VAERS Reports #FH8020

VAERS 2707253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 31.10.2023
Impfdatum: 19.11.2021
Beginn: 19.09.2023
Tage bis Beginn: 669,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anaemia Asthma Blood folate Blood iron Blood pH decreased Blood urea normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Coagulation test Computerised tomogram thorax abnormal Condition aggravated Cough Dyspnoea Echocardiogram Ejection fraction normal

Symptomtext

Patient is a 84 years old female patient of, DO with history of chronic hypoxic respiratory failure, COPD, CAD, HTN, HLD, and depression presented to Hospital with shortness of breath, cough. Admitted and being managed for acute on chronic hypoxic respiratory failure, pneumonia COVID COPD exacerbation. Not much significant success with weaning off supplemental oxygen complicated by patient's inability to expel sputum. Acute on chronic hypoxic respiratory failure, COVID-19 infection COPD/Asthma with mild acute exacerbation Pulmonary HTN, presumed Group 3 Bacterial pneumonia Presented with 1 week history of non-productive cough and worsening SOB. Patient fully vaccinated and 1 booster Afebrile, HR 77, RR 15, BP 125/71, satting >94% on 2L NC (2L qHS at home) Initial CBC w slight leukocytosis to 11.76. Hgb 10.5. ProBNP 3.2K CXR: No vascular congestion or consolidation PFT 2016: FEV/FVC 0.54, FEV1 39% (22% reversible), TLC 201% Echo 3/2023 with EF 72%, TRVmax 3.59 m/s (RVSP 62) VBG showed pH of 7.25 with PCO2 66.2 Chest x-ray done showed left infrahilar streaky opacity likely represent focal pneumonia and/or aspiration. CT of the chest without contrast showed development of a peripheral airspace consolidation left lower lobe and to a lesser extent peripheral IVs in the dependent right lower lobe which may indicate aspiration and/or pneumonia. There is also numerous scattered bilateral multilobar tree-in-bud nodular opacity indicating underlying small airway inflammatory changes. Switch IV Solu-Medrol to Decadron IV if in case COVID infection contributed to lung finding. Patient started on Zosyn on 9/22, started on vancomycin but stopped as MRSA screen is negative Cont supplemental O2 to maintain goal SpO2 > 88-90% Continue Mucinex, ipratropium DuoNeb . Fluctuating oxygen requirement, wean down to 2 L baseline Scheduled Mucinex added. Acapella, bedside incentive spirometry Acute normocytic Anemia Presumed ABLA from UGIB Melena Pt reports 3 month of black, tarry stool with worsening fatigue and SOB Denies chronic NSAID use. Pt takes eliquis and plavix Initial Hgb 10.5 (from 12.3 in 7/2023), plts 295. BUN 16. +FOBT Last colonoscopy 11/2020: benign, per patient Type and screen, coags, LFTs Monitor with serial labs, transfuse for Hgb < 7 Additional IVFs as needed Protonix 40mg IV bid Surgery consulted for scope Iron study showed iron of 13, ferritin is 260, iron saturation is 5%, TIBC is 201, folate 9.8 Hemoglobin remained stable, it is 10.5, was 10.5 on 9/19 Continue home iron tablet. NSTEMI, likely type 2 due to demand HTN, HLD Non-obstructive CAD HFpEF, compensated Paroxysmal afib with RVR HDS on admission, complaining of SOB but denies chest pain or palpitations Initial trop 38 Keep on cardiac monitor 2D echo on 3/25/2023 showed EF of 72% Continue home statin, propafenone, metoprolol and Eliquis GERD Continue protonix Anxiety Stable will continue home xanax Severe malnutrition POA Hypoalbuminemia Cachexia, underweight; BMI 17.56 Encourage nutritional intake. Deconditioning weakness Benefit from extensive rehabilitation PT OT evaluation in progress. Hypophosphatemia Supplemented with Neutra-Phos Hypocalcemia In the setting of hypoalbuminemia Corrected serum calcium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2674299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 21.08.2023
Impfdatum: 19.10.2021
Beginn: 30.01.2023
Tage bis Beginn: 468,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Symptom recurrence

Symptomtext

ACUTE NON ST ELEVATION MI 1/29/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2665718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: FL
Alter: 86,0
Geschlecht: F
Eingang: 03.08.2023
Impfdatum: 20.10.2021
Beginn: 15.07.2023
Tage bis Beginn: 633,0
Dosis: 3
Route/Site: SYR / UN

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

Acute respiratory failure COVID-19

Symptomtext

Hospitalization for Acute hypoxic respiratory failure due to COVID-19 on dates 7/15/2023-7/20/2023. Treated with dexamethasone, baricitinib, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

Weitere VAERSDATA-Felder

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

VAERS 2660044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 24.07.2023
Impfdatum: 14.10.2021
Beginn: 02.06.2022
Tage bis Beginn: 231,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy Aspiration Barium swallow abnormal Bifascicular block Blood gases abnormal Blood pH decreased COVID-19 Carbon dioxide increased Cerebrovascular accident Dysphagia Dyspnoea Echocardiogram abnormal Ejection fraction normal Electrocardiogram abnormal Headache SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient is a 79 y.o. male with a history of CVA with left hemiplegia, prostate cancer and recent admission 5/12/23?5/15/23 for acute CVA who presented to RMH 6/2/2023 with progressive shortness of breath and positive COVID at facility. 1. COVID-19 Infection: Symptom onset 5/29/23 with headache, tested positive 6/2/23 at SNF. Decadron x 10 days continued; weaned off O2. Isolation per protocol. 2. Acute on Chronic Respiratory Failure: ABG on admit showed pH 7.33 and CO2 56.9 indicative of chronic retention. SaO2 88% on admit due to COVID; weaned off O2 gradually. 3. Elevated Troponin: Prior troponin 24, 25 noted in 2019. Troponin 25 on 6/2/23. Suspected demand. EKG 6/2/23 showed bifascicular block without ST changes noted. No further evaluation necessary. 4. Bifascicular Block: Noted on EKGs prior to admission with RBBB and LAFB. s/p loop recorder 2016 and 2019. Follows with Dr. (EP)TTE 5/14/23 with slightly abnormal septal wall motion, EF 55%. 5. Dysphagia: Due to CVA in 5/2023. MBS 5/13/23 showed aspiration and patient placed on nectar thick liquids. SLP followed. 6. CVA: Multiple with residual left hemiplegia (requiring wheelchair) and residual dysphagia. Follows with Dr. (PMR) and, CNP (Neuro). Home ASA, Plavix and statin resumed. 7. Hypothyroidism: S/p thyroidectomy in 1995. Home medications resumed. 8. Prostate Adenocarcinoma: Per history. Follows with Dr. 9. Code status: Full code, patient transitioned to DNR-CCA prior admission but was uncertain this admit. 10. DVT Prophylaxis: Lovenox

Weitere VAERSDATA-Felder

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

VAERS 2644737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 27.10.2021
Beginn: 10.12.2022
Tage bis Beginn: 409,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Neuropathy peripheral

Symptomtext

PERIPHERAL NEUROPATHY ACUTE HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2638443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 30.05.2023
Impfdatum: 11.07.2022
Beginn: 21.08.2022
Tage bis Beginn: 41,0
Dosis: 4
Route/Site: - / -

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

Acute myocardial infarction

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE NON ST ELEVATION MI

Weitere VAERSDATA-Felder

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

VAERS 2621618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 26.04.2023
Impfdatum: 09.11.2021
Beginn: 01.06.2022
Tage bis Beginn: 204,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2621455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 87,0
Geschlecht: M
Eingang: 26.04.2023
Impfdatum: 19.10.2021
Beginn: 22.06.2022
Tage bis Beginn: 246,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Hypoxia

Symptomtext

J96.00 ACUTE RESPIRATORY FAILURE 6/12/2022 ACUTE RESPIRATORY FAILURE WITH HYPOXIA R09.02 HYPOXEMIA 6/12/2022 ACUTE RESPIRATORY FAILURE WITH HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2620738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 13.10.2021
Beginn: 07.02.2022
Tage bis Beginn: 117,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Chronic respiratory failure Respiratory failure Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE RESPIRATORY FAILURE CHRONIC HYPERCAPNIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 2/24/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2616090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: WI
Alter: 79,0
Geschlecht: M
Eingang: 17.04.2023
Impfdatum: 02.11.2021
Beginn: 08.04.2023
Tage bis Beginn: 522,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Death Disease complication

Symptomtext

Unknown of any adverse events from the vaccine in 2021. However, per medical examiner, patient died of COVID-19 complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: OSC: UTI; CKD stage 3; DM2; PVD; renal carcinoma; prostate carcinoma; HTN; HLD; dementia; morbid obesity
Vorgeschichte: OSC: UTI; CKD stage 3; DM2; PVD; renal carcinoma; prostate carcinoma; HTN; HLD; dementia; morbid obesity
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2611646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 95,0
Geschlecht: M
Eingang: 07.04.2023
Impfdatum: 16.06.2022
Beginn: 13.07.2022
Tage bis Beginn: 27,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure Asthma Hypoxia Leukocytosis Pulmonary embolism Pulmonary infarction

Symptomtext

PULMONARY EMBOLISM W INFARCTION, UNSPECIFIED 7/26/2022 LEUKOCYTOSIS ACUTE RESPIRATORY FAILURE 7/26/2022 LEUKOCYTOSIS HYPOXIA 7/26/2022 LEUKOCYTOSIS PULMONARY EMBOLISM W INFARCTION, UNSPECIFIED 7/26/2022 ASTHMA, UNSPECIFIED ACUTE RESPIRATORY FAILURE 7/26/2022 ASTHMA, UNSPECIFIED HYPOXIA 7/26/2022 ASTHMA, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2590275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MN
Alter: 88,0
Geschlecht: F
Eingang: 02.03.2023
Impfdatum: 11.04.2022
Beginn: 03.12.2022
Tage bis Beginn: 236,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 COVID-19 pneumonia Confusional state Cough Death Dysphagia Encephalopathy Pneumonia aspiration Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient brought to the ED by EMS on 12/3/22 for generalized weakness, persistent cough, and confusion. En route to the ED, patient's oxygen sats was 88% so was placed on oxygen. She tested positive for COVID by PCR in the ED, and was admitted on 12/3/22 for hypoxic respiratory failure due to COVID-19 pneumonia, dysphagia and possible aspiration pneumonia, among other problems. She initially required O2 and was on decadron, however was able to be weaned off oxygen. Her COVID pneumonia resolved during her admission. Patient has received the COVID primary vaccine series and two boosters. Of note, during admission patient continued to have persistent encephalopathy, dysphagia, and suspected LLL aspiration pneumonia. Ultimately she was transitioned to comfort focused care on 12/27, and expired in the hospital on 12/30/22. Cause of death documented in the chart is respiratory failure secondary to aspiration pneumonia.

Weitere VAERSDATA-Felder

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

VAERS 2569994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 28.01.2023
Impfdatum: 02.12.2021
Beginn: 22.12.2022
Tage bis Beginn: 385,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Asthenia Blood creatinine increased COVID-19 Cardiac failure congestive Cardiac resynchronisation therapy Chronic kidney disease Computerised tomogram thorax abnormal Condition aggravated Decubitus ulcer Diuretic therapy Dysphagia Dyspnoea Echocardiogram Ejection fraction normal Haemodialysis Hypoxia

Symptomtext

Clinical Summary Patient is a 86 y.o. male with a history of CAD, HFpEF, CKD-4, recently dx with COVID 12/17/22, who presented to hospital 12/22/22 with progressive dyspnea, weight gain, generalized weakness and abdominal/lower extremity edema. Found to have acute CHF. Hospital course complicated by worsening CKD started on HD, pneumonia and dispo/goals of care. After GOC discussions plan was to transition to inpatient hospice. 1. Acute on Chronic HFpEF: S/p PPM, with pHTN. Follows with Dr. TTE 12/14/22 with EF 57%, pHTN. Admit ProBNP 31K. Started on IV diuresis then switched to Lasix gtt, now on dialysis. Meds completed for CC. 2. AKI on CKD-4: Follows Dr. (nephrology). Baseline Cr recently ~3 but on admission Cr >4. Nephrology began trial of CRT 12/30/22. IR placed line 12/30/22. Pt already has outpt chair set up for T-R-S, however family requested twice a week given weakness - Nephro following labs. Patient declined HD and transitioned to hospice. 3. COVID-19: Symptom onset 12/16/22. Tested positive 12/17/22. Had persistent hypoxia, so obtained CT Chest 12/24/22, showed multifocal PNA. Completed decadron and Azithromycin 1/2/22. Resolved. 4. Acute Resp Failure: used to be on O2 at baseline, but last few months has not used it. Required 3L on admit, titrate for comfort. 5. DM-2: by hx. Insulin completed. 6. CAD: Follows with Dr. (cardiology). CABG 1992 and also stent. ASA and statin completed. 7. History of Heart Block: Complete heart block s/p PPM implant with generator change during hospitalization 12/2021. Recent device interrogation almost 100% RV pacing without significant arrhythmia 8. Dysphagia: new problem noted 1/1/22- recommended regular solids, thin liquids 9. Sacral pressure injury stage 2: wound care completed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 19,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 06.04.2021
Beginn: 05.10.2022
Tage bis Beginn: 547,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Aortic dissection Asthenia COVID-19 Computerised tomogram thorax Ex-tobacco user Fatigue Renal aneurysm SARS-CoV-2 test positive

Symptomtext

Pt admitted to Hospital with a dissection of his descending thoracic aorta. While there he developed acute respiratory insufficiency that required high flow oxygen therapy. Concomitantly he was also noted to have a infrarenal aneurysm measuring up to 5.7 to 6 cm in diameter. Radiology measurements were 5.4 cm but not deemed accurate because of the measurement technique. He states he is now not smoking. He is fatigued but otherwise slowly regaining strength. His infrarenal aneurysm was not treated during that admission due to his other acute problems. His thoracic aortic dissection actually appeared to be improving on subsequent CT imaging.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 10/7 SARS-CoV-2 -COVID-19, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2522567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 03.12.2022
Impfdatum: 19.11.2021
Beginn: 07.10.2022
Tage bis Beginn: 322,0
Dosis: 3
Route/Site: IM / LA

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

Accidental overdose Acute kidney injury Acute respiratory failure Anxiety Blood creatinine increased COVID-19 Chronic obstructive pulmonary disease Circadian rhythm sleep disorder Condition aggravated Confusional state Dyspnoea Epistaxis Hypercapnia Hypotension Hypoxia Mental status changes Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

Patient is a 64 y.o. female patient of CNP with history of COPD on 4L NC chronically along with BiPAP at night time, paroxysmal AFib, chronic hypotension, hypothyroidism, and RLS presented with mental status changes in setting of likely unintentional overdose. COVID-19 viral infection Tested positive on routine check for SNF placement delaying discharge for 10 days Completed course of steroids for ACOPDE Completed 10 days of isolation Acute toxic metabolic encephalopathy, resolved In setting on unintentional overdose with hypercapnia and ACOPDE Regulate sleep/wake cycle Continue management as below Acute on chronic respiratory failure with hypoxia and hypercapnia COPD exacerbation Discharged on steroid taper following last admit; baseline O2 ~4L NC Significant expiratory wheezing on admission requiring BiPAP Completed course of Azithromycin and steroids Bronchodilators (Symbicort and Spiriva), BiPAP HS and with naps Improved- on nasal cannula this morning Overdose, unintentional Per hospice RN notes, pt appears to have taken ~24mg of Haldol between 3am and 7am Suspecting confusion due to hypercapnia lead patient taking more than indicated Evaluated by BH and cleared. Anxiety Likely multifactorial due to dyspnea and hospitalization Started on Buspirone due to adverse events on Haldol (will be held at discharge) Morphine PRN Epistaxis Noted to have right anterior epistaxis ENT consulted. S/p FloSeal instilled in left nasal cavity due to prominent left caudal nasal vessel by Dr.. If re-rebleeds, apply 4-5 sparys of Afrin followed by nasal clamp for 20 mins. Resolved AKI, resolved Cr 1.2 on presentation Baseline creatinine wnl Resolved with IV fluids Atrial fibrillation Recent diagnosis for patient, rate controlled Continue home Toprol-XL, and Eliquis Diltiazem held this admission due to hypotension. Defer to PCP when safe to resume Chronic HFrEF No evidence of volume overload on exam Takes Lasix PRN Continue Toprol-XL Hypotension Chronic hypotension due to likely being on prolonged steroids Continue Florinef RLS Takes Gabapentin 300mg HS PRN Hypothyroidism Continue Synthroid GERD Unclear as to why on both PPI and H2 blocker BID Continue Famotidine only at this time Goals of care Given potential suicide attempt, code status was changed to full code briefly BH cleared of suicide precautions Changed code status back to DNR-CC after discussion with POA Goals are hospice

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 35,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2468274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: OH
Alter: 82,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 19.11.2021
Beginn: 12.09.2022
Tage bis Beginn: 297,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Affective disorder Asthenia Bladder catheterisation Bladder dilatation C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray normal Clavicle fracture Computerised tomogram head normal Computerised tomogram thorax abnormal Condition aggravated Confusional state Delirium Dementia Alzheimer's type Fall Leukopenia

Symptomtext

Clinical Summary 83 yo M with a h/o dementia who has had increased confusion over the last 48 hours. The patient's wife cannot care for him in his current condition. The patient also recently suffered a clavicle fx from a fall. Delirium on baseline Alzheimer's dementia Likely aggravated by COVID-19 infection Follows up with Dr. of neurology. Believes the patient has Alzheimer's and some mood disorder Could be normal waning of dementia, delirium, or adverse effect of medications. CT head-no acute intracranial abnormality Reduce memantine back to 5 mg BID. (Dose increased 8/11) Consulted PT/OT. Recommended SNF. SNF accepted and waited for pre-CERT but unfortunately got denied. Discussed with wife. Wife decided to take patient home. DC home with home health care Covid-19 Virus Infection Acute respiratory failure Date of onset of symptoms: No symptoms other than baseline symptoms symptoms present on admission: None. Day after admission spiked low-grade fever. No fever since then Date of covid positive test: 9/13/2022 Vaccination status: vaccinated Imaging: Chest x-ray unremarkable Oxygen requirements: 2 L of oxygen>RA Medical therapy: Started dexamethasone 9/14/22 and continued at discharge to complete 7 days course Anticipated special isolation end date: 9/18/2022 CRP 34.9, ferritin 337. Mild leukopenia Checked O2 requirement prior to discharge. Qualified for 2 L of oxygen with exertion COPD Pulmonary fibrosis Follows up with Dr. as outpatient PFT from 2021-moderate obstruction. FEV1 (% predicted) 62 Continue home medications BPH Continue Flomax 0.4 mg daily Left clavicle Fx Distal third Sling (for comfort) Consulted orthopedic surgery. Recommended outpatient follow-up in 10 days Supportive care The patient was discharged to home and the family brought him back to the ED in less than 24 hours and he was readmitted Clinical Summary Patient is a 83 y.o. male patient of MD with history of dementia, nephrolithiasis, osteoarthritis, appendectomy, back surgery and hernia repair who was discharged home from this facility on 9/16/2022 with delirium, COVID-19 infection, acute respiratory distress and left clavicle fracture, was brought back to the emergency department by his wife for worsening confusion and weakness Delirium, improving Baseline dementia Delirium due to COVID-19 He was admitted to hospital from 9/12/22 through 09/16/2022 with worsening delirium in the setting of COVID-19 infection. Initially he was recommended to go to SNF, after waiting for SNF pre-CERT got denied. Finally his wife decided to take the patient home with home health care. Unfortunately the patient's delirium has failed to clear, and the patient has become weaker PT/OT still recommends 5 days of therapy DC to nursing home for continued therapy History of nephrolithiasis and moderate left-sided hydronephrosis. Urinary retention Patient noted to have distended bladder on examination and Foley catheter was placed. Fortunately kidney function is currently stable Consulted urology. Plan was for ureteroscopy, laser lithotripsy and stent placement. But holding off now considering COVID-19 and pneumonia DC Foley catheter and was able to void without difficulty Patient to follow-up with Dr. in 1-2 weeks Covid-19 Virus Infection Complicated by pneumonia Date of onset of symptoms: Unclear due to dementia Date of covid positive test: 9/13/2022 Vaccination status: vaccinated CT chest-asymmetric RLL infiltrate concerning for possible pneumonia Oxygen requirements: 2 L No fever since 96 hours prior to discharge Medical therapy: Completed 10 days course of dexamethasone Anticipated special isolation end date: 9/23/2022 Levaquin 750 mg daily x7 days for pneumonia Fall While ambulating to bathroom patient felt weak and PSA had to make him sit on the floor on 9/23/2022. Did not fall to the floor, hit his head or lost consciousness Patient examined after the fall. No reports of pain COPD Pulmonary fibrosis Follows up with Dr. as outpatient PFT from 2021-moderate obstruction. FEV1 (% predicted) 62 Continue home medications BPH Continue Flomax 0.4 mg daily Left clavicle Fx Distal third Sling (for comfort) Consulted orthopedic surgery. Recomended outpatient follow-up in 1 week Supportive care Moderate malnutrition Consulted dietitian Continue dietary supplementation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2465440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MN
Alter: 70,0
Geschlecht: M
Eingang: 30.09.2022
Impfdatum: 29.10.2021
Beginn: 25.09.2022
Tage bis Beginn: 331,0
Dosis: 3
Route/Site: IM / RA

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

Anticoagulant therapy COVID-19 Chest pain Cough Deep vein thrombosis Pain in extremity Peripheral vein occlusion Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID on 9/14 - he was experiencing some coughs but overall felt symptomatically improved. However on 9/24 he was seen in the ED for right leg pain and some chest pain. He tested positive again for COVID while in the ED. He was found to have an occlusive right femoral DVT with scattered pulmonary emboli. Patient was admitted from 9/24-9/25 for vascular consultation due to acute DVT. Per vascular surgery consult, the provider felt the right femoral DVT was likely secondary to COVID-19 infection. Patient was started on Eliquis at discharge. Additionally, he has received the COVID vaccine and one booster.

Weitere VAERSDATA-Felder

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

VAERS 2464451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: WI
Alter: 79,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 23.10.2021
Beginn: 21.09.2022
Tage bis Beginn: 333,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Death on 09/21/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID test on 09/20/2022
Aktuelle Erkrankungen: -
Vorgeschichte: UTI; OSC; COVID-19; Hx of C. diff,; acute on chronic renal failure; COPD; RA; HTN; HLD; obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2374933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: WI
Alter: 72,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 26.10.2021
Beginn: 06.01.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: UN / UN

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

Acute respiratory failure COVID-19 pneumonia Death

Symptomtext

Patient admitted to Medical Center 1/6/2022. Per Death abstracted submitted by the state Patient Died 1/16/2022 at 14:04 of Covid pneumonia acute hypoxic respiratory failure. public health has no further information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: unknown.
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2290625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: WA
Alter: 76,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 22.10.2021
Beginn: 15.05.2022
Tage bis Beginn: 205,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Exposure to SARS-CoV-2 Inappropriate schedule of product administration SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 2/28/21 (lot # EN6198), 3/26/21 (lot # ER8732), and 10/22/21 (lot # FH8020). On 5/15/22, patient admitted to our inpatient facility with acute respiratory failure with hypoxia due to COVID-19 pneumonia. Patient lives with multiple family members, all of whom were recently tested positive for COVID19. Patient was admitted to our med/surg unit and discharged home on 5/17/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: COVID status positive 5/15/22.
Aktuelle Erkrankungen: -
Vorgeschichte: With history of hypertension, type 2 diabetes, ESRD on HD, A. fib on Coumadin, and recent left MCA stroke with aphasia and right hemiparesis (3/2022)
Andere Medikamente: acetaminophen, amlodipine, calcium carbonate, vitamin d3, insulin nph, labetalol, losartan, omeprazole, pysllium, rosuvastatin, sevelamer carbonate, vitamin b complex with c and folic acid (Nephrocaps), warfarin
Allergien: aspirin, simvastatin
Vorherige Impfungen: -

VAERS 2278379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MA
Alter: 50,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 29.10.2021
Beginn: 10.02.2022
Tage bis Beginn: 104,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Cardiac function test Cerebrovascular accident Computerised tomogram Magnetic resonance imaging Magnetic resonance imaging head abnormal Scan with contrast

Symptomtext

On Feb 10, 2022 I was rushed to the hospital via ambulance and ultimately diagnosed with a stroke. Follow up with Neurologist highlighted I had a previous stroke 3 - 6 months prior to Feb 10 (as shown on my MRIs). I have had significant testing and follows with doctors and they are unable to find a medical reason why I had the strokes. I am 51yo. Hematologist says it could be related to vaccines given time frames and all medical test results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: 2/10-2/11/22 - hospitalized. Cat scan, multiple MRIs, heart tests, blood work, neurologist assessment, Hospital 3/16/22 - MRI with contract Hospital 5/9/2022 - hematologist ( 25 vials of blook)
Aktuelle Erkrankungen: No
Vorgeschichte: none
Andere Medikamente: Fluoxetine 20 mg
Allergien: no just seasonal allergies
Vorherige Impfungen: -

VAERS 2235927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 07.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / AR

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

Blood test Coronary arterial stent insertion Loss of personal independence in daily activities Myocardial infarction Tissue injury

Symptomtext

On 12/05/2021, I had a heart attack. I called an ambulance and was taken to the hospital. On I had a stent on 12/07/202. I stayed 4 days in the hospital. I was told it was a widow maker heart attack. My heart tissues were damaged. I am now taking several medications due to the heart attack. I am a vegetarian and no one in my family has heart issues. This is very unusual. Three weeks before the vaccine, I had blood work and it indicated that my blood work was good. I now go to rehab three days a week. This has affected my life and can not do the things I use to.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Blood work
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes controlled non-insulin dependent
Andere Medikamente: Metformin; Vitamin C; Lisinopril; Lipitor
Allergien: None
Vorherige Impfungen: -

VAERS 2206456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 23.02.2021
Beginn: 29.03.2022
Tage bis Beginn: 399,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 Dyspnoea SARS-CoV-2 test positive Upper respiratory tract infection

Symptomtext

Pt has a history of CAD, status post CABG, history of lung cancer status post lobectomy, diabetes, and obesity. She has had 8 days of increased work of breathing at which time she states she caught a URI. She is COVID positive and admitted with acute hypoxic respiratory failure.

Weitere VAERSDATA-Felder

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

VAERS 2184369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

kritisch

Staat: TN
Alter: 68,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 05.11.2021
Beginn: 17.03.2022
Tage bis Beginn: 132,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Death Vaccine breakthrough infection

Symptomtext

COVID-Related death- Breakthrough case. Not all LOT#'s available

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 28,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2184193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

kritisch

Staat: KY
Alter: 86,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 21.01.2021
Beginn: 17.02.2022
Tage bis Beginn: 392,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

pt received covid vaccines. later diagnosed with covid on 02/07/2022, and passed on 02/17/2022

Weitere VAERSDATA-Felder

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

VAERS 2184143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

kritisch

Staat: OH
Alter: 78,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 02.12.2021
Beginn: 10.02.2022
Tage bis Beginn: 70,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Death

Symptomtext

Pt was admitted to the hospital with Covid post vaccination. Patient had Covid Pneumonia and the patient expired on 02/10/22 due to Covid complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CKDD, HF, ASHD, Depression
Andere Medikamente: amlodipine, atenolol, vitamin D3, B-12, fish oil, gabapentin, Isosorbide mono, sertraline, simvastatin, spironolactone
Allergien: Codeine, Furosemide, latex
Vorherige Impfungen: -

VAERS 2180647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: AZ
Alter: 74,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 03.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / AR

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

Glaucoma Visual field defect

Symptomtext

My ophthalmologist was suspecting that I may develop glaucoma before my booster but could not diagnose it as such until it got worse after my booster. This was discovered in 12/2021 because of loss of visual field in test. Was prescribed Timolol Maleate which I found was allergic to. Alphagan P was prescribed to replace it and I have been using it for two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Glaucoma
Hospital-Tage: -
Labordaten: 12/2021 Visual field test (glaucoma discovered)
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic Type 1, Mitral valve stenosis, Seasonal Allergies, Environmental Allergies, Osteoporosis w/spinal fracture, hypothyroidism, Factor V Leiden
Andere Medikamente: Humalog, Warfarin, Rosuvastatin, Synthroid, Prolia, Aspirin, Calcium, Magnesium, B complex w/folic acid, C, D3, Glucose tabs, Chamomile
Allergien: Sulfa, lactose intolerant, perfume, scents(chemical base), Timolol Maleate
Vorherige Impfungen: 1st and 2nd dose of COVID Vaccine by Pfizer, 02/20/2021 and 03/13/2021, 72age, I had gout after both regular shots but not after

VAERS 2154590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 03.03.2022
Impfdatum: 26.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Catheterisation cardiac abnormal Chest pain Electrocardiogram abnormal Myocardial infarction

Symptomtext

Acute STEMI presentation - initial cath with no culprit lesion identified. with history of type 2 diabetes, permanent atrial fibrillation with intrinsically controlled heart rates, and long term anticoagulation with Xarelto, Obesity, hypertension , hyperlipidemia, DVT and right sided carotid endarterectomy admitted for further evaluation of chest pain progressively worsening since receiving COVID vaccine booster 2 days prior. ECG was consistent with anterior STEMI. Initial emergent LHC was felt to show TIMI 3 flow in all vessels and moderate diffuse disease - the films were reviewed by multiple interventionalists and the consensus was that no culprit vessel could be identified. ED and hospital admission was within 2 days of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2148439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 15.10.2021
Beginn: 17.12.2021
Tage bis Beginn: 63,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Back pain Cerebrovascular accident Computerised tomogram Hypertension Hypoaesthesia Laboratory test Magnetic resonance imaging Vision blurred

Symptomtext

I had a small stroke. I began to have blurred vision, pain in back, numbness in fingers and very High Blood pressure. I called 911. Once, I got to ER and test were ran, I was told by doctor that I had a stroke due to AFIB but had never had heart issues before vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: MRI, CT scan, Labs
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Trazadone 50 mg, Zyrtec, Omeprazole, Vitamin D3
Allergien: Flagyl
Vorherige Impfungen: -

VAERS 2140102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: KY
Alter: 62,0
Geschlecht: M
Eingang: 25.02.2022
Impfdatum: 12.11.2021
Beginn: 28.12.2021
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: IM / RA

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

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

Symptomtext

COVID pneumonia , acute respiratory failure with hypoxia, sepsis, and dementia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: positive COVID lab 12-28-2021
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2131465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: NV
Alter: 29,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 29.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Angiogram Blood test Cardiac stress test abnormal Chest X-ray Chest pain Dizziness Dyspnoea Echocardiogram abnormal Electrocardiogram abnormal Electrocardiogram ambulatory Heart rate increased Hypertension Hypoaesthesia Insomnia Magnetic resonance imaging heart Myocarditis Nausea Palpitations

Symptomtext

Monday Nov 1, 2021, I was vomiting, dizzy, and nauseous. I stayed at home next day, could not sleep, chest pain, and SOB. I went to the ER. While at ER, I had blood work that stated I had pulmonary embolism blood clot and low white blood cell count. That was ruled out but something triggered that. Was discharged from ER with a referral to cardiologist. I also went back to the ER due to fast heart rate above 170 and high blood pressure with numbness in my arm. I wanted to make sure I was not having a heart attack. While in ER, I received another EKG, chest x-ray, and blood work. I had went to cardiologist and had a stress test which I failed. More testing was done with echocardiogram, EKG, CTA, a cardiac MRI, and Holter monitor. I have mild palpitation and myocarditis determined from the EKG and echocardiogram. I just had a cardiac MRI today so no results yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Blood work, EKG, CTA, cardiac MRI, Holter monitor, echocardiogram, and chest x-ray.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin, Sulfa, Cephlasporin
Vorherige Impfungen: -

VAERS 2110326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MD
Alter: 95,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 13.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / UN

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

Affective disorder Amnesia Aphasia Balance disorder Barium swallow abnormal Chest X-ray Computerised tomogram abdomen Computerised tomogram head Confusional state Death Disorientation Dysarthria Dysgraphia Dysphagia Electroencephalogram abnormal Fall Gait disturbance Hallucination

Symptomtext

Over a 3 month period (10/13/22 until 1/30/33, patient experienced mood disturbances, loss of social/safety judgement ability, a sudden and significant increase in memory loss, slurred speech and difficulty swallowing, CVA-type " word loss", complete loss of reading and writing ability, disorientation and confusion, hallucinations, balance & gait disturbance which caused severe increase in unsteadiness and falls, myoclonus, and debilitating tremors. On 1/17/22, he fell and was admitted to hospital with no injuries from fall, but developed aspiration pneumonia related to inability to swallow. He died on 1/30/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: Testing from 1/17 until 1/30 included cspine xrays and head CTscan related to a fall, CXRs , an EEG for suspected seizures, multiple chem panels, swallowing tests and barium swallow test (failed), CTscan of abdomen to determine feeding tube placement
Aktuelle Erkrankungen: none
Vorgeschichte: mild hypertension 1st deg AV block CAD hyperlipidemia
Andere Medikamente: Amlodipine, aspirin, atovastatin, Dorzolomide/Timilol eyedrops, multivitamin,Pantoprozol, terazosin, Prozac
Allergien: none
Vorherige Impfungen: -

VAERS 2099367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: OH
Alter: 42,0
Geschlecht: M
Eingang: 09.02.2022
Impfdatum: 02.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 20,0
Dosis: UNK
Route/Site: - / -

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

Arteriosclerosis Cardiac stress test abnormal Catheterisation cardiac normal Chest pain Coronary arterial stent insertion Coronary artery disease Hyperhidrosis Myocardial infarction Pain in extremity

Symptomtext

Had heart attack on 11/22/21 .no heart issues ever in my lifetime prior .had sever chest pain and pain in my arms and was sweating during attack.was admitted to hospital and observed overnight and again overnight till transporting me to their larger hospital .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Did heart cath on 11/24/21 and could not find anything obvious wrong .heart looked healthy.normal plaque.used nuclear stress test.found plaque that seemed to be cut by something flapping in artery in heart.they took a recording of it.dr did heart cath and took video and recording..decided to put stent in the area where he recorded video of after consulting with one of his peers.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ibuprofen on occasion
Allergien: None
Vorherige Impfungen: -

VAERS 2050788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

kritisch

Staat: NC
Alter: -
Geschlecht: U
Eingang: 05.02.2022
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Cardiac arrest

Symptomtext

Sudden Cardiac Arrest/My heart stopped beating for 20 minutes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 25Oct2021 15:30 (Lot number: Fh8020) as dose number unknown (booster), single 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 completed, dose number unknown, MANUFACTURER UNKNOWN), for COVID-19 immunization. The following information was reported: CARDIAC ARREST (hospitalization, medically significant) with onset 25Oct2021 17:00, outcome "unknown", described as "Sudden Cardiac Arrest/My heart stopped beating for 20 minutes". The patient was hospitalized for cardiac arrest (start date: 25Oct2021, discharge date: 05Nov2021, hospitalization duration: 11 day(s)). Therapeutic measures were taken as a result of cardiac arrest (an ICD (Implantable defibrillator) was implanted in my upper-left chest). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

kritisch

Staat: NC
Alter: -
Geschlecht: U
Eingang: 05.02.2022
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Cardiac arrest

Symptomtext

Sudden Cardiac Arrest/My heart stopped beating for 20 minutes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 25Oct2021 15:30 (Lot number: Fh8020) as dose number unknown (booster), single 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 completed, dose number unknown, MANUFACTURER UNKNOWN), for COVID-19 immunization. The following information was reported: CARDIAC ARREST (hospitalization, medically significant) with onset 25Oct2021 17:00, outcome "unknown", described as "Sudden Cardiac Arrest/My heart stopped beating for 20 minutes". The patient was hospitalized for cardiac arrest (start date: 25Oct2021, discharge date: 05Nov2021, hospitalization duration: 11 day(s)). Therapeutic measures were taken as a result of cardiac arrest (an ICD (Implantable defibrillator) was implanted in my upper-left chest). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2082702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: IL
Alter: 82,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 15.10.2021
Beginn: 27.01.2022
Tage bis Beginn: 104,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Asthenia COVID-19 Cerebrovascular accident Chest X-ray abnormal Computerised tomogram head normal Inappropriate schedule of product administration Interstitial lung disease Magnetic resonance imaging head normal Pneumonitis Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccine on 3/10/21, 4/7/21 and 10/15/21. Presented to ER on 1/27/22 and found to be COVID positive. presented with generalized weakness suspected CVA. CT head & MRI-brain -negative for stroke. COVID positive 01/27/2022 , patient was vaccinated. initially was requiring 2 L NC oxygen Dexamethasone, remdesivir was started. Clinically improved. Now on room air. Medication discontinued. AKI- hydrochlorothiazide -triamterene on hold. AKI improved with hydration. Dischaged to home health care on 2/1/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 5,0
Labordaten: 1/27/22 COVID19: positive 1/27/22 chest xray: Chronic interstitial lung markings are re-identified. Mild superimposed interstitial edema or inflammation is also possible. Recommend clinical correlation.
Aktuelle Erkrankungen: -
Vorgeschichte: Atherosclerosis of native coronary artery of native heart with angina pectoris (7/22/2016), Chronic combined systolic and diastolic heart failure (6/13/2020), Compression fracture of lumbar vertebra, Coronary atherosclerosis of native coronary artery, Cough, Diabetes, Former smoker (7/22/2016), Graves disease (10/30/2019), Interstitial lung disease, Ischemic cardiomyopathy( Severe LV dysfunction) (6/13/2020), Mixed hyperlipidemia, Old inferior wall myocardial infarction, Osteoporosis, Prostate cancer, S/P PTCA/Stent x 2 Mid LAD/Proximal RCA 2008 (7/22/2016), and Skin cancer. He also has no past medical history of Anesthesia complication.
Andere Medikamente: acetaminophen 500 MG Tabs Commonly known as: TYLENOL 1,000 mg, Oral, EVERY 8 HOURS PRN apixaban 5 MG Tabs Commonly known as: ELIQUIS 5 mg, Oral, 2 TIMES DAILY carvedilol 3.125 MG Tabs Commonly known as: COREG 3.125 mg, Oral, 2 TIMES DAI
Allergien: none
Vorherige Impfungen: -

VAERS 2025063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: IL
Alter: 58,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 12.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: SYR / RA

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

Computerised tomogram Deep vein thrombosis Interchange of vaccine products Pulmonary embolism Ultrasound Doppler

Symptomtext

DVT and bilateral PE. Taking Xarelto 20 mg. Pfizer was my booster. My original vaccine was J&J

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CT Scan 12/10 Doppler US 12/17
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Prempro, Multi Vitamin, Biotin, B12, CoQ-10, Vitamin C
Allergien: amoxicillin
Vorherige Impfungen: -

VAERS 2014009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 22.10.2021
Beginn: 19.11.2021
Tage bis Beginn: 28,0
Dosis: UNK
Route/Site: IM / RA

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

Acute myocardial infarction Chest pain Dyspnoea exertional

Symptomtext

Known history of ASCVD. The patient was admitted for further evaluation and treatment of acute STEMI associated with symptoms of chest pain and shortness of breath with exertion. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2010719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: WA
Alter: 61,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Delirium Encephalopathy Exposure to SARS-CoV-2 Metabolic encephalopathy SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient received Pfizer COVID vaccine on 12/29/20 (lot EL1284), 2/9/21 (lot EN6201), and 10/15/21 (lot FH8020). Patient lives on adult facility living. On 1/3/22, patient tested positive for COVID (exposure due to a big outbreak in the adult living facility). On 1/4/22, patient admitted to our inpatient unit with acute hypoxic respiratory failure secondary to COVID-19 pneumonia(breakthrough/reinfection) currently on high flow oxygen and acute encephalopathy, toxic metabolic/ delirium in the context of COVID-19. As of today (1/6/22), patient is still admitted in our med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: COVID status positive 1/3/22.
Aktuelle Erkrankungen: -
Vorgeschichte: history of COVID-19 requiring hospitalization in April 2020, COPD, coronary artery disease, diabetes mellitus type 2, prior CVA with right-sided hemiparesis and contractures, peripheral arterial disease and prior AKA on left, schizophrenia, cognitive impairment
Andere Medikamente: acetaminophen PRN, aripiprazole, baby aspirin, baclofen, bisacodyl suppository, calcium carbonate, vitamin d3, clonazepam, clopidogrel, divalproex dr, famotidine, finasteride, gabapentin, insulin glargine pen, magnesium, MVI, omega-3, prava
Allergien: Milk
Vorherige Impfungen: -

VAERS 1999427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 09.10.2021
Beginn: 27.12.2021
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: UN / UN

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

Acute respiratory failure Agitation Angiogram pulmonary abnormal Aortic arteriosclerosis Aortic valve thickening Arteriosclerosis Atelectasis Bronchiectasis COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Condition aggravated Death Deep vein thrombosis Discomfort Dyspnoea Echocardiogram

Symptomtext

Patient expired after 5 days hospitalization. 73y Male pm hx ESRD/kidney transplant 2018, CAD, HTN, PHTN, DM-2 - Presented to BWED 12/27 w/dyspnea - dx'd COVID - HFNC/NRM. Imaging without significant infiltrates c/w COVID - suspect pHTN uncontrolled. Transferred to ICU 12/31 and placed on Veletri. Oxygenation worsened after Veletri increased from 30 to 50 ng - suspected secondary to developing pulmonary edema from increased vasodilation. Patient became encephalopathic - trying to pull off his mask. Code status changed to DNR/DNI. Respiratory status then improved after Veletri decreased back to 30 ng, placed on BiPAP and given a dose of Lasix. Precedex started for agitation. Now having fever - cultures ordered and antibiotics initiated. With his ongoing work of breathing and discomfort the patient's family ultimately transitioned the patient to comfort care "to ease his suffering". Patient was pronounced dead on 1/1/22 at 18:30 p.m. Medical Examiner Case Assessment Select Applicable Patient Criteria: Does not meet any of the listed criteria

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: USV Venous Upper Extremity Duplex Bilateral Resulted: 01/01/22 0946 Order Status: Completed Updated: 01/01/22 0948 Narrative: EXAMINATION: Complete Bilateral Upper Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 1/1/2022 9:28 AM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left upper extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: fever COMPARISON: None _____________________ Right Upper Extremity Findings: Right Internal Jugular Vein: No thrombus. Right Subclavian Vein: No thrombus. Right Axillary Vein: No thrombus. Right Brachial Vein: No thrombus. Right Radial Vein: No thrombus. Right Ulnar Vein: No thrombus. Superficial Veins: Right Basilic Vein: No thrombus. Right Cephalic Vein: Dilation of the cephalic vein within the upper arm. Chronic appearing echogenic mural-based foci suggesting mural calcifications or chronic sequela of thrombophlebitis. Age-indeterminate thrombus within the right medial cubital vein. Left Upper Extremity Findings: Portion of the distal upper arm and elbow obscured by bandage. Left Internal Jugular Vein: No thrombus. Left Subclavian Vein: No thrombus. Left Axillary Vein: No thrombus. Left Brachial Vein: No thrombus. Left Radial Vein: No thrombus. Left Ulnar Vein: No thrombus. Superficial Veins: Left Basilic Vein: No thrombus. Left Cephalic Vein: Thrombosed within the distal upper arm. ADDITIONAL FINDINGS: Normal cardiac pulsatility is present in the subclavian veins. _____________________ Impression: There is no sonographic evidence for deep venous thrombosis in the visualized deep veins of the right or left upper extremity. Superficial thrombophlebitis of the left cephalic vein within the upper arm. Chronic appearing changes of the cephalic vein on the right with dilation within the upper arm and likely chronic wall calcifications or chronic thrombus. Age indeterminant thrombus present within the median cubital vein on the right. USV Venous Lower Extremity Duplex Bilateral Resulted: 01/01/22 0939 Order Status: Completed Updated: 01/01/22 0941 Narrative: EXAMINATION: Complete Right and Left Lower Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 1/1/2022 9:29 AM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left lower extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: fever COMPARISON: None _____________________ Right Lower Extremity Findings: Right Common Femoral Vein: No DVT. Right Femoral Vein: No DVT. Right Popliteal Vein: No DVT. Right Posterior Tibial Veins: No DVT. Right Peroneal Veins: No DVT Right proximal Greater Saphenous Vein: No thrombus. Left Lower Extremity Findings: Left Common Femoral Vein: No DVT. Left Femoral Vein: No DVT. Left Popliteal Vein: No DVT. Left Posterior Tibial Veins: No DVT. Left Peroneal Veins: No DVT Left proximal Greater Saphenous Vein: No thrombus. Duplex Doppler: The common femoral vein waveforms are abnormally pulsatile. This finding may be seen with elevated central venous pressure from heart failure, tricuspid valve regurgitation, pulmonary hypertension, or right heart dysfunction. Additional Findings: None. _____________________p Impression: There is no sonographic evidence for deep venous thrombosis in the visualized deep veins of the right or left lower extremity. Reflected cardiac pulsations are present in the common femoral vein waveforms. This finding may be seen with elevated central venous pressure from heart failure, tricuspid valve regurgitation, pulmonary hypertension, and elevated right heart pressures or dysfunction. * DR CHEST SINGLE VIEW Resulted: 01/01/22 0758 Order Status: Completed Updated: 01/01/22 0800 Narrative: EXAMINATION: Single View Chest EXAM DATE: 1/1/2022 5:26 AM TECHNIQUE: Single view chest INDICATION: acute hypoxic respiratory failure COMPARISON: December 31, 2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Bilateral lung opacifications continue appearing mildly improved about the right base. Blunting of the bilateral costophrenic angles just a small amount of bilateral pleural fluid. No visualized pneumothorax. Heart appears enlarged in similar fashion. Hilar and mediastinal borders appear grossly stable with atherosclerosis, limited evaluation due to adjacent opacification. No new tubes or catheters are evident. Overlying support devices limits evaluation. _________________________ Impression: Bilateral lung opacities continue, there appears to be mild clearing at the right base. Bilateral small pleural effusions are suspected. DR CHEST SINGLE VIEW Resulted: 12/31/21 2328 Order Status: Completed Updated: 12/31/21 2330 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/31/2021 11:22 PM TECHNIQUE: Single view chest INDICATION: acute hypoxic respiratory failure COMPARISON: Chest x-ray of 12/31/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: There is extensive bilateral pulmonary space consolidation, which has significantly increased since the prior exam. Cardiac size is within normal limits. No pneumothorax. No appreciable pleural fluid. Bones appear stable. _________________________ Impression: Extensive bilateral pulmonary space consolidation which has increased since the prior exam, consistent with worsening pneumonia. The Orange significant findings protocol was initiated at 12/31/2021 11:27 PM. DR CHEST SINGLE VIEW Resulted: 12/31/21 0906 Order Status: Completed Updated: 12/31/21 0908 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/31/2021 7:22 AM TECHNIQUE: Single view chest INDICATION: COVID pneumonia COMPARISON: 12/29/2021 12/28/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Interstitial prominence minimal streaky changes. No significant change. No consolidation. Cardiac silhouette is stable. No pneumothorax. No definite pleural effusion. _________________________ Impression: No significant change. DR CHEST SINGLE VIEW Resulted: 12/29/21 0810 Order Status: Completed Updated: 12/29/21 0812 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/29/2021 7:05 AM TECHNIQUE: AP portable semiupright views chest INDICATION: resp failure hypoxemia COMPARISON: 12/28/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: No supporting lines or tubes. There is no evidence of pneumothorax. Stable cardiomegaly. No change in the pulmonary vasculature or hilar regions. Stable aorta and superior mediastinum. Small left effusion without definite right effusion, essentially unchanged. Atelectasis at the peripheral left base improved. Mild increase in opacities in the medial left base retrocardiac region and right base, likely atelectasis. Mid to upper lungs unchanged. Osseous structures are unchanged. Multiple skinfolds demonstrated. _________________________ Impression: Minimal change in the chest. There is some improvement in peripheral left base atelectasis with slight increase in atelectasis elsewhere in the lung bases. Stable small left effusion. CV Echo Limited with Contrast Collected: 12/27/21 1810 Order Status: Completed Updated: 12/28/21 1717 Narrative: Heart Center LIMITED ECHOCARDIOGRAPHY REPORT Name: Study Date: 12/27/2021 MRN: Patient Location: DOB: Patient Class: Inpatient Gender: Male Ordering Physician: Age: 73 yrs Height: 178 cm Performed By: RDCS Weight: 64 kg Resting HR: 77 BSA: 1.8 m2 Resting BP: 141/92 mmHg Reason For Study: Pulmonary HTN History/Symptoms: Hypertension,Pulmonary Hypertension,Dyslipidemia,Former Smoker,Dyspnea on exertion (DOE),End stage Renal Disease (ESRD),Cardiomyopathy (non-ischemic),Coronary artery disease,Chronic Obstructive Pulmonary Disease,Covid 19,Renal transplant Electronically signed by: MD on 12/28/2021 05:16 PM Interpretation Summary The left ventricle size and thickness are normal. All wall segments contract normally. The left ventricular ejection fraction is 55%. The LV ejection fraction is normal. The left ventricular wall motion is normal. There is no thrombus. Right ventricle function is moderately decreased. The estimated right ventricular systolic pressure is 65 mmHg. There is severe pulmonary hypertension. There is moderate tricuspid regurgitation. There is mild to moderate aortic valve thickening. There is trace mitral regurgitation. No pericardial effusion. There is no comparison study available. STUDY PERFORMED/QUALITY: AORTIC VALVE: A two-dimensional transthoracic There is mild to moderate aortic valve echocardiogram with color flow and thickening. There is no aortic valve spectral flow Doppler was performed in stenosis. limited views only. The technical quality of the exam was limited due to MITRAL VALVE: suboptimal acoustic windows. The The mitral valve is normal in technical quality of the exam was structure and function. There is no fair. Location: Portable. Due to mitral valve stenosis. There is trace limited acoustic windows, Definity was mitral regurgitation. administered. LEFT VENTRICLE: TRICUSPID VALVE: The left ventricle size and thickness The tricuspid valve is normal in are normal. All wall segments contract structure and function. There is no normally. The LV ejection fraction was tricuspid stenosis. The estimated determined utilizing Simpson's Biplane right ventricular systolic pressure is method. The left ventricular ejection 65 mmHg. There is severe pulmonary fraction is 55%. The LV ejection hypertension. There is moderate fraction is normal. The left tricuspid regurgitation. ventricular wall motion is normal. There is no thrombus. PULMONIC VALVE: The pulmonic valve is not well visualized. LEFT ATRIUM: The left atrium is not well visualized. The interatrial septum is not well visualized. RIGHT ATRIUM: The right atrium is moderately dilated. RIGHT VENTRICLE: The right ventricle is moderately dilated. Right ventricle function is moderately decreased. PERICARDIUM/PLEURAL: No pericardial effusion. No pleural effusion. AORTA/PULMONARY ARTERY: The aortic root is not dilated. INFERIOR VENA CAVA: The inferior vena cava was not visualized during the exam. Right Ventricle Tricuspid Valve TAPSE.: 1.6 cm TR max vel: 3.98 m/sec RVDs: 9.9 cm TR max PG: 63.6 mmHg RVFW S' Max Vel: 0.08 m/sec ______________________________________________________________________________ Great Vessels IVC diam: 2.6 cm Reference Table: Normal Mild ModerateSevere Men LVEF > 52% 41-51% 30-40% <30% Women LVEF > 54% 41-53% 30-40% <30% Men LVIDd 4.2-5.8 5.9-6.3 6.4-6.8 >6.8 Women LVIDd 3.8-5.2 5.3-5.6 5.7-6.1 >6.1 LA Volume (ml/m^2) < 34 35-41 42-48 >48 ______________________________________________________________________________ Electronically signed by: MD on 12/28/2021 05:16 PM All sources of data reside in the Cardiology EJECTION FRACTION ECHO Collected: 12/27/21 1810 Order Status: Completed Updated: 12/28/21 1717 EJECTION FRACTION ECHO 55 % DR CHEST SINGLE VIEW Resulted: 12/28/21 0719 Order Status: Completed Updated: 12/28/21 0721 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/28/2021 6:10 AM TECHNIQUE: Single view chest INDICATION: resp failure hypoxemia COMPARISON: Yesterday 1149 hours ENCOUNTER: Not applicable _________________________ FINDINGS: Inspiration is mildly more shallow. Heart is mildly enlarged with mildly prominent size of the central pulmonary arteries. Mildly increased central and basilar interstitial markings. Patchy and streaky atelectasis/infiltrate in the left mid and lower lung zone, mildly increased. Slight blunting of the left CP angle persists. _________________________ Impression: Mildly more shallow inspiration. Mildly increased probable subsegmental atelectasis in the left lower lung zone. CT ANGIO THORAX WITH IV CONTRAST Resulted: 12/27/21 1601 Order Status: Completed Updated: 12/27/21 1603 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 12/27/2021 3:24 PM TECHNIQUE: Standard protocol CT angiogram images were obtained through the chest following the administration of intravenous contrast. Coronal and sagittal MIP 3-D reformations were performed. CONTRAST: 80 mL Isovue 370 QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: PE suspected, high prob. Additional history: Covid-19 pneumonia with acute on chronic respiratory failure. COMPARISON: 8/11/2020, 5/26/2016 ENCOUNTER: Not applicable ____________________ FINDINGS: 1. Lungs/pleura: * Interval development of mild peripheral groundglass opacities and bibasilar subsegmental consolidation and atelectasis. * Minimal right pleural effusion. No diffuse septal thickening or centrilobular groundglass opacities. * Previous bibasilar subsegmental atelectasis/scarring is less well-visualized due to the acute changes but, probably unchanged. * Mild cylindrical bronchiectasis and mild mosaic attenuation. No centrilobular or suspicious random nodules. 2. Mediastinum: * No pulmonary embolus. Chronic pulmonary artery dilation compatible with pulmonary hypertension. No gross right heart strain. * Development of mild mediastinal and bilateral hilar lymphadenopathy. Coalescent right hilar nodes measure up to 20 mm. Subcarinal nodes 15 mm. Smaller nodes are seen along the lower right and left paratracheal, para-aortic and left hilum. * Trace pericardial effusion. Mild calcified aortic plaque without aneurysm. * Suspected small hiatal hernia without esophageal dilation. 3. Musculoskeletal/upper abdomen: * No significant bone lesions. * Bilateral chronic renal cortical atrophy. Calcified splenic granulomas. __________________________ Impression: 1. No pulmonary embolus. Chronic pulmonary hypertension. 2. Bilateral groundglass and lower lobe subsegmental consolidation/atelectasis compatible with Covid 19 pneumonia. Findings are superimposed on chronic lower lobe scarring/subsegmental atelectasis and cylindrical bronchiectasis. 3. Mild mediastinal and hilar lymphadenopathy is likely reactive. DR CHEST SINGLE VIEW Resulted: 12/27/21 1238 Order Status: Completed Updated: 12/27/21 1241 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/27/2021 12:05 PM TECHNIQUE: Single view chest INDICATION: SOB COMPARISON: Chest x-ray August 3, 2020 ENCOUNTER: Not applicable _________________________ FINDINGS: The heart is enlarged, mild pulmonary vascular prominence is present. Hyperaeration changes are again demonstrated. Subtle increase in ill-defined right greater than left basilar pulmonary opacities. Upper lungs appear clear. No large pleural effusion or pneumothorax. _________________________ Impression: 1. Mild bibasilar airspace disease. No dominant consolidation. 2. Mild cardiomegaly with mild pulmonary vascular prominence. 3. Hyperaeration changes. Collected: 12/27/21 1136 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 12/27/21 1240 COVID-19 PCR Detected Abnormal Not Detected Influenza A PCR Not Detected Not Detected Influenza B PCR Not Detected Not Detected RSV PCR Not Detected Not Detected
Aktuelle Erkrankungen: Stage 4 COPD
Vorgeschichte: Respiratory Moderate COPD (chronic obstructive pulmonary disease) Multiple pulmonary nodules Dyspnea on exertion Acute respiratory failure with hypoxia Circulatory Essential hypertension Coronary artery disease involving native coronary artery of native heart without angina pectoris Non-ischemic cardiomyopathy Pulmonary hypertension Deep venous insufficiency Superficial vein thrombosis Pulmonary HTN digestive Hepatitis C Genitourinary ESRD on hemodialysis Endocrine/Metabolic History of prediabetes Dyslipidemia Other History of prostate cancer Renal transplant, status post
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 5 MG tablet Apoaequorin (PREVAGEN PO) APPLE CIDER VINEGAR PO aspirin 81 MG chewable tablet calcium carbonate (TUMS) 500 MG chewable tablet carvedilol
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1981012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: CA
Alter: 74,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

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

Anticoagulant therapy Computerised tomogram abnormal Electrocardiogram ST-T segment abnormal International normalised ratio abnormal Pulmonary embolism

Symptomtext

Bilateral Saddle Pulmonary Emboli, treated with heparin, hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: INR, CT confirmed right heart strain with Saddle Emboli
Aktuelle Erkrankungen: none
Vorgeschichte: ALS, GE reflux
Andere Medikamente: none
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1957997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: WI
Alter: 52,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 23.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Blood pressure increased Blood pressure measurement Burning sensation Dizziness Dyspnoea Feeling hot Feeling of body temperature change Hypersensitivity Lethargy Migraine Nausea Oropharyngeal pain Oxygen saturation Pain Palpitations Peripheral swelling Pharyngeal swelling Respiratory arrest

Symptomtext

severe allergic reaction; arm was still running hot; on the verge of a sinus infection; arm swelling went down to her bicep on her right arm; neck swelling; running hot and cold. She would be burning up and then she would be freezing cold; Migraine headache; right shoulder blade was burning/arm burning; felt like her breathing was starting to restrict, like when she gets stung by a bee; having the sensation like she couldn't breath; Nauseous; lightheaded; burning pain; injection site was running super hot; her heart was pounding in her chest; wheezing; blood pressure was 120/80 which for her that's very high; lethargic; Sore throat; swelling had reached the base of her throat; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52 year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), administration date 23Nov2021 13:20 (Lot number: FH8020) at the age of 52 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "allergic to milk" (unspecified if ongoing); "Mold allergy" (unspecified if ongoing); "had the same kind of breathing problem" (unspecified if ongoing), notes: when she had the antivenom and anti-swelling injections to counteract a bee string; "bee string" (unspecified if ongoing); "runny nose" (unspecified if ongoing), notes: from mold allergies; "reactiorn to the anti-swelling medicine" (unspecified if ongoing). There were no concomitant medications. The following information was reported: HYPERSENSITIVITY (medically significant), outcome "unknown", described as "severe allergic reaction"; RESPIRATORY ARREST (medically significant) with onset 23Nov2021, outcome "unknown", described as "felt like her breathing was starting to restrict, like when she gets stung by a bee"; DYSPNOEA (medically significant) with onset 23Nov2021, outcome "unknown", described as "having the sensation like she couldn't breath"; NAUSEA (non-serious) with onset 23Nov2021, outcome "unknown", described as "Nauseous"; DIZZINESS (non-serious) with onset 23Nov2021, outcome "unknown", described as "lightheaded"; PAIN (non-serious) with onset 23Nov2021, outcome "not recovered", described as "burning pain"; VACCINATION SITE WARMTH (non-serious) with onset 23Nov2021, outcome "unknown", described as "injection site was running super hot"; PALPITATIONS (non-serious) with onset 23Nov2021, outcome "unknown", described as "her heart was pounding in her chest"; WHEEZING (non-serious) with onset 23Nov2021, outcome "unknown", described as "wheezing"; BLOOD PRESSURE INCREASED (non-serious) with onset 23Nov2021, outcome "unknown", described as "blood pressure was 120/80 which for her that's very high"; LETHARGY (non-serious) with onset 23Nov2021, outcome "unknown", described as "lethargic"; PERIPHERAL SWELLING (non-serious) with onset 24Nov2021, outcome "unknown", described as "arm swelling went down to her bicep on her right arm"; SWELLING (non-serious) with onset 24Nov2021, outcome "unknown", described as "neck swelling"; PHARYNGEAL SWELLING (non-serious) with onset Nov2021, outcome "unknown", described as "swelling had reached the base of her throat"; FEELING OF BODY TEMPERATURE CHANGE (non-serious) with onset 24Nov2021, outcome "not recovered", described as "running hot and cold. She would be burning up and then she would be freezing cold"; OROPHARYNGEAL PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "Sore throat"; SINUSITIS (non-serious) with onset 24Nov2021, outcome "unknown", described as "on the verge of a sinus infection"; MIGRAINE (non-serious) with onset 23Nov2021, outcome "not recovered", described as "Migraine headache"; BURNING SENSATION (non-serious) with onset 23Nov2021, outcome "unknown", described as "right shoulder blade was burning/arm burning"; FEELING HOT (non-serious), outcome "unknown", described as "arm was still running hot". The events "severe allergic reaction", "felt like her breathing was starting to restrict, like when she gets stung by a bee", "having the sensation like she couldn't breath", "arm swelling went down to her bicep on her right arm", "neck swelling" and "swelling had reached the base of her throat" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (23Nov2021) 120/80, notes: normal blood pressure in mid-90s/68; oxygen saturation: (23Nov2021) 100; sars-cov-2 test: (Nov2021) negative. Therapeutic measures were taken as a result of hypersensitivity, respiratory arrest, dyspnoea, blood pressure increased, burning sensation. The clinical course was reported as follows: the patient vaccine was administered on 23Nov2021 at about 1:20 PM in the afternoon at the (name) and within 15 minutes she felt nauseous and lightheaded to where she needed to lay down. The nurse had called back someone else and gave that person their vaccine and when the nurse came out the patient must have looked pretty dang bad because the nurse took the patient straight back to tend to her. By that time her right shoulder blade was burning, it was a burning pain at the top of her shoulder blade and it went all around. The injection site was running super hot and her heart was pounding in her chest. To her it felt like her breathing was starting to restrict, like when she gets stung by a bee. In the past when she had the antivenom and anti-swelling injections to counteract a bee string she had the same kind of breathing problem. The nurse checked her pulse ox and the nurse was surprised that it was still at 100, which means that her airway wasn't closing but she was still having the sensation like she couldn't breath and like it was cut off. The patient felt like she was wheezing. She was laying down and the nurse took her blood pressure. Normally the caller has a low blood pressure and it was 120/80 which is probably the biggest reason why she appeared to have major problems because for her that's very high. Her normal blood pressure in mid-90s/68. She had ice applied to her forehead and the nurse monitored her vitals and helped get her breathing to calm down and the nurse continued to monitor her pulse ox. The patient didn't know how long she was in the back with the nurse until the nurse felt that she was stable enough to move back to the lobby where she had to wait until 3:20 in the afternoon before she was feeling well enough to drive herself home. The nurse was still nervous sending the caller home at that point because the patient had ice on her arm for 2 hours and it was still burning up. Later that night she became very lethargic and she went to bed at 9:00 PM, her arm was still on fire, she still had the burning pain, her breathing was still similar to other allergic reactions that she has had in the past. She woke up at 9:00 AM the next day and the arm swelling went down to her bicep on her right arm and to her neck. At some point during that day or maybe the next day the swelling had reached the base of her throat where her shoulder attaches to her neck. By Monday, when she went to see her chiropractor, acupuncturist and her massage therapist they all said that they couldn't believe the amount of swelling that she had. Her arm was still running hot and by that point she was running hot and cold. She would be burning up and then she would be freezing cold. It has been all day from 24Nov2021 and it is still happening, it is just not as frequent. She had a sore throat. She normally has a runny nose from mold allergies but that has gone from being clear and runny to white and sticky and she is on the verge of a sinus infection. She had a migraine headache after receiving the vaccine, that is getting better now but up until a couple of days ago it was constant. She had the sore throat to the point that they thought that she actually had COVID and she had to go in for a COVID swab, it came back negative. She went to her primary care provider on 01Dec2021 because normally 7 days after something like this her body is able to start fighting it and her body couldn't deal with it so she had to get medical help. On Monday her acupuncturist had to treat her lungs to open them up to get her breathing stabilized from the injection. She also had to have other herbal supplements added to her regimen to help her liver and spleen process whatever Pfizer put into this thing. She has been allergic to milk and they identified it as an allergy to the protein in milk. Her primary care doctor said that she had an immediate reaction to something that Pfizer has in the drug and her prolonged situation is because she is allergic to the protein in the vaccine. Based on the injectables that she had with her first bee string she literally walked out of the emergency room looking like the Michelin man in 1981 from all of the stuff that they were trying to do to counteract her bee sting. This agent may not believe her but she will not take an EpiPen because of her reaction to the anti-swelling medicine. If she were stuck with an EpiPen it may kill her because it's a lot stronger than the anti-swelling medication is. She can't have Benadryl, amitriptyline, flexeril, the muscle relaxer stuff and she can't have an anti- something for when you have an upset stomach. Like when they would make you take Prilosec. She also can't have Tylenol. Patient stated another medication that was provided too fast for this agent to capture and when this agent attempted to get patient to repeat the medications she refused to do so and said basically she just can't have any prescription drugs. They all make her sick and make her sick in this way. She knew that these symptoms that she was having are definitely an allergic reaction. The problem is that she didn't know which ingredient is causing her side effects and her allergist will keep clearing her to have the vaccine because she didn't know which one specifically that she is allergic to.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: Test Date: 20211123; Test Name: blood pressure measurement; Result Unstructured Data: Test Result:120/80; Comments: normal blood pressure in mid-90s/68.; Test Date: 20211123; Test Name: pulse oximeter; Result Unstructured Data: Test Result:100; Test Date: 202111; Test Name: COVID swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to molds; Arthropod bite; Breathing difficult (when she had the antivenom and anti-swelling injections to counteract a bee string); Drug allergy; Milk allergy; Runny nose (from mold allergies)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1948426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: GA
Alter: 56,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 21.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: IM / LA

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

Alanine aminotransferase increased Areflexia Aspartate aminotransferase increased Blood creatinine increased Blood electrolytes abnormal Bradycardia Cardiac arrest Cardio-respiratory arrest Coma Computerised tomogram Corneal reflex decreased Dialysis Electrocardiogram abnormal Electrolyte imbalance Endotracheal intubation Hyperglycaemia Hypokalaemia Hypotension

Symptomtext

Cardiopulmonary arrest; shock 56-year-old female with a past medical history significant for ESRD in the setting of diabetes and hypertension, chronic diastolic heart failure, and other medical problems, who received hemodialysis treatments on a Monday, Wednesday, Friday regimen at dialysis facility, followed by Doctor. The patient became hypotensive and bradycardic during a routine outpatient dialysis session on 11/05/2021, and had struggled with this for several weeks according to outpatient dialysis nursing staff. In the past, she has responded to IV fluid bolus when her blood pressure gets low although on this occasion she was persistently hypotensive receiving 2-3 L of IV fluid prior to discontinuation of her treatment and arrival of EMS. The patient was arrested en route to the ED and was redirected to Hospital, where she was intubated, received one dose of ketamine, and started on Levophed, per report. Upon arrival, she was found to have systolic blood pressures in the 120 to 130 range on Levophed at >20 mcg's per minute. This was subsequently down titrated and she was on 2-6 mcg per minute with an SBP in the 130-150 range. Unfortunately she was found to be unresponsive with no spontaneous movement noted since her arrival, with no sedation administered since leaving the emergency department in Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Per neurology on 11/5/21: Patient is intubated and comatose. Patient's son and daughter at bedside, and history was therefore, collectively obtained from the patient?s family at bedside, from the nursing staff and from reviews of available medical records. The patient is a critically ill, 56 years old, Female, unknown handedness, with known multiple complex medical co-morbidities listed below including, but not restricted to, ESRD on hemodialysis, CHF, and metabolic syndrome, who was flown today from Hospital for further evaluation and management of cardiac arrest. Apparently the patient was undergoing hemodialysis this morning at an outside facility where she became severely hypotensive, bradycardic, followed by cardiac arrest of at least 5 to 10 minutes or more down time duration, before pulse obtained. It is important to note that no documentations are available on the exact details. She was intubated, not sedated, but remains unresponsive, with non-reactive pupils, absent corneal, and gag reflexes, and absent motor movements or response to noxious stimuli. Hence neurology service is consulted for prognostication. NCHCT reviewed and negative for acute, subacute or space occupying lesions. EKG showed evidence of MI as per cardiology attending. Labs reviewed and remarkable for elevated high sensitivity troponin 253, and evidence of renal failure Cr 3.9, electrolytes imbalance including hypokalemia 3.2, hyperglycemia 477 mg/dL, mild leukocytosis 11.3, and transaminities ALT 221, AST 369.
Aktuelle Erkrankungen: n/a
Vorgeschichte: Insulin-Dependent Diabetes Mellitus; Peripheral Neuropathy; ESRD (HD on MWF at Hospital); Chronic low back pain/sciatica; Osteoarthritis; Dyslipidemia; Fibromyalgia; PAD; History of seizure disorder; Obesity; GERD; Glaucoma; Anxiety
Andere Medikamente: ProAir (albuterol) inhaler; apixaban 5mg BID; atorvastatin 40mg daily; Symbicort inhaler; calcium acetate 667mg 2 caps TID; citalopram 20mg daily; cyclobenzaprine 10mg daily; diphenhydramine 25mg daily; docusate 100mg BID; ferrous sulfate 3
Allergien: chlorhexidine (hives); doxycycline (rash); betadine (itching); xalatan; paper/silk tape (itching); polysulfone-based dialyzers (itching)
Vorherige Impfungen: -

VAERS 1940501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8020

kritisch

Staat: CA
Alter: 89,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 05.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Angiogram pulmonary normal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Death Decreased appetite Dyspnoea Fatigue General physical health deterioration SARS-CoV-2 test positive

Symptomtext

Date of Admission: 11/10/2021 Date of Death:11/21/2021 Reason for Hospital Admission (Admitting Diagnosis): Covid pneumonia, acute hypoxic respiratory failure 89 Y male with purported dementia (per family, not clear if formally diagnosed), hypertension, hyperlipidemia, glaucoma, had recent covid booster on 11/5 who presented to ED on 11/10 with fatigue, shortness of breath, cough, anorexia. Found to have covid pneumonia with acute hypoxic respiratory failure. CXR with multifocal pneumonia. Covid pneumonia/acute hypoxic respiratory failure: Symptom onset 11/5, covid positive 11/10. Pt received 5 day course of redemsivir (11/11-11/15/21), dose of tocilizumab (11/13/21), and high dose steroids. Otherwise CTA of chest on 11/13 was negative for PE. Despite the aforementioned treatments, pt continued to deteriorate with escalating oxygen requirements up to 60L and 100% high flow oxygen. Family decided to forego ICU care and mechanical intubation. After further discussions with family (grandson served as family spokesperson), they made difficult decision for comfort care on 11/19/21. High flow oxygen removed, placed on morphine drip, and limited family members were allowed to visit. Patient subsequently expired at 14:46 on 11/21/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: purported dementia (per family, not clear if formally diagnosed), hypertension, hyperlipidemia, glaucoma,
Andere Medikamente: beta-carotene,A,-vits C,E/mins (OCUVITE ORAL) Take by mouth ? Timolol Maleate (TIMOPTIC) 0.5 % Opht Drop Instill 1 drop in right eye 2 times a day 10 mL 6
Allergien: Chocolate, wine
Vorherige Impfungen: -

VAERS 1902207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: AZ
Alter: 68,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 15.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / AR

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

Cerebrovascular accident Magnetic resonance imaging abnormal

Symptomtext

Stroke, two, small, frontal lobe 1.3 cm and 1.5 cm on MRI. Stroke occurred 2 weeks after vaccination .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: MRI x3
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Hypoparathyroidism
Andere Medikamente: Insulin, bit D3,tums,multivitamin,creon,a Lodi pine,Flovent, albuteral,calcitriol,
Allergien: Augmenting, ofloxacin, fluconazole
Vorherige Impfungen: -

VAERS 1854515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: TX
Alter: 78,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray Computerised tomogram Confusional state Intensive care Lethargy Mechanical ventilation Oxygen saturation decreased Pulmonary embolism Respiratory distress

Symptomtext

In 24 hours the resident became confused, lethargic and in respiratory distress. Saturations could not be kept above 90 on 5 liters. She subsequently ended up in the ICU on a ventilator and was diagnosed with 2 large pulmonary embolisms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 8,0
Labordaten: CXR, CT Scan at the hospital
Aktuelle Erkrankungen: Urinary Tract Infection
Vorgeschichte: COPD, CHF, DM, Anxiety, Dementia
Andere Medikamente: Proventil, Tramadol, Simvastatin, Abilify, Linzess, Apixaban, Gabapentin
Allergien: Codeine, Lactose
Vorherige Impfungen: -

VAERS 1854325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MN
Alter: 69,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 27.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure COVID-19

Symptomtext

Dose 1 COVID on 2/27/21, dose 3 on 3/20/21, and dose 3 of COVID vaccine. PAtient admitted with COVID acute resp failure on 11/5/21, and patient remains hospitalized on 11/9/21.

Weitere VAERSDATA-Felder

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

VAERS 1817609

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac disorder Chest discomfort Chest pain Flushing Hyperhidrosis Myocardial infarction

Symptomtext

Systemic: Cardiac Disorder (diagnosed by MD)-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Heart Attack-Severe, Additional Details: Patient suffered a massive myocardial infarction 12 hours post vaccination. She was hospitalized and received stent. Patient was in remarkably good health and had no issues prior to vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1798299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: LA
Alter: 64,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 14.10.1957
Beginn: 14.10.1957
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anaphylactic reaction Eye swelling Anaphylactic shock

Symptomtext

Received the flu shot and the Covid booster on the same day (five minutes apart). Later that day had dinner that included seafood and mollusks. Previously, no allergic reactions to seafoods or mollusks. Went into anaphylaxic shock. Spent night in hospital receiving IV and steriods.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, High blood pressure
Andere Medikamente: Metformin, Losartan
Allergien: None
Vorherige Impfungen: -

VAERS 1794349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

kritisch

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Cerebrovascular accident Computerised tomogram head Hypertension Sleep disorder Tachycardia Tinnitus Urine analysis normal

Symptomtext

10/15/21: Awoken from sleep with severe tinnitus, 911 call, ambulance to nearest hospital due to tachycardia, hypertension, concern for stroke. Severe tinnitus resolved within an hour? Discharged following morning with recommendation to see Neurologist. Milder tinnitus on 10/16/ 21 pm managed at home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: 10/16/21: Including but not limited to Electrolytes, cardiac enzymes, urinalysis, head CT: all normal. Observed for approximately 10 hours in the Emergency Dept.
Aktuelle Erkrankungen: none
Vorgeschichte: Bipolar disorder
Andere Medikamente: seroquel multivitamin
Allergien: Kiwi
Vorherige Impfungen: -

VAERS 2674220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 21.08.2023
Impfdatum: 23.10.2021
Beginn: 27.03.2022
Tage bis Beginn: 155,0
Dosis: 2
Route/Site: IM / RA

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

Coagulopathy Deep vein thrombosis Hypotension Symptom recurrence

Symptomtext

COAGULOPATHY, UNSPECIFIED TYPE ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN HYPOTENSION 4/11/2022, 5/18/2022, 6/4/2022, 6/12/2022, 8/7/2022, 8/31/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2673467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 09.11.2021
Beginn: 24.10.2022
Tage bis Beginn: 349,0
Dosis: 2
Route/Site: IM / RA

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

Deep vein thrombosis

Symptomtext

ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN

Weitere VAERSDATA-Felder

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

VAERS 2527839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 18.02.2021
Beginn: 08.11.2022
Tage bis Beginn: 628,0
Dosis: 1
Route/Site: IM / UN

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

Arthralgia COVID-19 Discoloured vomit Intensive care Lethargy Mental status changes Productive cough Respiratory distress SARS-CoV-2 test positive

Symptomtext

Pt to ED 11/8 for AMS, lethargy. Pt COVID+ 11/8. 11/9 pt in resp distress, transfer to ICU. 11/12 pt coughing up a moderate amount of brown/tan Phlegm, thick. Also emesis noted small amount times one dark green in color. 11/15 Pt a/o x4, room air, complaints of chronic pain in left hip, vital signs stable, afebrile. Pt discharged 11/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 14,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Acute respiratory failure with hypoxia (CMS/HCC) Acute respiratory failure with hypoxia (CMS/HCC) Oropharyngeal dysphagia Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxemia (CMS/HCC) Nausea and vomiting Morbid obesity with BMI of 50.0-59.9, adult (CMS/HCC) Cellulitis of right lower extremity Pain Bradycardia Morbid obesity (CMS/HCC) Toxic metabolic encephalopathy Acute renal failure with tubular necrosis (CMS/HCC) Hyperkalemia, diminished renal excretion Metabolic acidosis, increased anion gap Atrial fibrillation with RVR (CMS/HCC) UTI due to extended-spectrum beta lactamase (ESBL) producing Escherichia coli Wounds, multiple Acute blood loss anemia Acute deep vein thrombosis (DVT) of right upper extremity (CMS/HCC) Septic shock (CMS/HCC) COVID-19 virus infection Hypomagnesemia Hyperkalemia Acute renal failure with acute tubular necrosis superimposed on stage 3a chronic
Andere Medikamente: acetaminophen (TYLENOL) 500 MG PO Tab apixaban acetaminophen (TYLENOL) 500 MG PO Tab apixaban (ELIQUIS) 5 MG PO Tab bumetanide (BUMEX) 2 MG PO Tab calcitriol (ROCALTROL) 0.5 MCG PO Cap chlorthalidone (HYGROTON) 25 MG PO Tab cyclobenzaprine
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2522018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 71,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 01.12.2021
Beginn: 21.05.2022
Tage bis Beginn: 171,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Blood immunoglobulin G increased Blood test abnormal Fatigue Muscle operation Orthosis user Peripheral swelling SARS-CoV-2 test negative Thrombosis Ultrasound Doppler abnormal

Symptomtext

I did not have an adverse reaction to the vaccine. I had to have a hamstring repair on my left leg and was in a brace for six weeks. In May 2022, I developed a blood clot in my left leg which was probably caused by the brace. On July 5., 2022, I received my 2nd booster. We went on a trip on 07/22/2022 and arrived back home on 08/02/2022. I felt very tired, and I tested for COVID-19 and it was negative. I had a follow-up appointment with my doctor for my surgery. I had some bloodwork and the IGG antibody was elevated. A few days later I noticed my right calf was swollen and contacted my doctor. I had an ultrasound, and I had a distal vein thrombosis in my right calf. I am currently on blood thinners.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Fish Oil; Multivitamin; Restasis
Allergien: Soy; Adhesive Tape; Environmental Allergies
Vorherige Impfungen: -

VAERS 2509462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CO
Alter: 59,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 16.11.2021
Beginn: 24.09.2022
Tage bis Beginn: 312,0
Dosis: 3
Route/Site: SYR / UN

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

Autopsy Eosinophilic myocarditis Histology

Symptomtext

Post-mortem examination of cardiac tissue revealed eosinophilic myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eosinophilic myocarditis
Hospital-Tage: -
Labordaten: Post-mortem autopsy (09/28/2022), microscopic histology study
Aktuelle Erkrankungen: Unknown
Vorgeschichte: None
Andere Medikamente: Trazedone 100mg daily, Escitalopram 20mg
Allergien: None
Vorherige Impfungen: -

VAERS 2461637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Pericarditis Pneumonia Pneumothorax

Symptomtext

Pericarditis; Partially Collapsed Lung Resulting in Pneumonia; Partially Collapsed Lung Resulting in Pneumonia; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), in Nov2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 54 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE , Batch/Lot No: EW0151), administration date: Apr2021, when the patient was 53 years old, for COVID-19 immunization; Bnt162b2 (DOSE 1, SINGLE , Batch/Lot No: FH6204), administration date: Mar2021, when the patient was 53 years old, for COVID-19 immunization. The following information was reported: PNEUMONIA (hospitalization), PNEUMOTHORAX (hospitalization) all with onset Nov2021, outcome "unknown" and all described as "Partially Collapsed Lung Resulting in Pneumonia"; PERICARDITIS (hospitalization) with onset Nov2021, outcome "unknown". The patient was hospitalized for pericarditis, pneumonia, pneumothorax (hospitalization duration: 3 day(s)). The events "pericarditis" and "partially collapsed lung resulting in pneumonia" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of pericarditis, pneumonia, pneumothorax. Additional information: The patient had pericarditis & partially collapsed lung resulting in pneumonia. But the most concerning was pericarditis. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. The patient received the fourth dose of BNT162b2 (lot number: FM0173 9122) in Jun2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2454697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 85,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SC / LA

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

Asthenia Blood culture Computerised tomogram abdomen Computerised tomogram head Computerised tomogram thorax Cough Electrocardiogram Erythema Full blood count Headache Laboratory test Loss of consciousness Pain Swelling Vomiting

Symptomtext

localized swelling, redness and pain, 2 days later, started having headache. 7 days later, started having cough, 9 days later, the patient vomited, passed out and having generalized weakness, which required hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 4,0
Labordaten: CBC, CHME 13, EKG, blood cultures, CT head, CT chest, abdomen and pelvis
Aktuelle Erkrankungen: none
Vorgeschichte: HTN,HLD,DM1 ,Aortic valve stenosis
Andere Medikamente: Finasteride (PROSCAR) 5 mg Oral Tab Metoprolol Tartrate (LOPRESSOR) 25 mg Oral Tab Tamsulosin (FLOMAX) 0.4 mg Oral Cap Nystatin (MYCOSTATIN) 100,000 unit/gram Top Powd cloNIDine HCL (CATAPRES) 0.1 mg Oral Tab Lisinopril (PRINIVIL/ZESTR
Allergien: Augmentin
Vorherige Impfungen: -

VAERS 2430096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

schwer

Staat: IN
Alter: 24,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 12.10.2021
Beginn: 21.02.2022
Tage bis Beginn: 132,0
Dosis: 1
Route/Site: IM / RA

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

Intensive care Maternal exposure before pregnancy Pre-eclampsia Premature delivery

Symptomtext

Severe Preeclampsia. Born 35weeks 5days due 3/28/22. 5lbs 9oz. 18 days in NICU due to prematurity. Magnesium needed for 36 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal vitamin Iron supplements
Allergien: None
Vorherige Impfungen: -

VAERS 2292781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CT
Alter: 70,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 04.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / AR

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

Acute left ventricular failure Anxiety Cardiac failure congestive Condition aggravated Dyspnoea Electrocardiogram abnormal Familial risk factor Fear Hyperlipidaemia Hypertension Nervousness Positive airway pressure therapy Rales Respiratory distress Rheumatoid arthritis Rhonchi SARS-CoV-2 test Tachycardia

Symptomtext

On November 14, 2021 we were taking a walk around our neighborhood at around 6:00 PM and after about 1/4 of a mile the patient started having trouble breathing. We stopped for a short time to rest and the breathing did not get any better. The patient started to get very nervous so we returned to the house. Once inside she tried sitting for a few minutes and she then showed symptoms of anxiety and indicated that she was scared so I (spouse) got her into the car and headed for the Hospital (about 20 minutes away). Upon arrival at the hospital they immediately admitted her to the Emergency room where they performed many tests and put her on medications to get her stabilized after about 2 hours and many test. She was doing much better and was breathing without mask assistance. She stayed in the hospital for a total of 3 days. Scheduled follow-up with cardiologist. She is now on Entresto and Metoprolol Succinate ER. Her cardiologist has indicated that her heart muscles are stronger now and are improving. They found no blockages and no damage as a result of the episode. I can provide medical records from the hospital stay if necessary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 3,0
Labordaten: ED Provider Notes at 11/14/2021 9:08 PM History Chief Complaint -Patient presents with Difficulty Breathing I personally evaluated the patient. I reviewed the AP's or resident's findings, supervised the management of the patient, and I agree with the treatment and plan. History provided by: The patient Chief Complaint: Shortness of breath Associated symptoms and Additional history: Patient in normal state of health earlier today but this evening had rapid onset of severe shortness of breath. No cough. No history of CHF, COPD, or lung disease. No history of heart failure or heart disease known. No chest pain corresponding to shortness of breath. No peripheral weakness, numbness, or edema. No history of this in the past. No recent health changes. Physical Exam BP (!) 191/100 (BP Location: Left arm, Patient Position: Sitting) | Pulse (!) 124 | Temp 97.1 ?F (36.2 ?C) (Tympanic) | Resp 18 | LMP 08/27/2003 (Within Years) | SpO2 100% Physical Exam Constitutional: Alert and oriented but in moderate respiratory distress. Only couple words able to be spoken at a time due to dyspnea. HENT: Head: Atraumatic MMM Eyes: PERRL, EOMI Neck: Normal ROM. Question slight JVD bilaterally though difficult to assess due to redundant tissue in neck. Cardiovascular: Tachycardic at 110-120 bpm. No extra sounds appreciated. Grossly regular rhythm. Pulmonary: Diffuse rales/rhonchi throughout lung fields. Scant wheezing with overall limited airflow equally throughout lung fields. Chest: Chest wall: No gross chest wall ttp. Abdominal: Soft, NT/ND Musculoskeletal: Normal gross ROM, no evidence of focal trauma. Lymphadenopathy: No unilateral or diffuse peripheral edema. Skin: Normal color, no rashes Neurological: AAO with normal cognition, No gross deficits Psychiatric: Anxious but cooperative and appropriate on exam. MDM: Clinical Impression Notes: Patient with rapid onset of severe shortness of breath. Rales and rhonchi on exam with limited airflow. Question flash pulmonary edema though patient has no history or significant risk factors. Will treat presumptively in the interim due to level of distress. Patient placed on BiPAP and respirations slowing and much improved. Will add nitroglycerin at this time. Stat portable chest x-ray ordered and to be performed by radiology tech. If x-ray confirms edema, will start nitroglycerin drip. Patient will require admission. No concern acute ACS or pneumonia. Critical Care: Critical care provided by me for the care of this patient totalling 35 minutes, exclusive of other billable procedures. MD 11-15-2021 - Dr. Assessment 1. Acute diastolic heart failure 2. Abnormal ECG 3. Abnormal high-sensitivity troponin 4. Rheumatoid arthritis 5. Hypertension with suboptimal control 6. Hyperlipidemia 7. Family history of coronary artery disease and congestive heart failure Suggest 1. Telemetry, cycle cardiac enzymes 2. Aspirin 81 mg daily 3. Continue rosuvastatin 4. Furosemide 20 mg IV once daily with daily chemistry panel 5. If remains hypertensive resume amlodipine 5 mg once daily +/- olmesartan 6. Transthoracic echocardiography for evaluation of ventricular and valvular substrate 7. Given new congestive heart failure, persistently abnormal electrocardiogram, elevated high-sensitivity troponin and family history of coronary artery disease I would favor definitive evaluation for obstructive coronary artery disease with coronary angiography. Concomitant right heart catheterization can be performed to assess for pulmonary hypertension elevated pulmonary capillary wedge pressure given her presentation and history of rheumatoid arthritis. Risks and rationale reviewed and she is in agreement with proceeding. Thank you for the consultation. Please contact me anytime with questions. Addendum ( 6:51 AM): I spoke with her husband, for an update and reviewed above. Notified attending hospitalist via text Addendum (3:!5 pm): Unfortunately, delay to coronary angiography today based on COVID-19 test not yet resulted / Cath Lab protocol. Discussed with interventional cardiology. Sign: MD 11/15/2021 6:26 AM
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis
Andere Medikamente: Xeljanz,Crestor,Celebrex,Folic Acid,Vascepa,Dymista,Timolol
Allergien: None
Vorherige Impfungen: -

VAERS 2264969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 11.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / LA

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

Deep vein thrombosis Thrombectomy

Symptomtext

DVT , Double thrombectomy performed 11/28/2021 by Dr.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 4,0
Labordaten: Hospitalization, double thrombectomy performed by Interventional Radiology on 11/28/2021.
Aktuelle Erkrankungen: adverse reaction to Juardiance
Vorgeschichte: diabetes, sleep apnea, hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 18.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Allergy to chemicals Blood cholesterol increased Blood test Cardiac monitoring Computerised tomogram normal Dizziness Dysmenorrhoea Echocardiogram normal Fatigue Feeling abnormal Hangover Head discomfort Heart rate increased Hypersensitivity Hypertension Menstruation irregular Migraine Ocular discomfort

Symptomtext

I had my last booster and flu shot on same date. Since then I have had to call the emergency number 3 times due to my heart beating super fast. It was worse than heart palpitations. The last time I called was last week. I think that it was a change in my blood pressure. I was light headed and felt I would pass out and my vision was blurry. I also had pressure in the top of my head. The medics came over and checked my blood pressure. They determined it was high but it was ok. I still asked to be taken to the ER. They kept me there for 4 or 5 hours and gave me a prescription for migraine. The symptoms returned shortly after they gave me the medicine. I was sent to have a CT scan performed. The results were normal. I scheduled an appointment with my doctor after that. He referred me to an ophthalmologist. The ER prescribed 2 medications for migraines but I have not taken them. In November I had a heart ultrasound done and was placed on a heart monitor for 1 week. I went to see a cardiologist. He advised the heart ultrasound was normal. I called the ER because my heart was beating like crazy for more than a minute. I had no stress factors that contributed. I have also been experiencing extreme fatigue so I had a full panel blood test and determined that my Vitamin D was low and that cholesterol was slightly high. I do still the pressure in my head and my eyes. It feels like my eyes have changed and it comes and goes. I have also experienced brain fog and extreme fatigue. I had a change in my periods. They are extremely painful and they are showing up a week earlier. When I drink wine, it seems that I am having an allergic reaction. After having half a glass of wine, I started having the palpitations and feeling like I am having a hangover.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: CT Scan-normal Heart ultrasound-normal Blood panel
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2254814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 13.10.2021
Beginn: 17.03.2022
Tage bis Beginn: 155,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Delivery Exposure during pregnancy Foetal heart rate abnormal Foetal vascular malperfusion Pyrexia SARS-CoV-2 test positive Stillbirth Umbilical cord thrombosis

Symptomtext

I got the third dose (booster) while I was just a few weeks pregnant, while I did not know I was pregnant at the time, I found out 2-weeks later. I had a very normal and healthy pregnancy until my 25 week appointment where they could no longer find the heartbeat of my baby and I delivered her stillborn the next day on 3/18/22. After the placenta report and the autopsy, we found that everything was normal aside from blood clotting found in the umbilical cord and in the placenta, believed to be from my positive COVID infection. While I was in the hospital to deliver my daughter, I tested positive for COVID and a couple of hours later, I had a fever of 102, which again, is believed to be from my COVID infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Umbilical cord thrombosis
Hospital-Tage: 2,0
Labordaten: positive COVID test 3/17/22; placenta report 3/18/22; autopsy 3/18/22
Aktuelle Erkrankungen: n/a
Vorgeschichte: migraines (treated with sumatriptan)
Andere Medikamente: sumatriptan
Allergien: bactrim
Vorherige Impfungen: -

VAERS 2211276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: IL
Alter: 89,0
Geschlecht: M
Eingang: 01.04.2022
Impfdatum: 27.10.2021
Beginn: 24.03.2022
Tage bis Beginn: 148,0
Dosis: 3
Route/Site: SYR / -

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

Dysarthria Facial paralysis Hemiparesis

Symptomtext

Patient admitted to Hospital on 3/24/2022 with left sided weakness, left facial droop and slurred speech.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 01.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: SYR / RA

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

Dermatitis allergic Nausea Syncope Urticaria Vaccination complication Dermatitis Rash SARS-CoV-2 test Viral rash Vomiting

Symptomtext

acute rash/ weals rash; wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet; wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date Dec2021 (Lot number: FE3594) at the age of 68 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Irritable bowel syndrome" (unspecified if ongoing); "Known allergies: pennicillen" (unspecified if ongoing). Concomitant medication(s) included: CYMBALTA; DULOXETINE. Past drug history included: Codeine, reaction(s): "Allergy"; Ibufrofen, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 1 at 01:15 PM (Batch/Lot No: pfizer FH8020) Location of injection: Right Arm), administration date: Dec2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: RASH (non-serious) with onset 24Dec2021 14:30, outcome "not recovered", described as "acute rash/ weals rash"; URTICARIA (non-serious), DERMATITIS (non-serious) all with onset 24Dec2021 14:30, outcome "not recovered" and all described as "wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash, urticaria, dermatitis. Additional information: Patient received second dose on unspecified date in Dec2021 at 02:30 PM at hospital. No other vaccine in four weeks. Adverse event: acute rash/ weals rash/ wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet. No Covid prior vaccination. Patient had Covid test post vaccination. Patient received Medrol prednisone 6 day dose pack/ hydroxyzine as treatment for adverse event. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20211230; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Irritable bowel syndrome; Penicillin allergy
Andere Medikamente: CYMBALTA; DULOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 2165676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Angiogram normal Blood test normal Dry eye Electric shock sensation Feeling abnormal Head discomfort Moaning Nausea Pain Sleep disorder

Symptomtext

Adverse Event that happened: 11/18/2021 I was woken up out of my sleep by my brain feeling like it was being electrocuted. It was extremely painful, i thought I was going to die. All I could do was moan and pray for it to stop. It continued for approximately 2 minutes and kept coming back for 10- 15 second shocks. This happened for 30 minutes. They continued throughout the day. 11/19/2021 - one at approx 9:45 am. 2 pm. another zap. 7:10 p.m. Lasted approx. 2 minutes, I remember my dog staring at me. 11/20/2021 woken at 3:30 a.m for approx. 2 minutes with zaps, 6:30 am woken for another 2 zaps, one came and then when it ended another one started. 6:40 a.m. another zap for approx 1 minute, 10:08 a.m. a few more zaps lasting 10-15 seconds 11/21 7:37 am - a short one, 6:36 p.m. a 10 second zap, 6:47 p.m. a 7 second zap, 7:50 p.m. another 15 second zap, 9:18 p.m. a 20 second zap, 9:25 p.m. a 10 second zap, 9:42 p.m. 8 second zap and 11:17 p.m. 5 second zap. 11/22 some happened during the day too busy to write down all 11/22. 4:15 10 seconds 11/22 11:20 pm 15 seconds 11/22 11:28 been having them off and on for last 8 minutes 11:38 pm 1 minute 11/23 8:31 am. 8 seconds 11/23 9:37 am 11/23 9:54 am 11/23 2:34 pm 11/23 3:06 pm 11/23 3:14 pm 11/23 6:11 pm More happened but didn?t keep track 11/24. 6:03 am. 11/24 10:09 am 11/24 11:07 am 11/24 1:49 pm 11/24 3:50 11/24 6:50 11/24 8:04 11/24 9:27 11/24 9:57 11/25. 1 am 11/25 4:30 am. 20 seconds 11/25 4:50 11/25 4:56 11/25 3 more times 11/26 sometime during the night 11/26 11:41 am 11/26 7:31 pm 11/26 11:00 pm off an on for 15 minutes 11/27 woken up a few times through the night 11/27 9:17 am lasted at least 30 seconds. 11/28 - no zaps 11/29 10:37 pm Pressure on right side of brain. 11/30. 12:51. A few zaps 11/30. 9:52 pm. About 5 in a row 12/1 9:33 am top back of right side 12/2 sometime during the night 12/2 3:41 a couple of zaps 12:2 3:50 12/3. 10:25 am they are quick shocks now not the long and bad ones at first. More toward the back top right corner of my head. 12/5 4:30 pm had a little pressure on the left side and then went to the right ride 12/6. 4:05 pm 12/7. 8:21 pm. A few quick jolts. Right above right ear toward the back of the head 12/7. 11:09. Pressure on top right side of head and behind right eye 12/7. 11:29. Quick zap 12/8. 9:44 am couple of zaps 12/9- 12/12 I didn?t keep track 12/13. 8:25 very strong one The largest one felt like someone was electrocuting my brain from the inside out. I had pressure behind my right eye after. Its always on the right side. My right eye has constantly been dried out. Not usual. Been wearing contacts for years. A little nauseous at times. Treatment, went to see Dr. (neurologist), she processed blood tests and had me get an MRA. Both the tests came back normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Dr. (neurologist), she processed blood tests and had me get an MRA. Both the tests came back
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma and hypothyroidism
Andere Medikamente: L-Thyroxine (Synthroid) 75 mcg, Estradiol/Norethindrone Acetate Tables 1.0mg/0.5 mg, Vitamin C Supplement 1000 mg, Super B-Complex Supplement
Allergien: prednisone, erythromycin, pineapple, adhesive
Vorherige Impfungen: -

VAERS 2129397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: -
Alter: 87,0
Geschlecht: M
Eingang: 21.02.2022
Impfdatum: 15.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Atrioventricular block complete Bradycardia Cardiac pacemaker insertion Hypotension Intensive care

Symptomtext

Patient admitted with Symptomatic bradycardia. He was given a dose of atropine at facility, monitored in CCU on admission. EP was consulted and he underwent PPM placement. Due to his low BP and complete heart block, carvedilol and amlodipine were discontinued on admission. Will continue to hold for now until PCP and cardiology follow up. BP is fairly stable. He was seen by PT and OT, recommended home. ED visit and hospital admission were within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2128693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 20.02.2022
Impfdatum: 09.12.2021
Beginn: 09.02.2022
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: IM / LA

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

Epistaxis Erythema Pain Peripheral swelling Skin warm Thrombosis Tinnitus

Symptomtext

Arm swelled and large (2?) red raised circle around injection spot. Lasted for over 2 weeks. Hot to the touch. Painful to raise arm. Ears ringing . Bloody nose and constant dried blood clots in nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: None. Just put ice on arm every day to help with pain. Took Alieve.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2119159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 01.11.2021
Beginn: 05.02.2022
Tage bis Beginn: 96,0
Dosis: 3
Route/Site: IM / -

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

Blood glucose increased Influenza A virus test Influenza B virus test SARS-CoV-2 test Syncope

Symptomtext

multiple syncopal episodes, high blood sugar

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: -
Vorgeschichte: ? Acquired hypothyroidism ? Anemia, normocytic normochromic ? Anxiety ? Arthritis ? Bilateral leg edema ? CKD stage 3 due to type 2 diabetes mellitus (CMS/HCC) ? Decreased thyroid stimulating hormone (TSH) level ? Depressive disorder ? Diabetic peripheral neuropathy associated with type 2 diabetes mellitus (CMS/HCC) ? Essential hypertension ? Hyperlipidemia ? Memory deficits ? Mild intermittent asthma, uncomplicated ? Morbid obesity with BMI of 40.0-44.9, adult (CMS/HCC) ? Muscle cramps ? Obesity, Class I, BMI 30-34.9 ? Obesity, Class II, BMI 35-39.9 ? Overweight (BMI 25.0-29.9) ? Parkinson's disease ? Sprain of left shoulder ? Uncontrolled type 2 diabetes mellitus with hyperglycemia ? Vitamin D deficiency
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2116007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: WI
Alter: 74,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 09.11.2021
Beginn: 05.02.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Device kink Dialysis Endotracheal intubation Intensive care Resuscitation SARS-CoV-2 test positive Tachycardia Unresponsive to stimuli

Symptomtext

Pt presents to Facility on 02/05/2022 via Ambulance from dialysis after becoming unresponsive. He is intubated upon arrival. Art line was kinked during dialysis. Became tachycardic. Transported by Ambulance to ER ER - CPR for two minutes -Incidentlly found to be COVID positive on admission to ICU

Weitere VAERSDATA-Felder

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

VAERS 2096020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: KY
Alter: 69,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 03.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / RA

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

Activated partial thromboplastin time normal Albumin globulin ratio decreased Angiogram pulmonary abnormal Ascites Blood albumin decreased Blood calcium decreased Blood chloride decreased Blood fibrinogen normal Blood lactate dehydrogenase normal Blood lactic acid normal Blood magnesium decreased Blood potassium decreased Blood sodium decreased Brain natriuretic peptide normal C-reactive protein increased COVID-19 Carbon dioxide normal Chemotherapy

Symptomtext

1/10/22 70 yr/o female who presents with covid. HPI 70 y/o F here with nausea, HA. PT was dx'ed with covid this AM. PT has been sick since last admission (12/23). Last chemo was while inpatient in Dec (24th). Patient denies any history of blood clots, heart disease. States she has had ongoing issues since recent hospitalization of fatigue, headache. Has had some mild shortness of air. This is not worsening. Denies any chest pain. Has had a slightly productive cough and did vomit recently. No diarrhea or constipation. No signs of GI bleed otherwise. 1/15/22 Hospital Course: Patient is a 70-year-old female with a past medical history of asthma, arthritis, hypertension, hyperlipidemia, kidney stones, atrial fibrillation, ovarian and endometrial cancer on chemotherapy, malignant ascites, urinary tract infections, GERD, and vitamin D deficiency. She presented to emergency department with complaints of known COVID-19 positive, nausea, and headache. She reports she has been sick since last admission on 12/23/21, and was diagnosed with COVID yesterday morning. She is currently followed by Dr. with Oncology, with her last chemotherapy treatment on December 24. She reports having continued fatigue, headache, and shortness of breath since being discharged. She has had a productive cough but no nausea, vomiting, or diarrhea. Upon further work-up in the ED her labs showed sodium 134, potassium 3.2, chloride 93, CO2 30, albumin 2.6, calcium 8.3, D-dimer 6180, RBC 3.59, hemoglobin 10.7, hematocrit 32, with a CT head showing no acute abnormalities, urinalysis with 30 protein, CTA chest for PE with no evidence of pulmonary embolism or aortic dissection, new interstitial pulmonary infiltrate and mild groundglass opacity infiltrates, mild pulmonary edema, new small to moderate left pleural effusion, moderate to large right pleural effusion concerning for metastatic disease, CT abdomen and pelvis with mild thickening of the peritoneal surfaces, moderate to large abdominal and pelvic ascites, persistent, relatively stable retroperitoneal and mesenteric lymph nodes concerning for metastatic disease. She was given fluid bolus, IV Zofran, and initiated on IV remdesivir while in the ED with plans for admission for further evaluation and treatment. Upon assessment this morning she is resting in bed comfortably. She appears in no acute distress at this time. Review of Systems Constitutional: Negative for chills and fever. HENT: Negative for congestion, nosebleeds, postnasal drip, rhinorrhea, sinus pressure, sinus pain, sneezing and sore throat. Eyes: Negative for pain and visual disturbance. Respiratory: Positive for cough and shortness of breath. Negative for chest tightness. +sputum production Cardiovascular: Negative for chest pain and leg swelling. Gastrointestinal: Positive for nausea and vomiting (a few days ago). Negative for abdominal pain, anal bleeding, blood in stool and diarrhea. Genitourinary: Negative for flank pain and vaginal bleeding. Musculoskeletal: Negative for arthralgias, back pain, myalgias and neck pain. Skin: Negative for rash. Neurological: Positive for headaches. Negative for dizziness, syncope, speech difficulty, weakness, light-headedness and numbness. All other systems reviewed and are negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 5,0
Labordaten: No COVID test result at hospital facility. 1/10/22 CBC W/DIFF - Abnormal; Notable for the following components: Result Value Red Blood Count 3.59 (*) Hemoglobin 10.7 (*) Hematocrit 32.1 (*) Lymphocyte % 13.8 (*) Immature Granulocyte% 2.0 (*) Immature Granulocyte Abs 0.12 (*) All other components within normal limits COMPREHENSIVE METABOLIC PANEL (CMP) - Abnormal; Notable for the following components: Sodium 134 (*) Potassium 3.2 (*) Chloride 93 (*) Carbon Dioxide 30 (*) Albumin 2.6 (*) Albumin/Globulin Ratio 0.7 (*) Calcium 8.3 (*) All other components within normal limits URINALYSIS - Abnormal; Notable for the following components: Protein-Urine 30 (*) Urobilinogen-Urine 4.0 (*) All other components within normal limits COMPREHENSIVE METABOLIC PANEL (CMP) - Abnormal; Notable for the following components: Sodium 134 (*) Potassium 3.3 (*) Chloride 95 (*) Total Protein 5.9 (*) Albumin 2.4 (*) Albumin/Globulin Ratio 0.7 (*) Calcium 7.9 (*) All other components within normal limits C-REACTIVE PROTEIN - Abnormal; Notable for the following components: C-Reactive Protein 4.2 (*) All other components within normal limits D-DIMER,QUANTITATIVE - Abnormal; Notable for the following components: D-DIMER 6,180 (*) All other components within normal limits CBC W/DIFF - Abnormal; Notable for the following components: Red Blood Count 3.45 (*) Hemoglobin 10.1 (*) Hematocrit 31.1 (*) Neutrophils % 84.1 (*) Lymphocyte % 6.2 (*) Metamyelocyte % 0.9 (*) Lymphocyte-Absolute 0.32 (*) Metamy-Absolute 0.05 (*) Poikilocytosis 1+ (*) Toxic Granulation PRESENT (*) Burr Cells 1+ (*) All other components within normal limits FERRITIN - Abnormal; Notable for the following components: Ferritin 1,291.1 (*) All other components within normal limits MAGNESIUM - Abnormal; Notable for the following components: Magnesium 1.2 (*) All other components within normal limits LIPASE TROPONIN B-TYPE NATRIURETIC PEPTIDE LACTIC ACID PROCALCITONIN B-TYPE NATRIURETIC PEPTIDE FIBRINOGEN PROTIME-INR PARTIAL THROMBOPLASTIN TIME LACTATE DEHYDROGENASE(LDH) 1/10/22 CT Angiogram Chest For PE IMPRESSION: 1.Mild thickening of the peritoneal surfaces which may reflect peritonitis or metastatic disease. Stable, moderate to large abdominal and pelvic ascites. 2.Omental stranding and nodularity highly concerning for metastatic omental caking. 3.Persistent, relatively stable retroperitoneal and mesenteric lymph nodes concerning for metastatic disease. 4.Colonic diverticulosis with no evidence of diverticulitis
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis o Asthma o Eyes sensitive to light o Hyperlipidemia o Hypertension o Mass of colon 03/11/2021 o New onset atrial fibrillation 08/13/2021 SAW DR ONCE IN ER. PATIENT REPORTS WILL TRY TO SEE AFTER HYST o Osteopenia o Ovarian cancer o Pleural effusion, right 03/11/2021 o PONV (postoperative nausea and vomiting) DENIES--REPORTS N/V FROM COLONOSCOPY BOWEL PREOP o Seasonal allergies o Stroke 2001 right weak at time (pt described TIA); underwent percutaneous PFO closure Dr. transiently treated with coumadin 2001. o Unspecified nonsenile cataract o Vitamin D deficiency
Andere Medikamente: amiodarone (PACERONE) 200 MG tablet Take 1 tablet by mouth daily. o amitriptyline (ELAVIL) 75 MG tablet Take 1 tablet by mouth nightly. o amLODIPine (NORVASC) 5 mg tablet TAKE 1 TABLET EVERY DAY o aspirin EC 81 MG EC tablet Take 1 tab
Allergien: Adhesive, Barium sulfate, Topamax
Vorherige Impfungen: -

VAERS 2076058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 75,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 27.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Anxiety Computerised tomogram Haemorrhagic stroke Magnetic resonance imaging

Symptomtext

Patient suffered from anxiety for 2 days following the Booster injection and then a hemorrhagic stroke on the afternoon of 11/3/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Haemorrhagic stroke
Hospital-Tage: 4,0
Labordaten: CT Scans (2) MRI (1)
Aktuelle Erkrankungen: None
Vorgeschichte: HBP
Andere Medikamente: Lisinopril 20mg, Aspirin 81mg, One A Day Vitamin, Atorvastatin 20mg
Allergien: None
Vorherige Impfungen: -

VAERS 2075662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 61,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 03.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: - / RA

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

Bell's palsy Eyelid function disorder Facial paralysis Herpes zoster oticus

Symptomtext

DIAGNOSED WITH BELLS PALSY VS. RAMSAY HUNT SYNDROME. MY FACE IS PARALYZED ON THE RIGHT SIDE AND I CANNOT CLOSE MY RIGHT EYE. NO KNOWN TREATMENT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NUTS
Vorherige Impfungen: -

VAERS 2047510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CT
Alter: 26,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 21.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Blood test Computerised tomogram Heart rate increased Hypoaesthesia Hypotension Intensive care Porphyria Ultrasound scan Urine analysis

Symptomtext

Severe abdominal pain (lasting 7 days, hospitalized every month since October), low blood pressure (80/74),high heart rate (162), Admitted to ICU on last visit to hospital (1/22) Numbness in left leg and foot. Unofficially diagnosed with Porphyria.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 14,0
Labordaten: Cat scans, ultrasounds, blood work, urine test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2043377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MO
Alter: 54,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 08.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

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

Electroencephalogram Laboratory test Magnetic resonance imaging Migraine Neurological examination Partial seizures

Symptomtext

multiple migraines vs focal seizures 1-2/week which continue to this date. Neurological evaluation including MRI, EEG, lab work completed. Multiple migraine medications as well as seizure medications have been tried but symptoms continue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: -
Labordaten: MRI 11/11/2021 EEG, lab work 12/13/2021
Aktuelle Erkrankungen: Hypertension Hypothyroidism
Vorgeschichte: -
Andere Medikamente: Benicar 20 mg daily levothyroxine 50 mcg daily estradiol 1 mg daily
Allergien: Penicillan, Sulfa antibiotics
Vorherige Impfungen: -

VAERS 2039457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: WA
Alter: 57,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 07.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: SYR / RA

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

C-reactive protein increased Echocardiogram Echocardiogram abnormal Inflammation Pericardial effusion Pericarditis

Symptomtext

Pericarditis 3 days in hospital Taking Colchicine 0.6 mg twice daily Had Ecocardigran C Reactive Protein was 233, far above normal. Still have an issue. lots of inflammation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 3,0
Labordaten: ECHO LIMITED - Details Study Result Narrative ? Left Ventricle: Left ventricle size is normal. Normal wall thickness. Normal systolic function. LV EF is 57 % , assessed by visual estimation. ? Right Ventricle: Right ventricle size is normal by visual estimation. Normal systolic function. TAPSE measures 2.1 cm. ? Pericardium: Small pericardial effusion is present. This is predominantly posterolateral to the left ventricule with maximal dimension of 1.3 cm. There is trivial anterior effusion. No evidence of hemodynamic effect. ? Right Sided Pressures: The IVC diameter is </=21 mm with a >50% collapse with inspiration suggesting a right atrial pressure of 3 mmHg. Unable to assess pulmonary artery systolic pressure due to insufficient doppler signal. ? Since the echocardiogram 9/16/21 the pericardial effusion is smaller. Images Scan on 9/17/2021 11:50 AM Component Results Component Your Value Standard Range Flag Vitals Height 180 Vitals Weight 124.005 Vitals BSA 2.41 Vitals BMI 38.27 Vitals BP Systolic 148 Vitals BP Diastolic 70 Vitals Heart Rate Rest 93 LVIDd 4.86 cm cm LVPW Diastolic Thickness MM 0.96 cm cm LV Systolic Diameter MM 3.4 cm cm IVS Diastolic Thickness MM 0.88 cm cm FS 30 % % TAPSE 2.12 cm cm RA PRESSURE 3 mmHg mmHg LVEF-TTE TRANSTHORACIC ECHO 57 % % C-REACTIVE PROTEIN - Details Component Results Component Your Value Standard Range Flag CRP 233.0 mg/L 0.0 - 5.0 mg/L H Performed by Lab
Aktuelle Erkrankungen: psoriatic arthritis GERD
Vorgeschichte: psoriatic arthritis GERD Obesity
Andere Medikamente: gabapentin 300 mg capsule pantoprazole 40 mg tablet famotidine 20 mg tablet HUMIRA PEN 40 mg/0.4 mL injection (pen)
Allergien: None
Vorherige Impfungen: -

VAERS 2014493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: IL
Alter: 38,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Alanine aminotransferase increased Aspartate aminotransferase normal Blood folate Blood magnesium normal C-reactive protein normal Electric shock sensation Electrocardiogram normal Full blood count normal Injection site pain Mobility decreased Pain Red blood cell count normal Tremor Vitamin B12 normal

Symptomtext

Pain at injection site, pain traveled to shoulder and deltoid, causes a decrease in mobility and tender to touch. Uncontrollably shaking/movement, electrical feeling in bones (legs area), right hand began to tremble randomly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Blood folic acid - NORMAL Vitamin B 12 - NORMAL Magnesium - NORMAL CRP - NORMAL RBC - NORMAL CBC - NORMAL MCGH - 25.6 SGOT - 32 SGPT - 78 Electrocardiogram - NORMAL
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Penicillin.
Vorherige Impfungen: flu vaccination/ cerebral palsy

VAERS 1993597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NY
Alter: 91,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 15.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain Arachnoid web Back pain Blood test abnormal Bone scan abnormal Computerised tomogram abdomen abnormal Confusional state Echocardiogram abnormal Laboratory test Magnetic resonance imaging abnormal Osteoarthritis Painful respiration Pericarditis Pleural effusion Pleurisy Red blood cell sedimentation rate increased Spinal column injury Weight increased

Symptomtext

Eleven days after vaccine, patient started abdominal pains that went on and off. Four days later on Oct 29, patient went to see Dr. He diagnosed possible appendicitis, and recommended to go straight to the hospital. Patient went to Hospital, after tests they were ready for surgery to remove the appendix, but realized he takes Eliquis for his heart condition. So instead of surgery, he was given antibiotics and had four nights in hospital recovering. Before being released he was given a Flu shot on 11/2/21. On November 21 at 11pm, patient found breathing painful. Then went back to Hospital for the day and diagnosed Pleurisy and sent back home. Then he was gaining about a pound a day of fluid. He started taking Furosimide 20-40mg and 12.5mg Spironolactone, but surprisingly was not losing weight, but continued to gain weight. Since patient had severe back pain, the doctor had back x-ray done, and nothing notable, so then he had an MRI done of his back. Fluid around the lungs was scene and and arachnoid web at T3 zone. Then December 8th patient complained of pain in his abdomen again, and also had been having severe back pain as well. So off we went to Hospital again. After tests, they found his appendix looked better than the month previous, but the echo cardiogram showed fluid around the heart(pericarditis) and fluid around the lungs. You would have to confirm with the hospital what all was given, but I believe he was given prednisone. He did come home on prednisone and colchicine and diuretics. It took about two weeks for patient to gain 20 pounds of fluid, and about 10 days to take off the 20 pounds when he was given the anti-inflammatory medications. Patient was released on December 11th. The first night home was bad! Back pain and confusion. He needed help into his PJ's and had to sleep in a recliner. Today patient has much improved, but still recovering. He is still on prednisone, but it is on a taper. Being decreased as the sed rate continues to decrease. In the hospital patient's sed rate was up over 130! It kept decreasing each week, and this week it tested at 28. A repeat echo cardiogram done December 20 showed that the fluid was off the heart now. patient's back pain is much improved, but still is an issue. The doctor's saw an injury at the T9 zone and he has osteoarthritis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Tests were extensive: Hospital from Oct 29 - Nov 2, 2021. ER at Hosp on Nov. 22. Back xray 12/1 at Imaging . MRI on 12/3/21 of back with fluid around the lungs. Arachnoid web at T3. Again at Hosp Dec 8 - 11, 2021. Cat scan of abdomen - appendix was improved from the end of October. Echo-cardiogram showed fluid around the heart and lungs. With the severe back pain a nuclear bone scan was done on his back. Some old injury was seen on the left side of the back ribs, and also a compression injury at T9. Patient had blood tests done with the ESR rate over 138 and that is decreasing while on Prednisone.
Aktuelle Erkrankungen: Recovered from bronchitis about one month prior to vaccination
Vorgeschichte: A-fib, Diabetes, Hypertension, Regurgitation, Aortic Stenosis, Tricuspid Regurgitation, Rheumatic Heart Disease, CKD, BPH, HLD, CHF, Mitrovalve Disease, CRI.
Andere Medikamente: Eliquis 2.5mg x 2, Spironolactone 12.5mg 3 x per week, 1 a day; vitamin, vitamin C 500mg x2, Arthro-7 2 capsules, GlipisideER 5mg 1 per day, GlipisideER 2.5mg 1 per day, vitamin D3 2000IU x2,Rosuvastatin Cal. 10mg MWF, Miralax 17g in eveni
Allergien: Codeine
Vorherige Impfungen: -

VAERS 1972662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: PA
Alter: 13,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

PATIENT WAS GIVEN A PFIZER VACCINE AT AROUND 10:15AM AT A HEALTH CLINIC. SHE WAS ANXIOUS AND NERVOUS AT THE TIME. AFTER THE INJECTION SHE WAS SITTING IN THE WAITING AREA WITH HER FAMILY . AFTER A FEW MINUTES WE WERE INFORMED SHE NEEDED SOME WATER . OUR VOLUNTEER MEDICAL DOCTOR WENT OVER WITH THE WATER AND OBSERVED HER WITH NO FURTHER ISSUES. WE WERE INFORMED ON 12/21 BY DEPT OF PUBLIC HEALTH THAT SHE HAD GONE TO VISIT DOCTOR LATER THAT DAY AND WAS DIAGNOSED WITH SYNCOPE.

Weitere VAERSDATA-Felder

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

VAERS 1971924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Aphasia Arthralgia Chills Dyskinesia Gait inability Mobility decreased Myalgia Nausea Seizure Sleep disorder Tremor

Symptomtext

Severe involuntary, uncontrollable seizure-like shaking started at 11 PM, exactly 14 hours after I got Pfizer booster shot on Thurs, Dec 9, 2021. Up until that time, I had no negative side effects. Lasted for two hours. Unable to walk. Unable to talk adequately. Severe chills. Unable to sleep. On Day 2, Sat, Dec 10, 2021, I was only able to be up to walk to the bathroom. Also on Day 2, severe muscle and joint pain that made it difficult to move and walk. Nausea--ate & drank only saltine crackers & Ginger Ale. Day 3 - much improved but only able to be up for 1.5 hours at breakfast and had to rest remainder of day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Levothyroxine 75 mcg, Centrum Silver Women 50+, B Complex, Calcium-Magnesium, Vitamin D, Vitamin E, Zinc Citrate
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1963385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 26.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

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

Anticoagulant therapy Blood test C-reactive protein Condition aggravated Deep vein thrombosis Dyspnoea Full blood count Haematoma Infection Intra-abdominal haematoma Lethargy Pain Pain in extremity Peripheral swelling Pyrexia Thrombophlebitis septic Ultrasound Doppler abnormal X-ray

Symptomtext

One week after vac. I had pain and large sore bump in my left calf. I began to run a fever and body pain on 11/13. Ambulance took me ER. Tests indicated I had septic thrombophlebitis in left calf behind knee. This happened even though I had been on warfarin for 15+years for DVT and PE (8/2003). There was never a problem until I got the vaccine. Hospitalized from 11/14/21- 11/19/21 on lovenox 120mg 2x a day now . Antibiotics IV and oral contained the infection. Now, numerous hematomas on my legs and abdomen, shortness of breath and extreme lethargy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 30,0
Labordaten: 11/14/21-1119/2021 CBC, c-reactive, leg ultra sound indicated DVT behind left knee. x rays heparin blood tests.
Aktuelle Erkrankungen: Arthritis Atrial fib, flutter. Murmur Kidney stone Septic UTI Depression. Hernia
Vorgeschichte: Asthma. Arthritis. Atrial fib& flutter. Depression UTIs obesity. Hernia.
Andere Medikamente: Warfarin, cardizem, fluoxetine, acifex, digoxin, vitamin D
Allergien: Phenobarbital Penicillin Statins Levaquine Tylenol. Tramadol
Vorherige Impfungen: -

VAERS 1962387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 21.04.2021
Beginn: 30.05.2021
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: SYR / LA

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

Amenorrhoea Anxiety Blood magnesium Blood thyroid stimulating hormone Chest X-ray Differential white blood cell count Echocardiogram Electrocardiogram Full blood count Human chorionic gonadotropin Metabolic function test Migraine Palpitations Presyncope Thyroxine free Troponin Urine analysis

Symptomtext

Daily rapid heart racing, heart rates over 110 bpm daily, missed periods, migraines, increased anxiety due to heart racing, vasovagal syncopal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: 6/1/2021 Increased intermittent heart palpitations, CBC with differential, Comprehensive Metabolic panel, magnesium, troponin, tsh reflex free t4, pregnancy serum, ecg 12 lead, urinalysis, XR chest, EKG. 7/16/2021 Echo Complete
Aktuelle Erkrankungen: n/a
Vorgeschichte: hypothyroidism
Andere Medikamente: Claritin, Armor thyroid, vitamin d, magnesium
Allergien: Demerol, Sulfa, latex
Vorherige Impfungen: -

VAERS 1961756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MI
Alter: 16,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Decreased appetite Dizziness Feeding disorder Impaired driving ability Migraine Nausea Neurological examination Pain Photophobia Syncope

Symptomtext

She was light headed and dizzy passed out the next day after injection, started getting migraines, was nauseated, has 10 lbs. Can't eat, doesn't want to eat, light sensitive, hurts when she walks and can't drive anymore. She has never had migraines or experienced any of these symptoms before her second injection of the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Neurologist - 12/15/2021 No tests have been run but EEG is scheduled
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth Control
Allergien: None
Vorherige Impfungen: -

VAERS 1959690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Amnesia Body temperature increased Chills Computerised tomogram head normal Confusional state Dysarthria Fatigue Feeling abnormal Incontinence Laboratory test Pain Pain in extremity Pyrexia Seizure like phenomena Urine analysis

Symptomtext

Day 1 post vaccine - fatigue, sore arm, low grade fever, mild body aches Day 2 post vaccine - fatigue, sore arm, T Max 102.6, chills, significant body aches Day 3 post vaccine - confusion, seizure like activity, rigors, slurred speech, incontinence, periods of ?lost time? - ambulance ride to ER, ER doc said he can?t confirm a seizure because it was not witnessed and CT was negative but did endorse a significant immune response to 3rd dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: 12/3/21- CT head, labs including UA. Unsure of exact tests as I did not see my medical record and had some lingering brain fog at time of discharge.
Aktuelle Erkrankungen: None
Vorgeschichte: HTN
Andere Medikamente: Benicar, Wellbutrin, Buspar, Paxil
Allergien: Cinnamon, hydromet
Vorherige Impfungen: -

VAERS 1959483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CO
Alter: 18,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

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

Angiogram abnormal Anticoagulant therapy Coagulation test Headache Hypoaesthesia Infarction Intensive care Laboratory test normal Magnetic resonance imaging abnormal Muscular weakness Platelet count normal Seizure Superior sagittal sinus thrombosis Thrombectomy Venogram abnormal

Symptomtext

Patient received x2 Pfizer Covid vaccines on 4/7/21 and 4/29/21 with out any adverse events. She then received her 3rd shot (booster) on 12/10/21. On 12/11/21, she developed a headache. Over the course of the next several days, she started having intermittent numbness on the right side of her body on 12/15. She presented to emergency department on 12/15 PM where she then had a seizure. MR, MRA, MRV showed extensive thrombus of saggital sinus. She was started on Keppra and heparin drip and was admitted to the ICU. Lab testing was unremarkable, including platelets which were normal. The patient also has a family history of VTE and was on birth control pills. On 12/16, she had LUE and BLE weakness. Repeat MRI on 12/16 showed increased volume of cortical acute infarction so patient was taken to interventional radiology for superior sagittal sinus thrombectomy with resultant good flow through SSS. . On 12/17, the patient reports headache is improved. BLE and LUE weakness improved after procedure. Hypercoag labs sent. Plan is to stop oral contraceptives permanently and patient is to be worked up for hypercoagulable state (some workup will need to be completed outpatient). No evidence of ongoin seizures. The patient will be treated with heparin drip and ultimately will be converted to warfarin for anticoagulation. On day of this report (12/17/21), the patient remains hospitalized and is transferring from ICU to general medicine floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: See summary of event. 12/15 platelets 366, 12/17 platelets 270.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Junel FE 1/20 PO daily
Allergien: Lactose intolerant
Vorherige Impfungen: -

VAERS 1952301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 23.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / RA

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

Arrhythmia Cardiac failure Chest pain Myocarditis

Symptomtext

39-year-old man with chest pain and low level stable elevated cardiac biomarkers with imaging findings consistent withuncomplicated idiopathic myocarditis. Borderline LVSF on TTE without other abnormalities. Normal ejection fraction on MRI without evidence of heart failure or dysrhythmia. Only mild LGE on CMR. Nearly asymptomatic now. Regarding etiology, unclear at this point. Routine evaluation of common infectious etiologies including fungal, viral, and tuberculosis was unremarkable. Vaccine related myocarditis secondary to either the COVID, influenza, or both vaccines is a possibility. Symptoms started 7 days after the vaccine, and he presented for care 3 days later after symptoms escalated. Plan for 3 months of exercise restriction. If patient is doing well at that time, repeat TTE. If normal, assess symptoms and functional status with GXT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: Denies
Vorgeschichte: Anxiety, depression, OSA
Andere Medikamente: Loratadine, propranolol, tizanidine, trazodone, venlafaxine.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1951263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: PA
Alter: 30,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Dizziness Panic attack Syncope White blood cell count increased

Symptomtext

Faint/dizzy. Occurred day of shot. Three days after shot very strong that caused a panic attack. Faint/dizzy lasted for a week straight. Spells come up randomly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Routine blood work at doctor to check all levels. Blood work came back normal but high white blood cells.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Ceclor & Amoxicillin.
Vorherige Impfungen: -

VAERS 1943786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 22.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Acidosis Acute kidney injury Anaemia Azotaemia Blood creatinine Cough End stage renal disease Face oedema Fatigue Glomerulonephritis Haematuria Haemodialysis Hypercholesterolaemia Hyperkalaemia Hypertension Hypoalbuminaemia Hypocalcaemia Intensive care

Symptomtext

Patient with no past medical history received Covid vaccine Pfizer booster on 10/22/21 from community pharmacy. Student originally no childhood illnesses, who reported ~ 2 weeks prior to presentation she had a "flu" with subjective fevers, fatigue, dry cough, myalgias. Lasted a few days and self resolved. 7 days ago she noted some facial/periorbial edema that progressed and she presented on 11/2. There she was noted to Have HTN, AKI w/ Cr of 19, hyperkalemia, hypertension, hypocalcemia and anemia. Pt then was discharged and presented to ED for further care on 11/4. She admitted for 11 days, including ICU level care, and was diagnosed with IgA glomerulonephritis. Given extent of scarring on biopsy, renal has determined she now requiring three times weekly hemodialysis. Previous Covid vaccines also from Pfizer documented on 3/5/21 (lot EN6199) and 3/27/21 (lot EP6955)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 11,0
Labordaten: Labs on admission to Medical Center on 11/4/21: Pertinent results include: AKI, mild acidosis, uremia, anemia, hematuria, with nephrotic glomerular proteinuria, hypoalbuminemia, hypercholesterolemia. Hypocalcemia 138 95* 141* / 109 4.0 22 18.10* \ Cai: .7 Alb: 2.3 10.4 \ 9.1* / 193 / 25.8* \ UPR/UCR: 8025g UA: <500 protein
Aktuelle Erkrankungen: No past medical history
Vorgeschichte: -
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1851048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: IN
Alter: 42,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Anaphylactic reaction Arrhythmia Blood bilirubin increased Blood test abnormal Asthenia Dyspnoea Hyperhidrosis Hypoaesthesia Throat tightness Chest pain Computerised tomogram abdomen Dehydration Echocardiogram Electrocardiogram abnormal Electrocardiogram ambulatory abnormal Myocardial injury Ultrasound biliary tract

Symptomtext

About 5 minutes after receiving the second dose of Pfizer vaccine I had a severe anaphylactic reaction. I couldn't breathe was sweating my throat was closing. I was in ministered the EpiPen in the doctor's office and was rushed to the local ER. Posterial oropharyngeal a Arrhythmia. Benadryl injection 25 mg pepcid injection 20 mg saline 9% bolus 1000 ml Benadryl injection, Tylenol. Was told to follow up with my PCP in 2 days. So my PCP on November 10th. Was in urgent Care on the 12th - EKG performed November 14th return to the ER with severe abdominal pain, chest pains, shortness of breath numbness of the fingers and hands and severe dehydration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Blood work- elevated white blood cell count, elevated bilirubin, depleted of vitamin d, B12, Holter monitor - showed symptomatic PVCs Echo 2D Doppler- show damage to two lower ventricles CAT scan abdomen Ultrasound of the gallbladder and kidneys EKG - showed PVCs
Aktuelle Erkrankungen: Hypothyroidism
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid 100 mcg Zyrtec
Allergien: Dairy, Eggs, adhesives
Vorherige Impfungen: -

VAERS 1851048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: IN
Alter: 42,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain Anaphylactic reaction Arrhythmia Blood bilirubin increased Blood test abnormal Asthenia Dyspnoea Hyperhidrosis Hypoaesthesia Throat tightness Chest pain Computerised tomogram abdomen Dehydration Echocardiogram Electrocardiogram abnormal Electrocardiogram ambulatory abnormal Myocardial injury Ultrasound biliary tract

Symptomtext

About 5 minutes after receiving the second dose of Pfizer vaccine I had a severe anaphylactic reaction. I couldn't breathe was sweating my throat was closing. I was in ministered the EpiPen in the doctor's office and was rushed to the local ER. Posterial oropharyngeal a Arrhythmia. Benadryl injection 25 mg pepcid injection 20 mg saline 9% bolus 1000 ml Benadryl injection, Tylenol. Was told to follow up with my PCP in 2 days. So my PCP on November 10th. Was in urgent Care on the 12th - EKG performed November 14th return to the ER with severe abdominal pain, chest pains, shortness of breath numbness of the fingers and hands and severe dehydration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Blood work- elevated white blood cell count, elevated bilirubin, depleted of vitamin d, B12, Holter monitor - showed symptomatic PVCs Echo 2D Doppler- show damage to two lower ventricles CAT scan abdomen Ultrasound of the gallbladder and kidneys EKG - showed PVCs
Aktuelle Erkrankungen: Hypothyroidism
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid 100 mcg Zyrtec
Allergien: Dairy, Eggs, adhesives
Vorherige Impfungen: -

VAERS 1788461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: FL
Alter: 13,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 11.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / -

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

Chest pain Myocarditis Troponin increased

Symptomtext

Developed chest pain 3 days after vaccination, and was seen at ER. Testing at ER showed signs of acute heart inflammation. Was hospitalized for 2 days (10/15/21-10/17/21).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: On 10/15/21 (4 days after vaccination) had elevated troponin levels of 4.68 (normal less than 0.045) that improved during hospital stay to 2.9.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma Autism ADHD
Andere Medikamente: Quillichew ER 30mg Guanfacine 1mg Cyproheptadine 10mg
Allergien: -
Vorherige Impfungen: -

VAERS 1923364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: OH
Alter: 28,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Blindness Deafness Dizziness Feeling hot Hyperhidrosis Presyncope Tinnitus Vision blurred

Symptomtext

Began feeling hot, sweaty and somewhat lightheaded. Attempted to "walk it off" but after approximately 5 minutes I had to sit down on the floor with my legs crossed to prevent fainting. Loss of vision (cloudy/white light) and hearing (loud ringing.) After approximately 30-45 seconds I regained my hearing and vision and was able to stand again. Continued to walk around the pharmacy, then left and sat in my vehicle until I felt normal again. Total time passed between nearly fainting and feeling normal enough to drive was approximately 15 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Flu, sinus infection within one month
Vorgeschichte: ADHD, Generalized anxiety disorder, Major depressive disorder
Andere Medikamente: 450mg Wellbutrin daily, 10mg Buspar 3x a day. One-A-Day Men's multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1921216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 15.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Anaphylactic reaction Rash

Symptomtext

Anaphylaxis and full rashes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none that i know of
Vorherige Impfungen: -

VAERS 1919258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: FL
Alter: 35,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 22.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Thrombosis

Symptomtext

Within 1 week of vaccination developed blood clot to 4th finger of left hand. No prior history of clotting disorders or other medical conditions or medication use. No adverse reactions to first or second Phizer COVID vaccination. This event was triggered by the third dose. Treatment course includes initiation of Aspirin 325 daily.

Weitere VAERSDATA-Felder

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

VAERS 1912754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: VT
Alter: 55,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 08.10.2021
Beginn: 28.11.2021
Tage bis Beginn: 51,0
Dosis: 3
Route/Site: IM / LA

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

Magnetic resonance imaging heart Myocarditis Ventricular tachycardia

Symptomtext

Developed symptoms of V-tach arrest during a bike ride. Myocarditis was diagnosed in the left ventricle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: Cardiac MRI completed on 11/30
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1897918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: WI
Alter: 95,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Feeling hot Musculoskeletal stiffness Pallor Syncope Thirst

Symptomtext

We had an incident of Post Vaccination Syncope at store 4677. I gave an elderly lady her Pfizer Booster shot and asked her to wait in the post vaccination benches. Since she got the shot at 1:30 pm (the pharmacy closed at lunch) I told the patient I will be keeping an eye on how she is doing even though the doors are closed . When i went outside to see how the patient is doing her grandson who is a nurse told me that the patient is feeling warm and thirsty. When I looked at the patient she looked very Pale and stiff. She wasn't comprehending very well when I asked her how she is doing. With the help of her grandson, we made the patient lie down on the benches and elevated her feet. Code white was alerted and I gave patient Cold Compress on her forehead and around the neck area. Shortly after doing cold compress patient started talking and she stated she is feeling better. We gave her some water and she waited in the pharmacy for about half an hour. Patient was very happy with the care she got throughout the episode and was very thankful!!

Weitere VAERSDATA-Felder

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

VAERS 1888160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

schwer

Staat: LA
Alter: 54,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 16.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Electric shock sensation Tinnitus

Symptomtext

Feeling of waves in ears and back of head. Started last night and has been constant

Weitere VAERSDATA-Felder

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

VAERS 1887826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NJ
Alter: 38,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Arthralgia Bone pain Electric shock sensation SARS-CoV-2 test

Symptomtext

This is a spontaneous report from a contactable consumer, the patient. A 38-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FH8020) via an unspecified route of administration in the left arm on 03Nov2021 at 13:00 (at the age of 38-years-old) as a single dose for COVID-19 immunisation. Medical history included known allergies to walnuts and pecans. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included multivitamins (one a day) (MANUFACTURER UNKNOWN) for an unknown indication from an unknown date and unknown if ongoing. The patient did not receive any other vaccine within four weeks prior to the COVID-19 vaccine. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2290) via an unspecified route of administration in the left arm on 13Oct2021 at 13:00 (at the age of 38-years-old) as a single dose for COVID-19 immunisation. On 04Nov2021 at 08:00, the patient experienced burning sensations in her joints hands, wrists, ankles and knees, traveling bone pain, bones in hands and wrists hurt and electricity-like nerve zaps in muscles and joints. The events resulted in doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient had been tested for COVID-19. On 05Nov2021, the patient underwent BinaxNOW (nasal swab) test and the result was negative. No therapeutic measures were taken as a result of the events. The clinical outcome of the events burning sensations in the joints hands, wrists, ankles and knees, traveling bone pain, bones in hands and wrists hurt and electricity-like nerve zaps in muscles and joints was not resolved at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Date: 20211105; Test Name: BinaxNOW; Test Result: Negative; Comments: Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts (Known allergies: Walnuts, Pecans.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1885900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: IL
Alter: 19,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Syncope

Symptomtext

Syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Lightheaded and syncope
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: No
Allergien: None
Vorherige Impfungen: -

VAERS 1885266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: TX
Alter: 32,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Chest pain Myocarditis

Symptomtext

Moderate Myocarditis. Chest pain lasted for approximately 7 days

Weitere VAERSDATA-Felder

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

VAERS 1885094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: OH
Alter: 82,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 12.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram cerebral normal Anticoagulant therapy Arteriogram carotid normal Blood glucose increased Chest X-ray normal Computerised tomogram head normal Confusional state Dysarthria Full blood count Haemoglobin decreased Hypertension International normalised ratio normal Ischaemic stroke SARS-CoV-2 test negative Troponin normal White blood cell count normal

Symptomtext

11/18/21: pt presents to ED with slurred speech and confusion for an hour pt was worked upi with following note: ] "Acute ischemic stroke (HCC) Hypertension, unspecified type Diagnosis management comments: Patient presents to the emergency department slurred speech. Brain attack protocol was initiated. CT the brain shows no acute intracranial findings. Chest x-ray shows limited evaluation with no radiographic evidence of acute cardiopulmonary disease. CTA head and neck shows1. No hemodynamically significant stenosis at the extracranial carotid or vertebral arteries. 2. No intracranial large vessel occlusion or flow-limiting stenosis. CBC shows a normal white count and hemoglobin 11.7. INR is normal. Chemistry shows a glucose of 124 otherwise normal. Troponin is normal. Covid is negative. Brain attack protocol was initiated. The eICU neurologist evaluated the patient and felt that he should get TPA. She discussed with wife at bedside and consulted for the TPA. Patient and wife did agree to the TPA. " - TPA given 11/18/21 14:05

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 1,0
Labordaten: CT Head: Unremarkable. No hemorrhage or acute changes. CTA Head: Unremarkable. No large vessel occlusion. No high grade stenosis. No aneurysm. CTA Neck: Unremarkable. No large vessel occlusion. No high grade stenosis. No dissection
Aktuelle Erkrankungen: s/p lumbar spinal fusion 10/5/21
Vorgeschichte: hyperlipidemia, hypothyroid, hypertension, DVT (~2011), CAD, carpel tunnel, arthritis, 3 cardiac stents placed ~2003
Andere Medikamente: amlodipine/benazepril, ascorbic acid, aspirin, atenolol, atorvastatin, celecoxib, cyclobenzaprine, glucosamine/chondroitin, levothyroxine, misoprostol, multivitamin, nystatin, omeprazole, Senna, trazadone
Allergien: codeine
Vorherige Impfungen: -

VAERS 1881295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 08.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Fatigue Fibrin D dimer increased Glomerular filtration rate decreased Hypotension Hypoxia Somnolence Syncope Ventilation/perfusion scan

Symptomtext

immediately after the vaccine the patient fatigued and was somnolent on day 5 after the vaccine she had a syncopal episode during dinner requiring 911

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: acute on chronic kidney failure- GFR down to 11 from baseline of 50's d-dimer elevate - negative v/q scan hypotensive hypoxic
Aktuelle Erkrankungen: anemia
Vorgeschichte: stage 3 ckd, htn, adhd, anxiety, chronic pain, spinal stenosis, depression, fatigue, hemochromatosis, gerd, hx of breast ca, hx of seizure in 2018, hyperlipidemia, memory changes, muscle cramps, ocular migraine, ptsd, vitamin D
Andere Medikamente: adderall ER 10mg, omeprazole 40mg, buspirone 15mg, clonazepam 1mg, citalopram 40mg, amlodipine 5mg, hctz 25mg, lisinopril 40mg, terazosin 2mg, narcan prn, morphine sulfate er 15mg, oxycodone 5mg, topiramate 25mg, atorvastatin 40mg, tizanidi
Allergien: codeine, pcn
Vorherige Impfungen: -

VAERS 1877374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: OH
Alter: 27,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Syncope

Symptomtext

patient fainted 6 minutes after vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: bp check
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: nka
Vorherige Impfungen: -

VAERS 1870090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: OH
Alter: 22,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Blood test Chest X-ray Dizziness Electrocardiogram Fatigue Hyperhidrosis Loss of consciousness Motion sickness Nausea Pain in extremity

Symptomtext

An hour and thirty minutes after getting vaccine I got nauseous, and having black out, pouring sweat, dizzy, almost like motion sickness. I was taken to the ER. They gave me IV fluids, medication for nausea, and dizziness. I'm having joint pain, fatigue, soreness in my arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood Work EKG Chest X-Ray
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Birth Control
Allergien: N/A
Vorherige Impfungen: -

VAERS 1867374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 65,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Immunisation Interchange of vaccine products Off label use Paralysis SARS-CoV-2 test

Symptomtext

lower body paralysis; Brand=Pfizer/ Dose number=3; prev dose brand, Moderna; prev dose brand, Moderna; This is a spontaneous report from a contactable Consumer. A 65- years- old male patient had received bnt162b2 (Pfizer-biontech covid-19 vaccine, Solution for injection, Batch/lot number: FH8020) via an unspecified route of administration on 30Oct2021 as DOSE 3 (BOOSTER), SINGLE for covid-19 immunization (at an age of 65 years).The patient medical history had included diabetes, neuropathy, heart condition and allergic to Fentanyl and Niacin.The patient concomitant medication had included Influenza vaccine (FLU) for unknown indication on 29-SEP-2021 and Flupentixol dihydrochloride, Melitracen hydrochloride(U) for unknown indication from unspecified date and ongoing: unknown. The patient previously took MODERNA COVID-19 VACCINE Batch/lot number: 026A21A) via an unspecified route of administration on 06Mar2021 as DOSE 1, SINGLE for covid-19 immunization (at an age of 64 years)and also took MODERNA COVID-19 VACCINE Batch/lot number: 0188218) via an unspecified route of administration on 06Apr2021 as DOSE 2, SINGLE for covid-19 immunization(at an age of 64 years). It was reported that patient did not have Covid-19 prior to covid-19 vaccination. The patient underwent for covid test after receiving the vaccination. On 30Oct2021at 20:00 the patient had experienced lower body paralysis .On 01Nov the patient underwent lab test and procedures which included SARS-CoV-2 nasal swab test and diagnosed with negative value. Therapeutic measures were taken for the AE and treatment was given with IV. The patient visited emergency room for the AE and was hospitalized for two days. The clinical outcome of the event was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: 2,0
Labordaten: Test Date: 20211101; Test Name: Covid-19 virus test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes (Other medical history: diabetes, neuropathy, heart condition); Heart disorder (Other medical history: diabetes, neuropathy, heart condition); Neuropathy (Other medical history: diabetes, neuropathy, heart condition)
Andere Medikamente: U
Allergien: -
Vorherige Impfungen: -

VAERS 1865006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: WI
Alter: 56,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 28.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / -

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

Facial paralysis X-ray

Symptomtext

facial nerve paralysis left side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: xr face 11/12/21
Aktuelle Erkrankungen: no
Vorgeschichte: diabetes and obesity. asthma well controlled.
Andere Medikamente: albuterol, fexofenadine, atorvastatin, levothyroxine, vitamin D, Vit E
Allergien: penicillin G
Vorherige Impfungen: -

VAERS 1864515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: TX
Alter: 32,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Seizure-Mild.

Weitere VAERSDATA-Felder

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

VAERS 1861588

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8020

schwer

Staat: CA
Alter: 43,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Deep vein thrombosis Fibrin D dimer Pain in extremity Peripheral swelling Ultrasound Doppler abnormal

Symptomtext

Pain in my right foot began on Wed. morning. Pain and swelling spread from foot to lower right leg. Intense pain Friday night. Symptoms were similar to blood clot, and a blood clot was suspected so I went to the ER Saturday (11-6). DVT was confirmed (11-6).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: D-dimer and ultrasound were preformed to evaluated whether it was a clot (Sat. morning, Nov. 6). Tests indicated that is was.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 1857154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: NC
Alter: 33,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SC / LA

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

Syncope

Symptomtext

Systemic: patient fainted after injection regained conciousness in few seconds-Mild, Additional Details: faintedafter injection

Weitere VAERSDATA-Felder

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

VAERS 1854356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: PA
Alter: 35,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 03.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Blood test Chest X-ray Chest pain Dyspnoea Echocardiogram Myalgia Myocardial necrosis marker Myocarditis Pain in extremity Pericarditis Pyrexia SARS-CoV-2 test Troponin increased

Symptomtext

Wednesday November 3rd 2 pm (after 2nd shot) arm hurting. Thursday November 4th, joint muscle pain full body. Thursday night fever/chills. Friday November 5th minor chest pains, slight fever. Saturday November 6th 4 am major chest pain, unable to breathe. Went to emergency room. Diagnosed as pericarditis myopericarditis due to 2nd covid shot. High levels of troponin released by heart due to inflammation of heart lining and possible muscle damage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Heart enzyme blood tests, regular blood tests, covid 19 tests, chest X-rays, heart ultrasound all performed at Hospital in on November 6th 2021 and November 7 2021.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1848751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: IL
Alter: 38,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Seizure

Symptomtext

Systemic: Seizure-Mild, Additional Details: Patient was sitting down after the covid vaccine and pt's wife came up and said that she noticed that the patient seemed like he has a mini seizure as he was sitting down. When i went to check on the patient, he was alert and said he was feeling ok. Wife stated that pt has history of epilepsy and has not had a seizure in over 3 years. Called pt's neuroligist to make doctor aware of what had happened after the vaccine. Nurse from MD's office instructed pt's wife to monitor him at home

Weitere VAERSDATA-Felder

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

VAERS 1848546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: TN
Alter: 71,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 21.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Abdominal pain Fall Loss of consciousness Pain

Symptomtext

then blacked out and fell between the tub and bathroom vanity/unconscious; Severe paid in the abdomen just below my ribs; then blacked out and fell between the tub and bathroom vanity; Severe pain in my left side due to the impact with the vanity cabinet; This is a spontaneous report from a contactable consumer (patient himself). A 71-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number FH8020), via an unspecified route of administration, on 21Oct2021 14:30 (at the age of 71-year-old) at single dose for COVID-19 immunisation. Historical vaccine includes the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number FF2589) via intramuscular in the left arm, on 30Sep2021 (at the age of 71-year-old) for COVID-19 immunisation and developed welts. The patient did not have a medical history and concomitant medications were provided. No known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Just over 48 hours after the second dose, on 23Oct2021 at 18:00, while in the shower, he had severe pain in the abdomen just below his ribs, then blacked out and fell between the tub and bathroom vanity. Not sure how long he was unconscious but finally managed to get his legs down from the tub and get on his feet. Severe pain in his left side due to the impact with the vanity cabinet. No treatments were given for the events. Pre-vaccination and post-vaccination COVID tests were not performed. The patient was recovering from the events.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101440721 Same reporter, different vaccine dose (1st dose), different event

Weitere VAERSDATA-Felder

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

VAERS 1847150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: SC
Alter: 15,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Loss of consciousness Pallor Seizure

Symptomtext

PT. LOST CONSCIOUSNESS AFTER RECEIVING COVID -PFIZER VACCINE. PT SEEMS HAD A SEIZURE FOR FEW SECONDS. AFTER A MINUTE OR TWO, PT. GAINED CONCIUSNESS AND ASKED, "WHAT HAPPENED?" PT. WAS ALERT AND LOOKED PALE. PT'S MOM DECLINE VITALS CHECK FROM RESCUE. MOM SAID THAT HER DAUGHTER IS OKAY AND DOES NOT NEED TO SEEN IN ER. RESCUE ACCOMPANIED THE PT. ON THEIR WAY OUT.

Weitere VAERSDATA-Felder

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

VAERS 1846788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 21,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood glucose normal Dizziness Electrocardiogram Electrocardiogram T wave amplitude increased Hyperhidrosis Loss of consciousness Pallor

Symptomtext

Pt experienced dizziness 5-10 minutes after vaccine administration. Pt lost consciousness and was diaphoretic and pale. Blood pressure was 73/42. Pulse was 44. Blood glucose 66. 4-lead EKG - slightly elevated T waves (per first responders). Pt slowly resolved to a more stable state. Color returned. BP - 107/77. Pulse 70. Patient refused transport and decided to return home about 1 hour after his vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None stated.
Vorgeschichte: None stated
Andere Medikamente: Not specified
Allergien: Not specified
Vorherige Impfungen: -

VAERS 1845787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MN
Alter: 21,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Dizziness Injection site pain Seizure like phenomena Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: seizure like symptoms-Severe, Additional Details: pt has hx of this event since birth from shots/blood draws

Weitere VAERSDATA-Felder

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

VAERS 1845356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Confusional state Facial paralysis Limb injury Peripheral swelling Speech disorder

Symptomtext

right eye lower than left; Arm swollen; could not close hand; confusion; Problem/difficulty speaking; This is a spontaneous report from a contactable consumer (patient). A 40-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: fh8020), via an unspecified route of administration, administered in right arm on 14Oct2021 (at the age of 40-years-old) as dose 2, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination. The patient previously took ibuprofen and experienced allergy. Historical vaccine included BNT162B2 (Lot number: fe3592), via an unspecified route of administration, administered in right arm on 23Sep2021 (at the age of 40-years-old) at dose 1, single for COVID-19 immunization. Prior to vaccination, the patient did not have COVID-19 infection and did not receive any other vaccine in four weeks. The patient reported that next day at 6 pm, her arm was swollen, could not close hand, had confusion, problem/difficulty speaking, and right eye was lower than left. No treatment was received for the events. The patient was not COVID tested post-vaccination. Outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1837203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: FL
Alter: 95,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Fall Loss of consciousness

Symptomtext

Patient briefly passed out and fell. No other adverse effects. No apparent injuries.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood Pressure taken: 130/78
Aktuelle Erkrankungen: none
Vorgeschichte: skin cancer
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1837081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 59,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 18.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Eating disorder Fluid intake reduced Lip disorder Ophthalmoplegia Paralysis Speech disorder

Symptomtext

About a week ago patient noticed slight sag in lip. Now she has paralysis of left mouth and eye impeding speech, eating and drinking. She is following up with MD today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: Meeting doctor today
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's Grave's disease
Andere Medikamente: Alphagan Eye Drops Levothyroxine Lisinopril Rosuvastatin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1833811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: OH
Alter: 88,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 25.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blood alkaline phosphatase increased Blood calcium decreased Blood chloride decreased Blood sodium decreased C-reactive protein increased Chest X-ray abnormal Computerised tomogram thorax normal Dyspnoea Endotracheal intubation Fatigue Fibrin D dimer Haematocrit decreased Haemoglobin decreased Intensive care Lung opacity N-terminal prohormone brain natriuretic peptide increased Pleural effusion

Symptomtext

The patient reports that about 2 days after vaccination with his Pfizer booster shot, he began feeling weak and fatigued. Patient is acutely short of breath. On initial presentation to the ED, patient was 94% on RA, but patient continuously decompensated during ED stay progressing from RA, to nasal cannula, to high flow nasal cannula, and finally to requiring intubation. The patient has received dexamethasone and is admitted to ICU.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: 11/1/21 COVID-19 rapid: positive Chest X-ray: extensive bilateral airspace opacities, with small right pleural effusion HGB: 11.4; HCT: 34 D-dimer: 1.62 pro-BNP: 12,838 Calcium: 8.2; Sodium: 128; chloride: 93 High sensitivity troponin: 63 Procalcitonin: 0.18 CRP: 37.6 CT PE: no evidence of PE Alk phos: 158
Aktuelle Erkrankungen: -
Vorgeschichte: CHF stage D, atrial fibrillation, actinic keratosis, BPH, Bowen's disease, macular degeneration, hypertension, hyperlipidemia, lymphoma, IBS
Andere Medikamente: acyclovir, amiodarone, atorvastatin, clopidogrel, digoxin, furosemide, midodrine, glucosamine-chondroitin, Preservision, Benefiber
Allergien: niacin
Vorherige Impfungen: -

VAERS 1831896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 22.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / AR

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

Angiogram pulmonary abnormal Anticoagulant therapy Diastolic dysfunction Echocardiogram abnormal Ejection fraction decreased Hepatic lesion Hepatic steatosis Mitral valve incompetence Pulmonary valve incompetence Scan with contrast normal Splenic artery thrombosis Splenic infarction Tricuspid valve incompetence Ultrasound Doppler abnormal

Symptomtext

splenic artery thrombosis and splenic infarction treated with anticoagulation unclear cause, not cardioembolic based on ECHO

Weitere VAERSDATA-Felder

Praegender Schweregrund: Splenic artery thrombosis
Hospital-Tage: 3,0
Labordaten: CT angiogram chest 10/26 IMPRESSION: 1. Partially visualized infarct involving a large portion of the spleen. Distal branches of the splenic artery are thrombosed. 2. No acute pulmonary embolism to the level of the subsegmental pulmonary arteries. 3. The lungs are clear. 4. Diffuse hepatic steatosis. There are 2 arterially enhancing lesions within the right lobe measuring 7 mm each. See below for recommendations. Given hepatic steatosis, suggest further evaluation with MRI liver with contrast. ECHO 10/28/21 Left Ventricle: The left ventricular cavity size is decreased. The left ventricular wall thickness is normal. The visually estimated left ventricular ejection fraction is 60-65%, which is normal. Spectral Doppler shows grade I diastolic dysfunction. Right Ventricle: Normal right ventricular size, wall thickness, and systolic function. Left Atrium: The left atrium volume index is normal. Right Atrium: The right atrium is normal in size and structure. Pericardium: There is no evidence of pericardial effusion. Mitral Valve: Structurally normal mitral valve, with normal leaflet excursion; without any evidence of mitral stenosis. Physiologic mitral valve regurgitation seen by color Doppler observation. Tricuspid Valve: Structurally normal tricuspid valve, with normal leaflet excursion. Trace tricuspid regurgitation is visualized. The pulmonary artery systolic pressure cannot be estimated, due to lack of tricuspid regurgitant doppler signal. Aortic Valve: The aortic valve is trileaflet and structurally normal, with normal leaflet excursion; without evidence of aortic stenosis. No evidence of aortic valve regurgitation is seen. Pulmonic Valve: The pulmonic valve was not well visualized. There is physiologic pulmonic valve insufficiency. Aorta: There is no dilatation of the aortic annulus. The aortic sinus dimension, adjusted for age and estimated BSA, is normal. There is no dilatation of the ST junction. The ascending aorta dimension, adjusted for patients age and estimated BSA, is normal. Pulmonary Artery: The pulmonary artery is not well seen. Shunts: Agitated saline contrast was given intravenously to evaluate for intracardiac shunting. Saline contrast bubble study was negative, with no evidence of any intracardiac shunt.
Aktuelle Erkrankungen: uncontrolled hypertension and diabetes
Vorgeschichte: uncontrolled hypertension and diabetes
Andere Medikamente: none
Allergien: fluoxetine
Vorherige Impfungen: -

VAERS 1831576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: TX
Alter: 50,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Arterial stent insertion Arterial thrombosis

Symptomtext

10/27/2021. 99% blood clot in main artery widow maker. I was able to get to the emergency room in time to get treatment , moved to hospital where stint was placed that same night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arterial thrombosis
Hospital-Tage: 2,0
Labordaten: Placed stint in artery.
Aktuelle Erkrankungen: Baricardia, enlarged heart due to being a runner
Vorgeschichte: Nome
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2649730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: -
Alter: 25,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Deafness Dizziness Syncope

Symptomtext

On October 20th, 2021, Patient presented to the pharmacy for the 1st Dose of the FDA Approved Pfizer-BioNTech COVID-19 Vaccine. Prior to administration that patient said that he was afraid of injections but during administration the patient stated that he did not feel the needle being administered for the vaccination. After administration, the patient said he was dizzy and that he needed a bottle of water, after retrieving the bottle of water the patient woke up from fainting and stated that he fainted and was not able to hear during the time that I went to retrieve the bottle of water. The other pharmacist and technicians kept watch on him for 15 minutes and he felt okay afterwards and left the pharmacy in a healthy state.

Weitere VAERSDATA-Felder

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

VAERS 1829056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NV
Alter: 19,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain Syncope Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: Pt fainted for about 30 seconds at 12:17pm before regaining consciousness. We monitored pt for about an hour afterward and recorded the follow vitals: at 12:17pm HR113, BP 86/51, 12:32pm HR112, 87/47, at 12:38pm HR 111 BP 89/42. Pt then walked 30 minutes home and called us from home to notify us that she is safe and sound.

Weitere VAERSDATA-Felder

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

VAERS 1825568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 43,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Chest X-ray Electrocardiogram Loss of consciousness Seizure Dizziness Feeling hot Laboratory test normal Malaise

Symptomtext

Patient received vaccine and waited the required 15 minutes after the administration. He was fine when he left here. Approximately 10 minutes later he reported not feeling well, feeling hot and commented to his wife that he felt like he was going to pass out. He then did pass out and wife describes it as he was having a seizure. Ambulance was called and picked him up (not at our pharmacy). He was passed out for a minute or so before he came back around. He was stable when transported to the hospital. EMT couldn't get a BP reading, but his heart rate was 40 and his O2 was 84 before transport to hospital. Hospital did tests without findings. Discharged from hospital and advised to follow up with PCP.

Weitere VAERSDATA-Felder

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

VAERS 1824845

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: FL
Alter: 25,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Disorientation Dizziness Flushing Hyperhidrosis Hypotension Pulse abnormal Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Hypotension-Mild, Additional Details: Patient was talking to RN after vaccine administered when he was observed slumping in his chair with head down. He did not respond to verbal/ touch cues. Pulse thready. This lasted less than 30 seconds. RN called pharmacist. Patient became diaphoretic with beads of sweat on face & arms after regaining consciousness. Disorientation resolved quickly and he could recollect previous conversation. BP 91/34 and this resolved with 2 bottles of water. Patient stable after 15mins, remained for 30.

Weitere VAERSDATA-Felder

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

VAERS 1815040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: KY
Alter: 72,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Blood test normal Computerised tomogram normal Electroencephalogram normal Feeling abnormal Illness Impaired driving ability Magnetic resonance imaging normal Nausea Seizure Vomiting

Symptomtext

Patient received pfizer booster and then started to suffer from seizures and was in the ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: patient went to ER
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: PANTOPRAZOLE SOD 40MG TAB
Allergien: n/a
Vorherige Impfungen: -

VAERS 1815040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: KY
Alter: 72,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Blood test normal Computerised tomogram normal Electroencephalogram normal Feeling abnormal Illness Impaired driving ability Magnetic resonance imaging normal Nausea Seizure Vomiting

Symptomtext

Patient received pfizer booster and then started to suffer from seizures and was in the ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: patient went to ER
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: PANTOPRAZOLE SOD 40MG TAB
Allergien: n/a
Vorherige Impfungen: -

VAERS 1822156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: NY
Alter: 26,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

The patient had waited their 15 minutes and was setting up their 2nd dose appointment when they fainted. His girlfriend caught him so he didn't hit the floor. By the time I got to him he was sitting up and was alert. I had a code white paged. I sat with him for 10 minutes on the floor then moved him to the chair for another 20 minutes. He didn't state he had issues with shots in the past (as per his consent form but said he hadn't eaten much today), I checked on him every 5 minutes. He stated he was feel better. I informed him that his girlfriend needed to drive home.

Weitere VAERSDATA-Felder

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

VAERS 1822024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CT
Alter: 25,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Hyperhidrosis Loss of consciousness Malaise Pallor

Symptomtext

Patient said she started to feel dizzy then passed out for ~1 minute, patient was hot, sweaty, color drained from face, felt sick, did not throw up. Recovered completely and left store after ~30min. Patient was with her boyfriend.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None-- no rxns ever to anything
Vorgeschichte: None-- no rxns ever to anything
Andere Medikamente: Birth control
Allergien: None-- no rxns ever to anything
Vorherige Impfungen: -

VAERS 1821837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 25,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

Less than 5 minutes after the vaccination, patient fainted and began vomiting. He was conscious less than a minute after fainting and remained as so until EMS arrived.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: Patient stated that he faints "after every vaccine" he receives

VAERS 1821547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NC
Alter: 36,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Dizziness Dyspnoea Flushing Hyperhidrosis Hypoaesthesia Nausea Pallor Paraesthesia Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Mild, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Shakiness-Mild, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Patient became pale in color while sitting in the chair following the Pfizer Covid shot. He said he felt nauseas and then laid on the floor. He was sweating and complained of chest pain. He then said his arms felt tingling. 911 was called immediately. Wet rag was applied to his forehead and 2 pharmacists stayed with him until EMS arrived. The sypmtoms began midway thru the 15 minute waiting period. He said he had not had any food today.

Weitere VAERSDATA-Felder

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

VAERS 1821541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Generalised tonic-clonic seizure

Symptomtext

Systemic: Seizure-Severe, Additional Details: Patient had Grand Mal Seizure approximately 2 minutes after injection. She does have a history of seizures.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1815697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CT
Alter: 80,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 06.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Cardiomyopathy Chest pain Electric shock sensation Electrocardiogram Immunodeficiency

Symptomtext

Patient started having an electrical feeling/chest pain. She went to see her doctor and he diagnosed her with cardiomyopathy.

Weitere VAERSDATA-Felder

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

VAERS 1814357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NH
Alter: 29,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Nausea Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: Nausea-Mild, Additional Details: Patient has a history of fainting when receiving vaccinations. She fainted roughly 1-3 minutes after vaccine was administered, while sitting in her chair. Her mother was present and helped pharmacist lie patient on the ground and elevate her legs on a chair. Patient was given a lollipop and water while she recovered from the event. She left the pharmacy around 30 minutes after event with her mother stating that she no longer felt faint and was okay to leave.

Weitere VAERSDATA-Felder

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

VAERS 1814006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: WA
Alter: 20,0
Geschlecht: M
Eingang: 24.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

C-reactive protein increased Chest X-ray normal Chest pain Dizziness Electrocardiogram normal Fibrin D dimer normal Presyncope Troponin I normal

Symptomtext

Chest pains experienced in upper left chest afternoon after received vaccines and continued into following morning. On day following vaccination at approx. 12 noon, experienced lightheadedness, dizziness, and felt like was going to pass out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: XR CHEST 2 VW (10/21/2021), lungs clear and no abnormalities. EKG 12 LEAD (10/21/2021), "NORMAL SINUS RHYTHM WITHIN NORMAL LIMITS WHEN COMPARED WITH ECG OF 18-FEB-2020 16:02, NO SIGNIFICANT CHANGE WAS FOUND" C_Reactive Protein (10/21/2021), 15.9 mg/L TROPONIN_I (10/21/2021), <0.03 ng/mL D_Dimer, Quant (10/21/2021), 0.31 ug{FEU}/mL
Aktuelle Erkrankungen: None
Vorgeschichte: Generalized anxiety disorder; ADHD, predominantly inattentive type; Tachycardia; Allergic rhinitis; Childhood asthma
Andere Medikamente: Fluoxetine HCl; Azelastine Hydrochloride and Fluticasone Propionate Nasal Spray; Montelukast; Amphetamine/Dextroamphetamine Extended Release
Allergien: None
Vorherige Impfungen: -

VAERS 1813860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NY
Alter: 31,0
Geschlecht: M
Eingang: 24.10.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Hyperhidrosis Lethargy Syncope Tremor Vomiting

Symptomtext

Patient received 2nd dose of Pfizer and as he is seated waiting for his 15 minutes patient became lethargic and started fainting. Patient also experienced sweating, perspiration, shaking and vomiting. Ambulance was called and was taken to the hospital .

Weitere VAERSDATA-Felder

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

VAERS 1813750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MA
Alter: 29,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 23.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature increased Chills Feeling of body temperature change Headache Loss of consciousness Muscular weakness Nausea Pain Pyrexia

Symptomtext

Woke up at 2AM with full-body aches and chills, nausea, headache. Alternating hot and cold, and muscle weakness. Patient blacked out twice, at 2:30 and 8:30 AM, for approximately 20 seconds each time. Temperature was slightly elevated at 99.1. Currently (11 AM) patient is sore and feeling feverish, with a headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple sclerosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: 2nd Pfizer covid shot, similar symptoms to a lesser extent, and no blacking out.

VAERS 1807564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: VA
Alter: 37,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Dizziness Fatigue Lethargy Nausea Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Mild, Systemic: Nausea-Medium, Systemic: Weakness-Medium, Additional Details: patient was given second shot and about 3 to 5 minutes later he passed out for less than a second and then reported dizziness and nausea. re was drinking some water and then passed out for less than a second a second time

Weitere VAERSDATA-Felder

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

VAERS 1967198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: OH
Alter: 79,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Endotracheal intubation Pulse absent Resuscitation Syncope Tachycardia

Symptomtext

Approx 1300 pt was SOB then collapsed at golf club facility. No pulse, Bystander started CPR, EMS arrived 2 rounds of epinephrine and intubated. Arrived at ER @ 1334 Tachycardia rhythm, pulses lost, CPR restarted. Pt given Epinephrine, Sodium bicarbonate and calcium gluconate. Return of spontaneous circulation. @ 1336 1mg Epinephrine IV Push @ 1336 50 mEq Sodium Bicarbonate 8.4% IV push @ 1344 1g Calcium gluconate IV push @ 1347 1 liter over 1 hr 0.9% Sodium Chloride @ 1446 8mg/500ml levophed in 05w started at mcg/min @ 1503 1mg Epinephrine IV push, @ 1504 50 mEq Sodium Bicarbonate 8.4% @ 1506 1mg Ephinephrine IV push @ 1509 50 mEq Sodium Bicarbonate 8.4% @ 1512 1mg Epinephrine IV push @ 1517 1mg Ephinephrine/250 ml 0.9% Sodium Chloride via gravity feed 200cc total given until end of code @ 1523 compressions @ 1524 1mg Epinephrine IV push @1527 no pulse @1528 1mg Epinephrine IV push @1529 no pulse @1531 no pulse @1532 1mg Epinephrine IV push @1533 no

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: hypertension
Vorgeschichte: -
Andere Medikamente: Losartan 25mg QD, Xanax 0.25mg QD, Sertraline 25mg QD, Allopurinol 300mg QD, Cardizem CD 130mg QD
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1801667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: MA
Alter: 17,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Pallor Syncope

Symptomtext

As soon as vaccine was given patient became pale, nauseous, dizzy, and fainted

Weitere VAERSDATA-Felder

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

VAERS 1797494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient was in waiting room after receiving the vaccine and informed me that she fainted. This was approximately 10 minutes after receiving the vaccine. The patient was awake and alert. She did not fall after fainting, she was sitting down so she just slumped down in her chair.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NA
Vorgeschichte: anxiety/depression allergies
Andere Medikamente: buproprion
Allergien: NA
Vorherige Impfungen: -

VAERS 1793838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: SC
Alter: 69,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Speech disorder Syncope Feeling abnormal Hypotension Loss of consciousness

Symptomtext

Fainted twice, threw up twice. Had to be taken to ER. Couldn't even speak. Depleted of all energy. Very frightening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, high cholesterol
Andere Medikamente: Synthroid 75 mcg Nexletol Pantoprazole 40 mg
Allergien: Various food sensitivities, allergic to penicillin
Vorherige Impfungen: -

VAERS 1794302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: VA
Alter: 59,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Electric shock sensation Pain in extremity Sleep disorder

Symptomtext

I am not totally sure if this is a side effect of the vaccine. But, it is unusual. I am experiencing, intermittently a sharp pain on my left outer mid thigh. It happened last night and woke me up and now that I am relaxing for the evening it comes and goes without a warning. It feels like a Nerve as it sends a sort of shock to the system and I actually say "oww" when it happens.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Elevated blood pressure
Andere Medikamente: Omeprazole DR 20 MG 1x day Escitalopram 20 MG 1 x day Buspirone 10mg 1 x day Losartum 50mg 1 x day Montelukast Sodium 10mg 1 x day Multiple Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1793990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: OH
Alter: 20,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient fainted and fell but was conscious and alert. EMT service was called and patient was evaluated. Patient was feeling better and did not need to be transported to ER. Patient was taken home by his mother. A follow up call to the patient was made 3 hours later. Mom inform Rph that patient was feeling fine and everything was OK.

Weitere VAERSDATA-Felder

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

VAERS 1793985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: MA
Alter: 25,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Additional Details: Pt passed out but recovered and felt fine after

Weitere VAERSDATA-Felder

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

VAERS 1793752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Flushing Head injury Hyperhidrosis Hypotension Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Shakiness-Mild, Additional Details: Patient received Pfizer Booster on R-Deltoid and Flu Vaccine (Afluria) on L-Deltoid. Pt moved to waiting area and 3 minutes later fainted. RPh heard a thump and the verbal response of another patient who was waiting her 15 minutes. When Rph ran out immediately, patient was conscious. Pt bumped right forehead on neighboring chair. Took blood pressure which was 95/70. Pt requested water and granola bar. Pt stated he felt better after 30 minutes and stated this has happened previously.

Weitere VAERSDATA-Felder

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

VAERS 1788909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: ID
Alter: 15,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Hyperhidrosis Loss of consciousness Pallor Seizure

Symptomtext

Patient was nervous about getting the vaccine to start but she seemed fine right after the shot. She walked over to another chair to sit down. About a minute or two after sitting down in the chair she passed out and started having a seizure. Myself and another adult in the room got her safely to the floor. The seizure lasted just a few seconds but she was sweating and white. We called 911 and kept her calm and sitting while waiting for the paramedics to arrive. She slowly regained color in her face and was feeling better by the time paramedics arrived.

Weitere VAERSDATA-Felder

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

VAERS 1785784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: NY
Alter: 23,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

The patient fainted after about 10 minutes after vaccination was administered. Patient was aware and alert and did not loose consciousness at any time during the process. Patient stood up and approach the pharmacy counter and at that time fainted. patient did not want any medical attention . Patient left 30 minutes later with a parent.

Weitere VAERSDATA-Felder

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

VAERS 1783097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

schwer

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Syncope Vomiting

Symptomtext

Patient stated that she fainted after 1st dose and wanted to let me know. Patient immediately fainted and vomited after second dose. She was given an ice pack, had some water, and rested for 15-20 minutes. Was able to leave on her own per her request. Counseled patient on seeking emergency medical attention if she started showing signs of an allergic reaction. Patient was accompanied by a group of friends who agreed to watch for any symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1775650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

schwer

Staat: OK
Alter: 24,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Balance disorder Dizziness Feeling hot Injection site pain Joint range of motion decreased Loss of consciousness Lymph node pain Lymphadenopathy Pyrexia Skin test Swollen tongue

Symptomtext

I had the pfizer vaccination administered in my left arm and the flu vaccination administered in my right arm at the same time. Within 10 minutes of my injection, the under side of my tongue began to swell. This only lasted 5-10 minutes. Throughout the afternoon/evening I was frequently lightheaded and imbalanced on my feet. My left arm was difficult to lift which was normal for a shot. The next morning I woke up very light headed and thought that if I could just get some food and fluid in me I would be ok. I began to pass out twice while moving about my kitchen, taking a break to sit after the first instance, and having to move all the way to the floor with my legs in the air on the second instance. I laid on the floor for roughly 10 minutes before being able to move to the couch. I was unable to take more than a few steps on my own for the next 2-3 hours without feeling severely lightheaded again. I also noticed from the time I woke up that my left arm (pfizer) hurt significantly worse than my right arm (flu) and that something was wrong with the lymph nodes in my left armpit. Throughout the day I would take my right hand and try to massage my lymph node from my left elbow down to my left ribs to encourage lymph fluid mobility. By early afternoon 10/9 the lightheadedness and arm pain had decreased and I was able to move freely around the house; however, around 6pm I noticed myself feeling hot and lightheaded running a 99.9 degree fever (my standard temperature is close to 97.5 degrees). I spent the rest of the evening in bed, lymph node pain worsening, and my temperature reached 100.3 degrees. My fever broke between 1-5am on 10/10. On 10/10 the only persistent symptom was the lymph node pain at which point I noticed my lymph node in the left armpit was visibly swollen. As of 3pm 10/10 my lymph node is still swollen despite my efforts (massage, stretching, and heat therapy) to reduce the swelling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 2/10/21 was the day of my skin test with the pfizer vaccination which determined I am not actually allergic to the vaccination
Aktuelle Erkrankungen: -
Vorgeschichte: severe seasonal allergies, occasional skin rashes of unknown causes
Andere Medikamente: allegra, singular, lo-lestrin, flexeril, claritin
Allergien: I had an allergic reaction to the first pfizer dose. It should already be in the system from my allergist reporting it. The under side of my tongue turned fuzzy like a peach at ~10 minutes after the injection and at ~12 minutes after the injection my injection arm and up to my chest/neck turned bright red and hot to the touch. The reaction subsided on without medical intervention within 30 minutes. I completed a skin test with the pfizer vaccine through my allergist, was determined to not be allergic to the pfizer vaccine, and was able to receive my 2nd dose of the pfizer vaccination without any abnormal reactions.
Vorherige Impfungen: 01/20/21 reaction to 1st dose of the pfizer vaccination lot number EK9231 when the pt was 23. Adverse event described earlier i

VAERS 2708096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 55,0
Geschlecht: F
Eingang: 07.11.2023
Impfdatum: 15.03.2021
Beginn: 01.06.2021
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Computerised tomogram head Condition aggravated Echocardiogram normal Insomnia Mitral valve disease Palpitations Vestibular migraine Pain Sleep disorder

Symptomtext

Increase in severity and duration of vestibular migraines.; Increase in severity and duration of vestibular migraines.; Mitral valve disease; I currently have palpitations; Sometimes I am up the entire night; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 15Mar2021 as dose 2, single (Lot number: EN199gh v c) at the age of 55 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Mitral valve disease" (unspecified if ongoing), notes: stable and no issues until vaccine; "Allergy to Sulfa" (unspecified if ongoing); "Allergy to mold" (unspecified if ongoing); "migraines" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: bnt162b2 (Dose Number: 1, Batch/Lot No: EN6200, Location of injection: Arm Left), administration date: 22Feb2021, when the patient was 55-year-old, for Covid-19 Immunization. The following information was reported: PALPITATIONS (disability) with onset Jun2021, outcome "not recovered", described as "I currently have palpitations"; VESTIBULAR MIGRAINE (disability), CONDITION AGGRAVATED (disability) all with onset Jun2021, outcome "not recovered" and all described as "Increase in severity and duration of vestibular migraines."; MITRAL VALVE DISEASE (disability) with onset Jun2021, outcome "not recovered"; INSOMNIA (disability) with onset Jun2021, outcome "not recovered", described as "Sometimes I am up the entire night". The events "increase in severity and duration of vestibular migraines.", "mitral valve disease", "i currently have palpitations" and "sometimes i am up the entire night" required physician office visit. Therapeutic measures were taken as a result of vestibular migraine, condition aggravated. Therapeutic measures were not taken as a result of mitral valve disease, palpitations, insomnia. Clinical course: Increase in severity and duration of vestibular migraines: patient always had migraines, but they increased from perhaps one per week to several per week, lasting days. No pain reliever works. Sometimes patient was up the entire night. she take Ibuprofen and Tylenol and even decongestants offer some relief. She continue to suffer these episodes. The doctor's suggestion was migraine meds. PT told her vestibular and while her manual PT did work, she cannot afford to go 2x per week, which was the only way she had some relief. Heart palpitations: she had an underlying heart condition (Mitral valve disease) and was told by her cardiologist that it was fine to take the vaccine. she was concerned reading about possible vaccine issues affecting the heart, but followed his advice. She saw a cardiologist in 2021, but there was nothing conclusive. He denied that the vaccine could have harmed her heart further. She currently have palpitations, which happen a lot of the time when she get her migraines. Seeing new cardio soon.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300354136 Same patient, same drug/different dose, different AEs.;US-PFIZER INC-202300354135 Same patient, same drug/different dose, different AEs.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to molds; Migraine; Mitral valve disease (stable and no issues until vaccine); Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2640237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 94,0
Geschlecht: M
Eingang: 02.06.2023
Impfdatum: 18.10.2021
Beginn: 01.08.2022
Tage bis Beginn: 287,0
Dosis: 1
Route/Site: IM / LA

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

Dementia Alzheimer's type Hydronephrosis Hypotension Organ failure Sepsis

Symptomtext

I95.9 HYPOTENSION 1/27/2023 HYDRONEPHROSIS I95.9 HYPOTENSION 1/27/2023 SEVERE SEPSIS W ACUTE ORGAN DYSFUNCTION I95.9 HYPOTENSION 1/27/2023 ALZHEIMERS DISEASE

Weitere VAERSDATA-Felder

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

VAERS 2614658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 13.04.2023
Impfdatum: 26.10.2021
Beginn: 04.04.2023
Tage bis Beginn: 525,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia Blood creatinine increased Blood pressure systolic decreased Cardiorenal syndrome Dizziness postural Nephropathy toxic Orthostatic hypotension Renal impairment Troponin

Symptomtext

Discharge Provider: MD Primary Care Provider: PA Admission Date: 4/4/2023 Discharge Date: Apr 8, 2023 PRESENTING PROBLEM: AKI (acute kidney injury) (HCC) HOSPITAL COURSE: Patient is a 72 y.o. male with past medical history significant for severe CAD s/p CABG and PCI, ischemic cardiomyopathy with combined systolic and diastolic heart failure s/p ICD in 2018, atrial fibrillation on anticoagulation, hypertension, lung cancer, CKD3, type 2 diabetes presents with complaints of increased dizziness with standing and generalized weakness. Patient was admitted from March 16-17th after having ICD shocks that were occurring over a period of 3 weeks prior. Patient was then re-admitted to the hospital again from March 18-26th with AHRF due to CHF and COVID. His respiratory status improved with diuresis. He has an AKI that failed to improve and his creatinine remained around 2.5-2.9 throughout his admission. Nephrology at that time reported that his kidney function was likely a combination of cardiorenal syndrome and contrast nephropathy. They recommended further diuresis and started torsemide 20mg daily. He has been compliant with this since discharge. He attempted to contact cardiology for assistance who took prolonged time getting back to him and did not give him advice on fluid intake vs restriction. Ultimately contacted nephrology who recommended increased fluids, but given worsening symptoms, presented to the ER for evaluation. Patient was evaluated by cardiology. They attributed his troponins to AKI and signed off without further input. Nephrology evaluated patient. His torsemide was held. He was given gentle IV fluids. He attempted to work with PT/OT and upon standing systolic BP dropped from 120 to 50's. Later worked with PT/OT and able to go home. As he gentle accumulated fluid, first with IV fluid help, then later only with removal of fluid restriction, his weight slowly increased, renal function drastically improved, and patient felt much improved. Nephrology graciously agreed to be the primary manager of his diuretics moving forward to help with patient's outpatient needs. As he improved he no longer had positive orthostatic vitals. He was discharged in stable condition on 4/8/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Pancreatic cyst (History of) Laryngeal cancer (HCC), s/p chemo-RT in 2017 S/P CABG x 2 ASHD (arteriosclerotic heart disease) Ischemic cardiomyopathy HTN (hypertension) Dyslipidemia Type 2 diabetes mellitus with stage 3 chronic kidney disease, with long-term current use of insulin (HCC) Acute on chronic combined systolic and diastolic CHF (congestive heart failure) (HCC) Shortness of breath CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) Paroxysmal ventricular tachycardia Mitral valve insufficiency, unspecified etiology ICD (implantable cardioverter-defibrillator), dual, in situ History of GI bleed Abdominal aortic aneurysm (AAA) (HCC) AF (paroxysmal atrial fibrillation) (HCC) Malignant neoplasm (Adenocarcinoma) of upper lobe of right lung (HCC) diagnosed 2023 History of tobacco abuse Left inguinal hernia ICD (implantable cardioverter-defibrillator) discharge Ventricular fibrillation (HCC)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 100 MG tablet amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG tablet atorvastatin (LIPITOR) 40 MG tablet escitalopram (
Allergien: LisinoprilDiarrhea ScopolamineConfusion BupropionOther, Nausea Only Selective Serotonin Reuptake InhibitorsOther, Headache, Nausea Only ParoxetineUnknown
Vorherige Impfungen: -

VAERS 2588562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MN
Alter: 92,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 22.04.2022
Beginn: 06.12.2022
Tage bis Beginn: 228,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Dyspnoea Fall SARS-CoV-2 test positive Wheelchair user

Symptomtext

Patient brought in by EMS to ED on 12/6/22 for weakness and shortness of breath. To note, patient fell transferring to wheelchair the morning of 12/6. COVID PCR test done in the ED was positive, and he notably tested positive for COVID the day before. Ultimately, patient admitted to the hospital 12/6/22 - 12/8/22 for COVID-19 and generalized weakness attributed to COVID-19 infection, among other problems. Patient has received the COVID primary vaccine series and two boosters.

Weitere VAERSDATA-Felder

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

VAERS 2585632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: AL
Alter: 63,0
Geschlecht: F
Eingang: 22.02.2023
Impfdatum: 03.01.2023
Beginn: 04.01.2023
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Cough Dyspnoea Feeling cold Feeling hot Headache Pain Tremor

Symptomtext

Chills, shakes, cold, hot, cough, headaches, hard to breathe, all over body pain (not so much the left arm).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: The week of 01/15/2023.
Aktuelle Erkrankungen: None
Vorgeschichte: Pelvic-floor Dysfunction, GERD
Andere Medikamente: Pristiq, Nexium, Linzess, Gabapentin - for nerve pain, Pepcid, Ozempic - for hyperinsulinemia, Relpax/Maxalt - for occasional migraines
Allergien: Compazine, Nickle, Adhesive Tape
Vorherige Impfungen: -

VAERS 2565039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 20,0
Geschlecht: F
Eingang: 21.01.2023
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain Amnesia Angina pectoris Arthralgia Balance disorder Bladder pain Breast pain Burning sensation Cardiac flutter Dissociation Disturbance in attention Dyskinesia Dysphagia Dyspnoea Erythema Fatigue Feeling abnormal Feeling hot

Symptomtext

Immediate allergic reaction occurred after receiving the 2nd dose. The left side of my face and neck broke out in red wepts and went completely numb. I was told to take Benadryl which I did. I developed symptoms over time and I will provide a full list of my symptoms that I deal with now every single day. As of today 1/21/2023, I am the sickest I have ever been in my entire life and that started when I received my second shot. My daily symptoms are: Warmness in my head that comes and goes. Burning on the inside of whole left side of body. Severe burning on the inside of left side of head. Severe burning in left side of chest. Severe burning in left arm/armpit. Head Pressure. Off Balance. Feelings of being zoned out almost all the time. Feelings of being disassociated with the world at times. Blurry Vision. Cheeks burn and turn red. Nerve Pain in head, neck, back, arms, & legs. Joint pain. Abdominal Pain. Cramping in bladder area after peeing. Heart Palpitations, flutters, Tachycardia, heart rate rises high when I sit up from laying down and when I stand on my feet from sitting. Sharp pains in middle of heart and on left lower side of my heart/breast area. Chronic Fatigue. Hands and Feet turn Cherry Red and Burn. Brain Fog. Short Term Memory Loss. Unable to process or get out what I need to say at times. Trouble Concentrating. Throat fullness/puffy feeling. Extremely hard to swallow. Shortness of breath. Quivering/Tremor like on the inside of my lower chest/stomach. Tremors in my left leg. Jerks in my neck and head from time to time. Extreme Food Allergies. I now have Mast Cell Activation Syndrome. I have received no treatment because no one knows how to treat this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: My D-Dimer level is always super elevated since receiving the shot.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Albuterol for Asthma as needed.
Allergien: Bananas, Carrots, Squash, Peaches, & Whey.
Vorherige Impfungen: -

VAERS 2559686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 08.11.2021
Beginn: 14.12.2022
Tage bis Beginn: 401,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy Asthenia Atelectasis Blood lactic acid decreased Blood magnesium normal Blood osmolarity decreased Blood potassium decreased Blood sodium decreased COVID-19 Chest X-ray abnormal Condition aggravated Constipation Culture urine negative Dehydration Diarrhoea Hyperglycaemia Hypokalaemia Hyponatraemia

Symptomtext

Patient is a 83 y.o. female patient of, MD with history of COVID 19 ( 12/11/22), DM, HTN presented to Hospital with nausea, emesis, and diarrhea Hyponatremia Secondary to dehydration from vomiting / COVID Corrected sodium on admission 124 Patient was given 1 L NS bolus in ED BMP every 6 hours 12/14/22 Na+ 122. Stop hydrochlorothiazide and spirolactone Ur osm 360, Ur Na 46 Ser Osm 272 0.9NS at 75cc/hr completed Na fluctuating 126 (12/18/22), not much improvement with IV hydration. Added salt tabs Continue salt tabs. Na improving 130 12/19 => 134 12/20 TSH nl Will check bmp in 1 week COVID-19 Infection Generalized weakness Symptoms onset 12/9/22, positive test date 12/11/22 No current oxygen demand Continue paxlovid Anticoagulation: Heparin SQ Consider discontinuation of isolation 12/21/22 PT recommended intensity of skilled Therapy5 to 7 days per week/Duration 10 - 30 days. Swing bed likely 12/20 Sepsis without organ dysfunction - resolved Secondary to COVID-19 and possible left lower lobe PNA & POA Presented with tachycardia and leukocytosis. QSOFA score 0 Hemodynamically stable, not requiring vasopressors. Lactic acid 2.0 Pro calc nl Received 1 L NS bolus in ED. Workup: CXR with left lower lobe atelectasis and/or airspace disease Blood cultures NGTD urine culture neg Completed Ceftriaxone and azithromycin. Hypokalemia-resolved 3.1 on presentation Magnesium 1.6 Replace and recheck K of 4.1 (12/18) DM2 with hyperglycemia Hold home oral medication, Diet Special; Diabetic, Cardiac; Carbohydrate Consistent 60g/meal (1500-2000 kCal equivalent) diet, sensitive SSI + BG checks ACHS, hypoglycemic protocol, and target BG 140-180 Added Lantus 30 units (12/18) titrate based on BG Continue home meds HTN Elevated blood pressure Continue nifedipine, clonidine, and aldactone Constipation - resolved Reports no BM since admission Added schedule laxative and senna s

Weitere VAERSDATA-Felder

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

VAERS 2557495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 21.01.2021
Beginn: 14.12.2022
Tage bis Beginn: 692,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/14/22 presents to ED for "SOB". PMHx of "prostate cancer, status postradiation colonic tubular adenomas, and diverticulosis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/14/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2546948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 21.03.2021
Beginn: 18.12.2022
Tage bis Beginn: 637,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chest X-ray normal Culture urine positive Leukocytosis Mental status changes Pyrexia SARS-CoV-2 test positive Sepsis Tachycardia Urinary tract infection Urine analysis abnormal White blood cell count increased

Symptomtext

In the ER she tested positive for COVID with no hypoxia and no findings of acute infiltrate on CXR. She was also noted to be septic with tachycardia, fever and leukocytosis with a UA showing a UTI. She was admitted on COVID isolation. COVID was treated with daily Remdesivir but no steroids as no hypoxia. She will need COVID isolation through 12/27/22. For her UTI she was treated with IVF and ceftriaxone. Her WBC normalized on 12/19. Fever resolved after admission. Mental status improved daily and for the last several days of hospital stay she was at her baseline MS. Urine culture grew mixed flora but she improved on ceftriaxone so she was changed to Vantin to complete a full course - last day is 12/27/22. PT saw the patient and she was transferred to on 12/22/22. Hospital course otherwise without complication.

Weitere VAERSDATA-Felder

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

VAERS 2544603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 29.10.2021
Beginn: 28.11.2022
Tage bis Beginn: 395,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Headache Idiopathic intracranial hypertension Lumbar puncture Maternal exposure before pregnancy Post lumbar puncture syndrome Pregnancy SARS-CoV-2 test positive

Symptomtext

Date of Admission: 11/28/2022 Date of Discharge: 12/4/2022 Admission Diagnosis: Pregnant state, incidental [Z33.1] Labor and delivery indication for care or intervention [O75.9] Intractable headache Hospital Principal Problem (Discharge Diagnoses): Idiopathic intracranial hypertension Spinal Headache following LP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Idiopathic intracranial hypertension
Hospital-Tage: -
Labordaten: 11/28 Contains abnormal data SARS-COV-2 (COVID-19) by NAA, Micro
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2529416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 69,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 05.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Condition aggravated Influenza SARS-CoV-2 test

Symptomtext

ringing in her ear; icky-flu general side effects; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient received BNT162b2 (BNT162B2), on 05Nov2021 as dose 3, single (Lot number: FH8020) at the age of 69 years for covid-19 immunisation. The patient's relevant medical history included: "Mastectomy" (unspecified if ongoing), notes: Had a mastectomy for breast cancer 19 years ago; "Breast cancer" (unspecified if ongoing); "Prediabetic" (unspecified if ongoing), notes: Is at a 5.6-5.7 prediabetic level; "lymph node removal" (unspecified if ongoing); "peripheral neuropathy" (unspecified if ongoing). Concomitant medication(s) included: TAXOL taken for breast cancer; TAXOTERE taken for breast cancer. Vaccination history included: Bnt162b2 (Dose 1: 11Mar2021, LOT: EN6207, Got it at the (withheld) clinic), for Covid-19 immunization, reaction(s): "icky-flu general side effects", "ringing in her ear". The following information was reported: CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "ringing in her ear"; INFLUENZA (non-serious), outcome "unknown", described as "icky-flu general side effects". Relevant laboratory tests and procedures are available in the appropriate section. She had the first three vaccines and had icky-flu general side effects afterwards like most people do. Had a mastectomy for breast cancer 19 years ago, so had a lot of scar tissue around that area. Didn't know if she had swollen lymph nodes, because her nodes were taken out with the mastectomy. She was a 70 year old female in good health in spite of cancer. Never had cancer again. Takes care of herself. Was at a 5.6-5.7 prediabetic level which she was managing with diet and exercise. Didn't usually get sick. Got it (dose 2) at the (withheld) clinic. Got the vaccine in her right arm because the breast cancer with the mastectomy and lymph node removal made it so so all shots were given in her right arm. Used up all all her Covid tests. They were all negative. Wanted to make sure it was the side effects from the shot and not something else. Had tinnitus from breast cancer drugs. It was hissing in her ears. When she got stressed, it was louder. She noticed that the tinnitus was worse now and as the days went on. She did all kinds of stuff to control her body and brain. She controlled it through means of less stress. She didn't get sick from the other Covid-19 vaccines, but the ringing in her ear was intensified after each shot. She knew why she had it, but didn't know why the vaccines would aggravate it. Chemo drugs she was on were Taxol and Taxotere. NDC, LOT, EXP: Unknown. They were common breast cancer drugs that were used back then. They were very terrible. She was over treated. Had 33 round so chemo even though there was no cancer in her body after the mastectomy. Were treating her just to make money. Was a Guinea pig and lab rate. Had chemo induced peripheral neuropathy. Should've stopped treatment when she first had neuropathy. Today, they stop treatment when neuropathy occurred. Her doctor knew about her's from the third treatment. Facility was closed down for maltreat. Were shut down because they were over treating people and she was one of them. Did pet scans and there no cancer and were treating her just in case. She did it because just wanted to live because her children were little. No prior vaccinations within four weeks prior to the first administration date of the suspect vaccine. Family Medical History Relevant to Adverse Events was not provided. No follow-up attempts are possible. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201352992 Same /reporter/patient, same drug/different dose, same AE;US-PFIZER INC-202201352991 Same /reporter/patient, same drug/different dose, same AE;US-PFIZER INC-202201352934 Same reporter/patient, same drug/different dose, different AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Covid test; Test Result: Negative ; Comments: They were all Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer; Lymphadenectomy; Mastectomy (Had a mastectomy for breast cancer 19 years ago); Peripheral neuropathy; Pre-diabetic (Is at a 5.6-5.7 prediabetic level)
Andere Medikamente: TAXOL; TAXOTERE
Allergien: -
Vorherige Impfungen: -

VAERS 2505642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 70,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 23.11.2021
Beginn: 08.11.2022
Tage bis Beginn: 350,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 Dyspnoea

Symptomtext

Hospitalization for shortness of breath due to COVID-19 on dates 11/8/22- still hospitalized. Treated with dexamethasone, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: levofloxacin, sulfa (sulfonamide antibiotics)
Vorherige Impfungen: -

VAERS 2504545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 71,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 29.10.2021
Beginn: 17.09.2022
Tage bis Beginn: 323,0
Dosis: 3
Route/Site: UN / UN

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

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

Symptomtext

Tested positive for COVID-19 and admitted to hospital. Symptoms include chills and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: Nasopharyngeal swab collected 9/18/2022 tested positive for 2019 Novel Coronavirus RNA on 9/18/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic lung disease.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2496688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 30.10.2021
Beginn: 03.10.2022
Tage bis Beginn: 338,0
Dosis: 3
Route/Site: UN / UN

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

Chest pain Dyspnoea Respiratory tract congestion Wheezing

Symptomtext

congestion, SOB, wheezing, chest pain

Weitere VAERSDATA-Felder

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

VAERS 2496662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: SC
Alter: 63,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Adverse reaction Injected limb mobility decreased Loss of personal independence in daily activities Periarthritis X-ray limb abnormal

Symptomtext

patient had adverse reaction with her left arm to upper shoulder. Patient could not lift arm, had trouble doing daily activites

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: x-rays, results said shoulder was "frozen"
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Atovastatin, Lexapro, ibuprofen
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2496421

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FH8020

moderat

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 15.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Biopsy skin abnormal Blister Burning sensation Condition aggravated Impaired quality of life Impaired work ability Insomnia Joint effusion Joint fluid drainage Joint swelling Loss of personal independence in daily activities Magnetic resonance imaging abnormal Pain Pain in extremity Pruritus Psoriasis Psoriatic arthropathy Skin exfoliation

Symptomtext

1st vaccine 10/15/21 few days after first vaccine palms developed tiny almost blisters mainly right hand burning intense itching sensation i notified occupational health and was still advised i had to receive second vaccine in order to be compliant 2nd vaccine 11/5/21 my hands continued with reaction to the point my skin started peeling off the intensity of pain became so unbearable i had a heartbeat in palm of hand unable to sleep called in to work at 12/20/21 to seek help went to dermatologist 12/20/21 he prescribed oral,topical steroids and steriod injection and was unfamiliar with covid vaccine side effects and thought perhaps it would subside with steroids or possibly psoriasis he wasnt sure of auto immune system response with covid vaccination. at the same time my right knee swelled however no injury .fast forward another dermatologist stelera did not help or steroids currently skyrizi has not helped today my palm has never healed severe painful cracks it limits my daily functions had biopsy and is palmar psoriasis which is life long .i was referred to rheumatologist by orthopedic my large right knee effusion seen on MRI and x-ray 80ml of fluid was drained/collected rheumatologist stated i had psoriatic arthritis which is life long. I expressed my concerns for exemption prior to vaccine since I had two autoimmune diseases and Dr. our hospital physician deemed that I be vaccinated and even the second vaccine after expressing reaction concerns. Since this Vaccine my quality of life has dramatically changed pain, physical, emotional, not to mention this will never go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: palm biopsy 6/30/2022 confirmed palmar psoriasis knee effusion drainage 6/18/2022 rheumatologist stated psoriatic arthritis
Aktuelle Erkrankungen: none
Vorgeschichte: psoriasis, hashimotos thyroiditis
Andere Medikamente: stelara injection, armour thyroid, vit -d, adderall
Allergien: none
Vorherige Impfungen: -

VAERS 2494173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 15.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / RA

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

Chills Tremor Urinary tract infection Urine analysis abnormal

Symptomtext

I thought I had a UTI and I started having extreme chills. The chills weren't normal, but it was like someone was shaking my body and it lasted for about 45 min and I took XANAX as soon as I got home, and it did calm the shaking. They tested for the UTI and they said I did have a UTI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: UTI test
Aktuelle Erkrankungen: Uncertain
Vorgeschichte: Anemia; Anxiety; Depression; Asthma; Hypertension; Fatigue; GERD; DVT; Hyperlipidemia; Impaired Glucose Tolerant; LUPAS Systemic Erythematous; Fibromyalgia Syndrome; Sjogren's Syndrome; Raynaud's syndrome; migraines; Central Sleep apnea; Hiatal Hernia; Eczema; IBS; Conjunctivitis; Osteoarthritis; PsychoGenic Nonepileptic Seizures; Cellulitis; C-diff; Post Traumatic Stress Disorder; Costochondritis
Andere Medikamente: ASPIN; azelastine eye drops; BENLYSTA infusions; BREO ELLIPTA; chlorthalidone; duloxetine; esomeprazole: folic acid; hydroxychloroquine; ZYRTEC; vitamin C; manganese; netrin; valacyclovir.
Allergien: Sulfa; ranitidine; sumatriptan; succinate; CELEBREX; DEPAKOTE; KEPPRA; levetiracetam; tizanidine; topiramate; lisinopril
Vorherige Impfungen: Flu shot gave me a frozen shoulder and it lasted for a long time (2016 or 2017)

VAERS 2494037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: AZ
Alter: 59,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 28.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: SYR / LA

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

Brain oedema COVID-19 Dyspnoea Fatigue Feeling abnormal Hypertension Nasopharyngitis SARS-CoV-2 test positive Vomiting

Symptomtext

COVID-19 positive on 1/5. My whole family was positive. I had minor cold symptoms for a few days. By 1/9 I was feeling really bad with shortness of breath and throwing up so I went to the hospital for 9 days. My blood pressure was so high that it was causing swelling of my brain and I was placed on seizure mediation. They kept me in the hospital until I was testing negative. Today I still have a little bit of exhaustion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 9,0
Labordaten: COVID-19 - positive;
Aktuelle Erkrankungen: No
Vorgeschichte: Fibromyalgia; Chronic pain; High blood pressure; Gastrointestinal disease
Andere Medikamente: Morphine; Riddling; Lisinopril; Propanol; Anatriptoline; Paxil; Clonidine; Estradiol; Vitamin B100; Calcium; Vitamin D; Magnesium; Potassium
Allergien: No
Vorherige Impfungen: -

VAERS 2488278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: SC
Alter: 51,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 29.10.2021
Beginn: 15.11.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Joint lock Joint noise Joint range of motion decreased Mobility decreased Myalgia

Symptomtext

I work from home and as I was typing I reached for a pen and my shoulder locked up. Began to have muscle aches, joint popping, decreased range of motion, and weakness. Began receiving chiropractic care which relieved symptoms but they return. Having significant issues with weakness and mobility. When I am able to go to the chiropractor the relief lasts 2.5 days. I take TYLENOL and ADVIL for the pain which help make it tolerable. I am in the process of following up with PCP and try to get into PT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure; high cholesterol
Andere Medikamente: Hydrochlorothiazide; lisinopril; amlodipine; phenyl fibrate; TYLENOL arthritis; ICY HOT; VYVANSE; VOLTAREN; JUNEL; METAMUCIL; CENTRUM
Allergien: Kale
Vorherige Impfungen: -

VAERS 2483921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IL
Alter: 41,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 19.10.2021
Beginn: 15.07.2022
Tage bis Beginn: 269,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Chest X-ray Electrocardiogram abnormal Electrocardiogram ambulatory Hypokalaemia Palpitations Panic attack Tachycardia

Symptomtext

On 07/15/2022, I was vacuuming and my heart began racing as it turned out it was a panic attack, I had called 911 and was taken to the local hospital ER. I was given a chest X-ray, EKG, blood profile. Diagnosis was tachycardia palpitations, hypokalemia. A Holter monitor was ordered for 24 hours. I returned to the ER two additional times after this event and was diagnosed with anxiety and panic attacks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Chest X-ray, EKG results slightly abnormal but benign.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2479421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: AZ
Alter: 62,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 18.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: - / RA

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

Condition aggravated Rash erythematous Skin disorder Vitiligo

Symptomtext

Sudden onset of skin issues; Red itchy rash that calmed followed by white patches; Intensified by sunlight; vitiligo/calmed followed by white patches; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Nov2021 at 09:30 as dose 3 (booster), single (Lot number: FH8020) at the age of 62 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Chronic lymphocytic leukaemia" (unspecified if ongoing); "Known allergies: sulfa antibiotics" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN + HIDROCLOROTIAZIDA. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EN6202, Location of injection: Arm Right, Vaccine Administration Time: 10:00 AM), administration date: 28Feb2021, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EL9263, Location of injection: Arm Right, Vaccine Administration Time: 10:00 AM), administration date: 25Feb2021, for Covid-19 immunization. The following information was reported: CONDITION AGGRAVATED (disability) with onset Feb2022, outcome "not recovered", described as "Intensified by sunlight"; RASH ERYTHEMATOUS (disability) with onset Feb2022, outcome "not recovered", described as "Red itchy rash that calmed followed by white patches"; SKIN DISORDER (disability) with onset Feb2022, outcome "not recovered", described as "Sudden onset of skin issues"; VITILIGO (disability) with onset Feb2022, outcome "not recovered", described as "vitiligo/calmed followed by white patches". The events "sudden onset of skin issues", "red itchy rash that calmed followed by white patches", "intensified by sunlight" and "vitiligo/calmed followed by white patches" required physician office visit. Clinical course: Adverse event: Dr. suspects vitiligo. Adverse event start time: 06:00 AM. The patient did not receive any other vaccine in four weeks. Other medications in two weeks: Losartan- HCTZ 50-12.5. If covid prior vaccination: No. If covid tested post vaccination: No. The patient received fourth dose of BNT162b2 (Lot Number: FM0173) on 11Jul2022 at 10:00 AM, in right arm and fifth dose of BNT162b2 (Lot number: GJ2524) on 06Oct2022 at 09:15 AM, in left arm for Covid-19 immunization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic lymphocytic leukemia; Penicillin allergy; Sulfonamide allergy
Andere Medikamente: LOSARTAN + HIDROCLOROTIAZIDA
Allergien: -
Vorherige Impfungen: -

VAERS 2464614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 19.11.2021
Beginn: 21.09.2022
Tage bis Beginn: 306,0
Dosis: 3
Route/Site: UN / UN

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

Appetite disorder Chest pain Chills Cough Dyspnoea Fatigue Myalgia Oropharyngeal pain Pyrexia Respiratory tract congestion Upper-airway cough syndrome

Symptomtext

appetite change, chills, fatigue, fever, congestion, postnasal drip, sore throat, cough, SOB, chest pain, myalgias

Weitere VAERSDATA-Felder

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

VAERS 2456115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: CA
Alter: 90,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 05.04.2022
Beginn: 04.09.2022
Tage bis Beginn: 152,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 pneumonia

Symptomtext

? (Principal) COVID-19 PNEUMONIA

Weitere VAERSDATA-Felder

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

VAERS 2456115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: CA
Alter: 90,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 05.04.2022
Beginn: 04.09.2022
Tage bis Beginn: 152,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 pneumonia

Symptomtext

? (Principal) COVID-19 PNEUMONIA

Weitere VAERSDATA-Felder

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

VAERS 2450141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NJ
Alter: 52,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 13.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Heart rate Heart rate increased Palpitations Tachycardia

Symptomtext

Palpitations; Tachycardia; Increased heart rate; the side effects was worst with the booster; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 53-year-old female patient received BNT162b2 (BNT162B2), on 13Nov2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 52 years, in left deltoid for covid-19 immunization. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: BNT162b2 (the second shot I got on 29Jan2021,Single, Lot: EL3247), administration date: 29Jan2021, for Covid-19 Immunization, reaction(s): "Palpitations", "Tachycardia", "Increased heart rate"; Covid-19 vaccine (Dose 1, Single, manufacturer Unknown), for Covid-19 Immunization. The following information was reported: PALPITATIONS (non-serious), outcome "unknown"; TACHYCARDIA (non-serious), outcome "unknown"; HEART RATE INCREASED (non-serious), outcome "unknown", described as "Increased heart rate"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "the side effects was worst with the booster". The events "palpitations", "tachycardia", "increased heart rate" and "the side effects was worst with the booster" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of palpitations, tachycardia, heart rate increased, condition aggravated. Additional information: It was reported that Tachycardia; Increased heart rate, lasted for a month after the vaccine and the side effects was worst with the booster then with the second shot. Doctor stated that No treatment was taken because nothing was diagnosed. So he did go to the doctor and did not go through testing but this was not in the past two weeks." Age at time of vaccination was reported as 52 and she was 53 and by the time of vaccination I was 52." Lot#: Doctor stated the lot number one given on 29Jan was EL3247 and the one given in Nov was FH8020." No follow-up attempts are required. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Heart Rate; Result Unstructured Data: Test Result:Increased
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 48,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 29.03.2021
Beginn: 12.08.2022
Tage bis Beginn: 501,0
Dosis: 3
Route/Site: - / -

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

Ageusia Anosmia Bacterial test positive Blood lactic acid abnormal COVID-19 Chest discomfort Computerised tomogram thorax normal Electrocardiogram normal Lactic acidosis Palpitations Procalcitonin SARS-CoV-2 test positive Troponin normal Urine analysis

Symptomtext

49y.o. female presenting with palpitations, chest pressure. Upon presentation she had significant lactic acidosis 7.0. She also tested positive for COVID, however she was recently positive less than 2 months ago, CT chest was negative for PE as well as any signs of viral pneumonia. She was given large fluid resuscitation in the EC. Her lactic acid improved to normal levels. Additionally, cardiac work-up including troponin and EKG was negative. She had some bacteria on UA, however no urinary symptoms, fever, leukocytosis. Antibiotics were not given. By the following day, she had improved almost completely with fluid resuscitation alone. Noted procalcitonin 0.9, however without signs of active infection she was managed expectantly. She was then stable for discharge home with instructions to maintain aggressive oral hydration. She was additionally given information on isolating for positive COVID test. I attempted to contact microbiology lab to obtain cycle threshold from her positive test, however I was unable to contact them. Patient was recommended for continued COVID isolation at home with repeat testing. If she has 2 consecutive negative rapid tests, this is reassuring that her PCR was a hold over from previous positive infection and isolation can be successfully removed. On a final note, patient asked for appetite stimulant. She stated that cannabis-derived appetite stimulants were not successful for her in the past including Marinol. Main barrier to her nutrition is her lack of taste and smell which is secondary to previous chemotherapy. She was given a trial of low-dose Remeron. Patient was discharged home in stable condition with no restrictions on diet or activity to continue medications and follow up with physicians as listed below.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 3,0
Labordaten: 8/12 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2431003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 27.01.2021
Beginn: 03.08.2022
Tage bis Beginn: 553,0
Dosis: 3
Route/Site: - / -

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

Blood culture negative COVID-19 Chemotherapy Chest pain Echocardiogram abnormal Ejection fraction Febrile neutropenia Haematocrit decreased Haemoglobin decreased Heart valve incompetence Hyperdynamic left ventricle Metabolic function test Neutrophil count decreased Oropharyngeal pain Platelet count decreased Platelet transfusion Pyrexia Red blood cell count decreased

Symptomtext

78 year old male with history significant for AAA (stable), HTN, HLD, DM type II, recent Covid-19 (7/21/22) presents to the hospital with chest pain. Cardiology consulted for further evaluation. Echocardiogram completed, revealing LVEF 70%. The left ventricular appears hyperdynamic. No segmental wall motion abnormalities are identified. There is moderately increased thickness of the interventricular septum without significant obstruction to outflow. There is trace valvular regurgitation. There is no pericardial effusion. Pt discharged to home. well. She received half dose of Neulasta after chemotherapy. Physical examination was only remarkable for in injected pharynx. Labs on presentation showed WBC of 0.2, RBC 2.69, Hct 25.2, RDW 16, Platelets 45, neutrophil 0.1, Hb 8.8 and CMP was within normal limits. Afterwards, blood culture were sent from oncology, normal saline fluid bolus initiated in clinic, and patient received first dose of cefepime at 14: 30 in clinic. And patient was started on Paxlovid (nirmatrelevir & ritonavir)1 dose orally twice per day. Patient was diagnosed with febrile neutropenia and was admitted to the inpatient ward to continue IV antibiotics, fluids and for monitoring. On 08/04 at midnight, patient developed a fever of 100.7 and was started on Tylenol. Aftwerwards, her congestion and sore throat improved and patient has been afebrile since. On 08/05, patient was doing well with no fevers, chills or night sweats. However, patient's platelet count decreased to 27 and was given 1 dose of platelet transfusion and no transfusions reactions occured. Furthermore, blood cultures showed no growth at 1 day. Patient was deemed stable for discharge on 08/05 to home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: 8/3 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 65,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 06.09.2022
Beginn: 25.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / LA

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

Colitis microscopic Colonoscopy abnormal Cough Diarrhoea Endoscopy Feeling abnormal Feeling hot Gastritis Pain Palpitations Stress

Symptomtext

The diarrhea began by 7 pm & felt like I had a 105 degree temp! I didn't thankfully, but I ached & my heart raced, etc.! I almost called 911. It is horrible & I have bad allergies & started coughing & wondered if I was going to die! It took a few days but I lived!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: On 4/8/22 I had a colonoscopy & endoscopy & the gastritis was from stress about this & the colonoscopy showed Collagenous, Colitis, & the diarrhea has been horrid!! I already cornered the market on Imodium & now even more! I've had to eliminate many more foods from my diet, thanks to this!
Aktuelle Erkrankungen: IBS the diarrhea form
Vorgeschichte: IBS & Migraines
Andere Medikamente: The list is too long & now I mostly live on Imodium!
Allergien: penicillin & some other antibiotics, onion, garlic, cayenne pepper & anything hotter!
Vorherige Impfungen: T-Dap, earlier in 2021.

VAERS 2420124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 73,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 06.11.2021
Beginn: 24.08.2022
Tage bis Beginn: 291,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Diarrhoea Faeces discoloured Gastrointestinal haemorrhage Hypotension Malaise Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Hospitalization: admitted 8/17/2022; discharged 8/24/2022. Presentation to the ED: weakness, malaise, nausea, vomiting, diarrhea, hypotensive. Patient had black stools. COVID-19 + date: 8/24/2022 Treatment: patient was treated for acute GI bleeding. COVID prophalyxis was not administered. Discharge to: SNF

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, renal failure, tobacco use, alcohol consumption.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2405681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 02.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Contusion Electromyogram abnormal Injection site mass Magnetic resonance imaging head normal Nerve compression Orthosis user Pain Tremor X-ray limb

Symptomtext

Starting a week after receiving the vaccine, I got a big lump at the injection site and then I developed a bruise which is unusual for me. I developed soreness and weakness which I connected to the lump. When the lump disappeared the symptoms persisted and I was more concerned. I started developing tremors and weakness making it difficult to type. I contacted my PCP and they referred me to orthopedics and neurology. Due to a family death, I was unable to follow up until after that. They first thought it may be an early onset Parkinson's but ruled it out. So, when neurology did an EMG recently it was determined that I had an entrapped nerve on the right side. They classified it as an atypical carpel and cubital nerve entrapment since it starts at the wrist and goes up the arm. They said they will treat it with braces/rest. As time goes on, it is slowly getting better so they want to watch it and not do any surgery unless it does not improve. Usually these are painful conditions, but I am not having any pain at this moment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: EMG (07/25/2022): atypical carpel and cubital nerve entrapment extending from the wrist to the upper arm; x-ray of wrist, shoulder and elbow (06/24/2022); MRI of brain (11/22/2021): normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Acid Reflux
Andere Medikamente: Omeprazole; multivitamin; vitamin D; calcium
Allergien: Latex; nitrile
Vorherige Impfungen: -

VAERS 2404573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MN
Alter: 87,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 22.11.2021
Beginn: 04.08.2022
Tage bis Beginn: 255,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID on 8/4/22 with sx of cough and SOB. Treatment includes oxygen and IV medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, CAD, COPD A fib
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2367850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 19,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 24.11.2021
Beginn: 30.04.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: UN / UN

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

Cough Dyspnoea Fatigue Respiratory tract congestion

Symptomtext

fatigue, congestion, cough, sob

Weitere VAERSDATA-Felder

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

VAERS 2359526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 04.11.2021
Beginn: 24.06.2022
Tage bis Beginn: 232,0
Dosis: 3
Route/Site: - / -

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

Atelectasis Blood culture positive COVID-19 COVID-19 pneumonia Chest X-ray abnormal Confusional state Cough Culture urine positive Cystitis Dyspnoea Fatigue Hypoxia Klebsiella test positive Lung infiltration Nitrite urine present Respiratory symptom SARS-CoV-2 test positive Staphylococcus test positive

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 6/24/2022 Discharge Date: Jun 26, 2022 PRESENTING PROBLEM: Acute confusion [R41.0] Hypoxia [R09.02] Acute cystitis without hematuria [N30.00] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: 78-year-old female with past medical history significant for hypothyroidism, autoimmune hepatitis who presented to emergency department on 06/24 with upper respiratory symptoms including dyspnea, cough, fatigue. In emergency department she appears slightly confused. She was found to be hypoxic requiring 2 L nasal cannula. Labs were relatively unremarkable. COVID test did return positive. Urinalysis showed positive nitrites and small leukocytes with 16 wbc's concerning for infection. Chest x-ray showed patchy infiltrates versus atelectasis in the right lung base. Patient was admitted to Medicine Service for further assessment management COVID pneumonia. She was treated with dexamethasone with improvement in respiratory status and symptoms. Blood cultures obtained grew 1/2 coag-negative staph likely contaminant. Urine cultures growing Klebsiella confirming urinary tract infection. Patient had been started on Rocephin and this was continued while inpatient. Symptoms improved by the following morning. She was no longer confused. Felt stronger. Urine cultures susceptibilities resulted and patient was transitioned to Keflex to complete an additional 3 days of discharge. Physical therapy work with patient and recommended home with assist. Patient discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Autoimmune hepatitis (HCC) Hypothyroidism, unspecified type Obesity (BMI 30-39.9) Anxiety Hypothyroidism due to Hashimoto's thyroiditis Peripheral polyneuropathy Fatigue, unspecified type Chronic bilateral low back pain without sciatica Other chest pain Dyspnea on exertion Splenic infarct Hydronephrosis, unspecified hydronephrosis type Kidney cysts Fat necrosis of peritoneum (HCC) Pulmonary emphysema, unspecified emphysema type (HCC) Obstructive sleep apnea Hypersomnia Elevated diaphragm Morbid obesity with BMI of 40.0-44.9, adult (HCC) Primary osteoarthritis of both knees Primary insomnia Pneumonia due to COVID-19 virus
Andere Medikamente: Ascorbic Acid (VITAMIN C PO) Cyanocobalamin (VITAMIN B-12 PO) fluticasone (FLONASE) 50 MCG/ACT nasal spray guaifenesin (ROBITUSSIN) 100 MG/5ML liquid liothyronine (CYTOMEL) 5 MCG tablet MAGNESIUM PO Niacin (VITAMIN B-3 PO) Omega-3 Fa
Allergien: None
Vorherige Impfungen: -

VAERS 2344767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 27.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / AR

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

Eye swelling Hypersensitivity Immunisation reaction Lip swelling Oral pruritus Paraesthesia Pharyngeal swelling Sleep disorder Speech disorder Swollen tongue

Symptomtext

I got the vaccine on October 27, 2021. On November 5 at about 01:00AM, I woke up with an itchy mouth and my face started to tingle. My lips, eyes, tongue, and throat started to swell up. I took some Benadryl as soon as I started to feel symptoms and monitored. The symptoms persisted despite the Benadryl, so we went to the Emergency Department and we waited for 3 hours. They called me back and took my vitals and they agreed that it was an allergic reaction. I was not able to talk well, but my husband did tell them that I had a response to the 2nd Moderna vaccine with the overreaction in my arm. The doctor at the ER did not seem to think it was related in the moment. They gave me prednisone on site at 02:45AM. We left with a prescription for an epi pen and prednisone. We left after the symptoms had gone down and after the prednisone. I took prednisone for 2-3 days after. They did refer me to an allergy specialist, and I called my healthcare provider and they said it was most likely a response to the vaccine since there wasn?t anything to have an allergic reaction to. Along with my reaction to the other dose. I did not do further testing for the allergies, and I was told to call the CDC. I?m currently due for my next booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Mirena IUD
Allergien: None
Vorherige Impfungen: 2nd COVID-19 Moderna vaccine on 02/28/2021 - Around 2 weeks after the injection, arm swelled to twice its size. Took Benadryl an

VAERS 2329150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 14.12.2021
Beginn: 16.06.2022
Tage bis Beginn: 184,0
Dosis: 3
Route/Site: UN / UN

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

Aortic valve incompetence Aortic valve sclerosis Atelectasis Brain natriuretic peptide increased COVID-19 Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Dyspnoea Dyspnoea paroxysmal nocturnal Echocardiogram Exposure to SARS-CoV-2 Hypervolaemia Hypoxia Inferior vena cava dilatation Left atrial dilatation Left ventricular dilatation Left ventricular dysfunction

Symptomtext

The patient is a 67 y.o. with past and current medical history of ICM EF 15-20% chronic systolic heart failure, CAD with hx of anterior STEMI in 2016 with PCI LAD, with 70-80% RCA not intervened at the time, EF25% at that time. He has followed with Cardiology but was referred to another healthcare facility Feb 2022. He presented to the ED 6/15 with edema, dyspnea, orthopnea, and PND for 1-2 weeks prior to admission. He had admitted weight gain about 20-25 lbs. In the ED, CXR with pulmonary congestion, BNP 5k. He was admitted to care service for diuresis. An echo was updated on admit that showed severely dilated LV with EF 15%. He was diuresed aggressively with a lasix drip. He threatened to leave AMA multiple times, but ended up staying, lasix gtt transitioned to PO torsemide 40mg bid. His fluid status and symptoms greatly improved with aggressive diuresis. GDMT; his coreg was cotninued. Lisinopril was continued but later held and transitioned to entresto on discharge. He reported a hx of dizziness with aldactone but this was trailed while inpatient and tolerated well. SGLT2i cost was prohibitive, therefore not prescribed. Patient reported that his wife recently testes positive for COVID, he took a home test and was positive, PCR was positive on admit 6/16. Internal medicine was consulted to help treat COVID. He was hypoxic, unclear how much was from COVID vs fluid overload. He was treated with remdesivir x5 doses. He was offered decadron but declined due to possible edema side effects. He qualified for home oxygen, especially required it at night, he initially refused home O2 due to the copay, but later okay with a lower copay and was delivered oxygen tanks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: CV Echo Limited Collected: 06/17/22 0743 Order Status: Completed Updated: 06/17/22 0834 Narrative: ECHOCARDIOGRAPHY REPORT Study Date: 06/17/2022 Patient Location: PORTABLE Patient Class: Inpatient Gender: Male Age: 67 yrs Height: 188 cm Weight: 113 kg Resting HR: 70 Resting BP: 144/77 mmHg BSA: 2.4 m2 Reason For Study: ., HF, ICM History/Symptoms: CAD, ischemic cardiomyopathy, MI, CHF, COVID 19 (6/16/2022), history of EF 15% (no reports of this found) Electronically signed on 06/17/2022 08:33 AM Interpretation Summary The left ventricle is severely dilated. There is normal left ventricular wall thickness. The left ventricular ejection fraction is 15% .Severe global left ventricular systolic dysfunction with minor regional variation is noted. The right ventricle is not well visualized. There is mild aortic valve sclerosis. There is no aortic valve stenosis. There is mild mitral regurgitation. There is no comparison study available. STUDY PERFORMED/QUALITY: AORTIC VALVE: A complete transthoracic There is mild aortic valve sclerosis. echocardiogram was performed without There is no aortic valve stenosis. spectral or color flow doppler. The Trace (trivial) aortic regurgitation. technical quality of the exam was fair. Images from the parasternal window were difficult to obtain and MITRAL VALVE: are suboptimal in quality. The apical There is mild mitral annular views were difficult to obtain and are calcification. There is mild mitral suboptimal in quality. The subcostal valve thickening. There is no mitral views were difficult to obtain and are valve stenosis. There is mild mitral suboptimal in quality. Definity was regurgitation. not given because patient refused. TRICUSPID VALVE: The tricuspid valve is not well LEFT VENTRICLE: visualized. The left ventricle is severely dilated. There is normal left PULMONIC VALVE: ventricular wall thickness. The left The pulmonic valve is not well ventricular ejection fraction is 15%. visualized. There is no pulmonic The LV ejection fraction was valvular stenosis. Trace pulmonic determined utilizing Simpson's Biplane valvular regurgitation. method. Severe global left ventricular systolic dysfunction with minor regional variation is noted. LEFT ATRIUM/ATRIAL SEPTUM: The left atrium is mildly dilated. RIGHT ATRIUM: Right atrium not well visualized. RIGHT VENTRICLE: The right ventricle is not well visualized. PERICARDIUM/PLEURAL: No pericardial effusion. INFERIOR VENA CAVA: The IVC is dilated (>2.1 cm) with less than 50% collapse during patient sniff. The estimated RA pressure is 15 mm Hg (10-20 mm Hg). Left Ventricle Great Vessels IVSd: 0.68 cm IVC diam: 3.2 cm LVPWd: 1.2 cm LVIDd: 7.7 cm LVIDs: 7.2 cm ______________________________________________________________________________ ______________________________________________________________________________ Reference Table: Normal Mild ModerateSevere Men LVEF > 52% 41-51% 30-40% <30% Women LVEF > 54% 41-53% 30-40% <30% Men LVIDd 4.2-5.8 5.9-6.3 6.4-6.8 >6.8 Women LVIDd 3.8-5.2 5.3-5.6 5.7-6.1 >6.1 LA Volume (ml/m^2) < 34 35-41 42-48 >48 LVEDVI (mL/m2) Male 34-74 75-89 89-100 >100 LVEDVI (mL/m2) Female 29-61 62-70 70-80 >80 ______________________________________________________________________________ Electronically signed on 06/17/2022 08:33 AM All sources of data reside in the Cardiology Dept EJECTION FRACTION ECHO Collected: 06/17/22 0743 Order Status: Completed Updated: 06/17/22 0834 EJECTION FRACTION ECHO 15 % DR CHEST 2 VIEWS FRONTAL AND LATERAL Resulted: 06/16/22 1131 Order Status: Completed Updated: 06/16/22 1133 Narrative: EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 6/16/2022 11:12 AM TECHNIQUE: Frontal and lateral views INDICATION: dyspnea, elevated bnp. COMPARISON: 6/7/2022 ENCOUNTER: Not applicable _________________________ FINDINGS: Stable cardiomegaly. Mild CHF appears similar to the prior exam and seen to asymmetrically involve the right lung relative to the left. Linear bibasilar atelectasis. Slight hazy opacity in both lung bases without convincing pleural effusions. No measurable pneumothorax. _________________________ Impression: Similar prominent cardiomegaly with right greater than left lung field CHF. COVID-19 PCR (Abnormal) Collected: 06/16/22 1253 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 06/16/22 1412 COVID-19 PCR Detected
Aktuelle Erkrankungen: -
Vorgeschichte: Circulatory Coronary artery disease involving native coronary artery of native heart without angina pectoris Ischemic cardiomyopathy, EF 15% Mediastinal lymphadenopathy Chronic systolic heart failure Infectious/Inflammatory COVID-19 Other History of gout
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 100 MG tablet aspirin 81 MG enteric coated tablet bisacodyl (DULCOLAX) 5 MG enteric coated tablet carvedilol (COREG) 12.5 MG tablet
Allergien: Lorsartan
Vorherige Impfungen: -

VAERS 2323959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: PA
Alter: 47,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 29.10.2001
Beginn: 15.11.2021
Tage bis Beginn: 7.322,0
Dosis: 1
Route/Site: - / -

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

Blood test Bradyphrenia Colonoscopy Electrocardiogram Fatigue Headache Hyporesponsive to stimuli Impaired work ability Laboratory test Scan Sleep disorder Tremor

Symptomtext

I have been tested and tested. I have been scanned. Everyone gives different reasons. Some say it happens! Some say a sleep disorder, Some say they want to do all kinds of unnecessary mental tests. Some say it was is just a coincidence. Nothing helps from any doctor. This is effecting my income. There are no real answers. I was told by most doctor's that I will have to wait it out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Heart scans, EKG, colonoscope, blood work, many trips to my local Doctor. There are so many dates that I would have to get form my doctor. This is all in the last 6 months.
Aktuelle Erkrankungen: -
Vorgeschichte: Fatigue, headaches, shaking, stopped thinking or answering questions for a second. Unable to work.
Andere Medikamente: duloxetine, omeprazole, amlodipine, lisinopril, Vitamin D
Allergien: Shell fish
Vorherige Impfungen: -

VAERS 2315625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CO
Alter: 91,0
Geschlecht: M
Eingang: 10.06.2022
Impfdatum: 19.12.2021
Beginn: 29.05.2022
Tage bis Beginn: 161,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

Pt admit to hospital 5/29-6/1 with COVID PNA (tested positive for COVID 5/29/22). Pt received 3 COVID19 vaccines prior to admit (3/10/21 - moderna, 4/7/21 - moderna, and 12/19/21 - Pfizer)

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2301116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 20.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Blood test Body height decreased Disease recurrence Dysphonia Fall Body height COVID-19 Drug ineffective Endoscopy Feeling abnormal Gastrooesophageal reflux disease Illness Paraesthesia SARS-CoV-2 test Weight Swelling

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group, Program ID: Unknown. The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 01Apr2021 as dose 2, single (Lot number: EW015), in left arm and on 20Oct2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 71 years, in left arm for Covid-19 immunisation; CoviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), in left arm for Covid-19 immunisation. The patient's relevant medical history included: "GERD" (unspecified if ongoing), notes: Note: GERD; "Hemithyroidectomy", start date: 2011 (unspecified if ongoing), notes: Note: Hemithyroidectomy. Concomitant medication(s) included: LEVOTHYROXINE taken for thyroidectomy. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "She already have first and second dose of the Covid-19 Vaccine as well as the booster dose, so tested positive". The patient underwent the following laboratory tests and procedures: Blood test: (unspecified date) Negative; Body height: (unspecified date) 5.25; Endoscopy: (unspecified date) Unknown results, notes: I am going to have a endoscopy something I want to find out, its going on for 3 years now; SARS-CoV-2 test: (unspecified date) Unknown results, notes: I have used 3 of them now because I had different test it didn't work; (unspecified date) Unknown results, notes: I have used 3 of them now because I had different test it didn't work; (unspecified date) Unknown results, notes: I have used 3 of them now because I had different test it didn't work; (unspecified date) Positive; (Apr2022) Negative; (Apr2022) Negative; Weight: (unspecified date) 118; (unspecified date) 115. Additional Context: "I have caller on hold she is a consumer, she mentioned that she already have first and second dose of the Covid-19 Vaccine as well as the booster dose. So tested positive and also had some adverse events just tingling of feet and she tested positive so, she wants to know the expiration date for the whole test kit that she has and where to get another box for whole test kit." Consumer stated, "Hold on just for a sec I need to turned it down a little bit hold on. I got till you were giving me list of called and above could you just says those again slowly. Right so I have a thing called Clinitest rapid Covid-19 antigen self-test there were five its from (Withheld) and there are five test and I have used 3 of them now because I had different test it didn't work. I knew I was getting sick after two an half years I am very careful, I went to an art exhibit and most of the people they were not wearing mask and I two couple days later 2-3 days later I started felling unusual things and I figured that I had Covid and had some tested and handed it out free here in my community and they showed I was negative. But then I have ordered before I got those test because I didn't know they were available I sent way to government and find some government test and afterwards I had got this mail and when I got Covid I had both types of test and the one I had alterably found out I had Covid from Clinitest rapid and even I did the everything on the same day the other one said I was negative this was only the one worked so I wanted to get some more of this because I have a friend who got Covid twice and even after she have two initial vaccines and booster (Further information was not available over the call hence, split was not made). So I have those and I am 76 so I wanted to make sure if I feel sick again and I have some symptoms I don't know if they are from the virus or from the vaccination. I have been read on upon from the side effects from the vaccination and I was deprived to see that some of the other things I have been experiencing on that list so, I just didn't even think they could be associated with the vaccine itself the shot. "Consumer stated, "You have no way to track this remaining two test still good you don't know how to do that or you don't have capability of doing that. Date of birth: "I am 76 years old that's what I tell you I don't give out my date of birth because people can track you in fraudulently. Start Date of adverse event: Consumer stated, "It was in April I think because I wrote it down hold on I think I now where I got it. I didn't experienced I had it treated afterwards. So I went to art exhibit April 6th and most of the people attending the exhibit didn't have mask on and masking was take it way in prior month February. The day I started experiencing symptoms were Saturday the month of April and than I took a test Sunday that was first day when I took this and it was negative and I had other test that I am trying to get more of and that was the test it that was rapid Covid-19 antigen self test I tested positive than I on the 10". Height and weight, consumer stated, "I lost some height I am 5.25 (Further clarification unknown hence, captured as event) now and I weight about my weight varies my weight about let see I don't know let say 118, 115." (Further the height and weight is not clarified hence, not captured in tab). Facility name, consumer stated, "Where I got it I told you I got at art exhibit the (Withheld) of art I went to see exhibit lot of people there probably." Facility name, consumer stated, "(Hospital Name Withheld)." LOT# for 2nd dose, consumer stated, "2nd one I got in April and lot# EW0151 and its was 01Apr2021 same location (Withheld)." LOT# for booster 1st dose, consumer stated, "The LOT# FH8020 and the date was 20Oct2021 and I got it at (Withheld) and that's it I didn't get the second booster yet whatever question I was hoping to answered today. You were the person that was going to answer but I was miss lead by prior person I thought I was going to reconnect to someone and ask some question". Informed about Pfizer Medical Information: Consumer stated, "Say that again. This is the right department or the wrong department? Okay so I can ask you question. Okay so you can't help me with expiration date. So that's what I really need to know but I wanted to know since I got Covid and you have the dates of my vaccination and my age. I wanted to know, my understanding is you have 5 months between first vaccination and second one where you can get the second one but since I have had Covid in between I am just wondering I am still should be getting the second booster. Now as I think I am eligible now in May but I was told that we were probably going to have another search in the fall so I was thinking that it might be better for me to wait and because I don't know if there is going to be third booster may be wait until just before the fall. Whenever they think the search is starting to happen. Whether I should wait to get my second booster until then. Can you answer that question?" Consumer was informed about the role of Pfizer Drug Safety, consumer stated, "For what question can you answer. I don't want to waste your time. What sort of question as a Pharmacist are you able to answer. Side effects? Are you able to answer side effects question. Yes or No. You just file a report. Okay since you can't answer my question and why don't you ask me any of the other question that you need to know and the I can try to get the hold of them although they are not going to be available until probably Monday till Tomorrow. Do you have any other questions that you need to know from me. Okay let's wrap it up Because I have been on Phone long time now and nobody has helped me here so. Okay go ahead what else you need to know." LOT# Confirmation, consumer stated," Okay so I can't verify them, it's like get it them all again. Why don't you just assume that you got it all right." Anatomical site, consumer stated, "The first one was in my left. They were both, the first two were in my left because I was in my Car so they were in my first. And the second one I am not sure I did it at (Pharmacy Withheld) So I was sitting in chair. I don't remember." Other medication and Other Medical condition, consumer stated, "Am I suffering from any other medical condition ad what was the second part? Am I taking any medication? Any of my own medication separate from the virus medication Is that what you are asking? Okay I take Levothyroxine (25microgram, once a day, a tablet), And the reason I take it is Hemithyroidectomy in 2011." Treatment, consumer stated, "For the side-effects that I have from the virus I have experienced and that was the reason I wanted to look up my dates. I have been having some problems I don't think that they were associated with vaccine but I was doing some reading today and saw that all my symptoms were on the list and there were many symptoms and my symptoms could be from something else but I had tingling in my feet, for a long time I didn't know what it was and I had swelling with the first test , when I first noticed I had tingling my legs swelled up below my Knee my whole from my ankle to my knee I had swelling, numbness and tingling in my feet I still have it. The swelling I went to the Emergency hospital and they told me that I am negative for lot of thing but I needed to be sure that I slept in prone position because I had just moved and falling from feet on the chair a lot of time and I needed to put some constrictive stocking and elevate my feet to get the flowing to go down. So I went out and bought some stocking and then wore it for maybe for 3 or 4 weeks and the swelling did finally go down. And I tried to elevate my leg as much as I could but I was moving and not getting around. And the I had raspiness in my throat which got worsen since I got Covid this raspiness gotten down into my chest since I have kind of cough, a deep cough that sounds like the kind of cough when you have cold, kind of like and I have had little bit of. So it effects my voice and I am singer and my speaking voice it feels like sand paper when I talk like right now. So I am doing some test to find out if something is going on in my esophagus I use to have GERD. You know what GERD is right. So I took some medication for few years after my Hemithyroidectomy, I had some Raspiness as then and then they took the medication off the market that I was taking called Ranitidine I stopped taking for a while and then because raspiness is a kind of gone away and it came back and I got new prescription the drug may be few weeks after that was taken off the market so I stopped taking it. Medication for my GERD so it has come back something is happening in my esophagus and I am having some test at the end of months variant so I am going to have a endoscopy something I want to find out, its going on for 3 years now. I did have so you wanna things I lot a had Covid now still happening is that what you wanna know is that you want to know both. I have been taking I just went to a doctor about two weeks ago a new doctor and she gave me this is after months and months these things going on this is new doctor two doctor now. He gave me two prescriptions one I have been taking and other one called Protonix its a 40 milligram tablets I take one a day doctor gave me for weeks doses of a day that's for my throat, probably of GERD or whatever is causing something in my coming up my stomach acid, I am not sure and they gave me another for my feet but I have not start taking it yet because when I read the contraindication it said that if people are trying to suicide or start have thought of suicide. (Further clarification unknown) when I take it should take it or should stop taking it and it sound it pretty well so my doctor is on vacation he is coming back tomorrow and I have appointment with him to find out I careful about what I take because of my age. I don't want to start taking something have some wired side effect you know what I mean so I am going to talk to him before start taking it or may not take it what he says. So these only the two things I had for my symptoms and my symptoms may or may not be related to the virus or vaccination I don't think about these vaccines but when I started reading I started taking the dates of my symptoms and it was after I moved here and that was right after those two first vaccination thinking about nobody is able to say what going on with me I wonder if I have side effects with vaccination. I will say the list I saw was not from Pfizer list it was from (Brand name withheld) list but there was list thing kind of common side that people I don't know what is causing my symptoms I had lot of blood test I thought may be diabetic something my in family had symptoms on feet but all tested negative so that was the interesting thing that may be thinking caused by vaccinated that is the reason I called you guys." Is there a product complaint to report? Yes. Description of Product Complaint: Call was transferred from Pfizer Support by (Name Withheld) (CEP ID: Unknown). Employee stated, "I have caller on hold she is a consumer, she mentioned that she already have first and second dose of the Covid-19 Vaccine as well as the booster dose. So tested positive and also had some adverse events just tingling of feet and she tested positive so, she wants to know the expiration date for the whole test kit that she has and where to get another box for whole test kit." When paraphrased above concern, C stated, " Right so I have a thing called Clinitest rapid Covid-19 antigen self test there were five its from (Withheld) and there are five test and I have used 3 of them now because I had different test it didn't work. I knew I was getting sick after two an half years I am very careful, I went to an art exhibit and most of the people they were not wearing mask and I two couple days later 2-3 days later I started felling unusual things and I figured that I had Covid and had some tested and handed it out free here in my community and they showed I was negative. But then I have ordered before I got those test because I didn't know they were available I sent way to government and find some government test and afterwards I had got this mail and when I got Covid I had both types of test and the one I had alterably found out I had Covid from Clinitest rapid and even I did the everything on the same day the other one said I was negative this was only the one worked so I wanted to get some more of this because I have a friend who got Covid twice and even after she have two initial vaccines and booster. So I have those and I am 76 so I wanted to make sure if I feel sick again and I have some symptoms I don't know if they are from the virus or from the vaccination." LOT# for 2nd dose, consumer stated, "2nd one I got in April and lot# EW015." LOT# for booster 1st dose, consumer stated, "The LOT# FH8020." This is a notification generated from the system. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in system. Refer to the below table for details: AE Ref No. (CC): # PR ID (CR):. Product- Description (CR): Compound BNT162B2 Covid-19 vaccine suspension for intramuscular 2ml multiple dose vial x 1. Lot-# (CR): EN6199. Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EN6199 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EN6199, fill lot EN5331, and the formulated drug product lot EN5320. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: #. PR Link (Previously Investigated CR):. AE Ref No. (CC): # PR ID (CR):. Product- Description (CR): Compound BNT162 Covid-19 Vaccine Suspension for Intramuscular 2ml Multiple Dose Vial X 1. Lot-# (CR): EW0151. Conclusion of Previously Completed Investigation (FCI/SI/OffCI)*: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE INJECTABLE lot EW0151 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot EW0151, fill lot EP8691, and the formulated drug product lot EP8588. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: #. PR Link (Previously Investigated CR): #. AE Ref No. (CC): # PR ID (CR): #. Product- Description (CR): Compound BNT162 Covid-19 Vaccine Suspension for Intramuscular 2ml Multiple Dose Vial X 1. Lot-# (CR): EL3247. Conclusion of Previously Completed Investigation (FCI/SI/OffCI)*. The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE INJECTABLE lot FH8020 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FH8020, fill lot FG3521, and the bulk formulated drug product lot FH0137. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: #. PR Link (Previously Investigated CR): #. When more than one investigation is found in the family, the Conclusion field could result in repeating rows for the CR in the table. If the Conclusion is blank in the table above, then the investigation record is likely an Offline Contractor Investigation and the conclusion must be obtained directly from the child investigation record(s) of the linked Complaint Record. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Blood test; Test Result: Negative; Test Name: Height; Result Unstructured Data: Test Result:5.25; Test Name: Endoscopy; Result Unstructured Data: Test Result: Unknown results; Comments: I am going to have a endoscopy something I want to find out, its going on for 3 years now.; Test Name: Clinitest rapid Covid-19 Antigen self test; Result Unstructured Data: Test Result: Unknown results; Comments: I have used 3 of them now because I had different test it didn't work; Test Name: Clinitest rapid Covid-19 Antigen self test; Result Unstructured Data: Test Result: Unknown results; Comments: I have used 3 of them now because I had different test it didn't work; Test Name: Clinitest rapid Covid-19 Antigen self test; Result Unstructured Data: Test Result: Unknown results; Comments: I have used 3 of them now because I had different test it didn't work; Test Name: Clinitest rapid Covid-19 Antigen self test; Test Result: Positive; Test Date: 202204; Test Name: Covid-19; Test Result: Negative; Test Date: 202204; Test Name: Covid-19; Test Result: Negative; Test Name: Weight; Result Unstructured Data: Test Result:118; Test Name: Weight; Result Unstructured Data: Test Result:115.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD (Note: GERD); Hemithyroidectomy (Note: Hemithyroidectomy)
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2301116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 20.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Blood test Body height decreased Disease recurrence Dysphonia Fall Body height COVID-19 Drug ineffective Endoscopy Feeling abnormal Gastrooesophageal reflux disease Illness Paraesthesia SARS-CoV-2 test Weight Swelling

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group, Program ID: Unknown. The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 01Apr2021 as dose 2, single (Lot number: EW015), in left arm and on 20Oct2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 71 years, in left arm for Covid-19 immunisation; CoviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), in left arm for Covid-19 immunisation. The patient's relevant medical history included: "GERD" (unspecified if ongoing), notes: Note: GERD; "Hemithyroidectomy", start date: 2011 (unspecified if ongoing), notes: Note: Hemithyroidectomy. Concomitant medication(s) included: LEVOTHYROXINE taken for thyroidectomy. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "She already have first and second dose of the Covid-19 Vaccine as well as the booster dose, so tested positive". The patient underwent the following laboratory tests and procedures: Blood test: (unspecified date) Negative; Body height: (unspecified date) 5.25; Endoscopy: (unspecified date) Unknown results, notes: I am going to have a endoscopy something I want to find out, its going on for 3 years now; SARS-CoV-2 test: (unspecified date) Unknown results, notes: I have used 3 of them now because I had different test it didn't work; (unspecified date) Unknown results, notes: I have used 3 of them now because I had different test it didn't work; (unspecified date) Unknown results, notes: I have used 3 of them now because I had different test it didn't work; (unspecified date) Positive; (Apr2022) Negative; (Apr2022) Negative; Weight: (unspecified date) 118; (unspecified date) 115. Additional Context: "I have caller on hold she is a consumer, she mentioned that she already have first and second dose of the Covid-19 Vaccine as well as the booster dose. So tested positive and also had some adverse events just tingling of feet and she tested positive so, she wants to know the expiration date for the whole test kit that she has and where to get another box for whole test kit." Consumer stated, "Hold on just for a sec I need to turned it down a little bit hold on. I got till you were giving me list of called and above could you just says those again slowly. Right so I have a thing called Clinitest rapid Covid-19 antigen self-test there were five its from (Withheld) and there are five test and I have used 3 of them now because I had different test it didn't work. I knew I was getting sick after two an half years I am very careful, I went to an art exhibit and most of the people they were not wearing mask and I two couple days later 2-3 days later I started felling unusual things and I figured that I had Covid and had some tested and handed it out free here in my community and they showed I was negative. But then I have ordered before I got those test because I didn't know they were available I sent way to government and find some government test and afterwards I had got this mail and when I got Covid I had both types of test and the one I had alterably found out I had Covid from Clinitest rapid and even I did the everything on the same day the other one said I was negative this was only the one worked so I wanted to get some more of this because I have a friend who got Covid twice and even after she have two initial vaccines and booster (Further information was not available over the call hence, split was not made). So I have those and I am 76 so I wanted to make sure if I feel sick again and I have some symptoms I don't know if they are from the virus or from the vaccination. I have been read on upon from the side effects from the vaccination and I was deprived to see that some of the other things I have been experiencing on that list so, I just didn't even think they could be associated with the vaccine itself the shot. "Consumer stated, "You have no way to track this remaining two test still good you don't know how to do that or you don't have capability of doing that. Date of birth: "I am 76 years old that's what I tell you I don't give out my date of birth because people can track you in fraudulently. Start Date of adverse event: Consumer stated, "It was in April I think because I wrote it down hold on I think I now where I got it. I didn't experienced I had it treated afterwards. So I went to art exhibit April 6th and most of the people attending the exhibit didn't have mask on and masking was take it way in prior month February. The day I started experiencing symptoms were Saturday the month of April and than I took a test Sunday that was first day when I took this and it was negative and I had other test that I am trying to get more of and that was the test it that was rapid Covid-19 antigen self test I tested positive than I on the 10". Height and weight, consumer stated, "I lost some height I am 5.25 (Further clarification unknown hence, captured as event) now and I weight about my weight varies my weight about let see I don't know let say 118, 115." (Further the height and weight is not clarified hence, not captured in tab). Facility name, consumer stated, "Where I got it I told you I got at art exhibit the (Withheld) of art I went to see exhibit lot of people there probably." Facility name, consumer stated, "(Hospital Name Withheld)." LOT# for 2nd dose, consumer stated, "2nd one I got in April and lot# EW0151 and its was 01Apr2021 same location (Withheld)." LOT# for booster 1st dose, consumer stated, "The LOT# FH8020 and the date was 20Oct2021 and I got it at (Withheld) and that's it I didn't get the second booster yet whatever question I was hoping to answered today. You were the person that was going to answer but I was miss lead by prior person I thought I was going to reconnect to someone and ask some question". Informed about Pfizer Medical Information: Consumer stated, "Say that again. This is the right department or the wrong department? Okay so I can ask you question. Okay so you can't help me with expiration date. So that's what I really need to know but I wanted to know since I got Covid and you have the dates of my vaccination and my age. I wanted to know, my understanding is you have 5 months between first vaccination and second one where you can get the second one but since I have had Covid in between I am just wondering I am still should be getting the second booster. Now as I think I am eligible now in May but I was told that we were probably going to have another search in the fall so I was thinking that it might be better for me to wait and because I don't know if there is going to be third booster may be wait until just before the fall. Whenever they think the search is starting to happen. Whether I should wait to get my second booster until then. Can you answer that question?" Consumer was informed about the role of Pfizer Drug Safety, consumer stated, "For what question can you answer. I don't want to waste your time. What sort of question as a Pharmacist are you able to answer. Side effects? Are you able to answer side effects question. Yes or No. You just file a report. Okay since you can't answer my question and why don't you ask me any of the other question that you need to know and the I can try to get the hold of them although they are not going to be available until probably Monday till Tomorrow. Do you have any other questions that you need to know from me. Okay let's wrap it up Because I have been on Phone long time now and nobody has helped me here so. Okay go ahead what else you need to know." LOT# Confirmation, consumer stated," Okay so I can't verify them, it's like get it them all again. Why don't you just assume that you got it all right." Anatomical site, consumer stated, "The first one was in my left. They were both, the first two were in my left because I was in my Car so they were in my first. And the second one I am not sure I did it at (Pharmacy Withheld) So I was sitting in chair. I don't remember." Other medication and Other Medical condition, consumer stated, "Am I suffering from any other medical condition ad what was the second part? Am I taking any medication? Any of my own medication separate from the virus medication Is that what you are asking? Okay I take Levothyroxine (25microgram, once a day, a tablet), And the reason I take it is Hemithyroidectomy in 2011." Treatment, consumer stated, "For the side-effects that I have from the virus I have experienced and that was the reason I wanted to look up my dates. I have been having some problems I don't think that they were associated with vaccine but I was doing some reading today and saw that all my symptoms were on the list and there were many symptoms and my symptoms could be from something else but I had tingling in my feet, for a long time I didn't know what it was and I had swelling with the first test , when I first noticed I had tingling my legs swelled up below my Knee my whole from my ankle to my knee I had swelling, numbness and tingling in my feet I still have it. The swelling I went to the Emergency hospital and they told me that I am negative for lot of thing but I needed to be sure that I slept in prone position because I had just moved and falling from feet on the chair a lot of time and I needed to put some constrictive stocking and elevate my feet to get the flowing to go down. So I went out and bought some stocking and then wore it for maybe for 3 or 4 weeks and the swelling did finally go down. And I tried to elevate my leg as much as I could but I was moving and not getting around. And the I had raspiness in my throat which got worsen since I got Covid this raspiness gotten down into my chest since I have kind of cough, a deep cough that sounds like the kind of cough when you have cold, kind of like and I have had little bit of. So it effects my voice and I am singer and my speaking voice it feels like sand paper when I talk like right now. So I am doing some test to find out if something is going on in my esophagus I use to have GERD. You know what GERD is right. So I took some medication for few years after my Hemithyroidectomy, I had some Raspiness as then and then they took the medication off the market that I was taking called Ranitidine I stopped taking for a while and then because raspiness is a kind of gone away and it came back and I got new prescription the drug may be few weeks after that was taken off the market so I stopped taking it. Medication for my GERD so it has come back something is happening in my esophagus and I am having some test at the end of months variant so I am going to have a endoscopy something I want to find out, its going on for 3 years now. I did have so you wanna things I lot a had Covid now still happening is that what you wanna know is that you want to know both. I have been taking I just went to a doctor about two weeks ago a new doctor and she gave me this is after months and months these things going on this is new doctor two doctor now. He gave me two prescriptions one I have been taking and other one called Protonix its a 40 milligram tablets I take one a day doctor gave me for weeks doses of a day that's for my throat, probably of GERD or whatever is causing something in my coming up my stomach acid, I am not sure and they gave me another for my feet but I have not start taking it yet because when I read the contraindication it said that if people are trying to suicide or start have thought of suicide. (Further clarification unknown) when I take it should take it or should stop taking it and it sound it pretty well so my doctor is on vacation he is coming back tomorrow and I have appointment with him to find out I careful about what I take because of my age. I don't want to start taking something have some wired side effect you know what I mean so I am going to talk to him before start taking it or may not take it what he says. So these only the two things I had for my symptoms and my symptoms may or may not be related to the virus or vaccination I don't think about these vaccines but when I started reading I started taking the dates of my symptoms and it was after I moved here and that was right after those two first vaccination thinking about nobody is able to say what going on with me I wonder if I have side effects with vaccination. I will say the list I saw was not from Pfizer list it was from (Brand name withheld) list but there was list thing kind of common side that people I don't know what is causing my symptoms I had lot of blood test I thought may be diabetic something my in family had symptoms on feet but all tested negative so that was the interesting thing that may be thinking caused by vaccinated that is the reason I called you guys." Is there a product complaint to report? Yes. Description of Product Complaint: Call was transferred from Pfizer Support by (Name Withheld) (CEP ID: Unknown). Employee stated, "I have caller on hold she is a consumer, she mentioned that she already have first and second dose of the Covid-19 Vaccine as well as the booster dose. So tested positive and also had some adverse events just tingling of feet and she tested positive so, she wants to know the expiration date for the whole test kit that she has and where to get another box for whole test kit." When paraphrased above concern, C stated, " Right so I have a thing called Clinitest rapid Covid-19 antigen self test there were five its from (Withheld) and there are five test and I have used 3 of them now because I had different test it didn't work. I knew I was getting sick after two an half years I am very careful, I went to an art exhibit and most of the people they were not wearing mask and I two couple days later 2-3 days later I started felling unusual things and I figured that I had Covid and had some tested and handed it out free here in my community and they showed I was negative. But then I have ordered before I got those test because I didn't know they were available I sent way to government and find some government test and afterwards I had got this mail and when I got Covid I had both types of test and the one I had alterably found out I had Covid from Clinitest rapid and even I did the everything on the same day the other one said I was negative this was only the one worked so I wanted to get some more of this because I have a friend who got Covid twice and even after she have two initial vaccines and booster. So I have those and I am 76 so I wanted to make sure if I feel sick again and I have some symptoms I don't know if they are from the virus or from the vaccination." LOT# for 2nd dose, consumer stated, "2nd one I got in April and lot# EW015." LOT# for booster 1st dose, consumer stated, "The LOT# FH8020." This is a notification generated from the system. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in system. Refer to the below table for details: AE Ref No. (CC): # PR ID (CR):. Product- Description (CR): Compound BNT162B2 Covid-19 vaccine suspension for intramuscular 2ml multiple dose vial x 1. Lot-# (CR): EN6199. Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EN6199 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EN6199, fill lot EN5331, and the formulated drug product lot EN5320. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: #. PR Link (Previously Investigated CR):. AE Ref No. (CC): # PR ID (CR):. Product- Description (CR): Compound BNT162 Covid-19 Vaccine Suspension for Intramuscular 2ml Multiple Dose Vial X 1. Lot-# (CR): EW0151. Conclusion of Previously Completed Investigation (FCI/SI/OffCI)*: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE INJECTABLE lot EW0151 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot EW0151, fill lot EP8691, and the formulated drug product lot EP8588. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: #. PR Link (Previously Investigated CR): #. AE Ref No. (CC): # PR ID (CR): #. Product- Description (CR): Compound BNT162 Covid-19 Vaccine Suspension for Intramuscular 2ml Multiple Dose Vial X 1. Lot-# (CR): EL3247. Conclusion of Previously Completed Investigation (FCI/SI/OffCI)*. The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE INJECTABLE lot FH8020 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FH8020, fill lot FG3521, and the bulk formulated drug product lot FH0137. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: #. PR Link (Previously Investigated CR): #. When more than one investigation is found in the family, the Conclusion field could result in repeating rows for the CR in the table. If the Conclusion is blank in the table above, then the investigation record is likely an Offline Contractor Investigation and the conclusion must be obtained directly from the child investigation record(s) of the linked Complaint Record. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Blood test; Test Result: Negative; Test Name: Height; Result Unstructured Data: Test Result:5.25; Test Name: Endoscopy; Result Unstructured Data: Test Result: Unknown results; Comments: I am going to have a endoscopy something I want to find out, its going on for 3 years now.; Test Name: Clinitest rapid Covid-19 Antigen self test; Result Unstructured Data: Test Result: Unknown results; Comments: I have used 3 of them now because I had different test it didn't work; Test Name: Clinitest rapid Covid-19 Antigen self test; Result Unstructured Data: Test Result: Unknown results; Comments: I have used 3 of them now because I had different test it didn't work; Test Name: Clinitest rapid Covid-19 Antigen self test; Result Unstructured Data: Test Result: Unknown results; Comments: I have used 3 of them now because I had different test it didn't work; Test Name: Clinitest rapid Covid-19 Antigen self test; Test Result: Positive; Test Date: 202204; Test Name: Covid-19; Test Result: Negative; Test Date: 202204; Test Name: Covid-19; Test Result: Negative; Test Name: Weight; Result Unstructured Data: Test Result:118; Test Name: Weight; Result Unstructured Data: Test Result:115.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD (Note: GERD); Hemithyroidectomy (Note: Hemithyroidectomy)
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2302077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 48,0
Geschlecht: F
Eingang: 30.05.2022
Impfdatum: 30.11.2021
Beginn: 09.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / AR

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

Dizziness Headache Hypertension

Symptomtext

Headaches and dizziness observed but not attributed to vaccination until dangerously high blood pressure readings while attempting to donate blood. Blood pressure reading was confirmed by pharmacy and physician and treatment prescribed. Reviewed blood pressure history and see trend of slight increase after first dose of Pfizer Covid vaccine, another slight increase after 2nd dose then major spike after third dose.

Weitere VAERSDATA-Felder

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

VAERS 2296435

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 22.11.2021
Beginn: 25.05.2022
Tage bis Beginn: 184,0
Dosis: 3
Route/Site: UN / UN

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

Chemotherapy Dyspnoea Lung opacity Pneumonia

Symptomtext

Hospitalized with new ground glass opacities pneumonia, increased dyspnea but no need for O2. Given monoclonal antibodies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Lung malignancy, hx PE, on chemotherapy since Mar 2022
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 14.04.2021
Beginn: 08.02.2022
Tage bis Beginn: 300,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/08/22 presents to ED for "Breathing Problem". PMHx of "non-Hodgkin's lymphoma (on chemo), empyema, Afib, asthma"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/08/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2266078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WA
Alter: 67,0
Geschlecht: M
Eingang: 06.05.2022
Impfdatum: 04.11.2021
Beginn: 10.04.2022
Tage bis Beginn: 157,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Chest discomfort Chest pain Chills Cough Dyspnoea Ear infection Fatigue Headache Malaise Myalgia Nausea Pulmonary congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 4/10/2022 with symptoms of cough, fever, severe headache, chest congestion, ear infections in both ear, chest pain/tightness, shortness of breathe, lost sense of taste and smell, fatigue, myalgia, chills, nausea, and I was ill for 18 days before the symptoms began to resolve. I have lingering symptoms of cough, headache, and sense of taste and smell are still muted but are returning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 PCR nasal swab was positive 4/19/2022
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma BPH
Andere Medikamente: Caersitin 500mg Multivitamin Diltiazem 120mg Daily Bupropion 300mg Daily Atorvastatin 20mg Daily Hydrochlorothiazide Finasteride 5mg Tamsulosin 0.4mg Daily Aspirin 325mg
Allergien: Lisinopril Epinephrine
Vorherige Impfungen: Flu shots last dose 1993, experienced flu like symptoms lasting 2 to 3 weeks.

VAERS 2263953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: SC
Alter: 20,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chest X-ray normal Chest pain Chills Confusional state Electrocardiogram normal Myalgia Somnolence

Symptomtext

On Oct 11, 2021 I had extreme 24 hour symptoms of chills, drowsiness, confusion, and muscle pains and aches. I had major chest pain accompanied with the muscle aches. No treatment was necessary. The pain lasted throughout the weekend.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Normal chest x-ray; normal EKG
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity
Andere Medikamente: Tylenol Advil Caffeine
Allergien: Allergic to all allergy medication Sulfa and Penicillin family Onions Corn Mint
Vorherige Impfungen: -

VAERS 2262140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NH
Alter: 33,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 29.10.2021
Beginn: 05.01.2022
Tage bis Beginn: 68,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Feeling abnormal Migraine Myalgia SARS-CoV-2 test positive

Symptomtext

On January 5, 2022, it started with severe migraines at nighttime in bed. When I woke up the next day I woke up with muscle aches and feeling really crappy. I tested myself on January 6, 2022, with my at home test and I tested positive. I contacted my doctor on Thursday or Friday that same week, to let them know that I tested positive for COVID-19. My doctor sent me a inhaler just in case I needed it. On January 17, 2022, I tested negative for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: COVID-19 at home test done on January 6, 2022 and I tested positive.
Aktuelle Erkrankungen: None
Vorgeschichte: I have Hepatitis
Andere Medikamente: I take Lexapro 20mg; Topamax 50mg; Suboxone 8 over 2 mg
Allergien: None
Vorherige Impfungen: -

VAERS 2261927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 28,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 01.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 39,0
Dosis: 2
Route/Site: SYR / RA

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

Blood cholesterol increased Blood test abnormal Hypertension Photopsia Tinnitus Visual impairment

Symptomtext

Around December 10, 2021, I had started hearing a squeaking noise in my ear. I thought that it was because of a call I was on at the time, but when I got off and took off my headphones, I could still hear the squeaking sound. It sounded like a kitten was making noise. The last week of December 2021 when I woke up, I would see blue and green flashes in my eyes. I would see it if I stood up or moved my head quickly. My whole vision would be a blue and green flash, and then it would go away. On January 19, 2022, I went to the doctor and they diagnosed me with Pulsatile Tinnitus. They also told me that I have high blood pressure and high cholesterol. On October 21, 2022, before I had the COVID vaccine my blood pressure and cholesterol were normal. Early March 2022 is when I stopped noticing any of those symptoms anymore. As I got better with my vision the blue and green flashed started to become blue and green spots and then it went away completely over time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Blood work - cholesterol was high
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; High Cholesterol
Andere Medikamente: BENADRYL
Allergien: None
Vorherige Impfungen: -

VAERS 2257023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 28.03.2022
Beginn: 28.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Condition aggravated Dizziness Immediate post-injection reaction Migraine

Symptomtext

Lightheadedness immediately following vaccination. Increase in migraine headaches since vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Migraine Headaches Hypothyroidism Cystic Acne
Andere Medikamente: Buproprion, Levothyroxine, Singulair, Spironolactone, Rizatriptan, Vitamin D, Tumeric
Allergien: Vicodin
Vorherige Impfungen: -

VAERS 2249594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 54,0
Geschlecht: M
Eingang: 23.04.2022
Impfdatum: 19.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 11,0
Dosis: UNK
Route/Site: IM / RA

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

Arteriosclerosis coronary artery Cardiac stress test abnormal Cardiac ventricular disorder Carotid artery stenosis Catheterisation cardiac abnormal Chest discomfort Coronary artery disease Dyspnoea Electrocardiogram ambulatory abnormal Palpitations Ultrasound Doppler

Symptomtext

Felt heaviness/weight on chest, difficulty breathing around midnight on 10/30/21 - had been having "palpitations" for a couple weeks prior; felt same symptoms around 3:30am on same day. Contacted PCP who referred for a stress test and holter monitor. Failed both tests, so referred to a cardiologist. Had appointment on 11/18/21, and cardiologist performed heart catheterization on 12/14/21. Final impression: 1. Nonobstructive CAD with 30% proximal LAD plaquing, otherwise patent coronary arteries 2. Mildly elevated LV filling pressures, with LVEDP of 20 mmHg 3. Normal LV systolic function, with LVEF of 55% by LV gram Increased atorvastatin from 10mg/day to 40mg/day. Also had carotid doppler ultrasound on 1/14/22 - final impression: right carotid vasculature - fibrous plaque at the proximal ICA results in a less than 50% stenosis; left carotid vasculature - fibrous plaque at the proximal ICA results in a less than 50% stenosis; vertebral arteries - antegrade flow is seen at the bilateral vertebral arteries.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid; low testosterone; high blood pressure; depression; anxiety; PTSD; back pain
Andere Medikamente: Ranolazine 1000 mg 2x/day; Losartan potassium 100mg; atorvastatin 40mg; testosterone cypionate 0.5ml/2 wks.; bupropion HCL 450mg; clonazepam 1mg 3x/day; levothyroxine 50mcg; multivitamin; baby aspirin; glucosamine chondroitin; vitamin D3; m
Allergien: Gabapentin; prednisone
Vorherige Impfungen: -

VAERS 2245740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 50,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Adverse event Blood test normal Cardiac flutter Chest pain Dyspnoea Echocardiogram normal Incomplete course of vaccination

Symptomtext

Starting a few hours after receiving the vaccine, my heart felt like it was fluttering. It was mild at first but then over the next couple of days it increased. It would take my breath away for a second. Then, it would come and go for a few days at a time or less and vary in intensity for about a 3 week period of time. Then, I considered it as going away. I went to the same pharmacy for the 2nd and they told me that likely it was an adverse event and I needed to get evaluated before I could have the 2nd dose. I ended up going to see my cardiologist and he said, since it had been 4 weeks since the last event, it would not show up in blood work but it sounded like I had a mild case of myocarditis. The doctor had seen side effects in his practice. I was concerned about getting COVID-19 so I discussed with him about getting the 2nd dose. He advised me that I should get it but warned me that there is no cure for myocarditis so he left the decision up to me. When I saw my PCP and my neurologist, they both advised against receiving another vaccine due to my reaction. For the past few months I've been having intermittent chest pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood work: nothing abnormal, Echocardiogram: negative for myocarditis.
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines; PVCs; Degenerative Disc Disease
Andere Medikamente: I did not take any of these the day of the vaccine to ensure no interaction; Vitamin D 50000IU weekly; Clarinex 5mg QD; Xyzal PRN; Linzess QD; vitamin E 400mg QD; EpiPen PRN; Inhaler PRN
Allergien: Cephalosporin; Sulfa; Penicillin; Cipro; Topomax; NSAIDs; Steroids; Toradol; Propafol; Eggs; all Nuts; Basil; Gluten Sensitivity; Red Dye
Vorherige Impfungen: -

VAERS 2243724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IL
Alter: 44,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 13.10.2021
Beginn: 11.02.2022
Tage bis Beginn: 121,0
Dosis: 3
Route/Site: SYR / LA

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

Asthma COVID-19 Chills Condition aggravated Electrocardiogram T wave abnormal Electrocardiogram abnormal Feeling cold Oropharyngeal pain SARS-CoV-2 test positive X-ray normal

Symptomtext

I had chills and sore throat and could not get warm and just traveled for work for the first time and took a home test and tested positive and the next morning I was having allergy induced asthma and I called the after hours line for my physician and was advised to get to the hospital to be checked out. I had an abnormal EKG.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG with T wave abnormality; X rays clear no abnormalities
Aktuelle Erkrankungen: None
Vorgeschichte: Allergies; Hypertension; Colectomy
Andere Medikamente: Mirtazapine 15 mg Montelukast 10mg Amlodipine 5mg Quivira Inhaler 80 mcg Flonase Nasal Spray Mariana IUD
Allergien: Sulfa; pet dander
Vorherige Impfungen: -

VAERS 2220285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Aphthous ulcer Coating in mouth Condition aggravated Dizziness Feeling abnormal Fibrin D dimer normal Flank pain Glossodynia Headache Hemiparesis Hypoaesthesia Impaired work ability Injection site pain Lymph node pain Lymphadenopathy Mastication disorder Mobility decreased Mouth haemorrhage

Symptomtext

History of adverse reaction to COVID vaccine December 16, 2021 - 1st dose of Pfizer vaccine in left arm. Felt tingling and pins and needles in face and extremities, left arm soreness. These symptoms continue for a three-week period. This seems odd that the symptoms are lasting longer than a few days. January 6, 2022 ? 2nd dose of Pfizer The day after the second dose, I am unable to move for a day. I feel like I have a huge hangover. I have a headache, I am sore, I cannot move, flat on my back. I missed work on that Friday. I feel tingling and pins and needles in face and extremities. The left arm is very sore at the injection site. Left lymph node started feeling ?full? or swollen. Intermittent tingling and prickly feeling on face and extremities over the next 2 months. It feels like something is circulation through the body, and my body does not like it. However, the tingling remains in the background. March 10, 2022 - I saw NP for annual checkup, complained of fullness in lymph nodes, especially left lymph node. March 11, 2022 On this day, I felt my left lymph node release, meaning that it felt less full all of a sudden. It felt like something drained out of it. March 12, 2022 - I started feeling lymph nodes in my neck getting activated and swollen. It kind of felt like I was getting a common cold. Weirdly, however, I started getting tons of mouth sores. But at first, it felt like a piece of food was stuck in my teeth way in the back of mouth, or like I had burned myself on hot food and a piece of skin was loose. However, within a couple days, this feeling gave way to an explosion of painful canker sores. The tongue started bleed. The tongue was covered with painful, tingling sores. There were red, bloody blotches on my tongue and all over the inside of my mouth. Most of my tongue turned white. However, there were some red blotches. (This looked like covid tongue on the internet). The sores in the back of my mouth were white. I could not chew or brush my teeth, as it was too painful. I had to eat mushed up food for one week. It was painful to smile. The lymph nodes under my neck were swollen and sensitive to the touch. It was difficult to drink water because it was uncomfortable and painful to swallow fluid. My mouth was extremely sensitive to almost every flavor except the most bland food, like rice or water. For example, I could not drink orange juice as it was too painful. I had hives on my extremities (red dots on my hands, feet, arms, legs, feet). I had to eat only soft foods and try to mush the food with my tongue, as anything with sharp edges caused too much pain against the inflamed gums. March 14, 2022 - I get tested for COVID, thinking that maybe I have a new variant. March 15, 2022 ? I received a negative COVID test. I try to make an appointment for March 16 but the next appointment is March 17. March 17, 2022 ? I see drs. I start the steroid taper and do the hydrogen peroxide mouth rinse. Within 5 days, I feel a lot better. I can eat again without much pain. The inflammation in the mouth subsides greatly. However, the lymph nodes in my neck still feel full, activated and slightly swollen. I do not feel like the healing crisis is over but the extreme mouth sores are healing up. March 24, 2022 ? I am given the results of the D-Dimer test, they are negative March 24, 2022 to April 5, 2022 ? My tongue starts tingling again; face and extremities start tingling. Left arm feels sore again in the same location as the shot, like I just got the shot yesterday. Left lymph node starts feeling full again. Now the right under arm lymph node feels activated, whereas before there was nothing wrong there. Now both right and left under arm lymph nodes now feel occasionally sore. Not painful to the touch or sharp pain, but more of a dull fullness or sometimes a more acute internal ?pulling? or pinching sensation or fullness. There was also a swollen "pocket" or grape-like protuberance on the inside of my mouth on the inside of the "goatee area" of the chin (under the bottom lip). There was a painful swelling on the inside of the mouth that seemed to get worse on this second wave. By April 5, 2022, the mouth has healed up significantly since I made the appointment last approximately Wednesday, March 30. NP was not available until April 6, 2022, so I am not sure what she is going to find during my appointment on April 6, 2022. I started to use the BEMER light on my mouth starting on April 3, 2022, which I think contributed significantly to the healing process of the mouth sores. I have started doing hot yoga at home in order to detox, and I also try to bike a few times a week in order to increase lymph circulation. April 6, 2022 I saw NP, (who is my regular GP), at Medical Center April 7, 2022 At the time of this report, the mouth ulcers are pretty much healed up, but I have been now experiencing dizziness and vertigo, and a general weakness in the right side of my body, there is a very faint numbness of the right half of the head area, including the face. The right arm feels weaker and "deader." There is also the continued "activated" or pinching or pulling feeling in both lymph nodes underneath the armpits on right and left side. The swollen lymph nodes in the neck seem to have gone down a little bit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: March 15, 2022 negative COVID test results received March 17, 2022 doctor's visit to Medical Center March 17, 2022 VAERS report made by patient (self report) March 24, 2022 negative D-Dimer test results received April 6, 2022 doctor's visit to Medical Center
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 2220285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Aphthous ulcer Coating in mouth Condition aggravated Dizziness Feeling abnormal Fibrin D dimer normal Flank pain Glossodynia Headache Hemiparesis Hypoaesthesia Impaired work ability Injection site pain Lymph node pain Lymphadenopathy Mastication disorder Mobility decreased Mouth haemorrhage

Symptomtext

History of adverse reaction to COVID vaccine December 16, 2021 - 1st dose of Pfizer vaccine in left arm. Felt tingling and pins and needles in face and extremities, left arm soreness. These symptoms continue for a three-week period. This seems odd that the symptoms are lasting longer than a few days. January 6, 2022 ? 2nd dose of Pfizer The day after the second dose, I am unable to move for a day. I feel like I have a huge hangover. I have a headache, I am sore, I cannot move, flat on my back. I missed work on that Friday. I feel tingling and pins and needles in face and extremities. The left arm is very sore at the injection site. Left lymph node started feeling ?full? or swollen. Intermittent tingling and prickly feeling on face and extremities over the next 2 months. It feels like something is circulation through the body, and my body does not like it. However, the tingling remains in the background. March 10, 2022 - I saw NP for annual checkup, complained of fullness in lymph nodes, especially left lymph node. March 11, 2022 On this day, I felt my left lymph node release, meaning that it felt less full all of a sudden. It felt like something drained out of it. March 12, 2022 - I started feeling lymph nodes in my neck getting activated and swollen. It kind of felt like I was getting a common cold. Weirdly, however, I started getting tons of mouth sores. But at first, it felt like a piece of food was stuck in my teeth way in the back of mouth, or like I had burned myself on hot food and a piece of skin was loose. However, within a couple days, this feeling gave way to an explosion of painful canker sores. The tongue started bleed. The tongue was covered with painful, tingling sores. There were red, bloody blotches on my tongue and all over the inside of my mouth. Most of my tongue turned white. However, there were some red blotches. (This looked like covid tongue on the internet). The sores in the back of my mouth were white. I could not chew or brush my teeth, as it was too painful. I had to eat mushed up food for one week. It was painful to smile. The lymph nodes under my neck were swollen and sensitive to the touch. It was difficult to drink water because it was uncomfortable and painful to swallow fluid. My mouth was extremely sensitive to almost every flavor except the most bland food, like rice or water. For example, I could not drink orange juice as it was too painful. I had hives on my extremities (red dots on my hands, feet, arms, legs, feet). I had to eat only soft foods and try to mush the food with my tongue, as anything with sharp edges caused too much pain against the inflamed gums. March 14, 2022 - I get tested for COVID, thinking that maybe I have a new variant. March 15, 2022 ? I received a negative COVID test. I try to make an appointment for March 16 but the next appointment is March 17. March 17, 2022 ? I see drs. I start the steroid taper and do the hydrogen peroxide mouth rinse. Within 5 days, I feel a lot better. I can eat again without much pain. The inflammation in the mouth subsides greatly. However, the lymph nodes in my neck still feel full, activated and slightly swollen. I do not feel like the healing crisis is over but the extreme mouth sores are healing up. March 24, 2022 ? I am given the results of the D-Dimer test, they are negative March 24, 2022 to April 5, 2022 ? My tongue starts tingling again; face and extremities start tingling. Left arm feels sore again in the same location as the shot, like I just got the shot yesterday. Left lymph node starts feeling full again. Now the right under arm lymph node feels activated, whereas before there was nothing wrong there. Now both right and left under arm lymph nodes now feel occasionally sore. Not painful to the touch or sharp pain, but more of a dull fullness or sometimes a more acute internal ?pulling? or pinching sensation or fullness. There was also a swollen "pocket" or grape-like protuberance on the inside of my mouth on the inside of the "goatee area" of the chin (under the bottom lip). There was a painful swelling on the inside of the mouth that seemed to get worse on this second wave. By April 5, 2022, the mouth has healed up significantly since I made the appointment last approximately Wednesday, March 30. NP was not available until April 6, 2022, so I am not sure what she is going to find during my appointment on April 6, 2022. I started to use the BEMER light on my mouth starting on April 3, 2022, which I think contributed significantly to the healing process of the mouth sores. I have started doing hot yoga at home in order to detox, and I also try to bike a few times a week in order to increase lymph circulation. April 6, 2022 I saw NP, (who is my regular GP), at Medical Center April 7, 2022 At the time of this report, the mouth ulcers are pretty much healed up, but I have been now experiencing dizziness and vertigo, and a general weakness in the right side of my body, there is a very faint numbness of the right half of the head area, including the face. The right arm feels weaker and "deader." There is also the continued "activated" or pinching or pulling feeling in both lymph nodes underneath the armpits on right and left side. The swollen lymph nodes in the neck seem to have gone down a little bit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: March 15, 2022 negative COVID test results received March 17, 2022 doctor's visit to Medical Center March 17, 2022 VAERS report made by patient (self report) March 24, 2022 negative D-Dimer test results received April 6, 2022 doctor's visit to Medical Center
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 2218147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 67,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 06.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Blood test abnormal Condition aggravated Electrocardiogram ambulatory abnormal Herpes simplex Hypersensitivity Supraventricular extrasystoles Urticaria

Symptomtext

Total body hives for 3 months treated with topical and oral steroids and oral antihistamines. Severe nasal allergy symptoms treated with antihistamines. X 3 months. New onset herpes simplex type1 treated with oral Valtrex. Severe PACs treated with Atenolol and Xanax symptoms remain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Holster monitor for PACs. 1/21/2022. Blood tests for herpes 2/21/2022
Aktuelle Erkrankungen: None
Vorgeschichte: PSVT, PACs, hypothyroidism, seasonal allergies, Eczema, insomnia, high cholesterol, chronic back and hip pain, diverticulitis , chronic dry eyes
Andere Medikamente: Atenolol, Synthroid, Lipitor, Xyzal, Temazepam, Lorazepam, Mobic, Probiotics, Vitamin D, Vitamin E, Turmeric, Calcium, Biotin, Estrace cream
Allergien: Metamucil, Cats, Bees, latex, Doxycycline, Sulfa
Vorherige Impfungen: -

VAERS 2213353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: PA
Alter: 63,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Chest discomfort Chills Fatigue Headache Malaise Mobility decreased Pyrexia

Symptomtext

approximately 8 hrs. later experienced chills and low fever again. joint pain.uncomfortable feeling in upper chest. worn out and felt as if i were hit by truck. next day bad headache only relieved by migraine medicine. in bed again. took 3 days to recover.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: migraine
Andere Medikamente: effexor, ativan
Allergien: none
Vorherige Impfungen: 1st pfizer covid dose on 03/06/2021,age 62 chills,fever,achey,headache, 2nd pfizer 03/27/2021 age 62 dizzy after 15 mins. same

VAERS 2209310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IL
Alter: 83,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 01.05.1938
Beginn: 27.03.2022
Tage bis Beginn: 30.646,0
Dosis: 3
Route/Site: SYR / -

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

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

Symptomtext

Patient admitted to hospital 3/28/22 with SOB and cough. Some diarrhea is reported but no chest pain, vomiting, fever or chills.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: SARS COV2 COVID19 NAAT positive 3/27/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2206492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 29.03.2021
Beginn: 16.07.2021
Tage bis Beginn: 109,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac flutter Chest pain Echocardiogram abnormal Electrocardiogram abnormal Heart valve incompetence Immediate post-injection reaction Sinus arrhythmia

Symptomtext

I immediately had heart flutters after receiving each vaccine. Administrator of vaccine stated it might be nerves but I was not nervous. I had chest pains intermittently and sought care at an urgent care facility in July 2021. EKG showed sinus arrhythmia. CHest pains continued and saw a Cardiologist in December 2021. Echocardiogram showed a leaky tricuspid valve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG-July 2021 EKG -December 2021 Echocardiogram-January 2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Omeprazole, Vitamin D and Tylenol PM
Allergien: Penicillin and CLindamycin
Vorherige Impfungen: -

VAERS 2204984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 22.10.2021
Beginn: 10.01.2022
Tage bis Beginn: 80,0
Dosis: 3
Route/Site: SYR / -

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

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

Symptomtext

I had a sore throat, slight fever, fatigue on 01/10/22. I took rapid and PCR lab test on 01/11/22. Both came back negative. I had fatigue, a fever, sore throat and started coughing on 01/15. I lost my voice and had trouble breathing. I tested positive for Covid 19 on 01/21/22. I continued coughing and had trouble breathing through 02/19/22. I was only worked two 8 hour shifts from 01/11 through 02/19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Negative rapid and lab Covid test 01/11/22. Positive rapid Covid test 01/21/22 and PCR lab test on 01/24/22.
Aktuelle Erkrankungen: None
Vorgeschichte: Degenerative disk disease. Arthritis in both knees. Waiting for knee replacement on right knee
Andere Medikamente: Nexium, Prevacid, iron, tumeric, zinc, dicyclomine, duloxtine, Norco, propanol, one a Day multi-vitamin and Vitamin D
Allergien: Codine and Nsaids
Vorherige Impfungen: -

VAERS 2204226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 20.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Echocardiogram Influenza virus test positive Parainfluenzae virus infection Pneumonia Respiratory viral panel

Symptomtext

Pneumonia of both lungs due to infectious organism. She was admitted inpatient, empirically treated with IV antibiotics for pneumonia, respiratory panel returned positive for parainfluenza. Repeat echocardiogram was done, results as above. She was weaned off supplemental oxygen. Discharged home. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2194390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 30.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Dyspnoea Nasopharyngitis Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had running nose, sore throat, and SOB. It was like a mild cold. These lasted for about 10 days. On Jan 5th, I tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood; Asthma; Gait; GERD
Andere Medikamente: N/A
Allergien: Hydrocodone
Vorherige Impfungen: -

VAERS 2193872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TN
Alter: 78,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Discomfort Insomnia Limb discomfort Mobility decreased Pain in extremity Product administered at inappropriate site

Symptomtext

I have discomfort; Difficult to sleep on affected arm; Difficult to sleep on affected arm; Pain; limited mobility; the dose was administered to his tendon and not to his muscle; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 78 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 18Oct2021 13:00 (Lot number: FH8020) at the age of 78 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Barrett's esophagus" (unspecified if ongoing); "Cardio respiratory issues Senior citizen" (unspecified if ongoing); "Cardio respiratory issues Senior citizen" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose number: 1, Date/Time: 20Mar2021, Time : 10:00 AM, Anatomical site of injection : Right Arm, Route of administration : Intramuscular, Batch/Lot number : ER8727), administration date: 20Mar2021, when the patient was 77 years old, for COVID-19 immunization; Bnt162b2 (Dose number: 2, Date/Time: 10Apr2021, Time : 10 AM, Anatomical site of injection : Right Arm , Route of administration : Intramuscular, Batch/Lot number : ER0151), administration date: 10Apr2021, when the patient was 77 years old, for COVID-19 immunization. The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 18Oct2021, outcome "unknown", described as "the dose was administered to his tendon and not to his muscle"; DISCOMFORT (non-serious), outcome "unknown", described as "I have discomfort"; LIMB DISCOMFORT (non-serious), INSOMNIA (non-serious), outcome "unknown" and all described as "Difficult to sleep on affected arm"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Pain"; MOBILITY DECREASED (non-serious), outcome "unknown", described as "limited mobility". Additional information: Caller received his Comirnaty booster and the dose was administered to his tendon and not to his muscle. Caller asked if this interfered with the uptake of the vaccine, if he needs to get another dose, or what the effect of this administration is. Patient was not very happy. He always respected Pfizer but this is definitely not one of the respectful things that they've done so he was gonna hang up now as it seemed to him that's an irresponsibility on Pfizer's part. Patient won't be taking the survey. In Oct, he went to a branch of the local Health Department for his booster, which was put the in his tendon, not the muscle. He had discomfort and he was seeing a physical therapist. As a senior with pulmonary and cardio issues, will there be follow on injections. This report was not related to a study or programme. No investigation assessment. Reporter states he had no problems with the first two shots. He got his booster shot at the health department and the stupid nurse put it into his tendon and not his muscle. Caller states that he attempted to go online, but it referred him to call this number. Caller states that calling has been frustrating because he just wants a fast answer and has had to go through all of these options. Caller verifies that he was speaking about the booster dose of the Pfizer Covid Vaccine. Caller states that he has been doing physical therapy for was arm. Says it was very difficult to sleep on the affected arm. Caller states that he has Barrett's esophagus and needs to sleep on his left side. States he tosses and turns a lot. At physical therapy they worked the mobility around well. States he does exercises at home. Caller says that his physical therapist was not satisfied with their progress and instructed the caller to keep working it at home. Caller says that he saw online there was a syndrome related to people who get injections wrong and 15 percent respond to follow up treatment. Caller states he was hoping to be in the 15 percent. Caller denies any other labs, testing, or treatments relevant to these events. Vaccination Facility Type was Public Health clinic/Veterans administration facility. No Prior vaccinations (within 4 weeks) were given. Health Department nurse administered the covid Booster into a tendon in the right arm. This necessitated the services of a physical therapist at results physiotherapy for several weeks. Pain and limited mobility were addressed. He was to return for further treatment if necessary. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Barrett's esophagus; Cardiac disorder NOS; Respiratory disorder NOS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2192251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 71,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 29.10.2021
Beginn: 15.12.2021
Tage bis Beginn: 47,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test COVID-19 Cough Dyspnoea Headache Hypertension Influenza virus test Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

I had body ache, coughing, SOB, congestive, headache, and running nose. These symptoms lasted for over a month. I contacted my doctor on Dec 27th. They did a COVID-19 and Flu test. I tested positive for COVID-19 on Dec 30th. I still was having SOB and high blood pressure. I went back to my doctor on Jan 17th. They did blood work and another COVID-19 tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test, Flu test, Blood work
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic stomach issue, heart mummer
Andere Medikamente: Takes a lots of medicine
Allergien: Shell fish
Vorherige Impfungen: Flu and Pneumonia

VAERS 2187751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 22.10.2021
Beginn: 10.02.2022
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Fatigue Feeling abnormal Mobility decreased Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

I had severe sore throat, stuffy nose, running nose, and very tired. I was in bed for about 6 day. I also had brain fog. The fatigue and sore throat was my biggest issue. These lasted for about 7 or 8 days. On Feb 13th, I tested positive for COVID-19. I went to urgent care, they also tested me for Strep, negative results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: COVID-19 test; Strep test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin
Allergien: White fish; Detergent
Vorherige Impfungen: -

VAERS 2184376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: LA
Alter: 56,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Fatigue Headache Mobility decreased Muscular weakness Myalgia Pyrexia

Symptomtext

Extreme fatigue accompanied by chest heaviness, severe muscle aches/ weakness , frontal headache and low grade fever( 99.7) I am normally very active with a BMI of 21.5. I spent the day in bed and at one point had to sit on the bathroom floor because I had a feeling of chest heaviness that felt as if I was going to stop breathing. I am an RN and kept telling myself this is just the vaccine side effects and did not want to embarrass myself by going to the ER. I think if I were a layperson I may have gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension Papillary thyroid cancer with (R) thyroid lobectomy and parathyroid removal secondary to adenoma ( 2018)
Andere Medikamente: levothyroxine 50mcg amlodipine 5 mg vitamin D fish oil
Allergien: doxycycline (hives) lisinopril (cough)
Vorherige Impfungen: -

VAERS 2184333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 06.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Aphthous ulcer Blood test Condition aggravated Dental discomfort Hypersensitivity Immediate post-injection reaction Insomnia Lymphadenopathy Malaise Mastication disorder Mouth ulceration Odynophagia Oropharyngeal pain Pain in extremity Paraesthesia Paraesthesia oral SARS-CoV-2 test negative Stomatitis

Symptomtext

Dose 1 (12/16/21): within a couple days of Dose 1, I experienced tingling in extremities, pins and needles feeling at various random places in body (including bottom of feet, hands, lips, face); left arm soreness; left lymphnode under arm felt "full" and sensitive to the touch (although it was not distended to the point of being noticeable) Does 2 (1/6/22): immediately after Dose 2, I was unable to move for 1 day. I missed work and stayed in bed with the following symptoms ("hangover" like symptoms: headache, flu like feeling, severe fatigue, lethargy). This acute flu-like feeling passed after a couple days. Immediately after Dose 2, my left arm was even sorer than after Dose 1. My left lymphnode felt "full" and like it was holding fluid. From 1/6/22 until March 10, I experienced sporadic tingling and prickling in the face, lips, hands, feet, and various other places. On March 10, I had an annual checkup with PA, I complained of swelling in the left lymphnode. She palpated the left lymphnode but did not notice that it was distended. However, I complained that it felt "full." On March 12, a severe allergic reaction happened. The left lymphode suddenly seemed to "release" because it felt less full. At the same time, the lymphnodes under my chin started to get swollen. I kind of felt like I was getting "sick" with a cold. I felt something in the back of my right back-most tooth. It felt like something was lodged in my teeth. I flossed well and brushed it, but it wasn't anything stuck. That back tooth area was the first mouth ulcer to form. Over the next few days, my mouth became full of white mouth sores. My tongue became white, with patchy red spots on the top and sides. My mouth burst with canker sores of various nasty colors and sizes. It was extremely painful to chew. I had to mash up my food because I could not put any pressure on my gums. I looked up some symptoms online and found that "Covid tongue" exactly captured what was happening. I wondered if I had Covid., but I got tested and I did not have Covid. My throat is sore especially on the left side. It is painful to swallow. I have been taking aspirin in order to sleep. On 3/17/22 I saw Dr. He said it looked like an allergic reaction, gave me steriod script, said to gargle with water and hydrogen peroxide, gave me a blood lab to rule out clotting issue, Dr said I would be able to be exempt from future requirements because the symptoms were correlated with the vaccine He said not to take the booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 3/15/22 negative covid test,
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2184333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 17.03.2022
Impfdatum: 06.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Aphthous ulcer Blood test Condition aggravated Dental discomfort Hypersensitivity Immediate post-injection reaction Insomnia Lymphadenopathy Malaise Mastication disorder Mouth ulceration Odynophagia Oropharyngeal pain Pain in extremity Paraesthesia Paraesthesia oral SARS-CoV-2 test negative Stomatitis

Symptomtext

Dose 1 (12/16/21): within a couple days of Dose 1, I experienced tingling in extremities, pins and needles feeling at various random places in body (including bottom of feet, hands, lips, face); left arm soreness; left lymphnode under arm felt "full" and sensitive to the touch (although it was not distended to the point of being noticeable) Does 2 (1/6/22): immediately after Dose 2, I was unable to move for 1 day. I missed work and stayed in bed with the following symptoms ("hangover" like symptoms: headache, flu like feeling, severe fatigue, lethargy). This acute flu-like feeling passed after a couple days. Immediately after Dose 2, my left arm was even sorer than after Dose 1. My left lymphnode felt "full" and like it was holding fluid. From 1/6/22 until March 10, I experienced sporadic tingling and prickling in the face, lips, hands, feet, and various other places. On March 10, I had an annual checkup with PA, I complained of swelling in the left lymphnode. She palpated the left lymphnode but did not notice that it was distended. However, I complained that it felt "full." On March 12, a severe allergic reaction happened. The left lymphode suddenly seemed to "release" because it felt less full. At the same time, the lymphnodes under my chin started to get swollen. I kind of felt like I was getting "sick" with a cold. I felt something in the back of my right back-most tooth. It felt like something was lodged in my teeth. I flossed well and brushed it, but it wasn't anything stuck. That back tooth area was the first mouth ulcer to form. Over the next few days, my mouth became full of white mouth sores. My tongue became white, with patchy red spots on the top and sides. My mouth burst with canker sores of various nasty colors and sizes. It was extremely painful to chew. I had to mash up my food because I could not put any pressure on my gums. I looked up some symptoms online and found that "Covid tongue" exactly captured what was happening. I wondered if I had Covid., but I got tested and I did not have Covid. My throat is sore especially on the left side. It is painful to swallow. I have been taking aspirin in order to sleep. On 3/17/22 I saw Dr. He said it looked like an allergic reaction, gave me steriod script, said to gargle with water and hydrogen peroxide, gave me a blood lab to rule out clotting issue, Dr said I would be able to be exempt from future requirements because the symptoms were correlated with the vaccine He said not to take the booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 3/15/22 negative covid test,
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2183766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 02.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

numbness and tingling in both arms n hands, entire arms fall asleep; numbness and tingling in both arms n hands, entire arms fall asleep; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 02Nov2021 17:30 (Lot number: FH8020) at the age of 39 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Ulcerative Colitis" (unspecified if ongoing); "Covid-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?:Yes. Concomitant medication(s) included: LIADIA; VYVANSE. The following information was reported: HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious) all with onset 05Nov2021, outcome "unknown" and all described as "numbness and tingling in both arms n hands, entire arms fall asleep". Additional information: The patient received second dose of BNT162B2 (lot number: 33025BD) via unspecified route on 04Jan2022 18:30 on arm right for covid-19 immunization. Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. On 02Nov received 1st of Pfizer, 3 days following patient had numbness and tingling in both arms and hands, entire arms fell asleep and currently waiting to see a neurologist. The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. Just received 2nd dose of Pfizer on 04Jan2022 and day 6 she was having chest tightness, shortness of breath, rapid heartbeat. Waiting to see a doctor today 11Jan2022. Currently waiting for treatment. Since the vaccination, the patient had not been tested for COVID-19. Known allergies: Not that patient was aware of. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes); Ulcerative colitis.
Andere Medikamente: LIADIA; VYVANSE.
Allergien: -
Vorherige Impfungen: -

VAERS 2181641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / RA

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

Blood pressure measurement Blood test Burning sensation Condition aggravated Cyst Mammogram Melanocytic naevus Skin irritation

Symptomtext

A mole/cyst like thing underneath the skin of her left breast, and after receiving the vaccine it doubled and became marble like size.; A mole/cyst like thing underneath the skin of her left breast, and after receiving the vaccine it doubled and became marble like size.; A mole/cyst like thing underneath the skin of her left breast, and after receiving the vaccine it doubled and became marble like size.; Cyst was burning; Irritation; 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 54 year-old female patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 08Nov2021 11:35 (Lot number: FH8020) at the age of 55 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Diabetes" (ongoing), notes: Diabetes is really high and they keep switching her diabetes medication.; "Hypertension" (ongoing), notes: In 2009 or 2010, numbers are usually 136/85-90. If does not take medication or stress it goes up.; "Hypothyroidism" (ongoing); "Hyperthyroidism" (ongoing); "Cyst" (ongoing), notes: Cyst has been present for well over a year prior to receiving her COVID-19 vaccine; "Hysterectomy", start date: 2018 (unspecified if ongoing), notes: Had uterus, cervix, right ovary and tubes that go with it removed. She still has her left ovary. Concomitant medication(s) included: LEVOTHYROXINE taken for thyroid disorder, hyperthyroidism, hypothyroidism, start date: 2001 (ongoing); ALOGLIPTIN taken for diabetes mellitus, start date: 2021 (ongoing); GLIMEPIRIDE taken for diabetes mellitus (ongoing); BASAGLAR taken for diabetes mellitus, start date: Sep2021 (ongoing); JANUVIA. Past drug history included: Metformin for Diabetes, reaction(s): "Itching", notes: Reports having to stop Metformin due to itching and red boils on skin sometime around 2009 or 2010.; Metformin for Diabetes, reaction(s): "Red boils on skin", notes: Reports having to stop Metformin due to itching and red boils on skin sometime around 2009 or 2010. Vaccination history included: Flu vaccine (Unsure but 3 weeks prior to COVID-19 vaccine), for Immunization. The following information was reported: CYST (non-serious), MELANOCYTIC NAEVUS (non-serious), CONDITION AGGRAVATED (non-serious) all with onset 09Nov2021, outcome "not recovered" and all described as "A mole/cyst like thing underneath the skin of her left breast, and after receiving the vaccine it doubled and became marble like size."; BURNING SENSATION (non-serious) with onset 09Nov2021, outcome "unknown", described as "Cyst was burning"; SKIN IRRITATION (non-serious) with onset 09Nov2021, outcome "unknown", described as "Irritation". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient was diagnosed with hypertension in 2009 or 2010. Numbers were usually 136/85-90. If did not take medication or stress it went up. The patient did not have any family medical history relevant to adverse events. The patient was taking Levothyroxine because her thyroid was taken out in 2001. Took thyroid out and replacement for thyroid. She was hyperthyroid, now she was hypothyroid. She was getting older so dose went up. After she had her thyroid taken out she started at 5mcg. The patient was taking Januvia but then was switched to alogliptin. She was no longer taking Januvia. It was not working very well and she did remember why they stopped this medication. The patient was taking 20 units of Basaglar at night but after bloodwork dose was switched. She still had her left ovary. She was informed needed one ovary for calcium. No additional vaccines were administered on same date of the Pfizer suspect. The patient received her first dose of the COVID-19 vaccine and was going to get her second dose of the COVID-19 vaccine. The patient stated that she had a cyst on her skin after taking her first COVID-19 vaccine and now wanted to know if this had something to do with the vaccine and if she should get her second dose. The cyst was under her skin and was the size of a mole and then the day after receiving her COVID-19 vaccine, 09Nov2021, she noticed irritation in that area and that the cyst was burning and was then the size of a marble, it had gotten bigger. Cyst on skin size of mole and now the size of a marble. It started with a little burning. She started touching it. The cyst was very small then like a mole. The cyst was on the base of her right breast. It had been recommended that she should see a dermatologist but she had not seen one yet. The cyst didn't grow outside. It grew inside and under the skin. Something fed it and it got big. The patient initially stated that she noticed this the following day. Also mentioned, within 10 days it was big like a marble. She did not know if she may be allergic to the COVID-19 vaccine because of this. The caller wanted to know if since the cyst got larger, whether she should she get the second vaccine. She asked if the cyst was a concern; she didn't get her second vaccination on the 29th because of the cyst on her skin and had not yet seen a recommended dermatologist. The adverse events did not require a visit to Emergency Room or Physician Office. No relevant tests were done. There was a Product complaint. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:136/85-90; Comments: Hypertension; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown results; Test Date: 202110; Test Name: Mammogram; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: Cyst (Cyst has been present for well over a year prior to receiving her COVID-19 vaccine); Diabetes (Diabetes is really high and they keep switching her diabetes medication.); Hypertension (In 2009 or 2010, numbers are usually 136/85-90. If does not take medication or stress it goes up.); Hyperthyroidism; Hypothyroidism
Vorgeschichte: Medical History/Concurrent Conditions: Hysterectomy (Had uterus, cervix, right ovary and tubes that go with it removed. She still has her left ovary.)
Andere Medikamente: LEVOTHYROXINE; ALOGLIPTIN; GLIMEPIRIDE; BASAGLAR; JANUVIA
Allergien: -
Vorherige Impfungen: -

VAERS 2176260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Loss of personal independence in daily activities Pain

Symptomtext

Been in pain ever since receiving booster dose vaccine; The patient can hardly use her arm; the booster dose Pfizer Vaccine but the pain has gotten worse.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Oct2021 (Lot number: FH8020) at the age of 48 years as dose 3 (booster), single for covid-19 immunisation; methoxy polyethylene glycol-epoetin beta (MIRCERA), administered in arm right, administration date 18Oct2021 (Lot number: X405R, Expiration Date: Mar2024) as unk unk, single. Relevant medical history included: "Dialysis", start date: 2019 (ongoing), notes: Verbatim: Dialysis (Patient began dialysis two years ago, peridenal). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 2nd, Lot: PF1725, Route of administration: Right arm), administration date: 06Feb2021, when the patient was 48 years old, for Covid-19 immunization; Bnt162b2 (Dose: 1st, Lot: EL1284, Route of administration: Right arm), administration date: 16Jan2021, when the patient was 48 years old, for Covid-19 immunization. The following information was reported: PAIN (non-serious) with onset 18Oct2021, outcome "not recovered", described as "Been in pain ever since receiving booster dose vaccine"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 2021, outcome "unknown", described as "The patient can hardly use her arm"; CONDITION AGGRAVATED (non-serious) with onset 2021, outcome "unknown", described as "the booster dose Pfizer Vaccine but the pain has gotten worse.". Therapeutic measures were taken as a result of pain. Additional information: After receiving booster dose patient had localized pain and it got worsen and she was taking Tylenol (lot: SDA002) and that helped her shorter period of time and also put salonpas patch (lot: X5087, expiration: APR-2024) on and a heating pad, patient received micera vaccine on right side as same day of booster dose to do with blood for anemia. The patient doesn't visit emergency room. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Dialysis (Verbatim: Dialysis (Patient began dialysis two years ago, peridenal))
Vorgeschichte: -
Andere Medikamente: MIRCERA
Allergien: -
Vorherige Impfungen: -

VAERS 2170767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 10.03.2022
Impfdatum: 22.10.2021
Beginn: 04.03.2022
Tage bis Beginn: 133,0
Dosis: 3
Route/Site: OT / OT

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

Dyspnoea

Symptomtext

shortness of breath

Weitere VAERSDATA-Felder

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

VAERS 2162750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: PA
Alter: 52,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Blood pressure increased Cardiac disorder Cardiac stress test Electrocardiogram Palpitations

Symptomtext

Heart palpitations, blood pressure elevated at random times heart issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG stress test
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, heart stent
Andere Medikamente: Metformin plavix metropolol
Allergien: -
Vorherige Impfungen: -

VAERS 2150815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 19.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Dizziness Fall Memory impairment Paraesthesia X-ray

Symptomtext

fell twice; Caller states she is getting forgetful right now; Tingling; she is currently dizzy, and feels "dizzy to the left."; 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 70 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Oct2021 (Lot number: FH8020) at the age of 70 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing); "Verbatim: allergic to every grass tree or weed she could be allergic to" (unspecified if ongoing). Concomitant medication(s) included: SERUM DERIVED BOVINE IMMUNOGLOBULIN/PROTEIN ISOLATE; IGG; FISH OIL. Vaccination history included: Bnt162b2 (Dose 1, LOT: EN6203), administration date: 04Mar2021, when the patient was 70 years old, for COVID-19 immunization, reaction(s): "neuropathy", "had a bad fall twice", "tingling sensations", "had really cold toes and fingers", "had problems with swallowing", "felt dizzy", "feels like she would choke"; Bnt162b2 (Dose 2, LOT: ER8733), administration date: 25Mar2021, when the patient was 70 years old, for COVID-19 immunization, reaction(s): "neuropathy"; Bnt162b2 (Dose 2, LOT: ER8733), administration date: 25Mar2021, when the patient was 70 years old, for Covid-19 immunization, reaction(s): "had a bad fall twice", "tingling sensations", "had really cold toes and fingers", "had problems with swallowing", "felt dizzy", "feels like she would choke"; Flu shot (She has not had a flu shot since last Nov2020), administration date: Nov2020. The following information was reported: DIZZINESS (non-serious) with onset Oct2021, outcome "not recovered", described as "she is currently dizzy, and feels "dizzy to the left.""; PARAESTHESIA (non-serious) with onset 19Oct2021, outcome "unknown", described as "Tingling"; FALL (non-serious), outcome "unknown", described as "fell twice"; MEMORY IMPAIRMENT (non-serious), outcome "unknown", described as "Caller states she is getting forgetful right now". The event "fell twice" was evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of dizziness, paranesthesia, fall, memory impairment. Additional Information: Patient sates that she was slightly dizzy and it sounds weird but, she was only dizzy to the left. When it happened, she felt like her head was swirling. She states it felt weird, and she was having another dizzy moment. As she sat down, she started feeling a little more tingling, like a circulation tingling. She lives by herself, so she has to be cautious. Tingling: She just started experiencing this now and she hadn't thought about it before, but it is in both feet. The right foot is more pronounced. It feels like it is tingling in her face. It feels a little tingly in the right fingers and the left hand, she is holding the phone with so, that might be a distraction. It was not uncomfortable but it is tingling and she can feel it in the chin and tip of the nose. Caller states that the tingling just started during this call, today 19Oct2021. The dizziness kind of faded and she hadn't related it to the vaccine. She had fallen down twice. Patient takes vitamins, fish oil and takes DHA and suggested Turmeric. Caller states that the other ingredient listed underneath immunoglobulin was lactoferrin. No Prior Vaccinations (within 4 weeks). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: X-ray; Result Unstructured Data: Test Result:They did an X-ray and it was not broken; Comments: She did go the first time she fell because she didn't want to break a hip. They did an X-ray and it was not broken
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Grass allergy
Andere Medikamente: SERUM DERIVED BOVINE IMMUNOGLOBULIN/PROTEIN ISOLATE; IGG; FISH OIL
Allergien: -
Vorherige Impfungen: -

VAERS 2147269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 63,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 06.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Condition aggravated SARS-CoV-2 test Vision blurred Visual impairment Vitreous adhesions

Symptomtext

Vision got blurrier; Vitreo Adhesion in right eye got worse (open area in scan doubled - pulled away even further).; my vision went wavy, got a wave to it and it turned out that I had a macular hole/vision in left eye got wavier; when I got the third shot it got much worse; 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 63 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 06Nov2021 (Lot number: FH8020) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Interstitial Cystitis" (unspecified if ongoing); "Irritable Bowel" (unspecified if ongoing); "Fatty Liver" (unspecified if ongoing); "High Cholesterol" (unspecified if ongoing); "Obesity" (unspecified if ongoing); "Neuropathy gums/teeth 13, 14, 15" (unspecified if ongoing); "Osteoarthritis Neck, Back, Knee" (unspecified if ongoing); "Osteoarthritis Neck, Back, Knee" (unspecified if ongoing); "Osteoarthritis Neck, Back, Knee" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing). The patient was allergic to Generic Silod. The patient did not have covid prior vaccination. Concomitant medication(s) included: RAPAFLO; CLONAZEPAM; ADDERALL. The patient did not take any other vaccine in four weeks. Past drug history included: Known allergies: multiple - ssri's, reaction(s): "Allergies: Multiple - SSRI's"; Known allergies: fluoroquinolones, reaction(s): "Allergies: Fluoroquinolones"; Known allergies: elmiron, reaction(s): "Allergies: Elmiron"; Known allergies: lamictal, reaction(s): "Allergies: Lamictal"; Known allergies: uroxytrol, reaction(s): "Allergies: Uroxytrol"; Known allergies: trimetoprim, reaction(s): "Allergies: Trimetoprim". Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot: EN6202 , Anatomical location: left arm, lot number= EN6202, vaccine location=Left arm), administration date: 26Feb2021, when the patient was 62 years old, for Covid-19 Immunization, reaction(s): "my vision went wavy, got a wave to it and it turned out that I had a macular hole", "my vision went wavy, got a wave to it and it turned out that I had a macular hole"; Bnt162b2 (DOSE 2, SINGLE, lot: ER8730, Anatomical location: left arm, lot number=ER8730, vaccine location=Left arm), administration date: 26Mar2021, for Covid-19 Immunization, reaction(s): "my vision went wavy, got a wave to it and it turned out that I had a macular hole", "when It got worse but that's when they discovered that I had a Macular hole". The following information was reported: VISION BLURRED (disability, medically significant), outcome "not recovered", described as "Vision got blurrier"; VITREOUS ADHESIONS (medically significant), outcome "not recovered", described as "Vitreo Adhesion in right eye got worse (open area in scan doubled - pulled away even further)."; VISUAL IMPAIRMENT (medically significant) with onset 2021, outcome "not recovered", described as "my vision went wavy, got a wave to it and it turned out that I had a macular hole/vision in left eye got wavier"; CONDITION AGGRAVATED (medically significant) with onset 2021, outcome "not recovered", described as "when I got the third shot it got much worse". The events "vision got blurrier", "vitreo adhesion in right eye got worse (open area in scan doubled - pulled away even further).", "my vision went wavy, got a wave to it and it turned out that i had a macular hole/vision in left eye got wavier" and "when i got the third shot it got much worse" were evaluated at the physician office visit. She reported like when 'retinol gel pull out' and get stuck, that happened after the second shot, the first and the second shot also then when she got the third shot it got much worse. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (Jan2022) negative, notes: Nasal Swab; (Sep2021) negative, notes: Nasal Swab; (Oct2021) negative, notes: Nasal Swab; (Nov2021) negative, notes: Nasal Swab; (16Dec2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of vision blurred, vitreous adhesions, visual impairment, condition aggravated with vitrectomy left eye and monitoring right eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 202201; Test Name: Antigen - Home Test x2; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202109; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202110; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 202111; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211216; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cystitis interstitial; Fatty liver; High cholesterol; Irritable bowel; Neuropathy; Obesity; Osteoarthritis; Osteoarthritis knee; Osteoarthritis of neck; Sulfonamide allergy
Andere Medikamente: RAPAFLO; CLONAZEPAM; ADDERALL
Allergien: -
Vorherige Impfungen: -

VAERS 2137662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 29.10.2021
Beginn: 28.01.2022
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Dyspnoea Fatigue Feeling abnormal Nasal congestion Respiratory tract congestion SARS-CoV-2 test positive Wheezing

Symptomtext

Coughing, wheezing, difficulty breathing, congestion, stuffiness, fatigue, brain fog

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: PRN Covid + test on February 1, 2022
Aktuelle Erkrankungen: Sinus/allergies
Vorgeschichte: Thyroid disease, hidradenitis supprativa
Andere Medikamente: Armour Thyroid, Cytomel, spironolactone, mulitivitamin, Vitamin D, Magnesium
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2118760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MA
Alter: 29,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 15.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Asthenia Cough Diarrhoea Dyspnoea Feeling abnormal Headache Increased appetite Lethargy Menstruation irregular Nasopharyngitis Respiratory tract congestion SARS-CoV-2 test

Symptomtext

I started my period for the 3rd time in 1 month on 10/22/21; head cold; chest congestion; lethargy; cough; brain fog; headaches; diarrhea; increased appetite; weakness; shortness of breath; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 15Oct2021 16:30 (Lot number: FH8020) at the age of 29 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Chronic Migraine" (unspecified if ongoing); "OCD" (unspecified if ongoing); "PTSD" (unspecified if ongoing). Concomitant medication(s) included: CAMILA taken for contraception; ZOLOFT; ZYRTEC [CETIRIZINE HYDROCHLORIDE]. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FF8841, Location of injection: Arm Left, Vaccine Administration Time: 04:00 PM), administration date: 24Sep2021, for Covid-19 Immunization. The following information was reported: MENSTRUATION IRREGULAR (non-serious) with onset 22Oct2021, outcome "unknown", described as "I started my period for the 3rd time in 1 month on 10/22/21"; NASOPHARYNGITIS (non-serious) with onset Oct2021, outcome "unknown", described as "head cold"; RESPIRATORY TRACT CONGESTION (non-serious) with onset Oct2021, outcome "unknown", described as "chest congestion"; LETHARGY (non-serious) with onset Oct2021, outcome "unknown", described as "lethargy"; COUGH (non-serious) with onset Oct2021, outcome "unknown", described as "cough"; FEELING ABNORMAL (non-serious) with onset Oct2021, outcome "unknown", described as "brain fog"; HEADACHE (non-serious) with onset Oct2021, outcome "unknown", described as "headaches"; DIARRHOEA (non-serious) with onset Oct2021, outcome "unknown", described as "diarrhea"; INCREASED APPETITE (non-serious) with onset Oct2021, outcome "unknown", described as "increased appetite"; ASTHENIA (non-serious) with onset Oct2021, outcome "unknown", described as "weakness"; DYSPNOEA (non-serious) with onset Oct2021, outcome "unknown", described as "shortness of breath". The events "i started my period for the 3rd time in 1 month on 10/22/21", "head cold", "chest congestion", "lethargy", "cough", "brain fog", "headaches", "diarrhea", "increased appetite", "weakness" and "shortness of breath" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. It was unknown if therapeutic measures were taken as a result of menstruation irregular, nasopharyngitis, respiratory tract congestion, lethargy, cough, feeling abnormal, headache, diarrhoea, increased appetite, asthenia, dyspnoea. Additional Information: Facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. Reported Event: Menstruated normally from 23Sep2021- 27Sep2021. But then she had her next period a week later from 07Oct21-13Oct2021 and it was heavier and longer and more physically draining/demanding than ever. She started her period for the 3rd time in 1 month on 22Oct2021. She also had a head cold with head and chest congestion, lethargy, cough, brain fog, headaches, diarrhea, increased appetite, weakness, shortness of breath. This started 3 days after the vaccine. She was tested for Covid on 21Oct2021 and it was Negative. Prior to vaccination, patient was not diagnosed with Covid-19. Since the vaccination, patient has been tested for Covid-19. Patient did not receive any other vaccines within 4 weeks prior to the Covid vaccine. Patient received other medications within 2 weeks of vaccination. No known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211021; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Chronic migraine; Depression; Obsessive-compulsive disorder; Post-traumatic stress disorder
Andere Medikamente: CAMILA; ZOLOFT; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2116875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 78,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 18.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / RA

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

Blood test normal Cardiac stress test normal Computerised tomogram normal Dyspnoea exertional Electrocardiogram normal Laboratory test normal Magnetic resonance imaging normal Urine analysis normal

Symptomtext

Minimal exertion and I had a hard time breathing. I had to correct by sitting down and control my breathing to catch my breath. When I told my doctor he said it will be fine and prescribed Albuterol. Saw a cardiologist and had ECG, Stress test(nuclear), MRI, blood work, uranalysis, ect. Basically the whole gambit and found it all to normal. Still struggle sometimes when exerting myself.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: ECG, Stress Test, MRI, Blood work, Uranalysis, CT Scan, (All come back normal)
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal Allergies, Acute Anaphylaxis, Atopic Dermatitis, PVC's, Childhood asthma(age 14 stopped)
Andere Medikamente: Albuterol, Amiodaron, Benadryl, Tessalon, Claritin D, Clobetasol, Crestor, Budesonide, EpiPen, Fludrocortisone, Fluticasone, Omeprazole, Paroxetine, Singulair, Synthroid, Neuriva
Allergien: Penicillin, Avocados, Melons, Latex
Vorherige Impfungen: -

VAERS 2113099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 01.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: UN / LA

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

Blood thyroid stimulating hormone Cardiac stress test Dyspnoea Electrocardiogram abnormal Full blood count Glycosylated haemoglobin Lipids Low density lipoprotein Palpitations Thyroxine Tri-iodothyronine Ventricular extrasystoles

Symptomtext

A month after getting the shots I started experiencing heart palpitations, heart racing rapidly and shortness of breath around January 9 or 10th of 2022. The shortness of breath had been ongoing before due to lingering effects from covid that I got in January of 2021 but now the heart was racing and palpitating. Saw my family doctor January 11th. She discovered on the stethoscope pvc's were happening and sent me to a cardiologist immediately. Saw Dr. and had a heart monitor for a week, ectocardiogram and stress test. I have pvc's randomly due to the covid shots was the probable cause. I still have the problem currently at random times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CBC, Hemoglobin A1C, Lipid panel with reflex to direct LDL, Stress test, T4 free, TSH, T3, CV Trans-thoracic Electrocardiogram. Seeing PVC's in heart beat 2, pauses, beats 3,4.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Levothyroxine 200 mg
Allergien: Penicillin, Codeine, Latex
Vorherige Impfungen: -

VAERS 2203727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dyspnoea

Symptomtext

Narrative: Pt received 1st dose of COVID-19 VACCINE (Pfizer) on 12/27/21. Within 10 mins, complained of "knot in chest" and some "difficulty breathing." Reported to ED, ECG done and no STEMI. No meds or treatment given, improved on own and discharged home.

Weitere VAERSDATA-Felder

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

VAERS 2088670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 67,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Hypotension

Symptomtext

Morning after booster injection blood pressure was 87/52 (measured with 2 devices) Previously BP was typically measuring 140/70 with medication in months previous - was 87/51 two weeks later Sustained low blood pressure over 2 months - has stabilized in range of 110/63 AM to 125/75 beginning of Feb 2022. Generally consistent measurements show Systolic seems 20 to 30 points lower and Diastolic seems 10 points higher

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: BP measured twice daily with upper arm cuff Omron unit I have two that I use to check against one another if a reading seems out of normal range (wife is RN & supervises)
Aktuelle Erkrankungen: none
Vorgeschichte: High Blood Pressure
Andere Medikamente: hydroCHLOROthiazide 25 MG tab Spironolactone 50 MG AmoLODIpine, AmoLODIpine 10mg Tab Benazepril 40mg Tab Carvedilol 25 MG tab (2x daily rest of Rx are daily) Aspirin 325 MG tab Rosuvastatin 40 MG Tab Potassium Chloride 10 MEQ ER cap Allopu
Allergien: none known
Vorherige Impfungen: -

VAERS 2075802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NM
Alter: 62,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Eyelid infection Feeling abnormal Headache Infection Migraine Photopsia

Symptomtext

Pfizer-BioNTech Dose 3 - 10/21/2021. Lunch time evening 9pm worse migraine, in duration lasted all night into the next day it lingered. Symptoms was low level headache and light show, pounding and brain fog, the day unsure of taking the medication at the onset to cut the intensitive and duration from 4-8 hours, did not get a chance to take the medication and intensitive Symptom in 08/09 symptom get infection in eye lids and right nostril that was infected as secondary issue. Daily masked all day long for a full month. Took care of the migraines with medication, PRN medication that was prescribed by doctor on report. Last year 9 different occasions of the migraine. Same date as booster Vaccination 3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: No test.
Aktuelle Erkrankungen: No
Vorgeschichte: -
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2075593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 10.11.2021
Beginn: 28.01.2022
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Dyspnoea Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

SOB, feeling unwell, , COVID pneumonia, fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: COVID-19 PCR test positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NJ
Alter: 64,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 05.11.2021
Beginn: 30.01.2022
Tage bis Beginn: 86,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 Cough Decreased appetite Dyspnoea Knee arthroplasty SARS-CoV-2 test positive

Symptomtext

64-year-old male with a PMH of DM type 2, HTN HLD who recently underwent a left knee replacement with an Orthopedics office at an outside facility, he subsequently went to rehab and was released 2 days ago but did test positive for COVID-19 prior to his release on 01/24 and presents today with increasing weakness, cough, SOB and poor appetite.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: 01/30/2022 - SARS-CoV-2 Antigen (++)
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, Dyslipidemia, HTN.
Andere Medikamente: DULoxetine (Cymbalta) 60 mg capsule,delayed release(DR/EC) Directions: 1 capsule oral daily (Active) gabapentin 600 mg Tablet Directions: 1 tablet oral three times a day (Active) insulin glargine (Lantus Solostar U-100 Insulin) 100 un
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2075488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IN
Alter: 40,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea exertional Echocardiogram normal Headache Oxygen saturation decreased Rash macular Tachycardia

Symptomtext

The patient stated that on the evening of the day when she received the vaccine she developed a generalized macular, non-pruritic rash. She had no fever or chills. The next day she started experiencing headaches and exertional dyspnea, desaturating into the 80s with minimal exertion. She presented to the ED on December 3 where she was found to have tachycardia and oxygen desaturation with exertion such as standing up (heart rate 140-150, O2 SATS in the 70s). Patient was admitted for observation. The day following admission her symptoms were markedly improved and she was discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: 1,0
Labordaten: Echocardiogram - normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Pulmonary Hypertension, Irritable bowel disease, Migraine, Celiac Disease
Andere Medikamente: Bupropion, Carvedilol, HCTZ, Hyoscyamine, Spironolactone
Allergien: Gluten, Furosemide, Bupivacaine
Vorherige Impfungen: -

VAERS 2075473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 71,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 12.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac stress test abnormal Catheterisation cardiac abnormal Condition aggravated Coronary artery disease Echocardiogram Exercise tolerance decreased Hypertension Paraesthesia

Symptomtext

Several weeks after the Pfizer Covid-19 booster, which was my first Pfizer vaccine as previous shots were Moderna, I experienced two episodes of tingling sensations across my chest when riding my bike, upper back and shoulders. I went to my cardiologist Dr. as reported above, and he conducted a stress test and echo cardiogram. The stress test showed possible blockage so I had a cardio catheter done by Doctor and this was negative for blockage but showed some arterial disease and I was prescribed I rosuvastatin. I renewed riding my bike and these strange symptoms persisted. Review of possible causes points to Thoracic outlet syndrome and I am going to see a neurologist about this. In parallel, following the Pfizer vaccine my hypertension has worsened and my related meds have been elevated. It is possible this vaccine caused these problems!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: Contact my Doctor for cardio test results.
Aktuelle Erkrankungen: Elevated blood pressure
Vorgeschichte: Crohns, hypertension
Andere Medikamente: Telmisartan, amlodipine, balsalazide disodium, Flonase, Cialis
Allergien: Codeine and NSAIDS
Vorherige Impfungen: -

VAERS 2071672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 33,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Anxiety Dizziness Electrocardiogram ambulatory abnormal Fatigue Hypoaesthesia Immediate post-injection reaction Laboratory test Magnetic resonance imaging head normal Palpitations Ventricular extrasystoles

Symptomtext

Within minutes of receiving my booster I became dizzy and felt as I was about to lose consciousness, I also felt heart palpitations. I was not anxious about the shot, as I work for a health system, and this was just another thing I had to do in my busy day. The symptoms were very sudden and intense. I was taken by a nurse for observation. I was able to calm down within minutes. Throughout the day following my booster I felt heart palpitations coming and going. After 4 days I had another episode of feeling as I was about to pass out. I went to the ER and nothing significant was found. I was asked to wear a Holter monitor for 48hours, only benign PVCs were found. A week following the vaccine, I gradually started feeling numbness on the left side of my body, beginning with face, then hand, and leg. I was ordered a brain MRI where nothing abnormal was found. It has been two months after my vaccine, and I still feel numbness on the left side of my body, sometimes more intense, sometimes less. Occasionally I feel dizziness, however not as intense as directly after the vaccine. I feel fatigued and anxious. Anxiety is directly related to the intensity of my symptoms. As of right now, there is no plan of action to my symptoms. Physicians who were able to see me, believe these are side effects of the vaccine which with time they hope will resolve. I am concerned as it has been two months and still having significant intensity of numbness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Brain MRI, Holter Monitor, A number of lab tests in the ER
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2071074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OR
Alter: 60,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 26.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

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

Arrhythmia Electrocardiogram abnormal Palpitations

Symptomtext

Heart palpitations, irregular heart rhythm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Abnormal EKG at physicians office
Aktuelle Erkrankungen: None
Vorgeschichte: Crohn's Dx
Andere Medikamente: mesalamine, vitamin D 2000 IU, vitamin B12
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2228008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 35,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Depression Dyspnoea Electrocardiogram normal

Symptomtext

RespDepression chest tightness Narrative: Pt received 1st dose of COVID-19 vaccine (Pfizer) on 12/27/21, WIthin 10 mins, complained of "know in chest" and some "difficulty breathing." Reported to ED, ECG done and no STEMI. No meds or treatment given, improved on own and discharged home.

Weitere VAERSDATA-Felder

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

VAERS 2068727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: AZ
Alter: 52,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 09.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 53,0
Dosis: 3
Route/Site: IM / RA

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

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

Symptomtext

1/1/2022 Sore throat, cough, short of breath, fever of 101.7? On 01/04 called my doctor and he called in a prednisone pack. And as a (Privacy), I knew I had to Tylenol and Motrin, Cold medicines (Mucinex day and night), Zinc. I got a Covid PCR on 01/05 and it came back positive on the 01/06. Recovery from this took until 1/10 and I am fully recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/05 Covid PCR (positive)
Aktuelle Erkrankungen: None
Vorgeschichte: Environmental and Seasonal Allergies
Andere Medikamente: ZYRTEC; FLONASE; C; VITAFUSION; VIACTIV CALCIUM w/D
Allergien: Sulfa
Vorherige Impfungen: 1/21/2021, Covid 2nd dose, Pfizer, 52yr old, Short of breath, Chest pain, under arm pain, fever, fatigue. Missed 2day of work, r

VAERS 2065575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: MD
Alter: 48,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 09.10.2021
Beginn: 06.12.2021
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: - / RA

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

COVID-19 Dizziness Dyspnoea Headache Pain SARS-CoV-2 test positive

Symptomtext

Headache short breath dizzy body aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Positive Covid test
Aktuelle Erkrankungen: None
Vorgeschichte: PTSD hypothyroidism depression anxiety allergies
Andere Medikamente: Claritin, synthesis, topamax, magnesium, potassium, calcium, vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2065440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NJ
Alter: 97,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 22.10.2021
Beginn: 25.01.2022
Tage bis Beginn: 95,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain Cough Dyspnoea Hypophagia SARS-CoV-2 test positive

Symptomtext

This is a 97 year old, frail, elderly male, patient of Dr. with past medical history significant for CAD, s/p CABG, HTN, HLP, Hypothyroidism, Barretts Esophagus, Depression, Bells Palsy with residual Left side facial droop/weakness, who presented to the ED with complaints of SOB, CP, Cough, poor po intake. Apparently this started several days ago per his family.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: 01/25/2022 - SARS-COV-2 Antigen (++)
Aktuelle Erkrankungen: -
Vorgeschichte: Depression, Dyslipidemia, HTN, Hypothyroidism; Addt'l Med History Barretts Esophagus CAD, s/p CABG. Significant Surg Hx As Listed Common CABG, R THA; Addt'l Surgical History Hernia repair.
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2065316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 11.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Herpes simplex Oral herpes

Symptomtext

After both the booster shot and a subsequent mild case of Covid (onset: December 26, 2021) I experienced a reoccurrence of herpes simplex. The first time my entire upper palate was affected; I saw my periodontist. The second time (after the illness) the problem was milder lasting four days and then healed. I first had herpes simplex in 1962; since then, have had very few outbreaks until Covid vaccine and then the actual Covid illness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Herpes simplex
Andere Medikamente: Xarelto, Klonopin
Allergien: None
Vorherige Impfungen: -

VAERS 2050498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Chills Dizziness Dysphagia Dyspnoea Fatigue Flushing Headache Hyperhidrosis Injection site pain Lethargy Throat tightness

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Chills-Severe, Systemic: Dizziness/Lightheadedness-Severe, Systemic: Exhaustion/Lethargy-Severe, Systemic: Flushed/Sweating-Severe, Systemic: Headache-Medium, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

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

VAERS 2048056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 50,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 15.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / AR

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

Abdominal pain C-reactive protein increased Colitis ulcerative Condition aggravated Faecal calprotectin Lipase increased Neutrophil percentage increased Pancreatitis Pyrexia Red blood cell sedimentation rate increased White blood cell count increased

Symptomtext

Ulcerative colitis flare and pancreatitis. Started developing abdominal pain 3 days after COVID vaccine that progressively worsened over 1 week. Then developed a fever and was seen in the ED when pancreatitis and colitis flare were diagnosed. At the time, I was receiving mesalamine, which was stopped. Started on clear liquid diet and symptoms improved within 24 hours. Discharged home on Uceris and low fat diet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 1,0
Labordaten: 10/26/2021: WBC 13.3 (79% neutrophils), CRP 3.8, ESR 30, Lipse 1774, fecal calprotectin 959
Aktuelle Erkrankungen: Ulcerative colitis (stable, managed)
Vorgeschichte: Ulcerative colitis
Andere Medikamente: Mesalamine
Allergien: None
Vorherige Impfungen: -

VAERS 2047711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 68,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Headache Hypoaesthesia oral Paraesthesia Paraesthesia oral Pyrexia

Symptomtext

After my vaccine my lips tingled. It was at the pharmacy. My lips went numb with pins and needles. When I got home, I got a fever and had a bad headache. I had a headaches on and off for a good month and felt very tired. Today I have no symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: None
Allergien: Amoxicillin
Vorherige Impfungen: Flu shot vaccine- fever, aching sensation to my body.

VAERS 2047601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 41,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 27.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / RA

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

Abdominal pain upper Bedridden Blood test Chest pain Computerised tomogram Cyst removal Electrocardiogram Endoscopy Feeding disorder Impaired work ability Magnetic resonance imaging Motor dysfunction Oesophageal disorder Oesophageal manometry Pruritus Salivary hypersecretion X-ray

Symptomtext

Extremely itchy hands lasting for about two weeks; debilitating chest/upper abdominal pain; intense esophageal issues; large amounts of constant saliva; frequent necessary ER visits; admission to hospital; surgery and removal of cyst to determine if that was the source of the problem (which it was not) ; still ongoing issues - no remedy or conclusive diagnosis thus far; cannot eat regularly or consistently; practically bed ridden and cannot work or function normally because of the ongoing issues PCP 11/16/2021? Hospital admission: 11/20 through 11/29/2021 Hospital ER Visits General Hospital: 11/19/2021, 12/06/2021, 12/09/2021, 12/13/2021, 12/14/2021, 12/23/2021, 12/26/2021, 12/28/2021, 01/03/2022 Hospital ER Visit Hospital: 12/17/2021 Additional visits to Gastro Doctors; Outpatient Urgent care facilities; phone consults with doctors

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 9,0
Labordaten: November to current, too many to list dates: Bloodwork, XR, EKGs, cat scans, MRI, endoscopes (both upper and lower), esphogeal manometry
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, bronchitis
Andere Medikamente: none
Allergien: nuts and some shellfish
Vorherige Impfungen: -

VAERS 2047402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: WI
Alter: 74,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 05.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Chest pain Laboratory test Rash

Symptomtext

developed rash over neck, chest back and top of head. Eventually it mostly disappeared but some spots still remain. Recommended to see dermatologist if does not totally disappear. Also developed chest pain and just completed routine of wearing a Zio patch to see if there is any cardiac issues developed or just pain. No results have been returned yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Wore zio patch over heart waiting on results
Aktuelle Erkrankungen: similar rash developed after second dose this was the booster
Vorgeschichte: hernia discs in lower back, intercostal cartilage torn off right rib cage, rheumatoid arthritis in back, and both wrists/hands
Andere Medikamente: atenolol, prilozec, ezembid, allergy generic, flonase, hydroxychloroquine
Allergien: statins
Vorherige Impfungen: seasonal flu shot developed short term amnesia

VAERS 2042309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: AL
Alter: 49,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Breast pain Chest pain Immunisation

Symptomtext

Sore, painful: from left breast toward the middle of chest, heart area, was sore and painful.; Sore, painful: from left breast toward the middle of chest, heart area, was sore and painful.; booster; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 15Nov2021 (Lot number: FH8020) at the age of 49 years as dose 3, (booster) single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU. Vaccination history included: Bnt162b2 (Dose 1, Lot: EV or EN 6208, handwritten, Expiration: Jun2021, Site: right arm, First and Second: hospital vaccine site), administration date: 22Mar2021, when the patient was 49 years old, for Covid-19 Immunization, reaction(s): "mild temperature"; Bnt162b2 (Dose:2, Lot: looks like EW0150, handwritten, Expiration: Jul2021, Site: right arm, First and Second: hospital vaccine site), administration date: 12Apr2021, when the patient was 49 years old, for Covid-19 Immunization, reaction(s): "Tired", "achy". The following information was reported: IMMUNISATION (non-serious) with onset 15Nov2021, outcome "unknown", described as "booster"; BREAST PAIN (non-serious), CHEST PAIN (non-serious) all with onset 16Nov2021, outcome "recovered" (17Nov2021) and all described as "Sore, painful: from left breast toward the middle of chest, heart area, was sore and painful.". Additional Information: AE(s) require a visit to Emergency Room and Physician Office Follow-Up (04Jan2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2031517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 27,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 22.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Vitiligo

Symptomtext

I was born with vitiligo on my right leg (pattern was unchanged for my entire life, never spread, never changed). After my covid vaccination, the two covid injection sites now have over a quarter sized vitiligo mark that has stayed for months and gotten more prominent. I have been absolutely traumatized by the way it looks. I can not wear tops that show my arms anymore. I have never had this kind of reaction from any other vaccine (including flu) and I haven?t had this reaction when having covid naturally.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid
Vorgeschichte: Vitiligo
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2020672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 64,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

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

Gait disturbance Joint stiffness Joint swelling Paraesthesia

Symptomtext

I had a Left KNEE replacement on February 23, 2021 right after the shot there was a tingling sensation right to my left knee. I had been doing Great walking with no issues. Now my knee is stiff and swallow everyday and I am having issues walking. My knee has not been the same. Saw the Dr. and I am taking anti flammatory meds which should not be.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Taking Anti Flammatory Meds daily Meloxicam
Aktuelle Erkrankungen: NONE
Vorgeschichte: Knee replacement on February 23, 2021, tingling right after the shot to my Left knee immediately. Has not been the same since swells up and stiff. I had been doing Fantastic and now I am have issues!!
Andere Medikamente: Synthroid 88 MCG, Vitamins: One A day, B 12, Bition, C, Calcium w/D, Probiotic
Allergien: Cyclor
Vorherige Impfungen: -

VAERS 2019423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cardiac stress test normal Chest pain Cough Discomfort Dyspnoea Nasal congestion Nausea Pain Palpitations Productive cough Pyrexia

Symptomtext

36-year-old female with history adult onset diabetes onset approximately 5 years ago presents with complaint of anterior chest pain which has occurred almost daily since early November at which time she took her first Covid vaccine. She states typically she has 3-5 episodes per day but since 4 days ago has had many episodes. Patient has been seen and evaluated by cardiology, and has had previous nuclear stress test which by history was normal. States over the past few days has had 10-12 episodes of pain and typically relieved with nitroglycerin. She describes the discomfort as heaviness and sharp with average duration 5 to 10 minutes with associated shortness of breath, nausea, and palpitations. No provocation factors. Patient also gives history of having cough productive of scant clear sputum along with fever and nasal congestion since Monday or Tuesday. Chest pain is worse with cough. Patient's son was diagnosed with Covid infection on Monday. No hx DVT/PE. Fam Hx Long QT syndrome. Last normal menstrual December 15

Weitere VAERSDATA-Felder

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

VAERS 2019106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NV
Alter: 37,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Fatigue Malaise Pyrexia Tachycardia

Symptomtext

101 degree Fahrenheit Fever, malaise, tachycardia, dizziness, fatigue. Experienced when alarm sounded at 6:00am the day after receiving the COVID-19 Vax injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: No test or lab results
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2018180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 44,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Dysphagia Headache Immunisation Lymphadenopathy Migraine Nausea Photophobia Tonsillar hypertrophy

Symptomtext

significant cervical, auricular, occipital lymphadenopathy; bilateral L>R, w/enlarged R tonsilar, submental lymph; dysphagia; burning diffuse headache with photo phobia; burning diffuse headache with photo phobia; nausea; w/associated migraine symptoms R temporal; Booster; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 44 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 20Oct2021 12:00 (Lot number: fh8020) at the age of 44 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "migraine" (unspecified if ongoing), notes: Other medical history: migraine, hashimoto, rocky mountain spotted fever; "hashimoto" (unspecified if ongoing), notes: Other medical history: migraine, hashimoto, rocky mountain spotted fever; "rocky mountain spotted fever" (unspecified if ongoing), notes: Other medical history: migraine, hashimoto, rocky mountain spotted fever. The patient's concomitant medications were not reported. Past drug history included: Haldol, reaction(s): "Known allergies: Haldol", notes: Known allergies: Haldol. Vaccination history included: Bnt162b2 (Prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Prev dose lot unknown: True, Prev dose lot unknown reason: Unable to locate or read the details, Prev dose administration date: 05Feb2021, Prev dose dose number: 2, Prev dose vaccine location: Left arm), administration date: 05Feb2021, when the patient was 43 years old, for Covid-19 Immunization; Bnt162b2 (Prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Prev dose lot unknown: True, Prev dose lot unknown reason: Unable to locate or read the details, Prev dose administration date: 08Jan2021, Prev dose administration time: 05:00 PM, Prev dose dose number: 1, Prev dose vaccine location: Left arm), administration date: 08Jan2021, when the patient was 43 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 20Oct2021 12:00, outcome "unknown", described as "Booster"; LYMPHADENOPATHY (non-serious) with onset 22Oct2021, outcome "recovering", described as "significant cervical, auricular, occipital lymphadenopathy"; TONSILLAR HYPERTROPHY (non-serious) with onset 22Oct2021, outcome "recovering", described as "bilateral L>R, w/enlarged R tonsilar, submental lymph"; DYSPHAGIA (non-serious) with onset 22Oct2021, outcome "recovering", described as "dysphagia"; HEADACHE (non-serious), PHOTOPHOBIA (non-serious) all with onset 22Oct2021, outcome "recovering" and all described as "burning diffuse headache with photo phobia"; NAUSEA (non-serious) with onset 22Oct2021, outcome "recovering", described as "nausea"; MIGRAINE (non-serious) with onset 22Oct2021, outcome "recovering", described as "w/associated migraine symptoms R temporal". The events "significant cervical, auricular, occipital lymphadenopathy", "bilateral l>r, w/enlarged r tonsilar, submental lymph", "dysphagia", "burning diffuse headache with photo phobia", "burning diffuse headache with photo phobia", "nausea" and "w/associated migraine symptoms r temporal" were evaluated at the physician office visit. Therapeutic measures were taken as a result of lymphadenopathy, tonsillar hypertrophy, dysphagia, headache, photophobia, nausea, migraine. Additional Information: Prior vaccination within 4 weeks was reported as none. Prior to vaccination patient was not diagnosed with COVID-19 and since the vaccination, the patient had not been tested for COVID-19. Treatment for adverse event was reported as high dose prednisone, chiropractic/massage. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hashimoto's disease (Other medical history: migraine, hashimoto, rocky mountain spotted fever); Migraine (Other medical history: migraine, hashimoto, rocky mountain spotted fever); Rocky mountain spotted fever (Other medical history: migraine, hashimoto, rocky mountain spotted fever)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: HI
Alter: 44,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 19.11.2021
Beginn: 24.12.2021
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Dyspnoea Fatigue Influenza like illness Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had fever, fatigue, SOB, light cough, and difficulty breathing. I had a sore throat and flu like symptoms. These lasted for about 10 days. I did a at home Covid-19 test, positive results. I went to my doctor after that. She did a physical exam and just asked about my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid-19 test.
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2010776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 47,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Arthralgia Burning sensation Chest pain Fatigue Heart rate increased Hypoaesthesia Muscle twitching Palpitations Paraesthesia Vision blurred

Symptomtext

I received the 2 dose Pfizer vaccine on 10/3/21 and 10/25/21. The day after my 1st dose I experienced my heart rate increase, chest pains and fatigue. The day after I received my second dose , I woke up in the am panicing bc both my hands and both feet were tingling, burning, with a sensation of pins and needles. They also felt numb, as when your arm or leg falls asleep and is limp. I experienced twitching in my eye and my vision was very blurry. I had palpitations and my heart felt like it was racing out of my chest, and chest pains. I was extremely fatigued and my joints were very painful. I am still experiencing parasthesia in both my hands and both feet. I can't hold my phone or surface laptop for long periods of time because the sensations worsen when I do this. I have intermitent episodes of chest pains and my joint feel painful still have heavy fatigue. I am setting up an appointment with a specialist in my area to consult with about my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None available at this time
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal asthma, migraines
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 1999207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 43,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Dyspnoea Somnolence

Symptomtext

I was in the gym working on calves the following morning 12/10/2021 @ approximately 5:15am when I started experiencing severe chest pain and shortness of breath. I left my workout early and when home where I slept most of the day. The chest pain lasted approximately 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Protein, creatine, pre-workout, vitamins, BCAAs.
Allergien: None
Vorherige Impfungen: -

VAERS 1998830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TN
Alter: 57,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 17.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Condition aggravated Musculoskeletal stiffness Pain in extremity

Symptomtext

My arm was sore a day after my last vaccine, then faded away as it did with my first two injections. It returned two to three weeks later and remains unusually sore, stiff and painful in my shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa and penicillin antibiotics
Vorherige Impfungen: -

VAERS 1975350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 02.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: SYR / LA

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

Condition aggravated Tinnitus

Symptomtext

It made my tinnitus a lot worse.

Weitere VAERSDATA-Felder

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

VAERS 1966273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: KS
Alter: 36,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fear Nausea Palpitations Pruritus Rash erythematous Rash papular Rash pruritic Swelling

Symptomtext

10-20-2021: Event 1 was an extreme reaction to kinesio tape on my belly; wherever the adhesive was became very itchy, red, raised and swollen. The rash became worse and worse until I removed the tape and washed off the adhesive. 10-28-2021: Event 2 was a red, raised, itchy, swollen rash on my face and neck. It became worse and worse throughout that day. I apply cortisone cream from the drug store throughout the evening, but it doesn't seem to help and feels like its making me feel worse. 10-29-2021: Early AM, I awoke feeling dizzy, nauseated, very itchy (face and neck were worse, more swollen and red and raised) and my heart was racing. I was scared I was having a very bad reaction to something but I didn't know what to do. I called a friend that was a nurse and my boss as I was traveling. 10-30-2021: Rash continues, but other symptoms start to improve 10-31-2021: Rash continues 11-01-2021: Rash continues 11-02-2021: Rash continues, I see my primary care provider. She prescribes an antihistamine (2nd gen, breastfeeding safe) and a stronger topical cortisone cream. 11-03-2021: Rash begins to resolve 11-06-2021: Rash returns, worse than before 11-13-2021: Rash returns, worse than before 11-23-2021: Appointment to test for food allergies as food diary shows rash is linked to possible allergy of apples and/or tomatoes. Testing shows no allergies to food but allergy to latex. 12-04-2021: Rash returns, worse than before within 30 minutes of having eaten take out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 11-02-2021: Primary care provider appointment. She prescribes an antihistamine (2nd gen, breastfeeding safe) and a topical cortisone cream. 11-23-2021: Appointment to test for food allergies as food diary shows rash is linked to possible allergy of apples and/or tomatoes. Testing shows no allergies to food but allergy to latex.
Aktuelle Erkrankungen: None
Vorgeschichte: Generalized anxiety, irritable bowel syndrome (in remission since 2018)
Andere Medikamente: Pre-natal vitamins (breastfeeding)
Allergien: None to my knowledge
Vorherige Impfungen: -

VAERS 1963620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 23.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

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

Blister Herpes zoster Pain in extremity Palpitations

Symptomtext

Side effects after my booster (3rd shot): Very sore arm the day of the shot, which lasted for about a week. On day three, I felt strong heart palpitations that lasted for a few minutes, a couple times throughout the day. These daily heart palpitations lasted for two weeks. I developed shingles the day after my shot. I have a group of blisters on the right-side of my neck. It is now Dec 20th, and they have not gone away. Now I have blisters showing up on my face (cheeks).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin D, Vitamin C, Magnesium, Zinc, NAC
Allergien: -
Vorherige Impfungen: -

VAERS 1963497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / AR

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

Blood thyroid stimulating hormone Pain in extremity Paraesthesia

Symptomtext

my feet and hands started tingling which has progressed and now my hands are painful

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: my level of tsh was , but started taking levelthyroxine more regular , and has not made a difference , this was diagnosed by my primary , wh said to folow up with dr
Aktuelle Erkrankungen: sjogren's syndrome , mixed connective tissue disease
Vorgeschichte: same as above
Andere Medikamente: none
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1963458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NE
Alter: 43,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Bronchitis Condition aggravated Cough Fatigue Influenza virus test negative Lymphadenopathy Nerve compression Productive cough Pyrexia SARS-CoV-2 test negative Sinus congestion

Symptomtext

24 hours later - Fatigue lasting 3 days 24-48 hours later fever 102+ 24 hours to 5 days after swollen lymph nodes (under the right armpit) to the extent I over-utilized my left arm and ended up with a pinched nerve 3.5 weeks after booster - sinus congestion, cough - negative COVID test 5.5 weeks after booster shot - cough became productive. Negative COVID, Influenza Test. DX: Bronchitis. Prescribed Prednisone and Antibiotics - cleared up within 7 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 12/7 COVID Test (Negative) 12/13 COVID Test (Negative) 12/13 Influenza Test (Negative)
Aktuelle Erkrankungen: Swollen Lymph nodes for 5 days following booster shot Fever (102+) 24-48 hours after receiving booster Bronchitis - Dec 2021. I get this pretty much every December so that's probably not related to the booster.
Vorgeschichte: Asthma, Acid Reflux, Anxiety
Andere Medikamente: Celexa, Zyrtec, Vit. D, Priolsec
Allergien: Sulfa
Vorherige Impfungen: Pfizer COVID Jan 2021 - Migraine Headache Pfizer COVID Feb 2021 - Migraine Headache and Fatigue

VAERS 1962447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: MD
Alter: 45,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Arthralgia Blood test Dyspnoea exertional Fatigue Muscle spasms Muscle tightness Sleep disorder Trismus

Symptomtext

For the first dose I got extreme cramping in my jaw in front of my left and right ear. It would tighten really bad then pop. The left side was a little worse than the right side. This went away after about a week. I also got tightness on the left side of my neck. The tightness felt like it was in the muscles used to swallow. It did not hinder me from swallowing so I did not go to the doctor. The neck tightness went away about a week after the shot. The second dose (administered on 11/16/21) is where I had and am still having bad side effects. About a day after the second dose I the jaw tightness came back to only the left side. It is less extreme, but has not gone away. When I whistle it tightens then pops. So it is mostly an annoyance. The main problems is that from my belt line to my belly button (all the way around my core) I get very severe pain when I lay down. It affects my sleep causing me to wake up during the night. Likewise, I have a raw (like tendonitis) pain on the inner side of my left elbow. I get cramping in my left wrist (especially when playing guitar which I never had before). And worse of all I seem to fatigue very quickly, like my muscles are not getting enough oxygen. I was running before the first shot, so I know this was not an issue before. Now I breath hard when walking. This has continued till today and has not lessened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: I just had blood work done last week. I am still waiting on test results.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1942093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: GA
Alter: 22,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal discomfort Abdominal distension Abdominal pain Blood creatinine increased Blood urea normal C-reactive protein increased Computerised tomogram abdomen abnormal Condition aggravated Constipation Differential white blood cell count normal Dyspepsia Fatigue Flank pain Full blood count Haematocrit normal Haemoglobin normal Headache Human chorionic gonadotropin normal

Symptomtext

Fatigue, myalgias, HA, right flank pain, RLQ cramps, constipation, sore arm, nausea, indigestion started an progressed on day of vaccine. 12/17: Flank pain gone, nausea and indigestion improved but not resolved. Constipation worse. Bloating, mild diffuse abd discomfort. No f/c/s. Fatigue persists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: U/A- normal urine HCG-neg CBC: WBC: 5.1, H/H: 13.3/39, normal diff, PLT: 235 ESR: 8; CRP: 3 CMP: normal except Cr: 1.3. BUN: 14 Urine C&S pending CT abd: normal except large stool burden and bilateral ovarian follicular cyst
Aktuelle Erkrankungen: None known
Vorgeschichte: IBS-C (stable for about 3 years) Allergic Rhinitis Auditory Processing D/O Nut Allergy Eczema
Andere Medikamente: Ultraflora immune health Lo Loestrin Fe Multivitamin Mometasone Furoate
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1954742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IL
Alter: 23,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Chest discomfort Chest pain Headache

Symptomtext

Slight headache and chest pain around the heart. Happened around 9pm that night. Chest would squeeze that around near my heart and made it hard to move. Anxiety would kick as well and make it worst. Slowly tamper off when days went by but still have the effect until now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Went to an emergency care on Nov 8th. Nothing wrong but was told if I felt.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1948135

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Chills Dyspnoea Pulmonary congestion Wheezing

Symptomtext

I experienced chills, shortness of breath, congestion in my lungs, severe wheezing, and severe joint pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Hypothyroidism, Thyroiditis, and Kidney Stones
Andere Medikamente: Yes
Allergien: I am allergic to Latex, Sulfa, Iodine. IVP Dye, Eggs, Bees and Wasps.
Vorherige Impfungen: -

VAERS 1939669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OR
Alter: 34,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 07.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Dyspnoea Fatigue Lymphadenopathy Pyrexia

Symptomtext

day of- fever, fatigue 2 weeks after and continued to present: swelling of lymph nodes in right axillary. Same reaction after dose 2 completed, lasted 6months. - 1 week after lasting 1 month: SOB worse on exacerbation, no relief with rescue inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Ultrasound run after doses 1 and 2 when lymph node pain severe and cause unknown, was also treated for shingles in case that was the cause of pain, gabapentin treated the pain as NSAIDs did not help with the pain
Aktuelle Erkrankungen: -
Vorgeschichte: pseudotumor/increased intracranial pressure, SVT, asthma
Andere Medikamente: Diamox, Gaba, 5Htp, Cetrizine
Allergien: -
Vorherige Impfungen: -

VAERS 1939336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IN
Alter: 41,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Chills Fatigue Feeling abnormal Headache Myalgia Nausea Speech disorder Tremor

Symptomtext

At exactly 12 hours after the shot at 1:30am I had uncontrollable shaking and chills. I was shaking so bad I could hardly speak. At the same time I felt nauseous but never vomited. The violent shaking lasted about 30 minutes and only after I put on a sweater, sweatpants, wool socks, two blankets and my husband provided his body heat did I finally stop having chills and shaking uncontrollably. I didn?t have any other chills after that. Additionally I had a terrible headache the next day, felt like my head was in a fog, had full body muscle aches, and was extremely fatigued. I took an afternoon nap and felt slightly better. I also took Tylenol every 6 hours.

Weitere VAERSDATA-Felder

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

VAERS 1938826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Eczema Epistaxis Feeling abnormal Immunisation Muscle twitching Pain Parosmia SARS-CoV-2 test Tinnitus

Symptomtext

Muscle twitching; Tinnitus; Intense nose bleeds for about 3 days; Eczema I had on my arms flared up; Eczema I had on my arms flared up; Eczema I had on my arms flared up, causing intense pain; Brain fog; Phantom smells (when you smell something that's not there, such as smoke or sewage).; Dose received: 3; This is a spontaneous report received from contactable reporter (consumer or other non-HCP). The reporter is the patient. A 27-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 19Oct2021 (Lot number: FH8020) at the age of 27 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "COVID-19" start date: an unknown date in Mar2020 (unspecified if ongoing), notes: Long Covid/ Prior to vaccination, was the patient diagnosed with COVID-19?:Yes; "Asthma" (unspecified if ongoing); "Eczema" (ongoing); "Cranial nerve sensory neuropathy" (unspecified if ongoing), notes: post viral vagal neuropathy; "EBV infection reactivation" (unspecified if ongoing), notes: Reactivated EBV; "Human herpesvirus 6 infection reactivation" (unspecified if ongoing), notes: Reactivated HHV 6; "Brain injury" (unspecified if ongoing), notes: Brain injury (due to covid) and "Post-traumatic stress disorder" (unspecified if ongoing), notes: PTSD. Concomitant medications included: FLU SHOT taken for Immunisation on 29Sep2021; PINDOLOL; LEXAPRO and SYMBICORT. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number : EM9810), administration date: 19Feb2021, when the patient was 27 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number : EM6202), administration date: 12Mar2021, when the patient was 27 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 19Oct2021, outcome "unknown", described as "Dose received: 3"; MUSCLE TWITCHING (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (22Oct2021), described as "Muscle twitching"; TINNITUS (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (22Oct2021), described as "Tinnitus"; EPISTAXIS (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (22Oct2021), described as "Intense nose bleeds for about 3 days"; ECZEMA (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (an unknown date in 2021), described as "Eczema I had on my arms flared up"; CONDITION AGGRAVATED (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (an unknown date in 2021), described as "Eczema I had on my arms flared up,"; PAIN (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (an unknown date in 2021), described as "Eczema I had on my arms flared up, causing intense pain"; FEELING ABNORMAL (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (an unknown date in 2021), described as "Brain fog"; PAROSMIA (non-serious) with onset 19Oct2021 at 22:00, outcome "recovered with sequelae" (an unknown date in 2021), described as "Phantom smells (when you smell something that's not there, such as smoke or sewage)". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of eczema and condition aggravated. Additional Information: Prior to the vaccination, the patient was diagnosed with COVID-19. The patient received other vaccine within four weeks prior to COVID vaccine. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Treatment included Elidel cream for eczema. It was reported that patient was a long Covid patient and had symptoms every day since Mar2021. Her eczema had gone down extremely slowly and had not returned to a manageable point yet. Since the vaccination, the patient had been tested for COVID-19. The patient underwent the following laboratory tests and procedures which included: SARS-CoV-2 test (PCR) by test type nasal swab on 03Dec2021 and the result was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211203; Test Name: PCR; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: Eczema
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Brain injury (Brain injury (due to covid)); COVID-19 (Long Covid/ Prior to vaccination, was the patient diagnosed with COVID-19?:Yes); Cranial nerve sensory neuropathy (post viral vagal neuropathy); EBV infection reactivation (Reactivated EBV); Human herpesvirus 6 infection reactivation (Reactivated HHV 6); Post-traumatic stress disorder (PTSD)
Andere Medikamente: PINDOLOL; LEXAPRO; SYMBICORT
Allergien: -
Vorherige Impfungen: -

VAERS 1937034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain

Symptomtext

Still ongoing effects after two weeks of the shot, my chest still hurts I go over 114 pulse and it will hurt or below 60 pulse. I can take Tylenol but it doesn?t help as much. Started hurting early morning on 11/27/2021 and continues I am seeing my doctor o. 12/13/2021 for the issue as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Chest pains, insomnia, and sometimes tiredness
Vorgeschichte: Heart murmur, Small leaking valve in in heart not noticeable as the heart doctor told me. Clinically known for depression, lower back issues, shoulder pain registered due to my old job.
Andere Medikamente: Multivitamin for men, Tylenol
Allergien: Hydrocoidene
Vorherige Impfungen: -

VAERS 1936580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: KY
Alter: 32,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 21.10.2021
Beginn: 07.12.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Chest pain Constipation Cough Decreased appetite Diarrhoea Dyspnoea Exposure during pregnancy Exposure to SARS-CoV-2 Fatigue Haematemesis Haematochezia Headache Melaena Myalgia Nausea Palpitations Respiratory tract congestion

Symptomtext

12/7/21 Pt is a 32 yr/o who presents to the ED complaining of fatigue, myalgias, mild HA, nausea, vomiting and loss of appetite for 3 days. Pt has covid and is concerned about her pregnancy. She denies any cough, congestion, dyspnea, chest pain, palpitations, hematemesis, diarrhea, constipation, hematochezia, melena, vaginal bleeding, vaginal discharge or abdominal pain. She does report being exposed to Covid and she is currently 27 weeks pregnant. She does not have any medications at home for nausea and has not contacted her OB/GYN today but was seen in the office yesterday. She does not believe she has lost taste or smell but states that throughout her pregnancy she has had alteration in taste and intermittent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/7/21 COVID-19 Result Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Biotin 10 MG Caps TAKE 1 CAPSULE BY MOUTH EVERY MORNING
Allergien: Amoxicillin, eggs or egg derived products, latex
Vorherige Impfungen: -

VAERS 1936447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest pain Computerised tomogram Dyskinesia Hemiparesis Magnetic resonance imaging head Magnetic resonance imaging spinal Magnetic resonance imaging thoracic Pain Scan with contrast

Symptomtext

The first and second dose, I had full body rash, body aches, fever, and chills. The booster shot (3rd dose), I had chest pain that started the following morning and it progressively got worse. I eventually throbbing pain on my left chest and my left side of the body couldn't move the way I wanted it to; it was very weak. I went to the emergency room, and was admitted into the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: They completed CAT scan with contrast of chest, Chest X-ray, blood test for clots, Brain and spinal cord MRI with contrast, Chest MRI with contrast
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergy to Amoxicillin
Vorherige Impfungen: -

VAERS 1932547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 77,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood thyroid stimulating hormone normal Discomfort Full blood count normal Hypoaesthesia Metabolic function test Paraesthesia Sensitisation Vitamin B12 normal

Symptomtext

Patient developed numbness and tingling in her feet. It came on suddenly and has progressed up her legs to below the knees. She has sensitivity and discomfort. No weakness. Nothing makes it worse or better. No treatment. No abnormal physical exam findings-no abnormal weakness, sensation intact, normal vibratory sensation, and reflexes intact. Symptoms are persistent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: B12, TSH, CMP and CBC normal 12/7/21. EMG ordered but not yet done.
Aktuelle Erkrankungen: none
Vorgeschichte: COPD, osteoporosis, hypothyroidism, and HLD
Andere Medikamente: Aspirin 81 mg, famotidine 20 mg daily, flonase nasal spray prn, levothyroxine 75 mcg qd, pravastatin 10 mg qd, serevent diskus 50 mcg BID, spiriva 18 mcg once daily, combivent prn and vitamin D 400 units daily.
Allergien: Codeine, pseudoephedrine, IV contrast
Vorherige Impfungen: -

VAERS 1929415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 37,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 30.10.2021
Beginn: 22.11.2021
Tage bis Beginn: 23,0
Dosis: UNK
Route/Site: IM / LA

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

Blood test Chest X-ray Chest pain Costochondritis Electrocardiogram

Symptomtext

Experienced chest pain on patient left side from 11/22-11/28/21. Visited ER on 11/28/21 and was diagnosed with costochondritis, treated with advil and rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: At ER on 11/28/21: ECG, chest x-ray, bloodwork were used to rule out other conditions
Aktuelle Erkrankungen: none
Vorgeschichte: migraine
Andere Medikamente: Nurtec ODT, Mirena IUD, sumatriptan, multivitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1928721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CO
Alter: 34,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Dyspnoea Nausea Pain Pyrexia Vomiting

Symptomtext

nausea, vomiting, extreme chills, body ache, high temp, breathing problem

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: high blood pressure and cholesterol
Vorgeschichte: blood pressure cholesterol elevated
Andere Medikamente: tylenol
Allergien: none
Vorherige Impfungen: -

VAERS 1928694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 32,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Dizziness Gastrooesophageal reflux disease

Symptomtext

Patient received Pfizer dose 1 today. Reports burning in chest at 11:29am and dizziness 5 minutes after getting vaccinated. Patient describes burning in chest as acid reflux. Offered medication, water, ice pack and crackers. Patient declined. Patient declined laying down. Patient had her 2 young children with her. VS: 11:41am 120/62 99 84 At 11:48am dizziness subsided. Discharged 11:55am. Advised to monitor burning in chest and contact primary with questions/concerns. Advised to take medications at home if needed. Patient agreed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: clindamycin - anaphylaxis; diclofenac - throat swelling
Vorherige Impfungen: -

VAERS 1928565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: NY
Alter: 31,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Blood pressure fluctuation Chest pain Dizziness Electrocardiogram Heart rate irregular

Symptomtext

When I first got the shot I got a tad lightheaded. After sitting I was fine, I went home and had bad chest pain it was light and got worse over the next few days. I went to a Dr about a week after due to chest pain. I was told it may be pericarditis/ pleurisy and was given steroid and amoxcillin. For 7 days I took these and Symptoms were worse, I have burning chest pain that has developed more. My heart and blood spike for just standing up and feel like I'm going to pass out everytime. My bpm and BP are reading high at times fluctuating randomly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Ekg
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1924761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 44,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

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

Chest pain

Symptomtext

Chronic chest pain which continues as of 11/20/2021 which was the last contact I had with this patient. She was seen by a cardiologist who ruled out myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: none
Vorgeschichte: multiple chemical and environmental sensitivities
Andere Medikamente: none
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1923769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CO
Alter: 61,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 26.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

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

Diarrhoea Dizziness Dyspnoea exertional Epistaxis Full blood count Haemoglobin decreased Red blood cell count decreased

Symptomtext

Lightheadedness, Dizziness, Low Hemoglobin, Low Red Blood Cells, labored breathing upon physical exertion, diarrhea, nosebleeds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: CBC- Nov 15, 2021
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure High cholesterol Dupuytren's contracture
Andere Medikamente: Irbesartan 300 mg 1/day Rosuvastatin 20mg 1/day Bayer Baby Aspirin 81 mg 1/day Omeprazole 20 mg 1/day
Allergien: Bee stings
Vorherige Impfungen: Typical side effects of the second shingles vaccine

VAERS 1923758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 51,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Malaise Nausea Pain Paraesthesia

Symptomtext

Tingling on the left side of the face, feeling unwell, dizziness, nausea, body aching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Adverse reaction to the first covid shot
Vorgeschichte: None
Andere Medikamente: None
Allergien: Bee stings, penicillin
Vorherige Impfungen: Flu shot (5-8 years ago?) and Covid shot on 10/07/2021

VAERS 1920762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 87,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 14.10.2021
Beginn: 02.12.2021
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 Decreased appetite Dyspnoea Hypophagia Productive cough SARS-CoV-2 test positive

Symptomtext

Patient is fully vaccinated against COVID (Pfizer-BioNTech): Dose 1 given 2/17/21, Dose 2 given 3/10/21, and Dose 3 given 10/14/21. Patient subsequently admitted to Health System for COVID-19 & related symptoms ( onset of productive cough, dyspnea, and decreased appetite with decreased p.o. intake, generalized weakness)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 PCR (Positive)
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic kidney disease, osteoarthritis,
Andere Medikamente: -
Allergien: Tetanus vaccines and toxoid - noted in 2008, note says "40+ years ago, happened at work, had to go to ER" - Had a systemic rash reaction. Severity not specified.
Vorherige Impfungen: Tetanus toxoid vaccine; systemic rash; Seen in ER when patient was in 20s -

VAERS 1917082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 03.03.2021
Beginn: 02.09.2021
Tage bis Beginn: 183,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac stress test Chest X-ray Chest pain Computerised tomogram thorax Dyspnoea Echocardiogram Fatigue Fibrin D dimer Palpitations

Symptomtext

chess Pains, Heart papitations, shorness of breath, fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: CT scasn Chess, Xray Chess. E cocardiogram, heart stress test, D dimer test. all done at the ER 0n 09/092021 and 09/10/2021.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: sumatriptan. Acyclovir
Allergien: unknowed
Vorherige Impfungen: -

VAERS 1916872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: GA
Alter: 32,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / LA

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

Blood pressure increased Blood test Bundle branch block left Chest pain Diarrhoea Discomfort Ejection fraction decreased Electrocardiogram abnormal Gastrooesophageal reflux disease Headache Heart rate increased

Symptomtext

I started having diarrhea and what felt like acid reflux two days after. I became so uncomfortable and had a horrible headache, so I went to the emergency room. BP and heart rate were elevated, and had three abnormal EKGs but was sent home following bloodwork and told to follow up with cardiologist. Ended up having to return to the ER five days later due to chest pains and rapid heart rate. BP was 178/120. Was admitted to the hospital for 3 days where they found that I have a left bundle branch block and EF of 35%. Now treating with beta blockers and ARBs until more is known from upcoming cardiac MRI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Apri birth control
Allergien: latex
Vorherige Impfungen: -

VAERS 1916708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WA
Alter: 62,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Back pain Chest pain Chills Cough Fatigue Myalgia Night sweats Productive cough Pyrexia

Symptomtext

Started out with night sweats, fever and chills, extreme fatigue and muscle soreness. By Sunday morning, I had also developed a deep cough with Phlegm in the back of my throat.. The cough was so deep and strained that I had piercing pain in my chest at my lumpectomy surgical site. I still have pain in my chest and lower back when I cough. I'm still having fever and chills that come and go - 101 last night, down to 100.4 to 98.4 - temperature. I'm tired and don't have my normal energy. Will this ever end?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I visited ARNP on 11/30/21. He hadn't seen a cough associated with the booster shot and recommended I take Delsym, and the "usual" care for a virus. I contacted him again today because I have more Phlegm in my throat and fever but haven't heard back.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Tamoxifen, Vitamin D
Allergien: Wasp, Hornet, Yellow Jackets, Latex
Vorherige Impfungen: -

VAERS 1913697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

C-reactive protein increased Chest discomfort Chest pain Dyspnoea Pain in extremity

Symptomtext

On Friday 11/12/21 she took her first dose of COVID vaccine (Pfizer). The following day she started having sharp pain in her left arm and left chest, and could not take a deep breath due to discomfort in her chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/17/21: C-reactive protein elevated at 12.5mg/L
Aktuelle Erkrankungen: none known
Vorgeschichte: irritable bowel syndrome, unspecified type
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1913136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 83,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 14.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Neck pain Nerve compression Pain in extremity Paraesthesia X-ray

Symptomtext

Neck pain, pain going down right arm, numbness, tingling of finger. Saw Dr., 11/18/21. Pinch nerve. About 3 -4 weeks since started. Told to continue to rotate Tylenol and ASA. Use heating pad , schedule physical therapy , scheduled for 1 available appointment, December 13th. Saw on 12 day course of prednisone. , restarted 2nd course of prednisone 11/30/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Had neck X-rays done at appointment. 11/18/21
Aktuelle Erkrankungen: The incident that had happened was a pinched nerve in neck, that is why answer was yes for an incident, maybe it should have been no. Don?t think this had anything to do with the vaccine, but was being honest about answering the question.
Vorgeschichte: Meriere?s disease, arthritis.
Andere Medikamente: Pantoprazole, tamsulosin, HCTZ, Meloxicam, prevagen, domperidone, baby asa, Atorvastatin, losartan, asa, Tylenol, prednisone, meclizine, ondansetron.
Allergien: Naprosyn, morphine, gabapentin, lisinopril.
Vorherige Impfungen: -

VAERS 1912787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: GA
Alter: 20,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Echocardiogram Electrocardiogram Electrocardiogram ambulatory Laboratory test Tachycardia

Symptomtext

Tachycardia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Echogram, halter monitor, labs, ekg
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Nova Ring
Allergien: -
Vorherige Impfungen: -

VAERS 1836717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MA
Alter: 40,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abnormal dreams Amnesia Angioedema Chills Fatigue Dyspnoea Hyperacusis Rash Lethargy Malaise Muscle spasms Muscular weakness Myalgia Nervous system disorder Pyrexia SARS-CoV-2 test Tinnitus

Symptomtext

Angioedema/swelling in face + neck (angioedema); Tinnitus; Rash on face, neck and abdomen developed; Hyperacusis; Muscle weakness; Fatigue; Fever; Chills; Muscle aches; lethargy; Abnormally vivid dreams; Memory loss; Extreme muscle cramping; Functional neurological disorder; Severe malaise; This is a spontaneous report from a contactable pharmacist (patient). A 40-years-old female non-pregnant patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number: FH8020, Expiration date was not reported), via intramuscular in arm left on 24Oct2021 at 12:30 PM (at the age of 40-years-old) as a dose 1, single for COVID-19 immunization. The patient's medical history included COVID-19, ongoing COVID long haulers from 04Jul2020, pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues from 04Jul2020 and ongoing. The patient's concomitant medication(s) received within 2 weeks of vaccination included lisdexamfetamine mesilate (VYVANSE), via oral, taken for binge eating disorder (reported as B.E.D) from an unspecified start date and ongoing, fexofenadine hydrochloride (ALLEGRA), via oral, taken for allergies from an unspecified start date and ongoing, fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]), via nasal, taken for allergies from an unspecified start date and ongoing, norethindrone acetate, via oral, taken for birth control from an unspecified start date and ongoing. The patient was not pregnant at the time of vaccination. The patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior vaccinations were reported as none. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, has the patient been tested for COVID-19 was reported as no. On 24Oct2021 at 23:00, the patient experienced severe malaise, abnormally vivid dreams, memory loss, functional neurological disorder, extreme muscle cramping. On 25Oct2021 at 11:00, the patient experienced hyperacusis, on 25Oct2021 at 09:00, the patient had muscle weakness/fatigue/fever/chills. On 26Oct2021 at 14:00, the patient had experienced tinnitus. On 06Nov2021 at 09:00, the patient experienced angioedema and resulted in physician office visit. It was reported that, the vaccine was given on 24Oct2021, beginning on 25Oct2021, the patient experienced fever chills, muscle aches & lethargy continuing every day through 04Nov2021. Beginning on 26Oct2021, rash on face, neck and abdomen developed with swelling in face + neck (angioedema) Benadryl 50mg Q5h, famotidine 20mg BID Started. Stated that, symptoms were worsening over the following 24 hrs. Topical Betamethasone applied and prednisone 40mg oral started on 28Oct2021, increased to 60mg on 27Oct2021 with tapering of 40mg, 20mg, 10 mg, 5mg over the next 2 weeks. Albuterol inhaler used for Sob. Hyperacusis began on 25Oct2021 and continued until present day has not resolved. Tinnitus began 26Oct2021 and lasted them on 29Oct2021. The reporter seriousness for the events hyperacusis, muscle weakness/fatigue/fever/chills, angioedema, tinnitus was reported as non-serious. Stated that, the patient provided information regarding the reported adverse event(s) with the use of the product was reported as yes and the Pfizer product had a causal effect to the adverse event was reported as yes. Stated that, the patient had weakened immune system due to Covid long haulers. The events hyperacusis, muscle weakness/fatigue/fever/chills and tinnitus did not require the initiation of new medication/other treatment/ procedure. Treatment medication included ibuprofen. The event angioedema required the initiation of new medication/other treatment/ procedure was reported as yes, Prednisone, Pepcid, EpiPen, topical Betamethasone, Benadryl 50 mg Q4, Albuterol. Therapeutic measures were taken as a result of angioedema/swelling in face + neck, severe malaise, abnormally vivid dreams, memory loss, extreme muscle cramping, functional neurological disorder. Hospitalization prolonged was reported as no. The specific relevant test for thromboembolic with thrombocytopenia was reported as none. On 28Jul2020, the patient underwent lab tests and procedures which included Covid (SARS-CoV-2 test), resulted as false negative, MD confirmed false negative. The device date was on 27Oct2021. The outcome of the events for severe malaise, hyperacusis, abnormally vivid dreams, memory loss, functional neurological disorder, extreme muscle cramping and lethargy was not recovered and events angioedema/swelling in face + neck, muscle weakness, fatigue, fever, chills and tinnitus was recovering while for the other events rash on face, neck and abdomen developed and muscle aches was unknown.; Sender's Comments: Based on the current limited available information and the drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of event angioedema cannot be excluded. The case will be reassessed if additional information becomes available. 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: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20200728; Test Name: Covid; Result Unstructured Data: Test Result:False Negative; Comments: MD confirmed false negative
Aktuelle Erkrankungen: Hair loss (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Long COVID-19 (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Loss of smell (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Loss of taste (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Memory impairment (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Shortness of breath (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes)
Andere Medikamente: VYVANSE; ALLEGRA; FLONASE [FLUTICASONE PROPIONATE]; NORETHINDRONE ACETATE
Allergien: -
Vorherige Impfungen: -

VAERS 1836717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MA
Alter: 40,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Abnormal dreams Amnesia Angioedema Chills Fatigue Dyspnoea Hyperacusis Rash Lethargy Malaise Muscle spasms Muscular weakness Myalgia Nervous system disorder Pyrexia SARS-CoV-2 test Tinnitus

Symptomtext

Angioedema/swelling in face + neck (angioedema); Tinnitus; Rash on face, neck and abdomen developed; Hyperacusis; Muscle weakness; Fatigue; Fever; Chills; Muscle aches; lethargy; Abnormally vivid dreams; Memory loss; Extreme muscle cramping; Functional neurological disorder; Severe malaise; This is a spontaneous report from a contactable pharmacist (patient). A 40-years-old female non-pregnant patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number: FH8020, Expiration date was not reported), via intramuscular in arm left on 24Oct2021 at 12:30 PM (at the age of 40-years-old) as a dose 1, single for COVID-19 immunization. The patient's medical history included COVID-19, ongoing COVID long haulers from 04Jul2020, pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues from 04Jul2020 and ongoing. The patient's concomitant medication(s) received within 2 weeks of vaccination included lisdexamfetamine mesilate (VYVANSE), via oral, taken for binge eating disorder (reported as B.E.D) from an unspecified start date and ongoing, fexofenadine hydrochloride (ALLEGRA), via oral, taken for allergies from an unspecified start date and ongoing, fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]), via nasal, taken for allergies from an unspecified start date and ongoing, norethindrone acetate, via oral, taken for birth control from an unspecified start date and ongoing. The patient was not pregnant at the time of vaccination. The patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior vaccinations were reported as none. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, has the patient been tested for COVID-19 was reported as no. On 24Oct2021 at 23:00, the patient experienced severe malaise, abnormally vivid dreams, memory loss, functional neurological disorder, extreme muscle cramping. On 25Oct2021 at 11:00, the patient experienced hyperacusis, on 25Oct2021 at 09:00, the patient had muscle weakness/fatigue/fever/chills. On 26Oct2021 at 14:00, the patient had experienced tinnitus. On 06Nov2021 at 09:00, the patient experienced angioedema and resulted in physician office visit. It was reported that, the vaccine was given on 24Oct2021, beginning on 25Oct2021, the patient experienced fever chills, muscle aches & lethargy continuing every day through 04Nov2021. Beginning on 26Oct2021, rash on face, neck and abdomen developed with swelling in face + neck (angioedema) Benadryl 50mg Q5h, famotidine 20mg BID Started. Stated that, symptoms were worsening over the following 24 hrs. Topical Betamethasone applied and prednisone 40mg oral started on 28Oct2021, increased to 60mg on 27Oct2021 with tapering of 40mg, 20mg, 10 mg, 5mg over the next 2 weeks. Albuterol inhaler used for Sob. Hyperacusis began on 25Oct2021 and continued until present day has not resolved. Tinnitus began 26Oct2021 and lasted them on 29Oct2021. The reporter seriousness for the events hyperacusis, muscle weakness/fatigue/fever/chills, angioedema, tinnitus was reported as non-serious. Stated that, the patient provided information regarding the reported adverse event(s) with the use of the product was reported as yes and the Pfizer product had a causal effect to the adverse event was reported as yes. Stated that, the patient had weakened immune system due to Covid long haulers. The events hyperacusis, muscle weakness/fatigue/fever/chills and tinnitus did not require the initiation of new medication/other treatment/ procedure. Treatment medication included ibuprofen. The event angioedema required the initiation of new medication/other treatment/ procedure was reported as yes, Prednisone, Pepcid, EpiPen, topical Betamethasone, Benadryl 50 mg Q4, Albuterol. Therapeutic measures were taken as a result of angioedema/swelling in face + neck, severe malaise, abnormally vivid dreams, memory loss, extreme muscle cramping, functional neurological disorder. Hospitalization prolonged was reported as no. The specific relevant test for thromboembolic with thrombocytopenia was reported as none. On 28Jul2020, the patient underwent lab tests and procedures which included Covid (SARS-CoV-2 test), resulted as false negative, MD confirmed false negative. The device date was on 27Oct2021. The outcome of the events for severe malaise, hyperacusis, abnormally vivid dreams, memory loss, functional neurological disorder, extreme muscle cramping and lethargy was not recovered and events angioedema/swelling in face + neck, muscle weakness, fatigue, fever, chills and tinnitus was recovering while for the other events rash on face, neck and abdomen developed and muscle aches was unknown.; Sender's Comments: Based on the current limited available information and the drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of event angioedema cannot be excluded. The case will be reassessed if additional information becomes available. 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: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20200728; Test Name: Covid; Result Unstructured Data: Test Result:False Negative; Comments: MD confirmed false negative
Aktuelle Erkrankungen: Hair loss (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Long COVID-19 (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Loss of smell (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Loss of taste (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Memory impairment (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues); Shortness of breath (Pertinent details: Hair loss/Non growth SOB, loss of taste/smell, memory issues)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes)
Andere Medikamente: VYVANSE; ALLEGRA; FLONASE [FLUTICASONE PROPIONATE]; NORETHINDRONE ACETATE
Allergien: -
Vorherige Impfungen: -

VAERS 1906000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: SC
Alter: 71,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 16.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Ear disorder Fatigue Injection site nodule Lacrimation increased Pain in extremity Pruritus SARS-CoV-2 test negative Sneezing Vertigo

Symptomtext

initially had really sore arm and a knot at the site of injection and very tired. approximately 3 days later started sneezing and itchy, watery eyes. about 5 days after injection started having severe vertigo when rolling over in bed. while I have had vertigo before, it has never been this bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: doctor suggested having a rapid Covid test just to be careful. Test was negative. While I had a slight temp that was rising before going to the doctor, it was normal by the time they saw me. doctor checked my ears and said that the left ear was slightly pink. doctor prescribed meclizine for the vertigo. November 24 was the visit to the doctor.
Aktuelle Erkrankungen: COPD, IBS, arthritis in right TMJ
Vorgeschichte: COPD, IBS, arthritis in right TMJ
Andere Medikamente: Spiriva, Synthroid, LIpitor, Bentyl, HZTZ, Klor-Con, Nexium, Furosemide, Pro-Air, Refresh Optive, Probiotic, Zyrtec, Stress-B Complex vitamin, Mucinex, Citrical +D3, Vitamin C, Phazyme, Tylenol As needed: Mylanta, Mupiricin
Allergien: Sulfa, Cipro, Omnicef, Zofran, Ultram, Hydrocodone, Donnatal, Flonase, possibly penicillins, black pepper, raspberries
Vorherige Impfungen: -

VAERS 1905732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: TX
Alter: 51,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthritis Blood test Carpal tunnel syndrome Dizziness Feeling abnormal Headache Muscle atrophy Muscle spasms Musculoskeletal chest pain Tinnitus Weight increased

Symptomtext

arthritis, brain fog, carpal tunnel (today), headaches, weight gain/ muscle loss, extreme pain under rib cage esp. right side, tinnitis- always had it but seems louder, Charley horse one episode so extreme it felt like a bubble from the leg to the heart felt like a pop then dizziness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: blood test awaiting results
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroid
Andere Medikamente: synthroid Adderall Lisinopril vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 1904409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MA
Alter: 73,0
Geschlecht: M
Eingang: 28.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Balance disorder Fall Gait disturbance Lethargy Tremor Unresponsive to stimuli

Symptomtext

following morning after injection, fall out of bed, weak, lethargic, did not respond well to questions, impaired walking and balance, shaky knees, following morning fall off the couch

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: 3,0
Labordaten: sent to hospital on 11/12/21 emergency room was admitted then discahrged 11/15/21 to rehab then home 11/27/21.
Aktuelle Erkrankungen: none
Vorgeschichte: Traumatic brain injury 1972, HLD, CVA, Rhobdomyosis, depression, right sided hemiparesis
Andere Medikamente: simvastatin 40mg daily, namenda 20mg daily, zyrtec 10mg daily as needed, aspirin 325mg daily, multivitamin daily, vitamin d 400u daily, celexa 10mg daily, miralax as needed, trazodone 75mg bedtime, vitamin c 500md twice daily, baclofen 10mg
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1904074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IL
Alter: 29,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Dizziness Dyspnoea Hyperhidrosis Nausea Tremor

Symptomtext

1500- 1st dose Pfizer administered (lot #FH8020). Client is employee of host site 1507- patient complained of nausea and went into bathroom adjoining the clinic. NP followed client into bathroom. Diaphoretic. Attempts to vomit. Spits in toilet and takes sips of water. Chair brought into bathroom and clients sits. 1508- Ice packs applied, radial pulse 90s, BP 149/99, RR 22 Client denies allergies, hx of HTN, or medication use today. Says she has DM2. does not take insulin, but does take metformin. refuses graham crackers. 1510- Client says there is no improvement in nausea and now feels lightheaded. BP 170/98. RR 20, pulse 98, spO2 98% 1515- Client says she feels better and moves back to the room of the clinic. Drinking water and eating graham crackers. Does not want to lay down on yoga mat at this time. NP and RN in close proximity. 1525- Client says she is feeling increasingly lightheaded. Assisted to yoga mat x2. feet raised on chair. HR 105, systolic pressure 128, RR 26, shaky, A&0x 4. Breath sounds clear. 1527- Client says she feels SOB laying down. EMS called. now sitting up on mat. Breath sounds clear. No stridor in upper airway. skin appropriate color. no urticaria/ angioedema. Radial pulse 2+ , sp02 98% 1540- fire dept arrive, take vitals BP 120/70. HR 90s, spO2 98%. They ask client if she wants to go to the hospital and she says yes. 1545- EMS arrives. Patient unsure if she wants to go to one Hospital or the other as she is leaving site via stretcher

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none reported
Vorgeschichte: DM2
Andere Medikamente: denies taking any medication at that time but does take Metformin for DM2
Allergien: NKA
Vorherige Impfungen: -

VAERS 1903731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MS
Alter: 58,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 11.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Condition aggravated Hypersensitivity Pruritus

Symptomtext

My hand is still itching; The itching started yesterday but it got worse; I had an allergic reaction; I had it broken all over my face, all over my arms and my legs; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: FH8020), dose 1 via an unspecified route of administration, administered in left arm on 11Nov2021 (at age of 58-year-old) as dose 1, single for covid-19 immunization. Medical history included thyroid cancer and blood pressure from an unspecified date and unknown if was ongoing. Concomitant medications included levothyroxine (LEVOTHYROXINE) for an unspecified indication and amlodipine besilate (NORVASC) taken for blood pressure measurement start and stop dates are not reported for both. The patient did not receive any prior vaccinations within 4 weeks. The patient said, my hand is still itching, the itching started yesterday but it got worse on 12Nov2021, I had an allergic reaction; I had it broken all over my face, all over my arms and my legs (all medically significant) on Nov2021. The patient stated, "Yeah, I got my COVID shot Thursday, my Pfizer COVID shot, first shot Thursday at work and just today, I had been to emergency room. I had an allergic reaction. I had it broken all over my face, all over my arms and my legs and in the emergency room they gave me Benadryl and stuff and 'not clear'. My hand is still itching. That's why I called because I had an allergic reaction when I took the shot." Patient stated, "Yes I took my first. I will take my second 02Dec." Treatment for side effects (Other than Benadryl) was none. Patient stated, " Benadryl; No, they gave me in the emergency room. I don't know how many doses they gave me. They gave it my arm. They gave me an IV, so I don't know how many." For reassurance, patient stated, "No, that's it." Reporter seriousness for the events was unspecified. The outcome of events my hand is still itching, the itching started yesterday but it got worse not recovered, I had an allergic reaction; I had it broken all over my face, all over my arms and my legs was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Thyroid cancer (Verbatim: Thyroid cancer)
Andere Medikamente: LEVOTHYROXINE; NORVASC
Allergien: -
Vorherige Impfungen: -

VAERS 1903706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 35,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Chest pain Chills Headache Immunisation Lymph node pain Lymphadenopathy Pain Pyrexia

Symptomtext

Fever 103; headache; swollen/very painful lymph node under armpit; swollen/very painful lymph node under armpit; pain irradiated into chest; body aches; chills; booster; This is a spontaneous report from a contactable consumer. This 35-year-old female consumer (patient) reported that she received 3rd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, FH8020) booster dose single on 09Nov2021 02:30 PM at left arm for COVID-19 immunization at the age of 35 years old. Medical history included known allergies; Sulfa meds. Historical vaccine included 1st dose of BNT162B2 (lot EN6202) on 02Mar2021 at 07:00 AM at left arm and 2nd dose of BNT162B2 (lot EN6203) on 23Mar2021 07:30 AM at left arm both for COVID-19 immunization at the age of 34 years old. Concomitant drugs included diazepam, isopropamide iodide (VALTRAX), ethinylestradiol, norethisterone acetate (JUNEL) and cetirizine hydrochloride (ZYRTEC ALLERGY). The patient experienced fever 103, swollen/very painful lymph node under armpit, pain irradiated into chest, body aches, chills, headache on 09Nov2021 08:00 PM. No treatment was received for the events. The outcome of the events was not resolved. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211109; Test Name: Fever; Result Unstructured Data: Test Result:103
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: VALTRAX; JUNEL; ZYRTEC ALLERGY
Allergien: -
Vorherige Impfungen: -

VAERS 1903696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IA
Alter: 63,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Cough Dyspnoea Heart rate increased Immunisation Pain in extremity Throat irritation

Symptomtext

booster; Left arm really hurts; heart rate is 116 currently; cough; short of breath; Keeps clearing throat; This is a spontaneous report from a contactable consumer (patient). A 63-year-old female patient received bnt162b2 (COMIRNATY- formulation: solution for injection, Batch/Lot Number: FH8020), dose 3 via an unspecified route of administration, administered in Arm Left on 09Nov20211, (at the age of 63-year-old) as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation. The patient medical history and concomitant medications reported as none. The patient's historical vaccine included first dose of bnt162b2 (COMIRNATY- formulation: solution for injection, Batch/Lot Number: EN6206), dose 1 via an unspecified route of administration, on 05Mar2021, as DOSE 1, SINGLE for covid-19 immunisation and second dose of bnt162b2 (COMIRNATY- formulation: solution for injection, Batch/Lot Number: EN6204), dose 2 via an unspecified route of administration, on 26Mar2021, as DOSE 2, SINGLE for covid-19 immunisation. The patient experienced cough, short of breath, keeps clearing throat on 10Nov2021, and left arm really hurts, heart rate is 116 currently and booster on an unspecified date. Caller (patient) reported that, her Pfizer COVID-19 vaccine booster dose yesterday on 09Nov20211, around 14:30 she is complaining of a deep cough and having to clear her throat and while on the phone looked at her watch and her resting heart rate is 116 currently and since she is coughing so much right now is starting to get short of breath. She is wondering if this could be a possible side effect of the booster. She said she is just wondering, because she hasn't read it anywhere, if these are possible side effects. Patient denies any other medications, medical conditions, labs, testing, or treatments relevant to events. Patient stated that she does take medications, she doesn't think they are relevant because she took them before. Caller states that these symptoms started today. The patient underwent lab tests and procedures which included heart rate increased: 116 on an unspecified date. No therapeutic measures were taken as a result of the events. The outcome of the events was reported as unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: heart rate is 116 currently; Result Unstructured Data: Test Result:116
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1898175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: AL
Alter: 40,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Adverse reaction Chest discomfort Condition aggravated Dyspnoea exertional Ear pain Fatigue Heart rate increased Lip erythema Lip swelling Pruritus Tinnitus

Symptomtext

Immediately after the booster, I went to sit in the waiting area to wait 30 minutes. After just a few minutes, my left side of my jaw started itching really bad and my heartrate spiked. I monitored it on my watch, and it was 156bpm. I called the nurse over and my chest was feeling tight, and they observed me. Since then, I have had itching on the right side of my face. My bottom lip also swelled up and became red. It was not bad enough to go to the emergency room. I was monitored for 2 hours and then went home once my symptoms subsided. I also had extreme fatigue for days following. I also had a lot of ear pain in both ears, especially my left. My doctor prescribed a steroid cream called Mometasone 0.1% ointment. It does not completely help. I also have ear ringing occasionally. I still have difficulty breathing when exerting myself. I had bad reactions to all three Pfizer vaccines but the third was the worst.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Mitral Valve Prolapse
Andere Medikamente: Albuterol Sulfate 2.5 mg as needed Atrovent HFA 12.9g daily Azelastine HCI 0.1% daily via nostril Budesonide 1mg/2mL as needed Citalopram 10mg daily Flovent HFA 220mcg two puffs twice daily Ipratropium Bromide 0.5mcg as needed/ nasal solut
Allergien: Dairy Cefprozil Sensitive to: Divalproex Levaquin Nortriptyline Singulair Topamax Wellbutrin Zoloft
Vorherige Impfungen: Pfizer dose 1- 02/28/2021 and dose 2- 03/21/2021. I had been diagnosed with Pleurisy after both shots and had chest tightness. T

VAERS 1897593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: KY
Alter: 35,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Dyspnoea Fatigue

Symptomtext

The next day I began feeling fatigued and short of breath. It has been about 4 weeks and I am still feeling these symptoms. I thought it was my fibromyalgia, but this is worse than before, especially the shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia, long covid
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1896392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 43,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood test Hypoaesthesia Immunisation Lymph node pain Lymphadenopathy Off label use Paraesthesia

Symptomtext

The next day i also have swelling in my left lymph node and it still hurts; The next day i also have swelling in my left lymph node and it still hurts; tingling; numbness in both my legs and feet for several hours; booster; booster; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 43-year-old non pregnant female patient received bnt162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), dose 3 via an unspecified route of administration, administered in Arm Left on 07Nov2021 at 12:00 (Batch/Lot Number: FH8020) as DOSE 3 (BOOSTER), SINGLE (at the age of 43-year-old) for covid-19 immunisation. The patient was not pregnant at the time of vaccination. The patient medical history and concomitant medications were not reported. The patient did not have COVID prior to vaccination. Historical vaccine included first dose of bnt162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Batch/lot number: EL3247), via an unspecified route of administration on 01Mar2021 (at the age of 42-year-old) as dose 1, single and second dose of bnt162b2 PFIZER BIONTECH COVID-19 mRNA VACCINE, Batch/lot number: EL3247), via an unspecified route of administration on 22Mar2021 (at the age of 42-year-old) as dose 1, single for covid-19 immunisation. The patient did not receive other vaccine in four weeks. On 07Nov2021, the patient got all the same symptoms reported from first shot and adverse event plus tingling and numbness in both my legs and feet for several hours. The next day on 08Nov2021, the patient had swelling in left lymph node and it still hurts, that was patient observing. It was unknown if Covid tested post vaccination or not. The patient underwent lab tests and procedures which included blood test: unknown result on an unspecified date. The outcome of events reported as recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: Blood test; Result Unstructured Data: Test Result:Unknown Result
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2570361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chest discomfort Dyspnoea Electrocardiogram normal Troponin normal

Symptomtext

Narrative: Pt presented to ED with chest tightness and SOB that started morning after his 3rd dose. EKG was normal. He is currently experiencing a sensation of chest pressure in the middle of his sternum, he denies any neck or arm pain, no nausea, vomiting or diaphoresis. He feels slightly short of breath 2/2 chest pressure, not related to exertion. He has no cough or sputum production. Denies any fevers or chills. 71 year old male who presents with chest pressure and shortness of breath. Reassuring that his EKG is unchanged. Delta trop negative. Physical exam was also unrevealing. Overall seems pt's symptoms most consistent with post-vaccination physioloic response.

Weitere VAERSDATA-Felder

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

VAERS 1894038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 08.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram Angiogram abnormal Aortic arteriosclerosis Atelectasis Bronchial wall thickening Chest pain Echocardiogram Echocardiogram normal Electrocardiogram abnormal Hiatus hernia Mucosal hypertrophy Pericardial effusion Pleuritic pain Pulmonary fibrosis Pulmonary mass Troponin normal

Symptomtext

Atypical Chest pain Pleuritic Chest pain Pt presents with pleuritic chest pain in context of recent RT treatment CTA negative, initial trop neg, initial EKG w/out signs of acute ischemia Repeat EKG (11/14) showing diffuse ST elevations D/W on call cardiology (see significant event note) Lexiscan without signs of ischemia> current concern for Pericarditis No viral prodrome, did receive COVID booster a couple days ago (unsure if re;ated at this point) Will start course of NSAID/PPI + prednisone taper, (drug interaction between colchicine and coreg) Cycle trop> neg, recent TTE performed no sig WMA, CTA with trace pericardial effusion Cardiology/ PCP follow up consults placed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CTA Chest FINDINGS: Tubes, catheters and devices: A port catheter terminates in the lower SVC. The port reservoir overlies the right pectus musculature. Pulmonary arteries: Bolus timing is insufficient for definitive exclusion of small peripheral pulmonary emboli. Within these confines no definite pulmonary embolism appreciated. Aorta: Moderate atherosclerotic disease of the aorta without dissection or aneurysm. There is a common origin of the brachiocephalic and left common carotid arteries resulting in a 2 vessel aortic arch morphology. Lungs: No dominant pulmonary mass or discrete airspace consolidation. Dependent atelectasis and areas of pulmonary scarring are appreciated. Suspected subtle developing peribronchial nodular opacities and mild bronchial wall thickening in the right upper lobe and left lung base. Although this could reflect post treatment changes, in the acute setting developing multifocal bronchiolitis should be considered. Consider short interval follow-up imaging in 3 months to confirm resolution. Pleural spaces: Unremarkable. No pneumothorax. No pleural effusion. Heart: Heart size is stable. However there is a trace pericardial effusion. Lymph nodes: No enlarged lymph nodes. Previous left axillary lymph node dissection. Diaphragm: A 2.2 cm hiatal hernia with mild distal esophageal mucosal thickening is redemonstrated. Intraperitoneal space: Limited assessment of the upper abdomen. Within these confines no acute inflammatory change appreciated. Bones/joints: Diffuse demineralization. No definite acute fracture. Soft tissues: Interval left axillary dissection with surgical clips and residual soft tissue scarring. New postsurgical left chest wall thickening status post mastectomy. IMPRESSION: 1. No definite evidence of an acute pulmonary embolism. 2. Suspected subtle developing peribronchial nodular opacities and mild bronchial wall thickening in the right upper lobe and left lung base. Although this could reflect post treatment changes, in the acute setting developing multifocal bronchiolitis should be considered. Consider short interval follow-up imaging in 3 months to confirm resolution. 3. Evidence interval left mastectomy and left axillary dissection. Lexiscan Conclusion Normal global and regional wall motion in all territories. Abnormal EKG. Normal rest and stress perfusion. . LVEF= 76%. Given abnormal EKG and no evidence of ischemia conisder echocardiogram is not done if pericarditis is suspected.
Aktuelle Erkrankungen: Malignant neoplasm L breast , estrogen receptor positive 3/22/2021
Vorgeschichte: Hypercholesterolemia w/o hypertriglyceridemia 3/17/2018 STEMI involving left anterior descending coronary artery 3/14/2018 Severe Hypertension 3/14/2018 CAD 4/2/2018 Iron def. anemia 4/29/2021 s/p left mastectomy 9/10/2021
Andere Medikamente: Aspirin 81 mg daily Atorvastatin 20 mg daily Calcium Vit D3 500mg-200 unit tab daily Carvedilol 3.125 mg bid Isorbide mononitrate 30 mg daily Loratadine 10 mg daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 1893454

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: MD
Alter: 77,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 26.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chest pain Dizziness Flushing Hyperhidrosis

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium

Weitere VAERSDATA-Felder

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

VAERS 1893120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: GA
Alter: 73,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood creatine phosphokinase Blood creatine phosphokinase MB Chest pain Full blood count Immunisation Interchange of vaccine products Metabolic function test Off label use Product use issue SARS-CoV-2 test

Symptomtext

Chest pain left side of chest; Dose Number: 1 Moderna /Dose Number: 2 Moderna/ Dose Number: 3 Pfizer; Dose Number: 1 Moderna /Dose Number: 2 Moderna/ Dose Number: 3 Pfizer; Dose Number: 1 Moderna /Dose Number: 2 Moderna/ Dose Number: 3 Pfizer; vaccine received same date: Moderna; This is a spontaneous report from a contactable consumer (patient). A 73-year-old male patient received the third dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: FH8020), in arm left on 25Oct2021 14:15 (at the age of 73-years-old) at dose 3 (booster), single for COVID-19 immunisation; COVID-19 vaccine MRNA (MRNA 1273) (MODERNA COVID-19 VACCINE; lot number: 012M20A) in arm left on 25Oct2021 at dose 3, single (reported as Dose Number: 1) for COVID-19 immunisation. Medical history included high blood pressure, cholesterol, prostate. The patient had not known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included unspecified medications received within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received second dose of MODERNA vaccine (lot number: 024M20A) in arm left on 03Mar2021 11:00 (at the age of 73-years-old) and first dose of MODERNA vaccine (lot number: 012m20A) in arm left on 27Jan2021 07:45 (at the age of 73-years-old), both for COVID-19 immunisation. The patient experienced chest pain left side of chest on 26Oct2021 07:00 AM. The event was reported as serious due to hospitalization for 1 day. The event resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care visit. The patient underwent lab tests and procedures, which included nasal swab on 25Oct2021 with unknown results; since the vaccination, the patient had been tested for COVID-19; in Oct2021 complete blood count (CBC) with auto differential, creatine phosphokinase (CK) total and CKMB, comprehensive metabolic panel (CMP), all with unknown results. An unspecified treatment was received for the event. The patient had not recovered from chest pain left side of chest, the outcome of the other event was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Test Date: 202110; Test Name: CK total; Result Unstructured Data: Test Result:Unknown results; Test Date: 202110; Test Name: CKMB; Result Unstructured Data: Test Result:Unknown results; Test Date: 202110; Test Name: CBC with auto differential; Result Unstructured Data: Test Result:Unknown results; Test Date: 202110; Test Name: CMP; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211025; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood cholesterol abnormal; Blood pressure high; Prostatic disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1893113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TN
Alter: 77,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Bursitis Condition aggravated Immunisation

Symptomtext

administered in Arm Left on 04Nov2021 11:30 as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation.; Dysfunctional left hip, I regarded as a disabling bursitis flare-up (I cannot walk now) of a non-disabling painful condition that had been annoying for about 1-2 mo.; Dysfunctional left hip, I regarded as a disabling bursitis flare-up (I cannot walk now) of a non-disabling painful condition that had been annoying for about 1-2 mo.; This is a spontaneous report from a contactable physician (patient). A 77-year-old (age at vaccination) male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 3 via an unspecified route of administration, administered in Arm Left on 04Nov2021 11:30 (Batch/Lot Number: FH8020) as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation. Medical history included prostate cancer (Prostate ca (treatment seems to be successful). MI in 1995) from 1995 to an unknown date, dysfunctional left hip from an unknown date. Concomitant medications included abiraterone acetate (ZYTIGA); denosumab (XGEVA); prednisone and metoprolol all taken for an unspecified indication, start and stop date were not reported. The patient received the first dose (at 77-years-old) of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) administered in right arm on 12Apr2021 10:15 (Batch/Lot number: ER8729) and the second dose (at 77-years-old) administered in left arm on 03May2021 10:30 (Batch/Lot number: EN6205) for covid-19 immunisation. The patient experienced dysfunctional left hip, which he regarded as a disabling bursitis flare-up (he cannot walk now) of a non-disabling painful condition that had been annoying for about 1-2 months on 04Nov2021 22:30. The event was considered disabling. The patient did not receive treatment for the event. The patient did not recover from the event.; Sender's Comments: Based on the information currently available,The casual association between the reported events and suspected vaccine BNT162B2 cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Joint dysfunction; Prostate cancer (Prostate ca (treatment seems to be successful). MI in 1995)
Andere Medikamente: ZYTIGA; XGEVA; PREDNISONE; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1888491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: SC
Alter: 22,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Bradycardia Dyspnoea Extrasystoles Tachycardia Tremor Vision blurred

Symptomtext

Heart became tachycardic ( 140 - 160 beats/min) then It would become bradycardic (50 beats/min) and sometimes skip a beat. During this time, I was short of breath and had blurry vision. I also experienced tremors of both hands. This lasted approximately 15 minutes before bedtime at 10:30pm the SAME day I received the shot. Heart rate and SpO2 was measured by pulse oximetry and palpitating pulses. SpO2 would go from about 85% to 100% on room air.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None performed
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None before time of vaccination
Allergien: None
Vorherige Impfungen: -

VAERS 1887890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: GA
Alter: 74,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Flushing Hyperhidrosis Nervousness Tremor

Symptomtext

Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Mild, Additional Details: pt is diabetic, was very nervous prior to vaccine administration. states she has not eaten in several hours. pt given water and piece of candy in case blood sugar low. pt fine at time of leaving

Weitere VAERSDATA-Felder

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

VAERS 1882631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 58,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal discomfort Abdominal pain upper Adnexa uteri pain Angina pectoris Biliary colic Dizziness Dysgeusia Hepatic pain Hot flush Migraine Nausea Oropharyngeal pain Tonsillar hypertrophy

Symptomtext

Migranes, hot flashes, dizziness, nausea, stomach upset, pin pain heart, swollen tonsils, pin pain gallbladder, pin pain area liver, pin pain area pancreas, chemical taste, sore throat, pain both side of ovaries.

Weitere VAERSDATA-Felder

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

VAERS 1882621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 43,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 27.09.2021
Beginn: 27.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Fatigue Headache Heart rate irregular Vaccine positive rechallenge

Symptomtext

Severe headache, irregular heartbeat, tiredness and fatigue since first shot and getting worse after second shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1881288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MA
Alter: 60,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 09.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Dry mouth Paraesthesia oral

Symptomtext

Pfizer Booster Vaccine given. At 9:13am the pt reported dry mouth. Pt encouraged to drink water. Pt then reported tingling lips and feeling anxious. Pt escorted to nursing station. VS - BP - 134/75, HR 87, 02 98%. Pt encouraged to continue to drink and deep breath. Continued to monitor. Pt reported symptoms resolved and requested to return to her vehicle. Pt escorted to vehicle. Continued to monitor. Pt reported feeling good to go after 30 mins of observation. Pt was reassessed and cleared to leave clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: OTC Vitamins
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 1880672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: PA
Alter: 44,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chills Fatigue Headache Injection site pain Musculoskeletal stiffness Impaired work ability Loss of personal independence in daily activities Migraine Neck pain Pain

Symptomtext

Within four hours of the vaccine, she developed severe migraine, neck pain and stiffness , extreme fatigue and chills. She was prescribed steroids and recommended Ganoderma Lucidum for it's anti-inflammatory effects. She could not go to work for 7 days after the vaccine. There are lingering migraine and the worst symptom is fatigue, limiting her ability to take care of herself and her daily work. She sleeps 12 hours per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's Thyroiditis, Thyroid nodule, Iron deficiency, Chronic migraine with aura, GERD, Mycoplasma pneumoniae infection, Magnesium deficiency, Mixed hyperlipidemia, Vitamin B12 and folate deficiency, Abnormal weight loss, Muscle weakness, Benign paroxysmal vertigo.
Andere Medikamente: Tylenol, Vit C.
Allergien: Allergic to peas. Sensitivity to corn , eggplants, gelatin , pollen and tree allergy. Allergic to Polysorbate per testing done on 11/4/2021.
Vorherige Impfungen: In 2019, she developed a severe neuroimmune reaction after Influenza vaccine. She was 42 years old. Other information about the

VAERS 1877724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / LA

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

Blood test normal Blood thyroid stimulating hormone normal Computerised tomogram head normal Dizziness Electrocardiogram normal Lymphocyte count normal Lymphocyte percentage decreased Nausea Neutrophil count increased Neutrophil percentage increased Paraesthesia Paraesthesia oral Vertigo White blood cell count increased

Symptomtext

Dizziness/vertigo, nausea (started on 11/6 and has been present since tingly cheeks/chin/lips (started 11/16) Emergency room via ambulance on 11/8 due to extreme dizziness when driving - treated with fluids and antivert 25mg and released. Had bloodwork, head ct, ekg - all normal Saw Neurologist 11/10 PT- started 11/16

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Head ct : normal Ekg: normal Blood work: relatively normal Thyroid stimulating hormone : 4.586 White blood cells : 12.3 Neutrophils, percent: 82.7 Neutrophils, absolute: 10.2 Lymphocytes, percent: 10.7 Lymphocytes, absolute: 1.3
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Paxil: 10mg Ativan: .05 mg as needed
Allergien: Adverse reaction to pseudoephedrine
Vorherige Impfungen: -

VAERS 1877711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: PA
Alter: 52,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia Body temperature increased Chills Decreased appetite Disturbance in attention Dizziness Dyspnoea Fatigue Feeling cold Gait disturbance Headache Impaired work ability Influenza like illness Malaise Oropharyngeal pain Pain Poor quality sleep SARS-CoV-2 test negative

Symptomtext

Sunday Nov 7th-In the morning I felt tired around 12PM. I got the chills, it got worst, had 3 blankets, head hurting, and body aching. I felt like I had the flu. Temperature 99.8. Slept for 4 hours, woke up, and still felt sick. Then slept most of the day. I could barely walk. Was too dizzy to walk. Got in the shower, felt dizzy and lightheaded in the shower, also felt faint. Went back to slept for the evening, kept tossing and turning, and drank water. No appetite but had a little soup. Monday Nov 8th- Head hurting, chills had a blanket on me. Temperature 99.2. Went to a job site at 3:20PM, felt shortness of breath so left to go home. Went home still felt lightheaded, body aches, and cold. Tuesday Nov 9th- Went to work with a sore throat, felt tired, achy and weak but no temperature. Couldn't focus and sneezed a few times. Wednesday Nov 10th- Went to work couldn't keep my eyes open, achy, and sore throat. Thursday Nov 11th-Didn't go to work. Still had lack of energy. Nov 12th, 13th, 14th -Didn't go to work. Felt better Friday. Returned to work on Nov 15th.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Called doctor Nurse line Nov 11th= Told me to get an over-the-counter COVID-19 test - Negative Patient first on Nov 11th=They administer the COVID-19 Test - Negative
Aktuelle Erkrankungen: High Blood Pressure Pre-diabetes Underactive Thyroid
Vorgeschichte: High Blood Pressure Pre-diabetes Underactive Thyroid
Andere Medikamente: Lisinopril 10mg 1xday Levothyroxine 112 mcg 1xday Hydrochloride 2.5mg 1xday
Allergien: Penicillin Bactrim Erythromycin Cipro Latex
Vorherige Impfungen: -

VAERS 1877101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 31.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test normal Burning sensation Disturbance in attention Electrocardiogram normal Impaired work ability Lymphadenopathy Migraine Paraesthesia Pruritus Urine analysis normal Vaccine positive rechallenge

Symptomtext

For 3 days under my armpit/lymph nodes like oval. 7 November Sunday night Feet started burning, and on Monday am my feet felt like it's on fire, legs were tingly and itchy, and Wednesday burning on the skin of tummy. Couldn't focus and migraines. I couldn't even work from home. Telehealth on Monday. I thought it was antibiotic and drink lots of water and Benadryl. 10 went to ER. Had the second, I had the same reaction for 2nd dose, and it was worst this time. EKG, Bloodwork, urine test, Pain and uninflammatory Sunday evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: EKG Bloodwork Urine Test Results all normal
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: None
Allergien: No
Vorherige Impfungen: Polio vaccine on my right thigh, and I was paralyzed for a while and recovered.

VAERS 1877035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 56,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Musculoskeletal stiffness Peripheral swelling Tremor

Symptomtext

On 10/17/2021 hands started to shake so bad that spilling hot things on myself, that lasted till this day. Fatigue, joint pain, both ankles and toes are stiff, all joints are painful, swelling in the top part of left foot-still ongoing as of today. My doctor is on vacation till 11/29, I have an appointment scheduled for 11/30 to get tests done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Diabetes High Blood Pressure High Cholesterol
Andere Medikamente: I took Metoprolol 100mg twice a day Jardiance 10mg once a day Montelukast Sodium 10mg Gabapentin 300mg three times a day
Allergien: Aspirin Penicillin NSAIDS
Vorherige Impfungen: 04/17/2021 Pfizer-hard time breathing

VAERS 1876520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IN
Alter: 29,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Chest discomfort Chest pain Dyspnoea Heart rate increased Hypoaesthesia Palpitations Paraesthesia Pyrexia Wheezing

Symptomtext

Fever, Wheezing, Tightness in Chest, trouble breathing, fast heart beat, weakness, numbness and tingling, chest pain, shortness of breath, heart pounding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: N/a
Allergien: N/a or Known
Vorherige Impfungen: -

VAERS 1872809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TN
Alter: 23,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 22.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Body temperature Condition aggravated Cough Incorrect dose administered Nasal congestion Nausea Rhinorrhoea

Symptomtext

Patient was given an incorrect dose of the Pfizer Covid 19 vaccine. We were giving booster doses and the staff member administering patients vaccine though that Pfizer vaccine was like the Moderna vaccine and the booster doses were only half the amount of the initial and secondary doses. Due to this error patient was given 0.6ml of Pfizer Covid 19 vaccine. Her symptoms post vaccine were simiilar to her initial vaccine symptoms with temp, cough, stuffy/runny nose, nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: NOne
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: None reported
Vorherige Impfungen: -

VAERS 1869018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 42,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Adverse reaction Blood glucose normal Electrocardiogram normal Pharyngeal paraesthesia Throat irritation

Symptomtext

Client received 1st dose of vaccine at 8:58 am via IM to L deltoid. She is a 42 y/o female in observation area complaining of tingling sensation and itching to the back of the throat noted. Encouraged client to rest and relax. County Fire Rescue arrived to the scene for further evaluation. Vital signs: BP 120/78, HR 66, Temp. 98.6, O2 98% via room air, Blood Sugar 96 and EKG normal sinus. Client observed for an additional 15 min. Client states allergy but unable to state specifically what she is allergic to. Post additional 15 min. observation time client states that tingling sensation and itching to the back of the throat has subsided and refused hospitalization and left observation area and recovered at 9:45am. Client noted with no difficulty breathing or any additional adverse reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: BP 120/78, HR 66, BS 96, O2 98%, T 98.6 and EKG NS.
Aktuelle Erkrankungen: n/a
Vorgeschichte: HTN
Andere Medikamente: n/a
Allergien: Pt. states unknown allergy
Vorherige Impfungen: -

VAERS 1868851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CT
Alter: 45,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

Shortness of breath. Went away after 48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Obesity
Andere Medikamente: Patel Multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 1814157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: PR
Alter: 23,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Blood glucose increased Malaise Palpitations Blood glucose normal Feeling abnormal

Symptomtext

Patient of 23 years comes to the vaccination center at 6:55 to be evaluated since she felt palpitations. Patient indicates after receiving her booster dose of Pfizer at 5:34 she went shopping and at 6:50 she started feeling unwell. Patient is taken to treatment and observation area to be evaluated by EMT and her vital signs were 11/70b/p 114 pulse and 122dxt Case was consulted with Dr and refers to transport patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1868289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: KS
Alter: 31,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthma Dysmenorrhoea Dyspnoea Extra dose administered Impaired work ability

Symptomtext

Asthma attack - difficulty breathing, used rescue inhaler. Asthma was controlled prior to vaccination. Severe Dysmenorrhea - missed two days of work. Typically, first day of menstruation is worst. This occurred on the 3rd and 4th days of menstruation after booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Endometriosis, asthma, allergies
Andere Medikamente: Pepcid complete, montelukast, melatonin, vitamin D, Tylenol
Allergien: Zyrtec, corn, cucumbers, oats, almonds
Vorherige Impfungen: Syncope age 18 hpv vaccine second dose

VAERS 1867360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MA
Alter: 58,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Abdominal pain upper Body temperature Diplopia Fatigue Headache Migraine Muscular weakness Myasthenia gravis Nausea Pyrexia

Symptomtext

Exacerbation of Myasthenia Gravis (flare) drooping left eye; stomach pain; Fever 103.1 for 10 hours then fever 100.0-101.4 for 24 hours; muscle weakness; fatigue; seeing double; headache; migraine; nausea; This is a spontaneous report from a contactable consumer (patient). A 58-years-old female patient received bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection; Batch/Lot Number: FH8020), via an unspecified route of administration, administered in Arm Right on 28Oct2021 at 10:00 (at the age of 58 years old) as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation. Medical history included myasthenia gravis, lupus cystitis, scleroderma, raynaud's phenomenon, intervertebral disc degeneration, fructose intolerance. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Concomitant medications included prednisone, diltiazem, pyridostigmine, bromide, hydrochlorothiazide, triamterene and ezetimibe. The patient received second dose of BNT162B2 (PFIZ-ER-BIONTECH COVID-19 VACCINE, Lot number: ER2613) in right arm on 18March2021 at 2:30 for covid-19 immunisation. The patient received first dose of BNT162B2 (PFIZ-ER-BIONTECH COVID-19 VACCINE, Lot number: EN6200) in right arm on 22Feb2021 at 11:15 for covid-19 immunisation. bnt162b2 for covid-19 immunisation, lyrica and experienced drug hypersensitivity, gabapentin and experienced drug hypersensitivity. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient experienced exacerbation of myasthenia gravis (flare) drooping left eye, stomach pain, fever 103.1 for 10 hours then fever 100.0-101.4 for 24 hours, muscle weakness, fatigue, seeing double, headache, migraine, nausea on 28Oct2021 14:00. 4 hours after vaccine -Fever 103.1 for 10 hours then fever 100.0-101.4 for 24 hours. Exacerbation of Myasthenia Gravis (flare) drooping left eye and muscle weakness, fatigue, seeing double, headache, migraine, nausea, stomach pain. The patient underwent lab tests and procedures which included body temperature result was 103.1 on 28Oct2021, body temperature result was 100.0-101.4 for 24 hours on 28Oct2021. The patient did not receive any treatment for the events. Facility type Vaccine result was Hospital. The outcome of exacerbation of myasthenia gravis (flare) drooping left eye, stomach pain, fever 103.1 for 10 hours then fever 100.0-101.4 for 24 hours, muscle weakness, fatigue, seeing double, headache, migraine and nausea was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20211028; Test Name: Body Temperature; Result Unstructured Data: Test Result:103.1; Test Date: 20211028; Test Name: Body Temperature; Result Unstructured Data: Test Result:100.0-101.4 for 24 hours
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Degenerative disc disease; Drug allergy (Allergy); Fructose intolerance (Allergy); Lupus cystitis; Myasthenia gravis; Raynauds; Scleroderma
Andere Medikamente: PREDNISONE; DILTIAZEM; MESTINON; DYAZIDE; EZETIMIBE
Allergien: -
Vorherige Impfungen: -

VAERS 1865041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Anxiety Blood test Blood thyroid stimulating hormone Decreased appetite Depersonalisation/derealisation disorder Dizziness Dyspnoea Fatigue Hypovitaminosis Panic attack Serum ferritin

Symptomtext

Beginning on Friday Nov 5th, fatigue, daily debilitating panic attacks and uncontrollable anxiety. Lightheadedness, loss of appetite, shortness of breath, depersonalization. Still ongoing till today November 12.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Vitamin deficiency panel, TSH, ferritin, blood sugar level, tested on November 11, all came out good.
Aktuelle Erkrankungen: Anxiety, depression, gastrointestinal issues (constipation, sensitivity to food)
Vorgeschichte: Anxiety, depression, gastrointestinal issues (constipation, sensitivity to food)
Andere Medikamente: Over the counter Probiotic, women's multi vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1865001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 42,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 18.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac flutter Extrasystoles Palpitations

Symptomtext

Heart skipped a beat, then fluttered, then was beating extremely hard for over 24 hours. I went to the ER, they were unable to find anything wrong. I did not feel better for several days

Weitere VAERSDATA-Felder

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

VAERS 1864536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 24,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Arthralgia Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1861567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: SC
Alter: 56,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Condition aggravated Fatigue Headache Interchange of vaccine products Oedema peripheral Pyrexia

Symptomtext

1 day after vaccine, experienced swelling in left armpit. Chills, fever, fatigue, headache. Swelling in armpit is continuing through second day followimg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ulcerative Colitis, Depression, Anxiety disorder
Andere Medikamente: Lorazepam, Trintellix, vitamin B12, D
Allergien: Erythromycin
Vorherige Impfungen: Moderna covid, 2020, similar side effects.

VAERS 1861384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 16.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Confusional state Impaired work ability Injected limb mobility decreased Joint swelling Mass Muscle swelling Peripheral swelling

Symptomtext

After my second shot I have had swollen muscles and joints. Day two after my shot I had a lump start on my left arm above my wrist on right side and was unable to move or work on my job that I was designated to do that day. My left middle finger has been swelling up and making my job more difficult to do. Also I was feeling confusion for a week or two on and off.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Just told my doctor during physical.
Aktuelle Erkrankungen: N/A
Vorgeschichte: -
Andere Medikamente: Metroprolol 100 MG, hyoscyamine .25mg
Allergien: Morphine
Vorherige Impfungen: -

VAERS 1861253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: SC
Alter: 48,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Dizziness Feeling hot Heart rate increased Tachycardia

Symptomtext

Symptoms experienced within 3-5 minutes of vaccine administration: rapid heart rate of 130=140 bpm, regular rate, palpated right radial pulse. Chest heaviness, lightheaded, feeling warm. The above symptoms were experienced with the 1st dose, too.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Took Atenolol 12.5 mg for tachycardia. Rapid heart rate subsided within 15 min. No EKG, went home. Took Aspirin 81 mg. Will have Holter Monitor placed.
Aktuelle Erkrankungen: No chronic illness.
Vorgeschichte: Covid-19 in December 2020. Intermittent tachycardia at times.
Andere Medikamente: None on the day prior to vaccination.
Allergien: Sulfa, PCN, Ativan.
Vorherige Impfungen: Yes, with 1st dose of Covid-19 vaccine. Pfizer on 03/15/2021, age:47.

VAERS 1858439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 26.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / AR

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

Abdominal pain Asthenia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram abdomen normal Cough Dyspnoea Fatigue Gastrointestinal disorder Hypoxia Laboratory test normal Lung opacity Mobility decreased SARS-CoV-2 test positive Troponin increased

Symptomtext

Hospitalized (11.5.21); COVID-19 positive (11.5.21); fully vaccinated PLUS booster Admission Date: 11/5/2021 Discharge Date: 11/6/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Weakness [R53.1] Elevated troponin [R77.8] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: 85 yo M hx CAD, HLD, NHL, T2DM presented to ER on 11/5 with several days of fatigue, weakness, poor mobility, shortness of breath and cough. He had recently received his COVID19 booster shot approximately 2 weeks ago. On arrival to ER he is found to be hypoxic and placed on supplemental oxygen. His COVID19 PCR came back positive. CXR showed groundglass patchy opacities that could be of viral etiology. A CT Abdomen was obtained due to vague complaints of gastrointestinal issues, this imaging test was unremarkable. Labs were also unremarkable. Patient was admitted to Medicine service for further management of COVID19 pneumonia. He was started on decadron. Over the course of the following day, patient's symptoms improved drastically, particularly after initiation of steroids. His fatigue, abdominal pain, shortness of breath were resolved. He was able to wean from oxygen to room air and maintained his saturations. PT and OT recommended home with assist and home care. Patient is discharging home to complete 3 more days of decadron, during which time he has been advised to take 4 additional units of long acting insulin. Home health services will be set up. He will follow up with his primary care physician.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary artery disease Hyperlipidemia Hypertension Type 2 diabetes mellitus Ischemic cardiomyopathy Facial palsy LV (left ventricular) mural thrombus without MI Pneumonia due to COVID-19 virus
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler carvedilol (COREG) 12.5
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1857411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NV
Alter: 59,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Breast tenderness Injection site bruising Injection site pain Injection site swelling Lymphadenopathy Musculoskeletal chest pain Tenderness

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: swelling and tenderness in armpit/left side of breast/ left side of ribs-Medium, Systemic: Lymph Node Swelling-Medium, Additional Details: pt stated rxn started about 48 hours after receiving third booster of pfizer, previous 2 doses were pfizer, she states tenderness and swelling in left armpit area, on side of left breast and down left side of her ribs. She states no worsening of symptoms ( since 11/07/2021) and that ibuprofen helps with the pain. no limitation in mobility but tender/ and feels swollen. counselled pt to reach out to MD to look at, especially if symptoms worsen.

Weitere VAERSDATA-Felder

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

VAERS 1857159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Chest discomfort Chest pain Dizziness Fatigue Lethargy Nervous system disorder

Symptomtext

Systemic: Abdominal Pain-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Neurological Disorder (diagnosed by MD)-Severe

Weitere VAERSDATA-Felder

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

VAERS 1854873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: SC
Alter: 41,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Fatigue Mobility decreased Pain Pyrexia

Symptomtext

On Tuesday, 8 hours after the shot, extreme body aches, soreness, and over all tiredness began. Very weak and had issues climbing stairs and moving from a resting position. This lasted through the night, all day Wednesday, and most of Thursday, finally tapering off on Friday. Fever began Tuesday night about 10 hours after the shot and lasted about 12 hours until Wednesday afternoon. Body Aches/soreness/weakness - ~54 hours total over 3 days. Fever - ~12 hours Treatments - Rest, hydration, and two Advil twice a day. As of today Tuesday November 9 I feel back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None, at home care only with electronic conversations with primary care doctor.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Nexium
Allergien: None
Vorherige Impfungen: -

VAERS 1854808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WA
Alter: 50,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 23.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / AR

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

Blood test Chest pain Differential white blood cell count Electrocardiogram Fibrin D dimer Full blood count Influenza A virus test negative Influenza B virus test Platelet count SARS-CoV-2 test negative

Symptomtext

Chest pain, possibly costochondritis related to Asthma, but d-dimer tests returned with flag and elevated/abnormal WBC and platelet count suggesting mild local (non-systemic) infection. Emergency Room visit to rule out PE in relation to d-dimer tests. Broad spectrum immune support to treat mild infection systems. Still resolving, but better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: To many to list here, but from memory d-dimer tests, then during ER visit ~ 11/2 Influenza A/B, COVID etc. (all negative), CBC w/ differential, Platelet and EKG.
Aktuelle Erkrankungen: None that I knew of.
Vorgeschichte: Asthma (non-acute cough)
Andere Medikamente: To many dietary supplements to list here that have never before been problematic.
Allergien: Antibiotics cause gut distress and occasionally rash.
Vorherige Impfungen: -

VAERS 1853457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 28.09.2021
Beginn: 05.10.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Dyspnoea Headache Musculoskeletal pain Neck pain Pain in extremity Swelling face Urticaria

Symptomtext

Headache, shortness of breath, face swelling, body hives, upper torso - neck, shoulder, arm and shoulder blade pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Allergies and asthma
Vorgeschichte: N/A
Andere Medikamente: Zyrtec
Allergien: Benzoyl peroxide
Vorherige Impfungen: -

VAERS 1852035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NJ
Alter: 51,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest discomfort Dyspnoea Spirometry Wheezing

Symptomtext

I received the vaccine at approximately 7:45pm. At approximately 3:00am, I awoke with shortness of breath and my lungs felt heavy. I was also wheezing. I used my inhaler, but it did not alleviate my symptoms. I waited to see if the symptoms would go away on their own; however, they did not. Six days later I went to see the Dr. and he prescribed a course of prednisone and told me to continue using my inhaler as needed. After I was finished taking the prednisone, I did feel better; however, I do still experience shortness of breath from time to time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: On October 26, 2021, when I saw the Dr., they did a chest exam, blood work, a chest xray, amd a spirometry breathing test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma, High Blood Pressure, Gout
Andere Medikamente: Amlodipine, Allopurinol, Albuterol
Allergien: Aspirin
Vorherige Impfungen: -

VAERS 1851619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MI
Alter: 19,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 17.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chest X-ray Chest pain Dyspnoea Electrocardiogram Heart rate increased Hypertension Palpitations Pyrexia

Symptomtext

Shortness of breath, chest pain, high blood pressure and BPM, fever, chest pounding

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, chest xray, IV
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1851120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Magnetic resonance imaging head normal Migraine Pain Photophobia Photopsia Visual impairment

Symptomtext

The evening that I got my third dose of the vaccine, I got a pounding Migraine. After the first dose, I had a mild headache. I do not get headaches or Migraines normally. I went to the Urgent Care on the third day, after and the Toradol shot, and it did help. I returned to the ER the next day and they gave me a cocktail of painkillers. It did not really help the pain. The migraine finally subsided on 10/17/2021. When I woke up that morning, I had flashing lights in my vision. I now have a variety of vision problems after a month. I have since had a two-hour eye exam and an MRI of my Brain. All tests have been negative, except that that they want to test my vision angles, which could have been due to inflammation. I see flashes of light, and I am very sensitive to light, as well as flashing lights at the edge of my vision. It does not seem to be improving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 10/13/2021- Urgent Care 10/14/2021-ER, Hospital- MRI Optometry Dose 1: 02/27/2021 EN6201 Dose 2: 03/20/2021 EN6207
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Wellbutrin 150mg
Allergien: N/A
Vorherige Impfungen: -

VAERS 1850938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Condition aggravated Hypoaesthesia Hypoaesthesia oral Paraesthesia Paraesthesia oral

Symptomtext

Vitals: 11/08/21 1037 11/08/21 1042 BP: (!) 155/90 125/81 Pulse: 67 66 Resp: 18 15 SpO2: 100% 100% Vital signs at 1058 BP 122/80, HR at 66, sat 99% in room air 1037 Patient c/o numbness and tingling in the lips and right fingertips. Taken to gurney. Checked vital signs. Please see vital signs. Denies pain, denies SOB, no redness, no swelling in lips, tongue or throat. No rash noted. Speaks in full sentences. No audible wheezing noted. Patient states the same thing happen on his first dose, benadryl helped per patient. 1040 bendaryl given 25mg ORAL x1 1042 patient states the numbness in the lips is going away, but numbness to fingers still present Vital signs remain stable at this time 1053 remains stable. Denies pain, denies SOB, no redness, no swelling in lips, tongue or throat. Speaks in full sentences. No audible wheezing noted. 11:00 patient states he is having chest pain. 1/10. New onset, never happened before per patient. Vital signs stable. 130/76, 64HR 100% in roomair. Afebrile. Placed in 2LNC Paramedics called Taken via gurney to ER for further eval

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: anxiety
Vorgeschichte: anxiety
Andere Medikamente: vit d
Allergien: reaction to 1st dose pfizer, numbness and tingling in tongue and lips. vital signs stable. allergist suggested patient to take anti allergy prior to appt. patient denies
Vorherige Impfungen: -

VAERS 1849483

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 59,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Paraesthesia

Symptomtext

Tingling in lower legs, sometimes in feet also started morning after vaccine. Periods of dizziness started 2nd day after vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None done. It is the weekend and I have not notified my Primary Care Physician yet. I plan to call Monday morning if still have these side effects.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1848660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 55,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Tachycardia

Symptomtext

Systemic: Tachycardia-Medium, Additional Details: told her to go to hospital immediately for observation and evaluation. I told her son she shouldn't be driving and if he was unable to bring her to call for an ambulance immediately.

Weitere VAERSDATA-Felder

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

VAERS 1848581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: VA
Alter: 50,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Blood pressure measurement Dizziness Hypertension Nasopharyngitis Tremor

Symptomtext

High blood pressure if 206; Dizziness; Uncontrollably Shaking; Cold; This is a spontaneous report from a contactable consumer (patient). This 50-year-old female patient (not pregnant) received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number FH8020) at single dose via an unknown route in right arm on 29Oct2021 11:30 at 50-year-old for Covid-19 immunization. Prior to vaccination, the patient was not diagnosed with COVID-19. Medical history included diabetes. Patient received other medications the patient received within 2 weeks of vaccination; did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Past drug history included Ace inhibitors and celecoxib (CELEBREX) and experienced allergy. Patient experienced dizziness, uncontrollably shaking, cold, high blood pressure "if 206" (as reported) on 29Oct202111:30. The adverse event result in doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient had not been tested for COVID-19. No hospitalization involved. No treatment was received. Outcome of the events was unknown. The report was assessed as serious with seriousness criteria of life threatening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20211029; Test Name: Blood pressure; Result Unstructured Data: Test Result:206; Comments: High
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1846911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: -
Alter: 43,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood pressure increased Chest discomfort Chills Dizziness Dysgeusia Eye pain Head discomfort Headache Heart rate increased Hot flush Hypoaesthesia Injection site hypoaesthesia Muscle tightness Muscular weakness Pain in extremity Palpitations Rash macular Throat tightness

Symptomtext

ten minutes after injection - metal/bloody taste in mouth, pain in both arms and hands, then numbness starting in hands, heart palpitations, increased heartrate, tightness of chest, tightness of throat, uncontrolled full body shaking, full body numbness with injection location exacerbated (with no feeling upon injection), blotchy skin, dizziness, headache, eye ache, muscle tension throughout, pressure in head and chest, muscle weakness, chills, hot flashes, lasted for about an hour and a half for most - then tightness of the chest, dizziness, headache, eye ache, pressure throughout continued for days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: day of injection - since done at a pharmacy, they didn't do anything , offered me water and a poptart, when i called primary care, they told me to ride it out. day 2 after injection, called doctor again - told to wait it out, not concerned with reaction at pharmacy, was advised doc would call back day 3 after injection, no doctor call back, called again, was told would call back day 4 after injection, called doctor and was seen - nurse told me i should expect to ride it out, blood pressure slightly elevated above norm, doctor provided exemption based on description of extreme reaction
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1845771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: NC
Alter: 52,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Injection site pain Loss of personal independence in daily activities Paraesthesia Tremor

Symptomtext

Site: Pain at Injection Site-Medium, Additional Details: Right arm tingling & shaking all the way down to patient's hand making it difficult to perform day-to-day activities

Weitere VAERSDATA-Felder

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

VAERS 1962499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: VA
Alter: 74,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Mobility decreased Pain Pain in extremity

Symptomtext

- arm pain, throbbing stabbing pain from fingers to shoulders - cannot lift arms - No redness or swelling Advised pt to contact MD in morning

Weitere VAERSDATA-Felder

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

VAERS 1843900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: PA
Alter: 53,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Condition aggravated Gout Headache Pain

Symptomtext

head ache, body ache, chills. Gout was made intense, more than I've ever felt, in my left foot and in multiple locations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Urgent care for treatment.
Aktuelle Erkrankungen: gout
Vorgeschichte: -
Andere Medikamente: fish oil, daily vitamin, magnesium, D3, L-Tyrosine, St John's wort, ginko
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1843876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: UT
Alter: 55,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Chest discomfort Crying Dyspnoea Hypoaesthesia oral

Symptomtext

The patient stated that she was driving when she noticed her chest feeling tight, SOB, and the right side of her lips were going numb. She drove back to the clinic. I took her vitals: BP 164/93, HR 68, O2 98, RR 22, temp 98.4. I gave her Benadryl 25mg PO and told her to wait for another 30min for observation. Towards the end of the 30 mins, she got on the floor in the child pose manner and started crying saying she couldn't breathe. I stayed with her while another nurse went to get a wheelchair. When the WC came back I got her in it and took her to the ED. While in the ED she received 4LO2 via NC, and an IM injection of Epi.

Weitere VAERSDATA-Felder

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

VAERS 1843170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 78,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 21.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Cough Culture urine negative Dyspnoea Lung disorder Malaise Platelet count increased SARS-CoV-2 test negative Thrombocytosis

Symptomtext

patient with h/o polycythemia rubra vera, followed by heme and has monitoring CBC almost weekly to q2weeks. day prior to pfizer #2, platelets increased to 757. previous value 10/12/21 at 95. ranges low with high of 1176. h/o thrombocytosis when she is ill with COPD/pneumonia in past. started on hydroxyurea 9/21 and had complaints of diarrhea, but improved. then 10/27, platelets were 1558. minimal symptoms. urine culture negative. seen in my office 10/29/21 and just started with worsening SOB and cough. RLL lung findings and started on augmentin. covid test negative. Seen 11/4/21 for f/u and plt now down to 511. Thrombocytosis could be due to infection, resolving with antibiotics, but just wanted to report for possible link with pfizer vaccine. thanks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: see above
Aktuelle Erkrankungen: 1. Hypertension. 2. Carotid stenosis- followed by vascular surgery 3. Hyperlipidemia 4. Allergic rhinitis 5. Tobacco abuse, quit 3/15 6. Hyperparathyroidism 7. COPD 8. Osteopenia 9. Anxiety 10. CAD, followed by cards (RCA stent 03/2015. NSTEMI. Subsequent cath demonstrated left main and circumflex mild nonobstructive CAD, LAD mid 50 and RCA had a proximal 70 that had a drug-eluting stent.) 11. PAD (4/15- LE ABI's) 12. Polycythemia rubra vera, followed by heme 13. Adrenal insufficieny with Long-term steroid use. 14. GERD with h/o UGIB 15. CKD 16 .Diabetes
Vorgeschichte: see above
Andere Medikamente: tylenol, proair, azithromycin 3/week, pulmicort, coreg bid, vitamin D, plavix, colace, repatha, flonas, asix, bevespi, hydroxyurea, atrovent neb, protonix, prednisone 10, trazodone
Allergien: ace inhibitors, codeine
Vorherige Impfungen: -

VAERS 1843157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Chest discomfort Dyspnoea Fatigue SARS-CoV-2 test

Symptomtext

About 20 minutes after shot, I felt pressure in my chest. I felt like I could not catch my breath. I went to the pharmacist, she ask if I had I felt like something was in my throat. I told her no. She said then I am not having a anaphylactic reaction. Then she if I wanted her to call emergency services. I went and sat back down. These symptoms continued on for about a week. When I walked or do any activities it would get worse. I was also very fatigue and tired that whole week as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin Dilaudid Rhubarb Wheat Grass
Vorherige Impfungen: Flu

VAERS 1842979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 24,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Decreased appetite Diarrhoea Extra dose administered Feeding disorder Feeling abnormal Headache Illness Insomnia Nausea Pain Pain in extremity Pyrexia Rash

Symptomtext

Got the on Tuesday and in the evening -soreness on arm, body pains and fever. Next am rash on chest and neck, wed nausea and diarrhea - fever and headache. Shooting pain in my arms to finger on the both arms and especially left and couldn't eat and couldn't sleep and urgent care on Thursday, sick 5-6 days. In urgent care, they said I was having a reaction to the vaccine and gave me Zofran -4milligrams. I loss my appetite and still not feeling back to my normal. 1st and 2nd dose was Moderna and I had reaction for the 2nd dose - with rash on my neck. face and chest and the pharmacist said I could take the Pfizer booster to since I had a reaction to Moderna 2nd dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: None
Allergien: Cephalexin Bee stings
Vorherige Impfungen: Moderna dose 2 - rash on your neck, chest and face

VAERS 1842643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chest pain Dyspnoea Hypersensitivity Interchange of vaccine products Laboratory test normal

Symptomtext

Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Additional Details: This was reported by patient's wife. She stated pt has difficulty breathing and chest pain after his vaccine. they took him to an urgent care who ran tests and stated patient was "fine". They gave him some type of shot (steroids?) and pt felt better the next day. This was patient's booster--first vaccine was Janssen.

Weitere VAERSDATA-Felder

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

VAERS 1841180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 37,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 22.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Hypertension Tachycardia

Symptomtext

prolonged Hypertension/high blood pressure, periods of Tachycardia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: APS - Anti-phospholipid Syndrome PCOS - Polycystic Ovarian Syndrome
Andere Medikamente: Metformin probiotic vitamins B12 complex, C, D Niacin Zinc Zyrtec Low dose aspirin
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1840707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: -
Alter: 30,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Dizziness Hyperhidrosis Pallor Paraesthesia

Symptomtext

5 mins after Pfizer vaccine given at 1:45pm pt became pale, diaphoretic, tingling to hands/ feet. felt lightheaded. bp check 99/61 hr 103, placed in a lying position. contacted MD. BP recheck 105/69 hr 103. 1402 pt c/o cp. contacted the MD again who gave order to call 911. 911 called, 1417- ambulance arrived and transferred to the ED

Weitere VAERSDATA-Felder

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

VAERS 1840554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 30,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Chest discomfort Dyspnoea Pruritus Rash

Symptomtext

Patient complained of itchiness, rashes, shortness of breath and tightness in chest.

Weitere VAERSDATA-Felder

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

VAERS 1840077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NV
Alter: 40,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Hypertension Tachycardia Wheezing

Symptomtext

Pt came in for 2nd Pfizer vaccine. Pt had previously had anaphylactic reaction to 1st Pfizer vaccine. During first dose visit, pt was administered epinephrine, solu-medrol and diphenhydramine by staff and MD. Pt was then transported to ER. Upon return for 2nd visit 21 days later, the pt stated to LPN that she had experienced an anaphylactic reaction to the 1st dose, which is a direct contraindication to receive the second dose. Pt also stated to LPN that ER doctor during her first visit, had said to receive the 2nd dose regardless of reaction. Per protocol, any anaphylaxis history needs to be reported to charge RN for closer observation. LPN administered 2nd dose of vaccine without informing charge RN. Approximately 5 minutes after administration, pt began to have severe shortness of breath and chest tightness. RN, and Charge RN, proceeded to recognize pt distress and began to take vital signs. Pt exhibited hypertension of 139/110, tachycardia of < 135 beats per minute, and expiratory wheezes bilaterally in all lung field posteriorly. Pt was transferred to wheel chair and moved to secluded area for further medical treatment. Occupational MD was called and arrived approximately 5 minutes later. Pt did take one puff of her prescribed albuterol inhaler in those minutes. Occupational Health MD arrived and 0.3ml of Epinephrine was administered. Repeat vital signs were taken 5 minutes later and vital signs showed improvement. Pt stated she experienced a decrease in shortness of breath and expiratory wheezes decreased upon auscultation. Pt was taken to ER for further evaluation and observation and instructed by health MD not to receive the 3rd dose due to severe anaphylaxis. LPN was pulled aside after incident and re-educated on POD protocol and CDC guidelines with anaphylaxis reactions to COVID shots. Follow up email was sent to rest of POD nurses with POD guidelines and protocols.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: GERD, chronic vertigo, eczema, fibromyalgia, asthma
Vorgeschichte: -
Andere Medikamente: Albuterol, prednisone, montelukast, hydroxyzine, levothyroxine, pantoprazole, famotidine, ketotifen oph soln, meclizine,
Allergien: Anaphylaxis to Pfizer 1st dose, sumatriptan, influenza, Percocet, latex, saccharin, aspartame,
Vorherige Impfungen: Influenza - anaphylaxis

VAERS 1839647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 73,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Mild

Weitere VAERSDATA-Felder

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

VAERS 1836958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: SC
Alter: 59,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypertension

Symptomtext

Systemic: Hypertension-Mild

Weitere VAERSDATA-Felder

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

VAERS 1836893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IN
Alter: 61,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Hypoacusis Tinnitus

Symptomtext

5 minutes after injection my tinnitus started ringing loud. Approx 20 years ago I had steroidal eye drops that set off raging tinnitus that only allowed me to sleep 20 minutes at a time. Discussion of cutting acoustic nerve even had but couldn?t guarantee would decrease tinnitus. Found alternative doctor that able to turn it down with alternative treatments whereas convention med had only Valium to offer. I cannot risk it getting louder yet again with the second shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Increase in hard of hearing due to ringing in ears loud. It hasn?t subsided or decreased since the shot.
Aktuelle Erkrankungen: None
Vorgeschichte: Allergic responses to select masks, gloves, blue dye such as Dawn makes skin peel.
Andere Medikamente: Zinc, aspirin
Allergien: PCN
Vorherige Impfungen: -

VAERS 1836424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WA
Alter: 41,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 14.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Eczema Rash

Symptomtext

I began to get a major eczema flair up, rash on my left arm, right arm, left calf, it is constantly getting worse. I went to see Dermatologist, they started me on a new medication, pimecrolimus, to combat this flair up, eczema is starting to improve some of the areas however it is still bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Depression, eczema, and asthma
Andere Medikamente: Famotidine 20mg, D3 125mcg, methylphenidate 20mg, acetaminophen and aspirin, duloxetine 90 mg, Montelukast 5mg, fluticasone nasal spray, azelastine nasal spray, Betamethasone topical ointment, setyrazene
Allergien: I am allergic to Wellbutrin, reglan, nuts, peanuts, fennel, licorice, coconut, anise, balsamic vinegar, red wine,
Vorherige Impfungen: Pfizer dose #2, 40, Skin became sensitive to sunlight.

VAERS 1833330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NC
Alter: 54,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Cardiovascular symptom Catheterisation cardiac abnormal Chest pain Coronary artery disease Echocardiogram Electrocardiogram QT prolonged Electrocardiogram T wave abnormal Electrocardiogram T wave inversion Haemoptysis Hypotension Ischaemia Neoplasm malignant Surgery Systolic dysfunction Troponin increased

Symptomtext

On 10/27/21, 54 yo immunocompromised M was admitted after experiencing hypotension during an outpatient procedure. On 10/28 at 1223, pt was administered booster dose of COVID-19 vaccine (PFIZER-BIONTECH COVID-19 VACCINE) 0.3 mL IM. Pt had no prior cardiac history. On evening of 10/28, pt developed chest pain with elevated troponins and new T wave inversions on EKG. On 10/29, pt underwent LHC and TTE showing new evidence of RV systolic dysfunction. with Wells Score 3.5 (active malignancy, surgery, hemoptysis). Pt was started on atorvastatin 40 mg PO daily and aspirin 81 mg PO daily. MD unclear of cause of cardiac symptoms and whether COVID vaccination was contributory. Evaluation ongoing. Pt was discharged home on 10/31 with plans to follow up in Cardiology clinic in 4 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 29-OCT-2021 21:48:29 Clinic-EKG ROUTINE RECORD Normal sinus rhythm T wave abnormality, consider anterolateral ischemia Markedly prolonged QT interval Abnormal ECG When compared with ECG of 29-OCT-2021 09:14, T wave abnormality, consider lateral ischemia is now present Prolonged QT is more prominent I reviewed and concur with this report. Electronically signed by: on 10/30/2021 1:08:44 PM 25mm/s 10mm/mV 150Hz 9.0.7 12SL 241 HD CID: 88 Cardiac Catheterization Report 10/29/21 Nonobstructive CAD noted-right dominant coronary system Normal LVEDP on left heart catheterization
Aktuelle Erkrankungen: HIV (on HAART), prostate cancer (diagnosed 10/21, no active treatment), depression, bipolar I disorder
Vorgeschichte: HIV (on HAART), prostate cancer (diagnosed 10/21, no active treatment), depression, bipolar I disorder
Andere Medikamente: bictegravir-emtricitabine-tenofovir alafenamide (BIKTARVY) 50-200-25 mg tablet Take 1 tablet by mouth once daily cholecalciferol (VITAMIN D3) 2,000 unit tablet Take 2,000 Units by mouth once daily FLUoxetine (PROZAC) 20 MG capsule Take 20
Allergien: Sulfa Beef-containing products
Vorherige Impfungen: -

VAERS 1833246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

COVID-19 Chest X-ray Chest pain Cough Dyspnoea Fatigue Full blood count Headache Laboratory test Oxygen saturation decreased Pneumonia Pyrexia SARS-CoV-2 test positive Troponin

Symptomtext

Shortness of Breath, low oxygen levels, fatigue, severe headache, chest pain, cough, low fever Visited ED following Thursday (10/28/21), pneumonia and COVID positive confirmation tests

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CXR, CBC, chem panel, Troponin, vital signs 10/28/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Men's daily vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1832624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: FL
Alter: 47,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Back pain Chest discomfort Dyspnoea Electrocardiogram normal

Symptomtext

Client is a 47 y/o male observed in observation area slump over in seat in car. Responds to verbal stimuli. He complained of tightness in chest and shortness of breath. Fire Rescue arrived to further evaluate client. V/S taken BP 109/63, HR 100, Temp 98.7, RR 18, O2 97%, Via room air BS 150. EKG performed and showed normal sinus with no acute changes noted. Client complains of weakness and lower back pain and refused hospitalization despite paramedics and nurses encouragement to seek medical attention. He continued to refuse hospitalization and remained in observation for an additional 15 min for observation. Client left observation area at 4:40 pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG: NS no acute changes T 98.7, BP 109/63, RR 18, O2 97%, HR 100
Aktuelle Erkrankungen: skin cancer (melanoma)
Vorgeschichte: HTN Diabetes Cancer (skin)
Andere Medikamente: -
Allergien: n/a
Vorherige Impfungen: -

VAERS 1832324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NV
Alter: 39,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Adnexa uteri pain Balance disorder Blister Chest discomfort Discomfort Feeling hot Gait disturbance Headache Herpes virus infection Hyperhidrosis Limb discomfort Migraine Nausea Pain Pyrexia Rash Vaginal haemorrhage Visual impairment

Symptomtext

The next day in the morning , I had a headache and my arm felt heavy. Closer to the afternoon I started to feel hot, fever like symptoms, my body was aching. Towards the afternoon was when it was getting worst, I was sweating, I could not hold food down and vomit, my lower body was aching severely it was a struggle to get up and walk. As I attempted to walk I would lose my balance. Towards the night my headaches became sharp migraines on the left temporals it felt like a drill passing through my brain, I couldn't see clearly. I found a small vaginal bleeding and then I ended up with a herpes blister. As I tried to sleep, my chest felt heavy and I started wheezing and my ovary felt as someone was stepping or squeezing on them feeling much pressure and pain. The next morning (today) I did have a rash behind my left ear but it soon went away, I still have that blister, I still have the headache and I am still unable to hold food down as I get nauseous and my body still aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: yaz
Allergien: dairy , egg whites
Vorherige Impfungen: -

VAERS 1832161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 26,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Ear pain Fatigue Headache Pain

Symptomtext

Body aches (stomach, arms and legs, back, abdomen), chest pain, fatigue, strong headache, ear pain in both ears Not yet resolved after 1 dose of extra strength tylenol 1 hr ago

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Sleep apnea, migraine with aura
Andere Medikamente: Zoloft 25mg, Colace, Vitamin D 2000IU (every day 1x per day)
Allergien: -
Vorherige Impfungen: -

VAERS 1831967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: VA
Alter: 50,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Disorientation Dizziness Hypotension Pain Pallor

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Hypotension-Mild, Additional Details: 5 mins after giving the vaccine, patient felt lightheaded, dizzy, about to faint, looked paled. BP 82/49, pulse=45. pt drank some water & apple juice. after 15 mins took BP 113/74, pulse 59. advised pt to take ibuprofen, rest, and drink water. Follow up with pt the next day 10/30/21, she stated at home she felt disoriented at one point and took advil for soreness. today feel better

Weitere VAERSDATA-Felder

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

VAERS 1831818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TN
Alter: 37,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Amnesia Anxiety Dizziness Feeling abnormal Headache Hypoaesthesia Palpitations Panic attack Tremor

Symptomtext

Right sided body numbness, brain fog, anxiety, tremors, memory loss, panic attacks, headaches, dizziness, heart racing,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: none- Referred to higher level of care
Aktuelle Erkrankungen: none
Vorgeschichte: IBS
Andere Medikamente: None
Allergien: Perfume
Vorherige Impfungen: -

VAERS 1831648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: UT
Alter: 12,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Feeling hot Headache Hyperhidrosis Migraine Oropharyngeal pain Pyrexia

Symptomtext

Migraine headache ( pain described as ring around the top of the head with the greatest pain at the top of forehead) Excessive heat and sweating Low grade fever Temporary sore throat

Weitere VAERSDATA-Felder

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

VAERS 1831542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: KY
Alter: 39,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Back pain Chills Dizziness Dyspnoea Fatigue Headache Pain Paraesthesia Pyrexia

Symptomtext

Fever over 102? for two days, severe body aches, lower back pain, headache, shortness of breath, chills, very fatigued and weak, dizziness, tingling sensation in arms and legs. All of these symptoms occurred the entire next day after receiving the booster shot. Went to sleep in the evening (the day after booster) and woke up the following morning with a fever still, body aches, headache and fatigue. Today is day three following the booster and the only symptoms still lingering are faint body aches but still very fatigued and weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Conducted an at home rapid test with extra precautions to follow the tests instructions perfectly. The results were negative for Covid-19.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Hydrocodone 10/325, Men's Multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1829864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 43,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Cold sweat Dyspnoea Pain in extremity Pruritus Urticaria

Symptomtext

Hives on right arm with pain and itching on arm and left hand. Body cold with sweats with heavy breathing.

Weitere VAERSDATA-Felder

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

VAERS 1829071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IN
Alter: 86,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Flushing Hyperhidrosis Hypertension Musculoskeletal stiffness Nausea Vomiting

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Stiff arm-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Hypertension-Mild, Systemic: Nausea-Medium, Systemic: Vomiting-Medium

Weitere VAERSDATA-Felder

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

VAERS 1825387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MN
Alter: 52,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Chest discomfort Chills Cough Cyanosis Headache Neck pain Oropharyngeal pain Pallor Pyrexia Sinus congestion Tremor

Symptomtext

Chills, UNCONTROLABLE SHAKING, fingers and toes were white and blue, sinus congestion, sore neck, headache, cough, chest discomfort, sore throat, fever 101.7 and weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Zero negative RA and Hypothyroid
Vorgeschichte: Zero negative RA and Hypothyroid
Andere Medikamente: Hydroxychloroquine, folic acid, Celebrex, methotrexate, baby aspirin, Fish oil, Zyrtec, zinc, turmeric, Calcium,
Allergien: Erythromycin, oxycodone,
Vorherige Impfungen: -

VAERS 1823621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WA
Alter: 63,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 12.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Chest discomfort Dyspnoea Lip swelling Migraine Paraesthesia oral Respiration abnormal Swollen tongue

Symptomtext

Short of breath; because of migraine my eyes I have hard time to read; lips were swelling; my tongue was swollen and tingling; my tongue was swollen and tingling; tight chest; I am still using my accessory muscles, high in the chest to breathe; This is a spontaneous report from a contactable nurse (patient). A 63-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: FH8020), intramuscular, administered in Arm Left on 12Oct2021 at the age of 63-year-old as dose 1, single for covid-19 immunisation. Medical history included allergic to phosphate, sulphate, total right shoulder replacement surgery in June end, gained weight since going off with Topiramate (The reason of going off patient was 180 in January) and patient had stage three kidney disease which was apparently from Tramadol and 'Omni Prozac' generic 45% (not clarified, Patient nephrologist told me, in January with Psychiatrist, put down dose from 200 milligram and patient finished the last dose a month ago and she went from 3 tramadol a day to 2 and next time it will be moved down to one). The patient was on a lot of medication. On 12Oct2021 patient received vaccination, she stayed there for 30 minutes and was already having the migraine as she was leaving and 30 minutes after, she was having shorter breath and the tight chest and took the quick acting inhaler and it helped to open up the tightness but remains short of breath for 6 hours. The patient's lips were swollen and tongue was swollen and tingling. She have been taking a 100 mg of Benadryl since before the shot. They were out of Moderna and Pfizer has Phosphate in it. So, her doctor told to bring Benadryl and quick acting inhaler. she had short of breath and needed the quick inhaler three times since 12Oct2021. Patient took 100 milligrams of Benadryl about every 6 to 8 hours and quick acting inhaler (Levalbuterol Tartrate HFA) that does not have Sulphate in it. Patient still using accessory muscles, high in the chest to breathe. Patient was concerned about the 2nd dose in a month, and it will be right after her physical therapy appointment. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shoulder arthroplasty; Stage 3 acute kidney injury (apparently from Tramadol and 'Omni Prozac' generic); Weight gain
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1821451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 84,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypertension Musculoskeletal pain

Symptomtext

Patient became hypertensive and was experiencing right scapular pain. Hypertension did not resolve with rest. Patient was sent to emergency room via ambulance for further evaluation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Synthriod, Catapres, Neurotin, Apresline, Aldactone, Ventolin, Alvesco,
Allergien: Cozaar, HcTz, Hydralazine, Lisinopril, Metoprolol, Nifedipine, Xanax, Tetracycline, Chorthalidone,
Vorherige Impfungen: -

VAERS 1818290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 44,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest pain Computerised tomogram Dizziness Electrocardiogram Headache Inflammation

Symptomtext

10/15/21 (day of shot): 9pm - left side chest pain and headaches. Chest pain has been continuous since 10/15/21 but the severity has differed. 10/16 & 10/17: episodes of severe stabbing chest pain. 10/17: went to ER and they confirmed inflammation in or around heart, given Ibuprofen 600mg. Ibuprofen alleviated the pain until it would wear off. 10/18: contact PCP Dr.: she advised to continue Ibuprofen and contact her if not better by day 10. 10/18-10/22: I experienced episodes of lightheadedness while sitting at my desk working. These episodes were severe to the point I thought I'd blackout and lasted 30 min or so. On 10/25 I contacted Dr. as the chest pain had not gotten better and had in fact gotten worse because the ibuprofen was no longer effectively addressing the pain. She prescribed prednisone that I'm currently taking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 10/17/2021: EKG, CT with contrast, bloodwork - inflammation/inflammation of left atrial
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1816467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8020

moderat

Staat: NC
Alter: 20,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy Atrial fibrillation Cardiac monitoring Chest discomfort Dyspnoea Hyperhidrosis Hypertension Hypoaesthesia Immediate post-injection reaction Laboratory test Nausea Pallor Palpitations

Symptomtext

Immediately after the vaccine he became nauseous turned white and started sweating profusely. Then his chest felt heavy and he was having a hard time breathing. After that his hand started to go numb and his heart started pounding very hard. At that point the pharmacist came over and put him on the blood pressure machine, his pressure was extremely high! The pharmacist then had him sit for a few minutes and took his blood pressure again and it was still high but he told us we could go home. An hour after being home his heart was still pounding extremely fast and hard so I took him to the emergency room. When we got there they hooked him up to machines and started an IV and reported that he was in atrial fibrillation! They could not normalize his heart for 24 hours while they were trying to get him a hospital bed. There were no hospital beds available after 24 hours so they finally gave him 3 AFib pills which eventually brought his heart into a normal rhythm. He went home shortly after his heart normalized which was approx 26 hours after the initial event. Nobody in the emergency room had ever seen a young, healthy 20-year-old boy go into AFib after having the vaccine. He saw a cardiologist three days after the event and that doctor has no idea what happened and he?s never seen anything like this before with a young person with no underlying health issues but believes it had something to do with the vaccine. This event needed to be reported and investigated ASAP because this was extremely serious and a possible side effect that is extremely rare. It was a very frightening event especially because there is no explanation for why it happened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: All the tests were done in the ER and includes but not limited to heart monitor, IV fluids, blood thinners, and other medication?s to try to stabilize his heart.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: Amoxicillin, Omnicef
Vorherige Impfungen: -

VAERS 1815652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: AK
Alter: 45,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 15.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / RA

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

Chest pain Headache Hypertension Myalgia

Symptomtext

Symptoms- Chest Pain, Headaches, high blood pressure , Myalgia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Was seen at the Emergency Room on 10/21/2021 due to symptoms
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Telmisatan 80mg, hydrochlorothiazide 25 mg , Magnesium, Potassium, Zinc, Iron and B Complex, probiotic
Allergien: Steroids
Vorherige Impfungen: -

VAERS 1815058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NY
Alter: 71,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Hypoaesthesia Injection site pain Lethargy Neuralgia Pain Paraesthesia Sciatica

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Exhaustion / Lethargy-Severe, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Patient is having sciatica like pain, nerve radiating pain down arm and up into the neck area. It comes and goes but is still persisting after 9 days.

Weitere VAERSDATA-Felder

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

VAERS 1814673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: VT
Alter: 37,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 18.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Fatigue Headache Migraine with aura Nausea

Symptomtext

Approximately 3 days following the vaccine, I developed a severe migraine (aura, severe headache and nausea) that lasted for about 4 hours followed by 24 hours of fatigue and weakness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine with aura
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pfizer COVID-19 vaccine, 01/09/2021. Same migraine symptoms happened after 2nd Pfizer dose.

VAERS 1814040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: MD
Alter: 53,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Cough Dyspnoea Headache Injection site pain Muscle spasms Pain Respiratory tract congestion

Symptomtext

Injection site pain, body aches, leg cramps, shortness of breath, coughing, congestion, headache continuing on day two after vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hashimotos thyroiditis, sjogren's syndrome disease
Vorgeschichte: Thyroid disease
Andere Medikamente: Atenolol, Levothyroxin
Allergien: Latex, iodine, betadine, shellfish, sulphur antibiotics
Vorherige Impfungen: -

VAERS 1813733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 53,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Chest discomfort Condition aggravated Dizziness Dyspnoea Dysstasia Fatigue Gait disturbance Headache Muscular weakness Pain in extremity Peripheral swelling Skin warm Wheezing

Symptomtext

headache, arm lot of pain swollen and hot, very dizzy , VERY exhausted VERY weak VERY hard to even just stand walking only few steps knees going VERY weak. Wheezing & hard to breath hard to speak chest heavy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: lung cancer
Andere Medikamente: Tylenol
Allergien: Penicillin
Vorherige Impfungen: both 1 & 2 covid 19 shots 12/23/2020 & 01/12/2021 Pfizer very sick for 3 days after each shot VERY bad sent to ER I would not

VAERS 1813218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 29,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Dehydration Diarrhoea Dizziness Extra dose administered Feeding disorder Hyperhidrosis Malaise Myalgia Nausea Pain Vaccine positive rechallenge

Symptomtext

Dizziness, nausea, diarrhea, headache, body aches (muscle and joint), fever Felt sick a couple hours after injection, had first round of diarrhea Went to bed with a 100.3 fever Woke up Saturday around 4:30am completely soaked in sweat Kept falling asleep involuntarily (during a shower, while sitting upright watching a video) and realized I was probaby dehydrated from the fever, diarrhea, and not having been able tot eat/drink anything besides a couple of crackers since the shot Had trouble finding a phone number for a nurse line because I had just changed insurance and kept falling asleep Went to urgent care as soon as they opened Was treated with 1000ml saline IV and an anti nausea medication Went home and waited out the rest of the reaction Returned to feeling normal Tuesday morning

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: synthetic epinephrine caffeine pineapple menthol
Vorherige Impfungen: 2nd covid shot (also Pfizer), similar symptoms

VAERS 1808458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: WI
Alter: 77,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Blood pressure increased Blood thyroid stimulating hormone Brain natriuretic peptide Chest X-ray Condition aggravated Electrocardiogram Full blood count Heart rate increased Metabolic function test Micturition urgency Palpitations Thyroxine Tinnitus Troponin

Symptomtext

!. Beginning at 3:30 a.m. urgent need to utinate every 30-45 minutes until approx 8;30 am. (Had same response with my second dose given on 2/21/2021.) At approx 9:00, while resting and listening to soft music, noticed a pounding in both ears and felt sporadic heart palpitation. My sport watch indicated my heart rate at 103 (my normal rate is 60-70 bpm. Checked heart rate and blood pressure using in-house automated equipment. Initial BP 200/130 Pulse 103; repeated after 10 min: still 199/120, pulse 130. I have never before had any indication of hypertension. Usual BP is 110-130/60-70. After consulting with our resident nurse, I was transported to a nearby emergency clinic for evaluation and treatment. After a two hours at the ER, my BP was still 195/100, pulse 103. I was administer a beta-blocker tablet and by 3:30 pm my BP had dropped to 148/85, but my pulse rate remained above 100.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG (2), Basic metabolic panel, ISAT Troponin & ISAT BNP, TSH Refex T4,Cbc W auto differential, Chest Xray
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: divalproex/doxazosin/methamazole/ omeprazole/simvastatin/B12/D
Allergien: none
Vorherige Impfungen: Second Pfizer Covid shot, age 77 (02/21/2021) Frequent urination, fever, rapid heartbeat, sore muscles, did not check bp or seek

VAERS 1807784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

moderat

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain upper Chills Cough Fatigue Injection site erythema Injection site pruritus Injection site swelling Lymphadenopathy Muscle spasms Productive cough Pyrexia Tenderness Tremor Urticaria

Symptomtext

Red swollen itchy at injection site about the size of a baseball Hives on neck and arms ,better with benedryl, gone as of 10/20 Coughing with phlegm since the shot Swollen glands in neck , still swollen today and tender Exhaustion-still Chills, fever, shakes first 3 days after the shot Full body cramps and stomach pains- first 2 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: Penicillin Flexeril Naproxen Codeine
Vorherige Impfungen: -

VAERS 1807568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 17.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1804701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 17.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Axillary pain Back pain Fatigue Headache Joint noise Joint range of motion decreased Lymph node pain Lymphadenopathy Musculoskeletal pain Neck pain Pain Pain in extremity Paraesthesia

Symptomtext

10/17/21: Vax @ 1120am= no s/s. At 1600 typical arm soreness w/ HA (expected even though I did not get any s/s w/ 1st vax. Fatigue 10/18/21: arm/shoulder/neck sore affecting ROM, pain in armpit- from neck radiating down to shoulder, palpable lympn nodes in arm at clavical/pectorus/left upper breast, back pain, tingling in afternoon in shoulder/arm. Popping shoulder. Body soreness, fatigue. 10/19/21: above s/s slightly better. Popping worse. 10/20/21 palpable node in armpit with pain/tingling. Neck/shoulder less sore. Small bursts of pain to scapula. 10/21/21: symptoms almost gone ( weird sensation in armpit). Shoulfer soreness 2/10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Called facility (PCP group) for earliest appt for 10/27/21, message left with MD's MA & NP MA. No testing done yet.
Aktuelle Erkrankungen: None
Vorgeschichte: -Chronic allergic rhinits. -asthma (allergy related- to asthma).
Andere Medikamente: Cetrizine 10mg bid (taken1.5 hours prior to vaccine) for chronic allergic rhinits. Routine: -Actif prenatal (prior to pregnancy). IUI done 10/20/2021 -Vitmain D3 50,000 IU qWed weekly. -Pregynl 10000 Units IM (to right buttocks) once for t
Allergien: None
Vorherige Impfungen: -

VAERS 1801562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Chest pain Dyspnoea

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: shortness of breath not allergy related-Medium

Weitere VAERSDATA-Felder

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

VAERS 1801271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: NV
Alter: 51,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Arthralgia Asthenia Chest discomfort Chest pain Chills Dizziness Dysphagia Dyspnoea Fatigue Headache Lethargy Nausea Pain Pyrexia Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Chills-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fever-Severe, Systemic: Headache-Severe, Systemic: Joint Pain-Severe, Systemic: Nausea-Severe, Systemic: Weakness-Severe, Additional Details: PT CAME TO PHARMACY COMPLAINING ABOUT REACTION SHE GOTTEN AFTER VACINATION INFORM HER TO GO TO HOSPITAL OR URGENT TO GET CHECK

Weitere VAERSDATA-Felder

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

VAERS 1800887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 13.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Axillary pain Condition aggravated Lymphadenopathy Oedema peripheral Pain Pain in extremity Pyrexia Skin sensitisation

Symptomtext

This was my second dose of the Pfizer-BioNTech COVID-19 vaccine. The first injection on 9/22/21, I only had severe arm pain lasting about two days. After this second vaccine, I began feeling feverish on 10/14, and my arm started to hurt, but not as much as the first time around. I woke up on Saturday morning, 10/16/21, with pain on the upper right side of my body where I got the vaccine, it felt like the vaccine pain and soreness had literally gone through my arm and reached my armpit and below my armpit. I later looked in the mirror and saw that my armpit, near my right breast, was very swollen that felt like I had swollen lymph nodes, but was and is too swollen to discern if any are in my armpit. I later discovered a very hard swollen lymph node on the right side of my right breast. It's hard and sensitive. I haven?t visited the doctors office yet as apparently getting swollen lymph nodes in your armpits is normal, but this is in the breast area, so I want to report it as a side effect. I am a healthy adult with no breast cancer in my family, and no history of any such thing, so it is very obvious this arose from vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Not yet.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: SSRI for OCD, Armodafinil for Excessive Sleepiness Disorder. Not new medications, been on them for several years. Multi-vitamin by Nature's Plus Source of Life, taken for years as well.
Allergien: N/A
Vorherige Impfungen: -

VAERS 1795311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8020

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Fatigue Hypomenorrhoea Nausea Pain Palpitations

Symptomtext

fatigue, all-over body aches, nausea starting about 12 hours after x 24 hours, intermittent heart palpations x 3-4 days; light menstrual period beginning, continues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: not applicable
Aktuelle Erkrankungen: not applicable
Vorgeschichte: not applicable
Andere Medikamente: lexapro 5mg
Allergien: nkda
Vorherige Impfungen: on file after COVID #1, COVID #2

VAERS 1794544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: NV
Alter: 31,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 17.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Muscle spasms Palpitations

Symptomtext

Systemic: patient at first said a palpitation then he thought it may be a muscle spasm-Mild.

Weitere VAERSDATA-Felder

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

VAERS 1794271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 51,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
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 Fatigue Headache Migraine Myalgia Paraesthesia

Symptomtext

About 10 mins after injection there was a tingling and zinging sensation down the left arm on the underside. It started in the arm pit and traveled down to the wrist. This went on for about 2 hours post injection. About 12:15pm muscle pain and joint pain started through out the whole body. A very intense headache started shortly after. There is also a feeling of complete exhaustion. I went to bed after taking some Exedrine Migraine to try to quell the INTENSE headache. That really did not help the headache at all. It was the most intense migraine like headache I've ever had. I had the feeling of chills but never registered a fever. I can not get warm. The headache and achy feeling has lasted for 2 days so far. It is not as intense as Friday and Saturday but I still do not feel well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: I called Sunday for a doctors appointment was was referred to this site to report my symptoms. I am going to see a doctor tomorrow as recommended by doctor.
Aktuelle Erkrankungen: none
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine, Estrodiol, Lexapro, Vit D, Cranberry extract, Probiotic
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1793906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: VT
Alter: 24,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Chest pain Dyspnoea Flank pain Pyrexia

Symptomtext

Right sided chest pain, right sided flank pain, right knee pain, fever of 101. F, dyspnea while ambulatory. Easier not to talk

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: HTN
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1793821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: IL
Alter: 50,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Fall Hyperhidrosis Orthostatic hypotension

Symptomtext

Patient was given 2nd dose of pfizer, walked out of room and sat in chair for observation. Within minutes patient fell out of chair and fell to the floor. Pharmacist ran to assist patient and within seconds patient came to. 911 was called. Patient sat back up in chair and starting sweating profusely. Ice pack was applied to back of neck. Patient stated that he was having "head rushes" . Paramedics arrived and checked the patient out, ran vitals and told patient he was ok to leave as long as he wasnt driving. Patient family member drove him home. Paramedics left and patient stayed for another 15 minutes and then left

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: -
Labordaten: Paramedics did vitals however do not have those numbers but advised patient was ok to leave
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: Patient denies any medication however did disclose that he uses marijuana
Allergien: none
Vorherige Impfungen: -

VAERS 1785284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

moderat

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Herpes ophthalmic Injection site pain

Symptomtext

Site: Pain at Injection Site-Mild, Additional Details: flare up of pre-existing herpes in eye

Weitere VAERSDATA-Felder

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

VAERS 1784919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: OH
Alter: 35,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cold sweat Dizziness Immediate post-injection reaction Pallor Tremor Unresponsive to stimuli

Symptomtext

Patient became very pale, clammy and started shaking immediately after vaccination. Patient almost passed out. The shaking became worse and she was not responding to questions so the paramedics were contacted to attend to the patient.

Weitere VAERSDATA-Felder

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

VAERS 1778890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

moderat

Staat: MD
Alter: 26,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 06.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Chest pain Chills Nausea Pain Pyrexia Vomiting

Symptomtext

FEVER FROM 10/7/21-10/10/21, NAUSEA AND VOMITING FROM 10/8/21-10/11/21, ACHES AND CHILLS FROM 10/7/21-10/11/21, CHEST AND ABDOMINAL PAIN FROM 10/8/21-10/12/21. TREATED WITH TYLENOL AND PEDIALYTE.

Weitere VAERSDATA-Felder

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

VAERS 2723543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: TX
Alter: 30,0
Geschlecht: F
Eingang: 13.12.2023
Impfdatum: 22.10.2021
Beginn: 27.12.2021
Tage bis Beginn: 66,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chills Cough Respiratory tract congestion

Symptomtext

Mild cough, congestion, chills. "acute symptomatic Covid infection".

Weitere VAERSDATA-Felder

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

VAERS 2671532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NM
Alter: 21,0
Geschlecht: F
Eingang: 15.08.2023
Impfdatum: 29.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / AR

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

Blood folate Blood test Fatigue Full blood count Glycosylated haemoglobin Metabolic function test Polydipsia Polyuria Vitamin B12 Vitamin D Weight decreased

Symptomtext

Fatigue, extreme weight loss, polydipsia,polyuria

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Blood work : CBC,CMP,, T-SHIRT, Vit B12 &D, HbA1c, folate Jan.3, 2022
Aktuelle Erkrankungen: DVT in left leg
Vorgeschichte: -
Andere Medikamente: Xarelto
Allergien: None
Vorherige Impfungen: DVT left leg, Janssen Covid vaccine, age 20, vaccination date 4/9/21

VAERS 2667113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 07.08.2023
Impfdatum: 21.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Arthralgia Lethargy

Symptomtext

sore shoulder; lethargy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received BNT162b2 (BNT162B2), on 21Oct2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 68 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, Anatomical Site of Injection: left arm, Route of administration: Intramuscular, Batch/Lot number: EN4202), administration date: 02Mar2021, when the patient was 67-year-old, for COVID-19 IMMUNIZATION, reaction(s): "sore shoulder", "Lethargy"; BNT162b2 (DOSE 2, Anatomical Site of Injection: left arm, Route of administration: Intramuscular, Batch/Lot number: EP6955), administration date: 23Mar2021, when the patient was 67-year-old, for COVID-19 IMMUNIZATION, reaction(s): "sore shoulder", "Lethargy". The following information was reported: ARTHRALGIA (non-serious), outcome "unknown", described as "sore shoulder"; LETHARGY (non-serious), outcome "unknown". Additional information: I rarely have even mild reactions (sore shoulder; a day of lethargy) after each dose.

Weitere VAERSDATA-Felder

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

VAERS 2653800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 07.07.2023
Impfdatum: 19.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Brain fog Fatigue SARS-CoV-2 test

Symptomtext

3rd one in October was very similar to 1st one/1st one she felt a little foggy and maybe just a little tired; 3rd one in October was very similar to 1st one/1st one she felt a little foggy and maybe just a little tired; 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), on 19Oct2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history included: "arthritis" (unspecified if ongoing); "left branch bundle blockage" (ongoing), notes: L branch bundle blockage had all her life. takes no medication for this and there is no treatment; "Suffers greatly for anxiety" (ongoing); "has panic attacks for no reason" (unspecified if ongoing); "Asthma" (ongoing), notes: she developed asthma; "Osteoporosis" (ongoing), notes: Diagnosed 7 years ago. Concomitant medication(s) included: XANAX taken for anxiety, start date: 2004 (ongoing); ALBUTEROL [SALBUTAMOL SULFATE] taken for asthma (ongoing); PROLIA subcutaneous taken for osteoporosis. Vaccination history included: BNT162b2 (Dose: 1, lot number: ER2613), administration date: 19Mar2021, when the patient was 67-year-old, for Covid-19 Immunization, reaction(s): "1st one she felt a little foggy and maybe just a little tired", "1st one she felt a little foggy and maybe just a little tired"; BNT162b2 (Dose: 2, lot number: EW0153), administration date: 09Apr2021, when the patient was 67-year-old, for Covid-19 Immunization, reaction(s): "2nd one a lot more fatigued". The following information was reported: BRAIN FOG (non-serious), FATIGUE (non-serious), outcome "unknown" and all described as "3rd one in October was very similar to 1st one/1st one she felt a little foggy and maybe just a little tired". Relevant laboratory tests and procedures are available in the appropriate section. Additional information : Covid vaccine: 1st one she had was Oct2021. Clarified she thought first one was 19Mar2021. She had 3 in 2021. March, April and October. All were Pfizer Covid vaccines. 1st one she felt a little foggy and maybe just a little tired. 2nd one a lot more fatigued. 3rd one in October was very similar to 1st one. Then had more, the 04Apr2022. Nothing remarkable about it. A little fatigued and a little soreness at site. Then had another one in May2023 and doesn't recall feeling anything but fatigue. Just felt kinda wiped out and tired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: did test; Test Result: Negative ; Comments: Negative covid
Aktuelle Erkrankungen: Anxiety; Asthma (she developed asthma); Bundle branch block left (L branch bundle blockage had all her life. takes no medication for this and there is no treatment); Osteoporosis (Diagnosed 7 years ago)
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Panic attack
Andere Medikamente: XANAX; ALBUTEROL [SALBUTAMOL SULFATE]; PROLIA
Allergien: -
Vorherige Impfungen: -

VAERS 2634981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 95,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 18.10.2021
Beginn: 26.11.2021
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Hypoxia

Symptomtext

R09.02 HYPOXIA 11/26/2021 ABDOMINAL PAIN

Weitere VAERSDATA-Felder

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

VAERS 2628717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

mild

Staat: NH
Alter: 66,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 20.09.2022
Beginn: 22.09.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Feeling abnormal Pain SARS-CoV-2 test positive

Symptomtext

Received booster shot on 9/20/2022,Felt ok 9/21/2022,started to feel bad on the 22nd, really felt bad on the 23rd, took a at home test, and tested positive for Covid. Have know idea how I got it or where it came from. On the 26th I started the 5 day treatment of paxovid. I don't seem to have any long term effects. I did have a dry cough,body aches,very tired.

Weitere VAERSDATA-Felder

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

VAERS 2624729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: FL
Alter: 55,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 23.11.2021
Beginn: 25.04.2023
Tage bis Beginn: 518,0
Dosis: 3
Route/Site: SYR / UN

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

Malaise

Symptomtext

Hospitalization for COVID-19 symptoms on dates 4/25/2023- 4/30/2023. Treated with hydrocortisone PO, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: levofloxacin, metoclopramide, prochlorperazine, codeine, estrogens, sumatriptan, teriparatide, buspirone, doxepin, erythromycin, lactose, olive extract.
Vorherige Impfungen: -

VAERS 2621879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 27.04.2023
Impfdatum: 03.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Fatigue Pain in extremity Vaccination site pain

Symptomtext

fatigue; arm soreness; injection site soreness in the arm soreness; 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 67-year-old male patient received BNT162b2 (BNT162B2), on 03Nov2021 as dose 3 (booster), single (Lot number: FH8020) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, lot: EN6204), administration date: 18Mar2021, for Covid-19 immunization, reaction(s): "fatigue", "arm soreness", "injection site soreness in the arm soreness"; BNT162b2 (DOSE 2, SINGLE, lot: EN6204), administration date: 08Apr2021, for Covid-19 immunization, reaction(s): "fatigue", "injection site soreness in the arm soreness", "injection site soreness in the arm soreness". The following information was reported: FATIGUE (non-serious), outcome "unknown"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm soreness"; VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "injection site soreness in the arm soreness". Additional information: Caller wanted to know if the Pfizer COVID-19 Bivalent Vaccine meant the vaccine was wearing off, the shelf life for the Pfizer COVID-19 Bivalent Vaccine, if there was safety information for the Pfizer COVID-19 Bivalent Vaccine administered after its beyond use date, if the side effects he experienced with the Pfizer COVID-19 Bivalent Vaccine meant the vaccine was working and if the Pfizer COVID-19 Bivalent Vaccine is different from the Monovalent. Per agent, caller got 4 covid vaccines, primary dose, 2 boosters, and bivalent booster, all of them from Pfizer. He mentioned that he usually felt fatigue and arm soreness for a while. He wanted to know if someone else has experienced this for this long and what to do to feel better. If there was a difference in the formulation that could have caused this. He also mentioned that he didn't have any COVID-19 symptoms, but that if one could get the vaccine with a previous infection of COVID-19 in case he had the infection without being aware. He also wanted to know why sometimes the expiry was placed as 6 months and other times as 10 weeks, given that his vaccine expires on 14May2023. He also wanted to know if his side effects meant that the vaccine was working and if the fact that we're constantly needing boosters means that the vaccine is wearing off. Typically, with the other injections, a few hours later, he started feeling fatigue and then later in the evening injection site soreness in the arm soreness. He had previously taken his original Pfizer Covid vaccinations when they first came out. He got the first two vaccines 2 weeks apart. Then, in 6-8 months he got his first booster. Then, 6-8 months later her got a second booster. He had relatively the same side effects for those. His side effects were common and expected. They all cleared up by the following evening by the most part. Sender's Comments: Linked Report(s): US-PFIZER INC-202300163844 same patient/event, different vaccine dose.

Weitere VAERSDATA-Felder

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

VAERS 2596076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 56,0
Geschlecht: F
Eingang: 14.03.2023
Impfdatum: 12.10.2021
Beginn: 17.04.2022
Tage bis Beginn: 187,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Fatigue Feeling cold Malaise Oropharyngeal pain Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

4/17/2022 that evening I felt like I was getting a cold. I had a sore throat, achy, tired and a runny nose. The next day, it was worse. I took an at home COVID test that was positive. I had an urgent care visit and discussed PAXLOVID, but my symptoms were mild and the nurse practitioner did not think I needed it. I was sick for about a week. I continued to have chest congestion and a runny nose for two weeks. Then I recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID at home test, positive
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma; Obesity; Depression
Andere Medikamente: Citalopram; ZYRTEC; FLOVENT; amlodipine; WELLBUTRIN; albuterol
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2585928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 23.02.2023
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Body height Pain in extremity

Symptomtext

just a sore arm; 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 74-year-old female patient received BNT162b2 (BNT162B2), on 22Oct2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 74 years for covid-19 immunisation. The patient's relevant medical history included: "Cirrhosis From Hepatitis C" (unspecified if ongoing), notes: Hepatitis C She got this from a hospital 40 years ago; "Cirrhosis From Hepatitis C" (unspecified if ongoing), notes: she got cirrhosis.; "Car accident" (unspecified if ongoing), notes: She was in a car accident; "Encephalopathy" (ongoing), notes: Encephalopathy. Concomitant medication(s) included: XIFAXAN taken for encephalopathy, start date: 2020 (ongoing); ZINC; GENERLAC taken for hepatic cirrhosis; LACTULOSE taken for hepatic cirrhosis. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot: EN6199, NDC/Expiry: Unknown, this is not on the CDC vaccine record card.), administration date: 06Mar2021, when the patient was 73-year-old, for COVID-19 immunization, reaction(s): "Just a sore arm"; BNT162b2 (DOSE 2, SINGLE, Lot: ER8733, NDC/Expiry: Unknown, this is not on the CDC vaccine record card., Administered at 14:00.), administration date: 30Mar2021, when the patient was 73-year-old, for COVID-19 immunization, reaction(s): "Just a sore arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 22Oct2021, outcome "recovered" (2021), described as "just a sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity. Additional information: patient reported she got hepatitis C from a hospital 40 years ago. She was in a car accident and they didnt screen the blood for Hepatitis C, they didnt even know Hepatitis C existed yet. When she got this, it kind of messed up her liver, so she got cirrhosis.Theres too much ammonia that goes into the brain, messes your brain up. If not for Xifaxan and Generlac would probably be in a home, because ended up in hospital; couldnt figure out how to go to bathroom. She knew she had to go, couldnt figure out how to do it, didnt know own name or name of president.They just loaded her up with Generlac and that was about it. Xifaxan really, really helps, she wouldnt be able to function without it; It has to do with gut, kills bad bacteria, thats why it works. Patient did not take a dose of Xifaxan because nauseous, didnt want to be more nauseous. Generlac: If the pharmacy is out of this they will give her Lactulose instead since its the same. Tastes really sweet, if youre trying not to eat sugar, theres no sugar or corn syrup, its a good sugar fix.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300073682 same patient, different dose and event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:shrunk; Comments: She used to be 5 feet and 4 and 3/4 inches, but she shrunk
Aktuelle Erkrankungen: Encephalopathy (Encephalopathy)
Vorgeschichte: Medical History/Concurrent Conditions: Automobile accident (She was in a car accident); Hepatic cirrhosis (she got cirrhosis.); Hepatitis C (Hepatitis C She got this from a hospital 40 years ago)
Andere Medikamente: XIFAXAN; ZINC; GENERLAC; LACTULOSE
Allergien: -
Vorherige Impfungen: -

VAERS 2575825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CT
Alter: 49,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 21.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Fatigue Seronegative arthritis Swelling COVID-19 Disease recurrence SARS-CoV-2 test Vaccination failure

Symptomtext

joint pain; swelling; seronegative inflammatory arthritis; fatigue; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 49-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 21Oct2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 49 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 2, Single, Lot# EL3247, ), administration date: 19Jan2021, when the patient was 48-year-old, for COVID-19 immunization; BNT162b2 (Dose 1, Single, Lot# EL0140, ), administration date: 26Dec2020, when the patient was 48-year-old, for COVID-19 immunization. The following information was reported: FATIGUE (non-serious) with onset 06Nov2021, outcome "not recovered"; SERONEGATIVE ARTHRITIS (medically significant) with onset Mar2022, outcome "not recovered", described as "seronegative inflammatory arthritis"; ARTHRALGIA (non-serious) with onset Jul2022, outcome "not recovered", described as "joint pain"; SWELLING (non-serious) with onset Jul2022, outcome "not recovered". The events "seronegative inflammatory arthritis", "fatigue", "joint pain" and "swelling" required physician office visit. Therapeutic measures were taken as a result of seronegative arthritis, fatigue, arthralgia, swelling. Clinical course: The Facility type vaccine was Hospital. The patient received no other vaccine in four weeks or other medications in two weeks. In Nov2021 developed severe fatigue, Jan2022 developed joint pain and swelling, Mar2022 diagnosed with seronegative inflammatory arthritis. Treatment included Plaquenil, Prednisone, methotrexate, Humira. The patient did not have covid prior vaccination. The patient had no known allergies or other medical history. Patient occupation was Nurse; Sender's Comments: The causal association between the event seronegative inflammatory arthritis and the suspect drug BNT162b2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-202300048109 same patient, different vaccine dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No adverse event (Other medical history: No known allergies No)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 03.12.2021
Beginn: 13.02.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Fatigue Illness Impaired work ability SARS-CoV-2 test positive Sinus congestion

Symptomtext

I received my first Pfizer COVID-19 booster on 12/3/2021. On 2/13/2022, I began to experience sinus congestion. On 2/14/2022, I took a home antigen test and got a positive result. On 2/15/2022, I went to the local office of the facility I work for and underwent a rapid test, which also yielded a positive result. During the first two days, I had sinus congestion and fatigue. On the third or fourth day, I lost my senses of taste and smell. The loss of taste and smell lasted for maybe a little over a week. The worst symptom was the fatigue, because I would get exhausted just walking across the room. During my illness, I took a vitamin C-zinc combination supplement. The sinus congestion lasted for about two weeks, and the fatigue ultimately lasted for over a month. I was finally able to return to work on 3/3/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 2/7/2022 rapid test, negative result; 2/14/2022 home antigen test, positive result; 2/15/2022 rapid test, positive result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension; Asthma; Sleep Apnea; Obesity.
Andere Medikamente: Carvedilol; clonidine; hydrochlorothiazide; losartan; terazosin; VENTOLIN inhaler; FLOVENT inhaler; FLONASE; BENADRYL; KIRKLAND signature ALLERCLEAR; KIRKLAND signature ALLER-TEC; acetaminophen; vitamin B12; calcium; coQ10; iron; KIRKLAND s
Allergien: Codeine; erythromycin; ciprofloxacin; morphine.
Vorherige Impfungen: After my first Pfizer booster, I had a small knot at the injection site. It was tender, but it wasn't too painful. It went away

VAERS 2551449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 11.03.2021
Beginn: 15.11.2022
Tage bis Beginn: 614,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chills Cough Headache Pyrexia SARS-CoV-2 test positive

Symptomtext

11/15/22 presents to EC ED for "worsening HA, cough, fever/chills". PMHx of "DM, HTN, HLP"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 11/15/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MI
Alter: 92,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 20.01.2021
Beginn: 28.09.2022
Tage bis Beginn: 616,0
Dosis: 3
Route/Site: - / -

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

Asthenia Beta haemolytic streptococcal infection Blood creatinine increased Blood magnesium normal Blood potassium normal Blood sodium normal COVID-19 Chest X-ray abnormal Cough Culture urine positive Fatigue Haemoglobin decreased Hypophagia Lung opacity Platelet count normal Procalcitonin normal Renal impairment SARS-CoV-2 test positive

Symptomtext

Pt is a 94 yo female w/ hx of HTN, HLD, AAA, CKD, DM, neuropathy, ILD, spinal stenosis, TIA who presented to ED secondary to weakness. Over the past week, pt w/ weakness, fatigue. She tested positive for COVID on 9/25. She had progressive sx, poor PO intake, cough, She was brought to ED for further care as she lives alone. Upon arrival to ED, BP 150/53, HR 62, afebrile, no hypoxia, no leukocytosis, Hgb 10.7, plts 218. Na 136, K 4.4, Cr 1.37. MG 1.7. Repeat UA concerning for UTI. +COVID. CXR w/ similar interstitial opacities. Pt given IVFs. Abx initiated for UTI. Pt admitted for further care. Stable on RA, afebrile. ID consulted. Cont 5 day course of paxlovid. Urine cx w/ strep agalactiae. Was on Rocephin, transitioned to Keflex BID to complete 7 days total. Procal WNL. Nephro followed, renal function improved w/ IVFs. PT/OT rec home w/ therapies, physical assist. Pt stable for Dc home w/ home therapies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 9/28 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MO
Alter: 82,0
Geschlecht: M
Eingang: 29.11.2022
Impfdatum: 14.05.2022
Beginn: 25.11.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Fall Knee arthroplasty Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Surgery

Symptomtext

symptoms: fever, congestion Admitted to hospital for scheduled knee replacement on 11/04/2022, slipped out of chair, required more surgery on 11/22/2022, tested positive for COVID-19 11/25/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: unable to access that information due to regulations
Aktuelle Erkrankungen: this information was not provided
Vorgeschichte: high blood pressure
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2517932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 88,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 21.09.2022
Beginn: 28.11.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / -

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

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

Symptomtext

Resident presents with non-productive cough and sore throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Rapid Covid Test completed results POSITIVE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Morphine, Capsaicin
Vorherige Impfungen: -

VAERS 2509449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 49,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 15.11.2021
Beginn: 05.07.2022
Tage bis Beginn: 232,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Cough Fatigue Malaise Myalgia Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I did not have a reaction to the vaccine. On 07/05/2022, I wasn't feeling well with fatigue, muscle aches, chills, cough and sore throat. On 07/06/2022, I tested positive for COVID-19. I contacted my doctor and was not given a prescription for PAXLOVID because of my age. I am a physician and prescribed myself PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 06JUL2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Scleritis
Andere Medikamente: ZOLOFT; KLONOPIN
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2499161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 07.10.2021
Beginn: 26.10.2022
Tage bis Beginn: 384,0
Dosis: 3
Route/Site: IM / -

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

Anion gap Asthenia Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate decreased Blood bilirubin decreased Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium decreased Blood urea normal COVID-19 Fall Fatigue Haematocrit normal Haemoglobin normal

Symptomtext

COVID+ 10/26/22. Vaccination status - Pfizer x3 Discharge Date: Oct 28, 2022 Admission Date: 10/26/2022 Discharge Diagnoses: Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 virus infection 10/26/2022 Yes ? Generalized weakness Details of Hospital Stay PRESENTING PROBLEM: COVID-19 virus infection HOSPITAL COURSE: 89-year-old male who presented after having a fall at home. He had felt fatigued for 2 weeks prior to admission when multiple other family members have been sick with COVID-19. While ambulating at home, his legs gave out and he fell to the ground hitting the right side of his head and right arm. He suffered a right ear and right forearm laceration. He was brought to the emergency department for evaluation. His right ear and right forearm lacerations were sutured and closed with Dermabond, respectively. He tested positive for COVID-19. He was evaluated for PT and OT evaluation. He did well with therapy elevation. He although he remained weaker than her baseline, he was able to tolerate ambulating 300 ft with a walker. Patient was discharged home with home health care and to continue home therapy. Patient was advised to use a walker for now until he is back to baseline functioning status.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 2,0
Labordaten: PERTINENT LABS AND STUDIES: Recent Labs 10/26/22 1349 10/27/22 0457 WBC 6.14 7.70 HGB 15.7 15.6 HCT 45.4 45.4 PLATELET 118* 108* INR 1.1 -- Recent Labs 10/26/22 1349 10/27/22 0457 SODIUM 132* 139 POTASSIUM 3.7 4.3 CHLORIDE 100 103 HCO3 19* 28 ANIONGAP 13 8* CREATININE 0.99 1.17 BUN 13 13 GLUCOSE 149* 93 CALCIUM 8.4* 8.5* TOTALPROTE 5.8* 5.8* ALBUMIN 3.0* 3.1* BILIRUBINT 0.8 0.7 ALKALINEPH 82 80 Recent Labs 10/26/22 1349 NTPROBNP 1,127
Aktuelle Erkrankungen: -
Vorgeschichte: Hx of colonic polyps Coronary artery disease involving native coronary artery of native heart without angina pectoris Myocardial infarction, apical Essential hypertension Elevated low density lipoprotein (LDL) cholesterol level History of Empyema, left H/O diverticulitis of colon Mild persistent asthma without complication Gastroesophageal reflux disease without esophagitis Other seasonal allergic rhinitis LV (left ventricular) mural thrombus following MI Senile nuclear cataract, bilateral Myopia of both eyes Urinary frequency Easy bruising BPH with obstruction/lower urinary tract symptoms Degeneration of macula and posterior pole of retina Pancreatic cyst Late onset Alzheimer's dementia without behavioral disturbance Coronary artery disease with stable angina pectoris, unspecified vessel or lesion type, unspecified whether native or transplanted heart
Andere Medikamente: Albuterol Sulfate 108 (90 Base) MCG/ACT 1-2 puffs Inhalation Every 4 hours PRN Aspirin 81 mg Oral Daily Patient taking differently: Take 81 mg by mouth Every 48 hours. Atorvastatin Calcium 40 mg Oral Daily Beclomethasone Dipropionate 80 M
Allergien: AugmentinDiarrhea CiprofloxacinDiarrhea Sertraline Vibramycin
Vorherige Impfungen: -

VAERS 2494655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: PA
Alter: 68,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 03.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Pain in extremity

Symptomtext

Pain in her arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP),. The reporter is the patient. A 69-year-old female patient received BNT162b2 (BNT162B2), on 03Nov2021 as dose 2, single (Lot number: FH8020) at the age of 68 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Lot: 30135BA), administration date: 13Oct2021, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "Pain in her arm". The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Pain in her arm". Additional information: COVID vaccine history: All Pfizer First vaccine: given: 13Oct2021 Lot: 30135BA, second vaccine: given 03Nov2021 lot: FH8020. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2489986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: VA
Alter: 43,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 25.10.2021
Beginn: 05.08.2022
Tage bis Beginn: 284,0
Dosis: 3
Route/Site: IM / AR

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

Bedridden COVID-19 Nasopharyngitis Pyrexia SARS-CoV-2 test positive Sinus headache

Symptomtext

I went to a concert, a day and a half later I had a really bad sinus headache. I was bed ridden, I had a slight fever and head cold. I used a home COVID-19 test that came back positive, I went into an Urgent Care the next day. I was given a rapid COVID-19 test that came back positive and prescribed Paxlovid. I started taking it immediately and it took a week and a half before I started feeling normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Home COVID-19 positive; rapid antigen COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamin; Wellbutrin; Zyrtec
Allergien: No
Vorherige Impfungen: -

VAERS 2488444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

mild

Staat: NC
Alter: 51,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 31.05.2022
Beginn: 25.08.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / AR

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

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

Symptomtext

Developed sore throat and slight congestion. Tested positive for COVID on Aug. 26. Symptoms worsened slightly over weekend. Started feeling better about 4 days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID PCR test positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: famotidine 40 MG
Allergien: -
Vorherige Impfungen: Vertigo after 2nd shot

VAERS 2488421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CO
Alter: 32,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 22.10.2021
Beginn: 22.09.2022
Tage bis Beginn: 335,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Body temperature fluctuation COVID-19 Chronic sinusitis Dysphonia Fatigue Headache Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative SARS-CoV-2 test positive Urticaria

Symptomtext

Since vaccination I was diagnosed with chronic hives and chronic sinusitis. Then my COVID-19 symptoms were lost of taste, temperature changes, fatigue, congestion, runny nose. It began with a hoarseness and headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 09/22/2022 home COVID-19 test positive; 09/28/2022 home COVID-19 test negative.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin
Allergien: Fish; environmental allergies
Vorherige Impfungen: -

VAERS 2486101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 22.10.2022
Impfdatum: 05.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Body temperature Pain in extremity SARS-CoV-2 test

Symptomtext

achiness to the injection arm, put ice on it and it was gone within an hour; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient received BNT162b2 (BNT162B2), on 05Nov2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 72 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (ongoing), notes: Diagnosed for 20 years; "High cholesterol" (ongoing), notes: for the last 10 years; "Arthritis" (unspecified if ongoing), notes: Diagnosed for last 5 years. Concomitant medication(s) included: LISINOPRIL taken for hypertension; SIMVASTATIN taken for blood cholesterol increased. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, NDC: Unknown, Lot: EM9810, Exp: Unknown, Dose and Route: Unknown dose, injection given in arm), administration date: 04Mar2021, when the patient was 71-year-old, for COVID-19 Immunization, reaction(s): "slight Headache", "Had achiness to the injection arm"; BNT162b2 (DOSE 2, SINGLE, NDC: Unknown, Lot: ER2613, Exp: Unknown, Dose and Route: Unknown dose, injection given in arm), administration date: 25Mar2021, when the patient was 71-year-old, for COVID-19 Immunization, reaction(s): "slight Headache", "Had achiness to the injection arm". The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "recovered", described as "achiness to the injection arm, put ice on it and it was gone within an hour". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain in extremity. Additional information: Patient had high cholesterol Sort of has high cholesterol. States it wasn't really high, she had a stressful job. Had high cholesterol for the last 10 years and Arthritis Diagnosed for last 5 years. It's been bothering her. She just has an ache to the arm and maybe a slight fever to other vaccines, but does not provide any product names. She has taken many vaccinations as she travels a lot. Has never gotten really sick. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201240143 Same patient and drug, different event separated in time;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:101 degrees; Test Date: 20220630; Test Name: COVID-19 test; Test Result: Positive ; Comments: Clarified she tested positive for COVID-19 on 30Jun2022; Test Date: 20220715; Test Name: COVID-19 test; Test Result: Negative ; Comments: COVID-19 negative 15Jul2022; Test Name: PCR test; Test Result: Positive ; Comments: Positive with the PCR test; Test Name: PCR test; Test Result: Negative ; Comments: got a COVID-19 test there and was told her PCR was negative; Test Date: 20220714; Test Name: rapid COVID-19 test; Test Result: Positive ; Comments: was positive on a rapid COVID-19 test.
Aktuelle Erkrankungen: Blood pressure high (Diagnosed for 20 years); High cholesterol (for the last 10 years)
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis (Diagnosed for last 5 years)
Andere Medikamente: LISINOPRIL; SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2452031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MN
Alter: 35,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 20.09.2021
Beginn: 12.09.2022
Tage bis Beginn: 357,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive Vomiting

Symptomtext

VOMITING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: 2,0
Labordaten: COVID POSITIVE 9/12/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Keflex [Cephalexin], Naproxen Sodium (Bulk)
Vorherige Impfungen: -

VAERS 2440114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: IL
Alter: 16,0
Geschlecht: M
Eingang: 11.09.2022
Impfdatum: 05.09.2021
Beginn: 12.09.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Decreased appetite Diarrhoea Gastrointestinal pain Nausea

Symptomtext

Unrelenting gastrointestinal pain, loss of appetite, weight loss, nausea, and diarrhea since then. NO other medical history.

Weitere VAERSDATA-Felder

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

VAERS 2436296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 18.11.2021
Beginn: 03.09.2022
Tage bis Beginn: 289,0
Dosis: 3
Route/Site: UN / UN

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

Cough Diarrhoea Upper-airway cough syndrome

Symptomtext

Postnasal drip, cough, and diarrhea.

Weitere VAERSDATA-Felder

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

VAERS 2431023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 30.07.2021
Beginn: 05.08.2022
Tage bis Beginn: 371,0
Dosis: 5
Route/Site: - / -

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

Abdominal lymphadenopathy Alpha 1 foetoprotein normal Ascites Back pain Biopsy COVID-19 Carbohydrate antigen 19-9 Computerised tomogram thorax abnormal Decreased appetite Full blood count normal Hepatic cirrhosis Hepatic lesion Hepatic mass Hepatocellular carcinoma Laboratory test abnormal Liver function test increased Metabolic function test normal Nausea

Symptomtext

70 yo M with PMH CAD, HTN, HLD who presents on 8/6 for n/v, decreased appetite x 1 week. He was evaluated by PCP who noted elevated LFT and was found to have liver lesions. Also with L lumbar back pain since June so he was taking 2 extra dose tylenol Q2-3H. On day PTA, took 6 tablets of tylenol at once. Pt was reading on tylenol OD so he came to EC for evaluation. Also notable for 20lb weight loss. On arrial to EC, CT a/p w lung nodules, severe liver cirrhosis and splenomegaly, ascites, R hepatic lobe and L hepatic lobe mass consistent with multifocal HCC, upper abdominal adenopathy indicating mets, lytic lesion L1. CBC, BMP unremarkable. HFT markedly elevated. Pt admitted for further w/u and oncology consult. Oncology, GI, hepatology consulted. AFP and CA-19-9 wnl. S/p CT guided bx of L1 on 8/12. FPRS consulted, started on methadone with improvement. Biopsy results pending at the time of dc. Pt instructed to f/u with oncology team for pathology results and further plan of care. Pt remained hemodynamically stable. He was discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: 10,0
Labordaten: 8/6 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2424051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: WV
Alter: 74,0
Geschlecht: F
Eingang: 30.08.2022
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Laboratory test Loss of personal independence in daily activities Muscle spasms Pain in extremity Sleep disorder X-ray

Symptomtext

Patient is having severe leg pain & cramps mainly in the thigh area. she states it has affected her everyday life even painful at sleep

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Labsm Xrays, ABI specialist consults ordered
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2404673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: IN
Alter: 70,0
Geschlecht: M
Eingang: 08.08.2022
Impfdatum: 22.10.2021
Beginn: 19.07.2022
Tage bis Beginn: 270,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Fatigue Pain Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I received my first Pfizer booster for COVID-19 on 10/22/2021. On 7/19/2022, I experienced fatigue and fever, which was about 99 degrees. I was out of town when I began having symptoms. These symptoms continued as I flew home on 7/21/2022, and I just slept through the flight. On 7/22/2022, my fever climbed to about 101 degrees, and I began having body aches. On 7/24/2022, I took a home test for COVID-19, and the result was positive. I called my doctor's office and spoke to a nurse, and I was advised to take OTC pain relievers, drink plenty of water, and ride it out. I alternated between taking Advil and Tylenol about every 6 hours to treat my symptoms, and they helped keep my fever in check and helped relieve some of the body aches. The symptoms continued until about 7/26/2022, and my fever stabilized at about 99 degrees. The body aches went away, though I still had some residual fatigue. In the meantime, I worked from home on 7/28/2022 and 7/29/2022. I then finally came out of isolation on 8/1/2022 and returned to the office. At the time of this writing, I feel fine and I have fully recovered from the breakthrough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 7/24/2022--Home Test for COVID-19--Positive Result; 7/28/2022--Home Test for COVID-19--Negative Result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension.
Andere Medikamente: St. Joseph Aspirin; Amlodipine/Valsartan; Simvastatin; Allopurinol; Multivitamin.
Allergien: Tree Moss; Hay Fever; Dust.
Vorherige Impfungen: -

VAERS 2394935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: VT
Alter: 55,0
Geschlecht: M
Eingang: 28.07.2022
Impfdatum: 30.04.2021
Beginn: 03.06.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / LA

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

Adverse drug reaction Allergy test negative Biopsy skin abnormal Drug eruption Eosinophilic cellulitis Glycosylated haemoglobin abnormal Heart rate increased Immunisation reaction Laboratory test normal Rash Rash vesicular Superficial inflammatory dermatosis

Symptomtext

Pt sent a message on 6/3 that he had developed a full-body blistering rash which was initially thought to be related to poison ivy. He was treated with a course of prednisone, which was moderately helpful. It was treated throughout the summer with intermittent topical steroids. However, the rash persisted in a waxing and waning fashion until after his booster on 10/28/2021. At that point the rash became markedly worse and did not respond to another course of steroids. On 11/23/2021 I did a punch biopsy which was consistent with a drug reaction. We stopped all of his medications at that point, and his rash got a little better. However, he started having runs of rapid heart beat so was started on diltiazem (assuming that the metoprolol was a cause), and then his A1c worsened and because he had been on metformin in the past, this was restarted. Nothing changed the presentation of the rash. He was referred for allergy testing and had that done 3/10/2022. This was negative. He was finally able to be seen by Dermatology on 5/12/2022 who determined his rash was secondary to the Covid vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: skin biopsy 11/23/2021: perivascular dermatitis with eosinophils most consistent with a drug-related eruption allergy panel 3/10/22: negative celiac testing 3/10/2022: negative
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, hypertension.
Andere Medikamente: albuterol HFA, Januvia 100 mg, metformin 500mg BID, metoprolol ER 25 mg
Allergien: PCN
Vorherige Impfungen: -

VAERS 2319034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 04.10.2021
Beginn: 23.05.2022
Tage bis Beginn: 231,0
Dosis: 2
Route/Site: - / -

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

Back pain COVID-19 Hypoaesthesia SARS-CoV-2 test positive

Symptomtext

5/23 36y.o. female with history of lumbar DDD and disc herniations s/p right L4-L5 discectomy who presents with acute on chronic low back pain, associated with intermittent numbness in her L leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: 5/23 SARS-CoV-2 Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2306587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 03.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Pain in extremity

Symptomtext

sore arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient received BNT162b2 (BNT162B2), on 08Apr2021 as dose 1, 0.3 ml single (Lot number: EW0151, Expiration Date: 31Jul2021), in left arm, on 30Apr2021 as dose 2, 0.3 ml single (Lot number: EW0167, Expiration Date: 31Aug2021), in left arm and on 03Nov2021 as dose 3 (booster), 0.3 ml single (Lot number: FH8020, Expiration Date: 31Jan2022) at the age of 61 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "sore arm".

Weitere VAERSDATA-Felder

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

VAERS 2301107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 44,0
Geschlecht: F
Eingang: 28.05.2022
Impfdatum: 05.11.2021
Beginn: 23.05.2022
Tage bis Beginn: 199,0
Dosis: 3
Route/Site: - / RA

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

Diarrhoea Drug ineffective Faeces discoloured Suspected COVID-19

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Yellow stool; diarrhea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 45-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Nov2021 as dose 3 (booster), single (Lot number: FH8020) at the age of 44 years, in right arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (COVID-19 VACCINE MODERNA), on 06Apr2021 as dose 1, single (Lot number: 036B21A), in right arm and on 06May2021 as dose 2, single (Lot number: 025C21A), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Obesity" (unspecified if ongoing); "Known allergies: Sulfites" (unspecified if ongoing). Concomitant medication(s) included: VITAMIN D2, start date: 01Jan2021; FAMOTIDINE, start date: 01Jan2021; B12-VITAMIIN, start date: 12Jan2022; FOLIC ACID, start date: 01Jan2021; NORETHINDRONE [NORETHISTERONE], start date: 01Jan2021, stop date: 20May2022. The following information was reported: FAECES DISCOLOURED (non-serious) with onset 23May2022 at 11:00, outcome "unknown", described as "Yellow stool"; DIARRHOEA (non-serious) with onset 23May2022 at 11:00, outcome "unknown", described as "diarrhea"; DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, suspected covid-19 with Paxlovid (Lot number FY9918) from 21May2022 to 23May2022. Therapeutic measures were not taken as a result of faeces discoloured, diarrhoea. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE INJECTABLE lot FH8020 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FH8020, fill lot FG3521, and the bulk formulated drug product lot FH0137. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Obesity; Sulfonamide allergy
Andere Medikamente: VITAMIN D2; FAMOTIDINE; B12-VITAMIIN; FOLIC ACID; NORETHINDRONE [NORETHISTERONE]
Allergien: -
Vorherige Impfungen: -

VAERS 2294543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 19.11.2021
Beginn: 06.05.2022
Tage bis Beginn: 168,0
Dosis: 3
Route/Site: SYR / AR

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

COVID-19 Fatigue Headache Oropharyngeal pain SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case of COVID-19: I got COVID-19, I had to quarantine, I did not require any treatment. I had a headache and sore throat for three days; and felt very fatigued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Rapid PCR test positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal Allergies; COPD; Migraines
Andere Medikamente: Estradiol; fluticasone; multivitamins; vitamin D
Allergien: Sulfa; morphine
Vorherige Impfungen: -

VAERS 2294503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain

Symptomtext

PAIN IN ARM AT INJECTION SITE. PAIN LASTED IN MUSCLE FOR 5 MONTHS UNTIL END OF APRIL 2022. hE STATES HIS MUSCLE WAS AGITATED AND THE PAIN INCREASED OVER THE FIRST FEW WEEKS AND THEN STAYED THE SAME, DECREASING IN APRIL UNTIL IT WENT AWAY BY END APRIL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroid
Andere Medikamente: levothyroxine, fluoxetine, atorvastatin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2288082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 28.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: UN / LA

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

Asthenia Joint range of motion decreased Limb discomfort Muscular weakness Pain in extremity

Symptomtext

Since my third Pfizer shot, I have issues with my left arm. I have a limited range of motion, some pain and weakness. When I got my fourth shot, I told this nurse about this experience and she asked me to report it through this site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: No lab tests. I have mentioned it to my doctors when I was seeing them for other things and I have told my other about it
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis Low thyroid
Andere Medikamente: Levothyroxine Prolia
Allergien: None
Vorherige Impfungen: -

VAERS 2286953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 10.12.2021
Beginn: 16.05.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: IM / AR

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

Blood culture negative COVID-19 Chemotherapy Chest X-ray normal Oesophageal carcinoma Pancytopenia Platelet transfusion Pyrexia Red blood cell transfusion Respiratory symptom SARS-CoV-2 test positive Thrombocytopenia

Symptomtext

Hospitalized 05/16/2022-05/18/2022; COVID-19 positive 05/16/2022; fully vaccinated plus booster HOSPITAL COURSE Per H and P at the time of admission, this is 64-year-old male with a history of ischemic cardiomyopathy, coronary artery disease status post multiple stenting procedures, dyslipidemia, CVA, newly diagnosed metastatic esophageal small cell carcinoma, on active treatment, presented to the emergency room with upper respiratory symptoms and a fever for 3 days prior to his hospitalization, had 2 positive home COVID test, which was confirmed in the ED with a COVID PCR. Chest x-ray was completed which was negative. Blood cultures were obtained. He was given 1 unit of packed red blood cells and 1 unit of platelets. Denied any shortness of breath or chest pain. He was admitted for further evaluation and treatment. Blood cultures remained negative. He was started on cefepime and vancomycin. He was continued on cefepime while he was inpatient. It was noted that the patient got Neulasta outpatient on May 6 as part of his chemo regimen. He continues to be pancytopenic, which is likely secondary to recent chemo. Discussed with Service as well which also agree likely secondary to the recent chemo. Counts should recover, recommending close monitoring at this time. The patient will be offered a dose of Zarxio before he leaves to help improve his counts further. The patient was continued on his home medications. Aspirin was held due to his thrombocytopenia, may resume when his counts are normal. The patient declines to remain in the hospital to complete a 5-day course of remdesivir. He did receive a second dose this morning. Please see system for complete listing of discharge instructions, followup information. Discussed discharge plans with the attending who is aware of the patient being discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: Port a cath placement in Interventional radiology on 04/29/2022
Vorgeschichte: OSA (obstructive sleep apnea) Ischemic cardiomyopathy CAD (coronary artery disease) HTN (hypertension) Single ICD (implantable cardiac defibrillator) in place Chronic combined systolic and diastolic congestive heart failure Acute ischemic left MCA stroke Aphasia due to acute stroke Protein-calorie malnutrition, moderate Pancytopenia Alcohol abuse, continuous Stage 3b chronic kidney disease Dyslipidemia, goal LDL below 70 Memory loss Memory loss or impairment Irregular sleep-wake rhythm
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet benzonatate (TESSALON) 100 MG capsule carvedilol (COREG) 25 MG tablet guaiFENesin (MUCINEX) 600 MG 12 hr tablet losartan (COZAAR) 50 MG tablet nitroGLYCERIN (NITROST
Allergien: NKA
Vorherige Impfungen: -

VAERS 2266903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 10.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Cough Headache Insomnia Oropharyngeal pain Pyrexia COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

I had a fever; bad headache; sore throat; coughing; got very little sleep last night; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 43-year-old male patient received BNT162b2 (BNT162B2), on 10Oct2021 as dose 3 (booster), single (Lot number: FH8020) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 1, Lot Number: EL9264), administration date: 28Jan2021, for Covid-19 immunization; BNT162b2 (Dose Number: 2, Lot Number: EL9266), administration date: 20Feb2021, for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 2022, outcome "recovered" (2022), described as "I had a fever"; HEADACHE (non-serious) with onset 2022, outcome "recovered" (2022), described as "bad headache"; COUGH (non-serious) with onset 2022, outcome "unknown", described as "coughing"; INSOMNIA (non-serious) with onset 2022, outcome "unknown", described as "got very little sleep last night"; OROPHARYNGEAL PAIN (non-serious) with onset 2022, outcome "unknown", described as "sore throat". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (04May2022) Positive, notes: patient tested positive today, 04May2022, for COVID-19. It was reported that, patient tested positive today, 04May2022, for COVID-19. Patient had previously been vaccinated and boosted with the Pfizer BNT vaccine. Event took place after use of product. Patient was not feeling well today at the time of the report and will be offline. Patient wanted to share that he had tested positive for Covid-19 and will likely be offline for the rest of the week. It was reported that, yesterday I had a fever, bad headache and sore throat/coughing. I got very little sleep last night, but at least the headache and fever have subsided. I'm going to try and rest today and tomorrow. Product quality group providing Investigation results for lot FH8020: As part of the simplification process, the following Complaint Records were classified and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process. Refer to the below table for details: AE Ref No. Product Description (CR): COMPOUND BNT 162 COVID-19 VACCINE SUSPENSION FOR INTRAMUSCUL AR 2ML MULTIPLE DOSE VIAL was 1 The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot EL9264 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EL9264, fill lot EL9255, and the formulated drug product lot EL9246. A complaint sample was not returned. No related quality issues were identified during the investigation. There was no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Product quality group providing Investigation results for lot EL9264: As part of the LOE simplification process, the following Complaint Records were classified as Product and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process. Product Description (CR): COMPOUND BNT 162 COVID-19 VACCINE SUSPENSION FOR INTRAMUSCULAR 2ML MULTIPLE DOSE VIAL was 1 Lot- (CR): EL9264 Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot EL9264 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EL9264, fill lot EL9255, and the formulated drug product lot EL9246. A complaint sample was not returned. No related quality issues were identified during the investigation. There was no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Product quality group providing Investigation results for lot EL9266: As part of the LOE simplification process, the following Complaint Records were classified as Product and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process. Refer to the below table for details: Product-Description (CR): COMPOUND BNT 162 COVID-19 VACCINE SUSPENSION FOR INTRAMUSCULAR 2ML MULTIPLE DOSE VIAL X 1. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot EL9266 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EL9266, fill lot EL9257, and the formulated drug product lot EL9248. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. When more than one investigation is found in the family, the Conclusion field could result in repeating rows for the CR in the table. If the Conclusion is blank in the table above, then the investigation record is likely an Offline Contractor Investigation and the conclusion must be obtained directly from the child investigation record(s) of the linked Complaint Record. No follow-up attempts are possible. No further information is expected. Follow up (04May2022): New information received from a contactable consumer. This consumer reported in response to Non- HCP letter via Email follow-up activity: Updated information included: New events (I had a fever, bad headache, sore throat, coughing. I got very little sleep last night) were added. No follow-up attempts are possible. No further information is expected. Follow-up (06May2022): This is a follow-up spontaneous report from product quality group providing investigation results. This report included that: Updated Information Included: Batch and lot tested and found within specifications was checked.( All release testing performed prior to the release of the reported batch was within specifications.). Additional Information: This is a notification generated from the system. Follow-up (06May2022): This is a follow-up spontaneous report from product quality group providing investigation results. This report included that: Additional Information: This is a notification generated from the system. Follow-up (09May2022): This is a follow-up report from product quality group providing investigation results. This report included that: Updated information included: Batch/lot tested found within specifications ticked in product tab and investigational results were updated in narrative. Follow-up attempts completed. No further information expected. Follow-up (15May2022): This is a spontaneous follow-up report received in response to the mail trail sent regarding the confirmation below mentioned query. The response included: Updated information included: Dose 1 and 2 captured as Historical Vaccine. Events "Vaccination failure" and "Covid-19" removed as this case is for dose 3 with events insomnia, pyrexia, headache, cough, oropharyngeal pain as the events occurred in 2022 after dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20220504; Test Name: SARS-CoV-2 test; Test Result: Positive ; Comments: patient tested positive today, 04May2022, for COVID-19.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2280802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: LA
Alter: 60,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 13.11.2021
Beginn: 02.05.2022
Tage bis Beginn: 170,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Influenza like illness Pyrexia SARS-CoV-2 test positive Sinus operation

Symptomtext

-approximately 12 hours after shot I experienced flu like aches and low grade ( 99) fever for about 24 hours. - I contracted COVID on 05/02/2022 -I had minimal symptoms (flu like aches for about 48 hours, sinus drip for 14 days and minor cough due to sinus drip for 7 days) Never had fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: - Tested positive for COVID using OTC antigen test on May 5, 2022.
Aktuelle Erkrankungen: Not applicable
Vorgeschichte: Coronary atery disease with previous heart attack
Andere Medikamente: Losartan, atorvastatin
Allergien: Penicillin
Vorherige Impfungen: -flu like aches and low grade (99) fever for about 24 hours after each COVID vaccine.

VAERS 2275573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

mild

Staat: MO
Alter: 56,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 11.11.2021
Beginn: 29.04.2022
Tage bis Beginn: 169,0
Dosis: 3
Route/Site: IM / LA

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

Back pain COVID-19 Cough Myalgia Pain Pain in extremity SARS-CoV-2 test positive Sleep disorder

Symptomtext

I noticed pain in my lower back and front thigh area. I was achy with muscle pain. I developed a bronchitis like cough. When I woke up that Saturday morning I completed a home test and was positive. I treated myself with Advil and Tylenol and plenty of fluids. Coughing made it hard to get a good nights re st so I contacted my doctor and she prescribed Benzonatate 200 mg to take 3 times a day. That helped because by that Wednesday I was feeling better. I have a slight cough but I believe I have completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin C Cranberry supplement Vitamin D3 Cetirizine Imipramine
Allergien: none
Vorherige Impfungen: Shingles-I felt not well-achy and tired.

VAERS 2271874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: HI
Alter: 39,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 20.10.2021
Beginn: 07.05.2022
Tage bis Beginn: 199,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Asthenia Cold sweat Diarrhoea Discomfort Fatigue Pain Pruritus Pulmonary congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

On Saturday morning I started to have some minor chest congestion. As the day went on I was feeling really fatigue and started to get achy. I started to run a fever of 100 and so I took a rapid test and it came back positive. The following day my fever got up to 101. I took 2 Tylenol to help reduce the fever and that seemed to help. That evening I did experience cold sweats and I felt very uncomfortable. I started to feel very itchy and anxious. I would compare it as if I took a stimulant or had a lot of caffeine. I also experienced diarrhea for 2 days. On 05/10/2022 I did have a PCR test which also came back positive. My chest congestion has cleared up for the most part just feeling a little weak.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 05/10/2022: PCR: Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Mild high blood pressure
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2268984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NY
Alter: 26,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 22.10.2021
Beginn: 12.04.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: IM / RA

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

Coronavirus infection Cough Fatigue Influenza like illness Malaise Nasopharyngitis Oropharyngeal pain Pain Pyrexia

Symptomtext

I caught the novel coronavirus about 6 months after I received my booster dose. I was sick with minor cold/flu-like symptoms for about 8 days. During the worst part of the sickness, I had a fever of 101.6 and body aches. This only lasted about one day. The rest of the week I felt tired and had a sore throat with a mild, but painful, cough.

Weitere VAERSDATA-Felder

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

VAERS 2268145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MN
Alter: 41,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 08.04.2021
Beginn: 23.04.2022
Tage bis Beginn: 380,0
Dosis: 2
Route/Site: SYR / LA

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

Blood magnesium normal Decreased appetite Diarrhoea Full blood count normal Glycosylated haemoglobin Hepatitis C test negative Laboratory test normal Metabolic function test Red cell distribution width decreased SARS-CoV-2 test negative Stool analysis

Symptomtext

Diarrhea started around 4/23/2022. Progressively has gotten worse since then. After a week, I had a phone visit with Urgent care, and they told me to take Imodium and come back in a week if it wasn't better. I took Imodium for about a week. Once I stopped, diarrhea had gotten significantly worse, to the point where I can't eat any food. I called my PCP and they couldn't get me in, but got a phone appointment with a different doctor the next day, and an in person appointment with a PA-C 5 days later (5/10/2022). I'm now basically just eating white rice, bananas, and Gatorade. But no fever, no cough, still have taste and smell, and have gotten 2 negative COVID tests on rapid covid tests spaced a week apart. **Note that my epilepsy meds changed in 4/2022 -- I titrated to my current dose of 200mg am/200mg pm Vimpat, and 100mg am/200mg pm Zonegran -- the Zonegran has been messing with my appetite a lot).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Bloodwork on 5/5/2022 done while still on Imodium, but magnesium normal, CBC generally normal except RDW slightly low, metabolic bloodwork normal, A1C showed significant interference from HbF (though result was normal), Hepatitis C was negative, Zonisamide levels were within range. Still waiting on Vimpat levels; and for 5 days post-Imodium for stool test (will be done on 5/10/2022).
Aktuelle Erkrankungen: None
Vorgeschichte: Epilepsy, migraine, GERD, anemia, seasonal asthma, anxiety/depression
Andere Medikamente: Oxcarbazepine (750mg am, 900mg pm), Iron, Famotidine, Prilosec, QVar, Albuterol (as needed), fluticasone
Allergien: Lamictal, Brevital
Vorherige Impfungen: -

VAERS 2268056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: WI
Alter: 57,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 03.11.2021
Beginn: 04.05.2022
Tage bis Beginn: 182,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Chills Cough Fatigue Mucosal hypertrophy Oropharyngeal pain Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sleep disorder Vomiting

Symptomtext

On Wednesday, 05/04/2022, morning I had a cough. At bedtime I started to get congested and chills. Slept on the couch and stayed away from everyone. Thursday, 05/05/2022, I threw up all day, I had body aches, and the next morning I was able to drink water and kept it down and had toast. I did an at home COVID-19 test and tested positive 05/05/2022. I went to the clinic and had a PCR test on Thursday, 05/05/2022. And I kept throwing up all day Thursday. I had a lot of snot and drainage. The mucous was so thick, I could not lay down flat or I would gag on it. Friday morning, I kept food in. I received an email from the clinic and found out I tested positive for COVID-19. My doctor prescribed Paxlovid on Friday night. I still had body aches Friday night, threw up just a little bit and I have not thrown up since then. I still had a sore throat. Since taking the Paxlovid I am getting a little bit stronger. I am still having congestion, exhaustion, not as bad as it was. I can make a meal and then I am tired. All the other symptoms have dissipated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 05/04/2022- at home COVID-19 test- positive 05/04/2022 - PCR COVID-19 test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: Metals- break out from wedding ring and watches
Vorherige Impfungen: -

VAERS 2267923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NY
Alter: 28,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 10.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: IM / RA

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

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

Symptomtext

I woke up with a massive headache and a sore throat on day one. For the first 5 days I woke up to a splitting headache. Tuesday May 03, I took a 2nd COVID-19 test which was positive. At that point the sore throat was moderate. No congestion, My cough peaked around May 4 and 5th. The nasal and chest congestion started then as well. I am still testing positive. I went to the doctor on Wednesday May 04. They confirmed I was positive and recommended OTC medication. I have taken Excedrin just to tackle the headache. I still have mild chest congestion and a faint sore throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 Test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: 1 A Day Male Multivitamin Vitamin D3 25mg Minoxidil Finasteride
Allergien: None
Vorherige Impfungen: -

VAERS 2267616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

mild

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 01.12.2021
Beginn: 01.05.2022
Tage bis Beginn: 151,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Neuralgia

Symptomtext

Patient reported Significant joint and nerve pain that developed within 7 days of 1st Booster vaccine (pain primarily located behind knees and in wrists (on both sides of body)). Prescriber gave motrin, but symptoms still present currently (5/9/22).

Weitere VAERSDATA-Felder

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

VAERS 2266358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NM
Alter: 61,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 15.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: SYR / AR

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

Biopsy uterus normal Blood test abnormal Fatigue Feeling of body temperature change Thyroid disorder Thyroid function test abnormal Ultrasound thyroid abnormal Ultrasound uterus normal Vaginal haemorrhage

Symptomtext

After my vaccine I felt hot and cold for a few days and general fatigue that happens with every shot. Around 10/30/2021 I began to bleed vaginally and got in touch with my OBGYN and he stated that this seemed to be normal for elderly patients with vaccines being administered. The bleeding did stop after bout 4 days later and still got checked with my OBGYN. They did do an ultrasound and did not find anything out of the normal. Biopsies came back clear as well. The only other thing that came up was surrounding my thyroid. I went in for my physical on March 03rd and with blood work and my THX levels were way out of proportion and not within normal range. I was told to get it checked out as soon as possible, he ordered an ultrasound, a check in with endocrinology as well. Ultrasound did see areas that may be questionable and will be doing additional scans and found that thyroid is off. I am waiting for now a biopsy on Wednesday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Ultrasound: Showing no issues from OBGYN Ultrasound: Showing issues in thyroid Bloodwork: Showing THX levels out of normal range
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis in joints Melanoma Cancer twice Hx of SVT top two chambers of heart Hyperthyroidism
Andere Medikamente: Losartan Potassium Ibuprofen Trazodone HCL Vitamin D3 and K2 Magnesium Mucinex PRN
Allergien: Minor Allergy Shellfish Adhesive Products Metals Nylon
Vorherige Impfungen: Last Flu Shot I was almost hospitalized when I was younger due to very bad fevers.

VAERS 2263292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 01.11.2021
Beginn: 16.04.2022
Tage bis Beginn: 166,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Fatigue Headache Malaise Nasal congestion Nasopharyngitis Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

COVID-19 symptoms started the night of 04/16/22 with a sore throat. On 04/17/22, I felt the chills and I thought I was having a bad cold. On 04/18/22, I took a home test and it was positive. I had a stuffy head and a headache and took antiviral medications and felt fine. I was also tired. The fatigue lasted awhile but I'm not sure if it was COVID-19 or from taking care of people. The sore throat and stuffy head was done and I was just tired, but not any more than normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19- Home Test (04/18/2022- Positive)
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Thyroid Medication Birth control
Allergien: None
Vorherige Impfungen: -

VAERS 1853860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH 8020

mild

Staat: PA
Alter: -
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / -

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

Atrial fibrillation Atrial flutter Electrocardiogram abnormal Exercise tolerance decreased Fatigue Gait disturbance Heart rate increased

Symptomtext

Atrial fibrillation; Flutter; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An adult male patient received BNT162b2 (BNT162B2), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: ATRIAL FIBRILLATION (medically significant), outcome "unknown"; ATRIAL FLUTTER (non-serious), outcome "unknown", described as "Flutter". Clinical course: Customer verbatim: Pfizer BioNTech Covid Vaccine and Atrial fibrillation/flutter - a phase IV clinical study of CDC and FDA data Summary: Atrial fibrillation/flutter is found among people who get Pfizer BioNTech Covid Vaccine, especially for people who are male, 60plus old. Reporters husband developed this and they reported it but have not heard from them. Requested to be contacted to discuss this. 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: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2260595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 23.11.2021
Beginn: 14.01.2022
Tage bis Beginn: 52,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Myalgia Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive Sneezing Vaccine breakthrough infection

Symptomtext

COVID-19 breakthrough. The symptoms were like a mild cold. I had a runny nose, fatigue, sneezing and muscle aches. The cough was very severe, I seemed to be coughing all the time. I think I remember taking Ibuprofen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Gastritis Gastroesophageal Reflux Disease
Andere Medikamente: Zyrtec Singulair Pepcid Melatonin Multivitamin Ocuvite Ibuprofen Efudex
Allergien: Latex
Vorherige Impfungen: Shingles vaccine. Flu-like symptoms. 63 years

VAERS 2255074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MO
Alter: 30,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 24.10.2021
Beginn: 22.12.2021
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia Autoimmune disorder Blood test abnormal COVID-19 Cough Fatigue Feeling abnormal Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had fatigue, fever, loss of taste and smell. I also have congestive, brain fog and a cough. These lasted for about a week, but the cough lasted about a month and the brain fog lasted for about 2 months. On Dec 24th, I tested positive for COVID-19. And now I have been diagnosed with an autoimmune disease. I have had blood work done, that confirmed the autoimmune disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test, blood work.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Cyclopes
Vorherige Impfungen: -

VAERS 2254693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: OK
Alter: 50,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 10.11.2021
Beginn: 21.04.2022
Tage bis Beginn: 162,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia COVID-19 Cough Feeling abnormal Hyperhidrosis Influenza like illness Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I tested positive on 04/21/2022 for COVID-19 and my symptoms are moderate. I had a serve cough, running nose, joint ache, brain fog, sweats and sore throat. I had flu like symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: At home COVID-19 test.
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure
Andere Medikamente: Atenolol 25mg; Atorvastatin 10mg; Fluoxetine 60mg.
Allergien: No
Vorherige Impfungen: Dose 2 ER8729 04/08/2021

VAERS 2252213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 23.10.2021
Beginn: 05.03.2022
Tage bis Beginn: 133,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chest X-ray normal Cough Fatigue Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sleep disorder

Symptomtext

On March 5, 2022 woke with sore throat in am between 8:00-9:00AM. I had just got back from a trip overseas and they tested me the Wednesday 03/02/2022 and it was Neg. I took a home test 03/05/2022 and tested positive. I got worse over the next few days and got a fever, congestion, cough, and fatigued. I did go to an Urgent Care and did a remote visit on 03/21/2022 because my symptoms were manageable but my cough did not go away. I was prescribed Antibiotic ZPAK, Inhaler Albuterol, and Tessalon because the cough prevents me from being able to sleep at night. The inhaler made me cough more so I followed-up with my PCP 04/06/2022 who ordered a chest x-ray. He prescribed me more Tessalon and scheduled a follow up for 2-3 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 04/06/2022 Chest X-ray Normal and Clear; 03/02/2022 E-med COVID-19 Test -Results Negative; 03/05/2022 COVID-19 Test -Positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None.
Allergien: None
Vorherige Impfungen: -

VAERS 2252141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NH
Alter: 32,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 25.10.2021
Beginn: 24.04.2022
Tage bis Beginn: 181,0
Dosis: 2
Route/Site: SYR / LA

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

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

Symptomtext

I ended up with COVID-19 in April 2002. It started Saturday morning with a headache. It got work. to a home test. Started coughing the next day the test was negative at first. I went to work that day and at night I felt worst. took another test and it came out positive. I am in quarantine in has been 2 days so far. I spoke to doctor over the phone. I have been resting and drinking fluids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: D?cor; Sulfa
Vorherige Impfungen: -

VAERS 2252059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: VT
Alter: 36,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 21.10.2021
Beginn: 10.04.2022
Tage bis Beginn: 171,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Hyperacusis Nasopharyngitis Photophobia SARS-CoV-2 test positive Sinus disorder Vaccine breakthrough infection

Symptomtext

COVID-19 breakthrough. I started off with a wet cough in the back of the throat and it traveled up to my sinuses. I had sensitivity to light and sound. I was also extremely fatigued. Its been very similar to a sinus cold with an extra cough. The worst of it was from the 4/10/2022-4/14/2022. Now its pretty much just a lulling cough that I can take a cough drop for and be okay.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: Polycystic Ovarian Syndrome (PCOS)
Andere Medikamente: Birth control - Vienza; Olly Women's Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2250596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: AK
Alter: 37,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal distension Adenomyosis Blood test abnormal Fatigue Heavy menstrual bleeding Hysterectomy Laboratory test Liver disorder Mood swings Uterine leiomyoma

Symptomtext

Abnormal periods hemorrhaging, Adenomyosis, and development of fibroids. 12/28 uterus, ovaries, and cervix removed. Bloating, fatigue and mood swings.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Stenography, Blood Labs revealed liver issues as well.
Aktuelle Erkrankungen: No
Vorgeschichte: Early onset osteoarthritis
Andere Medikamente: Multivitamin; Vitamin D
Allergien: Penicillin; Sulfa; Celery; Blue cheese
Vorherige Impfungen: -

VAERS 2243208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 28.01.2021
Beginn: 09.08.2021
Tage bis Beginn: 193,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain COVID-19 Nausea SARS-CoV-2 test positive

Symptomtext

8/9/21 history of stage 3 CKD, HTN, presenting with acute onset abdominal pain and persistent nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 8/9/21 SARS-CoV-2 (COVID-19) by NAA Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2241038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MO
Alter: 68,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 19.10.2021
Beginn: 15.01.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: SYR / LA

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

Body temperature increased Fatigue Nasopharyngitis Respiratory tract congestion

Symptomtext

It was like I had a nasty cold congestion and feeling fatigued a little temperature.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: RSV
Vorgeschichte: Heart Failure
Andere Medikamente: Carvedilol; Lisinopril; Aspirin; Omega 3
Allergien: Pollen
Vorherige Impfungen: -

VAERS 2241022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: SC
Alter: 61,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 18.10.2021
Beginn: 25.03.2022
Tage bis Beginn: 158,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Blood test Fatigue

Symptomtext

I had extreme fatigue and exhaustion, it was unlike anything I've ever had. If I didn't have a dog to take out, I probably would have stayed in bed all day with little to no energy. It went on for weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Complete blood work panel 4/11
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity; Arthritis
Andere Medikamente: Meloxicam Trazodone Atorvastatin Baclofen
Allergien: None
Vorherige Impfungen: -

VAERS 2240848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: PA
Alter: 50,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 03.11.2021
Beginn: 15.12.2021
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: SYR / RA

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

Ear discomfort Ear disorder Ear pruritus

Symptomtext

December 15,2021 I started having issues with my ear. I went to the doctor on February 21, 2022. He prescribed ofloxacin, two drops in both ears 5 times a day for 5 days. I did it actually for 7 days. In a couple of days if felt okay. Then the itchy and moist feeling came back and I went back to the doctor on April 5 and saw a PA. She prescribed tobramycin, 1-2 drops every 2-4 hours a day for 7 days. She also prescribed clotrimazole, 1 drop 3-4 times daily for 14 days. I finished that up last week, my ears are still itchy, not totally resolved. I have good days and bad days. There are days it feels so dry and itchy, feels like a lot of moisture inside. Today doesn't feel like as much moisture. My next option is to go to an ENT.

Weitere VAERSDATA-Felder

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

VAERS 2240557

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Drug ineffective Fatigue Interchange of vaccine products Off label use Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 54-year-old female patient received BNT162b2 (COMIRNATY), on 27Oct2021 as dose 2 (initial Pfizer dose), single (Lot number: FH8020) at the age of 54 years for Covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Janssen (Dose 1), administration date: 15Mar2021, when the patient was 53-year-old, for COVID-19 Immunization. The following information was reported: OFF LABEL USE (medically significant) with onset 27Oct2021, outcome "unknown"; INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 27Oct2021, outcome "unknown"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "She tested positive for COVID-19 with an at home test"; PAIN (non-serious), outcome "unknown", described as "body aches"; PYREXIA (non-serious), outcome "unknown", described as "fever"; OROPHARYNGEAL PAIN (non-serious), outcome "unknown", described as "sore throat"; FATIGUE (non-serious), outcome "unknown". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: COVID-19 with an at home test; Test Result: Positive.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2239235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: AS
Alter: 37,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Blindness unilateral Bone pain Breast cancer stage IV Myalgia SARS-CoV-2 test

Symptomtext

the left eye stopped seeing; cancer of the 4th stage appeared; severe pains in the muscles, in the bones began; severe pains in the muscles, in the bones began; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 37-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Sep2021 as dose 1, single (Lot number: FH8020) at the age of 37 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "If covid prior vaccination: Yes" (unspecified if ongoing), notes: If covid prior vaccination: Yes; "Breast cancer 2 stage" (unspecified if ongoing). There were no concomitant medications. The following information was reported: BREAST CANCER STAGE IV (medically significant, life threatening) with onset 10Sep2021, outcome "not recovered", described as "cancer of the 4th stage appeared"; MYALGIA (life threatening), BONE PAIN (life threatening) all with onset 10Sep2021, outcome "not recovered" and all described as "severe pains in the muscles, in the bones began"; BLINDNESS UNILATERAL (medically significant, life threatening) with onset 10Sep2021, outcome "not recovered", described as "the left eye stopped seeing". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (25Dec2021) Negative, notes: Covid test type post vaccination=Nasal Swab. Therapeutic measures were taken as a result of blindness unilateral, breast cancer stage iv, myalgia, bone pain. Additional information: If other vaccine in four weeks: No. Other medications in two weeks.; Sender's Comments: Based on the information provided in the narrative, a causal association between the suspect drug and the events cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: Test Date: 20211225; Test Name: Nasal Swab; Test Result: Negative ; Comments: Covid test type post vaccination=Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer stage II; COVID-19 (If covid prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2231394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 57,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 12.10.2021
Beginn: 09.01.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Headache Impaired work ability Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

01/09/2022, in the mid- morning early afternoon the symptoms, I had chest congestion on my chest, cough, and headache. I kept testing positive for omicron. I tested positive for Omicron after my booster shot. I finally tested negative for omicron on Jan 18, 2022. I missed work. Jan 12, I did a home test it was positive. Jan 16, I was still positive. On the 18/2022, negative. I went back to work on the Jan 19, 2022. I still have the headache from the omicron it comes on and off.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure
Andere Medikamente: Omeprazole 20mg, Amlodipine baseplate 5mg
Allergien: Seasonal allergies, Imodium
Vorherige Impfungen: -

VAERS 2228819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MN
Alter: 36,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 15.10.2021
Beginn: 20.12.2021
Tage bis Beginn: 66,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chills Cough Headache Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I had congestive, running nose, sneezing, headache, fever, body ache, cough and chills. These lasted for about 3 day but the cough lasted for about 5 days. On Dec 21st, I tested positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec, Vitamin D
Allergien: N/A
Vorherige Impfungen: Flu

VAERS 2223022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 01.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: SYR / RA

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

Injection site bruising Injection site swelling Pain in extremity

Symptomtext

Couple of days after my booster shot my arm was sore then a week after the site of the shot you could ( can still see it ) see like a rectangle on my arm. Now it look like there's a bruise all along the site of the shot and the area is swollen. I have told my PCM about it over the phone and he told me that if it doesn't go away in a couple of months to report it to the CDC. So I am......

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Fibromyalgia IBS with Constipation RA Slow digestive system
Vorgeschichte: See above
Andere Medikamente: Singular Zyrtec Advair HFA Albuterol Nitroglycerin Aspirin 81mg Lipitor Dronabinols Fluoxetine Hyroxychloroquine Prednisone Topiramate Metoprolol
Allergien: None
Vorherige Impfungen: -

VAERS 2218090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NC
Alter: 39,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 25.03.2021
Beginn: 15.04.2021
Tage bis Beginn: 21,0
Dosis: UNK
Route/Site: SYR / -

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

Arthralgia Gait disturbance Laboratory test Pain Pain in extremity Rash Rheumatoid factor

Symptomtext

In July of 2021 I developed a rash on my left leg. I had pain in my left leg that steadily increased over the next 30 days. It was difficult to walk. It then increased to pain in my arms, legs, wrists, hands. The pain moved each day and gradually got worse. At first the pain would just start in the evenings and gradually get worse through the night to where it was difficult to get up and walk in the morning. The pain was subsided with medication and steroid treatment for inflammation but the root cause has not been determined and now the pain is starting to come back even with current medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Lyme, Lupus, rheumatoid arthritis, Chikungunya, RA
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: 10MG Amlodipine, Women's one a day vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 2214215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 09.09.2021
Beginn: 01.12.2021
Tage bis Beginn: 83,0
Dosis: 2
Route/Site: SYR / LA

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

Erythema Inflammation Pruritus Swelling Urticaria

Symptomtext

Constant inflammatory state. Hives on face and body. Only steroids will stop the hives which are red, swollen and itchty

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism
Andere Medikamente: synthroid
Allergien: none
Vorherige Impfungen: -

VAERS 2213616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 16,0
Geschlecht: F
Eingang: 03.04.2022
Impfdatum: 10.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Cough Full blood count normal Rash Rash pruritic Respiratory tract infection Skin warm Viral rash Viral test negative

Symptomtext

Patient was seen 11/15/2021 please see attached notes Patient here with mom for eruption that started 11/11 or 11/12 24-48hrs after her 2nd pfizer covid vaccine. The rash started on her left arm/elbow area (distal to the injection site, also left arm). The rash was initially reportedly itchy, but now "feels hot". She has taken benadryl, unclear if it helped. Patient is also on Augmentin rx'd by UC for an acute cough/respiratory illness (dx unclear, notes not available for review at time of visit) that she started on 11/1 and has not been taking as directed (she has missed doses). The appearance of the rash is most consistent with a viral exanthem, similar to a mono-type rash, also possibly caused by Augmentin. Discussed this with mom and pt. Recommended testing for mono, esp due to recent URI illness. Pt denies fatigue, no lymphadenopathy, no organomegaly. Pending lab test results will fill our VAERS paperwork if mono negative as this is possibly a vaccine reaction or an immune mediated response from vaccine (not necessarily "allergic reaction" or contraindication to future boosters if indicated). Ok to take zyrtec 10mg daily or benadryl. If needed may take 1-2 benadryl before bed with zyrtec, but not to exceed that dosing. F/u prn. Check CBC w/auto diff Check infectious mono qualitative Check epstein barr virus evaluation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: CBC - WNL Monospot, EBV Panel Neg
Aktuelle Erkrankungen: Upper Respiratory illness dx 11/1/2021
Vorgeschichte: patellofemroral stress syndrome
Andere Medikamente: AUGMENTIN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2209143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CT
Alter: 39,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 29.11.2021
Beginn: 30.03.2022
Tage bis Beginn: 121,0
Dosis: 3
Route/Site: IM / -

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

Fatigue Headache Respiratory tract congestion

Symptomtext

Headache, fatigue, congestion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Rapid Test at Docs - 3/30/22. Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2204937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: PA
Alter: 53,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 25.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / LA

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

Acoustic stimulation tests Injection site pain Tinnitus

Symptomtext

Received Pfizer booster and had only soreness at injection site. No other symptoms noted. About a week later I woke up with tinnitus in my left ear. Has been constant ever since -- 5 months now. In December, had physician check for other causes, had hearing test. No change.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: Jan 21 2022, had hearing test, prescribed antihistamine and nasal steroid. Told to take Lipo Flavonoids vitamins for the tinnitus. No change.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Xiidra eye drops
Allergien: -
Vorherige Impfungen: -

VAERS 2201785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CT
Alter: 91,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 29.11.2021
Beginn: 28.03.2022
Tage bis Beginn: 119,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Discomfort Fatigue Headache Nasal congestion SARS-CoV-2 test positive

Symptomtext

Headache, nasal congestion/pressure, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Rapid test 3/28/22 - Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertensive heart disease with heart failure mixed hyperlipidemia longstanding persistent atrial fibrilation chronic diastolic (congestive ) heart failure impaired fasting glucose hypothyroidism, unspecified gout, unspecified sprain of ligaments of lumbar spine, sequela
Andere Medikamente: Acetaminophen 500mg bumetanide 2mg coreg 12.5mg febuxostat 40mg levothyroxine 75 mg metolazone 5mg potassium chloride ER 10 sildenafil f/c 20mg sodium bicarbonate 10gr
Allergien: Penicillin G Potassium Septra
Vorherige Impfungen: -

VAERS 2196319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: TX
Alter: 76,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Feeling cold Headache Influenza like illness Pain

Symptomtext

I had a really bad headache, and I ached all over. It felt like the flu. I had terrible chills and couldn't get warm. This lasted about 12 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Advair, Singulair, Multivitamin, B-12, CQ10
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2189286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: WI
Alter: 45,0
Geschlecht: M
Eingang: 20.03.2022
Impfdatum: 22.02.2021
Beginn: 01.09.2021
Tage bis Beginn: 191,0
Dosis: 3
Route/Site: - / RA

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

Erythema Pain in extremity Pruritus Rash Sleep disorder Tendonitis

Symptomtext

Last year around sept. without doing anything the right heel started to ache (wondering if it is plantar fasciitis and it lasted for a month. Then, Feb.4 the ache in the heel came back and both feet has it. Everyday I do cold compress just to ease the pain and do some muscle stretching . Feb.15, I went to my doctor and reported that incident, her findings is Achilles tendinitis., and she gave me some PT exercises. Feb.28, my armpit started to have some rushes, itchy and reddish. After 5 days I started to apply sulpur hoping it will ease the problem since at night it bothers my sleep. I went to the derma on mar.9 and she said that the sulfur agitated the skin. She gave me oral medication to be taken for 7days and an ointment to be applied on the skin. Now it?s mar.20 there still some itchiness but the skin is slowly curing.

Weitere VAERSDATA-Felder

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

VAERS 2183032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 11.11.2021
Beginn: 11.01.2022
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: IM / -

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

Asthenia Blindness unilateral Blood test COVID-19 Computerised tomogram Exposure to SARS-CoV-2 Fatigue Nasopharyngitis Pain Retinal artery occlusion Rhinorrhoea Urine analysis

Symptomtext

I didn't have an symptoms at first, but I was exposed to COVID. When they tested positive I decided to take a rapid test and it came back positive. I was having cold like symptoms. Nose running, I was achy and tired. I didn't have much energy. I tested negative 8 days later. About a month later I noticed I lost vision in my right. I went to bed to see if it would get better in the morning. The next morning I woke up and it wasn't better. I call my treatment nurse and she told me to go to the emergency room. They did a head CT Scan, took blood, urinalysis. They sent me home and I had to make an appointment to see the ophthalmologist and he determined I had a stroke in my right eye.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: ER: 02/2022: CT Scan, blood work, urinalysis: No presence of an active stroke.
Aktuelle Erkrankungen: None
Vorgeschichte: Depression; Asthma; High Blood pressure; Hypertension; High Cholesterol; Melanoma Cancer; Survivor
Andere Medikamente: Atorvastatin 20mg once daily; Montelukast 10mg once daily; Paroxetine 40mg once daily; Losartan 50mg once daily; Levothyroxine unsure of dose because it just changed; Fluticasone; Baby Aspirin; Claritin.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2181863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 05.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Bedridden Decreased appetite Fall Malaise Memory impairment Pyrexia Swelling Urinary incontinence

Symptomtext

Swelling left arm; Urinated on herself; Fell up the stairs; Did not eat for 2 days; Stayed in bed for 2 days; Caller states she did not recognize her family.; feeling sick; after the first dose; fever; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A 67 year-old female patient received bnt162b2 (BNT162B2), administration date 05Jan2022 (Lot number: FH8020) at the age of 66 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Acid reflux" (unspecified if ongoing), notes: Verbatim: Acid reflux; "Covid", start date: Sep2021 (unspecified if ongoing), notes: had got Delta virus last Sep and whole month of Oct Further clarification Unknown.; "dealt and held in hospital whole month", start date: 2021 (unspecified if ongoing). The patient took concomitant medications. The following information was reported: MALAISE (non-serious) with onset 06Jan2022, outcome "not recovered", described as "feeling sick; after the first dose"; PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "fever"; SWELLING (non-serious), outcome "unknown", described as "Swelling left arm"; URINARY INCONTINENCE (non-serious), outcome "unknown", described as "Urinated on herself"; FALL (non-serious), outcome "unknown", described as "Fell up the stairs"; DECREASED APPETITE (non-serious), outcome "unknown", described as "Did not eat for 2 days"; BEDRIDDEN (non-serious), outcome "unknown", described as "Stayed in bed for 2 days"; MEMORY IMPAIRMENT (non-serious), outcome "unknown", described as "Caller states she did not recognize her family.". Therapeutic measures were taken as a result of malaise, pyrexia. Additional information: Patient said that she took the Pfizer Covid-19 Vaccine yesterday and she felt sick after the taken the Pfizer Covid-19 Vaccine, first dose." Consumer stated, "she got her first dose. She had Covid in Sep but didn't get hospitalized until Oct she dealt and held in hospital whole month (history). They give in her arm. Patient was on acid regimen (further not clarified), Nitro (further not clarified). Patient had acid reflex. Patient take lot of medication and told them whatever medication she was on." Patient had an accident and broke her ankle. Patient also stated that, she fell up the stairs but did not break her ankle. Patient scheduled to get her second dose on 26Jan2022. She stated, she got her first vaccine on 05Jan2022, and the next day, she urinated on herself, and then fell up the stairs. Caller stated she did not eat for 2 days and stayed in bed for 2 days. She did not recognize her family. Caller stated, her appointment for her second vaccine is 26Jan2022, and she does not drive. Also mentioned that, had got Delta virus last Sep and whole month of Oct (Further clarification Unknown). The report was related to a study or programme. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (oesophageal) (Verbatim: Acid reflux); COVID-19 (had got Delta virus last Sep and whole month of Oct Further clarification Unknown.); Hospitalization
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NC
Alter: 83,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 22.11.2021
Beginn: 16.02.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Drainage Pain Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

02/16/2022, coughing and I felt like I had drainage. I felt sore all over. I did have a slight temperature of 99, but it was not persistent. I took a rapid test and it came back negative. I still was cough so I decided to go to the clinic to get tested on 02/19/2022 and I tested positive for COVID-19. The PA suggested I do the monochromal infusion which I did and I started to feel a bit better that night. My coughing was not as intense. I contacted my doctor and told her I read that azithromycin would help and she prescribed it. I think it did help.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 02/16/2022 Rapid COVID-19 Test: Negative; 02/19/2022 COVID-19 test at the clinic: Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Bladder Condition that causes blood clots. 2019- Breast Cancer
Andere Medikamente: Multi Vitamins, Vitamin C, Zinc, Vitamin D, Potassium, Calcium, Garlic pill, Cholesterol and Blood Pressure vitamins, eye vitamins, Vitamin B, Benazepril 20mg once daily, Macrodantin 100mg once a day, baby aspirin Dropper of CBD, Claritin
Allergien: Levaquin
Vorherige Impfungen: -

VAERS 2179358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MA
Alter: 7,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Diarrhoea Product administered to patient of inappropriate age

Symptomtext

Diarrhea; Received their first dose of the Pfizer covid vaccine (adult dose from Gray cap); This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 7 year-old female patient received bnt162b2 (BNT162B2), administration date 16Dec2021 (Lot number: FH8020) at the age of 7 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 16Dec2021, outcome "unknown", described as "Received their first dose of the Pfizer covid vaccine (adult dose)"; DIARRHOEA (non-serious) with onset 17Dec2021, outcome "not recovered", described as "Diarrhea". Therapeutic measures were not taken as a result of diarrhoea. Additional information: Reporter stated that 3 patients received their first dose of the Pfizer covid vaccine (adult dose). First patient: 7 years old female ? experiencing diarrhea- lot number FH8020. Second patient: 10 years old male, lot number FH8020 (brother of the female). Third Patient :11 years male - lot number FL0007. Caller wanted to know any recommendation on what to tell the patient regarding what they need to look for. She stated she will be reaching out to disease control as well. Reporter stated the children were 11 and 10.5 and the third child was 7 and 60 pounds, she didn't know what weight pulls in to this. Caller states that she has talked to the parents and notified them. Caller states she is calling to report this and find out what else they should do and what guidelines they need to follow. Reporter stated she had the nurse check in with the patient's parents and they reported this morning she was having a lot of diarrhea but no vomiting and they were pumping her full of fluids. No follow-up attempts are possible. No further information is expected. .; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101815734 same reporter/drug, different patients.;US-PFIZER INC-202101815735 same reporter/drug, different patients

Weitere VAERSDATA-Felder

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

VAERS 2179099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 14.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Asthenia Dizziness Fatigue Feeling abnormal Illness Influenza like illness Myalgia Nausea SARS-CoV-2 test

Symptomtext

He has felt ill with muscle aches/feeling lousy with muscle aches; Flu-like symptoms; Nausea; Weakness; Dizziness; Fatigue; he is pretty sick; Feeling lousy; 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 69 year-old male patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 14Oct2021 (Lot number: FH8020) at the age of 69 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Heart Disease", start date: 2002 (ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (First dose, Lot Number: EL3249), administration date: 15Feb2021, when the patient was 69 years old, for COVID-19 immunization; Bnt162b2 (Second dose, Lot Number: EN9581), administration date: 09Mar2021, when the patient was 69 years old, for COVID-19 immunization, reaction(s): "Thought he had just caught a bug"; Flu vaccine, administration date: 2021. The following information was reported: MYALGIA (non-serious) with onset Oct2021, outcome "not recovered", described as "He has felt ill with muscle aches/feeling lousy with muscle aches"; INFLUENZA LIKE ILLNESS (non-serious) with onset Oct2021, outcome "not recovered", described as "Flu-like symptoms"; NAUSEA (non-serious) with onset Oct2021, outcome "not recovered", described as "Nausea"; ASTHENIA (non-serious) with onset Oct2021, outcome "not recovered", described as "Weakness"; DIZZINESS (non-serious) with onset Oct2021, outcome "not recovered", described as "Dizziness"; FATIGUE (non-serious) with onset Oct2021, outcome "not recovered", described as "Fatigue"; ILLNESS (non-serious) with onset Oct2021, outcome "not recovered", described as "he is pretty sick"; FEELING ABNORMAL (non-serious) with onset Oct2021, outcome "not recovered", described as "Feeling lousy". The events "he has felt ill with muscle aches/feeling lousy with muscle aches", "flu-like symptoms", "nausea", "weakness", "dizziness", "fatigue", "he is pretty sick" and "feeling lousy" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller stated States he is not sure what to think. He just got the booster on 14Oct2021 and the same thing that happened with his second dose of the vaccine happened again. States when he first got the third vaccine, he was fine the first couple of days. That Sunday he felt ill. Since then, he has been feeling lousy with muscle aches, flu, and nausea. States this has been ongoing since then. Confirmed that some of the patient's similar symptoms were reported such as fatigue and muscle aches. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Covid 19; Test Result: Negative ; Comments: He got tested for Covid 19 and it was Negative
Aktuelle Erkrankungen: Heart disease, unspecified
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NC
Alter: 12,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Dizziness Nausea Poor quality product administered Product temperature excursion issue

Symptomtext

Vaccine was diluted and in the vial stored at room temperature for 7 hours and then administered to a patient; Vaccine was diluted and in the vial stored at room temperature for 7 hours and then administered to a patient; nausea; dizziness; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. A 12 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 26Oct2021 16:00 (Lot number: FH8020, Expiration Date: 31Jan2022) at the age of 12 years as dose 1, 0.3 ml single for covid-19 immunisation. Relevant medical history included: "Generalized anxiety disorder" (unspecified if ongoing), notes: Verbatim: Generalized anxiety disorder; "Migraine" (unspecified if ongoing), notes: Verbatim: Migraine. There were no concomitant medications. The following information was reported: POOR QUALITY PRODUCT ADMINISTERED (non-serious), PRODUCT TEMPERATURE EXCURSION ISSUE (non-serious) all with onset 26Oct2021 16:00, outcome "unknown" and all described as "Vaccine was diluted and in the vial stored at room temperature for 7 hours and then administered to a patient"; NAUSEA (non-serious) with onset 26Oct2021, outcome "recovered" (26Oct2021), described as "nausea"; DIZZINESS (non-serious) with onset 26Oct2021, outcome "recovered" (26Oct2021), described as "dizziness". Additional information: The reporter stated that 12-year-old male patient received vaccine which was diluted and in the vial stored at room temperature for 7 hours and then administered to a patient, the vaccine was mixed, and it was out for over 6 hours. The vaccine was actually out for 7 hours instead. The vaccine was expired at 3PM and instead was given at 4PM. Caller states that the vaccine was diluted and was in the vial stored at room temperature for 7 hours and then administered to a patient. Caller asks if the patient needs to be revaccinated or for any recommendations or monitoring. No investigation assessment. The patient did complain of dizziness and nausea at the 15-minute mark, and there were no other reactions. Caller clarified that this event happened today and this was the first dose for the patient. The dizziness and nausea resolved, both only lasted for about a couple of minutes. The patient has no drug allergies. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Generalized anxiety disorder (Verbatim: Generalized anxiety disorder); Migraine (Verbatim: Migraine)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2177837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 30.11.2021
Beginn: 28.12.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Fatigue Influenza like illness Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test Sinusitis

Symptomtext

Nov30,2021, I got my booster on December 28/2021 in the evening around 5:00pm I started with tiredness, I left like a very bad flu. I have fever, body ache, fatigue, sore throat. It lasted a few days. A week after I called my doctor I told him what happened he said had sinus infection. He said I had omicron. He gave me antibiotics for 10 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estrogen, Progesterone
Allergien: None
Vorherige Impfungen: 2nd dose reaction for 2 days and it was gone after

VAERS 2176511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: CT
Alter: -
Geschlecht: U
Eingang: 12.03.2022
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Fatigue Vaccination site pain

Symptomtext

Fatigue; Injection site pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administered in arm, administration date 25Oct2021 (Lot number: FH8020) as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: TRI LO MARZIA (ongoing). Vaccination history included: Bnt162b2 (Dose number: 1, Anatomical site of injection: Arm, Batch/lot number: EL3247, Resolved within 24 hours with no further action taken, no medication used), administration date: 01Mar2021, for COVID-19 immunization, reaction(s): "pain was in the arm of vaccine injection"; Bnt162b2 (Dose number: 2, Anatomical site of injection: Arm, Batch/lot number: EP6955, Resolved within 24 hours with no further action taken, no medication used), administration date: 24Mar2021, for COVID-19 immunization, reaction(s): "pain was in the arm of vaccine injection". The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 25Oct2021 20:00, outcome "recovered" (26Oct2021), described as "Injection site pain"; FATIGUE (non-serious) with onset 26Oct2021, outcome "recovered" (26Oct2021), described as "Fatigue". Therapeutic measures were not taken as a result of vaccination site pain, fatigue. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: None
Andere Medikamente: TRI LO MARZIA
Allergien: -
Vorherige Impfungen: -

VAERS 2176509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: UT
Alter: 27,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 16.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: - / RA

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

Herpes zoster Rash Rash erythematous Rash pruritic

Symptomtext

Diagnosed with shingles; I noticed a red rash on the left side of my torso; It followed in a straight lint and itched; Was painful; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 27 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 16Oct2021 10:30 (Lot number: FH8020) at the age of 27 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ESCITALOPRAM. The following information was reported: HERPES ZOSTER (non-serious) with onset 03Nov2021 12:00, outcome "not recovered", described as "Diagnosed with shingles"; RASH ERYTHEMATOUS (non-serious) with onset 03Nov2021 12:00, outcome "not recovered", described as "I noticed a red rash on the left side of my torso"; RASH PRURITIC (non-serious) with onset 03Nov2021 12:00, outcome "not recovered", described as "It followed in a straight lint and itched"; RASH (non-serious) with onset 03Nov2021 12:00, outcome "not recovered", described as "Was painful". The events "diagnosed with shingles", "i noticed a red rash on the left side of my torso", "it followed in a straight lint and itched" and "was painful" were evaluated at the physician office visit. Additional information: Dose received -2: Most recent dose details: product=COVID 19, brand=Pfizer, lot number= FG3527, administration date=06Nov2021, administration time-10:45, vaccine location=left arm. Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. Did the patient receive any other vaccines within 4 weeks prior to the COVID vaccine: No. List of any other medications the patient received within 2 weeks of vaccination: Escitalopram. Reported Event: After the first dose of the vaccine About a week after patient noticed a red rash on the left side of his torso. It followed in a straight lint and itched and was painful. On 08Nov2021, 5 days after I noticed the rash he saw his primary care physician and was diagnosed with shingles. If covid prior vaccination: no. If covid tested post vaccination: no. Known allergies -no. Other medical history- none. Prior to vaccination, was the patient diagnosed with COVID-19: No. Since the vaccination, has the patient been tested for COVID-19: No. Device Date: 08Nov2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2176426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fh8020

mild

Staat: AZ
Alter: 71,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 22.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / RA

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

Rash Rash pruritic

Symptomtext

entire torso rash from neck to thigh. It was itchy; entire torso rash from neck to thigh. It was itchy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 22Oct2021 16:45 (Lot number: Fh8020) at the age of 71 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Celiac" (unspecified if ongoing); "Colitis" (unspecified if ongoing); "allergy" (unspecified if ongoing), notes: Known Allergy : Yes. Concomitant medication(s) included: BUDESONIDE; ROSUVASTATIN CALCIUM. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL9264, Location of injection: Arm Right, Vaccine Administration Time: 10:00 PM), administration date: 02Feb2021, when the patient was 70 years old, for Covid- 19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6202, Location of injection: Arm Right, Vaccine Administration Time: 02:30 AM), administration date: 26Feb2021, when the patient was 71 years old, for Covid-19 immunization. The following information was reported: RASH (non-serious), RASH PRURITIC (non-serious) all with onset 24Oct2021 10:00, outcome "recovered" (26Oct2021) and all described as "entire torso rash from neck to thigh. It was itchy". Therapeutic measures were taken as a result of rash, rash pruritic. Additional information: No other vaccine in four weeks was administered. Patient did not have COVID prior vaccination and COVID was not tested positive post vaccination. On 24Oct2021, entire torso rash from neck to thigh. It was itchy. Patient took Benadryl and it mostly went away after 48 hours, but was slightly itchy for a week. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Known Allergy : Yes); Celiac disease; Colitis
Andere Medikamente: BUDESONIDE; ROSUVASTATIN CALCIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2176213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NC
Alter: 59,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 19.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: OT / RA

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

Gait disturbance Nausea Pain

Symptomtext

nausea; moderate body aches; hard to walk; This is a spontaneous report received from contactable reporter(s) (Other HCP and Pharmacist). The reporter is the patient. A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in deltoid right, administration date 19Oct2021 16:20 (Lot number: FH8020) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "Viral infection" (ongoing). Concomitant medication(s) included: FLUZONE QUADRIVALENT taken for immunisation, administration date 04Oct2021; SHINGRIX taken for immunisation, administration date 04Oct2021; LEVOTHYROXINE taken for thyroid disorder, start date: Jul2021 (ongoing); VALACYCLOVIR [VALACICLOVIR] taken for viral infection, start date: Jul2021 (ongoing). Past drug history included: Morphine, reaction(s): "Known allergies: Morphine"; Demerol, reaction(s): "Known allergies: Demerol"; Phenergan, reaction(s): "Known allergies: phenergan"; Mobix, reaction(s): "Known allergies: Mobix". Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EK9231), administration date: 07Jan2021, when the patient was 59 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EK5730), administration date: 07Dec2020, when the patient was 58 years old, for COVID-19 Immunization. The following information was reported: NAUSEA (non-serious) with onset 21Oct2021, outcome "not recovered", described as "nausea"; PAIN (non-serious) with onset 21Oct2021, outcome "not recovered", described as "moderate body aches"; GAIT DISTURBANCE (non-serious) with onset 21Oct2021, outcome "not recovered", described as "hard to walk". Therapeutic measures were not taken as a result of nausea, gait disturbance. Therapeutic measures were taken as a result of pain. Additional information: Patient did not had covid prior vaccination and was not covid tested post vaccination. Reportedly, with the booster patient had nausea and moderate body aches. Had intense body aches that make it hard to walk. Patient was away from home and have taken Alieve but it doesnt really touch the pain. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Viral infection
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: LEVOTHYROXINE; VALACYCLOVIR [VALACICLOVIR]
Allergien: -
Vorherige Impfungen: -

VAERS 2175974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Chills Nausea Pain Pain in extremity

Symptomtext

Arm soreness; chills; body ache; nausea; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from a sales representative. The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date Oct2021 (Lot number: FH8020) at the age of 45 years as dose 3 (booster) , single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Unknown. Not available/provided to reporter at the time of report completion), for COVID-19 IMMUNIZATION; Bnt162b2 (Dose Number: 2, Batch/Lot No: Unknown. Not available/provided to reporter at the time of report completion), for COVID-19 IMMUNIZATION. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Oct2021, outcome "recovered" (2021), described as "Arm soreness"; CHILLS (non-serious) with onset Oct2021, outcome "recovered" (2021), described as "chills"; PAIN (non-serious) with onset Oct2021, outcome "recovered" (2021), described as "body ache"; NAUSEA (non-serious) with onset Oct2021, outcome "recovered" (2021), described as "nausea". Therapeutic measures were not taken as a result of pain in extremity, chills, pain, nausea. Additional information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Patient did not receive any medications within 42weeks prior to the COVID vaccine. Patient did not received treatment for AE. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1850766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 28.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: - / LA

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

Balance disorder Body height Dizziness Vertigo

Symptomtext

She was feeling a little off balance; Vertigo; She just had a little dizziness.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Oct2021 (Lot number: FH8020) at the age of 56 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Blood pressure high" (unspecified if ongoing), notes: She is on a high blood pressure medication. Concomitant medication(s) included: ENALAPRIL+HCTZ taken for hypertension (ongoing). Vaccination history included: Bnt162b2 (lot number 30155BA, left arm), administration date: 07Oct2021, when the patient was 56 years old, for Covid-19 immunization. The following information was reported: VERTIGO (non-serious) with onset 03Nov2021 11:00, outcome "not recovered", described as "Vertigo"; DIZZINESS (non-serious) with onset 03Nov2021, outcome "unknown", described as "She just had a little dizziness."; BALANCE DISORDER (non-serious), outcome "unknown", described as "She was feeling a little off balance". Relevant laboratory tests and procedures are available in the appropriate section. Follow-up (11Nov2021): Follow-up attempts completed. No further information expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:5' 4.25"; Comments: shrinking
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (She is on a high blood pressure medication)
Andere Medikamente: ENALAPRIL+HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 1850766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fh8020

mild

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 28.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Balance disorder Body height Dizziness Vertigo

Symptomtext

She was feeling a little off balance; Vertigo; She just had a little dizziness.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Oct2021 (Lot number: FH8020) at the age of 56 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Blood pressure high" (unspecified if ongoing), notes: She is on a high blood pressure medication. Concomitant medication(s) included: ENALAPRIL+HCTZ taken for hypertension (ongoing). Vaccination history included: Bnt162b2 (lot number 30155BA, left arm), administration date: 07Oct2021, when the patient was 56 years old, for Covid-19 immunization. The following information was reported: VERTIGO (non-serious) with onset 03Nov2021 11:00, outcome "not recovered", described as "Vertigo"; DIZZINESS (non-serious) with onset 03Nov2021, outcome "unknown", described as "She just had a little dizziness."; BALANCE DISORDER (non-serious), outcome "unknown", described as "She was feeling a little off balance". Relevant laboratory tests and procedures are available in the appropriate section. Follow-up (11Nov2021): Follow-up attempts completed. No further information expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:5' 4.25"; Comments: shrinking
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (She is on a high blood pressure medication)
Andere Medikamente: ENALAPRIL+HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 2163109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: SC
Alter: 78,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 08.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Cough Diarrhoea Fatigue SARS-CoV-2 test positive Weight decreased

Symptomtext

I had diarrhea, cough, fatigue, and loss of weight. I also lost my taste and smell. These lasted for about week. In Oct, I tested positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Normal prescription for High Blood Pressure; Cholesterol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2161493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NC
Alter: 34,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 09.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Vaccination site pain

Symptomtext

complaints of her left arm being sore after receiving the first dose of the purple cap Pfizer Covid-19 vaccine in her left deltoid; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. A 34 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 09Nov2021 (Lot number: FH8020, Expiration Date: 28Nov2021) at the age of 34 years as dose 1, 0.3 ml single for covid-19 immunisation. Relevant medical history included: "Hypertension", start date: 22Mar2019 (ongoing); "Sleep apnea", start date: 29Sep2020 (ongoing). Concomitant medication(s) included: LISINOPRIL taken for hypertension (ongoing). The following information was reported: VACCINATION SITE PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "complaints of her left arm being sore after receiving the first dose of the purple cap Pfizer Covid-19 vaccine in her left deltoid". Additional information: She said that her arm hurt really bad and she felt like it was going to fall off and that is why she wanted the second dose in the gluteal area. She did not have prior vaccinations (within 4 weeks). She did not have any AE(s) following prior vaccinations. She did not have any family medical history relevant to AE(s). The AE(s) did not require a visit to: emergency Room or physician office. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypertension; Sleep apnea
Vorgeschichte: -
Andere Medikamente: LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 2161403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: FL
Alter: -
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 21.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Blister Herpes zoster Pain in extremity Pruritus Rash

Symptomtext

shingles; States that it started with a rash; My arm started Itching; lower upper arm started hurting; blisters; 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 79-year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 21Oct2021 11:00 (Lot number: FH8020) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: AMBIEN taken for sleep disorder (ongoing); SYNTHROID taken for thyroid disorder (ongoing); DILTIAZEM taken for blood pressure measurement (ongoing). Vaccination history included: Bnt162b2 (Time: 2 PM, Anatomical Site of injection: left arm, Route of administration: Intramuscular, Batch/Lot number: EL3362), administration date: 20Jan2021, for covid-19 immunization; Bnt162b2 (Time: 11 AM, Anatomical Site of injection: left arm, Route of administration: Intramuscular, Batch/Lot number: EN6201), administration date: 10Feb2021, for Covid-19 immunization; Flu shot. The following information was reported: HERPES ZOSTER (non-serious), outcome "not recovered", described as "shingles"; RASH (non-serious), outcome "unknown", described as "States that it started with a rash"; PRURITUS (non-serious) with onset Oct2021, outcome "unknown", described as "My arm started Itching"; PAIN IN EXTREMITY (non-serious) with onset Oct2021, outcome "unknown", described as "lower upper arm started hurting"; BLISTER (non-serious) with onset Oct2021, outcome "unknown", described as "blisters". The events "shingles" and "states that it started with a rash" were evaluated at the physician office visit. Therapeutic measures were taken as a result of herpes zoster, pruritus, pain in extremity, blister. Additional information: Caller states that she had the Covid 19 shots, and she did fine with those, then she got the booster and now she has shingles, and she knows that it's related because there is no reason in the world that she would get shingles one week after getting the booster. States that it started with a rash. Got the 7-day prescription for antiviral medicine and gabapentin. Shingles: so, a month later no blisters occasional itching and continual pain taking Tylenol. Still having side effects from shingles. 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: -
Andere Medikamente: AMBIEN; SYNTHROID; DILTIAZEM
Allergien: -
Vorherige Impfungen: -

VAERS 2157921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 10.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Haematuria

Symptomtext

Mention to the Urologyst I feel tired, fatigue. Was found a hematosis in the urine. She suggested to reported because has other patients mention the same after the booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: crestor, Premarin, progesterone, fosteum, Estriol
Allergien: No allergies
Vorherige Impfungen: -

VAERS 2151628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: VA
Alter: 58,0
Geschlecht: M
Eingang: 02.03.2022
Impfdatum: 05.11.2021
Beginn: 19.01.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: IM / LA

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

Pain in extremity

Symptomtext

Left arm pain during sleeping

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Heart disease
Andere Medikamente: Crestor, Zetia, Metoprolol, Aspirin, Clopidrogel, multi vitamins
Allergien: none
Vorherige Impfungen: -

VAERS 2131122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 20.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / -

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

Catheter placement Fall Head injury Incisional drainage Oedema Pain Pyrexia Skin abrasion Swelling face Tenderness

Symptomtext

Patient fell and had swelling and a large abrasion to the forehead, extending into the scalp. ED visit; Patient given tramadol for pain with a small prescription for this. Hospital admission for history of progressive left vulvar edema tenderness and febrile sensation. Incision and drainage was performed with placement of a Word catheter. She was deemed to have achieved maximal benefit of inpatient therapy on the third postoperative day and discharged to home care on doxycycline. ED visit and hospital admission were separate and both within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2125826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NM
Alter: 72,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Rash

Symptomtext

Rash on legs; 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), administered in arm left, administration date Oct2021 (Lot number: FH8020) at the age of 72 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "HBP" (unspecified if ongoing), notes: HBP - 20mg lisinopril. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM, lot unknown reason=Unable to locate or read the details), administration date: Feb2021, when the patient was 72 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 2, lot unknown reason=Unable to locate or read the details, After 2nd dose: red spot rash over stomach, arms and legs.), administration date: Feb2021, when the patient was 72 years old, for Covid-19 immunization, reaction(s): "Red spot rash over stomach, arms and legs". The following information was reported: RASH (non-serious) with onset Oct2021, outcome "recovered with sequelae" (Oct2021), described as "Rash on legs". The event "rash on legs" was evaluated at the physician office visit. Therapeutic measures were taken as a result of rash. Additional information: Patient had no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient had been tested for COVID-19 via Nasal Swab in May2021 and result was negative. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (HBP - 20mg lisinopril)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2122634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NJ
Alter: 44,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Vaccination site erythema Vaccination site pain Vaccination site pruritus Vaccination site swelling

Symptomtext

the injection site was sore, red, and swollen; the injection site was sore, red, and swollen; the injection site was sore, red, and swollen; Besides that, the most concerning side effect which was the itchiness at the injection site; 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 received bnt162b2 (BNT162B2), administered in arm left, administration date 23Oct2021 13:00 (Lot number: FH8020) at the age of 44 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Alport Syndrome" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Known allergies: latex" (unspecified if ongoing). Concomitant medication(s) included: EFFEXOR; LAMICTAL; TRAZODONE; FISH OIL; VIT D [COLECALCIFEROL]. Vaccination history included: Bnt162b2 (lot umber=EP6955, dose number=1, vaccine location=Left Arm), administration date: 01Apr2021, when the patient was 44 years old, for COVID-19 immunization; Bnt162b2 (lot umber=EP7533, dose number=2, vaccine location=Left Arm), administration date: 22Apr2021, when the patient was 44 years old, for COVID-19 immunization; Flu, administration date: 13Oct2021. The following information was reported: VACCINATION SITE PAIN (non-serious), VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE SWELLING (non-serious) all with onset 23Oct2021 14:00, outcome "recovering" and all described as "the injection site was sore, red, and swollen"; VACCINATION SITE PRURITUS (non-serious) with onset 23Oct2021 14:00, outcome "recovering", described as "Besides that, the most concerning side effect which was the itchiness at the injection site". Therapeutic measures were not taken as a result of vaccination site pain, vaccination site erythema, vaccination site swelling, vaccination site pruritus. Additional information: If covid prior vaccination: No. If covid tested post vaccination: No. After receiving the booster on 23Oct2021 the injection site was sore, red, and swollen. Unlike the previous two injections, this third dose was noticeably more swollen and more painful than the other two. It has been 5 days and arm still shows signs of swelling and pain. Besides that, the most concerning side effect was the itchiness at the injection site which was very uncomfortable, almost as itchy as a mosquito bite. The itchiness was only on the injection site, the swollen area, and maybe an inch outside of the swollen area. It has also lasted 5 days. No medication was used for this symptom. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Alport's syndrome; Anxiety; Latex allergy
Andere Medikamente: EFFEXOR; LAMICTAL; TRAZODONE; FISH OIL; VIT D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2122632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

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

Myalgia Nausea Pyrexia

Symptomtext

fever; nausea; muscle pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from a sales representative. A 12 year-old male patient received bnt162b2 (BNT162B2), administration date 26Oct2021 (Lot number: FH8020) at the age of 12 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: 301451A), administration date: 05Oct2021, when the patient was 12 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 27Oct2021, outcome "recovered" (2021), described as "fever"; NAUSEA (non-serious) with onset 27Oct2021, outcome "recovered" (2021), described as "nausea"; MYALGIA (non-serious) with onset 27Oct2021, outcome "recovered" (2021), described as "muscle pain". Therapeutic measures were not taken as a result of pyrexia, nausea, myalgia. Additional Information: Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2122603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: LA
Alter: 46,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 24.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Headache Influenza like illness Nausea Pain Pyrexia

Symptomtext

flu like symptoms; 104 degree fever; body aches; nausea; head ache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 46-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 24Oct2021 11:00 (Lot number: FH8020) at the age of 46 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN2601, Location of injection: Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 11Feb2021, when the patient was 46 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL9263, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 21Jan2021, when the patient was 46 years old, for COVID-19 Immunization. The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset 25Oct2021 03:00, outcome "recovering", described as "flu like symptoms"; PYREXIA (non-serious) with onset 25Oct2021 03:00, outcome "recovering", described as "104 degree fever"; PAIN (non-serious) with onset 25Oct2021 03:00, outcome "recovering", described as "body aches"; NAUSEA (non-serious) with onset 25Oct2021 03:00, outcome "recovering", described as "nausea"; HEADACHE (non-serious) with onset 25Oct2021 03:00, outcome "recovering", described as "head ache". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of influenza like illness, pyrexia, pain, nausea, headache. Additional information: Seriousness Criteria-Results in death was reported as no. Seriousness Criteria-Life threatening was NO. Seriousness criteria-Caused/prolonged hospitalization was as no. Seriousness Criteria-Disabling/Incapacitating was NO. Seriousness criteria-Congenital anomaly/birth defect was reported as NO. Facility where the most recent COVID-19 vaccine was administered (withheld). the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No treatment ae. No known allergies. No other medical history. Prior to vaccination, was the patient diagnosed with COVID-19 was reported as No. Since the vaccination, has the patient been tested for COVID-19 was reported as no.? Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 20211025; Test Name: body temperature; Result Unstructured Data: Test Result:104; Comments: 104 degree fever
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2118731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: OT / LA

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

Body temperature Pyrexia

Symptomtext

Fever at 101 degrees; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 12 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 21Oct2021 17:00 (Lot number: FH8020) at the age of 12 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Known allergy: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: FLU taken for immunisation, administration date 18Oct2021. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FF2587, Location of injection: Arm Left, Vaccine Administration Time: 17.00, Route of Administration: Intramuscular), administration date: 30Sep2021, when the patient was 12 years old, for Covid-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 22Oct2021 07:00, outcome "unknown", described as "Fever at 101 degrees". The patient underwent the following laboratory tests and procedures: body temperature: (22Oct2021) 101 degrees. Therapeutic measures were not taken as a result of pyrexia. Additional information: Other vaccine 4weeks product Flu vaccine was taken. The patient had not covid prior vaccination. The patient had not covid tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 20211022; Test Name: Fever; Result Unstructured Data: Test Result:101 degrees
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2114187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: MD
Alter: 57,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 29.10.2021
Beginn: 17.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Burning sensation Chest X-ray normal Computerised tomogram normal Discomfort Nipple pain

Symptomtext

It started with topical pain from my left nipple to my left under-armpit. the pain became extremely uncomfortable because it felt like someone was ripping duct tape off my skin then setting fire to it. It would last for about 3 seconds. When I got into certain positions while sitting or standing or jogging it would trigger something and then it would start to burn. I wrapped my upper chest to keep compression around it to keep it from spasming. Ibuprofen 600 did not help, ice and heat did not help either. Then the pain moved to the other side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Cat scan came back negative. Chest X-ray came back negative Chiropractor- Used Graston technique to treat the pain and started making good progress
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Omega 3 Gabapentin Fenofibrate Joint Collagen
Allergien: -
Vorherige Impfungen: -

VAERS 2110819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: WI
Alter: 50,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Incorrect route of product administration Injection site pain Pain in extremity Shoulder injury related to vaccine administration

Symptomtext

Noticed that the injection felt to be in the wrong place and hurt more than usual. Have had pain in left arm, particularly elbow and shoulder, ever since. Went to physician, who tried a round of prescription strength NSAID, but that did not help. Physical Therapist diagnosed SIRVA. Currently undergoing PT, but continue to have pain in left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Evaluation by DPT and MD. Strength is normal, but continued pain in left arm.
Aktuelle Erkrankungen: none
Vorgeschichte: high LDL levels
Andere Medikamente: Rosuvastatin
Allergien: none known
Vorherige Impfungen: -

VAERS 2110421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 19.10.2021
Beginn: 07.02.2022
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain Chills Nausea Pyrexia

Symptomtext

Chills, fever, abdominal pain and nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2110323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: DE
Alter: 12,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal discomfort Headache Oropharyngeal pain SARS-CoV-2 test negative Streptococcus test

Symptomtext

The next day after patient's 2nd dose he experienced the following symptoms: Headache and was treated with Tylenol and hot shower and recovered right away and last week from the week of January 7th - 11th he was experiencing sore throat, and another headache, it was consistent for 1 week and was tested negative for COVID-19. His doctor advised to gargle with salt water, Take Tylenol, and cough drops for the sore throat. As of today, he still has a little bit of headache, his throat is feeling better, and stomach is a bit upset and he took Tylenol before he went to school.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Strep Test, COVID-19 Test.
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal Allergies
Andere Medikamente: None
Allergien: Lactose
Vorherige Impfungen: Headache for 3 days.

VAERS 2201209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 27.10.2021
Beginn: 15.12.2021
Tage bis Beginn: 49,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Chills Myalgia Nasal congestion SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 08/17, Pfizer, dose #1 10/27, Pfizer, dose#2 COVID swab, result: detected 12/25 pt cc: chills, myalgia, nasal congestion, exposure: unknown clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: (Included dates) 12/27 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2091153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: FL
Alter: 44,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 05.11.2021
Beginn: 21.01.2022
Tage bis Beginn: 77,0
Dosis: 3
Route/Site: OT / LA

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

COVID-19 Drug ineffective Interchange of vaccine products Nasal congestion Off label use Pain Pyrexia SARS-CoV-2 test

Symptomtext

tested positive for COVID; tested positive for COVID; fever of 102.3 F; body aches; congestion; Dose 1: Moderna, Dose 2: Moderna; Dose 1: Moderna, Dose 2: Moderna; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 44 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 05Nov2021 (Lot number: FH8020) at the age of 44 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: 039B21A, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 23Apr2021, when the patient was 43 years old, for COVID-19 immunization; Moderna (Dose Number: 1, Batch/Lot No: 031A21A, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 26Mar2021, when the patient was 43 years old, for COVID-19 immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 21Jan2022 01:30, outcome "recovering" and all described as "tested positive for COVID"; PYREXIA (non-serious) with onset 21Jan2022 01:30, outcome "recovering", described as "fever of 102.3 F"; PAIN (non-serious) with onset 21Jan2022 01:30, outcome "recovering", described as "body aches"; NASAL CONGESTION (non-serious) with onset 21Jan2022 01:30, outcome "recovering", described as "congestion"; OFF LABEL USE (non-serious), INTERCHANGE OF VACCINE PRODUCTS (non-serious) all with onset 21Jan2022 01:30, outcome "recovering" and all described as "Dose 1: Moderna, Dose 2: Moderna". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (20Jan2022) positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of drug ineffective, covid-19, pyrexia, pain, nasal congestion, off label use, interchange of vaccine products. Clinical information: The patient did not take other vaccine in four weeks and did not take other medications in two weeks. The patient did not have COVID prior vaccination and tested COVID positive post vaccination. On Thursday, 20Jan2022 (at approximately 5:24 PM), he tested positive for COVID. In the early morning of Friday, 21Jan2002 (at approximately 1:30 AM), he developed a fever of 102.3 F, body aches, and congestion. At the time that event was being submitted, he no longer have fever and the body aches had improved significantly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20220120; Test Name: COVID-19 TEST; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: No reaction on previous exposure to drug
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2090203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: NC
Alter: 74,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 17.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: - / LA

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

Rash erythematous Rash pruritic

Symptomtext

In mid December a new area appeared on my lower right leg/ All areas are still itchy and red; In mid December a new area appeared on my lower right leg/ All areas are still itchy and red; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 17Nov2021 15:00 (Lot number: FH8020) at the age of 74 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "peripheral Neuropathy" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing), notes: Known allergies: Sulfa; "High Blood pressure" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Valium, reaction(s): "Known allergies: Valium"; Codeine, reaction(s): "Known allergies: Codeine". Vaccination history included: Bnt162b2 (prev dose product: COVID 19, prev dose brand: pfizer Biotech, prev dose brand unknown: False, prev dose lot number: EN6208, prev dose lot unknown: False, prev dose administration date: 14Mar2021, prev dose administration time: 03:00PM , prev dose dose number: 2, prev dose vaccine location: Left arm), administration date: 14Mar2021, when the patient was 74 years old, for COVID-19 IMMUNIZATION, reaction(s): "Itchy rash", "red rash"; Bnt162b2 (prev dose product: COVID 19, prev dose brand: pfizer Biotech, prev dose brand unknown: False, prev dose lot number: EN6203, prev dose lot unknown: False, prev dose administration date: 21Feb2021, prev dose administration time: 03:00PM , prev dose dose number: 1, prev dose vaccine location: Left arm), administration date: 21Feb2021, when the patient was 74 years old, for COVID-19 IMMUNIZATION. The following information was reported: RASH ERYTHEMATOUS (non-serious), RASH PRURITIC (non-serious) all with onset Dec2021, outcome "not recovered" and all described as "In mid December a new area appeared on my lower right leg/ All areas are still itchy and red". The event "in mid december a new area appeared on my lower right leg/ all areas are still itchy and red" and "in mid december a new area appeared on my lower right leg/ all areas are still itchy and red" was evaluated at the physician office visit. Therapeutic measures were taken as a result of rash erythematous, rash pruritic. Additional information: Itchy, Red Rash. Appeared first on lower back (Late July). Then spread in late August/early September. It started and has continued on left arm, near elbow and spread up and down the arm. Then about a month later it spread to her chest. mostly right side; then to the back of her neck (at hair line and up into her scalp above the hairline). All rash areas-left arm, chest, and back of her neck have continued to irritate her. In mid-December a new area appeared on her lower right leg. All areas are still itchy and red except lower back, which has stopped itching. The patient took other medication in two weeks. There was no other vaccine in four weeks. Event treatment included Prednisone one shot then one course oral. The adverse event resulted in doctor or other healthcare professional office/clinic visit. The patient did not had covid prior vaccination and not tested covid post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Peripheral neuropathy; Sulfonamide allergy (Known allergies: Sulfa)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085292

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FH8020

mild

Staat: VA
Alter: 47,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 27.10.2021
Beginn: 19.01.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

TESTED POS 01/19/2022 07:15pm Tested because of Sore throat. I started Dayquil/Nyquil and Advil. I also used Flonase. I did virtual visit with a provider. High dose of Zinc and Vitamin C.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroidism, Seasonal allergies
Andere Medikamente: 1. Synthroid 2. Flonase 3. Zyrtec 4. Multi-Vitamin from Costco
Allergien: No
Vorherige Impfungen: -

VAERS 2085216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 21.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

Developed recurrent hives starting 2 days after vaccination, medicated with Zyrtec. Hives continued for a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HTN
Andere Medikamente: Losartan 25mg BID
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2080304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 08.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Balance disorder Dizziness Dizziness postural Nausea Vertigo

Symptomtext

I experienced extreme vertigo within 3 days of the first shot. Experienced dizziness laying down and sitting up from laying down position; experienced dizziness if looking upward when standing as well. The first 2 days of the vertigo experience, I was nauseated as well. Dizziness was severe enough when standing that I lost my balance on numerous occasions. The dizziness started to subside about 9 days after the first shot, but returned to the severe level within 24 hours of receiving the second shot. I tried two different vertigo "resolution" exercises as recommended by my doctor, but neither of those exercises resolved the dizziness. My doctor administered a shot of dexamethasone which provided moderate relief temporarily. The vertigo subsided approximately 30 days after the second shot but NEVER COMPLETELY WENT AWAY. I don't experience the vertigo when standing now, but still experience the vertigo when laying down at night going to bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: 300 mg well-butrin (daily)
Allergien: none
Vorherige Impfungen: -

VAERS 2080304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FH8020

mild

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 08.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

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

Balance disorder Dizziness Dizziness postural Nausea Vertigo

Symptomtext

I experienced extreme vertigo within 3 days of the first shot. Experienced dizziness laying down and sitting up from laying down position; experienced dizziness if looking upward when standing as well. The first 2 days of the vertigo experience, I was nauseated as well. Dizziness was severe enough when standing that I lost my balance on numerous occasions. The dizziness started to subside about 9 days after the first shot, but returned to the severe level within 24 hours of receiving the second shot. I tried two different vertigo "resolution" exercises as recommended by my doctor, but neither of those exercises resolved the dizziness. My doctor administered a shot of dexamethasone which provided moderate relief temporarily. The vertigo subsided approximately 30 days after the second shot but NEVER COMPLETELY WENT AWAY. I don't experience the vertigo when standing now, but still experience the vertigo when laying down at night going to bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: 300 mg well-butrin (daily)
Allergien: none
Vorherige Impfungen: -