang: 20.03.2023
Impfdatum: 04.11.2022
Beginn: 25.11.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: SYR / RA

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

Headache Photophobia Visual impairment

Symptomtext

On 11/04/2022 I received my Covid-19 vaccine. On 11/25/2022 I started having severs headaches visual issues and sensitivity to light. I am following up with my neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Rheumatoid arthritis; Migraines
Andere Medikamente: Risedronate SOD; Estradiol vaginal inserts; Rinvoq; Solifenacin; COQ10; Mag Tabs; Calcium; B12;
Allergien: N/A
Vorherige Impfungen: -

VAERS 2598604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VA
Alter: 74,0
Geschlecht: M
Eingang: 17.03.2023
Impfdatum: 15.09.2022
Beginn: 01.01.2023
Tage bis Beginn: 108,0
Dosis: 5
Route/Site: IM / LA

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

Blood pressure decreased COVID-19 Cough Diarrhoea Fatigue Malaise SARS-CoV-2 test positive Weight decreased

Symptomtext

I just wasn't feeling well, very tired, no fever, my blood pressure went down a little diarrhea. I used a home COVID-19 test that came back positive, I called my doctor, discussed my symptoms. He suggested the PAXLOVID, but with not being sure of when my symptoms really started, I decided against taking it. I did have a little coughing, that started during my five-day quarantine. I came of my blood pressure med as my blood pressure was low, I lost weight. I am recovered and feel much better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 00JAN2023 home COVID-19 positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: HUMIRA; levothyroxine; DAYVIGO; DIOVAN
Allergien: No
Vorherige Impfungen: -

VAERS 2596995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IL
Alter: 53,0
Geschlecht: F
Eingang: 15.03.2023
Impfdatum: 12.11.2022
Beginn: 20.02.2023
Tage bis Beginn: 100,0
Dosis: 4
Route/Site: SYR / LA

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

Blood test normal Diarrhoea Differential white blood cell count normal Full blood count normal Metabolic function test normal Nausea SARS-CoV-2 test

Symptomtext

I've had unexplained nausea and diarrhea periodically. It started before this vaccine, but this last episode lasted three days. The nausea lasted on and off for about two weeks. They had me take a COVID-19 test. Their machine was broken, and I did not get the results. They also did blood work. The results were normal. I was taking IMODIUM AD. They prescribed TESSALON and ZOFRAN-OBT. I took both three times a day for seven days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 02/21/2023 COVID-19 test results unavailable; 02/21/2023 Comprehensive Metabolic Panel, normal; 02/21/2023 CBC with differential, normal
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine
Allergien: Penicillin; codeine; PHENERGAN; walnuts; pecans
Vorherige Impfungen: 03/12/2022 COVID-19 Pfizer dose 3, Lot FK9895: Age 53, I've had unexplained nausea and diarrhea periodically.

VAERS 2596167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WI
Alter: 85,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 13.10.2022
Beginn: 25.12.2022
Tage bis Beginn: 73,0
Dosis: 5
Route/Site: UN / -

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

COVID-19 Chills Diarrhoea SARS-CoV-2 test positive

Symptomtext

Patient is fully vaccinated, boosted, and up to date on COVID-19 vaccinations. He was admitted to the hospital for treatment of COVID-19 on 12/25/2022. His onset of symptoms was on 12/24/2022 with chills and diarrhea. He tested positive for COVID-19 on 12/25/2022 at the hospital. No treatment information was provided. Submitter does not have access to further medical information on this case. If more information is needed, please contact the admitting hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Positive COVID NAA test on 12/25/2022
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hypertension
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2591864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IN
Alter: 74,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 21.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 9,0
Dosis: N/A
Route/Site: IM / RA

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

Anticoagulant therapy Asthenopia Burning sensation Pruritus Retinal artery occlusion Sensation of foreign body Vision blurred

Symptomtext

Pt developed right eye symptoms including blurred vision, itching/burning, and foreign body sensation on 10/30/22. She saw her optometrist on 11/2/22 and an inferior branch retinal artery occlusion of the right eye was diagnosed. ASA 81 mg daily was restarted at that time (pt had previously taken daily ASA but PCP had discontinued it at her annual wellness visit of 10/17/22). Pt returned to the optometrist for follow up on 12/13/22 and was still having blurred vision and a feeling of heaviness in the right eye and optometrist wrote in the visit note that the vision change was likely to be permanent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: OCT and exam done on 11/2/22. Bilateral carotid ultrasound ordered on 1/31/23 and is scheduled on 3/13/23.
Aktuelle Erkrankungen: none known
Vorgeschichte: HTN, CKD 3b, HLD, elevated Hgb A1c, left BBB, osteoarthritis, hx of endometrial Ca, hx posterior vitreous detachment
Andere Medikamente: Medication list as of 10/21/22: Lisinopril-HCTZ 20-12.5 mg: one tablet PO daily. Simvastatin 20 mg: one tablet PO nightly. Nifedipine ER 30 mg: one tablet PO daily. Fexofenadine 180 mg: one tablet PO daily. Clobetasol 0.05% cream: one appl
Allergien: poison ivy extract
Vorherige Impfungen: -

VAERS 2590926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 03.03.2023
Impfdatum: 28.01.2023
Beginn: 04.02.2023
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: IM / LA

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

Myalgia

Symptomtext

Pt came in about 11 days after the shot had been received complaining of significant muscle pain.

Weitere VAERSDATA-Felder

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

VAERS 2585314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: FL
Alter: 42,0
Geschlecht: M
Eingang: 22.02.2023
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Lip oedema Rash Urticaria

Symptomtext

my waist line and inside thighs in my groin area/extremely itchy and painful; A few weeks later my bottom lip blew up; urticaria/clear visible lumps; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Dec2022 at 17:45 as dose 4 (booster), single (Lot number: GH9697) at the age of 42 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "I had COVID-19 in Jun2022", start date: Jun2022 (unspecified if ongoing), notes: if covid prior vaccination: Yes, Patient had COVID-19 in Jun2022; "Kidney stone" (unspecified if ongoing); "Surgery on left knee (ACL reconstruction Plus meniscus repair)" (unspecified if ongoing), notes: Surgery on left knee (ACL reconstruction Plus meniscus repair); "Surgery on left knee (ACL reconstruction Plus meniscus repair)" (unspecified if ongoing), notes: Surgery on left knee (ACL reconstruction Plus meniscus repair); "high cholesterol" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose number: 3,, Lot number: FL3197,, Administration time: 06:15 PM,, Vaccine location: Left arm,), administration date: 13Jan2022, when the patient was 41-year-old, for COVID-19 Immunization; 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: LIP OEDEMA (disability) with onset 01Dec2022 at 19:00, outcome "recovering", described as "A few weeks later my bottom lip blew up"; RASH (disability) with onset 01Dec2022 at 19:00, outcome "recovering", described as "my waist line and inside thighs in my groin area/extremely itchy and painful"; URTICARIA (disability) with onset 01Dec2022 at 19:00, outcome "recovering", described as "urticaria/clear visible lumps". The events "my waist line and inside thighs in my groin area/extremely itchy and painful", "a few weeks later my bottom lip blew up" and "urticaria/clear visible lumps" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of rash, lip oedema, urticaria. Clinical course: Facility type vaccine was pharmacy or Drug Store. No other vaccine in fourweeks. Other medications in twoweeks no Just vitamins (multivitamin, ginko biloba). 2 hours after receiving the booster, patient had a severe rash on his waist line and inside thighs in his groin area. It was extremely itchy and painful with clear visible lumps (patient have pictures). Since then, patient continue to have this rash. almost daily. A few weeks later his bottom lip blew up as if he had an anaphylactic reaction and waited outside ER because patient was able to breathe. Patient went to urgent care and the APRN told him patient have urticaria and prescribed steroids. Since then, patient told his family doctor and patient taking 2 benadryl and applying calamine lotion whenever the rash occurs which was typically after dinner or after work around 5 pm daily. The urticaria was now moving to different locations on his body including his arm pit and penis now. Patient can't leave home without having benadryl and calamine lotion with him. Patient received treatment as Methylprednisone, daily Benadryl, calamine lotio. Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Disability or permanent damage. Covid prior vaccination was yes. Covid tested post vaccination no. Known allergies were not that patient was aware of. Patient was going to see an allergist in Feb. Patient had COVID-19 in Jun2022. Kidney stone. Surgery on left knee (ACL reconstruction plus meniscus repair), high cholesterol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anterior cruciate ligament reconstruction (Surgery on left knee (ACL reconstruction Plus meniscus repair)); COVID-19 (if covid prior vaccination: Yes, Patient had COVID-19 in Jun2022); High cholesterol; Kidney stone; Meniscus operation (Surgery on left knee (ACL reconstruction Plus meniscus repair))
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2584281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 03.12.2022
Beginn: 03.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Dermatitis Erythema Rash Rash macular Skin exfoliation Skin swelling Urticaria

Symptomtext

Body rash. Red, painful welts on abdomen, some welts on back with a spotted rash over entire back. Took Benadryl and used Cortizone-10 cream. Rash subsided but scaled and peeled. Since the December Vaccine different areas of the body, elbows, waste-line, portions of back, eyelids become red, inflamed and swollen, then scaly and peel. Dermatologist prescribed Pimecrolimus but it caused burning and increased irritation. Second cream prescribed Flucticasone Propionate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Bicuspid aortic valve, Stage One Melanoma approximately 8 years ago, Subglottic stenosis,
Andere Medikamente: None
Allergien: Antibiotics with sulfides, codeine
Vorherige Impfungen: Mild rash after Pfeizer shots 3 and 4

VAERS 2583357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: FL
Alter: -
Geschlecht: M
Eingang: 17.02.2023
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

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

Lip swelling Rash Urticaria

Symptomtext

Severe rash 2 hours after getting the Pfizer-BioNTech booster around my waist line and inner groin areas. I have now been diagnosed with Urticaria. I have the rashes almost daily now. The rash is now migrating across my body. I now have the rash at my arm pit, buttocks, testicles, and penis in addition to my waist line and other areas. I take 2 benadryl and apply calamine lotion to the affected areas as required. The rash subsides after 1 hr after taking benadryl an applying calamine lotion. In January, my right lower lip blew up as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: High cholesterol. Vitamin D deficiency.
Andere Medikamente: Now using 2x benadryl antihistamine when spontaneous urticaria occurs. Now started taking natire's bounty 1000 IU vitamin D, men's one-a-day multivitamin, nature's bounty apple cider vinegar
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2578958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NV
Alter: 51,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Chills Fatigue Injection site erythema Injection site pain Injection site swelling Injection site warmth Loss of personal independence in daily activities Myositis Pain in extremity Peripheral swelling Somnolence Tendonitis

Symptomtext

3-4 hours later I started to feel the pain at the injection site and chills on my all my body. I had to put on two blankets, two pajamas, and turn the heater on. All night long I had pain at the injection site but more pain. The next day in the morning I looked at the injection site and I had bump, redness, and hot at the injection site. I still felt chills. I felt really sleepy. All my body really tired. I could feel a pain in all of my joints. I was like that for two days at the beginning. After about two days, I felt my hand really rare and a lot of pain. I tried to open the milk and bottled water but I couldn't it was really painful. I had to ask my husband for help. I had pain on my whole body like that with pain for a couple days. The chills I had about 4 days. Later, I still feel my hands in constant pain. I wear compression socks because I walk too much at my job but I couldn't put them on. My husband had to put them on me. When I was working I bought compression gloves after that I still had the same pain for 24 hours a day on my hands. Every morning my hands felt swollen. I have a hard time working to pull, to carry, to grab. On November 12, 2022, I decided to go to the doctor. They told me to do ice pack, hot pack, elevate hands, and for pain to take TYLENOL but nothing worked. I tried putting arthritis ointment for pain. I went back to doctor on December 22nd, 2022 and they gave me prednisone for two weeks. The doctor told me I had muscular inflammation and tendonitis in both wrists. The medication helped but when I finished taking it the pain came back again. I have an upcoming appointment on February 22, 2023 with my doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: HX of back surgery; HX of Gall Bladder Removal; HX of Hysterectomy
Andere Medikamente: Metoprolol; omeprazole
Allergien: Acyclovir; citrus
Vorherige Impfungen: -

VAERS 2575200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: SC
Alter: 72,0
Geschlecht: M
Eingang: 03.02.2023
Impfdatum: 22.10.2022
Beginn: 18.12.2022
Tage bis Beginn: 57,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Cough Malaise Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I did not have an adverse event after receiving the vaccine. I began not feeling well on 12/18/2022, I had a runny nose, sore throat and a cough. I tested positive for COVID-19 on 12/19/2022. I contacted my nurse practitioner and I got a prescription for PAXLOVID. I tolerated the medication with no problem.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 19DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes; Coronary Artery Disease
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2574186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: GA
Alter: 44,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 02.11.2022
Beginn: 27.12.2022
Tage bis Beginn: 55,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Inflammation Malaise Pain SARS-CoV-2 test positive

Symptomtext

I was sick for one day after receiving the vaccine with body aches. I began not feeling well on 12/26/2022 with a cough. I tested positive for COVID-19 on 12/27/2022. I never went to the doctor, so I took over the counter medication to relieve my symptoms. I tested positive for fourteen days. I did go to the doctor because my cough was so bad, I got a steroid prescription. As of today, I still have inflammation and coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 27DEC2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid; Prozac
Allergien: Methimazole; Hyoscyamine
Vorherige Impfungen: -

VAERS 2572772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: WA
Alter: 69,0
Geschlecht: M
Eingang: 01.02.2023
Impfdatum: 05.10.2022
Beginn: 05.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Bursitis Gait disturbance Joint range of motion decreased Joint swelling Musculoskeletal pain Musculoskeletal stiffness Myalgia SARS-CoV-2 test Wrong product administered

Symptomtext

sudden onset of arthralgias in myalgias, hips, quadriceps; sudden onset of arthralgias in myalgias, hips, quadriceps; sudden onset of arthralgias in myalgias, hips, quadriceps; acutely swollen bursitis of the left knee; acutely swollen bursitis of the left knee; progressive difficulty ambulating; more than 100 200 yards morning stiffness unable to bend or get up from chairwithout two hands; more than 100 200 yards morning stiffness unable to bend or get up from chairwithout two hands; Pfizer bioNTech Bivalent/Dose Number: 1; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 69-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Oct2022 at 12:00 as dose 1 (bivalent), single (Lot number: GH9697) at the age of 69 years, in left arm for covid-19 immunisation. The patient didn't receive BNT162b2 (BNT162B2). The patient's relevant medical history included: "Peripheral neuropathy feet" (unspecified if ongoing), notes: Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired; "GERD" (unspecified if ongoing), notes: Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired; "traumatic injury to aorta" (unspecified if ongoing), notes: Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired; "heart repaired" (unspecified if ongoing), notes: Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired. Concomitant medication(s) included: BABY ASPIRIN; GABAPENTIN. Past drug history included: Tcy, reaction(s): "Known allergies: Tcy". The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 05Oct2022 at 12:00, outcome "unknown", described as "Pfizer bioNTech Bivalent/Dose Number: 1"; JOINT SWELLING (disability), BURSITIS (disability) all with onset 19Oct2022 at 07:00, outcome "recovered with sequelae" and all described as "acutely swollen bursitis of the left knee"; MUSCULOSKELETAL STIFFNESS (disability), JOINT RANGE OF MOTION DECREASED (disability) all with onset 19Oct2022 at 07:00, outcome "recovered with sequelae" and all described as "more than 100 200 yards morning stiffness unable to bend or get up from chairwithout two hands"; GAIT DISTURBANCE (disability) with onset 19Oct2022 at 07:00, outcome "recovered with sequelae", described as "progressive difficulty ambulating"; MUSCULOSKELETAL PAIN (disability), ARTHRALGIA (disability), MYALGIA (disability) all with onset 19Oct2022 at 07:00, outcome "recovered with sequelae" and all described as "sudden onset of arthralgias in myalgias, hips, quadriceps". The events "sudden onset of arthralgias in myalgias, hips, quadriceps", "acutely swollen bursitis of the left knee", "progressive difficulty ambulating" and "more than 100 200 yards morning stiffness unable to bend or get up from chairwithout two hands" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Oct2022) Unknown Result. Therapeutic measures were taken as a result of musculoskeletal pain, arthralgia, myalgia, joint swelling, bursitis, gait disturbance, musculoskeletal stiffness, joint range of motion decreased. Clinical courses is as follows: The patient didn't receive other vaccine in four weeks. No new medication's baby aspirin gabapentin hundre in two weeks. Two week status post immunization, sudden onset of arthralgias in myalgias, hips, quadriceps and acutely swollen bursitis of the left knee, progressive difficulty ambulating, more than 100 200 yards morning stiffness unable to bend or get up from chair without two hands. Scene by orthopedics, physiatry and family medicine. Finally Rheumatology who advised me yesterday it was due to the immunization. The events resulted in: Doctor or other healthcare professional office/clinic visit, Disability or permanent damage. The patient received treatment Prednisone 20 mg a day.; Sender's Comments: Based on the information provided, a causal relationship between the suspected drug and the reported events cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20221019; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown Result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD (Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired); Heart disorder (Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired); Injury to thoracic aorta (Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired); Peripheral neuropathy (Peripheral neuropathy, feet gerd traumatic injury to aorta and heart repaired)
Andere Medikamente: BABY ASPIRIN; GABAPENTIN
Allergien: -
Vorherige Impfungen: -

VAERS 2572204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: PA
Alter: 39,0
Geschlecht: M
Eingang: 31.01.2023
Impfdatum: 29.10.2022
Beginn: 10.01.2023
Tage bis Beginn: 73,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Headache Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I received my Covid-19 vaccine on 10/29/2022. On 01/10/I tested positive for Covid-19. I started getting a headache, sore throat and congestion. Symptoms were mild. Symptoms lasted about 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Covid-19
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma High cholesterol; Lichen Lanus
Andere Medikamente: FLOVENT; sertraline; rosuvastatin; hydroxyzine; budesonide; folate; melatonin; albuterol; ZADITOR; medical cannabis
Allergien: CECLOR; penicillin; GANTRISIN
Vorherige Impfungen: Moderna Covid-19 vaccine 2nd dose 04/17/2021; headache; age 38; headache

VAERS 2570573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: TX
Alter: 55,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 26.10.2022
Beginn: 20.12.2022
Tage bis Beginn: 55,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia COVID-19 Influenza virus test positive Pyrexia SARS-CoV-2 test positive Streptococcus test positive Throat irritation

Symptomtext

I was having a scratchy throat, so I took a COVID-19 Home Test, and it was negative. The next day I woke up with slight fever of 100.8 took Tylenol and called my PCP but they wanted to do a virtual appointment, so I went to an urgent care. The urgent care did not test for COVID-19 but did for influenza and strep and both were negative, so they sent me home with amoxicillin and an antibiotic shot. I took a nap and woke up and by that night I had a fever of 104. I had my husband bring me some soup and I could not taste it, so I had him bring me a test and I took a home test again and it was positive, I called my doctor's office back and the clinic back where I was seen and then i went to the ER. They tested again for flu, strep, and COVID and it was positive. They gave me a breathing treatment, ibuprofen and an inhaler to take home and then sent me home. On the 22nd I called to my PCP they put me on Paxlovid. My husband and son ended up positive for COVID-19 as well. I finally tested negative on December 26th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: COVID-19 Home Test; Influenza Test; Strep Test; COVID-19 PCR
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism; Osteoporosis; Vitamin D Deficiency
Andere Medikamente: Levothyroxine; Vitamin B12; Vitamin D3; Pantoprazole; Ozempic
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2569695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: GA
Alter: 60,0
Geschlecht: F
Eingang: 27.01.2023
Impfdatum: 11.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 82,0
Dosis: 5
Route/Site: IM / UN

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

COVID-19 Cough Decreased appetite Feeling of body temperature change Nasopharyngitis Pain Productive cough Respiratory tract congestion SARS-CoV-2 test positive Symptom recurrence

Symptomtext

I had a bad head cold. I had phlegm, hot, cold, body ache, and loss appetite. I tested positive for COVID-19 and my doctor prescribed me PAXLOVID. I tested negative for COVID-19 01/09/2023 and I ended up tested positive again on Wednesday. I had the same symptoms as the first time. I also had a cough, congestion, and worse body aches. My doctor gave me prednisone and cough syrup. I still have body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: COVID-19 test, 01/02/2023, 01/11/2023, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis
Andere Medikamente: SYNTHROID; LEXAPRO; losartan
Allergien: N/A
Vorherige Impfungen: -

VAERS 2569338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 27.01.2023
Impfdatum: 04.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Blood glucose fluctuation Blood test Chest X-ray Fatigue Pyrexia Respiratory symptom Sinusitis Urinary tract infection Urine analysis

Symptomtext

I started noticing I was having a low-grade fever in the evening, and this has been off and on since November. I also had a UTI and sinus infection and upper respiratory system issues, fatigue and low energy, blood sugar has been all over the place.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Chest X-ray, blood work, Urine Analysis
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic; Depression; Tachycardia
Andere Medikamente: Metformin; metoprolol; EFFEXOR; pantoprazole; RYBELSUS; baby aspirin; multivitamin; vitamin C; calcium with vitamin D; REEQUIP; simvastatin; eye drops timolol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2568299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 26.01.2023
Impfdatum: 19.01.2023
Beginn: 01.01.2023
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

Headache Motion sickness Nasopharyngitis Product use issue

Symptomtext

eceiving the 4th shot along with flu shot/receiving Pfizer with a Flu Shot at the same time; I began to feel like having cold; car sick; I'm still having a mild headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Jan2023 as dose 4 (booster), single (Lot number: GH9697), in right arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 19Jan2023 as dose number unknown, single (Batch/Lot number: unknown), in left arm for immunisation. The patient's relevant medical history included: "Known allergies: Penicillin (no memory, was told this)" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, single, Unknown Manufacturer), administration date: 2021, for COVID-19 Immunization; Covid-19 vaccine (Dose 2, single, Unknown Manufacturer), administration date: 2021, for COVID-19 Immunization; Covid-19 vaccine (Dose 3 (booster), Unknown Manufacturer), administration date: Nov2022, for COVID-19 Immunization. The following information was reported: NASOPHARYNGITIS (non-serious) with onset Jan2023, outcome "recovering", described as "I began to feel like having cold"; HEADACHE (non-serious) with onset Jan2023, outcome "recovering", described as "I'm still having a mild headache"; MOTION SICKNESS (non-serious) with onset Jan2023, outcome "recovering", described as "car sick"; PRODUCT USE ISSUE (non-serious) with onset 19Jan2023, outcome "unknown", described as "eceiving the 4th shot along with flu shot/receiving Pfizer with a Flu Shot at the same time". Additional information: Previous shots (2 in Mid-2021, 3rd on Nov2022) gave the patient little to no side effects after receiving, little to no impact of his daily activities. However, this time after receiving the 4th shot along with flu shot, the patient began to feel like having cold and was car sick. At the time of the report, it is the 3rd day after injection and he is still having a mild headache. Since all previous 3 shots barely affected me, the patient was unsure if this change is due to the updated Pfizer vaccine, or due to receiving Pfizer with a flu Shot at the same time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: TX
Alter: 71,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 01.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 31,0
Dosis: 5
Route/Site: SYR / LA

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

Arthralgia Blood pressure increased Computerised tomogram normal

Symptomtext

Pain in my shoulder that I had many years ago when I first took cholesterol medication prescribed to me. It is a mild pain all the time. I also have increased blood pressure now and my doctors are trying to figure out the source of it. The CT scan of my shoulder also showed that there was nothing there, so the pain is also unexplained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: CT scan of the shoulder
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Cholesterol medication
Vorherige Impfungen: -

VAERS 2566811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: KS
Alter: 67,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 22.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 40,0
Dosis: 5
Route/Site: IM / RA

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

Erythema Post-acute COVID-19 syndrome Pruritus

Symptomtext

Pinkish red areas about the size of a nickel to a quarter that were very itchy going up my neck down to my chest within about a four inch area. The steroid cream the doctor gave me went helped them go away in about two weeks but now they are over my right and inside both elbows and every now and then will pop back up on my neck. I did also have long haul COVID-19 symptoms from getting COVID-19 in January 26th, 2021 but the vaccine was not available to me until March 2021. I may now have auto-immune disease and will begin testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Aneurism; High Blood Pressure
Andere Medikamente: Valsartan; LUNESTA; VASCEPA; metoprolol; ZYRTEC; multivitamin; vitamin D3; vitamin C; magnesium and potassium supplement; zinc; fiber
Allergien: Penicillin; LEVAQUIN; sulfa
Vorherige Impfungen: After the 2nd COVID-19 Pfizer vaccine, I had the fever body aches for about 1 1/2 days

VAERS 2566728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WI
Alter: 30,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 07.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Differential white blood cell count normal Full blood count normal Lymph node pain Lymphadenopathy

Symptomtext

I received Moderna vaccines previously for vaccines 1 and 2 as well as booster 1. For booster 2, I was offered Pfizer and was told that mixing manufacturers was not a bad thing. For almost all of the COVID-19 injections, I had almost immediately experienced swollen lymph nodes in both armpits and breasts - these conditions resolved after about two weeks or so for every injection except for the last one, the most recent Pfizer booster received in November of 2022. It is now January 2023 and I am still experiencing sporadic lymph node pain in those areas of my body. The swelling never went away like the other vaccines. I made an appointment with my primary healthcare provider to get checked out and she told me not to panic but to report these symptoms to you as it was concerning they were lasting so long.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: Primary care health appointment, including breast exam (January 9, 2023) - no risks detected Complete blood count (CBC) with differential count (January 9, 2023) - no risks detected and blood counts were fine
Aktuelle Erkrankungen: (none)
Vorgeschichte: (none)
Andere Medikamente: birth control pill (LO LOESTRIN? FE)
Allergien: (none)
Vorherige Impfungen: Same lymph node swelling present with all other Moderna vaccines/boosters for COVID-19.

VAERS 2564956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: MD
Alter: 56,0
Geschlecht: M
Eingang: 21.01.2023
Impfdatum: 04.01.2023
Beginn: 04.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Chills Lymphadenopathy Malaise Pyrexia SARS-CoV-2 test

Symptomtext

got sick; fever; chills; swollen lymph nodes under left arm pits; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 56-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Jan2023 at 10:30 as dose 4 (booster), single (Lot number: GH9697) at the age of 56 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing); "Diabetes" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; TRADJENTA; LISINOPRIL; VIT D [COLECALCIFEROL]. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EL1284, Location of injection: Arm Left; Vaccine Administration Time: 08:30 AM), administration date: 28Dec2020, when the patient was 54-year-old, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: EL8982, Location of injection: Arm Left; Vaccine Administration Time: 08:00 AM), administration date: 15Jan2021, when the patient was 54-year-old, for Covid-19 immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: EW0196, Location of injection: Arm Left; Vaccine Administration Time: 08:00 AM), administration date: 15Oct2021, when the patient was 55-year-old, for Covid-19 immunization, reaction(s): "chills", "got sick", "swollen lymph nodes under left arm pits", "fever". The following information was reported: CHILLS (non-serious) with onset 04Jan2023 at 21:00, outcome "recovering"; PYREXIA (non-serious) with onset 04Jan2023 at 21:00, outcome "recovering", described as "fever"; MALAISE (non-serious) with onset 04Jan2023 at 21:00, outcome "recovering", described as "got sick"; LYMPHADENOPATHY (non-serious) with onset 04Jan2023 at 21:00, outcome "recovering", described as "swollen lymph nodes under left arm pits". The events "got sick", "fever", "chills" and "swollen lymph nodes under left arm pits" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300025237 same reporter/patient/AE, different dose.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20221123; Test Name: Covid test Binax Now; Test Result: Negative ; Test Date: 20220713; Test Name: Covid test Flow flex; Test Result: Negative ; Test Date: 20220521; Test Name: Covid test Or; Test Result: Negative ; Test Date: 20210624; Test Name: Covid test PCR; Test Result: Negative ; Test Date: 20210705; Test Name: Covid test PCR; Test Result: Negative ; Test Date: 20220527; Test Name: Covid test PCR; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Hypertension
Andere Medikamente: METFORMIN; TRADJENTA; LISINOPRIL; VIT D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2562271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: -
Alter: 88,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 04.11.2022
Beginn: 21.12.2022
Tage bis Beginn: 47,0
Dosis: 1
Route/Site: - / -

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

Asthenia COVID-19 Chest X-ray normal Computerised tomogram head normal Computerised tomogram spine Confusional state Dementia Fall Fatigue Hypophagia Hypoxia Mental status changes Metabolic encephalopathy SARS-CoV-2 test positive Thrombocytopenia

Symptomtext

A 88 year old female with no significant PMH who was brought to the HCF by her family from her apartment due to fall, poor oral intake and confusion. Patient was diagnosed with COVID 19 infection. Not hypoxic and therefore no treatment for COVID indicated. Mentation waxes and wanes with underlying dementia. Evaluated by PT/OT with recommendation for SNF placement. COVID-19 infection without Pneumonia Generalized weakness/fatigue Metabolic encephalopathy (resolved) Patient's generalized weakness, fatigue and some confusion is probably due to Covid-19 Virus Infection on background dementia Date of onset of symptoms: 12/20 Symptoms present on admission: fatigue, generalized weakness, confusion Date of covid positive test: 12/21 Vaccination status: not known Imaging: CXR. Does not show pneumonia Oxygen requirements on admission: none. Sats are 95% on RA Current oxygen requirements: None RA with sats 95-96% Medical therapy: not indicated Consultants following: none Anticipated special isolation end date: 12/31 Mentation tends to wax and wane Plan to discharge to SNF Hypoxia (resolved) Intermittently requiring oxygen Has not required most recently Saturation 95-98 on room air Thrombocytopenia Likely due to viral illness Stable No bleeding noted Fall -Secondary to generalized weakness. - CT brain and CT cervical spine did not show any fracture or intracranial bleed. PT/OT evaluated: Plan for SNF at discharge

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2562214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NJ
Alter: 59,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 18.10.2022
Beginn: 31.12.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / LA

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

Cough Decreased appetite Influenza virus test negative Pain Pyrexia Respiratory syncytial virus test positive Respiratory tract congestion SARS-CoV-2 test negative

Symptomtext

I was tested for COVID-19, RSV, and Flu and I ended up testing positive for RSV. I had loss of appetite, fever, cough, congestion, and body aches. My doctor told me that it should be gone in 5 days, but I still have a bad cough. It gets really bad when I lay down. I was prescribed benzonatate, 600mg ibuprofen, and a steroid injection while I was at the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 02JAN2023 COVID-19 test negative; 02JAN2023 Flu test negative; 02JAN2023 RSV test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD; Heart Disease
Andere Medikamente: Aspirin; lisinopril; metoprolol; isosorbide mononitrate; nortriptyline; gabapentin; XANAX; fish oil; calcium; multivitamin
Allergien: TOPAMAX
Vorherige Impfungen: -

VAERS 2560779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OR
Alter: 64,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 13.10.2022
Beginn: 19.12.2022
Tage bis Beginn: 67,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Dysphonia Headache Laryngitis Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing Symptom recurrence

Symptomtext

I had a headache and congestion. I had fever that was under 101 degrees, runny nose, hoarse voice, a lot of sneezing. Doctor prescribed PAXLOVID on Wednesday 12/21/2023-12/25/2023. Then I started to get better on 12/27/2023 and then on 12/29/2023 I experience a rebound experience same symptoms plus laryngitis but worse except I didn't have fever. While taking PAXLOVID, I was still taking all medications except.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 19DEC2023 COVID-19 at home, negative; 20DEC2023 COVID-19 at home positive; 21DEC2023 COVID-19 at home test positive; 22DEC2023 COVID-19 at home test positive; 23DEC2023 COVID-19 at home test positive; 24DEC2023 COVID-19 at home test positive; 25DEC2023 COVID-19 at home test positive; 26DEC2023 COVID-19 at home test positive; 27DEC2023 COVID-19 at home test positive; 28DEC2023 COVID-19 at home test negative; 29DEC2023 COVID19 at home test positive; 30DEC2022 COVID-19 at home test positive; 31DEC2022 COVID-19 at home test positive; 01JAN2023 COVID-19 at home test positive; 02JAN2023 COVID-19 at home test positive; 03JAN2023 COVID-19 at home test positive; 04JAN2023-COVID-19 at home test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic Cerebral Small Ischemic Disease; Coronary Artery Disease; HX of Heart Attack NSTEMI; 2 Stents inserted; Diabetes Type II; Fibromyalgia; High Blood Pressure; High Cholesterol; High Triglycerides; Non-Alcoholic Fatty Liver Disease Severe; Obesity; Obstructive Sleep Apnea; Osteopenia; Chronic Pain
Andere Medikamente: Gabapentin; losartan hydrochlorothiazide; metformin ER; metoprolol succinate; rosuvastatin calcium; acetaminophen; loratadine; low dose aspirin; vitamin D; lidocaine patches; nitroglycerine (has not needed to take since heart attack)
Allergien: Amitriptyline; atorvastatin; levofloxacin
Vorherige Impfungen: -

VAERS 2560061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 11.12.2022
Beginn: 12.12.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal distension Diarrhoea Flatulence

Symptomtext

Diarrhea, bloating and gas for over 4 weeks

Weitere VAERSDATA-Felder

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

VAERS 2558540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: GA
Alter: 69,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 10.10.2022
Beginn: 28.12.2022
Tage bis Beginn: 79,0
Dosis: 5
Route/Site: IM / LA

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

Arthralgia COVID-19 Diarrhoea Gastrointestinal disorder Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Skin exfoliation

Symptomtext

I had symptoms of a fever, a sore throat, body aches and joint pain on 12/27/2022. I tested myself at home and the result was positive on 12/28/2022. I reached out to my PCP and he called in Paxlovid for me. I started to take the medication right away. My whole GI tract seemed to become affected and I was experiencing diarrhea. It also seemed that my skin started to shed as well. I feel that I have recovered from COVID as of today, 01/12/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Covid-19
Aktuelle Erkrankungen: None
Vorgeschichte: HIV
Andere Medikamente: Combivere; Icentris; Prazista; Ritonavir; Lisinopril; Rosuvastatin; Low dose aspirin; OTC Antihistamine; Calcium; Fish Oil; Vitamin D; B-Complex; Testosterone Gel
Allergien: None
Vorherige Impfungen: -

VAERS 2556011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MD
Alter: 33,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 02.12.2022
Beginn: 26.12.2022
Tage bis Beginn: 24,0
Dosis: UNK
Route/Site: IM / RA

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

Chills Cough Diarrhoea Human rhinovirus test positive Malaise Nausea Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

I had nausea, chills, and three days of terrible diarrhea, then 3 days of not so bad diarrhea. This lasted for about a week. About seven days later I was feeling sick again and tested positive for Rhinovirus. I had a sore throat for two days, congestion and a cough. I contacted my doctor, but no medication was prescribed. I did take SUDAFED, eucalyptus oil and garlic honey lemon tea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 03JAN2023 Strep test negative; 03JAN2023 COVID-19 test negative; 03JAN2023 Rhinovirus positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: HIV; Cold sores
Andere Medikamente: N/A
Allergien: Penicillin; azithromycin; vitamin C supplements
Vorherige Impfungen: -

VAERS 2554846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: TX
Alter: 73,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 09.12.2022
Beginn: 05.01.2023
Tage bis Beginn: 27,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Nasal congestion Pain SARS-CoV-2 test positive

Symptomtext

I've been generally asymptomatic. Having spent time in an airport, I took a COVID-19 test to be on the safe side. The result was positive. Other than some slight nasal congestion, I've had no symptoms. I had brief and very mild body aches. I took ibuprofen. They cleared up in two hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 01/02/2022 at home COVID-19 test negative; 01/04/2022 at home COVID-19 test negative; 01/05/2022 at home COVID-19 test positive; 01/06/2022 at home COVID-19 test positive
Aktuelle Erkrankungen: C-Diff
Vorgeschichte: None
Andere Medikamente: Candesartan; PEPCID; rosuvastatin; omeprazole; CENTRUM SILVER; vitamin D3; FLORASTOR
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2554835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: TX
Alter: 58,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 07.10.2022
Beginn: 11.11.2022
Tage bis Beginn: 35,0
Dosis: 4
Route/Site: IM / LA

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

Blood test normal Burning sensation Groin pain Pollakiuria Urine analysis normal

Symptomtext

11/11/2022, I went to Dr. for a history of burning while urinating for several weeks. I had groin pain and frequent urination but no blood or discharge in the urine. He did urine and blood tests, negative. Levaquin was prescribed. After 2 weeks, symptoms came back. I was put on a high dose for 3 weeks. I was referred to a Urologist. I will see the Urologist this week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Groin pain
Hospital-Tage: -
Labordaten: 11NOV2022 - Urine Test - Normal 11NOV2022 - Blood Test - Normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; Coronary Artery Disease; Seasonal Allergies
Andere Medikamente: Repatha; Atorvastatin; Lysinopril; Aspirin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2554709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: GA
Alter: 69,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 06.10.2022
Beginn: 14.12.2022
Tage bis Beginn: 69,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Cough Dizziness Feeling hot Oropharyngeal pain Productive cough Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

My symptoms started but I thought it was the flu, on 12/14. I woke up feeling feverish, lightheaded, sore throat, bad cough, runny nose. I normally have a chronic dry cough but told the PA that this was a different cough, I was coughing up phlegm. I just stayed in bed. I don't remember taking any medicine, but if I did it was probably acetaminophen. I took my temperature a few times but it was never over 100 on my forehead, but I was too hot so I took temperature in my mouth and it was over 100. I went to urgent care on Friday morning and spoke with PA, they tested me for COVID-19 and I was positive. She prescribed PAXLOVID and a cough medicine. I followed the instructions to the letter. Stayed in a room upstairs for five days, had a separate bathroom, tried not to cross contaminate anything. I got the medicine late Friday, so I started Saturday morning and almost immediately started feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 16DEC2022 COVID-19 test positive; 22DEC2022 COVID-19 negative
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic constipation; High blood pressure; previous Stroke (10/22); Chronic GERD; High cholesterol; Slipped discs; Depression; Chronic Cough
Andere Medikamente: EQUATE women 50 plus; vitamin D3; MIRALAX; FLEET suppository; baby aspirin; coQ10; hydrochlorothiazide; omeprazole; simvastatin; clopidogrel; amlodipine besylate
Allergien: Morphine; droperidol; PHENERGAN; ibuprofen
Vorherige Impfungen: A flu vaccination in 1996, I don't remember exactly, but I just remember being really sick afterwards, my job put me in a spare

VAERS 2553152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: SC
Alter: 60,0
Geschlecht: F
Eingang: 07.01.2023
Impfdatum: 30.11.2022
Beginn: 31.12.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: SYR / LA

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

Breast mass Breast pain Glossodynia Lip pain Oral pain Sinusitis

Symptomtext

Sore knot under left breast and sinus infection. Dr prescribed antibiotic, zpack, to help with both. Size of knot under breast was reduced and soreness went away. After I finished antibiotics, mouth got sore. Left side of tongue and inside top lip. I am taking Benadryl, benzocaine lozenges, and Ambesol right now (started 1/7/2023).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: None yet for this booster. Will see doctor this coming week. Prior booster, I had cyst removed from top of left breast. It developed shortly after third Covid-19 Pfizer vaccination.
Aktuelle Erkrankungen: Flu - 11/1/2022 Sinus infection - 12/20/2022 Cyst - under left breast Mouth soreness - 12/2022
Vorgeschichte: High blood pressure
Andere Medikamente: Losartan hctz, montelukast, tramadol (as needed), vitamin D, potassium, multivitamin, azelastine, saline nasal spray.
Allergien: Clindomycin, penicillins, amoxicillin, ampicillin
Vorherige Impfungen: Covid-19 vaccine dose #3

VAERS 2544914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 34,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 15.11.2022
Beginn: 21.12.2022
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia COVID-19 Cough Fatigue Headache Illness Nausea Oropharyngeal pain SARS-CoV-2 test positive Somnolence

Symptomtext

I contracted COVID-19 on 12/21/22 with symptoms of sore throat, headache, nausea, cough, joint pain, grogginess, and fatigue. I was prescribed Paxlovid on 12/23/22. My symptoms have begun to resolve today, which is day 7 of illness, but have not fully resolved. The joint pain worsened on day 6 and 7. I am not recovered as of today day 7 of illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19 PCR test was positive on 12/22/22
Aktuelle Erkrankungen: N/A
Vorgeschichte: Epilepsy
Andere Medikamente: Lamictal Lamotrigine; Multivitamin; Magnesium Citrate
Allergien: Sulfa; Amoxicillin
Vorherige Impfungen: Pfizer Dose 2 I experienced dizziness on 12/05/21

VAERS 2537932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: NJ
Alter: 41,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 03.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Gastroenteritis viral Headache Pruritus Rash Rash vesicular Rhinorrhoea SARS-CoV-2 test positive Sneezing Vomiting

Symptomtext

The Sunday before the rash developed I came down with the stomach flu and was throwing up all day. Then I stopped and it followed with a headache on Monday. Wednesday I woke up to an itchy neck that had a blistery rash on my shoulder, neck and clavicle area. The doctor put me in on antiviral and pain relief medication. The rash lasted for 2 weeks. Now I have residual itchy feeling in that area some time. My husband wasn't feeling well a week ago and tested positive for COVID-19. This past Wednesday 12/14 I I took a test and it was positive. then the Sunday I started with symptoms of runny nose, sneezing, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Multiple sclerosis
Andere Medikamente: Multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2537255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 20.12.2022
Impfdatum: 11.12.2022
Beginn: 11.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / -

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

Abdominal discomfort Asthma Vomiting

Symptomtext

Asthma; I got sick to my stomach and was throwing; I got sick to my stomach and was throwing; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Dec2022 as dose 5 (booster), single (Lot number: GH9697) for covid-19 immunisation. The patient's relevant medical history included: "blood pressure" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: EL9264), administration date: 01Apr2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "First two shots, I fell and had hard time getting up Fall"; BNT162b2 (DOSE 2, SINGLE, Lot number: EW0171), administration date: 29Apr2021, when the patient was 70-year-old, for COVID-19 immunization, reaction(s): "I fell and had hard time getting up"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot number: 0308D), administration date: 10Dec2021, when the patient was 71-year-old, for COVID-19 immunization, reaction(s): "I got sick to my stomach and was throwing up", "I got sick to my stomach and was throwing up"; BNT162b2 (DOSE 4 (BOOSTER), SINGLE, Lot number: FJ4991), administration date: 12Apr2022, when the patient was 71-year-old, for COVID-19 immunization, reaction(s): "I got sick to my stomach and was throwing up", "I got sick to my stomach and was throwing up". The following information was reported: ABDOMINAL DISCOMFORT (non-serious), VOMITING (non-serious) all with onset 11Dec2022, outcome "unknown" and all described as "I got sick to my stomach and was throwing"; ASTHMA (non-serious), outcome "unknown". Therapeutic measures were not taken as a result of asthma, abdominal discomfort, vomiting. Additional information: The patient had adverse reaction to the first two shots and all three boosters. And then on the other ones, afterwards, couple of hours later, the patient got sick to stomach and was throwing up and those were not given as any of the side effects. The patient did not undergo any investigations. Sender's Comments: Linked Report(s): PFIZER INC-202201375592 same reporter/patient, different vaccine dose;

Weitere VAERSDATA-Felder

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

VAERS 2536053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 17.12.2022
Impfdatum: 02.12.2022
Beginn: 04.12.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Hypoaesthesia Pain in extremity

Symptomtext

2 days following vaccination patient experienced pain, numbness in right hand. persisted and pt went to see provider 12/16 at which time he received an rx to treat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: nka
Vorherige Impfungen: -

VAERS 2535387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 03.11.2022
Beginn: 12.12.2022
Tage bis Beginn: 39,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Exposure to SARS-CoV-2 Influenza virus test Pain Pyrexia Respiratory syncytial virus test Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I was around my son and we did not know he had COVID-19. A couple days later, I started showing symptoms of a cough. The next day, I started to feel stuffy, congested, had body aches and continued to cough. Later that night, I developed a fever. I took a rapid COVID-19 test and it came back negative. My physician contacted me and told me the PCR came back positive. He prescribed PAXLOVID for me. I have been taking PAXLOVID since 12/14/2022. I have not noticed any positive change so I was thinking that I may discontinue taking it. I had a tele-health appointment this morning and my physician told me to continue taking PAXLOVID because it is the only medication available for me to take.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Covid-19; flu; RSV
Aktuelle Erkrankungen: None
Vorgeschichte: Controlled high blood pressure
Andere Medikamente: Lisinopril; clonazepam; vitamin D; vitamin C; probiotic; multivitamin; fish oil.
Allergien: None
Vorherige Impfungen: -

VAERS 2535330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: IL
Alter: 18,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 15.12.2022
Beginn: 16.12.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Pyrexia Wrong product administered

Symptomtext

Pt came in for a flu shot Flucelvax and instead received a second updated Covid booster. Pt woke with fever 102. Dr was contacted and stated pt could take ibuprofen or acetaminophen and to seek her primary dr at school if needed any further care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: none
Allergien: peanuts
Vorherige Impfungen: -

VAERS 2529087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 17.11.2022
Beginn: 05.12.2022
Tage bis Beginn: 18,0
Dosis: 5
Route/Site: IM / -

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

COVID-19 Influenza like illness Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Caught COVID, felt like I had a cold coming on, antigen tested immediately and it came back positive. Felt flu-like for 3 days, then just feels like a cold. Mild congestion, runny nose, no fever after day 2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Home rapid test
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: acyclovir, levothyroxine, duloxetine , lamictil
Allergien: shellfood
Vorherige Impfungen: -

VAERS 2527814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WI
Alter: 11,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Injection site pain

Symptomtext

Was given the Pfizer bivalent booster for ages 12 and up, patient was 11 yo and should have gotten the Pfizer bivalent booster for 5-11yo patient had arm tenderness at injection site and no other side effects

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Adderall XR 15mg
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2525536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: AZ
Alter: 67,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 01.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 30,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Chills Feeling cold Malaise Nausea Oropharyngeal pain Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive Taste disorder

Symptomtext

I started feeling nauseous. I had a fever. It got up to 102-degrees at its highest. I had a very sore throat. I didn't lose my appetite or sense of smell, but I had a weird taste in my mouth. As the day progressed, I started feeling worse. I got chills and couldn't get warm. I tested for COVID-19 at home that evening. The first test I took was a false negative. I tested again, and it came back positive. It progressively got worse. My sore throat got really painful for the next two nights. My doctor prescribed PAXLOVID. I took my last dose this morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 12/01/2022 at home COVID-19 test negative; 12/01/2022 at home COVID-19 test positive; 12/02/2022 PCR COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tamsulosin; EMERGEN-C
Allergien: None
Vorherige Impfungen: -

VAERS 2525479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 71,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 21.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 10,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Fatigue Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

Sore throat; nasal congestion and fatigue for 2 days. I was prescribed 5 day course of PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 10/31/2022 home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Simvastatin; FLAMOXIDE
Allergien: None
Vorherige Impfungen: -

VAERS 2524325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Blood test normal Electromyogram abnormal Muscular weakness Myalgia Myopathy Nerve conduction studies abnormal

Symptomtext

On or about November 7, 2022, I began noticing significant increase thigh muscle and glut muscle pain. The doctors discovered some odd things such as a myopathy. I have seen a neurologist and a physical therapist, and they have both found muscle problems, significant bilateral weakness. I have another appointment in January 2023 with the neurologist, the rheumatologist in December 2022, and an infectious disease doctor in December 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Needle Electromyography, mildly abnormal, 11/2022; Nerve Conduction test, mildly abnormal, 11/2022; Blood panels appeared normal, 11/2022
Aktuelle Erkrankungen: Sjogren's Syndrome
Vorgeschichte: -
Andere Medikamente: Vitamin D; vitamin B12; potassium chloride; TYLENOL
Allergien: Erythromycin; sulfa; doxycycline; CIPRO; lidocaine; metronidazole; iodine; quinacrine; latex; omeprazole
Vorherige Impfungen: -

VAERS 2524120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 06.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Immediate post-injection reaction

Symptomtext

At 10-minute mark of post vaccine waiting period patient felt dizzy. patient was instructed to wait additional time to see if symptoms resolved. patient still felt dizzy, and provider notified for Evalution. patient advised to wait additional time frame prior to releasing.

Weitere VAERSDATA-Felder

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

VAERS 2524113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: NC
Alter: 56,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 27.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Arthralgia Bone pain Gait disturbance Headache Inflammation Injection site erythema Injection site warmth Muscle swelling Musculoskeletal stiffness Myalgia Pyrexia

Symptomtext

I experienced an extreme inflammatory response. I was hardly able to walk. I skipped showering the morning after as I was too stiff to raise my leg. I gingerly walked down the stairs when leaving for work. All joints and bones ached. I ran a fever at the 24 hour mark after injection. The fever lasted approximately five hours. As the soreness and stiffness wore off throughout the week. my joints were very sore. I have had persistent headaches. I had a perfect concentric red circle on my arm at the injection site x six days. The injection site was hot to touch for six days. At day three, I experienced soreness and swelling at the pectoralis muscle. No changes in color, no discharges from the breast. Overall a very unexpected inflammatory response. Tylenol was minimally helpful. I took 500 mg po q3H when symptoms would increase.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: HTN Diabetes
Andere Medikamente: Zinc
Allergien: Fructose Crab Shrimp Tetanus Soy All Trees Pollen Dust Grass Cochroaches
Vorherige Impfungen: Tetanus shot. Age 37, fever, hot to touch, unable to lift arm x 4 days

VAERS 2522465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VA
Alter: 41,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 02.12.2022
Beginn: 02.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Pain in extremity Rash papular Rash pruritic

Symptomtext

The arm the patient got the vaccine in, on the forearm was painful and had a not raised rash. Started small area, got better and then had a bigger rash on the other side of the same arm. Itchiness where the rash is but only local to the forearm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2519603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: WY
Alter: 34,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 15.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Pain in extremity Wrong product administered

Symptomtext

her arm hurt; She got the booster instead of the first dose of the primary series; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the patient. A 34-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Oct2022 as dose 1 (bivalent), single (Lot number: GH9697) at the age of 34 years, in left arm for covid-19 immunisation. The patient didn't receive BNT162b2 (BNT162B2). The patient had no relevant medical history. There were no concomitant medications. The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 15Oct2022, outcome "unknown", described as "She got the booster instead of the first dose of the primary series"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "her arm hurt". Additional information: Caller reported she received Pfizer BioNTech COVID-19 Vaccine Bivalent booster on 15Oct2022. Only received the Pfizer BioNTech COVID-19 Vaccine Bivalent Booster and had not received any primary series vaccinations. She was trying to get the second shot and no one was giving this to her; wanted the Moderna Vaccine. She had zero reactions except her arm hurt and that was it. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2518256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: NC
Alter: 10,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / LA

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

Nasal congestion Off label use Overdose Pain Product administered to patient of inappropriate age Product use issue Pyrexia

Symptomtext

fever; body aches; congestion; He got the flu shot today as well; He got the flu shot today as well; medical assistant reporting that a 10-year-old patient received the adult dose of Pfizer COVID vaccine bivalent for the booster dose.; medical assistant reporting that a 10-year-old patient received the adult dose of Pfizer COVID vaccine bivalent for the booster dose.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. A 10-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 31Oct2022 as dose 4 (booster), single (Lot number: GH9697, Expiration Date: 30Jun2023) at the age of 10 years intramuscular, in left deltoid for covid-19 immunisation; influenza vaccine inact split 3v (FLULAVAL), on 31Oct2022 as dose number unknown, single (Lot number: 72KJ4, Expiration Date: 30Jun2023) for immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1; unknown manufacturer), for Covid-19 immunization; Covid-19 vaccine (Dose 2; unknown manufacturer), for Covid-19 immunization; Covid-19 vaccine (Dose 3; unknown manufacturer), for Covid-19 immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 31Oct2022, outcome "unknown" and all described as "He got the flu shot today as well"; PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), OVERDOSE (non-serious) all with onset 31Oct2022, outcome "unknown" and all described as "medical assistant reporting that a 10-year-old patient received the adult dose of Pfizer COVID vaccine bivalent for the booster dose."; PAIN (non-serious) with onset 01Nov2022, outcome "recovered", described as "body aches"; NASAL CONGESTION (non-serious) with onset 01Nov2022, outcome "recovered", described as "congestion"; PYREXIA (non-serious) with onset 01Nov2022, outcome "recovered", described as "fever". Therapeutic measures were not taken as a result of pyrexia, pain, nasal congestion. Additional information: Caller was a medical assistant reported that a 10-year-old patient received the adult dose of Pfizer COVID vaccine bivalent for the booster dose. The caller wanted to know if it was safe for the patient. This report was not related to study or program. Other conditions and investigations reported as no. The patient received the adult dose bivalent formulation that was intended for the patient booster dose. The patient did not receive any treatment. Reporter stated, the patient got the vaccine here in the office, doctor's office. Any prior vaccination (within 4 weeks) reporter stated, he got the flu shot today as well. The patient did not received any other vaccine prior, no medical history and no relevant test performed. There was no hospitalization and no specific relevant test for thromboembolic events with thrombocytopenia. Follow-up attempts are completed. No further information is expected. Follow up (23Nov2022): This is a spontaneous follow-up report from a contactable consumer. This consumer reported in response to Non Hcp follow-up letter sent which Included that: Updated information included: Patient information (last name, Address, city, state and postal code) added. Historical vaccine (dose 01, 02 and 03). Vaccination Information (dose number, dose description, Route of administration, Anatomical Location) added. Vaccine Administered at Facility captured. New events (Fever, body aches, congestion). Concomitant Therapy.

Weitere VAERSDATA-Felder

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

VAERS 2517312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 26.11.2022
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Pain

Symptomtext

Systemic: Joint Pain-Severe, Additional Details: Pain on left side of body, in hip area. Started following vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2516755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 25.11.2022
Impfdatum: 14.10.2022
Beginn: 09.11.2022
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Cough Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

I had a terrible sore throat, fever, body aches and pains, and a very bad, dry cough that wouldn't go away. I had digestive issues, I vomited for two days. I called and told my doctor about my symptoms. I took several at-home COVID-19 tests which all came back positive. My doctor prescribed me PAXLOVID half-dose. It took a couple of days, but it helped reduce the symptoms. At this moment, it's been over two weeks and I'm starting to feel better. I finally got a negative COVID-19 test as of two days ago (11/23/2022).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 tests
Aktuelle Erkrankungen: Urinary Tract Infection
Vorgeschichte: N/A
Andere Medikamente: BYSTOLIC; vitamin E; vitamin C
Allergien: Penicillin; oral sulfa drugs
Vorherige Impfungen: -

VAERS 2515828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: NM
Alter: 45,0
Geschlecht: F
Eingang: 24.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / RA

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

Body temperature Chills Cough Decreased appetite Feeling hot Flushing Headache Interchange of vaccine products Investigation Malaise Menstruation irregular Nasopharyngeal swab Nausea Night sweats Pain Pyrexia

Symptomtext

Menstrual cycle started 7 days early; Night sweats; chills or being overheated; Coughing; Loss of appetite/ decreased intake; nausea with serving sizes greater than a cup; severe shivering/riggers on 2 occasions lasting 15-25 minutes; fevers (100.4 - 102.5) degrees; Hot/cold body flushing; Malaise; body aches; headache; Prev dose brand=Moderna; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the patient. A 45-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 at 07:45 as dose 4 (booster), single (Lot number: GH9697) at the age of 45 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "hypothyroid" (unspecified if ongoing). Concomitant medication(s) included: FLUCELVAX taken for immunisation, on 21Oct2022 as dose 1, single; LEVOTHYROXINE; CETIRIZINE. Vaccination history included: moderna (DOSE 1, SINGLE , Lot number=039K20-2A), administration date: 23Dec2020, when the patient was 43-year-old, for COVID-19 immunization; moderna (DOSE 2, SINGLE , Lot number=030L20A), administration date: 20Jan2021, when the patient was 43-year-old, for COVID-19 immunization; moderna (DOSE 3 (BOOSTER), SINGLE , Lot number=077C21B), administration date: 30Dec2021, when the patient was 44-year-old, for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 10Nov2022, outcome "unknown", described as "Prev dose brand=Moderna"; FLUSHING (non-serious) with onset 11Nov2022, outcome "not recovered", described as "Hot/cold body flushing"; MALAISE (non-serious) with onset 11Nov2022, outcome "not recovered"; PAIN (non-serious) with onset 11Nov2022, outcome "not recovered", described as "body aches"; PYREXIA (non-serious) with onset 11Nov2022, outcome "not recovered", described as "fevers (100.4 - 102.5) degrees"; HEADACHE (non-serious) with onset 11Nov2022, outcome "not recovered"; CHILLS (non-serious) with onset 11Nov2022, outcome "not recovered", described as "severe shivering/riggers on 2 occasions lasting 15-25 minutes"; DECREASED APPETITE (non-serious) with onset 13Nov2022, outcome "not recovered", described as "Loss of appetite/ decreased intake"; NAUSEA (non-serious) with onset 13Nov2022, outcome "not recovered", described as "nausea with serving sizes greater than a cup"; COUGH (non-serious) with onset 14Nov2022, outcome "not recovered", described as "Coughing"; NIGHT SWEATS (non-serious) with onset 15Nov2022, outcome "not recovered"; FEELING HOT (non-serious) with onset 15Nov2022, outcome "not recovered", described as "chills or being overheated"; MENSTRUATION IRREGULAR (non-serious) with onset 18Nov2022, outcome "not recovered", described as "Menstrual cycle started 7 days early". The events "severe shivering/riggers on 2 occasions lasting 15-25 minutes", "fevers (100.4 - 102.5) degrees", "hot/cold body flushing", "malaise", "body aches", "headache", "loss of appetite/ decreased intake", "nausea with serving sizes greater than a cup", "coughing", "night sweats", "chills or being overheated" and "menstrual cycle started 7 days early" required emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of chills, pyrexia, flushing, malaise, pain, headache, decreased appetite, nausea, cough, night sweats, feeling hot, menstruation irregular.Patient on day 10 of fevers (100.4 - 102.5) degrees Fahrenheit using oral thermometer. Requiring doses of acetaminophen 325mg plus ibuprofen 400mg every 4 hours. Hot/cold body flushing, shivering, severe shivering/riggers on 2 occasions lasting 15-25 minutes. Malaise, body aches, and headache not relieved by acetaminophen or ibuprofen. Loss of appetite started on day 4, nausea with serving sizes greater than a cup, and decreased intake. Coughing started on day 5; semi-controlled with dextromethorphan 30mg up to 4 dose/per day, plus lemon honey tea. Night sweats started day 6, sweats soak through clothing once a night requiring clothing changes, followed by additional dry awaking due to chills or being overheated. Menstrual cycle started 7 days early, on day 9, which has never happened before. Negative home COVID tests on day 5 and 9. Negative rapid Flu and COVID taken at Urgent Care on day 6, COVID send out also negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20221111; Test Name: fevers (100.4 - 102.5) degrees Fahrenheit; Result Unstructured Data: Test Result:(100.4 - 102.5) degrees Fahrenheit; Test Name: rapid Flu; Test Result: Negative ; Test Date: 20221114; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20221115; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20221119; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: LEVOTHYROXINE; CETIRIZINE
Allergien: -
Vorherige Impfungen: -

VAERS 2514097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Pallor

Symptomtext

Patient was seen to administer the FLU and Pfizer booster vaccines. She was accompanied by mother who consented to receiving both vaccines. Vaccine screening was complete, and no noted contraindications were noted. Vaccine possible side effects were reviewed. AT 10:14-10:15AM vaccines were administered following county guidance. She experienced dizziness within seconds of receiving both the FLU and Pfizer vaccines. She requested water post vaccination and was noted with paleness. I stayed with patient while calling for assistance to get cot, water and emergency bag. I immediately assisted her to lie down. She explains had not had breakfast as her and mom were rushing out to their appt. She reports not feeling anxious or nervous prior to the vaccine or having a similar incident in the past. 10:15am -10:20am She drank water, rested on the cot, applied ice pack to back of neck and took vital signs. She reported feeling much better right after lying on the cot. VS were as follows BP 110/78 P 75-82 R: 18 02: 98-100% RA. 10:25am She was assisted slowly to a sitting/dangled position and reported feeling "good". She then slowly sat up and tolerated. Mother was at her side the whole time. 10:30 Patient reported feeling well and ready to head out. Educated on staying hydrated and other possible side effects post vaccinated. Patient and mother verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None reported by patient and mother
Vorherige Impfungen: -

VAERS 2514056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 24.10.2022
Beginn: 15.11.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / LA

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

Conjunctivitis Fatigue Impaired work ability Nasopharyngitis Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative

Symptomtext

Last Tuesday I was having congestion, fever mild fever, runny nose, and by my performance on Saturday was feeling worse and worse and finally called out of work. I have tested for COVID-19 and that was negative, but this is a horrible cold. I am so tired and achy, and this is really hitting me hard. I have had COVID-19 before, and this feels worse than when I was positive with COVID, and this has been worse than that experience. I also developed pink eye on Sunday as well and think it may be from the runny nose and having a mask.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Herpes Type II
Andere Medikamente: Prenatal Vitamin; DHEA 25; Valtrex; NeoQ10; Magnesium; Xyzal
Allergien: N/A
Vorherige Impfungen: -

VAERS 2513489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: PA
Alter: 76,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 17.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: SYR / RA

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

Erythema Periorbital swelling Rash Rash pruritic Rhinorrhoea Swelling face

Symptomtext

1-2 days after vaccination patient started with erythema around the nose, rhinorrhea and itchy rash of nose. Then on 11/20-11/21 noted some slight facial swelling, cheeks and below the eye. Seen at PCP office 11/21/2022 noted to have mild facial edema without angioedema. No diffuse urticaria, airway not compromised. given antihistamines and topical steroid cream for rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no other illnesses Also received flu vaccine
Vorgeschichte: Diabetes, HTN, HLD,
Andere Medikamente: -
Allergien: Penicillin and sulfa both - itching and rash
Vorherige Impfungen: -

VAERS 2512929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: PA
Alter: 17,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 18.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Injection site erythema Injection site swelling Pruritus

Symptomtext

Red and swollen at injection site. Itching by 11/21/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Minocycline (acne), L-norest/eth (birth control), Fiber gummies and daily vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2512888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 20.10.2022
Beginn: 14.11.2022
Tage bis Beginn: 25,0
Dosis: UNK
Route/Site: IM / LA

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

Cough Ear pain Headache Illness Influenza virus test negative Oropharyngeal pain Pyrexia Respiratory disorder SARS-CoV-2 test negative

Symptomtext

Developed an upper respiratory illness. Severe ear pain. Cough, sore throat, headache. Fever of 101.5 on Tuesday, Wednesday and Thursday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: 3 negative covid antigen test. (15, 16 and 17) Negative flu test( 11/19).
Aktuelle Erkrankungen: no
Vorgeschichte: metabolic syndrome, restless leg, depression
Andere Medikamente: Metformin, Ropinerole, Vitamine C, Lithium
Allergien: Sulpha, SSRI's, SNRI's Heparin, and Seroquel
Vorherige Impfungen: -

VAERS 2512410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IL
Alter: 62,0
Geschlecht: F
Eingang: 19.11.2022
Impfdatum: 18.11.2022
Beginn: 18.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Rash Rash erythematous Rash papular Rash pruritic

Symptomtext

Patient developed rash on arms starting about 1 hour post-vaccination. Described rash as really red, bumpy, and slightly itchy; worse on right arm (vaccinated arm). Self-treated with benadryl.

Weitere VAERSDATA-Felder

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

VAERS 2512337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IA
Alter: 60,0
Geschlecht: F
Eingang: 19.11.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Site: Pain at Injection Site-Severe, Additional Details: Patient came in on 11/15 to pick up a prescription. She complained that she was still having moderate-severe arm pain from her covid injection on 10/20/22. She had had Pfizer previously and not reacted to other immunizations. I advised her if it continues she may want to have it evaluated for shoulder impingement/injury.

Weitere VAERSDATA-Felder

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

VAERS 2510623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VA
Alter: 47,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 26.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

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

Axillary mass Impaired work ability Oedema peripheral Pain in extremity

Symptomtext

After receiving my vaccines, I went home and went to sleep because I work nights. My arm was in pain which I expected. When I woke up, I felt like I had a cold, so I only worked a short shift. I went in at 04:00AM instead of 12:00AM. When I was getting ready for work the following night, while taking a shower, I noticed that under my left arm was swollen. When I checked it out after getting out of the shower, I noticed a large lump under my arm. On 10/28/2022, I went to a local clinic because the lump was still there and was still swollen. The physician there told me that it was a normal reaction and advised that I take TYLENOL and use warm compresses. I currently still have slight swelling, but it has gone down significantly, and it is no longer concerning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; High Cholesterol; Anxiety; Depression
Andere Medikamente: Atorvastatin; valsartan; bupropion; fluoxetine; aspirin; iron; DULCOLAX
Allergien: Azithromycin
Vorherige Impfungen: -

VAERS 2510452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NY
Alter: 17,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 12.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness Nausea

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Nausea-Mild

Weitere VAERSDATA-Felder

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

VAERS 2509501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: DC
Alter: 67,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / RA

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

Injection site discharge Injection site haemorrhage Injection site pain Product administration error Underdose

Symptomtext

There was an administration error. The Pharmacist gave the injection which was unusually painful. When she applied the bandaid, the pressure caused liquid to be expelled ( blood or vaccine. She jumped, made an audible sound of surprise, then wiped the dripping substance that was running down my arm. Within an hour the area around the injection site was extremely sore. The next morning when I removed the bandaid, there were multiple (3?) small blood spots on it. But, concerning, some clear liquid seemed to have run through them leaving some streaking! None of the customary tiredness on the 2nd or 3rd day following the booster. I am certain I did not get a full dose. I need to determine if I should repeat!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discharge
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Hypertension Hypothyroidism
Andere Medikamente: Januvia Hctz Lisinipril
Allergien: Not relevant
Vorherige Impfungen: -

VAERS 2508688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: TX
Alter: 76,0
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 15.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Hallucination Headache

Symptomtext

patient stated had headache and hallucinations a few hours later

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: LIDOCAINE, NOVOCAINE, BENZOCAINE
Vorherige Impfungen: -

VAERS 2506519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: DE
Alter: 74,0
Geschlecht: M
Eingang: 12.11.2022
Impfdatum: 18.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / RA

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

Blood cholesterol Blood test Drug hypersensitivity Fatigue Hypoacusis Magnetic resonance imaging

Symptomtext

he had a reaction similar to when he had atorvastatin, niaspan, and dyazide.; he felt exhausted; He has bad hearing/his hearing has been decreased even more; 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 74-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Sep2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 74 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "because of heart attacks he immediately had fibrillation in heart" (unspecified if ongoing), notes: Additional Information for Other medicines Pradaxa: been on it for years.; "because of heart attacks he immediately had fibrillation in heart" (unspecified if ongoing), notes: Additional Information for Other medicines Pradaxa: been on it for years.; "bilateral TIA like symptoms" (unspecified if ongoing), notes: The bilateral TIA like symptoms were originally discovered after open heart surgery in Jan2016; "had open heart surgery", start date: Jan2016 (unspecified if ongoing), notes: The bilateral TIA like symptoms were originally discovered after open heart surgery in Jan2016; "became unconscious", start date: 2016 (unspecified if ongoing); "His arm went numb/brain went numb/his hearing went numb", start date: 2016 (unspecified if ongoing); "had brain fog", start date: 2016 (unspecified if ongoing); "he had severe pain in legs", start date: 2016 (unspecified if ongoing); "hyperallergic to soy" (unspecified if ongoing), notes: hyperallergic to soy; "Hypermetabolism" (unspecified if ongoing). Concomitant medication(s) included: PRADAXA taken for myocardial infarction, cardiac fibrillation (ongoing); AMLODIPINE BESYLATE 10 taken for myocardial infarction (ongoing). Past drug history included: Statin, reaction(s): "he was allergic to statin", notes: That test determined that he was allergic to statin. Vaccination history included: BNT162b2 (First dose:, Date: 11Feb2021, LOT: EL926S, but he can't tell if that is really an S, EXP: unknown), administration date: 11Feb2021, when the patient was 72-year-old, for COVID-19 Immunization; BNT162b2 (Second dose:, Date 04Mar2021, LOT: EN6198, NDC: unknown, EXP: unknown), administration date: 04Mar2021, when the patient was 72-year-old, for COVID-19 Immunization; BNT162b2 (Pfizer Covid Vaccine Booster:, Date: 01Oct2021, LOT: SW0191 or could be EW0191 or could be FW0191, EXP: unknown), administration date: 01Oct2021, when the patient was 72-year-old, for COVID-19 Immunization; BNT162b2 (Pfizer Covid Vaccine Booster:, Date: 21Apr2022, LOT: FK9894, NDC: unknown, EXP: unknown), administration date: 21Apr2022, when the patient was 73-year-old, for COVID-19 Immunization. The following information was reported: DRUG HYPERSENSITIVITY (non-serious), outcome "unknown", described as "he had a reaction similar to when he had atorvastatin, niaspan, and dyazide."; FATIGUE (non-serious), outcome "unknown", described as "he felt exhausted"; HYPOACUSIS (non-serious), outcome "unknown", described as "He has bad hearing/his hearing has been decreased even more". The events "he had a reaction similar to when he had atorvastatin, niaspan, and dyazide.", "he felt exhausted" and "he has bad hearing/his hearing has been decreased even more" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of drug hypersensitivity, fatigue, hypoacusis. Additional information: Reporter did showed appreciation and stated, "He appreciated your product. He appreciated all you do and for those around the world. You folks had been wonderful. They were wonderful!" Reporter thanked Pfizer for keeping people all over the world and so many others alive due to this product.Was there any form of the preservative proline in the product or something similar.Reporter stated he had done his own research as well as with his cardiologist as he stated he had adverse reaction to medications due to his sensitivities. "Among other things, things normal people take for high blood pressure, He could not take any of those medication because he was hyper allergic to them." He accidently found out a cholesterol reducing medication, Repatha (injectable product BID), normal product for reducing cholesterol, he was hyper allergic to them. He had to discontinue - atorvastatin as he noted this product "almost killed him." Reptha which seemed to work ended up having proline, an amino acid preservative, this amino acid is essentially in significant amounts in soy, which he was hyper sensitive too. Did not reacted previously at all to the previous doses of his Pfizer COVID 19 Vaccinations however when he took the booster this time, he had a reaction similar to when he had atorvastatin, niaspan, and dyazide. Any significant soy products he also could not tolerate. Called about booster. Has had all Pfizer shots from day one. The boosters were fine, but with the last booster he had bad reaction. He was amazed because with the others he did not even know he had taken them. He wanted to let Pfizer know. He did research online. He was trying to find out if the booster, has any form of the preservative Proline in it. This preservative was for example in statins. When reporter was prescribed a statin because he was very allergic to Proline it almost killed him and took him years to get over it. Clarified booster that he had bad reaction to as Omicron Covid vaccine booster. He got it on 18Sep2022. Reporter was unique. He was a DES baby that was in his 70's. In the 40's DES was used. DES is Diethyl something, but he could not remember the whole thing. Was used in women who had miscarriage and later discontinued because it led to birth defects in children. Reporter's mother was given DES because she had a miscarriage. Reporter was not aware of birth defects in him. His DNA was screwed up and kidneys look like walnuts. Kidneys were not normal. His sinuses were not normal. Several of his bone joints had limited motion because the bone structures were not like normal hips and knees. Externally he seemed fine. It was after he had a heart attack and had open heart surgery they discovered because of the MRI what had happened to him. They were able to establish DES was the problem. Whatever screwed up his DNA caused him to be hyperallergic to soy and statins. He was also hyperallergic to Proline. That was why he was asking if there was any preservative in the Omicron Covid vaccine booster that might be the cause. When he looked at the chemical composition there did not seemed to be anything that would effect a DES baby that reporter could determine. They told him in the hospital he had bilateral TIA like symptoms. Reporter was thankful for Pfizer's work. He did not get sick with Covid and the vaccine was a good service. He was retired. Reporter clarified the bilateral TIA like symptoms was the bad reaction he had with a statin. The bilateral TIA like symptoms were originally discovered after he had open heart surgery in Jan2016. Approximately 6 months after that in the summer of 2016 he had the first event. He called (withheld) and became unconscious. He was a mess. He thought he was having another heart attack. His arm went numb, brain went numb and had brain fog, his hearing went numb, and he had severe pain in legs. It was described as bilateral TIA like symptoms. No one was sure what was going on. 3 months later it happened again. The hospital team assessed him and said something was going on. They did a blood test and it had to be sent to Clinic. That test determined that he was allergic to statin. They pulled it. He had been on the baby dose of the statin because of his previous history of reacting negatively to pharmaceutical. Clarified that the statin he had bad reaction and bilateral TIA like symptoms with was Atorvastatin. He forgets things now. From memory it was well within date code. He was religious about that. They told him he was allergic to Atorvastatin. Previously he had problem with Meniere's disease and had been put on Dyazide and Niaspan. Within 24 hours of taking those medications he was collapsing and was rushed to hospital. The only difference with the bad reaction he had with the Omicron Covid vaccine booster and Atorvastatin was he was not completely unconscious. He knew that something was wrong. His heart and chest were fine. He was not having heart attack. He was conscious enough to realize the symptoms. He drank a lot of water and it started getting better. Unfortunately he was out of town. Drove home and it took a week to get his act together. He called doctor about what happened. They checked him out and they said don't do that again. He had appointment last week with his general practitioner. General practitioner told reporter that reporter knew he was an odd duck and essentially if reporter thinks that was what happened that was probably what happened. It was an observation at that point. Reporter did so well with all the shots all along, but this one took him out completely. That surprised him. Reporter would visit cardiologist in about an hour. Up until that point, he did fine with all the Pfizer vaccines and did not expect to have a problem. After the first Pfizer Covid vaccine they had him wait an hour to make sure he did not have a reaction and was fine. He had first dose done at the hospital. Bad reaction: started about 16-18 hours later. The vaccine was given in afternoon and later that evening was when he was in deep trouble. It took about a week to feel normal. Within 24-48 hours he was up and about and he felt exhausted. He has bad hearing anyway, but he had been very conscious that after the event his hearing had been decreased even more. That was unusual. That was the only thing that had not fully recovered back to the average state it was. He was using hearing aid previously, but hearing has not return to his baseline. Concomitant Medications: he had taken them for years with no negative impact. He could remember on que the medication names and has to go get them. He also took some vitamins. DES he had no knowledge of the product. He was just aware his mother took it. They later found out, years later, about his deformities that they previously were not aware of. Hypermetabolism: Discovered 20 years ago. He processes food extremely fast. When he was on Dyazide for problems in ears with Meniere's they had said it will take 48-72 hours to have impact. He could not remember how much he had to take, but he took it and within 8 hours his wife found him unconscious on the floor. Cardiologist told him his blood pressure was 60/40. He was as close to being dead with out being dead. Because of that hypermetaoblism he reacts to medications differently than normal and also because of DES. He did not realize the implications until over time. Meniere's situation occurred in 2011. It was hard to say if the Meniere's is gone away because the doctor said it doesn't go away but recedes to where it was not as noticeable. He was in semi coma for 3 months. It was a terrible experience. Investigations: went for blood work and did not had results. He followed a heart healthy diet. Usually his blood work was spectacular. His total cholesterol was normally around 70. Treatment: none, continued heart healthy diet and made no changes. took him almost a week to feel semi-normal or refreshed or alive. the only thing had continued was impact on hearing. he could hear but it was 20-30% less than what it was before. Vaccine was not administered at Military Facility. Intensive Care Unit: no

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: cholesterol; Result Unstructured Data: Test Result:around 70; Comments: His total cholesterol is normally around 70; Test Name: Blood test; Result Unstructured Data: Test Result:he was allergic to statin; Comments: That test determined that he was allergic to statin; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: It was after he had a heart attack and had open heart surgery they discovered because of the MRI what had happened to him
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fibrillation cardiac (Additional Information for Other medicines Pradaxa: been on it for years.); Foggy feeling in head; Heart attack (Additional Information for Other medicines Pradaxa: been on it for years.); Hypermetabolism; Numbness; Open heart surgery (The bilateral TIA like symptoms were originally discovered after open heart surgery in Jan2016); Pain in leg; Soy allergy (hyperallergic to soy); TIA (The bilateral TIA like symptoms were originally discovered after open heart surgery in Jan2016); Unconsciousness
Andere Medikamente: PRADAXA; AMLODIPINE BESYLATE 10
Allergien: -
Vorherige Impfungen: -

VAERS 2506499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MD
Alter: 44,0
Geschlecht: F
Eingang: 12.11.2022
Impfdatum: 09.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Axillary mass Axillary pain Fear Injection site pruritus

Symptomtext

On 11/10/22 in the evening, I started to feel pain under my left and right armpits. Initially, I thought it was due to my bra, but the pain increased as time went on. I checked for lumps under both arms and researched side effects of the vaccine booster. It read that swollen lymph nodes are uncommon and could last for 10 days. I've had no reactions from the previous 3 Pfizer shots, but this one was itchy at the injection site hours later, and now I'm assuming my lymph nodes are swollen. It's either that or I'm scared I have cancer now (which does not run in my family). I also read that the effect is usually on the side where the injection was performed. In my case, it was both sides which prompted me to report this to you. As of today, 11/11/22, my right armpit is slightly less painful than the left side (injection was left arm), but the left armpit pain is still the same as last night.

Weitere VAERSDATA-Felder

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

VAERS 2506457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NV
Alter: 57,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 20.10.2022
Beginn: 03.11.2022
Tage bis Beginn: 14,0
Dosis: 5
Route/Site: IM / RA

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

Chills Myalgia Paranasal sinus discomfort Pyrexia

Symptomtext

I had a fever, chills and muscle aches with sinus pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: Penicilin
Vorgeschichte: rumortoid arthritis
Andere Medikamente: I was taking Hydroxclorquin: Presidone: Sulsasalazine; multivitamin: calcium supplement; D3 and biotin at the time of vaccination.
Allergien: Kelsex
Vorherige Impfungen: -

VAERS 2505248

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: PA
Alter: 11,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Abdominal pain upper Body temperature Contusion Fatigue Headache Nausea Overdose Pain Pain in extremity Product administered to patient of inappropriate age Pyrexia Vaccination site pain

Symptomtext

bruising; more achiness; Pain at injection (left arm); Stomach pain; Nauseous; Slight fever/more fever; Fatigue; arm soreness; Headache; they are 11 yeas old my kids, twins but they were given the adult doses; grabbed the wrong vial; they are 11 yeas old my kids, twins but they were given the adult doses; grabbed the wrong vial; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the parent. An 11-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 as dose 4 (booster), 0.3 ug single (Lot number: GH9697, Expiration Date: 10Jan2023) at the age of 11 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose: 3, Lot: FL8095), administration date: 08Aug2022, when the patient was 10-year-old, for COVID-19 immunization; Bnt162b2 (Dose: 1, Lot: FK5618), administration date: Nov2021, when the patient was 10 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, Lot: FK5127), administration date: Dec2021, when the patient was 10 years old, for COVID-19 immunization. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 04Nov2022, outcome "unknown", OVERDOSE (non-serious) with onset 04Nov2022, outcome "recovered" and all described as "they are 11 yeas old my kids, twins but they were given the adult doses; grabbed the wrong vial"; FATIGUE (non-serious) with onset 05Nov2022, outcome "recovered" (05Nov2022); HEADACHE (non-serious) with onset 05Nov2022, outcome "recovered" (06Nov2022); NAUSEA (non-serious) with onset 05Nov2022, outcome "recovered" (05Nov2022), described as "Nauseous"; VACCINATION SITE PAIN (non-serious) with onset 05Nov2022, outcome "recovering", described as "Pain at injection (left arm)"; PYREXIA (non-serious) with onset 05Nov2022, outcome "recovered" (06Nov2022), described as "Slight fever/more fever"; ABDOMINAL PAIN UPPER (non-serious) with onset 05Nov2022, outcome "recovered" (06Nov2022), described as "Stomach pain"; PAIN IN EXTREMITY (non-serious) with onset 05Nov2022, outcome "recovering", described as "arm soreness"; CONTUSION (non-serious), outcome "unknown", described as "bruising"; PAIN (non-serious), outcome "unknown", described as "more achiness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of overdose, fatigue, pain in extremity, abdominal pain upper, nausea, vaccination site pain. Therapeutic measures were taken as a result of pyrexia, headache. Additional information: Reporter stated that reporter was trying to, and walking kids to the pediatrician. They went and got their Pfizer Omicron boosters (Clarified as Pfizer COVID-19 Vaccine) yesterday. The pharmacy they went to wrote one thing down on the vaccination card but than, they are 11 yeas old kids, twins but they were given the adult doses not the child dose and reporter concern was, reporter talked to the pediatrician they were just having some, and patient daughter had like a 99 degree fever and they had just fatigue and arm soreness and a headache so nothing, and reporter asked about know more reaction they had on the kids dose. Reporter stated, that the kids got the wrong dose they got the adult one. Right, because the dose was told 30 micrograms. Caller would like to know the risk regarding that Resolutions. Gathered caller's concern/inquiry-Gathered. Advise provider stated that it will not going to affect the kids in the long term, understand side effects and know it was not dangerous. Possibly more side effect issues. Patient shot site hurts still and notes bruising as well. Patient seems fine. The father states, from all the studies, no adverse long-term effects that anyone has seen. Patient date of birth was told three times so there was no issue with the children. Son told them he was eleven and they wrote on the card Pfizer pediatric booster 6K1657, however 2-3 minutes after the shot they were standing in the aisle 15 minutes after the pharmacy tech gave the shot. Mentioned that she went in quick when she went in and got the vaccine. They had more reaction than the one in Aug2022. Clarified that patient arm hurting was over. Had more symptoms and fatigue over the weekend than any dose previously had. Called because he was trying to make sure that his kids okay over the weekend. Was told that it was the wrong dose paperwork that they gave him which said the Pfizer updated booster 5-11 NDC 59267-0565-01. she had pain at the site and stomach pain. Watched patient diet but no medical treatment. Later clarified that they kept her at breads and stuff for a couple of hours and by the end of the day was fine. For headache and slight fever patient treated with children's Tylenol. Patient had the original dose and then the booster in Aug2022. Clarified that they had the Pfizer vaccine in Nov2021 with a lot of FK5618 and the second Pfizer vaccine in Dec2021 with a lot of FK5127. Clarified that on 08Aug2022 they had the Pfizer Booster with a lot number of FL8095. NDC provided above was crossed out and underneath it was NDC 59267-0304-01. Product: Comirnaty, Pfizer-BioNTech COVID-19 Vaccine [Monovalent] and/or Bivalent Dose/Dosage Form: Gray cap, Original/Omicron BA.4/BA.5 (Bivalent),grater than equal 12 years 15/15 mcg per dos. Question: Caller states that his 11 year old kids were given the incorrect dosage for the Pfizer COVID Vaccine. He followed up with his pediatrician and they are fine. He notes this was on Friday. He is now calling Pfizer to double check his information that he has sought out over the weekend through the internet, his peds office and the (pharmacy withheld).; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201280900 same drug/AE, diferent patient;

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Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:99 Fahrenheit; Comments: my daughter had like a 99 degree fever; Test Name: fever; Result Unstructured Data: Test Result:99.4-99-7 Fahrenheit; Test Name: fever; Result Unstructured Data: Test Result:more fever Fahrenheit; Comments: his children have "more fever
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2505243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / RA

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

Arthralgia Cognitive disorder Euphoric mood Fatigue Myalgia SARS-CoV-2 test Tension Thirst Vaccination site pain

Symptomtext

feelings of euphoria/mood enhancement; improved cognitive function; fatigue; muscle soreness; tension; joint pain; thirst; the injection site pain started within 1 hr.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Nov2022 at 15:15 as dose 5 (booster), single (Lot number: GH9697) at the age of 67 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "osteoarthritis" (unspecified if ongoing); "hypertension" (unspecified if ongoing). Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, on 23Oct2022 as dose 1, single, flu vaccine senior dose; LISINOPRIL; MOTRIN [IBUPROFEN]. Vaccination history included: BNT162b2 (DOSE 4 (BOOSTER), SINGLE, Batch/Lot No: FK9893, Location of injection: Arm Left, Vaccine Administration Time: 04:00 PM), administration date: 05Apr2022, when the patient was 67-year-old, for COVID-19 immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Batch/Lot No: FC3184, Location of injection: Arm Right, Vaccine Administration Time: 05:00 PM), administration date: 27Sep2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Batch/Lot No: EP7534, Location of injection: Arm Right, Vaccine Administration Time: 01:15 PM), administration date: 22Mar2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (DOSE 1, SINGLE, Batch/Lot No: EN6201, Location of injection: Arm Left, Vaccine Administration Time: 08:15 AM), administration date: 26Feb2021, when the patient was 66-year-old, for COVID-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 03Nov2022 at 16:15, outcome "recovered" (04Nov2022 at 14:15), described as "the injection site pain started within 1 hr."; FATIGUE (non-serious) with onset 03Nov2022 at 22:00, outcome "recovered" (04Nov2022 at 20:00); ARTHRALGIA (non-serious) with onset 03Nov2022 at 22:00, outcome "recovered" (04Nov2022 at 20:00), described as "joint pain"; MYALGIA (non-serious) with onset 03Nov2022 at 22:00, outcome "recovered" (04Nov2022 at 20:00), described as "muscle soreness"; TENSION (non-serious) with onset 03Nov2022 at 22:00, outcome "recovered" (04Nov2022 at 20:00); THIRST (non-serious) with onset 03Nov2022 at 22:00, outcome "recovered" (04Nov2022 at 20:00); EUPHORIC MOOD (non-serious) with onset 04Nov2022 at 07:15, outcome "recovered", described as "feelings of euphoria/mood enhancement"; COGNITIVE DISORDER (non-serious) with onset 04Nov2022 at 07:15, outcome "recovered", described as "improved cognitive function". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of euphoric mood, fatigue, myalgia, tension, arthralgia, thirst, vaccination site pain, cognitive disorder. Additional information: The adverse events were initial fatigue, muscle soreness, tension, joint pain with some thirst within first 24 hours. The injection site pain started within 1 hour and other symptoms followed but disappeared 22 hours later. However adverse symptoms were temporary, and patient noticed mood enhancement, improved cognitive function, feelings of euphoria 16 hours after injection. The patient had no known allergies. In Mar2022 (post vaccination with third dose), the patient underwent covid test (Nasal Swab) and the results was negative.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 202203; Test Name: Covid 19 Test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Osteoarthritis
Andere Medikamente: LISINOPRIL; MOTRIN [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 2503883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 29.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Pain in jaw

Symptomtext

Severe 10/10 crushing and aching pain to maxilla and mandible areas. Distressing pain.; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 56-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 29Oct2022 at 20:15 as dose 4 (booster), single (Lot number: GH9697) at the age of 56 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: MIRALAX; COLACE; CLONOPIN; MAGNESSIUM CARBONATE; BEANO. Vaccination history included: Covid-19 vaccine (Primary immunization series complete; manufacturer unknown), for Covid-19 Immunization; Covid-19 vaccine (DOSE 3 (BOOSTER); manufacturer unknown), for Covid-19 Immunization. The following information was reported: PAIN IN JAW (non-serious) with onset 30Oct2022 at 23:45, outcome "recovered", described as "Severe 10/10 crushing and aching pain to maxilla and mandible areas. Distressing pain.". Therapeutic measures were taken as a result of pain in jaw.

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Praegender Schweregrund: Pain in jaw
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: No chronic illness
Andere Medikamente: MIRALAX; COLACE; CLONOPIN; MAGNESSIUM CARBONATE; BEANO
Allergien: -
Vorherige Impfungen: -

VAERS 2503872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: PA
Alter: 11,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Body temperature Contusion Fatigue Headache Overdose Pain Pain in extremity Product administered to patient of inappropriate age Pyrexia Vaccination site pain

Symptomtext

bruising; more fever; more achiness; shot site hurts; Fatigue; arm soreness/Arm hurting, left arm where the vaccine was given; Headache; they are 11 yeas old my kids, twins but they were given the adult doses; grabbed the wrong vial; they are 11 yeas old my kids, twins but they were given the adult doses; grabbed the wrong vial; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the parent. An 11-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 as dose 4 (booster), single (Lot number: GH9697, Expiration Date: 10Jan2023) at the age of 11 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose: 3, Lot: FL8095), administration date: 08Aug2022, when the patient was 10-year-old, for COVID-19 immunization; Bnt162b2 (Dose: 1, Lot: FK5618), administration date: Nov2021, when the patient was 10 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, Lot: FK5127), administration date: Dec2021, when the patient was 10 years old, for COVID-19 immunization. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), OVERDOSE (non-serious) all with onset 04Nov2022, outcome "unknown" and all described as "they are 11 yeas old my kids, twins but they were given the adult doses; grabbed the wrong vial"; FATIGUE (non-serious) with onset 05Nov2022, outcome "recovered" (05Nov2022); HEADACHE (non-serious) with onset 05Nov2022, outcome "recovered" (05Nov2022); PAIN IN EXTREMITY (non-serious) with onset 05Nov2022, outcome "recovered" (06Nov2022), described as "arm soreness/Arm hurting, left arm where the vaccine was given"; VACCINATION SITE PAIN (non-serious) with onset 05Nov2022, outcome "recovered" (06Nov2022), described as "shot site hurts"; CONTUSION (non-serious), outcome "unknown", described as "bruising"; PYREXIA (non-serious), outcome "unknown", described as "more fever"; PAIN (non-serious), outcome "unknown", described as "more achiness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of product administered to patient of inappropriate age, overdose, fatigue, pain in extremity, vaccination site pain. Therapeutic measures were taken as a result of headache. Additional information: The patient was given the adult doses not the child dose and had fever and they had just fatigue and arm soreness and a headache so nothing, more reaction they had on the kid dose when they had their last booster. Like 3 months ago but nothing critical. The caller was in the room and as per the caller she wrote down the child, but she just grabbed the wrong vial. The reporter stated that he would like to verify the lot number that was given to his children to confirm the dose of the product. He states they are 11 years and one month of age and they were given an adult dosage, rather than the child's. Caller notes the pharmacy will provide an updated vaccination card as well. The reporter stated he had concerned that data may come out in the future stating if you got an adult dose you would not need another dose for 12 amount of months, vs if you received a child's dose then you would need another one at say 6 months instead. He is concerned that someone will say in 6 months if you got a child dose to get another because its less than the adult dose. He noted he wanted to know the formulation for future progress. Caller stated thank God the kids are fine and discussed how they screwed up at the pharmacy and gave the adult dose to kids and they will go through their procedures. He had been advised by his provider, it's not going to affect the kids in the long term, understand side effects and know its not dangerous. Possibly more side effect issues. He proceeded to note he had been told and read through the news where people have received 2 doses at once due to errors while drawing the vaccines. The reporter noted that while his pediatrician did advise possible more side effects, his children had more fever more achiness and are now over it back to school and normal however he noted bruising as well. The father stated, from all the studies, no adverse long term effects that anyone has seen. My kid's shot site hurts still fine.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201280841 same drug/AE, diferent patient;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:more fever; Comments: his children have "more fever"
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (Other condition: No)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2502040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VT
Alter: 19,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Anxiety Dizziness Immediate post-injection reaction Nausea

Symptomtext

Pt came to the clinic to get her Flu & Covid Bivalent vaccines. Immediately after the administration of the 1st vaccine (Flu), pt. started to feel lightheaded and nauseous. She was transferred to a wheelchair and then to a cot to lay down. She was offered water/snack and vitals monitored. She advised she felt a bit anxious before coming in for the vaccines. Pt wanted to proceed with her 2nd vaccine (Pfizer Bivalent). That was administered at 1455 with no troubles. Pt was monitored for approximately 25 minutes after her last vaccine, and she advised she was feeling back to normal. Vitals all were within normal limits during the duration.

Weitere VAERSDATA-Felder

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

VAERS 2500489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: IL
Alter: 50,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 14.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / RA

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

Blood test abnormal Ear pain Labyrinthitis Protein urine present Urine analysis abnormal Vitamin D decreased

Symptomtext

A week after receiving my COVID-19 vaccine and 3 days after y yearly flu shot I woke up with an earache. Went in to doctor on 10/31/2022 and found out that I had an inner ear infection in both ears. Prescribed augmentin. After about 5 days on antibiotics I began to see improvement in my ears. Ears are much better but still not 100%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Blood work returned with low Vitamin D and UA returned with Protein in urine
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; breast cancer 10 years ago
Andere Medikamente: Trulicity; Prestique; simvastatin; metformin; Jardiance; Topamax;
Allergien: None
Vorherige Impfungen: -

VAERS 2500458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MO
Alter: 71,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Additional Details: After about 10 minutes after receiving the vaccine the patient was complaining of lightheadedness/dizziness. Patient remained in the pharmacy for up to 30 minutes after vaccination. After 30 minutes the patient said she was feeling better and lightheadedness had gone away.

Weitere VAERSDATA-Felder

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

VAERS 2499978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 05.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Nausea

Symptomtext

Patient sat down to get vaccines - gave flu shot vaccine first in Left Deltoid; Immunizing technician went to right deltoid to give Covid Booster shot and after Covid shot the patient stated she felt faint and that she was about to throw up. Technician gave her Trashcan and promptly grabbed the pharmacist. When pharmacist entered the immunization room - asked patient what was going on. got her some water and a fan to blow cool air on her. Patient heart rate was 87 bpm when rph came in immunization room at 3:41pm - heart rate lowered with in 2 min to 71 bpm (per patient's smart watch reading). Patient drank some water on her own and stated she was ready to stand up. RPh walked with patient to her car and she walked normally and she felt better. Patient had a driver to already to take her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None confirmed by patient
Vorgeschichte: none noted
Andere Medikamente: none noted
Allergien: None noted
Vorherige Impfungen: -

VAERS 2499752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 30.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / RA

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

Erythema Feeling hot Pruritus Swelling Vaccination site induration

Symptomtext

swelling; redness; hotness; itchiness; hardness at injection site; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 46-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 30Oct2022 at 10:00 as dose 4 (booster), single (Lot number: GH9697) at the age of 46 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "High cholesterol" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "Autoimmune gastritis" (unspecified if ongoing). Concomitant medication(s) included: FLUCELVAX QUAD taken for immunisation, on 12Oct2022; LEVOTHYROXINE; ROSUVASTATIN. Vaccination history included: Covid-19 vaccine (DOSE 3 (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN), for COVID-19 immunisation; Covid-19 vaccine (DOSE 3; MANUFACTURER UNKNOWN), for COVID-19 immunisation. The following information was reported: VACCINATION SITE INDURATION (non-serious) with onset 31Oct2022 at 18:00, outcome "not recovered", described as "hardness at injection site"; FEELING HOT (non-serious) with onset 31Oct2022 at 18:00, outcome "not recovered", described as "hotness"; PRURITUS (non-serious) with onset 31Oct2022 at 18:00, outcome "not recovered", described as "itchiness"; ERYTHEMA (non-serious) with onset 31Oct2022 at 18:00, outcome "not recovered", described as "redness"; SWELLING (non-serious) with onset 31Oct2022 at 18:00, outcome "not recovered". Therapeutic measures were not taken as a result of swelling, erythema, feeling hot, pruritus, vaccination site induration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune gastritis; High cholesterol; Hypothyroidism
Andere Medikamente: LEVOTHYROXINE; ROSUVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2499070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 21.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pruritus Rash Rash pruritic Sleep disorder

Symptomtext

Site: Itching at Injection Site-Severe, Systemic: Allergic: Itch (specify: facial area, extremeties)-Severe, Systemic: Allergic: Itch Generalized-Severe, Systemic: Allergic: Rash (specify: facial area, extremeties)-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: pt reported severe itching rash that gets worse at night but goes away in am-Severe, Additional Details: pt said rash itching all over body in patches got worse about a week after shot. he felt due to covid shot. he took benadryl which helped sleep but very bad at night goes away in am and then returns especially when he exercises. i told him to contact md. itching feels like coming from inside not on skin tried hydrocortisone does not help told to reach out to md and we would report it

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2498846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gh9697

mild

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 17.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Cough Fatigue Feeling cold Headache Malaise Pain

Symptomtext

Began about 5 hrs after injection, tired, achy, chills in the middle of the night, feeling achy the next day for the whole day, symptoms of feeling Sick with dry cough (cold feeling in chest) which continued the rest of the week, as well as being tired, also head pain on left side of head that lasted the whole day upon waking and went away the following day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None done
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: Not lactose tolerant
Vorherige Impfungen: -

VAERS 2498834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 28.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site pruritus Injection site swelling Injection site warmth

Symptomtext

Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: injection site is warm to touch and tender to touch. advised pt to draw a surrounding line and monitor and take benadryl. If not better see doctor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2498762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: NJ
Alter: 42,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 19.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Decreased appetite Fatigue Headache SARS-CoV-2 test Urticaria

Symptomtext

Days 1-3 headachy; tired/Days 4-9 fatigue; loss of appetite; hives/By end of day 10, hives have moved up and down body, particularly arms and legs. Day 11 hives spread to fully cover arms and legs, down to feet/toes and hands; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Oct2022 at 13:15 as dose 4 (booster), single (Lot number: GH9697) at the age of 42 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Previous dose details, Prev dose product=COVID 19,, Prev dose brand=Pfizer,, Prev dose brand unknown=False,, Is bivalent=False,, Prev dose lot number=331308A,, Prev dose lot unknown=False,, Prev dose administration date=08Dec2021,, Prev dose dose number=3,, Prev dose vaccine location=Left arm), administration date: 08Dec2021, when the patient was 41-year-old, for COVID-19 immunization, reaction(s): "tired (same as prev 3 doses)"; BNT162b2 (Prev dose product=COVID 19,, Prev dose brand=Pfizer,, Prev dose brand unknown=False,, Is bivalent=False, Prev dose lot number=EW0172, Prev dose lot unknown=False,, Prev dose administration date=26Apr2021,, Prev dose dose number=2,, Prev dose vaccine location=Left arm,), administration date: 26Apr2021, when the patient was 41-year-old, for COVID-19 immunization, reaction(s): "tired (same as prev 3 doses)"; Bnt162b2 (Prev dose product=COVID 19,, Prev dose brand=Pfizer,, Prev dose brand unknown=False,, Is bivalent=False, Prev dose lot number=EW0172, Prev dose lot unknown=False,, Prev dose dose number=1,, Prev dose vaccine location=Left arm), for COVID-19 immunization, reaction(s): "tired (same as prev 3 doses)". The following information was reported: HEADACHE (non-serious) with onset Oct2022, outcome "recovering", described as "Days 1-3 headachy"; URTICARIA (non-serious) with onset Oct2022, outcome "recovering", described as "hives/By end of day 10, hives have moved up and down body, particularly arms and legs. Day 11 hives spread to fully cover arms and legs, down to feet/toes and hands"; DECREASED APPETITE (non-serious) with onset Oct2022, outcome "recovering", described as "loss of appetite"; FATIGUE (non-serious) with onset Oct2022, outcome "recovering", described as "tired/Days 4-9 fatigue". The events "days 1-3 headachy", "tired/days 4-9 fatigue", "loss of appetite" and "hives/by end of day 10, hives have moved up and down body, particularly arms and legs. day 11 hives spread to fully cover arms and legs, down to feet/toes and hands" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache, fatigue, decreased appetite, urticaria.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: OTC (Don't remember); Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Skin reaction; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2497848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: MO
Alter: 32,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Vomiting

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Nausea-Medium, Systemic: Vomiting-Medium

Weitere VAERSDATA-Felder

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

VAERS 2497280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: MN
Alter: 14,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Irritability Product use issue Pyrexia

Symptomtext

irritability fever 100.1; irritability fever 100.1; Pfizer: 31Oct2022/Flu shot: 31Oct2022; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 14-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 31Oct2022 as dose 3 (booster), single (Lot number: GH9697) at the age of 14 years, in left arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 31Oct2022 as dose 3, single (Batch/Lot number: unknown), in left arm for immunisation. The patient's relevant medical history included: "Cerebral Palsy" (unspecified if ongoing); "rhizotomy shunt" (unspecified if ongoing); "spinal fusion" (unspecified if ongoing); "bilateral hip surgery" (unspecified if ongoing). Concomitant medication(s) included: IRON. Past drug history included: Vancomycin, reaction(s): "known allergies: Vancomycin". Vaccination history included: BNT162b2 (Dose 1, Lot number FC3182, Vaccine location: Left arm), administration date: 14Sep2021, for COVID-19 Immunization; BNT162b2 (Dose 2, Lot number FF2588, Vaccine location: Left arm), administration date: 04Sep2021, for COVID-19 immunization, reaction(s): "14Sep2021: Dose Number: 1/04Sep2021: Dose Number: 2". The following information was reported: PRODUCT USE ISSUE (non-serious) with onset 31Oct2022, outcome "unknown", described as "Pfizer: 31Oct2022/Flu shot: 31Oct2022"; PYREXIA (non-serious), IRRITABILITY (non-serious) all with onset 31Oct2022 at 12:00, outcome "not recovered" and all described as "irritability fever 100.1". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, irritability. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201270012 same patient/product, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20221031; Test Name: Fever; Result Unstructured Data: Test Result:irritability fever 100.1
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cerebral palsy; Hip surgery; Rhizotomy; Spinal fusion
Andere Medikamente: IRON
Allergien: -
Vorherige Impfungen: -

VAERS 2496422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VT
Alter: 61,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Burning sensation Insomnia Joint noise Ligament injury Limb discomfort Loss of personal independence in daily activities Pain Sensory disturbance

Symptomtext

this was an influenza vaccine.my shoulder and arm felt an intense burning sensation when I got the vaccine and the shoulder and upper arm have been hurting ever since.feels like the arm was pulled out of its socket and some ligaments were damaged.intense twinges of pain when moved certain ways and clicking that wasn?t there before.went to my doctor a week and a half after as it was not getting better and was making it very hard to sleep and do normal activities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None just a doctor visit
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pulmicort 180 mcg vitamin c 500 mg
Allergien: Latex,dairy,amoxicillin
Vorherige Impfungen: -

VAERS 2495260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: CO
Alter: 37,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 20.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / LA

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

Eye irritation Eye swelling Ophthalmological examination abnormal Pain Swelling of eyelid Visual impairment

Symptomtext

Six days after vaccine eye started feeling irritated, removed contacts and flushed eye with saline; Woke up next morning and eye was really swollen; Went to an eye doctor and had a full eye exam and saw that my vision was decreased in right eye; Prescribed levofloxacin and MAXITROL eye drops and told to use warm compresses on eye. Was told that eye was going to be more swollen then go down; it's starting to go down and the pain is gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Eye test, loss of vision in right eye.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Migraines; Acne; Anemia
Andere Medikamente: Spironolactone; TAZORAC topical; multivitamin
Allergien: Penicillin; CECLOR; BIAXIN.
Vorherige Impfungen: -

VAERS 2494636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: SC
Alter: 60,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Fatigue Somnolence

Symptomtext

Extremely drowsiness; Tiredness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 26Oct2022 at 16:30 as dose 4 (booster), single (Lot number: GH9697) at the age of 60 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High cholesterol" (unspecified if ongoing), notes: High cholesterol. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, on 21Oct2022 as dose number unknown, single. Vaccination history included: Covid-19 vaccine (Primary immunization was completed, unknown manufacturer), for Covid-19 immunization; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE), for Covid-19 immunization. The following information was reported: SOMNOLENCE (non-serious) with onset 26Oct2022 at 19:00, outcome "recovering", described as "Extremely drowsiness"; FATIGUE (non-serious) with onset 26Oct2022 at 19:00, outcome "recovering", described as "Tiredness". Therapeutic measures were not taken as a result of somnolence, fatigue. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient received flu vaccine within 4 weeks prior to the vaccination. The patient received other medications within 2 weeks. The patient had unspecified known allergies. Follow-up (31Oct2022): 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: High cholesterol
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: UT
Alter: 76,0
Geschlecht: M
Eingang: 29.10.2022
Impfdatum: 25.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: IM / LA

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

Movement disorder Pain in extremity Peripheral swelling

Symptomtext

Patient reported that their arm and hand had become swollen and painful and had lack of movement. Patient was informed that they should seek further medical attention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: MN
Alter: 72,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Decreased appetite Diarrhoea Interchange of vaccine products Vomiting

Symptomtext

diarrhea; vomiting; dose 1: 04MAR2021, Moderna; dose 2: 08APR2021, Moderna; dose 3: 31OCT2021, Moderna; dose 4: 06MAY2022, Moderna; dose 5: yesterday (25Oct2022), Pfizer Covid 19 Vaccine Bivalent; don't have a lot of appetite; 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 72-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 25Oct2022 at 10:30 as dose 5 (booster), single (Lot number: GH9697) at the age of 72 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: coviD-19 vaccine moderna (Dose: 01, Lot number: unknown), administration date: 04Mar2021, when the patient was 70-year-old, for COVID-19 immunization; coviD-19 vaccine moderna (Dose: 02, Lot number: unknown), administration date: 08Apr2021, when the patient was 70-year-old, for COVID-19 immunization; coviD-19 vaccine moderna (Dose: 03, Lot number: unknown), administration date: 31Oct2021, when the patient was 71-year-old, for COVID-19 immunization; coviD-19 vaccine moderna (Dose: 04, Lot number: unknown), administration date: 06May2022, when the patient was 71-year-old, for COVID-19 immunization. The following information was reported: DECREASED APPETITE (non-serious) with onset 25Oct2022, outcome "unknown", described as "don't have a lot of appetite"; INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 25Oct2022 at 10:30, outcome "unknown", described as "dose 1: 04MAR2021, Moderna; dose 2: 08APR2021, Moderna; dose 3: 31OCT2021, Moderna; dose 4: 06MAY2022, Moderna; dose 5: yesterday (25Oct2022), Pfizer Covid 19 Vaccine Bivalent"; DIARRHOEA (non-serious) with onset 25Oct2022 at 22:30, outcome "recovered" (26Oct2022), described as "diarrhea"; VOMITING (non-serious) with onset 25Oct2022 at 22:30, outcome "recovered" (26Oct2022). Therapeutic measures were taken as a result of diarrhoea, vomiting. Additional information: Caller stated the she received the shot at 10:30 a.m. and about 12 hours later she had diarrhea that lasted about 2-4 hours and a couple hours after that started she vomited her entire evening meal. Caller stated she did not have a reaction to her previous vaccines, but the others were Moderna. Treatment: Drank soda and put a pillow on her belly. The patient did not received any prior vaccinations within 4 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
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 2493277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OH
Alter: 40,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 25.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal distension Abdominal pain Alanine aminotransferase increased Aspartate aminotransferase increased Axillary pain Blood test C-reactive protein normal Diarrhoea Differential white blood cell count normal Fatigue Feeding disorder Full blood count abnormal Lipase normal Mean cell haemoglobin increased Metabolic function test abnormal Nausea Swelling

Symptomtext

Swollen right armpit, painful. Abdominal pain and bloating, loose stools, brief nausea, fatigue. Abdominal pain started 10/16 around 8pm, got much worse over night, communicated with my doctor on Thursday 10/27, that evening I thought about going to the ER the pain was so bad in my abdomen. Woke up to relief almost on 10/28, saw a Dr. in person who examined me and did blood work. All labs came back normal so no imaging was ordered. Fasted for 2 days and pain was relieved. Have not tried eating food yet. Hopefully it will be ok.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: Full CBC with differential COPC 10/28 - normal except for a slightly high MCH of 32.4 CRP COPC normal Comprehensive Metabolic Panel COPC -all normal except slightly high AST of 58 and ALT of 70 Lipase COPC - normal
Aktuelle Erkrankungen: None.
Vorgeschichte: Type 2 Diabetes; Celiac Disease; Diverticular Disease
Andere Medikamente: Synthroid; Turmeric; Garlic; Vitamin D; Calcium; Magnesium; Zinc; Potassium; Allergy pills
Allergien: Allergic to wheat, gluten, and surgical glue
Vorherige Impfungen: -

VAERS 2493107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: TN
Alter: 58,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness postural

Symptomtext

Dizziness upon standing up too quickly

Weitere VAERSDATA-Felder

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

VAERS 2492754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VT
Alter: 14,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Fall Feeling hot Hyperhidrosis Malaise Pallor

Symptomtext

Patient came to the vaccine clinic with his mom to get his Pfizer Bivalent booster dose. He received the dose at 3:50, while waiting in the waiting area he started to not feel well and walked to a family friend who is a vaccinator at 3:55. Patient was complaining of feel dizzy, warm, sweaty and pale. He started to fall to the ground and his mom lowered him. Mom does not believe there was LOC, he did not strike his head or any other body parts and has no additional complaints. At 3:59 patient was given water and a granola bar and advised he was feeling much better. Both he and his mom stayed with us for approximately 30 minutes to ensure he was feeling 100%.

Weitere VAERSDATA-Felder

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

VAERS 2491784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: WA
Alter: 78,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 12.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / UN

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

Blood test normal Computerised tomogram normal Dizziness Electrocardiogram normal Incontinence Vertigo Vomiting

Symptomtext

I had my vaccination on 10/12/2022. I woke up on 10/13/2022 with vertigo. As soon as I tried to sit up, I was overwhelmed with dizziness. I made several attempts to get up but threw up and had incontinence. I tried to drink water but vomited. I went back to bed and stayed there. I have had a history of vertigo but never this bad. It eased up on 10/14/2022. I went to the emergency room on 10/18/2022 and they prescribed me meclizine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Blood panel, CT scan, EKG 10/18/2022 all normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: COVID-19 positive 08/01/2022; Pacemaker 2019; Depression; Asthma
Andere Medikamente: Rosuvastatin; ADVAIR; FLONASE; spironolactone; vitamin 3; aspirin; dalbavancin
Allergien: ANEXSIA; SERZONE; omeprazole
Vorherige Impfungen: -

VAERS 2486869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: NJ
Alter: 60,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Fatigue Injection site pain Myalgia Pyrexia

Symptomtext

Starting 12 hours after injection and lasting until 36 hours post injection: low grade fever (99.9 F degrees), full body muscle aches, fatigue, injection site soreness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypothyroid
Andere Medikamente: Tirosint solution 88 mcg daily Cequa eye drops
Allergien: penicillin, augmentin, Cipro, tetracycline, Flagyl, NSAIDs, cafergot, IV contrast agents, shellfish, weeds/grasses.
Vorherige Impfungen: All previous Covid vaccines: age 58/59 yrs, Pfizer 03/31/2021, 04/21/2021, 11/21/2021. Shingrix Zoster vaccine 2nd dose: age

VAERS 2486581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: GA
Alter: 74,0
Geschlecht: M
Eingang: 23.10.2022
Impfdatum: 07.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Deafness unilateral Neck pain Peripheral swelling Pharyngeal swelling

Symptomtext

Patient stated that he had swelling of the throat and right hand with in 24 hours of vaccine. Patient then began experiencing right-sided neck pain and complains of complete hearing loss of the right ear. Patient called and visited his primary care physician. He was given a steroid shot and methylprednisolone 4mg twice daily. The steroids reduced the neck pain, throat swelling, and hand swelling with in 2-3 days of initiation. However, patient states the he is still experiencing hearing loss of the right ear two weeks after shot was received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neck pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no known
Vorgeschichte: -
Andere Medikamente: clindamycin gel, xarelt, hctz, anastrazole, clindamycin tabs, pregabalin
Allergien: no known
Vorherige Impfungen: -

VAERS 2485419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Chills Dizziness

Symptomtext

Pt reported cold chills in the upper extremeties and dizziness. Pt given ammonia inhalant. Denies chest pains Vitals: 9:45 145/69, 107, 18, O2 Sat 100% -- > 10:15 142/70, 102 -- > 88,18 pt sitting up w/ no dizziness. skin color pink Pt laid down w/ feet elevated. @10:00 w/ interpreter- pt denies major medical problems except anemia -- > takes iron pills Pt stable and released from the vaccination site w/ husband.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: anemia
Andere Medikamente: Medications: iron supplement
Allergien: Allergies: None
Vorherige Impfungen: -

VAERS 2483083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: CT
Alter: 58,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 08.09.2022
Beginn: 13.10.2022
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Fatigue Full blood count abnormal Platelet count decreased

Symptomtext

This last Thursday I was very tired till 5PM and thought maybe my platelets when down but couldn't get it checked at that time. The next day I had a draw and my platelets were down to 22, and the next day it was 28. Prior to the 4th dose vaccine my platelets were in the 40's when I had blood drawn the same day I had the 4th dose vaccine. I routinely get blood drawn before any vaccinations because I have ITT and that is when it was in 40's. So it went from 40's the day of the vaccine to 22 a week after the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Blood draw CBC, low platelet 22 the doctor advised if I feel bad again to go to the hospital
Aktuelle Erkrankungen: No
Vorgeschichte: Fatty liver disease; Low platelets; Overweight
Andere Medikamente: Metformin ER; calcium; vitamin D3; vitamin C; vitamin B12
Allergien: BYDUREON
Vorherige Impfungen: After the 1st dose COVID-19 vaccination my platelet count went from 37 to 28 six weeks after the shot and I was put on prednison

VAERS 2482519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

mild

Staat: IL
Alter: 63,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 13.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

Hypersensitivity Pruritus Urticaria Vaccination site swelling

Symptomtext

itching on his arm and back of his scapula.; swollen in the arm like a welt in the injection site; allergic reaction; a welt on his arm; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team, Program ID. A 63-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Oct2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 63 years, in arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose #4: , Date: 13May2022 , Lot: FP4554, NDC: unknown , Expiry: unknown), administration date: 13May2022, when the patient was 62-year-old, for COVID-19 immunization; BNT162b2 (Dose #3: , Date: 09OCt2021 , Lot: FF2590 , NDC: unknown , Expiry: unknown), administration date: 09Oct2021, when the patient was 62-year-old, for COVID-19 immunization; BNT162b2 (Dose #2: outside source, Date: 06Feb2021, Lot: EM9810, NDC: unknown , Expiry: unknown), administration date: 06Feb2021, when the patient was 61-year-old, for COVID-19 immunization; BNT162b2 (Dose #1: from an outside source, Date: 19Jan2021, Lot: EL3247 , NDC: unknown, Expiry: unknown), administration date: 19Jan2021, when the patient was 61-year-old, for COVID-19 immunization. The following information was reported: PRURITUS (non-serious), outcome "unknown", described as "itching on his arm and back of his scapula."; VACCINATION SITE SWELLING (non-serious), outcome "unknown", described as "swollen in the arm like a welt in the injection site"; HYPERSENSITIVITY (non-serious), outcome "unknown", described as "allergic reaction"; URTICARIA (non-serious), outcome "unknown", described as "a welt on his arm". Additional information: Caller was asking for the components of the vaccine. Agent also stated there was a complaint, caller said they usually get a list of components when they receive the boxes and for this vaccine nothing was in the boxes. Follow-up attempts are completed. No further information is expected. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2475941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: RI
Alter: 74,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 06.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia

Symptomtext

Pt complained of right hip pain directly after receiving the vaccine. Pt was immunized on the 2nd floor of hospital, pain began as he ambulated downstairs and continued for 2 days. Pt has no Medical Hx of arthritis, walks everyday 3.5 miles. This pain was new, directly after vaccine, took Ibuprofen and subsided after 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Hypercholesteremia, COPD, BPH
Andere Medikamente: 1) AMLODIPINE BESYLATE 10MG TAB TAKE ONE TABLET BY MOUTH ACTIVE EVERY MORNING FOR BLOOD PRESSURE DO NOT TAKE WITH GRAPEFRUIT JUICE 2) ARTIFICIAL TEARS PVA 1.4%/POVIDONE (PF) INSTILL 1 ACTIVE DROP BOTH EYES FOU
Allergien: HCTZ - hypokalemia
Vorherige Impfungen: -

VAERS 2475780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

mild

Staat: WI
Alter: 74,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 08.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Musculoskeletal stiffness Pain in extremity

Symptomtext

complains of right arm pain and stiffness. says shot was placed "too high" and plans to file claim.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: OR
Alter: 74,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 06.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Electrocardiogram Muscular weakness Pyrexia

Symptomtext

10/7/22: HIGH FEVER, FOLLOWED BY LOSS OF MUSCLE CONTROL, FEARFUL OF STROKE, CALLED PARAMEDICS HE RECEIVED AN EKG, AND RULED OUT STROKE. 10/10/22 FELT 100% BACK TO NORMAL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: EKG VIA PARAMEDICS 10/7/22
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: N/A
Allergien: INDOMETHACIN, AUGMENTIN, METRONIDAZOLE, HYDROMORPHONE
Vorherige Impfungen: -

VAERS 2473630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

mild

Staat: VT
Alter: 17,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 10.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Feeling hot Vomiting

Symptomtext

Patient post vaccinations c/o feeling warm and lightheaded, patient vomited x1 with resolution of symptoms. Patient was offered water and was continuously monitored. HR 76 strong/regular 1306 All symptoms resolved

Weitere VAERSDATA-Felder

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

VAERS 2718808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: KS
Alter: 71,0
Geschlecht: M
Eingang: 29.11.2023
Impfdatum: 12.01.2023
Beginn: 01.11.2023
Tage bis Beginn: 293,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Jan2023 as dose 4 (booster), single (Lot number: GH9697) at the age of 71 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 24Mar2021 as dose 1, single (Lot number: ER8732), on 21Apr2021 as dose 2, single (Lot number: EW0153) and on 22Nov2021 as dose 3 (booster), single (Lot number: FG3527) for covid-19 immunisation. The patient's relevant medical history included: "Prostate cancer" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Nov2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid from 07Nov2023 to 12Nov2023. Clinical course: Patient had no known allergies.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300396391 same patient/reporter, different drug/ events;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Prostate cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2698734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NJ
Alter: 37,0
Geschlecht: F
Eingang: 19.10.2023
Impfdatum: 19.10.2022
Beginn: 04.10.2023
Tage bis Beginn: 350,0
Dosis: 1
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 38-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Oct2022 as dose 1, single (Lot number: GH9697) at the age of 37 years for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant) all with onset 04Oct2023, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (04Oct2023) Positive; (12Oct2023) Negative; (14Oct2023) Negative; (15Oct2023) Positive. Therapeutic measures were taken as a result of covid-19, drug ineffective. Clinical course: No known allergies. Patient tested positive on Wednesday evening 04Oct2023, visited telemedicine doctor immediately and was prescribed Paxlovid. Began 5 day course evening 04Oct2023, ending Monday morning 09Oct2023. Treatment helped, symptoms improved steadily, eventually testing negative on Thursday 12Oct2023 and again on Saturday 14Oct2023. Symptoms began returning morning Sunday 15Oct2023 and test came back positive. Currently, symptoms are not severe and include runny nose and cough. Patient received COVID 19 Antiviral treatment orally with Paxlovid from 04Oct2023 to 09Oct2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20231004; Test Name: COVID-19; Test Result: Positive ; Test Date: 20231012; Test Name: COVID-19; Test Result: Negative ; Test Date: 20231014; Test Name: COVID-19; Test Result: Negative ; Test Date: 20231015; Test Name: COVID-19; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2698125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NH
Alter: -
Geschlecht: F
Eingang: 18.10.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test Wrong product administered

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; Wrong vaccine administered; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 as dose 1, single (Lot number: GH9697), in left arm for covid-19 immunisation. The patient didn't receive bnt162b2 (BNT162B2). The patient's relevant medical history included: "Known allergies: sulfa drugs" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 28Oct2022, outcome "unknown", described as "Wrong vaccine administered"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (11Oct2023) Negative; (unspecified date) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid from 05Oct2023 to 10Oct2023. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300330546 same patient, different SD/AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20231011; Test Name: COVID test/Covid-19 virus test; Test Result: Negative ; Test Name: antigen test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2694574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 12.10.2023
Impfdatum: 11.10.2022
Beginn: 23.09.2023
Tage bis Beginn: 347,0
Dosis: 5
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 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 66-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Oct2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 65 years, in right arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 04Mar2021 as dose 1, single (Lot number: EN6199), in right arm, on 26Mar2021 as dose 2, single (Lot number: EP6955), in right arm, on 04Sep2021 as dose 3 (booster), single (Lot number: FC3183), in right arm and on 15Jun2022 as dose 4 (booster), single (Lot number: FM7553), in right arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Penicillin" (unspecified if ongoing); "Cancer", start date: 2017 (unspecified if ongoing); "sensory hearing loss" (unspecified if ongoing); "vertigo" (unspecified if ongoing); "tinnitus" (unspecified if ongoing), notes: 20000. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 23Sep2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 (Paxlovid).

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer; Penicillin allergy; Sensory hearing loss; Tinnitus (20000); Vertigo
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2691538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NM
Alter: 57,0
Geschlecht: M
Eingang: 05.10.2023
Impfdatum: 20.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19; COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 58-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Oct2022 as dose 4 (booster), single (Lot number: GH9697) at the age of 57 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 08Apr2022 as dose 3 (booster), single (Lot number: FP4554), 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. The patient's concomitant medications were not reported. Past drug history included: Amoxicillin, reaction(s): "known allergies: Amoxicillin", notes: known allergies: Amoxicillin. The patient had rebound beginning with runny nose and mild sore throat on evening of Saturday, 30Sep2023 (was symptom-free the previous two days). Positive Binax antigen test on morning of Sunday, 01Oct2023 (this morning). Today, sore throat was gone, but runny nose persists, as does mild fatigue (a lot like a mild head cold). The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (01Oct2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid from 23Sep2023 to 27Sep2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300314846 Same reporter/patient, different drug/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20231001; Test Name: Binax antigen test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2682714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: 36,0
Geschlecht: M
Eingang: 15.09.2023
Impfdatum: 14.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Oct2022 as dose number unknown, single (Lot number: GH9697) at the age of 36 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2678294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OH
Alter: 60,0
Geschlecht: M
Eingang: 31.08.2023
Impfdatum: 26.10.2022
Beginn: 29.01.2023
Tage bis Beginn: 95,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19

Symptomtext

Hospitalization for COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2675969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 24.08.2023
Impfdatum: 11.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Body temperature COVID-19 SARS-CoV-2 test Vaccination failure Weight

Symptomtext

got at hospital because she was sick with Covid; got at hospital because she was sick with Covid; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Nov2022 as dose 4 (booster), single (Lot number: GH9697) for covid-19 immunisation; BNT162b2 (BNT162B2), on 17Mar2021 as dose 1, single (Lot number: EN6207), on 08Apr2021 as dose 2, single (Lot number: EW0151) and on 03May2022 as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Had Lyme a few years ago" (unspecified if ongoing); "ehrlichiosis, a tick disease" (unspecified if ongoing), notes: Had 2 tick disease 3 years ago, she is negative now, but she wonders; "Did affect her memory a little bit" (unspecified if ongoing), notes: Did affect her memory a little bit; "shingles" (unspecified if ongoing); "chicken pox" (unspecified if ongoing). Concomitant medication(s) included: ROSUVASTATIN; HYDROXYCHLOROQUINE. The following information was reported: VACCINATION FAILURE (hospitalization, medically significant), COVID-19 (hospitalization, medically significant), outcome "not recovered" and all described as "got at hospital because she was sick with Covid". The event "got at hospital because she was sick with covid" required physician office visit. The patient underwent the following laboratory tests and procedures: Body temperature: (20Aug2023) 101.5, notes: Last night fever 101.5; (21Aug2023) 100, notes: Today fever is about 100; SARS-CoV-2 test: (unspecified date) Positive, notes: She tested the next morning and tested positive; (20Aug2023) Positive, notes: Unit: Not Provided; Weight: (unspecified date) 92 and a half pounds. Therapeutic measures were taken as a result of vaccination failure, covid-19. Additional information: The patient's height was reported to be about 5 foot. The lot number for the 3rd Pfizer Covid vaccine looked like FM or FN 992Z. It's handwritten and the patient can't tell. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Body temperature
Hospital-Tage: -
Labordaten: Test Date: 20230820; Test Name: Fever; Result Unstructured Data: Test Result:101.5; Comments: Last night fever 101.5.; Test Date: 20230821; Test Name: Fever; Result Unstructured Data: Test Result:100; Comments: Today fever is about 100.; Test Name: Covid test; Test Result: Positive ; Comments: She tested the next morning and tested positive; Test Date: 20230820; Test Name: Covid test; Test Result: Positive ; Comments: Unit: Not Provided; Test Name: Weight; Result Unstructured Data: Test Result:92 and a half pounds
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chickenpox; Human ehrlichiosis (Had 2 tick disease 3 years ago, she is negative now, but she wonders); Lyme disease; Memory impaired (Did affect her memory a little bit); Shingles
Andere Medikamente: ROSUVASTATIN; HYDROXYCHLOROQUINE
Allergien: -
Vorherige Impfungen: -

VAERS 2670306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 11.08.2023
Impfdatum: 10.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 6
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

COVID-19 treatment; COVID-19 treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Oct2022 as dose 6 (booster), single (Lot number: GH9697) at the age of 54 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown), as dose 4 (booster), single (Batch/Lot number: unknown) and as dose 5 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID-19 treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient was treated with Paxlovid from 30Jul2023 to 04Aug2023. The patient experienced rebound COVID-19 infection on 09Aug2023 at 08:00 PM. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2665833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: MS
Alter: 53,0
Geschlecht: F
Eingang: 03.08.2023
Impfdatum: 14.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Oct2022 as dose 3 (booster), single (Lot number: GH9697) at the age of 53 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "depression" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2660118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 24.07.2023
Impfdatum: 24.10.2022
Beginn: 01.07.2023
Tage bis Beginn: 250,0
Dosis: 5
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Oct2022 at 11:00 as dose 5 (booster), single (Lot number: GH9697) at the age of 62 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Reactive airway" (unspecified if ongoing); "Bronchitis" (unspecified if ongoing); "Over weight" (unspecified if ongoing); "combination pain medications" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Levaquin, reaction(s): "Known allergies: Levaquin". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid (start date: 12Jul2023 and stop date: 16Jul2023.; Sender's Comments: Based on the information in the case report and known drug safety profile, a possible causal relationship between the events Drug ineffective, COVID-19 and suspect product cannot be completely excluded.,Linked Report(s) : US-PFIZER INC-202300257123 Same patient, different drug, different event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bronchitis; Drug allergy; Reactive airways disease; Weight increased
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2656426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 14.07.2023
Impfdatum: 19.10.2022
Beginn: 31.01.2023
Tage bis Beginn: 104,0
Dosis: 5
Route/Site: IM / LA

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

Neuropathy peripheral

Symptomtext

PERIPHERAL NEUROPATHY

Weitere VAERSDATA-Felder

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

VAERS 2656073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: WA
Alter: 50,0
Geschlecht: M
Eingang: 13.07.2023
Impfdatum: 05.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Nov2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 50 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 27Mar2021 as dose 1, single (Lot number: EP7534), in left arm, on 16Apr2021 as dose 2, single (Lot number: ER8734), in left arm, on 06Nov2021 as dose 3 (booster), single (Lot number: FH8027), in left arm and on 30Jul2022 as dose 4 (booster), single (Lot number: FP7150), in left arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Penicillin, sulfur products, trazodone" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19 included Paxlovid treatment from 05Jul2023 to 09Jul2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300249242 Same reporter/patient, different product/AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug hypersensitivity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 25.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 68,0
Dosis: 5
Route/Site: IM / LA

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

Hypoxia

Symptomtext

HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2648856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 23.06.2023
Impfdatum: 12.10.2022
Beginn: 02.11.2022
Tage bis Beginn: 21,0
Dosis: 5
Route/Site: IM / LA

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

Hypoxia

Symptomtext

HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2646321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 81,0
Geschlecht: M
Eingang: 16.06.2023
Impfdatum: 25.10.2022
Beginn: 31.12.2022
Tage bis Beginn: 67,0
Dosis: 4
Route/Site: IM / RA

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

Transient ischaemic attack

Symptomtext

TRANSIENT CEREBRAL ISCHEMIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Transient ischaemic attack
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2642331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 07.06.2023
Impfdatum: 05.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

I did not have an adverse reaction to the vaccine. In 2020, I had COVID-19 and since then my allergies and tinnitus have been worse. My allergies are worse each year from February to May. I have tinnitus in both, and the left is worse. I take allergy shots regularly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Urinary Blockage
Vorgeschichte: N/A
Andere Medikamente: Claritin; Flonase
Allergien: Seasonal Allergies; Animal Dander
Vorherige Impfungen: -

VAERS 2640544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CO
Alter: 59,0
Geschlecht: F
Eingang: 04.06.2023
Impfdatum: 27.10.2022
Beginn: 31.01.2023
Tage bis Beginn: 96,0
Dosis: 5
Route/Site: IM / LA

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

Tinnitus

Symptomtext

My ears started ringing after I got my vaccine. I don't have any hearing loss. It hasn't gotten any better. I found out about VAERS on the Radio. Please research this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: overweight
Andere Medikamente: Remifemin Osteo Bi-Flex Triple Strength + Tumeric Aspirin 81 mg Vitamin D 5000 IU Raw B Complex Multi vitamin Flaxseed Oil 1200 mg Omega 3-6-9
Allergien: LorTab
Vorherige Impfungen: -

VAERS 2640257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9*697

gering

Staat: MO
Alter: 57,0
Geschlecht: F
Eingang: 02.06.2023
Impfdatum: 26.05.2023
Beginn: 02.06.2023
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Thought the Expiration date was. 6/30/23, but it was the be used by 5/22/23. The vaccine was given on 5/26/23 . I did have njurse check with me before giving the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Losartan 25mg daily, Cyanocobalamin 1000IM monthly, Propranolol 10mg BID, Ropinirole 0.5mg @ HS, Hydrocodone 300-5mg as needed for pain..
Allergien: Phenobarbital
Vorherige Impfungen: -

VAERS 2639049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NE
Alter: 75,0
Geschlecht: M
Eingang: 31.05.2023
Impfdatum: 16.11.2022
Beginn: 28.03.2023
Tage bis Beginn: 132,0
Dosis: 5
Route/Site: SYR / LA

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

Unevaluable event

Symptomtext

none

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cancer of the parotide gland
Vorgeschichte: Deep Vein Thrombosis Pace Maker Small cell carsonoma of the parotide gland
Andere Medikamente: Losartan Hydrochlorothiazide Simvastatin Alogliptin B12 Montelukast Vitamin D3 Metformin
Allergien: None
Vorherige Impfungen: -

VAERS 2638699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 01.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Therapeutic response unexpected

Symptomtext

Caller mentioned she took a booster from Pfizer and her inflammation disappeared/Three weeks later, her inflammation was down at least 60%; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP) from medical information team, Program ID: The reporter is the patient. A 65-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Nov2022 as dose 4 (booster), single (Lot number: GH9697) for covid-19 immunisation. The patient's relevant medical history included: "Hashimotos" (unspecified if ongoing); "mixed connective tissue disease" (unspecified if ongoing); "psoriasis" (unspecified if ongoing), notes: Its just psoriasis on her ankle that she puts coconut oil on; "tendons" (unspecified if ongoing); "ligaments" (unspecified if ongoing); "autoimmune diseases" (unspecified if ongoing); "ear and sinus infections a year" (unspecified if ongoing); "ear and sinus infections a year" (unspecified if ongoing), notes: usually secondary from colds and allergies. The patient's concomitant medications were not reported. Past drug history included: Monolaurin, notes: for five years. Vaccination history included: BNT162b2 (Dose 1, Single, Lot: ER8733, did not have expiration dates on her immunization card), administration date: 25Mar2021, for Covid-19 immunization, reaction(s): "her inflammation disappeared"; BNT162b2 (Dose 2, Single, Lot: EW0153), administration date: 15Apr2021, for Covid-19 immunization, reaction(s): "her inflammation disappeared"; BNT162b2 (Dose 3 (Booster), Single, Lot: FJ8762), administration date: 10Dec2021, for Covid-19 immunization, reaction(s): "The effects of this one lasted a little bit longer". The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "Caller mentioned she took a booster from pfizer and her inflammation disappeared/Three weeks later, her inflammation was down at least 60%". Additional information: Caller has a history of autoimmune diseases, including Hashimotos, mixed connective tissue disease, and the other one is like no big deal, its annoying, but no one sees it. Its just psoriasis on her ankle that she puts coconut oil on. It just kind of soothes it so it doesn't get itchy. With her autoimmune disease, when she has one of them attacks, tendons and ligaments, they get inflamed and she can't move. Caller states she has no complaints about the vaccine. She sent an email to Pfizer last year to let them know of all the amazing benefits she got from the vaccine. She got a packet in the mail, but it was asking about adverse events and she didn't have any. She's been thinking about calling Pfizer for a long time because obviously sending the email explaining this didn't work because she's not getting negative effects. She received fourth dose of the Pfizer bivalent vaccine on 01Nov2022. Now in a few weeks it will have been 6 months and its been wearing off for the past couple weeks, and the pain is getting very severe again. Yesterday on 25May2023 she got the Moderna Covid vaccine. They told her she could get the Moderna or get nothing so she is giving the Moderna shot a chance. She doesn't know if its going to work the same way, she's never had it before. She's talked to her doctor, rheumatologist, pharmacist, about why this is happening. They can't think of any reason why. She came up with own theory, uneducated theory. She thinks that when you get the vaccine it freaks her immune system out and stops attacking her. Or there's some ingredient in the vaccine that is soothing her immune system. It lessens the attacks, there's got to be a reason for that. She has tried to look at research articles but they're all so far over her head she doesn't understand what its saying. When Covid first started, her primary care doctor told her that she was afraid that if because of her autoimmune and other stuff that if she got Covid she wouldn't survive. So she's been isolated since then and when she goes out she still wears a mask. She also isn't that afraid of getting Covid because she takes a supplement called Monolaurin. It penetrates bacteria and viruses that have a lipid membrane and deactivates it. And the Covid virus has a lipid membrane. She used to get 8, 10, 12 ear and sinus infections a year, usually secondary from colds and allergies. She's been on Monolaurin for 5 years, she has not had since, not any cold or flu since then at all. Sender's Comments: Linked Report(s): US-PFIZER INC-202300204260 same patient/event, different dose; US-PFIZER INC-202200016205 same patient/event, different dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Therapeutic response unexpected
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder; Ear infection; Hashimoto's disease; Ligament disorder; Mixed connective tissue disease; Psoriasis (Its just psoriasis on her ankle that she puts coconut oil on); Sinus infection (usually secondary from colds and allergies); Tendon disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2599852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: DE
Alter: 74,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 29.11.2022
Beginn: 01.04.2023
Tage bis Beginn: 123,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Vaccination failure Weight Hypoacusis Jaw disorder Tooth disorder

Symptomtext

In addition to my previous report, I began having difficult hearing in April 2023. Everything was muffled. I saw my doctor and was referred to an ENT. I have not seen the ENT yet. Also, in mid-May 2023, I saw a doctor due an issue with my wisdom tooth. My dentist said that my jawbone was growing out of the back of my mouth. An oral surgeon stated this was most likely caused by the drug I was taking for my osteoporosis. My dentist gave me some special mouthwash to help with care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anxiety; Cholesterol abnormal; Osteoporosis
Andere Medikamente: Atorvastatin; levothyroxine; escitalopram; alendronate sodium; vitamin D; calcium
Allergien: N/A
Vorherige Impfungen: -

VAERS 2599852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: DE
Alter: 74,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 29.11.2022
Beginn: 01.04.2023
Tage bis Beginn: 123,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Vaccination failure Weight Hypoacusis Jaw disorder Tooth disorder

Symptomtext

In addition to my previous report, I began having difficult hearing in April 2023. Everything was muffled. I saw my doctor and was referred to an ENT. I have not seen the ENT yet. Also, in mid-May 2023, I saw a doctor due an issue with my wisdom tooth. My dentist said that my jawbone was growing out of the back of my mouth. An oral surgeon stated this was most likely caused by the drug I was taking for my osteoporosis. My dentist gave me some special mouthwash to help with care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anxiety; Cholesterol abnormal; Osteoporosis
Andere Medikamente: Atorvastatin; levothyroxine; escitalopram; alendronate sodium; vitamin D; calcium
Allergien: N/A
Vorherige Impfungen: -

VAERS 2636203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 28.10.2022
Beginn: 17.11.2022
Tage bis Beginn: 20,0
Dosis: 5
Route/Site: IM / RA

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

Anaemia Coagulopathy Femoral neck fracture

Symptomtext

COAGULOPATHY, UNSPECIFIED TYPE 11/17/2022 LEFT FEMORAL NECK UNSPECIFIED TYPE FX, INIT COAGULOPATHY, UNSPECIFIED TYPE 11/17/2022 ANEMIA

Weitere VAERSDATA-Felder

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

VAERS 2634216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OH
Alter: 68,0
Geschlecht: F
Eingang: 19.05.2023
Impfdatum: 06.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 87,0
Dosis: UNK
Route/Site: SYR / LA

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

Autoimmune disorder Bile duct stenosis Biopsy liver abnormal Cholangitis sclerosing Cholelithiasis Endoscopic retrograde cholangiopancreatography Hepatic enzyme increased Immunoglobulin G4 related disease Scar Ultrasound biliary tract abnormal

Symptomtext

Lab work for annual physical showed elevated liver enzymes. Gallbladder ultrasound done. Gallstone and sludge found. Referred to gallbladder surgeon. She referred to liver specialist who referred for liver biopsy. This was done on February 9, 2023. Scarring was found in liver and bile ducts. Additionally, there were strictures and some thickening. Referred for ERCP scope. This was done on March 9, 2023. Two autoimmune diseases have been potentially identified: Primary Schlerosing Cholangitis and IgG4-related disease (liver).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Autoimmune disorder
Hospital-Tage: -
Labordaten: See above
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium, D3, Mutltivitamin, over 50, psyllium husk fiber
Allergien: Erthromycin
Vorherige Impfungen: -

VAERS 2633007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: IL
Alter: 63,0
Geschlecht: M
Eingang: 17.05.2023
Impfdatum: 16.11.2022
Beginn: 01.02.2023
Tage bis Beginn: 77,0
Dosis: 5
Route/Site: IM / RA

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

Acne Biopsy skin abnormal Blastomycosis COVID-19 Chest X-ray abnormal Fungal infection Inflammation Rhinorrhoea SARS-CoV-2 test positive Skin lesion Skin weeping

Symptomtext

In early February 2023, I had a couple of pimples on my chin and then became lesions with oozing. They did a biopsy and determined it was a fungal infection, blastomycosis. I had a chest X-Ray and found inflammation. They believe I breathed in a spore, and it moved from my chest to my chin. I have been taking antibiotics for a week and it didn't help. The infectious disease doctor gave me itraconazole and it seems to be helping. I have to get blood work every two weeks. The lesions have reduced in size. Also, in early January I tested positive for COVID-19 while we were on a cruise. My symptoms were just a slight runny nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acne
Hospital-Tage: -
Labordaten: X-Ray, chest, abnormal, 02/2023; Blood panel, abnormal, 02/2023; Biopsy of lesion on chin, abnormal, 02/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type II Diabetes; Hypertension; High Cholesterol
Andere Medikamente: Atorvastatin; doxycycline HYC; glipizide; hydrochlorothiazide; lisinopril; metformin; aspirin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2629461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Gh9697

gering

Staat: WA
Alter: 47,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 28.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Other HCP) from product quality group. The reporter is the patient. A 48-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 as dose 4 (booster), single (Lot number: Gh9697) at the age of 47 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 14Apr2021 as dose 1, single (Lot number: Er8731), in left arm, on 05May2021 as dose 2, single (Lot number: Ew0171), in left arm and on 14Jan2022 as dose 3 (booster), single (Lot number: 33130ba), in right arm for covid-19 immunisation. The patient's relevant medical history included: "DM" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing); "Morbid obesity" (unspecified if ongoing); "Known allergies: Yes" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19 including Paxlovid from 25Apr2023 to 30Apr2023.; Sender's Comments: Based on the given information , the possible contributory role of the suspect for the event vaccination failure and covid-19 cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Diabetes mellitus; High cholesterol; Morbid obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2626517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MN
Alter: 72,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 12.10.2022
Beginn: 15.02.2023
Tage bis Beginn: 126,0
Dosis: 4
Route/Site: IM / LA

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

Chest X-ray Ear infection Otitis media SARS-CoV-2 test negative Sinusitis

Symptomtext

So I went to urgent care and they prescribed two different antibiotic. I also had an ear infection. It took me weeks to get over it. I had sinus infection and a middle ear infection for over a month. It has been about two weeks since I have had no issues or problems with my sinuses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest X-ray
Hospital-Tage: -
Labordaten: Chest Xray Home COVID-19 test-Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Pulmonary Embolism
Andere Medikamente: Eliquis
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2621387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: TX
Alter: 75,0
Geschlecht: M
Eingang: 26.04.2023
Impfdatum: 21.10.2022
Beginn: 25.03.2023
Tage bis Beginn: 155,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Influenza Influenza virus test positive SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. I was exposed to COVID-19 from my wife after she returned from a trip. I tested positive for COVID-19 on 03/25/2023. I contacted a provider via telehealth visit and got a prescription Paxlovid, an antibiotic and Benzonatate. I tolerated the medication without any complications. I also tested positive for the flu on 04/23/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 25MAR2023 COVID-19 Test - Positive; 23APR2023 FLU Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Amlodipine; Atorvastatin; Multivitamin; Aleve; Vitamin D; Osteo Biflex
Allergien: N/A
Vorherige Impfungen: -

VAERS 2620095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 22.10.2022
Beginn: 01.03.2023
Tage bis Beginn: 130,0
Dosis: 4
Route/Site: SYR / LA

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

Hordeolum Ocular discomfort

Symptomtext

I had my vaccination on 10/22/2022. On 03/01/2023 I started to experience an sty in my right eye that has continued and become worse. My whole right eye is uncomfortable. They have prescribed Erythromycin ointment for my eye. It is very slowly getting better but after 2 months I am still not 100%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hordeolum
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Sertraline; Divigel; Progesterone; Multi Vitamin; Fish Oil; Estrovera ; Biotin; Cranberry;
Allergien: Sumatriptan
Vorherige Impfungen: -

VAERS 2618534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: MN
Alter: 41,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 10.04.2023
Beginn: 12.04.2023
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Order incident and administered what was thought to be Bivalent from the pharmacy but was Monovalent. Patient had no reaction and was notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2618027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 21.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Oct2022 as dose 4 (booster), single (Lot number: GH9697) at the age of 33 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 10Feb2021 as dose 1, single (Lot number: EL9266), in left arm, on 03Mar2021 as dose 2, single (Lot number: EN6205), in left arm and on 13Oct2021 as dose 3 (booster), single (Lot number: FF8841), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Ibuprofan for Known allergies: Ibuprofan; Asprin for Known allergies: Asprin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2613351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 12.11.2022
Beginn: 01.03.2023
Tage bis Beginn: 109,0
Dosis: 5
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

acute COVID; acute COVID; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Nov2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 67 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Inflammatory proctitis" (unspecified if ongoing); "Known allergies: Sulpha" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Mar2023, outcome "not recovered" and all described as "acute COVID". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08Apr2023) Positive, notes: 3 days after first negative test; (Mar2023) Positive; (Apr2023) Negative, notes: day 8. Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid from 29Mar2023 to 03Apr2023. Clinical course: Had acute COVID, and became negative day8 and symptoms resolved. Symptoms returned 3 days after first negative test and antigen test became positive again.; Sender's Comments: Based on the information provided in the narrative, a causal association between the events and the suspect drug cannot be completely excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230408; Test Name: Antigen test; Test Result: Positive ; Comments: 3 days after first negative test; Test Date: 202303; Test Name: COVID Test; Test Result: Positive ; Test Date: 202304; Test Name: COVID Test; Test Result: Negative ; Comments: day 8
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Proctitis; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2612558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 25.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 61-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 25Nov2022 as dose 5 (booster), single (Lot number: GH9697), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative; Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information: Report about Covid treatment yes, Reporter type patient, vaccine was received, No other medication in 2weeks, Product COVID 19 Treatment, start date 27Mar2023, stop date 01Apr2023. This is a notification generated from the system. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process. Refer to the below table for details. Product Quality Group Provided investigational results for Comirnaty the investigation included reviewing the involved batch records, deviation investigation, an analysis of the complaint history for the reported lot and product type. The final scope was determined to be the associated lot(s) of the reported lot GH9697. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality, regulatory, validation and stability. Agency concludes that the reported defect is not representative of the quality of the batch and the batch remains acceptable. The process determined that no regulatory notification was required. The reported defect could not be confirmed. No root cause or CAPA were identified as the complaint was not confirmed. 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 virus test; Test Result: Negative ; Test Name: COVID-19 virus 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 2610131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AL
Alter: 56,0
Geschlecht: M
Eingang: 05.04.2023
Impfdatum: 22.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / LA

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

Computerised tomogram normal Mass Neck dissection Papilloma viral infection Squamous cell carcinoma Ultrasound scan normal

Symptomtext

10/25/2022 I felt a small lump at left side of jaw. I saw my neurologist on the same day and it was probably a lymph node. A month later, it was growing and getting larger. I got on steroids, then ENT examined me and did a Ultrasounds and CT scan and it was all negative, Had a neck dissection on 3/6/2023 and it was diagnosed Squamous Cell Carcinoma HPV P16 on 3/9/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Computerised tomogram normal
Hospital-Tage: -
Labordaten: 2/6/2023 Ultrasounds and CT scan - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; High Cholesterol; Restless Legs Syndrome
Andere Medikamente: Pregabalin; Carvedilol; Telmisartan; Ropinirole; Vascepa; Vitamin D3; Vitamin B12
Allergien: N/A
Vorherige Impfungen: -

VAERS 2604026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: FL
Alter: 62,0
Geschlecht: F
Eingang: 27.03.2023
Impfdatum: 27.10.2022
Beginn: 26.03.2023
Tage bis Beginn: 150,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

patient hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2603374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 24.03.2023
Impfdatum: 13.10.2022
Beginn: 08.03.2023
Tage bis Beginn: 146,0
Dosis: 4
Route/Site: - / -

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

Asthenia Blood sodium decreased COVID-19 Chest X-ray normal Fall

Symptomtext

Discharge Provider: Private DO Primary Care Provider at Discharge: Private DO Admission Date: 3/8/2023 Discharge Date: 03/9/2023 PRESENTING PROBLEM: Debility [R53.81] Weakness [R53.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 75-year-old male with a past medical history significant for Alzheimer's dementia, seizure, hypertension, hyperlipidemia and diabetes who presented to the emergency department after a fall at home. In the emergency department, vital signs were stable. Lab work was obtained which revealed a sodium of 128. He was found to have COVID-19. Chest x-ray with no acute cardiopulmonary disease. Patient was admitted to the Internal Medicine Service for generalized weakness. PT/OT evaluated patient recommended home with home health care. The following day patient felt well. A 4ww was delivered to the hospital for patient to take home. He was recommended follow up his primary care physician. He was discharged home in stable condition

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Hypercholesterolemia Diabetes mellitus (HCC) Anxiety Coronary arteriosclerosis Seasonal allergic rhinitis Alzheimer's dementia without behavioral disturbance (HCC) Intraventricular hemorrhage (HCC) Debility
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ascorbic acid (VITAMIN C) 1000 MG tablet atorvastatin (LIPITOR) 80 MG tablet cyanocobalamin 1000 MCG tablet donepezil (ARICEPT) 10 MG tablet lacosamide (VIMPAT) 50 MG tablet lisinopril (PRINIVIL,ZESTRI
Allergien: Bee PollenSwelling
Vorherige Impfungen: -

VAERS 2599094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: TX
Alter: 7,0
Geschlecht: M
Eingang: 19.03.2023
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Product administered to patient of inappropriate age

Symptomtext

Error: Wrong Age for Vaccine Given-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2593786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MN
Alter: 51,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 29.11.2022
Beginn: 08.03.2023
Tage bis Beginn: 99,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient vaccinated against then tested positive for COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2593778

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge gh9697

gering

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 09.03.2023
Impfdatum: 11.11.2022
Beginn: 08.03.2023
Tage bis Beginn: 117,0
Dosis: 5
Route/Site: - / -

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

Unevaluable event

Symptomtext

hospitalization

Weitere VAERSDATA-Felder

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

VAERS 2592248

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 06.03.2023
Impfdatum: 06.03.2023
Beginn: 06.03.2023
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient received duplicate therapy of Pfizer Bivalent Updated Booster. Patient received first dose of Pfizer bivalent in September 2022 from a different pharmacy and patient received a second dose of Bivalent in March 2023. Patient was not aware that they were not supposed to get two doses of Bivalent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 2591899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: WI
Alter: 79,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 24.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

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

Extra dose administered No adverse event

Symptomtext

None Reported to us, I called the patient confirmed all the information matched so we had the correct patient and confirmed he had no adverse reactions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None, since there was no adverse reactions
Aktuelle Erkrankungen: None listed on Var, spoke to pt over the phone and they did not mention anything
Vorgeschichte: None listed or mentioned at time of phone conversation where patient was made aware of extra dose. Please note the form REQUIRES to put the date the adverse reaction occured to even submit this report. No adverse reaction was reported by the patient and I called him he said nothing was out of the ordinary and had no adverse reactions
Andere Medikamente: None Reported or on File, pt has only seen us for vaccines
Allergien: Only allergies on file are to Spironolactone.
Vorherige Impfungen: -

VAERS 2590845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OH
Alter: 29,0
Geschlecht: M
Eingang: 03.03.2023
Impfdatum: 02.03.2023
Beginn: 01.03.2023
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Pt accidentally received bivalent pfizer vaccine as his first dose series. Patient was panicking before I administered the vaccine and wanted to grab the vaccine card and not receiving the actual shot. I refused to do that and explained that the vaccine has more benefits than side effects. At the pharmacy we confirmed with patient that he is receiving his booster bivalent vaccine and he acknowledged that with us. After Patient was administered the booster he stated that he never received his first or second series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: No Known allergy
Vorherige Impfungen: -

VAERS 2589986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 02.03.2023
Impfdatum: 08.12.2022
Beginn: 09.12.2021
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Vaccine brand other= Moderna/Vaccine administration date= 09Dec2021, Vaccine dose number=3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Dec2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 53 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 17Mar2021 as dose 1, single (Lot number: EP7534), in left arm, on 07Apr2021 as dose 2, single (Lot number: EL8982), in left arm and on 19Jul2022 as dose 4 (booster), single (Lot number: EP7139), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 09Dec2021 as dose 3 (booster), single (Lot number: 007C21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "High cholesterol" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 09Dec2021, outcome "unknown", described as "Vaccine brand other= Moderna/Vaccine administration date= 09Dec2021, Vaccine dose number=3"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Feb2023, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Feb2023) Positive; (21Feb2023) Negative; (24Feb2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230214; Test Name: COVID rebound Tested; Test Result: Positive ; Test Date: 20230221; Test Name: COVID rebound Tested; Test Result: Negative ; Test Date: 20230224; Test Name: COVID rebound Tested; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2587249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: OH
Alter: 27,0
Geschlecht: F
Eingang: 25.02.2023
Impfdatum: 07.01.2023
Beginn: 01.02.2023
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 27-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Jan2023 as dose 4 (booster), single (Lot number: GH9697) at the age of 27 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 10Mar2021 as dose 1, single (Lot number: EN6199), in left arm and on 31Mar2021 as dose 2, single (Lot number: ER8732), in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 03Dec2021 as dose 3 (booster), single (Lot number: 3303080), in right arm for covid-19 immunisation. The patient's relevant medical history included: "asthma" (unspecified if ongoing); "depression" (unspecified if ongoing); "environmental allergies" (unspecified if ongoing); "generalized anxiety" (unspecified if ongoing); "acne" (unspecified if ongoing); "eczema" (unspecified if ongoing); "benign breast tumors" (unspecified if ongoing); "ankle arthroscopy surgery" (unspecified if ongoing). Concomitant medication(s) included: DAYQUIL, start date: 15Feb2023, stop date: 17Feb2023; SERTRALINE, start date: 02Feb2023, stop date: 21Feb2023; MINOCYCLINE, start date: 02Feb2023, stop date: 21Feb2023; CETIRIZINE, start date: 02Feb2023, stop date: 21Feb2023; ACETAMINOPHEN, start date: 13Feb2023, stop date: 13Feb2023. Past drug history included: Known allergies chorhexidine, reaction(s): "Known allergies chorhexidine". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Feb2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Dayquil (brand: Kroger CO), Sertaline (brand: Aurobindo pharma), Minocyline 100mg (Sun pharmaceuticals), cetirizine (brand: Kroger Co), Acetaminophen 500mg (brand: Kroger CO). The patient received Paxlovid from 16Feb2023 to 20Feb2023 for treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acne; Arthroscopy; Asthma; Breast tumor benign; Depression; Eczema; Environmental allergy; Generalized anxiety disorder
Andere Medikamente: DAYQUIL; SERTRALINE; MINOCYCLINE; CETIRIZINE; ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 2586243

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge GH9697

gering

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 23.02.2023
Impfdatum: 11.02.2021
Beginn: 18.02.2023
Tage bis Beginn: 737,0
Dosis: 4
Route/Site: - / -

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

Asymptomatic COVID-19 Femoral neck fracture SARS-CoV-2 test positive

Symptomtext

Pt was admitted on 2/18 due to a left femoral neck fracture. A COVID swab was taken on 2/22 due to transfer requirements to hospice care and pt was COVID positive, yet asymptomatic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: FL
Alter: -
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 01.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 treatment; COVID 19 treatment; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 47-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Nov2022 as dose number unknown (booster), single (Lot number: GH9697), in left arm for COVID-19 immunisation; COVID-19 vaccine (COVID-19 VACCINE), as dose number unknown, single (Batch/Lot number: unknown) for COVID-19 immunisation. The patient's relevant medical history was not reported. 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: Positive. Therapeutic measures were taken as a result of drug ineffective, COVID-19 which included Paxlovid from an unspecified date in Feb2023 to an unspecified date in Feb2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2581672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 01.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 30,0
Dosis: 4
Route/Site: IM / LA

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

Echocardiogram Heart rate increased

Symptomtext

It started after my third dose on November 2021, I had the vaccine around 10:30AM and noticed chills, fast heart rate and headache. I noticed it ever since; I ended up in the ER November 2021. Had my second booster November 2022, it began to get worst again so I went to see Dr. and he sent me to get an echocardiogram on February 2023 because my heart rate was 115BPM and I'm still waiting for the results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Echocardiogram
Hospital-Tage: -
Labordaten: 10FEB23 Echocardiogram, pending
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis
Andere Medikamente: Vitamin D; B-12; hormone replacement therapy
Allergien: None
Vorherige Impfungen: -

VAERS 2581116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 03.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Nov2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 54 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "known allergies: Mango" (unspecified if ongoing); "known allergies: seasonal pollens" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 including Paxlovid from 30Jan2023 to 03Feb2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fruit allergy; Hypothyroidism; Pollen allergy
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 2578600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: VT
Alter: 75,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 26.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 67,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 75-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 26Oct2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 75 years, in left arm for covid-19 immunisation; COVID-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "lumbar stenosis" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: COVID 19 Treatment; (02Feb2023) Negative; (04Feb2023) Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19: the patient received Paxlovid from 27Jan2023 to 01Feb2023 (lot number GG0052) for COVID-19 treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 20230202; Test Name: COVID-19; Test Result: Negative ; Test Date: 20230204; Test Name: COVID-19; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Lumbar spinal stenosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 08.02.2023
Impfdatum: 14.11.2022
Beginn: 29.12.2022
Tage bis Beginn: 45,0
Dosis: 5
Route/Site: - / -

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

Acute kidney injury COVID-19 Encephalopathy Hypernatraemia Influenza Mental status changes SARS-CoV-2 test positive Screaming Sedation Somnolence

Symptomtext

"Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: ""78-year-old female with dementia who presents with acute encephalopathy, somnolence. Suspect influenza with over-sedation. Wean down psychotropic medications. Her mental status improved although she did have outbreaks of yelling. Tamiflu x5 days. Hypernatremia and AKI resolved with IV fluids and was stable without IV fluids. Recommend outpatient neuropsych testing and psychiatric consultation. I suspect progression of patient's dementia is causing many of her symptoms. Incidentally tested positive for COVID on day of discharge, was negative on admission. Question if false positive as she had no change in her respiratory status."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute kidney injury
Hospital-Tage: 5,0
Labordaten: Covid PCR dectected on 01/03/2023
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular High blood pressure Hyperlipidemia Bilateral pulmonary embolism (HCC) Hypotension Endocrine Type 2 diabetes mellitus with stable proliferative retinopathy of both eyes, without long-term current use of insulin (HCC) Psychological Late onset Alzheimer's dementia with behavioral disturbance (HCC) Respiratory Influenza A Acute respiratory failure with hypoxia (HCC) Urinary AKI (acute kidney injury) (HCC) Other Retinopathy, hypertensive, right eye Obesity (BMI 30.0-34.9) Benign familial tremor Osteoporosis Weakness Chronic midline low back pain without sciatica Hypernatremia Viral sepsis (HCC) Toxic metabolic encephalopathy
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet Take 1 tablet by mouth every 4 (four) hours as needed for Pain. aluminum-magnesium hydroxide-simethicone (MAALOX) 200-200-20 mg/5 mL suspension Take 30 mLs by mouth every 4 (four) hours as needed for I
Allergien: No Know Allergies
Vorherige Impfungen: -

VAERS 2578001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 08.02.2023
Impfdatum: 14.10.2022
Beginn: 07.02.2023
Tage bis Beginn: 116,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

covid vaccine breakthrough case dose 1 Pfizer 1/13/21 EL3248 dose 2 Pfizer 2/3/21 EL9265 dose 3 Pfizer 9/27/21 FC3148

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ test on 2/7/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 08.02.2023
Impfdatum: 08.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: SYR / LA

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

Appendicitis Surgery

Symptomtext

12/03/22 went to urgent care, accute appendicits, then went to hospital for surgery within 2 hrs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Appendicitis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi Vitamin Alaya Collagen powder Calcium tablet
Allergien: None
Vorherige Impfungen: -

VAERS 2571271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CA
Alter: 23,0
Geschlecht: M
Eingang: 30.01.2023
Impfdatum: 06.01.2023
Beginn: 06.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Pfizer COVID-19 Bivalent vaccine incorrectly administered as a primary series monovalent dose. No signs or symptoms of ADRs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: No adverse reaction to Bivalent vaccine
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2570626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WA
Alter: 72,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 27.10.2022
Beginn: 15.01.2023
Tage bis Beginn: 80,0
Dosis: 4
Route/Site: SYR / RA

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

Chest discomfort

Symptomtext

I had my vaccination on 10/27/2022. I have a history of shortness of breath, near syncope and possible heart murmur. On 01/15/2023 I started to experience a thickness and heaviness in my chest. I have follow up with cardiology in 03/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest discomfort
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type II Diabetes; Herniated Disc 2020
Andere Medikamente: Glucotrol; Multivitamins; Insulin; Glipizide; Baby Aspirin
Allergien: Lactose Intolerance; Statin Medications; Augmentin; Metformin; Gabapentin; Cephalexin; Glucophage; Adhesive; Latex; Nichol; Wellbutrin; Atorvastatin; Effexor; Gluconate
Vorherige Impfungen: Tetanus 2022; redness at injections site

VAERS 2561334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MN
Alter: 79,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 10.11.2022
Beginn: 16.01.2023
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient vaccinated against then tested positive for COVID-19 in the ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2559468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: DE
Alter: 22,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 08.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: SC / -

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

Incorrect product formulation administered

Symptomtext

Patient given Pfizer Bivalent as first dose instead of the original

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: PATIENT GIVEN BIVALENT FOR FIRST DOSE INSTEAD OF ORIGINAL
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2559122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: OH
Alter: 61,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 14.10.2022
Beginn: 22.12.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: - / LA

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

Anaemia Blood test Haemoglobin Off label use Product use issue

Symptomtext

off label use; Product use for unapproved combination; Anemia; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID: The reporter is the patient. A 61-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Oct2022 as dose 3 (booster), single (Lot number: GH9697) at the age of 61 years, in left arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 14Oct2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation; varicella zoster vaccine (VARICELLA ZOSTER VACCINE), on 14Oct2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history included: "Pre Diabetic Blood Sugar Levels" (ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (1st dose: Date: 11Mar2021 Time: Not Provided Anatomical Site of injection: Not Provided Route of Administration: Not Provided, Batch/Lot number: EN6204), administration date: 11Mar2021, when the patient was 59-year-old, for COVID-19 immunization; BNT162b2 (2nd dose: Date: 06Apr2021 Time: Not Provided Anatomical Site of injection: Not Provided Route of Administration: Not Provided, Batch/Lot number: LW0151 or BW0151 or KW0151. States he can not make out the writing on the card of the first letter.), administration date: 06Apr2021, when the patient was 59-year-old, for covid-19 immunization. The following information was reported: ANAEMIA (non-serious) with onset 22Dec2022, outcome "recovering", described as "Anemia"; OFF LABEL USE (non-serious), outcome "unknown"; PRODUCT USE ISSUE (non-serious), outcome "unknown", described as "Product use for unapproved combination". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of anaemia. Additional information: Agent stated she had a patient on the line calling because he received the Covid Bivalent on 14Oct2022. On 19Dec2022, he went for a routine annual physical and discovered he was anemic. He said he was a regular blood donor and could demonstrate he had high hemoglobin up until the time he received his vaccination. He wanted to report it. Caller stated he became aware of the anemia on 22Dec2022. He reported he had subsequent labs drawn 2 weeks later and he has been taking iron and his levels have marginally improved but they are still in the sub therapeutic range. Caller stated he has observed findings on public forums that concur with this occurrence happening so this was not unique to him. Caller was offered to speak with Medical Information. He stated not if it is just education material about the events that transpired. Caller states unless they have documented studies that offer alternative treatments than he is currently doing, he declines transfer. Call handler advises caller she doesn't have the information on what type of information they have. Patient received prior vaccinations (within 4 weeks):Flu Shot and Shingles Vaccine. Family Medical History Relevant to Adverse Events (AEs) was None. Specific Relevant Test for Thromboembolic events with Thrombocytopenia were none or unknown. The event require the initiation of new medication/other treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaemia
Hospital-Tage: -
Labordaten: Test Name: routine annual physical; Result Unstructured Data: Test Result:anemic; Comments: discovered he is anemic; Test Name: hemoglobin; Result Unstructured Data: Test Result:high; Comments: had high hemoglobin up until the time he received his vaccination.
Aktuelle Erkrankungen: Diabetes mellitus
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NC
Alter: 71,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 14.10.2022
Beginn: 03.01.2023
Tage bis Beginn: 81,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Oct2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 71 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 02Feb2021 as dose 1, single (Lot number: EL9264), in left arm, on 23Feb2021 as dose 2, single (Lot number: EN6203), in left arm, on 08Oct2021 as dose 3 (booster), single (Lot number: FF2587), in left arm and on 01Apr2022 as dose 4 (booster), single (Lot number: FK9729), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing); "Known allergies: wool" (unspecified if ongoing), notes: Known allergies: wool; "Known allergies: dust" (unspecified if ongoing), notes: Known allergies: dust; "Known allergies: mold" (unspecified if ongoing), notes: Known allergies: mold. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 03Jan2023 at 10:00, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (29Dec2022) Negative, notes: Tested negative on home test on 29Dec2022; (03Jan2023) Positive, notes: 03Jan2023; took a home test and it was positive for Covid. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Information: Patient received the vaccine. Patient received other medications in 2 weeks. Antiviral details: Product: COVID 19 Treatment, Brand: Paxlovid, Treatment start date: 20Dec2022,Treatment stop date: 24Dec2022,Indication: Treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221229; Test Name: home test; Test Result: Negative ; Comments: Tested negative on home test on 29Dec2022; Test Date: 20230103; Test Name: home test; Test Result: Positive ; Comments: 03Jan2023; took a home test and it was positive for Covid
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to molds (Known allergies: mold); Allergy to wool (Known allergies: wool); Diabetes; Dust allergy (Known allergies: dust)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2550924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: WV
Alter: 42,0
Geschlecht: M
Eingang: 05.01.2023
Impfdatum: 27.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 27Nov2022 as dose number unknown (booster), single (Lot number: GH9697) at the age of 42 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 20Nov2021 as dose number unknown, single (Lot number: FF2590), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypercholesterolemia" (unspecified if ongoing), notes: other medical history: Hypercholesterolemia; "chronic acid reflux" (unspecified if ongoing), notes: other medical history: chronic acid reflux. Concomitant medication(s) included: ATORVASTATIN, start date: 01Jan2010; PANTOPRAZOLE, start date: 01Jan2017. 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. No known allergies.

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: Acid reflux (esophageal) (other medical history: chronic acid reflux); Hypercholesterolemia (other medical history: Hypercholesterolemia)
Andere Medikamente: ATORVASTATIN; PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2550207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 30.12.2022
Beginn: 30.12.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Pfizer Bivalent booster was given in error, patient had the Janessen/J&J COVID shot first.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2549501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: IL
Alter: 17,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 10.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Adverse reaction

Symptomtext

Patient came in with mother and had appointment for both the COVID-19 booster (Pfizer) and seasonal flu vaccine (Flucelvax). The patient and both vaccines were verified to be correct before administration with both the patient and guardian. Both vaccines were administered properly to the left deltoid. After the vaccines were administered, patient displayed no signs of distress. The guardian (mother) was vaccinated in the same manner confirming each vaccine before administration. Both patients were waiting for the administrating pharmacist to complete the vaccine cards. There was commotion as the cards were being completed and the vaccinating pharmacist was preparing shots for different patients. The patient in question was laying on the ground and we immediately contacted 9-1-1. The vaccinating pharmacist grab an Epipen out of the emergency response bag and ran to establish contact with the patient. Encouraged the patient to sit upright and the store manager offered complimentary waters as the paramedics were en route. Once paramedics arrived, responsibility was transferred to the paramedics. Patient and guardian were both escorted out by the paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no other illnesses at the time of vaccination reported by the patient or guardian
Vorgeschichte: gastrointestinal disease unspecified
Andere Medikamente: none as of patient profile
Allergien: No known allergies at the time of vaccination
Vorherige Impfungen: -

VAERS 2546915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 27.12.2022
Beginn: 27.12.2022
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

vaccine was administered past expiration date of 12/19/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2546888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 27.12.2022
Beginn: 27.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Expired product administered

Symptomtext

vaccination was administered past expiration date of 12/19/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 14.11.2022
Beginn: 20.12.2022
Tage bis Beginn: 36,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Fall Femur fracture SARS-CoV-2 test positive

Symptomtext

Patient up to date on COVID vaccines who fell and admitted for femur fracture with COVID detected PCR. No hypoxia noted during stay.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 4,0
Labordaten: COIVD Detected PCR on 12/21/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Hypertension Hyperlipidemia LDL goal <130 Internal hemorrhoids Digestive Lesion of cecum Colon polyp Multiple gastric ulcers GERD (gastroesophageal reflux disease) Endocrine Hypothyroidism Psychological Anxiety, generalized Respiratory Allergic rhinitis Shortness of breath Urinary Hydronephrosis, right E. coli urinary tract infection History of UTI Other Glaucoma Normocytic anemia Right ureteral stent retained Iron deficiency Diverticulosis of large intestine Osteoarthritis History of colonic polyps Menopausal and postmenopausal disorder Osteopenia Hyponatremia Debility Generalized weakness Nursing home resident Displaced intertrochanteric fracture of right femur, initial encounter for closed fracture
Andere Medikamente: -
Allergien: Ace Inhibitors
Vorherige Impfungen: -

VAERS 2545080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NY
Alter: 61,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 27.12.2022
Beginn: 27.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

vaccine was administered 8 days past use by date from corporate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2545071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 27.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

vaccine was administered 8 days past expiration based on when taken out of freezer

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2540697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NC
Alter: 44,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

PT CAME IN TO GET HER FIRST COVID VACCINE AND WAS GIVEN A BIVALENT VACCINE. PT HAD NOT PREVIOUSLY RECEIVED ANY COVID VACCINES

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: BACKPAIN
Vorgeschichte: HYPOTHYROIDISM, DIABETES MELLITUS, ACUTE BRONCHITIS, HTN, SMOKER, SERONEGATIVE RHEUMATOID ARTHRITIS OF MULTIPLE SITES,
Andere Medikamente: OTC VITAMIN D, FAMOTIDINE, FLUOXETINE, FUROSEMIDE, LISINOPRIL
Allergien: SUMATRIPTAN, TRAMADOL
Vorherige Impfungen: -

VAERS 2540697

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GH9697

gering

Staat: NC
Alter: 44,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

PT CAME IN TO GET HER FIRST COVID VACCINE AND WAS GIVEN A BIVALENT VACCINE. PT HAD NOT PREVIOUSLY RECEIVED ANY COVID VACCINES

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: BACKPAIN
Vorgeschichte: HYPOTHYROIDISM, DIABETES MELLITUS, ACUTE BRONCHITIS, HTN, SMOKER, SERONEGATIVE RHEUMATOID ARTHRITIS OF MULTIPLE SITES,
Andere Medikamente: OTC VITAMIN D, FAMOTIDINE, FLUOXETINE, FUROSEMIDE, LISINOPRIL
Allergien: SUMATRIPTAN, TRAMADOL
Vorherige Impfungen: -

VAERS 2540555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 02.11.2022
Beginn: 21.12.2022
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient vaccinated against then tested positive for COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2540143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: IN
Alter: 49,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 21.10.2022
Beginn: 06.12.2022
Tage bis Beginn: 46,0
Dosis: 5
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja 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 50-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Oct2022 at 19:00 as dose 5 (booster), single (Lot number: GH9697) at the age of 49 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Amputee" (unspecified if ongoing), notes: Other medical conditions: Amputee, Intracranial Pressure, SVT; "Intracranial Pressure" (unspecified if ongoing), notes: Intracranial Pressure; "SVT" (unspecified if ongoing), notes: I have SVT - where it went over 200 even while taking 50mg of metoprolol. Concomitant medication(s) included: METOPROLOL; ACETAZOLAMIDE; FERROUS SULFATE. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 06Dec2022, outcome "unknown" and all described as "Treatment of COVID-19". The event "treatment of covid-19" required emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (15Dec2022) Positive, notes: I had a PCR lab test done; (Dec2022) Faintly positive, notes: Was testing very faintly positive; (15Dec2022) positive, notes: also did two at home tests; (15Dec2022) positive, notes: also did two at home tests; (16Dec2022) positive, notes: Lab test came back positive today as well. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Anti-viral details: COVID 19 Treatment with Paxlovid. Treatment start date: 07Dec2022. Treatment stop date: 11Dec2022. Indication: Treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221215; Test Name: PCR lab test; Test Result: Positive ; Comments: I had a PCR lab test done; Test Date: 202212; Test Name: Testing; Result Unstructured Data: Test Result:Faintly positive; Comments: Was testing very faintly positive; Test Date: 20221215; Test Name: Testing; Test Result: Positive ; Comments: also did two at home tests.; Test Date: 20221215; Test Name: Testing; Test Result: Positive ; Comments: also did two at home tests.; Test Date: 20221216; Test Name: Testing; Test Result: Positive ; Comments: Lab test came back positive today as well.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Amputee (Other medical conditions: Amputee, Intracranial Pressure, SVT); Intracranial pressure monitoring (Intracranial Pressure); Supraventricular tachycardia (I have SVT - where it went over 200 even while taking 50mg of metoprolol.)
Andere Medikamente: METOPROLOL; ACETAZOLAMIDE; FERROUS SULFATE
Allergien: -
Vorherige Impfungen: -

VAERS 2531789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 14.12.2022
Impfdatum: 02.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: IM / LA

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

Herpes zoster

Symptomtext

Developed Herpes Zoster outbreak one week on my left side of body after receiving vaccine. I?ve never had this before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Hypertension OSA Elevated cholesterol
Andere Medikamente: Atorvastatin Amlodipine Allegra Albuterol
Allergien: None
Vorherige Impfungen: -

VAERS 2530142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 11.10.2022
Beginn: 13.12.2022
Tage bis Beginn: 63,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Vaccine breakthrough infection

Symptomtext

Fully vaccinated, COVID breakthrough infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 58,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 15,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 48,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 41,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 66,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 67,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 48,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 60,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 51,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 51,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 51,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 53,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 34,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 68,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 16,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 78,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 90,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 70,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 39,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 67,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: AZ
Alter: 62,0
Geschlecht: M
Eingang: 13.12.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
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

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2528958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 12.12.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / RA

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

Inappropriate schedule of product administration No adverse event Product administration error

Symptomtext

VACCINE ADMINISTRATINO ERRORS. BIVALENT BOOSTER WAS ADMINISTERED ON 10/22/22 HOWEVER ANTOHER BIVALENT BOOSTER WAS ADMINISTERED ON 12/12/22. NO ADVERSE EVENT REPORTED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2528328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: IL
Alter: 18,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

pt received bivalent Pfizer booster on 9/11/2022. she presented to pharmacy for another booster today and we administered bivalent Pfizer today

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 2527313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 20.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 12,0
Dosis: 5
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. A 70-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Oct2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 70 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "hypothyroidism" (unspecified if ongoing); "Hep B carrier" (unspecified if ongoing); "Anxiety" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Known allergies opoids, reaction(s): "Known allergies Opoids", notes: known allergies: Opoids. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Nov2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient previously receive a COVID-19 Vaccine. Paxlovid treatment started from 19Nov2022 to 23Nov2022. Device Date: 02Dec2022.; Sender's Comments: The vaccine efficacy varies from one patient to another and can be affected by different factors; however, a contributory role of the suspect vaccine BNT162B2 to its Lack of efficacy cannot be ruled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Hepatitis B carrier; Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2525405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 21.10.2022
Beginn: 07.12.2022
Tage bis Beginn: 47,0
Dosis: 5
Route/Site: - / -

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

Asymptomatic COVID-19 SARS-CoV-2 test positive

Symptomtext

asymptomatic- tested positive for covid on binax rapid antigen test done as f/u to new admission per regs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, OA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2524504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MD
Alter: 10,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 01.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

ADULT DOSE GIVEN TO PEDIATRIC PATIENT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2524299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gh9697

gering

Staat: MA
Alter: 71,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

No adverse event Product use issue

Symptomtext

Patient signed up for Covid Pifzer bivalent updated booster. Her vaccine was processed in the computer with her insurance. She was given the bivalent booster and pharmacist noticed after the vaccine was given, that she had already received the bivalent booster in the beginning of September 2022. This was then her 4th booster and her 2nd bivalent booster, which is not approved. I had her wait for at least 15 minutes after the vaccine and she felt fine upon leaving. I checked in with her in the afternoon and at 7 PM the same day and she felt fine, no adverse effets.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None I know.
Vorgeschichte: None I know.
Andere Medikamente: None I know.
Allergien: None I know.
Vorherige Impfungen: -

VAERS 2524286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 30.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 32,0
Dosis: 5
Route/Site: SYR / AR

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested positive for Covid on Dec 1, 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: At home test kit
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: pantoprazole, rosuvastatin, losartin, trelegy, vit d, vit c, multil vit, calcium, vit b, 81 mg asprin, fish oil, coq10
Allergien: latex, prednizone
Vorherige Impfungen: -

VAERS 2523758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 12.10.2022
Beginn: 21.11.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 46-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 at 11:00 as dose 4 (booster), single (Lot number: GH9697) at the age of 46 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 04Jan2021 as dose 1, single (Lot number: EH9899), on 25Jan2021 as dose 2, single (Lot number: EL3302) and on 01Nov2021 at 10:00 as dose 3 (booster), single (Lot number: ff2593), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Celiac dz" (unspecified if ongoing); "reactive airway dz" (unspecified if ongoing). There were no concomitant medications. The following information was reported: COVID-19 (medically significant), VACCINATION FAILURE (medically significant) all with onset 21Nov2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (21Nov2022) Positive. Therapeutic measures were taken as a result of covid-19, treatment failure. On day 1 took PAXLOVID 5 days (from 21Nov2022 to 25Nov2022) as COVID 19 Treatment. No follow-up attempts are possible. No further information is expected.; Sender's Comments: The vaccine efficacy varies from one patient to another and can be affected by different factors; however, a contributory role of the suspect vaccine BNT162B2 to its Lack of efficacy cannot be ruled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221121; Test Name: Covid test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Celiac disease; Reactive airways disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2523741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NC
Alter: -
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 29.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: OT / -

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

Burning sensation

Symptomtext

burning pain in the elbow to wrist; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 50-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 29Nov2022 as dose number unknown (booster), single (Lot number: GH9697, Expiration Date: 15Dec2022) intramuscular for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: BURNING SENSATION OF UPPER LIMB(medically significant) with onset 30Nov2022, outcome "not recovered", described as "burning pain in the elbow to wrist". Therapeutic measures were taken as a result of pain in extremity. Clinical course: Patient given a shot (to deltoid unspecified if left or right) yesterday and is now complaining of burning pain in the elbow to wrist. Has been about 24 hours since the shot. Didn't see anything on the package insert online other than extremity pain. Wants to know how common it is, management, or other information. Patient started taking ibuprofen to treat it. Doesn't know any further information other than what was on the text message he received.; Sender's Comments: Based on temporal association, there is reasonable possibility of causal association between the Reported events and the suspect drug. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 2521975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OH
Alter: 17,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2520950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MO
Alter: 59,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 26.10.2022
Beginn: 21.11.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: IM / LA

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

Cough SARS-CoV-2 test negative Sinus congestion

Symptomtext

I had no symptoms at all from the vaccination. On 11/21/22, I had sinus congestion and a very bad cough. I have taken 3 COVID-19 tests and they were all negative. I was prescribed guaifenesin with codeine, TYLENOL, and ciprofloxacin. I am still dealing with these symptoms at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: 21NOV2022 COVID-19 test negative; 24NOV2022 COVID-19 test negative; 26NOV2022 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic Kidney Disease; Chronic Allergic Rhinitis
Andere Medikamente: Melatonin; potassium chloride; MITIGARE; NEPHROCAPS; Q-NASAL; VIIBRYD; montelukast; torsemide; pantoprazole; amlodipine; olmesartan; potassium citrate; temazepam; SUDAFED
Allergien: Penicillin; ZYVOX
Vorherige Impfungen: I usually have heat and swelling at the injection site when I get a Flu vaccine.

VAERS 2520116

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GH9697

gering

Staat: IA
Alter: 62,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Technician gave a booster shot instead of primary series. No side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2517228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 26.11.2022
Impfdatum: 14.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Tinnitus

Symptomtext

Increased ringing in both ears; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162B2 OMI BA.4-5, on 14Nov2022 at 13:15 as dose 4 (booster), single (Lot number: GH9697) at the age of 69 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "depression" (unspecified if ongoing); "Ringing in ears" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; NOVOLOG; IRBESARTAN; ZOLOFT; LAMTRACET. Vaccination history included: Covid-19 vaccine (DOSE: 1, MANUFACTURER UNKNOWN), for Covid-19 Immunization; Covid-19 vaccine (DOSE: 2, MANUFACTURER UNKNOWN), for Covid-19 Immunization; Covid-19 vaccine (DOSE: 3, MANUFACTURER UNKNOWN), for Covid-19 Immunization. The following information was reported: TINNITUS (non-serious) with onset 15Nov2022, outcome "not recovered", described as "Increased ringing in both ears". Therapeutic measures were not taken as a result of tinnitus. Additional information: The patient had no known allergies. Prior vaccination, the patient was not diagnosed with COVID. Post vaccination, the patient had not tested COVID. The patient did not receive other vaccine in four weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Diabetes; Hypertension; Ringing in ears
Andere Medikamente: METFORMIN; NOVOLOG; IRBESARTAN; ZOLOFT; LAMTRACET
Allergien: -
Vorherige Impfungen: -

VAERS 2514113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 11,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 22.11.2022
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

11 years old Patient came accompanied by mother to receive Pediatrics Pfizer Bivalent booster, patient was given 12+ years Pfizer Bivalent booster. Vaccinating nurse adminsted Pfizer adult dose 12 years and above, med error was not caught until after patient had already left. Allergist notified and manager notified. Patient was mother was called and mother stated patient is okay and will monitor her for any reactions. Patient's mother stated no SOB, or any other respiratory issues, patient was educated that if any SOB or respiratory issues to go to nearest ED. Patient mother stated " I will continue to watch her"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2512420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WA
Alter: 11,0
Geschlecht: M
Eingang: 19.11.2022
Impfdatum: 19.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect dose administered No adverse event

Symptomtext

No adverse event; admin. error only. Pt was not to receive grey cap Pfizer bivalent booster and should have received the pediatric orange cap bivalent booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2512289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: CA
Alter: 8,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 05.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

PT RECIEVED ADULT PFIZER VACCINE INSTEAD OF PEDIATRIC PFIZER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2511307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: VA
Alter: 90,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Blood pressure abnormal Poor quality sleep

Symptomtext

We can not fall asleep; we were not sleepy; we were awake all night; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 90-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Nov2022 as dose 3 (booster), single (Lot number: GH9697) at the age of 90 years for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure high" (unspecified if ongoing); "Glaucoma" (unspecified if ongoing). Concomitant medication(s) included: CANDESARTAN [CANDESARTAN CILEXETIL] taken for hypertension. Vaccination history included: flu shot, administration date: 07Oct2022, when the patient was 90-year-old, for Immunization; 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: POOR QUALITY SLEEP (non-serious) with onset 11Nov2022, outcome "unknown", described as "We can not fall asleep; we were not sleepy; we were awake all night". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Reporter stated that, he just wants to report and sort of curious. He could not find anything on the computer about side effects and one that he would like to pursue was ability to fall asleep. Last night, his wife and he had some time and they haven't had their third booster yet, so they had the first two and now they wanted to get the third one for the Pfizer. So, they made an appointment at pharmacy for 7:15 and 7:30 and went there and they both had shots. They did not see the shot getting drawn up out of the bottle it came already in syringe and they asked him if it came from a bottle and he said yes and he didn't get about 6 of the bottles (Further not clarified, hence event captured as per the verbatim) and that's what they knew about it. He did not see if it came from refrigeration or anything. He didn't particularly want that kind of shot because those often to have a protection called some kind of a, he did not know the word. Basically, they could not fall asleep. He and his wife had this shot, they were awake all night. She had a very little high blood pressure, its only 132 extremely not high but she took a tremendous number of ocular medications, her problem was Glaucoma.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201300388 Same product/event; different patient;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure abnormal
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:132; Comments: She has very little high blood pressure, its only 132 extremely not high
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Glaucoma
Andere Medikamente: CANDESARTAN [CANDESARTAN CILEXETIL]
Allergien: -
Vorherige Impfungen: -

VAERS 2510323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NC
Alter: 81,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 09.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

Decreased appetite Illness

Symptomtext

Went to be and was sick all night long. Got up, forced herself to go to work. Left at 2PM, went home and went to bed. Has been in bed ever since.; Has not had anything to eat yet. Had once cracker yesterday. Is trying to eat.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 81-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 09Nov2022 at 14:30 as dose 5 (booster), single (Lot number: GH9697) at the age of 81 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, on 25Sep2022 as dose number unknown, single. Vaccination history included: BNT162b2 (DOSE:1, Pfizer Covid-19 vaccine:, First Dose: 05Feb2021, LOT: EL9264, NDC, EXP: Unknown), administration date: 05Feb2021, when the patient was 79-year-old, for COVID-19 immunization; BNT162b2 (DOSE: 2, Second Dose: 26Feb2021; 1115A, next to date on vaccine card, LOT: EN6203, NDC, EXP: Unknown), administration date: 26Feb2021, when the patient was 79-year-old, for COVID-19 immunization; BNT162b2 (DOSE: 3, Third Dose: 25Sep2021, LOT: FF2589, NDC, EXP: Unknown), administration date: 25Sep2021, when the patient was 79-year-old, for Covid-19 immunization; BNT162b2 (DOSE: 4, Fourth Dose, Booster: 04Apr2022, LOT: FJ6369 , NDC, EXP: Unknown), administration date: 04Apr2022, when the patient was 80-year-old, for Covid-19 immunization. The following information was reported: ILLNESS (non-serious) with onset 09Nov2022, outcome "recovering", described as "Went to be and was sick all night long. Got up, forced herself to go to work. Left at 2PM, went home and went to bed. Has been in bed ever since."; DECREASED APPETITE (non-serious) with onset Nov2022, outcome "recovering", described as "Has not had anything to eat yet. Had once cracker yesterday. Is trying to eat.". Therapeutic measures were taken as a result of illness, decreased appetite: Treatment: Took Tylenol. Additional information: Family Medical History Relevant to Adverse Events (AEs): No. Got flu shot 25Sep2022, was over 4 weeks prior to this last booster shot. Just takes her regular medications. At her age, does not want to be getting Covid. Patient has been in bed ever since and missed work today (at the time of report on 11Nov2022). Has been sick in bed at least 2 days with it. Got all the other 3 and never had this problem.

Weitere VAERSDATA-Felder

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

VAERS 2509717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WA
Alter: 69,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 27.10.2022
Beginn: 02.11.2022
Tage bis Beginn: 6,0
Dosis: 5
Route/Site: SYR / RA

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

Body temperature increased COVID-19 Cough Pulmonary congestion Respiratory disorder Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

Above vaccine received on Oct 27, 2022. On Nov 02, 2022 woke up with chest congestion/dry cough. Took home Covid-19 test = Negative. Went to local urgent care clinic, diagnosed withupper respratory illness. PCR Covid test = Positive. Sent home with 5 day Plaxovid regimen with instructions to self isolate/wear mask for 5 days. After completing 5 days Plaxovid regimen/isolation period on Nov 09, 2022 experienced "Plaxovid rebound", dry coughing, sneezing, runny nose, low grade temp of 99.8 degs. As of this date (Nov 16, 2022) self treatment has been self isolation, Day/Nyquil, temp = 98.4, slight lung congestion, dry cough. NOTE: Had annual 65+ flu vaccination administered on Oct 21, 2022 prior to C-19 vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Body temperature increased
Hospital-Tage: -
Labordaten: PCR Covid-19 test on Nov 02, 2022 - positive
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Rosuvastatin, OTC multivitamin, krill oil, glucosamine
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2509518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: NC
Alter: 44,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 16.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient given bivalent instead of second dose in inital series. No adverse effect reported or noted. Date of first vaccine was 10-26-2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: hypertension, hyperlipidemia
Andere Medikamente: Albuterol, Lipitor, Zyrtec, Flexeril, Hydodiuril, Lisinopril,
Allergien: amlodopinie, codeine
Vorherige Impfungen: -

VAERS 2506622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 12.11.2022
Impfdatum: 14.02.1994
Beginn: 15.10.2022
Tage bis Beginn: 10.470,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

PATIENT WAS GIVEN BIVALENT AS A PRIMARY SHOT. PATIENT DID NOT RECEIVED PRIMARY SERIES PREVIOUSLY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2505889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: IL
Alter: 68,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Wrong product administered

Symptomtext

The patient was scheduled for 4 vaccines, the shingrix, pnuemovax 23, fluad 65 and covid 19 booster. The fluad and pnuemovax were predrawn vaccines and required only a needle. The needles were attached to the predrawn syringes. I drew up the Covid 19 in a syringe appropriate for the patient. I then mixed the dilulent into the powdered shingrix and swirled. I picked up the predrawn syringes with needles attached and secured. I then proceeded and picked up the covid-19 booster. I didn't draw up the shingrix because I wanted to able to discern between the covid 19 and shingrix syringe. I grabbed what i thought was the shingrix vials along with the covid 19 and the two predrawn syringes and approached the patient for administration. I administered the Covid 19 to upper left arm and Pneumonia lower left. I then went to administer the shingrix but I noticed the vial was empty so I drew up from what I thought was Shingrix but it was actually Covid 19. I administered the vaccine. I thought it was Shingrix but I inadvertently brought out the covid 19 vial not the mixed Shingrix vial consequently administering a double dose. I gave the fluad lower right. When I returned to vaccine station in the back I saw the Shingles vaccine filled and realized I had taken out the wrong vial.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Degenerative Arthritis; Diabetes and Asthma
Vorgeschichte: Degenerative Arthritis, Asthma and diabetes
Andere Medikamente: HYDROCODONE/APAP 5MG/525, MEDROL DOSE PAK AND TIZANIDINE 4MG TABLETS
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2505889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: IL
Alter: 68,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered Wrong product administered

Symptomtext

The patient was scheduled for 4 vaccines, the shingrix, pnuemovax 23, fluad 65 and covid 19 booster. The fluad and pnuemovax were predrawn vaccines and required only a needle. The needles were attached to the predrawn syringes. I drew up the Covid 19 in a syringe appropriate for the patient. I then mixed the dilulent into the powdered shingrix and swirled. I picked up the predrawn syringes with needles attached and secured. I then proceeded and picked up the covid-19 booster. I didn't draw up the shingrix because I wanted to able to discern between the covid 19 and shingrix syringe. I grabbed what i thought was the shingrix vials along with the covid 19 and the two predrawn syringes and approached the patient for administration. I administered the Covid 19 to upper left arm and Pneumonia lower left. I then went to administer the shingrix but I noticed the vial was empty so I drew up from what I thought was Shingrix but it was actually Covid 19. I administered the vaccine. I thought it was Shingrix but I inadvertently brought out the covid 19 vial not the mixed Shingrix vial consequently administering a double dose. I gave the fluad lower right. When I returned to vaccine station in the back I saw the Shingles vaccine filled and realized I had taken out the wrong vial.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Degenerative Arthritis; Diabetes and Asthma
Vorgeschichte: Degenerative Arthritis, Asthma and diabetes
Andere Medikamente: HYDROCODONE/APAP 5MG/525, MEDROL DOSE PAK AND TIZANIDINE 4MG TABLETS
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2505838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NC
Alter: 10,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Patient was given the Pfizer bivalent 12+ instead of the Pfizer bivalent 5-11.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2504772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MA
Alter: 11,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

Patient is 11 years old but was given the Pfizer bivalent dose for patients 12 and over. No adverse events reported at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2504669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: FL
Alter: 75,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Petechiae

Symptomtext

Petechiae on palms of hands and fingers resolved in one day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Petechiae
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Atrial fib Hx of Graves? disease - tx with RIU 40 years ago
Andere Medikamente: Atenolol Xarelto Synthroid Rosuvastatin Estradiol patch Zolpidem 2.5mg
Allergien: None except maybe vibramycin
Vorherige Impfungen: Swollen lymph node after 1st booster

VAERS 2503888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: KY
Alter: 73,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / RA

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

Back disorder Blister Hypoaesthesia

Symptomtext

Has numbness; back problems; gotten a blister on buttocks; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 27Oct2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 73 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EL9269), administration date: 09Feb2021, when the patient was 72-year-old, for COVID-19 Immunization, reaction(s): "1st blister", "numbness", "back problems"; BNT162b2 (DOSE 2, SINGLE; Lot number: EN6198), administration date: 02Mar2021, when the patient was 72-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: FF8839), administration date: 27Sep2021, when the patient was 72-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 4 (BOOSTER), SINGLE; Lot number: FM7553), administration date: 17May2022, when the patient was 72-year-old, for COVID-19 Immunization. The following information was reported: BLISTER (non-serious) with onset 27Oct2022, outcome "unknown", described as "gotten a blister on buttocks"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "Has numbness"; BACK DISORDER (non-serious), outcome "unknown", described as "back problems". Therapeutic measures were taken as a result of blister. Additional Information: This is not 1st time but this is the 2nd time that caller has gotten a blister on buttocks.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201282459 same patient and event, different dose/drug;

Weitere VAERSDATA-Felder

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

VAERS 2502810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: WV
Alter: -
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 01.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Lymphadenopathy

Symptomtext

Swollen lymph node under left armpit; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), in Nov2022 as dose 3 (booster), single (Lot number: GH9697), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE , lot number: ER2613, vaccine location=Left arm), administration date: Apr2021, for COVID-19 Immunization; Bnt162b2 (DOSE 1, SINGLE , lot number: ER2613, vaccine location=Left arm), administration date: Mar2021, for COVID-19 immunization. The following information was reported: LYMPHADENOPATHY (non-serious), outcome "unknown", described as "Swollen lymph node under left armpit". Therapeutic measures were not taken as a result of lymphadenopathy. Additional information: The patient had no other vaccine in four weeks. The patient had no COVID prior vaccination. The patient had no COVID post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2501912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MO
Alter: 11,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 15.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered No adverse event

Symptomtext

No adverse event reported. Patient mistakenly received Pfizer bivalent for patients 12+, and not the product specific for patients 5-11.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: N/A
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2501486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: NJ
Alter: 79,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2500667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 07.11.2022
Impfdatum: 21.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 11,0
Dosis: 5
Route/Site: - / -

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

Herpes zoster

Symptomtext

Shingles developed 10 days after administration of both vaccines

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: HTN obesity HLD
Andere Medikamente: pantoprazole 40mg daily lisinopril 40mg dailyamlodipine 2.5mg daily atorvastatin 20mg daily levothyroxine 137mcg daily testosterone daily
Allergien: nkda
Vorherige Impfungen: -

VAERS 2500626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 15.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

The Pharmacy made a mistake. When I arrived on Saturday for what I thought would be the second doze. The Pharmacist told me they made a mistake. They never gave me the covid first doze. They gave me a buster. I do not even know what they gave me. The card states Pfizer GH9697 but not sure if that is accurate. This is the first time that I have the vaccine because my liver was not in good condition. I waited until my liver was healthier. Now I do not know what to do. I am not sure if Ok to take the second doze of covid vac. I need to have the correct vaccines to leave the country on the 23rd. Please help me!!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: I did not have an adverse reaction. I am reporting Pharmacy mistake and I need help figuring what to do before my trip. Thank you
Aktuelle Erkrankungen: I have a Fatty liver stage 3 diagnosis was before I lost 70 pounds. Blood tests tell me I am better, but I am being monitor
Vorgeschichte: Fatty liver stage 3 Because of the need to lose weight I had bariatric surgery. I am a bariatric patient mass in Pancreas (this mass is so small now that it cannot be detected) I am monitored. Needed colonoscopy every year because of the health issues
Andere Medikamente: no
Allergien: I am allergic to Prilosec
Vorherige Impfungen: -

VAERS 2500610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MD
Alter: 66,0
Geschlecht: M
Eingang: 07.11.2022
Impfdatum: 31.10.2022
Beginn: 02.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

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

Upper respiratory tract infection

Symptomtext

URI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Upper respiratory tract infection
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2499873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: SC
Alter: 10,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Error: Wrong Age for Vaccine Given-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2499847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

The pharmacist accidentally administered 2 doses of the Covid Pfizer Bivalent booster to the patient. Patient did not receive the flu shot. Pharmacy will call the patient daily to check on his condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2498716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: MN
Alter: 25,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Interchange of vaccine products Off label use Product use issue Wheezing

Symptomtext

wheezing as if I had Asthma; Pfizer: 28Oct2022. Moderna: 28Oct2022; Pfizer - Dose Number: 4; Moderna - Dose Number: 3; Pfizer: 28Oct2022. Moderna: 28Oct2022; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 25-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 at 15:00 as dose 4 (booster), single (Lot number: GH9697) at the age of 25 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), as dose 1, single (Lot number: 031C20H) for 1 day, as dose 2, single (Lot number: 003B21A) for 1 day and as dose 3 (booster), single (Lot number: 031H21H) for 1 day for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing). There were no concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 28Oct2022, outcome "unknown", described as "Pfizer - Dose Number: 4; Moderna - Dose Number: 3"; OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 28Oct2022, outcome "unknown" and all described as "Pfizer: 28Oct2022. Moderna: 28Oct2022"; WHEEZING (non-serious) with onset 30Oct2022 at 10:00, outcome "unknown", described as "wheezing as if I had Asthma". Therapeutic measures were not taken as a result of wheezing. Additional Information: It was reported that the patient went on a run two days after receiving the vaccine and she began wheezing as if she had asthma. She had never wheezed during a run before, and this type of run was a regular part of her routine. She had known allergies to Penicillin. Patient had no other vaccines in 4 weeks and no other medications in two weeks. Patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 post the vaccination. No treatment was received for the adverse event wheezing. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2498690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: MN
Alter: 25,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / LA

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

Inappropriate schedule of product administration Wheezing

Symptomtext

I began wheezing as if I had athsma; All Four doses of vaccine administered on 28 Oct 2022; This spontaneous case was reported by a patient and describes the occurrence of WHEEZING (I began wheezing as if I had athsma) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (All Four doses of vaccine administered on 28 Oct 2022) in a 25-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 031H21H) for COVID-19 prophylaxis. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. The patient's past medical history included COVID-19. Concurrent medical conditions included Penicillin allergy. On 28-Oct-2022, the patient received third dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and fourth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 28-Oct-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (All Four doses of vaccine administered on 28 Oct 2022). On 30-Oct-2022, the patient experienced WHEEZING (I began wheezing as if I had athsma). At the time of the report, WHEEZING (I began wheezing as if I had athsma) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (All Four doses of vaccine administered on 28 Oct 2022) outcome was unknown. Concomitant medication not reported. Co-suspect product also included Moderna Dose 1 (Batch number 031C20H) and Dose 2 (Batch number 003B21A) administered on same date 28 Oct 2022. Location of injection for vaccine was Arm. Since the vaccination, the patient was not tested positive for COVID-19. Patient went on a run two days after receiving the vaccine, and began wheezing as if she had asthma. Patient never wheezed during a run before, and this type of run was a regular part of her routine. Treatment medication not reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Penicillin allergy
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2497693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: IL
Alter: 35,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Inappropriate schedule of product administration Wrong product administered

Symptomtext

The patient was accidently given flu shot when they only needed covid vaccine. The patient had received a flu shot month and a half ago already. So, patient was double vaccinated for Flu shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2496773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WI
Alter: 36,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pharyngeal swelling

Symptomtext

I have never had a problem before, and I asked If I could just leave after the vaccine. When I was driving down the road, I started noticing swelling in my throat about 15 minutes after receiving my vaccine. I went to urgent care, and they told me to take BENADRYL, and to come back if things got worse. The BENADRYL cleared it up and I didn't have any other issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal swelling
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Seasonal allergies
Vorgeschichte: Type 3 Ehlers Danlos Syndrome
Andere Medikamente: N/A
Allergien: Penicillin; benzodiazepine; tobacco; cats; seasonal allergies
Vorherige Impfungen: -

VAERS 2496474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 31.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Erythema Immunisation reaction Peripheral swelling Skin warm Tenderness

Symptomtext

Covid arm. Swollen, sore/painful upon tactile stimulation, red, warm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Acne
Andere Medikamente: Spironolactone for acne, doxycycline for acne
Allergien: No
Vorherige Impfungen: -

VAERS 2495090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: GA
Alter: 52,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 14.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Heavy menstrual bleeding Ultrasound pelvis normal Ultrasound scan vagina normal

Symptomtext

On 10/17/22, I was going through my normal spotting during my cycle. Later that evening into 10/18/22 spotting picked up to heavy bleeding that continued until 10/26/22 until I received medication to get it to stop. I consulted with my physician's office and an appointment was made for me to have, a pelvic and cross vaginal ultrasound, nothing out of the ordinary was found. I am now taking hormones to keep the heavy bleeding from coming back and I was referred to a gynecologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Heavy menstrual bleeding
Hospital-Tage: -
Labordaten: Ultrasound negative
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: ALVESCO inhaler; albuterol; FLONASE; ZYRTEC
Allergien: CYMBALTA
Vorherige Impfungen: -

VAERS 2494521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
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 came in the store to receive a Flu vaccine (above information). However, a Covid vaccine was administered (Pfizer Bivalent Booster GH9697 12-02-22 in the left arm). No adverse effects at the time of the incorrect vaccine. Flu vaccine was administered right after since that was when the error was noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: Fish-derived products, iodides
Vorherige Impfungen: -

VAERS 2494053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 21.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Cough Fall Lethargy

Symptomtext

Lethargy, weakness, cough, fall

Weitere VAERSDATA-Felder

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

VAERS 2493987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WI
Alter: 10,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 30.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

Minor is 10yr 11 months old and received adult 12yo+ dose of pfizer bivalent instead of the authorized pediatric pfizer bivalent as instructed for 10 yo minor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2492275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: TX
Alter: 21,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 22.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: NY
Alter: 77,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 23.10.2022
Beginn: 23.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / -

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

Asthenia Blood test Culture urine Dysstasia Insomnia Sitting disability Speech disorder Thinking abnormal Urinary incontinence

Symptomtext

couldn't stand him up; speech wasn't right; he is so weak.; couldn't understand him and he couldn't sit up; couldn't understand him and he couldn't sit up; couldn't sleep; He urinated in his diaper three times, which he doesn't usually do that he usually uses the urinal; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 77-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Oct2022 as dose 5 (booster), single (Lot number: GH9697) at the age of 77 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "Deep brain stimulation" (unspecified if ongoing), notes: This was put in August 2022 or August 2021, she can't remember exactly.; "Parkinson's", start date: Apr2015 (unspecified if ongoing); "walked with a walker" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, LOT: ER8982), administration date: 28Jan2021, when the patient was 75-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, LOT: EN6201), administration date: 18Feb2021, when the patient was 75-year-old, for COVID-19 immunization; BNT162b2 (Dose 3 (Booster), LOT: FF8841), administration date: 06Oct2021, when the patient was 76-year-old, for Covid-19 immunization, reaction(s): "Walking difficulty", "Injection site discomfort"; BNT162b2 (Dose 4 (Booster), LOT: FJ9943), administration date: 19Apr2022, when the patient was 77-year-old, for COVID-19 Immunization. The following information was reported: URINARY INCONTINENCE (hospitalization) with onset 23Oct2022, outcome "unknown", described as "He urinated in his diaper three times, which he doesn't usually do that he usually uses the urinal"; INSOMNIA (hospitalization) with onset 23Oct2022, outcome "unknown", described as "couldn't sleep"; DYSSTASIA (hospitalization, disability) with onset 24Oct2022, outcome "unknown", described as "couldn't stand him up"; THINKING ABNORMAL (hospitalization), SITTING DISABILITY (hospitalization) all with onset 24Oct2022, outcome "unknown" and all described as "couldn't understand him and he couldn't sit up"; ASTHENIA (hospitalization) with onset 24Oct2022, outcome "unknown", described as "he is so weak."; SPEECH DISORDER (hospitalization, disability) with onset 24Oct2022, outcome "unknown", described as "speech wasn't right". The patient was hospitalized for dysstasia, speech disorder, urinary incontinence, asthenia, insomnia, thinking abnormal, sitting disability (start date: 24Oct2022). The events "couldn't stand him up", "speech wasn't right", "he urinated in his diaper three times, which he doesn't usually do that he usually uses the urinal", "he is so weak.", "couldn't sleep" and "couldn't understand him and he couldn't sit up" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: (24Oct2022) fine; Culture urine: (24Oct2022) fine. Additional information: Consumer calling about her husband who got the booster, the last one, and he landed up in the hospital yesterday. He got the vaccine at noon on Sunday and he came home and ate dinner and was fine, she put him to bed and got him up at seven and he had a snack and she laid him back down at midnight but he couldn't sleep so he went back up and was up all night. He urinated in his diaper three times, which he did not usually do that he usually used the urinal, but she couldn't stand him up in the morning and his speech wasn't right. She couldn't get him up and had to call the paramedics and they took him to the hospital which he is still there, and he was also a Parkinson's patient. Caller says her husband's Pfizer COVID-19 vaccine card information is handwritten. NDC/EXP were not provided on vaccine card for any of his doses. His last dose was the Pfizer COVID-19 bivalent vaccine, which was his first dose of that, on Sunday 23Oct2022. On 24Oct she woke him up at 07:30 in the morning actually he wanted to get up, but then she couldn't understand him and he couldn't sit up. She called the paramedics who took him to the hospital immediately. They did no treatment there, and they did blood and urine tests and said everything looked fine. He was admitted to the hospital 24Oct, and they may have to put him in rehab because he was so weak. It was like all the life went out of him after he got the vaccine. Before it he walked with a walker back and forth, then it seemed like after the shot the morning after they came home he ate and did his regular routine, then the next morning she couldn't get him up. Her husband went to a neurologist and urologist.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101342031 Same product, patient, different event, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: Test Date: 20221024; Test Name: blood test; Result Unstructured Data: Test Result:fine; Test Date: 20221024; Test Name: urine tests; Result Unstructured Data: Test Result:fine
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Deep brain stimulation (This was put in August 2022 or August 2021, she can't remember exactly.); Parkinson's disease; Walking aid user
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2489215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: PA
Alter: 75,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

No adverse event Wrong product administered

Symptomtext

No adverse event reported. The prescriber notified the pharmacy that PT had received PCV20 on 7/21/22 at the prescriber's office. Pt had come in on 10/18/22 requesting COVID19 bivalent booster, Shingrix dose#1, and PPSV23

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE NOTED
Vorgeschichte: NONE NOTED
Andere Medikamente: UNKNOWN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2488178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: CA
Alter: 20,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2487434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WA
Alter: 11,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 23.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 1,0
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

wrong vaccine was administered to the patient. Patient was only 11.5 years old but received Pfizer bivalent 12+ instead of kids bivalent 5-11

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: wrong vaccine was administered to the patient. Patient was only 11.5 years old but received Pfizer bivalent 12+ instead of kids bivalent 5-11
Allergien: -
Vorherige Impfungen: -

VAERS 2487422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: WA
Alter: 32,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 19.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

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

Heavy menstrual bleeding Menstrual disorder Vaccine positive rechallenge

Symptomtext

I experienced a disruption in my menstrual cycle. My period arrived almost three weeks early and was exceptionally heavy. This is something I have experienced after my second Pfizer dose, first booster, and this most recent booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Heavy menstrual bleeding
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Bipolar disorder
Andere Medikamente: Lithium Quetiapine Propranolol Levothyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 2487393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 09.09.2022
Beginn: 22.09.2022
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: SYR / UN

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

Gastrointestinal haemorrhage Herpes zoster Skin lesion

Symptomtext

I had my vaccination on 09/09/2022. On 09/22/2022 I had a spot on my back that looked like a burn. I saw my dermatologist on 09/27/2022 and stated that it was Shingles. I chose not to take the prescription. Two weeks after vaccination I also had gastrointestinal bleeding. I did see my primary doctor on 09/23/2022 and they are going to do a colonoscopy in 01/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gastrointestinal haemorrhage
Hospital-Tage: -
Labordaten: Colonoscopy 01/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Chronic back issues
Andere Medikamente: N/A
Allergien: Metformin; TEQUIN
Vorherige Impfungen: -

VAERS 2486883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MA
Alter: 16,0
Geschlecht: M
Eingang: 24.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

No adverse event Wrong product administered

Symptomtext

Pt given COVID bivalent booster as first dose in series. No adverse reaction, RN confirmed CDC recommendations and spoke with pts father regarding event. Father has no further questions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2486708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 16.10.2022
Beginn: 16.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: IA
Alter: 25,0
Geschlecht: F
Eingang: 23.10.2022
Impfdatum: 17.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series Given Too Early-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2484038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MS
Alter: 19,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered Medication error No adverse event

Symptomtext

Pfizer Bivalent vaccine was given as a first dose when Pfizer Monovalent Vaccine was ordered. No adverse reaction occurred. Patient was seen by the prmary care provider, medication error was discussed, reassurances given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2482180

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GH9697

gering

Staat: WA
Alter: 10,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Patient's age is 10 and Pfizer vaccine for 12+ was administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 2480275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 17.10.2022
Impfdatum: 13.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

COVID BREAKTHROUGH CASE

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID+ 10/15/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia Benign essential HTN CAD (coronary artery disease) of artery bypass graft Class 2 obesity Depression GERD without esophagitis HLD (hyperlipidemia) Obesity, Class I, BMI 30-34.9 Pancreatic pseudocyst Tobacco user
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 52,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 64,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 57,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 45,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 57,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: UT
Alter: 61,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 10.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

Deafness

Symptomtext

Lose of hearing in right ear.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Oct2022 at 10:45 as dose 4 (booster), single (Lot number: GH9697) at the age of 61 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The patient did not receive any other vaccine in four weeks. The patient did not have Covid prior to vaccination. The patient was not Covid tested post vaccination. The patient had no known allergies. Vaccination history included: Covid-19 vaccine (Dose: 3 (1st booster), MANUFACTURER UNKNOWN), for Covid-19 Immunization; Covid-19 vaccine (Dose: 2, MANUFACTURER UNKNOWN), for COVID-19 immunization; Covid-19 vaccine (Dose: 1, MANUFACTURER UNKNOWN), for COVID-19 Immunization. The patient experienced lose of hearing in right ear in Oct2022. No treatment was received for the event. The outcome of the event was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deafness
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 2479370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: LA
Alter: 75,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 04.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

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

Blister infected Lip swelling Oral herpes Scab

Symptomtext

the blister has been crusted up and was aggravating; The crusty area has pus attached to it and left a deep hole in her lip; lips were swollen; fever blister; 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 75-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Oct2022 at 05:00 as dose 3 (booster), 15 ug single (Lot number: GH9697) at the age of 75 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure abnormal"; "COVID", start date: 24Apr2022 (not ongoing), notes: She had been sick for 5 days when she tested positive for COVID. Concomitant medication(s) included: VALSARTAN taken for blood pressure abnormal (ongoing). Vaccination history included: Bnt162b2 (Dose 1), for Covid-19 immunization; Bnt162b2 (Dose 2), for Covid-19 immunization. The following information was reported: BLISTER INFECTED (non-serious) with onset 07Oct2022 at 06:00, outcome "unknown", described as "The crusty area has pus attached to it and left a deep hole in her lip"; ORAL HERPES (non-serious) with onset 07Oct2022 at 06:00, outcome "unknown", described as "fever blister"; LIP SWELLING (non-serious) with onset 07Oct2022 at 06:00, outcome "unknown", described as "lips were swollen"; SCAB (non-serious) with onset 11Oct2022, outcome "not recovered", described as "the blister has been crusted up and was aggravating". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of blister infected. Additional information: 2 and a half days after getting the 3rd booster dose, around 6 AM Friday morning (07Oct2022), she noticed that her lips were swollen and noticed 3 huge blisters on her lip and not on the cluster and was advised by her doctor that it might have been a fever blister. Today (11Oct2022), the blister has been crusted up and was aggravating for her since she never had anything like this happen to her in her life. The crusty area has pus attached to it and left a deep hole in her lip. She attempted to send a picture over to her physician but for some reason the air was not good for pictures; she was asking if this could be a side effect of her shot; he did not think so at the time but sent medication over for a fever blister. She is curious because this thing eventually just crusted up and made a huge scab on her lip, the scab this morning (11Oct2022) fell off on it is own and underneath it was pus and the hole in her lip is several layers deep. It confused her that the 3rd booster dose was her 5th shot (as reported, pending clarification). Follow-Up (14Oct2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blister infected
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal; COVID-19 (She had been sick for 5 days when she tested positive for COVID)
Andere Medikamente: VALSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2479312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 49,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 33,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 74,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 56,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 22,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 48,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: OK
Alter: 29,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Incorrect dose administered

Symptomtext

Error: Wrong Dose of Vaccine - Too High-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2481468

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Hyperhidrosis Thirst Tinnitus Vision blurred

Symptomtext

BlurredVision diaphoresis, thirsty, tinnitus Narrative: Reaction occurred within 5 minutes post vaccination and employee was taken to the ED, later discharged to home.

Weitere VAERSDATA-Felder

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

VAERS 2479687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GH9697

gering

Staat: KY
Alter: 75,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: -
Beginn: 12.10.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: SC / -

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

Depressed level of consciousness Gait inability Lethargy Neurological symptom Speech disorder

Symptomtext

After receiving the second and third COVID boosters patient had stroke like symptoms, unable to talk, stay alert, walk. She is slowly coming out of the symptoms but remains very lethargic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Depressed level of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: alzheimers and seizures
Andere Medikamente: Levothoroxine 88mg, Memantine 10mg twice daily, Buprprion HCL 23mg, Lacosamide 150 mg twice daily, Atorvastatin40mg, Pantoprazole 20 mg, Sertaline 200mg, Aripiprozole 4mg, Mertazapine 30mg, gabapentin 300mg, Melatonin 5mg, frolic Acid 400m
Allergien: -
Vorherige Impfungen: -

VAERS 2478455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gh9697

gering

Staat: MD
Alter: 59,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

He got double the dose of the pfizer bivalent covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2476320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Blood glucose increased

Symptomtext

Patient is a diabetic and currently using insulin pump. After getting her Pfizer bivalent booster vaccine at 5:00pm he experienced high blood sugar level of 200 at bedtime. She stated the previous night her blood sugar was at 97.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood glucose increased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Patient took 200mg of Ibuprofen prior to vaccination
Allergien: -
Vorherige Impfungen: -

VAERS 2476311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: WA
Alter: 56,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Blood glucose normal

Symptomtext

Patient is a diabetic and currently using insulin pump. After getting his Pfizer bivalent booster vaccine at 5:00pm he experienced high blood sugar level of 160 at bedtime. He stated that this high blood sugar event was very unusual for him and the previous night reading was 116. According to him his wife, also a diabetic, also experienced high blood sugar after her vaccination (I am reporting her event on a separate form).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood glucose normal
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Patient took 400mg of Ibuprofen prior to vaccination
Allergien: -
Vorherige Impfungen: -

VAERS 2476280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 12.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

No adverse event Product administration error Wrong product administered

Symptomtext

Client came to the pharmacy requesting Flublok flu vaccination. He had planned to separate his flu vaccination and his covid bivalent booster vaccinations by one week to decrease the intensity of side effects that might be more severe with co-administration. Due to the large number of people receiving flu vaccines and covid booster vaccines at the same time during this clinic, 2 syringes of Pfizer bivalent booster vaccine were in close proximity on the vaccinator table to the Flublok vaccine distributed by the pharmacists. In error, a Pfizer bivalent booster was administered instead of the Flublok. The client was informed as soon as the erroneous administration occurred. He decided to proceed with administration of the Flublok in the same right deltoid muscle, separated by more than an inch, as he wanted to avoid arm pain side effects bilaterally. This report is of the vaccine administration error. No other adverse effects have been reported related to this error.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None, and none expected
Aktuelle Erkrankungen: None known
Vorgeschichte: Asthma
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2475668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gh9697

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Extra dose administered Wrong product administered

Symptomtext

patient came in for COVID booster wife at chair side who also was getting the vaccine. Patient requested flu along with his COVID.. The patient in exam area wife siting outside curtain. RN brought in all 3 vaccines for the patient and wife. The RN administered Covid vaccine in patient's right deltoid. RN then administered what Rn believed to be the flu vaccine, however was discovered to be a second covid vaccine. RN administered 2 covid booster's, one in each arm of the patient, instead of the requested flu vaccine. RN then discussed with the pharmacist and the patient was brought to pharmacy's room to discuss the incident that occurred. The patient stated understanding of the incident and has been given instruction by pharmacist and RN to report any untoward side effects after leaving the facility. The patient was given the information on how to contact RN with any concerns. Pharmacist recommends patient now waiting at least a week before returning for the Flu vaccine. Patient was monitored per CDC guidelines. RN then reported the incident to manager on duty, charge RN was alerted as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2473715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GH9697

gering

Staat: MO
Alter: 11,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 08.10.2022
Beginn: 08.10.2022
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 No adverse event

Symptomtext

Patient is 11 years old. Instead of boosting with the Pfizer 5-11 vaccine, nurse administered Pfizer bi-valent (12+). Patient's mom reports no adverse effects as of 48 hours post-administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: n/a
Vorgeschichte: ankyloglossia, allergic rhinitis
Andere Medikamente: montelukast, fluticasone nasal, cetirizine
Allergien: n/a
Vorherige Impfungen: -