VAERS Reports GJ6665

VAERS 2728691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 29.12.2023
Impfdatum: 08.11.2022
Beginn: 06.11.2023
Tage bis Beginn: 363,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Atrial fibrillation COVID-19 Cardiac failure acute Cough Diuretic therapy Dyspnoea Dyspnoea exertional Hypertension Hypervolaemia Left ventricular failure Orthopnoea Peripheral swelling SARS-CoV-2 test positive Tricuspid valve incompetence

Symptomtext

Pt is a 90 y/o male with history noted above. Now presents with dyspnea over the last 7 days with cough. Reports nonproductive cough, worsening dyspnea on exertion. Also reports orthopnea with increased leg swelling, denies chest pain, fever or chills, n/v/d, abdominal pain. He denies recent sick contacts. Workup in ED: acute hypoxic respiratory failure on arrival. Found to be fluid overloaded and COVID positive. Admission for supportive care, continued O2 therapy, diuresis, ID and cardio consults. Clinical Summary Patient was weaned off oxygen for acute respiratory failure due to covid. Patient completed a course of remdesivir and has been stable. Placement has been an issue as patient requires care takers at home and they would not come into the home until patient is out of his quarantine period and SNF had reported the same. Patient is now 10 days out from testing positive and will be discharged to SNF with instructions to follow up with PCP. No medication changes were made and VS and labs have been stable otherwise. Discharge diagnosis Acute hypoxic respiratory failure COVID-19 infection without pneumonia Acute on chronic diastolic heart failure Valvular heart failure Severe tricuspid regurgitation Permanent atrial fibrillation Hypertension Seizure history

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2728550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 29.12.2023
Impfdatum: 09.11.2022
Beginn: 04.11.2023
Tage bis Beginn: 360,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray normal Chest pain Cough Full blood count abnormal Metabolic function test abnormal Mobility decreased Platelet count decreased SARS-CoV-2 test positive Thrombocytopenia Walking aid user

Symptomtext

Patient is a 77-year-old male with past medical history of coronary artery disease status post DES to the RCA, essential hypertension, subclavian artery stenosis, bleeding duodenal ulcer, type 2 diabetes, BPH who presented to the emergency department via squad from home due to increased cough and burning in the chest. Oxygen was noted to be 87% on room air and 2 L per nasal cannula was placed. Clinical Summary Clinical course Include/ Problem list Acute hypoxic respiratory failure secondary to Covid 19 pneumonia: -Last Vaccination: 11/2022; Symptom onset: 3 day PTA; Test positive: 11/4. -ED representation (11/4): CXR negative, 2.5 L oxygen->Now on 1L -Decadron: 11/5 -Remdesivir: 11/5 -Continue: albuterol inh qid, mucinex -Monitor daily CBC and BMP Mild thrombocytopenia -Secondary to COVID infection -Plt 125 -No evidence of bleeding bruising oozing Coronary artery disease -History of DES to the RCA. Documented 100% occlusion to the circumflex. Appears to be pending outpatient left heart catheterization with IFR to evaluate the LAD. -Continue aspirin and Plavix Essential hypertension -Recent addition of lisinopril 10 mg daily by cardiology. Stopped by PCP due to cough. Change to ARB and monitor. -Continue metoprolol 25 Subclavian artery stenosis -Follows with cardiology, apparent asymptomatic History of bleeding duodenal ulcer -Occurred after initiating dual antiplatelet therapy -On lifelong PPI twice daily. Type 2 diabetes -Levemir -Wound Sitagliptin?metformin BPH -ContinueFlomax, finasteride 11/6/2023 patient seen and examined at bedside. He is on room air is oxygen saturations with continuous pulse oximeter is 95 to 96%. Patient states that he has not been up much over the course the last day and a half but he is able to walk to the bathroom before walker has been placed. We will plan to discharge patient home today with a 3-day course of dexamethasone, will cover him with doxycycline for the next 5 days as well as send orders for inhalers x2. Patient declines home health care. He is instructed to return the emergency department if he feels that he needs to be evaluated or his condition worsens.

Weitere VAERSDATA-Felder

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

VAERS 2727624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 27.12.2023
Impfdatum: 14.10.2022
Beginn: 07.11.2023
Tage bis Beginn: 389,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19 Cardiac failure acute Chest X-ray abnormal Condition aggravated Dry lung syndrome Dyspnoea Fall Hip fracture Left ventricular failure Open reduction of fracture Periprosthetic fracture Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

89 y.o. male patient of MD with history of previous hip fracture and cva presented to Hospital with shortness of breath, covid and possible hip infection Acute Hypoxic Respiratory Failure Suspected combination of covid infection with possible heart failure exacerbation CXR with Pulmonary edema Will follow treatment of covid an HF as below Improved Covid-19 Virus Infection Date of onset of symptoms: 10/29 Symptoms present on admission: shortness of breath Date of covid positive test: 10/31 per son Vaccination status: vaccinated Imaging: CXR with Pulmonary edema Oxygen requirements on admission: 9L Current oxygen requirements: RA Medical therapy: steroids Consultants following: none Isolation precautions to end 11/12 Acute on Chronic HFpEF Suspected exacerbation CXR with Pulmonary edema 2L fluid and then lasix IV given in the ED Will favor dry lung with comorbid covid infection and possible heart failure Continue IV lasix, decreased dose I&O Discharge on small dose of lasix Right hip fracture, periprosthetic Patient fell during transferring and injured right hip on previous admission S/p open reduction internal fixation of femur on 10/31 Question possible possible post op infection initially Rocephin and Levaquin given in the ED - will change to vanc and zosyn Ortho consulted -- no concerns for infection -- stopping antibiotics CAD Last DES in April 2021 Continue aspirin, plavix and statin Celiac disease Gluten-free diet History of CVA Delirium With residual right sided weakness On ASA, plavix, statin at home

Weitere VAERSDATA-Felder

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

VAERS 2713263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MI
Alter: -
Geschlecht: M
Eingang: 15.12.2023
Impfdatum: 14.11.2022
Beginn: 08.09.2023
Tage bis Beginn: 298,0
Dosis: 5
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 Dyspnoea Hypercapnia Angiogram Encephalopathy Pneumonia Hypoxia Positive airway pressure therapy Sepsis

Symptomtext

Sepsis / Appeared septic; Acute respiratory failure with hypoxia and hypercapnia; Acute encephalopathy; Multifocal pneumonia; Covid-19; This spontaneous case from the United States was retrieved on 07-Dec-2023 from Vaccine Adverse Event Reporting System (VAERS) (reference number: 2713263-1) reported by other healthcare professional and concerned a male patient of unspecified age (discrepantly reported as 64 and 4-years-old). The patient's concurrent condition included unspecified mood disorder, essential (primary) hypertension, non-insulin-dependent type 2 diabetes, arteriovenous malformation (AVM), unspecified brain neurocognitive disorder, anxiety with agitation, paroxysmal atrial fibrillation, tremor, and benign prostatic hyperplasia (BPH). The patient's concomitant medications included Tylenol (paracetamol), Pacerone (amiodarone hydrochloride), Amoxil (amoxicillin), aspirin, Plavix (clopidogrel bisulfate), and cyanocobalamin, all used for unreported indications. The patient's historical condition included hemorrhagic stroke (cerebrovascular accident (CVA) due to intracerebral hemorrhage) with subsequent tremor. The patient's historical procedure included Watchman procedure. The patient had no allergies. It was reported that on 14-Nov-2022, the patient was vaccinated with Fluad Quadrivalent (influenza vaccine inact sag 4v; dose, route of administration, anatomical location, and indication: not reported). The batch number reported was AS3705B (reported batch number was identified by Seqirus to be linked to suspect product Afluria Quadrivalent (influenza vaccine inact split 4v) instead of reported suspect product Fluad Quadrivalent). Based on the reported batch number, the suspect product was changed to Afluria Quadrivalent. On the same date, the patient was vaccinated with non-company, co-suspect Covid-19 vaccine reported as Pfizer BioNTech COVID-19 vaccine, bivalent (active ingredient not specified; dose reported as '5', route of administration, anatomical location, and indication: not reported). The batch number reported was GJ6665. On an unspecified date in 2023, reported as about ten days prior 08-Sep-2023, an unknown amount of time after receiving Afluria Quadrivalent and non-company, co-suspect Covid-19 vaccine, the patient was diagnosed with Covid-19. On 08-Sep-2023, nine months and 25 days, after receiving Afluria Quadrivalent and non-company, co-suspect Covid-19 vaccine, the patient was brought to the emergency department (ED) and was admitted to hospital with concerns of acute encephalopathy and he appeared septic. On an unspecified day in Sep-2023, computed tomography angiography (CTA) of chest was performed and revealed concerning for extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia. The patient was diagnosed with severe sepsis and acute respiratory failure with hypoxia and hypercapnia. The patient had been residing in a skilled nursing facility on hospice care. The patient had court-appointed guardian and emergency department physician was able to get in touch with her, and she agreed that patient would want to revoke his hospice for hospitalization, but with no aggressive measures. The patient was treated with unspecified broad-spectrum antibiotics and was placed on positive airway pressure therapy (BiPAP) for increase of breathing. During next 24 hours the patient showed very minimal improvement. On 10-Sep-2023, after discussion with his guardian, the patient was made comfort measures. On 11-Sep-2023, nine months and 28 days after receiving Afluria Quadrivalent and non-company, co-suspect Covid-19 vaccine, the patient died. The causes of death were sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia. It was unknown if an autopsy was performed. The reporter did not provide a causality assessment. The events of sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia were assessed as serious due to the seriousness criterion of fatal outcome and hospitalization. Additionally, the events of sepsis, encephalopathy acute, acute respiratory failure, and pneumonia were considered to be medically significant by a Physician within Seqirus' Pharmacovigilance Department. Company comment: On 14-Nov-2022, a male patient of unspecified age (discrepantly reported as 64 and 4-years-old) was vaccinated with Fluad Quadrivalent and non-company, co-suspect Covid-19 vaccine. On 08-Sep-2023, the patient was brought to the emergency department (ED) and was admitted to hospital with concerns of acute encephalopathy and he appeared septic. Ten days before admission, the patient was diagnosed with Covid-19. Computed tomography angiography (CTA) of chest was performed and revealed concerning for extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia. The patient was diagnosed with severe sepsis and acute respiratory failure with hypoxia and hypercapnia. On 11-Sep-2023, the patient died. The causes of death were sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia. It was unknown if an autopsy was performed. Causal role of the suspect vaccine is assessed as not related for all events, based on biological and chronological implausibility.; Sender's Comments: On 14-Nov-2022, a male patient of unspecified age (discrepantly reported as 64 and 4-years-old) was vaccinated with Fluad Quadrivalent and non-company, co-suspect Covid-19 vaccine. On 08-Sep-2023, the patient was brought to the emergency department (ED) and was admitted to hospital with concerns of acute encephalopathy and he appeared septic. Ten days before admission, the patient was diagnosed with Covid-19. Computed tomography angiography (CTA) of chest was performed and revealed concerning for extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia. The patient was diagnosed with severe sepsis and acute respiratory failure with hypoxia and hypercapnia. On 11-Sep-2023, the patient died. The causes of death were sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia. It was unknown if an autopsy was performed. Causal role of the suspect vaccine is assessed as not related for all events, based on biological and chronological implausibility.; Reported Cause(s) of Death: Sepsis / Appeared septic; Acute respiratory failure with hypoxia and hypercapnia; Covid-19; Acute encephalopathy; Multifocal pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Test Date: 202309; Test Name: CTA chest; Result Unstructured Data: Extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia
Aktuelle Erkrankungen: Agitation; Anxiety; Arteriovenous malformation; Atrial fibrillation; BPH; Cognitive disorder; Mood disorder; Primary hypertension; Tremor; Type 2 diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Atrial appendage closure; Hemorrhagic stroke (Subsequent tremor)
Andere Medikamente: Tylenol; Pacerone; Amoxil; Aspirin; Plavix; Cyanocobalamin
Allergien: -
Vorherige Impfungen: -

VAERS 2713263

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge GJ6665

kritisch

Staat: MI
Alter: -
Geschlecht: M
Eingang: 15.12.2023
Impfdatum: 14.11.2022
Beginn: 08.09.2023
Tage bis Beginn: 298,0
Dosis: UNK
Route/Site: OT / -

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 Dyspnoea Hypercapnia Angiogram Encephalopathy Pneumonia Hypoxia Positive airway pressure therapy Sepsis

Symptomtext

Sepsis / Appeared septic; Acute respiratory failure with hypoxia and hypercapnia; Acute encephalopathy; Multifocal pneumonia; Covid-19; This spontaneous case from the United States was retrieved on 07-Dec-2023 from Vaccine Adverse Event Reporting System (VAERS) (reference number: 2713263-1) reported by other healthcare professional and concerned a male patient of unspecified age (discrepantly reported as 64 and 4-years-old). The patient's concurrent condition included unspecified mood disorder, essential (primary) hypertension, non-insulin-dependent type 2 diabetes, arteriovenous malformation (AVM), unspecified brain neurocognitive disorder, anxiety with agitation, paroxysmal atrial fibrillation, tremor, and benign prostatic hyperplasia (BPH). The patient's concomitant medications included Tylenol (paracetamol), Pacerone (amiodarone hydrochloride), Amoxil (amoxicillin), aspirin, Plavix (clopidogrel bisulfate), and cyanocobalamin, all used for unreported indications. The patient's historical condition included hemorrhagic stroke (cerebrovascular accident (CVA) due to intracerebral hemorrhage) with subsequent tremor. The patient's historical procedure included Watchman procedure. The patient had no allergies. It was reported that on 14-Nov-2022, the patient was vaccinated with Fluad Quadrivalent (influenza vaccine inact sag 4v; dose, route of administration, anatomical location, and indication: not reported). The batch number reported was AS3705B (reported batch number was identified by Seqirus to be linked to suspect product Afluria Quadrivalent (influenza vaccine inact split 4v) instead of reported suspect product Fluad Quadrivalent). Based on the reported batch number, the suspect product was changed to Afluria Quadrivalent. On the same date, the patient was vaccinated with non-company, co-suspect Covid-19 vaccine reported as Pfizer BioNTech COVID-19 vaccine, bivalent (active ingredient not specified; dose reported as '5', route of administration, anatomical location, and indication: not reported). The batch number reported was GJ6665. On an unspecified date in 2023, reported as about ten days prior 08-Sep-2023, an unknown amount of time after receiving Afluria Quadrivalent and non-company, co-suspect Covid-19 vaccine, the patient was diagnosed with Covid-19. On 08-Sep-2023, nine months and 25 days, after receiving Afluria Quadrivalent and non-company, co-suspect Covid-19 vaccine, the patient was brought to the emergency department (ED) and was admitted to hospital with concerns of acute encephalopathy and he appeared septic. On an unspecified day in Sep-2023, computed tomography angiography (CTA) of chest was performed and revealed concerning for extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia. The patient was diagnosed with severe sepsis and acute respiratory failure with hypoxia and hypercapnia. The patient had been residing in a skilled nursing facility on hospice care. The patient had court-appointed guardian and emergency department physician was able to get in touch with her, and she agreed that patient would want to revoke his hospice for hospitalization, but with no aggressive measures. The patient was treated with unspecified broad-spectrum antibiotics and was placed on positive airway pressure therapy (BiPAP) for increase of breathing. During next 24 hours the patient showed very minimal improvement. On 10-Sep-2023, after discussion with his guardian, the patient was made comfort measures. On 11-Sep-2023, nine months and 28 days after receiving Afluria Quadrivalent and non-company, co-suspect Covid-19 vaccine, the patient died. The causes of death were sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia. It was unknown if an autopsy was performed. The reporter did not provide a causality assessment. The events of sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia were assessed as serious due to the seriousness criterion of fatal outcome and hospitalization. Additionally, the events of sepsis, encephalopathy acute, acute respiratory failure, and pneumonia were considered to be medically significant by a Physician within Seqirus' Pharmacovigilance Department. Company comment: On 14-Nov-2022, a male patient of unspecified age (discrepantly reported as 64 and 4-years-old) was vaccinated with Fluad Quadrivalent and non-company, co-suspect Covid-19 vaccine. On 08-Sep-2023, the patient was brought to the emergency department (ED) and was admitted to hospital with concerns of acute encephalopathy and he appeared septic. Ten days before admission, the patient was diagnosed with Covid-19. Computed tomography angiography (CTA) of chest was performed and revealed concerning for extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia. The patient was diagnosed with severe sepsis and acute respiratory failure with hypoxia and hypercapnia. On 11-Sep-2023, the patient died. The causes of death were sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia. It was unknown if an autopsy was performed. Causal role of the suspect vaccine is assessed as not related for all events, based on biological and chronological implausibility.; Sender's Comments: On 14-Nov-2022, a male patient of unspecified age (discrepantly reported as 64 and 4-years-old) was vaccinated with Fluad Quadrivalent and non-company, co-suspect Covid-19 vaccine. On 08-Sep-2023, the patient was brought to the emergency department (ED) and was admitted to hospital with concerns of acute encephalopathy and he appeared septic. Ten days before admission, the patient was diagnosed with Covid-19. Computed tomography angiography (CTA) of chest was performed and revealed concerning for extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia. The patient was diagnosed with severe sepsis and acute respiratory failure with hypoxia and hypercapnia. On 11-Sep-2023, the patient died. The causes of death were sepsis, acute respiratory failure, Covid-19, encephalopathy acute, and pneumonia. It was unknown if an autopsy was performed. Causal role of the suspect vaccine is assessed as not related for all events, based on biological and chronological implausibility.; Reported Cause(s) of Death: Sepsis / Appeared septic; Acute respiratory failure with hypoxia and hypercapnia; Covid-19; Acute encephalopathy; Multifocal pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Test Date: 202309; Test Name: CTA chest; Result Unstructured Data: Extensive bilateral nodularity, ground-glass, areas of multifocal consolidation consistent with multifocal pneumonia
Aktuelle Erkrankungen: Agitation; Anxiety; Arteriovenous malformation; Atrial fibrillation; BPH; Cognitive disorder; Mood disorder; Primary hypertension; Tremor; Type 2 diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Atrial appendage closure; Hemorrhagic stroke (Subsequent tremor)
Andere Medikamente: Tylenol; Pacerone; Amoxil; Aspirin; Plavix; Cyanocobalamin
Allergien: -
Vorherige Impfungen: -

VAERS 2714161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 15.11.2023
Impfdatum: 10.11.2022
Beginn: 05.09.2023
Tage bis Beginn: 299,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Anal fistula Antinuclear antibody Biopsy kidney abnormal Blood creatinine increased Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Complement factor Condition aggravated Deep vein thrombosis Diabetic nephropathy Diuretic therapy Electrocardiogram normal End stage renal disease Glycosylated haemoglobin increased

Symptomtext

Patient is a 63 y.o. male patient of MD with history of CKD stage 3b, HTN, IDDM2 presented to Medical Center with abnormal renal labs. Hospital course complicated by COVID-19 pneumonia and worsening AKI on CKD. AKI on CKD stage 4 with ATN Metabolic acidosis - resolved Anemia of CKD - stable Cr 3.85 on admission (baseline 2.5-2.6), now 4.67 Recently established care with Nephrology, Dr. 7/2023 renal USG w/o obstruction, indicative of medical renal disease IFE, hepatitis, HIV, ANA & complements -ve Nephrology consulted: s/p renal bx 09/21: DM nephropathy, HTN nephrosclerosis, ATN S/P IV lasix prn per Nephro recs - given 9/25, stopped further doses, ok for discharge, IPR denied Plan for to discharge home with HHS likely next am after Eliquis pre-auth complete New onset RUE DVTs USG w/ complete occlusive acute DVT R radial v, partially occlusive acute DVT R ulnar v Was on heparin gtt, transitioned to DOAC 10/03, continue on discharge x3 mon ID preauthorization over the phone yesterday, Eliquis was approved Prescription was sent to his pharmacy, case management to verify coverage HTN urgency : resolved BP 210s/90s on admission Currently well controlled with 5 mg Norvasc and 100 mg Toprol Continue the same, outpatient follow-up with PCP Adjust as needed Elevated troponin 2/2 demand ischemia in assoc w/ AKI on CKD Trop 88>97 EKG w/o acute coronary change Denies chest pain Continue statin, BB Acute hypoxemic respiratory failure - Resolved COVID-19 Suspected CAP CXR B/L airspace opacities R>L edema vs infectious COVID +ve 9/8 BNP 10.6K in renal failure--diuresed w/ Bumex initially 2/2 fluid overload, COVID, and suspected CAP Pulm consulted, treated empirically with Levaquin PRN bronchodilators Initially hypoxic, req up to 4 L NC 09/19, dced IVFs, CXR w/ improvement, duoneb PRN, weaned to RA 09/20 COVID-19 COVID-19 +ve 9/8 Reports vaccination CXR R>L infiltrate 9/8 Finished course of Remdesivir/Decadron T2DM on insulin 8/2023 A1c 7.4% Metformin held, renal decline likely precludes further use at DC Adjusted home insulin dose based on inpatient dosing Close follow-up with PCP, adjust as needed Anemia of ESRD Baseline HGB ~9 Hgb 6.6 on 9/11 - transfused pRBC x 1 Venofer, Epo ordered per renal Hgb 9/30 stable and stopped daily labs Anal fistula F/w CRS, Dr Was scheduled for op intervention 9/7 Not cleared due to AKI Reschedule for later date as OP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 38,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2708164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: TN
Alter: 60,0
Geschlecht: M
Eingang: 01.11.2023
Impfdatum: 05.10.2022
Beginn: 05.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / -

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

Cardio-respiratory arrest Mechanical ventilation Pulse abnormal Pulse absent Pulse waveform abnormal Resuscitation

Symptomtext

RRT called and and patient bagged with 100% O2 changed to code blue with compressions for 15 minutes until patient s pulse returned and patient placed on vent for a few minutes then patients pulse and waveform dictated to continue CPR until NP called the code and CPR stopped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Osteomyelitis of vertebra of sacral region Stage 4 decubitus ulcer of sacral region Protein-calorie malnutrition Type 2 diabetes mellitus Quadriplegia
Vorgeschichte: Quadriplegia due to history of stroke and anterior cord syndrome with contractures Dysphagia with chronic PEG tube History of hypertension Type 2 diabetes mellitus Depression GERD Sacral ulcer History of Klebsiella ESBL UTI Neurogenic bladder
Andere Medikamente: -
Allergien: Ibuprofen iodine adhesive
Vorherige Impfungen: -

VAERS 2684630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 21.09.2023
Impfdatum: 11.11.2022
Beginn: 20.08.2023
Tage bis Beginn: 282,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 Chronic obstructive pulmonary disease Condition aggravated Cough Diarrhoea Dyspnoea Dyspnoea exertional Emphysema Malaise Pain Respiratory tract congestion

Symptomtext

This is a 72-year-old male with past medical history of former tobacco use, COPD, chronic respiratory failure (previously required home oxygen, currently cannot afford), hypertension, hyperlipidemia, PAD s/p aortoiliac stent/graft 2013, depression, prediabetes (A1c 6.0), who presents emergency department with progressive shortness of breath, cough for 1 week. Patient reports his symptom onset was past Sunday, started with chest congestion, increased cough, shortness of breath, worse with exertion, generalized malaise, body aches. Had intermittent diarrhea, denies nausea vomiting. Denies chest pain, lightheadedness, dizziness, bleeding issues, fever. Upon arrival patient was satting between 85 to 87% room air, p Upon arrival patient was satting between 85 to 87% room air, placed on 2 L nasal cannula oxygen with improvement. Received azithromycin, Solu-Medrol, bronchodilators, CTA showed no acute cardiopulmonary disease, did show advanced upper lobe predominant emphysema with 1.7 cm linear density within the right upper lung apex possibly scarring. He is otherwise nontoxic-appearing, CODE STATUS discussed full code. Clinical Summary Patient was admitted with above noted complaints. He was continued on supplemental oxygen as needed. He was started on Zithromax IV, remdesivir which was initiated with loading dose, bronchodilators, and Decadron IV for treatment of COVID-19 and COPD exacerbation. Patient has had significant improvement in symptoms and has remained hemodynamically stable. He has received a total of 4 doses of IV remdesivir and Decadron. He intermittently requires supplemental oxygen at rest therefore 6-minute walk test was completed which showed that oxygen saturation dropped to 87% on room air with activity. Patient will be discharged with oxygen at 2 L via nasal cannula. Patient has no concerns regarding discharge home today. Prescriptions provided for dexamethasone and Zithromax p.o. to complete course. Patient to follow-up with PCP in 3 to 5 days and also strongly encouraged to return to the ER if he develops any new or worsening symptoms. Discharge diagnosis Acute Hypoxic Respiratory Failure Acute COPD Exacerbation Acute COVID-19 Infection Chronic conditions include: Hypertension Hyperlipidemia PVD s/p aortoiliac stent Former tobacco use Prediabetes (A1c 6.0)

Weitere VAERSDATA-Felder

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

VAERS 2684566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 21.09.2023
Impfdatum: 25.10.2022
Beginn: 14.08.2023
Tage bis Beginn: 293,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Asthenia Atelectasis Back pain COVID-19 Cardiomegaly Chest X-ray abnormal Dysstasia Gait disturbance Hypotension Malaise Nausea Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient is a 84 y.o. female patient of MD with history of HTN, CVA, HLD, permanent atrial fibrillation, OSA not on CPAP and vertigo who presented with fevers and weakness after testing positive for COVID on a home test 8/14. Discharge Diagnoses: Covid-19 Virus Infection Acute Respiratory Failure with Hypoxemia Date of onset of symptoms: 8/11/2023 Symptoms present on admission: Weakness, nausea, malaise, body aches and fever Date of covid positive test: 8/14/2023 on home testing Vaccination status: vaccinated x3 Imaging: chest xray with mild cardiomegaly and atelectasis Oxygen requirements on admission: 2 L O2 Current oxygen requirements: 2 L O2 Medical therapy: Decadron 6 mg, Remdesivir. Albuterol PRN with pulmonary toilet. Antitussive as needed. Encourage self proning, use of incentive spirometer Weaned off to room air prior to discharge Will continue Decadron for several more days as outpatient Debility with Impaired Ambulation Normally utilizes Rollator for ambulation, now unable to stand PT/OT, fall risk and delirium precautions Home health care to follow on discharge Permanent Atrial Fibrillation Follows with Dr., continue home Eliquis 5 mg BID Chronic Back Pain NARx with Gabapentin 300 mg TID, will continue HTN Antihypertensives initially held on admission due to low normal blood pressures BP improved and will resume outpatient antihypertensives on discharge HLD Per history, continue home Lipitor 40 mg daily

Weitere VAERSDATA-Felder

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

VAERS 2667667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 88,0
Geschlecht: F
Eingang: 08.08.2023
Impfdatum: 13.10.2022
Beginn: 25.07.2023
Tage bis Beginn: 285,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure COVID-19 Condition aggravated Dyspnoea Exposure to SARS-CoV-2 Hyponatraemia Mental status changes Metabolic encephalopathy Positive airway pressure therapy Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient is a 88 y.o. female patient of, MD with a history of cough Discharge Diagnoses: Covid 19 Acute on chronic hypoxic respiratory failure - baseline 2 L NC Chronic Hyponatremia - baseline around 129 Metabolic encephalopathy - previous history of same; previous admissions with full neurology evaluation HTN COPD Overweight; POA BMI 35 Emphysema Patient presented to Hospital with SOB, AMS. Has known history of encephalopathy and hyponatremia noted on previous admissions. Currently stays at facility and roommate was + for Covid. Patient also noted to be Covid +; has had vaccinations and booster. Initially required Bipap from ED; deescalated to her ba Patient is a 88 y.o. female patient of, MD with a history of cough Discharge Diagnoses: Covid 19 Acute on chronic hypoxic respiratory failure - baseline 2 L NC Chronic Hyponatremia - baseline around 129 Metabolic encephalopathy - previous history of same; previous admissions with full neurology evaluation HTN COPD Overweight; POA BMI 35 Emphysema Patient presented to Hospital with SOB, AMS. Has known history of encephalopathy and hyponatremia noted on previous admissions. Currently stays at facility and roommate was + for Covid. Patient also noted to be Covid +; has had vaccinations and booster. Initially required Bipap from ED; deescalated to her baseline 2 L NC; pulmonary evaluated patient and recommended 10 day course of 6 mg Decadron. Patient will return to facility

Weitere VAERSDATA-Felder

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

VAERS 2663015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 30.07.2023
Impfdatum: 26.11.2022
Beginn: 02.07.2023
Tage bis Beginn: 218,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Asthenia Bladder catheterisation Blood culture negative Blood glucose increased Blood lactic acid normal Blood potassium increased COVID-19 COVID-19 pneumonia Cough Culture urine positive Escherichia test positive Eustachian tube dysfunction Fatigue Hyperglycaemia Hyperkalaemia Klebsiella test positive

Symptomtext

Patient is a 63 year-old female patient of, MD with history of hypothyroidism, and small fiber neuropathy/myelopathy who presented to Hospital on 7/2/23 with fatigue, weakness, and cough. Patient was found to be positive for COVID-19 with additional concerns for superimposed bacterial CAP. CTPA showing peribronchiolar airspace opacities in the right upper and lower lobes consistent with bacterial pneumonia so IV ceftriaxone and azithromycin were started. Patient also started on decadron. Patient required oxygen supplementation and was able to wean down to room air prior to discharge. Patient found to have UTI, symptoms improved with antibiotics. Acute hypoxemic respiratory failure COVID-19 viral pneumonia Suspected community acquired pneumonia Respiratory failure in setting of pneumonia, potentially combination of viral from COVID with bacterial superimposed given imaging findings Imaging: CTPA with peribronchiolar airspace opacities in the right upper and right lower lobes most confluent in the right upper lobe, no PE Medical therapy: IV Rocephin and Azithromycin, decadron. Transition to orals at discharge Urinary antigens negative for strep. pneumo and legionella Continue Mucinex and hycodan for cough Continue claritin for eustachian tube dysfunction Nasal Ocean Spray for congestion Sepsis Febrile and tachycardic on admission with normal lactate, likely due to pneumonia Blood cultures preliminary result showing no growth Continue COVID-19 treatment as above and antibiotics with ceftriaxone/azithromycin UTI - improved Urinary cultures positive for Klebsiella pneumonia and E. coli, likely 2/2 patient intermittent self catheterization, POA Patient already on rocephin therefore not starting new abx at this time, will continue to monitor Hyperglycemia Elevated glucose in the setting of infection and decadron use Improving since starting SSI Continue SSI Hyperkalemia Elevated potassium in the setting of potential dehydration, less likely medication induced Hold IVF in the setting of COVID infection Monitor K+, consider Lokelma if indicated Hypothyroidism Continue home levothyroxine Myelopathy Small fiber neuropathy Follows with neurology, chronically with lower extremity weakness and using walker Continue home pregabalin Underweight Body mass index is 19.22 kg/m?. In the setting of COVID and CAP Encourage PO intake

Weitere VAERSDATA-Felder

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

VAERS 2657375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: AZ
Alter: 90,0
Geschlecht: F
Eingang: 17.07.2023
Impfdatum: 28.10.2022
Beginn: 29.06.2023
Tage bis Beginn: 244,0
Dosis: 4
Route/Site: IM / RA

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

Anion gap Blood culture Blood culture negative COVID-19 Cerebral atrophy Cerebral small vessel ischaemic disease Chest X-ray normal Computerised tomogram head abnormal Computerised tomogram neck Death Electrocardiogram T wave abnormal Electrocardiogram T wave inversion Full blood count normal Haematocrit decreased Haemoglobin decreased Haemorrhagic stroke Laboratory test normal Lacunar infarction

Symptomtext

No adverse reaction to the vaccine itself, but patient presented with COVID & hemorrhagic stroke to the ED on 6/29/23. Patient was transferred the same day to a local Medical Center where she expired on 7/9/23. Tests/labs conducted on 6/29/23: CBC, CMP, urinalysis, blood cultures, head & neck CT, EKG, chest x-ray (unremarkable). EKG: rate 86, sinus, left axis, normal int4rvasl, t wave inversion in lead III, V4, V5, V6, no acute ST elevation. T wave cahgnes in v4-v6 new when compared to 10/12/16 CT head: small acute left thalamic hemorrhage, chronic left thalamic lacunar infarct, age appropriate supratentorial and infratentorial atrophy, moderate chronic white matter microvascular ischemic disease CT neck: 1. No acute extracranial vascular abnormality identified. 2. Nonspecific fluid distension of the midthoracic esophagus (reflux? distal obstruction?) Labs indicate a white count of 6.4, H&H 11.1 and 34 and platelets are 128. Patient has no previous labs within the last year for comparison. Patient also has a CMP with anion gap of 6. Urinalysis without any acute evidence of infection. Patient did have blood cultures obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: see above
Aktuelle Erkrankungen: unknown
Vorgeschichte: none documented in medical record, but provider note on 6/29/23 references hypothyroidism
Andere Medikamente: levothyroxine 25mcg daily
Allergien: none documented in medical record
Vorherige Impfungen: -

VAERS 2656726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

kritisch

Staat: AZ
Alter: 79,0
Geschlecht: M
Eingang: 16.07.2023
Impfdatum: 04.01.2021
Beginn: 05.01.2021
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / AR

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

Chest X-ray Computerised tomogram thorax Death Full blood count Hypertension Prostate cancer Pulmonary hypertension

Symptomtext

Developed prostate cancer, pulmonary hypertention, death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 5,0
Labordaten: Ct thorax Chest xrays Cbc
Aktuelle Erkrankungen: Copd, emphysema, stage 3 kidneyn developed cancer prostate, high blood pressure pulmonary hypertension from vaccine
Vorgeschichte: -
Andere Medikamente: First vaccination pfizer EK5730 01/04/2021 The day after 1st dose became very sick with flu like symptoms. Went to er. At a local HCF. Was told pt. had pneumonia. And because of his copd and emphysema he would need oxygen. Pt. was not on o
Allergien: Lyrica
Vorherige Impfungen: -

VAERS 2655885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 13.07.2023
Impfdatum: 24.10.2022
Beginn: 07.02.2023
Tage bis Beginn: 106,0
Dosis: 5
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2653650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 07.07.2023
Impfdatum: 14.11.2022
Beginn: 22.02.2023
Tage bis Beginn: 100,0
Dosis: 5
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2648885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 26.10.2022
Beginn: 10.11.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Embolic stroke Symptom recurrence

Symptomtext

ACUTE ST ELEVATION MI, ANTERIOR WALL ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/9/2022 -- 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 2645943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 15.06.2023
Impfdatum: 08.10.2022
Beginn: 22.12.2022
Tage bis Beginn: 75,0
Dosis: 5
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 NON ST ELEVATION MI

Weitere VAERSDATA-Felder

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

VAERS 2645336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

kritisch

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 14.06.2023
Impfdatum: 11.10.2022
Beginn: 14.04.2023
Tage bis Beginn: 185,0
Dosis: 5
Route/Site: IM / RA

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

Acute respiratory failure Bronchial hyperreactivity Obstructive sleep apnoea syndrome

Symptomtext

G47.33 ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE 5/1/2023 ACUTE RESPIRATORY FAILURE REACTIVE AIRWAY DISEASE, UNSPECIFIED J96.00 ACUTE RESPIRATORY FAILURE 4/14/2023 ACUTE RESPIRATORY FAILURE REACTIVE AIRWAY DISEASE, UNSPECIFIED J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/14/2023 ACUTE RESPIRATORY FAILURE REACTIVE AIRWAY DISEASE, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2644684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 07.10.2022
Beginn: 06.12.2022
Tage bis Beginn: 60,0
Dosis: 5
Route/Site: IM / LA

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

Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2642978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 08.06.2023
Impfdatum: 12.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Bacteraemia Dysphagia Dyspnoea Melaena

Symptomtext

ACUTE NON ST ELEVATION MI 4/6/2023 DYSPNEA ACUTE NON ST ELEVATION MI 4/6/2023 BACTEREMIA ACUTE NON ST ELEVATION MI 4/6/2023 MELENA ACUTE NON ST ELEVATION MI 4/6/2023 DYSPHAGIA

Weitere VAERSDATA-Felder

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

VAERS 2639680

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 01.06.2023
Impfdatum: 03.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 8,0
Dosis: 5
Route/Site: - / LA

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

Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2632550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: WI
Alter: 90,0
Geschlecht: M
Eingang: 16.05.2023
Impfdatum: 31.10.2022
Beginn: 09.05.2023
Tage bis Beginn: 190,0
Dosis: 5
Route/Site: UN / UN

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

Acute kidney injury Acute respiratory failure Atrial fibrillation Bradycardia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram head normal Confusional state Death Electrocardiogram abnormal Epistaxis General physical health deterioration Heart rate increased Hypoxia Intensive care Lung infiltration Mental status changes

Symptomtext

CLINICAL IMPRESSION: Altered mental status, COVID Hypoxia, Chronic atrial fibrillation, Chronic kidney disease, unspecified CKD stage Came to ED for evaluation of altered mental status. Patient's wife died yesterday morning as well. Heart rate is elevated and variable, hx atrial fibrillation. Scattered rhonchi. Patient in the emergency department last night for epistaxis. Anticoagulated on Eliquis due to history of atrial fibrillation. A nasal packing was placed in the right nostril which remains in place currently. Baseline use of O2- 1 to 2 L. Here he is requiring 3 to 4 L. On oxy mask rather than nasal cannula due to the presence of nasal packing. Patient given dose of dexamethasone due to hypoxia in the presence of COVID. He was also given a dose of diltiazem due to elevated heart rate. ASSESSMENT & PLAN: COVID c/b Hypoxia - Unclear day of symptom onset; PCR+ 5/9 - CXR - diffuse bilateral pulmonary infiltrates (but unchanged from 4/11) - Recently started wearing 2L O2 with activity - up to 5L in ED - wean as able - IV Decadron 10 mg x 3 days, then 6 mg x 7 days - Not a candidate for Remdesivir d/t borderline renal function, unclear onset - Mucinex BID - Isolation precautions Mon May 15 2023 Date of hospital admission: 5/9/2023 Date of death: 5/15/2023 Cause of death Interval 1. Acute hypoxic respiratory failure - 3 days 2. COVID-19 - 1 week Admitted with: Altered Mental Status, COVID-19 pneumonia, metabolic encephalopathy, mild AKI. Hospital Course: Patient on nightly oxygen as he cannot tolerate CPAP. Patient lost his wife just day before admission. Patient started on remdesivir and dexamethasone for COVID-19. Patient is high aspiration risk and speech therapy evaluated on admission. Despite optimal treatment, patient started worsening and oxygenation got worse and he was transferred to ICU on 15 L / 90% Vapotherm. Patient started becoming more confused. Patient was started on high-dose steroids, low-dose Precedex drip. Patient continued to worsen. He removed his own oxygen and was noted to have severe bradycardia. Family was notified and worsening status was related. Patient was transitioned to hospice care on the night of 5/14/2023. Patient expired soon after at 0220 on 5/15 /2023. Family at bedside. 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: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: 5/9/2023: COVID Screen Result: Positive PCR CMP with mild worsening in renal function. XR Chest 1 View Portable: Patchy bilateral infiltrates consistent with known COVID CT Head WO Contrast: No acute intracranial abnormality. EKG: atrial fibrillation with ventricular rate of 109 bpm. No acute ischemic changes noted.
Aktuelle Erkrankungen: unknown
Vorgeschichte: past medical history: mild cognitive impairment, obesity, depression, anemia, BPH, CKD 3, OSA (not on CPAP), HLD, HFpEF, and Afib on Eliquis
Andere Medikamente: unknown
Allergien: ? Lactose ? Bacitracin Rash Ointment ? Cefoxitin Rash ? Iodine Rash
Vorherige Impfungen: -

VAERS 2624865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MO
Alter: 52,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 26.10.2022
Beginn: 29.01.2023
Tage bis Beginn: 95,0
Dosis: 4
Route/Site: SYR / RA

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

Anticoagulant therapy Blood test normal Computerised tomogram normal Dyspnoea Echocardiogram normal Hypertension Oxygen saturation decreased Pulmonary embolism Therapy change Ultrasound Doppler normal X-ray normal

Symptomtext

On 01/29/2023 I went to the hospital at 01:00PM. I had shortness of breath, low blood oxygen level and high blood pressure. They did CT-Scan, blood work and X-RAY. They gave me with blood thinners and oxygen. At 03:00PM they diagnosed me as having Provoked Pulmonary embolism and they transferred me to another hospital. At the new hospital they did Ultrasound (No DVT's found) heart Echo and gave me more blood thinners. They also gave me oxygen. I was there for 3 days and released on 01/31/2023. I had to increase my blood pressure medication and taking blood thinners as of now. I am following up with hematologist, pulmonologist and cardiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 29JAN2023 CT scan test normal; 29JAN2023 Blood work normal; 29JAN2023 X-RAY normal; JAN2023 Ultrasound normal; JAN2023 Heart Echo test normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Depression
Andere Medikamente: Systolic; CYMBALTA; SYNTHROID; trazadone; BUSPAR
Allergien: CEPROTIN drugs
Vorherige Impfungen: -

VAERS 2624046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MO
Alter: 77,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 02.11.2022
Beginn: 21.03.2023
Tage bis Beginn: 139,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Death Respiratory distress SARS-CoV-2 test positive

Symptomtext

Patient admitted to hospital on 3/12/2023 for respiratory distress and tested positive for Covid. He subsequently died in the hospital on 3/21/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, DM type 2, HTN, Alzheimers dementia, Parkinson's Dz
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2621345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: WI
Alter: 86,0
Geschlecht: M
Eingang: 26.04.2023
Impfdatum: 31.10.2022
Beginn: 19.04.2023
Tage bis Beginn: 170,0
Dosis: 4
Route/Site: UN / UN

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

Aspiration Asthenia Blood thyroid stimulating hormone normal Bundle branch block left COVID-19 Chest X-ray normal Computerised tomogram head normal Computerised tomogram neck Death Electrocardiogram ST segment depression Electrocardiogram abnormal Fall Full blood count abnormal General physical health deterioration Productive cough Respiratory distress SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

4/19/2023: Admitted after fall, general weakness. Has activated HCPOA. Wife reported productive cough since the day before. COVID came back positive later on. Treated with Remdesivir 200 mg today 100 mg daily x 4 day. Not hypoxic with normal saturation on room air - dexamethasone deferred. Patient admitted, placed in isolation. 4/22/2023: He was treated empirically with Remdesivir, but deteriorated rapidly. He exhibited aspiration, prompting downgrade of diet to puree with nectar thick liquids. He exhibited episodic respiratory distress. His oxygen requirement increased progressively. Due to his Alzheimer's dementia, he frequently removed medically necessary devices such as supplemental oxygen. On 4/22/23, he was discharged to local facility for comfort cares per family wishes. He died on 4/24/2023. Submitter does not have access to further medical records or information on hospital course. If further information is needed, please contact the admitting hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 5,0
Labordaten: 4/19/2023: SARS-CoV-2 RNA Resp Ql NAA+probe Detected EKG -normal sinus rhythm with LBBB, ST depression in V5 and V6. Patient denies chest pain or shortness of breath on exam - will add a Trop but defer echocardiogram given POA does not want extensive work-up. CBC revealed stable chronic anemia. TSH normal. CXR unremarkable. CT of head negative, CT of neck negative
Aktuelle Erkrankungen: unknown
Vorgeschichte: past medical history significant for Alzheimer's disease, hypertension, hyperlipidemia, type 2 diabetes, and anemia
Andere Medikamente: unknown
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2616034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 17.11.2022
Beginn: 11.04.2023
Tage bis Beginn: 145,0
Dosis: 5
Route/Site: - / -

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

Acute myocardial infarction Brain natriuretic peptide increased COVID-19 Catheterisation cardiac abnormal Chest pain Coronary angioplasty Coronary arterial stent insertion Coronary artery disease Coronary artery occlusion Cough Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Hyperhidrosis Left ventricular dysfunction Left ventricular end-diastolic pressure increased Malaise Pain in extremity

Symptomtext

Heart Cath 4/11/2023, Dr 1. Coronary artery disease as follows: 100% distal right coronary artery culprit lesion, 70% mid LAD, 70-80% distal LAD, 50% mid circumflex artery, 50-60% mid 1st obtuse marginal branch. 2. Successful PTCA stent mid right coronary artery with a 3.55 x 18 mm drug-eluting stent, successful PTCA stent distal right coronary artery/PDA with a 3 mm x 38 mm drug-eluting stent. 3. Mild LV dysfunction with ejection fraction of 45-50% with severe inferior apical hypokinesis. 4. No significant mitral regurgitation. 5. No aortic stenosis. 6. Mildly elevated left ventricular end-diastolic pressure of 20 mmHg. Echo 4/11/2023 1. Left Ventricle: Left ventricle cavity appears normal. Wall thickness is normal. Systolic function is mildly decreased with an ejection fraction of 50 - 55%. Regional wall motion abnormalities present. Inferior wall hypokinesia There is no diastolic dysfunction. Hospital Course: Patient is a 71 year-old Male who presented via EMS due to complaints of crushing chest pain, Left arm pain, and diaphoresis that started at 4/11 at 800 when he was raking the leaves. EKG in field significant for STEMI in inferior posterior aspect. In the ED, Vitals : 97.2F, 56 HR, 18 RR, 121/76, 97% RA, Labs significant for Trope 2120-- >2823, BNP 389 and positive Covid-19 test. Patient admitted to cardiology team with emergent heart-cath. Heart cath performed by Dr showed complete RCA occlusion requiring 2x DES, notable 70% occlusion of mid LAD and 70-80% distal LAD, 50% mid circumflex and 0-60% obtuse marginal artery. Echocardiogram obtained showed EF of 50-55% with regional wall motion abnormalities, inferior wall hypokinesis with history of diastolic dysfunction. Patient was initiated on DAPT: ASA and Prasugrel, Lisinopril, and Metoprolol. Patients COVID symptoms remained stable with no significant symptomatology besides occasional cough. Pts hospital course not complicated and patient was discharged with instructions to follow-up with pcp, Cardiology while obtaining stress test and referral for cardiac rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: Positive COVID PCR 4/11/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2614526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 07.10.2022
Beginn: 22.02.2023
Tage bis Beginn: 138,0
Dosis: 5
Route/Site: IM / UN

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

Computerised tomogram abnormal Deep vein thrombosis Pulmonary embolism Ultrasound Doppler abnormal

Symptomtext

On Feb 22nd I was diagnosed with DBT clout in my right leg, on Feb 26th I was diagnosed pulmonary embolism in your left lung, I am in medication until the end of May and then the doctor will evaluate me. Ultrasound

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 22FEB2023 - Ultrasound - DBT; 26FEB2023 - CAT SCAN - Pulmonary Embolism
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Irbesartan; Zinc; Vitamin D; Vitamin C; D12
Allergien: N/A
Vorherige Impfungen: Flu Vaccine; 2021; Fever, Fatigue

VAERS 2607018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 08.11.2022
Beginn: 17.02.2023
Tage bis Beginn: 101,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Anion gap Arthralgia Blood creatine phosphokinase increased Blood creatinine increased Blood culture negative Blood ketone body COVID-19 COVID-19 pneumonia Cellulitis Computerised tomogram head normal Cough Culture urine negative Diabetic ketoacidosis Fall Hypophagia Injury Lactic acidosis

Symptomtext

Patient is a 68 y.o. female with a history of DM2, CAD, HTN, HFpEF, hyperlipidemia, CKD, chronic pain and OSA who presented to Hospital 2/17/2023 after mechanical fall out of bathtub and unable to get up for 3 days. Found to have DKA, leukocytosis of 20, lactic acidosis, covid positive, mildly elevated CPK at 1.2K. Trauma imaging negative. Hospital course complicated by progressive hypoxia. 1. COVID19 Pneumonia: DOP 2/17/23. Cough and congestion, sore throat. Mild o2 usage in ED. Will do remdesivir for now but cautious with renal function/GFR. Wean o2 as able. Isolation. Dexamethasone started 2/19/23 for worsening O2 sats. Procal 0.48 on 2/19/23. Ceftriaxone and azithro for possible CAP/superinfection x 5 days ending 2/22/23 2. Acute hypoxic respiratory failure: Due to above. High risk for progression as family requestng discharge home with O2 while patient recently titrated to 6lpm. Pulm hygiene ordered. Given COVID infection, patient may require chronic O2 on discharge pending recovery course. Improving and weaned to room air 2/21/23. 3. DKA: DM2 per history with likely DKA from acute stressors. Gap closed and ketones negative for 48 hours but limited by poor oral intake. Insulin transitioned to subcutaneous with steroids. Discharge on lantus 25 bid and lispro 16qac + ssi. May need titrated down with end of steroids and some instructions given. F/u with PCP. 4. Sepsis: Present on admission. COVID with suspected cellulitis and possible UTI will cover with rocephin. Blood cultures 2/17/23 NGTD x2. UCX no growth. 5. Fall with Elevated CPK: Mild with being down for 3 days. Improved with IVF. CT Head, CTL, CTAP negative for acute fractures. Right shoulder pain, XR 2/18/23 showed no fracture but degenerative changes, recommended ortho follow up as patient established for knees. 6. DM2: On metformin at home. Held. Management as above 7. CAD:Hx, statin bb continued. 8. HTN: Home coreg 25 reduced and losartan held. Titrate PRN. 9. HFpEF: Hx echo 9/2021 with ef 59% mild AS. No longer on diuretics at home. IVF completed. 10. Hyperlipidemia: home statin 11. CKD: CKD 3 per notes and suspect baseline creat 1.3-1.5. At baseline on admission. 12. OSA: Does not use cpap at home. 13. Code status: DNR CCA DNI on discussed with with patient with son at bedside.

Weitere VAERSDATA-Felder

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

VAERS 2606805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 14.11.2022
Beginn: 03.02.2023
Tage bis Beginn: 81,0
Dosis: 1
Route/Site: - / -

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

Abdominal pain Abdominal pain upper Acute respiratory failure Adhesiolysis Angiogram pulmonary abnormal Anticoagulant therapy Anticoagulation drug level above therapeutic Atrial fibrillation Blood albumin decreased Blood loss anaemia Blood magnesium normal Blood potassium normal COVID-19 Chest X-ray abnormal Chest pain Computerised tomogram abdomen abnormal Constipation Dyspnoea

Symptomtext

Patient is a 68 y.o. female patient of MD with history of anxiety, atrial fibrillation, cervical cancer, constipation, COPD, depression, fibromyalgia, glaucoma, IBS, lumbosacral disease, nephrolithiasis, osteoporosis, PTSD, peripheral neuropathy, seizure, spinal stenosis presented to the hospital with progressive shortness of breath Abdominal pain SBO-resolved P/w left sided sharp abdominal/flank pain. No CVAT or hematuria, urinary sxs. Suspected constipation however, patient w/ large BM but continued pain KUB: Stomach is distended. Overall nonobstructive bowel gas pattern. Large amount of stool in the right colon. In the left abdomen there is likely some artifactual lucency from superimposed bowel loops rather than abnormal gas within the bowel wall. CT: There is a high-grade partial-to-complete obstruction of the distal small bowel. Gastrograffin challenge: No passage of Gastrografin in the colon. Findings are very suspicious for high-grade small bowel obstruction. S/p exploratory laparotomy, converted to open, lysis of adhesions with Dr. 2/10 Removed NGT (2/12) Advanced to full liquid (2/14) 02/17 CT abdomen persistent postsurgical ileus, no obstruction Advanced to regular diet (2/18) tolerating well and having regulat BM's Atypical Chest Pain-resolved Patient reports LUQ abdominal pain that radiates to her back and into her left chest, worse with inspiration. Left chest TTP when auscultating heart sounds. EKG sinus tachycardia without acute ischemic changes Serial troponin normal CT PA without e/o PE, shows moderately sized layering bilateral pleural effusion partial consolidation of the lower lobes bilaterally (L>R) Suspect largely 2/2 MSK due to frequent retching PRN flexeril Acute on Chronic Hypoxic Respiratory Failure Bilateral Pleural Effusions Patient reports worse DOE than baseline and BLE edema CXR 2/13 with bilateral pleural effusions CT PA shows bilateral pleural effusions, as above Echo with EF 65% normal diastolic fxn. Could be due to low albumin/poor nutritional status and/or as a result of recent covid infection Encourage increased protein intake as able. Limited at this time due to full liquid diet Continue home lasix Strict I/O Sepsis, COVID-19 multifocal pneumonia - Resolved Superimposed Commnity Acquired Pneumonia - Resolved Date of onset of symptoms: Symptoms present on admission: SOB Date of covid positive test: 1/25 Vaccination status: vaccinated x5 Imaging: CTPA 2/3 multifocal pneumonia/pneumonitis in right middle lobe, RLL and left posterior medial base Oxygen requirements on admission: 3L NC (wears 2.5L NC at baseline) Current oxygen requirements: 3L NC Medical therapy: Completed course of remdesivir and Decadron Completed 5 days of ceftriaxone and azithromycin Out of isolation Hypokalemia-resolved K 3.6 (02/20) Normal Mag level Replace and recheck Monitor Acute blood loss anemia Hgb baseline 13-15 stable 10.1 (2/20) Paroxysmal A-fib Supra therapeutic INR - Resolved Currently in NSR Continued home metoprolol and Coumadin. Pharmacy to dose INR 2.9 on admit; s/p 4u plasma and vitK pre-op INR now subtherapeutic at 1.1; pharmacy to dose. No need to bridge peri-operatively Controlled heart rate 80's (02/18) Resume home coumadin, bridge with Lovenox for 3 days Follow up with coumadin clinic Hypothyroidism Continue home levothyroxine. Depression/anxiety Continue home Xanax as needed Severe protein calorie malnutrition BMI 15.34

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 17,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2606010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: WI
Alter: 89,0
Geschlecht: F
Eingang: 29.03.2023
Impfdatum: 31.10.2022
Beginn: 20.01.2023
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: UN / UN

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

Acute respiratory failure Atelectasis COVID-19 COVID-19 pneumonia Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Chronic kidney disease Condition aggravated Dyspnoea Lethargy Lung infiltration Positive airway pressure therapy Pyrexia Respiratory distress SARS-CoV-2 test positive Sepsis

Symptomtext

On 1/20/2023, patient presented to the emergency department via ambulance from the nursing home for evaluation of shortness of breath, increased need for supplemental oxygen use from 2 L to 6 L, fever, and lethargy. She had a recent hospital admission for influenza A. Patient was in respiratory distress in the ED, so she was placed on BiPAP which improved her respiratory status; She was given a COVID-19 NAA test which resulted positive; Her chest x-ray showed cardiomegaly, and atelectasis vs basilar infiltrate. Patient was treated with cefepime, azithromycin and vancomycin given the recent admission and influenza A. She was diagnosed with acute hypoxemic respiratory failure, severe sepsis secondary to possible hospital-acquired pneumonia, COVID-19 pneumonia, mild CHF exacerbation, and chronic kidney disease. Patient was admitted to the hospital for further evaluation and treatment. Submitter does not have access to further medical information on this case including discharge date. If more information is needed, please contact the admitting hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 1/20/2023 - positive COVID-19 NAA test; Chest x-ray showed cardiomegaly, and atelectasis vs basilar infiltrate.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Chronic atrial fibrillation, Coronary artery disease, Diastolic CHF, dual chamber pacemaker, hypertension, Irregular heartbeat, arthritis.
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2591883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6665

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 23.10.2022
Beginn: 26.01.2023
Tage bis Beginn: 95,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Aspiration Barium swallow abnormal COVID-19 pneumonia Cough Death Depression Diabetes mellitus Dysphagia Dyspnoea Feeding tube user Gastrointestinal tube removal General physical health deterioration Hyponatraemia Ileus Intestinal dilatation Lung disorder

Symptomtext

Patient admitted for acute hypoxic respiratory failure, multifocal pneumonia, COVID-pneumonia, aspiration pneumonia. He received treatment for COVID with remdesivir, steroids. During his stay he had worsening of his respiratory status with oxygen demand increased. He was noted to need BiPAP for improvement of oxygen. Due to his aspiration plans were for PEG tube however PEG tube was unable to be placed because of his poor respiratory status. Despite antibiotics, steroids BiPAP, nebs patient continued to deteriorate. Repeat imaging with CTA ruled out PE and confirmed worsening pneumonia. Patient and family eventually decided on DNR CCA and later DNR CC. Patient later passed away at 6:25pm 2/7/23 with family at bedside. RIP. Clinical Summary Assessment and Plan The patient is a 83 y.o. male with history of recently diagnosed dementia prostate cancer hyperlipidemia diabetes diverticulosis DVT status post 6 months of therapy GERD presented to the Hospital with worsening shortness of breath and cough from primary care's office. Acute respiratory failure with hypoxia, worsening Sepsis 2/2 Multifocal pneumonia Probably aspiration pneumonia Covid pneumonia Patient on BiPAP, wean as tolerated Completed remdesivir and dexamethasone Received duo nebs every 4 every 6 as needed ID consulted IV Zosyn Repeat CTA - no PE, worsening Lung disease DC bipap, transition DNRCC COVID PNA Completed remdesevir and decadron DC'd COVID isolation 2/5/23 Ileus- resolved KUB shows mild distention of small bowel large bowel with persistent contrast throughout the colon continue bowel regimen continue tube feeds Dysphagia with aspiration S/p modified barium swallow study No need for PEG tube now Remove NG tube- DNRCC Depression Mirtazapine DM Sliding scale Hyponatremia-resolved Mild, continue to monitor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2586963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MN
Alter: 91,0
Geschlecht: M
Eingang: 24.02.2023
Impfdatum: 07.11.2022
Beginn: 20.02.2023
Tage bis Beginn: 105,0
Dosis: UNK
Route/Site: IM / RA

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

Pulmonary embolism

Symptomtext

Patient was admitted to hospital on 2/20 with a diagosis of pulmonary embolism.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: Epistaxis
Vorgeschichte: MV regurgitation, Thrombocytopenia, anemia, HF with reduced EF: 45%, Chronic diarrhea.
Andere Medikamente: Vitamin D, anti-diarrheals and nasal sprays
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2546881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 27.01.2023
Impfdatum: 28.10.2022
Beginn: 17.12.2022
Tage bis Beginn: 50,0
Dosis: 4
Route/Site: - / -

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

Abdominal distension Abdominal pain Activated partial thromboplastin time normal Acute myocardial infarction Angiogram cerebral normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Condition aggravated Angiogram pulmonary normal Arteriogram carotid normal Arteriospasm coronary Bone disorder Cancer pain Cardiac disorder Catheterisation cardiac normal Chemotherapy Chest pain

Symptomtext

Patient up to date on COVID vaccines who admitted with COVID detected PCR. Provider d/c note: "64 yr old male with a past medical history significant for esophageal adenocarcinoma (s/p esophagectomy/ McKeown procedure on 03/2022) with current chemotherapy, diverticulosis, hyperlipidemia who presented to the hospital for left hand weakness and abdominal pain. CXR with left hemidiaphragm hiatal hernia and pulmonary vascular congestion. Patient placed on NG tube to suction for partial SBO. Tested COVID positive and suspected COVID pneumonia and started on dexamethasone, remdesvir. Repeat CXR on 12/26 with right basilar consolidation and pleural effusion, likely progression of COVID pneumonia vs aspiration pneumonia. Surgery rec transfer where patient had original surgery performed. Neurology consulted for left weakness, recommended oupatient follow-up and evaluation. Currently, stable for transfer. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 9,0
Labordaten: Covid PCR Detected 12/24/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Mixed hyperlipidemia Digestive Diverticulosis Erosive gastropathy Duodenal erosion Nodule of esophagus Malignant neoplasm of esophagus (HCC) Diarrhea of presumed infectious origin Esophageal adenocarcinoma (HCC) Drug-induced constipation Chemotherapy induced nausea and vomiting Small bowel obstruction (HCC) Hernia of small intestine Psychological Adjustment disorder with mixed anxiety and depressed mood Mood insomnia (HCC) Respiratory Dyspnea Difficulty breathing Acute respiratory failure with hypoxia (HCC) Urinary Urinary retention Overactive bladder Other Strain of musc/tend the rotator cuff of right shoulder, init Elevated blood-pressure reading without diagnosis of hypertension Family history of GI tract cancer Status post12/1/2020 right C4-5 and C6-7 foraminotomies Esophageal mass Pain Encounter for antineoplastic chemotherapy Fitting and adjustment of vascular catheter Dehydration Weight loss Nausea Chemotherapy-induced thrombocytopenia Leukopenia due to antineoplastic chemotherapy (HCC) Anemia due to antineoplastic chemotherapy Mediastinal adenopathy Nicotine dependence Anemia associated with chemotherapy Hiatal hernia Opiate analgesic use agreement exists COVID-19 Benign prostatic hyperplasia Anxiety Compression of left radial nerve
Andere Medikamente: albuterol sulfate (ProAir HFA) 90 mcg/actuation inhaler Inhale 2 puffs into the lungs every 4 (four) hours as needed for Wheezing or Cough. bisacodyL (DULCOLAX) 10 mg suppository Insert 1 suppository into the rectum daily as needed for cons
Allergien: Sulfa (Sulfonamide Antibiotics)Rash
Vorherige Impfungen: -

VAERS 2567856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: SC
Alter: 77,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 25.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 68,0
Dosis: 5
Route/Site: SYR / RA

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

Anticoagulant therapy Cardiac disorder Coronary arterial stent insertion Dizziness Fear General physical health deterioration Hypertension Myocardial infarction

Symptomtext

Since starting the COVID-19 vaccine in January 2021, I started having heart issues. I have a heart attack in May of 2022.It was mild, but I wasn't thinking much. I got a stint in place and been under cardiac care and they changed my blood pressure. I have been taking medicines for 6 or 7 months. Lately I have been declining in my health. I recently checked my blood pressure, and it was high, but I felt fine. This morning it was extremely high 189/185. I was scared and went on about my morning. I took my meds blood pressure and blood thinner. I have had another change in my health, a constant state of dizziness and this erratic blood pressure. This all very strange.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension, Gastrointestinal Reflux Disorder; Bullous Pemphigoid
Andere Medikamente: Primidone; Prednisone; Amlodipine; Omeprazole; Bicalutamide; Timolol
Allergien: Hydrochlorothiazide, Erythromycin
Vorherige Impfungen: -

VAERS 2561890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

kritisch

Staat: MO
Alter: 82,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 10.10.2022
Beginn: 24.11.2022
Tage bis Beginn: 45,0
Dosis: UNK
Route/Site: - / -

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

Cerebrovascular accident Laboratory test

Symptomtext

Stroke; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An 82-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Oct2022 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 82 years for COVID-19 immunization. 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: CEREBROVASCULAR ACCIDENT (hospitalization) with onset 24Nov2022, outcome "unknown", described as "Stroke". The patient was hospitalized for cerebrovascular accident (start date: 24Nov2022, discharge date: 27Nov2022, hospitalization duration: 4 day(s)). The patient underwent the following laboratory tests and procedures: Lab work: unknown result, notes: Lab work: Reporter stated, "Many (Further name and results of lab tests were not clarified over the call). Therapeutic measures were taken as a result of cerebrovascular accident. Clinical course: Reporter stated, he want to report an adverse reaction or he was not sure it is but he was reading on the CDC website and it said the new variant can cause Stroke.Then probed for the adverse event: Reporter stated, A stroke. And he was the one that had the stroke. Medical conditions and Concomitant medications Reporter stated, nothing, he has no health issues. Reporter stated, "Many (Further name and results of lab tests were not clarified over the call hence tab left unchecked). He was hospitalized. This event happened on 24Nov2022. Not today it happened. Treatment: Reporter stated, Nothing, you mean like TPA? He had no, no any sort of that kind of treatment. He is now taking a Baby Aspirin." Discharge date: Reporter stated, "Whatever, 4 days later. He was there 4 days, discharged on 27Nov2022 (27Nov2022) in the evening."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Test Name: Lab work; Result Unstructured Data: Test Result:unknown result; Comments: Lab work: Reporter stated, "Many (Further name and results of lab tests were not clarified over the call)
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 2560815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: LA
Alter: 35,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 30.11.2022
Beginn: 09.12.2022
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: IM / RA

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

Deep vein thrombosis Dyspnoea Pain in extremity Pulmonary embolism Right ventricular dysfunction

Symptomtext

12/09/2022: Pain to right lower leg, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: 12/10/2022 Right Leg DVT Extensive acute bilateral pulmonary embolism with evidence of right heart strain
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2559462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: NC
Alter: 82,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 04.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 8,0
Dosis: 5
Route/Site: IM / LA

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

Computerised tomogram thorax abnormal Pulmonary embolism

Symptomtext

Pulmonary Embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT scan confirmed PE 8 days after shot
Aktuelle Erkrankungen: none
Vorgeschichte: CAD HTN
Andere Medikamente: aspirin vitamin D losartan hctz ezetimibe hctz metoprolol omeprazole
Allergien: niacin toradol
Vorherige Impfungen: -

VAERS 2557594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 07.11.2022
Beginn: 02.01.2023
Tage bis Beginn: 56,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Brain natriuretic peptide normal COVID-19 Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Dyspnoea exertional Hypoxia Laboratory test normal Lung opacity Pulmonary fibrosis Tachypnoea White blood cell count increased

Symptomtext

DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute on chronic respiratory failure with hypoxia [J96.21] Chronic obstructive pulmonary disease, unspecified COPD type [J44.9] COVID [U07.1] COVID-19 [U07.1] HOSPITAL COURSE: HOSPITAL COURSE: Patient is a 70 y/o male with history of COPD, ILD and amiodarone toxicity, chronic oxygen use, DM, HTN and PAF. He presented to the ER on 1/2/2023 with increased dyspnea on exertion and hypoxia with exertion. He is on 3L NC at baseline and on arrival to the ER was requiring up to 6L NC. He tested positive for COVID at home on 12/24 and completed a course of Paxlovid outpatient on 1/1. In the ER he had CT that showed no PE, mild diffuse ground glass opacities superimposed upon pulmonary fibrosis which could be related to atypical pneumonia. He had slightly elevated WBC and normal BNP. His other labs were fairly unremarkable. He was admitted to the hospitalist team due to his increased oxygen needs. He was started on decadron in the ER. After admission his pulmonologist was contacted who recommended treatment with solumedrol 1mg/kg while hospitalized and transition to prednisone 60 mg daily at discharge. The patient's oxygen needs returned to baseline quickly. He has close follow up with pulmonology next week. He will be discharged home on daily prednisone 60 mg with a slow taper until he can follow up with his pulmonologist. He was also encouraged to follow up with his PCP after discharge. The patient verbalized understanding of these instructions and discharged home in stable condition. CONSULTANTS: Care management Pulmonology INPATIENT PROCEDURES: None BP 117/63 | Pulse 78 | Temp 36.5 ?C (Oral) | Resp 18 | Ht 1.702 m | Wt 125.1 kg | SpO2 90% | BMI 43.20 kg/m? Physical Exam Constitutional: General: He is not in acute distress. Appearance: He is obese. He is not diaphoretic. HENT: Head: Normocephalic and atraumatic. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Normal pulses. Heart sounds: Normal heart sounds. Pulmonary: Breath sounds: Normal breath sounds. Comments: Mild tachypnea after walking around Abdominal: Tenderness: There is no abdominal tenderness. Musculoskeletal: Right lower leg: No edema. Left lower leg: No edema. Skin: General: Skin is warm and dry. Neurological: Mental Status: He is alert and oriented to person, place, and time. Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory OSA on CPAP Restrictive lung disease secondary to obesity Lung nodules Moderate COPD (chronic obstructive pulmonary disease) Decreased diffusion capacity of lung Amiodarone pulmonary toxicity Multifocal bilateral airspace disease ILD (interstitial lung disease) Dyspnea on exertion Circulatory Essential hypertension Persistent atrial fibrillation Typical atrial flutter Mediastinal adenopathy Digestive Esophageal reflux Class 3 severe obesity in adult Nervous Cigarette nicotine dependence in remission Endocrine/Metabolic Hyperlipidemia Type 2 diabetes mellitus, with long-term current use of insulin Other Supraclavicular fossa fullness
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG TABS calcium-vitamin D (CALCIUM 600+D) 600-200 MG-UNIT TABS per tablet Coenzyme Q10 (COQ10)
Allergien: Hydrocodone Seasonal allergies, unspecified
Vorherige Impfungen: -

VAERS 2555134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 27.10.2022
Beginn: 09.12.2022
Tage bis Beginn: 43,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy Atelectasis Blood pressure abnormal Blood thyroid stimulating hormone normal COVID-19 Chest X-ray abnormal Chest pain Computerised tomogram head normal Computerised tomogram spine Dyspnoea Electrocardiogram normal Fall Gastric ulcer Haematochezia Haematocrit Haemoglobin decreased Hypotension

Symptomtext

Patient is a 85 y.o. male with history of MGUS, Peripheral Neuropathy, Glaucoma, CAD with DES to LAD and Cx in 2009, Ischemic Cardiomyopathy, Paroxysmal Afib on sotalol and xarelto, PVCs, HTN, HLD, Pacemaker in situ, Hypothyroidism presented to the Medical Center with Rectal Bleeding. Hospitalization was complicated by acute respiratory failure 2/2 HCAP/COVID. Acute hypoxic respiratory failure Likely Healthcare Associated Pneumonia Covid-19 Virus Infection Date of onset of symptoms: 12/13/22 Symptoms present: congestion, SOB, hypoxia Date of covid positive test: 12/13/22 Vaccination status: vaccinated Imaging: CXR - bilateral airspace opacities concerning for infection Oxygen requirements on admission: RA Current oxygen requirements: 2L Medical therapy: steroids, Cefepime, remdesivir Consultants following: None Anticipated special isolation end date: 12/23/22 MRSA probe negative Pt. Fortunately passed his home O2 eval does not qualify for oxygen Change Cefepime to Levaquin for 2 more days to complete abx discharge with Decadron to complete 10d total therapy Acute Upper GI Bleed Presented w/ large bloody BM and an episode of Tarry BM Enhanced by Xarelto Hgb 9.3 on admit (Hgb 14 a month ago) S/p K-centra at OSH GI follows. EGD with non bleeding gastric ulcers and clotted blood in cardia and fundus. Per GI, PPI BID for 2 months, repeat EGD in 2 months. Check H. Pylori stool antigen test and treat if positive. HGB 8.7,stable for 48 hrs therefore restarted home xarelto 12/12/22 (Discussed with GI) H/h stable Restarted ASA as hgb has been stable Syncope Could be related to Vasovagal and GI bleed and hypotension Check Orthostats when able BP already improving Monitor on Tele Paroxysmal Afib Home Regimen: Sotalol and Xarelto Continuee Sotalol and Xarelto Fall In setting of syncope CXR with bibasilar atelectasis CT head non acute CT C-spine: Non acute but with multilevel spondylosis CT T/L Spine: non acute but with degen changes w/o significant stenosis team assessed and signed off PT/OT re consulted and has no needs Hypothyroidism TSH 2.81 Continue synthroid HTN Initially held home BP meds due to hypotension Now hypotension resolved, resume home sotalol If BP continued to trend up, will restart home lisinopril BP controlled without lisinopril Resume Norvasc on discharge Hx of CAD s/p DES Holding ASA given above Iresume ASA on discharge as Hgb has been stable Check H&H o/p Chest Pain Troponin on admit neg x 2 EKG on admit w/o signs of acute ischemia Vague episode 12/10 night and EKG w/o signs of ischemia Monitor on Tele, follow up with Cardio o/p

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2550245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MO
Alter: 64,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 30.09.2022
Beginn: 18.11.2022
Tage bis Beginn: 49,0
Dosis: 5
Route/Site: IM / LA

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

Angiogram abnormal Asthenia COVID-19 Cerebral infarction Cerebrovascular accident Computerised tomogram Pyrexia SARS-CoV-2 test positive

Symptomtext

I had 2 episodes where I got really weak, and I went in to be seen in the ER. I advised them that I was weak and they did a CAT scan. I got a fever of 100.4 and I was admitted on November 18, 2022. They did a COVID-19 PCR, and it came back positive Sunday Morning I was given 3 days of remdesivir. I started Occupational and Physical therapy on November 19, 2022. I residual weakness. I remained in the hospital for 1 week and acute rehab for 1 week. I am still in physical rehab. I covered from the COVID-19 but not from the stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: COVID-19 PCR November 19, 2022 positive, Cat scan 18, 2022 residue of Hemorrhage but nothing else. MRI, a small stroke was detected, left frontal infarct December 19, 2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Parkinson's; Subarachnoid Hemorrhage in April 2022
Andere Medikamente: Multivitamin; SYNTHROID; SINEMET; midodrine; vitamin D3; TYLENOL
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2528536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: OR
Alter: 55,0
Geschlecht: F
Eingang: 11.12.2022
Impfdatum: 13.10.2022
Beginn: 16.11.2022
Tage bis Beginn: 34,0
Dosis: UNK
Route/Site: IM / -

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

Angiogram Blood test Chest pain Computerised tomogram Confusional state Depressed level of consciousness Electrocardiogram Myocardial infarction Myocarditis

Symptomtext

Chest pain 1 month later , unsure of onset because I was so depressed I was confusing physical symptoms as being mental

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 6,0
Labordaten: Angiography, EKG, CT scan, blood work, transferred to cardiology department. Myocarditis inflammation caused heart attack. Hospitalized for a week - no blockages to explain what happened.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, depression
Andere Medikamente: Lisinopril 10mg 2x day Buproprion 300- 450mg daily Eliquis 5mg 2x day
Allergien: None
Vorherige Impfungen: -

VAERS 2526153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: CA
Alter: 52,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 31.10.2022
Beginn: 02.12.2022
Tage bis Beginn: 32,0
Dosis: 5
Route/Site: IM / LA

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

Cerebral haemorrhage Computerised tomogram Magnetic resonance imaging head abnormal Peroneal nerve palsy

Symptomtext

On Friday my foot started dragging in the morning. I went to work, and it wasn't getting better. I went to the ER and they thought it was too severe to be a stroke. They did a CAT scan, and it was all clear, then they did MRI and found bleeding in the brain. I was put in the hospital a couple days later and I am in a acute care program now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 3,0
Labordaten: CAT scan, clear, 12/02/2022; MRI, bleeding in brain, 12/02/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Stoke 7 years ago; Type 2 Diabetic; Hypertension
Andere Medikamente: Nasal spray; eye drops; aspirin; VENTOLIN; BASAGLAR; HUMALOG; losartan; atorvastatin; gabapentin
Allergien: Penicillin; CELEXA
Vorherige Impfungen: -

VAERS 2521901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 02.12.2022
Impfdatum: 12.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / RA

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

Aphasia Burning sensation COVID-19 Cerebrovascular accident Computerised tomogram head abnormal Culture urine positive Cystitis Dehydration Disease susceptibility Dysuria Echocardiogram normal Escherichia test positive Hypotension Lethargy Magnetic resonance imaging head normal SARS-CoV-2 test positive Speech disorder Syncope

Symptomtext

COVID+ 11/28/22. Vaccination status - Pfizer x3 + Pfizer bivalent BRIEF OVERVIEW: Discharge Provider: Primary Care Provider: MD Admission Date: 11/28/2022 Discharge Date: Nov 30, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Aphasia [R47.01] Expressive aphasia [R47.01] Acute cystitis without hematuria [N30.00] COVID-19 [U07.1] HOSPITAL COURSE: 84 y.o. male presented from rehab after episode of lethargy, speech and visual distubrance during second therapy session of day.Found to be hypotensive with systolic pressures in the 60s. Neurologic status returned back to baseline by time he was seen in ED. Initially concern for TIA vs stoke. Neurology consulted. CTH revealed no acute intracranial abnormality with mild chronic microvascular ischemic changes. MRI brain unremarkable. Incidentally COVID positive. UA positive and urince culture grew E.coli, pan-susceptible. Patient endorsed burning with urination and was started on 7 day course of antibiotics for UTI treatment (ceftriaxone inpatient with transition to cefuroxime on discharge). On further evaluation initial presenting episode thought to be vasovagal syncope secondary to hypotension. Unclear etiology of hypotension but likely setting of dehydration, therapy, COVID infection and UTI. Patient without any recurrence of symptoms and normotensive throughout admission. Orthostatic vitals negative. Recent echo 08/2022 reviewed without any systolic or diastolic dysfunction, no aortic valve stenosis. PT/OT/PMR evaluated patient and recommended IPR. Patient medically stable for discharge to IPR 11/30. Pt currently active inpatient at inpt rehab 11/30/22-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Inpt 10/29/22-11/12/2022 at hospital for thoracic compression fracture
Vorgeschichte: Right leg weakness 10/31/2022 Unknown ? Left leg weakness 10/29/2022 Unknown ? Hydronephrosis of right kidney 03/22/2022 Unknown ? Impaired functional mobility and activity tolerance 03/22/2022 Unknown ? Prediabetes 02/21/2022 Unknown ? Back pain 01/26/2022 Unknown ? Pelvic fracture 06/22/2021 Unknown ? Dermatochalasis of both upper eyelids 05/22/2019 Unknown ? Elevated hemidiaphragm 01/22/2019 Unknown ? Preoperative cardiovascular examination 10/05/2015 Unknown ? Primary open angle glaucoma of both eyes, moderate stage 09/08/2015 Unknown ? Myopia of both eyes 09/08/2015 Unknown ? Senile nuclear cataract, bilateral 01/06/2015 Unknown ? Posterior vitreous detachment, bilateral 01/06/2015 Unknown ? Positional lightheadedness 02/25/2014 Unknown ? History of colonoscopy 02/14/2013 Unknown ? Muscle pain Unknown ? Mixed hyperlipidemia
Andere Medikamente: Acetaminophen 500-1,000 mg Oral Every 8 hours PRN / 500-1,000 mg Oral Every 6 hours PRN, Do not exceed 4000mg of Tylenol in 24 hours. If you are taking Norco it also has tylenol so adjust your Tylenol dose as needed. As you wean off of No
Allergien: ibuprofen
Vorherige Impfungen: -

VAERS 2515734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: WA
Alter: 80,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 09.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Cancer pain Condition aggravated Encephalopathy Hypoxia Lung neoplasm malignant Metastasis SARS-CoV-2 test positive

Symptomtext

Patient received Moderna COVID vaccine on 2/14/21 (lot #031L20A), 3/14/21 (lot #003A21A), 10/30/21 (lot #006D21A), and Pfizer bivalent COVID vaccine on 11/9/22. On 11/19/22, patient admitted to our inpatient facility (med/surgical unit) with pneumonia due to COVID-19 virus with acute hypoxemic respiratory failure due to COVID-pneumonia, acute encephalopathy secondary to hypoxia and pneumonia, and malignant neoplasm of lung with metastasis, with cancer associated pain. As of today (11/23/22), patient is still admitted in the med/surgical unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: COVID status positive 11/19/22.
Aktuelle Erkrankungen: -
Vorgeschichte: rehab facility resident who was recently hospitalized for pathological fracture of left femur and underwent ORIF on 11/2/2022 with metastatic lung cancer and cancer associated pain (chronic narcotic use), decubitus sacral area, BPH, and history of tobacco abuse
Andere Medikamente: acetaminophen, albuterol inh, atorvastatin, bisacodyl supp, calcium carbonate, vitamin d3, cyclobenzaprine, diphenhydramine, fish oil, dronabinol, lactulose, melatonin, morphine er, mvi w/minerals, ondansetron, oxycodone, prochlorperazine,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2511928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 11.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Death

Symptomtext

Patient expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, Nutritional deficiency, Hyperlipidemia, Hypertension, Alzheimer's Disease, Malaise, Osteoarthritis, Major depressive disorder, Dysphagia,
Andere Medikamente: Celebrex, Levothyroxine, Sertraline, Tylenol ES, Hydrocortisone Solutions 1%, Polyethylene glycol, Ensure Clear
Allergien: NKA
Vorherige Impfungen: -

VAERS 2503975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: CA
Alter: 36,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 26.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

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

Acute myocardial infarction Antiplatelet therapy Arterial occlusive disease Catheterisation cardiac abnormal Chest pain Coagulation test normal Coronary arterial stent insertion Coronary artery occlusion Coronary artery thrombosis Echocardiogram Electrocardiogram ST segment elevation Embolism Pain Pain in extremity Thrombectomy

Symptomtext

11/1/22 had STEMI thought to be due to embolic thrombi requiring aspiration thrombectomy. 11/2 /22 had another STEMI due to embolic thrombi requiring aspiration thrombectomy. Patient is a 36-year-old man with history of hypertension and possible MI (age 21, self-reported) who presented with acute onset substernal chest pain radiating to both arms and was found to have STEMI with 100% occlusions with thrombi (no underlying plaque) of both LAD and RCA now s/p aspiration and thrombectomy of both arteries on 11/1 c/b persistent ST elevation, then found to have 100% occluded posterolateral branch artery in the setting of heavy thrombus burden s/p second aspiration thrombectomy and stent placement on 11/2. He was then started on DAPT and apixaban, with plan for triple therapy (DAPT/apixaban) for a month (stop aspirin 12/1/22) followed by dual therapy (P2y12/DOAC) for at least 1 year. Hypercoagulable workup was unrevealing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 8,0
Labordaten: Left heart catheterization 11/1/22, 11/2/22 Transesophageal echocardiogram Transthoracic echocardiogram
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2494795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: ME
Alter: 64,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 07.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 22,0
Dosis: 5
Route/Site: IM / LA

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

Abscess drainage Anion gap Atelectasis Back pain Blood chloride decreased Blood creatinine increased Blood glucose decreased Blood lactic acid increased Blood potassium increased Blood pressure decreased Blood sodium normal Blood urea increased Carbon dioxide decreased Cervical cord compression Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Culture wound positive Death

Symptomtext

Presented with subacute back pain and difficulty walking, fatigue, malaise. Found to have epidural abscess and septic shock. Underwent surgical decompression/evacuation of abscess. Despite proper antibiotics and source control, septic shock worsened. She received levophed, vasopressin, phenylephrine, epinephrine, hydrocortisone, and angiotensin II. Despite this aggressive care, lactate continued to rise and blood pressure continued to fall. Patient died on 10/31/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: MRi brain, cervical spine,thoracic spine 10/30/22: cervical epidural abscess with cord compression CT chest/abd/pelvis 10/29/22 . Noncalcified subsolid nodular opacities throughout the bilateral upper lung fields may be infectious or neoplastic. The largest of these are in the lateral segment right middle lobe and measure 7 and 8 mm respectively. Recommend follow-up per Fleischner society criteria as given below. 2. Patchy bilateral airspace disease is likely atelectatic. 3. Mild interlobular septal thickening with lower zonal predilection represents interstitial pulmonary edema. 4. Chronic well-healed fracture of the manubrium. 5. Moderate to severe multilevel spondylosis and degenerative facet arthropathy throughout with disc height loss most pronounced at L1-2, L2-3, L3-4, and L5-S1. Lactate 28 WBc 15.5 Hb 7.7 Hct 25.8 PLT 40 Na 144 K 5.8 Cl 94 CO2 <7 Anion gap 43 glcose 74 BUN 65 Cr 3.61 wound culture: staphylococci
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: atorvastatin duloxetine
Allergien: penicillin tdap
Vorherige Impfungen: -

VAERS 2494118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: OR
Alter: 86,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 17.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Death

Symptomtext

Pt passed away the following morning

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Diastolic heart failure, chronic kidney disease, a-fib, peripheral venous insufficiency, pulmonary hypertension
Vorgeschichte: Diastolic heart failure, chronic kidney disease, a-fib, peripheral venous insufficiency, pulmonary hypertension
Andere Medikamente: Atorvastatin 20 mg, B12 1,000 mcg, Eliquis 5 mg, iron 325 mg, folic acid 1 mg, melatonin 5 mg, metoprolol succinate ER 100 mg, pantoprazole 40 mg, potassium chloride ER 10 mEq, torsemide 10 mg, trazodone 50 mg, b12 100 mg
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2489819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ 6665

kritisch

Staat: AR
Alter: 64,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 13.10.2022
Beginn: 16.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / RA

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

Angiogram Balance disorder Cerebrovascular accident Hemiparesis Mobility decreased Pain Vertebral artery occlusion

Symptomtext

Occlusion of right vertebral artery, stroke. Symptoms began the morning of October 16, went to hospital via ambulance, discharged to home on the 18th, though medical team wanted in patient rehab. Now homebound with severely compromised mobility, right sided weakness, pain , balance issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: Angiogram 10/16/22
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, asthma, depression
Andere Medikamente: Atenolol 25mg daily, esomeprazole 20mg daily, lisinopril 10mg daily, sertraline 25mg daily
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2486548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

kritisch

Staat: FL
Alter: 84,0
Geschlecht: F
Eingang: 23.10.2022
Impfdatum: 17.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Cerebrovascular accident

Symptomtext

Systemic: Stroke-Severe

Weitere VAERSDATA-Felder

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

VAERS 2481895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: PA
Alter: 83,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 07.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Anticoagulant therapy Chest pain Computerised tomogram Fatigue Laboratory test normal Pulmonary embolism

Symptomtext

On the morning of 10/10/2022, patient developed extreme fatigue. By early afternoon, she was in extreme pain in her upper right chest area. The PCP recommended going to the nearest emergency room. We arrived there shortly after 3:00. Around 6:00 she received tests to determine the source of the pain, including a CAT Scan and a test for DVT. DVT was not found, but a pulmonary embolism was found in the right lung. She was started on heparin and admitted. She was released Wednesday, October 12. She is home and has improved, and is now on Eliquis 5 mg 2 times daily and 1,000 mg Tylenol daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Heart disease; bypass surgery in 2007 Reduced kidney function High blood pressure Vertebral disc degeneration
Andere Medikamente: Aspirin (81 mg daily) B complex vitamin Lisinopril (30 mg daily) Multivitamin Osteo Biflex Pravastatin (40 mg daily) Ubiquinal (100 mg daily) Vitamin D3 (1,000 i.u. daily)
Allergien: Strawberries and other seeded berries; nausea Allopurinol (itching) Dilaudid (itching) Fentanyl (itching) Metoprolol Tartrate Pencillin G Propantheline Statin HMG COA reductase inhibitors Tramadol Vicodin Zoloft
Vorherige Impfungen: -

VAERS 2479750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj6665

kritisch

Staat: WA
Alter: 77,0
Geschlecht: M
Eingang: 16.10.2022
Impfdatum: 12.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

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

VAERS 2478836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: NY
Alter: 63,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 04.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / RA

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

Cardio-respiratory arrest Chest tube insertion Death Dialysis Mechanical ventilation

Symptomtext

Resident coded at / during Dialysis Treatment. Was transferred to MEDICAL CENTER and placed on a Ventilator with chest tubes per family. Resident was then transfered to Hospital on 10/6/22. Resident passed away on 10/10/22 at the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 4,0
Labordaten: Hospital
Aktuelle Erkrankungen: 9/8/22 Left arm Fistulagram w/ balloon angioplasty,
Vorgeschichte: ESRD, Idiopathic Urticaria, Hx Thromobosis fo Fistula, Pacreatitis, Atherosclerosis, IDDM, Pityriasis versicolor, CHF, Constipation, GERD, Hypothyroidism, Diverticulitis, Hx pneumonia, Nephrotic Syndrome
Andere Medikamente: Atorvastatin, Calcium Acetate cap 667, Creon DR, Hydralazine, Insulin, Latanoprost soln, Levocetirizine Dihydrochloride, Melatonin PRN, Metoclopramide, Midodrine, MiraLax, MVI, Oxycodone prn, Pepcid, ProAir Inhaler PRN, Ranolazine ER, Synth
Allergien: Lisinopril, Flexeril
Vorherige Impfungen: Res stated that he was not able to take the INFLUENZA Vaccine

VAERS 2473706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: MA
Alter: 90,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 05.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: IM / LA

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

Death

Symptomtext

Resident expired on 10/09/2022 No s/s leading up to it No adverse effects after vaccine administration

Weitere VAERSDATA-Felder

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

VAERS 2470896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

kritisch

Staat: NJ
Alter: 87,0
Geschlecht: M
Eingang: 06.10.2022
Impfdatum: 04.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Cerebrovascular accident

Symptomtext

No symptoms after vaccine administration on 10/4. Resident monitored as is normal practice, no symptoms noted on 10/5. On 10/6 at approximately 11:50am, resident experienced a cerebral vascular accident and was transferred and admitted to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Alzheimer's, hypertension, malignant neoplasm of prostate, anxiety disorder, discovery of specified B group vitamins, decreased mobility
Vorgeschichte: Alzheimer's, hypertension, malignant neoplasm of prostate, anxiety disorder, discovery of specified B group vitamins, decreased mobility
Andere Medikamente: amiodipine, aspirin, B-12, diclofernac, escital opram, losartan, meloxican, centrum, quetiapine, tolterodine, cimetidin, memantine, atorvastatin, ibuprofen, miraxlax
Allergien: Aricept
Vorherige Impfungen: -

VAERS 2724653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: ME
Alter: 17,0
Geschlecht: F
Eingang: 15.12.2023
Impfdatum: 07.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: IM / LA

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

Abnormal behaviour Abnormal sensation in eye Blood thyroid stimulating hormone increased Borrelia test negative C-reactive protein normal Compulsive handwashing Discomfort Dizziness Fatigue Fear Feeling abnormal Full blood count normal Gait disturbance Headache Impaired healing Incontinence Laboratory test normal Limb injury

Symptomtext

Swelling in hands ? November 2022 through January 2023 ? Altered feelings and discomfort with items at home ? started subtly in November 2022, progressed slowly until later in February and into beginning of March, then became intense ? Bilateral sciatica pain ? January 2023-beginning subtly in upper left gluteal area, spreading down left leg into foot and then right side, with spreading down right leg into foot by early March ? Open wound behind left knee ? February 2023- did not heal until early April ? Fainted March 2023 ? In late February and through March, Pt also began having focal seizures with her pupils dilated during the episodes. She believed she was in another location and called out to her parents without realizing we were with her. The episodes usually lasted about a minute. ? Swollen feet with pitting edema ? late March 2023 ? Lymphadenopathy- early March 2023 ? Bilateral peripheral neuropathy ? late March 2023 to present day ? Motor tremors in both hands and legs/feet ? March-May 2023 ? Persistent headache ? March 2023 Incontinence ? late March 2023 ? Feeling of coldness behind left eye ? April 2023 Dizziness ? February 2023 to current day Fatigue ? July 2023 to current day ? Obsessive compulsive disorder (fear of contamination from school of items at home, compulsive and ritualistic hand washing and showering, inability to walk in certain areas of home or touch certain objects) ? January 2023 to current day. Condition has improved after 3 month stay in residential mental health facility, but condition still exists and patient continues outpatient therapy for OCD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: 14,0
Labordaten: March 30, 2023 ? April 5, 2023 MRI of brain showed no tumors, MRI of spine and ultrasound of legs were normal. Blood tests for CBC, CMP, CRP, Lyme, anaplasma, sed rate, autoimmune dysautonomia panel were negative. TSH was elevated and free T4 was normal. August 2023 TSH normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Cetirizine, multi-vitamin , calcium supplement, epi-pen prn
Allergien: Severe allergies to furred animals, dogs in particular. Secondary allergy to amoxicillin.
Vorherige Impfungen: Covid vaccines 6/2/21 and 6/23/21 reported 12/14/23 E-Report Number: 1008111 and 1008116

VAERS 2712001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 09.11.2023
Impfdatum: 21.10.2022
Beginn: 02.08.2023
Tage bis Beginn: 285,0
Dosis: 4
Route/Site: - / -

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

Arteriogram carotid abnormal Asthenia Blood sodium decreased COVID-19 Cardiac telemetry Carotid artery stenosis Computerised tomogram head normal Condition aggravated Echocardiogram abnormal Ejection fraction Ejection fraction normal Electroencephalogram normal Fall Hypertension Hyponatraemia Loss of consciousness Magnetic resonance imaging head normal Magnetic resonance imaging spinal abnormal

Symptomtext

BRIEF OVERVIEW: Admission Date: 8/2/2023 Discharge Date: 8/4/2023 Discharge Disposition: home health care svc Active Issues Requiring Follow-up: Hyponatremia ? No future appointments. DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness [R53.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient presented to the ED on 8/2/2023 with concerns for brief loss of consciousness, bilateral lower limb weakness, seizure like activity and possible facial droop on the left side. Blood pressure at presentation was 194/76. NIH 4. We admitted for Loss of consciousness with possible left sided facial drop and seizure like activity: CT of the head showed no acute process. CTA showed high grade stenosis of the proximal right ICA and left common carotid and vertebral artery. We consulted neurology they recommended aspirin 81mg, permissive hypertension, MRI of the brain with and without contrast and continuous EEG. Both showed no acute process. We started patient on continuous telemetry and echo which shows LVEF of 62%. We also started patient on ASA + Plavix x 90 days, then ASA thereafter. Patient also complained of Generalized weakness and multiple falls at home. We ordered MRI lumber spine to rule out stenosis. No high-grade spinal canal stenosis was seen but there was multiple Mild to moderate stenosis of the neural foramina. PT/OT /SLP were consulted. They saw patient and recommended patient be discharged into skilled nursing facility. Patient preferred to be home with family. Patient has Hyponatremia on admission we discontinue the HCTZ medication he uses at home and we gave saline bolus and it improved. Blood sodium dropped the next day so we discharged patient home with sodium chloride salt and ordered a repeat lab in 2 days. We cc the PCP so that result could be followed-up. Patient examined today and discharged in stable condition. Follow-up instruction given to patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Mixed hyperlipidemia HTN (hypertension), benign ED (erectile dysfunction) Normocytic anemia History of colon cancer Ex-heavy cigarette smoker (20-39 per day) Lung nodule History of small bowel obstruction Coronary artery calcification COVID-19
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 10 mg tablet ascorbic acid (VITAMIN C) 1000 MG tablet aspirin 81 mg chewable tablet atorvastatin (LIPITOR) 40 mg tablet cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet clopidog
Allergien: Carvedilol Statins
Vorherige Impfungen: -

VAERS 2697895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 18.10.2023
Impfdatum: 14.11.2022
Beginn: 17.09.2023
Tage bis Beginn: 307,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury Asthenia Blood creatinine increased Blood culture negative Blood thyroid stimulating hormone normal Computerised tomogram abdomen abnormal Computerised tomogram head normal Computerised tomogram spine normal Fall Gait disturbance COVID-19 Cardiomegaly Chest X-ray abnormal Chronic kidney disease Colitis ischaemic Haemorrhage Hyperglycaemia Hypotension

Symptomtext

Patient is a 77 y.o. male who presented from home on 9/17/2023 with falls and weakness ,found to be COVID positive. Patient was not hypoxic, no need for steroid, antiviral therapies, continue supportive care, PT/OT for weakness and falls recommended skilled nursing therapy and sent to SNF. Patient had acute kidney injury on CKD stage IV that resolved with IV hydration and temporarily hold lisinopril and restarted on 9/24. COVID 19 Infection Generalized Weakness - Presented with: Weakness, fall - Symptom onset: Day of admission - Positive COVID-19: 9/17 at facility - Vaccination status: Vaccinated with Pfizer and boosted with Pfizer with booster dose on 11/2022 - CXR on admission showed borderline cardiomegaly, nonacute - Oxygen status: Room air - Decadron: Does not qualify due to SpO2>94% on RA. - Remdesivir: Does not qualify due to SpO2>94% on RA. - DVT prophylaxis: Subcutaneous heparin - Serial COVID labs ordered: No, given no hypoxia - Case Management/Social Services consulted: Yes -Supportive care and physical therapy and Occupational Therapy. AKI on CKD 4-resolved -Baseline creatinine of 1.9-2.5 -Cr worsened to 3.06 on 9/21 -He noted vomiting, and pre-syncope with hypotension yesterday -Appreciate nephrology Cr improving, no signed off -Resolved AKI with IVF and holding antiHTN meds -Resume lisinopril 9/24 Ischemic colitis Noted colitis on CT abd/pelvis from 9/20 -Suspect that this is ischemic over infectious or inflammatory. Patient has had some hypotensive episodes and noted some bleeding. -We will support blood pressure, check lactic acid and monitor abdominal pain -Less concerned for infection, blood cx ngtd, gi path panel cancelled per protocol Frequent Falls Patient does need a walker at home at baseline. Does not have any home health care services in place. Presented with falls at home. -Likely with exacerbation of weakness due to COVID, with baseline gait impairment 2/2 MS and deconditioning -CT cervical spine, head, and maxillofacial scan showing no acute injury. -PT and OT evaluation -Orthostatic positive on 9/20, likely also with slowed baroreceptors -TSH and b12 not deficient Essential HTN, uncontrolled RAS - pt with uncontrolled HTN secondary to bilateral RAS. S/p stent to L renal artery on 5/18/22, right renal artery stent placed on 6/17/2022 -Has had hypotensive episodes: hold parameters on his Norvasc and Coreg -Resume lisinopril 9/24, continue to hold hydralazine -Patient on aspirin Plavix, post stenting -Continue to monitor Diabetes mellitus type 2 with hyperglycemia -Continue home Januvia 25 mg QD MS - follows with Dr., OP follow up as scheduled -Not on any biologic therapy or DMARDs. - uses 4 wheeled walker at baseline -Neurology consulted for concern for possible worsening MS with LUE weakness: recommended supportive care of MS. Pulmonary HTN - mild, RVSP 40 mmHg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2672194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 16.08.2023
Impfdatum: 14.11.2022
Beginn: 08.12.2022
Tage bis Beginn: 24,0
Dosis: 4
Route/Site: IM / LA

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

Guillain-Barre syndrome Lumbar puncture abnormal Magnetic resonance imaging abnormal

Symptomtext

Guillain-Barre Syndrome

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: MRIs and Lumbar Tap supported GBS diagnosis
Aktuelle Erkrankungen: Head cold
Vorgeschichte: none
Andere Medikamente: Larin Fe (birth control)
Allergien: none
Vorherige Impfungen: -

VAERS 2643558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 09.06.2023
Impfdatum: 05.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 6,0
Dosis: 5
Route/Site: IM / LA

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

Thalamic stroke

Symptomtext

ACUTE STROKE OF THALAMUS, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2623914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MD
Alter: 31,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 27.10.2022
Beginn: 16.02.2023
Tage bis Beginn: 112,0
Dosis: 4
Route/Site: IM / LA

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

Bell's palsy Magnetic resonance imaging normal SARS-CoV-2 test negative

Symptomtext

I developed Bells? Palsy. I did not have any prior symptoms. I went to the doctor on 02/17/2023. I tested negative for COVID-19 twice and Lyme?s disease so we do not know why I got it. They also did an MRI to rule out anything else but everything was fine. I am still recovering from it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 16FEB2023 COVID-19 Test ? Negative; 16FEB2023 COVID-19 Test ? Negative; 17FEB2023 Lyme's Disease Test ? Negative; 22FEB2023 MRI- Normal
Aktuelle Erkrankungen: None
Vorgeschichte: Polycystic Ovarian Syndrome
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2620789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: CT
Alter: 75,0
Geschlecht: M
Eingang: 25.04.2023
Impfdatum: 14.10.2022
Beginn: 17.03.2023
Tage bis Beginn: 154,0
Dosis: 5
Route/Site: IM / -

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

Abscess limb Asthenia COVID-19 Computerised tomogram abnormal Cough Dysuria Feeling abnormal Intensive care Magnetic resonance imaging abnormal Malaise Mobility decreased Nausea SARS-CoV-2 test positive Urinary tract infection Walking aid user

Symptomtext

3/17/2023 I had a minor cough and not feeling quite right. The main symptom was just not feeling well. I took an at home COVID test and it was positive. I texted my doctor and went to bed early. Later I began feeling very nauseous and continued throughout the night feeling that way. I had trouble urinating. I just did not want to move. The next morning, I was terribly weak. The doctor called that morning and was going to prescribe Paxlovid and something for nausea. She called back and told me to go to the hospital I went to the hospital by ambulance. On the way, they said my oxygen level was about 86 and I was given something for nausea. After that, I was weak. After I got to the Emergency Room, they admitted me into ICU. They were watching my oxygen levels that fluctuated throughout my stay. I was given Paxlovid. While I was there I was given antibiotics for a UTI. I had a CT scan and an MRI and saw I had an abscess in my left buttocks. I was taken off Oxygen on 3/24/23. I was discharged on 3/26/23 with a walker because I was so weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 9,0
Labordaten: 17MAR23-At Home COVID Test-Positive; 18MAR23-COVID test-Positive; 18MAR23-MRI-Abscess on buttocks; 18MAR23-CT - Abscess on Buttocks
Aktuelle Erkrankungen: None
Vorgeschichte: Crones Disease, Diabetes Type 2, Hemochromatosis, Osteo Arthritis
Andere Medikamente: Alsace, Amitriptyline HCL, Diphenoxylate-Atropine, Doxazosin Mesylate, Glipizide, Finasteride, Hydrochlorothiazide, Lialda, Metformin, Methenamine HIPP, Montelukast SOD , Potassium Chloride, Prednisone, Tamsulosin HCL, Advil, Align, Vitami
Allergien: None
Vorherige Impfungen: -

VAERS 2614151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: TX
Alter: 64,0
Geschlecht: M
Eingang: 12.04.2023
Impfdatum: 07.10.2022
Beginn: 17.03.2023
Tage bis Beginn: 161,0
Dosis: 5
Route/Site: SYR / RA

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

Anticoagulant therapy Arthralgia Computerised tomogram abnormal Erythema Groin pain Magnetic resonance imaging abnormal Pain Pain in extremity Surgery Thrombectomy Thrombosis

Symptomtext

I had vaccination on 10/07/2022. On 03/17/2023 I ended up in the hospital. I had a small pinch in my calf a few days prior. I thought it was a sports injury. The pain radiated from calf to behind my knee cap with a red line. It was sore in that area. On 03/17/2023 the pain was from top of foot up the calf all the way up to my groin. The red line was visible. I went to the urgent care and they did a MRI and CAT Scan. I had a massive blood clot and I was rushed into surgery. The blood clot was pulled out but they couldn't get all of it. I am presently on blood thinners and I am being monitored with a specialist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 5,0
Labordaten: 03/17/2023 MRI and CAT Scan, positive for blood clot
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Prazosin; hydrazine; CETAPHIL; FLONASE
Allergien: N/A
Vorherige Impfungen: -

VAERS 2611988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 30.10.2022
Beginn: 01.04.2023
Tage bis Beginn: 153,0
Dosis: 4
Route/Site: IM / AR

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

Alanine aminotransferase Blood chloride Blood creatinine Blood electrolytes Blood glucose Blood potassium Blood sodium Brain natriuretic peptide C-reactive protein Carbon dioxide Chest X-ray Culture urine Differential white blood cell count Electrocardiogram Fibrin D dimer Full blood count Impaired work ability Inflammation

Symptomtext

Flu like symptoms that lasted a couple of days following days after vaccination. Now dealing with Pericarditis that started April 5th which caused me to miss work and I am prescribed steroid treatment and Naproxen to reduce inflammation. Still feeling consistent symptoms until this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: XR CHEST 2 VIEWS; Rapid COVID-19 (SARS-COV-2), Flu (Influenza A/B) (Local Center Approved); CREATININE; GLUCOSE; ELECTROLYTE PANEL (NA, K, CL, CO2); ALT; B-TYPE NATRIURETIC PEPTIDE (BNP); CBC W AUTOMATED DIFFERENTIAL; CRP (C-REACTIVE PROTEIN), NON-CARDIAC, HIGH SENSITIVITY; ERYTHROCYTE SEDIMENTATION RATE, AUTOMATED; TROPONIN I, HIGH SENSITIVITY; URINE CULTURE; URINALYSIS, AUTOMATED; D-DIMER FOR PULMONARY EMBOLISM, QUANTITATIVE; WBC AUTO DIFF; REFERRAL CARDIOLOGY; ECG, 12 Lead, Back Office, Now; Ketorolac Injection 60 mg (TORADOL); methylPREDNISolone Sod Succinate (PF) Injection 125 mg (Solu-Medrol PF); predniSONE 5 mg Oral Dose Pack Tab; Naproxen (NAPROSYN) 500 mg Oral Tab.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Latex
Vorherige Impfungen: Urgent care visit with similar symptoms following a month after initial series of Covid 19 Pfizer. Dates : 09/17/21, 10/08/21.

VAERS 2581494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

schwer

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 14.02.2023
Impfdatum: 28.10.2022
Beginn: 11.02.2023
Tage bis Beginn: 106,0
Dosis: 4
Route/Site: SYR / -

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

Alanine aminotransferase normal Angiogram pulmonary abnormal Anion gap Anticoagulant therapy Aspartate aminotransferase normal Aspiration pleural cavity Asthenia Atelectasis Auscultation Base excess Basophil count normal Basophil percentage Bladder scan Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate normal Blood bilirubin normal Blood calcium decreased

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: DO on February 12, 2023 00:28 Verified By: DO on February 12, 2023 00:28 Encounter Info: Hospital, Inpatient, 02/11/23 - * Final Report * Document Has Been Revised Chief Complaint Shortness of Breath History of Present Illness/Subjective 60-year-old male with a past medical history of chronic HFpEF CAD CVA DVT hypertension and type 2 diabetes presented to ED complaining of dyspnea that started the day prior to his presentation. He is well known to me, this provider admitted him for similar complaints and presentation Document Type: History and Physical Document Subject: History & Physical Note Performed By: DO on February 12, 2023 00:28 Verified By: DO on February 12, 2023 00:28 Encounter Info: Hospital, Inpatient, 02/11/23 - * Final Report * Document Has Been Revised Chief Complaint Shortness of Breath History of Present Illness/Subjective 60-year-old male with a past medical history of chronic HFpEF CAD CVA DVT hypertension and type 2 diabetes presented to ED complaining of dyspnea that started the day prior to his presentation. He is well known to me, this provider admitted him for similar complaints and presentation on 01/20/23, he was diuresed, had a therapeutic thoracentesis and was discharged. He returns saying he feels worse than before but labs, imaging suggest his pleural effusion is stable but likely has pulmonary edema. Please see H&P from 01/20/2023 for additional background hx. 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) 36.4 (36.4-36.4) Temp (FAHR) 97.5 (97.5-97.5), BP 187/100 (187-187)/(100-100), HR 87 (87-87), RR 18 (18-18), O2Sat 97 (97-97) Patient Weight Current Daily Weight: 133.9 kg 02/11/23 Patient Height Constitutional: No acute distress, well-nourished Eyes: PERRL, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs CTAB, no crackles, however some decreased breath sounds in left base Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: 2+ pitting edema in bilateral lower extremities extending to knee, no deformity Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Hypertensive crisis I16.9 resume home meds with the exception of amlodipine due to LE edema 2. Respiratory failure with hypoxia J96.91 likely 2/2 uncontrolled hypertension and recurrent pleural effusion/pulm edema cont supplemental o2, svns, diuresis 3. Recurrent pleural effusion on left J90 patient has had multiple thoracentesis this year, will attempt diuresis before obtaining consult for additional thoracentesis 4. (HFpEF) heart failure with preserved ejection fraction I50.30 cont home meds recent echo shows normal EF and was otherwise benign likely not in acute exacerbation given bnp being wnl cont diuresis 5. Bilateral lower extremity edema R60.0 possibly 2/2 chronic dvt vs chf 6. Generalized weakness R53.1 7. Physical deconditioning R53.81 likely due to pleural effusion, hypertensive crisis, as well as over all physical deconditioning from repeat admissions this month may need SAR upon discharge, patient is agreeable 8. Coronary artery disease I25.10 Noted. Cont home meds, control bp. trop negative and patient not experiencing chest pain makes ACS very unlikely 9. Hypertension I10 see plan above, cont home meds except amlodipine 10. Uncontrolled type 2 diabetes mellitus E11.65 poc glucose checks iss diabetic diet 11. Mixed hyperlipidemia E78.2 cont home meds, had recent lipid panel 12. History of DVT in adulthood Z86.718 obtain records from last LE doppler, patient states he had one this month and doesn't want another one if possible patient is not on anticoagulation and doesn't remember why not, possibility of obtain d-dimer 13. Proteinuria R80.9 noted. needs to follow up with nephrologist outpatient. Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 02/11/23 22:11:00 Dextrose 10% in Water 500 mL, Total Volume (mL) = 500, IV, 02/11/23 22:11:00, PRN - See Comments, Clinical Weight docusate, 100 mg, Orally, Capsule, BID, 02/12/23 9:00:00 furosemide, 40 mg, IV Push, Injection, Q12, 02/12/23 9:00:00 glucagon, 1 mg, IM, Injection, Unscheduled, PRN, Hypoglycemia, 02/11/23 22:11:00 glucose, Per Glucose Level, IV Push, Injection, Unscheduled, PRN, Low Blood Sugar, 02/11/23 22:11:00 heparin, 5,000 Units, Subcutaneous, Injection, Q8H, Routine, 02/11/23 23:00:00 hydroCODONE-acetaminophen, 1 Tablet, Orally, Tablet, Q6H, PRN, Pain, Moderate (4-6 out of 10), 02/11/23 22:48:00 insulin lispro, Sliding Scale, Subcutaneous, Injection, With Glucose Testing, PRN, Serum Glucose, 02/11/23 22:11:00 180 gm Carb per day Diet Admit to Inpatient CAH Aspiration Precautions Basic Metabolic Panel Bladder Scan BNP Pl QN Call (Specify) Call Blood Glucose 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 Call Urine Output Care Management Consult CBC w/Differential Digoxin SerPl QN Fall Precautions Fluid Intake Requirement Gluc-Strip POC Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Respiratory Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict Intake + Output Strict Level of Care Lipid Panel SerPl QN Magnesium SerPl QN Magnesium SerPl QN Medical Service Medication Message to Nursing Message to Nursing Message to Nursing Notify Provider Notify Provider Notify Provider Nutrition Consult Peripheral IV Insertion PT Evaluation and Treatment Reason for Not Ordering Long-acting Insulin Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Single Oxygen Saturation Sodium Ur Ran QN Telemetry Class III 24hr Recommendation Titrate FiO2 to Keep O2 Sat TSH w FreeT4 reflex Vital Signs Weight Weight Weight Code Status Resuscitation Status - Ordered -- 02/11/23 22:11:00, Full Code Chronic Problem List Anxiety and depression Chronic heart failure with preserved ejection fraction (HFpEF) Coronary artery disease Coronary artery disease without angina pectoris CVA (cerebrovascular accident) Deep vein thrombosis Generalized weakness Hypertension Long term use of drug Mixed hyperlipidemia Neck pain OSA (obstructive sleep apnea) Pharyngeal lesion Physical debility Pleural effusion Presence of drug coated stent in LAD coronary artery Proteinuria Psoriatic arthritis S/P gastric bypass Severe obesity Staphylococcus aureus septicemia Uncontrolled type 2 diabetes mellitus Procedure/Surgical History ocompound fracture repair R LE (1972) oGastric bypass operation opsa 2011 oRotator cuff repair oRotator cuff repair oUlnar nerve decompression Surgical History Internal 05/11/2021 Soft Tissue I and D MD Medications Home Medications (11) Active aspirin 81 mg oral delayed release tablet 81 mg = 1 Tablet, Orally, QAM atorvastatin 80 mg oral tablet 80 mg = 1 Tablet, Orally, At Bedtime carvedilol 6.25 mg oral tablet 3.125 mg = 0.5 Tablet, Orally, BID furosemide 40 mg oral tablet 20 mg = 0.5 Tablet, Orally, Daily gabapentin 800 mg oral tablet 800 mg = 1 Tablet, Orally, 4 Times Daily hydroCODONE-acetaminophen 10 mg-325 mg oral tablet 1 Tablet, PRN, Orally, Q6H Lantus (insulin glargine) SoloStar Pen 100 units/mL subcutaneous solution 60 Units, Subcutaneous, QAM losartan 100 mg oral tablet 100 mg = 1 Tablet, Orally, QAM nitroGLYCerin 0.4 mg sublingual tablet 0.4 mg = 1 Tablet, Sublingually, Q5min, not to exceed 3 doses/15 min--if pain persists, seek medical attention ProAir HFA 90 mCg/inh inhalation aerosol 2 Puff, PRN, Inhalation, 4 Times Daily Voltaren Topical 1% topical gel 2 GM, Topical, 4 Times Daily Active Scheduled Inpatient Medications docusate (docusate sodium), Capsule, 100 mg, Orally, BID, Start: 02/12/23 09:00:00 furosemide, Injection, 40 mg, IV Push, Q12, Start: 02/12/23 09:00:00 heparin (heparin 5,000 units/0.5 mL injectable solution), Injection, 5,000 Units, Subcutaneous, Q8H, Start: 02/11/23 23:00:00 Dextrose 10% in Water 500 mL IV PRN - See Comments One-Time Medications Given 02/11/23 00:00:00 TO 02/12/23 00:28:07 None Reported PRN Medications (0600 - 0559) from 02/11 - 02/12 acetaminophen, 650 mg, Orally, Q4H, 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, Q6H, 1 Dose(s) insulin lispro, Sliding Scale , Subcutaneous, With Glucose Testing, 0 Dose(s) Allergies NKA No Known Medication Allergies Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School disability Home/Environment Lives with Spouse. Living situation: Home/Independent. Alcohol abuse in household: No. Substance abuse in household: No. Smoker in household: No. Injuries/Abuse/Neglect in household: No. Nutrition/Health Diet: Regular. Wants to lose weight: Yes. Sleeping concerns: Yes. Feels highly stressed: No. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Cancer: Mother, Father and Sister. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 10.1 k/cumm (02/11/23 18:09:00) RBC: 4.35 million/cumm (02/11/23 18:09:00) Hgb: 12.2 GM/dL Low (02/11/23 18:09:00) Hct: 37.1 % Low (02/11/23 18:09:00) MCV: 85 fL (02/11/23 18:09:00) MCH: 28 pg (02/11/23 18:09:00) MCHC: 32.8 GM/dL (02/11/23 18:09:00) RDW: 14.8 % High (02/11/23 18:09:00) Platelet: 235 k/cumm (02/11/23 18:09:00) MPV: 6.5 fL Low (02/11/23 18:09:00) Neutrophils %: 72 % (02/11/23 18:09:00) Lymphocytes %: 18 % (02/11/23 18:09:00) Monocytes %: 5 % (02/11/23 18:09:00) Eosinophils %: 4 % (02/11/23 18:09:00) Basophils %: 1 % (02/11/23 18:09:00) Absolute Neutrophil: 7.3 k/cumm (02/11/23 18:09:00) Absolute Lymphocyte: 1.8 k/cumm (02/11/23 18:09:00) Absolute Monocyte: 0.5 k/cumm (02/11/23 18:09:00) Absolute Eosinophil: 0.4 k/cumm High (02/11/23 18:09:00) Absolute Basophil: 0.1 k/cumm (02/11/23 18:09:00) Chemistry: Sodium SerPl QN: 145 mmol/L (02/11/23 18:09:00) Potassium SerPl QN: 4 mmol/L (02/11/23 18:09:00) Chloride SerPl QN: 111 mmol/L High (02/11/23 18:09:00) Carbon Dioxide SerPl QN: 26 mmol/L (02/11/23 18:09:00) Anion Gap: 8 mmol/L (02/11/23 18:09:00) BUN SerPl QN: 31 mg/dL High (02/11/23 18:09:00) Creatinine SerPl QN: 1.39 mg/dL (02/11/23 18:09:00) Estimated GFR (CKD-EPI, no race): 58 mL/min/1.73m2 Low (02/11/23 18:09:00) Estimated CRCL (CG): 71 mL/min (02/11/23 18:09:00) Glucose SerPl QN: 186 mg/dL High (02/11/23 18:09:00) Calcium Total SerPl QN: 8 mg/dL Low (02/11/23 18:09:00) Alkaline Phos SerPl QN: 83 Units/L (02/11/23 18:09:00) ALT SerPl QN: 9 Units/L (02/11/23 18:09:00) AST SerPl QN: 14 Units/L (02/11/23 18:09:00) Bilirubin Total SerPl QN: 0.3 mg/dL (02/11/23 18:09:00) Total Protein SerPl QN: 5.9 GM/dL Low (02/11/23 18:09:00) Albumin SerPl QN: 3 GM/dL Low (02/11/23 18:09:00) Lipase SerPl QN: 19 Units/L (02/11/23 18:09:00) Troponin-I High Sensitivity: 12 ng/L (02/11/23 19:26:00) BNP Pl QN: 62 pg/mL (02/11/23 18:09:00) Gluc-Strip, POC: 111 mg/dL High (02/11/23 22:27:00) pH Bld Venous QN: 7.41 (02/11/23 18:09:00) PCO2 Bld Venous QN: 36 mmHg Low (02/11/23 18:09:00) PO2 Bld Venous QN: 146 mmHg High (02/11/23 18:09:00) Base Excess Bld Venous: -1 mmol/L (02/11/23 18:09:00) Bicarb Bld Venous Calc: 23 mmol/L (02/11/23 18:09:00) O2 Sat Bld Venous Calc: 99 % (02/11/23 18:09:00) Patient Temperature: 37 DegC (02/11/23 18:09:00) Coagulation: D-Dimer Pl QN: 367 ng/mL DDU High (02/11/23 18:09:00) Toxicology: Digoxin SerPl QN: <0.2 Low (02/11/23 22:31:00) All Other Labs: COVID 19 Specimen Source: Nasal (02/11/23 16:49:00) Coronavirus SARS-CoV2 Rapid: Not Detected (02/11/23 16:49:00) Diagnostics Radiology Results - Last 24 hours Across Visits 02/11/2023 19:14 - CTA Chest Pulm Embolism W/IV Contrast IMPRESSION:1. Negative for pulmonary embolism.2. Small-moderate left pleural effusion, slightly increased from CTcomparison.3. Bibasilar airspace opacities favored represent atelectasis.4. Pulmonary mosaic attenuation which is likely related to smallairway disease and air trapping.5. Noncalcified pulmonary nodules. One along the right major fissureis slightly enlarged and may represent an intrapulmonary lymph node.Another in the right upper lobe is new and is favoredinfectious/inflammatory. Recommend 3 month follow-up CT to documentstability and/or resolution.6. Mild mediastinal lymphadenopathy, favored reactive.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. Signature Line Electronically Signed on 02/12/23 00:28 ________________________________________________________ DO Electronically Signed on 02/12/23 00:30 ________________________________________________________ DO

Weitere VAERSDATA-Felder

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

VAERS 2578859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 09.02.2023
Impfdatum: 02.11.2022
Beginn: 20.12.2022
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram pulmonary normal Cerebral infarction Echocardiogram normal Implantable cardiac monitor insertion Ischaemic stroke Laboratory test normal Magnetic resonance imaging head abnormal Muscular weakness Paraesthesia

Symptomtext

Patient had been experiencing right upper extremity weakness and tingling in his hands and feet starting on 12/20/22. He presented to ER on 12/31/22 and underwent MRI brain revealed acute infarction within the left frontal and parietal lobes and left centrum semiovale. He underwent extensive testing including transesophageal echocardiogram, CT pulmonary angiography, implantable loop recorder, and limited hemeatologic workup which all returned broadly normal without causal evidence for this ischemic stroke.

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Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: -
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 27.10.2022
Beginn: 19.01.2023
Tage bis Beginn: 84,0
Dosis: 4
Route/Site: - / -

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

Angiogram cerebral normal Aphasia Bladder catheterisation Blood pressure increased Computerised tomogram head abnormal Confusional state Hemianopia Hypertensive urgency NIH stroke scale Perfusion brain scan normal Urinary retention

Symptomtext

1/19/2023 - 1/20/2023 (23 hours) Hospital Emergency CHIEF COMPLAINT: POSSIBLE STROKE The patient is a pleasant 85-year-old female who presents to the ER as a stroke alert. She was seen in the Trauma Bay hot spot along with Stroke Neurology. Patient reports that she was at home with her husband and around 16:30 today she started feeling confused. She felt like she was having difficulty getting some of her words out. Patient denies any unilateral numbness or weakness. No headaches. On initial exam, stroke scale is 3. Patient has some partial hemianopsia which appears chronic per previous records. Patient also had 1 point off for knowing her age as well as 1 for mild aphasia. After evaluation, patient is taken emergently to CT scan for CT head without contrast as well as advanced imaging. Patient's records were reviewed. Patient is on aspirin and Plavix. No other obvious blood thinners. In reviewing patient's records it does state she has had previous hemianopsia consistent with her symptoms today. Patient's blood pressure would intermittently spike into the 190s to 200 systolic. It would then come back down into the 160s. After CT scan, patient was taken back to an ER room. After speaking with the patient further, she feels more that she is confused rather than actually having difficulty speaking. CT head came back showing no acute abnormalities. CT angiogram and perfusion came back showing no large vessel occlusion or perfusion changes. At this point, we did discuss giving TNK to this patient for mild language changes. It does seem that patient's symptoms more consistent with confusion than actual dysarthria or aphasia. Also patient's blood pressure does intermittently spike into the 200. She is given IV labetalol. After discussion with Stroke Neurology, it was felt symptoms are most likely secondary to patient's confusion from hypertension urgency. However, we could have further discussion with the patient and shared decision making regarding giving IV TNK in the event of potential stroke. At this point, patient was continually complained that she had to urinate but could not go. At that point nursing staff did perform urine catheterization. Approximately 1 L of urine was removed. Patient did feel significantly improved after this. We did discuss risks and benefits with patient and family at bedside. In having these discussions, patient was actually able to speak quite fluently. She would intermittently problems remembering things but was having less problem with her speech. We did talk about risks and benefits of TNK and did offer this to the patient. Given that the patient is already on aspirin and Plavix, she was more concerned about potential risk of bleeding. Ultimately, she declined IV TNK. The patient will be admitted for further blood pressure management and further workup.

Weitere VAERSDATA-Felder

Praegender Schweregrund: NIH stroke scale
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Incomplete bladder emptying Post-void dribbling Subjective tinnitus.more on right Benign paroxysmal positional vertigo Right asymmetrical SNHL Mixed hyperlipidemia Type 2 diabetes mellitus Other chest pain Syncope, near Allergic rhinitis Gastroesophageal reflux disease Mild persistent asthma Anemia Anxiety Depression Essential hypertension Hypothyroidism Osteoarthritis of hip Palpitations Hypertensive emergency Carotid atherosclerosis, bilateral Stage 3a chronic kidney disease STEMI (ST elevation myocardial infarction) CAD (coronary artery disease)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet cetirizine (ZYRTEC) 10 MG tablet clopidogrel (PLAVIX) 75 MG tablet escitalopram (LEXAPRO) 5 MG tablet e
Allergien: Darvocet [Propoxyphene N-apap]Hives KeflexDiarrhea
Vorherige Impfungen: -

VAERS 2574355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: GA
Alter: 38,0
Geschlecht: M
Eingang: 02.02.2023
Impfdatum: 14.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Dyspnoea Fatigue Headache Nausea Pericarditis

Symptomtext

Pericarditis. Chest pain. Fatigue. Shortness of breath. Headache. Nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 1,0
Labordaten: I visited a Heart Specialist and was diagnosed, and treated for, pericarditis by a local Dr. . I also had to visit the ER and was diagnosed with pericarditis by the hospital doctor ( MD) there also.
Aktuelle Erkrankungen: None.
Vorgeschichte: IBS.
Andere Medikamente: None.
Allergien: Penicillin & Levaquin.
Vorherige Impfungen: Moderna Covid-19 08/27/2021 Previously reported to VAERS.

VAERS 2562381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: OH
Alter: 42,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 08.11.2022
Beginn: 19.12.2022
Tage bis Beginn: 41,0
Dosis: UNK
Route/Site: IM / RA

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

Angiogram cerebral Arteriogram carotid Cerebellar stroke Computerised tomogram head Ischaemic stroke Magnetic resonance imaging head

Symptomtext

cryptogenic ischemic stroke left superior cerebella artery distribution

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebellar stroke
Hospital-Tage: 4,0
Labordaten: CT head 12/19/22. CTA head and neck 12/19 MRI brain 12/19
Aktuelle Erkrankungen: none
Vorgeschichte: obesity, depression, add, insomnia
Andere Medikamente: adderall, ozempic,remeron, lunesta, celexa, mvi
Allergien: trazodone
Vorherige Impfungen: -

VAERS 2560152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: WV
Alter: 69,0
Geschlecht: M
Eingang: 14.01.2023
Impfdatum: 26.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / -

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

Blood test Hypoaesthesia Ischaemic stroke Scan

Symptomtext

Ischemic brain stroke with treatment, left side numbness face, arm, and leg. Emergency Room with admission to local hospital, for 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 3,0
Labordaten: Scans, bloodwork
Aktuelle Erkrankungen: none
Vorgeschichte: CAD with stent placement 14 years ago-no MI
Andere Medikamente: statin, aspirin, multi VIts, Vit D3
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2560031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MD
Alter: 58,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 19.12.2022
Beginn: 07.01.2023
Tage bis Beginn: 19,0
Dosis: UNK
Route/Site: IM / LA

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

Computerised tomogram head abnormal Magnetic resonance imaging head abnormal Scan with contrast abnormal Sensory disturbance Thalamic stroke

Symptomtext

Roughly twenty days after vaccination, I had a thalamic stroke, diagnosed by CT scan and MRI at Hospital. No underlying risk factors. Stroke caused sensory damage but no apparent mental or mobility effects. Having read the Reuters summary of the concerns about Pfizer bivalent I thought I should report this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thalamic stroke
Hospital-Tage: 2,0
Labordaten: Stroke diagnosed with CT w Contrast and MRI, Jan 8, 2023
Aktuelle Erkrankungen: none
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: Rosuvastatin 5mg daily, Trazodone 50mg intermittently for insomnia
Allergien: N/A
Vorherige Impfungen: -

VAERS 2546458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

schwer

Staat: TX
Alter: 74,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / RA

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

Blood test Fibrin D dimer Fibrin D dimer increased N-terminal prohormone brain natriuretic peptide Off label use Product use issue Thrombosis Ultrasound scan X-ray

Symptomtext

high D-dimer; blood clots/has 4 blood clots in 1 leg and 2 blood cots in the other leg; Comirnaty and Flu vaccine administered on same day; Comirnaty and Flu vaccine administered on same day; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 as dose 5 (booster), single (Lot number: GJ6665) at the age of 74 years, in right arm for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), on 28Oct2022 as dose number unknown, single (Lot number: UJ875AD), in right arm for immunisation. The patient's relevant medical history included: "blood vessel injuries" (unspecified if ongoing), notes: Had 2 blood vessel injuries.; "factor 2 Thrombophilia mutation" (unspecified if ongoing), notes: had a Boston Heart Test run by cardiologist. The patient's family history included: "Scleroderma", start date: 1977 (unspecified if ongoing), notes: Scleroderma. Obviously an autoimmune issue; "Pulmonary arterial hypertension" (unspecified if ongoing), notes: Pulmonary arterial hypertension. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (First Dose: Sars Cov2, Covid-19 Mrna LMP-S PF30mcg/0.3ml Pfizer Covid-19 vaccine, Date: 22Feb2021, LOT: EN6202, NDC/EXP: Unknown), administration date: 22Feb2021, when the patient was 72-year-old, for Covid-19 Immunization; BNT162b2 (Second Dose: Sars Cov2, Covid-19 Mrna LMP-S PF30mcg/0.3ml Pfizer Covid-19 vaccine, Date: 15Mar2021, LOT: EN6204, NDC/EXP: Unknown), administration date: 15Mar2021, when the patient was 72-year-old, for COVID-19 Immunization; BNT162b2 (Third Dose: First Booster: Covid-19 vaccine, Date: 18Oct2021, LOT: 301558A, NDC/EXP: Unknown), administration date: 18Oct2021, when the patient was 73-year-old, for COVID-19 Immunization; BNT162b2 (Fourth Dose: 18May2022, Covid-19 Mrna LNPSPF 30mcg/0.3ml TS Comirnaty, TS30mcg/0.3ml, LOT: FJ9943, NDC/EXP: Unknown), administration date: 18May2022, when the patient was 73-year-old, for Covid-19 immunization; tetanus shot (Vaccine Name: Tetanus shot, TDap (Adacel), Manufacturer: PMC Sanofi Pasteur Inc., LOT: 2CA18C1, EXP: Unknown, Route, Anatomical Location: think left arm), administration date: 21Oct2022, when the patient was 74-year-old. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 28Oct2022, outcome "unknown" and all described as "Comirnaty and Flu vaccine administered on same day"; THROMBOSIS (medically significant) with onset 15Dec2022, outcome "unknown", described as "blood clots/has 4 blood clots in 1 leg and 2 blood cots in the other leg"; FIBRIN D DIMER INCREASED (non-serious), outcome "unknown", described as "high D-dimer". The events "blood clots/has 4 blood clots in 1 leg and 2 blood cots in the other leg", "high d-dimer" and "comirnaty and flu vaccine administered on same day" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: (unspecified date) 16.74 mg/l, notes: Blood test came up on computer as 16.74 mg/l; Fibrin D dimer: (May2022) 1.12, notes: it was 1.12 ugr/ml; (06Dec2022) 16.74, notes: Result: 16.74; Unit: Not Provided; N-terminal prohormone brain natriuretic peptide: (May2022) 182, notes: Result: 182; Unit: Not Provided; (06Dec2022) 2026, notes: Result: 2026; Unit: pg/ml; Ultrasound scan: (unspecified date) she has 4 blood clots in 1 leg and 2 blood cots, notes: show that she has 4 blood clots in 1 leg and 2 blood cots in the other leg; X-ray: (unspecified date) she has 4 blood clots in 1 leg and 2 blood cots, notes: show that she has 4 blood clots in 1 leg and 2 blood cots in the other leg. Therapeutic measures were taken as a result of thrombosis. Clinical course: Clinical course: Scleroderma and was not an antivaxxer. Other Conditions: Yes. Investigations: Yes. Had 2 blood vessel injuries. One after trashed IV after surgery. Second one was after getting treatment for Lyme Disease.These were both a long time ago. Test results: 2 of these tests have names that are so similar but, reference ranges are so different. Family Medical History Relevant to Adverse Events (AEs): Mother had scleroderma, was on oxygen 24/7 and probably had pulmonary arterial hypertension. Other than that, no. Everybody had their issues. Caller and her mother are the only ones who had autoimmune problems. Caller has had multiple D-dimer tests in the past, since 2020. The fifth one she had on 06Dec2022 showed that she had 16.74, or something like that, in whatever the little scientific measurement is, the value, which generated a lot of activity. Does not have any blood clots in arms or in any emboli. When she talked to her pharmacist about D-dimer being so high, they told her that this was still experimental and that she needs to report this to Pfizer. Was last week when the D-dimer came back. Blood clots: Treatment: was now on Eliquis. The monkey wrench that she thought may be of interest, is that she had a Boston Heart Test run by cardiologist. That showed that she has factor 2 Thrombophilia mutation, which is also run by 23 and me. Concerning that it was the same position as being on gene mutation. Also on Lab core, and one from Baylor college that also run the Factor 2 gene.These are all related to Thrombophilia, which was blood clots. NT-ProBNP went really high.Previous reading in May2022 was 182 and sky rocketed on 06Dec2022 to 2026pg/ml. When she actually saw the report, she thought, not going to panic, refuses not to panic on this. Thought what she might have done to cause this. Then remembered she got the other booster shot. At that point, the only manufacturer that she knew to be implicated with blood clots was Moderna. Vaccination Facility Type: Pharmacy or Drug Store. On same day, 28Oct2022, had flu vaccine. Influenza high dose quadrivalent Fluzone high dose high dose quadrivalent. After getting through the ultrasound on both legs, they called radiologist to read results and caller was going to be brought to Emergency room but, her cardiologist told nurse that caller was prescribed Eliquis and she went home and did not end up going to emergency room. Thinking that the factor 2 genetic thing could play a part in this. For some other people who have gotten blood clots and also have a thrombophilia problem genetic in nature and may not know about it. Does not go around with little sign that says she has factor 2 but, maybe she should. Wondering if that should be something that is a suggestion to people that are researching. If this person has a genetic problem with thrombophilia. Should be asking someone if having genetic testing done, if having the factor 2 was on 23 and me or that they just happened to have other genetic studies that back it up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Name: Blood test; Result Unstructured Data: Test Result:16.74 mg/l; Comments: Blood test came up on computer as 16.74 mg/l.; Test Date: 202205; Test Name: D-dimer; Result Unstructured Data: Test Result:1.12; Comments: it was 1.12 ugr/ml; Test Date: 20221206; Test Name: D-dimer; Result Unstructured Data: Test Result:16.74; Comments: Result: 16.74; Unit: Not Provided; Test Date: 202205; Test Name: NT-proBNP; Result Unstructured Data: Test Result:182; Comments: Result: 182; Unit: Not Provided; Test Date: 20221206; Test Name: NT-proBNP; Result Unstructured Data: Test Result:2026; Comments: Result: 2026; Unit: pg/ml; Test Name: ultrasounds; Result Unstructured Data: Test Result:she has 4 blood clots in 1 leg and 2 blood cots; Comments: show that she has 4 blood clots in 1 leg and 2 blood cots in the other leg.; Test Name: X-rays; Result Unstructured Data: Test Result:she has 4 blood clots in 1 leg and 2 blood cots; Comments: show that she has 4 blood clots in 1 leg and 2 blood cots in the other leg.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Injury (Had 2 blood vessel injuries.); Pulmonary arterial hypertension; Scleroderma (Scleroderma. Obviously an autoimmune issue); Thrombophilia (had a Boston Heart Test run by cardiologist.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2537769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: IL
Alter: 94,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 21.11.2022
Beginn: 03.12.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / RA

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

Bell's palsy Facial paralysis

Symptomtext

drooping right eye lid and right side of mouth . Diagnosised as Bell's Palsy. Had the same reaction after 2nd dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: dementia, s/p fx ofleft femur, reflux disease, Hx of MRSA, dyspnea, chronic pain
Andere Medikamente: -
Allergien: Actonel, LNP-S, Myrbetrig, NSAIDS, Sulfa
Vorherige Impfungen: Pfizer given on 5/21/2021

VAERS 2536857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: WA
Alter: 71,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 28.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

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

Angiogram cerebral Arteriogram carotid Asthenia Dysarthria Dyskinesia Electrocardiogram Ischaemic stroke Laboratory test Metabolic function test Scan with contrast

Symptomtext

Taken by ambulance from home to hospital. Husband reports symptoms to be slurred speech, overall weakness in body, thrashing around in bed. Approx. 6am on 11-18-22. Admitted to hospital for 1 day and did testing. Diagnosis was Ischemic Stroke. Follow up with Primary physician and other specialists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 1,0
Labordaten: 11-18-22 Comprehensive Metabolic Panel 11-18-22 EKG 11-18-22 CT angio Head and Neck with and without contrast Many more - Please contact for complete list -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3 and Vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 2536822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

schwer

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 17.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: UN / UN

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

Anaphylactic reaction Angioedema Dysphagia Lip swelling Oral discomfort Pruritus Swelling face

Symptomtext

Patient presented to emergency department with complaint of bottom lip and cheek swelling, burning on lips, feeling itchy, and difficulty swallowing. No difficulty breathing. Patient was diagnosed with angioedema/anaphylaxis. Patient was treated with IV dexamethasone 4 mg every 8 hours. IV famotidine 20 mg twice daily. IV diphenhydramine 25 mg every 8 hours x3 doses. and IV fluids (lactated ringers). Patient improved over the course of about 12 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: None relevant
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: no allergies
Vorherige Impfungen: -

VAERS 2525530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

schwer

Staat: PA
Alter: 76,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Arthralgia Myalgia Pain Restlessness Scan Blood test Chest X-ray Electrocardiogram Electroencephalogram Magnetic resonance imaging COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test Scan brain Seizure Sleep disorder Weight

Symptomtext

They gave him a COVID test, on 19Nov2022 and it was positive; They gave him a COVID test, on 19Nov2022 and it was positive; Interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 76-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 as dose 5 (booster), single (Lot number: GJ6665, Expiration Date: 12Dec2022) at the age of 76 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 19Feb2021 as dose 1, single (Batch/Lot number: unknown), on 19Mar2021 as dose 2, single (Batch/Lot number: unknown), on 11Nov2021 as dose 3 (booster), single (Batch/Lot number: unknown) and on 20Apr2022 as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, start date: 05Oct2022, stop date: 05Oct2022. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 12Oct2022, outcome "unknown"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 19Nov2022, outcome "unknown" and all described as "They gave him a COVID test, on 19Nov2022 and it was positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Nov2022) Positive; Scan brain: (unspecified date) Negative; Weight: (unspecified date) losing. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: At the start of getting his COVID vaccines, he experienced pain in his right shoulder that radiated down his arm. That was going on for at least 18 months. He got his COVID booster shot. On, 15Nov2022, he had an episode where he couldn't wake from sleep. He went to the Emergency room where he was told it was a seizure. He briefly woke while the police and emt were there. They did brain scans and so one. Everything was negative. He unfortunately wasn't given a COVID test at the ER. That could be a symptom of COVID - not being able to awaken or seizure. So she doesn't know why they didn't test him. Then, two days after he was released on 16Nov2022. He had to go to a (withheld) ER in (withheld) due to a severe sore throat and muscle aches He started experiencing. It was 2 am he went to the (withheld) ER in (withheld). The doctor right away said he had flu and other viruses. He had a sore throat, muscle and joint aches. He had muscle, shoulder, and joint pain. That is why he went to the (withheld) ER on 19Nov2022. They gave him a COVID test, on 19Nov2022 and it was positive. For Country Only: Vaccination Facility Type: Pharmacy. Vaccine was not administered at military facility. Conclusion of Previously Completed Investigation on 08Dec2022: The complaint for "PFIZERBIONTECH COVID-19 VACCINE" was investigated. 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 GJ6665. A complaint sample was not returned. No related quality issues were identified during the investigation. There was no impact on product quality, regulatory, validation and stability. (Name) concludes that the reported defect was not representative of the quality of the batch and the batch remains acceptable. The Agency 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Test Date: 20221119; Test Name: Covid-19 test; Test Result: Positive ; Test Name: brain scans; Test Result: Negative ; Test Name: Weight; Result Unstructured Data: Test Result:losing
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2525530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

schwer

Staat: PA
Alter: 76,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / RA

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

Arthralgia Myalgia Pain Restlessness Scan Blood test Chest X-ray Electrocardiogram Electroencephalogram Magnetic resonance imaging COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test Scan brain Seizure Sleep disorder Weight

Symptomtext

They gave him a COVID test, on 19Nov2022 and it was positive; They gave him a COVID test, on 19Nov2022 and it was positive; Interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 76-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 as dose 5 (booster), single (Lot number: GJ6665, Expiration Date: 12Dec2022) at the age of 76 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 19Feb2021 as dose 1, single (Batch/Lot number: unknown), on 19Mar2021 as dose 2, single (Batch/Lot number: unknown), on 11Nov2021 as dose 3 (booster), single (Batch/Lot number: unknown) and on 20Apr2022 as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, start date: 05Oct2022, stop date: 05Oct2022. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 12Oct2022, outcome "unknown"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 19Nov2022, outcome "unknown" and all described as "They gave him a COVID test, on 19Nov2022 and it was positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Nov2022) Positive; Scan brain: (unspecified date) Negative; Weight: (unspecified date) losing. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: At the start of getting his COVID vaccines, he experienced pain in his right shoulder that radiated down his arm. That was going on for at least 18 months. He got his COVID booster shot. On, 15Nov2022, he had an episode where he couldn't wake from sleep. He went to the Emergency room where he was told it was a seizure. He briefly woke while the police and emt were there. They did brain scans and so one. Everything was negative. He unfortunately wasn't given a COVID test at the ER. That could be a symptom of COVID - not being able to awaken or seizure. So she doesn't know why they didn't test him. Then, two days after he was released on 16Nov2022. He had to go to a (withheld) ER in (withheld) due to a severe sore throat and muscle aches He started experiencing. It was 2 am he went to the (withheld) ER in (withheld). The doctor right away said he had flu and other viruses. He had a sore throat, muscle and joint aches. He had muscle, shoulder, and joint pain. That is why he went to the (withheld) ER on 19Nov2022. They gave him a COVID test, on 19Nov2022 and it was positive. For Country Only: Vaccination Facility Type: Pharmacy. Vaccine was not administered at military facility. Conclusion of Previously Completed Investigation on 08Dec2022: The complaint for "PFIZERBIONTECH COVID-19 VACCINE" was investigated. 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 GJ6665. A complaint sample was not returned. No related quality issues were identified during the investigation. There was no impact on product quality, regulatory, validation and stability. (Name) concludes that the reported defect was not representative of the quality of the batch and the batch remains acceptable. The Agency 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Test Date: 20221119; Test Name: Covid-19 test; Test Result: Positive ; Test Name: brain scans; Test Result: Negative ; Test Name: Weight; Result Unstructured Data: Test Result:losing
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2525530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: PA
Alter: 76,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / RA

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

Arthralgia Myalgia Pain Restlessness Scan Blood test Chest X-ray Electrocardiogram Electroencephalogram Magnetic resonance imaging COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test Scan brain Seizure Sleep disorder Weight

Symptomtext

They gave him a COVID test, on 19Nov2022 and it was positive; They gave him a COVID test, on 19Nov2022 and it was positive; Interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 76-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 as dose 5 (booster), single (Lot number: GJ6665, Expiration Date: 12Dec2022) at the age of 76 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 19Feb2021 as dose 1, single (Batch/Lot number: unknown), on 19Mar2021 as dose 2, single (Batch/Lot number: unknown), on 11Nov2021 as dose 3 (booster), single (Batch/Lot number: unknown) and on 20Apr2022 as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, start date: 05Oct2022, stop date: 05Oct2022. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 12Oct2022, outcome "unknown"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 19Nov2022, outcome "unknown" and all described as "They gave him a COVID test, on 19Nov2022 and it was positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Nov2022) Positive; Scan brain: (unspecified date) Negative; Weight: (unspecified date) losing. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: At the start of getting his COVID vaccines, he experienced pain in his right shoulder that radiated down his arm. That was going on for at least 18 months. He got his COVID booster shot. On, 15Nov2022, he had an episode where he couldn't wake from sleep. He went to the Emergency room where he was told it was a seizure. He briefly woke while the police and emt were there. They did brain scans and so one. Everything was negative. He unfortunately wasn't given a COVID test at the ER. That could be a symptom of COVID - not being able to awaken or seizure. So she doesn't know why they didn't test him. Then, two days after he was released on 16Nov2022. He had to go to a (withheld) ER in (withheld) due to a severe sore throat and muscle aches He started experiencing. It was 2 am he went to the (withheld) ER in (withheld). The doctor right away said he had flu and other viruses. He had a sore throat, muscle and joint aches. He had muscle, shoulder, and joint pain. That is why he went to the (withheld) ER on 19Nov2022. They gave him a COVID test, on 19Nov2022 and it was positive. For Country Only: Vaccination Facility Type: Pharmacy. Vaccine was not administered at military facility. Conclusion of Previously Completed Investigation on 08Dec2022: The complaint for "PFIZERBIONTECH COVID-19 VACCINE" was investigated. 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 GJ6665. A complaint sample was not returned. No related quality issues were identified during the investigation. There was no impact on product quality, regulatory, validation and stability. (Name) concludes that the reported defect was not representative of the quality of the batch and the batch remains acceptable. The Agency 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Test Date: 20221119; Test Name: Covid-19 test; Test Result: Positive ; Test Name: brain scans; Test Result: Negative ; Test Name: Weight; Result Unstructured Data: Test Result:losing
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2528577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 11.12.2022
Impfdatum: 29.11.2022
Beginn: 06.12.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Brain natriuretic peptide increased Chest discomfort Dyspnoea Echocardiogram abnormal Ejection fraction decreased Left ventricular dilatation Left ventricular dysfunction Magnetic resonance imaging heart Myopericarditis Pericardial disease Pyrexia Troponin White blood cell count increased

Symptomtext

Patient presented to the hospital on 12/6/2022 with 2 days of progressive shortness of breath as well as a sense of central chest pressure and squeezing and a nondescript left lower chest discomfort.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myopericarditis
Hospital-Tage: -
Labordaten: 12/6/2022 - troponin 0.32, BNP 1486, low grade fever up to 38.1C, WBC 10,200 12/6/2022- echo with severely dilated LV with severe systolic dysfunction, EF 20% 12/7/2022 - Cardiac MRI - Mild focal subepicardial enhancement within the lateral LV wall with abnormally elevated native T1 value, representing a nonischemic process such as myocarditis. Diffuse pericardial enhancement, suggesting acute pericarditis. Together, these findings indicate myopericarditis.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: History of basal cell carcinoma History of adenomatous polyp of colon Mixed anxiety depressive disorder Left bundle branch block (LBBB) Essential hypertension History of hepatitis C Hypercholesterolemia Hypertriglyceridemia Prediabetes Numbness of toes Otitis of left ear Sudden idiopathic hearing loss of both ears
Andere Medikamente: ascorbic acid (vitamin C) cholecalciferol (VITAMIN D3) amLODIPine (NORVASC) atorvastatin (LIPITOR) vitamin B complex (B COMPLEX 50 ORAL) docosahexanoic acid/epa (FISH OIL ORAL) wild alaskan fish oil - 1400 mg. L. acidophilus-L. rhamn
Allergien: None
Vorherige Impfungen: -

VAERS 2512379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MA
Alter: 16,0
Geschlecht: F
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: ja

Immediate post-injection reaction Syncope

Symptomtext

Patient fainted with 30 seconds of administration . Parents explained that patient did not have enough to eat or drink this morning . Parents and patient waited 15 minutes after vaccination and patient felt much better after ingestion food and water

Weitere VAERSDATA-Felder

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

VAERS 2509238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

schwer

Staat: CA
Alter: 73,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 07.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

Abdominal discomfort Asthenia Body temperature Chills Diarrhoea Muscle spasms Myalgia Nausea Off label use Pain Product use issue Relapsing fever SARS-CoV-2 antibody test Seizure

Symptomtext

The patient received the flu vaccine and Pfizer Bivalent vaccine on 07Nov2022; The patient received the flu vaccine and Pfizer Bivalent vaccine on 07Nov2022; upset stomach with nausea and cramping and diarrhea; upset stomach with nausea and cramping and diarrhea; upset stomach with nausea and cramping and diarrhea; upset stomach with nausea and cramping and diarrhea; chills; He hasn't been able to really get out of the bed. He has been weak too; pain all over the body; Muscle ache; the chills are like a seizure almost where his entire body shakes; relapsing fever; This is a spontaneous report received from a contactable reporter(s) (Physician) from medical information team. A 73-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Nov2022 as dose 5 (booster), single (Lot number: GJ6665) at the age of 73 years, in arm for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), on 07Nov2022 as dose number unknown, single (Batch/Lot number: unknown), in arm for immunisation. The patient's relevant medical history included: "Atrial fibrillation" (unspecified if ongoing), notes: He has A-fib, atrial fibrillation for which he has a pacemaker implanted. Concomitant medication(s) included: AMLODIPINE; CARVEDILOL; LOSARTAN; FINASTERIDE. Vaccination history included: Covid-19 vaccine (Dose 1), for COVID-19 immunization; Covid-19 vaccine (Dose 2), for COVID-19 immunization; Covid-19 vaccine (Dose 3), for COVID-19 immunization; Covid-19 vaccine (Dose 4), for COVID-19 immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 07Nov2022, outcome "unknown" and all described as "The patient received the flu vaccine and Pfizer Bivalent vaccine on 07Nov2022"; ASTHENIA (non-serious) with onset Nov2022, outcome "unknown", described as "He hasn't been able to really get out of the bed. He has been weak too"; MYALGIA (non-serious) with onset Nov2022, outcome "unknown", described as "Muscle ache"; CHILLS (non-serious) with onset Nov2022, outcome "unknown"; PAIN (non-serious) with onset Nov2022, outcome "unknown", described as "pain all over the body"; RELAPSING FEVER (medically significant) with onset Nov2022, outcome "unknown"; SEIZURE (medically significant) with onset Nov2022, outcome "unknown", described as "the chills are like a seizure almost where his entire body shakes"; ABDOMINAL DISCOMFORT (non-serious), NAUSEA (non-serious), MUSCLE SPASMS (non-serious), DIARRHOEA (non-serious) all with onset Nov2022, outcome "unknown" and all described as "upset stomach with nausea and cramping and diarrhea". The patient underwent the following laboratory tests and procedures: Body temperature: 99.5, notes: The fever by the way got up to 99.5. It was a low-grade fever; SARS-CoV-2 antibody test: Negative, notes: I tested him for COVID with the quick test, antibody test at home and he was negative for COVID. Therapeutic measures were taken as a result of relapsing fever, pain, myalgia. Clinical course: The Physician stated that the patient had initially upset stomach with nausea and cramping and diarrhea and that was the day after the injection and subsequently, so the injection and was on Monday, 07Nov2022. The side effects started 08Nov2022 and then from the 9th until today, he has had what the Physician would call a relapsing fever and chills. They were severe, the chills are like a seizure almost where his entire body shakes and the Physician had to put heating pad and multiple blankets on him and the fever had involved him sweating through all of his clothing and bed linens and kind of dripping in sweat. The fever by the way got up to 99.5. There seemed to be the chills particularly when he attempts to eat anything. All he had been able to keep down was liquid, no solid food. He had pain all over the body, muscle aches. The Physician wanted to report it but mentioned that this was for him the fifth Pfizer. So this was the Pfizer COVID-19 Bivalent vaccine. He was a senior and it was given concurrently with the Flu vaccine on the same arm. The Physician stated that both of his were given on same arm. The Physician gave the patient Advil. The Physician gave him 400 mg for the aches and fever. The fever by the way got up to 99.5. It was a low-grade fever. The Physician had tested the patient for COVID with the quick test, antibody test at home and he was negative for COVID. The Physician wanted to know since this was now the sixth day of the adverse effect, do they have any information about other people who reported similar adverse effects and how long they last. The Physician wanted to know how long they could expect him to remain ill. He hadn't been able to really get out of the bed. He had been weak too, maybe the Physician did mention about weakness but this was the sixth day. So the Physician wanted to know if there was an average link that these adverse effects last.; Sender's Comments: As there is limited information in the case provided, the causal association between the reported events: "Seizure", "Relapsing fever" and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available. 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: Seizure
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:99.5; Comments: The fever by the way got up to 99.5. It was a low-grade fever; Test Name: COVID-19 antibody test; Test Result: Negative ; Comments: I tested him for COVID with the quick test, antibody test at home and he was negative for COVID
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation (He has A-fib, atrial fibrillation for which he has a pacemaker implanted)
Andere Medikamente: AMLODIPINE; CARVEDILOL; LOSARTAN; FINASTERIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2508020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: KS
Alter: 44,0
Geschlecht: M
Eingang: 15.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Confusional state Dizziness Hypotension Presyncope Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe, Additional Details: Per wife had a vasovagal response, attempted method to provide circulation to the head but patient was barely responsive and had to call EMT

Weitere VAERSDATA-Felder

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

VAERS 2502269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: ID
Alter: 40,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 20.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RL

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

Abdominal discomfort Anxiety Asthenia Blood thyroid stimulating hormone increased Chest discomfort Computerised tomogram Decreased appetite Defaecation urgency Depression Discomfort Dizziness Electric shock sensation Electrocardiogram normal Full blood count normal Heart rate increased Hyperhidrosis Metabolic function test normal Pain

Symptomtext

Four days post-vaccination, had "jolts" to left side of chest during sleep, waking up multiple times in the evening. Morning after had heart palpitations and increased heart rate. Urgent Care visit with recommendation and subsequent visit to ER. ER visit ran routine labs and EKG, follow up with PCP recommended. After initial ER visit, two subsequent ER visits, two primary care visits, two urgent care visits. Symptoms include chest palpitations and pressure, constant increased heart rate, sweaty palms and feet, hollowness in stomach feeling, decreased appetite, frequent urination and bowel movement urges, general discomfort and body ache, lightheadedness, and occasional weakness and tingling in limbs. As a result of these symptoms there has been a significant increase in anxiety and increase in depression. Treatment includes: Propranolol10MG as needed, Metroprolol 25MG once daily, and ClonzaePAM .5MG as needed. Symptoms remain and not fully managed. Tests are ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: October 25, 2022: ER -EKG, CBC, Metabolic Panel, X-Ray. Results: Normal October 29, 2022: ER - EKG, CBC, Metabolic Panel, TSH, Urinalysis. Results: Elevated TSH. November 7, 2022: ER -EKG, CBC, Metabolic Panel, CT with and without contrast, TSH. Results: Normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Bupropion 150MG; Daily multi-vitamin.
Allergien: No
Vorherige Impfungen: -

VAERS 2497904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: IL
Alter: 6,0
Geschlecht: M
Eingang: 03.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Immediate post-injection reaction Seizure

Symptomtext

Seizure occurred about 5 minutes after receiving vaccination. Seizure lasted about 10 seconds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Ear infection
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2496850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: FL
Alter: 98,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Aggression Altered state of consciousness Seizure Troponin increased

Symptomtext

Seizure activity, aggressive behavior, change in LOC, sent to hospital via EVAC for evaluation and treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Troponin levels elevated / hospital reporting diagnosis as MI
Aktuelle Erkrankungen: COVID-19 (U07.1) on 9/9/22/Resolved on 9/19/22.
Vorgeschichte: DIFFICULTY IN WALKING, NOT ELSEWHERE CLASSIFIED (R26.2), MUSCLE WEAKNESS (GENERALIZED) (M62.81), ABNORMAL POSTURE (R29.3), COGNITIVE COMMUNICATION DEFICIT (R41.841), MUSCLE WEAKNESS (GENERALIZED) (M62.81), OTHER ABNORMALITIES OF GAIT AND MOBILITY (R26.89), HYPERLIPIDEMIA, UNSPECIFIED (E78.5) 3, MAJOR DEPRESSIVE DISORDER, SINGLE EPISODE, UNSPECIFIED (F32.9), REPEATED FALLS (R29.6) UNSPECIFIED DEMENTIA, UNSPECIFIED SEVERITY, WITHOUT BEHAVIORAL DISTURBANCE, PSYCHOTIC DISTURBANCE, MOOD DISTURBANCE, AND ANXIETY (F03.90)
Andere Medikamente: Acetaminophen Tablet 325 MG Give 2 tablet by mouth every 4 hours as needed, busPIRone HCl Tablet 5 MG Give 0.5 tablet by mouth every morning and at bedtime for anxiety, Colace Capsule 100 MG (Docusate Sodium) Give 1 capsule by mouth as need
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2493276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: WA
Alter: 17,0
Geschlecht: F
Eingang: 28.10.2022
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: ja

Altered state of consciousness Blindness Dizziness Loss of consciousness Pallor Presyncope

Symptomtext

Patient had a vasovagal vaccine reaction one minute after the vaccine was given. She started feeling dizzy and lightheadedness about half a minute after receiving the vaccine while seating down. I noticed her face color started to fade and turning to pale while, then began losing consciousness while seating down. I immediately called 911 and paramedics came within 5 minutes to check on patient. While waiting for paramedics to come, I noticed patient coming in and out of consciousness. She was able to verbal that she could not see but was breathing okay and able to make conversation with me and her mom. Paramedics came and checked vitals and made sure she was okay before they left. Vital signs were BP:108/78 mmHg, HR 78 bpm and Oxygen saturation 98%. The entire time from start to finish is about 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Vitals: BP: 108/78 mmHg, HR 78 bpm and Oxygen Saturation 98%
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2492020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: IL
Alter: 22,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Seizure

Symptomtext

Had seizure after 4 mins

Weitere VAERSDATA-Felder

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

VAERS 2491580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MN
Alter: 81,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 25.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Computerised tomogram head normal Seizure like phenomena

Symptomtext

Seizure like activity in nursing home transferred to ED where stroke was ruled out and transferred to a higher level of care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: CT on 10/27/2022
Aktuelle Erkrankungen: UTI - treated with Augmentin
Vorgeschichte: Dementia, depression, psychotic disorder with delusions, alzheimers, dysuria, angina, xerosis cutis, urinary retention, calculus of kidney, pulmonary edema, pain, shortness of breath, sleep apnea, COPD, benign prostatic hyperplasia. heart disease, GERD, anemia, osteoarthritis
Andere Medikamente: Abilify, Tylenol, Amitriptyline, Atorvastatin, Augmentin, Bisacodyl, Chlorthalidone, Citalopram, Donepezil, Finasteride, Glimepride, Humilin, Ibuprofen, Lasix, Loperamide, Losartan, Metformin, Metoprolol, Namenda, Norvasc, Multivitamin, Pan
Allergien: ambien
Vorherige Impfungen: -

VAERS 2486362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj6665

schwer

Staat: IN
Alter: 46,0
Geschlecht: M
Eingang: 22.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fall Loss of consciousness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Additional Details: Patient received the flu shot, then the pfizer vaccine, afterward he slowly fell forward and pased out for a few seconds. He then regained consciouness. His wife came in and calmed him down, EMS on the way, it was discovered he has a history of panic attacks. He declined going to the ER.

Weitere VAERSDATA-Felder

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

VAERS 2483109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MA
Alter: 16,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 15.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: PATIENT FAITED AFTER VACCINE ADMIN, HIT HEAD IN PHARMACY, TAKEN BY AMBULANCE TO EMERGENCY ROOM

Weitere VAERSDATA-Felder

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

VAERS 2483016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: PA
Alter: 15,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Blood glucose normal Disorientation Laboratory test Loss of consciousness Muscle rigidity Tonic clonic movements Urinary incontinence

Symptomtext

Patient lost consciousness, had tonic clonic movements of both upper extremeties and whole body rigidity, lost bladder control. Woke up after approx 30 seconds disoriented to time and place. Evaluated by pharmacist and paramedics. Transported to Hospital of via private vehicle per paramedic response team. Per father, patient evaluated with several tests in the emergency department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood sugar normal, other tests done at Hospital per father.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: syncope after several different vaccines

VAERS 2482217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge ##GJ6665

schwer

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 05.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Alanine aminotransferase Aspartate aminotransferase Blood calcium Blood creatine phosphokinase Blood magnesium Blood phosphorus Blood thyroid stimulating hormone Brain natriuretic peptide Differential white blood cell count Dyspnoea Electrocardiogram Full blood count Heart rate increased Laboratory test Lipase Muscle spasms Palpitations Pericarditis

Symptomtext

Rapid heartrate, pounding heartbeat for 2+ hours, shortness of breath, tongue swelling and severe muscle cramps in legs on Sunday, October 9, 2022. Admitted to local Emergency Room on Sunday, Oct. 9th and diagnosed with pericarditis. Treatment is rest and colchicine 0.6 mg 2x daily. Adverse event occured 4 days after Pfizer-Bivalent vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Testing in local Emergency Room on October 9th/10th: Troponin, EKG, Ultrasound, COVID (negative), magnesium, phosphate, CBC, white blood cell differential, AST, ALT, lipase, creatine kinase, TSH, BNP, Calcium, chemistry panel, prothrombin time
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Brimonidine Tartrate Ophthalmic Solution, Latanoprost Ophthalmic Solution
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2479720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

schwer

Staat: FL
Alter: 34,0
Geschlecht: M
Eingang: 16.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Hypotension Orthostatic hypotension Presyncope Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Additional Details: Patient experienced vasovagal response to covid booster vaccine dose which resulted in fainting for a few minutes. BP was monitored during episode and patient's caregiver requested to call 911. The paramedics came and checked bp which showed orthostatic hypotension. Patient was trasporoted to ER. Pt was followed up by the pharmacist, and informed by a patient that pt was discharged with 2 hours with all vitals back to normal. Patient is back to work the next day.

Weitere VAERSDATA-Felder

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

VAERS 2479654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

schwer

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 16.10.2022
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: ja Erholt: nein

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Additional Details: mom arrived to store in the evening claiming her son was vaccinated earlier that day and not told to wait after immunizing. The son, then left after being immunized and fell/fainted outside, ambulance was called, and the pt was injured (facial/skull fracture) per mom.

Weitere VAERSDATA-Felder

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

VAERS 2479648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

schwer

Staat: MA
Alter: 15,0
Geschlecht: M
Eingang: 16.10.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 2479615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 09.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Dizziness Myalgia Nausea Syncope

Symptomtext

Some soreness in the muscle for 24 hrs. Light-headed, nausea and fainted ~18 hrs. after the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None done.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Venlafaxine 75 mg, Rovustatin 10 mg, Vitamins, Calcium/Vit D.
Allergien: Vancomycin, Amoxicillin
Vorherige Impfungen: -

VAERS 2478322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 10.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: He was receiving two vaccine one for flu and other for bivalent covid pfizer vaccine. He got flu shot first and then when I administer the covid pfizer bivalent shot on other arm upon administration he fainted to the floor and was unresponsive for like 15 seconds

Weitere VAERSDATA-Felder

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

VAERS 2477976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: AZ
Alter: 12,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

On 10-13-22 at 4 pm patient received Pfizer-BioNTech Bivalent and tolerated that without adverse affects. Then after receiving Fluarix, patient fainted in chair. Patient did not lose consciousness. Patient's mother assisted pharmacist and confirmed she was ok. Patient stayed in sitted position with normal function of arms and legs. Patient's breathing was normal. Patient, mother, and sister were supporting patient by laughing and talking about how the patient in the past year has become more fearful of vaccines. Patient was able to stand on her own and walk without any help. Patient and mom did not have any concerns or requests. Patient care call was placed at 454 pm and 620 pm on 10-13-22 but no answer by the mother. Mother stated they were late for dinner and the opera. As of closing 10-13-22 no call back from patient/parent.

Weitere VAERSDATA-Felder

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

VAERS 2470291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

schwer

Staat: OR
Alter: 66,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 04.10.2022
Beginn: 05.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / -

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

Dizziness Muscle spasms Musculoskeletal stiffness Presyncope

Symptomtext

LIght headed - almost fainted. This lasted for about 10 minutes. I sat down and felt better a bit later. Cramping / stiffness in my right thumb that lasted for several minutes. Then after that, I had cramping / stiffness in my left index finger that lasted for several minutes. No pain, just could not move my fingers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep apnea, high blood pressure; pre-diabetes, high cholesterol
Andere Medikamente: Metformin 500mg; Irbesartan 300mg; Simvastatin 20mg; Vitamin D; Vitamin B12
Allergien: None
Vorherige Impfungen: -

VAERS 2716141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 21.11.2023
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Chills Cough Diarrhoea Lip swelling Paraesthesia Periorbital oedema Swelling face Vomiting

Symptomtext

TINGLING IN FACE AND ARMS, PERIORBITAL EDEMA, NEXT DAY FACIAL SWELLING, COUGH, VOMITING, DIARRHEA, CHILLS, LIPS FELT SWOLLEN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish oil, Vit D, Baby ASA, B complex
Allergien: Amoxicillin
Vorherige Impfungen: FACE TINGLING, 58 years old, 02/14/2022, PFIZER BIONTECH

VAERS 2712473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 10.11.2023
Impfdatum: 25.10.2022
Beginn: 03.09.2023
Tage bis Beginn: 313,0
Dosis: 4
Route/Site: - / -

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

Asthenia Balance disorder Blood alkaline phosphatase increased Blood bicarbonate normal Blood creatinine increased Blood lactic acid normal Blood pH increased Blood urea increased COVID-19 COVID-19 pneumonia Carbon dioxide increased Cough Fall Fatigue Head injury Leukocytosis Leukopenia Normocytic anaemia

Symptomtext

BRIEF OVERVIEW: Admission Date: 9/3/2023 Discharge Date: 09/08/2023 Discharge Disposition: home or self care DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Sepsis [A41.9] Multiple falls [R29.6] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is an 81-year-old male with history of T2DM, CKD and gastric B-cell lymphoma s/p radiation and now on alkylating chemotherapy presenting following a witnessed fall from home and found to have vital sign derangements concerning for sepsis secondary to COVID-19. Patient reported several months of functional decline with worsening generalized weakness (worse in lower extremities), balance issues, and fatigue. He has fallen several times in the last few weeks, never with loss of consciousness or severe head trauma. Timeline of symptoms is consistent with his chemotherapy regimen, which was initiated in March 2023. He has received 5 cycles of Bendamustine and Rituxan but had brief hiatus in August due to persistently low ANCs. Last cycle was two weeks ago. On 9/3, the patient had a fall and hit the back of his head against the bathroom wall. He did not lose consciousness. Wife encouraged him to be seen in the ED. His vital signs were mildly deranged, including tachycardia around 110 and tachypnea around 23, along with one-time fever of 39.5C. blood gas demonstrating partially compensated respiratory alkalosis with pH of 7.53, CO2 of 31 calculated bicarbonate of 26. Covid-19 PCR was positive. Chemistry was remarkable for elevated BUN and creatinine, though his renal labs have been variable lately, as well as an elevated alkaline phosphatase of 189. Complete blood count demonstrated stable normocytic anemia and normal white cell count with some neutrophilic predominance by differential; however, in the setting of very low ANC last month, this was seen as an acute leukocytosis (should be noted that the patient did receive peg-filgrastim in August 2023 for leukopenia that was holding up his chemotherapy). Because of the concern for sepsis in the setting of SIRS positivity, LA was obtained and was WNL. He was admitted to the hospital for further evaluation by his oncology providers and supportive management for his COVID-19 infection. In the inpatient setting, the patient's vitals normalized shortly after time of admission. He was stable throughout his stay, with no desaturations or oxygen requirement and minimal symptoms limited to a dry cough and persistent chronic feeling of weakness. He was evaluated by PT and OT, who recommended inpatient rehab facility transfer at time of discharge. He was also seen by Hematology/Oncology, who recommended trending CBC during admission and outpatient follow-up to discuss feasibility of continuing chemotherapy. He was discharged home in stable condition on 9/8 after finishing his course of IV remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: B-cell lymphoma of extranodal site Gastric lymphoma Macrocytic anemia Acute blood loss anemia Type 2 diabetes mellitus, without long-term current use of insulin Acute GI bleeding Essential hypertension Folate deficiency Unspecified severe protein-calorie malnutrition Enlarged prostate with lower urinary tract symptoms (LUTS) Iliac artery stenosis, right Elevated alkaline phosphatase level Thrombocytopenia Stage 3a chronic kidney disease
Andere Medikamente: atorvastatin (LIPITOR) 20 mg tablet candesartan (ATACAND) 8 MG tablet folic acid (FOLVITE) 1 mg tablet JANUVIA 50 MG tablet JARDIANCE 25 MG tablet metFORMIN-XR (GLUCOPHAGE-XR) 500 MG extended release 24 hr tablet pantoprazole (PROTONIX) 40
Allergien: MetforminDiarrhea
Vorherige Impfungen: -

VAERS 2689978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 03.10.2023
Impfdatum: 02.11.2022
Beginn: 16.09.2023
Tage bis Beginn: 318,0
Dosis: N/A
Route/Site: IM / LA

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

Asthenia COVID-19 COVID-19 pneumonia Dizziness Dysstasia Fall Hypoxia Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient was brought to the ED by EMS on 9/16/23 after sustaining a fall. He was getting up to use the bathroom, felt dizzy, and fell. He was unable to get up due to generalized weakness. His daughter, who he lives with, called EMS. In the ED, he was found to have hypoxia to 90% and fever to 100.4 F. A rapid COVID PCR test performed in the ED resulted positive. He was put on supplemental O2. Ultimately, the patient was admitted 9/16/23 - 9/18/23, with discharge diagnosis including COVID 19 pneumonia. During his admission, he was able to wean off supplemental oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2687256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 27.09.2023
Impfdatum: 28.10.2022
Beginn: 12.09.2023
Tage bis Beginn: 319,0
Dosis: N/A
Route/Site: UN / UN

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

COVID-19 Cough Decreased appetite Dyspnoea Dyspnoea exertional Ear pain Headache Oropharyngeal pain Rash Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

The patient has a history of stage III kidney disease and diet-controlled diabetes. She was seen in the ED on 9/12/23 for three weeks of congestion, sore throat, cough, and loss of appetite. She additionally endorsed shortness of breath on exertion, headache, right ear pain, a rash that started 6 days ago. In the ED, a COVID-19 PCR test was done which resulted positive. Ultimately, she was admitted 9/12/23 - 9/15/23 for COVID-19 infection, among other diagnoses. Of note, the patient has received the primary COVID vaccine series and two boosters.

Weitere VAERSDATA-Felder

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

VAERS 2607562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: OK
Alter: 53,0
Geschlecht: M
Eingang: 06.09.2023
Impfdatum: 11.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: SYR / RA

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

Amnesia Anxiety Burning sensation Cardiac disorder Cardiac monitoring Brain scan abnormal Feeling hot Laboratory test Loss of control of legs Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Feeling abnormal Headache Heart rate increased Hypertension Hypoaesthesia

Symptomtext

He had a Transient Ischemic Attack which lasted an hour and thirty minutes. He was rushed to the Medical Center Hospital for evaluation and then sent to City for further evaluation. He woke up that Thursday morning feeling different and stated that he couldn't move his left arm and leg. We dialed 911 and he was rushed in the ambulance to the hospital where he had several test. They include an CAT scan, MRI, EKG, TEE, and other physical exams. Since the TIA I have been experiencing severe breathing issues, severe headaches, anxie issues and lack of sleep, heart problems, body aches from head to toe, and I'm taking several different medications. These medications include Apixaban, Amlodipine, Aspirin, Atorvastatin, Plavix, Amoxicillin, Docusate, and others. He has also had the Intelliheart monitors sent to our house and had to wear them for 30 days to rule out AFIb. Before the the stoke, after retiring he worked out everyday, now he is limited to walking around the block 1 to 2 times a week. Since having the Trans Ischemic Attack, he has been to the ER 6 times for symptoms related to the stroke, those symptoms include rapid heart rate, headaches, insomnia and anxiety, high blood pressure, numbness and tingling in his left shoulder and arm, plus burning sensations all throughout his head. He has also experienced short term and long term memory loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2607562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: OK
Alter: 53,0
Geschlecht: M
Eingang: 06.09.2023
Impfdatum: 11.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 16,0
Dosis: UNK
Route/Site: IM / LA

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

Amnesia Anxiety Burning sensation Cardiac disorder Cardiac monitoring Brain scan abnormal Feeling hot Laboratory test Loss of control of legs Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Feeling abnormal Headache Heart rate increased Hypertension Hypoaesthesia

Symptomtext

He had a Transient Ischemic Attack which lasted an hour and thirty minutes. He was rushed to the Medical Center Hospital for evaluation and then sent to City for further evaluation. He woke up that Thursday morning feeling different and stated that he couldn't move his left arm and leg. We dialed 911 and he was rushed in the ambulance to the hospital where he had several test. They include an CAT scan, MRI, EKG, TEE, and other physical exams. Since the TIA I have been experiencing severe breathing issues, severe headaches, anxie issues and lack of sleep, heart problems, body aches from head to toe, and I'm taking several different medications. These medications include Apixaban, Amlodipine, Aspirin, Atorvastatin, Plavix, Amoxicillin, Docusate, and others. He has also had the Intelliheart monitors sent to our house and had to wear them for 30 days to rule out AFIb. Before the the stoke, after retiring he worked out everyday, now he is limited to walking around the block 1 to 2 times a week. Since having the Trans Ischemic Attack, he has been to the ER 6 times for symptoms related to the stroke, those symptoms include rapid heart rate, headaches, insomnia and anxiety, high blood pressure, numbness and tingling in his left shoulder and arm, plus burning sensations all throughout his head. He has also experienced short term and long term memory loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2667665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 08.08.2023
Impfdatum: 18.11.2022
Beginn: 21.07.2023
Tage bis Beginn: 245,0
Dosis: 1
Route/Site: - / -

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

Asthenia Blood pressure increased Bronchitis COVID-19 Chest X-ray normal Clostridium difficile infection Clostridium test positive Condition aggravated Cough Diabetic diet Diarrhoea Glycosylated haemoglobin normal Mobility decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient is a 78 y.o. male with PMH HTN, CKD, Prior CVA who presented from home on 7/21/2023 with generalized weakness due to COVID infection. He had a positive home test on 7/21, he subsequently was started on Paxlovid which he completed a total of 3 days. He remained stable on RA, not requiring Oxygen therapy or steroids. Hospitalization was further complicated by profound diarrhea and pt was tested and found positive for C-diff. Started him on PO Vancomycin x10 days, diarrhea slowly improving. PT/OT followed and recommended SNF. COVID infection Acute Bronchitis - Presented with: frequent cough, weakness, and fevers; (unable to get out of bed). Came to the hospital after recommendation from PCP - Symptom onset: 7/20/2023 - Positive COVID-19: 7/21/2023 at home kit, not tested on admit; positive family members as well - Vaccination status: Vaccinated with Pfizer with last dose 11/2022 - CXR on admission showed non-acute - Oxygen status: stable on RA - Decadron: Does not qualify due to SpO2>94% on RA. - Remdesivir: Does not qualify due to SpO2>94% on RA. - Completed 3 day course of Paxlovid - DVT prophylaxis:Lovenox - Serial COVID labs ordered: No - Case Management/Social Services consulted: Yes; PT/OT following with plan for SNF at DC - continue good pulmonary hygiene/IS C-Diff - pt reporting multiple days and episodes of watery diarrhea - tested positive for C-diff - started on PO Vancomycin x10 days Hypertension - elevated - home regimen includes Procardia, Coreg, Clonidine, losartan - resume home regimen, with hold parameters CKD Stage 3b - stable; 1.29 - Gentle iv fluids on admit - Avoid nephrotoxic meds as able History of stroke with residual cognitive and balance deficits Secondary parkinsonism - One in 2017 and one in 2021. Has ambulatory dysfunction since then and top of that patient has parkinsonism. -Continue Sinemet, rivastigmine, aspirin and statin Diabetes mellitus type 2 - A1c 6.4 -Diet controlled. Previously on Tresiba, metformin which have discontinued. - start SSI, monitor and adjust as needed - ADA diet at DC History of PE Chronic right lower extremity DVT -Treated with anticoagulation in the past - Lovenox for vte proph while here Hemochromatosis - per history; Follows with Ohio State hematology - Phlebotomy in the past. - monitor CBC daily Anxiety/depression - Continue home dose Celexa and Wellbutrin Vascular Dementia - Follows with Neurology - resume OP management Generalized Weakness Reduced mobility, PTA - In setting of known Parkinson's, now exacerbated by Covid infection - At baseline he uses a walker and is able to go up stairs (bedroom on 2nd floor of house) -On day of admit, was unable to get out of bed by himself - PT/OT recommending SNF at DC

Weitere VAERSDATA-Felder

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

VAERS 2664187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 01.08.2023
Impfdatum: 20.06.2023
Beginn: 21.06.2023
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Altered state of consciousness Condition aggravated Eye pruritus Eye swelling Irritable bowel syndrome Lip swelling Malaise Nervousness Neurological symptom Somnolence

Symptomtext

She got her vaccine, no reaction for the first time ever, no reaction, felt fine all day on the 20th, even her arm was fine. She woke up on 6/21/23 was fine, but by midday her lips were swollen, her eyes were swollen and itchy. She had not taken any NSAIDS and had not had any mangos. She had the classic symptoms she gets. She took a Claritin that night and by the next morning the symptoms were gone. She did not feel well on 6/22/23 and had an odd neurological reaction, had an altered state of consciousness, not a stroke or a TIA, did not loose consciousness, but it was odd. She felt like she was in two realities at the same time that lasted about 7 minutes. She was continuing to talk and acted normally. She did mention it to her neurologist, and it was like an aura. She did not feel well for the entire month, incredibly drowsy where she just wanted to sleep all the time. Her IBS symptoms were worse, which was normal give the circumstances. This makes her nervous about getting another one, but probably will.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: IBS flare.
Vorgeschichte: IBS.
Andere Medikamente: Prilosec, Lopressor. Injection day before of Ajove. Doxepin, Mirilax, Prevastatin
Allergien: NSAIDS, Mangos.
Vorherige Impfungen: Always gets sick, feeling like she has the flu for a few days, but this was different.

VAERS 2644346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: WA
Alter: 52,0
Geschlecht: M
Eingang: 12.06.2023
Impfdatum: 09.12.2022
Beginn: 11.01.2023
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: SYR / RA

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

Abdominal discomfort Abdominal pain upper Appendicectomy Appendicitis perforated Computerised tomogram abdomen abnormal Infection Mobility decreased Sensory disturbance

Symptomtext

On 10Jul2023 about 9PM, I felt like I had an air bubble in my stomach like I needed to pass gas. It was slowly getting uncomfortable, the longer I sat there the more it got uncomfterble. I layed down I felt better, I layed there for 2 hours it kept getting worsts it was so painful I couldn't get up. I went to the hospital and they found out I had appendix, that ruptured and was leaking inside of me. They did surgery and cleaned out the infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 21FEB2023- CT Scan- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2644208

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GJ6665

moderat

Staat: TX
Alter: 71,0
Geschlecht: M
Eingang: 12.06.2023
Impfdatum: 12.06.2023
Beginn: 12.06.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Blood test abnormal Hypoaesthesia Laboratory test normal Pain Paraesthesia Rheumatoid arthritis Sleep disorder

Symptomtext

Started to be awakened at night with numbness is different parts of my body. Sometimes sharp pains and sometime tingling. I have never experienced anything like that before and just waited for several months thinking it would go away. I went to my doctor and he suggested it was carpel tunnel and then saw my pain management doctor and he suggested the same thing. I had the test and it was determined that it was not carpel tunnel. My Primary doctor then did blood work and the work came back with a marker. I was then sent to see Dr. She started me on Methotrexate and folic acid. After about 6 months, at the third visit Dr. told me I have Rheumatoid Arthritis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Osteo arthritis knee replacement
Andere Medikamente: Fish Oil Citrizine Simvastatin Lisinopril Metoprolol Centrum Silver Tizanidine
Allergien: None
Vorherige Impfungen: -

VAERS 2641233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: OH
Alter: 50,0
Geschlecht: M
Eingang: 05.06.2023
Impfdatum: 30.11.2022
Beginn: 08.12.2022
Tage bis Beginn: 8,0
Dosis: 5
Route/Site: IM / AR

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

Arthralgia Bedridden Blood creatinine increased Blood pressure increased Blood test COVID-19 Chills Chronic kidney disease Cough Dyspnoea Fatigue Glomerular filtration rate Headache Hypertension Impaired work ability Myalgia Nasal congestion Oropharyngeal pain

Symptomtext

On 12/8/2022 at about 7-8 PM, I began to have a scratchy, sore throat. At around 6:30 AM on 12/9/2022, I woke up with a fever, chills, muscle aches, joint pain, headache, and nasal congestion. I then took a home antigen test and got a positive result. At 11:25 AM the same day, I also underwent a PCR test, and I got a positive result back on 12/10/2022. At this time, I began taking PAXLOVID. Later in the evening on 12/9/2022, I developed chest congestion and cough. On 12/10/2022, my symptoms continued to worsen, and I had some difficulty breathing. It was around this time that I began the PAXLOVID therapy. I was bedridden on 12/10/2022 and 12/11/2022. On 12/12/2022, my symptoms began to lessen. On 12/14/2022, I finished taking the PAXLOVID. By 12/15/2022, my symptoms had resolved. I was out of work between 12/9/2022 and 12/15/2022. On 12/16/2022, I did remote work. On 12/19/2022, I was able to return to the office. Sometime in January 2023, I began to develop mild hypertension. My blood pressure reading was around 130/80; before then, it was usually 120/70. By April 2023, it had increased to 150/90. On 4/19/2023, it was 170/100. At that time, my PCP did bloodwork. Everything was within range, except my serum creatinine had risen to 1.34, with a GFR of 64.5. My PCP then prescribed me losartan/HCT (50-12.5). In March-April 2023, I began to experience chronic fatigue and vascular headache. Despite having normalized blood pressure after beginning the losartan/HCT, I have continued to have chronic fatigue and vascular headache. As a result, on 5/25/2023, my PCP repeated bloodwork. My serum creatinine had risen to 1.41, and my GFR had dropped to 60.3. Because of that, I underwent a renal ultrasound on 5/31/2023, with additional testing. My PTH was notably elevated at 154.2. This means that I have now have chronic kidney disease, stage 2. I have a nephrology appointment in a few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09DEC2022 home antigen test, positive result; 09DEC2022 PCR test, positive result; JAN2023 Blood Pressure Reading 130/80; APR2023 Blood Pressure Reading 150/90; 19APR2023 Blood Pressure Reading 170/100; APR2023 Bloodwork, Serum Creatinine Elevated to 1. 34, GFR at 64.5; 25MAY2023 Bloodwork, Serum Creatinine Elevated to 1.41, GFR Dropped to 60.3; 31MAY2023 Renal Ultrasound, with additional testing, PTH Elevated at 154.2, Chronic Kidney Disease (Stage 2) indicated
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines; Enlarged Prostate; High Cholesterol; Chronic Depression; Insomnia
Andere Medikamente: EMGALITY injection; atorvastatin; finasteride; trazodone; VIIBRYD; vitamin D3; CLARITIN
Allergien: Fluoroquinolones; seasonal allergies (mainly grass)
Vorherige Impfungen: -

VAERS 2640980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 05.06.2023
Impfdatum: 29.11.2022
Beginn: 04.05.2023
Tage bis Beginn: 156,0
Dosis: 5
Route/Site: - / -

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

Asthenia COVID-19 Confusional state Failure to thrive Malaise Pneumonia SARS-CoV-2 test positive

Symptomtext

Discharge Provider: DO Primary Care Provider: MD Admission Date: 5/4/2023 Discharge Date: 5/11/2023 Clinical Narrative: 77 y/o M admitted for Pneumonia, failure to thrive, and increased confusion. He is debilitated with Parkinson's disease and has mild dementia and is cared for by his stepdaughter who noted increasing weakness. Patient tested + for COVID on admission, but has been sick for a several days prior to admission. The patient completed antibiotics prior to discharge. His discharge was held due to policies in Nursing Homes accepting patient's with COVID positivity. Facility was able to accept him on 5/11. He was medically stable for discharge. He will have SAR at the facility with eventual LTC placement to be determined by family and ECF and primary care staff. He has a vitamin B1 level to assess reversible causes of dementia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: 11/15/2022 - 11/18/2022 (3 days) HOSPITAL Debility Principal problem
Vorgeschichte: CLL (chronic lymphocytic leukemia) BPH with obstruction/lower urinary tract symptoms Essential hypertension GERD (gastroesophageal reflux disease) Polycythemia Normocytic anemia Parkinsonism Asymptomatic hyperuricemia Anemia Debility Moderate dementia Dysphagia Decreased oral intake Protein-calorie malnutrition, moderate
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet allopurinol (ZYLOPRIM) 300 mg tablet ascorbic acid (VITAMIN C) 1000 MG tablet aspirin EC 81 MG enteric coated tablet benztropine (COGENTIN) 0.5 MG tablet bisacodyl (DULCOLAX) 10 MG suppository calcium c
Allergien: None
Vorherige Impfungen: -

VAERS 2639042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CT
Alter: 59,0
Geschlecht: F
Eingang: 31.05.2023
Impfdatum: 29.11.2022
Beginn: 08.05.2023
Tage bis Beginn: 160,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Dyspnoea Ear discomfort Fatigue Feeling cold Nasal congestion Oropharyngeal pain Panic attack Pyrexia Rhinorrhoea SARS-CoV-2 test positive Streptococcus test

Symptomtext

I was feeling really cold and was having chills then was so tired that I just laid down on the floor. My nose started running and also got stuffed up. I then started having a fever and then having a sore throat, with pressure in my ears. Thursday, I woke up and I could not breath and this brought on a panic attack, and I went into the clinic and there they tested me for Strep and COVID-19 and I was positive for COVID-19. They gave me an inhaler and put me on Paxlovid as well. I did have the weird metal taste taking the Paxlovid, bad diarrhea and my stomach hurt, on Saturday I was not able to walk. It was like my legs did not work and I had to learn how to walk again, and my symptoms had not improved, and I went back to the clinic and learned this was common with the Paxlovid. I have tested negative, but I am still tired and fatigued,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 PCR Test; Strep Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Thyroid Issues
Andere Medikamente: Multivitamin; Omega Three; Vitamin C; Liothyronine; Levothyroxine
Allergien: Keflex
Vorherige Impfungen: -

VAERS 2636184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 08.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Bacterial infection Headache Malaise Mobility decreased Nasal disorder Pain in extremity Paranasal sinus discomfort Respiratory tract congestion Sinus headache Sinusitis Sputum discoloured Toothache

Symptomtext

I got the sore arm the evening of the vaccine, and on 11/09/2022, I had a headache about a day and a half after the vaccine. Pain scale would have been a 5 for my headache. And then for the sinus infection, on 11/08/2022, I got a sore tooth on the left upper molar from the pressure of the sinus right above it. And a lot of colored mucous, stuffy head, headaches, just not feeling well, just staying in bed and the chair kind of day, and it lasted about 3 weeks. I did get medication after 10 days. It was definitely a bacterial infection. I had that sinus headache. I got a couple of sores in my nose. They gave me amoxicillin and mupirocin an antibiotic ointment to use in my nose for my sores. The doctor told me after 10 days, they assume it is a bacterial infection. Within 24 hours of taking the amoxicillin I felt a whole lot better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Sixth Nerve Palsy on my Left Eye; High Blood Pressure; High Cholesterol; Arthritis
Andere Medikamente: Meloxicam; atenolol; simvastatin; losartan; ketotifen fumarate eye drops; magnesium; calcium; ALVESCO inhaler; multivitamin; vitamin D3
Allergien: Codeine; oxycodone; all pollen; walnuts; pecans
Vorherige Impfungen: -

VAERS 2636128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 06.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: SYR / UN

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

Blood test Chronic respiratory disease Computerised tomogram Dyspnoea Pneumonitis Pulmonary function test Pulmonary mass

Symptomtext

I had vaccination on 12/06/2022. On 12/10/2022 I started experience shortness of breath and I went to urgent care. I was diagnosed with chronic inflammatory lung disease. I was prescribed steroids. I had a follow up appointment in 03/2023 and had testing. I was diagnosed with nodules on my lungs with possible emphysema. I am on an inhaler and medication to help with the shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 03/2023 CAT Scan Pulmonary Function Test Blood Panel
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism; Chronic Pain
Andere Medikamente: Zoloft; Thyroid medication
Allergien: N/A
Vorherige Impfungen: -

VAERS 2632428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: VA
Alter: 59,0
Geschlecht: F
Eingang: 16.05.2023
Impfdatum: 15.11.2022
Beginn: 18.04.2023
Tage bis Beginn: 154,0
Dosis: 5
Route/Site: SYR / LA

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

Aphonia Asthma Bronchitis Chest discomfort Condition aggravated Environmental exposure Exposure to fungus Hypersensitivity Oropharyngeal pain Passive smoking Pyrexia Respiratory fume inhalation disorder

Symptomtext

I had allergies and astmha about a month ago contributing factors were smoke inhalation and pollen humidity and mold cigarette smoke while on vaction. 07MAY2023 I had a sore throat and tightness in my chest loosing my voice on10MAY2023 I began to get a fever and thenI called my Doctor and saw him on 12MAY2023 Bronchitis was diagnosed and Doxycycline was prescribed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Astmha; Allergies
Andere Medikamente: Flonase; Advair; Albutrerol; Spironolactone; Doxicillin; Multivitamin; Methyl-Sulfonyl-Methane; Bone UP Clacium; Vitamin D
Allergien: Sulfa; Benzyl
Vorherige Impfungen: -

VAERS 2629229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 47,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 27.10.2022
Beginn: 12.11.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / RA

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

Blood test abnormal Dyspnoea exertional Fatigue Haematocrit Haemoglobin Iron deficiency Laboratory test Mobility decreased Muscular weakness Serum ferritin decreased

Symptomtext

A few weeks after COVID booster on 10/27/22, I started developing extreme leg weakness and fatigue, some shortness of breath while running and walking/climbing hills and stairs. Thought it was just side effects but symptoms persisted to the point I had to stop mid-run, legs were extremely weak, could barely move them. Got a full set of bloodwork done beginning of December 2022, diagnosed with severe iron deficiency - ferritin was 2. Started ferrous sulfate 375 mg every other day, mid-March 2023 had repeat blood work, labs improved. Will get repeat blood work done in June 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: low ferritin, hgb, hct
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: over the counter B12 2500 mcg/week
Allergien: none
Vorherige Impfungen: -

VAERS 2628361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 08.05.2023
Impfdatum: 27.10.2022
Beginn: 12.04.2023
Tage bis Beginn: 167,0
Dosis: 5
Route/Site: - / -

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

Asthenia COVID-19 Cardiac failure Cellulitis Chronic obstructive pulmonary disease Condition aggravated Erythema Hyperkalaemia Metabolic function test SARS-CoV-2 test positive Swelling Vessel puncture site erythema Vessel puncture site swelling

Symptomtext

Discharge Provider: Primary Care Provider at Discharge: Admission Date: 4/12/2023 Discharge Date: 4/19/2023 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness [R53.1] COVID-19 [U07.1] HOSPITAL COURSE: The patient is a 69-year-old gentleman who presented the hospital complaints of weakness. The patient has multiple recent hospitalizations related to heart failure and chronic obstructive pulmonary disease exacerbation. Patient on presentation was stable from a respiratory standpoint but was noted to be testing positive for COVID-19. Patient's respiratory status remained stable throughout his hospitalization. No medication intervention was necessary related to patient's COVID-19. Patient was noted to have significant weakness during his hospitalization. Recommendations from physical and occupational therapy were for the patient to be sent for subacute rehab. Despite our recommendations and our concern for his ability to care for himself at home, the patient's insurance company did not authorize financial coverage for subacute rehab. Subsequent plan is to discharge patient home with home health services. During the patient's hospitalization he was noted to have some significant hyperkalemia. Patient's home Cozaar and Aldactone along with supplementary potassium were placed on hold. Patient's blood pressure remained stable and in an appropriate range without administration of Cozaar and Aldactone. Cozaar, Aldactone, and supplementary potassium are being held at discharge. Recommend a repeat BMP in follow-up. Additionally, the patient was noted to have erythema and swelling surrounding his IV site. Concern was noted for possible cellulitis. Patient was started on IV doxycycline and had significant improvement of traced area of erythema. Patient will be discharged home to complete a 1 week antibiotic course for suspected cellulitis of the left antecubital space. Patient is felt to be in stable condition at this time and is being discharged home with home health services

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: Ongoing Treatment of bilateral venous stasis ulcers 9/22/2022
Vorgeschichte: OSA (obstructive sleep apnea) CPAP/BiPAP dependent Morbid obesity DM type 2 (diabetes mellitus, type 2) HTN (hypertension) Restless leg syndrome Diabetic neuropathy Venous stasis ulcers of both lower extremities Venous stasis ulcer of left calf limited to breakdown of skin with varicose veins Venous stasis dermatitis of both lower extremities AKI (acute kidney injury) CHF (congestive heart failure), NYHA class II, chronic, diastolic Generalized weakness COVID-19 Iron deficiency anemia Atrial fibrillation Chronic left shoulder pain Leukocytosis Cellulitis Cellulitis of right lower extremity Thrombocytosis
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler benzonatate (TESSALON) 100 MG capsule budesonide/formoterol
Allergien: Ace InhibitorsCough Cefzil [Cefprozil] Theophylline
Vorherige Impfungen: -

VAERS 2624726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MO
Alter: 85,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 22.10.2022
Beginn: 07.04.2023
Tage bis Beginn: 167,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia COVID-19 pneumonia Fatigue Respiratory tract congestion

Symptomtext

Congestion, fatigue, weakness, COVID pneumonia. Hospitalized 04/07/203.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 8,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Cardiac pacemaker/defibrillator, diabetic, kidney disease.
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2624092

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 19.10.2022
Beginn: 24.03.2023
Tage bis Beginn: 156,0
Dosis: 4
Route/Site: IM / LA

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

Bone pain COVID-19 Chills Fungal infection Headache Hypotension Influenza Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

/24/23 I had low blood pressure, body aches, my bones ached, headache, chills, runny nose, but no fever. I took an at home COVID test and it was positive. It felt like flu symptoms. I called my doctor. She prescribed Paxlovid which I began taking it that day. It helped with the symptoms, but I ended up with a yeast infection. The side effects of Paxlovid were a little rough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: 24MAR23-At Home COVID Test-Posistive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pantoprazole, Losartan Potassium, Amlodipine, Clopidogrel, Vitamin B12, Vitamin D3, Calcium Lactate, Pro Symbiotic, , Multi Zyme, Zyrtec
Allergien: None
Vorherige Impfungen: -

VAERS 2623967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MO
Alter: 62,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 25.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: IM / LA

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

Arthritis Condition aggravated Pain Pain in extremity Peripheral swelling

Symptomtext

It seems like my arthritis pain has seemed to have gotten worse, especially in my feet, I thought I had broken my toe, it was swelling, I could not wear shoes, I had to but wide shoes to even be able to wear shoes comfortably. I made an appointment with the doctor who performed an exam, she said it wasn't broken, but it did feel like arthritis was in the toe. She gave me steroid shot, advised me take ibuprofen when I had a flare. I issue is not as bad but my feet do still hurt me, it's not as intense but the pain is there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Amlodipine; Bupropion
Allergien: Corn Products
Vorherige Impfungen: -

VAERS 2623200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 11.10.2022
Beginn: 11.03.2023
Tage bis Beginn: 151,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Diarrhoea Dyspnoea Fatigue Pyrexia SARS-CoV-2 test positive

Symptomtext

On March 11, 2023, I tested positive for COVID-19. I called my doctor. On the next day I had a mild fever and was coughing. I had tightness in my breathing, so I had to get another prescription for inhaled steroids. I also began taking Paxlovid on March 12th. For three weeks I was fatigued and had to take naps every afternoon. After 3 weeks I did have diarrhea for about a week. I took probiotics and it was resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19, positive, 03112023
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Breast Cancer
Andere Medikamente: Levothyroxine; Zyrtec; Super B Complex; Baby Aspirin; Collagen; Anastrozole; Calcium; Singular; Simvastatin;
Allergien: Sulfa; Bananas; Iodine; Nickel
Vorherige Impfungen: -

VAERS 2622328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 27.04.2023
Impfdatum: 11.10.2022
Beginn: 26.03.2023
Tage bis Beginn: 166,0
Dosis: 5
Route/Site: - / -

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

Asthenia Benign prostatic hyperplasia COVID-19 Catheter placement Condition aggravated Constipation Fall Micturition urgency Muscular weakness SARS-CoV-2 test positive Urinary retention

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 3/26/2023 Discharge Date: Mar 29, 2023 PRESENTING PROBLEM: Weakness [R53.1] Generalized weakness [R53.1] Constipation, unspecified constipation type [K59.00] HOSPITAL COURSE: 83 y.o. male with past medical history significant for panhypopituitarism, dyslipidemia, anxiety and depression, hypertension, GERD, hypothyroidism who presented with complaints of generalized weakness, recurrent falls. Previously living with wife who felt she could no longer care for him. Fall on morning of presentation. Patient admitted for further care. Reviewing chart, patient has been seen for multiple visits in the movement Disorders Clinic. Possible diagnosis of Parkinson's disease however testing returned intermediate on imaging. Patient with noted lower extremity weakness. In movement Disorder Clinic had been offered repeat electromyogram to better determine etiology and at that time patient refused. PT/OT evaluated patient and recommended skilled nursing facility. Patient has also been followed by Urology in the outpatient setting. Noted urinary retention BPH and urinary urgency. Patient initially cathed with 1 L urine removed. Continue to require intermittent straight catheterization. Urology consulted and recommended: Have pt up to void every 3-5 hours. 1. If the patients voids check bladder scan as PVR and if PVR greater than the amount voided, then st. Cath. 2. If the patient does not void, check bladder scan and if scan is greater than 350 ml, then st. Cath. Try to keep total bladder volume (void + cath) less than 500 ml (between 350 and 500 ml). If it is more than 500 ml, perform above more frequently. Follow-up in clinic. Screening COVID test returned positive however patient had had recent COVID-19 infection at the beginning of the month that had resolved. Patient strongly desires to return home and feels that he is able to manage at home with help of wife and walker unfortunately as family is unable to care for patient will be transferred to skilled nursing. Consider returned to movement Disorders Clinic for rediscussion on electromyogram to determine if results would lead to any meaningful intervention. Also noted patient has a baseline diagnosis of dysphagia and will be discharged on a dysphagia diet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Mixed hyperlipidemia Hypopituitarism Essential hypertension Hearing loss GERD (gastroesophageal reflux disease) Gout Hypothyroidism Chronic fatigue syndrome Raynaud disease Squamous cell carcinoma Pituitary adenoma TIA (transient ischemic attack) Polyneuropathy Major depressive disorder with single episode, in partial remission OSA (obstructive sleep apnea) Non-cardiac chest pain Calcification of abdominal aorta Other dysphagia Other constipation Angiomyolipoma of both kidneys with renal cysts Chronic obstructive pulmonary disease, unspecified COPD type Pulmonary air trapping At risk for osteoporosis Hyperparathyroidism Chronic right-sided low back pain with sciatica Continuous leakage of urine Frequent falls Poor balance Bilateral hip pain Chest pain Bradycardia Weakness Acute urinary retention BPH with obstruction/lower urinary tract symptoms Urinary urgency Movement disorder
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Aspirin (ASPIR-81 PO) Calamine Phenolated (THYMOL-MENTHOL-GLY-CALA) ointment Cholecalciferol (VITAMIN D) 2000 UNIT
Allergien: CephalexinHives HydromorphoneHives KeflexHives Niaspan [Niacin]Hives PenicillinsHives Sulfa DrugsHives
Vorherige Impfungen: -

VAERS 2621570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: IA
Alter: 68,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 27.10.2022
Beginn: 29.03.2023
Tage bis Beginn: 153,0
Dosis: 5
Route/Site: IM / RA

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

Aphonia Chronic obstructive pulmonary disease Condition aggravated Cough Gait inability Loss of personal independence in daily activities Mobility decreased

Symptomtext

I had a deep cough that caused me to lose my voice, it would be so bad that I could not even walk across the room. This lasted for three weeks. I was unable to even get out of bed to do my normal activities. Once I got into my doctor into my doctor, she said it was too late to test for COVID-19, RSV, Influenza. I was given a prescription for an inhaler and was told that my COPD had come back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Kidney Disease; Stomach Surgeries;
Andere Medikamente: Multivitamin; Bi-Flex; Escitalopram; Famotidine; Fentanyl Patch; Folic Acid; Iron; Levothyroxine; Lidocaine-Prilocaine Cream; Lyrica; Midodrine; Myrbetriq; Oxycodone; Pantoprazole; Prolia Injection every 6 months; Crestor; Solifenacin; Traz
Allergien: Penicillin; Vancomycin; Baclofen; Adhesives
Vorherige Impfungen: -

VAERS 2621511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: DC
Alter: 48,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 21.10.2022
Beginn: 23.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / RA

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

Burning sensation COVID-19 Fatigue Feeling abnormal Feeling hot Mobility decreased Pain SARS-CoV-2 test positive Throat irritation

Symptomtext

23OCT2022 I started with a scratchy throat associated with fatigue and body aches also I felt feverish but temperature was normal. 24OCT2022 I felt very bad inside my whole body burning sensation feverish body aches and generally felt horrible unable to get out of bed, I thought I was going to die.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 24OCT2022 COVID-19 Test-Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sprintpec
Allergien: None
Vorherige Impfungen: -

VAERS 2616869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: FL
Alter: 63,0
Geschlecht: M
Eingang: 18.04.2023
Impfdatum: 17.10.2022
Beginn: 30.03.2023
Tage bis Beginn: 164,0
Dosis: 5
Route/Site: IM / LA

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

Chills Cough Fatigue Mobility decreased Nasal congestion Night sweats SARS-CoV-2 test negative

Symptomtext

3/30/2023 it started like a dry cough. I took an at home COVID tests for 4 days and they all came back negative. On April 1, I was fatigued, coughing routinely and unable to get out of bed. I had chills and sweats that night. On 4/2,12 I went into the clinic. They did not want to give me the flu medication. I was given something for nasal congestion. I did not have any tests done. The next day, I was progressively getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 30MAR23 at home COVID test negative; 31 MAR23 at home COVID test, negative. 1APR23 at home COVID test, negative; 2APR23 at home COVID test, negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Baby aspirin; LIPITOR; losartan; amlodipine; milk thistle; vitamin D3
Allergien: A blood pressure medication that caused cough (doesn't know the name)
Vorherige Impfungen: -

VAERS 2616209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: ID
Alter: 58,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 14.10.2022
Beginn: 04.03.2023
Tage bis Beginn: 141,0
Dosis: 4
Route/Site: SYR / LA

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

Asthma COVID-19 Condition aggravated Cough Dysphonia Headache Impaired work ability Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had my vaccination on 10/14/2022. I started to have a runny hose and headache on 03/04/2023. I went to an appointment for a physical on 03/09/2023 and was told it was allergies. A few days later I had to leave work and go to the emergency room. I was given IV fluids and tested COVID-19 Positive on 03/12/2023. I was not provided medication as I was too young. I am still suffering from Asthma on 04/17/2023 and my voice is still hoarse with a dry cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 03/12/2023 test - COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia; Seasonal Asthma
Andere Medikamente: Multivitamins; Flonase; Beatriz; Allegra
Allergien: Composin; Pepcid
Vorherige Impfungen: COVID-19 chills flu like symptoms headache

VAERS 2616169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: OH
Alter: 52,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 05.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Back pain Chest pain Chills Cough Dyspnoea Incorrect product formulation administered Palpitations

Symptomtext

Patient came into Pharmacy to receive 1st dose (monovalent) Pfizer vaccine. Pharmacist did not indicate that this was the bivalent vaccine. Pt received this dose on 11/05/2022 and went home. At home patient immediately went to bed. Her bilateral joints were in excruciating pain, heart racing and had difficulty breathing. Her chest and back where in immediate pain even while lying in bed. She also started coughing and had intense chilling. Pt is unsure if she had a fever. These symptoms occurred for approximately 2 weeks. Pt did not call 911.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Pt did not take any medications or treatment for side effects.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2616045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 01.10.2022
Beginn: 27.03.2023
Tage bis Beginn: 177,0
Dosis: 4
Route/Site: SYR / RA

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

Caesarean section Exposure during pregnancy Full blood count abnormal Headache Hepatic enzyme increased Hypertension Vitreous floaters

Symptomtext

27MAR2023 I went to my OBGYN. I went to for what is designated as a non stress test, my blood pressure was high with a headache and I had floaters in my eye while in the hospital. My liver enzymes were high, they were elevated so that I was required to deliver my child the next days with a scheduled C section. The delivery weight of three pound fifteen ounces. Estimated date of delivery MAY2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: CBC blood profile showed elevated liver enzymes.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal vitamin prescription; vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 2614670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: WI
Alter: 82,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 11.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 82,0
Dosis: 5
Route/Site: IM / LA

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

Arteriogram coronary abnormal Arteriosclerosis coronary artery Bradycardia Coronary angioplasty Dizziness Fatigue Stent placement Surgery Tachycardia

Symptomtext

In January of 2023, I had to angioplasty procedure to replace five stents in my heart My cardiologist felt that with the with increase fatigue, lightheadedness, I needed to have an angiogram. The angiogram showed that my stents were in need of being replaced. They did the first of the replacements on January 13, 2023, the same day as the angiogram. The second surgery was on January 31, 2023. I am currently in cardiac rehab; I do have tachycardia and bradycardia now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: 13JAN2023 Angiogram positive for plaque build up
Aktuelle Erkrankungen: No
Vorgeschichte: Heart Disease; Chronic Bronchiolitis; Chronic Pneumonia
Andere Medikamente: LIPITOR; famotidine; calcium; alpha lipoic acid; ZYRTEC
Allergien: Penicillin; sulfa; amlodipine; trees; dust; mold
Vorherige Impfungen: -

VAERS 2613905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: AZ
Alter: 78,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 07.10.2022
Beginn: 30.01.2023
Tage bis Beginn: 115,0
Dosis: 5
Route/Site: IM / AR

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

Ageusia Anosmia COVID-19 Hypertension Mobility decreased Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Sinus headache

Symptomtext

I thought I had a sinus infection and a sinus headache. I had a fever 101.5. I was just down and in the bed. By the next day I lost my taste and smell and a sore throat, and I was giving PAXLOVID on 01FEB23. I was having high blood pressure a month later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 31JAN23 COVID test positive
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol
Andere Medikamente: Lisinopril; PRALUENT; ELIQUIS; rosuvastatin; levothyroxine; vitamin B12, vitamin D3
Allergien: Prednisone; iodine prep
Vorherige Impfungen: -

VAERS 2612946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: ME
Alter: 71,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 10.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 83,0
Dosis: 5
Route/Site: IM / LA

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

Dyspnoea exertional Respiration abnormal

Symptomtext

Recently when climbing stairs or bending down would keep me out of breath. It would take longer than usual for my breathing to get back to normal. I would have to take pumps of my inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Albuterol sulfate; Magnesium; Vitamin B12; Zinc; Vitamin D3; Garlic supplement; Vitamin C; Palmetto and light supplement
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 2612340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: ID
Alter: 26,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 09.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: SYR / UN

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

Blood test abnormal C-reactive protein increased Hypoaesthesia Paraesthesia Swelling

Symptomtext

I had my vaccination on 10/09/2022. Approximately in 01/2023 I started to experience tingling in legs and arms throughout the day. It may be a nerve thing but not circulatory. If I change position it will go away but can be scary when I am driving. I wake up every morning with one or both of my extremities being numb and sometimes swollen. I had tests done on 04/03/2023 to include a blood panel. All blood work was fine except the C Reactive protein was high. I am now being referred to a specialist. I am seeing specialist to be determined up to 3 weeks. I stopped taking the spironolactone to see if reaction to the medication last week but I am still experiencing the tingling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 04/03/2023 Blood panel
Aktuelle Erkrankungen: N/A
Vorgeschichte: Possible COVID-19 09/14/2023; Never tested positive and never developed symptoms; Depression; OCD; Spectrum Disorder; PTSD; IBS; Possible Celiac Disease
Andere Medikamente: Citalopram; amitriptyline; MIRENA IUD; multivitamin; vitamin D; spironolactone; clindamycin
Allergien: Amoxicillin; latex
Vorherige Impfungen: -

VAERS 2611925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: AZ
Alter: 34,0
Geschlecht: F
Eingang: 08.04.2023
Impfdatum: 05.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 15,0
Dosis: 4
Route/Site: SYR / RA

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

Cardiac monitoring Echocardiogram Supraventricular tachycardia

Symptomtext

Supra ventricular tachycardia occurring during intense exercise like hiking and shoveling snow

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: Heart monitor 48 hours, heart echocardiogram
Aktuelle Erkrankungen: N/A
Vorgeschichte: Autoimmune: occasional Sjogren's markers
Andere Medikamente: Hydroxychloroquine 150g/per day
Allergien: N/A
Vorherige Impfungen: -

VAERS 2610188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: WI
Alter: 92,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 06.12.2022
Beginn: 13.02.2023
Tage bis Beginn: 69,0
Dosis: 5
Route/Site: UN / UN

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

Acute left ventricular failure Blood sodium decreased COVID-19 Cardiac failure congestive Chest X-ray abnormal Cough Dyspnoea Electrocardiogram Fatigue Full blood count Haemoglobin decreased Hyponatraemia Metabolic function test Oedema peripheral Prohormone brain natriuretic peptide increased Respiratory tract congestion SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

2/13/2023 CLINICAL IMPRESSION: Hyponatremia, Shortness of breath, Bilateral edema of lower extremity Presents to the ED with chief complaint of shortness of breath, cough, congestion. The patient has had fatigue with bilateral lower extremity edema and a cough. On arrival here, the patient was afebrile with heart of 92, respiratory 26, blood pressure 137/74, pulse ox 96% on room air. On exam, the patient had some tachypnea with increased work of breathing but clear lung sounds, bilateral lower extremity edema. Principal Problem: Acute diastolic congestive heart failure (*) Active Problems: Peripheral vascular disease (*) Hypothyroidism due to acquired atrophy of thyroid (*) Chronic atrial fibrillation (*) Essential hypertension (*) Dual Chamber Cardiac pacemaker - Dr. [ 03/23/2014] Generalized anxiety disorder (*) Aortic valve stenosis, severe Resolved Problems: * No resolved hospital problems Submitter does not have access to further medical records or information on hospital course. If further information is needed, please contact the admitting hospital:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 2/13/2023: CMP- sodium of 126, down from 129 3 days ago, proBNP was elevated at 2500, CBC -white blood cell count of 9 with hemoglobin of 10.4 viral swabs are negative chest x-ray- possible tiny left pleural effusion but no focal consolidation. EKG -ventricular paced rhythm at 81 bpm 2/19/2023: SARS-CoV-2 RNA Resp Ql NAA+probe Detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: Past Medical History: Diagnosis Date ? Anemia 6/8/2015 ? Arrhythmia atrial fibrillation ? Arthritis ? Atherosclerosis of native arteries of the extremities with intermittent claudication 6/3/2009 ? Atrophic vaginitis ? Cataract ? Chronic back pain 1/9/2012 ? Gastro-esophageal reflux 06/20/2014 ? ? Hypercholesteremia ? Hypertension 11/12/2014 ? Hypothyroidism ? Incontinence FREQUENCY - ONLY AT NIGHT ? Intermittent claudication ? Lactose intolerance 11/12/2014 ? MEDTRONIC Dual Chamber Cardiac pacemaker - Dr. [ 03/23/2014 ] 03/23/2014 ? Mitral regurgitation moderate by echo 8/31/12 ? Osteoporosis ? Osteopenia by dexa November 2012 ? PAD (peripheral artery disease) ? Paroxysmal atrial fibrillation ? Peripheral vascular disease, unspecified 9/29/2009 ? Pseudophakia of both eyes ? PVD (peripheral vascular disease) ? Radiculopathy, lumbar region 8/30/2012 August 14, 2012 MRI epidural steroid injection Dr. ? SSS (sick sinus syndrome) ? Unspecified hearing los s 3/25/2011 ? Varicose veins 1/9/2012
Andere Medikamente: unknown
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2588515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MD
Alter: 69,0
Geschlecht: F
Eingang: 28.02.2023
Impfdatum: 28.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Blood test Cardiac stress test Dyspnoea Echocardiogram Electrocardiogram abnormal Exercise tolerance decreased Heart rate decreased Mobility decreased

Symptomtext

Myocardia shortness of breath soft heart beat exercise intolerance couldn't climb stairs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Stress, Echo, EKG, blood
Aktuelle Erkrankungen: Lacerated EHL tendon in left foot
Vorgeschichte: None
Andere Medikamente: Sulfamethoxazole; vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2583391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: GA
Alter: 57,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: 17.11.2022
Beginn: 27.01.2023
Tage bis Beginn: 71,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Chest discomfort Cough Dyspnoea Epistaxis Headache Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Sneezing

Symptomtext

On 11/17/2022 I received my Covid 19 vaccine. On 01/27/2023 I woke up with a severe sore throat with coughing and sneezing throughout the day. The next morning, I began to have nosebleed severe headache body aches and fevers. The symptoms began to progress. I took a home Covid test and was tested positive for Covid-19. I contacted my doctor and was prescribed molnupiravir for 5 days. The following Wednesday I was still coughing with tightness and trouble breathing so I contacted my doctor again and was prescribed albuterol and TESSALON PEARLS. Symptoms are still on going.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Kidney disease stage 3B; Diabetic
Andere Medikamente: Atenolol; enalapril; prednisone; allopurinol; levothyroxine; EFFEXOR; HUMULIN KWIK PEN
Allergien: Penicillin; KEFLEX; erythromycin; sulfa; codeine
Vorherige Impfungen: -

VAERS 2576373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 40,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 05.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Migraine Nasopharyngitis Oropharyngeal blistering Paranasal sinus discomfort SARS-CoV-2 test positive Sinus congestion

Symptomtext

I started getting migraines the day after the vaccine and lasted for 4 weeks. They finally went away after going to massage therapist and chiropractor 3 times. In January I went to urgent care I felt like I had a cold and they found white spots in my throat. I was given antibiotics. A few days later I took a Covid test and came back positive. I had sinus pressure and congestion and about a week and a half later it went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: MIRENA IUD; acid reflux medicine; multivitamin; probiotic; st. john's wort
Allergien: None
Vorherige Impfungen: -

VAERS 2576360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 01.12.2022
Beginn: 23.01.2023
Tage bis Beginn: 53,0
Dosis: 5
Route/Site: - / -

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

Atelectasis Blood folate normal Blood homocysteine increased Blood iron normal COVID-19 Computerised tomogram thorax abnormal Condition aggravated Glycosylated haemoglobin normal Haemoglobin decreased Hypotension Lethargy Lung opacity Metabolic encephalopathy Pyrexia SARS-CoV-2 test positive Somnolence Urinary tract infection Vitamin B12 normal

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: PA Admission Date: 1/28/2023 Discharge Date: 2/4/2023 Condition on discharge: Improving DETAILS OF HOSPITAL STAY: Patient is a 64-year-old female with history of end-stage renal disease on hemodialysis, Parkinson's disease with dementia, DM II, dilated cardiomyopathy with EF of 25%, s/p AICD, chronic pulmonary HTN, chronic megaloblastic anemia, chest lymphadenopathy, MDR recurrent UTI. She was transferred to Hospital from emergency room where she presented from a local subacute rehab facility with complaints of worsening lethargy/encephalopathy, fever onset the day prior to presentation. The patient was found to have a urinary tract infection which appeared to not have responded to outpatient antibiotic therapy. She was started on Zosyn and vancomycin upon arrival to hospital. Infectious disease switched her to ertapenem, to finish 7 days treatment (EOT 2/2/23). Patient was also found to be COVID-19 positive and was treated with 5 days of remdesivir. The patient responded well to antibiotic and antiviral therapy. Hemodialysis was continued per nephrologist. Next hemodialysis at hospital on 2/7/23. She had right side Permacath which is no longer used for hemodialysis at hospital (was used here) and RN requested removal. We tried to remove, but couldn't be done on time so patient was discharged. Permacath should be removed in hospital after discharge. The legal guardian, patient's family and the patient had a meeting with hospice on 1/30/2023. Guardian had discussion with outpatient nephrologist, who thought that due to frequent hypotension (despite midodrine), frequent inability do perform hemodialysis due to hypotension patient should sign with hospice and stop hemodialysis. However patient's guardian declined enrolment into hospice, and wished to continue hemodialysis. Subsequently we heard that she would enroll into hospice after discharge with continuation of hemodialysis due to CHF. Patient also had metabolic encephalopathy on and off during hospitalization. Discontinued Norco, avoid benzo, keep regular biorhythm. Still very sleep for most of the time, than wakes up and is good for couple hours. Anemia of ESRD, chronic megaloblastic anemia stable, Hgb 9.6 at discharge. Iron studies, B12, folate normal. Homocysteine elevated, could be due to ESRD. Vit B6 level was pending at the time of DC. PCP to follow up on it. Patient had extensive chest lymphadenopathy in 12/22. Repeat 3 months follow up CT of chest showed mild decrease in size of several mediastinal lymph nodes as described above. No enlarged axillary lymph nodes identified. Evaluation of the lungs is limited due to motion artifact. There appears to be multifocal scattered streaky opacities, favored to represent multifocal atelectasis. Dilated cardiomyopathy, chronic HFrEF (EF 25%) s/p AICD, chronic pulmonary HTN well controlled with hemodialysis and home meds. Net IO Since Admission: -9,051 mL [02/04/23 1309]. DM type II well controlled. Hgb. A1c 6.2% in Dec 2022. Discontinue insulin. Dementia d/t Parkinson's disease, continue supportive care, regular reorientation, normal sleep-wake cycle promotion. Continue Sinemet. Patient discharged on 2/4/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: 11/25/2022- Hospital Low Blood Sugar
Vorgeschichte: End-stage renal disease on hemodialysis Lymphadenopathy Sepsis COVID Controlled type 2 diabetes mellitus with chronic kidney disease on chronic dialysis, without long-term current use of insulin Multiple drug resistant organism (MDRO) culture positive Pneumonia due to COVID-19 virus Metabolic encephalopathy Anemia of chronic kidney failure, unspecified stage Dilated cardiomyopathy Systolic dysfunction with acute on chronic heart failure (EF 25%) Parkinsonism with dementia Goals of care, counseling/discussion
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet aspirin 81 MG chewable tablet bisacodyl (DULCOLAX) 10 MG suppository carbidopa-levodopa (SINEMET) 25-100 MG per tablet carvedilol (COREG) 3.125 MG tablet cyanocob
Allergien: Clarithromycin Rofecoxib
Vorherige Impfungen: -

VAERS 2575419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

moderat

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 03.02.2023
Impfdatum: 19.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Electrocardiogram Fatigue Headache Hypertension Pulse abnormal Tachycardia

Symptomtext

exhaustion, headache, hypertension, intermittent tachcardia, premature contractions, bounding pulse,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: ecg
Aktuelle Erkrankungen: -
Vorgeschichte: neck problem
Andere Medikamente: vitamin d
Allergien: -
Vorherige Impfungen: -

VAERS 2572194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 02.11.2022
Beginn: 25.01.2023
Tage bis Beginn: 84,0
Dosis: 5
Route/Site: - / AR

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

Arthralgia Bacterial test Blood culture Blood test COVID-19 Chest X-ray Cold sweat Cough Delirium febrile Diarrhoea Disorientation Dysphonia Ear pain Feeling of body temperature change Hyperhidrosis Hypertension Malaise Migraine

Symptomtext

My symptoms started on Wednesday of last week which was January 25. I had a dry cough, but I already have asthma and COPD. I requested albuterol thru a nebulizer treatment the night before. I had a progressively increasing sore throat and earache throughout the day. My blood pressure was high but better than it had been. I had just had my corticosteroids tapered from the medical dose back to the home dose. I do believe this weakened my immune system at that point. My voice had changed. By the next few hours, I was at the demonic toad way speaking. That night I had diarrhea, severe nausea, cold sweats and my temperature was at 99. I also had muscle aches. The next morning, I was coughing up clear solids from my lungs and throat. I had minor nasal congestion that required a change in oxygen mask. My urine became more concentrated and cloudier. My fever progressed to 102 with both hot and cold sweats and minor fever delirium. My lungs progressed to colored both yellow and brown. After doing my lung exercise, a chest x-ray was performed. I was not given the results. I was tested via blood and lung mucus for bacterial. My fever broke on Sunday morning and I was discharged to home and home health care. I was sent home. I did an intake with 2 nurses from home health. I am still symptomatic. I am still disoriented, have diarrhea, migraine joint and muscle pain, blurry vision. I'm on a prophylactic antibiotic called Levo Lexine.

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Praegender Schweregrund: Hypertension
Hospital-Tage: 1,0
Labordaten: COVID-19 PCR Test and Home Test-January 30, 2023-All Positive Chest Xray-January 28, 2023-unknown results Blood Culture to check for Sepsis-January 28, 2023-unknown result Sputum Culture-January 28, 2023-unknown results
Aktuelle Erkrankungen: Cold in Mid-October
Vorgeschichte: Addisons Severe; Immune Compromised; CIRS; MCAS; POCS; Invasive Candidiasis; ILD; Seizures; Miracidia Gravis; ME/CFS; Hypoxemic Dramatic Brain Injury; Hoshimotos Hypothyroidism; IBD; Leaky Gut; Heavy Metal Poisoning Traumatic Brain Injury; Neurological Apnea; Endometriosis; Diabetes; Hypoglycemia; Hypertension; Migraines; PTSD; Asthma; COPD
Andere Medikamente: IV Dextrose Plus Saline; Nebulized Albuterol Treatment; Hydrocortisone; Amino Acid; Atorvastatin; Diazepam; Cyclobenzaprine; Keto Econazole; Liothyronine; Amlodipine; Losartan Potassium; Eliquis; Minocycline; Montelukast; Nitrofurantoin; Fl
Allergien: Milk; Shellfish; Metal Based Multi-Vitamins; Metal Based Contrast Imaging; Mercury; IV Iodine; IV Chromium; Zinc; Botox
Vorherige Impfungen: -

VAERS 2569137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Dysgeusia Hypersensitivity Paraesthesia Swollen tongue

Symptomtext

PT c/o s/s allergic Rxn c/o metalic taste, tingling, & enlarged tongue. Prior Hxn allergic Rxn & Bees. Self admin Benedryl 25 mg PO. No effect. EMS called for continueing s/s. Care transferred to hospital. VS 152/96 99% Room Air, Lungs clear, 0 drooling. PT continued with normal conversation during episode.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNK
Vorgeschichte: Celiac, Osteopenia, Cobalamin def.
Andere Medikamente: Unk, Benedryl 25 po self admin
Allergien: Latex, Nuts (NOS), elavil, E-mycin; PCN BEE
Vorherige Impfungen: Hx BEE Allergy, self carry EPiPEN, Prednisone, Benedryl

VAERS 2568945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: MO
Alter: 72,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 25.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / RA

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

Blood disorder Blood test Chest pain Computerised tomogram Neck pain Pain Pruritus X-ray

Symptomtext

I had some pain and itching/I had lot of aching; I have had Bivalent Shot and then they give me the Flu shot on the other arm; I had some pain and itching; I have a neck pain; I couldn't move it and it would hurt so bad; I did get have one short pain in my chest; but they said that you have blood disorder; 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 female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 25Oct2022 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 72 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (ongoing), notes: Asthma. Concomitant medication(s) included: FLU [INFLUENZA VACCINE] taken for immunisation, on 25Nov2022 as dose number unknown, single. Vaccination history included: coviD-19 vaccine (Dose 1, unknown manufacturer, Intramuscular , Batch/Lot number: FJ8762), administration date: 27Dec2021, for COVID-19 immunization; coviD-19 vaccine (Dose 2, Unknown manufacturer, Intramuscular Batch/Lot number: FJ6369), administration date: 22Jul2022, for COVID-19 immunization. The following information was reported: CHEST PAIN (non-serious) with onset 2022, outcome "unknown", described as "I did get have one short pain in my chest"; PAIN (non-serious) with onset 2022, outcome "unknown", described as "I had some pain and itching/I had lot of aching"; NECK PAIN (non-serious) with onset 2022, outcome "unknown", described as "I have a neck pain; I couldn't move it and it would hurt so bad"; PRURITUS (non-serious) with onset 2022, outcome "unknown", described as "I have had Bivalent Shot and then they give me the Flu shot on the other arm; I had some pain and itching"; BLOOD DISORDER (non-serious) with onset 2022, outcome "unknown", described as "but they said that you have blood disorder". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of neck pain. Additional Information: Reporter stated, she was just have had Bivalent Shot (Later clarified as Pfizer COVID-19 Shot) on 25Oct and then they give me the Flu shot (further not clarified, hence captured as Unspecified Flu shot) on the other arm. Well, I had some pain and itching but she just, she was pretty well but then I noticed not worrying after she started to have, she had lot of aching and then her neck she have a neck pain then and well I did break my neck once back at my school, I never felt anything but this was really hurt and I would get my neck was actually stay, I couldn't move it and it would hurt so bad and it's still there I mean didn't going away. well, I have a pain doctor and I really go see him and I get done it X-Ray of my head and my neck and they said my X-Ray was okay but on the neck I should have that have followed by my pain doctor because it could get worse and it just and I wake up I will be in so much pain and I have to take well, a muscle relaxant (Intent: Treatment) I finally got my doctor to give me and then of course aching all over and then if I take my pain killer I feel good but really not in my neck ever completely it did go away for a while but it's still there. Other Medical Conditions and Other Medications: Consumer stated, Well, I am on lot of medication because I have Asthma so, I have to take that. Consumer stated, Not really, but when I am went to get my CAT scan, but they said that you have blood disorder, they keep saying that I don't know what it is. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine fluvax .

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: CAT scan; Result Unstructured Data: Test Result:unknown results; Test Name: X-Ray of my head; Result Unstructured Data: Test Result:okay; Comments: my X-Ray was okay; Test Name: X-ray of my neck; Result Unstructured Data: Test Result:on the neck I should have; Comments: on the neck I should have that have followed by my pain doctor because it could get worse; Test Name: blood test; Result Unstructured Data: Test Result:blood disorder NOS; Comments: they said that you have blood disorder, they keep saying that I don't know what it is.
Aktuelle Erkrankungen: Asthma (Asthma)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: NM
Alter: 63,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 24.10.2022
Beginn: 22.11.2022
Tage bis Beginn: 29,0
Dosis: 6
Route/Site: IM / RA

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

Back pain Cardiac function test abnormal Chest pain Differential white blood cell count normal Ejection fraction Electrocardiogram T wave inversion Electrocardiogram normal Full blood count normal Hypertension Lipids Low density lipoprotein increased Metabolic function test normal Scan myocardial perfusion abnormal

Symptomtext

I experienced severe back and chest pain. I thought I was having a heart attack. I took my blood pressure. It was around 185/110. I watched my blood pressure. It stayed high, but I went to sleep. The next day, I checked my blood pressure. It was still high, but it had improved. I took it easy and kept an eye on it. It kept improving. By Friday, it was normal, but I went to see a Cardiologist on December 14, 2022 anyway.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/14/2022 Blood pressure, normal; 12/14/2022 ECG 12 Lead, normal Sinus Right Access and Prior Inferior Infarct; 12/15/2022 CBC No Diff, normal; 12/15/2022 Lipid panel, LDL Cholesterol high; 12/15/2022 Comprehensive Metabolic Panel, normal; 01/03/2023 Stress test with Myocardial Profusion, Reversible Mild Small Inferior Defect, resolves with prone imaging, likely suggestive of soft tissue artifact, Left Ventricular Ejection Fraction: 68%, initial T-Wave Inversions that flip to normal with exercise
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Omeprazole
Allergien: Aspirin; codeine; penicillin; elm; seasonal
Vorherige Impfungen: -

VAERS 2565617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: DC
Alter: 41,0
Geschlecht: F
Eingang: 23.01.2023
Impfdatum: 21.10.2022
Beginn: 03.01.2023
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia COVID-19 Chest discomfort Dyspnoea Loss of personal independence in daily activities Myalgia Oropharyngeal pain SARS-CoV-2 test positive Sensitive skin

Symptomtext

I started having a sore throat and skin sensitivity all over muscle/joint aches all over. It hurt to put on pants, and this lasted for about 24 hours and then I did a COVID-19 test at home and, I was positive. I contacted a doctor as soon as I tested because I have asthma and chest/lungs were tight and I was having issues breathing. The doctor gave me PAXLOVID, and I was told to increase my inhaler uses and I was told to go to an urgent care center so they could listen to me. I started the medication January 4th. When I went to urgent care, they added methylprednisolone as well as my inhaler. Over time Jan11, I saw my doctor because the symptoms were weakening and to check my lung function. The doctor tested everything as far as my lungs and whatnot she increased PULMICORT because I was just about out. Then on 01/15 I woke up with worsening symptoms, so I tested again and except the sore throat these were all new symptoms. The COVID-19 test was very bold with a positive reading whereas the last test was positive a faint sign. So, 8 days later I tested again and was negative for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19, Peak test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Anxiety; Overweight
Andere Medikamente: Montelukast; XOPENEX; citalopram; cetirizine; bupropion; PULMICORT; probiotic; hair skin and nails
Allergien: Propofol; laughing gas
Vorherige Impfungen: -

VAERS 2561581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 15.10.2022
Beginn: 18.12.2022
Tage bis Beginn: 64,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Condition aggravated Fatigue Headache Pain Productive cough SARS-CoV-2 test positive

Symptomtext

Extreme fatigue and body aches for 12 hours. I tested positive for COVID-19 on 12/18/2022. I had a headache for the first 2 days. I have phlegm in my throat and was fatigue for 3 days. My provider prescribed medication LAGEVRIO. I did a telehealth visit with my provider over the phone.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 18DEC2022 COVID-19 positive, 25DEC2022 COVID-19 positive
Aktuelle Erkrankungen: Body pain; extreme fatigue
Vorgeschichte: Asthma; Thyroid Cancer
Andere Medikamente: Vitamin C; turmeric; levothyroxine
Allergien: VICODIN
Vorherige Impfungen: -

VAERS 2561448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: PA
Alter: 69,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 14.10.2022
Beginn: 15.12.2022
Tage bis Beginn: 62,0
Dosis: 5
Route/Site: SYR / LA

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

Cough Mobility decreased Nasal congestion Nasopharyngitis Pyrexia Throat irritation

Symptomtext

On 12/15/2022 I awoke with cold like symptoms stuffy nose, scratchy throat and a cough, on 12/16/2022-12/17/2022 I spent both days in bed and ran a slight fever of @ 101 degrees. By 12/18/2022 I was feeling a little better and no longer bedridden and by 12/19/2022 I feel I was better and recovered by 12/20/2022.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Detached retinas; Irregular Heartbeat; Enlarged Prostrate
Andere Medikamente: Rosuvastatin calcium; tamsulosin
Allergien: None
Vorherige Impfungen: -

VAERS 2558608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 12.10.2022
Beginn: 09.12.2022
Tage bis Beginn: 58,0
Dosis: 5
Route/Site: IM / RA

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

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

Symptomtext

I had a cough and chest pain. I did not get a fever. I was very tired. I did have rebound COVID-19 as well.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10DEC2022-COVID-19 - positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Congestive Heart Failure; Stroke; HX Breast Cancer; Lymphedema; Arthritis; CVA; Colon Polyps; Sleep Apnea; Dilated Cardiomyopathy; Acid Reflux, Stage III Chronic Kidney Disease; Atherosclerosis Aorta; TIA; Cataracts; Breast Cancer spread to Lymph Nodes; T2N1-- Breast Cancer; Mitral Valve Prolapse
Andere Medikamente: Spironolactone; Metoprolol Succinate; Sertraline; Pantoprazole; Atorvastatin; Plavix; Farxiga; Bupropion; Entresto; CBD Cream; Magnesium; Vitamin B12; Aspirin; Furofemide; Glucosamine; Multivitamin; Vitamin D3
Allergien: Docetaxel
Vorherige Impfungen: -

VAERS 2556152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MO
Alter: 72,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 07.10.2022
Beginn: 05.01.2023
Tage bis Beginn: 90,0
Dosis: 1
Route/Site: SYR / AR

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

Asthenia COVID-19 Cough Decreased appetite Dizziness Dysphonia Dyspnoea Dyspnoea exertional Fatigue Mobility decreased Nasal congestion Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 01/06/2023. My symptoms were hoarseness, lightheadedness, weakness and feeling very fatigued. I never had a fever. I didn't have much appetite and drinking a lot of fluids. I rested, and I had a bad dry cough which I still have and some hoarseness and raspiness in my throat. When I got up and walked around I was short of breath. I didn't move around much for 3 days. I had a stuffy nose. I also had body aches. My doctor offered for PAXLOVID but I opted not to. I took TYLENOL and CLARITIN D and MUCINEX for the cough and congestion. Yesterday, I was given a MEDROL dose pack because everything was congested. Everything was basically over the counter for treatment. I'm finally starting to feel a little better today. Fatigue and lightheadedness were some of the worst parts. Still in the process of recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 06JAN2023 at-home COVID test positive; 09JAN2023 at-home COVID test positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine; AREDS-2; calcium; vitamin D; vitamin C; multivitamin; FLONASE
Allergien: Environmental allergies
Vorherige Impfungen: -

VAERS 2554579

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GJ6665

moderat

Staat: MN
Alter: 57,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 17.10.2022
Beginn: 16.12.2022
Tage bis Beginn: 60,0
Dosis: UNK
Route/Site: IM / RA

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

COVID-19 Pneumonia SARS-CoV-2 test positive Sepsis

Symptomtext

Provider note states positive test on 12/21/22. No positive lab in chart. Currently hospitalized for sepsis and probable pneumonia. Tested again on 1/5/23 for COVID and found positive. Provider unsure why patient re-tested but not felt to have current positive COVID infection.

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Praegender Schweregrund: Pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, Diabetes
Andere Medikamente: -
Allergien: Piperacillin-tazobactam, sulfamethoprim DS, alendronate
Vorherige Impfungen: -

VAERS 2548418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: PA
Alter: 58,0
Geschlecht: F
Eingang: 02.01.2023
Impfdatum: 14.12.2022
Beginn: 16.12.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: SYR / LA

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

Cardiac flutter Electrocardiogram normal Palpitations

Symptomtext

Frequent heart flutters/palpitations noted within two days after vaccine, but patient did not initially consider any connection to vaccine. At a routine physical on 12/21/22, noted issue to doctor, who performed an in-office EKG which showed normal heart activity. Physician advised that heart flutters are a symptom of COVID19 but also may be a symptom of the vaccine. Heart flutters/palpitations have lessened over time and are much less frequent as of this writing, 2.5 weeks later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG 12/21/22 showed normal heart activity.
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: Flovent 110 mcg inhaler fish oil vitamin C 500 mg
Allergien: penicillin, amoxycillin and derivatives seasonal (tree/grass pollen) dust mite dander
Vorherige Impfungen: mild hives, initial Moderna COVID19 vaccine, age 57, 04-27-21

VAERS 2546970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 03.02.2021
Beginn: 17.12.2022
Tage bis Beginn: 682,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Culture urine positive Enterococcus test positive Fall Mobility decreased Urinary tract infection White blood cell count abnormal

Symptomtext

Hospital Course and Significant Findings: Patient is a 79 year old male with a history of dementia, NPH who lives alone with part time caregiver who presented with fall and inability to get up. Daughter called emergency number. In the ER patient found to have UTI and COVID. For his UTI he was treated with cipro with improvement in WBC and no fever. Urine culture grew Enterococcus. In terms of his COVID, he was not hypoxic so received no decadron. He did receive Remdesivir while in the hospital. He will go home on COVID isolation through 12/26/22.

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

VAERS 2545703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: VA
Alter: 42,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 14.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 7,0
Dosis: 6
Route/Site: SYR / RA

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

Back pain Blood test abnormal Food allergy Migraine Nausea

Symptomtext

I started having a lot of nausea, backpain and migraine headaches. I went to the Dr and was diagnosed with allergy to meats and this is new diagnosis since after the 6th dose because I was tested in July and was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Bloodwork - Alpha Gal syndrome
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Daily multivitamin; Fish oil
Allergien: Shellfish; Meat
Vorherige Impfungen: I break out in hives with the Flu vaccination

VAERS 2540577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 12.10.2022
Beginn: 17.12.2022
Tage bis Beginn: 66,0
Dosis: 4
Route/Site: - / -

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

Asthenia Blood chloride decreased Blood sodium decreased COVID-19 Chest X-ray normal Cough Hyponatraemia Respiratory tract congestion SARS-CoV-2 test positive Sneezing Tachycardia

Symptomtext

Discharge Provider: DO Primary Care Provider at Discharge: MD Admission Date: 12/17/2022 Discharge Date: 12/19/2022 COVID positive 12/17/2022 HOSPITAL COURSE: Patient is a 76-year-old female with history of moderate persistent asthma, GERD, OSA, anxiety and recent TIA who presented with increased weakness, congestion, cough and sneezing. In the ED, she tested positive for COVID-19. She was tachycardic, but otherwise hemodynamically stable. Chest x-ray was negative for pneumonia. Labs showed sodium 129, chloride 95. She was placed on observation for generalized weakness and hyponatremia related to COVID-19. Upon admission, she was placed on IV fluids. With hydration, her sodium and chloride normalized. Remainder of labs and vital signs remained stable. She was seen by PT and OT, who felt that she was safe to return home. Her respiratory status remained stable on room air, and she did not qualify for advanced therapies for COVID-19, including Decadron or Remdesivir. She was felt stable for discharge home on 12/19/22. She should follow-up with her PCP in 1 week. She will be followed by the COVID-at-home program at discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Hospital ED Observation CHIEF COMPLAINT: NUMBNESS Assessment/Plan DIAGNOSIS at time of disposition: 1. Right arm weakness 2. TIA (transient ischemic attack) Current Discharge Medication List ED Disposition: OBSERVATION HISTORY OF PRESENT ILLNESS: HPI 76-year-old female presenting to the emergency department for evaluation of transient right arm numbness and intraoral lesions. Patient was in her usual state of health preceding this. She states that she was at rest today and noticed her right arm was more weak and had paresthesias and numbness as well as paresthesias within the right side of her mouth similar to having a dental procedure done. This lasted for approximately 15 minutes. She endorses intermittent headaches for the last few weeks not enema the morning, no history of complex migraine. Usually responds well to Tylenol, took Tylenol this morning at approximately 6:00 a.m.. She denies any falls. Patient is being worked up in the outpatient setting for progressive cognitive decline and has an MRI ordered mid December to further work this up. 12/10/2022 ED visit notes: Hospital CHIEF COMPLAINT: ARM PAIN Assessment/Plan DIAGNOSIS at time of disposition: 1. Left arm pain ED Disposition: DISCHARGE MEDICAL DECISION MAKING: Supervising Physician: MD Patient presents with occasional chest tightness over last couple weeks and waking up with arm pain today. On examination the patient was able tolerate full range of motion of the left upper arm without any reproducible pain. No signs of trauma or bruising appreciated as well. No midline cervical spine tenderness. The rest of physical exam is unremarkable. Given patient's concern for cardiac cause, the patient was evaluated with an EKG which showed a normal sinus rhythm at a rate of 94 beats per minute. No ST segment elevation or depression. No T-wave inversions and no other ischemic changes. Patient will be evaluated with troponin, complete blood count, CMP and two view chest x-ray. CMP showed slightly low sodium and chloride. Kidney function was normal. No other major electrolyte derangements. Complete blood count was unremarkable. Initial troponin was 10. Given the duration of the patient's symptoms today a repeat was not obtained. Two-view chest x-ray was unremarkable for any acute pathology within the thorax. Patient's workup was discussed with her and family. Patient's workup was reassuring and overall her description of symptoms and examination did not appear consistent with ACS or coronary cause for her arm pain today. Return precautions were provided, and the patient was discharged in stable condition
Vorgeschichte: OSA (obstructive sleep apnea) mild Perennial allergic rhinitis Essential (primary) hypertension Raynauds syndrome Mitral valve prolapse Supraventricular tachycardia PAD (peripheral artery disease) Gastroesophageal reflux disease with stricture post dilation 11/8/2016 Generalized arthritis Monocytosis Subdural fluid collection Ocular migraine Pain in both lower extremities Right arm weakness Dyslipidemia Acute hyponatremia Anxiety Osteoarthritis Family history of coronary artery disease Osteopenia, unspecified location Insomnia, unspecified type Suspected sleep apnea Fatigue Statin started by Vascular Surgery with Rx to be taken over by patient's PCP Generalized weakness Abnormal CT scan, pelvis
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet calcium citrate-vitamin D (CITRACAL) 315-250 MG-UNIT tablet estradiol (ESTRACE) 0.1 MG/GM vaginal cream ferrous sulfate 325 (65 Fe) MG delayed release tablet flut
Allergien: NKA
Vorherige Impfungen: -

VAERS 2539347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: NE
Alter: 49,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 24.10.2022
Beginn: 07.11.2022
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Burning sensation Computerised tomogram head Electromyogram Head discomfort Headache Hypoaesthesia Magnetic resonance imaging head Neuropathy peripheral Paraesthesia

Symptomtext

Burning/numbness/tingling in both arms, hands and feet; severe headaches and pressure in head All symptoms are still on-going. Am taking gabapentin for neuropathy symptoms, hydroxyzine for sleep, and atenolol/Aleve for headaches and pressure in head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: EMG test on both arms; MRI/CT scan on head; blood tests
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium, omega-3, vitamin C, iron supplement
Allergien: None
Vorherige Impfungen: I was sick with flu-like symptoms after receiving the J&J shot on April 1, 2021. I was 48 at the time and recovered after less t

VAERS 2507524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: KY
Alter: 85,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Blood pressure fluctuation Fatigue Immediate post-injection reaction Nasopharyngitis Blood pressure increased Condition aggravated Feeling abnormal

Symptomtext

cold; arm was tired; It can be as low as 80 and as high as 220 / It just fluctuates; 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. An 85-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Oct2022 as dose 4 (booster), single (Batch/Lot number: unknown) at the age of 85 years for covid-19 immunisation. The patient's relevant medical history included: "blood pressure regulated" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN taken for hypertension; NIFEDIPINE taken for hypertension. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for COVID-19 immunization; Bnt162b2 (DOSE 2, SINGLE), for COVID-19 immunization; Bnt162b2 (DOSE 3 (BOOSTER), SINGLE), for COVID-19 immunization. The following information was reported: BLOOD PRESSURE FLUCTUATION (medically significant) with onset 24Oct2022, outcome "not recovered", described as "It can be as low as 80 and as high as 220 / It just fluctuates"; NASOPHARYNGITIS (non-serious), outcome "unknown", described as "cold"; FATIGUE (non-serious), outcome "unknown", described as "arm was tired ". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: highest reading at 220; hang around 187; 146 is lowest she can get it; It can be as low as 80. Therapeutic measures were taken as a result of blood pressure fluctuation. Clinical course included patient was a 85 years old female got her 4th dose; a Pfizer omicron booster dose. Patient reported that after she got it in October, her blood pressure has not been right since 24Oct2022. It fluctuates on 24Oct2022 with the highest reading at 220 but will hang around 187 (146 is lowest she can get it). said she has called before and was referred to CDC. Patient asking can the shot affect blood pressure. Patient stated she talked to 2 other people who experienced the same thing. Patient stated she has had all Pfizer covid 19 shots and date of last booster: 24Oct2022. States she had talked to many people about this; 2 other people she talked to landed in the ER with one man having a BP around 220. States she called Pfizer right after this happened. Caller has taken all of the COVID vaccines by Pfizer. Her last one was the Omicron COVID vaccine. She took the omicron shot the end of 24Oct2022, and her blood pressure has not been right since 24Oct2022. Everything was fine until this shot. She can only find 2 other people that this happened to. Ever since she got the last vaccine, her blood pressure has been going up and down on 24Oct2022. It has gotten up to 220 many times. It usually stays in the 180s. It just fluctuates. She had to switch pills around and added something else medication wise to help. It has not been 220 lately, but it is hanging around 187. 146 is the lowest she has seen the top number of her blood pressure. She takes her blood pressure in the mornings and evening. It can be as low as 80 and as high as 220. She received 4 doses though. She cannot read the information on the vaccine card. She had 4 doses. The last one was the Omicron shot. She got the last dose 24Oct2022, and the blood pressure issues started immediately. It just goes day to day She did not check her blood pressure last night. Her arm was tired from having the cuff on it. Her adding that blood pressure pill helped. Treatment included losartan- 100mg nifedipine - 30mg. She used to take losartan at night and nifedipine in morning, but now she is taking them together at night) hydrochlorothiazide- 25mg (to get the sodium out of her system). This cold she has was due to her not wearing socks on her cold floor. Originally she was on 75mg of losartan at night (for about 10 years), and nifedipine in the morning (she has been on that for about 10 years). Those products had her blood pressure regulated. When her blood pressure went high she did not have a headache or anything. The caller stated she probably should have went to the ER, but she just doubled down on her blood pressure medicine to bring it down. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201361208 Same reporter, same product, same event, different patient;US-PFIZER INC-202201361209 Same reporter, same product, same event, different patient;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Blood Pressure; Result Unstructured Data: Test Result:highest reading at 220; Test Name: Blood Pressure; Result Unstructured Data: Test Result:hang around 187; Test Name: Blood Pressure; Result Unstructured Data: Test Result:146 is lowest she can get it; Test Name: Blood Pressure; Result Unstructured Data: Test Result:It can be as low as 80
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high
Andere Medikamente: LOSARTAN; NIFEDIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2528354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 10.12.2022
Impfdatum: 01.12.2022
Beginn: 02.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SC / LA

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

Fatigue Migraine Nausea Pain Pain in extremity

Symptomtext

Terrible migraines; awful body aches all night, especially ribcage; nausea; exhaustion; and very sore upper arm for over a week after Covid booster shot, just like after previous Covid shots, except symptoms were the worst and the longest-lasting this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Fungal skin and toenail infections, tooth cavity, sore throat virus whose symptoms come and go.
Vorgeschichte: CFS/Fibromyalgia, sleep disorders, anxiety disorders, OCD, CPTSD, depression, Chronic Migraine, GERD
Andere Medikamente: Methadone, celecoxib, Lo Loestrin, polyethylene glycol, wheat dextrin (generic Benefiber)
Allergien: No known true allergies, but lactose intolerance, eczema rash from latex & parabens, and acid reflux from medication capsules and -mycin antibiotics.
Vorherige Impfungen: -

VAERS 2524105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 28.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Asthenia Chills Decreased appetite Gait inability Insomnia Gait disturbance Headache Migraine with aura Nausea Vomiting Sensory loss

Symptomtext

Migraine auras in my eyes; I had no appetite; I started getting chills, very very bad chills/my teeth were chattering and mostly all night that was going on; I couldn't sleep at all; I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs; I have been having problems walking; I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs; I have been having problems walking; I tried to have breakfast I threw it up; Its been very bad and all week I have been very weak; This is a spontaneous report received from a 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 28Nov2022 at 13:15 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 81 years for covid-19 immunisation. The patient's relevant medical history included: "border line diabetic" (unspecified if ongoing), notes: Not really,no I am border line diabetic I don't think so. I am going to go for some testing now, no. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation as dose number unknown, single. Vaccination history included: Covid-19 vaccine (Primary immunization series complete unknown manufacturer), for COVID-19 immunization. The following information was reported: MIGRAINE WITH AURA (non-serious), outcome "unknown", described as "Migraine auras in my eyes"; DECREASED APPETITE (non-serious), outcome "unknown", described as "I had no appetite"; CHILLS (non-serious), outcome "unknown", described as "I started getting chills, very very bad chills/my teeth were chattering and mostly all night that was going on"; INSOMNIA (non-serious), outcome "unknown", described as "I couldn't sleep at all"; GAIT INABILITY (non-serious), SENSORY LOSS (non-serious), outcome "unknown" and all described as "I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs; I have been having problems walking"; VOMITING (non-serious), outcome "unknown", described as "I tried to have breakfast I threw it up"; ASTHENIA (non-serious), outcome "unknown", described as "Its been very bad and all week I have been very weak". Therapeutic measures were taken as a result of migraine with aura, decreased appetite, chills, insomnia, gait inability, sensory loss, vomiting, asthenia. Additional information: I had two Migraine auras in my eyes when I got home that day and then at night starting around not after dinner I suppose I had no appetite. I started getting chills, very very bad chills, my teeth were chattering and mostly all night that was going on. I couldn't sleep at all and I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs. I had to get something, a walker to help me. And then when I woke up and I tried to have breakfast I threw it up. Its been very bad and all week I have been very weak and I have been having problems walking also and no appetite. Patient believes that she had taken Tylenol for the adverse events and does not have information relating to flu shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine with aura
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetic (Not really,no I am border line diabetic I don't think so. I am going to go for some testing now, no)
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2524105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 28.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / RA

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

Asthenia Chills Decreased appetite Gait inability Insomnia Gait disturbance Headache Migraine with aura Nausea Vomiting Sensory loss

Symptomtext

Migraine auras in my eyes; I had no appetite; I started getting chills, very very bad chills/my teeth were chattering and mostly all night that was going on; I couldn't sleep at all; I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs; I have been having problems walking; I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs; I have been having problems walking; I tried to have breakfast I threw it up; Its been very bad and all week I have been very weak; This is a spontaneous report received from a 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 28Nov2022 at 13:15 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 81 years for covid-19 immunisation. The patient's relevant medical history included: "border line diabetic" (unspecified if ongoing), notes: Not really,no I am border line diabetic I don't think so. I am going to go for some testing now, no. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation as dose number unknown, single. Vaccination history included: Covid-19 vaccine (Primary immunization series complete unknown manufacturer), for COVID-19 immunization. The following information was reported: MIGRAINE WITH AURA (non-serious), outcome "unknown", described as "Migraine auras in my eyes"; DECREASED APPETITE (non-serious), outcome "unknown", described as "I had no appetite"; CHILLS (non-serious), outcome "unknown", described as "I started getting chills, very very bad chills/my teeth were chattering and mostly all night that was going on"; INSOMNIA (non-serious), outcome "unknown", described as "I couldn't sleep at all"; GAIT INABILITY (non-serious), SENSORY LOSS (non-serious), outcome "unknown" and all described as "I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs; I have been having problems walking"; VOMITING (non-serious), outcome "unknown", described as "I tried to have breakfast I threw it up"; ASTHENIA (non-serious), outcome "unknown", described as "Its been very bad and all week I have been very weak". Therapeutic measures were taken as a result of migraine with aura, decreased appetite, chills, insomnia, gait inability, sensory loss, vomiting, asthenia. Additional information: I had two Migraine auras in my eyes when I got home that day and then at night starting around not after dinner I suppose I had no appetite. I started getting chills, very very bad chills, my teeth were chattering and mostly all night that was going on. I couldn't sleep at all and I couldn't walk. I had no feeling in my legs, hardly any feeling in my legs. I had to get something, a walker to help me. And then when I woke up and I tried to have breakfast I threw it up. Its been very bad and all week I have been very weak and I have been having problems walking also and no appetite. Patient believes that she had taken Tylenol for the adverse events and does not have information relating to flu shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine with aura
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetic (Not really,no I am border line diabetic I don't think so. I am going to go for some testing now, no)
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2525621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 20.10.2022
Beginn: 23.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain upper Chills Decreased appetite Dyspnoea Headache Influenza virus test negative Nausea Pyrexia SARS-CoV-2 test negative

Symptomtext

About three days after the dose 4 I began to have chills and feeling like I couldn't really catch my breath. I had a headache, and I had no appetite. I was nauseous. I had a fever, temp of 101.5. My stomach was really turning a lot. They symptoms began slowly and got worse. I am slowly recovering. Since I have asthma, I am still having trouble. I have taken two sets of steroids, one five-day and one-seven day. They said I had all the symptoms of RSV but they were unable to test me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Flu test, negative, 10/2022; COVID-19, negative, 10/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: DULERA inhaler; PROZAC; ibuprofen
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2525347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chest discomfort Chills Dyspnoea Fatigue Feeling abnormal Feeling hot Fibrin D dimer increased Headache Mobility decreased Pain Pyrexia Vertigo

Symptomtext

After I received the vaccine, I felt a warm sensation in my throat. Within 30 minutes of receiving the vaccine, I had a tightening in my chest, I started experiencing, chills and my body ached all over. Within 2 hours of receiving the vaccine, I was still experiencing the same symptoms but they were getting worse. Within 4 hours I felt I couldn't move and all I wanted to do was lay down.I slept for an hour. The symptoms were worse and I was short of breath and my head was swimming, I hurt all over, inside and out. I couldn't get up. I was like this for almost 16 hours. After 48 hours I was able to get to the bathroom and take a bath but symptoms were still there. After 6 more hours my fever broke. Its been 7 days and I am still experiencing a headache, body aches, chills, tightness of the chest, shortness of breath, my head is still swimming and I had no energy. I do not feel the same as I did before the vaccine and I am so tired all the time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: High D-Dimer
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ibuprofen
Allergien: morphine
Vorherige Impfungen: -

VAERS 2524334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MA
Alter: 79,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 28.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: SYR / LA

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

Dizziness Hypertension

Symptomtext

Starting a few weeks after receiving the vaccine, I developed some lightheadedness. I checked my blood pressure and it was sky high. For the next couple of days, I continued to monitor it. It was still high, but not as high as before (around 160/90). After 3-4 days, I contacted my PCP. The office told me to increase the dosage of the hydrochlorothiazide by 1/2 so take 1.5 tablets instead of 1. After that, I have had fewer days of high blood pressure but its still running high on occasion. I have an appointment with my doctor this Friday (12/09/2022) in regards to the blood pressure issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis; Borderline blood pressure
Andere Medikamente: Hydrochlorothiazide; calcium with vitamin D; vitamin C; zinc
Allergien: Dronate medications (for osteoporosis) like FOSAMAX
Vorherige Impfungen: Mild rash after the first Moderna vaccine

VAERS 2521913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: WI
Alter: 66,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 29.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Axillary pain Chest pain Fatigue

Symptomtext

Patient described waking up the day after vaccination around noon and having a sore armpit (possibly due to swollen lymph node). They also felt tired and their chest was sore. They described the soreness as a pulled muscle, but not chest pain. No difficulty breathing. By the next day the tiredness and chest soreness went away and just the armpit soreness remained. Today, 3 days later, the armpit is still sore. Patient will continue to monitor and contact the dr/ go to ER if anything worsens or if something concerning arises.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Synthroid, Sertraline, OTC/dietary/ herbal unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2517915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: PA
Alter: 79,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Blood glucose increased Dyskinesia Incoherent Nausea Pneumonia Vomiting

Symptomtext

Documented at 837am and was jerking motion and incoherent x 30 seconds. nausea w/emesis followed. Pt treated with Zofran IV, 200 cc NS. Blood glucose checked and was 226. Dr. was notified. Pt was stable on discharge and was discharged to home. Patient admitted next day with diagnosis of Pneumonia. MD not sure if any correlation. Patient already had existing issues with multiple recent hospitalizations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: CKD
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2517311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: OH
Alter: 71,0
Geschlecht: M
Eingang: 26.11.2022
Impfdatum: 17.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypoaesthesia Injection site swelling Paraesthesia Swelling

Symptomtext

Site: Swelling at Injection Site-Medium, Systemic: Numbness and swelling-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Numbness and swelling

Weitere VAERSDATA-Felder

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

VAERS 2515699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Differential white blood cell count Fatigue Full blood count Headache Malaise Vaccination site pain

Symptomtext

I started to have headaches, fatigue and feeling ill. I already had chronic headache and fatigue, but I haven't had headaches for a while and I barely use my medication for it. My arm was sore on vaccination site. On the 4th -7th I took several medications for headache because it wouldn't go away. I also used and ice pack for my migraines which works better than the medications. I drove to the urgent care on the 8th for my headache, which was better that day. My doctor ran some test, and I had an acute non-intractable headache. On 10th-14th I started having migraines again and I was taking medication for it. On the 16th-17th I had more headaches. I am waiting on my doctor to see if she wants me to get an MRI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CBC Differential, acute non-intractable headache, 11/08/2022
Aktuelle Erkrankungen: Scratchy throat
Vorgeschichte: Chronic Fatigue Syndrome; Migraines; Eye conditions Irritable Bowel Syndrome; Cholecystitis; Iliac; B12 Inefficacy; Hyponatremia; CMS-HCC
Andere Medikamente: Vitamin B; vitamin D; cholecalciferol
Allergien: Amitriptyline; diphenhydramine HCL; zaleplon; amoxicillin- pot clavulanate; penicillin; mirtazapine; chlorpheniramine-pseudoephedrine; omeprazole
Vorherige Impfungen: -

VAERS 2512392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MA
Alter: 35,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 11.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Mobility decreased Pyrexia Vaginal prolapse

Symptomtext

I noticed a significant vaginal prolapse while showering, 11/12/22, the day after of receiving a Pfizer bivalent vaccine 11/11/22. There was no prolapse 11/10/22 and I did not notice one 11/11/22. I did nothing different in between the time of the vaccine and the following evening. I spent most of my day laying on the cough with a low grade fever. The prolapse has subsided by the time I went to my visit my PCP on 11/17/22 so no labs were done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Never been pregnant and regular menstruation cycle
Vorgeschichte: Cardiovascular disease
Andere Medikamente: Enalapril, sotalol, and spironolactone
Allergien: Dust and lamb
Vorherige Impfungen: -

VAERS 2510460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 25.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Hypoaesthesia Injection site pain Mobility decreased Paraesthesia

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: TINGLING SENSATION/ NUMBENESS-Severe, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: PT REPORTS SHE COULD NOT MAKE A FIST WITH HER LEFT ARM. TINGLING SENSATION/ NUMBNESS THIS STARTED 24 HOURS POST VACCINE AND LASTED FOR ABOUT 2-3 MINS

Weitere VAERSDATA-Felder

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

VAERS 2510336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: FL
Alter: 83,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Asthenia Dyspnoea Electrocardiogram Wrong product administered

Symptomtext

Bivalent, Dose Number: 2; SOB; weakness; This is a spontaneous report received from a contactable reporter(s) (Nurse). An 83-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Nov2022 as dose 2, single (Lot number: GJ6665) at the age of 83 years intramuscular, in left arm for covid-19 immunisation. The patient didn't receive BNT162b2 (BNT162B2). The patient's relevant medical history included: "TIA" (unspecified if ongoing); "Heart Failure" (unspecified if ongoing); "Depression" (unspecified if ongoing); "Pax AFIB" (unspecified if ongoing). No known allergies. No other vaccine in four weeks. No covid prior vaccination. Was not covid tested post vaccination. Concomitant medication(s) included: COUMADIN; POTASSIUM CHLORIDE; DONEPEZIL; LEXAPRO. Vaccination history included: Covid-19 vaccine (Dose 1, Batch/Lot No: Unknown), for COVID-19 Immunization. The following information was reported: DYSPNOEA (medically significant) with onset 08Nov2022, outcome "recovering", described as "SOB"; ASTHENIA (medically significant) with onset 08Nov2022, outcome "recovering", described as "weakness"; WRONG PRODUCT ADMINISTERED (non-serious), outcome "unknown", described as "Bivalent, Dose Number: 2". The patient underwent the following laboratory tests and procedures: Electrocardiogram (EKG): unknown results. Therapeutic measures were taken as a result of dyspnoea, asthenia. Events treatment included oxygen and EKG. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: As there is limited information in the case provided, the causal association between the events dyspnoea, asthenia with the suspect product BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), cannot be excluded. The case will be reassessed once new information is available. 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: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: EKG; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Heart failure; Paroxysmal atrial fibrillation; TIA
Andere Medikamente: COUMADIN; POTASSIUM CHLORIDE; DONEPEZIL; LEXAPRO
Allergien: -
Vorherige Impfungen: -

VAERS 2507171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: VA
Alter: 74,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 05.10.2022
Beginn: 07.11.2022
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: SYR / RA

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

Anticoagulant therapy Atrial fibrillation Blood test abnormal Condition aggravated Electrocardiogram abnormal Heart rate irregular Tremor

Symptomtext

11/7/2022 I had a violent shaking on the inside of my body. I guess it was my heart or pulse and it was shaking my body. This lasted off and on along with my irregular heartbeat for a couple of hours. I went to the emergency room. I was hooked up to an EKG and had blood work. I was told I had A Fib. This could be related to Lyme's disease I had in the 90's. I was hospitalized. I was on an IV with medication that lowered my blood pressure really low. I am not sure what the medication was. My ELIQUIS and metoprolol were increased. I was released the next day. Since then, my heartbeat is briefly irregular.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: EKG, Afib, blood work, Afib
Aktuelle Erkrankungen: None
Vorgeschichte: Osteo Arthritis; Neuropathy; Tinnitus; Blood clot; 2 PE's and a DVT; A Fib; Hiatal hernia; Thyroid nodules; Partially torn rotator cuff in Left arm; left bundle block
Andere Medikamente: Gabapentin; ELIQUIS; metoprolol; olmesartan
Allergien: Amoxicillin; LEVAQUIN; codeine; sulfa
Vorherige Impfungen: -

VAERS 2506771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 13.11.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Impaired driving ability Impaired self-care Impaired work ability Injected limb mobility decreased Injection site nodule Injection site swelling Loss of personal independence in daily activities Pain Petechiae Pruritus Urticaria

Symptomtext

Once zyrtec was stopped post vaccination (taken as a pre-medication and two days post vaccine per past success with prior pfizer covid shots), a knot began to form in or under the left deltoid muscle, swelling into the bursa and causing similar range-of-motion limits to that of a torn rotator cuff. Left breast also developed intense itching consistent with hives (with petechiae). Pain and limited range of motion is ongoing as of this report. Uncertain if it will resolve or how fast, but I will seek care if it gets worse. For now I am stating below that it HAS caused disability, because I cannot use my arm for work, and it is limiting daily tasks like driving and self care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: none yet, as no life threatening anaphylaxis has developed at this time, and it is the weekend and I would rather not add to existing hospital overload - I will reach out to my PCP when they are open.
Aktuelle Erkrankungen: mild covid infection 1 month prior (faint indicator on home test), shoulder injury on opposite side of shot administration, seasonal rhinitis
Vorgeschichte: Mast Cell Disease, Ehlers Danlos Syndrome, Asthma, Arthritis, Fibromyalgia
Andere Medikamente: Xolair, Xopenex, Cromolyn Sodium, Quercetin, BC powder (aspirin/caffeine), b-12, methylfolate, zyrtec, tizanidine, tramadol, ketotifen
Allergien: corn, corn derivatives, rice, eucalyptus, Imitrex, Elavil, escitalopram, Tylenol, chlorhexidine gluconate, melons, kiwi, banana, chemical sensitivities
Vorherige Impfungen: -

VAERS 2503808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

moderat

Staat: OR
Alter: 61,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Injected limb mobility decreased Injection site bruising Injection site pain Loss of personal independence in daily activities

Symptomtext

Bruising and pain at injection site beginning shortly after administration. Pain continued from 10/7/22 until present with limited range of motion in left shoulder without pain. Pain has diminished some since injection, but is still causing discomfort in daily activities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2503198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: VA
Alter: 68,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 01.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Atrial fibrillation Chest pain Electrocardiogram abnormal Hypotension Influenza virus test negative Magnetic resonance imaging Pericardial effusion Pyrexia SARS-CoV-2 test negative Troponin Ultrasound scan Viral infection X-ray

Symptomtext

Starting 11/05/2022, I developed chest pain and a 102 fever. I ran a home EKG and was in afib. My heart rate was running 128-148. I went to the ER and my BP was so low that they were very concerned and couldn't believe it. They transported me to a specialty hospital via ambulance. They determined I had an effusion caused by an unknown virus. They tested for all COVID-19 and Flu Variants but all were negative. I am still in afib and still have an effusion. However, they are having me wait it out to see if it goes down on its own then they can give me blood thinner prophylactically to prevent stroke. Per the hospital, they could neither confirm nor deny that the vaccine may have played a part.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: EKG (at home and in the hospital): A-fib; Sonogram; MRI; X-ray; Troponin test (all at the hospital)
Aktuelle Erkrankungen: Pleurisy flare up
Vorgeschichte: Pleurisy; Asthma
Andere Medikamente: Rosuvastatin; baby aspirin; SYMBICORT; testosterone
Allergien: Antibiotic (unknown name)
Vorherige Impfungen: -

VAERS 2502567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 08.11.2022
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: nein

Paraesthesia

Symptomtext

Client presented to local Covid Vaccination Site on 11/01/2022 to receive Pfizer Bivalent COVID vaccine Lot#GJ6665 on left arm. At approximately 13:53 while sitting in the observation area client reported to lead nurse ?tingling sensation of both hands.? Client reports this has never happened with previous COVID vaccines. Client denies dizziness, shortness of breath and pain. Client was able to transfer to gravity chair without assistance. At approximately 1355 vital signs were taken by nurse; BP:110/79 mmHg, HR:96, RR:14, O2:97%. Client reports no known allergies a history of insomnia and is taking medication for insomnia (medication not specified.) Client reported she had breakfast around 8 in the morning. At approximately 1405 vital signs were taken by nurse; BP:112/72mmHg, HR:86, O2:98%. Client reported left hand improved, some tingling sensation on right hand. Client rested for ten more minutes in gravity chair. At 1615 vital signs were taken by nurse; BP:113/73mmHg, HR:86, O2: 98%. Client reported to PHN that both hands had improved. Client rested for approximately ten more minutes. At approximately 1625 vital signs were taken by nurse; BP:115/79mmHg, HR:82, O2:97%. Client reported to PHN that tingling sensation on left hand had resolved, right hand sensation was there but it had improved from when she reported. Client reported she felt good to leave. Client reported she was not driving, that she was accompanied by someone. PHN educated client on when to seek medical care. Client verbalized understanding. Client left the facility with a steady gait.

Weitere VAERSDATA-Felder

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

VAERS 2501322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: TX
Alter: 87,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / -

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

Decreased appetite Fatigue Feeling cold Nausea Somnolence Tremor Weight decreased

Symptomtext

adds loss of appetite; Began violently shaking, her full body and felt cold; Began violently shaking, her full body and felt cold; Felt not overwhelming nausea; felt she should not be eating.; Slept for 24 hours/sleepy; Lost weight/lost 6 pounds recently; Tired; sleepy; This is a spontaneous report received from contactable reporter (Nurse). The reporter is the patient. An 87-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: GJ6665) at the age of 87 years for prophylaxis. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU VACCINE VII, in Oct2022 as dose number unknown, single. Vaccination history included: BNT162b2 (Dose 1, Anatomical Site of injection: left arm, Route of Administration: intramuscular, Batch/Lot number: EL9262), administration date: 24Jan2021, when the patient was 85-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, Anatomical Site of injection: left arm, Route of Administration: intramuscular, Batch/Lot number: EL9266), administration date: 14Feb2021, when the patient was 85-year-old, for COVID-19 immunization; BNT162b2 (Dose 3, Anatomical Site of injection: left arm, Route of Administration: intramuscular, Batch/Lot number: FF8839), administration date: 02Nov2021, when the patient was 86-year-old, for COVID-19 immunization; BNT162b2 (Dose 4, Anatomical Site of injection: left arm, Route of Administration: intramuscular, Batch/Lot number: FK9893), administration date: 27Apr2022, when the patient was 86-year-old, for COVID-19 immunization, reaction(s): "lost 20 pounds prior to the bivalent booster.". The following information was reported: TREMOR (medically significant), FEELING COLD (medically significant) all with onset 27Oct2022, outcome "recovered" (28Oct2022) and all described as "Began violently shaking, her full body and felt cold"; NAUSEA (medically significant) with onset 27Oct2022, outcome "recovered" (30Oct2022), described as "Felt not overwhelming nausea; felt she should not be eating."; WEIGHT DECREASED (medically significant) with onset 27Oct2022, outcome "recovered" (30Oct2022), described as "Lost weight/lost 6 pounds recently"; SOMNOLENCE (medically significant) with onset 27Oct2022, outcome "recovered with sequelae" (28Oct2022), described as "Slept for 24 hours/sleepy"; FATIGUE (medically significant) with onset 27Oct2022, outcome "recovering", described as "Tired; sleepy"; DECREASED APPETITE (medically significant), outcome "recovering", described as "adds loss of appetite". Clinical course details: 8 hours after getting the vaccine she began violently shaking, her full body and felt cold. Felt not overwhelming nausea; felt she should not be eating. Stayed in bed and slept for 24 hours, except for the bathroom breaks. States she lost lost 6 pounds recently and lost 20 pounds prior to the bivalent booster. It was reported that, the patient had not had any reactions before that.; Sender's Comments: Considering the plausible drug-event temporal association, there is a reasonable possibility that reported events were related to BNT162B2 vaccine administration. Case will be reassessed upon receipt of additional information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

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

VAERS 2500104

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ6665

moderat

Staat: WA
Alter: 79,0
Geschlecht: F
Eingang: 06.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Dizziness Gait disturbance Mobility decreased

Symptomtext

A few minutes after receiving the vaccine, the customer felt faint and dizzy and was sitting in the waiting area. She reported some weakness and dizziness. Her spouse was with her and we called Emergency services for evaluation. They came and checked her out and said they need to take her to the hospital for further checks. Apparently, she had a history of stroke and was evaluated for that at the store. The next day I called the spouse and the patient had already been discharged to home. The episode had resolved and no further information was available. The patient was responding normal and could walk and move as before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Hospital evaluation - no data available
Aktuelle Erkrankungen: Had previous stroke according to spouse
Vorgeschichte: -
Andere Medikamente: -
Allergien: Sulfa Medications
Vorherige Impfungen: -

VAERS 2498269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ 6665

moderat

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 03.11.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Palpitations Tremor

Symptomtext

Extreme shaking at 7 hours after Vax with racing heart 120 bpm from 1:00 am til 12:00 pm. Forced Dr visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: CLL/SLL diagnosed 10/14/2021.
Andere Medikamente: Calquence 100 mg twice daily to treat CLL/SLL.
Allergien: None known.
Vorherige Impfungen: -

VAERS 2497747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 02.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Arthralgia Arthritis Condition aggravated Pain in extremity

Symptomtext

PATIENT STARTED TO GET ACHE IN BACK OF HAND LIKE ARTHRITIS WORKED UP ARM INTO SHOULDER AREA. CURRENTLY STILL ACHES AT TOP OF SHOULDER BLADE , DIDN'T DO ANYTHING PHYSICAL TO INFLAME ARTHRITIS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: NO
Aktuelle Erkrankungen: NO
Vorgeschichte: DIABETES, HEART ATTACK, ARTHRITIS
Andere Medikamente: METFORMIN, PLAVIX, VIT D, PANTOPRAZOLE, LEVOTHYROXINE, LISINOPRIL, BETAPACE, NORCO, ELIQUIS, PRAVACHOL
Allergien: CODEINE
Vorherige Impfungen: -

VAERS 2497719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

moderat

Staat: MA
Alter: 77,0
Geschlecht: M
Eingang: 03.11.2022
Impfdatum: 24.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Cyanosis Dyspnoea

Symptomtext

Shortness of breath, cyanotic- Epinephrine and Benadryl administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Pneumonia treated at beginning of October
Vorgeschichte: CHF, Dementia, COPD, BPH, restless leg syndrome, hypothyroidism, depression, hyperlipidemia
Andere Medikamente: Probiotic Oral Capsule, Ferrous Sulfate, Synthroid, Aggrenox Capsule Extended Release, Acetaminophen, Sertraline, tramadol, lipitor, Trelegy Ellipta Aerosol Powder Breath, Furosemide
Allergien: Moderna vaccine
Vorherige Impfungen: Moderna vaccine

VAERS 2495725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Discomfort Paraesthesia

Symptomtext

My left shoulder has been feeling achy, tingly sometimes - I thought it was just musculoskeletal so I have been getting a massage regularly for a year, I always wonder where I got it. Then when I had my fourth vaccination, the discomfort became even more intense, so I realized I probably got the original ache from my third shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Metformin, CoEnzyme Q 10, DHEA
Allergien: Theraflu
Vorherige Impfungen: -

VAERS 2494991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

moderat

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 17.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / RA

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

Anxiety Condition aggravated Depression Feeling abnormal Insomnia Irritability Panic attack

Symptomtext

About a week after receiving the omicon covid booster (3 prior covid vaccines were moderna) I began to notice irritability, anxiety, and trouble sleeping. I then noticed depression symptoms. I doubled my dose of mirtazapine to 15 mg and increased my exercise which is usually enough to prevent a flare up. The symptoms got worse with depression severe enough to make it difficult to function, severe insomnia, anxiety and panic attacks (I have not had panic attacks in the past even with bad flare ups). My doctor gave me trazodone to add to the increased dose of mirtazapine, the depression symptoms are beginning to ease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No tests. Antidepressant dose increased from 7.5 mg up to 15 mg mirtazapine. Trazodone added.
Aktuelle Erkrankungen: no symptoms
Vorgeschichte: Depression, well controlled for years on 7.5 mg mirtazapine once daily at bedtime. Mild intermittent asthma, no symptoms x years, no medication. Breast cancer survivor, in remission.
Andere Medikamente: mirtazapine 7.5 mg at bedtime tamoxifen 20 mg each morning vitamin D3 1000 units when remembered (not daily) multivitamin when remembered (not daily)
Allergien: betadine - rash
Vorherige Impfungen: Rash at injection site after 1st Moderna covid vaccine.

VAERS 2494987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 28.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Chills Decreased appetite Fatigue Headache Mobility decreased Pyrexia Vaginal haemorrhage

Symptomtext

Fever chills fatigue headache inappetance unable to get out of bed for 3 days Heavy vaginal bleeding despite being menopausal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known
Vorherige Impfungen: Same reaction after second Covid vaccine also Pfizer but not first or third

VAERS 2494190

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

moderat

Staat: MA
Alter: 60,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 17.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: IM / RA

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

Asthma Atrial flutter Blood test Cardioversion Condition aggravated Cough Dyspnoea Electrocardiogram Palpitations

Symptomtext

I always get a cough from the Covid vaccine and my asthma acts up, requiring albuterol at times and regular wexela doses for up to one month following vaccination. Although I seemed to be coughing less than with previous Covid vaccines, I seemed more out of breath than with the other doses. I received the vaccine on Monday 10/17, along with the FLU vaccine. On Friday 10/1 I was awoken by my heart racing , registering 140 on my Fitbit. This continued on throughout the day and night and into Saturday. I called the doctor on Saturday afternoon and was sent to urgent care. From there I was sent by ambulance to the hospital for Atrial Flutter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: ECGs on 10/22, 10/23, 10/24. Atrial Flutter Blood work on 10/22, 10/23, 10/24. Cardioversion to regain normal sinus rhythm Plan is for outpatient ablation in January 2023.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, fibromyalgia, high cholesterol, s/p sarcoidosis
Andere Medikamente: Cymbalta, Lipitor, wixela, singular, Tylenol, colac, multivitamin
Allergien: Benzoin, Vicodin
Vorherige Impfungen: -

VAERS 2494171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 28.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Burning sensation Condition aggravated Headache Limb discomfort Neuropathy peripheral Pain Pain in extremity Pyrexia

Symptomtext

My peripheral neuropathy has been under good control for over a year, with Gabapentin. The day after the vaccine was given, I had a very painful, severe almost 24 hour period of pain in both feet exactly like my neuropathy was over a year ago. Gabapentin and Tylenol provided no relief. There was burning and stinging in both feet, worse in the hallux. This went away in less than 24 hours, but was severe for over 12 hours. I have not had this severity of pain (8/10) in over a year. I did have 103 fever, body aches and headache the day after the vaccine all of which subsided within 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: 1. Gaucher disease 2. Type 2 DM 3. Idiopathic peripheral neuropathy 4. Hypertension
Vorgeschichte: All items listed in 11.
Andere Medikamente: Bisoprolol, Gabapentin, Chlorthalidone, Lisinopril,Metformin,Atarax,Multivit,Lipitor,Pantoprazole, Potassium 20 meq, Carafate, and PRN Tizanidine, Magnesium
Allergien: Tetracycline
Vorherige Impfungen: Only fever, body ache and headache from prior Pfizer Covid vaccines

VAERS 2493923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CO
Alter: 31,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 07.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / RA

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

Allergy test positive Anxiety Breast feeding Depression Dyspnoea Fatigue Impaired driving ability Intrusive thoughts Sleep disorder

Symptomtext

I just started feeling very tired, like I would fall asleep while driving. After a few days of this I started with deep depression and anxiety. I couldn't breathe properly and started waking up in the middle of the night which I don't normally do. Then I started having very intrusive thoughts that I don't feel like are mine. I have an active H-Pylori infection I'm working with an allergist to treat and just stared antibiotic. I am breast feeding also. I started having antihiatic reactions in August which I never had and then had a food allergy test. I had COVI-19 in May and my heart rate was really high and it took 3 weeks for it to get back to normal. Then after COVID I had another virus and a zpack. The COVID-19 symptoms I had were a dry cough and a faucet of a runny nose. The cough lasted a few days and runny nose for a few weeks. For a few days I had a severe fever and body aches that I managed with Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Food allergy skin test - 20 food allergies found.
Aktuelle Erkrankungen: I have an active H-Pylori infection
Vorgeschichte: No
Andere Medikamente: Vitamin D3 K2; Monolaurin-Avail; Zinc balance; Vitamin C
Allergien: Nonsteroidal anti-inflammatories; Red dye; Shrimp; Banana; Blueberry; Asparagus; Cauliflower; Cherry; Cranberry; Cucumber; Walnut; Cashew; Hazelnut
Vorherige Impfungen: -

VAERS 2493397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 07.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: SYR / LA

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

Blood magnesium normal Blood pressure increased Blood test normal Chest X-ray normal Chest pain Dyspnoea Electrocardiogram normal Fibrin D dimer normal Heart rate increased Injection site pain International normalised ratio normal Metabolic function test normal Neck pain Pain in extremity Prothrombin time normal Troponin normal

Symptomtext

10/8/22 -Pain at injection site & also achy pain under arm 10/21/22-pain in left chest up to neck, bad chest pain on inhaling (worse on any exertion & after laying down), shortness of breath, high BP, fast pulse

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/21/22 ECG, blood work-Initial Troponin, Protime INR, D-Dimer quantitative, Magnesium, Comp Metabolic Panel, 90 minute Troponin, X-ray chest *ALL NORMAL RESULTS
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension-controlled
Andere Medikamente: Lisinopril 20 mg, multi-vitamin, vitamin D
Allergien: Epinephrine, nickel
Vorherige Impfungen: After 2nd Covid shot on 3/29/2021?Phizer lot# ER-8730. Age 59. Chest throbbing/palpitations on bending forward, shortness of bre

VAERS 2492609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: ME
Alter: 68,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 27.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Asthenia Blood pressure increased Chills Dyspnoea Heart rate increased Pyrexia Tremor Vomiting

Symptomtext

FEVER 102F, Shortness of breath, oxygen saturation 77% on room air, shaking and chills, vomiting, weakness, elevated heart rate and elevated BP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: ACUTE AND CHRONIC RESPIRATORY FAILURE WITH HYPOXIA, PNEUMONIA, UNSPECIFIED ORGANISM, TYPE 2 DIABETES MELLITUS WITH FOOT ULCER , TYPE 2 DIABETES MELLITUS WITH DIABETIC NEUROPATHY, UNSPECIFIED, TYPE 2 DIABETES MELLITUS WITH MILD NONPROLIFERATIVE DIABETIC RETINOPATHY WITH MACULAR EDEMA, UNSPECIFIED EYE, ACUTE RESPIRATORY FAILURE WITH HYPOXIA, HYPERTENSIVE HEART AND CHRONIC KIDNEY DISEASE WITH HEART FAILURE AND STAGE 1 THROUGH STAGE 4 CHRONIC KIDNEY DISEASE, OR UNSPECIFIED CHRONIC KIDNEY DISEASE, NON-PRESSURE CHRONIC ULCER OF UNSPECIFIED HEEL AND MIDFOOT WITH UNSPECIFIED SEVERITY, ANEMIA IN CHRONIC KIDNEY DISEASE, HYPOTHYROIDISM, GASTRO-ESOPHAGEAL REFLUX DISEASE WITHOUT ESOPHAGITIS, GOUT, CHRONIC PAIN SYNDROME, CELLULITIS OF RIGHT LOWER LIMB, PERIPHERAL VASCULAR DISEASE, ACUTE ON CHRONIC DIASTOLIC (CONGESTIVE) HEART FAILURE, CHRONIC KIDNEY DISEASE, STAGE 4 (SEVERE)
Vorgeschichte: ACUTE AND CHRONIC RESPIRATORY FAILURE WITH HYPOXIA, PNEUMONIA, UNSPECIFIED ORGANISM, TYPE 2 DIABETES MELLITUS WITH FOOT ULCER , TYPE 2 DIABETES MELLITUS WITH DIABETIC NEUROPATHY, UNSPECIFIED, TYPE 2 DIABETES MELLITUS WITH MILD NONPROLIFERATIVE DIABETIC RETINOPATHY WITH MACULAR EDEMA, UNSPECIFIED EYE, ACUTE RESPIRATORY FAILURE WITH HYPOXIA, HYPERTENSIVE HEART AND CHRONIC KIDNEY DISEASE WITH HEART FAILURE AND STAGE 1 THROUGH STAGE 4 CHRONIC KIDNEY DISEASE, OR UNSPECIFIED CHRONIC KIDNEY DISEASE, NON-PRESSURE CHRONIC ULCER OF UNSPECIFIED HEEL AND MIDFOOT WITH UNSPECIFIED SEVERITY, ANEMIA IN CHRONIC KIDNEY DISEASE, HYPOTHYROIDISM, GASTRO-ESOPHAGEAL REFLUX DISEASE WITHOUT ESOPHAGITIS, GOUT, CHRONIC PAIN SYNDROME, CELLULITIS OF RIGHT LOWER LIMB, PERIPHERAL VASCULAR DISEASE, ACUTE ON CHRONIC DIASTOLIC (CONGESTIVE) HEART FAILURE, CHRONIC KIDNEY DISEASE, STAGE 4 (SEVERE)
Andere Medikamente: Allopurinol Tablet 100 MG, Ascorbic Acid Tablet 500 MG, Aspirin 81 MG, Bactrim DS Tablet 800-160 MG, buPROPion HCl ER (XL) 300 MG, Colchicine Capsule 0.6 MG, Fluticasone Propionate Suspension 50 MCG/ACT, Levothyroxine Sodium Tablet 100MCG,
Allergien: LISINOPRIL, KEFLEX
Vorherige Impfungen: -

VAERS 2492450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

moderat

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Dizziness Injection site pain Tachycardia

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Tachycardia-Medium

Weitere VAERSDATA-Felder

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

VAERS 2491792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: NV
Alter: 59,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 01.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 9,0
Dosis: 5
Route/Site: IM / LA

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

Back pain Balance disorder Burning sensation Dizziness Paraesthesia

Symptomtext

On or about October 10, 2022, I started having tingling down both arms, tingling in my left cheek and a burning sensation in my back. I also felt lightheaded and off balance. I started taking ibuprofen for the inflammation and it helped a little bit. I saw the doctor on October 14th and they recommended physical therapy for my back pain. I was also referred to a pain management doctor. I have seen him on October 20th and 26th and they will do an epidural soon. As of today, my symptoms are still the same by my back pain is now lower towards my tail bone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: History of Bronchitis
Andere Medikamente: Vitamin D3; Vitamin B12; Vitamin C; Ultimate Eye Support Vitamin; Magnesium
Allergien: Flonase Nasal Spray
Vorherige Impfungen: -

VAERS 2491227

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GJ6665

moderat

Staat: MA
Alter: 56,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 24.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / RA

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

Body temperature increased Hypotension Tachycardia Unresponsive to stimuli

Symptomtext

Unresponsive, Tachycardia, Low bp, Temp 104 (sent to Er)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: QUADRIPLEGIA, DIABETES MELLITUS
Andere Medikamente: Zofran Tablet 4 MG ,Neurontin Capsule 100 MG, Multivitamin Tablet, Baclofen Tablet 5 MG, Pepcid Tablet 20 MG (, Wellbutrin SR Tablet Extended Release 12 Hour 100 MG , Tylenol Tablet 325 MG, metFORMIN HCl Tablet 500 MG, Colace Capsule 100 M
Allergien: Gentamicin, Bactrim, Mycamine, neomycin sulfate
Vorherige Impfungen: -

VAERS 2490164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: GA
Alter: 66,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 11.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / AR

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

Hypertension Muscle spasms Tremor

Symptomtext

A few days after having the shot, I experienced some things at another doctor visit. My blood pressure was high and on the same day, I began to feel tremors and muscle spasm in the arm where this continued for several days. They determined that it was an anomaly as far as the spike. They took it on another area of my arm and the blood pressure was in normal range. I have not had an opportunity to speak with the doctor about the muscle spasms yet. They are not as frequent as before, but they still show up. I'm not sure whether I have completely recovered but I don't recall feeling the spasm in the last 12 hours, but it does come and go. The doctor indicated that they would continue to monitor the blood pressure to see if there are additional issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Prostate; Pinched Nerve; Lymphedema
Andere Medikamente: Atorvastatin; Finasteride; Tamsulosin; Vitamin D; Vitamin B3; Stool Softener; Metamucil; Emergen-C
Allergien: Sulfa; Perma Quin; Ciprofloxacin
Vorherige Impfungen: COVID 19 Vaccine-3rd or 4th-Tingling and muscle spasms. Participant indicates he already reported

VAERS 2489272

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 24.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Abdominal pain Chest pain Fatigue Gastrointestinal pain Headache Nausea Pain Pyrexia

Symptomtext

I did not seek treatment for the reactions but I had a fever, fatigue, chest pains, severe abdominal pain, pain in my lower intestine, headache, aches, and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none I did not seek any treatment for these events
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Methylphenidate, Atomoxetine, Guanfacine, Omeprazole
Allergien: none known
Vorherige Impfungen: -

VAERS 2488494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: NY
Alter: 77,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 01.10.2022
Beginn: 02.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Chest X-ray abnormal Cough Fatigue Headache Inflammation Lymphadenopathy Malaise Mobility decreased Nausea Pneumonia Pyrexia Respiratory tract congestion SARS-CoV-2 test negative Sleep disorder Speech disorder Throat irritation

Symptomtext

I had fever, headache, fatigue, nausea, swollen glands, my throat was so inflamed I could hardly talk, I was coughing so bad I couldn't sleep, and had terrible chest congestion. I did a steam inhalation to break the congestion up. I was so sick I could hardly get out of bed. My relatives insisted that I go to Urgent Care. I tested negative for COVID-19 on 10/22/2022. When they listened to my lungs, they knew that something was wrong. They did a chest X-ray on 10/21/22 and it showed that I had Pneumonia. I have to go back in 2 weeks for another chest X-ray. I will be taking antibiotics until 11/1/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 Test - 10/22/22 - Negative; Chest X-ray - 10/21/22 - Pneumonia
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: I got the flu after getting a Flu vaccine about 10 years ago. Now, I get the weaker dose and I don't have an issue.

VAERS 2488428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 02.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / LA

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

Blood culture negative Blood test abnormal Computerised tomogram abnormal Condition aggravated Culture urine Diverticulitis Flatulence Ketosis Metabolic function test abnormal Skin induration Urine analysis abnormal

Symptomtext

Starting Wednesday morning I felt gas pains in lower colon area. It progressed and by Thursday morning the 20th of October I knew I was having an episode of diverticulitis. My doctor was unavailable. An urgent care doctor called me. My abdomen was hard to the touch. I went to ER that afternoon. I didn't have a fever, just pain. I had some tests. I had a high blood cell count and diverticulitis event but no ruptures. I was prescribed AUGMENTIN. I was discharged was Friday at 7:00AM. I began to get better but on Saturday the 22nd the ER called me back in because my cultures showed an abnormality. They did two more cultures and monitored me to ensure I did not have signs of a blood infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CT scan, abnormal, 10202022; blood panels, abnormal, 10202022; Urine test with culture, ketosis, 10202022; Metabolic panel, abnormal, 102022; blood cell count, abnormal, 10202022; blood cultures and metabolic, normal, 10222022; blood cell count, abnormal, 10222022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diverticulitis; Arthritis; Rosacea
Andere Medikamente: SOOLANTRA; TYLENOL; ZYRTEC
Allergien: N/A
Vorherige Impfungen: -

VAERS 2488267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: WI
Alter: 65,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

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

Back pain Blood pressure increased Chest X-ray Chest pain Electrocardiogram Fibrin D dimer Full blood count Hypertension Metabolic function test Pain Pain in jaw Troponin

Symptomtext

Patient states she had her COVID booster on 10/12 at about 4 p.m.. 3-4 hours later she developed a chest pain that started on the right side of her chest, and radiates to the left. At times it radiates up into her jaw. Patient states she is had this pain intermittently since the shot and thought it was getting better a few days ago but now seems that it has been worse. Patient states since 7 p.m. last night pain has been constant. She describes it as an ache, across her anterior chest. At times will go into her neck, and upper back. No radiation to the arms. No nausea, vomiting, shortness of breath or diaphoresis. Does not worsen with exertion. No history of this prior to the COVID booster shot. She is had prior COVID boosters, 3, with no symptoms. Patient also also concerned as she took her blood pressure this morning and noted it to be high. Denies any previous history of hypertension. On no medications. Denies vaping or smoking, does drink 2 alcoholic drinks a day. No new medications. Patient states today, with her elevated blood pressure, and ongoing chest pain she called the nurse line, who told her to come in to be evaluated. Patient herself denies cardiac history but states her mom had some cardiac symptoms but not aware of her having stents placed or any significant cardiac history. Patient had a DVT following childbirth many years ago and was on anticoagulation for a short time. Patient was started on amlodipine 5 mg daily for elevated blood pressure with instructions to appropriately follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: BMP, CBC, D-dimer, troponin, ECG, and chest X-ray were all obtained/performed on 10/25/22
Aktuelle Erkrankungen: none
Vorgeschichte: depression, gingivostomatitis herpes simplex, diverticulitis, hypothyroidism (not on any medications), bilateral varicose veins, fibroid uterus, congenital malformation of inferior vena cava, history VTE
Andere Medikamente: fiber supplement, calcium + vitamin D supplement, as needed ibuprofen
Allergien: Latex
Vorherige Impfungen: -

VAERS 2486414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

moderat

Staat: UT
Alter: 79,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 17.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / AR

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

Dysarthria Feeling abnormal Mobility decreased

Symptomtext

Per the husband, the patient was walking and suddenly said she didn't feel good. Her speech became slurred and she nearly fell down but her husband caught her. He laid her down in bed and she could not move her arms or legs. Her speech remained slurred and gradually improved over the course of about 10 hours. The episode lasted about 10 hours and she feels fine now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: the patient did not seek medical care
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2483851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: KY
Alter: 38,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 19.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Mobility decreased Pain in extremity Peripheral swelling Skin discolouration

Symptomtext

PT complains of not being able to move her arm, pain from her shoulder to her hand, swelling in the hand, and discoloration compared to the other hand

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: arthritis, depression/anxiety
Andere Medikamente: omeprazole, ibuprofen, fluoxetine, escitalopram
Allergien: ketorolac, nitrofurantoin, gabapentin, estradiol, morphine, tramadol
Vorherige Impfungen: -

VAERS 2480633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: OR
Alter: 51,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Aphonia Asthenia Chills Decreased appetite Fatigue Headache Immediate post-injection reaction Malaise Migraine Nausea Pain Thirst

Symptomtext

Right when I received the vaccine, I got nauseous and a headache that was like a migraine. I felt immediately felt sick and tired. The next day I had chills, headache, loss of appetite, very fatigued. I continued feeling worse and had body aches. I lost my voice a little bit. As of today, I still have barely any energy and I cannot quench my thirst. I have not had an appetite, either.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Inner stem device for bladder; Herpes; ADD; Over Active Bladder; Bi Polar Disorder; Anxiety; Agoraphobia; Asthma
Andere Medikamente: Desvenlafaxine; Lansoprazole; Vraylar; Valacyclovir; Vitamin C; Concerta; Myrbetriq; Buspar; Zyrtec; Vitamin D; Ritalin; Atorvastatin; Montelukast
Allergien: -
Vorherige Impfungen: -

VAERS 2479950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: AZ
Alter: 73,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Autoimmune disorder Dyspnoea Injection site pruritus Lip swelling Myasthenia gravis Rash Urticaria

Symptomtext

Site: Itching at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash Generalized-Mild, Systemic: Autoimmune Disease (diagnosed by MD)-Mild, Additional Details: Patient states she had hives and swelling of upper lip. Did not require epinephrine a and onset was later in the evening after vaccince. states she has myasthenia gravis and believes reaction related to this, however, reported reaction and wanted pharmacy to be aware. No MD visit reported. Patient self medicated with benadryl. No reported difficulty breathing

Weitere VAERSDATA-Felder

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

VAERS 2478109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 10.10.2022
Beginn: 10.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Chills Discomfort Dyspnoea Hot flush Hyperhidrosis Pain

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Chills-Mild, Systemic: Flushed / Sweating-Mild

Weitere VAERSDATA-Felder

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

VAERS 2475836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MI
Alter: 24,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 07.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Blood test normal Chest X-ray normal Dyspnoea Electrocardiogram normal Palpitations

Symptomtext

On October 8th heart palpitations and breathlessness started midafternoon and got noticeably worse around 8 pm. I went to the emergency room to get it checked out. After tests, the doctor could find no cause other than the vaccine, and I was released. The palpitations lessened on October 9th and were almost non-existent on October 10th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood panel: normal (October 9th) chest x-ray: normal (October 9th) EKG: normal (October 8th)
Aktuelle Erkrankungen: None
Vorgeschichte: Exercise induced asthma, eczema
Andere Medikamente: 24 hour Claritin
Allergien: Penicillin, minocycline
Vorherige Impfungen: -

VAERS 2475664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: MN
Alter: 42,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 03.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Blood pressure increased Cardiac stress test Chest pain Computerised tomogram thorax Dizziness Electrocardiogram normal Muscle spasms Scan with contrast

Symptomtext

10/9/2022 new onset of intermittent left-sided chest and shoulder pain. Cramping/stabbing intermittent pain not associated or relieved by movement. Some lightheaded feeling. Has persisted with infrequent occurrence for 3 days now. Elevated Blood pressure with Diastolic readings as high as 100.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG 10/10/2022: Normal, no indication of recent or current cardiac event. Pending: Cardiac Stress Test, Chest CT w/ contrast.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Overweight, GERD (Barret's Esophagus).
Andere Medikamente: Pantoprazole 40mg
Allergien: Seasonal allergies: tree pollen.
Vorherige Impfungen: -

VAERS 2472887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: FL
Alter: 55,0
Geschlecht: M
Eingang: 09.10.2022
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: nein

Abdominal pain Anxiety Arthralgia Blood pressure increased Condition aggravated Dizziness Fatigue Headache Limb discomfort Muscle spasms Myalgia Nausea Pain Photophobia

Symptomtext

I immediately became lightheaded and dizzy upon receiving the Pfizer bivalent 4th booster. I received the booster at approximately 11:45 am. By 8pm I started experiencing moderate to severe body aches, joint and muscle pain, fatigue, nausea, abdominal pain around my liver, Severe headache with intense light sensitivity, and since the booster there has been a noticeable increase in my blood pressure. My blood pressure since booster has been on average about 157/103 and it is not going down. I am very concerned about the blood pressure and the severe headaches as the headaches are not subsiding and are interfering with my daily life and the blood pressure is very concerning. I am also having moderate cramping in left leg that is quite uncomfortable. I have taken blood pressure medication and it had been unable to bring down my bp since the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2471896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

moderat

Staat: WV
Alter: 30,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 05.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Blood pressure increased Electrocardiogram normal Pain Palpitations

Symptomtext

Heart Racing, Palpitations, increased Blood Pressure. Achy as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Urgent Care visit- ECG, then they recommended Emergency Room visit around 5pm - ECG, then sent home - Everything looks fine and ECG looks excellent. Felt relief when that was fine.
Aktuelle Erkrankungen: n/a
Vorgeschichte: Fibromyalgia, Type II Diabetes, Osteoarthritis, High Blood Pressure,
Andere Medikamente: Metformin ER 500mg, Naproxen Sodium 550mg, Cetirizine 10mg, Pimecrolimus 1%, Triamcinolone Cream 0.1%, Ketoconazole Shampoo, Sumatriptan 25mg, Basaglar, Duloxetine 60mg, Albuterol Inhaler HFA, Clobetasol 0.05% Ointment, Fluticasone NS, Lisi
Allergien: Sulfa Medications and Dairy Products
Vorherige Impfungen: -

VAERS 2724952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MN
Alter: 54,0
Geschlecht: F
Eingang: 18.12.2023
Impfdatum: 28.12.2022
Beginn: 17.12.2023
Tage bis Beginn: 354,0
Dosis: 4
Route/Site: IM / RA

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

Cough Oropharyngeal pain Pyrexia SARS-CoV-2 test Sinus disorder

Symptomtext

Fever, cough, sinus problem, sore throat

Weitere VAERSDATA-Felder

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

VAERS 2659594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 21.07.2023
Impfdatum: 02.11.2022
Beginn: 19.12.2022
Tage bis Beginn: 47,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Cough Dyspepsia Mechanical urticaria Nasopharyngitis Oropharyngeal pain Pruritus Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I began cold symptoms Dec. 19 with runny nose and sore throat. By 12/23/22 I had a bad cough and took an at home COVID test that was positive. Due to a family cruise on 12/27 (that we canceled) I went to an urgent care facility to be tested for proof of a positive test to submit to for travel insurance. They gave me Paxlovid and Zpac to prevent Covid pneumonia. I tested negative 12/31 at home and I ended with rebound Covid, testing positive on 1/2/23 with another at home test.1/11/23 I was finally testing negative with the at home test. I began having itchiness that I couldn't scratch to make it go away, it felt sub-dural and moved around the skin. It only affect my upper chest and head. Every day I'd wake to see where my skin felt itchy. My PCP's PA prescribed Atarax for it which helped minimally. Eventually I saw an allergy specialist who thinks the virus brought on Dermotographism and increased the Atarax which helped the itchiness to go away. Early February, out of the blue, I started having heartburn. I tried Prilosec 40mg 2x/day and it was still burning. A GI specialist changed me to Pantoprazole 40 mg/2x/day and that has improved greatly. I have GI scope and capsule implantation scheduled for 9/7/23. IDK if this was all triggered by contracting Covid (which I don't know where I picked it up from and was the only one in the home of 3 people with it) or if they are coincidences.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: 12/24/23 in office and PCR Covid tests were positive Blood work testing done
Aktuelle Erkrankungen: 33 days before vaccine I had Bacterial Vaginosis and was treated for it.
Vorgeschichte: Hashimoto's Thyroiditis-not currently on medication Back issues and in PT for it back then and still am
Andere Medikamente: Crestor 10 mg 1x/daily Estradiol 0.01% Cream 1x/weekly
Allergien: Sensitive to Tramadol; after first Shingles Vaccine I had Shingles symptoms within 24 hours and blisters in 48 hours. No food or other product allergies.
Vorherige Impfungen: Shingrex 8/19/20; Vaers case 883397

VAERS 2659554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 77,0
Geschlecht: F
Eingang: 21.07.2023
Impfdatum: 01.10.2022
Beginn: 15.06.2023
Tage bis Beginn: 257,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Nasopharyngitis Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

My symptoms began with a sore throat. I took a home COVID-19 test and it was negative. I had cold symptoms. I continued to have symptoms and tested positive on June 18, 2023. I had runny nose, cough and mild congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19, positive, 06/15/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Eliquis; Lasix; Multaq; Calcium; Vitamin D
Allergien: Amiodarone; Norco
Vorherige Impfungen: -

VAERS 2651106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: MA
Alter: 56,0
Geschlecht: F
Eingang: 29.06.2023
Impfdatum: 17.02.2023
Beginn: 22.02.2023
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: - / -

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

Blood test Rash pruritic

Symptomtext

rashes in the stomach/rash on her stomach and now has a full blown rash head to toe and/Rash: Serious. Very unsightly, unpredictable, and itchy.; The initial safety information received was reporting only non-serious adverse drug reaction. Upon receipt of follow-up information on 26Jun2023, this case contains serious adverse reaction, and all safety information is processed together. This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 56-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Feb2023 as dose 4 (booster), single (Lot number: GJ6665) at the age of 56 years for covid-19 immunisation. The patient's relevant medical history included: "Urinary tract infection" (unspecified if ongoing). Concomitant medication(s) included: CEFUROXIME taken for urinary tract infection, start date: Feb2023, stop date: Feb2023; CIPRO [CIPROFLOXACIN] taken for urinary tract infection, start date: 20Feb2023; NITROFURAZONE taken for urinary tract infection, start date: Feb2023, stop date: Feb2023. Vaccination history included: BNT162b2 (Dose: 01, Lot Number: ER8731 had a hard time reading LOT on vaccine card.), administration date: 15Apr2021, when the patient was 54-year-old, for COVID-19 Immunization, reaction(s): "feeling yucky"; BNT162b2 (Dose: 02, Lot Number: EW0199, NDC/EXPIRY: Not on vaccine card), administration date: 08May2021, when the patient was 54-year-old, for COVID-19 Immunization, reaction(s): "feeling yucky"; BNT162b2 (Dose: 03, Lot Number: FD0809, NDC/EXPIRY: Not on vaccine card), administration date: 15Dec2021, when the patient was 54-year-old, for COVID-19 Immunization, reaction(s): "feeling yucky". The following information was reported: RASH PRURITIC (medically significant) with onset 22Feb2023, outcome "not recovered", described as "rashes in the stomach/rash on her stomach and now has a full blown rash head to toe and/Rash: Serious. Very unsightly, unpredictable, and itchy. ". It was reported that the patient started breaking out rashes in the stomach and that this has been going on for four months. The patient was then prescribed prednisone and that all her blood work results turned out normal. Mentioned that the patient has already talked to all the doctors but thought that it was a side effect from the vaccine. Also stated that she would wake up totally clear and after five minutes of walking, her rashes will start to appear. The patient wanted to know if there were similar reports to this and if there is any relevant information to what she is experiencing now. Further stated that the patient started getting rashes on her stomach and now has a full-blown rash from head to toe and has been to her doctors. The doctors have done every blood test imaginable, and all the patient's numbers were coming back fine. The doctors thinks that the rashes were a side effect of the booster. The patient has an appointment with an allergist to do allergy testing. There is nothing different about her environment now and everything is pointing to the booster. The patient mentioned that the side effect has been going on for four months already. The patient has been prescribed prednisone by the HCP to address the rash. The rash was described as serious, very unsightly, unpredictable, and itchy. It as been staying the same, and over the last two weeks, it has gotten worse. It used to come and go throughout the day. Rash would be clear when she woke up then 15 minutes later would break out and be covered and then the rash would go away during the evening time. But now she wakes up with no rash and 10 to 15 minutes later breaks out, then the rash goes away for 2 hours, then comes back, then goes away and an hour later comes back. There is no rhyme or reason or anything triggering the rash. It was unpredictable. The patient was also on ciprofloxacin due to urinary tract infection but discontinued after a day and a half because she broke out in a rash and thought that it was an allergic reaction to ciprofloxacin. Stated that Nitrofurazone was started probably around 08Feb2023 or 09Feb2023 for 5 days. The events "rashes in the stomach/rash on her stomach and now has a full blown rash head to toe and/rash: serious. very unsightly, unpredictable, and itchy. " required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: (2023) All her numbers are coming back fine; (2023) Normal, notes: all her blood work results turns out normal. Therapeutic measures were taken as a result of rash pruritic.; Sender's Comments: Based on temporal association, the event rash pruritic is possibly related to BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5). The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash pruritic
Hospital-Tage: -
Labordaten: Test Date: 2023; Test Name: Blood test; Result Unstructured Data: Test Result:All her numbers are coming back fine; Test Date: 2023; Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Comments: all her blood work results turns out normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Urinary tract infection
Andere Medikamente: CEFUROXIME; CIPRO [CIPROFLOXACIN]; NITROFURAZONE
Allergien: -
Vorherige Impfungen: -

VAERS 2648479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: MS
Alter: 66,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 21.12.2022
Beginn: 01.01.2023
Tage bis Beginn: 11,0
Dosis: 5
Route/Site: IM / RA

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

Constipation Cough Muscle spasms Nasal congestion Oropharyngeal pain Pain in extremity Peripheral swelling Pharyngeal erythema Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative Throat irritation

Symptomtext

After I received the vaccine, my arm swelled for about three days and hurt. In 01/2023, I began having spasms in my back and I thought I was constipated. I drank lots of fluids and eventually felt better. I developed a cough that lasted for several weeks. In 04/2023, I had a very bad sore and red throat. I tested negative for COVID-19. I have had a lot of nasal congestion and drainage. As of today, I continue to have random days of my throat burning and congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Prediabetic; High Cholesterol; High Blood Pressure
Andere Medikamente: N/A
Allergien: Penicillin; Codeine
Vorherige Impfungen: 2nd Hepatitis vaccine, in 1991, I had a rash appear on my face.

VAERS 2644629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MN
Alter: 85,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 18.10.2022
Beginn: 10.06.2023
Tage bis Beginn: 235,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Chest X-ray Nausea SARS-CoV-2 test Vomiting

Symptomtext

Presented to ED on 6/11 with nausea and vomiting, along with weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: COVID 19 PCR 6/10/23, Chest Xray
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, CAD, Stents placed, HTN, OSA
Andere Medikamente: -
Allergien: Levaquin
Vorherige Impfungen: -

VAERS 2642994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: OR
Alter: 74,0
Geschlecht: F
Eingang: 08.06.2023
Impfdatum: 25.10.2022
Beginn: 11.05.2023
Tage bis Beginn: 198,0
Dosis: 5
Route/Site: IM / -

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

COVID-19 Cough Fatigue Poor quality sleep Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

In the evening I noticed my nose was running and I was very tired with a cough. I had fitful sleep that evening. This was just returning from a trip. 5/12 Symptoms stayed about the same. 5/13 I had overwhelming fatigue and tested with an At Home COVID-19 Test. Positive results. 5/15 Talked to doctor who proscribed Paxlovid. When I started taking Paxlovid, the fatigue and the runny nose really diminished. By 5/17 I felt much better, the nose had stopped running and there was very little coughing. Symptoms got gradually better until 5/22 I was felling recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 13May2023 At Home COVID-19 Test, Positive
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Atorvastatin; Benazepril; Vitamin D
Allergien: NA
Vorherige Impfungen: -

VAERS 2642249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 07.06.2023
Impfdatum: 12.10.2022
Beginn: 11.03.2023
Tage bis Beginn: 150,0
Dosis: 4
Route/Site: IM / RA

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

Nephrolithiasis Pain

Symptomtext

I did not have an adverse reaction to the vaccine. On 03/11/2023, I had to go to the emergency room and was diagnosed with kidney stones. I was given medicine for the pain and one to help pass the stones. I was able to pass the stones within two days. As of today, I have no lingering symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2638327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 30.05.2023
Impfdatum: 25.11.2022
Beginn: 08.05.2023
Tage bis Beginn: 164,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Chills Feeling cold Paranasal sinus discomfort Paranasal sinus hypersecretion Pyrexia SARS-CoV-2 test positive

Symptomtext

I woke up shivering and was cold. My sinus passages were stinging and when wakinfg up in the morning I felt like I had a temperature and it was two degrees higher than normal at nintey nine point eight. I took Tylenol which reduced the fever and remained low . My sinus es began to drain down my throat and the next morning I stillhad a fever and so I tested myself for COVID -19. My fever was gone by 12MAY2023 and by 20MAY2023 I was tetsing negative for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 10MAY2023 COVID-19 Test-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Lorradidine; Flutacazone; Qvar Inhaler;Lutein; Vitamin E; Vitamin D3; Calcium; Fish Oil; Over 50 Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2633036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OR
Alter: 73,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 06.10.2022
Beginn: 22.11.2022
Tage bis Beginn: 47,0
Dosis: 5
Route/Site: IM / LA

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

Blood test normal COVID-19 Colitis Colonoscopy abnormal Diarrhoea Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

In November 2022 my symptoms for the COVID-19 were body aches and runny nose. I started Paxlovid on November 24, 2022. The first day I felt good was December 9, 2022. In addition, beginning January 18th until April 26th, 2023, I have had diarrhea every day. I have visited the doctor and eventually I did have a 26th I had a colonoscopy, and I was diagnosed with colitis. I am now begin treated with Budesonide.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19, positive, 112022; Colonoscopy, abnormal, 042023; Blood panel, normal, 042023
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteoporosis
Andere Medikamente: Losartan; Lipitor; Aspirin; Vitamin C; Vitamin D3; Fosamax
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2630627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WV
Alter: 24,0
Geschlecht: F
Eingang: 11.05.2023
Impfdatum: 09.05.2023
Beginn: 09.05.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Rash Rash erythematous Rash pruritic

Symptomtext

Patient had itchy red rash to arms and trunk. Patient took 50mg benadryl 1x.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: cold symptoms weeks prior
Vorgeschichte: GERD GAD
Andere Medikamente: omeprazole 20mg norgestimate-ethinyl estradiol buspirone 15mg wellbutrin xl 300mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2630445

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 11.05.2023
Impfdatum: 05.10.2022
Beginn: 03.04.2023
Tage bis Beginn: 180,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Cough Fall Fatigue SARS-CoV-2 test positive

Symptomtext

04/03/23 presents to ED for "fatigue, falls, cough". PMHx of "Waldenstrom's macroglobulinemia, SIADH, atrial fibrillation, and obstructive sleep apnea"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 04/03/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2629795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: FL
Alter: 78,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 01.10.2022
Beginn: 03.01.2023
Tage bis Beginn: 94,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

1/3/23 I was having a little bit of congestion, slight aching and a slight fever. I took an at home COVID test and it was positive. I went to the Urgent Care. I was prescribed Paxlovid. I started taking it the next day for five days. On 1/8/23, I had a rebound. I had fever, congestion and aching like before, but only worse. This lasted until 1/16/23. I was better, but continued to have slight congestion for another 2-3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 3JAN23-At Home COVID-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Pace Maker, Caudo Neuropathy,
Andere Medikamente: Tamsulosen, Finasteride, Atorvastatin, Vitamin B12, Vitamin D3
Allergien: Hay Fever
Vorherige Impfungen: Every time I have the Flu Shot, Aching arm, slight fever, tiredness, sleeping lasting only a day.

VAERS 2629779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 10.05.2023
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Burning sensation Magnetic resonance imaging abnormal Pain in extremity Product administered at inappropriate site Tendon injury

Symptomtext

I have had all of my vaccinations with pharmacy. Almost immediately after receiving it, I could tell it was administered way too high up on the arm. Around an hour after receiving my vaccine, while at my next appointment, my arm became painful and was burning. I came home and iced my arm and just figured that it was administered too high up, but it just kept getting worse and worse. I've seen a joint surgeon and my primary care doctor. The joint surgeon stated that the vaccine went into the tendon. It has continued to get worse. He says that the tendons have shredded and I'm possibly looking at surgery for correction. He did and MRI, which is what led him to state that the tendons had become damaged. He has given me 2 Cortisone injections, but they have not really helped. I am seeing him again at the end of this week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: 29APR2023 - MRI - Damage To Tendon Found
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine; Furosemide; Irbesartan; MacuHealth; BioSil
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2629742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 54,0
Geschlecht: F
Eingang: 10.05.2023
Impfdatum: 05.11.2022
Beginn: 27.12.2022
Tage bis Beginn: 52,0
Dosis: 4
Route/Site: - / AR

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

Abdominal pain upper Abdominal tenderness Alopecia Areflexia Bacterial infection Brain fog COVID-19 Eustachian tube dysfunction Fatigue Feeling abnormal Headache Pain SARS-CoV-2 test positive Sinus disorder Sinusitis Vertigo Viral infection

Symptomtext

I previously tested positive for Influenza A and subsequently contracted the COVID-19 virus. 06JAN2023 Negative test I came off all the cold meds and was still having vertigo, sinuses, and a headache. 10JAN2023 doctors office visit I was diagnosed with a viral sinus infection now bacterial and Eustachian tube disfunction. Ten days of antibiotics ending 20JAN2023 09FEB2023 I was still having symptoms before and after this visit I had a long list of symptoms as previously mentioned, headache, stomach upset body aches, extreme fatigue, tender abdomen, bad gag reflex, mental fog, dizziness, loosing clumps of hair all above normal or strong symptoms. It was March 2023 before I was feeling anywhere close normal again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: 29DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Osteopenia; High Cholesterol
Andere Medikamente: SEROQUEL; CRESTOR; calcium; B12; magnesium; glucosamine chondroitin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2629491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: 73,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 02.12.2022
Beginn: 23.04.2023
Tage bis Beginn: 142,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Hypersomnia Malaise Nasopharyngitis Oropharyngeal pain Productive cough Pyrexia Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive Sneezing Throat irritation

Symptomtext

On 4/23/2023, I developed a scratchy throat. On 4/24/2023, I woke up with a scratchy throat and felt like I was catching a cold, but my cabin mate on the cruise ship I was travelling on felt even sicker than I did, so she called for medical assistance. She tested positive for COVID-19. I was also tested that day, and my results were negative, but I was feeling sicker instead of better as time progressed. On 4/26/2023, I was tested again, and I got a positive result. I felt like I had a bad head cold for the rest of the week. I had runny nose, cough, sneezing, and sore throat. The ship's doctor gave me a bottle of OTC cough syrup, which did not help much with my symptoms. On 4/29/2023, I came home from the cruise. I continued coughing, and it was a productive cough. I continued taking the cough syrup from the cruise ship, but I also started taking OTC ALKA-SELTZER plus cold and flu, which helped control the fever. On 5/3/2023, I called my PCP, who prescribed me an albuterol inhaler. After that, I gradually got better. I took a home antigen test on 5/7/2023 and finally got a negative result for the first time. At the present time, I feel fatigued and am sleeping a lot. However, I'm no longer coughing a lot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 24APR2023 COVID-19 test, negative result; 26APR2023 COVID-19 test, positive result; 07MAY2023 home antigen test, negative result
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis
Andere Medikamente: Trazodone; hydrocodone-acetaminophen; hydrochlorothiazide; duloxetine; metoprolol; atorvastatin; HYLAND LEG CRAMPS; vitamin B12; women's ONE-A-DAY multivitamin; famotidine; diphenhydramine
Allergien: Latex; lactose intolerance
Vorherige Impfungen: -

VAERS 2628547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MN
Alter: 54,0
Geschlecht: M
Eingang: 08.05.2023
Impfdatum: 28.10.2022
Beginn: 01.04.2023
Tage bis Beginn: 155,0
Dosis: 5
Route/Site: IM / LA

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

Dizziness Laboratory test normal

Symptomtext

I did not have an adverse reaction to the vaccine. On 04/01/2023, we had a heavy and wet snowstorm. On the street at my residence, we had a car that got stuck in the snow. I went out to help move the car and got lightheaded and laid down for about a minute. I got up and I still felt lightheaded. A neighbor recommended that I go to the emergency room. About 7 hours later, I did go to the emergency room. I was examined if I had a heart attack. All test was in normal range.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Ragweed; melons; strawberries; bananas
Vorherige Impfungen: -

VAERS 2626687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 13.10.2022
Beginn: 01.02.2023
Tage bis Beginn: 111,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Arthritis Muscle strain Myalgia Pain Tendon pain X-ray limb abnormal

Symptomtext

Late February, my shoulder, the muscle and tendons, began hurting when I reached behind it was very painful. On March 02, 2023, I went to the doctor, and she ordered an x-ray. The doctor thought I might be developing arthritis in my shoulder. She sent me to physical therapist for 4 to 6 weeks. It helped tremendously and I am fine also. The Physical Therapist, said the same thing, she thought I had pulled or strained a muscle in my upper arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 02MAR X-ray of shoulder, a little arthritis in my shoulder joint
Aktuelle Erkrankungen: None
Vorgeschichte: Controlled High Blood Pressure
Andere Medikamente: Losartan; levothyroxine; multivitamin; cranberry supplement; zinc
Allergien: None
Vorherige Impfungen: -

VAERS 2625667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 29.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal pain Back pain Burning sensation Clostridium test negative Colonoscopy abnormal Cough Diarrhoea Endoscopy abnormal Increased bronchial secretion Loss of personal independence in daily activities Polyp Polypectomy Walking aid user

Symptomtext

In early November I started having low back pain that is constant that feels like bone on bone. There are times it hurts so bad I have to use a cane to even get out of bed. It will ease up and I can do daily activities and then there are days I cannot do anything. Now I am having pain after I eat. Thirty to forty minutes after I eat, I start getting pains as if I have not eaten, a burning sensation, gurgling sounds, some diarrhea. I have had an endoscopy and colonoscopy they only showed polyps that I had removed, the pains still persist. I have been given PRILOSEC to help. I just started this medication; it is helping with my cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 00NOV2022 Endoscopy positive for polyps; 00NOV2022 Colonoscopy positive for polyps; 00APR2023 C-Diff negative
Aktuelle Erkrankungen: C-Diff in September
Vorgeschichte: Nodule on thyroid; Arthritis
Andere Medikamente: SYNTHROID; famotidine; RESTASIS; montelukast; VOLTAREN; AVENOVA spray; ASTEPRO; BIO FREEZE gel; TYLENOL; PHILIPS probiotic; biotin; super B complex; vitamin B-12; women's 50 plus ONE A DAY; vitamin D3; TUMS extra strength; ZYRTEC; REFRESH
Allergien: Latex; penicillin; millicin drugs
Vorherige Impfungen: All of my COVID-19 vaccines made me feel like I had the flu with a fever for 24 to 36 with the exception of the first dose. 2nd

VAERS 2625144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OR
Alter: 67,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 27.10.2022
Beginn: 24.11.2022
Tage bis Beginn: 28,0
Dosis: 5
Route/Site: IM / LA

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

Computerised tomogram abnormal Cystocele Endodontic procedure Feeling abnormal Infection Lymphadenopathy Malaise Oral mucosal erythema Proctalgia Rectal haemorrhage Respiratory syncytial virus infection Sinonasal obstruction Sinusitis Toothache

Symptomtext

About one month after dose 5, Holiday morning I woke up with pain and redness in my tooth. I went to the emergency department. The doctor at the emergency department confirmed it was an infection. I tried to get my dentist. The following Monday I saw my dentist and I had a mini root canal. It did not correct. The infection moved into my sinus. I got sick with RSV in January. During that time, I felt so horrible I saw my doctor. I had three rounds of Z-Pak. She found; my lymph nodes were swollen in my right neck. My sinus was blocked. During that time, I continued with RSV another virus in February and another in March. I saw the ENT and he said I needed surgery. I tried clindamycin. It helped but didn't clear. He cleaned out this sinus and rinsed it out. The ENT confirmed that infection from my tooth moved into my sinus and that is what caused the problem. In mid-March, my bladder prolapsed. I was brushing my hair and took a shower and then found that my bladder was hanging slightly out of my body. I was referred to a urologist. I have done the exercises that they gave me. I need a pessary, but I have not been able to get one. All of this causes my rectum to hurt, or I bleed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: CT Scan, abnormal, 12202
Aktuelle Erkrankungen: For several months prior I had pain in one of my back teeth that dentists said there was nothing wrong.
Vorgeschichte: Fibromyalgia; Cancer Survivor
Andere Medikamente: Kitimat; Lactaid; Tylenol
Allergien: Soy; Iodine; Fish; NSAIDS; Septra; Penicillin; Amoxycillin; Ceclor; Cefaclor; Cephalexin; Cipro; Codeine; Doxycycline; Erythromycin; Gabapentin; Moxifloxacin;
Vorherige Impfungen: -

VAERS 2624888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MO
Alter: 70,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 29.10.2022
Beginn: 15.01.2023
Tage bis Beginn: 78,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

It started with a postnasal drip and a slight sore throat only in my right nostril and the right side of my throat which lasted about 3 days. I also had a slight fever and cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: At home rapid COVID-19 test positive 1/15/2023
Aktuelle Erkrankungen: No
Vorgeschichte: Post pneumonia asthma; Acid reflex disease; Hypertension; Arthritis; History of anemia (watched clearly)
Andere Medikamente: Losartan; NEXIUM; amlodipine; famotidine; DYMISTA; PROAIR inhaler; EPIPEN; azelastine; IBGARD; ZYRTEC; TYLENOL arthritis; woman's multivitamin w/ iron; turmeric curcumin
Allergien: Penicillin; CIPRO; Z-PAK; red contrast dye; strawberries
Vorherige Impfungen: -

VAERS 2624689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MO
Alter: 73,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 26.10.2022
Beginn: 27.03.2023
Tage bis Beginn: 152,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Cough Ear discomfort Fatigue Headache Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Throat clearing Throat irritation

Symptomtext

3/27/2023 in the afternoon I got a tickle in my throat. Just the right side. I had trouble clearing my throat and my right ear felt full. I got a low-grade fever, 100. The next day, 3/28, I got a cough, the fever hit 102.3, chills, and a headache. I felt like I had lots of head congestion. Phone visit with doctor who prescribed PAXLOVID and advised to use DAYQUIL and NYQUIL. For the next week and a half, symptoms persisted, but gradually diminished. Felt recovered by 4/9, with fatigue being the final symptom to resolve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 28Mar2023 at home COVID-19 test, positive
Aktuelle Erkrankungen: NA
Vorgeschichte: Osteoarthritis; Cancer
Andere Medikamente: Multivitamin; MOBIC; vitamin D3; glucosamine; CLARITIN; calcium
Allergien: TC; PROLIA
Vorherige Impfungen: COVID-19 vaccine Moderna 2/4/2021 at 24 hours and 15 minutes after getting vaccine, I had a fever of 102, chills and body aches

VAERS 2624400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 21.10.2022
Beginn: 22.02.2023
Tage bis Beginn: 124,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chest X-ray abnormal Cough Diaphragmatic disorder Diarrhoea Electrocardiogram normal Feeling abnormal Headache Pyrexia SARS-CoV-2 test positive

Symptomtext

02/22/203, I felt generally poor, headache, fever and cough. I tested on 02/22/2022 with aCOVID-19 Home Test and the results were positive. The evening of the 02/22/2023, I went to an urgent care. They did an EKG, chest x-ray, and they prescribed a cough medicine, and I chose not to take the Paxlovid after I heard the pros and cons of taking it. After I started feeling better, I had a couple of days of diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 22FEB2023 - COVID-19 Home Test - Positive; 22FEB2023 - EKG - Normal; 22FEB2023 - Chest X-ray - Slight Elevated Hemidiaphragm; No focal Infiltrate for Cardiomegaly
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; High Cholesterol; GOUT; Low Thyroid; GERD; Anxiety; Urine Flow; Large Prostate; Acromegaly; Pre-Diabetes; Pre-ventricular Contractions
Andere Medikamente: Fish Oil; Aspirin; Vitamin D3; Vitamin C; Crestor; Tamsulosin; Lisinopril; Levothyroxine Sodium; Amlodipine Besylate; pantoprazole Sodium; Finasteride; Allopurinol; Escitalopram; Injectable Every 8 Weeks Medication Sandostatin Lar Depo; Os
Allergien: None
Vorherige Impfungen: -

VAERS 2623278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CT
Alter: 39,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 27.10.2022
Beginn: 01.03.2023
Tage bis Beginn: 125,0
Dosis: 3
Route/Site: IM / UN

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

Injection site pain

Symptomtext

After Vaccination pain at the injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's thyroiditis
Andere Medikamente: Levothyroxine
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2623144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 27.10.2022
Beginn: 02.04.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Chills Fatigue Pyrexia SARS-CoV-2 test positive Sneezing Somnolence

Symptomtext

COVID-19 symptoms started on 04/02/2023 in the afternoon. I had abnormal fatigued. I felt tired and wanted to take nap which I wasn't used to . On 04/03/2023 I was sneezing, and I was fatigued. I tested myself with a home test at 08:00pm which was negative. I had chills and fever during the night . On 04/04/2023 I did another home test which was positive. I called my doctor's office in the morning at 10;00am and did a telehealth with my doctor's partner in the practice. He prescribe me Paxlovid and advised me to hold on to Lipitor. I tested negative on 04/13/2023. As of today I still have fatigued but I have recovered 97% out of 100%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 03APR2023 COVID-19 Test- Negative; 04APR2023 COVID-19 Test- Positive; 13APR2023 COVID-19 Test- Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Lipidemia
Andere Medikamente: Multivitamins 50 +; Ocuvite Vision Supplements; Persulfate; Vitamin D3; Fish Oil; Flax Seed Oil; Melatonin; Miralax
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2620870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 25.04.2023
Impfdatum: 24.10.2022
Beginn: 01.04.2023
Tage bis Beginn: 159,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chills Cough Headache Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19 with headache, cough, slight fever, chills, congestion and very runny nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 01April2023 - COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Rosacea Topical
Allergien: N/A
Vorherige Impfungen: -

VAERS 2620850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: WA
Alter: 55,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 24.10.2022
Beginn: 02.04.2023
Tage bis Beginn: 160,0
Dosis: 4
Route/Site: SYR / RA

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

Abdominal pain Abdominal pain upper Back pain COVID-19 Cough Fatigue Head discomfort Nausea Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing Streptococcus test negative Swollen tongue Throat irritation Tongue eruption

Symptomtext

I contracted covid. I woke up with alittle scratchy throat but felt exhausted. I had a really intense pressure in my head. I didn't have any sinus congestion, it just felt like my head was swelling. i had a fever of 103. I had a stomachache, nausea, an ache in lower abdomen and my heart and low back. everything lasted for a few days. I was also prescribed paxlovid. after taking the meds, the sore throat became extreme. My tongue also swelled up and had red bumps on it. I went to urgent care and tested me for strep- negative. by day 4, I felt pretty good after that but I was still testing positive. I then started getting sick again with runny nose, sneezing, congestion, developed a bit of cough in my chest. energetically I feel fine but im still experiencing some throat/ congestion issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: covid test; strep test
Aktuelle Erkrankungen: Respiratory illness
Vorgeschichte: none
Andere Medikamente: Valacyclovir; Levophyroxine
Allergien: None
Vorherige Impfungen: -

VAERS 2620832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 24.10.2022
Beginn: 20.03.2023
Tage bis Beginn: 147,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia Asthenia Conjunctivitis Cough Deafness bilateral Fatigue Muscular weakness Nasopharyngitis Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative

Symptomtext

I experienced a head cold, sore throat, coughing and decided to get tested for COVID-19 and tested negative however, I experienced loss hearing in my ears, pink eye, congestion, loss of taste and fatigue. I'm used to working out but my muscles in my legs feel very weak when I walk up stairs and that is unusual to me because I'm used to having stamina and now I don't.

Weitere VAERSDATA-Felder

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

VAERS 2620756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IL
Alter: 69,0
Geschlecht: M
Eingang: 25.04.2023
Impfdatum: 31.10.2022
Beginn: 18.01.2023
Tage bis Beginn: 79,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Influenza like illness Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Throat clearing

Symptomtext

I had a mild sore throat; it was a little different than sore throats in the past. I wanted to cough to get my throat cleared, I was very tired, I wanted sleep, like when I have the flu, a low-grade fever that lasted a little more than a day. I tested for three days in a row, and it was not until day three that it came back positive, by then I felt as if my symptoms were starting to wane. I called my doctor to have a telehealth visit to discuss my positive test result, and my symptoms. I was able to take the Paxlovid and was feeling much better in 2 days. Ten days later I got rebound COVID-19, I did test negative ten days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 18JAN2023 Home COVID-19 test - negative; 19JAN2023 Home COVID-19 test - negative; 20JAN2023 Home COVID-19 test - positive; 02FEB2023 Home COVID-19 test - positive; 12FEB2023 Home COVID2023 test - negative
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; High Cholesterol
Andere Medikamente: Fenofibrate Acid DR; Lipitor; Amlodipine Besylate; Low Dose Aspirin
Allergien: Cat Dander
Vorherige Impfungen: -

VAERS 2620130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 15.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / RA

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

Arthralgia Back pain Brain fog COVID-19 Cough Dandruff Dry skin Fatigue Malaise Oropharyngeal pain Rash Rash erythematous Rash papular Rash pruritic Rhinorrhoea Rosacea SARS-CoV-2 test positive Skin exfoliation

Symptomtext

In October in 2022 I noticed I had a rash on my breastbone. It was raised, red, itchy bumps. It appears different on my chest than on my face. On my face it looks more like acne with white heads and would become dry and scaly. It started to appear on my face in February 2023. It got worse as I got emotionally stressed. I finally went to the doctor in April 2023 and diagnosed with dandruff on chest and face in addition to rosacea on my face. I received prescriptions for Doxycycline, face wash, Sodium Fulsacetamide Wash, Ketoconazole cream for my face. I began noticing symptoms for COVID-19 on February 4, 2023, and tested positive on the 6th. My symptoms were severe fatigue, joint pain, back pain, coughing and a runny nose. The symptoms progressed within 36 hours, and I had a bad cough and sore throat. I had a telehealth appointment and was prescribed Paxlovid. I felt better within the first day. I just remained fatigued and had brain fog for about another week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19, positive, 02042023
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Trigeminal Neuralgia; Herpes
Andere Medikamente: Acyclovir; Simpalta; Hydrochlorothiazide; Spironolactone; Vitamin D; Vitamin C; Calcium; Multi Vitamin; Fiber Supplement; Epi Pen as needed
Allergien: Bee Sting
Vorherige Impfungen: -

VAERS 2620011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OR
Alter: 72,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 22.10.2022
Beginn: 03.04.2023
Tage bis Beginn: 163,0
Dosis: 4
Route/Site: SYR / -

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

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

Symptomtext

I had vaccination on 10/22/2022. I had a slight fever having both vaccinations of about 100 for 2 days. On 04/03/2023 I started to experience dry cough headache dizziness and fever. I tested COVID-19 positive on 04/04/2023 and I called my doctor office. I was prescribed PAXLOVID. I feel ok but still feel wiped out a little bit and I still have a cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 04/04/2023 test COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Eye drops; vitamins; turmeric
Allergien: N/A
Vorherige Impfungen: Flu; fever

VAERS 2618977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TN
Alter: 39,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 20.10.2022
Beginn: 12.02.2023
Tage bis Beginn: 115,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Muscular weakness X-ray limb normal

Symptomtext

2/12/23 I had done something to my left shoulder and unsure what it is. I am having shoulder pain and weakness. I went to the doctor and had an x-ray, which was normal, and had a steroid injection into the bursa area of my shoulder which did not help. I have an MRI scheduled.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 18APR23 X-Ray of shoulder, normal
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic low pain
Andere Medikamente: Tramadol; ZANAFLEX; LIPITOR; levothyroxine; propranolol; vitamin D
Allergien: Pollen
Vorherige Impfungen: -

VAERS 2618535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 52,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 17.10.2022
Beginn: 04.01.2023
Tage bis Beginn: 79,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Dry throat Myalgia Nasal congestion Nasopharyngitis Pyrexia SARS-CoV-2 test positive Throat irritation Upper-airway cough syndrome

Symptomtext

On 01/06/2023, I tested positive for COVID-19. My symptoms began on 01/04/2023. My throat was dry and scratchy and I had post-nasal drip. It felt like a cold, with nasal congestion, muscle aches and low grade fever. I called to report it to my doctor. She prescribed PAXLOVID but I did not take it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: 06JAN2023 Covid-19 test, positive; 12JAN2023 COVID-19 test, negative; 15JAN2023 COVID-19 test, negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; fish oil; bioidentical hormone replacement therapy
Allergien: N/A
Vorherige Impfungen: -

VAERS 2618531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: AK
Alter: 67,0
Geschlecht: U
Eingang: 20.04.2023
Impfdatum: 20.09.2022
Beginn: 27.02.2023
Tage bis Beginn: 160,0
Dosis: 5
Route/Site: SYR / LA

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

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

Symptomtext

I had vaccination on 09/20/2022. I started to experience headache and feeling unwell on 02/27/2023. I tested COVID-19 positive on 02/28/2023. I was prescribed PAXLOVID. The symptoms went away really quickly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 02/28/2023 test, COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: COVID-19 Moderna; made me really sick to include vomiting headache fever chills.

VAERS 2618296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 69,0
Geschlecht: M
Eingang: 20.04.2023
Impfdatum: 26.10.2022
Beginn: 02.03.2023
Tage bis Beginn: 127,0
Dosis: 5
Route/Site: IM / LA

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

Asthma COVID-19 Influenza Malaise

Symptomtext

It felt like I had a flu coming on. I tested that evening, and it was positive. I called the doctor the next day. I had a prescription for PAXLOVID already due to precautions due to me traveling. I started taking it within a day of feeling symptoms. After taking it my symptoms were extremely mild. It was probably a week to ten days before I tested negative. I was using an albuterol and steroidal inhaler. I had little to no asthmatic symptoms. I was well for a couple of days and then I had a rebound. That was worse than the original COVID-19 symptoms. That was harder to get over. The rebound was a little longer than the initial symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: MAR2023 COVID-19 test positive; MAR2023 COVID-19 test negative; MAR2023 COVID-19 test positive; MAR2023 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Benign prostatic hyperplasia
Andere Medikamente: LEXAPRO; pantoprazole
Allergien: CIPRO
Vorherige Impfungen: -

VAERS 2617525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NC
Alter: 66,0
Geschlecht: F
Eingang: 19.04.2023
Impfdatum: 18.10.2022
Beginn: 23.02.2023
Tage bis Beginn: 128,0
Dosis: 5
Route/Site: IM / AR

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

Cough Influenza virus test negative Nasopharyngitis Pyrexia Respiratory syncytial virus test negative Respiratory tract congestion SARS-CoV-2 test negative Throat irritation

Symptomtext

2/23/23 I felt like I was getting a cold. I had a little tickle in my throat, a mild cough and a little congested. Over the next week, it became worse. My cough and congestion were worse. I had 101.5 to 102 fever. I did four at home COVID tests that were all negative. On 3/4/23 I went to Urgent Care because of my fever. I was tested for RSV, Flu and COVID and all were negative. I got a prescription for an antibiotic because they felt like I had pneumonia in one lung. A side effect for this antibiotic was ruptured tendons. After two or three doses, I woke up early in the morning with a pain in the back of my ankle. I stopped taking the medication. I went back to the Urgent Care and told them I would not take the antibiotic anymore. My lungs sounded clear, the fever was gone, but I still had some cold symptoms that were improving. By March 11,2023, I felt well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 24FEB23-At Home COVID Test-Negative; 25MAR23-At Home COVID Test-Negative; 27FEB23-At Home COVID Test-Negative; 4MAR23-At Home COVID Test-Negative; 4MAR23-Flu Test-Negative; 4MAR23-RSV Test-Negative; 4MAR-COVID Test-Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Minor Chronic Coughing Asthma
Andere Medikamente: Daily Multi Vitamins
Allergien: Penicillin, Sulfa Drugs, Novocain, Kee wee Sensitivity
Vorherige Impfungen: -

VAERS 2616288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NE
Alter: 73,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 14.10.2022
Beginn: 03.02.2023
Tage bis Beginn: 112,0
Dosis: 5
Route/Site: SYR / UN

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

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

Symptomtext

I was positive for COVID-19 on 03FEB2023, I had a lot of congestion and a little bit of a cough. Also, a little bit of a headache but nothing severe. I contacted my doctor, he gave me PAXLOVID. I started feeling better the day I saw him but fully better about 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 03FEB2023 COVID-19 test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Epilepsy; Irritable bowel syndrome
Andere Medikamente: Lamotrigine; dicyclomine; finasteride; VIVISCAL PRO; cod liver oil; fiber
Allergien: N/A
Vorherige Impfungen: -

VAERS 2616272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 74,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 14.10.2022
Beginn: 30.03.2023
Tage bis Beginn: 167,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Fatigue Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sleep disorder

Symptomtext

I had vaccination on 10/14/2022. On 03/30/2023 I started to have an achy body with low grade fever. On 03/31/2023 I tested COVID-19 Positive at home. I called the clinic and I was prescribed Lagevrio mucous relief over the counter medication and a steroid. I was prescribed an inhaler but I didn't have it filled. I am still fatigued and have congestion on 04/17/2023. I am sleeping better and feeling better each day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 03/31/2023 test - COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Environmental Allergies; Diverticulosis
Andere Medikamente: Atorvastatin; Losartan; Testosterone; Baby Aspirin; Vitamin D3; Vitamin D12; COq10; Krill Oil; Multivitamin
Allergien: Penicillin; Anything in the cillin category
Vorherige Impfungen: -

VAERS 2615368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OR
Alter: 72,0
Geschlecht: F
Eingang: 14.04.2023
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

Arthralgia Joint range of motion decreased Laboratory test normal Magnetic resonance imaging abnormal Musculoskeletal stiffness Myalgia Pain Pain in extremity Rotator cuff syndrome X-ray limb normal

Symptomtext

I had pain in my right shoulder and then about a week or two after that I started having pain in my muscles and joints. It was pain and stiffness throughout my right shoulders the to my calf, heels, foot or both of my legs. I waited a couple of weeks to see if it would go away. I couldn't raise my arm and it was painful. I had a Xray, and it showed nothing wrong. Then after being sent to a orthopedic doctor. I was having more pain increasing throughout my body. My PCP did order a bunch of lab work and stuff. Nothing was found in significance she everything looked good. Then after I saw her, she had me stop my Atorvastatin. After the Ortho doctor I was given a MRI of my shoulder. It showed a partial tear in my rotator cup, I received a cortisone injection in my shoulder and the pain went away in my shoulder and the rest of my body. He has now been about two weeks. My aches and pain in my body is coming back, but the shoulder pain is not. I going to contact my doctor this week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 20MAR2023 MRI - Torn Rotator Cup
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol
Andere Medikamente: Alendronate; Atorvastatin; Calcium; Vitamin D3; Joint Oil; Omeprazole; Perse vision
Allergien: N/A
Vorherige Impfungen: -

VAERS 2615288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 69,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 05.10.2022
Beginn: 02.04.2023
Tage bis Beginn: 179,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

I started getting sick on 04/02/2023. I did not contact the doctor until that Tuesday because I did not realize it could be COVID-19. When I contacted the doctor, they suggested I take MUCINEX. They would not prescribe me PAXLOVID because of my kidney function.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Cholesterol; Rapid Heart Rate
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2615262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 13.10.2022
Beginn: 02.04.2023
Tage bis Beginn: 171,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I tested positive for COVID-19 on 4/2/23. I had a fever, runny nose, sneezing, and a cough. I contacted a doctor and was prescribed PAXLOVID. This lasted for about 10 days. I am feeling better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 02APR2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Enlarged Heart
Andere Medikamente: Calcium
Allergien: N/A
Vorherige Impfungen: -

VAERS 2614693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 12.10.2022
Beginn: 18.01.2023
Tage bis Beginn: 98,0
Dosis: 5
Route/Site: IM / LA

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

Computerised tomogram head normal Dizziness Gait inability Hypoaesthesia Magnetic resonance imaging head normal Myocardial necrosis marker normal

Symptomtext

I was extremely dizzy, I could not walk, I was unable to feel anything on my left side. My daughter drove me to the emergency room, I was uncertain of knowing if I was having a stroke or something with my heart. Once I got into the emergency room, they did a complete blood panel to check for a heart attack, they did a CT scan to check for stroke. I was kept overnight for observation and to have an MRI to also check for a stroke. All tests came back negative. I have a follow up MRI coming up on May 13, 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 1,0
Labordaten: 18JAN2023 CT scan - negative for stroke; 18JAN2023 Complete blood panel- negative for enzymes of heart attack; 19JAN2023 MRI - negative for stroke
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Albuterol Inhaler; Albuterol Nebulizer; Atorvastatin; Plavix; Protonix; Multivitamin; Calcium; Magnesium; Turmeric; Biotin; Vitamin B-12; Ginger as needed; Digestive Health Probiotic
Allergien: No
Vorherige Impfungen: -

VAERS 2613979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 41,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 07.10.2022
Beginn: 09.02.2023
Tage bis Beginn: 125,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia Blood test abnormal COVID-19 Laboratory test abnormal Malaise Post-acute COVID-19 syndrome Pyrexia SARS-CoV-2 test positive Sinus disorder Sinus headache White blood cell count increased

Symptomtext

I experienced COVID-19 after my vaccine. I tested positive for COVID-19 on 02/09/2023. I was sick for ten days, did do a telemedicine on Day4 or 5, but then about two weeks after still had sinus symptoms, using saline sprays, got alot of sinus headaches. I also had slight fever for a few days and lost taste and smell for quite awhile. I got blood done which they told me white count was elevated. They put me on a Z-pack for 5 days, Flonase spray for two weeks and probiotic. I have been basically fine since then and have recovered. I still can not smell certain things, like things being burned like popcorn. Iam part of research program for long term covid. I did not get anit-virals. I will be having a taste and smell test in the June 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 09FEB2023 COVID-19 Test-Positive; Lab Work-white count elevated
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: Keflex
Vorherige Impfungen: -

VAERS 2613945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: 69,0
Geschlecht: M
Eingang: 12.04.2023
Impfdatum: 11.10.2022
Beginn: 03.04.2023
Tage bis Beginn: 174,0
Dosis: 5
Route/Site: IM / RA

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

Arthralgia COVID-19 Dysgeusia Dysuria Headache Night sweats Pain Poor quality sleep Pyrexia SARS-CoV-2 test positive

Symptomtext

This started with joint pains in Hips, knee, and ankle. The next day, all joints hurt. The next day, I awoke with a bad headache, I had body pain everywhere. I also had fever and night sweats. At Home COVID-19 test positive on 4/6. Televisit with doctor, who proscribed Paxlovid. Joint pain significantly decreased by 4/8, but I slept poorly due to horrible taste from Paxlovid. 4/6 had difficulty passing urine, but no trouble since then. Symptoms diminishing over time with the night of 4/11-12 being the first night with no night sweats and slept through the night. I am still recovering at time of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 6April2023 At Home COVID-19 test positive
Aktuelle Erkrankungen: No
Vorgeschichte: Hemolytic Anemia; Psoriasis; Enlarged Prostate
Andere Medikamente: Finasteride; Terazosin; Atorvastatin; Tadalafil; Omeprazole; Vitamin D3; Vitamin B12; Azelastine
Allergien: No
Vorherige Impfungen: -

VAERS 2613903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 80,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 06.10.2022
Beginn: 21.12.2022
Tage bis Beginn: 76,0
Dosis: 5
Route/Site: SC / LA

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

COVID-19 Cough Exercise tolerance decreased Headache Lung disorder Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had a coughing. It was just coughing. It caught my attention because in the December previous I had RSV. I tested positive for COVID-19. I developed fever, headache, the coughing and congestion. I contacted my doctor right away and filled out a form online and got a answered back and called the tele health nurse and doctor. I was offered Paxlovid, my husband had had tested positive and had it before me, I noticed the tablets and told them I could not swallow them. The arranged for me to get another medicine intravenously at the clinic called Remdesivir. There were 3 appointments for December 23rd 24th and 25th. It was wonderful, it was immediate relief. I got two bags on the first day, so I had relief the on the 2nd day with one bag. and other on the third. By the 26th I was good, but my lung compacity was a little weak, I walk 4 miles a day, but I waited a month to go back to my routine. I was praised for getting this treatment it helps with hydration and the medicine working faster. I feel great today. I walked this morning and worked out at the Gym.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arterial Sclerosis; Cervical Bone Spurs; Nodules Thyroid; Osteoporosis, Lung Nodules
Andere Medikamente: Calcium D3, Multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2613096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 22.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Chest X-ray normal Chest discomfort Cough Fatigue Haemoptysis Headache Lower respiratory tract infection Malaise Pain Pyrexia Respiratory tract congestion

Symptomtext

Within 24 hours after having my vaccine, I had headaches, chest pressure, congestion, fever, loss of taste, fatigue and smell and body aches. When I caught COVID-19 February 25, 2023, I had all of the same symptoms I had for after my vaccine, but for eight weeks long. I still have some residual coughing. My taste and smell are finally starting to come back. I had a chest infection form as well and had to cough up blood. I also have chronic congestion. I take a nasal spray to try to keep the coughing from getting extreme.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 27FEB2023 - Pneumonia Chest X-Ray - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Back Injury; High Cholesterol
Andere Medikamente: Atorvastatin; Celebrex; Magnesium Oxide; Riboflavin; CoQ10; Zinc; Vitamin D3
Allergien: N/A
Vorherige Impfungen: -

VAERS 2612443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 08.10.2022
Beginn: 27.02.2023
Tage bis Beginn: 142,0
Dosis: 4
Route/Site: IM / -

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

COVID-19 Chills Fatigue Headache Nausea Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Vomiting

Symptomtext

I had a really big headache. I had chills during the day and a fever during the night. I had a lot of head congestion, very fatigue and a runny nose. The next day, I started feeling queasy and threw up once. I was prescribed Paxlovid and the medicine started to help a lot. When I got done taking the RX after day 5, the fatigue returned.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: at home rapid COVID-19 test- positive 2/27/2023
Aktuelle Erkrankungen: No
Vorgeschichte: SLE; Gurde; Depression; Anxiety
Andere Medikamente: Citalopram; Famotidine; Hydroxytoluene
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2612375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 27,0
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 06.10.2022
Beginn: 10.03.2023
Tage bis Beginn: 155,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Pain

Symptomtext

I have joint pain and it worsens with exercise. I take ALEVE, multivitamins, and fish oil for my symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2612281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: SD
Alter: 75,0
Geschlecht: F
Eingang: 10.04.2023
Impfdatum: 04.10.2022
Beginn: 30.03.2023
Tage bis Beginn: 177,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Headache Malaise Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Somnolence Taste disorder

Symptomtext

My grandson came over to visit on my birthday, he was not feeling well. I started not feeling well, I had a massive headache, a cough, runny nose. body ache, my taste became very intense, extremely tired, sleepiness. I used a home COVID-19 test, that came back positive. I called my doctor, had a virtual visit, discussed my symptoms. I was prescribed, Paxlovid that I started taking immediately. I have recovered I am just very fatigued and congestioned.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 30MAR2023 Home COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Arthritis; Osteoarthritis; Fibromyalgia
Andere Medikamente: Low-Dose Aspirin; Allegra; Omeprazole; Prozac; Levothyroxine: Memantine; Benazepril; Singular
Allergien: Codeine; Shellfish; Opioids
Vorherige Impfungen: -

VAERS 2611613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MO
Alter: 74,0
Geschlecht: M
Eingang: 07.04.2023
Impfdatum: 06.10.2022
Beginn: 05.02.2023
Tage bis Beginn: 122,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Infection Influenza like illness Musculoskeletal stiffness Myalgia Pyrexia SARS-CoV-2 test positive

Symptomtext

I had a break through case of Covid-19. I has chills muscle ache and stiffness, had a high fever the after two days It felt like severe flu symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: home test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Coenzyme; Fish Oil; Atorvastatin; Flonase; Pseudoephedrine
Allergien: None
Vorherige Impfungen: -

VAERS 2611564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: ME
Alter: 47,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 08.10.2022
Beginn: 14.03.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: IM / UN

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

COVID-19 Fatigue Nasal congestion Respiratory tract congestion Vaccine breakthrough infection

Symptomtext

I had a breakthrough case of Covid-19. Nasal and chest congestion with a lot of fatigue low oxygen level.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Heart Aneurism; Rheumatoid Arthritis; Asthma
Andere Medikamente: None
Allergien: Prednisone; amoxicillin; promethazine; ZOLOFT; beta blockers; fentanyl
Vorherige Impfungen: -

VAERS 2611526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 06.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: SYR / AR

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

Arthralgia Chills Cough Muscle spasms Pyrexia Retching SARS-CoV-2 test negative Viral infection

Symptomtext

This was my first Pfizer vaccine; the previous ones were Moderna. I had a viral infection that was tested as COVID-19 negative twice. This infection has been going on for at least a month now. In the beginning of November, it started with fever and chills. I would then develop coughing spasms; I couldn't quit until I gagged. The fever got to 102 and lasted with chills for about 3 days. The cough stayed and after I tested for COVID-19 it was negative. I went to the urgent and negative and had told me to take over the counter medications. 10 days later I went back to the urgent care because I was feeling worse. They gave me a Z PAK that did not impact this virus at all. It all continued for 6 weeks. I was told it was nothing I could do about this; it was a virus going around. My husband got it in January 6 weeks after I had gotten better. Now I am fine. I have noticed my joints are achy, but that could be my age.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: NOV2022 COVID-19 test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; vitamin D; triphala; hormone patch
Allergien: Aspirin; crabs; salicylate
Vorherige Impfungen: -

VAERS 2611388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: GA
Alter: 32,0
Geschlecht: F
Eingang: 07.04.2023
Impfdatum: 05.10.2022
Beginn: 15.03.2023
Tage bis Beginn: 161,0
Dosis: 4
Route/Site: IM / LA

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

Body temperature increased COVID-19 Cough Fatigue Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

March 15 had mild scratchy throat and a little tired. The next morning was very fatigued, low grade temperature, congestion, cough, sore throat. Tested positive on 03/17. Telehealth visit and was told to rest and hydrate. Symptoms resolved in 14 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home COVID-19
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Topical Tretinoin
Allergien: None
Vorherige Impfungen: -

VAERS 2611224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CO
Alter: 66,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 19.10.2022
Beginn: 01.04.2023
Tage bis Beginn: 164,0
Dosis: 4
Route/Site: IM / AR

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

COVID-19 Cough Headache Nasal congestion Pyrexia SARS-CoV-2 test positive Throat irritation

Symptomtext

It started as a scratchy throat. That night became nasal congestion, cough, and a headache. The next day I called the doctor to try and get on Paxlovid. I probably had a slight fever but didn't take my temperature. I was able to do a Telehealth visit and was prescribed Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 02APR2023 - COVID-19 At Home Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; Glucosamine Chondroitin; Vitamin C; Vitamin D; Fish Oil; Vitamin Multi B-Complex
Allergien: N/A
Vorherige Impfungen: -

VAERS 2611039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 05.10.2022
Beginn: 23.03.2023
Tage bis Beginn: 169,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chills Fatigue Headache Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 3/23/23. I had a sore throat, headache, chills, fatigue, and a runny nose. I contacted my doctor sand was prescribed Paxlovid. I am still dealing with fatigue and a slight runny nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 23MAR2023 COVID-19 Test - Positive; 01APR2023 COVID-19 Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Meniere's Disease; Hypothyroidism; Migraines
Andere Medikamente: Benadryl; Vitamin D3; COQ10; Vitamin B12; Levothyroxine; Maxzide; Topamax; Crestor; Rizatriptan
Allergien: Cipro; Sulfa; Pseudoephedrine; Atorvastatin; Simvastatin
Vorherige Impfungen: -

VAERS 2610932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 11.10.2022
Beginn: 19.11.2022
Tage bis Beginn: 39,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Nasal congestion Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I went to an amusement park on 11/18/2022 and did not have any COVID-19 symptoms. On 11/19/2022, I had a runny nose. The runny nose continued on 11/20/2022 and 11/21/2022, and it was not accompanied by any other symptoms. On 11/22/2022, my symptoms worsened. I began having coughing and mostly head congestion. The runny nose was gone, but it was stuffy. I took a home antigen test and got a positive result. The worst symptoms, which were head congestion and fatigue, continued for about two weeks. I also still had a cough, but it wasn't a heavy or severe cough. On 11/22/2022, I contacted my doctor, who prescribed me a Z-Pak and Molnupiravir, which I began taking that night. I tested positive for three weeks. During the third week, my main symptom was fatigue. Since I have asthma, we were concerned that the congestion would settle in the chest area, but it remained mostly in my head area. On 12/2/2022, my doctor prescribed me doxycycline and methylprednisolone. The cough lasted for five to six days. The fatigue lasted for about two and a half weeks. On 12/10/2022, I tested negative for COVID-19 on a home test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 22NOV2022 - Home Antigen Test - Positive Result; 02DEC2022 - Home Antigen Test - Negative Result
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Environmental Allergies; Sleep Apnea; Obesity
Andere Medikamente: Montelukast; Pepcid AC; Vitamin D; Vitamin C; Fish Oil; Meloxicam; Iron
Allergien: Vistaril; Phenergan
Vorherige Impfungen: -

VAERS 2610673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 01.10.2022
Beginn: 26.03.2023
Tage bis Beginn: 176,0
Dosis: 4
Route/Site: SYR / RA

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

Ageusia Diarrhoea Dry mouth Headache Lethargy Oesophageal achalasia Sensory disturbance Swollen tongue

Symptomtext

I starting having aches, headaches diarrhea, lethargic and swollen tongue. I didn't know what was happening, I started brushing my teeth and use hydrogen peroxide. My mouth was so dry I could even brush my teeth, I contacted my doctor he gave me steroids, I couldn't taste food or feel if it was hot or not. It did improve but I still have weird sensations with different foods.

Weitere VAERSDATA-Felder

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

VAERS 2609533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 71,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 03.10.2022
Beginn: 07.11.2022
Tage bis Beginn: 35,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

11/07/2022 tested positive for COVID-19. I had chills and a headache. My symptoms were relatively mild so I did not seek medical care. Symptoms lasted 2-3 days. No medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 07Nov2022 COVID-19 home test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin; PreserVision eye drops; Calcium Vitamin; Multi Vitamin
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2609529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 03.10.2022
Beginn: 19.02.2023
Tage bis Beginn: 139,0
Dosis: 4
Route/Site: SYR / RA

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

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

Symptomtext

I had my vaccination on 10/03/2022. I started to experience extreme muscle and joint aches and pains on 02/19/2023. I tested COVID-19 Positive on 02/22/2023. I contacted my physician on 02/24/2023 and was stated because my case was mild. I was not prescribed Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 02/22/2023 - test COVID-19 Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Microvalve Prolapse
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2609184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VT
Alter: 77,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 30.09.2022
Beginn: 19.01.2023
Tage bis Beginn: 111,0
Dosis: 5
Route/Site: SYR / LA

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

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

Symptomtext

I tested positive for Covid-19 on January 19, 2023 I experienced runny nose and fatigue I was prescribed Paxlovid for my symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2609066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 02.11.2022
Beginn: 12.02.2023
Tage bis Beginn: 102,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal discomfort COVID-19 Chest X-ray Decreased appetite Dizziness Electrocardiogram Pain SARS-CoV-2 test positive Vomiting

Symptomtext

I would say it started the week of the 12th. I was achy and dizzy. My stomach was upset, and I threw up once in a while. I thought it was the stomach flu, but it wouldn't go away. So, I went to get a COVID-19 test. We went on that PAXLOVID and that took care of it. I didn't really have an appetite. I couldn't get over how achy I was. I went to the emergency room because thought I was having a heart attack; this was before we tested positive. They did an EKG and chest x-ray. they gave me some fluids. Then I came home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 20FEB2023 COVID-19 positive; FEB2023 Chest X-ray; FEB2023 EKG
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure
Andere Medikamente: Fish oil; vitamin D3; verapamil HCLER; paroxetine; lisinopril; chlortalidone; famotidine
Allergien: TYLENOL 3; sulfa drugs
Vorherige Impfungen: -

VAERS 2608517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CO
Alter: 66,0
Geschlecht: M
Eingang: 03.04.2023
Impfdatum: 02.10.2022
Beginn: 24.01.2023
Tage bis Beginn: 114,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Subdural abscess

Symptomtext

I tested positive for COVID-19 and was put on Paxlovid by the infectious diseases doctor at the hospital while I was being treated for a Subdural Abscess which did not have anything to do with the COVID-19 vaccine. I am experiencing painful sore throat, slight fever of 99 degrees off and on (sometimes it is 98 - 99 degrees). I am currently on Day 2 of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: 20,0
Labordaten: 04APR2022 - COVID-19 Rapid Test - Tested positive
Aktuelle Erkrankungen: None
Vorgeschichte: Controlled Hypertension
Andere Medikamente: Multi-vitamins; Vitamin D-3; Iron; Timolol; Amlodipine; Endostatin; Trazodone
Allergien: None
Vorherige Impfungen: -

VAERS 2608429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: FL
Alter: 69,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 05.10.2022
Beginn: 25.03.2023
Tage bis Beginn: 171,0
Dosis: 5
Route/Site: IM / AR

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

Abdominal pain Blood test abnormal Computerised tomogram abnormal Inflammation Urine analysis abnormal

Symptomtext

I had severe abdominal pain that started on March 25, 2023. I called and made an appointment to see the gastrointestinal doctor, once I arrived since I was a new patient, they sent me to the emergency room. Once I arrived at the emergency room I had a CAT scan, a lot of blood work, and urinalysis that came back positive for inflammation negative for infection. I was given CIPRO and FLAGYL and so far, I am feeling much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 28MAR2023 CAT scan positive for inflammation negative infection, 28MAR Blood work positive for inflammation negative infection, 28MAR2023 Urinalysis positive for inflammation negative infection
Aktuelle Erkrankungen: No
Vorgeschichte: Ulcerative Colitis
Andere Medikamente: NORVASC; sulfasalazine; calcium with vitamin D; multivitamins
Allergien: PERCOCET
Vorherige Impfungen: -

VAERS 2608358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 76,0
Geschlecht: M
Eingang: 03.04.2023
Impfdatum: 30.09.2022
Beginn: 09.03.2023
Tage bis Beginn: 160,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

I started feeling sick and called my doctor. I tested for COVID-19 at home and the results came back positive. The doctor prescribed me with Paxlovid and I began feeling better between 24-36 hours after taking the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 Testing; Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; Prostate Cancer;
Andere Medikamente: Pravastatin; Flomax; Finasteride; Calcium Citrate; Zolpidem; Famotidine;
Allergien: N/A
Vorherige Impfungen: -

VAERS 2604896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: UT
Alter: 68,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 05.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Ear pain Headache Myalgia Pain Pyrexia

Symptomtext

Muscular pain that continues as of 03/28/2023, but is improving For a few days after vaccine= fever and chills, body aches and headaches, headaches tendering with earache but also gradually improving

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: DM, HTN, HLP, OA, Obese, depression, anemia, RLS, Anxiaty, sleep disordered, breathing
Andere Medikamente: Novolog, levemir, janumet, benzapril, APAP, atorvastatin, escitalopram, ropiner, ASA, Vitamin D, fluticasone, pantoprazole, famotidine, iron, meloxicam
Allergien: HCTZ
Vorherige Impfungen: -

VAERS 2603085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: IN
Alter: 64,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 22.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Chemical burn Nail disorder Pain Rash macular Skin discolouration COVID-19 Drug ineffective Skin exfoliation

Symptomtext

gained COVID back in the emergency; gained COVID back in the emergency; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). 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 22Oct2022 as dose 3 (booster), 0.3 ml single (Lot number: GJ6665, Expiration Date: 06Dec2022) at the age of 64 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 26Apr2021 as dose 1, single (Lot number: EWO161, Expiration Date: 01Jul2021) and on 17May2021 as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Depression" (unspecified if ongoing); "Arthritis" (unspecified if ongoing); "Degenerative bone disease" (unspecified if ongoing), notes: Degenerative bone disease; "Insomnia" (unspecified if ongoing); "COPD" (unspecified if ongoing); "PTSD" (unspecified if ongoing); "Emphysema" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (hospitalization, medically significant), COVID-19 (hospitalization, medically significant) all with onset 2022, outcome "unknown" and all described as "gained COVID back in the emergency". The patient was hospitalized for drug ineffective, covid-19 (start date: Nov2022, discharge date: Nov2022, hospitalization duration: 3 day(s)). The event "gained covid back in the emergency" required emergency room visit. Additional information: Consumer stated, "They tried a few things on me, but they could not figure out what it was because, so they were treating me because they could, the CDC could not figured it out, the center could not figure out. Dermatologist could not figure out. I left home but with no answers and it is just recently I was reading some of the effects from COVID shots, side effects on people of my age and it was stating for some of them that they could become as long as 23 to 30 days after the injections. I asked about the time I was into the emergency the first time and then within a day and a half I gained COVID back in the emergency as being kept. So, when I spent 3 days in there, everybody came and checked on me. All I took was my regular med, basically in pain medication. So much pain. Name of the medication, consumer stated, "The pain medication they gave me? I honestly do not know." 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: Pain
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; COPD; Degenerative bone disease; Depression; Emphysema; Insomnia; Post-traumatic stress disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2593913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 18.10.2022
Beginn: 06.12.2022
Tage bis Beginn: 49,0
Dosis: 5
Route/Site: SYR / UN

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

Abdominal discomfort Abdominal pain upper Blood test Computerised tomogram abdomen abnormal Diverticulum

Symptomtext

I had my vaccination on 10/18/2022. I had been feeling pain in my stomach for a couple weeks. On 12/06/2022 I sought medical attention for the intense pain and discomfort in my stomach. They ran a CT scan of my abdomen. They diagnosed me with Diverticulosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: CT Scan Blood Panel 12/06/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Celiac Disease; Psoriasis; Arthritis; Stills Disease; Autoimmune Thyroid Disease; Osteoarthritis; Pulmonary Disfunction
Andere Medikamente: COSENTYX injections; hydrochloride; IMITREX; ZOFRAN; WIXELA; albuterol; TYLENOL; ZYRTEC; vitamin B; vitamin C; vitamin D; magnesium; turmeric; eye vitamin
Allergien: Sulfa; KEFLEX; shellfish
Vorherige Impfungen: -

VAERS 2588552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 50,0
Geschlecht: F
Eingang: 28.02.2023
Impfdatum: 25.11.2022
Beginn: 18.01.2023
Tage bis Beginn: 54,0
Dosis: 5
Route/Site: SYR / AR

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

Cough Dysphagia Feeding disorder Glossitis Glossodynia Impaired work ability Oropharyngeal pain Productive cough Rhinorrhoea SARS-CoV-2 test negative Secretion discharge Sputum discoloured Sputum retention Streptococcus test negative Swollen tongue Tongue erythema

Symptomtext

On 01/18/2023 in the evening, I developed a moderate to severe sore throat. I had a low grade sore throat and runny nose until 01/23/2023. By 01/24 I thought I would be getting better and then I went into severe coughing. It was uncontrollable dry coughing with occasional production. The phlegm was difficult to expectorate and it was yellow to green. I went to urgent care 5 days later. I was taking ADVIL cold and sinus which helped with the snot. My cough was very challenging, so I went to urgent care. They gave me benzonatate on 02/06/2023 and prescribed a lidocaine liquid number because my throat was severely painful, but I didn't take that. The cough suppressant really helped. I took that for about 10 days and the medicine helped. It seemed like I was really improving. My tongue hurt really bad the entire time and it was bright red. The papillae were really inflamed. I couldn't brush my tongue with a toothbrush because it really hurt. It was hard to swallow. At urgent care they did a strep throat test and it was negative. After about a week, I thought I was getting much better. I woke up on 02/16/2023 and again my throat was severely sore. I went back to urgent care that day. The right side of my throat was super sore and the right side of my tongue was visibly swollen. The doctor said that's not normal. She thought I had maybe an abscess or something going on. She prescribed amoxicillin and I took that for 5 days. My throat improved. I was unable to eat before I went to urgent care. They did another strep test which was negative. By 02/23/2023 was when I started to turn a corner and feel better. Yesterday 02/27/2023 was when I felt like I'm starting to feel like myself. I did miss more than a week of work. I also had to use about 20 cough drops a day to stop coughing so I could talk. I was also using an N-95 mask majority of the time. It was over a month to recover. I did have other family members in the house during the time that I was sick, and I was the only one who was sick throughout this event. I did stay away from them while I was sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 25JAN2023 COVID-19 test negative; 06FEB2023 Strep test negative; 16FEB2023 Strep test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: WELLBUTRIN; SYNTHROID; fish oil; HCL tablets; melatonin; DIOVASC; hormone protect supplement; high dose methylated folic acid; vitamin D
Allergien: Penicillin; lanolin
Vorherige Impfungen: -

VAERS 2587028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 29.12.2022
Beginn: 26.01.2023
Tage bis Beginn: 28,0
Dosis: 6
Route/Site: SYR / AR

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

Asthenia COVID-19 Cough Dry throat Dysgeusia Headache Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Taste disorder

Symptomtext

The symptoms started with a runny nose that was constant and clear. I started taking Mucinex. A day later, the I also developed a dry sore throat. The next day, I developed a severe headache and a cough. On day three, I tested positive for COVID-19. I reported it to my doctor via MyChart. She scheduled a telehealth appointment. I received a prescription to Paxlovid due to my high-risk status. I was told to stop taking Atorvastatin while on Paxlovid. I began taking the Paxlovid about 5 days after my symptoms started. I took three in the morning and three at night for five days. My symptoms improved almost immediately. By the second day, the symptoms were going away totally. I experienced a nasty metallic taste in my mouth for the full five days. On day 7 or 8 after testing positive for COVID-19, I tested negative. COVID-19 also effected my taste and energy levels and that has lingered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 01/28/2023 At Home COVID-19 Test - Positive; 02/02/2023 At Home COVID-19 Test - Positive; 02/06/2023 At Home COVID-19 Test - Negative
Aktuelle Erkrankungen: Foot Surgery for Hammer Toe and Bunions
Vorgeschichte: Spinal Stenosis; Pemphigoid; Osteoarthritis; Torn Rotator Cuff; Type 1 Diabetes
Andere Medikamente: Amlodipine Besylate; Amoxicillin; Atorvastatin Calcium; Celecoxib; Doxycycline Monohydrate; Duloxetine; Enalapril Maleate; Ketoconazole 2% Shampoo; Mycophenolate Mofetil; Naltrexone; Nystatin Powder; Synthroid; Humalog Insulin
Allergien: Codeine; Bee Stings; Latex; Tramadol; Hydrochlorothiazide; Gadobutrol Iodine; Hydrocodone;
Vorherige Impfungen: -

VAERS 2585985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 22.02.2023
Impfdatum: 21.11.2022
Beginn: 27.01.2023
Tage bis Beginn: 67,0
Dosis: 4
Route/Site: IM / UN

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

Erythema Pruritus Skin swelling Urticaria

Symptomtext

I had full body hives. They were red, raised, itchy, and they come and go. When I went to the doctor, and they said they didn't know what cause them. They also started me on a couple medication and referred me to a dermatologist. I am still having problems with the hives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Genetic High Cholesterol; GERD
Andere Medikamente: Rosuvastatin; ZYRTEC; PEPCID; multivitamin; BLISOVI FE
Allergien: Adhesive
Vorherige Impfungen: -

VAERS 2585519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 64,0
Geschlecht: M
Eingang: 22.02.2023
Impfdatum: 06.12.2022
Beginn: 22.12.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Nasal congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

A couple of weeks after getting the shot, I had a brief fever and nasal congestion at night. The fever only lasted about an hour, but the congestion lasted for some nights. I treated the nasal congestion with a nasal spray. I decided to take an at-home COVID-19 test on 12/22/2022 which came back positive. The next morning, I contacted my doctor to inform her on my positive test and was prescribed molnupiravir 200mg for treatment. After a couple of days of treatment, I made a pretty fast recovery and doing well now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 22DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes; Asthma; Emphysema; High Blood Pressure; Heart Dysrhythmia; Obesity; High Cholesterol
Andere Medikamente: Metformin; ADVAIR; SINGULAIR; albuterol; fenofibrate; metoprolol; amlodipine; losartan; tamsulosin; fish oil; multivitamin; vitamin D; zinc; vitamin C; fluticasone
Allergien: Penicillin; NEOSPORIN
Vorherige Impfungen: -

VAERS 2579639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 83,0
Geschlecht: M
Eingang: 10.02.2023
Impfdatum: 20.02.2021
Beginn: 02.02.2023
Tage bis Beginn: 712,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cholelithiasis Exposure to SARS-CoV-2 Mental status changes Pyrexia SARS-CoV-2 test positive Transaminases increased

Symptomtext

85-year-old male, resident of boarding care facility, history of diastolic heart failure, benign neoplasm of the pituitary gland, history of gastrointestinal stromal tumor/stomach cancer, GERD with esophageal stricture, previous lacunar infarct, HLD, male hypogonadism failure on long-term testosterone, who presented from skilled nursing facility on 02/01 due to change in mental status along with fever. Although he tested negative for COVID at the boarding care facility, he tested positive in the ED 02/01. No further information it is revealed that his roommate was positive. Onset of his own symptoms was not clear. He was noted to have elevation of transaminases but no hypoxemia. Hence he was started on remdesivir but not steroid. Ultrasound of his right upper quadrant revealed the presence of cholelithiasis which were previously known without thickening of the gallbladder wall but they were unable to assess for Murphy sign sonographically. Clinically he did not not meet criteria for cholecystitis. Transaminase elevation improved significantly. His mental status also improved dramatically within 24 hours.

Weitere VAERSDATA-Felder

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

VAERS 2578938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NV
Alter: 75,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 09.11.2022
Beginn: 18.12.2022
Tage bis Beginn: 39,0
Dosis: 5
Route/Site: IM / LA

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

Cough Influenza virus test negative Malaise Nasopharyngitis Respiratory tract infection viral Rhinorrhoea SARS-CoV-2 test negative

Symptomtext

I didn't feel great for a day or two after receiving the vaccine. I took an Aleve about an hour after receiving the vaccine which helped. On 12/28/2022 I began not feeling well with symptoms of a head cold. It felt like a someone turned on the facet in my nose. I went to the clinic on 12/30/2022 and I was diagnosed with viral respiratory illness. I tested for COVID-19 and the flu. I did not retest for COVID-19. I took NyQuil for my symptoms so I could rest. As of today, I will have a cough, but I do feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 30DEC2022 COVID-19 Test - Negative; 30DEC2022 FLU Test - Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2578106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: 76,0
Geschlecht: M
Eingang: 08.02.2023
Impfdatum: 07.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 24,0
Dosis: 5
Route/Site: IM / AR

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

Back pain Pyrexia Rash Rash pruritic Tenderness

Symptomtext

I had no adverse reaction to the vaccine. In late December 2022, I developed a rash in my right shoulder and on the right side of my neck. The rash is little bumps, tender to the touch and itchy. I'm not taking anything for the symptoms. Recently I had lower back pain and a high temperature, and I went to the emergency room. I was observed and discharged. The symptoms resolved within 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Kidney Transplant; Coronary Artery Disease
Andere Medikamente: N/A
Allergien: TAMIFLU; morphine
Vorherige Impfungen: -

VAERS 2576899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WV
Alter: 34,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Pain Pain in extremity X-ray normal

Symptomtext

The next day all of my joints started to hurt. 2 days after the injection my right leg (knee and ankle) started throbbing and hurting when I would walk or take steps. When o do steps now my right leg starts to ache at the joints. Now when I stand for a long period of time! Bend over to pick anything up or do steps my right knee hurts. If I extend my right foot my ankle hurts as well. I have done home exercise in case it was something I can prevent or treat alone that did not help.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I have had an X ray so far that was normal. My dr is sending me to an orthopedic dr and getting an MRI scheduled now.
Aktuelle Erkrankungen: NA
Vorgeschichte: I have chronic back pain due to 2 previous back surgeries with a fusion and decompression of L5S1.
Andere Medikamente: I take hydrocodone 10/325 4 times a day. A multi vitamin and
Allergien: Bee stings
Vorherige Impfungen: The other 3 vaccines made me sick with flu like symptoms and some body aches but this only lasted 2-3 days after the shot.

VAERS 2576536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 04.11.2022
Beginn: 27.12.2022
Tage bis Beginn: 53,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Feeling abnormal Malaise Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

The symptoms started on Tuesday, 12/27/2022. I was feeling miserable with sinus drainage and coughing. When I still had symptoms the next morning, I used a home test and I was positive. I scheduled the Telehealth visit and my goal was to get PAXLOVID. The nurse practitioner agreed and after examining me over the telehealth and looking at my throat, she prescribed my PAXLOVID that day and within a couple days I was feeling a lot better. I never had a fever. I was given the expectation that I would have gotten a metallic taste, but it was really just a bad taste in the mouth. I was more tired than usual and that lasted longer than the other symptoms. Others I've talked to noted to continue to rest and they were correct. I had a get together for Christmas Eve, and after I tested positive, I contacted everyone that was there to inform them. Only one other person had noted they were positive 12 to 24 hours after I tested. I am unsure of who I was infected by, but they may have been asymptomatic. My wife did not get sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 28DEC2022 at home COVID-19 test positive; 06JAN2023 at home COVID-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Overweight
Andere Medikamente: Lisinopril HCTZ combination; atorvastatin; amlodipine; FLONASE; turmeric; generic PEPCID AC; low dose aspirin; adult multivitamin; omega 3; vitamin B12; coQ10; guaifenesin; ALEVE
Allergien: Environmental allergies; some bandages; lactose intolerance
Vorherige Impfungen: -

VAERS 2575182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 03.02.2023
Impfdatum: 03.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: SYR / LA

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

Injection site pain Rotator cuff syndrome

Symptomtext

Had prolonged should pain. Primary care doctor referred me to a sports medicine clinic. Saw doctor and was diagnosed with Left Shoulder Impingement Syndrome. Given a cortisone injection and about to start Physical Therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: FLONASE
Allergien: N/A
Vorherige Impfungen: -

VAERS 2575070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 03.02.2023
Impfdatum: 03.11.2022
Beginn: 14.01.2023
Tage bis Beginn: 72,0
Dosis: 5
Route/Site: SYR / UN

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

Abdominal X-ray Abdominal pain upper Computerised tomogram abnormal Diverticulitis

Symptomtext

I received my Pfizer Bivalent Booster on 11/03/2022. My adverse event started on 01/14/2023 in the morning as soon as I woke up around 07:00AM. I had severe pain in my stomach. It wasn't like a normal pain. It was on my left side. I tried to go to my doctor's office on the 01/16/2023 but since it was a holiday I had to schedule it for 01/17/2023 at 11:00AM. They asked me what was going on and about different issues I had with my stomach. They told me to get a X-ray done. It was normal. They also asked me to get a CT scan on 01/18/2023. When the results came in they diagnosed me with diverticulitis. They gave me IV with saline solution and also antibiotics. I went back for the rest of the week for IV infusion. They gave me an oral antibiotics to take as well. They prescribed with clindamycin which I started taking on 01/21/2023 for 10 days. They also told me to take probiotics over the counter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: 17JAN2023 X-ray test normal; 18JAN2023 CT scan test abnormal
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; dust allergies
Andere Medikamente: Lisinopril; allopurinol; calcium; famotine; ZYGEL
Allergien: BIAXIN; diltiazem; thiazide drug
Vorherige Impfungen: Flu vaccine, localized rash for 3-4 days

VAERS 2573151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IN
Alter: 59,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 01.11.2022
Beginn: 01.01.2023
Tage bis Beginn: 61,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Cough Injection site pain Malaise SARS-CoV-2 test positive Sneezing

Symptomtext

I had soreness at the injection site for a couple of days. I began not feeling well on 12/27/2022 with sneezing and coughing. I thought my allergies were acting up. On 01/01/2023 I tested positive with a home test for COVID-19. I was out of state when I tested positive for COVID-19 and contacted my doctor's office over the phone. I got a prescription for Paxlovid five hours later. I started feeling better, but it all returned with a vengeance. I started taking over the counter medication to relieve my symptoms. I was sick for 19 days. As of today, I still have a cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: 01JAN2023 COVID-19 Home Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Bystolic; Estradiol; Progesterone; Lysine; Vitamin D
Allergien: N/A
Vorherige Impfungen: 20-25 years ago, I had a flu vaccine and got really sick. Kidney infection and high fever.

VAERS 2570628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: AL
Alter: 69,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 27.10.2022
Beginn: 08.12.2022
Tage bis Beginn: 42,0
Dosis: 5
Route/Site: IM / LA

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

Cough Dysphonia Fatigue Influenza Influenza virus test positive Nasal congestion

Symptomtext

I experienced the flu with tiredness, stuffy nose, cough and hoarseness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: FLU test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2570583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 43,0
Geschlecht: M
Eingang: 30.01.2023
Impfdatum: 18.10.2022
Beginn: 08.12.2022
Tage bis Beginn: 51,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Feeling abnormal Headache Pain SARS-CoV-2 test positive

Symptomtext

On December 8, I started having a slight headache I felt rundown and just not good. Friday morning, I started having body aches. I went to the walk in clinic and was negative and then Saturday I tested again and was positive, I was prescribed prednisone and didn't get worse just body aches and coughing but I didn't get worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2570566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: GA
Alter: 75,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 28.10.2022
Beginn: 18.01.2023
Tage bis Beginn: 82,0
Dosis: 5
Route/Site: IM / LA

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

Aphonia Chills Headache Nausea Oropharyngeal pain Pyrexia SARS-CoV-2 test

Symptomtext

I lost my voice and had a sore throat. I had a fever with some chills and a slight headache, some nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home rapid COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: -
Andere Medikamente: Atorvastatin; hydrochlorothiazide sorazide; potassium chloride ER; losartan; chewable aspirin
Allergien: Nicainoprol
Vorherige Impfungen: -

VAERS 2570516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 45,0
Geschlecht: M
Eingang: 30.01.2023
Impfdatum: 05.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Pruritus Rash

Symptomtext

Rash, similar to poison ivy/sumac, but without the oozing or pussing. Itching over a very large portion of my body including but not limited to biceps, thighs, under arms, hips. Treated with calamine to soothe the itch (because I thought it was poison ivy/sumac) After ~48-72 hours I woke up and the rash was completely gone with no symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: No tests or labs I did receive a flu shot at the same time.
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep apnea
Andere Medikamente: None. I did receive a flu shot at the same time: FLUZONE QUAD 2022-2023 SYRINGE SANOFI-PASTEUR UT7741NA 0.5ml
Allergien: Doxycycline
Vorherige Impfungen: -

VAERS 2569453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TN
Alter: 89,0
Geschlecht: F
Eingang: 27.01.2023
Impfdatum: 08.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / RA

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

Biopsy skin Mass Pruritus Rash Urticaria

Symptomtext

extremely, horribily itchy hives/rash/welt areas that pop up sporadically at random places on torso (front and back), arms, fingers, hands, neck, head, eyelid, ears, and legs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Dermatologist (M.D.) took skin graft from one of the very large masses on arm and sent it off for culturing and testing. He basically said "there arent any finding which makes me go "huh???". It seems he int willing to go any further into delving and medical research to try and determine what might be the cause. He ought to have filed this report. But, I realize doctors get extremely busy. So, i am submitting the report. Dr contact info is reported.
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoarthritis, dramatic blood pressure swings, old age
Andere Medikamente: amilodipine(5mg), losarten(50mg), metroprolol(50mg), omeprazol ommeprolol(50mg), repinirole(.5mg), hydralazine(25mg), baby asprin(81mg), Vitamin D(1,000mg), calcium citrate zeta, preservision aved 2, CoQ10, melatonin, benadryl, amitriptylin
Allergien: prdnizone, tetnus, sulfa drug, cipaflexine, azithrom, most recent COVID 19 vaccine by BiValent
Vorherige Impfungen: tetnus shot (local large swelling and redness),

VAERS 2569132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 07.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Anxiety Blood pressure increased Dysgeusia Headache

Symptomtext

Fifteen minutes post vaccination, patient complained of metallic taste in her mouth and headache. Patient was provided with a glass of water and was assessed by RN. Vital signs were taken and monitored by RN. Blood pressure was 160/70, heart rate was 87, and oxygen 97%. Patient denied history of high blood pressure, but stated she had a busy stressful day. Blood pressure was repeated about 5 minutes later and read 148/72. Patient denied any shortness of breath, chest pain, palpitations, rash or itchiness. Patient reported feeling better after finishing her glass of water, and taking a few deep breaths. Patient reported feeling less anxious after this. Patient was advised to seek immediate medical attention at Emergency Department if symptoms return, or any new symptoms arise in the next few hours or days. Patient left vaccine clinic alert, oriented, and stable with her husband around 2:35PM. All symptoms resolved prior to patient leaving vaccine clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Type 2 Diabetes Mellitus
Vorgeschichte: Type 2 Diabetes Mellitus
Andere Medikamente: Atorvastatin 40mg, Escitalopram 20mg, Glipizide ER 5mg Metformin 1,000 MG, pioglitazone 15MG, Ambien 10MG, Vitamin D3 5,000
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2568615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 26.10.2022
Beginn: 08.01.2023
Tage bis Beginn: 74,0
Dosis: 5
Route/Site: IM / LA

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

Blood test normal Cough Culture stool negative Diarrhoea Influenza virus test negative Malaise Pyrexia Rhinorrhoea SARS-CoV-2 test negative X-ray normal

Symptomtext

I started feeling ill on 1/8/23. I didn't go to the doctor right away, but when I went, they believed that I had the Flu. I had a cough, runny nose, and a fever. Then I got diarrhea. The fever only lasted for about three days. I was prescribed benzonatate for my cough. I also took FLONASE, CLARITIN D, and ROBITUSSIN. I am still not 100 percent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 19JAN2023 Flu test negative; 19JAN2023 COVID-19 test negative; 19JAN2023 X-Ray normal; 19JAN2023 Blood panel normal; 20JAN2023 Stool culture normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Migraines
Andere Medikamente: AIMOVIG; amitriptyline; calcium; vitamin D; vitamin B12; multivitamin; probiotic; topiramate; ospemifene
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2567818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: 75,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 14.10.2022
Beginn: 23.11.2022
Tage bis Beginn: 40,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

I went on a cruise, and I got the Covid before boarded or so I assume I got on the ship. Because it was a requirement to even board is why I believe I was positive before getting on. I started feeling sick by the end of November and I was so tired and having so much fatigue. I went to see a medic while on the ship because I didn't trust my COVID-19 cabin test. The medic tested me and I was positive so I was stuck in isolation on the cruise in my cabin for 2 days. The cruise dates where 11-22-2022 to 12-06-2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Allegoristic; Arthritis
Andere Medikamente: Alendronate; azelastine HCL; ESTRING; hydroxychloroquine; calcium + D3; fluticasone propionate; multivitamin; extra vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 2567690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MN
Alter: 63,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 18.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 44,0
Dosis: 5
Route/Site: IM / AR

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

Back pain Endoscopy Hepatic cyst Magnetic resonance imaging abdominal abnormal Pancreatic cyst Pancreatitis Renal cyst X-ray abnormal

Symptomtext

I had gone for a scan of my back in May 2022 and there were no complications found. After receiving the Pfizer Bivalent vaccine, I started to experience extreme back pain. I went to see the specialist and they noticed that there wasn't anything wrong around my back, but that I did have cysts located on my pancreas, liver and both kidneys. The only change between May 2022 and November 2022 was the Pfizer Bivalent vaccine. I had more scans completed and they were able to tell that the cysts were not cancerous. I'm very thankful for that, but I was very surprised with what they found. At the present moment, The Endoscopic specialist stated that there was no need for a routine visit to look at the cysts. My pancreas is inflamed, but my PCP does not feel any need to progress with anything at the moment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: MRI; X-Ray; Endoscopy
Aktuelle Erkrankungen: None
Vorgeschichte: Heart Failure Disease; Asthma; Spinal Stenosis; Anxiety; Insomnia.
Andere Medikamente: TRELEGY inhaler; ALLEGRA; aspirin; azelastine (nasal inhaler); benzonatate: losartan; FLONASE; HCTZ; JARDIANCE; metoprolol; methocarbamol; MUCINEX; montelukast; NEXIUM; ondansetron; sertraline; simvastatin; albuterol inhaler; topiramate; AM
Allergien: AUGMENTIN; amlodipine desolate; baclofen; carvedilol; CLARITIN; LIPITOR; lisinopril; phenadrine; SPIRIVA; trazadone; animal dander; mold; pollen; dust mites.
Vorherige Impfungen: The second Pfizer vaccine, 2021, I ended up in the ER because I couldn't stop clearing my throat and I was having trouble breath

VAERS 2566855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NH
Alter: 70,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 24.10.2022
Beginn: 13.12.2022
Tage bis Beginn: 50,0
Dosis: 5
Route/Site: IM / LA

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

Cough Lower respiratory tract infection Malaise Wheezing

Symptomtext

I did not have an adverse reaction to the vaccine. I woke up on 12/13/2022 with a bad cough and things progressed from there. I saw my doctor on 12/19/2022 and he heard a wheezing sound in my lungs. I was diagnosed with a lower respiratory infection. I was prescribed an inhaler. I was sick for 15 days.

Weitere VAERSDATA-Felder

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

VAERS 2564539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CO
Alter: 70,0
Geschlecht: F
Eingang: 20.01.2023
Impfdatum: 20.10.2022
Beginn: 17.12.2022
Tage bis Beginn: 58,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Feeling abnormal Headache Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Started feeling bad 12/17/2022; severe headache body ach;cough; fever and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: home covid test-positive
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Atorvastatin; Cyclobenzaprine; estradiol; patch fioricet; trazodone
Allergien: aspirin
Vorherige Impfungen: -

VAERS 2603730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 17.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Chills Dialysis Diarrhoea Hyperkalaemia Immunisation reaction Injection site pain Nausea Pain Treatment noncompliance Vomiting

Symptomtext

Narrative: A 61yo male with PMH of multiple medical problems including Hypercholesteremia, Cholecystectomy, Gout, GERD, HTN, OA of Knee, Cervicalgia, BPH without urinary obstruction, OSA, ESRD and Right Inguinal Hernia. Per ED documentations; On October 19, 2022 the patient presented to the ED with chief complaint of vaccine reaction having pain at the injection site and body aches with chills , nausea, vomiting and watery diarrhea x 3 days. The patient reported he took some Pedialyte with mild relief and diarrhea improved slightly. Vaccine administering RN's documentation showed the patient received both Covid - 19 and Flu vaccine on the same day on 10/17/22. The patient also reported he missed his dialysis, which was due the previous day. He was found to be hyperkalemic and got admitted for hyperkalemia management and dialysis. On October 23, 2022, the attending on unit reported an observed ADR of Diarrhea post patient admission for vaccine reaction on 10/20/22. Patient's immunization record showed he's had four Pfizer Covid - 19 vaccine shots prior to this (On April 16, 2021, May 7, 2021, August 27, 2021 and April 11, 2022),

Weitere VAERSDATA-Felder

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

VAERS 2563370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IA
Alter: 72,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 17.10.2022
Beginn: 18.01.2023
Tage bis Beginn: 93,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Injection site pain Malaise Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

I had a little tenderness at the injection site for one day. I started feeling sick on 01/17/2023 like I was getting a bad cold. I tested positive for COVID-19 with a home test on 11/18/2023. I contacted my doctor and started me on Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: 13OCT2022 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: COPD; Arthritis; High Blood Pressure
Andere Medikamente: N/A
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2561576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 16.10.2022
Beginn: 24.12.2022
Tage bis Beginn: 69,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Influenza virus test negative Lymphadenopathy Malaise Oropharyngeal pain Pain Respiratory syncytial virus test negative SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

I started feeling achy on the 24th. I had a low grade fever at around 99.1 and a sore throat. I had lymph node enlargement with a bad cough as well. I completed a home test which was negative. I completed a COVID 19 PCR test at the doctors office and it was positive. I was prescribed both PAXLOVID and azithromycin. It took about 4 days before I started feeling better at all. It took a long time for them to get better. I think I had a rebound case 1 week later. I was prescribed methylprednisolone and TESSALON PERLES for my symptoms. My symptoms improved in about 5 days. I still cough every day but it's not as bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 PCR 12/26/2022 positive, Flu 12/26/2022 negative, RSV 12/26/2022 negative, Strep 12/26/2022 negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Multiple Sclerosis; Migraines; Depression
Andere Medikamente: GILENYA; desvenlafaxine: gabapentin; ALLEGRA; vitamin D3; AIMOVIG injection
Allergien: N/A
Vorherige Impfungen: -

VAERS 2561515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 27,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 17.01.2023
Beginn: 01.01.2023
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Blood pressure decreased Nausea Pallor Vomiting

Symptomtext

PATIENT EXPERIENCED NAUSEA AND VOMMITING AND TURNED PALE A FEW MINUTES AFTER ADMINISTERING VACCINE. WE CALLED 911 AND THE EMT MENTIONED HIS BLOOD PRESSURE WAS IN THE LOW 100'S TOOK THE PATIENT TO THE HOSPITAL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: HAD NAUSEA LAST DOSE 1/8/22 WHEN HE RECEIVED Moderna VACCINE
Vorherige Impfungen: -

VAERS 2561462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NH
Alter: 71,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 17.10.2022
Beginn: 15.11.2022
Tage bis Beginn: 29,0
Dosis: 5
Route/Site: IM / UN

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

Headache Neck pain Sleep disorder X-ray normal

Symptomtext

After my vaccine, I don't remember exact time, I started to get a very back pain on the eft of my neck, I couldn't sleep. I saw my doctor, they took X-ray, and it did not show anything at that point, but since then it's getting worst and I get headaches in the whole area around my head, daily, it keeps awake at night. I called the doctor and requested a 2nd appointment which I don't have yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 11NOV2022 -X-RAY - Normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: RLS; IBS; Sleep Apnea
Andere Medikamente: Bupropion; Linzess; Pregabalin; Methadone ; Vitamin D
Allergien: Statin; Keflex
Vorherige Impfungen: -

VAERS 2561390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: IN
Alter: 65,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 17.10.2022
Beginn: 02.11.2022
Tage bis Beginn: 16,0
Dosis: 5
Route/Site: SYR / RA

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

Erythema Pruritus Sensitive skin Urticaria

Symptomtext

I can scape my self lightly and eventually get Welt if I scratch it I would get more welts just from a small cut; my skin is also red and very itchy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Heart Failure; Bipolar Depression
Andere Medikamente: Entresol; Carvedilol; Lamartine; Cingular; Claritin; Atorvastatin; Dicycloverine; Vitamin D; Flonase
Allergien: Penicillin; Clindamycin; tetracycline; Lobster
Vorherige Impfungen: -

VAERS 2560818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 14.10.2022
Beginn: 10.12.2022
Tage bis Beginn: 57,0
Dosis: 4
Route/Site: SYR / AR

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

Arthralgia Asthenia COVID-19 Cough Headache Myalgia Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

My symptoms were severe headache, congestion, consistent dry cough, body aches, and general weakness with muscle/joint pain. That started on 12/10/22. I originally thought it was allergies until the body and joint pain started. I took it easy over the weekend, lots of fluid. The body and joint pains started to increase even with medication, so before I went to work on Monday I took an at home COVID-19 test, it was positive. I had a tele-health appt with my PCP that same day, and he prescribed PAXLOVID. I picked it up same day, and that night my body aches got even worse. Then after 24 hours that subsided, I just had the metallic taste in my mouth from the medication. My symptoms kept getting less and I just stayed home for 5 days. I had to report to work my temperature everyday, and I never had a fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 2022DEC12 COVID-19 (positive)
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Women's multivitamin; every other day allergy shots; NASONEX; ZYRTEC; LUPRON every 3 months; CORE for women probiotics
Allergien: Tree pollens; grass; cats; horses; cockroaches; molds
Vorherige Impfungen: -

VAERS 2559994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: 57,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Administration site pain Bursitis Immunisation reaction Ultrasound scan X-ray limb abnormal

Symptomtext

Vaccine recipient w pain x 2.5 months in shoulder where vaccine was administered, starting on day of vaccination. Recipient was eventually diagnosed with vaccine-induced bursitis requiring treatment with steroid injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Administration site pain
Hospital-Tage: -
Labordaten: - ultrasound - xrays eventual diagnosis of bursitis
Aktuelle Erkrankungen: unknown
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2559528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: OR
Alter: 59,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Chest X-ray Grip strength decreased Magnetic resonance imaging Neuralgia Pain in extremity X-ray limb

Symptomtext

Neuralgia and pain right arm with decreased grip strength.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: XR Humerous XR Forearm XR Chest MRI Shoulder MRI Upper arm
Aktuelle Erkrankungen: Vertigo Colonic Fistula Coronary arteriosclerosis Diverticulitis Elevated liver enzyme
Vorgeschichte: Obesity Hypertension COPD Hyperlipidemia
Andere Medikamente: albuterol sulfate HFA 90 mcg/actuation aerosol inhaler amLODIPine 10 mg tablet aspirin 81 mg tablet,delayed release atorvastatin 80 mg tablet diclofenac 1 % topical gel dicyclomine 20 mg tablet ergocalciferol (vitamin D2) 1,250 mcg (50,000
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2559516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CT
Alter: 32,0
Geschlecht: M
Eingang: 13.01.2023
Impfdatum: 13.10.2022
Beginn: 09.01.2023
Tage bis Beginn: 88,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Headache Myalgia Restlessness Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On Monday I started having runny nose and a cough not really tired just restless. I also had sore muscles and I tested the next day in which I was positive for COVID-19. I started having a headache Aleve and it did eliminate the pain. I called the doctor, and they did prescribe Paxlovid, and I haven't taken because everything is kind of going away on their own. Its really strange how I got it I have been wiping everything down and staying away from people.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Underdeveloped Lungs
Andere Medikamente: Albuterol Sulfate; Fluticasone; Robitussin; Mucinex
Allergien: N/A
Vorherige Impfungen: -

VAERS 2558572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 12.10.2022
Beginn: 07.01.2023
Tage bis Beginn: 87,0
Dosis: 5
Route/Site: IM / LA

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

Aphonia COVID-19 Cough Dysphagia Headache Heart rate increased Oropharyngeal pain Pain Pyrexia SARS-CoV-2 RNA increased SARS-CoV-2 test positive Sinus pain Sleep disorder

Symptomtext

After the vaccine I had headache for three days. (Cross reference to V-safe). I got COVID-19 last Saturday Jan 7th, at 4:00AM , I had very painful sore throat, so painful it was difficult to swallow, later on the day I had fever (101.7), sinus pain, headache, body ache, I had a home COVID-19 test and it was positive (very dark), I called my doctor, I requested PAXLOVID, I was told I had to speak to someone tele health appointment the next day, Sunday Jan 8th, I had the appointment with the TA and he prescribed PAXLOVID and ibuprofen, I never picked it up until that evening, the first dose 8PM January 8th. I am still taking PAXLOVID. I am on day 4th, symptoms are improving. On Monday Jan 9th coughing about 100 times a day. On Tuesday night January 10th at 9PM I started dry rapid pulse, take me from sleeping. Last night January 11th I took the first cough medicine, I called my doctor back, I lost my voice. The nurse told me that due to my symptom and my test results I had a huge Viral Load. She thinks I got the new Omicron Variant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 07JAN2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Migraine; Thyroid Disease
Andere Medikamente: N/A
Allergien: Airborne pollen
Vorherige Impfungen: -

VAERS 2557752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 55,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 11.10.2022
Beginn: 12.12.2022
Tage bis Beginn: 62,0
Dosis: 5
Route/Site: SYR / LA

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

Body temperature decreased COVID-19 Chills Headache Malaise Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Starting 12/12/2022, I developed a cough in the wee hours of the morning, and I felt fine for the rest of the day until about 4:30 in the afternoon. I began to feel sick with general malaise and some mild aches. Once I got home, I took my temperature and it was lower than usual. I took an at-home COVID-19 test which was negative. After taking a shower, I developed severe chills but no fever. The next morning I woke up with a fever of 101.1 and chills, and I took an at-home COVID-19 test which was positive. I contacted my doctor but they couldn't do telehealth until the next day. I called a pharmacy and they called me back. I had chills, headache and a fever. An hour after talking to them, I developed congestion that was very severe. I would continue feeling poorly until Wednesday afternoon when I started feeling better. I was prescribed PAXLOVID but I did not take it. By Friday afternoon (12/16/2022), I felt almost completely fine except for some mucous and cough that lasted until just right before the new year.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At-home COVID-19 test (12/12/2022): negative; at-home COVID-19 test (12/13/2022): positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fiber; vitamin B12; vitamin D
Allergien: OMNIPAQUE 3000
Vorherige Impfungen: -

VAERS 2557506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: PA
Alter: 62,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 11.10.2022
Beginn: 27.12.2022
Tage bis Beginn: 77,0
Dosis: 5
Route/Site: IM / LA

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

Fatigue Pain Pyrexia Respiratory tract congestion

Symptomtext

I experienced a slight fever, body aches, fatigue and congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Paroxysmal supraventricular tachycardia
Andere Medikamente: Bisoprolol fumarate; flecainide; atorvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2557496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 56,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 11.10.2022
Beginn: 06.01.2023
Tage bis Beginn: 87,0
Dosis: 5
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Cough Malaise Nasal congestion Pyrexia SARS-CoV-2 test positive Sneezing Throat irritation

Symptomtext

I was not feeling well that evening, I felt a little stuffy, and thought I may be coming down with a cold. The next day I had a starchy throat and was sneezing. I had plans to go out Saturday night, so I took a COVID-19 home test just to be safe and it was positive. I did have a coworker who was out before that with COVID as well. I ended up having a low-grade fever, lots of nasal congestion, and a minimal dry cough. I did have loss of taste and smell as well but fortunately have not had fatigue. I went to an urgent care connected to my work and got a rapid test and that confirmed the home test. I was put on Paxlovid, and I am on day four at this point and it is helping. I did have my flu shot on the same day that I got my COVID-19 vaccine, but I do not have the information on that as it is at work, and I am home with COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Elevated Blood Pressure; Exercise Induced Asthma; Depression; Anxiety
Andere Medikamente: Baby Aspirin; Allegra; Effexor; CoQ10; Probiotic; Tums; Red Yeast Rice; Vitamin D; Hydrochlorothiazide; Biotin; Magnesium Citrate; Pepcid; Flonase
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2557493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / LA

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

COVID-19 Cough Discharge Fatigue Headache Malaise SARS-CoV-2 test positive Sinus disorder

Symptomtext

I first noticed symptoms on 12/23/2022 and I thought it was a sinus event but on 12/24/2022 I took a COVID-19 test which resulted in a positive. I called my Physician by phone and was prescribed Paxlovid and I took a five day course of that. My symptoms were mostly around my sinuses, coughing from drainage with headache and fatigue they lasted on and off until 01/07/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test result was positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity
Andere Medikamente: Propranolol; Fluoxetine; Clobetasol; Fexofenadine; Hydroxyzine; Multivitamin; Vitamin C; Vitamin D; Fish Oil; Cinnamon; Prerevision
Allergien: None
Vorherige Impfungen: -

VAERS 2556790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: DC
Alter: 83,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 15.12.2022
Beginn: 16.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Site: Pain at Injection Site-Medium

Weitere VAERSDATA-Felder

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

VAERS 2556000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 10.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Cough Ear pain Fatigue Injection site erythema Injection site swelling Paranasal sinus discomfort Sinus congestion Sinus pain Throat clearing

Symptomtext

At the time I had redness and swelling on the left arm where I got my injection at. I was also fatigue. My most recent visit to the provider's I was prescribed medication. It is an antibiotic named cefuroxime axetil, nasal spray and generic ADVAIR. I am having symptoms now sinus congestion, pressure and pain. I also have a dry cough and a lot of throats clearing. I am also developing some pain in my ears as well. The provider states I might have a sinus affection and if I am not feeling better in 7-10 days. I will be referred to a ear, throat doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Allergies
Andere Medikamente: PRILOSEC OTC; FLONASE; cetirizine; furosemide; amlodipine besylate; lactate tablets
Allergien: N/A
Vorherige Impfungen: -

VAERS 2555046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 12.10.2022
Beginn: 24.11.2022
Tage bis Beginn: 43,0
Dosis: 1
Route/Site: - / LA

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

Axillary pain Burning sensation Myalgia Off label use Product use issue COVID-19 Drug ineffective SARS-CoV-2 test Wrong product administered

Symptomtext

Covid -19; Covid -19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 79-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 as dose 1 (bivalent), single (Lot number: GJ6665) at the age of 79 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 24Nov2022, outcome "unknown" and all described as "Covid -19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (24Nov2022) Positive, notes: Nasal Swab.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300002074 Same product, patient and different AEs;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Test Date: 20221124; Test Name: COVID-19 test; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 12.10.2022
Beginn: 24.11.2022
Tage bis Beginn: 43,0
Dosis: UNK
Route/Site: - / LA

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

Axillary pain Burning sensation Myalgia Off label use Product use issue COVID-19 Drug ineffective SARS-CoV-2 test Wrong product administered

Symptomtext

Covid -19; Covid -19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 79-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 as dose 1 (bivalent), single (Lot number: GJ6665) at the age of 79 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 24Nov2022, outcome "unknown" and all described as "Covid -19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (24Nov2022) Positive, notes: Nasal Swab.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300002074 Same product, patient and different AEs;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Test Date: 20221124; Test Name: COVID-19 test; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2555126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 07.10.2022
Beginn: 02.01.2023
Tage bis Beginn: 87,0
Dosis: 5
Route/Site: SYR / UN

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

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

I had my vaccination on 10/07/2022. I started to experience fatigue on 01/02/2023. I tested COVID-19 positive on 01/03/2023. I was not put on any medication because of excellent health. I had biked 37 miles on 01/02/2023. The nurse practitioner sent in the prescription but I didn't take as I was feeling better by day 3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 01/03/2023 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Herpes
Andere Medikamente: Vitamin C; vitamin B12
Allergien: N/A
Vorherige Impfungen: All COVID-19 vaccinations, fever, chills

VAERS 2554859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 04.01.2023
Beginn: 05.01.2023
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Atrial fibrillation Chills Hyperhidrosis Pain Pain in extremity

Symptomtext

Chills body aches AFIB event sweats very sore arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: No tests were done only a verbal communication with my cardiologist
Aktuelle Erkrankungen: No
Vorgeschichte: AFIB paroximal
Andere Medikamente: SOTALOL 100 mg at 7:00am Xarelto 20 mg at 6:00PM
Allergien: N0
Vorherige Impfungen: -

VAERS 2554821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 33,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 07.10.2022
Beginn: 23.12.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Dizziness Fatigue Headache Myalgia Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

My first symptoms were a sore throat and being tired on December 23, 2022. The next day I developed a fever, bad muscle aches, headache, dizziness and being very tired. On the morning of December 25, I tested positive for COVID-19. I reached out to my provider who prescribed PAXLOVID and advised me to take ibuprofen over the counter. I started the medication on the 26th and by the 28th the symptoms started improving. The worst of it was over while on PAXLOVID. I lost sense of taste and smell on the 28th of December. I am totally back to normal since the 6th of January.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: COVID-19 home test December 25, 2022 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: CYMBALTA; TRUVADA; gabapentin; XANAX; TREMFYA; VYVANSE
Allergien: Codeine
Vorherige Impfungen: Flu vaccine, experienced a breakthrough case of flu, date unknown

VAERS 2552417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 55,0
Geschlecht: M
Eingang: 06.01.2023
Impfdatum: 06.10.2022
Beginn: 05.12.2022
Tage bis Beginn: 60,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Paranasal sinus hypersecretion Pyrexia SARS-CoV-2 test positive Sinusitis

Symptomtext

I woke up the morning of December 5th, I had sinus drainage, on Tuesday I developed a fever (99.5) and then other times when I had a sinus infection it lasted 3 days, but on Wednesday fever went to 100.5. I had a home COVID-19 test, and it was positive. I went to Urgent Care facility, and I had another test, and it was also Positive, they recommended prescription, on Wednesday I started taking Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 06DEC2022 - COVID-19 TEST - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levothyroxine; Pepcid; Vitamin C; Iron; B-12; Folic Acid
Allergien: N/A
Vorherige Impfungen: -

VAERS 2551514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 18.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / RA

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

Acoustic stimulation tests abnormal Deafness Dizziness Immunisation reaction Influenza Magnetic resonance imaging Tinnitus Vertigo

Symptomtext

She got her vaccine she felt a little bit like she had flu symptoms, they were mild so they did not stop her. She woke up and she could not hear. A couple of days later she felt liquid like swishing noise around teh right ear. She went to the doctor who gave her Allegra to take. She took it and it did not help. The liquid stopped swishing around. All of a sudden she started getting dizzy but before she took the Allegra and had Meclizine and took that up until yesterday 1/4/23. She took the Allegra for 5 days and stopped taking it as it did not help. She went back to see her doctor and saw an audiologist to see if she had hearing loss and she did and was pretty bad, and she went to an ENT yesterday. He felt that her reaction was from the vaccine. Today she is scheduled for an MRI. The vertigo is very bad, but was given Prednisone dose pack yesterday and this has helped the vertigo but she still cannot hear. She did not have any hearing problems prior to the vaccine. She had seen an ENT in the past for nasal issues but that was 3 years ago. She had a pneumococcal shot a few weeks before the COVID shot. She did not have any reaction to that vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Hearing test, MRI today.
Aktuelle Erkrankungen: None.
Vorgeschichte: Arthritis.
Andere Medikamente: Hydrocodone 10/325 mg, Famotidine 20 mg, Celexa 10 mg, Zanaflex 4 mg, Amlodipine 5 mg.
Allergien: Aspirin (jittery).
Vorherige Impfungen: -

VAERS 2550801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NC
Alter: 73,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 30.09.2022
Beginn: 10.12.2022
Tage bis Beginn: 71,0
Dosis: 5
Route/Site: SYR / LA

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

Cellulitis Injection site swelling SARS-CoV-2 test negative Soft tissue disorder

Symptomtext

My adverse event started on 12/10/2022 in the evening. On left upper forearm it was swelling over the next few days it got bigger. it had no pain. I went to my doctor on 12/23/2022 she diagnosed as localized soft tissue swelling ( cellulitis). She prescribed Cephalexin for 5 days. As of today 01/04/2023 it decreased in size but still there. The doctor said if any changes occur on the swelling to contact her right away. If the swelling decreases to let my doctor know as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site swelling
Hospital-Tage: -
Labordaten: 04JAN2023 COVID-19 Test- Negative
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; Rosacea
Andere Medikamente: Amlodipine
Allergien: None
Vorherige Impfungen: -

VAERS 2550365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 60,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 13.12.2022
Beginn: 23.12.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / RA

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

C-reactive protein Differential white blood cell count Full blood count Injection site erosion Injection site erythema Injection site scab Laboratory test Rash Rash macular Rash maculo-papular Red blood cell sedimentation rate Skin lesion Treponema test

Symptomtext

The patient was noted to have "red circular spots" on the left arm, darkened scab area on the left upper arm, and "circle-like red spots" in the abdominal area. No pain or itching was reported. No respiratory distress was noted or reported." Maculopapular rash concentrated on the trunk (abd/chest/back) with a few scattered similar lesions on Bilat UE. LUE with 1 solitary lesion that appears larger excoriated with central dark scab & Minimal surrounding erythema.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erosion
Hospital-Tage: -
Labordaten: C-reactive Protein CBC auto differential RPR (Diagnosis) with Reflex to Titer and Confirmatory Testing Sedimentation Rate by Modified Westergren
Aktuelle Erkrankungen: N/A
Vorgeschichte: Alcohol use disorder HTN
Andere Medikamente: hydrochlorothiazide thiamine multivitamin
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2550033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 28.11.2022
Beginn: 26.12.2022
Tage bis Beginn: 28,0
Dosis: 5
Route/Site: IM / LA

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

Arthralgia Asthenia COVID-19 Exposure to SARS-CoV-2 Eye pain Headache Impaired work ability Malaise Nausea Pain Respiration abnormal SARS-CoV-2 test positive

Symptomtext

My granddaughter told me she tested positive last Thursday. I went to work, but on Monday my breathing wasn't right, I felt weak; I work on a place that I can't sit I couldn't stand straight, but I couldn't work anymore, I went to the bathroom for 10 minutes to rest, I had to do this three times; I took apple juice and energy drink. At 5:00PM I couldn't make it to the car to drive back home. Yesterday, when woke up I couldn't breathe, my eyes hurt, I had nausea, I had head and body ache, my joints hurt. I felt so sick I called to the doctor and took the COVID-19 test at the pharmacy (yesterday at 4:30PM) and it was positive. I have to quarantine for 5 days. I spoke to the doctor today and called the pharmacy for a prescription. I will start taking it today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 03JAN2023 COVID test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: CALTRATE; vitamin E; iron; turmeric
Allergien: N/A
Vorherige Impfungen: -

VAERS 2547054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 17.11.2022
Beginn: 26.12.2022
Tage bis Beginn: 39,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Diarrhoea Oropharyngeal pain SARS-CoV-2 test positive Upper-airway cough syndrome

Symptomtext

My husband tested positive for COVID-19 on December 13, 2022. I woke up on Monday, December 26, 2022, with a slight sore throat and a larger amount of postnasal drip than usual. I thought it was a cold, but, as a precaution, I took a COVID-19 test. The result was positive. I received a prescription for PAXLOVID and started taking it on December 27, 2022. Since then, the sore throat is completely gone. I still have a considerable amount of postnasal drip, but that is typical for me. I was taking BENADRYL as needed to keep it under control. I still have five doses of PAXLOVID left. I haven't had a fever at all. I've had slight diarrhea, but I'm not sure if it's due to the virus or the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 12/26/2022 at home COVID-19 positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; Chronic Sinusitis
Andere Medikamente: Lisinopril; low dose aspirin; MUCINEX; vitamin C; vitamin D3; folic acid; fish oil; OCUVITE; biotin
Allergien: Seasonal; narcotics; sulfa drugs; kiwi; cucumber
Vorherige Impfungen: -

VAERS 2545772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NV
Alter: 70,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 09.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 5,0
Dosis: 5
Route/Site: SYR / RA

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

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

Symptomtext

I received my 5th dose on 12/09/2022. My COVID-19 symptoms started on 12/14/2022 at night around 10:00PM. I had a sore throat. The next day 12/15/2022 I had cough, fatigue, chills, fever, severe headaches, and body aches. On 12/19/2022 I did a COVID-19 home test which was positive. In the afternoon I called doctor around 3:00PM. He prescribed with PAXLOVID for 5 days and TESSALON PERLES.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 29DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic back pain; Migraines; hypertension; 1981 Cancer fully treated
Andere Medikamente: Moprolol; NEURONTIN; hydrochlorothiazide; PERCOCET; rizatriptan
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2537886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 20.12.2022
Impfdatum: 04.10.2022
Beginn: 11.12.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: - / -

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

Adult failure to thrive Agitation Asthenia Blood glucose decreased Blood glucose increased COVID-19 Chest X-ray normal Computerised tomogram head normal Confusional state Fall Hallucination Hypoglycaemia Hypophagia Pyrexia SARS-CoV-2 test positive X-ray of pelvis and hip normal

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 12/11/2022 Discharge Date: Dec 14, 2022 COVID positive Date 12/12/2022 PRESENTING PROBLEM: Weakness [R53.1] Failure to thrive in adult [R62.7] Low blood glucose measurement [E16.2] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 65-year-old male with a past medical history of coronary artery disease s/p PCI in 2019, pulmonary embolism, T2 Diabetes, diabetic neuropathy, Parkinson's disease, stage 3 chronic kidney disease, GERD who presented from an outside living facility after episodes of hypoglycemia and a witnessed fall without loss of consciousness. On arrival to the emergency department, he was found to be febrile with a temperature of 38.3?. Glucose was low at 66, left otherwise within normal limits. He was without leukocytosis. Imaging, including pelvis x-ray, chest x-ray, and head CT were negative without any signs of acute abnormalities. On routine screening he was found to be positive for COVID, and was subsequently admitted to medicine for management of hypoglycemia in the setting of COVID infection. Patient's hypoglycemia was thought to be due to poor oral intake, and he was started on a D5 LR infusion. After approximately 12 hours, his blood sugars normalized in the mid 150s to 200s, and the infusion was subsequently stopped. Patient did have intermittent episodes of confusion and hallucinations throughout his hospital stay. Spoke with patient's son, who requested discontinuation of Artane, who stated he had given patient hallucinations and confusion in the past. Despite discontinuation, patient continued to have persistent episodes of confusion, agitation, and hallucination. He received p.r.n. Seroquel during these episodes. It was arranged for him to return to his care facility despite his COVID 19 positive status, and he was subsequently discharged with plans for PCP and neurology follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Essential hypertension Coronary artery disease GERD (gastroesophageal reflux disease) Failure to thrive in adult Parkinson disease Type 2 diabetes mellitus with peripheral neuropathy Left-sided weakness Parkinson's disease dementia Dementia with agitation Kidney stones Stage 3a chronic kidney disease Type 2 diabetes with nephropathy Mixed hyperlipidemia Erectile dysfunction due to diseases classified elsewhere
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 10 MG tablet aspirin EC 81 MG enteric coated tablet clopidogrel (PLAVIX) 75 MG tablet docusate (COLACE) 100 MG capsule esomeprazole (NEXIUM) 20 MG delayed release capsule fenofibrat
Allergien: Artane [Trihexyphenidyl] Azithromycin
Vorherige Impfungen: -

VAERS 2537286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: TX
Alter: 13,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 13.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Body temperature Nausea Pyrexia Vomiting

Symptomtext

fever (tmax 101.5); severe nausea and vomiting; severe nausea and vomiting; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the parent. A 13-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Dec2022 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 13 years for covid-19 immunisation. The patient's relevant medical history included: "Down Syndrome" (unspecified if ongoing); "mild sleep apnea" (unspecified if ongoing), notes: mild; "congenital heart defect" (unspecified if ongoing), notes: congenital heart defect. Concomitant medication(s) included: MIRALAX. Vaccination history included: Covid-19 vaccine (Primary immunisation complete, manufacturer unknown), for Covid-19 immunisation. The following information was reported: PYREXIA (non-serious) with onset 14Dec2022, outcome "unknown", described as "fever (tmax 101.5)"; NAUSEA (non-serious), VOMITING (non-serious) all with onset Dec2022, outcome "unknown" and all described as "severe nausea and vomiting". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: On evening of 14Dec2022 she developed a fever (tmax 101.5) and about 40 hours after the dose developed severe nausea and vomiting. Event took place after use of product.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Test Date: 20221214; Test Name: Temperature; Result Unstructured Data: Test Result:101.5; Comments: tmax, fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Down's syndrome; Sleep apnea (mild); Unspecified congenital anomaly of heart (congenital heart defect)
Andere Medikamente: MIRALAX
Allergien: -
Vorherige Impfungen: -

VAERS 2536142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 14,0
Geschlecht: F
Eingang: 18.12.2022
Impfdatum: 17.12.2022
Beginn: 17.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Rash Urticaria

Symptomtext

Rash and hives

Weitere VAERSDATA-Felder

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

VAERS 2533309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 12.12.2022
Beginn: 13.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Headache Myalgia Nausea

Symptomtext

Similar to prior reactions, muscle and joint pain, nausea, headache... I took Percocet, Benadryl and Ibuprofen... eventually it got a little better, but It took me days to get over these symptoms completely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Qulipta, Gabapentin
Allergien: -
Vorherige Impfungen: T-dap/Flu a few years ago, and similar reaction to the second and third doses of COVID vaccines.

VAERS 2533152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 35,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 11.11.2022
Beginn: 09.12.2022
Tage bis Beginn: 28,0
Dosis: 4
Route/Site: IM / LA

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

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

Symptomtext

I started off with a sore throat and general fatigue. That lasted about 3 days and I treated myself with over-the-counter medications. I tested myself on December 12, 2022, and I was positive for COVID-19. I was prescribed PAXLOVID due to hypertension and hyperthyroidism. I have been taking this every since then. I have lingering congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home December 12, 2022 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Enalapril; SYNTHROID
Allergien: N/A
Vorherige Impfungen: -

VAERS 2531698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: NJ
Alter: 61,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 18.11.2022
Beginn: 18.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Chills Fatigue Lymphadenopathy

Symptomtext

lymph node under her left arm next to her breast swelled up/warm and red; Fatigue; Chills; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). 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 18Nov2022 as dose 4 (booster), single (Lot number: GJ6665) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure" (ongoing), notes: Medical History (MedDRA code): Blood pressure, Continuing: true, Comments: Blood pressure; "Cholesterol" (ongoing), notes: Medical History (MedDRA code): Cholesterol, Continuing: true, Comments: Cholesterol. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (3rd dose: , Date: 06Dec2021 , Time: Not Provided , Anatomical Site of injection: Not Provided , Route of Administration: Not Provided), administration date: 06Dec2021, when the patient was 60-year-old, for Covid-19 Vaccination; BNT162b2 (1st dose: , Date: 20Mar2021 , Time: Not Provided , Anatomical Site of injection: Not Provided , Route of Administration: Not Provided , Batch/Lot number: EN6206), administration date: 20Mar2021, when the patient was 59-year-old, for Covid-19 Vaccination; BNT162b2 (2nd dose: , Date: 10Apr2021 , Time: Not Provided , Anatomical Site of injection: Not Provided , Route of Administration: Not Provided , Batch/Lot number: EW0151), administration date: 10Apr2021, when the patient was 59-year-old, for Covid-19 Vaccination. The following information was reported: CHILLS (non-serious) with onset 18Nov2022, outcome "recovered" (25Nov2022); FATIGUE (non-serious) with onset 18Nov2022, outcome "recovered" (25Nov2022); LYMPHADENOPATHY (non-serious) with onset 19Nov2022, outcome "recovered" (24Nov2022), described as "lymph node under her left arm next to her breast swelled up/warm and red". Additional information: Vaccination Facility Type was Hospital. Vaccine was not Administered at Military Facility. Patient wanted to report she had a reaction to it or a side effect. Her lymph node under her left arm next to her breast swelled up the next day and stayed swollen for about 5 days, at one time into the third day, it was warm and red. States it was in the same arm that she got the shot in. She also reports she had fatigue and chills. Treatment: she did call the CDC and spoke to a nurse specialist on 21Nov2022 and was told to drink plenty of water. Prior Vaccinations (within 4 weeks) was none. Family Medical History Relevant to Adverse Events was none.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure (Medical History (MedDRA code): Blood pressure Continuing: true Comments: Blood pressure); Cholesterol (Medical History (MedDRA code): Cholesterol Continuing: true Comments: Cholesterol)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2530971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NJ
Alter: 59,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 22.11.2022
Beginn: 11.12.2022
Tage bis Beginn: 19,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chills Cough Nasal congestion Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Sneezing

Symptomtext

On 12/11/2022 I noticed a little sore throat around 08:00PM. I woke up later that night and could tell I was stuffy. While getting ready for work the next day, I tested myself for COVID-19. To my surprise, it was positive. That same day, I went into work for a PCR test which was also positive. I spoke with a fellow healthcare provider from work. We discussed that my symptoms did not seem sever enough for antiviral treatment. As the day wore on, I began to feel worse. I took some ADVIL 2 at least twice that day. Monday night, I had a fever and chills. I went to get THERAFLU the next day and have been taking it every six to eight hours. When I don't take it, I get sneezing, coughing and body aches but the medication does seem to be helping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 12DEC2022 at home COVID-19 test positive; PCR COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis
Andere Medikamente: Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2528301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

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

Asthenia Dizziness

Symptomtext

dizziness, weakness

Weitere VAERSDATA-Felder

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

VAERS 2526738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 59,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 26.10.2022
Beginn: 05.12.2022
Tage bis Beginn: 40,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Chills Nausea Pyrexia SARS-CoV-2 test positive

Symptomtext

I started having bad chills and a fever of 102. The next day, I woke up and didn't feel any better. I took a rapid test on 12/6/22 and tested positive. I called the doctor, and they prescribed 5 days' worth of PAXLOVID. I have been feeling better up until today. I have had the metallic taste in my mouth that everyone talks about. Since lunchtime today, I have been feeling a little nauseated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 06DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Sleep Apnea
Andere Medikamente: Atorvastatin
Allergien: Eggplant
Vorherige Impfungen: -

VAERS 2526631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 06.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lip pain Lip swelling

Symptomtext

patient bottom lip started swelling morning after receiving covid shot, and painful. today symptoms have decreased but still a little swolleln

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lip pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: lisinopil 5mg daily
Allergien: no allergies
Vorherige Impfungen: -

VAERS 2526600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: AR
Alter: 62,0
Geschlecht: M
Eingang: 08.12.2022
Impfdatum: 26.10.2022
Beginn: 03.12.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Influenza virus test negative Nasal congestion Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

My adverse event started on 12/03/2022 around noon time. I had stuffy head, minor sore throat, fatigue, non productive cough, and runny nose. I went to the Urgent Care on 12/05/2022. They did FLU which was negative and I was positive for COVId-19 Infection. I took over the counter medications such as Severe Cold & Flu, Tylenol as per needed, and Robitussin DM for cough. I took all the medication yesterday but I feel good today so I didn't take any. As of today 12/08/2022 I am recovering from my COVID-19 Infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 08DEC2022 COVID-1p Test- Positive
Aktuelle Erkrankungen: Headaches
Vorgeschichte: None
Andere Medikamente: Atorvastatin; Omeprazole; Gabapentin; Alprezamin; Tylenol as per needed
Allergien: Procaine
Vorherige Impfungen: -

VAERS 2525449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 39,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 06.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Fatigue Injection site pain Myalgia

Symptomtext

Pain in arm at injection site, sore muscles, chills, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity, high blood pressure
Andere Medikamente: Birth Control Pills, daily women's vitamin gummy
Allergien: None
Vorherige Impfungen: -

VAERS 2525235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: -
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Deafness unilateral Ear pain Tinnitus

Symptomtext

I received my 2nd Pfizer Booster shot for the covid vaccine on November 29th. My ear started hurting very badly the next day. On December 1st, I lost hearing in my right ear along with an addition of severe tinnitus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: eosinophilic esophagitis
Andere Medikamente: triamcinolone for eczema, valtrex when needed; kirkland multivitamins, omega 3 cod liver oil, cerave moisturizing lotion,
Allergien: cats, penicillin, sulfa, (antibodies against: eggs, almonds, hazelnut, grass)
Vorherige Impfungen: -

VAERS 2524265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: PA
Alter: 80,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 30.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Asthenia Dizziness Dizziness postural Laboratory test Nystagmus Posture abnormal Vestibular function test

Symptomtext

Patient is a 80 y.o. male presenting to the ED with chief complaint of persistent dizziness, patient's been having dizziness over the past couple days he describes the dizziness lightheadedness especially when he gets up and moves around. This occurred after he got his COVID vaccination, he denies any speech difficulty or vision changes no arm or leg complaints, has had some weakness with the dizziness. Vestibular testing significant for positive head thrust to the left And positive LEFT sided brandt-daroff test with upbeating rotary nystagmus and reposition of sympotms. Orthostatic positive.

Weitere VAERSDATA-Felder

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

VAERS 2523130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: AZ
Alter: 66,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 27.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 35,0
Dosis: 5
Route/Site: SYR / AR

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

Rash Urticaria

Symptomtext

12/01/2022 I noticed I had a rash, like hives on my arms, legs and back. It continued to get worse until I could not stand it. I went to the doctor on 12/4/22. She gave me a prescription for prednisone. I have not been able to start the medication because I have not been able to fill the prescription. I have not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; high blood pressure
Andere Medikamente: Amlodipine besylate; duloxetine; furosemide; montelukast; naproxen; olmesartan; rosuvastatin; multiple vitamin; NATURES BOUNTY sleep 3; probiotic; vitamin C; fish oil
Allergien: None
Vorherige Impfungen: -

VAERS 2520903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NJ
Alter: 72,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 19.10.2022
Beginn: 24.11.2022
Tage bis Beginn: 36,0
Dosis: 5
Route/Site: IM / LA

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

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

Symptomtext

After receiving the vaccine, I had body aches and felt tired for about 24 hours. On 11/24/2022 I started not feeling well with congestion, so I took a COVID-19 test and it was negative. On 11/25/2022, I took another COVID-19 home test and it was positive. I contacted my doctor and was given a prescription for PAXLOVID and they recommended that I take an expectorant. After three doses of PAXLOVID, I started feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 25NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: N/A
Allergien: Iodine dye
Vorherige Impfungen: -

VAERS 2520535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 01.12.2022
Impfdatum: 29.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Arthralgia Headache Insomnia Joint injury Nerve compression Pain in extremity Swelling

Symptomtext

My left shoulder still hurts. It hurts and my left elbow all the way down stretch when I twist it/ my left shoulder, it is my left arm, it goes through all the way down to my arm over to my head; left elbow all the way down stretch when I twist it; Headache/sore area in the left lower part of my head/soreness of back left head; my head is even more swollen/swollen exterior left head; it looks like a typical type of a cervical spine issue. Looks like it might have hit some kind of nerve that runs from your shoulder to your head and down to your left fingers in your left hand; My left shoulder still hurts. It hurts and my left elbow all the way down stretch when I twist it/ my left shoulder, it is my left arm, it goes through all the way down to my arm over to my head; I haven't slept in 2 weeks; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 29Oct2022 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 68 years for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ROSUVASTATIN; CARVEDILOL; LOSARTAN POTASSIUM; FENOFIBRATE; ASPIRIN [ACETYLSALICYLIC ACID]; CLOPIDROGREL; AMLODIPINE. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: HEADACHE (medically significant) with onset 2022, outcome "unknown", described as "Headache/sore area in the left lower part of my head/soreness of back left head"; INSOMNIA (non-serious) with onset 2022, outcome "unknown", described as "I haven't slept in 2 weeks"; PAIN IN EXTREMITY (medically significant), ARTHRALGIA (medically significant) all with onset 2022, outcome "not recovered" and all described as "My left shoulder still hurts. It hurts and my left elbow all the way down stretch when I twist it/ my left shoulder, it is my left arm, it goes through all the way down to my arm over to my head"; NERVE COMPRESSION (medically significant) with onset 2022, outcome "unknown", described as "it looks like a typical type of a cervical spine issue. Looks like it might have hit some kind of nerve that runs from your shoulder to your head and down to your left fingers in your left hand"; JOINT INJURY (medically significant) with onset 2022, outcome "unknown", described as "left elbow all the way down stretch when I twist it"; SWELLING (medically significant) with onset 2022, outcome "unknown", described as "my head is even more swollen/swollen exterior left head". The events "my left shoulder still hurts. it hurts and my left elbow all the way down stretch when i twist it/ my left shoulder, it is my left arm, it goes through all the way down to my arm over to my head", "left elbow all the way down stretch when i twist it", "headache/sore area in the left lower part of my head/soreness of back left head", "my head is even more swollen/swollen exterior left head", "it looks like a typical type of a cervical spine issue. looks like it might have hit some kind of nerve that runs from your shoulder to your head and down to your left fingers in your left hand" and "I haven't slept in 2 weeks" required physician office visit. Therapeutic measures were taken as a result of pain in extremity, joint injury, headache, swelling, nerve compression, arthralgia. Clinical course: It was stated, "he have side effects from Pfizer Booster vaccine he was given on 29Oct." Stated, "His left shoulder still hurts. It hurts and his left elbow all the way down stretch when he twist it. he haven't slept in 2 weeks. He have a little sore area in the left lower part of his head. He woke up today and now his head, the back of his left side, his head was even more swollen. He went to his primary care doctor. He tried to go to a neurologist but then it looks like a typical type of a cervical spine issue. Looks like it might have hit some kind of nerve that runs from your shoulder to your head and down to your left fingers in your left hand." Stated, "he didn't just say elbow, his left shoulder, it was his left arm, it goes through all the way down to his arm over to his head, headache, swollen exterior left head, soreness of back left head, occipital cervical spine nerve, what the physician said." On confirming if the consumer only wants to report or needs any information, Other medical conditions and concomitant medications: stated, "Well, he take medications. No prior vaccinations within 4 weeks." Treatment in response to adverse event: stated, "he had a shot. He said it wasn't, it was Cortisone like but he said it wasn't Cortisone, into his C6 area of his neck, his primary care physician, Friday morning." No follow-up attempts are needed. No further information is expected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ROSUVASTATIN; CARVEDILOL; LOSARTAN POTASSIUM; FENOFIBRATE; ASPIRIN [ACETYLSALICYLIC ACID]; CLOPIDROGREL; AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2519230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 73,0
Geschlecht: M
Eingang: 29.11.2022
Impfdatum: 12.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Back pain Chills Headache Pain in extremity

Symptomtext

headaches, Right upper back pain, Left arm pain, chills. headaches still present, but improving

Weitere VAERSDATA-Felder

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

VAERS 2518817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 29.11.2022
Impfdatum: 09.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pruritus Interchange of vaccine products Irritability Pruritus Rash Urticaria

Symptomtext

Site: Itching at Injection Site-Medium, Systemic: Allergic: Itch Generalized-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Additional Details: Patient reports recurrent itching and hives since immunization. Previously received Moderna, but received bivalent Pfizer. Hives are relieved with diphenhydramine, but come back when dose wears off. Advised patient to seek treatment from primary care physician. Not severe or limiting activities, but irritating and unclear why they keep returning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 28.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Immediate post-injection reaction Injection site pruritus Pruritus

Symptomtext

Patient states previously had a non-severe allergic RXN to Covid vaccines (hives), but denies any severe allergic RXN (SOB, Wheezing, swelling, etc.). Approximately 10 mins after receiving Covid vaccine (at 14:20), patient did experience itchiness on hands, at injection site, and legs- gave Benadryl 25 mg PO, counseled patient that can cause drowsiness and instructed patient to go to ER if any worsening SXS. Patient was observed for 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2517944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: KS
Alter: 60,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 21.10.2022
Beginn: 22.11.2022
Tage bis Beginn: 32,0
Dosis: 4
Route/Site: IM / UN

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

COVID-19 Ear discomfort Ear pain Headache Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Sinus headache Tinnitus

Symptomtext

I started having symptoms on 11/22/22. I had a runny nose. It developed into a sinus congestion and my ears filled up really quick. I could hear a whirling noise in my ears, and it caused an ache in my ears and head. It was 24 hours of a sinus headache. I took a home testing kit after I had a fever of 100.2 on the 11/24/222. I took a at home test and tested positive for COVID-19 on 11/25/222. I started taking over the counter relief to help with my symptoms. I feel fine now, I was dragging a bit the other day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Metoprolol; Hormone Replacement therapy Compound
Allergien: N/A
Vorherige Impfungen: -

VAERS 2517327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OH
Alter: 19,0
Geschlecht: M
Eingang: 26.11.2022
Impfdatum: 26.11.2022
Beginn: 26.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Erythema Pruritus Skin warm

Symptomtext

after receiving the bivalent pfizer vaccine patient's arm started to itch and he had some redness up and down arm. it was then warm. i advised him to take benadryl and watch it closely. if it gets worse to go to urgent care/ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: BIAXCIN, AMOXICILLIN, MACROLIDES
Vorherige Impfungen: -

VAERS 2515414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: TN
Alter: 44,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 05.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Headache Lymphadenopathy

Symptomtext

Patient reported headache and swollen lymph node in left axilla

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 2515356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: ID
Alter: 24,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pain in extremity

Symptomtext

Pt complained of arm pain/soreness in the arm that the vaccines were administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Mild intermittent asthma, anxiety, tachycardia, arthritis, fibromyalgia, conjunctival lesion
Vorgeschichte: Mild intermittent asthma, anxiety, tachycardia, arthritis, fibromyalgia, conjunctival lesion
Andere Medikamente: Elavil, Atarax, Lopressor
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2515306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 28,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 10.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Chlamydial infection Injection site bruising Injection site induration Injection site swelling

Symptomtext

Patient reports that as of 11/23/2022 at site of MPV vaccine it is indurated, swollen, bruised.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: chlamydia and treated 11/17/2022 with Doxycyline 1 tab BID for 7 days.
Vorgeschichte: HIV
Andere Medikamente: Biktarvy
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2513633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: PA
Alter: 45,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 15.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / LA

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

Chills Cough Fatigue Headache Hyperhidrosis Pain

Symptomtext

Chills; fatigue; sweating; headache; body aches; cough; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Nov2022 at 13:00 as dose 4 (booster), single (Lot number: GJ6665) at the age of 45 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Covid" (unspecified if ongoing), notes: If covid prior vaccination: Yes. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN), for COVID-19 immunisation; Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN), for COVID-19 immunisation; Covid-19 vaccine (DOSE 3 (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 immunisation. The following information was reported: CHILLS (non-serious) with onset 16Nov2022, outcome "recovering"; PAIN (non-serious) with onset 16Nov2022, outcome "recovering", described as "body aches"; COUGH (non-serious) with onset 16Nov2022, outcome "recovering"; FATIGUE (non-serious) with onset 16Nov2022, outcome "recovering"; HEADACHE (non-serious) with onset 16Nov2022, outcome "recovering"; HYPERHIDROSIS (non-serious) with onset 16Nov2022, outcome "recovering", described as "sweating". Therapeutic measures were not taken as a result of chills, fatigue, hyperhidrosis, headache, pain, cough. Additional information: The patient did not receive other vaccines within four weeks prior to COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2513009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 27.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

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

Injection site erythema Injection site vesicles Pain in extremity Peripheral swelling

Symptomtext

REPROTED BY PATIENT: I have a blister where I received the Covid booster and Pneumonia shot on Thursday 10/27. There is a red ring around it. My arm feels better today as it was very sore and swollen the last 3days. The blister started Saturday. Just checking if I should do anything special. I am being careful no to break it

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: 10/26/2022 VIRAL GASTROENTERITIS
Vorgeschichte: CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (CMS/HCC) Mild non proliferative diabetic retinopathy (CMS/HCC) M obesity BMI 50.0-59.9, adult (CMS/HCC) Well controlled type 2 diabetes mellitus (CMS/HCC) Recurrent major depressive disorder, in full remission (CMS/HCC) Dyspepsia Essential hypertension Pure hypercholesterolemia Uric acid stone in urine AK (actinic keratosis) History of gastroenteritis
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG tablet Take 1 (one) tablet by mouth 2 times daily aspirin (ASPIRIN) 325 MG tablet Take 325 mg by mouth once daily Blood Glucose Monitoring Suppl (ONE TOUCH ULTRA SMART) W/DEVICE KIT Use 1 Device once daily.
Allergien: ERTHROMYCIN
Vorherige Impfungen: -

VAERS 2512806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CT
Alter: 79,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 18.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Dizziness Fall Head injury Nausea Vomiting

Symptomtext

Abrupt onset of severe disabling dizziness, I believe it was not vertigo. I was seated at home, my head crashed to the table and I was unable to lift my head up because of dizziness for 4.5 hours; vomited once, regretted lunch, nausea. If I had been driving, I would have crashed. If I had been in public, I would have been carted off to a hospital. Not a stroke, not the flu. Recovered by today with slight residual nausea and slight dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Post nasal drip
Vorgeschichte: Arthritis
Andere Medikamente: None
Allergien: Sensitive to epi; allergic to raw apples, lobster
Vorherige Impfungen: -

VAERS 2512799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OH
Alter: 70,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 27.10.2022
Beginn: 11.11.2022
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain lower Dysuria Pollakiuria Urinary tract infection Urine analysis abnormal

Symptomtext

I was having frequent urination, burning while urinating, lower belly pain. I had this for about 6 days before I went to the doctor. She tested my urine and found that I had a Urinary Tract Infection. I was prescribed nitrofurantoin, and fluconazole. I am feeling much better after taking the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: -
Labordaten: 16NOV2022 Urine test positive, Urinary Tract Infection.
Aktuelle Erkrankungen: Urinary Tract Infection
Vorgeschichte: Hypothyroid; Diabetic; High Cholesterol
Andere Medikamente: Levothyroxine; JANUMET; FARXIGA; glimepiride; losartan; atorvastatin; calcium; fish oil; baby aspirin; ZYRTEC; multivitamin; FLONASE; ALIGN
Allergien: N/A
Vorherige Impfungen: -

VAERS 2512458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 20.11.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Injection site erythema Injection site pruritus Injection site swelling Pruritus Rash

Symptomtext

Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash Generalized-Medium, Additional Details: Patient came to the pharmacy on 11/16 to report the reaction she experienced after the Pfizer bivanlent vaccine. The pharmacist on duty, Gave her benadryl cream to calm the rashes and itchiness. Will follow up with patient in a couple of days!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2512449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: AL
Alter: 47,0
Geschlecht: F
Eingang: 19.11.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Decreased appetite Diarrhoea Fluid intake reduced Headache Hypersensitivity Injection site erythema Injection site rash Pain Pyrexia Rash pruritic Sinus operation Skin warm Somnolence Tenderness

Symptomtext

4th vaccine, day one got sore and feverish took Tylenol. Tuesday fever 100 treated with Tylenol arm was extremely tender like it had broken glass in it. By Wednesday there was a huge red rash almost from my shoulder to my elbow fever 101+ more Tylenol slept all day and night., Thursday was going to show morning pharmacist but was told if it didn?t start to go down that day or the next to sho show the other pharmacist so I went back home fever was back down to 99 taking Tylenol. Throughout the whole time I had no appetite could barely make myself drink and had diarrhea and a headache. Went to my doctors office first thing Friday and saw the NP. He immediately told me it was an allergic reaction and ordered a steroid shot and prescribed 3 days of 20 mg steroids 2x daily an Benadryl at night. I?ve also had a lot of sinus drainage an got Sudafed to help with that. Today?s is Saturday the rash is itching and less tender no fever, the rash is still feverish though.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: RA, Fibromyalgia, Spinal Stenosis, Osteoarthritis, Raynaud's Syndrome, Bipolar, ADD
Andere Medikamente: Acidophilus probiotic Calcium Citrate w/D3 Celebrex Depakote Dicyclomine Famotidine Fiber Therapy Equate for FiberCon Fish Oil Gabapentin Geodon/Ziprasidone Hair Skin and Nails Leflunomide/Arava Metoprolol Tartr/Lopressor SUCC ER Miralax O
Allergien: Abilify, Ceftin(Cefuroxime) ,LISINOPRIL, LEVAQUIN, SEROQUEL, Restoril, SURGICAL Tape with tegaderm
Vorherige Impfungen: -

VAERS 2512416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: NH
Alter: 57,0
Geschlecht: M
Eingang: 19.11.2022
Impfdatum: 14.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Injection site discomfort Injection site mass

Symptomtext

Patient came in with a quarter sized lump on his arm where the vaccine was given. He stated that it only caused discomfort when he pressed on it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discomfort
Hospital-Tage: -
Labordaten: no tests done. told to seek help from MD if problem did not resolve
Aktuelle Erkrankungen: no
Vorgeschichte: diabetes
Andere Medikamente: patient is diabetic, no medications on file for him
Allergien: NSAIDS
Vorherige Impfungen: -

VAERS 2512144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: MI
Alter: 56,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 07.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Bladder pain Cystitis Decreased appetite Inflammation Insomnia Pain Pollakiuria Reaction to excipient Urine analysis White blood cell count increased White blood cells urine

Symptomtext

they never told her about the inactive ingredients of the vaccine, and she believed those ingredients were the reason of her side effects; couldn't sleep; thought she had a bladder infection; 48 hours after receiving her fourth dose of the Pfizer-BioNTech Covid 19 Vaccine, she has been experiencing inflammation; horrible pain 48 hours after the last injection/ excruciating pain; horrible bladder pain; can barely eat anything/ couldn't eat or drink; constantly urinating; extremely high number of white blood cells in urine without an infection; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP) from medical information team. The reporter is the patient. A 55-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Oct2022 (in the morning, exact time unknown) as dose 4 (booster), single (Lot number: GJ6665) at the age of 56 years, in arm (either left or right arm) for covid-19 immunisation. The patient's relevant medical history included: "interstitial cystitis" (unspecified if ongoing), notes: prior to receiving any doses of the vaccine; "Hunner's ulcers" (unspecified if ongoing), notes: prior to receiving any doses of the vaccine; "extreme allergies to preservatives and medications" (unspecified if ongoing), notes: prior to receiving any doses of the vaccine; "allergies to inactive ingredients and preservatives" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: 8734 (as only seen on vaccination card), anatomical site of injection: either left or right arm, time: in the morning, exact time unknown), administration date: 02Apr2021, when the patient was 54-year-old, for COVID-19 Immunization, reaction: "did not have side effects"; BNT162b2 (DOSE 2, SINGLE, Lot number: TW0162, anatomical site of injection: opposite arm from the 1st time, time: in the morning, exact time unknown), administration date: 23Apr2021, when the patient was 54-year-old, for COVID-19 Immunization, reaction: "did not have side effects"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot number: FH8027, anatomical site of injection: either left or right arm, time: in the morning, exact time unknown), administration date: 26Nov2021, when the patient was 55-year-old, for COVID-19 Immunization, reaction: "did not have side effects". The following information was reported: BLADDER PAIN (non-serious) with onset 07Oct2022, outcome "not recovered", described as "horrible bladder pain"; INFLAMMATION (non-serious) with onset 09Oct2022, outcome "not recovered", described as "48 hours after receiving her fourth dose of the Pfizer-BioNTech Covid 19 Vaccine, she has been experiencing inflammation"; PAIN (non-serious) with onset 09Oct2022, outcome "not recovered", described as "horrible pain 48 hours after the last injection/ excruciating pain"; DECREASED APPETITE (non-serious) with onset Oct2022, outcome "not recovered", described as "can barely eat anything/ couldn't eat or drink"; POLLAKIURIA (non-serious) with onset Oct2022, outcome "not recovered", described as "constantly urinating"; WHITE BLOOD CELL COUNT INCREASED (non-serious) with onset Oct2022, outcome "not recovered", described as "extremely high number of white blood cells in urine without an infection"; REACTION TO EXCIPIENT (non-serious), outcome "unknown", described as "they never told her about the inactive ingredients of the vaccine, and she believed those ingredients were the reason of her side effects"; INSOMNIA (non-serious), outcome "unknown", described as "couldn't sleep"; CYSTITIS (non-serious), outcome "unknown", described as "thought she had a bladder infection". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient was calling about the last injection that she received of the Pfizer COVID vaccine. There were horrible side effects the patient was continuing to have and calling to see if there was a doctor in the state for treating people. The patient normally never accepts any injections, but it was the patient's understanding that the Pfizer COVID vaccine would not have any inactive ingredients or preservatives in the injection. The patient had horrible pain 48 hours after the last injection. The patient learned that there was a list of chemicals in the injection she never heard of before, just the 1st chemical listed that she could understand was potassium chloride; she said if she had known potassium chloride was in the injection, she never would have accepted the injection. This last vaccine that the patient had received was a very different vaccine than the first dose she received. She told the doctor and 3 people at the facility that she would not be getting a flu shot. The patient cannot accept injections due to allergies to inactive ingredients and preservatives. The patient confirmed that she had interstitial cystitis with Hunner's ulcers and extreme allergies to preservatives in medications prior to receiving any doses of the vaccine, but after the vaccine, the side effects had skyrocketed, she can barely eat anything, constantly urinating, and in excruciating pain. The patient confirmed that the 3 prior doses were also the Pfizer COVID vaccine, all 4 doses had been the Pfizer COVID vaccine and all doses were administered at the same facility. The patient was told to get a vaccine, and was told that the more people who get the vaccine, the less likely to mutate, so all were supposed to participate in getting vaccinated. Since having the vaccine, the patient had an extremely high number of white blood cells in urine without an infection. The patient has had these urinalysis' done multiple times from the beginning, because at first she thought she had a bladder infection, and did not think after waking up 48 hours after the latest dose of the vaccine that her horrible bladder pain would be continuing to this date, never crossed her mind that the vaccine would be doing this to her. The patient had the 3 doses of the vaccine prior and did not have these side effects prior to getting the 4th dose. The vaccination facility was at the pharmacy or drug store. The vaccine was not administered at the military facility. The patient had no other vaccinations within four weeks prior to the first administration date of the suspect vaccine. She had not received any additional vaccines, nothing had changed since her 1st dose, then everything changed in her life after the 4th dose. The patient required a pharmacologist or a specialist regarding the inactive ingredients of the vaccine. She also knew that some universities were doing research with the reported adverse events of the vaccine and would like to know which universities were doing it. She would like the reports of people that have reported similar adverse events as her in order to make a decision of what type of treatment would be the best for her. The patient would also like to know how long the inactive ingredients were going to be in her body. She complained that Pfizer should know if universities were doing specific research of the Pfizer-BioNTech Covid 19 Vaccine and that the information should be shared with all the people. They never told her about the inactive ingredients of the vaccine, and she believed those ingredients were the reason of her side effects. It had been 6 weeks since she received the vaccine and she's still in horrible condition. She couldn't sleep, eat or drink because of her side effects. She mentioned she has medical condition and also had heard that people have died because of the vaccine. The patient assessed the events as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bladder pain
Hospital-Tage: -
Labordaten: Test Name: urinalysis; Result Unstructured Data: Test Result:Unknown Results; Comments: has had these urinalysis' done multiple times from the beginning; Test Date: 202210; Test Name: white blood cells in urine; Result Unstructured Data: Test Result:extremely high number without an infection; Comments: since having the vaccine
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to drug excipient; Hunner's ulcer (prior to receiving any doses of the vaccine); Intestinal cyst (prior to receiving any doses of the vaccine); Reaction to drug preservatives (prior to receiving any doses of the vaccine)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2511927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IA
Alter: 64,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 14.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Chills Headache Hyperhidrosis Pain Pyrexia Vomiting

Symptomtext

rxn -- severe headache, chills, fever, sweats, vomiting, body aches - 36 hours before starting to feel better

Weitere VAERSDATA-Felder

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

VAERS 2511857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: IL
Alter: 75,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain Pain in extremity

Symptomtext

Site: Pain at Injection Site-Medium, Additional Details: patient states he has a lot of pain on his right arm. States he did go to the doctor for his annual visit and informed the doctor. He recommended him to apply some warm cloths

Weitere VAERSDATA-Felder

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

VAERS 2511320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: NE
Alter: 42,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 28.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Chills Dizziness Heart rate Heart rate increased Nausea Pain in extremity

Symptomtext

racing resting heart rate; dizzy; sore arm; chills; nauseous; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 at 14:30 as dose 4 (booster), single (Lot number: GJ6665) at the age of 42 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Chronic neck pain" (unspecified if ongoing), notes: other medical history: Chronic neck pain. Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, in Sep2022 as dose number unknown, single; LYRICA. Vaccination history included: Covid-19 vaccine (Dose: 1st, Manufacturer unknown), for Covid-19 immunization; Covid-19 vaccine (Dose: 2nd, Manufacturer unknown), for Covid-19 immunization; Covid-19 vaccine (Dose: 3rd, Manufacturer unknown), for Covid-19 immunization. The following information was reported: CHILLS (medically significant) with onset 29Oct2022 at 01:00, outcome "unknown"; DIZZINESS (medically significant) with onset 29Oct2022 at 01:00, outcome "unknown", described as "dizzy"; NAUSEA (medically significant) with onset 29Oct2022 at 01:00, outcome "unknown", described as "nauseous"; HEART RATE INCREASED (medically significant) with onset 29Oct2022 at 01:00, outcome "unknown", described as "racing resting heart rate"; PAIN IN EXTREMITY (medically significant) with onset 29Oct2022 at 01:00, outcome "unknown", described as "sore arm". The events "racing resting heart rate", "dizzy", "sore arm", "chills" and "nauseous" required emergency room visit. The patient underwent the following laboratory tests and procedures: Heart rate: (29Oct2022) racing resting. Therapeutic measures were taken as a result of heart rate increased, dizziness, pain in extremity, chills, nausea. Clinical course: Other medications in two weeks: Lyrica, Mounjaro 5 mg. Within 10 hours post vaccine she experienced a sore arm, chills, and a racing resting heart rate that was picked up 6 times by (name withheld) watch. She was unable to get her heart rate to lower and began to feel nauseous and dizzy. She then went to the ER. AE treatment: IV fluids and Tylenol. Prior to vaccination, the patient was not diagnosed with covid-19. Post vaccination, the patient had not been tested for covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20221029; Test Name: heart rate; Result Unstructured Data: Test Result:racing resting
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Neck pain (other medical history: Chronic neck pain)
Andere Medikamente: LYRICA
Allergien: -
Vorherige Impfungen: -

VAERS 2510940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 25.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Headache Myalgia Pain Pain in extremity Pyrexia

Symptomtext

I usually have a bad day after the Covid shots where my whole body hurts, fever and headache. My left leg started hurting and hasn't stopped hurting. It's not joint pain. Its in the center of my left thigh and radiates out. In feels like a deep ache in the muscle. Not soreness but aching. It starts the moment I wake up and last all day long. When I was younger I would get what they called "growing pains in both legs." Stopped getting them at 18 and never had it since. Now I am 45 and the day after I get my second booster the same pain comes back. Now only in one leg and last all day long everyday for 4 weeks. Something is going on but not sure what.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: No
Allergien: None
Vorherige Impfungen: -

VAERS 2510928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NJ
Alter: 53,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Feeling hot Nausea

Symptomtext

Patient complained of nausea and feeling hot. Patient was given Benadryl 50mg and then symptoms resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD, HTN, CHF, Obesity, Ischemic Cardiomyopathy, obstructive sleep apnea.
Andere Medikamente: -
Allergien: Lisinopril
Vorherige Impfungen: -

VAERS 2510923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NJ
Alter: 58,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 10.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I was sneezing and I thought it was allergies. I had a really bad runny nose. My husband had COVID-19 so I took a test and the line appeared bright. I then called the doctor did a telehealth appointment and then he called instead. We talked about how I was sneezing, and he prescribed PAXLOVID. Within two days I started to notice a turnaround from taking the medication. I did get a slight fever 99.4 was the peak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Tremors
Andere Medikamente: Propranolol; trazodone
Allergien: Penicillin; naproxen
Vorherige Impfungen: -

VAERS 2510350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Interchange of vaccine products Off label use Product use issue Pruritus Rash erythematous

Symptomtext

face started itching suddenly; face and neck was red rash; She had the COVID-19 Vaccine Booster and Flu Shot; She had the COVID-19 Vaccine Booster and Flu Shot; Did have the Moderna COVID-19 Vaccines the first time around in April, May, and December.; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 70-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 as dose 4 (booster), single (Lot number: GJ6665) at the age of 70 years, in arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 09Mar2021 at 14:00 as dose 1, single (Batch/Lot number: unknown), in left arm, on 05Apr2021 at 14:00 as dose 2, single (Batch/Lot number: unknown), in left arm and on 29Dec2021 at 11:30 as dose 3 (booster), single (Lot number: 070H21A), in left arm, all intramuscular for covid-19 immunisation; influenza vaccine (FLU [INFLUENZA VACCINE]), on 28Oct2022 as dose number unknown, single (Batch/Lot number: unknown), in arm for immunisation. The patient's relevant medical history included: "Type 2 Diabetes" (ongoing), notes: thinks dx at 41 HCP was debating if she had juvenile diabetes or type two diabetes (diagnosed); "High blood pressure" (ongoing), notes: diagnosed at about maybe 40 years old. At 40 everything went downhill.; "Tested positive for COVID-19 in August or Sep2020", start date: 2020 (unspecified if ongoing), notes: in August or Sep2020, confirmed she tested positive before receiving any COVID-19 Vaccines.; "scratchy throat", start date: 2020 (unspecified if ongoing); "Fever", start date: 2020 (unspecified if ongoing), notes: for two different non-consecutive nights, reached 101 degrees Fahrenheit. The patient took concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 28Oct2022, outcome "unknown", described as "Did have the Moderna COVID-19 Vaccines the first time around in April, May, and December."; PRODUCT USE ISSUE (non-serious), OFF LABEL USE (non-serious) all with onset 28Oct2022, outcome "unknown" and all described as "She had the COVID-19 Vaccine Booster and Flu Shot"; RASH ERYTHEMATOUS (non-serious) with onset 08Nov2022, outcome "recovering", described as "face and neck was red rash"; PRURITUS (non-serious) with onset 08Nov2022, outcome "recovering", described as "face started itching suddenly". Therapeutic measures were taken as a result of pruritus. Additional Context: On 28Oct2022 patient had the COVID-19 Vaccine Booster and Flu Shot. She described the flu shot as the Old Age Lady Flu Shot for over 65 years old or whatever. Patient thinks she has had a reaction to the COVID-19 Vaccine Booster. Tuesday, 10 days after the COVID-19 Vaccine Booster, her face started itching suddenly and yesterday got her face and neck was red. Patient doesn't know if it is an actual reaction but she is still itching and is still has a rash today. Itching outcome: Happens in spells. Starts itching, goes away for a long time, then starts back again, intermittently. Patient clarified that it doesn't itch near as much as first day and has subsided some, clarified that it has improved. Itching Treatment: Still washing her face with the same cleansing cream and same moisturizers, hasn't stopped using her normal products. Patient clarified she was using the cleansing cream and moisturizers before the COVID-19 Vaccine Booster and itching with rash. Patient has been using the cleansing cream and moisturizers for 20 years. Face and neck was red rash: Start Date: 28Oct2022, aware this is discrepant as caller previously provided her face and neck were red yesterday. Documented as provided and confirmed by caller. Outcome: It is splotchy, not everywhere. It has gotten lighter, improved, doesn't seem to be as red as it was on Tuesday. Rash is not anywhere else on the body, not on stomach or arms. It was reported that it happened 10 days after the COVID-19 Vaccine Booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Blood pressure high (diagnosed at about maybe 40 years old. At 40 everything went downhill.); Type 2 diabetes mellitus (thinks dx at 41 HCP was debating if she had juvenile diabetes or type two diabetes (diagnosed))
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (in August or Sep2020, confirmed she tested positive before receiving any COVID-19 Vaccines.); Fever (for two different non-consecutive nights, reached 101 degrees Fahrenheit.); Scratchy throat
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2506955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: OH
Alter: 29,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Accidental overdose Dizziness Incorrect dose administered

Symptomtext

accidently gave me a double dose of Pfizer (Covid 19 vaccine bivalent) instead of Pfizer (Covid 19 vaccine bivalent) and Flu shot (Unspecified Flu Shot); little light headed; 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 29-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 at 17:05 as dose number unknown (booster), single (Lot number: GJ6665, Expiration Date: Jun2023) at the age of 29 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Seasonal allergy" (unspecified if ongoing), notes: Seasonal allergy medication (not clarified). Concomitant medication(s) included: IBUPROFEN; ALBUTEROL [SALBUTAMOL] taken for asthma. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 Immunization. The following information was reported: DIZZINESS (non-serious) with onset 10Nov2022, outcome "recovering", described as "little light headed"; ACCIDENTAL OVERDOSE (non-serious) with onset 10Nov2022 at 17:05, outcome "unknown", described as "accidently gave me a double dose of Pfizer (Covid 19 vaccine bivalent) instead of Pfizer (Covid 19 vaccine bivalent) and Flu shot (Unspecified Flu Shot)".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Seasonal allergy (Seasonal allergy medication (not clarified))
Andere Medikamente: IBUPROFEN; ALBUTEROL [SALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2506955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: OH
Alter: 29,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Accidental overdose Dizziness Incorrect dose administered

Symptomtext

accidently gave me a double dose of Pfizer (Covid 19 vaccine bivalent) instead of Pfizer (Covid 19 vaccine bivalent) and Flu shot (Unspecified Flu Shot); little light headed; 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 29-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 at 17:05 as dose number unknown (booster), single (Lot number: GJ6665, Expiration Date: Jun2023) at the age of 29 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Seasonal allergy" (unspecified if ongoing), notes: Seasonal allergy medication (not clarified). Concomitant medication(s) included: IBUPROFEN; ALBUTEROL [SALBUTAMOL] taken for asthma. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 Immunization. The following information was reported: DIZZINESS (non-serious) with onset 10Nov2022, outcome "recovering", described as "little light headed"; ACCIDENTAL OVERDOSE (non-serious) with onset 10Nov2022 at 17:05, outcome "unknown", described as "accidently gave me a double dose of Pfizer (Covid 19 vaccine bivalent) instead of Pfizer (Covid 19 vaccine bivalent) and Flu shot (Unspecified Flu Shot)".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Seasonal allergy (Seasonal allergy medication (not clarified))
Andere Medikamente: IBUPROFEN; ALBUTEROL [SALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2508920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: PA
Alter: 68,0
Geschlecht: M
Eingang: 15.11.2022
Impfdatum: 24.10.2022
Beginn: 13.11.2022
Tage bis Beginn: 20,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chest discomfort Cough Feeling hot Headache Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

It started out with headache, slight cough, felt hot, tightness in chest, and running nose. I tested positive for COVID-19 at home. Then I went to the urgent care to confirm and, I was positive. My doctor prescribed me PAXLOVID when I called. I started taking that yesterday. Today I have a sore throat and a more serious cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test, 11/13/2022, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Allopurinol; multivitamin; calcium; fish oil
Allergien: N/A
Vorherige Impfungen: -

VAERS 2508208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: MI
Alter: -
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Pain Swelling

Symptomtext

Corminaty- use for COVID-19 under Emergency Use Authorization (EAU):Patient bivalent covid vaccine on 11/4/2022 and began experiencing pain and swelling over the next 24 hours. Patient saw their primary physician 11/11/2022 and has a follow up appointment with them.

Weitere VAERSDATA-Felder

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

VAERS 2507850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NC
Alter: 66,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / RA

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

Pain

Symptomtext

Within hours of receiving the vacination my pain levels from the pre-existing injuries increased from a level of 1/10 to 8/10. The pain became more managable after 24 hours and returned to normal levels within 48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Pelvis and Ribs Cracked, Collar bone strained in Auto Collisio
Vorgeschichte: Hypertension
Andere Medikamente: Aliskirin,Advil,hydroCHLROthiazide,metoprolol tartrate,amlodipine besylate,methocarbamol,Gabapentin,tamsulosin HCL,Ergocalciferol VitD2,rosuvastatin Calcium.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2507364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 14.11.2022
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

Dizziness

Symptomtext

Patient presented to community mobile team on 11/10/22 to receive Pfizer COVID Bivalent Booster dose at 1030AM. Previously, the patient had received two full doses for Pfizer COVID vaccine primary series 03/30/21 Lot #EN6203 and 04/24/21 Lot # EW0179 and a Pfizer COVID vaccine booster on 11/9/21 Lot# 301358A. The patient was currently taking Allopurinol 200mg BID for gout and Propanolol TID for migraines. The patient was allergic to ampicillin which causes hives and IV contrast dye which results in hives as well. She reported having a history of gout, migraines and a nephrectomy. Patient answered no to all the pre-screening questions, reported she has done well with vaccines in the past and no history of fainting. The patient received a Pfizer Bivalent booster vaccine (0.3 ml dose) Lot#GJ6665 in the left arm by RN at 10:36 AM. At 10:42 AM patient reported feeling dizzy while sitting in the observation area. RN advised patient to sit in gravity chair and lay down while taking vitals. Vitals were taken at 10:42 AM BP 100/60, HR 62 SpO2 97. Patient sat in gravity chair for ten minutes and reported feeling better. Vitals were taken again at 10:51 AM BP 100/62 ,HR 56, SpO2 96. Patient reported only having soup this morning and was given water and ate nutrigrain bar. She returned to her seat and a third set of vitals were taken. Vitals at 11:00 AM BP 98/62 ,HR 63, SpO2 96. Patient reported feeling better, no other side effects and left in a steady gait.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 11/10/22 Vitals were taken at 10:42 AM BP 100/60, HR 62 SpO2 97. 11/10/22 Vitals were taken again at 10:51 AM BP 100/62 ,HR 56, SpO2 96. 11/10/22 Vitals at 11:00 AM BP 98/62 ,HR 63, SpO2 96.
Aktuelle Erkrankungen: n/a
Vorgeschichte: gout and migraines
Andere Medikamente: allopurinol 200 mg BID and Propranolol TID
Allergien: ampicillin causes hives and IV contrast dye causes hives
Vorherige Impfungen: -

VAERS 2507276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: ID
Alter: 66,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 09.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Autoscopy Chest X-ray normal Dizziness Electrocardiogram normal Metabolic function test normal Thinking abnormal

Symptomtext

At ~47h post vaccination, pt went to ER d/t feeling woozy and experienced an unprecedented "outer body" episode w/ unrelated mental thoughts to current activity that lasted ~10 seconds. ~1.5h later, experienced same episode. ER did CXR, EKG, and blood work that all returned negative and discharged same day. All sx resolved ~4d post vaccination and received reassurance from PCP via email/text.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Self reported 11/11/22: CXR, EKG, CMP (all negative)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tylenol 500 mg, Advil 400 mg, Zinc 15mg, B complex, 1 a day multivitamin, C 500mg, fish oil 1200mg, D 25mcg, CoQ10100mg, mega red 750mg, turmeric 1500mg, probiotic 10
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2507223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 30,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 12.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Body temperature increased Ear swelling Erythema Fatigue Injection site pain No reaction on previous exposure to drug Pruritus Rash Urticaria

Symptomtext

Have not had any reaction to the previous Pfizer/BioNTech vaccinations. Received #4 vaccine at approx. 8:10am 11/12 and stayed for monitoring for 15 minutes following. Normal reaction to vaccination as previously experienced was soreness at injection site, slight fatigue, and slight body temp. rise. At approx. 9:20pm 11/12, felt itching on back. Overnight, itching continued and at 5:30am 11/13, full body rash/hives were present. Redness and swelling of both ears also present. As the day continued, redness and rash continued to progress and spread to arms/hands and legs/feet. Full-body rash and itching still present as of 11:20am 11/14. Treatment sought at urgent care facility and included prescription antihistamines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: common cold
Vorgeschichte: none
Andere Medikamente: Benadryl for seasonal allergies
Allergien: none (that I know of, esp. at time of vaccination)
Vorherige Impfungen: -

VAERS 2507193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: AR
Alter: 59,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 12.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Pruritus Rash Rash erythematous Rash papular Urticaria

Symptomtext

PATIENT CALLED AND STATED THAT SHE HAD RECEIVED 2 VACCINES THIS WEEKEND AT OUR PHARMACY. WHEN SHE TOOK OFF HER CLOTHING LATER THAT EVENING, SHE NOTICED AN ENTIRE BODY RASH, MOSTLY ON THE TOPS OF HER THIGHS, CONSISTING OF WHEALS AND WELTS THAT WERE DIME TO QUARTER SIZED AND SLIGHTLY RAISED. SHE SAID THEY WERE RED, BUT ARE SLOWLY STARTING TO LIGHTED. SHE SAID ABOUT AN HOUR AFTER THE VACCINE THE SKIN ON HER NECK GOT SLIGHTLY ITCHY, BUT SHE DIDN'T THINK MUCH ABOUT IT. NO BREATHING ISSUES HAVE OCCURED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: PATIENT STATED THAT SHE TAKES FISH OIL, D3, AND CO-Q10
Allergien: PATIENT STATED THAT SHE HAD NO FOOD OR MEDICATION ALLERGIES
Vorherige Impfungen: -

VAERS 2498719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 88,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 24.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 5,0
Dosis: UNK
Route/Site: IM / RA

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

Back pain Body height Gait disturbance Illness Weight Flank pain Malaise

Symptomtext

Patient reports she got sick five days after receiving the vaccine and still does not feel well. She reports back and side pain and difficulty walking. She says she went to the ER and was checked out and sent home. She contacted pfizer to report this. Pharmacy staff recommended she follow up with primary care as well.

Weitere VAERSDATA-Felder

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

VAERS 2506509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: PA
Alter: 47,0
Geschlecht: M
Eingang: 12.11.2022
Impfdatum: 06.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Chills Headache Musculoskeletal stiffness Nasal congestion Off label use Pain Pain in extremity Product use issue

Symptomtext

Chills; Headache; Congestion nasal; Stiff neck; sore legs; generalized soreness; Off Label Use; Drug Use for Unapproved Combination; This is a spontaneous report received from a 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), on 06Nov2022 at 17:30 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 47 years, in left deltoid for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU VACCINE VII taken for influenza, on 06Nov2022 as unk unk, single. Vaccination history included: BNT162b2 (dose 1,, Lot: EL3247 , Expiry date: May2021, Site: Unknown), administration date: 24Feb2021, when the patient was 46-year-old, for Covid-19 vaccinations; BNT162b2 (dose 2, Lot: EN6203 , Expiry date: Jun2021 , Site: Unknown), administration date: 17Mar2021, when the patient was 46-year-old, for Covid-19 vaccinations; BNT162b2 (3rd dose:, Lot: FE3592 , Expiry date: Unknown), administration date: 01Oct2021, when the patient was 46-year-old, for Covid-19 vaccinations. The following information was reported: PRODUCT USE ISSUE (non-serious) with onset 06Nov2022, outcome "unknown", described as "Drug Use for Unapproved Combination"; OFF LABEL USE (non-serious) with onset 06Nov2022, outcome "unknown"; CHILLS (non-serious) with onset 07Nov2022, outcome "recovering"; NASAL CONGESTION (non-serious) with onset 07Nov2022, outcome "not recovered", described as "Congestion nasal"; HEADACHE (non-serious) with onset 07Nov2022, outcome "not recovered"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 07Nov2022, outcome "not recovered", described as "Stiff neck"; PAIN (non-serious) with onset 07Nov2022, outcome "not recovered", described as "generalized soreness"; PAIN IN EXTREMITY (non-serious) with onset 07Nov2022, outcome "not recovered", described as "sore legs". Additional information: Got the injection at about 17:30 and sometime at night the chills hit him with the headache along with everything else. This was in the early morning hours of 07Nov2022. Caller clarified that he had nasal congestion. Also reported that he had sore legs and generalized soreness. Chills are improved, he is still cold, but is not shivering anymore. He had no problems with the other 3 injections, but for some reason this one got him. He received the flu vaccine at the same time, but in the right deltoid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 2505742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: UT
Alter: 55,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: -
Beginn: 13.10.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Erythema Immediate post-injection reaction Pruritus Sensory disturbance

Symptomtext

Immediately felt like an insect bite. I had a very itchy red arm for longer than a week. I took an antihistamine for a couple of days, but I did not see a doctor. It took about 2 weeks 2 stop itching. It hurt a slight amount for a total of 3 weeks. I have since completely recovered from these symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin D3; vitamin B6; magnesium; calcium; folate; omega 3 fish oil; vitamin C; zinc
Allergien: Oral typhoid vaccine
Vorherige Impfungen: Oral typhoid around 1993, vomiting and diarrhea.

VAERS 2505441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NE
Alter: 47,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Pain Pyrexia

Symptomtext

Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Fever-Medium, Systemic: Joint Pain-Mild

Weitere VAERSDATA-Felder

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

VAERS 2505249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: DE
Alter: 44,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 04.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Arthralgia Chills Influenza like illness Lethargy Lymph node pain Myalgia Pyrexia Vaccination site pain

Symptomtext

flu-like symptoms; lethargy; lingering pain in left arm pit lymph node; Soreness at injection site; fever/chills; fever/chills; whole body muscle/joint aches; whole body muscle/joint aches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 at 19:00 as dose 4 (booster), single (Lot number: GJ6665) at the age of 44 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: FLU [INFLUENZA VACCINE] taken for immunisation, on 28Oct2022 as dose 1, single; TDAP taken for immunisation, on 28Oct2022 as dose 1, single; SYNTHROID; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; MIDNITE; AIRBORNE. Past drug history included: Neosporin, reaction(s): "known allergies: Neosporin"; Possibly aspirin, reaction(s): "Known allergies: possibly aspirin". Vaccination history included: Bnt162b2 (DOSE 1), for COVID-19 Immunization; Bnt162b2 (DOSE 2), for COVID-19 Immunization, reaction(s): "Joint pain", "Tiredness", "Headache", "Migraine", "Stiff neck", "Shaky feelings", "Ache", "Vomiting"; Bnt162b2 (DOSE 3 (BOOSTER)), for COVID-19 Immunization, reaction(s): "Arthralgia", "Back pain", "COVID-19", "Chills", "Exposure to SARS-CoV-2", "Hyperhidrosis", "Hypoaesthesia", "Lymph node pain", "Lymphadenopathy", "Pain", "Vaccination failure". The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 05Nov2022 at 06:00, outcome "recovering", described as "Soreness at injection site"; CHILLS (non-serious), PYREXIA (non-serious) all with onset 05Nov2022 at 06:00, outcome "recovering" and all described as "fever/chills"; INFLUENZA LIKE ILLNESS (non-serious) with onset 05Nov2022 at 06:00, outcome "recovering", described as "flu-like symptoms"; LETHARGY (non-serious) with onset 05Nov2022 at 06:00, outcome "recovering"; LYMPH NODE PAIN (non-serious) with onset 05Nov2022 at 06:00, outcome "recovering", described as "lingering pain in left arm pit lymph node"; MYALGIA (non-serious), ARTHRALGIA (non-serious) all with onset 05Nov2022 at 06:00, outcome "recovering" and all described as "whole body muscle/joint aches". Therapeutic measures were taken as a result of influenza like illness, lethargy, lymph node pain, vaccination site pain, chills, pyrexia, myalgia, arthralgia. Additional information: Zero prior events (four Pfizer shots). Soreness at injection site and flu-like symptoms (whole body muscle/joint aches, lethargy, fever/chills) resolved by Tylenol, lingering pain in left arm pit lymph node. Tylenol rapid release every 6-8 hours. Covid was not tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: SYNTHROID; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; MIDNITE; AIRBORNE
Allergien: -
Vorherige Impfungen: -

VAERS 2504558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 19.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / RA

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

Biopsy skin abnormal C-reactive protein increased Henoch-Schonlein purpura Pain Rash Swelling

Symptomtext

2-3 days after pt received vaccine she developed bilateral lower extremity, flat rash which originally was on the dorsum of both feet and legs. It spread proximally to above the ankles. She has bilateral swelling and pain. Was biopsied and was diagnosed with IGa vasculitits

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: CRP elevated and biopsy of rash pos for IGA vasculitis on 10/26/22 by rheum
Aktuelle Erkrankungen: none
Vorgeschichte: Gerd, Barretts esophagus,hyperlipidemia, asthma
Andere Medikamente: none
Allergien: grass, pollen
Vorherige Impfungen: -

VAERS 2504396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WI
Alter: 78,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 01.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: UN / UN

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

Anion gap Asthenia Back pain Blood bicarbonate normal Blood creatinine increased Blood glucose normal Blood potassium normal COVID-19 Computerised tomogram head normal Confusional state Dysarthria Haemoglobin decreased International normalised ratio increased Laboratory test Lipase normal Liver function test normal SARS-CoV-2 test positive Troponin normal

Symptomtext

Per web report received by Public Health Department and per state Immunization Registry; Presented 11/03/2022 to Hospital ED for evaluation of sudden onset of slurred speech and confusion that started at 3 PM. Patient was last known to feel well at bedtime yesterday. In the emergency department, symptoms spontaneously improved. Patient was positive for COVID-19 per 4-plex PCR. Patient is vaccinated: Denies having cough, shortness of breath, congestion, or sore throat. Patient has generalized weakness with confusion. Saturating well on room air, no indication for initiating antibiotic management or steroid therapy -Isolation per protocol, plan for 10 days of isolation starting from 11/3/2022. Pfizer 02/02/2021 lot EN5318; Pfizer 02/23/2021 lot EN6200; Pfizer 09/22/2021 lot 301308A; Pfizer BvlntBstr 12+ 11/01/2022 lot GJ6665 Per web report this Patient was recently started on Zanaflex for back pain, 11/03/2022 is day 3 of using Zanaflex. Urinalysis negative for UTI. WBC 8.9, hemoglobin 11.6, random blood sugar 142, creatinine 1.5/consistent with previously, potassium 4.3, anion gap 8, bicarbonate 28, normal liver function test, normal initial troponin, lipase 31, INR 2.2CT. note stated head stroke protocol negative for acute findings. Differential diagnosis of metabolic encephalopathy, infection, TIA/CVA, medication reaction, other. Stroke protocol initiated. CT head negative. The patient was not a tPA candidate because patient is on daily Xarelto. INR 2.2. Symptoms essentially completely resolved. Patient also had a COVI D-19 vaccination 11/1/2022. Patient given 4 baby aspirin. Per web report there was no evidence of UTI or other infections. Patient was admitted to the hospital to continue care. Public Health Department has no further information on this patient?s hospitalization or outcome. Please contact provider for any additional information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Lab work, Head CT
Aktuelle Erkrankungen: unknown
Vorgeschichte: paroxysmal A. fib on chronic Xarelto use, type 2 diabetes mellitus, CAD, hypothyroidism
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2504374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: PA
Alter: 53,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 05.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia COVID-19 Cough Diarrhoea Dysstasia Headache Malaise Pulmonary congestion SARS-CoV-2 test positive Sleep disorder

Symptomtext

On 10/29/2022 in the morning I woke up coughing. I thought I just had a cold. The next day on 10/30/2022 I started feeling sick and I was coughing more. On 10/31/2022 I was feeling the same symptoms along with severe cough. I took 2 home COVID-19 tests which were positive, and I also went to the pharmacy for a PCR test which was positive too. I messaged my doctor after testing positive. A nurse from her office reached out to me and advised me if my situation gets worse to go to the ER. On 11/01/2022 I was feeling very weak. I couldn't even stand up. On 11/02/2022 I was having diarrhea. I took over counter MUCINEX. On Monday I woke up with a headache so for all my symptoms I started taking TYLENOL, vitamin C, vitamin D, zinc and MUCINEX. I'm recovering from COVID-19, but I still have lingering cough and chest congestions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 10NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Major Depressive Disorder; Anxiety; Arthritis; Achilles Tendinopathy
Andere Medikamente: FETZIMA; trazodone; LYRICA; tizanidine; magnesium; vitamin D; melatonin; multivitamins; ADVIL
Allergien: Codeine; tetracycline; mold
Vorherige Impfungen: -

VAERS 2503892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: WA
Alter: 55,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / -

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

Body temperature Illness Off label use Pain Product use issue Pyrexia

Symptomtext

I received the vaccination I also got the Flu vaccine at the same time; I received the vaccination I also got the Flu vaccine at the same time; I was horribly sick; body ache; high, high fever; 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 31Oct2022 at 10:40 as dose 5 (booster), single (Lot number: GJ6665, Expiration Date: 30Jun2023) at the age of 55 years for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 31Oct2022 as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing), notes: I have Asthma and I do not want to go too far on my own medical history.". The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE 1; UNKNOWN MANUFACTURER), for Covid-19 immunization; Covid-19 vaccine (DOSE 3 (BOOSTER); UNKNOWN MANUFACTURER), for Covid-19 immunization; Covid-19 vaccine (DOSE 4 (BOOSTER); UNKNOWN MANUFACTURER), for Covid-19 immunization; Covid-19 vaccine (DOSE 2; UNKNOWN MANUFACTURER), for Covid-19 immunization. The following information was reported: ILLNESS (non-serious) with onset 2022, outcome "unknown", described as "I was horribly sick"; PAIN (non-serious) with onset 2022, outcome "unknown", described as "body ache"; PYREXIA (non-serious) with onset 2022, outcome "unknown", described as "high, high fever"; OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 31Oct2022, outcome "unknown" and all described as "I received the vaccination I also got the Flu vaccine at the same time". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of illness, pain, pyrexia. Additional information: the patient did not had any investigations in last two weeks. It was reported as I was horribly sick starting Tuesday to somewhat today but you now very, very situation better then now (at the time of report). The patient was treated with Tylenol cold and Ibuprofen. The patient I think it was my left arm, but they did one on the one side and one in the other, so I am not sure which one went where but it was top of arm." For Anatomical site of administration it was reported as I think it was my left arm, but they did one on the one side and one in the other, so I am not sure which one went where but it was top of arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Name: fever; Result Unstructured Data: Test Result:High; Comments: High Fever
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (I have Asthma and I do not want to go too far on my own medical history.")
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2503269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 09.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Headache Neck pain

Symptomtext

significant occipital headache and neck ache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: endometriosis, obesity, anxiety with depression, hypothyroidism, insomnia, reactive airway disease (mild intermittent)
Andere Medikamente: birth control, bupropion, fluoxetine, levothyroxine. B-100 complex, vitamin D
Allergien: amoxicillin, sulfa
Vorherige Impfungen: -

VAERS 2502057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 26,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 04.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / -

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

COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

Patient developed COVID infection after vaccination. Symptoms started on same day of vaccination. 11/4 booster, 11/4 symptoms in PM, 11/6 tested positive, 11/7 treated with paxlovid. Our facility didn't administer this vaccine. We are the pt's primary care. Clinician prescribed paxlovid. We called pfizer to ask if there was a minimum time between immunization and paxlovid. We were informed that this is a reportable event for Pfizer, so we decided to file a VAERS as well. The state immunization database, doesn't reflect site of vaccine administration. It was administered at her place of business, per pt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: covid at home test 11/6/22
Aktuelle Erkrankungen: unknown
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2501303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: MO
Alter: 69,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Asthenia Cardiac flutter Heart rate irregular Pruritus Throat tightness

Symptomtext

throat closing; heart flutters; Itching; fluctuation in heart; weak; This is a spontaneous report received from 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 31Oct2022 at 14:30 as dose 5 (booster), 0.3 ml single (Lot number: GJ6665) at the age of 69 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "She has Hashimoto's" (unspecified if ongoing); "She has many allergies to medicine" (unspecified if ongoing). Concomitant medication(s) included: DIPHTHERIA VACCINE taken for immunisation, on 28Sep2022 as dose number unknown, single; TETANUS VACCINE taken for immunisation, on 28Sep2022 as dose number unknown, single. Vaccination history included: BNT162b2 (Dose: 4 (2nd booster), Lot provided as both numbers on card: BNT162, FJ6369, expiration is unknown. Injected in left arm.), administration date: 08Apr2022, when the patient was 69-year-old, for COVID-19 immunization; BNT162b2 (Dose: 3 (1st booster), Lot is unknown, expiration is unknown. Injected in left arm.), administration date: 12Nov2021, when the patient was 68-year-old, for COVID-19 immunization; BNT162b2 (Dose: 2, Lot is unknown, expiration is unknown. Injected in left arm.), administration date: 06Mar2021, when the patient was 68-year-old, for COVID-19 immunization; BNT162b2 (Dose: 1, Lot is unknown, expiration is unknown. Injected in left arm.), administration date: 13Feb2021, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "Headache". The following information was reported: HEART RATE IRREGULAR (non-serious) with onset 2022, 1 month 4 days after the suspect product(s) administration, outcome "unknown", described as "fluctuation in heart"; ASTHENIA (non-serious) with onset 2022, 1 month 4 days after the suspect product(s) administration, outcome "unknown", described as "weak"; PRURITUS (non-serious) with onset 31Oct2022, outcome "recovering", described as "Itching"; CARDIAC FLUTTER (medically significant) with onset 31Oct2022, outcome "not recovered", described as "heart flutters"; THROAT TIGHTNESS (non-serious), outcome "unknown", described as "throat closing". Therapeutic measures were taken as a result of pruritus, throat tightness. Additional information: Received call from consumer regarding the Pfizer Bivalent vaccine. She had first 2 and then the 2 boosters because she is 69 years old. They were all with the Pfizer and she had no problems. Had Bivalent and is on 3rd day of Benadryl and heart flutters. She dug into it and saw that the ingredients changed. She just said they should let people know because her doctor said there were no changes other than the MRNA should target the Omicron. It was just a few days ago. Trying not to go out because there is COVID everywhere. Had shot on Halloween and started 2 hours after is when it started. Itching has improved, but the fluctuation in heart has not. It is not enough for her not to be able to move, but she gets weak easily. She has not been to the doctor for any treatment. She tries to handle things at home first because when she goes in, something else usually happens. She has Hashimoto's which was diagnosed many years ago and prior to receiving any of the Pfizer COVID vaccines. She has many allergies to medicine and needs to know when they change something. She has a lot of medicines she is allergic to. The event itching and heart flutters started about 2 hours after receiving it. She stated with the first Pfizer COVID vaccine, she only had a headache. She did not have the lot or expiration for that one. It could cause someone a death. She breaks open a Benadryl as soon as she feels her throat closing. Other people might not know this. Is a sample of the product available to be returned, if requested (Y/N): no Packaging sealed and intact? not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy; Hashimoto's disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: CT
Alter: 37,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 05.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Pruritus

Symptomtext

pt states that she had itching on her palm the next morning after the vaccine

Weitere VAERSDATA-Felder

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

VAERS 2501060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 55,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 04.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Fatigue Injection site rash Pain Rash Rash erythematous Rash papular Rash pruritic

Symptomtext

Received Pfizer COVID Bivalent booster on 11/4/22. On 11/5/22 developed fatigue, body aches. On 11/5/22, also developed rash that started just above injection site at right deltoid. Over the next 48 hours the rash spread to right upper arm, right side of neck, across upper back, and top portion of chest. The fatigue and body aches resolved within 24 hours. The rash was scattered red papules and was itchy.

Weitere VAERSDATA-Felder

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

VAERS 2500594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MN
Alter: 66,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 09.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Fatigue Feeling abnormal Feeling cold Feeling hot Irritability Nasopharyngitis Psychomotor hyperactivity SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19. When I first developed the symptoms on day one, I felt very tired and hyper. I felt crabby and very warm. On day 2, I felt like I had a head cold. I felt like I was in a fog. I would feel warm and then cold. That was when I took a COVID-19 test and tested positive. I spoke to my doctor and she prescribed me PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 1Nov2022 home COVID-19 test positive; 6Nov2022 home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: N/A
Vorherige Impfungen: -

VAERS 2500571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 03.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

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

Injection site rash

Symptomtext

rash at injection site for 4 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Levothyroxine
Allergien: salfa
Vorherige Impfungen: -

VAERS 2499975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 26.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: SC / RA

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

Computerised tomogram head normal Herpes virus infection Laboratory test normal Nausea Vertigo Vestibular neuronitis Vomiting

Symptomtext

Vestibular Neuritis started 3 days after vaccine. Disease likely caused by herpes viral infection where dormant virus was reactivated by the Covid vaccine. Severe vertigo x 24 hours with nausea and vomiting requiring Emergency Room treatment. Issue resolved 5 days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Lab tests, CT of Brain 10-31-22 were normal
Aktuelle Erkrankungen: -
Vorgeschichte: History of Herpes Simplex
Andere Medikamente: Synthroid, multi-vitamin
Allergien: Sulfa, Cipro
Vorherige Impfungen: -

VAERS 2499868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: MO
Alter: 67,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 30.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Erythema Flushing Hyperhidrosis Injection site erythema Injection site pain Injection site swelling Joint swelling Lymphadenopathy Pain

Symptomtext

Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: PT COMPLAINS OF GENERAL BODY ACHES, PAIN AND SWELLING IN JOINTS, REDNESS ALL OVER BODY-Mild, Systemic: Flushed / Sweating-Severe, Systemic: Joint Pain-Severe, Systemic: Lymph Node Swelling-Severe

Weitere VAERSDATA-Felder

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

VAERS 2499405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IL
Alter: 68,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 22.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Body temperature increased Pain Somnolence

Symptomtext

After vaccine started to feel weak, achy, had a temper and my body hurt really bad. Slept a long time, and continued to feel weak. Would have gone to the ER but I didn't have anyone to take me. Called my doctor because the pain was so bad, advised me to take my regular pain medication and rest. One week later I started feeling a little better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia; Myelodysplastic Syndrome; Obesity.
Andere Medikamente: NORCO; ALEVE; vitamin C; vitamin B-12; multivitamin; vitamin D-3; magnesium; fish oil; XANAX; acetate eye drops.
Allergien: Contrast dye; generic opioid medication
Vorherige Impfungen: Flu shots in the past have caused me to get Pneumonia in the past.

VAERS 2498724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: IN
Alter: 61,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 27.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Chills Fatigue Headache Illness Myalgia Nausea Pain in extremity Vaccination site erythema Vaccination site induration Vaccination site mass Vaccination site swelling Vaccination site warmth

Symptomtext

felt sick like with Covid; Huge, red area where injection was, swollen, has a lump and hot; Arm is really sore and painful/Painful lump in arm; hard, swollen, lump, huge red area on her injection site; hard, swollen, lump, huge red area on her injection site; hard, swollen, lump, huge red area on her injection site; hard, swollen, lump, huge red area on her injection site; severe muscle and joint pain; extreme chills; headache; nausea; overall just wiped out, extreme fatigue; joint pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 61-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 27Oct2022 as dose 3 (booster), single (Lot number: GJ6665) at the age of 61 years 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: Says lot number is FG3527, the 2 could be Z), administration date: 22Nov2021, for COVID-19 Immunization; Johnson and johnson covid vaccine (DOSE 1, SINGLE), for COVID-19 Immunization, reaction(s): "sick". The following information was reported: CHILLS (non-serious) with onset 28Oct2022, outcome "recovered" (30Oct2022), described as "extreme chills"; HEADACHE (non-serious) with onset 28Oct2022, outcome "recovered" (30Oct2022); ARTHRALGIA (non-serious) with onset 28Oct2022, outcome "recovered" (30Oct2022), described as "joint pain"; NAUSEA (non-serious) with onset 28Oct2022, outcome "recovered" (30Oct2022); FATIGUE (non-serious) with onset 28Oct2022, outcome "recovered" (30Oct2022), described as "overall just wiped out, extreme fatigue"; MYALGIA (non-serious) with onset 28Oct2022, outcome "recovered" (30Oct2022), described as "severe muscle and joint pain"; VACCINATION SITE INDURATION (non-serious) with onset 29Oct2022, outcome "unknown", VACCINATION SITE SWELLING (non-serious), VACCINATION SITE MASS (non-serious), VACCINATION SITE ERYTHEMA (non-serious) all with onset 29Oct2022, outcome "not recovered" and all described as "hard, swollen, lump, huge red area on her injection site"; ILLNESS (non-serious), outcome "unknown", described as "felt sick like with Covid"; VACCINATION SITE WARMTH (non-serious), outcome "not recovered", described as "Huge, red area where injection was, swollen, has a lump and hot"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Arm is really sore and painful/Painful lump in arm". Additional information: Caller requested for medical treatment recommendation for the side effect she experienced after getting the Pfizer biontech covid-19 Bivalent booster Gray cap vaccine. Consumer stated that she received her Pfizer biontech covid-19 Bivalent booster Gray cap vaccine last 27Oct2022 and noticed 2 days later (29Oct2022) a hard, swollen, lump, huge red area on her injection site. No other conditions and investigations. When caller got the shot, was odd, shot didn't hurt at all, but the next day felt sick like with Covid, knows how that feels because caller had Covid before. Clarified and confirmed caller had Covid prior to having any vaccine doses. Calling to report caller had severe muscle and joint pain, extreme chills, headache, nausea, overall just wiped out, extreme fatigue. Huge, red area where injection was, swollen, has a lump and hot: Then started feeling better but not callers arm, arm is getting terrible, huge, red area where injection was, swollen, has a lump and hot, doesn't know what to do for that, can Pfizer help with suggestions? Arm is really sore and painful. Hoping arm will continue getting better, but red spot started out the size of probably a quarter and now red spot is probably the size, can't think, maybe the size of a Coke can, the circumference of a Coke can. Painful lump in arm is why caller is calling, never had that happen before, caller gets sore after any kind of shot, but has never seen the red, warmth, or lump. Start date of adverse event: Does not think really started bothering caller until that night, woke up that morning sick and terrible, so guess would say arm started the next day, Saturday, 29Oct2022. Was bright red at first when started but is paler, so does not know if that means anything, as it has spread the color is more pink instead of bright red. Upon further clarifying, caller clarified that the vaccine caller was calling in regards to is the new vaccine, had the booster before, thinks this one caller just received is the new Pfizer vaccine. Upon further clarification, caller said caller never had this vaccine, whatever Pfizer just came out with. Caller had an original vaccine, then a booster vaccine, this was callers 3rd COVID shot total since last year. Confirmed this was callers 3rd dose total. Upon further attempting to clarify which vaccine caller received and is calling about, caller looked at vaccination card and clarified and confirmed caller received the Pfizer BioNTech COVID-19 vaccine bivalent for callers 3rd dose. COVID-19 vaccine bivalent placed in formal field. 1st dose was Johnson and Johnson COVID vaccine, was the 1 shot and done thing, was terrible, got really sick, but didn't get the arm issue. First COVID shot caller had caller went to race track to get done. Then the 2 booster doses, confirmed 2nd dose and 3rd dose, were at the doctors office. Doctor recommended the Pfizer vaccine. What happens to this information, Caller was not making a complaint or anything. Does not want to file a complaint against callers doctor, loves callers doctor, shot didn't hurt at all, just concerned about arm, the last shot was painful too but not hard, red, and hot. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2498226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: UT
Alter: 77,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 31.10.2022
Beginn: 02.11.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Injection site rash Injection site swelling

Symptomtext

Rash and swelling on upper arm under the injection site. Started on 11/2 and continued up to mid-day 11/3 at time of notification. Patient had not taken anything for the condition at time of notification.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: cephalexin, trazodone, levothyroxine
Allergien: sulfa antibiotics
Vorherige Impfungen: -

VAERS 2497918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 07.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Erythema Immunisation reaction Peripheral swelling Pruritus Skin warm

Symptomtext

COVID arm (left arm) Symptoms: Red, swollen, hot, mildly itchy 8.5 cm width x 7 cm height Onset: less than 24 hours. Duration: approximately 1 week Treatment: Applied cold compresses and sparing amounts or either hydrocortisone or betamethasone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N?A
Aktuelle Erkrankungen: Environmental allergies Equivocal/borderlin Rheumatoid Arthritis
Vorgeschichte: Environmental Allergies Food Allergies
Andere Medikamente: Montelukast, Cetirizine, LDN, Vitamin D3, Magnesium Glycinate, Zince, Evening Primrose, Omega Fish Oil, AdvaClear, Quercetin, Vitamin C with Bioflavonoid, Bromelain, Ostinol
Allergien: Too many food allergies and sensitivities
Vorherige Impfungen: -

VAERS 2497905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 11,0
Geschlecht: F
Eingang: 03.11.2022
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: ja

Malaise Product administered to patient of inappropriate age Pyrexia Wrong product administered

Symptomtext

11y10m female given 12+ bivalent pfizer gray cap rather than 5-11 bivalent pfizer orange cap. pt had fever and malaise post vaccination but still able to participate in activities. aware of error. PCP Dr aware.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: multivitamin
Allergien: nka
Vorherige Impfungen: -

VAERS 2497213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: 70,0
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: unbekannt Erholt: nein

Erythema Rash Rash pruritic

Symptomtext

Patient came into vax clinic to report a mild redness/rash that appeared on her cheeks and chin yesterday evening. Yesterday she received both a flu and bivalent covid vaccine. Patient says rash is itchy but not painful; she has not tried anything for it yet. Denied any swelling of face, neck, hands or trouble breathing. Explained that an allergic reaction can be a side effect after receiving a covid vaccine. Recommended she take a benadryl tab before bedtime and to use benadryl cream on the face during the day to help prevent drowsiness at work. Instructed her to go to ER (or call 911 if necessary) if face/neck start to swell or she has trouble breathing. She approved of the plan and went to go check to see if she could be seen by a provider today.

Weitere VAERSDATA-Felder

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

VAERS 2496970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 18,0
Geschlecht: F
Eingang: 02.11.2022
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

Injection site discharge

Symptomtext

Patient's caregiver stated that when patient removed bandage the evening of the shot, that clear liquid ran down her arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discharge
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Injection site bruising Injection site discharge Injection site swelling

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Error: Leaking from Injection Site-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 01.10.2022
Beginn: 01.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Headache Inappropriate schedule of product administration Overdose

Symptomtext

A pharmacist at reporter's store administered 2 doses of the product to the patient on the same day; A pharmacist at reporter's store administered 2 doses of the product to the patient on the same day; nonstop headache; This is a spontaneous report received from contactable reporter(s) (Pharmacist). A 45-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), in Oct2022 as dose number unknown (booster), single (Lot number: GJ6665, Expiration Date: May2023) at the age of 45 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious), OVERDOSE (non-serious) all with onset Oct2022, outcome "unknown" and all described as "A pharmacist at reporter's store administered 2 doses of the product to the patient on the same day"; HEADACHE (non-serious) with onset Oct2022, outcome "not recovered", described as "nonstop headache". Additional information: NDC number of Pfizer COVID Booster was 59267-0304-02. The caller had no reference as the staff on duty at time of reporting was not there. This Pharmacist called regarding Pfizer COVID Booster, adult gray cap bivalent multidose vial formulation. A pharmacist at reporter's store administered 2 doses of the product to the patient on the same day. The patient was reporting nonstop headache for the last 48 hours. The patient did not want to take any over the counter products for the nonstop headache like Tylenol or Ibuprofen. She called to ask how long they should expect the nonstop headache to last; how long to wait to go to the doctor; and what the patient could take for the nonstop headache. She was reading any studies to see if it was known how long headaches should last and kind of got the idea it was about a week, a person could have on and off headaches.

Weitere VAERSDATA-Felder

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

VAERS 2493516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: GA
Alter: 34,0
Geschlecht: F
Eingang: 30.10.2022
Impfdatum: 30.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Immediate post-injection reaction Injection site haemorrhage Injection site pain Pain

Symptomtext

Blood squirting out of the injection site immediately after the needle was removed from the deltoid. I applied pressure to the site and bleeding stopped. Patient was observed in the waiting area for 30 minutes. She said that she felt sore and throbbing at the injection site. I advised her to apply ice and take Tylenol when she gets home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 30.10.2022
Impfdatum: 20.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 2,0
Dosis: N/A
Route/Site: - / LA

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

Erythema Injection site erythema Injection site warmth Pain Peripheral swelling Pyrexia

Symptomtext

R arm swelling, redness, pain, tactile fever on 10/22. Took Ibuprofen, Dayquil, and Nyquil. Pt seen on 10/25 for follow up visit regarding test results from visit on 10/17 for evaluation of urticaria/facial edema and mentioned having received the PPSV23 vaccine on 10/20 with reaction beginning 10/22, slowly improving with Ibuprofen, Dayquil, Nyquil. Exam of RUE on 10/25: large area of erythema, mild warmth, mild ttp, no edema, no abcess, no cellulitis, able to raise RUE above her head, normal ROM R elbow

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Recurrent urticaria and Facial edema and history of mild intermittent asthma
Vorgeschichte: none other than that mentioned above
Andere Medikamente: ALBUTEROL BCP CETIRIZINE HCL 10 MG TABS; ONE TABLET Q AM DIPHENHYDRAMINE HCL 25 MG CAPS; 1 CAPSULE (25 MG) ORALLY DAILY AT BEDTIME AS NEEDED FOR HIVES/SWELLING FAMOTIDINE 20 MG TABS; 1 TABLET (20 MG) ORALLY DAILY 30 MINUTES BEFORE MEAL
Allergien: NKDA or food allergies. Was seen on 10/17 for Recurrent urticaria and Facial edema
Vorherige Impfungen: -

VAERS 2493455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 29.10.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Nausea Pyrexia Retching

Symptomtext

Patient was running a fever just under 101 F and having dry heaves and nausea.

Weitere VAERSDATA-Felder

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

VAERS 2493236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: NV
Alter: 78,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 13.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 9,0
Dosis: 5
Route/Site: IM / LA

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

Fatigue Nausea Pain Productive cough SARS-CoV-2 test negative

Symptomtext

About 9 days I woke up with body aches, fatigue, nausea, and phlegmy cough. I took a COVID-19 test at home and it was negative. I tested several test after and it was still negative. I called doctor and she didn't know what it was and she prescribed me an antibiotic to see if it goes away. It is the third day of the antibiotic and I am starting to feel a little. I still have the cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Test, Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Low Potassium; Etc
Andere Medikamente: Levothyroxine; Potassium; Pravastatin; Omeprazole; Ibuprofen; Losartan; Hydrochlorothiazide; Amlodipine; Eye Drops
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2492596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: SD
Alter: 42,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Malaise Nasal congestion Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

Fever and body aches one day after. I had nasal congestion and pain two days after, illness continued. I took a Covid test five days later due to continued illness and was positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Covid test on 10/26
Aktuelle Erkrankungen: -
Vorgeschichte: Allergies and asthma
Andere Medikamente: Trazodone, Singulair, and Allegra-D
Allergien: None
Vorherige Impfungen: -

VAERS 2492118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 23.10.2022
Beginn: 23.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Off label use Pain in extremity Product use issue

Symptomtext

flu shot on same date vaccine; flu shot on same date vaccine; paint in upper left arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Oct2022 at 12:00 as dose 4 (booster), single (Lot number: GJ6665) at the age of 54 years, in left arm for covid-19 immunisation; influenza vaccine (FLU [INFLUENZA VACCINE]), on 23Oct2022 as dose 1, single (Batch/Lot number: unknown), in left arm for immunisation. The patient's relevant medical history included: "chronic migraines" (unspecified if ongoing); "known allergies: PCN" (unspecified if ongoing), notes: known allergies: PCN; "known allergies: latex" (unspecified if ongoing), notes: known allergies: latex. Concomitant medication(s) included: IBUPROFEN; NYSTATIN; VIT D [COLECALCIFEROL]; VIT B12. Past drug history included: Amoxicllin, reaction(s): "known allergies: amoxicllin", notes: known allergies: amoxicllin. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTUERER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 2; MANUFACTUERER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 3; MANUFACTUERER UNKNOWN), for COVID-19 Immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 23Oct2022, outcome "unknown" and all described as "flu shot on same date vaccine"; PAIN IN EXTREMITY (non-serious) with onset 23Oct2022, outcome "recovering", described as "paint in upper left arm". Therapeutic measures were not taken as a result of pain in extremity. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. 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: Medical History/Concurrent Conditions: Latex allergy (known allergies: latex); Penicillin allergy (known allergies: PCN); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: chronic migraines
Andere Medikamente: IBUPROFEN; NYSTATIN; VIT D [COLECALCIFEROL]; VIT B12
Allergien: -
Vorherige Impfungen: -

VAERS 2492112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: PA
Alter: 34,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 16.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / LA

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

Lip blister Oral herpes Urticaria

Symptomtext

hives; fever blister; blister on top lip; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 34-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Oct2022 at 17:00 as dose 4 (booster), single (Lot number: GJ6665) at the age of 34 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "covid" (unspecified if ongoing), notes: if covid prior vaccination: Yes. Concomitant medication(s) included: INFLUENZA VACCINE taken for immunisation, on 05Oct2022 as dose number unknown, single. 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: LIP BLISTER (non-serious) with onset 19Oct2022, outcome "recovering", described as "blister on top lip"; ORAL HERPES (non-serious) with onset 19Oct2022, outcome "recovering", described as "fever blister"; URTICARIA (non-serious) with onset 23Oct2022, outcome "recovering", described as "hives". The events "fever blister", "blister on top lip" and "hives" required physician office visit. Therapeutic measures were taken as a result of oral herpes, lip blister, urticaria. Additional Information: The patient had received Influenza vaccine within four weeks of covid-19 vaccine. After receiving the 4th bivalent vaccine, he developed a fever blister on top lip which appeared to be similar to hsv1 type lesion (no personal history of fevers blister or any previous lip lesions) and on 23Oct after eating out at a restaurant (grits, shrimp, bacon, mushroom, onion, coffee, white potato) within 30 minutes broke out in hives. The patient had no previous history of food allergies or similar type reactions and had no medical history. The patient was treated with Abreva, Claritin 10 mg Benadryl 50 mg famotidine 40 mg for adverse events. The patient had Covid-19 prior to vaccination and was not tested for Covid-19 post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2491540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: GA
Alter: 35,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 13.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / UN

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

Blood cholesterol Blood triglycerides Chills Herpes zoster Hot flush Pain

Symptomtext

I got Shingles, Hot flashes chills, body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: cholesterol: triglyceride finger stick
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2491522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: ID
Alter: 28,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 25.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Injection site pain Injection site swelling Pain in extremity Swelling

Symptomtext

Patient received COVID Bivalent booster on 10/25/2022 in left deltoid. Noted pain in arm and armpit the same night. Yesterday felt swelling and increased pain in the left shoulder and arm pit. She took Tylenol and Ibuprofen with fair to moderate relief. Today the swelling has increased to the size of a baseball in her left arm pit and is extremely painful. No relief with OTC pain reliever. Has been taking mostly Tylenol today because she has no Ibuprofen. Patient denies rash, fever, swelling of mouth, lips eyes, tongue or throat. Is having no difficulty breathing or swallowing. Recommended patient be seen right away. States she cannot leave work but will go when she is off. I highly recommended she leave as soon as possible . Patient verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None by triage and advice only. See above
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2491503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: AZ
Alter: 77,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 21.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / RA

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

Injection site cellulitis Injection site erythema

Symptomtext

redness at the injection site caused cellulitis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site cellulitis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: arthritis
Vorgeschichte: arthritis
Andere Medikamente: unknown
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2491255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 93,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 24.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Diarrhoea

Symptomtext

Diarrhea, weakness,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: (CONGESTIVE) HEART FAILURE ) HYPERTENSION
Andere Medikamente: Rosuvastatin Calcium Tablet 10 MG Gabapentin Capsule 100 MG Melatonin Tablet 3 MG ClonazePAM Tablet 0.5 MG Multiple Vitamins-Minerals Tablet Esomeprazole Magnesium Capsule Delayed Release 20 MG acetaminophen Tablet 325 MG Sertraline HCl
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2491249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 77,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 19.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Body temperature increased Chest X-ray Cough Culture urine Erythema Full blood count Injection site warmth Laboratory test Metabolic function test Urine analysis

Symptomtext

Weakness, elevated temp, redness, warmth at site of injection, cough

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site warmth
Hospital-Tage: -
Labordaten: chest x ray, cbc, bmp, u/a c&s
Aktuelle Erkrankungen: -
Vorgeschichte: PERIPHERAL VASCULAR DISEASE, HYPERTENSION CHRONIC OBSTRUCTIVE PULMONARY DISEASE CHRONIC KIDNEY DISEASE, STAGE 5 HEART FAILURE OBESITY
Andere Medikamente: Paricalcitol Capsule 1 MCG Fleet Enema Enema ACETAMIN TAB 325MG ZINC OXIDE OIN 20% SERTRALINE TAB 50MG ATORVASTATIN TAB 40MG DOCUSATE SOD CAP 100MG Ocuvite Eye + Multi Tablet SYMBICORT AER 160-4.5 MiraLax Powder Mucus Relief Table
Allergien: Rocephin, Penicillin,Sulfa,Cephalsporin, plastic ID bracelet
Vorherige Impfungen: -

VAERS 2490843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / LA

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

Body temperature Chills Fatigue Malaise Myalgia Nausea Pain Pyrexia

Symptomtext

After I went to bed, I started developing chills; I spent all day, Saturday in bed. I was just that tired.; a low grade fever of 99.3; Achiness; generalized muscle pain; nausea; general unwell feeling; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). 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 21Oct2022 as dose number unknown (booster), single (Lot number: GJ6665, Expiration Date: 30Jun2023) at the age of 65 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Anxiety" (unspecified if ongoing), notes: Comments: Anxiety; "Stress" (unspecified if ongoing), notes: Comments: Stress; "High Blood Pressure" (unspecified if ongoing), notes: Comments: High Blood Pressure; "Hypothyroidism" (unspecified if ongoing), notes: Indication for use in the case: Hypothyroidism; "Cholesterol" (unspecified if ongoing), notes: Indication for use in the case: Cholesterol. Concomitant medication(s) included: LEVOTHYROXINE taken for hypothyroidism; SYNTHROID taken for hypothyroidism; PRAVASTATIN taken for blood cholesterol; METOPROLOL SUCCINATE taken for hypertension; ALENDRONATE SODIUM taken for bone disorder. Vaccination history included: Covid-19 vaccine (primary immunization series completed, unknown manufacturer), for COVID-19 Immunization. The following information was reported: PAIN (non-serious) with onset 22Oct2022, outcome "unknown", described as "Achiness"; CHILLS (non-serious) with onset 22Oct2022, outcome "not recovered", described as "After I went to bed, I started developing chills"; FATIGUE (non-serious) with onset 22Oct2022, outcome "unknown", described as "I spent all day, Saturday in bed. I was just that tired."; PYREXIA (non-serious) with onset 22Oct2022, outcome "recovered", described as "a low grade fever of 99.3"; MALAISE (non-serious) with onset 22Oct2022, outcome "unknown", described as "general unwell feeling"; MYALGIA (non-serious) with onset 22Oct2022, outcome "unknown", described as "generalized muscle pain"; NAUSEA (non-serious) with onset 22Oct2022, outcome "unknown". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: It was reported that she just wanted to report some very mild side effects, she received Covid Bivalent Booster shot (Clarified as: Pfizer Covid-19 Vaccine Bivalent). She received it on Friday in the early afternoon and she was just fine all Friday, came back home, did everything. But after she went to bed, she started developing chills, a low grade fever of 99.3, achiness, generalized muscle pain, nausea, no vomiting, and just a general unwell feeling. She spent all day, Saturday in bed. She was just that tired. She would get up, attend to her cats and go back to bed. On Sunday, She was feeling a little bit better but she took the precaution of calling in for work tomorrow because She was still not feeling a 100 percent, She still felt chills, She did not check her temperature but she said probably. She do not know, if she was normal yet or not? But they are all very mild, nothing that she would be terribly concerned about but she though. Treatment: Consumer reported that No. she stayed home and in bed. She was doing the same except she was actually managing to get out of bed and just maintaining good fluids, drinking some orange juice, lots of water, keeping herself warm since she was still experiencing the chills though she did check her temperature, she do not have a fever at that point. But still have the chills. She had the temperature up to 78 Degrees in her house but she was still feeling cold. Other medical conditions and concomitant medications: Consumer reported that she took other medications and yes one of them is for High Blood Pressure. Her prescription medications she took Synthroid or Levothyroxine 50mcg for Hypothyroidism(not clarified hence, captured both), Pravastatin 40mg, that's for Cholesterol, Buspar Hydrocloride' 5mg (further not clarified). One Tablet twice a day that's for Anxiety and stress, Metoprolol Succinate 25 mg, One Tablet, Twice a day for High Blood Pressure and Alendronate Sodium otherwise known as Fosamax 70 milligrams, getting her bones back to their good health. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20221022; Test Name: Body temperature; Result Unstructured Data: Test Result:99.3; Comments: a low grade fever of 99.3
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety (Comments: Anxiety); Blood pressure high (Comments: High Blood Pressure); Cholesterol (Indication for use in the case: Cholesterol); Hypothyroidism (Indication for use in the case: Hypothyroidism); Stress (Comments: Stress)
Andere Medikamente: LEVOTHYROXINE; SYNTHROID; PRAVASTATIN; METOPROLOL SUCCINATE; ALENDRONATE SODIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2490827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: MA
Alter: 53,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Arthralgia Back pain Lymph node pain Lymphadenopathy Off label use Product use issue

Symptomtext

Swollen painful lymph nodes - both under-arms and neck; Swollen painful lymph nodes - both under-arms and neck; lower back pain; joint pain; Other vaccine same date product: Flu, Other vaccine same date vaccine date: 21Oct2022; Other vaccine same date product: Flu, Other vaccine same date vaccine date: 21Oct2022; 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 21Oct2022 at 19:00 as dose 4 (booster), single (Lot number: GJ6665) at the age of 53 years, in left arm for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), on 21Oct2022 as dose 1, single (Batch/Lot number: unknown), in left arm. The patient's relevant medical history included: "Heart palpitations (SVT)" (unspecified if ongoing); "Heart palpitations (SVT)" (unspecified if ongoing); "Allergy to shellfish" (unspecified if ongoing). Concomitant medication(s) included: PROPRANOLOL; NAPROXEN; AMBEREN; BIOTIN. Vaccination history included: BNT162b2 (Dose 1 Single, Batch/Lot No: EW0150, Location of injection: Arm Left), administration date: 10Apr2021, when the patient was 52-year-old, for COVID-19 immunization, reaction(s): "The morning after: some joint pain, severe pain in spine but only lasted a couple of hours", "The morning after: some joint pain, severe pain in spine but only lasted a couple of hours", "About 24 hours after shot: swollen hands and feet but was gone by the second morning", "About 48 hours after shot: sore, swollen lymph nodes, also stabbing pains in the lymph nodes (neck, armpits, left side of chest and groin)", "About 48 hours after shot: sore, swollen lymph nodes, also stabbing pains in the lymph nodes (neck, armpits, left side of chest and groin)"; BNT162b2 (Dose 2 Single, Batch/Lot No: EW0170, Location of injection: Arm Left), administration date: 02May2021, when the patient was 52-year-old, for COVID-19 immunization, reaction(s): "swollen lymph nodes"; BNT162b2 (Dose 3 Single, Batch/Lot No: FJ8762, Location of injection: Arm Left), administration date: 08Dec2021, when the patient was 52-year-old, for COVID-19 immunization, reaction(s): "lymph nodes were swollen". The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 21Oct2022, outcome "unknown" and all described as "Other vaccine same date product: Flu, Other vaccine same date vaccine date: 21Oct2022"; LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 22Oct2022 at 17:30, outcome "recovering" and all described as "Swollen painful lymph nodes - both under-arms and neck"; ARTHRALGIA (non-serious) with onset 22Oct2022 at 17:30, outcome "recovering", described as "joint pain"; BACK PAIN (non-serious) with onset 22Oct2022 at 17:30, outcome "recovering", described as "lower back pain". Therapeutic measures were not taken as a result of lymphadenopathy, lymph node pain, back pain, arthralgia. Additional information: The patient did not know the lot number of other vaccine given on same date. The patient did not receive other vaccine in four weeks. The patient was not diagnosed with covid prior to vaccination. The patient was not tested for covid post vaccination. Adverse event: Swollen painful lymph nodes-both under-arms and neck, lower back pain, joint pain. For the first 2 shots the swollen lymph nodes lasted 3 weeks but almost all lymph nodes were swollen for the first few days, then only my neck and left underarm. The 3rd shot, the lymph nodes were swollen for less than a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Palpitations; Shellfish allergy; Supraventricular tachycardia
Andere Medikamente: PROPRANOLOL; NAPROXEN; AMBEREN; BIOTIN
Allergien: -
Vorherige Impfungen: -

VAERS 2490199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 24.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Nausea

Symptomtext

weakness, nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Parkinson disease , diabetes, Afib
Andere Medikamente: abilify , amitriptyline ,rivaroxaban, cetirizine, clonazepam , potassium chloride ER, bumetanide, lidocaine patch 5%, ondansetron hcl, lansoprazole, Sinemet, amlodipine, simvastatin, Cymbalta, calcium carbonate, cholecalciferol, lactobacill
Allergien: Apixaban, Aspirin, Baclofen, carBAMazepine, Cephalexin, Chlorhexidine, Ciprofloxacin, Clindamycin, dilTIAZem, Doxycycline, Gabapentin, Haloperidol, Lactose (Intolerance), lamoTRIgine, Lisinopril, Losartan, Metoprolol, Omeprazole, Oxcarbazepine, Penicillin, predniSONE, traZODone, Vancomycin, Flonase, NSAIDs, Penicillins, Sulfa Antibiotics, Scallop, Turmeric, Acai, Acetylcarnitine, ADHESIVE, aloe vera, ciprocinonide, Magnesium Citrate, Magnesium Sulfate, Neomycin-bacitracin-polymyxin
Vorherige Impfungen: -

VAERS 2488473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 11,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Malaise Pallor

Symptomtext

After patient received both vaccines from LVN, pt started to complain of dizziness and "not feeling well". pt appeared pale. Pt was given water and juice, remained completely alert and oriented with age-appropriate mentation. Pt denied pain, difficulty breathing, rash, or itching. Pt was able to ambulate from a chair to a gurney where he was observed for another 10 min with parent standing by. Pt reported then that he felt better and parent expressed that she felt comfortable with taking patient home. patient ambulated out of vaccine clinic with a steady gait, accompanied by parent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none were reported by parent
Vorgeschichte: none were reported by parent
Andere Medikamente: pt has Rx for epi-pen
Allergien: amoxicillin, pine nut
Vorherige Impfungen: -

VAERS 2488425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 07.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Chills Pain Pyrexia

Symptomtext

101 fever Body aches Chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Raynauds
Andere Medikamente: Multi vitamin Vitamin d Fish oil
Allergien: Penicillin Erythromycin Septra
Vorherige Impfungen: Pfizer Covid 19 3/11/21 Pfizer Covid 19 4/01/21 Pfizer Covid 19 11/19/21 Fever Muscle aches Chills

VAERS 2487902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 25.10.2022
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

Nausea Vomiting

Symptomtext

Systemic: Nausea-Mild, Systemic: Vomiting-Mild

Weitere VAERSDATA-Felder

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

VAERS 2487223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 66,0
Geschlecht: M
Eingang: 24.10.2022
Impfdatum: 10.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Body temperature increased Chills Choking sensation Feeling abnormal Feeling hot Impaired work ability Malaise Muscle tightness Pain Tinnitus

Symptomtext

At or around five AM I had chills and my body ached in addition I felt like someone had their hand around my neck, like it was being choked or squeezed, I checked my temperature as I felt hot it was 99.8 I drank a lot of liquids and took ibuprofen. I had to miss work due to not feeling good upon returning to work I have still not felt well and I have been running a low grade or elevated temperature that has lasted until 10/23/2022 in addition I have a ringing in my ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Levothyroxine; Androgel
Allergien: Zoloft; Sulfa
Vorherige Impfungen: -

VAERS 2486680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: AR
Alter: 64,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 11.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 9,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal pain upper Blood test Cholecystectomy Computerised tomogram Dizziness Laboratory test Laparoscopic surgery Ultrasound scan Weight decreased

Symptomtext

10.20.2022 PATIENT CAME IN FOR DIZZINESS, WEIGHT LOSS, AND ABDOMINAL PAIN IN RIGHT UPPER QUADRANT. PATIENT WAS ADMITTED AND HAD A LAPROSCOPIC CHOLECYSTECTOMY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: BLOOD LABS, CT SCAN, ULTRA SOUND ON 10.20.2022
Aktuelle Erkrankungen: WEIGHT LOSS, DIZZINESS, FATIGUE
Vorgeschichte: ANXIETY, PAIN, EMPHYSEMA, HYPERTENSION, HYPOTHYROIDISM, OSTEOPOROSIS
Andere Medikamente: ALBUTEROL, CITALOPRAM, FLUOXETINE, ADVAIR, FUROSEMIDE, LEVOTHYROXINE, LOSARTAN, OMEPRAZOLE, POTASSIUM CHLORIDE, SPIRONOLACTONE, FORTEO, SPIRIVA
Allergien: BENICAR, PENICILLIN, STRAWBERRY
Vorherige Impfungen: -

VAERS 2486593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 11,0
Geschlecht: F
Eingang: 23.10.2022
Impfdatum: 18.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered Vaccination site pain

Symptomtext

Father brought his daughter, patient, for her latest Pediatric Pfizer Bivalent Booster and instead one of the nurse at our clinic administered her Adult Pfizer Bivalent Booster. I called the father as soon as the error was discovered but could not reach him until the more than 24 hours later. Father assured me that patient was doing well and only experienced mild soreness of the arm where the vaccine was given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: Not necessary.
Aktuelle Erkrankungen: None mentioned by her father.
Vorgeschichte: None mentioned by her father.
Andere Medikamente: Father brought his daughter, patient, for her latest Pediatric Pfizer Bivalent Booster and instead one of the nurse at our clinic administered her Adult Pfizer Bivalent Booster. I called the father as soon as the error was discovered but c
Allergien: None mentioned by her father.
Vorherige Impfungen: -

VAERS 2486439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: WA
Alter: 30,0
Geschlecht: M
Eingang: 23.10.2022
Impfdatum: 20.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Injection site joint pain

Symptomtext

Join pain in the left shoulder

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site joint pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, high cholesteral, Seasonal pollen allergies
Andere Medikamente: Fish oil, Fenofibrate, Fexofenadine, vitamin D supplement
Allergien: Zithromycin, Minocycline
Vorherige Impfungen: -

VAERS 2486340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: SC
Alter: 74,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 19.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Chills Erythema Pain Peripheral swelling Pyrexia

Symptomtext

Fever, chills, with redness, pain, and swelling of arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Afib, paemaker
Andere Medikamente: -
Allergien: Pt has a long list of allergies, I do not have the complete list.
Vorherige Impfungen: -

VAERS 2486254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 13.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Injection site erythema Injection site pain

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 06.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Incorrect dose administered Pain in extremity

Symptomtext

5th booster dose of BNT162B2 administered; sore arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Oct2022 at 16:00 as dose 5 (booster), single (Lot number: GJ6665) at the age of 76 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Seasonal allergies" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6204), administration date: 11Mar2021, when the patient was 74-year-old, for COVID-19 Immunization, reaction(s): "sore arm"; BNT162b2 (DOSE 2, SINGLE; Lot number: ER8733), administration date: 31Mar2021, when the patient was 74-year-old, for COVID-19 immunization, reaction(s): "sore arm"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot number: EW0172), administration date: 15Nov2021, when the patient was 75-year-old, for COVID-19 Immunization, reaction(s): "sore arm"; BNT162b2 (DOSE 4 (BOOSTER), SINGLE; Lot number FJ6369), administration date: 25Apr2022, when the patient was 75-year-old, for COVID-19 Immunization, reaction(s): "sore arm"; flu (With the flu shot, just a sore arm, nothing to whine or complain about.), administration date: 26Oct2021, when the patient was 75-year-old, for Immunization, reaction(s): "sore arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 06Oct2022, outcome "recovered" (07Oct2022), described as "sore arm"; INCORRECT DOSE ADMINISTERED (non-serious) with onset 06Oct2022 at 16:00, outcome "unknown", described as "5th booster dose of BNT162B2 administered". Additional information: It was reported the person got bivalent vaccine and had no side effects other than sore arm. She had no problems with the first 4 doses, there was a bit of sore arm and she had less of a sore arm with this one and it was maybe just overnight and by the next night was fine. It was nothing she really noticed that evening and when she went to bed was when she noticed it, it was a little less than the others. It was totally gone at most in 24 hours. No additional vaccines administered on same date of the Pfizer suspect. The adverse events did not require a visit to emergency room and physician office.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201241911 same reporter/patient/AE, different dose;US-PFIZER INC-202201241912 same reporter/patient/AE, different dose;US-PFIZER INC-202201241913 same reporter/patient/AE, different dose;US-PFIZER INC-202201241914 same reporter/patient/AE, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seasonal allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2485791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: IN
Alter: 48,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 13.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Back pain Fatigue Musculoskeletal pain

Symptomtext

Sore back, debilitating. Mostly between and below shoulder blades . No neck pain. No paint at waist. Also fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Ulcerative Colitis
Andere Medikamente: Stelara 90mg/ml syringe, every 8 weeks
Allergien: -
Vorherige Impfungen: Flu-like symptoms, fatigue. age 47, 05Mar2021 Pfizer EJ6198, 07Jul2021 Pfizer ER8730, 31Oct2021 Pfizer booster FC3181. age 48,

VAERS 2485626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MI
Alter: 38,0
Geschlecht: F
Eingang: 21.10.2022
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

Eyelid oedema Eyelids pruritus

Symptomtext

Left eyelid edema with slight itching

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eyelids pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Parvovirus
Vorgeschichte: -
Andere Medikamente: B complex, vitamin c, zinc, vitamin d
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2485506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 31,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 15.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Eye pain Headache Influenza virus test Myalgia Pyrexia Respiratory syncytial virus test SARS-CoV-2 test

Symptomtext

On 10/18 I started feeling weak; ophthalmalgia; 101-degree fever; headache and muscle aches for 4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Influenza; COVID and RSV
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi Vitamin; Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2485438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered Injection site pain Injection site swelling

Symptomtext

Pt recevied J and J vaccine on 4/12/21 and Moderna 11/9/21 and came to clinic for the bivalent Pfizer vaccine on 10/18/22. Due to mix up of the Pfizer monovalent and bivalent vaccine- she may have gotten either the monovalent or bivalent Pfizer vaccine. She has some pain and swelling of the upper arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Squamous cell ca of skin, hypothyroidism, GERD, Migraine, PTSD
Andere Medikamente: -
Allergien: Bactrim, Morphine, Seafood, Rubber, Prevnar 13
Vorherige Impfungen: -

VAERS 2485417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 62,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 03.10.2022
Beginn: 03.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Headache Injection site erythema Injection site hypoaesthesia Injection site nodule Injection site swelling Injection site warmth Night sweats Pyrexia

Symptomtext

Evening: night sweats Day 2: 100F fever in a.m., headache in afternoon Day 3: large (2-3 in diameter) red welt at injection site; raised skin was warm and slightly numb. Fever and headache gone. Day 4: welt reduced in size, no longer warm or numb. Day 5: all symptoms resolved. Treatment: test, acetaminophen Days 1 and 2, lots of fluid all days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Graves, Myasthenia Gravis
Andere Medikamente: Metformin 500MG 1X daily Atorvastatin 20 MG 1X daily Levothyroxine 50 mcg 1x daily (discontinued now) Vitamin D3 125 mcg (5000 IU) 1X daily Centrum for Einen multivitamin (every other day)
Allergien: None
Vorherige Impfungen: Server headache for one solid day after 2nd Pfizer shot in two-dose covid series; age 61, 04182021, Lot EW0151 at local Vaccinat

VAERS 2485152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 21.10.2022
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

Chills Pain Pyrexia

Symptomtext

Extreme body aches that lasted 20 hours and did not respond to Ibuprofen. Chills. Low-grade fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothroxine; Timolol
Allergien: None
Vorherige Impfungen: -

VAERS 2483515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 08.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Injection site reaction Lymph node pain

Symptomtext

Severe lymph pain right shoulder x10 days not subsiding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Attention Deficit Disorder GERD Facet Joint Syndrome Arthritis
Andere Medikamente: Lisinopril/HCZ Ritalin Prevacid Vitamin D Claritin Multivitamin B12
Allergien: Bactrim Bacitracin Sodium Laurel Sulfate Colophony Hydrocortisone Amidoamine
Vorherige Impfungen: -

VAERS 2481998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj6665

mild

Staat: GA
Alter: 22,0
Geschlecht: F
Eingang: 18.10.2022
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: ja Erholt: nein

Feeling abnormal Flushing Nausea Pruritus Swelling

Symptomtext

pt came back after receiving both vaccines stating she is feeling weird. She has a history of serious allergic reaction to red dye but not the flu shot or the first two covid doses of pfizer. She started feeling flush, nauseous, itchy and then developed swelling in neck. Pt was given 150 mg of liquid benadryl and we started her breathing treatment with albuterol. EMS was called and 1 dose of 0.3 epinpen was given in right thigh. Pt reported the need of a second dose which was given in the left thigh 15 minutes later. EMS arrived and pt was passed off and taken to local hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: severe allergies, gastroparesis, insomnia
Vorgeschichte: severe allergies
Andere Medikamente: breo, gabapentin, allegra, olopatadine, auvi-q
Allergien: ibuprofen, milk, red dye
Vorherige Impfungen: -

VAERS 2481320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 83,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Injection site pain Resuscitation

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Additional Details: patient got both shots and complaint of dizziness i told him to keeping seating while a call 911. The paramentics came in started cpr and took the patient away to the hospital

Weitere VAERSDATA-Felder

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

VAERS 2481176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: CT
Alter: 26,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 08.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Body temperature Pyrexia

Symptomtext

Fever of 103.9 all day Sunday; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 26-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Oct2022 at 17:30 as dose 4 (booster), single (Lot number: GJ6665) at the age of 26 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: LAMICTAL; CLONIDINE. 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: PYREXIA (non-serious) with onset 09Oct2022 at 00:30, outcome "not recovered", described as "Fever of 103.9 all day Sunday". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia. Additional information: Fever of 103.9 all day Sunday, did respond to Tylenol and Advil but spiked again 4-6 hours later. No covid prior vaccination. Not covid tested post vaccination. No known allergies. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20221009; Test Name: Fever; Result Unstructured Data: Test Result:103.9 Fahrenheit; Comments: Fever of 103.9 all day Sunday
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LAMICTAL; CLONIDINE
Allergien: -
Vorherige Impfungen: -

VAERS 2480462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NH
Alter: 60,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 07.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Injection site pain Myalgia

Symptomtext

1 week and 1 day after the vaccination was administered, my upper left arm became extremely sore (muscle achiness, but without any swelling, redness or heat). This lasted for 2 days and resolved by the third day. I took Advil to reduce the pain. I had received 3 Moderna vaccines before this Pfizer Bivalent booster and never had this type of a reaction.

Weitere VAERSDATA-Felder

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

VAERS 2480414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 54,0
Geschlecht: M
Eingang: 17.10.2022
Impfdatum: 01.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Diarrhoea Discomfort Lethargy Malaise Nasal congestion SARS-CoV-2 test positive Sinus pain

Symptomtext

Began experiencing symptoms on October 8th. Began with nasal congestion, sinus pain, and pressure. By Monday I began having extreme lethargy. Possible low grade fever. On Wednesday and Thursday began having diarrhea. Began taking PAXLOVID on Monday October the 10th. Symptoms persisted until 10/15.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Positive at home COVID-19
Aktuelle Erkrankungen: No
Vorgeschichte: Mold allergy
Andere Medikamente: ALLEGRA; SINGULAIR; vitamin C; fish oil; multivitamin; OCUVITE for vision
Allergien: Sulfa; mold allergy
Vorherige Impfungen: -

VAERS 2479932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: MD
Alter: 83,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 16.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / LA

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

Rash

Symptomtext

Rash on left arm, 139/78 Blood pressure Pulse 64 temp 99.9

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Arthritis, Borderline elevated blood pressure
Andere Medikamente: None
Allergien: -
Vorherige Impfungen: Swelling, sore arm

VAERS 2479752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: NM
Alter: 52,0
Geschlecht: F
Eingang: 16.10.2022
Impfdatum: 12.10.2022
Beginn: 15.10.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Cellulitis Hyperhidrosis Inflammation Pain Pain in extremity

Symptomtext

Patient experienced excessive sweating, pain and inflammation in right arm. Inflammation from shoulder to hand. Patient went to Emergency room where she was prescribed cephalexin and acetaminophen for cellulitis and pain. All events happened 10/15/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: None aware
Vorgeschichte: GERD, Depression, Anxiety
Andere Medikamente: Quetiapine, oxcarbazepine
Allergien: chlorotrianisene, tramadol, imidazole antifungals, penicillins
Vorherige Impfungen: -

VAERS 2479741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CO
Alter: 61,0
Geschlecht: F
Eingang: 16.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Headache Injection site discolouration Vision blurred

Symptomtext

PATIENT REPORTS WHITE 1/2" PATCH ON INJECTION SITE, BLURRED VISION FOR 24 HOURS AND HEADACE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: OSTEOPENIA
Vorgeschichte: OSTEOPENIA
Andere Medikamente: NASONEX, ASTELINE, ALLEGRA 24 HOUR ALLERGY DROPS, SINGULAR, FLOVENT, VITAMIN D3.
Allergien: FRAGRENCES, ENVIRONMENTAL
Vorherige Impfungen: NOT SURE BUT SHE HAS ADVERSE REACTION TO OTHERS

VAERS 2479636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: OR
Alter: 40,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 06.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Back pain Headache Herpes zoster Pain Rash

Symptomtext

6-7 days post injection developed rash that progressed and was diagnosed immediately as Shingles. Was not immunocompromised, ill, or on immunosuppressants at time of vaccination. Three days after start of shingles outbreak developed severe headache and back pain when walking near shingles dermatome nerve root. Received and have just as of 10/15 started vancyclovir treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Went to Urgent care for diagnosis. No skin tests but the herpetic outbreak in classic mid-torso dermatomal pattern and symptoms was part of a clear diagnosis from the physician. Currently undergoing treatment. I am a Vaccine Nurse at the pharmacy I work with, so while I prepare and administer these vaccines, the pharmacist administered mine to me- there was no administration error and the dosing was correct.
Aktuelle Erkrankungen: No known illnesses in this time prior to vaccination. Flu vaccine 4 weeks earlier. No signs/symptoms of acute or oncoming illness.
Vorgeschichte: Premenstrual Dysphoric Disorder Depression ADD
Andere Medikamente: Citalopram Vitamin C, B6, Selenium, Biotin, etc Diazepam PRN
Allergien: None
Vorherige Impfungen: -

VAERS 2478810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: IN
Alter: 51,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 05.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Dysphonia Fatigue Headache Injection site pain Oropharyngeal pain

Symptomtext

10/07/2022 experienced mild symptoms; fatigue, pain at injection site; headache; sore throat and hoarseness symptoms. I contacted my Physician via telehealth and was prescribed antibiotics.

Weitere VAERSDATA-Felder

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

VAERS 2478025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: NJ
Alter: 53,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 07.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / RA

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

Ageusia Measles Oropharyngeal pain Rhinorrhoea Vaccination site pain

Symptomtext

general measles; Runny nose; sore arm at the sight of injection; sore throat; Loss of taste; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). The reporter is the patient. A 53-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Oct2022 as dose number unknown (booster), single (Lot number: GJ6665) at the age of 53 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing), notes: I am taking hypertension medication . The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer), for COVID-19 immunisation. The following information was reported: AGEUSIA (non-serious) with onset 08Oct2022, outcome "not recovered", described as "Loss of taste"; MEASLES (medically significant), outcome "unknown", described as "general measles"; RHINORRHOEA (non-serious), outcome "unknown", described as "Runny nose"; VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "sore arm at the sight of injection"; OROPHARYNGEAL PAIN (non-serious), outcome "unknown", described as "sore throat". Therapeutic measures were not taken as a result of measles, ageusia, rhinorrhoea, vaccination site pain, oropharyngeal pain. Additional information: The patient had question if its possible to get a loss of taste as a side effect from the new booster shot. Had just got the new booster, the bivalent booster on Friday and experienced some loss of taste as well and wondered if that was a possible side effect from the booster shot. The patient takes other hypertension medication. The patient took covid, the home test this morning and it was negative. The patient stated it's defiantly persistent because this morning her family, she make breakfast and everybody was saying it's too sweet and it didn't taste sweet to her that's why, thought that she had loss sense of taste and yesterday it was salty, didn't taste that too. Patient calling for loss of taste, runny nose and then sore arm at the sight of injection and for the sore throat from this also and just the general measles and nothing patient have you to worried Follow-up attempts are completed. No further information is expected.; Sender's Comments: Based on the known information available the event MEASLES and is due to viral infection and not related to the suspect drug

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension (I am taking hypertension medication)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 52,0
Geschlecht: F
Eingang: 12.10.2022
Impfdatum: 11.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Arthralgia Neuralgia

Symptomtext

Starting around 1AM this morning, intermittent jolting pain in elbow- along path of ulnar nerve- feels like nerve pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic moderate adult onset asthma
Andere Medikamente: Symbicort Montelukast Cetirizine Vitamin D3
Allergien: N/A
Vorherige Impfungen: -

VAERS 2475773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: VA
Alter: 73,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 05.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Asymptomatic COVID-19 Blood pressure increased Dizziness Headache Injection site bruising Injection site induration Injection site pain Injection site swelling Injection site warmth SARS-CoV-2 test positive

Symptomtext

Patient stated she had a very large baseball size bump where vaccine as given. She described the bump as being bruised, hot to the touch, hard, painful. She was feeling dizzy, light headed, and had a head ache after getting the vaccine. Her blood pressure increased and she had the EMTs come to her house and she did go to the ER. The doctors stated she had a possible hematoma at the injection site. Doctor stated her side effects could be related to being asymptomatic COVID+ recently thus having an adverse reaction to the vaccine. Patient is feeling better but still a bit dizzy.

Weitere VAERSDATA-Felder

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

VAERS 2474500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 05.10.2022
Beginn: 06.10.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: ID / LA

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

Administration site urticaria Incorrect route of product administration Laboratory test Product administered at inappropriate site Urticaria Vaccination site cellulitis Vaccination site erythema Vaccination site pain Vaccination site reaction Vaccination site warmth

Symptomtext

Narrative: Patient received Pfizer COVID-19 Vaccine, Bivalent 0.3 ml 10/5/22 at 0757 AM. Administration site was not reported upon completion of clinical reminder. Per follow up evaluation, vaccine was administered incorrection-give ID rather then indicated IM. To note, clinical reminder does state IM but administration site was not indicated. On 10/6 he called to report a welt "golf ball" in size at administration site. Patient reported to the ED on 10/6m reporting vaccine was given in the left forearm and now the site is red hot and painful. He reported it was placed in his left forearm like a PPD snot. Per ER notes, "He does state that he did have lab work in his left antecubital fossa after the vaccination, but he states you can visibly see that puncture site is without any reactions, and his vaccination site is below his antecubital fossa in hi forearm." Supportive care was provided and area was traced with a pen to mark rash. He reported again on 10/7/22 as redness seemed to be spreading outside of the border of the pen marking and seem to be increasingly warm. He was prescribed cephalexin for cellulitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Administration site urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2473751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: TX
Alter: 93,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 06.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 1,0
Dosis: 6
Route/Site: IM / RA

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

Asthenia Extra dose administered Malaise Fatigue

Symptomtext

My mother had the new booster administered on 9/14/22 at hospital, then when Pharmacy came to give the flu and COVID booster, she was given the new booster again after only 3 weeks! She is feeling weak and very unwell since the following morning. I am very concerned about the short timeframe between the two boosters.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Heart issues, low blood pressure, anxiety and depression
Andere Medikamente: Midodrine, Atoravastatin, Multi-vitamin, Super B Complex vitamin, baby aspirin
Allergien: Latex
Vorherige Impfungen: -

VAERS 2473697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

mild

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 08.10.2022
Beginn: 08.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Fatigue Myalgia Pyrexia

Symptomtext

tired, sore muscles, aches throughout body, fever of 100 lasting 12 hours +; overall symptoms ongoing for 36 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Liothyronine, HRT replacement therapy
Allergien: sulpha drugs
Vorherige Impfungen: Pfizer BioNTech EN6201 3/5/2021

VAERS 2473429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

mild

Staat: CA
Alter: 75,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / RA

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

Body temperature abnormal Erythema Headache Inflammation Injection site erythema Injection site pruritus Injection site swelling Pruritus Skin swelling Tenderness

Symptomtext

It seemed to be the usual tenderness and slight redness and puffy. Size = small a dime size maybe. Friday 10/7 Then in a few hours some itching, headache, mild temperature.Saturday 10/8 - I slept and when I woke I was REALLY itchy and looked at the sight. It was Very red and TERRIBLY itchy and swollen and the size was about 1.5 - 1.75 inches. It looked "mean". I took another tylenol and allegra as above. Then on Sunday 10/9 the red patch looked inflamed, itchy as before and a feeling of hives in my left hand*. Meds taken as before. 10/10 - The size of the red spot remained about 1.5 inches. The itching lessened and while still red swelling reduced.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: AFib, mild asthma, allergies
Andere Medikamente: 50 mg metoprolol 1 x day, Centrum Silver vitamin 1 x day, took a 500 mg tylenol for headache and an allegra for itching after vaccination
Allergien: shell fish, fin fish, strawberries, salicylates, iodine etc. preservatives in Restasis, adhesives on bandaids and relates products, surgical glue, wool
Vorherige Impfungen: -

VAERS 2726588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: NJ
Alter: 69,0
Geschlecht: F
Eingang: 22.12.2023
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; vaccine brand other=moderna/ vaccine brand=Pfizer / BioNTech/ vaccine brand other=moderna; This is a spontaneous report received from a Consumer or other non HCP. A 70-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Oct2022 at 14:00 as dose number unknown, single (Lot number: GJ6665) at the age of 69 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 20Jun2022 as dose number unknown, single (Lot number: 056A22A), in left arm and on 21Sep2023 at 11:00 as dose number unknown, single (Lot number: 3030368), in left arm for covid-19 immunisation. The patient's relevant medical history included: "glaucoma" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing). Concomitant medication(s) included: VALACYCLOVIR [VALACICLOVIR], start date: 09Oct2012, stop date: 18Dec2023; ATORVASTATIN, start date: 04Oct2018, stop date: 18Dec2023. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 18Oct2022 at 14:00, outcome "unknown", described as "vaccine brand other=moderna/ vaccine brand=Pfizer / BioNTech/ vaccine brand other=moderna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid from 08Dec2023 to 12Dec2023. Clinical course: Patient had no known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Glaucoma; High cholesterol
Andere Medikamente: VALACYCLOVIR [VALACICLOVIR]; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2723895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: TN
Alter: 41,0
Geschlecht: F
Eingang: 14.12.2023
Impfdatum: 04.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

Moderna 01Dec2021 / Pfizer / BioNTech 04Dec2022; 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 42-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Dec2022 at 12:00 as dose 4 (booster), single (Lot number: GJ6665) at the age of 41 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 15Mar2021 at 12:00 as dose 1, single (Lot number: 032M20A), in left arm, on 16Apr2021 at 12:00 as dose 2, single (Lot number: 027B21A), in left arm and on 01Dec2021 at 12:00 as dose 3 (booster), single (Lot number: O30H21B), in right arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "Treatment of COVID-19"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown", described as "Moderna 01Dec2021 / Pfizer / BioNTech 04Dec2022". Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2720785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: AL
Alter: 64,0
Geschlecht: F
Eingang: 04.12.2023
Impfdatum: 08.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / UN

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

Lymphadenopathy Musculoskeletal stiffness

Symptomtext

swollen Lymph nodes on collar bone; stiff neck

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymphadenopathy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: ace inhibitors
Vorherige Impfungen: -

VAERS 2713510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: OR
Alter: -
Geschlecht: F
Eingang: 14.11.2023
Impfdatum: 12.10.2022
Beginn: 26.10.2023
Tage bis Beginn: 379,0
Dosis: 5
Route/Site: - / -

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

Blood test COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Pfizer vaccines dose 1,2,3,4,5 and Moderna vaccine; Caller reports all her prior COVID-19 vaccinations were Pfizer but one may have been Moderna/she tested positive on 26Oct2023 while in the hospital; Caller reports all her prior COVID-19 vaccinations were Pfizer but one may have been Moderna/she tested positive on 26Oct2023 while in the hospital; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team and product quality group. The reporter is the patient. An 80-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 as dose 5 (booster), single (Lot number: GJ6665) for covid-19 immunisation; bnt162b2 (BNT162B2), on 09May2022 as dose 4 (booster), single (Lot number: FJ4991) for covid-19 immunisation; bnt162b2 (BNT162B2), on 29Jan2021 as dose 1, single (Lot number: EN6202), on 17Mar2021 as dose 2, single (Lot number: EN6208) and on 11Oct2021 as dose 3 (booster), single (Lot number: FE3292) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), as dose 6 (booster), single (Lot number: RA5325) for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), in Sep2023 as dose number unknown, single (Batch/Lot number: unknown) for influenza immunisation. The patient's relevant medical history included: "High cholesterol" (unspecified if ongoing). Concomitant medication(s) included: SIMVASTATIN taken for blood cholesterol increased. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 26Oct2023, outcome "unknown" and all described as "Caller reports all her prior COVID-19 vaccinations were Pfizer but one may have been Moderna/she tested positive on 26Oct2023 while in the hospital"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown", described as "Pfizer vaccines dose 1,2,3,4,5 and Moderna vaccine". The patient underwent the following laboratory tests and procedures: Blood test: (26Oct2023) Normal; SARS-CoV-2 test: (26Oct2023) Positive, notes: when she tested positive on 26Oct2023. Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Test Date: 20231026; Test Name: blood work; Result Unstructured Data: Test Result:Normal; Test Date: 20231026; Test Name: tested for COVID; Test Result: Positive ; Comments: when she tested positive on 26Oct2023
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol
Andere Medikamente: SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2699633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: CA
Alter: 71,0
Geschlecht: M
Eingang: 21.10.2023
Impfdatum: 12.10.2022
Beginn: 05.09.2023
Tage bis Beginn: 328,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Oct2022 at 10:45 as dose 5 (booster), single (Lot number: GJ6665) at the age of 71 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 20Apr2022 at 13:00 as dose 4 (booster), single (Lot number: FP4554), in right arm for covid-19 immunisation; covid-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "GERD" (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 05Sep2023, outcome "recovered" (14Sep2023) and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Sep2023) Negative, notes: Began to test negative via home test on 14Sep2023. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid from 07Sep2023 to 12Sep2023. Clinical course: Patient did not have known allergies.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300333390 same patient, different drug/AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230914; Test Name: Covid-19 virus test/ home test; Test Result: Negative ; Comments: Began to test negative via home test on 14Sep2023
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2695283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 13.10.2023
Impfdatum: 03.10.2022
Beginn: 01.09.2023
Tage bis Beginn: 333,0
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 contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Oct2022 at 16:30 as dose 4 (booster), single (Lot number: GJ6665) at the age of 61 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 10Jun2022 as dose 3 (booster), single (Lot number: FM0173), in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 05Mar2021 as dose 1, single (Lot number: EP6955), in left arm and on 26Mar2021 as dose 2, single (Lot number: EP6955), in right arm for covid-19 immunisation. The patient's relevant medical history included: "T2 diabetes" (unspecified if ongoing); "migraines" (unspecified if ongoing); "obesity" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: MELATONIN, start date: 01Jul2021; TRUBIOTICS ONE A DAY, start date: 01Oct2021; ZOLMITRIPTAN, start date: 06Jul2005. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Sep2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Patient received Paxlovid from 22Sep2023 to 27Sep2023 for the treatment of Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Migraine; Obesity; Penicillin allergy; Type 2 diabetes mellitus
Andere Medikamente: MELATONIN; TRUBIOTICS ONE A DAY; ZOLMITRIPTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2691339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: VA
Alter: 64,0
Geschlecht: M
Eingang: 05.10.2023
Impfdatum: 03.10.2023
Beginn: 03.10.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SC / LA

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

Agitation Irritability

Symptomtext

During the evening, overnight and the following day until Noon, I was hyper-agitated and hyper-irritable. It started abruptly and ended abruptly. Nothing in my routine had changed or was non-typical except for the booster shot. It felt very intense during that 12 hour period.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Agitation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Light typical Covid Booster side effects short lived

VAERS 2690909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: CO
Alter: 66,0
Geschlecht: M
Eingang: 04.10.2023
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test Wrong product administered

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; Wrong vaccine administered; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 25Oct2022 at 12:30 as dose 1, single (Lot number: GJ6665) at the age of 66 years, in left arm for covid-19 immunisation. The patient didn't receive bnt162b2 (BNT162B2). The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 25Oct2022 at 12:30, outcome "unknown", described as "Wrong vaccine administered"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2023, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures as Paxlovid were taken as a result of drug ineffective, covid-19 from 19Sep2023 to 23Sep2023. The information on the batch/lot number for bnt162b2 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300315083 same patient, different drug and different AE.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 17,0
Geschlecht: F
Eingang: 02.10.2023
Impfdatum: 20.07.2023
Beginn: 20.07.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 41,0
Geschlecht: F
Eingang: 02.10.2023
Impfdatum: 10.07.2023
Beginn: 10.07.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 63,0
Geschlecht: F
Eingang: 02.10.2023
Impfdatum: 07.12.2022
Beginn: 07.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 44,0
Geschlecht: F
Eingang: 02.10.2023
Impfdatum: 13.12.2022
Beginn: 13.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 69,0
Geschlecht: M
Eingang: 02.10.2023
Impfdatum: 13.12.2022
Beginn: 13.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 45,0
Geschlecht: M
Eingang: 02.10.2023
Impfdatum: 16.12.2022
Beginn: 16.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Product storage error

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 47,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 03.07.2023
Beginn: 03.07.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 36,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 27.06.2023
Beginn: 27.06.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 13,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 27.06.2023
Beginn: 27.06.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 13,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 14.06.2023
Beginn: 14.06.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 21,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 09.06.2023
Beginn: 09.06.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 19,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 17.05.2023
Beginn: 17.05.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 33,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 17.05.2023
Beginn: 17.05.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 42,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 16.05.2023
Beginn: 16.05.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 57,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 05.05.2023
Beginn: 05.05.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 19.04.2023
Beginn: 19.04.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688537

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ6665

gering

Staat: NJ
Alter: 50,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 11.04.2023
Beginn: 11.04.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 17,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 19.12.2022
Beginn: 19.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 55,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 20.12.2022
Beginn: 20.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 63,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 27.12.2022
Beginn: 27.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Product storage error

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 45,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 27.12.2022
Beginn: 27.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 06.04.2023
Beginn: 06.04.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688508

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 39,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 03.04.2023
Beginn: 03.04.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 78,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 29.12.2022
Beginn: 29.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 63,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 30.12.2022
Beginn: 30.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 65,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 04.01.2023
Beginn: 04.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 49,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 04.01.2023
Beginn: 04.01.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 66,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 04.01.2023
Beginn: 04.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 30,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 06.01.2023
Beginn: 06.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 59,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 06.01.2023
Beginn: 06.01.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 06.01.2023
Beginn: 06.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 63,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 06.01.2023
Beginn: 06.01.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 19,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 06.01.2023
Beginn: 06.01.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 28,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 09.01.2023
Beginn: 09.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 40,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 12.01.2023
Beginn: 12.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 61,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 65,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 13.01.2023
Beginn: 13.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 35,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 18.01.2023
Beginn: 18.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 76,0
Geschlecht: F
Eingang: 29.09.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 79,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 62,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 24.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 45,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 25.01.2023
Beginn: 25.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 61,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 27.01.2023
Beginn: 27.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 39,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 30.01.2023
Beginn: 30.01.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2688454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ6665

gering

Staat: NJ
Alter: 35,0
Geschlecht: M
Eingang: 29.09.2023
Impfdatum: 10.02.2023
Beginn: 10.02.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient received COVID 19 vaccine that had been stored beyond the Beyond Use Date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -