VAERS Reports FF2590

VAERS 2728535

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FF2590

kritisch

Staat: -
Alter: 52,0
Geschlecht: M
Eingang: 29.12.2023
Impfdatum: 14.10.2021
Beginn: 05.11.2023
Tage bis Beginn: 752,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Agitation Anaemia Anxiety Atelectasis Azotaemia Bacillus test positive Blood culture positive Blood gases abnormal Blood lactic acid Blood thyroid stimulating hormone increased COVID-19 Central venous catheterisation Computerised tomogram head abnormal Computerised tomogram thorax abnormal Condition aggravated Decubitus ulcer Echocardiogram

Symptomtext

Assessment and Plan Patient is a 54 y.o. male patient of DO with history of end-stage renal disease, dialysis, diabetes, hypertension, hyperlipidemia, spina bifida presented on 11/5/2023 with AMS and acute respiratory failure. Was seen by palliative care, made a DNR CC and transferred to hospice. Acute Metabolic Encephalopathy-resolved DDx: Metabolic v. Hypoxia/hypercapnea v. Infxn v. Rx v. Uremia CTH: No acute brain pathology. Opacification of the nasal airways and sphenoid sinusitis. Awake, alert and interactive during my exam Transitioned to DNR CC today 11/12 Continue prn morphine for pain Prn ativan for anxiety, prn haldol for agitation Prn ani-emetics Prn robinul for secretions Palliative care seeing patient today, await further recommendations Acute Respiratory Failure with hypoxia COVID-19 Respiratory Acidosis 2/2 V/Q mismatch (PNA) CT PE 11/5: There is no central PE but further distally evaluation is quite limited. Moderate scattered atelectasis. Consolidation at the left lung base ED started Zosyn and vancomycin ABG shows respiratory acidosis with inability to compensate metabolically secondary to renal failure Patient initially intubated and sedated Requested meeting with family regarding plan, he wishes to be extubated which was done today 11/12-- >patient also transitioned to DNR CC. Palliative care seeing patient today, await further recommendations Septic Shock Leukocytosis Secondary to PNA SIRS criteria: febrile, HR >90, RR >20, Leukocytosis Initial Lactic Acid 3.2 MRSA positive Blood cultures 11/5: 4/4 significant for G+ Bacilli Repeat blood cultures 11/7: NGTD Levophed and abx discontinued due to DNR CC status ESRD Hyperphosphatemia HD TTS Tunneled HD cath left chest F/w Dr. Nephrology following, recommend Prisma until pressor requirements decrease Transitioned to DNR CC Chronic Myocardial Injury Likely secondary to ESRD, possible volume related TTE: EF 70%, RV not well visualized Elevated troponin 114, repeat EKG, repeat troponin showed no signs of acute ischemia Troponin peaked 152, now down trending Elevated TSH Home med discontinued due to DNR CC status Anemia Hemoglobin of 9.8, has been stable History of diabetes mellitus Insulin discontinued Pt DNR CC Sacral pressure injury Stage 3 POA HAGMA-resolved Lactic Acidosis-resolved

Weitere VAERSDATA-Felder

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

VAERS 2728533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 29.12.2023
Impfdatum: 12.11.2021
Beginn: 09.11.2023
Tage bis Beginn: 727,0
Dosis: 2
Route/Site: - / -

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

Acute respiratory failure Asthenia Benign prostatic hyperplasia Brain natriuretic peptide normal COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Cough Depression Dyspnoea Emphysema Fatigue Full blood count normal Hypertension Intensive care Lactic acidosis Lung opacity

Symptomtext

Patient is a 63 y.o. male patient of MD with history of severe COPD, chronic respiratory failure on 6 L of oxygen at home, hypertension, anxiety, depression, BPH, cachexia, history of tobacco use presented on 11/9/2023 with shortness of breath. Patient found to be in acute exacerbation of COPD as well as have COVID. Acute on chronic hypoxic respiratory failure Acute exacerbation of COPD History of severe COPD Patient with history of severe COPD presented with shortness of breath, tested positive with COVID-19 History of chronic respiratory failure on 6 L of oxygen, requiring BiPAP in the ER. Patient on breztri and albuterol inhalers at home Patient initially admitted to ICU, however was weaned down to 6 L while in the ER and was deemed to be stepdown appropriate where he stayed until discharge Initial CBC unremarkable, lactic acidosis 2.8, troponin and BNP within normal range Blood cultures 11/9: NGTD In the ER received azithromycin and ceftriaxone CXR with severe bullous emphysema, new hazy and patchy right basilar density suspicious for infiltrate/pneumonia Treated with azithromycin, steroids, and treatment of COVID as below. Home inhalers, breathing treatments continued at discharge. Covid-19 Virus Infection Date of onset of symptoms: 2 weeks prior to admission Symptoms present on admission: Shortness of breath, cough, fatigue, generalized weakness Date of covid positive test: 11/9/23 Vaccination status: vaccinated, no booster Imaging: CXR?severe bullous emphysema. New hazy and patchy right basilar density suspicious for infiltrate/pneumonia. Oxygen requirements on admission: BIPAP Oxygen requirements on discharge: 6L nasal cannula (baseline) Medical therapy: remdesivir, steroids, azithromycin, tocilizumab Procal negative Patient stable on home O2 requirements x48 hours prior to discharge Hypertension Home carvedilol restarted at time of discharge Anxiety/Depression Continued citalopram BPH Continued Flomax Cachexia In setting of severe COPD BMI 14.2 Dietitian consulted and followed during admission; received Boost BID in addition to meals

Weitere VAERSDATA-Felder

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

VAERS 2727300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 44,0
Geschlecht: M
Eingang: 26.12.2023
Impfdatum: 21.10.2021
Beginn: 14.10.2023
Tage bis Beginn: 723,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Blood bicarbonate increased Blood lactic acid Blood pH normal Bradycardia C-reactive protein increased COVID-19 Cardiac stress test Cardiac telemetry abnormal Chest X-ray abnormal Compression garment application Dyspnoea Echocardiogram Essential hypertension Insurance issue Lung opacity Obesity Obstructive sleep apnoea syndrome

Symptomtext

Patient. is a 46 y.o. male who is a patient of MD with significant medical history of asthma and hypertension presented to Hospital with shortness of breath. Acute hypoxemic respiratory failure COVID-19 virus infection Patient with symptom onset on 10/9/2023 after having attended a Buckeye's game. SPO2 90% on room air and at Pickerington freestanding ED, SPO2 88% on room air on admission CRP 12.2, lactic acid 1.3 on admission VBG pH 7.37/PCO2 54.6/PO2 30/HCO3 31.3/sats 45.2% FiO2 2 L CXR marginal inspiration, questionable faint opacities noted bilaterally Decadron plus remdesivir started on admission Monitor closely pulse ox and titrate oxygen needs accordingly DVT prophylaxis with Lovenox Incentive spirometry, self proning Lasix IV 20 mg x 1 ordered on 10/15 Room air > past 24 hours Bradycardia, asymptomatic While patient is asleep Most likely related to untreated sleep apnea Discussed with cardiology who reviewed telemetry showing sinus bradycardia without associated heart block Patient recently had echocardiogram and stress test as outpatient Plan to reevaluate need for repeat echocardiogram once patient is out of isolation Encourage patient to utilize CPAP at night. Peripheral edema, BLE due to Chronic venous insufficiency Patient is dependent on compression stockings Elevate legs Recommend compression stocking use Obesity BMI 33 Essential hypertension BP 164/101 Continue eplerenone, formulary equivalent of Benicar Will hold Bystolic in the setting of bradycardia Add as needed hydralazine History of asthma Continue albuterol inhaler (neb at home, covid precludes this) Cont steroid for 10 days, mucinex OSA Patient says insurance not approving CPAP, unclear why Patient declined CPAP while inpatient on admission 10/15 after discussion regarding bradycardia and unmanaged sleep apnea, patient agreeable to nocturnal CPAP which was ordered but not utilized

Weitere VAERSDATA-Felder

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

VAERS 2700961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MN
Alter: 93,0
Geschlecht: M
Eingang: 24.10.2023
Impfdatum: 02.11.2021
Beginn: 09.10.2023
Tage bis Beginn: 706,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Asthenia COVID-19 Cough Nasal congestion Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient was seen in the ED on 10/9/23 for fever (103.5 F), cough, nasal congestion, and weakness for the past two days. He reported that his wife recently tested positive for COVID-19. A COVID PCR test performed in the ED also resulted positive for the patient. Ultimately, the patient was admitted 10/9/23 - 10/11/23 with diagnoses including acute hypoxic respiratory failure due to COVID-19. During his admission, the patient required supplemental O2 but was weaned to room air by discharge. Additionally, the patient was on dexamethasone. Of note, the patient has received three doses of the Pfizer monovalent COVID vaccine (given 2/2/2021; 2/23/2021; 11/2/2021).

Weitere VAERSDATA-Felder

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

VAERS 2684639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 21.09.2023
Impfdatum: 20.10.2021
Beginn: 29.07.2023
Tage bis Beginn: 647,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure COVID-19 COVID-19 pneumonia Dysphagia Endotracheal intubation Fungal infection Haematemesis Intensive care Pneumonia bacterial Respiratory failure Sepsis Septic shock Sputum culture positive

Symptomtext

1. Acute hypoxic hypercapnic respiratory failure, ARDS: -Pulmonology consulted and following. -7/31 intubated -8/4 extubated -8/16 re-intubated 2. COVID-pneumonia: -Infectious disease consulted -+7/31 COVID -Decadron, remdesivir completed 3. Sepsis, septic shock, bacterial PNA: -Receiving antibiotics -Received pressors -sputum cx with yeast, started on diflucan 4. Recent transesophageal fistula, status post esophageal stent placement, history esophageal cancer: -Prior admission found to have transesophageal fistula and transferred to hospital, hospital placed esophageal stent -ICU team discussed with recent CT surgeon at hospital -Follows with clinic for immunotherapy 5. AKI: -Monitor labs -Hold nephrotoxic agents, IV fluids 6. Coffee ground emesis: -GI consulted -no plan for EGD at this time d/t high risk re-intubation -cont PPI BID 7. Dysphagia: -unable to tolerate tube feeds, recurrent aspiration -TPN restarted 8. Other chronic medical conditions: History anxiety, history of asthma, history of non-Hodgkin's lymphoma, depression history, hypothyroidism, OSA History of Present Illness: Patient is a 46 y.o. female Despite all medical treatment and attempt to transfer patient to clinic. Patient continued to decline medically. Patient and family followed by palliative care and decision made to transition to hospice. Patient admitted to IP hospice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 23,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2670916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 14.08.2023
Impfdatum: 12.01.2022
Beginn: 10.04.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission/patient expired Pfizer 3/17/21 lot# ER2613; Pfizer 4/7/21 Lot# EW0150; Pfizer 1/12/22 Pfizer FF2590

Weitere VAERSDATA-Felder

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

VAERS 2660033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MN
Alter: 92,0
Geschlecht: F
Eingang: 24.07.2023
Impfdatum: 21.10.2021
Beginn: 10.05.2023
Tage bis Beginn: 566,0
Dosis: N/A
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Cardiac failure acute Dyspnoea Infection Left ventricular failure Pneumonia Pneumonia pneumococcal SARS-CoV-2 test positive

Symptomtext

The patient has a history of COPD, CHF, and chronic kidney disease. She was seen in the ED on 5/10 with gradually worsening shortness of breath over the past several days. In the ED, her O2 sats were at 88%; she was placed on 2L supplemental O2 with improvement. A COVID PCR test done in the ED resulted positive. Of note, the patient previously tested positive on 2/28, however had resolution of symptoms in early March. Ultimately, the patient was admitted 5/10/23 - 5/13/23. Discharge diagnoses include acute hypoxic respiratory failure, acute on chronic diastolic heart failure, suspect pneumonia likely hospital-acquired secondary to strep pneumoniae, and COVID-19 infection, among other diagnoses. Of note, during admission she was able to be weaned off supplemental oxygen.

Weitere VAERSDATA-Felder

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

VAERS 2640269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MN
Alter: 95,0
Geschlecht: M
Eingang: 02.06.2023
Impfdatum: 19.10.2021
Beginn: 20.02.2023
Tage bis Beginn: 489,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 COVID-19 pneumonia Death Fall General physical health deterioration Lethargy Pneumonia bacterial Pyrexia SARS-CoV-2 test positive Superinfection

Symptomtext

Patient with history of atrial fibrillation, dementia, CKD, and stroke. He was brought to the ED by EMS on 2/20/23 for lethargy and weakness as noted by his nursing home staff. Per EMS, the patient had a fall the day prior but was evaluated by EMS and was determined he could stay home. He was found to have a fever with a temp of 104.2. A COVID PCR test performed in the ED resulted positive. He was admitted 2/20-2/28. He was diagnosed with COVID-pneumonia and superimposed bacterial pneumonia. Initially he was treated with broad spectrum antibiotics and steroids with improvement in symptoms, however the patient's condition worsened on 2/25. He had increased oxygen needs during his admission, and ultimately was transitioned to comfort cares on 2/27. He passed away on 2/28/23. The patient received the primary COVID vaccine series and one booster dose.

Weitere VAERSDATA-Felder

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

VAERS 2634554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 20.05.2023
Impfdatum: 21.10.2021
Beginn: 08.03.2023
Tage bis Beginn: 503,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Aortic aneurysm Blood creatinine Blood lactic acid increased Blood sodium decreased COVID-19 COVID-19 pneumonia Computerised tomogram neck Computerised tomogram pelvis abnormal Cough Depressed mood Diverticulum oesophageal Dysphagia Dysphonia Dyspnoea Gastrointestinal tube insertion Gastrointestinal tube removal

Symptomtext

Patient is a 80 y.o. male who presented from home on 3/8/2023 with shortness of breath and cough. Found to have COVID19 PNA. Improved with dexamethasone and antibiotics. Course complicated by chronic dysphagia. SLP followed. Cor flo placed 3/13. GI consulted for PEG placement which occurred on 3/20. Neurology consulted for evaluation of possible MG, with plans to follow up outpatient. He received IVIG inpatient x5 days and minimal improvement after IVIG. Patient appropriate for discharge on 3/21. SNF acceptance 3/22. Plan for outpatient follow up with Neurology, ENT, GI. Repeat CMP in one week Dysphagia/dysphonia Possible Myasthenia Gravis Unilateral vocal cord paralysis. Per history. Established with ENT. -MBS on 3/12 demonstrated severe dysphagia in the pharyngeal region, compared to the previous study on 2/2/2023 there has been a significant decline in the pharyngeal swallow function -admissions previously for dysphagia in 2022 with some suspicion of TVC paralysis, dysmotility, possible cricopharyngeal bar and reflux -1/26/22 s/p flexible fiberoptic laryngoscopy; diagnosed with left TVC paralysis with Dr. -Esophagram 1/26/22 also revealed large cricopharyngeal bar but no findings of obstruction -MBS (2/1/22) with moderate pharyngeal and esophageal dysphagia with recommendations for ground mechanical diet and thin liquids. Noted to have osteophyte at C3/4 impacting pharyngeal contraction; also noted to have suspected cricopharyngeal bar -CT neck (1/31/22) without evidence for soft tissue mass or enhancement -s/p EGD 2/15/22 showing diverticulum in the middle third of the esophagus, suggestive of esophageal dysmotility. No mass, ring, stricture noted. - CorFlo placed 3/13. Removed withPEG placement 3/20 by GI. Neurology followed for possible MG; IVIG empirically x5 completed 3/20. Stopped mestinon due to nausea. Unable to fully tolerate EMG. Serologies PENDING on discharge. ENT recommending OP follow up. Neuro recommending OP follow up. Continue speech therapy Sepsis due to COVID-19 infection - resolved COVID-19 associated multifocal pneumonia - resolved Acute hypoxemic respiratory failure - resolved Onset of illness unclear. Patient was feeling ill for several weeks. Positive test on admission. He is vaccinated. -Requiring supplemental oxygen on admission, weaned to room air on 3/10 -Dexamethasone 6 mg daily x10 days total. Remdesivir was stopped on day of admission. -Completed 5 day Rocephin course. -Isolation removed. Hyponatremia Likely pseudohyponatremia from IVIG. Possible component of diminished PO intake and tube feeding - Na 132 on discharge - repeat CMP one week from DC Elevated transaminase - improving Likely secondary to COVID19 virus. No abdominal symptoms -ALT 57 on discharge - repeat CMP one week from DC Severe Malnutrition, POA Secondary to above. Dietician following - CorFlo placed 3/13 switched to PEG placement on 3/20. Dietician followed. Diet recs on discharge: NPO with PEG tube feeds Depression - Home med includes lexapro 10mg, continued inpatient - Patient's significant other does relay concerns about the patient being significantly depressed. She has mentioned this a few times up to this point has not been endorsing SI. She states that he becomes very withdrawn and has been having difficulty since he has been experiencing decline in his health. - No SI/HI - titrate regimen outpatient Essential hypertension Home medications include metoprolol. -Held metoprolol on discharge, normotensive Non hodgkin's lymphoma of Neck - Diagnosed in 2015 - Completed rituximab. - Follows with Dr., last seen 11/22. Continue follow up Ascending Thoracic Aortic Aneurysm - Follows outpatient with cardiothoracic surgery - CT dissection 1/29/23 with pelvis shows 4.4 x 4.4 diffuse aneurysmal dialation - Continue to follow up with CT Surgery Dr AKI - resolved Prerenal, secondary to above. -Baseline SCR around 0.9. SCR on admission 1.3. -S/p fluid bolus in the emergency department. -Repeat Cr normalized Elevated lactic acid - resolved Secondary to above, without acidosis. -Lactic acid 6.0 on admission. S/p fluid bolus in the emergency department. -Repeat lactic acid 1.8.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2628457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 16.10.2021
Beginn: 13.05.2022
Tage bis Beginn: 209,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Hypoxia Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA 5/20/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2626541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 04.03.2022
Beginn: 27.11.2022
Tage bis Beginn: 268,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Hypotension Hypoxia Obstructive sleep apnoea syndrome Respiratory failure

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ADULT OBSTRUCTIVE SLEEP APNEA ACUTE NON ST ELEVATION MI HYPOTENSION ACUTE RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2624657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: TN
Alter: 76,0
Geschlecht: M
Eingang: 02.05.2023
Impfdatum: 29.10.2021
Beginn: 29.04.2023
Tage bis Beginn: 547,0
Dosis: 1
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

admitted to Medical Center, 4.19.2023 as a transfer from another Med Center expired 4.29.2023 no time of death noted at present positive 4.17.2023 from the Med Center, tested 4.20-positive

Weitere VAERSDATA-Felder

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

VAERS 2618310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 87,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 20.10.2021
Beginn: 02.03.2023
Tage bis Beginn: 498,0
Dosis: 3
Route/Site: - / LA

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

Acute respiratory failure Hypoxia Respiratory failure

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2614664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 13.04.2023
Impfdatum: 06.10.2021
Beginn: 24.03.2023
Tage bis Beginn: 534,0
Dosis: 3
Route/Site: - / -

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

Alanine aminotransferase increased Anal incontinence Anion gap Aspartate aminotransferase increased Asthenia Blood creatinine increased Blood culture Blood lactic acid Blood potassium decreased Blood urea increased Breath sounds absent COVID-19 Cardiomegaly Chest X-ray abnormal Confusional state Cough Death Decreased appetite

Symptomtext

Discharge Provider: DO Primary Care Physician at Discharge: MD Admission Date: 3/24/2023 PRESENTING PROBLEM: SIRS (systemic inflammatory response syndrome) (HCC) [R65.10] HOSPITAL COURSE: I was called to patient?s bedside by RN to pronounce that the patient had passed. No spontaneous movements were present. There was not response to verbal or tactile stimuli. Pupils were mid-dilated and fixed. No breath sounds were appreciated over either lung field. No carotid pulses were palpable. No heart sounds were auscultator over entire precordium. Patient pronounced deceased at 21:15 on 4/4/23. No family was present at bedside. RN and hospice Rn to notify family. Patient is a 83 y.o. male with past medical history of end-stage renal disease on peritoneal dialysis, renovascular hypertension, chronic anemia, GERD, and GAD who presents today with lethargy, confusion. History is obtained from daughter and son at bedside as patient is able to answer only a few questions (name, DOB). The patient was recently admitted 03/15 through 3/17 with weakness and confusion. He was found to have COVID-19. He remained on room air and did not qualify for any medical therapy. He was noted to have dark stools and GI was consulted for possible bleeding. His hemoglobin remained stable and did not drop. They felt the color of the stools was likely related to his iron supplement. He does have baseline intermittent confusion and short-term memory difficulties. He does continue to drive short distances and grocery shop. His son pays his bills and his daughter does his peritoneal dialysis/cooking. He is normally able to do his own ADLs. She states that he has been improving since being discharged in relation to his COVID-19. He still has a mild cough. She states that he has had a very poor appetite ever since having COVID 19 and is barely eating. He had an episode where he pulled on his PD tube and was placed on Keflex by his dialysis company for possible tube site infection. This is radically improved on the Keflex. The patient takes docusate sodium, MiraLax daily with p.r.n. lactulose for bowel movements. His daughter states that his bowel movements the to be soft for him to have successful peritoneal dialysis. She states that today he has had 5, black, incontinent episodes of diarrhea. He did take lactulose, MiraLax and docusate sodium yesterday. The patient is not complaining of any abdominal pain. She states that he did have some retching when he had episode of diarrhea as it was quite odorous and mucous-like. Family does note that they have noticed that he is a bit more confused at night at baseline. The patient's son at bedside states that he has noticed him being very fidgety and somewhat hard to arouse at night. His daughter states that he has been taking Xanax for years. He is prescribed 0.25 mg to take 2 times a day, however he has always taken 0.5 nightly only. In the ER the patient was febrile with a temperature of 38.4? C, hypotensive with a blood pressure of 101/52, respiratory rate 24, tachycardic with a pulse of 108. Labs significant for potassium 3.3, anion gap 21, BUN 104, creatinine 7.42, AST 54, ALT 41, lactic acid 2.8-- >1.2, WBC 11.8, hemoglobin 11.8, UA with protein, 1 WBC, <1 RBC. CXR with cardiomegaly and interstitial prominence which could reflect mild edema or atypical infection. Slightly increased density in the right midlung zone peripherally favored to represent artifact from the chest wall soft tissues, less likely infiltrate. Blood cultures were collected. The patient was given 2 L of IV fluid. He was given 1 g of IV Tylenol.

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Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: 9/13/2021 Hospitalist Urinary tract infection without hematuria, site unspecified Dx
Vorgeschichte: Chronic kidney disease (CKD), stage V (HCC) Peritoneal dialysis catheter in place (HCC) Preop cardiovascular exam Renovascular hypertension Non-intractable vomiting with nausea, unspecified vomiting type Constipation, unspecified constipation type Chronic GERD COVID Generalized weakness Acute metabolic encephalopathy Black stools, chronic anemia C. difficile colitis Atrial fibrillation, new onset (HCC) Diarrhea of infectious origin Moderate protein-calorie malnutrition (HCC) End of life care
Andere Medikamente: ALPRAZolam (XANAX) 0.5 MG tablet amLODIPine (NORVASC) 5 MG tablet B Complex-C-Folic Acid (RENAL-VITE) 0.8 MG TABS calcitRIOL (ROCALTROL) 0.5 MCG capsule cinacalcet (SENSIPAR) 30 MG tablet Docusate Sodium (DSS) 100 MG capsule escitalopram (L
Allergien: OxycodoneNausea and Vomiting Gramineae Pollens Pollen CodeineNausea Only
Vorherige Impfungen: -

VAERS 2565184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 22.01.2023
Impfdatum: 20.07.2022
Beginn: 01.11.2022
Tage bis Beginn: 104,0
Dosis: 4
Route/Site: SYR / LA

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

Angiogram pulmonary abnormal COVID-19 Chest X-ray abnormal Computerised tomogram abnormal Diarrhoea Dyspnoea Fatigue Feeling abnormal Fibrin D dimer increased Hypotension Impaired driving ability Laboratory test abnormal Malaise Pain Pulmonary embolism Pulmonary hilar enlargement Ultrasound Doppler normal

Symptomtext

Though not due to the vaccine, I came down with COVID-19 on 11/1/2022 Became ill on 11/1/22, tested positive for COVID on 11/3/22, Received/started Nirmatrelvir-Ritonavir on 11/5/22. Symptoms: tired, ached, diarrhea, foggy brain, difficulty breathing. Was sick for two solid weeks, after which I experienced low blood pressure (to the point I felt unsafe to drive). Spoke with Dr. on 11/16/22. A week later I started having difficulty breathing. It progressively got worse. Called Dr.'s office who referred me to the emergency room on 11/28/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: In the emergency room initial lab work showed an elevated D-dimer. Chest x-ray showed new finding of asymmetric bulbous enlargement of the right pulmonary hilum which could represent enlarged pulmonary artery versus lymphadenopathy/mass. CT recommended for further evaluation. CT angiogram showed multiple small peripheral pulmonary emboli involving all lobes of the right lung. No large central pulmonary emboli identified. Incidental finding of a large lymph node versus mass in the upper mediastinum near the thoracic inlet level. Bilateral lower extremity venous duplex ultrasound did not show any evidence of deep vein venous thrombosis in either lower extremity.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Overweight, high blood pressure, arthritis, mild asthma
Andere Medikamente: Valsartan-Hydrochlorothiazide 160-12.5 mg per tablet, one tablet per day
Allergien: N/A
Vorherige Impfungen: -

VAERS 2563488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 13.05.2022
Beginn: 02.11.2022
Tage bis Beginn: 173,0
Dosis: 3
Route/Site: IM / RA

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

Arteriogram coronary abnormal COVID-19 pneumonia Cardiac failure Cardiac failure acute Coronary artery bypass Coronary artery stenosis Death Dyspnoea Haemoptysis Oedema peripheral SARS-CoV-2 test positive

Symptomtext

Patient with history of diabetes, CKD stage III, and COPD. He was seen in the ED on 10/25 for shortness of breath and difficulty breathing over the past week. He additionally reported lower extremity edema. While in the ED, patient tested negative for COVID-19. He was admitted on 10/25 for acute on chronic HFrEF. On 10/28, patient underwent a coronary angiogram and was found to have 99% stenosis of the ostial LAD. On 11/1 patient had new onset of hemoptysis. COVID test was ordered on 11/2 and patient tested positive for COVID-19 by PCR. On 11/3 patient underwent CABG. On 11/5, patient had shortness of breath with increased oxygen requirements and coughing. IV dexamethasone was started for suspected Covid pneumonia. Ultimately, patient was transitioned to comfort measures, and passed away on 11/12/22.

Weitere VAERSDATA-Felder

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

VAERS 2561965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: AZ
Alter: 79,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 27.09.2022
Beginn: 14.10.2022
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / LA

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

Amnesia Bradycardia Cerebral ischaemia Confusional state Dizziness Electrocardiogram abnormal Electroencephalogram Magnetic resonance imaging head abnormal Metamorphopsia Myocardial infarction Thalamic infarction Transient ischaemic attack Vision blurred

Symptomtext

Bivalent shot given on 9/27/2022. Suffered TIA on 10/14/2022 with Vision blurred and distorted, dizzy, confused, short term memory loss. Seen at Hospital the night of 10/14/2022 for Stroke protocol. EEG, MR without contrast. Seen by Dr on 11/21/2022 with slight light headed and short term memory loss. Vision appears to have returned to normal. MRI, EEG, Labs performed and reviewed by Dr. MRI impression: Moderate to severe chronic microvascular ischemic disease with small chronic infarct in the left thalamus. No preferential hippocampal volume loss. Symptoms of short term memory loss persists.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: 10/14/22 EKG SINUS BRADYCARDIA WITH SINUS ARRHYTHMIA INFERIOR MYOCARDIAL INFARCTION, PROBABLY OLD WITH POSTERIOR EXTENSION Abnormal ECG Compared to ECG 09/02/2011 23:39:43 Myocardial at Neurology Care 11/21/22 EEG Awake and Drowsy MR - BRAIN WITHOUT CONTRAST W/NEUROQUANT W/3D RENDERING, At Diagnostic Radiology 12/2/22 MRI Brain without contrast and volumetric analysys (neuroguant/icobrain) Impression: Moderate to severe chronic microvascular ischemic disease with a small chromic infarct in the left thalamus. No preferential hippocampal volume loss. Doctor review finds short term memory loss remains.
Aktuelle Erkrankungen: no illiness
Vorgeschichte: High Blood Presssure, Anxiety, high coloresterol, over weight
Andere Medikamente: Alprazolam, Atenolol, Amlodipine, Benzapril, B12, Omega3, D3
Allergien: Sulfa, Loriditine, Zyrtec
Vorherige Impfungen: -

VAERS 2525199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FF2590

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 18.02.2022
Beginn: 03.10.2022
Tage bis Beginn: 227,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure COVID-19 COVID-19 pneumonia Diarrhoea Dyspnoea Hypoxia Respiratory depression SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received three doses of Pfizer COVID 19 vaccine Feb/Mar/Nov 2021. The patient tested positive for COVID 19 on 3 October 2022. Patient presented to ED at Medical Center with shortness of breath. The patient was admitted with COVID pneumonia, Acute Hypoxic Respiratory Failure, currently on 2L of O2. The patient was treated with remdesevir, ceftriaxone and Zithromax for possible bacterial pneumonia. The patient left against medical advice on 4 Oct 2022. The patient presented to the hospital on 8 October 2022 with shortness of breath and diarrhea. The patient was admitted with COVID pneumonia and hypoxia. The patient was treated with supportive treatment, dexamethasone and oxygen. The patient was discharged on 12 Oct 2022 on dexamethasone and oxygen. The patient was re-admitted on 21 October with respiratory depression and acute kidney injury. The patient was discharged on prednisone and oxygen on 29 October 2022. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2514230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 28.10.2021
Beginn: 20.10.2022
Tage bis Beginn: 357,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Asthenia Blood creatinine increased C-reactive protein increased COVID-19 pneumonia Cough Dyspnoea Fluid intake reduced Hyperhidrosis Pneumonia bacterial Pyrexia Urine output

Symptomtext

Patient is a 51 y.o. female patient of MD with history of lupus, rheumatoid arthritis, asthma, migraine, depression, anxiety transferring to to Medical Center with acute hypoxemic respiratory failure due to COVID pneumonia. Acute hypoxemic respiratory failure Secondary to recent COVID PNA, underlying OSA/OHS Requiring 3L NC on admission, no baseline requirement CTPA 10/20 w/patchy bilateral infiltrates Aggressive pulmonary hygiene Wean O2 as able to maintain SpO2 88-92% Qualified for home O2 10/22, F2F completed Pulm/CC consulted Covid-19 Virus Infection Date of onset of symptoms: 9/29 Symptoms present on admission: SOB, cough, weakness Date of covid positive test: 9/29 Vaccination status: Vaccinated, booster x1 Imaging: CTA w/patchy bilateral interstitial infiltrates Oxygen requirements on admission: 6L Current oxygen requirements: 3L Medical therapy: Decadron Consultants following: Pulmonary, ID CRP elevated 308 No indication for ongoing isolation Bacteria PNA Pt reports subjective fevers and diaphoresis No SIRS/Sepsis criteria on admission MRSA probe, PCR antigens pending Cefepime, Flagyl ordered on admission Flagyl stopped 10/21 Changed to Levaquin on DC, to complete 7D total AKI, resolved Likely pre-renal secondary to poor intake Cr 1.28 on admission, baseline WNL Cr normalized 10/21 UOP remains adequate Limit nephrotoxins as able Daily RFP Asthma, w/o acute exacerbation Stable, at baseline Continue Symbicort, Singulair Needs PFT as OP History of lupus History of rheumatoid arthritis Continue home medications; Plaquenil and Arava Methotrexate recently discontinued, has not started Baricitinib Multimodal pain management History of depression Continue home medications History of migraine headaches Sumatriptan as needed GERD Cont pantoprazole OSA/OHS Suspected based on snoring, non-restful sleep Home PSG per Pulm Morbid Obesity BMI 53.27 Weight loss, lifestyle modifications encouraged

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

VAERS 2399163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: WI
Alter: 75,0
Geschlecht: M
Eingang: 02.08.2022
Impfdatum: 18.04.2022
Beginn: 21.07.2022
Tage bis Beginn: 94,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cardiac arrest Cardio-respiratory arrest Intensive care SARS-CoV-2 test positive

Symptomtext

Patient is a 75 y.o. year old male with complex medical history including bladder cancer receiving palliative chemo, and percutaneous nephrostomy tubes and urostomy, CKD, CAD with hx of CABG, GERD, admitted after cardiac arrest in the field, coded and ROSC, now in CCU, also found to be covid + on admission.

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

VAERS 2270779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: WI
Alter: 64,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 26.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 5,0
Dosis: UNK
Route/Site: IM / AR

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

Anticoagulant therapy Blood test Chest X-ray Computerised tomogram Dyspnoea Dyspnoea exertional Feeling abnormal Gait disturbance Oxygen saturation decreased Pulmonary embolism SARS-CoV-2 test negative

Symptomtext

"heavy load pulmonary emboli all lobes" On Saturday 1/31/2021 I felt poorly while exercising so I stooped on Thursday 1/6/2022 in the evening I felt very poorly and out of breath. My wife took me to Hospital. They tested me for COVID and it was negative and they discharged me despite low oxygen (95 -I was very fit). On Saturday morning 1/8/2022 I could barely walk without becoming extremely out of breath so my wife took me back to the hospital. At triage my oxygen level was 88. They did tests and told me that I had pulmonary emboli. I was hospitalized and am now on Eliquis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: Need records - CT scan and chest xray blood work
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Forgot which ones; would need to check
Allergien: None
Vorherige Impfungen: -

VAERS 2254665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 20.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 73,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Death Dyspnoea Hepatocellular carcinoma Pyrexia SARS-CoV-2 test positive Tachycardia Terminal state

Symptomtext

pt terminally ill with hepatocellular carcinoma; had a positive COVID test on 1/24/22; admitted to hospital on 2/1/22; tachycardia, fever, dyspnea; O2 supplementation; hospice GIP due to terminal disease process; hospice addressing sx; Fentanyl patch, Keppra, Ativan and Morphine given; pt passed away in the hospital

Weitere VAERSDATA-Felder

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

VAERS 2231603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MD
Alter: 66,0
Geschlecht: M
Eingang: 13.04.2022
Impfdatum: 11.10.2021
Beginn: 01.02.2022
Tage bis Beginn: 113,0
Dosis: 3
Route/Site: SYR / RA

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

Electrocardiogram abnormal Laboratory test Myocardial infarction

Symptomtext

Myocardial infarction (heart attack), very mild. No direct treatment, but additional drugs (atorvastatin and clopidogrel) prescribed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 1,0
Labordaten: EKG and lots of other things.
Aktuelle Erkrankungen: afib
Vorgeschichte: afib, BPH
Andere Medikamente: Pradaxa, metoprolol succinate ER, tamsulosin, finasteride, glucosamine, vitamin D3, esomeprezole, diclofenac gel
Allergien: None
Vorherige Impfungen: -

VAERS 2223704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: SD
Alter: 62,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 01.11.2021
Beginn: 07.02.2022
Tage bis Beginn: 98,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 Cough Death Dyspnoea Inappropriate schedule of product administration Intensive care SARS-CoV-2 test positive Terminal state Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 03/04/2021, 03/30/2021, and 11/01/2021. They presented to emergency department on 02/07/2022 with primary complaints of shortness of breath and cough. They tested positive for COVID-19 and were admitted to hospital (ICU) same day. The individual had stage IV metastatic lung cancer that had spread to the brain (diagnosis approx 4 months earlier) and was on palliative care at the time. They were discharged to a hospice facility on 02/11/2022. An additional COVID-19 test was positive on 02/17/2022. They died on 02/18/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Positive COVID-19 tests x2 despite being vaccinated and boosted
Aktuelle Erkrankungen: -
Vorgeschichte: At the time of the adverse event, the individual was terminally ill with stage IV lung cancer that had metastasized to the brain. They were on palliative care at the time of the adverse event. Chart notes medical conditions of: Lung Adenocarcinoma, Brain Metastasis, Neoplasm Causing Mass Effect, Anemia, Acute Hypoxic Respiratory Failure, Mediastinal Adenopathy, Vasogenic Brain Edema, Saddle Pulmonary Embolism, Asthma, Graves Disease, Autoimmune Hepatitis
Andere Medikamente: Radiation therapy for cancer (diagnosis in Oct 2021)
Allergien: Amoxicillin (Reaction: Rash), Clavulanic Acid (Reaction: Rash); Dog Dander (Reaction: Itchy Eyes); Dust Mites (Reaction: Unknown)
Vorherige Impfungen: -

VAERS 2223347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 17.11.2021
Beginn: 17.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Interstitial lung disease Pneumonia Respiratory failure

Symptomtext

ILD (interstitial lung disease) - He was treated for acute on chronic hypoxic respiratory failure secondary to interstitial lung disease also for pneumonia. He was evaluated by pulmonary specialist also was treated with oxygen and antibiotics. Patient was treated adequately and to stay discharged home with follow-up with the primary care physician as well as cardiology. Patient needs to continue oxygen at home this was explained to the patient. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2201653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: TN
Alter: 81,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 15.10.2021
Beginn: 27.02.2022
Tage bis Beginn: 135,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Pfizer vaccine x 3. Tested positive for Covid on 02/27/2022. Admitted to Hospital on 02/27/2022. Expired on 03/18/2022 while still hospitalized.

Weitere VAERSDATA-Felder

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

VAERS 2198697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 25.03.2022
Impfdatum: 11.10.2021
Beginn: 18.03.2022
Tage bis Beginn: 158,0
Dosis: 3
Route/Site: UN / UN

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

Angiogram pulmonary abnormal Arteriosclerosis Arthropathy Asthenia Bronchial secretion retention Bronchial wall thickening COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cholelithiasis Coma scale Cough Diffuse idiopathic skeletal hyperostosis Dyspnoea Fatigue General physical health deterioration Hepatic cyst Hepatic lesion

Symptomtext

Patient is a 83 y.o. male who presents today with cough, fatigue and shortness of breath. Patient was ill with upper respiratory infection type symptoms on March 11, 2022. Patient tested positive for COVID-19. Patient was being treated with vitamin-C, aspirin and doxycycline. Patient states that he continues to worsen. Patient presented to the emergency department tachypneic with room air saturation of 84%. He appeared to be in acute, moderate respiratory distress on arrival. No objective fever or chills. No nausea, vomiting or diarrhea reported. No abdominal pain, rash or lower extremity swelling. No focal neuro deficit. GCS 15. Patient has frequent nonproductive cough. Patient is vaccinated against COVID-19 and also had a booster. It appears to be a breakthrough case. Patient vital signs are otherwise stable. No evidence of acute sepsis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma scale
Hospital-Tage: 7,0
Labordaten: Procedure Component Value Ref Range Date/Time DR CHEST 2 VIEWS FRONTAL AND LATERAL Resulted: 03/25/22 0849 Order Status: Completed Updated: 03/25/22 0851 Narrative: EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 3/25/2022 8:36 AM TECHNIQUE: Frontal and lateral views INDICATION: Persistent hypoxia. Covid infection. COMPARISON: Chest x-ray 3/22/2022. CT angiography thorax 3/19/2022. ENCOUNTER: Not applicable _________________________ FINDINGS: Patchy peripheral left lung infiltrates are again noted, slightly increased. There is a small left pleural effusion. Heart size and pulmonary vasculature are within normal limits. _________________________ Impression: Slight increased peripheral left lung patchy infiltrates. Small left pleural effusion. DR CHEST SINGLE VIEW Resulted: 03/22/22 0617 Order Status: Completed Updated: 03/22/22 0619 Narrative: EXAMINATION: Single View Chest EXAM DATE: 3/22/2022 6:00 AM TECHNIQUE: Single view chest INDICATION: Resp failure/Covid infection COMPARISON: March 26, 2019 ENCOUNTER: Not applicable _________________________ FINDINGS: Lung volumes are diminished. Patchy airspace disease bilaterally seen to the greater extent on the left has a peripheral predominance. Mild blunting of the left costophrenic angle may represent a small pleural effusion. No visualized pneumothorax. The patient is lordotic in position. Heart size is likely within normal limits for lordotic positioning, low lung volumes, and portable technique. Hilar and mediastinal borders appear grossly stable with atherosclerosis. Old rib fractures again evident on the right. There are degenerative changes of the spine, chronic appearing widening of the acromioclavicular joint on the left. Postsurgical change of the left shoulder again evident. Study limited by overlying support devices. _________________________ Impression: Patchy peripherally based airspace disease, greater on the left. Short-term follow-up recommended. Possible small left pleural effusion. Imaging features can be seen with viral pneumonia, though are nonspecific and can occur with a variety of infectious and noninfectious processes. CT ANGIO THORAX WITH IV CONTRAST Resulted: 03/19/22 0203 Order Status: Completed Updated: 03/19/22 0205 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 3/19/2022 1:22 AM 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: The amount and type of contrast are recorded in the medical record. 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: Weakness, hypoxia.. COMPARISON: CT thorax 10/26/2020. ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: There is no mediastinal or hilar lymph node enlargement. Small hiatal hernia. Cardiovascular: The heart has a normal size and atherosclerotic plaque is present on the coronary arteries. There is no pericardial effusion. The thoracic aorta is not aneurysmal and there is no dissection. Mild diffuse atherosclerotic plaque. There is no evidence for right heart strain. Pulmonary Arteries: No pulmonary embolism is present. Lungs & Airways: Small amount of frothy respiratory secretions are seen in the trachea and mainstem bronchi. Scattered distal mucus plugging in the bilateral lower lobes. Diffuse bronchial wall thickening. Scattered diffuse groundglass opacities bilaterally. Small solid nodule in the right upper lobe (6:139) is unchanged from prior. Pleural Space: Small bilateral pleural effusions. No pneumothorax. Upper Abdomen: Cholelithiasis in a nondistended gallbladder. No gallbladder wall thickening or pericholecystic fluid. No evidence of biliary dilatation. Multiple low-density hepatic cystic lesions are similar in size and appearance to prior exam. Multiple large exophytic left renal cortical cysts are also similar to prior. Chest Wall & Musculoskeletal: Multilevel generative changes in the thoracic spine including diffuse anterior osteophytes at several levels compatible with diffuse idiopathic skeletal hyperostosis (DISH). No suspicious osseous lesions. ____________________ Impression: 1. No acute pulmonary embolism. 2. Scattered diffuse groundglass opacities bilaterally is compatible with COVID 19 pneumonia. 3. Small amount of respiratory secretions in the trachea and mainstem bronchi with scattered subsegmental mucus plugging in the bilateral lower lobes.
Aktuelle Erkrankungen: -
Vorgeschichte: Hospital Pneumonia due to COVID-19 virus Essential hypertension Electrolyte imbalance Class 2 severe obesity with serious comorbidity in adult Acute respiratory failure with hypoxemia D-dimer, elevated Non-Hospital BPH with obstruction/lower urinary tract symptoms Testicular pain, right Personal history of urinary calculi Kidney stone Renal cyst, left
Andere Medikamente: acetaminophen (TYLENOL) 650 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ascorbic acid (VITAMIN C) 500 MG tablet aspirin 81 MG chewable tablet carvedilol (COREG) 6.25 MG tablet cholecalcife
Allergien: Norco [Hydrocodone-acetaminophen]Nausea Only
Vorherige Impfungen: -

VAERS 2192200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: AZ
Alter: 93,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 16.03.2021
Beginn: 19.01.2022
Tage bis Beginn: 309,0
Dosis: 3
Route/Site: IM / RA

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

Acute kidney injury Ammonia Blood ethanol Blood gases Blood glucose COVID-19 Computerised tomogram head Computerised tomogram spine Cystitis Encephalopathy Full blood count Hypoglycaemia International normalised ratio Metabolic function test Prothrombin time SARS-CoV-2 test positive Sepsis Septic shock

Symptomtext

1/19/22: Patient admitted for: Acute cystitis without hematuria Sepsis with encephalopathy and septic shock, due to unspecified organism Hypoglycemia Elevated troponin Acute kidney injury COVID-19 positive

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 3,0
Labordaten: Covid test CBC/CMP POCT Glucose PT/INR Ammonia level, ethanol level BGA CT spine/head
Aktuelle Erkrankungen: UTI, foley catheter problem
Vorgeschichte: Hyperlipidemia Impaired fasting glucose Sick sinus syndrome due to SA node Presence of pacemaker BPH Obesity HTN Hx DVT
Andere Medikamente: Tamsulosin Lisinopril Atorvastatin Aspirin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2192149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 12.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Anticoagulant therapy Catheterisation cardiac abnormal Coronary artery disease Percutaneous coronary intervention Stent placement

Symptomtext

Patient admitted with NSTEMI. S/p cardiac cath with RCA 99% lesion in proximal 67% lesion with successful PCI DES for both lesions - ASA, Plavix, Coreg, lisinopril, atorvastatin. Hemodynamics stabilized and patient returned to baseline. She was discharged to f/u with cardiology and PCP. ED visit to hospital admission within 6 weeks 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 2189992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MA
Alter: 76,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 21.11.2021
Beginn: 06.01.2022
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac monitoring Cerebrovascular accident Computerised tomogram Echocardiogram Magnetic resonance imaging

Symptomtext

Stroke occurred January 5 , 2022. Admitted to hospital January 7 to January 22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 17,0
Labordaten: CT, MRI, Echocardiagram, continuing heart monitor
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ARMOUR Thyroid 30 mg. Vitamin C, D, B
Allergien: -
Vorherige Impfungen: -

VAERS 2189942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: SD
Alter: 81,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 06.10.2021
Beginn: 05.02.2022
Tage bis Beginn: 122,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 Death Feeding disorder General physical health deterioration SARS-CoV-2 test positive Speech disorder Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 01/05/2021, 01/26/2021, and 10/06/2021. The individual tested positive for COVID-19 on 02/05/2022 but COVID-19 symptoms were not the primary complaint on admission to hospital. The individual was in overall declining health at this time. It is not known if the individual had a specific symptom onset date as they had been non-verbal for a number of weeks, having suffered a CVA some time previous. The individual had been receiving end-of-life comfort cares at home but was brought to hospital on 02/05/2022 because the family no longer thought they were able to manage their condition and keep the individual comfortable at home. The individuals' end-of-life, comfort cares were continued in the hospital until their death on 02/06/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: Positive COVID-19 test on 02/05/2022 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Recent CVA, non-verbal in the weeks prior to the adverse event, in overall declining health. At the time of the adverse event, family had been providing comfort cares at home but the individual's condition necessitated hospitalization in order to keep them comfortable. The individual had not eaten for 5 days at the time of the adverse event. The individual was hospitalized with the intent of continuing end-of-life comfort care until the time of natural death. The individual also had underlying medical conditions of diabetes mellitus which was not well managed, hypertension, hyperlipidemia, and previous history of a small bowel obstruction.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 22.10.2021
Beginn: 29.11.2021
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / RA

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

Cerebrovascular accident

Symptomtext

Patient presented to the ED and was subsequently hospitalized for CVA within 6 weeks of receiving covid vaccination booster.

Weitere VAERSDATA-Felder

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

VAERS 2177033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MO
Alter: 59,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

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

Aphasia Cerebrovascular accident SARS-CoV-2 test

Symptomtext

Stroke like symptoms; aphasia; This is a spontaneous report received from contactable nurse. The reporter is the patient. A 59 year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: FF2590), on 12Oct2021, when the patient was 59 years, as single dose for covid-19 immunisation. Relevant medical history included diabetes and high blood pressure (HBP), and COVID prior to vaccination from unspecified dates. The patient took unspecified concomitant medications. Vaccination history included first dose of BNT162B2 (Lot number: 301308A), on 19Sep2021, when the patient was 59 years old, for covid-19 immunization. On 13Oct2021, the patient experienced stroke like symptoms and aphasia, which were serious as they were life-threatening, and involved hospitalization. The patient was noted as desperately in need of insight. The events were evaluated at the physician office visit and emergency room visit. The patient underwent laboratory tests and procedures, which included unknown results from a COVID test, post vaccination. Clinical details were as follows: Stroke like symptoms-aphasia-then total incapacity occurred. The patient was currently hospitalized, and noted as "desperately in need of insight ". The events involved hospitalization, and were life-threatening illness. There was no immediate risk of death from the event, and the patient was noted as hospitalized for 31 days. The patient had not recovered and treatment involved unspecified multiple interventions. The clinical outcome of stroke like symptoms and aphasia was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 31,0
Labordaten: Test Name: Covid; Result Unstructured Data: Test Result:Unknown results; Comments: if covid tested post vaccination: Yes
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; COVID-19 (covid prior to vaccination); Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2168892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: KY
Alter: 74,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 08.10.2021
Beginn: 12.01.2022
Tage bis Beginn: 96,0
Dosis: 3
Route/Site: UN / UN

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

Abdominal pain Acute respiratory failure Alanine aminotransferase normal Albumin globulin ratio Anion gap Aspartate aminotransferase normal Basophil count decreased Basophil percentage decreased Blood albumin decreased Blood alkaline phosphatase increased Blood bilirubin increased Blood calcium decreased Blood chloride increased Blood creatinine increased Blood glucose normal Blood potassium normal Blood sodium normal Blood urea increased

Symptomtext

1/24/22 Chief Complaint Patient presents with o HOT o Respiratory Distress Per EMS called resp distress, low-mid 80s on10L pt diagnosed with covid on 1/11. Pt increased WOB. hx of colon ca. 75 yr/o male who presents with abdominal and chest pain. He was recently diagnosed with Covid. His wife says that he has been confused since Thursday of last week. His O2 sats have been low at home. He was complaining of abdominal and chest pain and EMS was called to transport the patient to our facility. He was vaccinated against Covid, including a booster. Admission Diagnoses: Acute respiratory failure due to COVID-19 Hospital Problems: Principal Problem: Acute respiratory failure due to COVID-19 Active Problems: S/P thoracic aortic aneurysm repair (4/19/2012) Chronic anticoagulation (3/12/2015) CKD (chronic kidney disease) (5/20/2018) Malignant neoplasm of urinary bladder Discharge Diagnoses: Acute hypoxic respiratory failure secondary to COVID-19 PNA Sepsis, POA Acute on CKD III Hx of bladder cancer Hospital Course: 75 y/o male with hx of bladder cancer, who was vaccinated against COVID-19, was admitted to the hospital for acute hypoxic respiratory failure secondary to COVID-19 PNA. He was placed on high flow oxygen and started on IV Abx and IV steroids. On the evening of 1/25, he kept pulling off his oxygen and made it clear to me that he didn't want to fight anymore. I talked to him and called his wife. We discussed options of continuing aggressive medical care with DNR order vs transitioning to comfort care. Patient said he just wanted comfort care. He was started on prn IV dilaudid and versed. His family arrived, he was kept comfortable, and passed away at 14:45 on 1/26/2022. Cause of death is acute hypoxic respiratory failure secondary to COVID-19 PNA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: 1/12/22 COVID Result IPOC PCR Detected Abnormal CBC w/Diff Collection Time: 01/24/22 8:34 PM Result Value Ref Range White Blood Count 15.15 (H) 4.5 - 11.0 10*3/uL CBC w/Diff Collection Time: 01/24/22 8:34 PM Result Value Ref Range White Blood Count 15.15 (H) 4.5 - 11.0 10*3/uL Red Blood Count 3.90 (L) 4.5 - 5.9 10*6/uL Hemoglobin 11.5 (L) 13.5 - 17.5 g/dL Hematocrit 36.9 (L) 41.0 - 53.0 % Mean Corpuscular Volume 94.6 80.0 - 100.0 fL Mean Corpuscular Hemoglobin 29.5 26.0 - 34.0 pg Mean Corpuscular HGB Conc 31.2 31.0 - 37.0 g/dL Red Cell Distribution Width-CV 14.6 12.0 - 16.8 % Platelet Count 140 140 - 440 10*3/uL Mean Platelet Volume 10.0 8.4 - 12.4 fL Diff Type Hospital CBC w/AutoDiff (arb'U) Neutrophils % 90.4 (H) 45 - 80 % Lymphocyte % 3.4 (L) 15 - 50 % Monocyte % 3.0 0 - 15 % Eosinophil% 2.2 0 - 7 % BASO% 0.1 0 - 2 % Immature Granulocyte% 0.9 0.0 - 1.0 % Nucleated RBC % 0 0 /100(WBC) Neutrophil Abs 13.69 (H) 2.0 - 8.8 10*3/uL Lymphocyte-Absolute 0.51 (L) 0.7 - 5.5 10*3/uL Monocyte Absolute 0.46 0.0 - 1.7 10*3/uL EOS-Absolute 0.34 0.0 - 0.8 10*3/uL Basophil Abs 0.02 0.0 - 0.2 10*3/uL Immature Granulocyte Abs 0.13 (H) 0.00 - 0.10 10*3/uL Comprehensive Metabolic Panel (CMP) Collection Time: 01/24/22 8:34 PM Result Value Ref Range Sodium 136 136 - 145 mmol/L Potassium 3.7 3.5 - 5.1 mmol/L Chloride 109 (H) 98 - 107 mmol/L Carbon Dioxide 13 (L) 22 - 29 mmol/L Anion Gap 14 (H) 5 - 13 (arb'U) Glucose 104 (H) 74 - 99 mg/dL Blood Urea Nitrogen (BUN) 40 (H) 8 - 26 mg/dL Creatinine-Blood 2.41 (H) 0.73 - 1.18 mg/dL BUN/Creatinine Ratio 16.6 RATIO Estimated GFR 26 (L) >60 /1.73 m2 Estimated GFR if (Privacy) 32 (L) >60 /1.73 m2 Total Protein 7.1 6.2 - 8.0 g/dL Albumin 3.2 3.2 - 4.6 g/dL Globulin 3.9 1.5 - 4.5 g/dL Albumin/Globulin Ratio 0.8 (L) 1.1 - 2.5 RATIO Calcium 8.0 (L) 8.4 - 10.2 mg/dL Total Bilirubin 1.1 0.2 - 1.2 mg/dL AST/SGOT 21 5 - 34 U/L ALT/SGPT 10 0 - 55 U/L Alkaline Phosphatase 148 40 - 150 U/L Troponin Collection Time: 01/24/22 8:34 PM Result Value Ref Range Troponin 0.011 0.000 - 0.034 ng/mL B-Type Natriuretic Peptide Collection Time: 01/24/22 8:34 PM Result Value Ref Range B-Type Natriuretic Peptide 123.8 4 - 254 pg/mL Protime-INR Collection Time: 01/24/22 8:35 PM Result Value Ref Range Prothrombin Time 25.0 (H) 10.3 - 13.3 s INR 2.1 INR 1/24/22 CT Chest Wo Contrast IMPRESSION: Paraseptal and centrilobular emphysema. Scattered reticular and ground glass opacities likely infectious. INCIDENTAL FINDINGS: A few scattered calcified pulmonary nodules. Calcified mediastinal and hilar lymph nodes, likely remote granulomatous infection. No pleural effusion or pneumothorax. Calcified granuloma within the spleen and liver. Gallbladder is surgically absent.
Aktuelle Erkrankungen: -
Vorgeschichte: Anticoagulated on Coumadin chronic following aneurysm repair o Anxiety and depression o Arthritis o Arthritis HANDS, FEET KNEES o Asthma o Bladder cancer (CMS/HCC) o Blood transfusion 2009 BLADDER CANCER WITH CHEMO o Bruises easily o Cancer (CMS/HCC) o Decreased range of motion LEFT SHOULDER o GERD (gastroesophageal reflux disease) o Gout o H/O heat stroke 08/2017 o Hearing loss o History of concussion 2010 NECK SPRAIN /MVA o HIT (heparin-induced thrombocytopenia) (CMS/HCC) 2006 FOLLOWING KNEE SURGERY o Insomnia o Kidney stones PASSED WITHOUT INTERVENTION o Left shoulder pain X1 MONTH/FALL AT HOME o Neuropathy FEET o Obesity o Pneumonia 08/2017 MULTIPLE o PONV (postoperative nausea and vomiting) HAS DONE WELL WITH SCOPALAMINE PATCH o Restless leg syndrome o Seasonal allergies o Sepsis (CMS/HCC) 3/2018 from UTI o Slow to wake up after anesthesia o Snoring o Urinary tract infection MULTIPLE
Andere Medikamente: albuterol HFA (VENTOLIN HFA) 108 (90 Base) MCG/ACT inhaler albuterol HFA (VENTOLIN HFA) 108 (90 Base) MCG/ACT inhaler Inhale 2 puffs into the lungs every 6 (six) hours as needed o dexamethasone (DECADRON) 2 MG tablet Take 1 tablet by mouth
Allergien: Heparin, plastic tape, adhesive, Advil, sulfa antibiotics, amb ativan, bactrim, benadryl, codeine, diphehydramine, lunesta, morphine, restoril, temazepam, xanax, zolpidem
Vorherige Impfungen: -

VAERS 2168319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 29.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Arterial disorder Catheterisation cardiac abnormal Hypoxia Stent placement

Symptomtext

Acute respiratory failure with hypoxia - Patient had right and left heart catheterization which showed 65% proximal to mid LAD culprit lesion treated with drug-eluting stent on 11/10/2021. Hypoxia persisted requiring escalation of IV steroids with subsequent improvement. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2168078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 28.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Blood gases abnormal Chronic obstructive pulmonary disease Condition aggravated Confusional state Intentional medical device removal by patient Respiratory failure

Symptomtext

Patient presented with confusion. ABG showed acute on chronic respiratory failure with hypoxia and hyp patient was treated with ceftriaxone and azithromycin for possible superimposed bacterial pneumonia as well as COPD exacerbation with IV methylprednisolone and duo nebs. Patient self extubated on 11/7/2021 but was able to avoid reintubation as oxygen levels were weaned down. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2168005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: TX
Alter: 79,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 08.11.2021
Beginn: 01.03.2022
Tage bis Beginn: 113,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Abdominal wall haematoma Acute respiratory failure Anticoagulant therapy COVID-19 Chronic obstructive pulmonary disease Condition aggravated Death General physical health deterioration Haematoma Hypercapnia Hypoxia Inappropriate schedule of product administration Mental status changes Red blood cell transfusion Respiratory failure SARS-CoV-2 test positive Transfusion

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccine on 3/18/21, 4/15/21, and 11/08/2021. Admitted 2/9 - 19/22 for acute on chronic COPD exacerbation, tested Covid+ 2/9. Presented back to ED 2/20/22 for worsening pain in abdomen 2/2 abdominal wall hematoma 2/2 anticoagulation, TX'd w/2 uRBCs and 1 uFFP. Course c/b acute on chronic hypoxic respiratory failure. Continued to decline with hypoxia and hypercapnia with worsening mentation. Transitioned to comfort care and transferred to local Care Unit. Expired on 3/01/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: 02/09/22-This sample was analyzed using the SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen: -
Vorgeschichte: mitral valve replacement, squamous cell carcinoma of lung-stage III, COPD, OSA, AFib, hypothyroidism, CKD, HTN, anxiety, severe aortic stenosis, CHF
Andere Medikamente: Tylenol, albuterol, vitamin c, biotin, budesonide, buspirone, calcium carbonate/vitamin D3, calcium polycarbophil, cetirizine, diltiazem, docusate, enoxaparin, ferrous sulfate, fluticasone, lactobacillus rhamnosus, levothyroxine, multivitam
Allergien: Citrus, Wool
Vorherige Impfungen: -

VAERS 2147564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: FL
Alter: 84,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 03.03.2021
Beginn: 19.02.2022
Tage bis Beginn: 353,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Bronchitis C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Diarrhoea Hypokalaemia Lung opacity Nausea SARS-CoV-2 test positive Vaccine breakthrough infection Vomiting Walking distance test normal

Symptomtext

Patient was hospitalized due to breakthrough infection. Patient received the Moderna vaccine (2nd dose completed on 03/31/2021) and a Pfizer vaccine booster (11/09/2021). Patient was hospitalized from 02/19/2021 - 02/21/2021. Below is copied from discharge summary: Hospital Course: 85 yo F with COVID bronchitis/pneumonia with N/V/D #COVID pna/ acute resp failure - CXR w bl opacities -dc rocephin -s/p solumedrol, will complete w dexamethasone for 10 days -weaned off o2 this am -walking test done and passed, remained above 95% -crp elevated now downtrending -supportive tx #COPD - cont advair 250, budesonide BID, oxygen therapy to titrate >90% -+COVID -as above #CHF - ef 55-60% 12/18 with RV pacemaker, LAE -dc ivf #HTN -better controlled -cont home meds #CAD s/p CABG and pacemaker, h/o SMA stenosis -cont aspirin/plavix -cont lipitor -cont coreg #glaucoma - cont eye drops #hypokalemia - Potassium 100 total (s/p 40) Likely d/t N/V/D resolved Patient is discharged in stable condition with stable vital signs. All questions rearding hospital course and plan of care after discharge have been answered to satisfaction. Prescriptions for medications needed to be taken after discharge have been given to patient. Patient has been instructed to follow up with PCP and MD within the next 7 days after discharge. Patient verbalizes understanding all given instructions and has no further doubts regarding discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: SARS-COV-2, NAA, Detected: 02/19/2022
Aktuelle Erkrankungen: -
Vorgeschichte: ? Asthma ? CAD (coronary artery disease) ? Cancer (CMS-HCC) skin cancer right hand, left leg 2018 ? CHF (congestive heart failure) (CMS-HCC) ? COPD (chronic obstructive pulmonary disease) (CMS-HCC) ? Glaucoma ? High cholesterol ? Hypertension ? PNA (pneumonia)
Andere Medikamente: albuterol (PROAIR HFA;VENTOLIN HFA) 108 (90 Base) MCG/ACT IN Aerosol Solution Inhale every 6 hours as needed for wheezing. Information, Historical aspirin 81 MG Tablet Take by mouth daily. Information, Historical atorvastatin (L
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2113647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MO
Alter: 58,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 27.01.2022
Beginn: 02.02.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Death Malaise Vaccination complication

Symptomtext

Unknown. Reported via email by county coroner that patient was found deceased on 2/4/22. He stated in the email that it was reported by family members/friends, to the coroner, that the patient was ill after receiving his Pfizer Booster vaccine on 1/27/22. The coroner stated that it was his "opinion" that the patient died "as a result of complications from the COVID booster shot. The manner of the death is natural." Unknown if the patient attempted to medical advice from his physician.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma - reported by Coroner
Andere Medikamente: Inhaler - Reported by Coroner
Allergien: -
Vorherige Impfungen: -

VAERS 2113308

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FF2590

kritisch

Staat: KY
Alter: 64,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 16.11.2021
Beginn: 31.01.2022
Tage bis Beginn: 76,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Computerised tomogram head abnormal Computerised tomogram thorax abnormal Constipation Dyspnoea Fibrin D dimer increased General physical health deterioration Hypercalcaemia Hypotension Intensive care Ischaemic hepatitis Lactic acidosis Lung adenocarcinoma

Symptomtext

Pt rec'd Pfizer 3/4/21 and 3/25/21 both from facility, then Moderna booster 11/16/21. Pt to ED 1/31/22 c/o SOB. Dx acute hypoxic resp failure. CXR and CT show large mass encroaching on R mainstem bronchus. Admitted to ICU and placed on vent. Pos COVID Pcr in ED. Hypotensive with pressors. After continued deterioration changed to DNR/DNI. Discharge dx: septic shock, acute hypoxic and hypercapnic resp failure, poorly differentiated adenocarcinoma of lungs with distal metastasis, pleural effusion, COPD exacerbation, COVID-19 pneumonia, lactic acidosis, tobacco use disorder, moderate hypercalcemia, D dimer elevated, abnormal head CT (mets), pericardial efusion w/o tamponade, acute renal failure/anuric, metabolic acidosis, respiratory acidosis, constipation, shock liver

Weitere VAERSDATA-Felder

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

VAERS 2105123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 93,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 24.02.2021
Beginn: 02.02.2022
Tage bis Beginn: 343,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Chest X-ray normal Chills Cough Delirium Drainage Gait disturbance General physical condition abnormal Hypertension Metabolic encephalopathy Oropharyngeal pain Oxygen saturation decreased PO2 decreased Pyrexia

Symptomtext

94 yr old fully vaccinated (3 shots) patient present back to the ED after his son states he got him home and he was too weak to ambulate on his own and noted his pulse oximetry was low. Began having sore throat and drainage w cough 1/31, then developed fever that next am. Son states the patient does not leave his home and he and other family members have had mild URI symptoms for a couple weeks so they are getting tested, assuming they gave it to him. CXR does not look bad but paO2 is <60 and looks ill. Was prescribed Paxlovid last night but son has not filled yet. 1. Acute respiratory failure with hypoxia 2. Pneumonia due to COVID-19 virus 3. Acute delirium, acute metabolic encephalopathy 4. Fever and chill symptoms 1/31 and febrile so pretty acute fully vaccinated CXR not bad started Dex, RDSV - both completed day 3 on 2/4 - considered initiating IL-6 inhibitor if O2 needs increasing but is now on room air will not continue RDSV or Dex as room air and any risk > benefit at this point 5. HTN resume his ARB and amlodipine at higher doses PT recommended SNF but also acknowledges he has a very supportive family in the the home He has no interest in SNF and he and son both feel they can manage at home

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: 544269
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 11.10.2021
Beginn: 22.01.2022
Tage bis Beginn: 103,0
Dosis: UNK
Route/Site: IM / -

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

Acute respiratory failure Back pain COVID-19 Chills Condition aggravated Dyspnoea Nausea Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient is a 75 y male with a history of hypertension, CAD on Eliquis, COPD, lung cancer on immunotherapy, and Asthma presenting to the ED with complaints of worsening shortness of breath. He states he has chronic shortness of breath, worse with exertion, using 2 L home oxygen as well as a chronic cough but was needing more oxygen up to 4 L. Pt also reports a fever, chills, and generalized body aches that is worse in his back for one week, as well as nausea. Acute hypoxemic respiratory failure due to COVID-19.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: Positive COVID-19 test on 1/22/22
Aktuelle Erkrankungen: Unknown
Vorgeschichte: 4/23/20 Malignant neoplasm of lung, unspecified laterality, unspecified part of lung 4/7/20 Adrenal mass 8/20/19 Lung mass 09/11/2009 Bladder cancer Date Unknown Arthritis Date Unknown Asthma Date Unknown CAD (coronary artery disease) Date Unknown Cancer Date Unknown COPD (chronic obstructive pulmonary disease) Date Unknown History of kidney stones Date Unknown HTN (hypertension) Date Unknown Hyperlipidemia Date Unknown Prophylactic antibiotic Date Unknown Sleep apnea
Andere Medikamente: acetaminophen (TYLENOL EXTRA STRENGTH) 500 MG tablet albuterol (PROAIR HFA) 108 (90 BASE) MCG/ACT HFA inhaler apixaban (ELIQUIS) 5 MG TABS tablet aspirin (ECOTRIN) 81 MG EC tablet Cholecalciferol (VITAMIN D3) 2000 UNIT TABS Fluticasone
Allergien: Tape, Haloperidol.
Vorherige Impfungen: -

VAERS 2076023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: KS
Alter: 68,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 02.11.2021
Beginn: 16.12.2021
Tage bis Beginn: 44,0
Dosis: 3
Route/Site: - / -

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

Aneurysm ruptured Angiogram abnormal Angiogram cerebral normal Angiogram pulmonary abnormal Anticoagulant therapy Arteriosclerosis coronary artery Atelectasis Atrial fibrillation Blood culture Cardiomegaly Coagulopathy Computerised tomogram head abnormal Dilatation atrial Endotracheal intubation Endotracheal intubation complication Extubation Gastrostomy Headache

Symptomtext

clotting, PE RLL seg and subseg, L calf vein, R SCV, brach and ax v, radial art, bleeding aneurysmal at T10, w/ assoc thrombus and poss myelitis, e/o SAH My plan is agree w/ IVC filter, and holding AC at this time, would avoid further covid vaccines w/ quite extensive clotting w/in wks of getting booster, unexpected w/ his prior hx, though his mom did die of a stroke in her late 80s The patient was admitted and the following issues were addressed during this hospitalization: (with pertinent details including admission exam/imaging/labs). 12/15: Transferred from hospital for non-aneurysmal SAH/IVH 12/16: CT head/ MRI head ordered 12/17: Distal R radial artery occlusion, IR and Vascular surgery consulted 12/20: Extubated. Alkalotic, not tolerating so reintubated. CTA showing PEs. PERT activated. AFIB with RVR - metoprolol and cardizem. Blood cultures sent and antibiotics widened 12/21: IVC filter placed in IR. Heme consulted. ID workup. 12/22: CT head. Antibiotics stopped. 12/27: Trach at bedside 12/28: MRI T-spine, PEG tube in IR 12/30: Trach shield. 1/3: Progressed to tele status. PT/OT/SLP involved. 1/5 Rehab Medicine consulted. 1/6: Trach removed by patient. involved; working towards placement. 1/18: Discharged to facility with plan to see in 1 month with repeat imaging of spinal AVM

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: from heme consult on 12/21/21 -- 68 yo male with PMH of afib, retinal detachment s/p surgery X 2 (most recent 12/10/21) who presented to facility with mailaise, h/a, afib in RVR. Transferred for concerns for ruptured spinal AVM. Intubated 12/13 for concerns of respiratory failure. 1. Right radial artery occlusion/PE/ RUE DVT/ LLE DVT -12/17/21 RUE arterial U/S: Short segment occlusion of the right radial artery near the level of the wrist. Right upper extremity arterial Doppler is otherwise normal. (per RN had a right radial arterial line @ hospital) -12/21/21 BUE U/S: Acute occlusive/near occlusive catheter associated thrombus throughout the right subclavian, axillary, and single proximal brachial veins. No deep vein thrombus in the left upper extremity. -12/21/21 BLE U/S: Acute deep vein thrombus isolated to the left calf within one of the peroneal veins. No extension into the left popliteal or femoral veins. No right DVT. -12/20/21 CTA C: Multiple right lower lobe subsegmental and segmental pulmonary emboli, with additional right middle lobe and right upper lobe subsegmental PE. 2. Findings consistent with mild right heart strain, RV to LV ratio mildly elevated at 1.1. 3. Mild bilateral lower lobe dependent atelectasis. Additional mild left lower lobe inferior dependent groundglass opacities are present and favored for additional atelectasis, though infectious pneumonia/aspiration could be superimposed (given secretions in the trachea and left airways with a left lower lobe predominance). 4. Mild cardiomegaly and at least moderate coronary artery calcifications. -no AC due to ruptured spinal aneurysm 2. Neuro -transferred for concerns for ruptured spinal AVM -CT head was obtained OSH due to the patient unable to move his right leg: showed concern for posterior fossa subarachnoid hemorrhage while on heparin drip and reversed with protamine -Cerebral angiogram OSH negative. MRI scans of the spine which showed evidence of subarachnoid blood in a area of hematoma centered around the T11-12 region. He then underwent spinal angiogram which showed evidence of a aneurysmal dilatation of the artery of Adamkiewicz. -12/16/21 MRI T&L spine: Persistent extensive complex subarachnoid fluid throughout the thoracic and lumbar spinal canal with superimposed enhancement suspected focal thrombus at T10. Fluid findings are favored for subacute subarachnoid hemorrhage. Enhancement related to infectious meningitis cannot be excluded. No AVM or fistula is identified on time resolved MR a performed through the thoracic spine. Focal T2 hyperintense signal abnormality in the dorsal and right lateral cord at T10. This may represent a small amount of cord edema which may be from localized compression of hemorrhage or focal myelitis. 3. ID -concerns for PNA per CTA Chest -Tmax 39.3 on 12/20 @ 1300 with HR 132 -blood and sputum cx ntd -zosyn, vancomycin Recommendations: -Agree with holding AC and placement of temporary IVC filter -overall clinical picture looks dismal; if he should make a dramatic improvement please re-consult us for future anticoagulation planning.
Aktuelle Erkrankungen: (Principal) Spinal arteriovenous malformation Atrial fibrillation Cauda equina compression Acute urinary retention Paraplegia Hemorrhage into subdural space of spine Subarachnoid hemorrhage Acute hypoxemic respiratory failure Retinal detachment, right Intraventricular hemorrhage Primary hypertension Acute encephalopathy NSTEMI (non-ST elevated myocardial infarction) Dyslipidemia Anemia Radial artery occlusion, right Pulmonary emboli Atelectasis Acute deep vein thrombosis (DVT) of right upper extremity Acute deep vein thrombosis (DVT) of left peroneal vein Hypokalemia Diarrhea Agitation Delirium Resolved Problems RESOLVED: Renal insufficiency RESOLVED: Transaminitis RESOLVED: Elevated CK RESOLVED: Acute pulmonary edema RESOLVED: Hypertensive emergency RESOLVED: Fever RESOLVED: Constipation RESOLVED: Hypernatremia RESOLVED: Haemophilus influenzae pneumonia RESOLVED: Sepsis RESOLVED: Leukocytosis RESOLVED: Hypophosphatemia RESOLVED: Hypotension
Vorgeschichte: -
Andere Medikamente: n/a
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2074934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 15.12.2021
Beginn: 29.01.2022
Tage bis Beginn: 45,0
Dosis: 1
Route/Site: IM / LA

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

Abortion spontaneous Foetal death Maternal exposure during pregnancy

Symptomtext

Intrauterine fetal demise (miscarriage)

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Praegender Schweregrund: Foetal death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/a
Vorgeschichte: Anxiety/depression Anemia
Andere Medikamente: Aspirin, ferrous sulfate, prenatal vitamin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2059394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

kritisch

Staat: AZ
Alter: 51,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 23.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Acute myocardial infarction Cardiac disorder Catheterisation cardiac abnormal Chest pain Coronary arterial stent insertion Coronary artery occlusion Electrocardiogram Myocardial necrosis marker

Symptomtext

vaccine booster received 10/23/2021. 10/27/21 experienced chest pain, went to ED, STEMI verified. Transferred to cath lab and had 2 stents place in R coronary artery. Definite heart disease prior to MI but concern that vaccine may have accelerated occlusion with a clot.

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: 10/27/2021 EKG, Cardiac enzymes, cath lab
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: simvastatin
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2046294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 17.02.2021
Beginn: 14.07.2021
Tage bis Beginn: 147,0
Dosis: 3
Route/Site: - / -

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

Arterial stent insertion Myocardial infarction

Symptomtext

Not sure if this is related. I had a Heart Attack July 14, 2021

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Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Stent placed in artery.
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Levothyroxine Bupropion Hydrochoride XL Ubrelvy Myrbetiq Vitamin D Vitamin B12 Multivitamin
Allergien: Pencillian Codeine Amoxicillian Banana
Vorherige Impfungen: -

VAERS 2040458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: CA
Alter: 73,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 12.10.2021
Beginn: 17.11.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / RA

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

Cardiac failure Cerebrovascular accident Computerised tomogram Dizziness Echocardiogram Ejection fraction Electrocardiogram Magnetic resonance imaging Mobility decreased Myocarditis Supraventricular tachycardia

Symptomtext

Acute CVA with some permanent loss of left arm functionality. Heart Failure with evidence of myocarditis. 51% LV ejection fraction. Frequent Supraventricular Tachycardia events resulting in dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: MRI - 11/17/2021, Echocardiology -11/17/2021, CT Scan - 11/17/2021, continuous 14-day EKG
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Terazosin
Allergien: none
Vorherige Impfungen: -

VAERS 1995517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: NC
Alter: 22,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Illness Near death experience

Symptomtext

complex with potential life threatening condition which was monitored closely in the office with frequent re-evaluation for over an hour.; Life threatening illness; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 03Nov2021 15:45 (Lot number: FF2590) at the age of 22 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. Patient had no known allergies. Prior to vaccination, patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The following information was reported: NEAR DEATH EXPERIENCE (life threatening) with onset 03Nov2021 16:15, outcome "recovered" (2021), described as "complex with potential life threatening condition which was monitored closely in the office with frequent re-evaluation for over an hour."; ILLNESS (life threatening) with onset 03Nov2021 16:15, outcome "recovered" (2021), described as "Life threatening illness". Immediate risk of death from the event. Since the vaccination, patient had not been tested for COVID-19. The events "complex with potential life threatening condition which was monitored closely in the office with frequent re-evaluation for over an hour." and "life threatening illness" were evaluated at the emergency room visit. Therapeutic measures were taken as a result of near death experience, illness with Antihistamines and Steriods.

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Praegender Schweregrund: Near death experience
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 1982960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: NH
Alter: 78,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 25.10.2021
Beginn: 17.12.2021
Tage bis Beginn: 53,0
Dosis: 2
Route/Site: SYR / AR

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

Cerebral thrombosis Cerebrovascular accident Gait disturbance Pain Platelet count decreased Syncope

Symptomtext

First shot given 10/04/21. Second shot given 10/25/21. Patient had pains starting at 430am. Had difficulity walking, collapsed. Was able to regain strength, rested but later collapsed again. Went by ambulance to emergency room. Stayed 24 hours in hospital. In hospital diagnosed with 1 CVA (cerebrovascular accident). Blood clot found in brain/had stroke. Low platelet count.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Type II
Andere Medikamente: Metformin 500mg oral tablet
Allergien: None
Vorherige Impfungen: -

VAERS 1981624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 25.10.2021
Beginn: 05.12.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: UN / UN

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

Asthenia Brain natriuretic peptide normal C-reactive protein increased COVID-19 Cough Death Decreased appetite Dyspnoea Fatigue General physical health deterioration Haematuria Haemoptysis Hypoxia Inflammatory marker increased Pain Procalcitonin normal Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

The patient is a 89y.o. female who presented on 12/9/2021 complaining of chest congestion and body aches. She had a history of dementia, HTN, A fib, COPD, hodgkin lymphoma, IBS and thyroid disease and Was having cough and body aches for the past few days and they did a at home COVID test that was found to be positive. She was also having some sputum production, fatigue, generalized weakness and decreased appetite. She was also having some SOB. She was afebrile, normotensive and hypoxic on RA. BNP was within normal limits for age. She was COVID positive in ED. CRP and inflammatory markers were elevated on admission. She was started on IV steroids and ID and pulmonology were consulted. Pro calcitonin was within normal limits. On 12/11 she had marked deterioration in her condition compared to day prior and was on HFNC 60L as well as non rebreather she was having some bloody sputum and hematuria as well. She was treated for possibly superimposed bacterial pneumonia She did get monoclonal antibody treatment day prior and tolerated it without issues. She was continued on steroids and antibiotic. She continued to have increasing oxygen requirements and family ultiamtely decided to withdrawal care and proceed with comfort measures. Patient was transitioned to NC from non rebreather and HFNC and comfort medications were ordered other medications were stopped. STAT hospice consult and SW consult were placed by service. Patient ultimately passed 12/14 at 03:40 am. I was contacted by the medicine resident

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diagnosis Date ? Arrhythmia AFIB RVR ? Arthritis generalized ? Atrial fibrillation ? Chronic obstructive pulmonary disease ? Coronary artery disease ? Disorder of thyroid ? Hiatal hernia ? Hodgkin lymphoma DIAGNOSED 13YRS AGO ? Hypertension ? IBS (irritable bowel syndrome) ? Intrauterine pessary ? Kidney calculi ? Memory loss PT STATES SHE HAS MEMORY LOSS AFTER ANESTHESIA ADMINISTRATION ? Thyroid disease ? Tumors above liver, in right clavicle, face
Vorgeschichte: Diagnosis Date ? Arrhythmia AFIB RVR ? Arthritis generalized ? Atrial fibrillation ? Chronic obstructive pulmonary disease ? Coronary artery disease ? Disorder of thyroid ? Hiatal hernia ? Hodgkin lymphoma DIAGNOSED 13YRS AGO ? Hypertension ? IBS (irritable bowel syndrome) ? Intrauterine pessary ? Kidney calculi ? Memory loss PT STATES SHE HAS MEMORY LOSS AFTER ANESTHESIA ADMINISTRATION ? Thyroid disease ? Tumors above liver, in right clavicle, face
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN) (2.5 MG/3ML) 0.083% nebulizer solution 2.5 mg 2.5 mg Inhalation RT-QID ? apixaban (ELIQUIS) tablet 2.5 mg 2.5 mg Oral Q 12 H ? carvedilol (COREG) tablet 3.125 mg 3.125 mg Oral BID ? DULoxetine (CYMBALTA)
Allergien: Rivaroxaban Other Bleeding; diarrhea
Vorherige Impfungen: -

VAERS 1839651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

kritisch

Staat: MA
Alter: 52,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood disorder Chest discomfort Chest pain Chills Fatigue Blood test Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Immunisation Laboratory test Pulmonary embolism Pulmonary infarction Lethargy Pain Pyrexia

Symptomtext

Bilateral Pulmonary Emboli; Left lung infarct; shortness of breath; Booster; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 52 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 12Oct2021 14:00 (Lot number: FF2590) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Overweight" (unspecified if ongoing); "he dose not smoke" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 2 Lot EL3246, expiration Apr2021. Intramuscular injection right deltoid.), administration date: 08Jan2021, when the patient was 52 years old, for Covid-19 immunization, reaction(s): "'He did not feel good with first two Pfizer COVID vaccines", "Low grade fever", "muscle aches", "nausea", "headache"; Bnt162b2 (Dose 1, Lot EH9899, . Intramuscular injection right deltoid), administration date: 16Dec2020, when the patient was 52 years old, for Covid-19 immunization, reaction(s): "He did not feel good with first two Pfizer COVID vaccine", "Low grade fever", "muscle aches", "nausea", "headache". The following information was reported: IMMUNISATION (hospitalization) with onset 12Oct2021 14:00, outcome "unknown", described as "Booster"; PULMONARY EMBOLISM (hospitalization, medically significant) with onset 29Oct2021, outcome "unknown", described as "Bilateral Pulmonary Emboli"; PULMONARY INFARCTION (hospitalization, medically significant) with onset 29Oct2021, outcome "unknown", described as "Left lung infarct"; DYSPNOEA (hospitalization) with onset 29Oct2021, outcome "recovered with sequelae" (2021), described as "shortness of breath". The patient was hospitalized for immunisation, pulmonary embolism, pulmonary infarction, dyspnoea (start date: 29Oct2021, discharge date: 01Nov2021, hospitalization duration: 3 day(s)). The events "bilateral pulmonary emboli", "left lung infarct" and "shortness of breath" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: unknown results; computerised tomogram: bilateral pulmonary embolism and left lung infarct; echocardiogram: unknown results; electrocardiogram: unknown results; laboratory test: unknown results. Clinical course: He had a bilateral pulmonary emboli and left lung infarct after getting the booster dose. When asked to provide outcome of his hospitalization, he stated he was still out of work and had shortness of breath, but was getting better slowly. He first thought he may have been admitted on 28Oct2021, but then said it was early morning of 29Oct2021, around 3am. Causality not provided. He was on no other medications and just had a physical. He was in perfect health. He was overweight, but he did not smoke or drink or do drugs. There were no Additional Vaccines Administered on Same Date of the Pfizer Suspect. At 03:30-04:00 for diagnosis of Left lung infarct and bilateral pulmonary embolisms. They did a tremendous amount of lab work, blood work, pulmonary CT Scan, EKG, and Cardiac Echo. He was then admitted to hospital after CT scan showed bilateral pulmonary embolism and left lung infarct. Prior Vaccinations (within 4 weeks), there were no any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s). Father had heart disease but was always a smoker and mom was a diabetic.; Sender's Comments: Based on the available information in the case provided, the causal association between the events Pulmonary embolism, Pulmonary infarction, Dyspnoea and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Name: pulmonary CT Scan; Result Unstructured Data: Test Result:bilateral pulmonary embolism and left lung infarct; Test Name: Cardiac Echo; Result Unstructured Data: Test Result:Unknown results; Test Name: EKG; Result Unstructured Data: Test Result:Unknown results; Test Name: lab work; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Nonsmoker; Overweight
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1839651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MA
Alter: 52,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Blood disorder Chest discomfort Chest pain Chills Fatigue Blood test Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Immunisation Laboratory test Pulmonary embolism Pulmonary infarction Lethargy Pain Pyrexia

Symptomtext

Bilateral Pulmonary Emboli; Left lung infarct; shortness of breath; Booster; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 52 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 12Oct2021 14:00 (Lot number: FF2590) at the age of 52 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Overweight" (unspecified if ongoing); "he dose not smoke" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 2 Lot EL3246, expiration Apr2021. Intramuscular injection right deltoid.), administration date: 08Jan2021, when the patient was 52 years old, for Covid-19 immunization, reaction(s): "'He did not feel good with first two Pfizer COVID vaccines", "Low grade fever", "muscle aches", "nausea", "headache"; Bnt162b2 (Dose 1, Lot EH9899, . Intramuscular injection right deltoid), administration date: 16Dec2020, when the patient was 52 years old, for Covid-19 immunization, reaction(s): "He did not feel good with first two Pfizer COVID vaccine", "Low grade fever", "muscle aches", "nausea", "headache". The following information was reported: IMMUNISATION (hospitalization) with onset 12Oct2021 14:00, outcome "unknown", described as "Booster"; PULMONARY EMBOLISM (hospitalization, medically significant) with onset 29Oct2021, outcome "unknown", described as "Bilateral Pulmonary Emboli"; PULMONARY INFARCTION (hospitalization, medically significant) with onset 29Oct2021, outcome "unknown", described as "Left lung infarct"; DYSPNOEA (hospitalization) with onset 29Oct2021, outcome "recovered with sequelae" (2021), described as "shortness of breath". The patient was hospitalized for immunisation, pulmonary embolism, pulmonary infarction, dyspnoea (start date: 29Oct2021, discharge date: 01Nov2021, hospitalization duration: 3 day(s)). The events "bilateral pulmonary emboli", "left lung infarct" and "shortness of breath" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: unknown results; computerised tomogram: bilateral pulmonary embolism and left lung infarct; echocardiogram: unknown results; electrocardiogram: unknown results; laboratory test: unknown results. Clinical course: He had a bilateral pulmonary emboli and left lung infarct after getting the booster dose. When asked to provide outcome of his hospitalization, he stated he was still out of work and had shortness of breath, but was getting better slowly. He first thought he may have been admitted on 28Oct2021, but then said it was early morning of 29Oct2021, around 3am. Causality not provided. He was on no other medications and just had a physical. He was in perfect health. He was overweight, but he did not smoke or drink or do drugs. There were no Additional Vaccines Administered on Same Date of the Pfizer Suspect. At 03:30-04:00 for diagnosis of Left lung infarct and bilateral pulmonary embolisms. They did a tremendous amount of lab work, blood work, pulmonary CT Scan, EKG, and Cardiac Echo. He was then admitted to hospital after CT scan showed bilateral pulmonary embolism and left lung infarct. Prior Vaccinations (within 4 weeks), there were no any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s). Father had heart disease but was always a smoker and mom was a diabetic.; Sender's Comments: Based on the available information in the case provided, the causal association between the events Pulmonary embolism, Pulmonary infarction, Dyspnoea and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Name: pulmonary CT Scan; Result Unstructured Data: Test Result:bilateral pulmonary embolism and left lung infarct; Test Name: Cardiac Echo; Result Unstructured Data: Test Result:Unknown results; Test Name: EKG; Result Unstructured Data: Test Result:Unknown results; Test Name: lab work; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Nonsmoker; Overweight
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1962304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: VA
Alter: 77,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 23.01.2021
Beginn: 21.09.2021
Tage bis Beginn: 241,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blindness unilateral Cardiac monitoring normal Cerebrovascular accident Chills Fatigue Nausea Resuscitation SARS-CoV-2 test negative Thirst

Symptomtext

After the first dose, my Mother suddenly lost the sight in her right eye. We went to Hospital where they told us she had a stroke in her eye. Then after the second dose on September 22 she had a serious medical emergency where I had to perform CPR to bring her back to life. When she was rushed to the hospital they had no explanation for the incident. She was thoroughly checked and they couldn't explain it. She wore a heart monitor for a month and that was normal. After the booster on 10/21/21, she has had no energy, severe chills and shaking, extreme nausea, and extreme fatigue with no fever.. She has had 3 COVID tests which were negative, and extreme thirst.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: The two hospitalizations did not have any conclusive reasons for these reactions.
Aktuelle Erkrankungen: -
Vorgeschichte: Blood pressure
Andere Medikamente: Blood pressure medication
Allergien: -
Vorherige Impfungen: -

VAERS 1939820

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: IA
Alter: 57,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Blindness Cerebral haemorrhage Headache

Symptomtext

Booster dose of Pfizer given on 11/29/21. Was out with a friend on 11/30/21 and developed a severe headache and loss of sight. Went to local ER and was then transferred to the Hospital. DX of brain bleed. Was inpatient for 2 days. Is back at home and doing well at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 2,0
Labordaten: Unknown
Aktuelle Erkrankungen: None
Vorgeschichte: Gastric bypass
Andere Medikamente: Sucralfate 1 mg QID Omeprazole 40 mg 1 daily Famotidine 20 mg BID Multivitamin daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 1939756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: IN
Alter: 35,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 22.10.2021
Beginn: 02.12.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: IM / LA

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

Coronary arterial stent insertion Coronary artery occlusion Echocardiogram Electrocardiogram Myocardial infarction

Symptomtext

On Thursday evening 12/02/2021, I experienced a heart attack. I went to the emergency room that night. The doctor noticed a blockage in the artery. Two stents were placed. This was all shocking to me because I have no prior history of heart problems or heart disease. I am a vegan and a runner.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 3,0
Labordaten: EKG; Echo; First stent - mid lad; Second stent - mid lad. I will be getting a cardiac MRI soon.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Chronic back pain
Andere Medikamente: Orsythia; Vitamin D
Allergien: N/A
Vorherige Impfungen: -

VAERS 1933614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

kritisch

Staat: AZ
Alter: 77,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Cardiac arrest Myocardial infarction

Symptomtext

Cardiac arrest due to suspected myocardial infarction <36 hours after receiving Covid-19 booster shot. Had previously recieved second dose of Moderna Covid vaccine on 2/24/21 without complication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Was given medical okay earlier in the week. Pharmacy only checked patients temperature. Deceased on additional medications for pre-existing conditions.
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, kidney disease
Andere Medikamente: HYDROCORTISONE, FLUDROCORTISONE, METOPROLOL, SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1915917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: AZ
Alter: 39,0
Geschlecht: F
Eingang: 02.12.2021
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: ja Erholt: nein

Anaphylactic shock Heart rate increased Immunisation Rash Swelling Throat tightness

Symptomtext

Booster; Anaphylactic Shock; throat closure; rash; swelling; rapid heart rate; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 15Nov2021 14:00 (Lot number: FF2590) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Type 1 Diabetes" (unspecified if ongoing); "Rhuematoid Arth" (unspecified if ongoing); "Celiac Disease" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "allergy to Poultry" (unspecified if ongoing); "allergy to Eggs" (unspecified if ongoing); "allergy to gluten" (unspecified if ongoing); "COVID-19" (unspecified if ongoing). Concomitant medications included: LANTUS; HUMALOG; ENBREL; SINGULAIR; LISINOPRIL. Past drug history included: Dimetapp, reaction(s): "Allergy"; Guaifenesin, reaction(s): "Allergy"; Erythromycin, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EP7534, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 02Apr2021, when the patient was 38 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8734, Location of injection: Arm Right, Vaccine Administration Time: 02:00 PM), administration date: 23Apr2021, when the patient was 38 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (medically significant), outcome "unknown", described as "Booster"; ANAPHYLACTIC SHOCK (medically significant) with onset 15Nov2021 14:30, outcome "recovering", described as "Anaphylactic Shock"; THROAT TIGHTNESS (medically significant) with onset 15Nov2021 14:30, outcome "recovering", described as "throat closure"; RASH (medically significant) with onset 15Nov2021 14:30, outcome "recovering", described as "rash"; SWELLING (medically significant) with onset 15Nov2021 14:30, outcome "recovering", described as "swelling"; HEART RATE INCREASED (medically significant) with onset 15Nov2021 14:30, outcome "recovering", described as "rapid heart rate". The events "anaphylactic shock", "throat closure", "rash", "swelling" and "rapid heart rate" were evaluated at the emergency room visit. Therapeutic measures were taken as a result of anaphylactic shock, throat tightness, rash, swelling, heart rate increased included Epipen, Benadryl 75 mg, steroids, pepcid, fluids. She had Covid prior vaccination, no Covid tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to animals; Asthma; Celiac disease; COVID-19; Egg allergy; Gluten sensitivity; Rheumatoid arthritis; Type 1 diabetes mellitus
Andere Medikamente: LANTUS; HUMALOG; ENBREL; SINGULAIR; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1903734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 06.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / LA

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

Fatigue Myalgia Near death experience Pain

Symptomtext

I feel like I am dying; Muscular pain; Fatigue; I am in so much pain; I feel like I am dying, in a lot of pain; This is a spontaneous report from a contactable consumer (patient). A 46-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection; Batch/Lot Number: FF2590), via an unspecified route of administration, administered in Arm Left on 06Nov2021 (at the age of 46-year-old) as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient did not receive prior vaccinations within 4 weeks. On Monday, 08Nov2021 the patient experienced i feel like i am dying, muscular pain, fatigue, i am in so much pain; i feel like i am dying, in a lot of pain. It was reported that, patient had muscular pain and fatigue. She was in so much pain. felt like she was dying, in a lot of pain and she could not wait. She was just going to the doctor or a hospital. She went to the doctor Thursday. He said did not take medicine. Drink teas and soup and a lot of liquid. The patient did not receive any treatment. Report was not related to a study or programme. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1901724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 18.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: UN / UN

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

Abdominal pain Acquired diaphragmatic eventration Acute kidney injury Acute respiratory failure Asthenia Blood creatinine Blood culture negative C-reactive protein COVID-19 Cardiomegaly Central venous catheterisation Chest X-ray abnormal Cholecystectomy Chronic kidney disease Computerised tomogram head normal Condition aggravated Cough Dehydration

Symptomtext

Patient currently admitted at (5) days inpatient starting on 11/21/2021. Patient is a 79 y.o. male who presents today with weakness and diarrhea. The patient has a history of renal transplant, diabetes, CKD 3, HTN, HLD, COPD. The patient speaks another language and his son at bedside assists with translation. The patient is fully vaccinated for COVID and he was getting his booster shot on 11/18. Later that day he developed symptoms of fatigue and weakness. He then developed diarrhea and abdominal pain, fever and cough. He has some shortness of breath with activity. He came to the ER for evaluation. In the ER the patient was COVID positive. He was found to be hypoxic requiring 2L NC. His CXR was negative for any acute abnormalities. He had labs showing AKI and hypokalemia. He was given decadron and potassium supplement. The hospitalist team was contacted for admission and further management. ASSESSMENT / PLAN: * Acute hypoxemic respiratory failure Assessment & Plan Secondary to COVID, no infiltrates noted on CXR at this time Symptom onset: 11/18 Isolation: Severe Respiratory, if improved/afebrile antipyretics consider deescalation on 12/8 due to immune compromised status Vaccination Status: Fully vaccinated, got his booster shot on the day of symptom onset Continue supplemental O2, Titrate/wean to maintain SpO2>92% Continue Dexamethasone 1/10 Continue Remdesivir 1/5 Encourage Self Prone, IS, deep breathing and ambulation as tolerated Symptomatic Treatment: Anti Tussives, Anti Emetics, Analgesics VTE PPx: Lovenox 40mg SQ q24 Daily CBC, CMP, CRP, D-Dimer Monitor I/O, daily weight, creatinine Maintain net neutral to negative fluid balance q24 Code Status: Full AKI (acute kidney injury) Assessment & Plan Likely due to dehydration with poor PO intake and diarrhea History of renal transplant Monitor renal function closely Hold home lasix and lisinopril COVID-19 virus infection Assessment & Plan Tested positive 11/21 Fully vaccinated, got booster the same day as symptom onset See plan above COPD (chronic obstructive pulmonary disease) Assessment & Plan Continue inhalers No wheezing on exam Chronic kidney disease (CKD), stage III (moderate) Assessment & Plan Now with AKI Continue to monitor renal function closely Dyslipidemia Assessment & Plan Continue statin HTN (hypertension) Assessment & Plan BP stable Continue home metoprolol and hydralazine, hold home lisinopril and lasix with AKI History of renal transplant Assessment & Plan Continue home tacrolimus, mycophenolate Renal function worse than baseline, monitor closely Type 2 diabetes mellitus Assessment & Plan Last A1c 7.2, repeat pending Transition home levemir to lantus Monitor blood sugars and adjust insulin as needed, anticipate hyperglycemia with steroid use

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: Procedure Component Value Ref Range Date/Time DR ABDOMEN FLAT PLATE - AP (KUB) Resulted: 11/26/21 0703 Order Status: Completed Updated: 11/26/21 0705 Narrative: EXAMINATION: Abdomen Single View EXAM DATE: 11/26/2021 5:05 AM TECHNIQUE: Single AP portable limited abdomen for tube placement INDICATION: NG tube placement. COMPARISON: CT angiography chest 9/15/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Bowel: Gastric tube tip is likely in the fundus of the stomach with the fundus of the stomach located higher than expected because of marked elevation of the left hemidiaphragm which is also seen on CT of 9/15/2021. There is some gas in the stomach. There are multiple dilated gas-filled small bowel loops. No extraluminal air. Abnormal Calcifications: There is some atherosclerotic calcification in the splenic artery visible. Bones: No acute osseous findings. Other Findings: Cholecystectomy clips right upper quadrant. Please see separate chest x-ray report for chest findings. _________________________ Impression: Gastric tube in the stomach. The stomach is positioned high beneath an elevated left hemidiaphragm. DR CHEST SINGLE VIEWResulted: 11/26/21 0356 Order Status: Completed Updated: 11/26/21 0358 Narrative: EXAMINATION: Single View Chest EXAM DATE: 11/26/2021 2:47 AM TECHNIQUE: Single view chest INDICATION: Line placement COMPARISON: Chest x-ray dated November 24, 2021 _________________________ FINDINGS: A left sided central line has been placed with tip in the SVC. Endotracheal tube and NG tube remain in stable position. The heart remains significantly enlarged. The pulmonary vasculature is stable. Lung volumes remain decreased and there is significant elevation of the left hemidiaphragm and left basilar atelectasis. Patchy airspace density throughout the left lung and right lung remain stable over the past hour. There are no significant pleural effusions and there is no evidence of a pneumothorax. _________________________ Impression: 1. Interval placement of a left-sided central venous catheter with tip in the SVC and no evidence of a complication 2. The tip the NG tube remains in the distal esophagus 3. Stable extensive bilateral airspace disease DR CHEST SINGLE VIEW Resulted: 11/26/21 0151 Order Status: Completed Updated: 11/26/21 0153 Narrative: EXAMINATION: Single View Chest EXAM DATE: 11/26/2021 12:59 AM TECHNIQUE: Single view chest INDICATION: intubation COMPARISON: Chest x-ray of 11/24/2021 and 11/21/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Endotracheal tube is present, with tip lying approximately 5 cm above the carina. Nasogastric tube is present, with tip lying in the distal esophagus. The stomach is severely distended with gas. Lung volumes are decreased compared to the prior exam. Even accounting for this, there is significantly increased left pulmonary airspace consolidation, and stable, extensive right pulmonary airspace consolidation. No pneumothorax. No appreciable pleural fluid. Bones appear stable. _________________________ Impression: 1. Appropriately positioned endotracheal tube. 2. The nasogastric tube tip overlies the distal esophagus. This should be advanced when possible. 3. Severe gaseous distention of the stomach. 4. Extensive bilateral pulmonary airspace consolidation, which has slightly increased since the prior exam. The Orange significant findings protocol was initiated at 11/26/2021 1:50 AM. CT HEAD WITHOUT IV CONTRAST Resulted: 11/26/21 0130 Order Status: Completed Updated: 11/26/21 0132 Narrative: EXAMINATION: CT Head without Contrast EXAM DATE: 11/26/2021 1:22 AM TECHNIQUE: Multiple axial images were obtained from the skull base to the vertex without contrast. Coronal and sagittal reformatted images were generated for review. INDICATION: Head trauma, mod-severe, fall with head trauma and code. COMPARISON: None ENCOUNTER: Not applicable HAND DOMINANCE: Right. _________________________ FINDINGS: The ventricles are normal in size. There is no evidence of mass, mass effect, midline shift, acute intracranial hemorrhage, acute transcortical infarct, or extra-axial fluid collection. There are no depressed calvarial fractures. Visualized paranasal sinuses are clear. ___________________________ Impression: No acute intracranial abnormality. DR CHEST SINGLE VIEW Resulted: 11/24/21 0802 Order Status: Completed Updated: 11/24/21 0805 Narrative: EXAMINATION: Single View Chest EXAM DATE: 11/24/2021 7:57 AM TECHNIQUE: Single view chest INDICATION: worsening hypoxia COMPARISON: 11/21/2021. ENCOUNTER: Not applicable _________________________ FINDINGS: Unchanged severe elevation of the left hemidiaphragm. Unchanged cardiomegaly. The pulmonary vasculature is obscured. There are new/increasing airspace opacities in both lungs, worse in the right upper lobe. Unchanged chronic atelectasis in the left lower lobe. No significant pleural effusion. No obvious pneumothorax. _________________________ Impression: Increasing/new bilateral airspace disease, greater on the right. DR CHEST SINGLE VIEW Resulted: 11/21/21 1528 Order Status: Completed Updated: 11/21/21 1530 Narrative: EXAMINATION: Single View Chest EXAM DATE: 11/21/2021 3:13 PM TECHNIQUE: AP portable upright views chest INDICATION: Viral upper respiratory infection like symptoms COMPARISON: 7/13/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Chronic severe elevation of the left diaphragm compared to right. Stable cardiomegaly. Pulmonary vasculature grossly within normal limits. No hilar adenopathy or mass. Superior mediastinum within normal limits. Stable chronic aortic dilation tortuosity and calcification. Right lung and pleural space grossly clear. Opacities overlying the elevated left diaphragm most likely represent atelectasis similar to the previous study, left upper lung clear. No definite left effusion. There is no evidence of pneumothorax. No acute osseous findings. _________________________ Impression: Chronic severe elevation of the left hemidiaphragm. There is chronic atelectasis of the left lower lung overlying the elevated diaphragm similar to the previous study. No definite evidence of acute cardiopulmonary disease. Procedure Component Value Ref Range Date/Time Peripheral Blood Culture Collected: 11/24/21 1612 Order Status: Completed Specimen: Blood, Venous Updated: 11/25/21 2101 Cult Blood Peripheral No Growth 24 hours Peripheral Blood Culture Collected: 11/24/21 1612 Order Status: Completed Specimen: Blood, Venous Updated: 11/25/21 2101 Cult Blood Peripheral No Growth 24 hours COVID-19 PCR - Rapid (Abnormal) Collected: 11/21/21 1437 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 11/21/21 1452 COVID-19 PCR Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Hospital Immunocompromised Admitted to intensive care unit Type 2 diabetes mellitus History of renal transplant HTN (hypertension) COPD (chronic obstructive pulmonary disease) Acute hypoxemic respiratory failure COVID-19 virus infection Acute kidney injury superimposed on chronic kidney disease Diarrhea CAP (community acquired pneumonia) Cardiac arrest Shock Fall Non-Hospital Lumbar radiculopathy Dyslipidemia Chronic kidney disease (CKD), stage III (moderate) Chronic anemia Acute congestive heart failure
Andere Medikamente: acetaminophen (TYLENOL) 650 MG tablet amLODIPine (NORVASC) 10 MG tablet aspirin EC 81 MG enteric coated tablet Calcium Carbonate-Vitamin D (CALCIUM PLUS VITAMIN D PO) cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) tablet cinacalcet (SEN
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1865389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: GA
Alter: 16,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac arrest Cardiac dysfunction Chemotherapy Death Electrocardiogram Q waves Electrocardiogram T wave peaked Heart rate increased Hypoxia Livedo reticularis Mechanical ventilation Multiple organ dysfunction syndrome Oxygen saturation decreased Poor peripheral circulation Pulmonary haemorrhage Resuscitation Thrombocytopenia

Symptomtext

Patient with progressive hypoxemia throughout the day despite multiple changes in ventilator settings/modes. HFOV discussed with family, but functional oscillator not available and was awaiting arrival of donor oscillator. She is not a candidate for ECMO due to pulmonary hemorrhage and thrombocytopenia with recent chemotherapy as well as BMI (morbidly obese). Trial on nitric oxide performed with minimal improvement (sats increased from 60% to 65-68%). She was noted to have increasing peaked T waves as well as development of Q waves concerning for hyperkalemia and worsening cardiac function consistent with multiorgan failure; perfusion was quite poor with mottled extremities and difficult to palpate central pulse

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Pt expired 11/11/21 (Continued) despite vasopressor support. She was given a dose of bicarbonate with some brief improvement in saturations to 70s and increased heart rate but subsequently became asystolic and CPR was started. She was given epi x 2 doses as well as a dose of bicarbonate and was hand ventilated; there was significant blood backing up into her ETT. Parents at the bedside requested cessation of resuscitation efforts at that point and the patient was pronounced dead at 2036 on 11/11/21. The doctor of the heme/onc service made aware of the patient's death; she had been at the bedside earlier in the day and involved with the conversations regarding the patient's decline.
Aktuelle Erkrankungen: ALL, hypertension, obesity, Type 2 Diabetes, Cdiff
Vorgeschichte: ALL phase DI of treatment, hypertension, Diabetes, obesity
Andere Medikamente: Bactrim, dexamethasone, Ketorolac, Vanc, sodium chloride
Allergien: NKA
Vorherige Impfungen: -

VAERS 1832317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Abdominal pain upper Angina pectoris Arthralgia Chest X-ray Diarrhoea Blood test Chest discomfort Electrocardiogram Fatigue Headache Immunisation Extra dose administered Myocardial infarction Pain in extremity Limb discomfort SARS-CoV-2 test Vomiting Troponin I

Symptomtext

I vomited several times; exhaustion, experienced severe fatigue; pain in my arm, shoulder; discomfort in my arm and chest; discomfort in my arm and chest; pain in my heart; I thought I might be having a heart attack; I had a pretty bad headache; I had diarrhea and arm pain; I had diarrhea and arm pain; Booster; This is a spontaneous report from a contactable consumer (patient). A 49-year-old non-pregnant female patient received BNT162B2 (PFIZER BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot number: FF2590), via an unspecified route of administration, administered in arm left on 26Oct2021 16:45 as DOSE 3 (BOOSTER), SINGLE (at the age of 49-year-old) for covid-19 immunisation. The patient was not pregnant at the time of vaccination. Medical history included high cholesterol from an unknown date and unknown if ongoing. The patient previously took codeine and experienced known allergies: codeine. Concomitant medications included estradiol, fenofibrate, valaciclovir hydrochloride (VALTREX), rosuvastatin (ROSUVASTATIN), all taken for an unspecified indication, start and stop date were not reported. Historical vaccine included the patient received first dose of BNT162B2 (PFIZER BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot number: EN6205), via an unspecified route of administration, administered in arm left on 04Mar2021 15:30 as DOSE 1, SINGLE (at the age of 48-year-old), second dose BNT162B2 (BNT162B2, Solution for injection, Lot number: ER2613), via an unspecified route of administration, administered in arm left on 25Mar2021 15:30 as DOSE 2, SINGLE (at the age of 48-year-old), both doses for covid-19 immunisation. The patient had no other vaccine in four weeks. The patient not had covid prior vaccination. On 27Oct2021 (also reported as Wednesday), the patient had a pretty bad headache. On 27Oct2021, the patient had diarrhea and arm pain. On 28Oct2021, She woke up Thursday morning at 2:30 AM with pain in heart went to the ER because she thought she might be having a heart attack, discomfort in my arm and chest. The ER doctor stated that her heart was a muscle, and it was a reaction to the vaccine. He told me to take ibuprofen every 4-6 hours. On 29Oct2021, friday through Sunday, the patient continued to have diarrhea, exhaustion and pain in arm, shoulder and heart. On 31Oct2021, the patient had vomited several times early Sunday morning and experienced severe fatigue all day Sunday and Monday. I still have pain and felt moderately fatigued. She took a covid test on Sunday and it came back negative last night. The patient had a doctor appointment today to follow up regarding my heart issue. The adverse event was treated with Aleve. On an unspecified date, the patient underwent lab tests and procedures which included blood test: unknown result (2 blood test (Troponin-I)), chest x-ray and EKG: unknown result. On 31Oct2021, the patient had sars-cov-2 test: negative (nasal Swab). Therapeutic measures were taken as a result for all the events. Outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Name: blood test; Result Unstructured Data: Test Result:Unknown result; Comments: 2 blood test (Troponin-I); Test Name: Chest X-Ray; Result Unstructured Data: Test Result:Unknown result; Test Name: EKG; Result Unstructured Data: Test Result:Unknown result; Test Date: 20211031; Test Name: Covid-19 Aegis PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol
Andere Medikamente: ESTRADIOL; FENOFIBRATE; VALTREX; ROSUVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1854541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 06.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 20,0
Dosis: 3
Route/Site: IM / AR

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

Abscess drainage Acute kidney injury Acute myocardial infarction Anticoagulant therapy Antiplatelet therapy Asthenia Bacterial test negative Blood culture positive COVID-19 COVID-19 pneumonia Chills Computerised tomogram abdomen abnormal Condition aggravated Cough Dehydration Diarrhoea Drain placement Dyspnoea

Symptomtext

Hospitalized 10/29/2021; COVID-19 positive 10/26/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: DO Admission Date: 10/29/2021 Discharge Date: 11/3/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Dehydration [E86.0] Hypokalemia [E87.6] Transaminitis [R74.01] Severe sepsis [A41.9, R65.20] AKI (acute kidney injury) [N17.9] Pneumonia due to COVID-19 virus [U07.1, J12.82] COVID-19 [U07.1] Sepsis [A41.9] HOSPITAL COURSE: 75 yo male with history of CAD, PE/DVT, prostate CA, and Gilbert's syndrome. He presented to Hospital on 10/29 with symptoms of dyspnea cough, fever, weakness. His code PCR was positive on 10/26. In the emergency department the patient was found to be hypoxemic requiring 3 L of oxygen, hypotensive despite 3 L of fluids and therefore was started on norepinephrine and admitted to intensive care unit for further management of septic shock. Other labs are notable for an acute kidney injury, elevated troponin and elevated procalcitonin. Patient was started on IV antibiotics. Infectious Disease were consulted. Blood cultures were drawn. Epinephrine was able to be weaned down by the following day. CT imaging revealed a hepatic abscess for which Interventional Radiology were consulted and patient underwent image guided drain placement on 10/31. Cultures from the drain did not grow any bacteria. Her blood cultures did return positive for fusobacterium nucleatum. Antibiotics were adjusted to ceftriaxone and Flagyl while in the hospital. Infectious Disease recommended a 4 week course of levofloxacin and Flagyl on discharge. They will follow up with patient in 3 weeks in their clinic. Of note, patient's blood cultures were not back yet at the time of discharge, however telephone discussion with Infectious Disease Service today felt to be okay to discharge on above regimen and will follow up on susceptibilities, notify patient if any changes need to be made. Regarding his covid diagnosis, patient was treated with the severe and will complete a ten-day course of Decadron at home. He was able to wean off of oxygen and remained comfortable on room air without additional COVID-like symptoms during the last days of his hospitalization. Cardiology were consulted for NSTEMI, recommended heparin drip with transition to dual anti-platelet therapy for 1 year with possible outpatient stress testing on follow-up appointment. Patient is being discharged home in stable and improved condition. He has been instructed to follow up with interventional Radiology for drain removal in the next couple of weeks. He will follow up with primary care physician for regular health maintenance. His losartan was held on discharge due to lower blood pressures, this could be resumed in the outpatient setting if tolerable.

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: Office visit 10/26/2021: Assessment / Plan: 1. Contact with and (suspected) exposure to covid-19 - COVID-19 PCR; Future - COVID-19 PCR 2. Fever, unspecified fever cause - Influenza (Flu) A/B PCR; Future - Influenza (Flu) A/B PCR Will check covid and influenza tests. If symptoms worsen he will need to go into the emergency room for evaluation. Subjective: Patient ID: Patient is a 75 y.o. male Chief Complaint: FATIGUE (since saturday ), DIARRHEA, CHILLS, FEVER, and COVID-19 HPI: The patient presents to the clinic with fatigue, diarrhea, chills, and fever times 3 days. He went over the weekend with 10 other guys and on the way back started feeling ill. He took ibuprofen with some relief in his fever. He denies any cough, congestion, shortness of breath, abdominal pain, or loss of taste or smell. He had 3 doses of the covid vaccine and received his flu vaccine last month.
Vorgeschichte: CAD in native artery Essential hypertension Liver mass COVID-19 Septic shock Calcium oxalate kidney stones Acute kidney injury Mixed hyperlipidemia Primary osteoarthritis involving multiple joints Elevated troponin
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet clopidogrel (PLAVIX) 75 MG tablet levoFLOXacin (LEVAQUIN) 750 MG tablet metoprolol tartrate (LOPRESSOR)
Allergien: lisinopril
Vorherige Impfungen: -

VAERS 1851250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Back pain Blood magnesium Chest X-ray Chest pain Computerised tomogram thorax abnormal Culture urine Differential white blood cell count Electrocardiogram Erythema Flushing Full blood count Human chorionic gonadotropin Hypertension Metabolic function test Pulmonary embolism Scan with contrast abnormal Tachycardia Troponin

Symptomtext

Tachycardia a consistent heart rate of 90 to 120 bpm with a resting heart rate of 79 bpm. Flushing/red check. High blood pressure, chest pain, back pain. Follow up with Cardiologist December 20th 2021

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: CBC Auto Differential Comprehensive Metabolic Panel w/ Reflex to MG HCG Qualitive Serum Micro Uranalysis Troponin Urinalysis Reflex to Culture CT Chest Pulmonary Embolism with Contrast XR Chest Portable EKG 12 Lead
Aktuelle Erkrankungen: Covid 19 positive September 20th 2021
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1834249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: ME
Alter: 93,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 18.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

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

Acute myocardial infarction Cerebrovascular accident Computerised tomogram normal Dizziness Hemiparesis Magnetic resonance imaging head abnormal Troponin Urinary tract infection

Symptomtext

Ischemic CVA and N-STEMI type 2 cardiac event 5 days post injection. Dizziness and left-sided weakness. Admitted to hospital, transferred to rehab unit on day 3, discharged home day 8.

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 8,0
Labordaten: CT scan negative. MRI - two recent ischemic events. Elevated troponin 0.047 on admission, dropped to 0.043 after a few hours. UTI during inpatient stay.
Aktuelle Erkrankungen: irritable bowel
Vorgeschichte: diabetes, hypertension
Andere Medikamente: metoprolol 25mg 1/2 bid; glimepiride 1mg 1/2 bid; losartin 50mg 1/day; furosemide 20mg 3/week; diltiazem 120mg 1/day; acidophilus 1/day; AREDS vitamins bid; glucosamine/chondroitin 1/day; multivitamin 1/day; peppermint oil 1/day; cholestyr
Allergien: atenolol, codeine, lisinopril, dairy products
Vorherige Impfungen: -

VAERS 2638101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Death Intracranial aneurysm

Symptomtext

Narrative: Patient with a history COPD, HTN, hyperlipidemia, diabetes, gout, and episode of syncope Sept 2020 (possible orthostatic hypotension). The day after COVID booster and influenza vaccine, patient was taken to an outside hospital by family at 6 am where he later died due to an brain aneurysm per report from the patient's son. The outside hospital did not think the brain aneurysm was related to vaccinations, per report from the patient's son.

Weitere VAERSDATA-Felder

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

VAERS 1821681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: MS
Alter: 89,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Angiogram cerebral normal Arteriogram carotid normal Central nervous system lesion Cerebral haemorrhage Computerised tomogram head abnormal Disorganised speech Haematocrit decreased Haemoglobin decreased International normalised ratio normal Intracranial mass Nausea Neutrophil count normal Prothrombin level normal Vomiting

Symptomtext

On 10/22/21, resident noted with unclear, jumbled speech, nausea and vomiting. Sent to local ER. Returned at family request. Family declines aggressive treatement including MRI.

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Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: 10/22 CT - abnormal increased density apex Rt post. parietal region. I can not exclude a mass. Hemorrhage less likely but can't completely be excluded. CTA neck/head - the lesion in the cortex Rt post parietal region does not enhance. MRI necessary for further evaluation of lesion. 10/22/21 H/H 9.2/28.3, ANC 7,600, PT/INR 12.4/1.0
Aktuelle Erkrankungen: ---
Vorgeschichte: OA, Hyperlipidemia, HTN, GERD, Alzheimer's, PVD
Andere Medikamente: Vit c 500 mg bid, Pepcid 20 mg dly, Senna 8.6 mg bid, Namenda 10 mg bid, Zocor 40 mg q hs, Iron, 325 mg qod, Losartan 50 mg dly, Miralax dly, MVI with minerals dly,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1795506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

kritisch

Staat: NJ
Alter: 92,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Death Dyspnoea Fall Oxygen saturation decreased

Symptomtext

10/16 patient falls from sob and low 02 level. Patient sent to ER and passed away 10/17/21.

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

VAERS 2543673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: OH
Alter: 67,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 06.10.2021
Beginn: 16.12.2022
Tage bis Beginn: 436,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory distress syndrome COVID-19 Confusional state Diarrhoea Dyspnoea Mental status changes Pyrexia SARS-CoV-2 test positive

Symptomtext

Tested COVID-19 positive, resulted in hospital admission and ARDS. Symptoms included fever, shortness of breath, diarrhea, and confusion or mental status.

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Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: -
Labordaten: Nasopharyngeal swab collected 12/16/2022 tested positive for SARS-CoV-2 Antigen on 12/16/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease, hypertension, and current smoker.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2493090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 14.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Anticoagulant therapy Atrial fibrillation Bell's palsy Cardiac stress test Echocardiogram Electrocardiogram Electrocardiogram ambulatory Laboratory test Palpitations Supraventricular extrasystoles Ventricular extrasystoles

Symptomtext

Development of heart palpitations (Informed was Atrial Fib with PVC's/PAC's), as well as Bells Palsy of the right side of my face. Was put on Aspirin therapy until further testing was done.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 12-Lead EKG, 24 hour Holter Monitor, 30 Day Holter Monitor, Lab Work, Cardiac Stress Test, Echocardiogram.
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: Occasional Melatonin for sleeplessness
Allergien: None Known
Vorherige Impfungen: -

VAERS 2477665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 13.10.2022
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Burning sensation Cardiac monitoring normal Catheterisation cardiac Chest pain Condition aggravated Confusional state Coronary arterial stent insertion Cyst Discomfort Dizziness Ear pain Electric shock sensation Erythema Eye irritation Facial pain Feeling abnormal Haemorrhage Headache

Symptomtext

10/13/2022 Patient Vaccine Adverse Reactions Thursday, October 7th 2021 Received the 1st Pfizer Covid vaccine. By bedtime, I had a mild headache. Friday, October 8th 2021 Woke about 4:00am feeling headache and body aches typical of a flu. Symptoms increased throughout the day to severe headache, dizziness and fever. Began taking 2 Tylenol every 4 hours for the fever and pain. Saturday, October 9th 2021 Woke about 6:00am with strong pain/numbness in my right ear/face. A dull pain/numbness in my right arm and the toes of my right foot. A strange sensation on the right side below ribs. Dizziness, confusion and altered senses. My thoughts were vanishing moments after they came. Sunday, October 10th 2021 About the same symptoms as Saturday. Rested and did little else. Monday, October 11th 2021 Arrived at work at 6:00. I felt unsafe driving in, but could not decide to stop. Dizziness suddenly set in, and I began to see the letters on the computer monitor rolling to the left, and off of the screen. Stairs had turned into a fast moving escalator. Everything in my vision was floating and moving. After about an hour, I left work and made an afternoon appointment at urgent care. At the urgent care, I explained my symptoms and expressed worry that I had suffered a stroke. I was examined and told to continue taking Tylenol and return to work on Thursday. Here, the technician noted my blood pressure was high, 158/98. Tuesday, October 12th 2021 I made a follow up appointment with the family physician office. Gave the same symptoms and concerns. I asked if I could have something for high blood pressure, and was prescribed Lisinopril 10 mg. Later, about 4-5 hours after taking the first blood pressure tablet, I recall a sudden release of headache pain. It changed from a strong, sharp pain to a milder, dull ache. Wednesday, October 13th 2021 Same symptoms, but fever diminished. Blood pressure 120/75 (taken at home). Thursday, October 14th 2021 Returned to work. Continued symptoms. Blood pressure consistently normal taking Lisinopril. Also, a cyst (pea sized) behind my right ear began to hurt and bleed. The cyst had formed some 20 years prior and remained without any change. It bled for a couple days and then stopped. After a couple weeks, the cyst was gone. Monday, October 18th 2021 Received Flu vaccine ("Seqirus Lot Number: P100363319") Had typical flu symptoms for about a week. Longer than my usual 24 hour reaction. Tuesday, November 9th 2021 Received 2nd Pfizer Covid vaccine Unlike the 1st covid vaccination, I felt pain everywhere within 15 minutes of this injection. The pain is hard to describe. I began having random sensations starting at the top of my head, and flowing evenly downward through my body. As the sensation flowed downward, it removed all feelings where it had passed. For some moments after, maybe 20 seconds, bodily feelings are not there. Wednesday, November 10th 2021 Went to work in pain. Left early. At home, I laid down in bed to rest. As I was laying on my back, the sensation above returned, but this time remained for 2 hours. I could not move. My eyes were open, but stuck fixed on the ceiling. I was unable to move. My body and mind were not connected. My only comprehension of the passing time was that our clock illuminates on the ceiling. At the end of the 2 hours, my abilities suddenly returned. At that point my eyes began burning, and I realized my pillow was wet on each side of my face. Apparently, tears had been draining because I had not blinked for those 2 hours. Friday, November 12th 2021 Another symptom appeared. The palms of both hands had turned red and burned. The burning pain and redness would increase and decrease for days. The same burning then appeared on the bottoms of my feet, middle and upper back. After some days, the redness calmed but the burning sensation is now permanent. Friday, November 19th 2021 About 30 minutes after falling asleep, I awoke with a terrible pain in the right side of my upper chest. It was a burning/electrocution pain. My wife called EMS. They arrived minutes later and connected a heart monitor. The technician said that the heart testing turned out normal, but my blood pressure was again high, 170/100. It had been in the 120's/70's each day after starting Lisinopril. He suggested my wife could drive me to the hospital. That the pain may be nerve related and not cardiac. At the hospital, I was examined, told my Troponin levels were high and was scheduled for a heart catherization. Received cardiac stents November 20th, and released from hospital November 21st. Current Status 9/25/2022 Outside of the fevers and strong headache, the symptoms have remained constant. Pain is ever present. I always feel physically sick and mentally unwell. These dates and times are should be accurate. This is written from notes and receipts. My apologies for any errors. Urgent Care Visit 10-11-2021: Doctor's Office Visit 10-12-2021: ER/Hospital Visit 11-19-2021

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 2,0
Labordaten: I was not given any tests related to my original complaints. The results of tests done at the hospital are unavailable to me.
Aktuelle Erkrankungen: No illness
Vorgeschichte: None
Andere Medikamente: Prilosec 20mg/day
Allergien: None
Vorherige Impfungen: -

VAERS 2426589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 16.10.2021
Beginn: 30.07.2022
Tage bis Beginn: 287,0
Dosis: 2
Route/Site: IM / LA

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

Bell's palsy Facial paralysis

Symptomtext

Diagnosed with Bell's Palsy due to Facial paralysis

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: visual confirmation of Facial paralysis
Aktuelle Erkrankungen: none
Vorgeschichte: None
Andere Medikamente: Tums
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2359722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: IL
Alter: 64,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 08.12.2021
Beginn: 16.06.2022
Tage bis Beginn: 190,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Aspiration pleural cavity Asthenia COVID-19 COVID-19 pneumonia Cardiomegaly Lung opacity Pleural effusion Pulmonary oedema Right ventricular failure SARS-CoV-2 test positive

Symptomtext

Patient received pfizer vaccine on 5/5/21, 5/26/21 and 12/8/21. Presented to ER on 6/16/22 and found to be COVID positive. Patient is a 64-year-old male with past medical significant for chronic diastolic CHF, paroxysmal atrial fibrillation on Xarelto admitted on June 16th with generalized weakness x 3 days. CT angio chest was done which showed no evidence of PE, but showed cardiomegaly with evidence of right heart failure and pulmonary edema. Ground-glass opacities typical for COVID-19 pneumonia, large layering right pleural effusion and small left pleural effusion was also seen. Patient underwent thoracentesis and 1850 mL fluid was removed. Patient oxygen was gradually tapered down and now is doing well on room air. Has finished course of IV Rocephin, doxycycline for COVID pneumonia. Discharged on room air on 6/29/22

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Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 13,0
Labordaten: 6/16/22 COVID19: positive 6/16/22 CT chest: Ground-glass opacities predominantly throughout the left lung appearing typical for COVID-19 pneumonia.
Aktuelle Erkrankungen: -
Vorgeschichte: ? Atrial flutter (HCC) ? Diabetes (HCC) ? Diabetes mellitus (HCC) ? Hx of gout ? Hyperlipidemia ? Hypertension
Andere Medikamente: allopurinol 100 MG Tabs Commonly known as: ZYLOPRIM Take 100 mg by mouth daily. aspirin 81 MG Chew Take 81 mg by mouth daily. atorvastatin 20 MG Tabs Commonly known as: LIPITOR Take 20 mg by mouth nightly. furosemide 40 MG Tabs Common
Allergien: Penicillins and sulfa
Vorherige Impfungen: -

VAERS 2319046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: AZ
Alter: 60,0
Geschlecht: M
Eingang: 14.06.2022
Impfdatum: 29.04.2021
Beginn: 29.11.2021
Tage bis Beginn: 214,0
Dosis: 2
Route/Site: SYR / LA

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

Anticoagulant therapy Antiphospholipid syndrome Thrombosis

Symptomtext

Antiphospholipid Syndrom and Thrombosis of the liver, causing blood clots in various places in my body. Two month hospital stay on blood thinners. Am now taking Eliquis, a blood thinner.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: 60,0
Labordaten: Would need release of medical records to provide accurate information.
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Multi vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2249367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: WA
Alter: 80,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 28.10.2021
Beginn: 04.01.2022
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: OT / RA

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

Chills Paralysis Tremor COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID Nasal swab testing: positive tests; COVID Nasal swab testing: positive tests; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-healthcare professional). The reporter is the patient. An 80-year-old female patient received BNT162b2 (BNT162B2), on 20Dec2020 at 10:00 as dose 1, single (Lot number: EJ1685), in right arm, on 12Jan2021 at 10:00 as dose 2, single (Lot number: EK9231), in right arm and on 28Oct2021 at 10:00 as dose 3 (booster), single (Lot number: FF2590) at the age of 80 years, in right arm, all intramuscular for covid-19 immunisation. The patient relevant medical history included: "Penicillin (Later developed allergy)" (unspecified if ongoing), notes: Illness/AE: Pneumonia, Onset date: 1996, Stop date: 1996, Pertinent details: Treated with Penicillin (Later developed allergy), "Pneumonia" (unspecified if ongoing), notes: Illness/AE: Pneumonia, Onset date: 1944, Stop date: 1944, Pertinent details: Treated with sulfa (later developed allergy), Illness/AE: Pneumonia, Onset date: 1963, Stop date: 1963, Pertinent details: Treated with Penicillin, Illness/AE: Pneumonia, Onset date: 1996, Stop date: 1996, Pertinent details: Treated with Penicillin (Later developed allergy). Concomitant medication(s) included: HYDROCHLOROTHIAZIDE oral taken for hypertension, start date: 1996 (ongoing); BENAZEPRIL oral taken for hypertension, start date: 2006 (ongoing). Past drug history included: Sulfa for Pneumonia, reaction(s): "later developed allergy", notes: Illness/AE: Pneumonia, Onset date: 1944, Stop date: 1944, Pertinent details: Treated with sulfa (later developed allergy). The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 04Jan2022, outcome "unknown" and all described as "COVID Nasal swab testing: positive tests". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (04Jan2022) Positive, notes: Test: COVID Nasal SWAB testing. Date: 04Jan2022. Result: Through 28Jan2022 daily testing because of positive test (80 residents tested with only a few positives) my results were 100% negative. Clinical course: Please complete the section below for 3rd administration. Booster dose due to high risk of frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 Complications). This is the shot that caused the reaction. The 1st 2 shots were only minor redness and chills. Vaccination facility type: Nursing Home/ Senior Living Facility. Medical history relevant to AE(S): Father died after many strokes (over years) in his 80'S. Mother had malignant hypertension and COPD Died at 90. Both parents were heavy smokers most of their adult lives. (I started at age 18 and smoked for 20 years) but basically since birth? is it safe for me to get further vaccinations? No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: Test Date: 20220104; Test Name: COVID Nasal SWAB testing; Test Result: Positive ; Comments: Test: COVID Nasal SWAB testing Date: 04Jan2022 Result: Through 28Jan2022 daily testing because of positive test (80 residents tested with only a few positives) my results were 100% negative.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Pneumonia
Andere Medikamente: HYDROCHLOROTHIAZIDE; BENAZEPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 2270621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: GA
Alter: 59,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 27.10.2021
Beginn: 21.11.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: - / RA

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

Pain in extremity Thrombosis Ultrasound scan

Symptomtext

felt the blood clot coming up her leg and it was very painful.; saw something coming up her leg and she stated that this is a blood clot; Blood clot bouncing around her whole entire body; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient received BNT162b2 (BNT162B2), on 27Oct2021 as dose 2, single (Lot number: FF2590, Expiration Date: 31Mar2022) at the age of 59 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Developed an allergy to shellfish" (unspecified if ongoing); "peanut butter" (unspecified if ongoing); "Obase" (unspecified if ongoing), notes: Onset Date: Obese: Not provided. Concomitant medication(s) included: FLU. Vaccination history included: BNT162b2 (Dose 1, Single, Lot number: EW0176, Expiry: Nov2021), administration date: 06Oct2021, when the patient was 59-year-old, for COVID-19 Immunization; Flu shot (Caller states she received the flu shot last year and received this year also), administration date: 2021. The following information was reported: THROMBOSIS (hospitalization, medically significant) with onset 21Nov2021, outcome "recovered" (Dec2021), described as "Blood clot bouncing around her whole entire body"; THROMBOSIS (hospitalization, medically significant) with onset 21Nov2021, outcome "recovered" (Dec2021), described as "saw something coming up her leg and she stated that this is a blood clot"; PAIN IN EXTREMITY (hospitalization, medically significant), outcome "unknown", described as "felt the blood clot coming up her leg and it was very painful.". The events "saw something coming up her leg and she stated that this is a blood clot", "blood clot bouncing around her whole entire body" and "felt the blood clot coming up her leg and it was very painful." required emergency room visit. The patient underwent the following laboratory tests and procedures: Ultrasound scan: (21Nov2021) Blood Clot, notes: Result: Blood Clot / Hematoma; Unit: Not Provided. Therapeutic measures were taken as a result of thrombosis, thrombosis, pain in extremity. Clinical course: It was reported that the patient had blood clot developed in her right leg, then came through her groin. She was calling because she was being tracked down for a medical bill because she got her shot on 10Oct2021 and a follow up shot on 27Oct2021.Caller states on 21Nov2021 she had a blood clot develop in her leg at work. Caller states she went to the Emergency Room and had an ultrasound. Caller clarified that the Emergency Room requested an ultrasound, they did the ultrasound and said there was a blood clot. Caller states she had never had a blood clot before and has never had one after. Caller states the Emergency Room said there was nothing they could do and gave her three pain pills and said that was all they could do. States they told her it would dissolve in her body. Caller states she felt the blood clot bouncing around her whole entire body, when it came from her groin in her leg and it pushed out through something and was bouncing around. Caller states it developed in her groin. Caller states that the blood clot is still bouncing around. Caller clarified that the blood clot dissolved. Caller states she does not know how long after it dissolved, a couple days, maybe a couple weeks. States she has not had any problems since then. She was at one hospital for 8 hours and they did nothing and so she went to another. Caller states the other hospital within 30 minutes she had an ultrasound. States she could have probably died at the other one. States they are also coming after her for a bill even though they didn't do anything in the ER and she was at the first hospital from 9 to 3 and then she went to another hospital. Caller clarified the times to 9am to 3pm. Caller states that she had a long wait, especially for a blood clot. Blood clot in right leg Start Date: Caller states it was a day before Holiday. Caller clarified that the date was November something. Caller states she knows it was a Tuesday. Caller clarified the date to 21Nov2021. Caller states the blood clot came through her groin then it was in her body. Caller states the blood clot dissolved. Caller states she didn't feel the blood clot in her body for maybe a month even, not even. Caller states she doesn't want to give an exact date. Caller states the blood clot dissolved between November and December. Caller states the blood clot might still be there. Caller clarified end date to Dec2021. Caller states that she received the flu shot after the doses of COVID 19 Vaccine. Caller states she received the flu shot last year. Caller clarified the flu shot was received this year, just a regular flu shot and she had no problems with that. She developed an allergy to shellfish and peanut butter, onset Age: 46, she had to do basic shots for healthcare. Pfizer COVID 19 Vaccine Dose 1, Vaccine Lot Number: EW0176, Vaccine Lot Expire Date: Nov2021.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20211121; Test Name: Ultrasound; Result Unstructured Data: Test Result:Blood Clot; Comments: Result: Blood Clot / Hematoma; Unit: Not Provided.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Obesity (Onset Date: Obese: Not provided); Peanut allergy; Shellfish allergy
Andere Medikamente: FLU
Allergien: -
Vorherige Impfungen: -

VAERS 2266906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: MA
Alter: 65,0
Geschlecht: M
Eingang: 07.05.2022
Impfdatum: 11.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: OT / LA

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

Abdominal abscess Constipation Mesenteric vein thrombosis SARS-CoV-2 antibody test

Symptomtext

SMV/IMV thrombosis; constipation; bacteria filled abscess in abdomen; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the parent. A 65-year-old male patient received BNT162b2 (BNT162B2), on 11Oct2021 at 13:15 as dose 3 (booster), single (Lot number: FF2590) at the age of 65 years intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: Unknown. Not listed on medical record, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 31Mar2021, when the patient was 64-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EN6208, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM, Route of Administration: Other), administration date: 17Mar2021, when the patient was 64-year-old, for COVID-19 immunization. The following information was reported: MESENTERIC VEIN THROMBOSIS (hospitalization, medically significant, life threatening) with onset 01Nov2021, outcome "not recovered", described as "SMV/IMV thrombosis"; ABDOMINAL ABSCESS (hospitalization, medically significant, life threatening) with onset 01Nov2021, outcome "not recovered", described as "bacteria filled abscess in abdomen"; CONSTIPATION (hospitalization, life threatening) with onset 01Nov2021, outcome "not recovered". The patient was hospitalized for mesenteric vein thrombosis, constipation, abdominal abscess (hospitalization duration: 20 day(s)). The events "smv/imv thrombosis", "constipation" and "bacteria filled abscess in abdomen" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 antibody test: (03May2022) Negative, notes: Nasal Swab. Therapeutic measures were not taken as a result of mesenteric vein thrombosis, constipation, abdominal abscess. Clinical Course: The patient tested for covid post vaccination. no known allergies and no other medications were received with in two weeks of covid vaccination.; Sender's Comments: Based on the information provided there is a reasonable possibility of causal association between the events with the suspect product bnt162b2. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mesenteric vein thrombosis
Hospital-Tage: 20,0
Labordaten: Test Date: 20220503; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: Other medical history: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2260368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: UT
Alter: 70,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 05.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Balance disorder Computerised tomogram Disability Disorientation Fatigue Hemiparesis Hypoaesthesia Impaired work ability Joint lock Joint range of motion decreased Loss of personal independence in daily activities Magnetic resonance imaging Movement disorder Muscular weakness Paraesthesia Scan with contrast Sluggishness

Symptomtext

She got her vaccine, just felt a little tired, nothing unusual, little sluggish like coming down with a cold which lasted a couple of days. Within a few days started noticing some weakness in her right leg but nothing profound. She started noticing that her balance was kind of off a little bit, and by 11/20/21 she felt extreme pain in her lower back, kind of across her lower back, funny pins and needles like a numbness. She noticed that her right leg was getting very weak, and felt kind of wobbly, disoriented feeling. She went to go and get her husband to tell him that she needed to go to the ER and collapsed onto the floor. Her right leg went under her, could not use her right arm or hand at all, and he called 911. She was rushed to local Hospital. The pain in her lower back was extreme. After the extreme pain was a bizarre numbness, strange kind of numb feeling. At the hospital they thought she had a stroke. They did a CAT scan, and gave her an aspirin. She was totally coherent, never lost her cognitive ability, and knew what was going on. They told her they were going to put dye in her veins, and had the IV. She was put into a CAT scan and kept asking her other neurologic questions and did an MRI. The first MRI was done the first night. The next day she had another MRI for her back as she told them she was having pain. They did about 1 1/2 hour MRI then. The next day she was released to care unit. They had a transport come to take her to local Health facility. That morning (Neurologist) who came in and told her that they had no explanation of what happened to her. She did not have a stroke, had all of her mental capabilities and lost all muscle power in both her right arm and leg. She was not able to lift her right arm up. That evening around 5:00 she was transported for rehab. She was in rehab (local Health) for 2 weeks, which she needed to be in their longer but due to Medicare she had to be sent home. She continues to do therapy and has home health care. She saw a spine specialist for her back for all the nerves to make sure there was no nerve damage and that was a 2 1/2 MRI, and he could find nothing that showed any nerve damage that would contribute to the paralysis. She also saw a 2nd neurologist and she said that she was a mystery and that they did not know what happened to her. She asked when she got her COVID shot and would not say whether she felt it was due to that or not. She went to her PCP who asked her when she had the COVID vaccine, but again said that they did not know what happened to her. She is improving with therapy, using a cane, and was informed it will be a long process, about a year or two. She has a walker to use. Patient feels like she has made some progress. She had no neurologic issues prior to the vaccine. She worked full time as a loan officer and was employee of the year and is on a disability leave at the present time. In November they will access where she is at and whether she needs to keep her job or not. She has no coming from that job at this point. Due to her age she is not able to get disability. Financially this has been devastating. Her shoulder is now locked and she has someone come in twice a week and shower her and wash her head. There is a wellness service for the elderly and they take her to her Dr. appointments. She did not have any reaction to the first two vaccines other than tiredness, and took a day off from work and took it easy. She feels like somebody has dropped her off in the wilderness and said good luck. Nobody seems to care and give her answers as to what has happened and what to do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: Multiple as above.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypothyroidism, high blood pressure (borderline).
Andere Medikamente: Levothyroxine, Hydrochlorothiazide, Amlodipine Besylate, Nexium.
Allergien: Dairy products (sinus headaches/bad headaches), corn (headaches), mushrooms (glands swell), Sulfa, Penicillin (hives with both).
Vorherige Impfungen: -

VAERS 2256705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 05.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 13,0
Dosis: UNK
Route/Site: SYR / LA

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

Cardiac stress test normal Chest pain Echocardiogram Electric shock sensation Electrocardiogram Gastrointestinal scan Implantable cardiac monitor insertion Implantable cardiac monitor removal Postoperative wound complication

Symptomtext

13 days following the first booster, had pain in left chest beginning sporadically around approximately 3pm. By 6pm the pain was continuous. It felt like a charley horse or electrical shock in my heart. I went to an ER. The last thing I remember was being given morphine. I was hospitalized until Monday November 22nd. I underwent numerous tests including a stress test and GI related tests. All results were inconclusive. An electrophysiologist recommended implanting a loop recorder. I chose to do this on an outpatient basis. Had the procedure done on February. Had the device explanted a week later because the incision opened and the device began backing itself out of the open incision area. Am now recording my symptoms with the Kardiamobile device and patiently waiting for someone to figure out the solution to the ongoing cardiac symptoms I?m experiencing since (probably) having Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 5,0
Labordaten: As mentioned above, I had numerous tests while inpatient including an upper GI scan, nuclear stress test, echo, and EKGs.
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-existing seasonal allergies Long Covid symptoms- (probable Covid in March 2020 was unable to be tested) have been under medical care since then for breathing issues and erratic heart rhythm
Andere Medikamente: Diltiazem (90mg AND 180xr) both daily QVAR Redihaler Olapatidine nasal spray Mometasone nasal spray Culterelle Fish oil Pepcid
Allergien: Prednisone
Vorherige Impfungen: -

VAERS 2252238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: MI
Alter: 35,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 01.12.2021
Beginn: 12.04.2022
Tage bis Beginn: 132,0
Dosis: 1
Route/Site: IM / RA

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

Anticoagulant therapy Gait inability Pain in extremity Peripheral swelling Thrombosis Ultrasound Doppler abnormal

Symptomtext

Pain and swelling in calf. Unable to walk. Started on oral Xarelto. Improvement of symptoms noted, but not 100%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ulstrasound done to confirm clot.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2209529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: -
Alter: 87,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 15.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / UN

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

Concussion Loss of consciousness Pelvic fracture

Symptomtext

Patient presented to the ED and was subsequently hospitalized for Closed fracture of multiple pubic rami and Concussion with loss of consciousness of 30 minutes or less within 6 weeks of receiving covid vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2206936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: AZ
Alter: 19,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Depressed level of consciousness Presyncope

Symptomtext

Patient had vagal response with decreased LOC after immunization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EMS notified and transferred to medical center E.R.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Iron supplement
Allergien: none
Vorherige Impfungen: -

VAERS 2204259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 09.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: - / -

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

Cellulitis Debridement Thrombosis Ultrasound scan abnormal Wound haematoma

Symptomtext

Cellulitis of right leg - He was given vancomycin, Zosyn and transferred to local hospital where nurse set a iodoform wick to facilitate mechanical debridement of non viable clot and allow for healing by secondary intention. The patient has been instructed on daily wound care and will discharge home ncomycin and zosyn were continued. Ultrasound showed a 1 x 2.5 cm evolving hematoma at the site of prior blood blister. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2201714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: MT
Alter: 60,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 28.10.2021
Beginn: 20.01.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: IM / LA

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

Alcohol withdrawal syndrome COVID-19 Confusional state Cough Intensive care Nosocomial infection Pyrexia SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

Case vaccinated and boosted against Covid by October 2021,. He contracted Covid while hospitalized for non-covid issues in January 2022. Hospitalized at: Hospital. COVID-19 virus infection Assessment & Plan Noted febrile 1/20. COVID test turned +. Likely nosocomial as he had been admitted 10 days. Placed in contact/droplet isolation. On room air. Seemed more confused late last week, this is probably why. Is fully vaccinated against covid. Chronic liver disease probably places him at higher risk for severe disease. -Discussed use of monoclonal abs with the ID service and his transplant team, both prefered he receive so administered 1/21 without adverse reaction -Coughing frequently but held off on CXR given normal oxygen levels -No indication for specific covid treatments otherwise -Continue isolation. Discussing discharge options with family, but has high-risk elder at home, also vaccinated and boosted per report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 11,0
Labordaten: Ordered Test: Coronavirus (CoVID-19), NAA Ordered Test Codes: 94309-2 (LN LOINC)/ Status: Corrected Accession Number: Specimen Source: Tissue Specimen Site: Specimen Collection Date/Time: 2022-01-20 08:27:00.0 * Resulted Test: SARS CORONAVIRUS 2 RNA:PRTHR:PT:RESPIRATORY:ORD:PROBE.AMP.TAR Coded Result: Detected (LOCAL) Numeric Result: Units: Text Result: Reference Range From: Not Detected Reference Range To: Performing Facility Details: Date/Time: 2022-01-21 08:47:29.0 Performing Facility: Facility ID: Interpretation: Very abnormal Result Method: Status: Final Test Code: 94500-6 (LN LOINC)/ Result Code: 260373001 (SCT/Detected (L LOCAL)
Aktuelle Erkrankungen: Alcoholism (HCC) 09/11/2017 severe ETOH withdrawal during admission requiring icu transfer for precedex gttp; no seizures. Ascites paracentesis 2/2020 Calcium pyrophosphate crystal disease Cirrhosis (HCC) presumed ETOH induced; viral serologies neg. Esophageal varices (HCC) see on EGD 9/2017; grade I; no stigmata of bleeding GI bleed 09/11/2017 gastritis, duodenitis, Hpylori neg Hepatic encephalopathy (HCC) 3/1/2020 Hyperlipidemia Hypertension Macrocytic anemia 02/2020 B12/folate normal, likely due to EtOH, liver disease, and potentially occult GI bleeding
Vorgeschichte: Alcoholism (HCC) 09/11/2017 severe ETOH withdrawal during admission requiring icu transfer for precedex gttp; no seizures. Ascites paracentesis 2/2020 Calcium pyrophosphate crystal disease Cirrhosis (HCC) presumed ETOH induced; viral serologies neg. Esophageal varices (HCC) see on EGD 9/2017; grade I; no stigmata of bleeding GI bleed 09/11/2017 gastritis, duodenitis, Hpylori neg Hepatic encephalopathy (HCC) 3/1/2020 Hyperlipidemia Hypertension Macrocytic anemia 02/2020 B12/folate normal, likely due to EtOH, liver disease, and potentially occult GI bleeding
Andere Medikamente: ? cyanocobalamin (VITAMIN B-12) 500 mcg tablet Take 500 mcg by mouth Daily. ? diazePAM (VALIUM) 2 mg tablet Take 1-2 tablets by mouth once daily prior to flight. ? escitalopram (LEXAPRO) 10 mg tablet Take 10 mg by mouth Daily. ? folic
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2074786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: ME
Alter: 32,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 08.10.2021
Beginn: 14.01.2022
Tage bis Beginn: 98,0
Dosis: 2
Route/Site: IM / AR

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

Blood fibrinogen Delivery Exposure during pregnancy Intensive care

Symptomtext

I was 7 months pregnant when I received the first dose of the vaccine. My son was born normal term with a VERY rare bleeding disorder with no family history and a heterzygous gene mutation (indicating disease was not inherited). He was diagnosed with Factor 1 deficiency. We were hospitalized Medical center in NICU for 29 days and currently are followed by Children's Cancer care and hematology clinic. We have all documentation and I'm just not sure who to reach out to notify CDC. I am currently a nurse practitioner at cancer care and hematology clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: fibrinogen assay? not sure what to write here.
Aktuelle Erkrankungen: none
Vorgeschichte: newborn born with rare bleeding disorder after I (mother) received covid vaccine while pregnant, no family history
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2074786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

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Staat: ME
Alter: 32,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 08.10.2021
Beginn: 14.01.2022
Tage bis Beginn: 98,0
Dosis: 2
Route/Site: IM / LA

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

Blood fibrinogen Delivery Exposure during pregnancy Intensive care

Symptomtext

I was 7 months pregnant when I received the first dose of the vaccine. My son was born normal term with a VERY rare bleeding disorder with no family history and a heterzygous gene mutation (indicating disease was not inherited). He was diagnosed with Factor 1 deficiency. We were hospitalized Medical center in NICU for 29 days and currently are followed by Children's Cancer care and hematology clinic. We have all documentation and I'm just not sure who to reach out to notify CDC. I am currently a nurse practitioner at cancer care and hematology clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: fibrinogen assay? not sure what to write here.
Aktuelle Erkrankungen: none
Vorgeschichte: newborn born with rare bleeding disorder after I (mother) received covid vaccine while pregnant, no family history
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2182432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 08.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / LA

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

Blood sodium decreased Chest X-ray abnormal Confusional state Hyponatraemia Intensive care Pulmonary congestion

Symptomtext

Patient admitted for severe hyponatremia with sodium of 111 with associated confusion. He was admitted in the ICU and started on 3% saline and DDAVP. IV ceftriaxone and azithromycin were started for possible pneumonia. CXR revealed pulmonary vascular congestion. He completed a course of azithromycin and ceftriaxone for CAP coverage. He made good progress and O2 was weaned down to about 2-3L. He was discharged to SNF, where O2 will be attempted to be weaned off. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: WI
Alter: 72,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 13.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Haematemesis Haemoglobin normal Loss of consciousness Malaise Presyncope Transfusion Ulcer

Symptomtext

I was feeling weak after I woke up. I took a shower, and then I nearly fainted. I dried off and then laid on the sofa. I felt sick and threw up blood so I went to the ER. When I was at the ER I had passed out. I was given IV fluids and they repaired 2 ulcers I had. I was hospitalized for 3 days. They did a blood transfusion and IV liquids. I was prescribed pantoprazole 40 mg 2 x day and sucralfate 1gm. When the doctor checked my hemoglobin it was fine now. I don't believe the vaccine had anything to do with what happened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Infodema
Andere Medikamente: Atorvastatin; montelukast; cephalexin; Flovent; antihistamine; gabapentin; baby aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2085375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: MA
Alter: 50,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 25.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

C-reactive protein normal Chest discomfort Chest pain Imaging procedure artifact Magnetic resonance imaging heart Myocarditis Renal cyst Troponin increased

Symptomtext

Patient received 3 pfizer covid vaccines on 2/2/21, 2/23/21, and 10/25/21. Patient had cardiology visit on 11/4/21 due to recent episode of chest pain in the setting of an upcoming marathon participation. On 10/28/21, patient experienced a sudden-onset, left-sided, pressure like chest pain of 8/10 in severity and went to the ED. Troponin on 10/28: 32-- >33-> 31 11/4: 32 CRP: 1.7 cardiac mri done on 11/5/21: Normal biventricular function. The pattern of late gadolinium enhancement is most likely secondary to myocarditis. Cardiac sarcoidosis is considered unlikely given the absence of arrhythmia or evidence of extracardiac sarcoidosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 11/5/21 mri cardiac impression: 1. The left ventricular size and function are normal by visual assessment. Quantitative assessment was not possible due to artifact. There are no regional wall motion abnormalities of the left ventricular wall. 2. There is no resting first pass myocardial perfusion defect. Normal myocardial gadolinium kinetics with appropriate nulling of the blood pool prior to the myocardium. There is small amount of mesocardial late gadolinium enhancement in the mid-inferoseptal wall and inferior RV insertion point. There is no evidence of focal myocardial edema by T2 weighted imaging. Native T1 values are normal: 1146 - 1194 ms (Normal range: 1200 +/- 80 ms on 3T scanner). 3. The right ventricular size is normal. Global right ventricular function is normal. There are no regional wall motion abnormalities of the right ventricular wall. There is no late gadolinium enhancement of the right ventricle. 4. Left atrial size is normal. Right atrial size is normal. 5. Left renal cyst measuring up to 9 mm.
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: amitriptyline, cyclobenzaprine, etodolac, tizanidine
Allergien: oxycodone
Vorherige Impfungen: -

VAERS 2082213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: KY
Alter: 70,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 27.10.2021
Beginn: 29.01.2022
Tage bis Beginn: 94,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Intensive care

Symptomtext

COVID-19 hospitalization/ICU stay

Weitere VAERSDATA-Felder

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

VAERS 2043773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: AZ
Alter: 26,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 11.10.2021
Beginn: 13.12.2021
Tage bis Beginn: 63,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Cerebral venous thrombosis Computerised tomogram normal Headache Magnetic resonance imaging head abnormal Migraine Musculoskeletal disorder Nausea Pain Vomiting

Symptomtext

On 12/13/2021 at 3 PM, I felt a very severe headache at the top center of my head. The severity of the headache led to nausea and vomiting starting at 10 PM. At 6 AM on 12/14/2021, I went to the ER for the headache, nausea, and vomiting. They took a CT scan which came back normal. After given pain and nausea medication and an IV, I was discharged with the diagnosis of migraine/headache, and I was sent home with medicine to treat migraines. The medicine did not improve my headache or nausea conditions at all, so I went to the ER again at 5 PM. Again, after an IV, I was sent home with medicine to treat migraines and to follow up with my PCP. On 12/16/2021, I began to lose function of my right leg. By 12/17/2021 at 11 AM while at my PCP, I no longer had any function of my right leg, and I was immediately sent to the ER. On 12/17/2021 at 10 PM, I was admitted to the hospital and an MRI was taken. On 12/19/2021, I was diagnosed with cerebral venous thrombosis of cortical vein. Treatment consisted of heparin for blood thinning and acetaminophen to treat pain. Function of the right leg returned after several days of treatment and physical therapy. Discharged from hospital at 12/22/2021 at 6 PM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous thrombosis
Hospital-Tage: 6,0
Labordaten: On 12/14/2021, CT scan taken which returned normal. On 12/17/2021, MRI taken which resulted in identification of the blood clot.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Zyrtec, Flonase, Viorele
Allergien: none
Vorherige Impfungen: -

VAERS 2039365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: KY
Alter: 92,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 18.11.2021
Beginn: 15.01.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory distress syndrome COVID-19 SARS-CoV-2 test positive

Symptomtext

COVID-19 infection resulting in hospitalization, ARDS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: 3,0
Labordaten: COVID-19 PCR (+) 1/13/22
Aktuelle Erkrankungen: NONE
Vorgeschichte: Chest pain ? Coronary artery disease involving native coronary artery of native heart with unstable angina pectoris ? Difficulty walking ? Elevated troponin ? Hyperlipidemia ? Hypothyroidism ? Lightheadedness ? Pulmonary edema ? Third degree AV block
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet Nursing Home Yes Yes Take 650 mg by mouth Every 4 (Four) Hours As Needed for Mild Pain . aluminum-magnesium hydroxide-simethicone (Antacid) 200-200-20 MG/5ML suspension Nursing Home Yes Yes T
Allergien: Shellfish-derived products, Shrimp flavor, Azithromycin, and Codeine
Vorherige Impfungen: -

VAERS 2035530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature increased Burning sensation Condition aggravated Coordination abnormal Dizziness Headache Hypoaesthesia Hypotonia Impaired driving ability Injection site hypoaesthesia Limb discomfort Musculoskeletal stiffness Nausea Orthostatic hypertension Pain Pain in extremity Palpitations Presyncope

Symptomtext

I was administered the Pfizer Booster approximately at 15:20 on my left arm, I was given a timer with 30 min. Sometime during that period I felt a slight numbness on the injection site that radiated all the way down to the wrist (top portion of the arm only), but I disregarded it due to be though to be related to the needle size since they used the drawing needle for administration. I left the clinic with no other symptoms and walked to my car where I took (2) 500mg Tylenol since I did experience fever, flu like symptom and headaches with the second dose (symptoms lasted 3 days and the headache about 10 days post 2nd shot -I did not report these at that time). I left the parking structure and within 5 minutes I began to feel a pulsating sensation on the outer-upper-left side of my left calf (2.5-3inches below the back of the knee), increasing numbing sensation on the arm and mild lightheadedness. At 15:55, I pulled over and ate a mini kind bar, drank some water and walked around for a few minutes in case symptoms were to be r/t hypoglycemia and cramping. I resumed driving at 16:00 but symptoms got progressively worse with severe left calf pulsation on the same area, calf tightness with now a new burning sensation on the outer side of the left heel (below the ankle bone) and moderate dizziness. At 16:05 my arm and legs became extremely heavy, I could feel my heart pounding out of chest and a systemic burning sensation of blood rushing down my lower extremities (the burning can be described as similar to that of medication being injected into the injection site however this was felt like my blood was burning through my veins as it traveled down), I became overwhelmingly dizzy and nauseous, my vision became hazy and finally my arms and legs went completely limp. I managed to stop the vehicle; my coordination was poor (I took approx. 3 minutes to unlock my phone to call for assistant). It took 9 min for help to arrive, I was given oral fluids in the form of water and sugary drinks and applied cold compress to back of my head and forehead. At 16:47 I was finally feeling well enough to leave however still moderately dizzy. The dizziness remained for 3 days, as of today (1/14/2022) I am still experiencing orthostatic hypotension and tachycardia. My reaction has later been diagnosed as a Near Syncope. For the 2 days following the booster administration I experienced moderate to severe headaches and fever ranging between 102.7-103.1 that would not go lower than 102 with medication. The third day my temperature remained around 100.9-101.1 and the headache from mild to moderate. Footnote: Vaccine Administration time is reported based on appointment time; actual administration time might have range between 2-5 minutes after. All other times have been abstracted from my own cell records so accuracy of times can be considered extremely accurate. I have not been able to schedule a primary physician appointment due to the high volume of patients however I did speak with 2 providers that I personally know following the event and they both agree on the near syncope diagnosis. My primary physician appointment at pcp is scheduled for 01/28/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: No done yet
Aktuelle Erkrankungen: n/a
Vorgeschichte: ITP - Asymptomatic - No medication required
Andere Medikamente: (2) Tylenol Extra Strength prophylactic for post booster vaccine symptoms
Allergien: NKA
Vorherige Impfungen: 01/07/2021 Pfizer 2nd dose EK9231 At age 42 Post vaccine flu like symptoms and fevers up to 103+F for 3 days after administratio

VAERS 2035251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: PA
Alter: 47,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Chest discomfort Dizziness Dyspnoea Echocardiogram Electrocardiogram ambulatory Feeling abnormal Laboratory test Loss of consciousness Ultrasound Doppler

Symptomtext

After receiving the vaccine I was there for 45 mins after I received injection. I had tightness of chest, shortness of breath, dizziness, and light headed. They gave me a drink and candy to try to help while I was there. I was extremely dizzy and light headed. They were going to drive me home because I felt that bad. I didn't feel right for the rest of that day and a couple days after. I still dizziness and lightheadedness. I passed out from receiving the vaccine as well. I saw a PA and she ordered some test. I had a U/S Carotid Bilateral test done. I also had extended Holter monitor for 14 days and an echo cardiogram. I went for a follow up yesterday for a physical and I am being referred to an ENT and for some blood work because I am still having issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: U/S Carotid Bilateral test, Holter monitor, echo cardiogram
Aktuelle Erkrankungen: NA
Vorgeschichte: Tachycardia, Paralyzed Diaphragm, Medullary Sponge Kidney, Gastroparesis
Andere Medikamente: Saxenda, Topamax ( daily- 25mg - 3 tabs a day ), Linzess ( 290mcg 1 daily )
Allergien: NA
Vorherige Impfungen: -

VAERS 2024373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

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Staat: CT
Alter: 32,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 08.10.2021
Beginn: 29.12.2021
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: - / LA

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

Bell's palsy SARS-CoV-2 test

Symptomtext

Sudden Bell's palsy to the right side of my face; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 08Oct2021 (Lot number: Ff2590) at the age of 32 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Von willebrands disease" (unspecified if ongoing); "thyroid disease" (unspecified if ongoing). Concomitant medication(s) included: VYVANSE; TRILEPTAL; DOXEPIN; EUTHYROX; PAXIL [PIROXICAM]. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: Fd8448, Location of injection: Arm Left), administration date: 11Sep2021, when the patient was 31 years old, for Covid-19 immunization. The following information was reported: BELL'S PALSY (disability, medically significant) with onset 29Dec2021, outcome "recovering", described as "Sudden Bell's palsy to the right side of my face". The event "sudden bell's palsy to the right side of my face" was evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (30Dec2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of bell's palsy. Patient did not receive other vaccine in four-weeks. AE treatment medication included Antibiotics, steroids, medications. Patient did not have covid prior vaccination. No Known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20211230; Test Name: Rapid Covid test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Thyroid disorder; Von Willebrand's disease
Andere Medikamente: VYVANSE; TRILEPTAL; DOXEPIN; EUTHYROX; PAXIL [PIROXICAM]
Allergien: -
Vorherige Impfungen: -

VAERS 2024368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: ME
Alter: 72,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Deep vein thrombosis Immunisation

Symptomtext

Development of Deep Venous Thrombosis Right lower extremity; Booster; This is a spontaneous report received from contactable Consumer. The reporter is the patient. A 72 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 16Oct2021 (Lot number: FF2590) at the age of 72 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: Lot EL9269. NDC: 59267 100001, Location of injection: Arm Left), administration date: 20Feb2021, when the patient was 71 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: Lot EL9269 NDC: 59267 10001, Location of injection: Arm Left), administration date: 30Dec2020, when the patient was 71 years old, for Covid-19 Immunization. The following information was reported: IMMUNISATION (medically significant,hospitalization, disability, life threatening) with onset 16Oct2021, outcome "unknown", described as "Booster"; DEEP VEIN THROMBOSIS (medically significant,hospitalization, disability, life threatening) with onset 18Oct2021 15:00, outcome "recovering", described as "Development of Deep Venous Thrombosis Right lower extremity". The events "booster" and "development of deep venous thrombosis right lower extremity" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of deep vein thrombosis with Rx for Eliquis. Clinical course: the patient had no Covid prior vaccination, the patient was not tested for Covid post vaccination. Patient had no known allergies. No other vaccine in four weeks.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: none significant
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: -
Alter: -
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Inappropriate schedule of product administration Seizure

Symptomtext

seizure; Dose 1 was on 04Sep2021 and Dose 2 was on 06Nov2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 15 year-old male patient received bnt162b2 (BNT162B2), administration date 06Nov2021 (Lot number: FF2590) as dose 2, single for covid-19 immunisation. Relevant medical history included: "autism" (unspecified if ongoing), notes: Her son is a 15 year old male with Autism. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1, Lot: FD8448, he got an ear infection on both ears with perforation and bleeding after the first dose), administration date: 04Sep2021, for COVID-19 immunization, reaction(s): "ear infection", "got an ear infection on both ears with perforation and bleeding ", "may have been getting sick cause of the vaccine". The following information was reported: SEIZURE (medically significant) with onset 10Dec2021, outcome "unknown", described as "seizure"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 06Nov2021, outcome "unknown", described as "Dose 1 was on 04Sep2021 and Dose 2 was on 06Nov2021". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autism (Her son is a 15 year old male with Autism)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2018661

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Dizziness Hyperhidrosis Immunisation Loss of consciousness Mental impairment Nausea Syncope

Symptomtext

blacked out; was almost fainting; could barely think of what to do; very dizzy; I also thought I was going to vomit; sweating; Dose received: 3; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55 year-old female patient received BNT162b2 (BNT162B2), administered in arm right, administration date 01Dec2021 (Lot number: FF2590) at the age of 55 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulpha" (unspecified if ongoing). There were no concomitant medications. The patient did not receive any other vaccine within four weeks. The patient did not have covid before vaccination. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0173, Location of injection: Arm Right), administration date: 06May2021, when the patient was 54 years old, for COVID-19 immunization, reaction(s): "I got very dizzy and almost blacked out.", "almost blacked out.", "I was sweating and could barely think of what to do because I was almost fainting.", "almost fainting."; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0161, Location of injection: Arm Right), administration date: 11Apr2021, when the patient was 54 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (medically significant); LOSS OF CONSCIOUSNESS (medically significant) with onset 02Dec2021 06:30, outcome "recovered" (Dec2021), described as "blacked out"; SYNCOPE (medically significant) with onset 02Dec2021 06:30, outcome "recovered" (Dec2021), described as "was almost fainting"; MENTAL IMPAIRMENT (medically significant) with onset 02Dec2021 06:30, outcome "recovered" (Dec2021), described as "could barely think of what to do"; DIZZINESS (non-serious) with onset 02Dec2021 06:30, outcome "recovered" (Dec2021), described as "very dizzy"; NAUSEA (non-serious) with onset 02Dec2021 06:30, outcome "recovered" (Dec2021), described as "I also thought I was going to vomit"; HYPERHIDROSIS (non-serious) with onset 02Dec2021 06:30, outcome "recovered" (Dec2021), described as "sweating". The patient reported that after the 2nd and 3rd vaccines, upon waking up the following day, she got very dizzy and almost blacked out. She was sweating and could barely think of what to do because she was almost fainting. She also thought she was going to vomit when it happened after the 3rd vaccine (next day) but she didn't. She sat with her head down between her legs and the symptoms faded. Therapeutic measures were not taken as a result of loss of consciousness, syncope, mental impairment, dizziness, nausea, hyperhidrosis. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1964462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: OK
Alter: 46,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 01.11.2021
Beginn: 16.12.2021
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: SYR / RA

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

Bell's palsy

Symptomtext

Bell's Palsy

Weitere VAERSDATA-Felder

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

VAERS 1957826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: WA
Alter: 23,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 13.11.2021
Beginn: 14.12.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: SYR / LA

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

Chest pain Electrocardiogram Pericarditis

Symptomtext

Diagnosed with pericarditis after having chest pains

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: EKG preformed on 12/16/2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1954283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: LA
Alter: 77,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Amniocentesis Endocrine neoplasm malignant Immunisation Loss of consciousness Lung neoplasm malignant Mass Neoplasm progression Pain in extremity Pulmonary oedema

Symptomtext

The right lung had fluid; booster; passed out; had spread to his bones so fast; endocrine cancer; Lung cancer; hurt arm; mass; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 77 year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm right, administration date 13Oct2021 (Lot number: FF2590) at the age of 77 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Dialysis", start date: 18Oct2021, stop date: 22Nov2021; "back aches" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (1st dose, right arm, Lot: EL9265), administration date: 06Feb2021, when the patient was 76 years old, for Covid-19 Immunization; Bnt162b2 (2nd dose, right arm, Lot: EM9810), administration date: 23Feb2021, when the patient was 76 years old, for Covid-19 Immunization, reaction(s): "Inappropriate schedule of vaccine administered". The following information was reported: IMMUNISATION (death, hospitalization, medically significant) with onset 13Oct2021, outcome "fatal", described as "booster"; ENDOCRINE NEOPLASM MALIGNANT (death, medically significant) with onset 18Nov2021, outcome "fatal", described as "endocrine cancer"; LUNG NEOPLASM MALIGNANT (death, medically significant) with onset 18Nov2021, outcome "fatal", described as "Lung cancer"; PULMONARY OEDEMA (hospitalization, medically significant) with onset Nov2021, outcome "unknown", described as "The right lung had fluid"; LOSS OF CONSCIOUSNESS (hospitalization, medically significant) with onset Nov2021, outcome "unknown", described as "passed out"; NEOPLASM PROGRESSION (non-serious), outcome "unknown", described as "had spread to his bones so fast"; PAIN IN EXTREMITY (non-serious) with onset Nov2021, outcome "recovered" (Nov2021), described as "hurt arm"; MASS (non-serious) with onset Nov2021, outcome "unknown", described as "mass". The patient was hospitalized for loss of consciousness (start date: 14Nov2021, discharge date: 17Nov2021, hospitalization duration: 3 day(s)). The events "endocrine cancer", "lung cancer", "the right lung had fluid", "passed out", "had spread to his bones so fast" and "mass" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: amniocentesis: unknown results. Therapeutic measures were taken as a result of pain in extremity. The patient date of death was 22Nov2021. The reported cause of death was neoplasm malignant, lung neoplasm malignant. No autopsy was performed. Clinical course reported as: consumer reported husband just passed away from endocrine cancer and she thought it was because of the booster shot, he didn't have it a year. Consumer stated his hurt arm, this would last 3 days and was treated with Tylenol. After the booster shot he passed out and was taken to the emergency room on 14Nov2021, admitted and then discharged after 3 days; they didn't know what was wrong. Relevant Tests: amniocenteses on lung while in the hospital but the date was unknown. The right lung had fluid and there was a mass. The doctors didn't know how it happened so fast and had spread to his bones so fast. There was nothing in his records to show he had cancer. Patient passed away on 22Nov2021 from endocrine and lung cancer, he was diagnosed 18Nov2021.; Reported Cause(s) of Death: lung cancer; endocrine cancer

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Name: Amniocentesis; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back pain; Dialysis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 24.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Blood pressure diastolic decreased Dizziness Fatigue Heart rate increased Heart rate irregular Immunisation Orthostatic hypotension Sinus disorder Sinus pain Syncope Throat irritation Throat tightness

Symptomtext

booster; Orthostatic Hypotension, I collapsed upon standing; Orthostatic Hypotension; sinus and throat irritation and sensation of closing; sinus and throat irritation and sensation of closing; sinus and throat irritation and sensation of closing; sinus and throat irritation and sensation of closing; my diastolic blood pressure kept dropping into the low 50's, and then normalizing, then dropping again; dizziness; racing then slow heartbeat; racing then slow heartbeat; extreme fatigue; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 24Nov2021 (Lot number: FF2590) at the age of 39 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Celiac disease" (unspecified if ongoing); "Chronic fatigue" (unspecified if ongoing), notes: Chronic fatigue(unspecified); "Autism" (unspecified if ongoing); "Bipolar disorder" (unspecified if ongoing); "Migraines" (unspecified if ongoing); "Low iron" (unspecified if ongoing); "Thyroid nodule" (unspecified if ongoing); "uterine fibroid" (unspecified if ongoing); "2 brain injuries" (unspecified if ongoing). Concomitant medication(s) included: LAMOTRIGINE; TOPAMAX; CETIRIZINE; FAMOTIDINE; LYSI COD LIVER OIL. Past drug history included: Prochlorperazine, reaction(s): "known allergy: Prochlorperazine"; Known allergy: doxycycline, reaction(s): "allergy"; Known allergy: iodinated contrast media, reaction(s): "allergy"; Known allergy: gadolinium, reaction(s): "allergy"; Known allergy: escitalopram, reaction(s): "allergy"; Known allergy: shiitakes, reaction(s): "allergy". Vaccination history included: Bnt162b2 (Dose Number: 2, lot number=EW0173, vaccine location=Right arm), administration date: 04May2021, when the patient was 39 years old, for covid-19 immunization; Bnt162b2 (Dose Number: 1, lot number=ER2613, vaccine location=Left arm), administration date: 23Mar2021, when the patient was 38 years old, for covid-19 immunization. The following information was reported: IMMUNISATION (Medically significant) with onset 24Nov2021 13:45, outcome "unknown", described as "booster"; SYNCOPE (medically significant) with onset 24Nov2021 13:45, outcome "recovering", described as "Orthostatic Hypotension, I collapsed upon standing"; ORTHOSTATIC HYPOTENSION (medically significant) with onset 24Nov2021 13:45, outcome "recovering", described as "Orthostatic Hypotension"; THROAT IRRITATION (non-serious), SINUS DISORDER (non-serious), SINUS PAIN (non-serious), THROAT TIGHTNESS (non-serious) all with onset 24Nov2021 13:45, outcome "recovering" and all described as "sinus and throat irritation and sensation of closing"; BLOOD PRESSURE DIASTOLIC DECREASED (non-serious) with onset 24Nov2021 13:45, outcome "recovering", described as "my diastolic blood pressure kept dropping into the low 50's, and then normalizing, then dropping again"; DIZZINESS (non-serious) with onset 24Nov2021 13:45, outcome "recovering", described as "dizziness"; HEART RATE IRREGULAR (non-serious), HEART RATE INCREASED (non-serious) all with onset 24Nov2021 13:45, outcome "recovering" and all described as "racing then slow heartbeat"; FATIGUE (non-serious) with onset 24Nov2021 13:45, outcome "recovering", described as "extreme fatigue". The events "orthostatic hypotension, i collapsed upon standing", "orthostatic hypotension", "sinus and throat irritation and sensation of closing", "sinus and throat irritation and sensation of closing", "sinus and throat irritation and sensation of closing", "sinus and throat irritation and sensation of closing", "my diastolic blood pressure kept dropping into the low 50's, and then normalizing, then dropping again", "dizziness", "racing then slow heartbeat", "racing then slow heartbeat" and "extreme fatigue" were evaluated at the physician office visit. It was unknown if therapeutic measures were taken as a result of immunisation, syncope, orthostatic hypotension, throat irritation, sinus disorder, sinus pain, throat tightness, blood pressure decreased, dizziness, heart rate irregular, heart rate increased, fatigue. Vaccination facility: Doctors office/urgent care. Patient had not received any other vaccine in four weeks. Clinical Course: Orthostatic Hypotension, she collapsed upon standing, her diastolic blood pressure kept dropping into the low 50's, and then normalizing, then dropping again. Also, extreme fatigue, dizziness, racing then slow heartbeat, sinus and throat irritation and sensation of closing, like a mild sulfite allergy. Patient not had covid-19 prior to vaccination. patient was not tested for covid-19 post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autism; Bipolar disorder; Brain injury; Celiac disease; Chronic fatigue (Chronic fatigue(unspecified)); Iron low; Migraine; Thyroid nodule; Uterine fibroid
Andere Medikamente: LAMOTRIGINE; TOPAMAX; CETIRIZINE; FAMOTIDINE; LYSI COD LIVER OIL
Allergien: -
Vorherige Impfungen: -

VAERS 1944421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: AZ
Alter: 38,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 26.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: SYR / -

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

Bell's palsy Computerised tomogram Head discomfort Pain Sinusitis

Symptomtext

Diagnosed with Bells Palsy at ER. Treatment was 60mg prednisone once daily and 1gm Valacyclovir 3 x a day both for 7 days. Bells Palsy cleared up within 12 days but while being treated for bells palsy head pressure and pain occurred and was diagnosed with a sinus infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: ER Docto diagnosed Bells Palsy on November 16 2021 Sinus infection was diagnosed by CT scan on November 12 2021
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol, Herpes Simplex, Sinusitis
Andere Medikamente: None
Allergien: Tramadol
Vorherige Impfungen: -

VAERS 1940695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: KS
Alter: 21,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 07.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / -

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

Blood folate Blood iron normal Cholelithiasis Computerised tomogram thorax abnormal Condition aggravated Deep vein thrombosis Haemoglobin decreased Iron binding capacity total normal Lung opacity Lymphadenopathy Magnetic resonance imaging normal Mean cell volume increased Mycobacterium tuberculosis complex test Pain Pleural effusion Pneumonia Pulmonary mass Serum ferritin increased

Symptomtext

pfizer vaccine 11/7/2021, and she had u/s on 11/11/21 showing RUE DVT, Near the elbow at the site of a previously placed peripheral IV there is a a short segment acute appearing occlusive DVT within the more anterior of the paired brachial veins. Note from 30 Nov 2021: 21 yo female with PMH of SSA, avascular necrosis R hip s/p arthroplasty, hx acute chest, LE DVT on Xarelto admitted for acute pain. She has had a prolonged hospitalization and been treated with high doses of oral and parenteral opioids. She has had multiple local interventions to attempt to control the pain including trigger point injection. She declined exchange transfusion after discussion 1. SSA -follows with Dr. -discharge 11/7/21 after admission for pain crisis -Hgb 9.1, MCV 113 on Hydrea 1000mg po daily, folic acid 1mg po daily -PTA tylenol 650mg prn, neurontin 400mg 4 times daily, motrin 600mg prn q6hrs, oxycodone 15mg q4hr prn -retic much better- 120 -TB 0.5 -B12 296, folate >22 -ferritin 609, TIBC 332, % sat 46, iron 152 -CT Chest per #3 -We discussed outpatient management of sickle cell disease including the possibility of pulmonary transplant, which she would be willing to reconsider 2. LLE DVT/RUE DVT -9/5/21 LLE U/S: Thrombosed calf veins without femoral-popliteal deep venous thrombosis. -covid + 8/23/21 -PTA Xarelto-admits to compliance -covid vaccine 7 Nov 2021 -11/11/21 RUE U/S: Near the elbow at the site of a previously placed peripheral IV there is a a short segment acute appearing occlusive DVT within the more anterior of the paired brachial veins. 3. ID -11/11/21 CT Chest: No evidence of acute central or major segmental pulmonary embolism. Evaluation of the pulmonary arteries limited despite repeated attempts. Development of clustered nodular and groundglass opacities in the left upper lobe consistent with pneumonia. Trace left pleural effusion, likely reactive. Development of mild right axillary lymphadenopathy, likely reactive from reported recent COVID-19 vaccination in the right arm. Cholelithiasis. Stable osseous findings of sickle cell disease. -normal WBC, afebrile, no cough/SOB or hypoxia -pulmonary consulted, completed 5 day course of doxycycline 4. Avascular necrosis -MRI 11/25/2021: Evidence of prior bone infarctions, with no new bone infarctions identified -Appreciate orthopedic surgery evaluation, she will have outpatient follow-up Recommendations: -Appreciate pain service assistance, agree with current pain management -Will continue Hydrea at 1000mg po daily at d'c, to be adjusted outpatient -Continue Xarelto -B12 298, continue replacement 1000mcg po daily -continue folic acid 1 mg po daily

Weitere VAERSDATA-Felder

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

VAERS 1936356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: AZ
Alter: 27,0
Geschlecht: F
Eingang: 09.12.2021
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: nein

Blood test Chest pain Electrocardiogram Muscle spasms Myocarditis

Symptomtext

I received my third Pfifer shot on 11/05/2021. I had previously had an adverse reaction with my second shot 03/22/21 where I developed very painful pleurisy and went to the hospital. Because of this reaction to the second dose, I went to my doctor and asked if I should get the third. I was advised that there was a study researching long-term issues amongst males 18-40 but since I was not in this demographic and my issues did not go past the one day, that it would be safe for me to get the third vaccine. A few days after my third shot I developed chest pain and cramps. It was similar to the pain I had when I went to the hospital, but not painful enough to go to the hospital. I went to family practice again where I had blood tests done and an ekg. I was also prescribed a medication to address myocarditis. The pain persisted with medication but at the following appt I was given pain medication and recommended to use an inhaler. I have a pending echocardiogram but am switching doctors before scheduling. I continued to have pains after this

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Blood test EKG
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/a
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Pfizer Dose 2

VAERS 1935775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: IL
Alter: 24,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 02.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / -

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

Angiogram pulmonary normal Chest pain Echocardiogram normal Ejection fraction normal Myocarditis Troponin increased Vaccination complication

Symptomtext

Patient presented to ED on 10/13/21 with complaint of intermittent chest pain x 3 days. Patient has no past medical history. Patient received COVID-19 vaccine about one week prior to start of chest pain. CTA chest was negative for PE. Initial troponin was elevated at 13.17, troponin peaked at 23.84. Echo revealed LV ejection fraction of 68% with normal RV systolic function. No tachy or brady arrhythmias noted during hospitalization. Patient diagnosed with myopericarditis likely secondary to recent COVID-19 vaccine.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: none
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1928719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CT
Alter: 79,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 07.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / UN

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

Aortic valve incompetence Arrhythmia Arteriogram coronary normal Atrioventricular block Cardiac imaging procedure abnormal Dizziness Echocardiogram Echocardiogram abnormal Ejection fraction Ejection fraction decreased Electrocardiogram ambulatory normal Electrocardiogram normal Feeling abnormal Headache Left ventricular dysfunction Malaise Mobility decreased Myocardial bridging

Symptomtext

A few hours after the vaccine was administered patient had severe malaise. She laid in bed for approximately 20 hours. She got up the morning after the vaccine and had a headache. She went to take Tylenol but syncopated while standing in her bathroom. She continued to experience episodes of lightheadedness and brain fog. ECG and 3-day Holter monitor were unremarkable. Echocardiogram showed depressed ejection fraction (43%) and wall motion abnormalities. Coronary angiogram showed no coronary artery disease to explained these findings. Cardiac MRI showed improved ejection fraction and improving (although not fully normal) wall motion. Patient has experienced an improvement in her symptoms, but not full return to normal. This episode and imaging findings are suspicious for stress induced (Takotsubo) cardiomyopathy. Patient will get a repeat echocardiogram in 3 months to ensure resolution of wall motion abnormalities.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: ECG 10/13/21- sinus bradycardia at a rate of 50 bpm; 3 Day Holter 11/11/2021; 1. The patient's baseline rhythm during the monitoring period was normal sinus rhythm; 2. Heart rate varied from 38 bpm to 101 bpm. The patient?s average heart rate was 61 bpm; 3. Holter monitor analyzed duration was for 3 days 1 hours; 4. The patient had 0.02% ventricular ectopic activity (56 total beats) in the form of 56 isolated PVCs; 5. The patient had 0.07% supraventricular ectopy in the form of 193 singlets; 6. Other evidence of heart block or arrhythmia: None; 7. Patient diary: No reported events; Transthoracic echocardiogram 11/19/2021; The mid/distal septum, anterior, apical, and distal lateral walls are akinetic. Left ventricular systolic function is mildly decreased. The quantitative EF by 2D Simpson biplane is 43%; Right ventricular systolic function is normal; There is mild aortic regurgitation; There is no previous study for comparison in our system; Coronary angiogram 11/24/2021; Left Main; Large caliber vessel that birfucates into a left anterior descending and left circumflex artery. The left main is free of any angiographically significant coronary artery disease; Left Anterior Descending; There is a large-caliber vessel that coursed along the anterior interventricular groove and tapers as it reaches to the apex. The LAD gives off 1 large caliber diagonal branch in its proximal portion and a series of small caliber diagonal branches. In the mid LAD there is approximately 30 mm segment of myocardial bridging. There are mild luminal irregularities in the LAD however there is no angiographically significant coronary artery disease; Left Circumflex; Large-caliber nondominant vessel that gives off a large caliber obtuse marginal branch. The left circumflex system is free of any angiographically significant coronary artery disease; Right Coronary Artery; Large-caliber dominant vessel that gives off a PDA and PL branch. The RCA system is free of any angiographically significant coronary artery disease; CMR 12/4/2021; Preserved biventricular resting systolic function. LVEF 64%, RVEF 62%; There is mild hypokinesis of the left ventricular apex, with no abnormal late gadolinium enhancement to suggest inflammation, infiltration or scarring. In the appropriate clinical setting, findings could represent (recovering) Takotsubo cardiomyopathy.
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism; hyperlipidemia; accelerated idioventricular rhythm
Andere Medikamente: cholecalciferol; levothyroxine; metoprolol succinate; rosuvastatin; omega 3; multivitamin; vitamin K
Allergien: sulfa antibiotics
Vorherige Impfungen: Patient had similar profound malaise after her second covid vaccine but no syncope

VAERS 1925417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NH
Alter: 66,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 27.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy

Symptomtext

Patient now has Bells Palsy (Right side of Face)....

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: pravastatin viagra
Allergien: none
Vorherige Impfungen: -

VAERS 1916574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: ID
Alter: 73,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 29.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Back pain C-reactive protein normal Chest X-ray normal Chest pain Costochondritis Differential white blood cell count normal Dizziness Echocardiogram normal Electrocardiogram normal Fatigue Full blood count normal Loss of personal independence in daily activities Metabolic function test Syncope

Symptomtext

Pain in chest and back for two weeks, black out Nov. 13, 2021 and went to hospital ER thought I was having a heart attack, EKG normal and blood work came back normal and diagnose with Syncope. Weakness, fatigue, dizziness, light headed, and continued chest pain that I couldn't do normal activities. Went to GP Nov. 16, 2021, scheduled more blood tests and Echocardiogram. All test results came back normal. Saw GP Nov. 23, 2021. Diagnosed with Costochonditis and given 10 day supply of meloxicam. Slowly day by day symptoms are leaving, but still have fatigue. Dec. 1, 2021 saw GP and will take another 10 day of meloxicam.

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Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG Normal, Nov. 13, 2021; Comprehensive Metabolic Panel, Normal Nov. 13, 2021,,CBC W/ Auto Differential Normal, Nov. 13, 2021; Echocardiogram Normal, Nov. 19, 2021, Chest X-ray Normal and C-Reactive Protein Normal Nov.24,2021.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Calcium; Vitamin D 300 UI.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 1851291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NY
Alter: 13,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 19.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: - / -

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

Aphasia Asthenia Depression Electroencephalogram abnormal Encephalitis Blood test Fall Headache Lumbar puncture Magnetic resonance imaging Feeding disorder Gastrointestinal tube insertion Immunoglobulin therapy Plasmapheresis Seizure Mechanical ventilation Status epilepticus

Symptomtext

Patient presented in status epilepticus on 10/25, 6 days after receiving her COVID vaccine. She had been noted to have increasing depression and potential weakness over the week prior to presentation. Prior, she had been previously healthy and developmentally normal. After prolonged treatment course including multiple anti-epileptics, she began treatment for suspected acute encephalitis. In addition to seizure, she has become nonverbal, unable to eat, and does not follow commands. She received 6 rounds of plasmapheresis, and has completed two courses of 2g/kg of IVIG, and 1x Rituximab. She has received 2 rounds of burst seizures and is now currently tapering on her steroids. At this time, 12/2 she is currently on Vimpat 250mg BID, Keppra 1500mg BID for seizures. She has had 2 seizures in the past week, one subclinical noted on EEG, and 1 lasting ~30seconds. She is currently receiving all feeds via NG as she is not take anything by mouth. On current exam, awake, will open eyes, can move all extremities, will not follow commands, she can take steps with assistance with PT.

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Praegender Schweregrund: Seizure
Hospital-Tage: 38,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: She had mood changes, and clumsiness for 1 week after first dose of Pfizer

VAERS 1919971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 21.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cardiac failure Chest X-ray Cough Dyspnoea Pleural effusion Pneumonia Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 09/30, Pfizer, dose #1 10/21, Pfizer, dose #2 09/28 pt admit to medicine cc: shortness of breath dx: Community Acquired pneumonia LOS: 1 day 09/28 CXR impression: Multifocal pneumonia. Continued follow-up after treatment. 11/03 CXR impression: Multifocal consolidations have improved. There is a small amount of residual hazy opacity in the right lung base. The cardiac and mediastinal silhouettes are within normal limits. No pleural effusion or pneumothorax. 11/09 CXR impression: New findings of mediastinal interstitial pulmonary edema since 6 days ago, in keeping with congestive heart failure. This would account for the patient's dyspnea. Bilateral pleural effusions, RIGHT larger than LEFT, increased in volume since 11/3/2021. 11/05 pt cc: dyspnea, cough exposure: unknown 11/09 COVID swab, result: detected 11/10 COVID swab, result: detected 11/15 pt admit to medicine cc: SOB dx: Acutely decompensated systolic HF LOS: 5 days

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Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: 09/28 CXR impression: Multifocal pneumonia. Continued follow-up after treatment. 11/03 CXR impression: Multifocal consolidations have improved. There is a small amount of residual hazy opacity in the right lung base. The cardiac and mediastinal silhouettes are within normal limits. No pleural effusion or pneumothorax. 11/09 CXR impression: New findings of mild interstitial pulmonary edema since 6 days ago, in keeping with congestive heart failure. This would account for the patient's dyspnea. Bilateral pleural effusions, RIGHT larger than LEFT, increased in volume since 11/3/2021. 11/09 pt cc: dyspnea exposure: unknown 11/09 COVID swab, result: detected 11/10 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 21.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Diplopia Ophthalmological examination abnormal VIth nerve paralysis Visual impairment

Symptomtext

I noticed some vision changes October 28, 2021 which became obvious November 2, 2021 while I experienced binocular double vision while driving. On November 22, 2021 I was examined by Dr. who diagnosed me with right sixth nerve palsy. I researched online November 29, 2021 and discovered there were other instances of sixth nerve palsy in otherwise healthy people after the Pfizer Covid vaccine.

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Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: Optical exams on November 4th, 2021 and November 22, 2021.
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Amlodipine, Zetia, Vit D3, Fish Oil, Vit B12, Neuriva
Allergien: Aspirin, NSAIDS
Vorherige Impfungen: -

VAERS 1906712

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FF2590

schwer

Staat: TX
Alter: 21,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram Blood test Computerised tomogram Discomfort Dizziness Electric shock sensation Electroencephalogram abnormal Epilepsy Gait disturbance Headache Lethargy Magnetic resonance imaging Seizure Skin burning sensation Urinary incontinence

Symptomtext

I started feeling light headed at the time of receiving my first dose. I was not kept for the observation period and was released immediately . The next night i got home after a long day at work. I was brushing my teeth and on facetime with my boyfriend. One second I was there and talking the next I was on the floor and had urinated myself. I had experienced the first seizure i have ever had in my life.. I came around pretty quickly and called my mom. She then called my dr, who has been taking care of me since i was 3 years old, through the medical exchange. He contacted my mom very quickly and we were advised that it could have been me being tired or other factors. my mom then drove 3 hours to come take care of me and monitor me. I felt very heavy and lethargic, ,my head felt like it was on fire and my body felt like there was electricity pumping through my veins. I had to crawl to the door and unlock it for my mom while she was on the way. The next day went fine, I was alert and oriented x4. Exactly 24 hours after my first incident, I had another seizure. I was on a call with my friends and my webcam was on. My mom called ems and I was transported to the hospital. The ER Dr. who was on call spoke with me and immediately admitted me to run a whole course of tests. I had 2 EEG done, CT Scan, MRI, MRA, and bloodwork. They decided that I needed further testing and sent me to the hospital. I had a 48 hour monitored EEG done and they found abnormal activity.

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 5,0
Labordaten: I had a 48 hour monitored EEG done and they found abnormal activity in my brain. I was officially diagnosed with epilepsy and was placed on 2 anti seizure medication.
Aktuelle Erkrankungen: Was fully healthy. After receiving the first dose of the Pfizer vaccine, started to feel a headache coming on.
Vorgeschichte: ADHD PDD Anxiety PTSD Depression
Andere Medikamente: Zoloft, Trazadone, Mirtazapine,
Allergien: blueberries Azitgromycin benadryl clavulanic acid diphenhydramine erythromycin
Vorherige Impfungen: -

VAERS 1903722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

schwer

Staat: AZ
Alter: 39,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Laboratory test Myalgia Thrombosis Vaccination site pain Vaccination site swelling

Symptomtext

The next day, 12Nov2021, I went to my doctor and he told me it was a blood clot that I had in my armpit; the next day, 11Nov2021, I started with muscle pain in my back and legs, and by night I realized that I had a large swelling on the armpit of the same side of the vaccine; the next day, 11Nov2021, I started with muscle pain in my back and legs, and by night I realized that I had a large swelling on the armpit of the same side of the vaccine; patient received 3rd dose; On 10Nov2021, with dose 3 I felt more pain in the site of the application; This is a spontaneous report from a contactable Other HCP (patient herself). A 39 years old male patient received dose 3 of BNT162B2(PFIZER BIONTECH COVID VACCINE, solution for injection, lot number=Ff2590) via unspecified route of administration in arm left on 10Nov2021 at 14:30 PM as DOSE 3 (BOOSTER), SINGLE (age at vaccination 39 years) for covid 19 immunization. Patient had shrimp allergy from unknown date and unknown if ongoing. The concomitant medications were not reported. Patient previously received dose 2 of BNT162B2 (PFIZER BIONTECH COVID VACCINE, solution for injection, lot number: El1283) via unspecified route of administration in arm left on 10Feb2021 at 12:15 PM as dose 2, single (age at vaccination 38 years) and dose 1 of BNT162B2 (PFIZER BIONTECH COVID VACCINE, solution for injection, lot number:El1283) via unspecified route of administration in arm left on 20Jan2021 at 01:15 PM as dose 1, single (age at vaccination 38 years)for covid 19 immunization. Patient had covid prior to vaccination and Covid test result positive on 25Jan2021. Patient received 3 rd dose on 10Nov2021 at 02:30 PM (Immunisation). On 10Nov2021 patient experienced more pain in the site of the application and on next day 11Nov2021 experienced muscle pain in my back and legs, and by night I realized that I had a large swelling on the armpit of the same side of the vaccine and on 12Nov2021 patient went to his doctor and doctor told patient blood clot in his armpit, and doctor did tests on him and Patient had an appointment with the doctor for Monday 15Nov2021 to review results. Patient received treatment with aspirin. Adverse event resulted in patient Visit to doctor's office or other healthcare professional. Patient underwent covid test post vaccination: Nasal swab (sample): Negative on 17Aug2021. On 12Nov2021 patient underwent laboratory test result were was blood clot that in his armpit, and patient had an appointment with the doctor for Monday 15Nov2021 to review results. The outcome of more pain in the site of the application, muscle pain in my back and legs, and by night I realized that I had a large swelling were not recovered.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20211112; Test Name: he did tests on me; Result Unstructured Data: Test Result:Unknown results; Comments: 12Nov2021, I went to my doctor and he told me it was a blood clot that I had in my armpit, and he did tests on me and I have an appointment with the doctor for Monday 15Nov2021 to review results.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If Covid prior vaccination: Yes); SARS-CoV-2 test (Nasal swab (sample) : Negative on 17Aug2021); Seafood allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1893253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NC
Alter: 79,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 06.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: - / LA

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

Arthropathy Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Pulmonary thrombosis Ultrasound scan

Symptomtext

out of breath; blood clots in her lungs; felt a knot on the back of her knee.; This is a spontaneous report received from a contactable consumer (patient) from a Pfizer sponsored program. A 79-year-old female patient received the third dose of BNT162B2 (PFIZER COVID VACCINE) via an unspecified route of administration on the left arm on 06Oct2021 (Batch/Lot Number: FF2590; Expiration Date: Unknown) at the age of 79-year-old as single dose for COVID-19 immunization. Medical history included thyroid, diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes) and obesity. Prior vaccination (within 4 weeks) was none. Years ago, she worked in admissions in a small hospital. Concomitant medication included ongoing levothyroxine for thyroid. The patient previously received the first dose and the second dose of BNT162B2, the first dose on 28Jan2021 (Lot Number: EL9263), the second dose on 16Feb2021 (Lot Number: EN6201), both via an unspecified route of administration as single dose for COVID-19 immunization and experienced a little bit of feeling tired with those. In 2021, the patient was being treated for blood clots in her lungs. A couple of days later, she felt a knot on the back of her knee. She made an appointment on 12Oct2021 with her doctor. Her doctor said he didn't think much of it. Then, when she was walking around on 19Oct2021 she was out of breath. They also did an ultra sound of her legs, and did find a clot where the knot was. She was calling because she figured Pfizer is still doing research. She is pro vaccine, and always promotes it. It is wonderful. This could or could not be related, but she wanted to report just in case. She did not have a prescribing doctor. She just made an appointment at the pharmacy. She got out of the hospital on the evening of the 22Oct2021. She has another week of Lovenox, and then she is going on Eliquis for 6 months. She has seen a hematologist. She is still on oxygen at home at night. The handwriting was so tiny. Relevant tests included list other relevant diagnostic and confirmatory test results for event(s), for example, from blood tests, cerebrospinal fluid culture, bacterial sero-type, diagnostic imaging, (e.g., chest X-ray, MRI). They did a CT scan, ultra sound, echocardiogram, and EKG. Everything looked fine. The only medication she takes is for her thyroid. She takes Levothyroxine 50mcg. She knows Pfizer was working 24 hours a day to get the vaccine ready. She is very thankful. She is getting better everyday. The events resulted in emergency room and physician office. The events resulted in hospitalization from 19Oct2021 to 22Oct2021. Investigation assessment was none. The outcome of No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 4,0
Labordaten: Test Name: CT scan; Result Unstructured Data: Test Result:Looked fine; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Looked fine; Test Name: EKG; Result Unstructured Data: Test Result:Looked fine; Test Name: Ultra sound; Result Unstructured Data: Test Result:Looked fine; Test Name: Ultra sound of her legs; Result Unstructured Data: Test Result:Find a clot where the knot was
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Chromosome abnormality; Diabetes; Endocrine disorder; Immune system disorder; Obesity; Respiratory disorder NOS; Thyroid disorder
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1888204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: TN
Alter: 38,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Blood pressure decreased Eye movement disorder Hyperhidrosis Loss of consciousness Panic attack Unresponsive to stimuli

Symptomtext

Patient had a panic attack after admin of shot. He lost consciousness and had sweating and a drop in BP. He also had rapid eye movements and was unresponsive. 911 was called and paramedics came top assist. He was given fluids and then returned to the pharmacy for observation as he denied a ride to the hospital.

Weitere VAERSDATA-Felder

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

VAERS 1816464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: OR
Alter: 16,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 25.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Concussion Lethargy Pruritus Seizure Unresponsive to stimuli Syncope Urticaria

Symptomtext

A seizure and very lethargic and unresponsive for majority of the day. Included a concussion.. itchiness and hives

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Waiting on EEG but all other documentation showed clear.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1816464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

schwer

Staat: OR
Alter: 16,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 25.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Concussion Lethargy Pruritus Seizure Unresponsive to stimuli Syncope Urticaria

Symptomtext

A seizure and very lethargic and unresponsive for majority of the day. Included a concussion.. itchiness and hives

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Waiting on EEG but all other documentation showed clear.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1877532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 18.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: IM / -

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

Anticoagulant therapy Cerebral venous sinus thrombosis Magnetic resonance imaging head abnormal Seizure Thrombectomy

Symptomtext

Patient with seizure at home, no prior history of seizures, presented to ED, MRI done, patient found to have L transverse dural sinus thrombosis, underwent emergent thrombectomy, continues now on anticoagulation. Patient with no prior history of blood clots, no prior injury, surgery, travel, or other possible clot provoking factor aside from vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous sinus thrombosis
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: iron supplement
Allergien: none
Vorherige Impfungen: -

VAERS 1875903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 17.11.2021
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: ja

Body temperature Chills Immunisation Loss of consciousness Pyrexia SARS-CoV-2 test

Symptomtext

loss of conciousness; chills; fever of 102F; third dose; This is a spontaneous report from a non-contactable nurse (patient). A 55-year-old non-pregnant female patient received the third (booster) dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; lot number: FF2590), via an unspecified route of administration on 18Oct2021 (at the age of 55-years-old) at dose 3 (booster), single in the left arm for COVID-19 immunization. The patient has no medical history and concomitant medications. Historical vaccine includes the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Batch/Lot No: EL0142) received on 29Dec2021 (at the age of 54-years-old),and the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Batch/Lot No: EL1283) received on 15Jan2021 (at the age of 54-years-old); both for COVID-19 immunization. The patient was not pregnant at the time of vaccination. The patient has no known allergies, did not receive any other vaccines within 4 weeks prior to the COVID-vaccine, and has no other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. On 18Oct2021 at 22:00, the patient experienced loss of consciousness, chills, and fever of 102F. No treatment was received for the events. The patient underwent lab tests and procedures which included: Body temperature on 18Oct2021: 102 Fahrenheit; and COVID-19 nasal swab on 23Sep2021: negative. Outcome of the events was recovered on Oct2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender's Comments: Based on the information available and temporal association, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events . The case will be reassessed once new information is 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: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20211018; Test Name: body temperature; Result Unstructured Data: Test Result:102 Fahrenheit; Test Date: 20210923; Test Name: COVID-19 Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Blood test Cardiac monitoring Chest X-ray Loss of consciousness Syncope

Symptomtext

I don't think this is related to the vaccine, but I was asked by the CDC to fill this out. 26 days after getting my COVID-19 booster (Pfizer-BioNTech), I was out at the theater, at first feeling fine. Then my stomach bothered me so I went to the lobby. In the lobby I fainted three times in the span of about 30 minutes. The paramedics took me to the nearest ER, where my heart was monitored, bloodwork was done, and chest was x-rayed. They did not find anything to explain the episode of multiple losses of consciousness. I will be meeting with my primary care physician two days from now to follow up. I do not have the doctor's name at the ER nor any of the records from the tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: I do not have any of the records from the paramedics or ER. They hooked me up to a heart monitor, blood pressure, and pulse; they did blood work and a chest x-ray in the ER.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1872878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: KY
Alter: 52,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 14.10.2021
Beginn: 09.11.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: - / -

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

Condition aggravated Deep vein thrombosis

Symptomtext

unprovoked DVT in right posterior tibial vein

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: h/o of DVT in 2001
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1870900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: GA
Alter: 17,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Syncope

Symptomtext

Patient received 1st dose of Pfizer vaccine and after sitting for about 10 mins, patient felt faint and passed out, falling off his chair and onto the floor. Pharmacist rushed to the patient and assisted in comforting him and making sure he was ok. He was able to get back up after a few mins and sit back in chair. He was given water and paramedics arrived to check all vitals, which were normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Vitals were taken by paramedics
Aktuelle Erkrankungen: Congenital Adrenal Hyperplasia
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: Described having had felt faint or passed out from other vaccines in past

VAERS 1867329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NM
Alter: 50,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Abdominal pain Anaphylactic reaction Arthralgia Diarrhoea Fatigue Haemoptysis Myalgia

Symptomtext

anaphylactic reaction; lung producing bloody phlegm (when waking up in morning); sore muscle (deltoid) / muscle pain; abdomen pain (lower left); diarrhea; fatigue; joint pain; This is a spontaneous report from a contactable consumer (patient). A 50-year-old female patient received dose 3 of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in right arm on 29Oct2021 10:00 (Batch/Lot Number: FF2590) (at the age of 50 years old) as dose 3 (booster), single for Covid-19 immunisation. Medical history included asthma, hypertension, degenerative disc degeneration (DDD), attention deficit hyperactivity disorder (ADHD), and bee sting allergy. Concomitant medication included influenza vaccine (FLU VACCINE VII) taken for immunization, start and stop date were not reported. The first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) was administered on 16Mar2021 10:00am in left arm (Batch/Lot No: GN6206) (at the age of 50 years old); and second dose on 06Apr2021 10:00am in left arm (Batch/Lot No: FR8730) (at the age of 50 years old); for COVID-19 immunization. The patient previously took metformin and levothyroxine and experienced allergy. After the third dose, on 29Oct2021 at 16:00, the patient experienced anaphylactic reaction, lung producing bloody phlegm, sore muscle (deltoid), abdomen pain (lower left), diarrhea, fatigue, and muscle and joint pain. No treatment received for the events. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Outcome of the events was not recovered. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD; Asthma; Bee sting hypersensitivity; Degenerative disc disease; Hypertension
Andere Medikamente: FLU VACCINE VII
Allergien: -
Vorherige Impfungen: -

VAERS 1857419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CT
Alter: 61,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Anaphylactic reaction Angioedema Cardiac stress test abnormal Chest discomfort Chest pain Discomfort Echocardiogram normal Electrocardiogram Lipids Nausea Headache Lip dry Paraesthesia Stomatitis Oropharyngeal swelling Paraesthesia oral Periorbital swelling Positron emission tomogram

Symptomtext

Pfizer booster administered at Covid vaccine clinic 5 minutes after administration, patient c/o dry lips, headache, and feet/hands tingling Placed in reclining chair by RR nurses for observation RR nurses asked patient several times how she was feeling and patient reported that she was experiencing mild nausea and felt like "my tongue is thick". Denied: SOB, abd pain, throat swelling, lips swelling. Alert and oriented x 3 throughout Skin warm and dry. No cyanosis No resp distress No vomiting. O2 Sat 100% Temp 97.3 Pulse 87 and regular Patient made several phone calls while resting. Contacted AC clinician to discuss Clinician advised admin EpiPen due to 2 body systems involved Patient initially refused Discussed with patient 911 transport to ED for continued evaluation, even if she continued to refused EpiPen. Patient refused EpiPen several times. Patient then began complaining of "cheeks feel like they are getting closer to my teeth." Patient then agreed to EpiPen. Administered into left outer thigh 911 called Patient reported condition was not worsening after EpiPen administered. At no point did patient present as unstable or in distress. Patient was walked to the ambulance by EMS Transferred to ED via Ambulance. Accompanied by spouse. Additional Documentation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: tingling hands and feet 9/9/2021
Vorgeschichte: Trauma Closed nondisplaced fracture of head of right radius, initial encounter Female stress incontinence Hyperlipidemia Osteopenia Subclinical hypothyroidism Vitamin D deficiency Rosacea Meningioma (HC Code) (HC CODE) Postconcussion syndrome Hx of allergy Chronic constipation Dry eye syndrome Senile nuclear sclerosis Diverticulosis Esophageal reflux Symptomatic menopausal or female climacteric states Conductive hearing loss, unilateral OAB (overactive bladder) Mixed stress and urge urinary incontinence Palpitations Allergic Rhinitis
Andere Medikamente: albuterol (PROVENTIL HFA;VENTOLIN HFA;PROAIR HFA) 90 mcg/actuation HFA inhaler (Expired) aspirin 81 mg EC delayed release tablet calcium carbonate (CALCIUM 500) 1250 mg (500 mg calcium) tablet cholecalciferol (VITAMIN D) 1,000 unit tablet E
Allergien: Amoxicillin -Hives Cat/feline Products Latex, Natural Rubber -Rash
Vorherige Impfungen: -

VAERS 1858461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 73,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 08.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy Facial paresis Hypoaesthesia

Symptomtext

L facial weakness and numbness - mild Bell's palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Exam by physician - took 10 day course of prednisone
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension - controlled with lisinopril hypothyroidism (Graves disease status post radioactive iodine ablation years ago) - on replacement
Andere Medikamente: lisinopril 30 mg daily levothyroxine 0.1 mg daily ASA 80 mg daily
Allergien: none
Vorherige Impfungen: -

VAERS 1857917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: OH
Alter: 13,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient fainted after standing and walking away. Patient was then seen by NP in the clinic next to our pharmacy.

Weitere VAERSDATA-Felder

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

VAERS 1856806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 01.10.2021
Beginn: 01.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Contusion Diarrhoea Dizziness Eye movement disorder Face injury Fall Feeding disorder Haemorrhage Head injury Illness Immunisation Loss of consciousness Nausea

Symptomtext

Booster; in the pool of blood; passed out; eyes rolled back to head; because in the fall; feeling a bit light headed/ Dizzy; badly bruised; diarrhea; felt very nauseous; very sick; not able to eat; hit her head; hit jaw so badly; This is a spontaneous report from a contactable consumer (patient). This 66-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on Oct2021 at age of 66-year-old (Batch/lot number FF2590) as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation. Concomitant therapy was none. None other Vaccine (Prior to 4 weeks of COVID Vaccine). The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at age of 66-year-old for covid-19 immunisation and experienced sore arm. The patient previously received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at age of 66-year-old for covid-19 immunisation and experienced low grade fever, tired, sore arm. The patient had booster shot last Tuesday and woke up on Wednesday, when woke up on Wednesday morning on Oct2021, she was feeling a bit light headed and dizzy and the next thing she knew she was on the bathroom floor in the pool of blood and then she got herself up and she did not, When she was on the floor she did not know how she got there, when she got herself up, she passed out again, she had never passed out in life. Obviously she am badly bruised and whatever from the fall but she just, she don't know if other people have reported this but she think it is just important because this is the new vaccine and people have made aware of, you know what can happen. She got self on, she was not actually the good thing is she take care of her mother who was 94 and care giver ran upstairs, she heard the patient go down and helped but care giver was very nervous, care giver said the patient eyes rolled back to head, she then because she need to get to the bathroom where she could see, then had diarrhea felt very nauseous and very sick from this from this and the first two vaccine the patient was, you know other than sore arm except second shot she had very, very low grade fever and was just tired you know she thought was not big deal she thought she can take that and this booster shot though absolutely, she actually just wasn't killed, she know this sounds like she have added but you know she hit her head and whatever. Few days after the patient just took some Advil because the not able to open, not able to eat because in the fall the patient hit jaw so badly, so the only thing the patient had been taking was some Advil, the patient took absolutely before vaccine and took nothing for two or three days after vaccine. Outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101465991 Same patient and drug, different events separated in time;US-PFIZER INC-202101465992 Same patient and drug, different events separated in time

Weitere VAERSDATA-Felder

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

VAERS 1854856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 49,0
Geschlecht: M
Eingang: 09.11.2021
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: unbekannt

Dizziness Syncope

Symptomtext

Patient received his first dose of Pfizer Covid vaccine and experienced syncope. Patient while in waiting area post vaccine injection reported feeling dizzy. He set down on the chair and the nurse took his vitals and gave him water. He was laid down on his back since still experiencing dizziness. Patient at this time reports same type of reaction after every injection. Vaccination consent was reviewed was patient prior to injection but he didn't disclose this information. A bytander called ED and the EMT took over the care of the patient. Patient was against calling ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Vitals
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: Patient reports all injections

VAERS 1851128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: WA
Alter: 55,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Condition aggravated Face injury Joint injury Loss of consciousness Pyrexia

Symptomtext

Severe chills, 102F fever after 12 hours; loss of consciousness after 20 hours - resulted in chipped jaw and injured knee

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vit D
Allergien: None
Vorherige Impfungen: 101.5F fever, general malaise, age 55, 1/15/2021 dose #2 Pfizer COVID

VAERS 1850822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: NJ
Alter: 22,0
Geschlecht: M
Eingang: 08.11.2021
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: ja

Amnesia Hyperhidrosis Loss of consciousness Tremor

Symptomtext

after administrating second shot customer customer become extremely sweaty and start to shake . it last about 1 minute. he wake up from this right away and start asking whats happend to him. he said he was really anxious about shots and was very nervous. he described it as anxiety attact. i call 911 and emt came in 5 minutes. customer was siting in immunization room and i provide him with bottle of cold water. emt service checked the patient. all his vitals were normal bp, heart rate, they ask him if he wanted to go to hospital and patient said no. he moved to sit my pharmacy department another 20 minutes then he went home

Weitere VAERSDATA-Felder

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

VAERS 1850807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NE
Alter: 89,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Apraxia Facial paralysis Seizure like phenomena Speech disorder Wheelchair user

Symptomtext

Pt had no verbal response which is not normal for him was wheeling himself down the hallway and stopped and could not follow command even questioned drooping of face. Pt assisted to bed and while waiting for the ambulance had seizure like activity. Pt was transported per ambulance to the local Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 3,0
Labordaten: Unsure what was done at the hospital.
Aktuelle Erkrankungen: None
Vorgeschichte: Unspecified toxic encephalopathy, Benign prostatic hyperplasia, depression, type 2 diabetes, vit b12 deficiency, vit d deficiency, hyperlipidemia,
Andere Medikamente: Tylenol, artificial tears, aspirin, atorvastatin, cholecalciferol, Cyanocobalamin, ferrous sulfate, levetiracetam, multivitamin, Psyllium powder, Zoloft,
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1846592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: WA
Alter: 67,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Erythema Fatigue Feeling of body temperature change Heart rate increased Hyperhidrosis Lethargy Loss of consciousness Peripheral swelling Pyrexia

Symptomtext

Fever/Chills 12 hours after shot lasting 4 hours; changed to sweats & racing pulse lasting 30 minutes. Then on/off hot/cold for several hours. 24 hours after shot - heavy sweats and passed out for a few seconds. Very lethargic rest of day. Day 3: lightheaded, fatigued, left arm below shot sight starts to swell with redness & heat - this lasted for 2 days and subsided slowly on the following day. All issues gone by day 6. Similar event occurred with Phizer\BioN Tech shot EN6198 shot #2 (2/28/21) - that time the sweats/racing pulse after fever/chills ended me in ER, with the diagnosis that I must have had some kind of reaction. Not sure as it was early days if the ER reported the event. And I didn't know there was a reporting system at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: MCAS diagnosed after Phizer Vaccine #2.
Andere Medikamente: Losartan; Allegra; Benadryl; Vitamin C; Vitamin B; Vitamin D; Isoquercetin; Fish oil; Magnesium
Allergien: Sensitivities
Vorherige Impfungen: Described in Item 18

VAERS 1846481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: IL
Alter: 30,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient began to feel dizzy about 5 minutes after vaccination. Patient then passed out. Patient regained consciousness about 2 minutes after passing out. Emergency EMT were called and reported to the scene. Vitals were taken and patient denied further medical care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood pressure taken by EMT
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: fainting

VAERS 1844304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff-2590

schwer

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 15.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy Computerised tomogram head abnormal Embolism Magnetic resonance imaging head abnormal Neurological symptom

Symptomtext

presented in my garage with stroke symptoms and summoned the paramedics where they performed stroke protocol and took me to local hospital where they did the same and administered tPA. From onset of symptoms to tPA was approximately 45 minutes. CT and MRI showed narrowing where embolic debris lodged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolism
Hospital-Tage: 1,0
Labordaten: CT and MRI of head on 10/29 and 30. results available to VAERS upon request
Aktuelle Erkrankungen: -
Vorgeschichte: mild hypertension
Andere Medikamente: valsartan 10/160, rosuvastatin 5mg, tadalafil 5mg, asa 81mg, pantoprazole 40mg, coq10 300mg
Allergien: none
Vorherige Impfungen: -

VAERS 1837708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Patient fainted about 1 minute after vaccination. Patient was unresponsive for about 10 seconds. Patient was given ice pack. EMS came and patient did not want to go get treatment

Weitere VAERSDATA-Felder

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

VAERS 1833309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 01.11.2021
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: nein

Blood calcium decreased Blood glucose normal Carbon dioxide decreased Dizziness Feeling hot Full blood count normal Head injury Hyperhidrosis Loss of consciousness Metabolic function test abnormal Pain Pyrexia

Symptomtext

Pt received vaccine 10/25/21. On Tuesday 10/26/21 had body aches & fever while going down the stairs to get some medication got hot, sweaty, lightheaded and passed out hit her head. Her fianc? called 911 and she was taken to the ER for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: CMP wnl except: CO2 - 21, glucose 103, calcium 8.2 CBC wnl
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1831059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 30.10.2021
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 Diarrhoea Dizziness Dysstasia Headache Illness Pain Presyncope Pyrexia Vomiting

Symptomtext

feeling faint/ feeling like she's going to faint; dizzy; Third dose: has pain throughout her body; She states it is hard to stand up; throwing up; headache; diarrhea; high fever/ temperature before she called was 103.5; She got the booster yesterday and she has been quite ill/ really sick right now; Third dose: she's so weak right now; This is a spontaneous report from a contactable consumer (patient). A 72-years-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration, administered in left arm on 14Oct2021 11:30 (Lot Number: FF2590) (at the age of 72-years-old) as dose 3 (booster), single for covid-19 immunisation. The patient no medical history. The patient's concomitant medications were not reported. Historical vaccine included bnt162b2 (COMIRNATY), via an unspecified route of administration, administered in left arm on 03Feb2021 (Lot Number: E51666) (at the age of 71-years-old) as dose 1, single for covid-19 immunisation; and bnt162b2 (COMIRNATY), via an unspecified route of administration, administered in left arm on 26Feb2021 (Lot Number: EN6206) (at the age of 71-years-old) as dose 2, single for covid-19 immunisation and experienced high fever, dizzy, was throwing up, headache, felt like needles and couldn't stand up after dose 2. Patient took vaccine because she works in healthcare, not as a clinician, but leads a national group. Patient got the booster a day before reporting and she has been quite ill with that one. After the third dose on 14Oct2021, she had those symptoms (high fever, dizzy, throwing up), as well as feeling faint, diarrhea, and a headache. She stated it was hard to stand up on 14Oct2021, and she had thought she was in pretty good shape for her age. She also mentioned that this was only the second time in her life she's had a headache; the first was after the second dose. Her fever was 103-104 F for 2.5 days in 2021. Now it was closer to 102-103 F. Her maximum temperature was 103.5 F on the morning of day of reporting. Patient stated that she was experiencing the same symptoms, but a little worse, now she can't stand up without feeling like she's going to faint, her temperature before she called was 103.5 F. She got the shot at 14Oct2021 11:30, and the symptoms started around and they got really bad at night on 14Oct2021, they are all ongoing and worsened. She stated she has a very high temperature, very dizzy, she had pain throughout her body, she never had headaches, but she has one. The patient stated that she doesn't take anything, she did take an ibuprofen last night 14Oct2021, she usually never takes anything, but she had gotten it just in case and she took one and that was it. The events did not require visit to emergency room and physician office. She stated just put that just she's really sick right now, she was so weak right now in Oct2021. The outcome of all events was not recovered. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Fever; Result Unstructured Data: Test Result:103-104 Fahrenheit; Test Date: 202110; Test Name: Fever; Result Unstructured Data: Test Result:102-103 Fahrenheit; Test Date: 20211015; Test Name: Fever; Result Unstructured Data: Test Result:103.5 Fahrenheit; Comments: morning
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1830016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: AZ
Alter: 27,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nervousness Pain in extremity Palpitations Syncope

Symptomtext

Five minutes after receiving vaccine patient felt light headed and dizzy and black out for approximately 15 seconds. He had self-described heart palpitations and 911 was called.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Paramedics arrived and determined patient likely had nervous reaction. They checked his blood pressure sitting and standing and was in normal range. His blood sugar was also checked and found to be in normal range. Patient stated he had not eaten all day and was very nervous about getting the vaccine. Spoke to patient today and has a sore arm but is otherwise feeling well.
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: Unknown
Allergien: None reported
Vorherige Impfungen: -

VAERS 1829488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: KY
Alter: 12,0
Geschlecht: M
Eingang: 29.10.2021
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

Condition aggravated Syncope

Symptomtext

Patient's Mom stated patient has a history of vasal syncope and any sharp pain can trigger the event. The event lasted approximately 5 minutes while in the counseling room. Patient then was seated at the waiting area for another 10 minutes before walking through the store. Mom confirmed at 5:50pm patient was feeling ok and then left the store.

Weitere VAERSDATA-Felder

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

VAERS 1829068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: KY
Alter: 25,0
Geschlecht: M
Eingang: 29.10.2021
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: ja

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Additional Details: pt walking in the aisle during the 15 minute requirement before leaving the pharmacy, his friend yelled he had fainted when out pt came back through didnt realize he fainted. he was given water and stayed for an additonal 30 minutes. said he felt fine had no more issues and left.

Weitere VAERSDATA-Felder

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

VAERS 1826032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: WA
Alter: 57,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Bell's palsy Ear pain Facial paralysis Headache Hypoaesthesia Lip disorder Pain Sensory disturbance

Symptomtext

HEADACHE ON RIGHT TEMPLE SHOOTING PAIN BELOW LEFT EAR ON THE EVENING OF THE 26TH AFTER THE INJECTION. WOKE UP ON THE 27TH AROUND 9:30 AM WITH MY LIPS AND FACE FEELING STRANGE. APPROXIMATELY 11 AM FACE FEELING NUMBNESS. WENT TO BED WITH HEADACHE AND NUMBNESS IN FACE. WOKE UP AT 8AM ON 28TH HAVING TROUBLE SPITTING (LIPS NOT WORKING PROPERLY) CALLED MY FAMILY DOCTOR WHO ADVISE I GO TO THE ER. WENT TO THE ER AND WAS EXAMINED BY DR. WHO STATED I HAV BELL'S PALSY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: EXAMINATION BY DR ON 10/28 APPROXIMATELY 10AM. HE STATED MY RIGHT SIDE OF MY FACE IS PARCIALY PARALIZED TO TO BELL'S PALSY. HE PRESCRIBED ME ARTIFICAL TEARS, PREDNINSON 20MG AND VALACYCLOVIR 1000MG
Aktuelle Erkrankungen: NONE
Vorgeschichte: ATHSMA; LOWER BACK PAIN; SCIATICA LEFT LEG
Andere Medikamente: OLMESARTAN-AMLODIPIN-HCTHIAZID 40-10-25; METOPROLOS SUCCINATE 100 MG; ALLOPURINOL 300 MG; CYLOBENZAPRINE 5MG WHEN NEEDED
Allergien: NONE
Vorherige Impfungen: -

VAERS 1825863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

schwer

Staat: NY
Alter: 31,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest pain Condition aggravated Mental impairment Muscle tightness Myocarditis Nausea Stress Syncope Vomiting

Symptomtext

Return of myocarditis and syncope (dull chest pain continuously abs tight stabbing pain attacks a few times daily from the second day 11/10/2021- continues til now (28/10/2021) Severe nausea (near constant lasting from the night of the injection until now - over 18 days- low rare is constant and several times each day I feel so nauseous I am faint ) and vomiting- for reference it is extremely unusual for me to vomit even with severe nausea. There has also been reduced capacity to think clearly and exaxustion but this is probably from the stress of the above and not independently correlated to the vaccine (I don?t have health insurance and so cannot go to doctor for care about this)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Venous insufficiency, chronic bradycardia, tachycardia, spyncopip and edema, intermittent myocarditis and pericarditis that had been gone for 4 years (first instance was at age 17 - that led to two cardiac incidents one in which no heart rate was detected - but resuscitation was not necessarily after this this flatline. Also autoimmune skin and eye issues around ecsema along with endometriosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: I had autoimmune (ecsema) flare following the Gaurdisl vaccine in 2007

VAERS 1814193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 24.10.2021
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

Computerised tomogram thorax Differential white blood cell count Dizziness Electrocardiogram normal Fatigue Feeling abnormal Fibrin D dimer Full blood count Loss of consciousness Movement disorder Pyrexia

Symptomtext

High fever, some dizziness, felt really awful, fatigue, couldn't get out of bed, lost consciousness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: CBC and differential for fainting, fatigue - 10/21/2021 D-Dimer, quantitative for fainting, fatigue - 10/21/2021 ECG 12 lead for fainting - 10/21/2021 - result normal CTA-Chest with contrast - 10/22/2021 - result negative
Aktuelle Erkrankungen: slight congestion in nose and ears
Vorgeschichte: IBS
Andere Medikamente: multivitamin, aspirin, calcium, Vitamin D3, Red Yeast Rice, Zinc
Allergien: none known
Vorherige Impfungen: Fatigue, chills; age 74, PfizerNBioTech vaccine 2/21/2021 and 3/14/2021

VAERS 1813771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: LA
Alter: 55,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Brain natriuretic peptide increased Cardiomegaly Chest X-ray abnormal Condition aggravated Dyspnoea Dyspnoea exertional Electrocardiogram T wave abnormal Electrocardiogram abnormal Gait inability Heart rate abnormal Intensive care Pain SARS-CoV-2 test negative

Symptomtext

From Provider H&P: "Patient is a 55 year old woman who presented with dyspnea on exertion for one month that worsened acutely today. Patient was admitted here in September with rapid atrial fibrillation and started on metoprolol XL 100 mg daily. She was rate controlled on discharge. Today she did not take her metoprolol before arriving here for work and was so short of breath she could not walk so presented to the ED where her HR was in the 140's. She was given IV metoprolol without improvement and has been started on a diltiazem drip with improvement in HR to around 110. Patient reports she is also aching all over and believes that is due to her second COVID vaccination that she received yesterday. Her labs are at baseline today. She is being admitted to the ICU on the diltiazem drip."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: BNP elevated at 240 pg/mL Covid SARs swab negative Chest X-ray: 1. No acute cardiopulmonary abnormality. 2. Cardiomegaly. EKG: Atrial fibrillation with rapid ventricular response; T wave abnormality, consider inferior ischemia; Abnormal ECG
Aktuelle Erkrankungen: "presented with dyspnea on exertion for one month that worsened acutely today"
Vorgeschichte: ? Chronic low back pain ? DDD (degenerative disc disease), lumbosacral 8/27/2020 ? Essential hypertension 12/9/2019 ? Eye injury right eye vision deficit ? Fibroids ? Hypertension ? Mild intermittent asthma without complication 3/13/2019 Overview: ? Morbid obesity ? OSA (obstructive sleep apnea) ? Paroxysmal atrial fibrillation ? Prediabetes ? Shoulder tendonitis, left ? Umbilical hernia without obstruction and without gangrene 5/3/2018 ? Ventral hernia with obstruction and without gangrene 9/28/2017
Andere Medikamente: ? albuterol (PROVENTIL/VENTOLIN HFA) 90 mcg/actuation inhaler Inhale 1 puff into the lungs every 4 (four) hours as needed for Wheezing or Shortness of Breath. ? amLODIPine (NORVASC) 10 MG tablet Take 1 tablet (10 mg total) by mouth once dai
Allergien: CEPHALEXIN; CLINDAMYCIN; IODIDES; IODINATED CONTRAST MEDIA; IODINE AND IODIDE CONTAINING PRODUCTS; NEOMYCIN-BACITRACIN-POLYMYXIN; SHELLFISH CONTAINING PRODUCTS; SULFAMETHOXAZOLE-TRIMETHOPRIM
Vorherige Impfungen: -

VAERS 1813547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NC
Alter: 56,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Disorientation Electric shock sensation Feeling abnormal Hypersomnia Mobility decreased Myalgia Pain Pyrexia

Symptomtext

I woke up around 3am and was extremely disoriented and feverish. I ached all over. I could not straighten my right leg to get off the bed. It felt like electricity surging thru it. Everytime i tried to straighten right leg, it felt as though something inside my inner right thigh would snap into. It lasted about 20 minutes until i was finally able to stand. I slept for 48 hours straight without food, beverage, medications. Missed 2 days of work. After the 48 hr mark, the brain fog and muscle aches slowly started easing off. I was nearly back to normal on 3rd day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: No medical treatment sought
Aktuelle Erkrankungen: Chronic joint pain, finished 12 weeks of epsclusa mid september 2021 for hep c
Vorgeschichte: Hep c for 20 years, now non detectable
Andere Medikamente: Celebrex, senna laxative, aleve, osteo biflex
Allergien: Just seasonal allergies
Vorherige Impfungen: -

VAERS 1808086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CT
Alter: 23,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Speech disorder Syncope

Symptomtext

Patient experienced syncopy within 15 to 30 seconds after vaccine (pfizer ) administration next patient was unable to respond noticed gargling but couldnt speak I administered an epipen and within seconds responded and alert . EMT/Perimedics came and brought her to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A/
Andere Medikamente: N/A
Allergien: Stated allergy to cocnut
Vorherige Impfungen: -

VAERS 1804731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: WA
Alter: 29,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / AR

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

Presyncope

Symptomtext

vasovagal reaction

Weitere VAERSDATA-Felder

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

VAERS 1804287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: AL
Alter: 14,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Inappropriate schedule of product administration Myoclonus Syncope

Symptomtext

Patient received 4 vaccines in this order: Pfizer BioNtech and fluzone quad in the right deltoid, then Adacel followed by Gardarsil-9 in the left deltoid. Within one minute of final vaccine administration patient had a syncopal episode while seated that involved myoclonus (aproximately 10 seconds). Patient regained consciousness and remained seated. Patient was dizzy for approximately 5 minutes. An ice pack was applied to the back of the neck while they drank a refrigerated fruit smoothie beverage. Patient recovered fully by the end of the15 minute post vaccine observation period. No other side effects or injuries were noted.

Weitere VAERSDATA-Felder

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

VAERS 1803852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: MA
Alter: 13,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Nausea Syncope Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Nausea-Mild, Systemic: Vomiting-Mild, Additional Details: Approximately 2-3min after injection, patient briefly fainted then became concious and experienced nausea/vomiting. Called paramedic, but the vitals were normal and patient didn't use emergency service. Called mother about 1-2 hours later at home, and patient eating, drinking and doing ok.

Weitere VAERSDATA-Felder

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

VAERS 1801016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: UT
Alter: 13,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Blindness Cold sweat Headache Loss of consciousness Pyrexia

Symptomtext

Pt.'s Mother states that after receiving the 2nd dose of Phizer 10/13/2021, started experiencing symptoms 10/14/2021 of fever, cold-sweats, loss of consciousness, and loss of vision. Came to with headache and fever, 10/14/2021 Primary visit with recommendations of Ibuprofen for fever and no Follow-Up of "Booster". Symptoms have subsided.

Weitere VAERSDATA-Felder

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

VAERS 1799143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: ND
Alter: 40,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Electrocardiogram Syncope

Symptomtext

Multiple fainting episodes when getting up during the night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Blood work, EKG, IV of fluids
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control Multi vitamin Generic lexapro Magnesium
Allergien: None
Vorherige Impfungen: -

VAERS 1795172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 18.10.2021
Impfdatum: 17.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Confusional state Dizziness Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Chills-Mild, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Hypotension-Mild, Systemic: Weakness-Mild, Additional Details: PT fainted for 1 second and regaine consciousness right away. he declined 911/paramedics and asked for water and something to fan himself with. pts bp taken was 92/68 , pusle 69. pt stated his level of uncomfortability was 10 (worse) to 2,4, then 1. dad/sis came pick him up after monitoring him for 30 mins

Weitere VAERSDATA-Felder

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

VAERS 1794281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: FL
Alter: 38,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 17.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

patient fainted while waiting on the post vaccination area

Weitere VAERSDATA-Felder

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

VAERS 1793868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: MO
Alter: 60,0
Geschlecht: M
Eingang: 16.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / RA

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

Anaphylactic reaction Chest discomfort Pharyngeal swelling Tonsillar hypertrophy

Symptomtext

Anaphylaxis or anaphylactic reaction started 5 to 10 minutes after injection. Sides, tonsil region and back of throat swelling. Duration of event 30 minutes. Pressure on right side of chest started approximately 4 hours after injection. Duration periodic over the next 13 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Medoxomil (blood pressure)
Allergien: Sulfer based medicaton
Vorherige Impfungen: -

VAERS 1789167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 15.10.2021
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: ja

Chest discomfort Cold sweat Loss of consciousness Pallor Seizure

Symptomtext

Ten minutes after getting the vaccine on the left deltoid, patient became unconscious for about 2 mins. Patient was seated in the pharmacy observation area and while he was unconscious had a very short seizure with head movement and arm movement (arm rotated clockwise and fully locked in an open position). Patient gained consciousness in 2 mins after which looked pale, clammy and had a little bit of chest tightness. After continuing to wait and rest for about another 20 mins, patient felt okay and was ready to leave. Paramedics were called initially but patient refused their service since he felt better.

Weitere VAERSDATA-Felder

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

VAERS 1788489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CO
Alter: 34,0
Geschlecht: M
Eingang: 15.10.2021
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: ja Erholt: nein

Chills Dizziness Feeling cold Flushing Hyperhidrosis Hypopnoea Loss of consciousness Nausea Pain Syncope Tremor Unresponsive to stimuli Vision blurred Visual impairment Vomiting

Symptomtext

Systemic: Body Aches Generalized-Mild, Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Mild, Systemic: Nausea-Severe, Systemic: Visual Changes/Disturbances-Severe, Systemic: Vomiting-Medium, Additional Details: Customer sitting next to the patient came to the pharmacist and reported a man had passed out. Rph went over to examine the patient. Patient was unresponsive apon arrival. Pulse 54, shallow breathing. Patient started to regain consciousness. Patient was shaking, sweating, cold, and vomiting. Pt stated "very nauseous, blurred vision, no trouble breathing." Pt symptoms were not resolving after a few minutes pass. Rph instrcuted tech to call 911. Rph waited with the patient until EMS arrived.

Weitere VAERSDATA-Felder

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

VAERS 1788447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 15.10.2021
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: ja Erholt: nein

Bell's palsy Hypoaesthesia Injection site pain Pain

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Bell's Palsy-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Additional Details: Patient returned approximately 1 hour after receiving Pfizer booster complaining of pain radiating from inject site up into left side of face. Advised to seek immediate medical attention. Returned with MD orders for Medrol dose pack.

Weitere VAERSDATA-Felder

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

VAERS 1785298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: FL
Alter: 26,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
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 Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient fainted while immunizer was giving vaccine to another patient. Patient's friend found him on the floor while she went to purchase water. Patient recovered and was conscious when Immunizer came out. Offered water and food because patient said he felt light headed. Did not call EMT. Patient left after few minutes when immunizer went out to check,

Weitere VAERSDATA-Felder

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

VAERS 1783178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient received the immunization. After about 5 minutes he felt dizzy and passed out. He woke right back up and was able to sit in a chair to be observed for 30 minutes.

Weitere VAERSDATA-Felder

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

VAERS 1782249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: GA
Alter: 23,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Anxiety Chills Dysphagia Feeling cold Throat tightness

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Chills-Mild, Additional Details: tightness started 30 minutes after reaction--pt received epi 3 minutes after reaction. Tightness gradually emerged, pt felt very cool. Sx subside after epipen given. Pulse read 98 bpm, pt has anxiety and started to feel anxious. Called 911--paramedic accessed. After assessment recommend to transport through ambulance but patient refused.

Weitere VAERSDATA-Felder

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

VAERS 1780791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Confusional state Dizziness Dyspnoea Hallucination Immediate post-injection reaction Injection site erythema Injection site pain Injection site swelling Nausea Pallor Presyncope Skin discolouration Speech disorder Vomiting

Symptomtext

Immediate Extreme dizziness and confusion Faintness, nausea, vomiting, hallucinations, restricted breathing, pale and discolored. Unable to speak and not able to think straight. Called 911 parademics

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Vitals, oxygen levels blood. Blood sugar. Normal .
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1780791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / -

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

Confusional state Dizziness Dyspnoea Hallucination Immediate post-injection reaction Injection site erythema Injection site pain Injection site swelling Nausea Pallor Presyncope Skin discolouration Speech disorder Vomiting

Symptomtext

Immediate Extreme dizziness and confusion Faintness, nausea, vomiting, hallucinations, restricted breathing, pale and discolored. Unable to speak and not able to think straight. Called 911 parademics

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Vitals, oxygen levels blood. Blood sugar. Normal .
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1778828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: NJ
Alter: 61,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 10.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Headache Pyrexia Sleep disorder Syncope

Symptomtext

The day after the shot, I developed a fever of 102.4. During the night, I developed a headache so bad I couldn't sleep. When I got up to take Tylenol, I fainted on the bedroom floor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Fainting the DAY AFTER receiving Pfizer Covid-19 vaccine shot #2.

VAERS 1775842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient fainted 10 to 15 minutes after receiving COVID vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1775838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: CA
Alter: 15,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 10.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose Dizziness Syncope

Symptomtext

Patient fainted after receiving COVID vaccine. Patients states feeling dizzy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: BP monitoring and blood glucose monitor
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None
Allergien: None reported
Vorherige Impfungen: -

VAERS 1768798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

schwer

Staat: CT
Alter: 69,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Mydriasis Skin warm

Symptomtext

During administration, patient jumped away from the needle, she felt like fainting. Proceeded to black out. Patient was warm to touch, sweating, eyes dilated. After about 30 minutes of laying on her side on the floor she started to feel better. She was capable of walking out to the car by herself.

Weitere VAERSDATA-Felder

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

VAERS 1765603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

schwer

Staat: WI
Alter: 15,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness Syncope Urinary incontinence

Symptomtext

Within 1 minute of receiving the vaccine, the patient lost consciousness & urinated herself. Within 1 minute she regained consciousness. Her vitals signs were normal after fainting & 30 min after vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2726704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 71,0
Geschlecht: M
Eingang: 20.12.2023
Impfdatum: 19.03.2021
Beginn: 21.08.2023
Tage bis Beginn: 885,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Asthenia COVID-19 COVID-19 pneumonia Cardiac failure acute Diarrhoea Dizziness Dyspnoea Fall Lethargy Respiratory depression Respiratory failure SARS-CoV-2 test positive Tachypnoea

Symptomtext

Reported Symptoms: 10012727:DIARRHEA; 10013573:DIZZINESS; 10038436:RENAL FAILURE ACUTE; 10038678:RESPIRATORY DEPRESSION; 10043088:TACHYPNEA; 10084380:COVID-19 PNEUMONIA; Narrative: Patient received five doses of Pfizer COVID 19 vaccine (Mar/Apr/Oct 21/Mar/Oct 22). The patient presented to the ED on 21 August 2023 with shortness of breath, falling, diarrhea, and weakness. The patient tested positive for COVID 19 on 21 August 2023. The patient was admitted with acute covid 19 infection and acute heart failure. The patient was treated with supportive care and furosemide. The patient was discharged on 23 August 23, but the patient was readmitted on 25 August 2023 with increased lethargy and COVID pneumonia, acute renal injury, and respiratory failure. The patient was treated appropriately and discharged on 6 Sep 23 in stable condition. Reported per EUA. Other Relevant HX: Other: covid pneumonia

Weitere VAERSDATA-Felder

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

VAERS 2725814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 82,0
Geschlecht: M
Eingang: 20.12.2023
Impfdatum: 28.07.2022
Beginn: 18.12.2023
Tage bis Beginn: 508,0
Dosis: 3
Route/Site: IM / LA

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

Chills Cough Diarrhoea Dyspnoea Pain Pyrexia SARS-CoV-2 test

Symptomtext

Cough, dyspnea, body aches, diarrhea, fever, chills

Weitere VAERSDATA-Felder

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

VAERS 2707249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 31.10.2023
Impfdatum: 20.10.2021
Beginn: 29.09.2023
Tage bis Beginn: 709,0
Dosis: 3
Route/Site: - / -

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

Asthenia Atelectasis Blood creatine phosphokinase increased Blood culture negative COVID-19 Cough Dysphagia Fluid intake reduced Infection Leukocytosis COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram neck Computerised tomogram normal Condition aggravated Mobility decreased Oropharyngeal pain Productive cough

Symptomtext

HMS DISCHARGE SUMMARY -- Hospital Admitted: 9/29/2023 Discharge Date: 10/02/23 PCP Handoff Recommended Outpatient Testing o None Results Pending At Discharge o None Clinical Summary Patient is a 72 y.o. male patient of MD with history of Parkinson's disease, hyperlipidemia presented to Hospital with cough, sore throat for a few days and severe weakness that started earlier today. Found to be COVID positive at PCP office. Found to have elevated CPK likely due to underlying COVID infection and decreased fluid intake. CPK trending down with IV fluids. Sore throat resolved. Read by therapy with no further recommendations. To be discharged home with outpatient follow-up Covid-19 Virus Infection with pneumonia Date of onset of symptoms: 9/27/23 Symptoms present on admission: Cough, sore throat Date of covid positive test: 9/29/23 Imaging: Chest x-ray 9/29 with minimal atelectasis of the left lung base Oxygen requirements on admission: None Current oxygen requirements: room air Medical therapy: Continued outpatient Paxlovid Anticipated special isolation end date: 10/7/23 Possible aspiration pneumonia/superimposed bacterial pneumonia Sepsis, POA (tachycardia, tachypnea, leukocytosis) Patient says he has some issues with swallowing related to the Parkinson's disease Weakness has been much worse due to the COVID Significant productive cough, sepsis on presentation Chest x-ray without any infiltrate CT soft tissue neck done for severe sore throat without any acute findings. Blood cultures no growth today SLP consulted for swallow evaluation-appreciate recommendations. No further speech therapy needs or diet modifications. Rhabdomyolysis Weakness Severe weakness that led to patient not being able to get up from the floor earlier on the day of admission CPK 18K on admission Appreciate neurology follow-up. PT/OT Parkinson's disease Continue home carbidopa levodopa, Artane Patient has had gradual weakness over the last few weeks. Appreciate neurology follow-up , continue home medications and follow-up with neurology as outpatient. Had brief episodes of altered state while inpatient likely due to acute infection versus steroid use. Symptoms now resolved Outpatient follow-up with neurology

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2683628

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FF2590

moderat

Staat: GA
Alter: 54,0
Geschlecht: F
Eingang: 19.09.2023
Impfdatum: 10.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / RA

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

Arrhythmia Cardiac monitoring Cardiac stress test Electrocardiogram Heart rate increased Palpitations

Symptomtext

I would like to report a possible adverse effect of Covid 19 because I have never experienced this kind of effect before until after COVID-19. I experienced an abnormal heart palpation or abnormal heart rhythm like no other palpations. I have experienced abnormal palpations before but sporadically. This recent heartbeat was fast and unusual. I was placed on another pill called Bisoprolol which I never had to take before and I am concerned about this effect because it appears I may have to take this medicine forever, and I don't want to take it at all. I want to know why there is a new fast palpation instead of being put on medications and left without any answers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: ECG, heart monitor, stress test
Aktuelle Erkrankungen: HBP
Vorgeschichte: HBP
Andere Medikamente: BP meds
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2660895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 26.07.2023
Impfdatum: 17.10.2021
Beginn: 08.01.2022
Tage bis Beginn: 83,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Dehydration Hyperkalaemia Hypophagia

Symptomtext

Presented with acute hyperkalemia related to dehydration and poor intake nephro consulted hyperkalemia treated. Incidental finding of COVID-19 infection and asymptomatic

Weitere VAERSDATA-Felder

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

VAERS 2634830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: VA
Alter: 12,0
Geschlecht: M
Eingang: 22.05.2023
Impfdatum: 11.10.2021
Beginn: 01.09.2022
Tage bis Beginn: 325,0
Dosis: 1
Route/Site: SYR / UN

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

Cardiac disorder Cardiac imaging procedure abnormal Cardiac stress test Cardiomyopathy Electrocardiogram Electrocardiogram ambulatory Hypertension

Symptomtext

Cardiomyopathy is being diagnosed - MRI confirms thickening of heart. Symptoms included high blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: EKG, ECG, MRI, Stress test, Holter monitoring completed at least once in the last 1.5 years
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2632539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 16.05.2023
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / AR

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

Audiogram abnormal Deafness bilateral Deafness neurosensory Dizziness Dizziness postural Mobility decreased Nausea Sleep disorder Tinnitus Vertigo

Symptomtext

I woke up at 2 AM on 10/23/2021 with severe vertigo; the room was spinning and I could not move my head without a feeling of dizziness and nausea. Any time I attempted to move I felt as if I was going to either throw up or pass out. After sitting on the bathroom floor for an hour I moved to sitting at the kitchen table with my head on the table. I stayed there for the next several hours, covered in a blanket. The sense of severe vertigo passed by 6 AM or so and I returned to bed. I still had mild vertigo for about a week and this was then followed by mild ringing in my right ear which progressed to moderate ringing in both ears. The bilateral tinnitus continues to this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 5/4/2022: Audiogram: BIlateral mild to moderate sensorineural hearing loss 3-8 kHz.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2616308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AR
Alter: 52,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 31.12.2021
Beginn: 05.06.2022
Tage bis Beginn: 156,0
Dosis: 3
Route/Site: IM / LA

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

Brain fog Bronchial disorder Bronchoscopy abnormal COVID-19 Chest X-ray abnormal Chest discomfort Electrocardiogram abnormal Fatigue Magnetic resonance imaging abnormal Malaise Pneumonia Post-acute COVID-19 syndrome Pulmonary function test abnormal SARS-CoV-2 test positive

Symptomtext

I ended up feeling sick and the next day I went into my doctor, and I took a COVID-19 PCR test, and it was positive. I was put on Paxlovid, and I really did not feel that bad while, I was positive. About three weeks later I had this heaviness in my chest, and I went back to my doctor, and I had an Xray in my chest and I had pneumonia. I ended up on a steroid. I was diagnosed with long COVID. I have an Bronchoscope, an MRI, and EKG, a Pulmonary Function Lab; they have found damage to my bronchial tubes but nothing conclusive other than that. I have brain fog and really can only do one thing a day and am always just tired and exhausted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: COVID-19 PCR Test; Bronchoscope; MRI; X-ray; Pulmonary Function La; EKG
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec; Levothyroxine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2596928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 47,0
Geschlecht: M
Eingang: 15.03.2023
Impfdatum: 13.10.2021
Beginn: 01.12.2021
Tage bis Beginn: 49,0
Dosis: UNK
Route/Site: - / -

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

Back pain Blindness Coccydynia Corrective lens user Dysstasia Magnetic resonance imaging Mobility decreased Pain Spinal X-ray

Symptomtext

I started losing my eye site and I now have to wear corrective lenses. Severe lower back/tailbone pain that started about 5 months after the second shot. Not able to sit for long periods of time. Very painful to stand from a sitting position.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-Rays for my back in 2022 and 2023, MRI in 2023. Vision test in 2022.
Aktuelle Erkrankungen: n/a
Vorgeschichte: Asthma, sleep apnea, issues sitting and standing from a sitting position that started in 2022 right after the vaccine
Andere Medikamente: ATORVASTATIN, CETIRIZINE, OMEPRAZOLE, FLUTICASONE, FISH OIL
Allergien: Unknown food
Vorherige Impfungen: -

VAERS 2584081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 19.02.2023
Impfdatum: 09.11.2021
Beginn: 23.01.2023
Tage bis Beginn: 440,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary normal Asthenia Blood sodium decreased COVID-19 Chronic obstructive pulmonary disease Chronic respiratory failure Condition aggravated Dyspnoea Fatigue Gait disturbance Hodgkin's disease Hyperglycaemia Hypertension Laboratory test abnormal Loss of personal independence in daily activities Malnutrition Obstructive sleep apnoea syndrome Respiratory failure

Symptomtext

Patient is 87 years old with past medical history of COPD, diabetes, GERD, hyperlipidemia, hypertension, obstructive sleep apnea presented to the hospital with a chief complaint of shortness of breath associated with fatigue and weakness. Patient had a recent admission to the hospital January 17 for COPD exacerbation. He was discharged home on oxygen. He has been encountering difficulty ambulating at home and fulfilling daily needs. Otherwise patient has no fever, chills, chest pain, abdominal pain, nausea, vomiting, diarrhea, constipation, difficulty urination, dysuria. In the ED, patient had CT angio of the chest which was negative for pulmonary embolism. Labs significant for mildly low sodium level. Clinical Summary Patient was admitted to the medical surgical unit due to chronic respiratory failure related to COPD exacerbation secondary to COVID-19 infection. He did not meet criteria for remdesivir. He was treated with steroids, azithromycin, and bronchodilators. On hospitalization day 3 patient was feeling improved and agreeable to discharge. He was assessed on his new baseline oxygen of 2 L and did well. He did not require further titration of his home oxygen. Notably, he did have an element of hyperglycemia during hospitalization related to steroid use. He is discharged on short course of sliding scale insulin while on steroids. He has a glucometer at home and understands how to check his glucose and insulin administration which was reinforced by myself and nursing. He has been started on a maintenance inhaler. He has an appointment with his primary care doctor on Monday. Patient denied further questions or concerns and was agreeable for discharge. Home health referrals been placed. Discharge diagnosis Acute exacerbation of COPD COVID-19 infection Chronic hypoxic respiratory failure Debility/generalized weakness Type 2 diabetes Hypertension Hodgkin's lymphoma Obstructive sleep apnea COVID-19 infection Protein calorie malnutrition next

Weitere VAERSDATA-Felder

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

VAERS 2577225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 93,0
Geschlecht: M
Eingang: 07.02.2023
Impfdatum: 02.11.2021
Beginn: 11.01.2023
Tage bis Beginn: 435,0
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

01/11/23 presents to ED for "shortness of breath". PMHx of "COPD, diabetes, hypertension, CVA, arrhythmia"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/11/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 26.10.2021
Beginn: 05.01.2023
Tage bis Beginn: 436,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Dyspnoea Laboratory test abnormal SARS-CoV-2 test positive

Symptomtext

01/05/23 presents to ED for "abnormal labs" "shortness of breath". PMHx of "chronic anemia, diabetes, hypertension"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/05/23 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2561352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 02.02.2021
Beginn: 18.12.2022
Tage bis Beginn: 684,0
Dosis: UNK
Route/Site: - / -

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

Asthenia COVID-19 Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

12/18/22 presents to EC ED for "weakness, fatigue, shortness of breath". PMHx of "CAD CHF A. fib, recently diagnosed DVT, PE on Eliquis, abdominal aortic aneurysm, hypertension hyperlipidemia, COPD, NPH GERD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/18/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 39,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / -

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

Autonomic nervous system imbalance Back pain Blood calcium Blood creatine phosphokinase Dysphagia Dyspnoea Electrocardiogram Erythema Fatigue Feeling hot Hyperventilation Hypoaesthesia Immediate post-injection reaction Immunology test Laboratory test Magnetic resonance imaging head Magnetic resonance imaging spinal Metabolic function test

Symptomtext

I immediately had numbness and tingling in my hands, feet, scalp, and face. I felt like I was having difficulty breathing and my face was very red and hot. After seeing my doctor and ruling out a histamine issue and asthma, I was diagnosed with hyperventilation syndrome and a vestibular ocular reflex dysfunction. I also had a difficult time swallowing. I saw a speech therapist and most of the throat discomfort has resolved. I still have heart palpitations, tingling/numbness, muscle twitches and spasms, muscle aches, general fatigue and back/neck pain, and difficulty regulating my breathing. I have been seeing a Butyeko breathing coach which has helped. I have dysautonomia as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 5/3/22 Breathing evaluation with Breathing Occupational Therapist 5/24/22 comprehensive metabolic panel 11/26/21 comprehensive metabolic panel 05/5/22 autoimmune panel 09/29/22 creatine kinase 12/13/22 voltage gated calcium 12/13/22 calcium level 12/13/22 B Vitamins 12/28/22 MRI of brain and spinal cord 01/09/23 EKG 1/11/23
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: prenatal vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 2557655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Body temperature increased COVID-19 pneumonia Dysstasia Fall Respiratory failure

Symptomtext

Patient brought to the ED by EMS on 11/2 for evaluation of a fall. The patient's wife found patient lying on the floor next to his bed, possibly down for two hours. Patient reported he rolled out of bed onto the floor. Patient was unable to get up, so EMS was called. While in the ED, he was found to have a temperature of 100.5 F and O2 sats around 89%. Additionally, his COVID PCR test came back positive in the ED. Patient was admitted 11/2 - 11/4 for evaluation of the fall/generalized weakness and mild hypoxic respiratory failure secondary to COVID-19 pneumonia. Patient was placed on 2L O2 but was quickly weaned off oxygen. He has received the primary COVID vaccine series and two boosters.

Weitere VAERSDATA-Felder

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

VAERS 2543783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 69,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 23.09.2022
Beginn: 16.12.2022
Tage bis Beginn: 84,0
Dosis: 5
Route/Site: SYR / AR

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

Blood test normal Chest X-ray normal Chest pain Electrocardiogram normal Pain Toothache

Symptomtext

Two months after vaccine started feeling dull tooth pain every 30 seconds on and off for a half hour; After 40 minutes back of chest started hurting; Went to urgent care and was given an EKG, chest X-ray and had blood work; No findings.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG negative; Chest X-ray negative; blood work.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism; High Cholesterol; Arthritis.
Andere Medikamente: Levothyroxine; simvastatin; coQ10; glucosamine chondroitin; vitamin B; vitamin D3; multivitamin; fish oil; turmeric.
Allergien: Cats; codeine; MOTRIN; erythromycin; naproxen; dust.
Vorherige Impfungen: -

VAERS 2536166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 60,0
Geschlecht: F
Eingang: 18.12.2022
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Heart rate increased Pain Tachycardia

Symptomtext

Elevated heart rate over 110 for 48 hours constant post vaccine. Body aches but mostly tachycardia was issue. Continues randomly post vaccine and has never neen a problem prior to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tylenol ibuorofen zinc
Allergien: None
Vorherige Impfungen: -

VAERS 2533184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 20.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia Atelectasis Blood creatinine increased Blood magnesium normal Blood urea increased COVID-19 Chest X-ray abnormal Chills Chronic kidney disease Condition aggravated Cough Diuretic therapy Dyspnoea Fatigue Fluid intake reduced Full blood count normal Influenza virus test negative

Symptomtext

The patient is a 91 y male presented to the ED with complaints of fatigue, chills and increased cough. Spoke with the patient's daughter over the phone for the patient's history. The patient comes today from his nursing home where he had a positive COVID-19 test yesterday. 2 of the staff at the home had recently tested positive. The patient has had generalized weakness and fatigue over the last few days. He has a chronic cough which has become productive. The patient is otherwise symptomatic. The patient's daughter stated that they wanted a confirmation of his COVID-19 through a PCR test, as he had his booster vaccination last week. COVID-19, RSV and Influenza tests and a chest x-ray were ordered for evaluation of the patient's fatigue and productive cough. An IV was established. The chest x-ray was reviewed by the ED physician and read by the radiologist showing mild left basilar atelectasis. COVID-19 was positive, RSV and influenza were negative. 1420: Spoke with the patient's daughter, who was informed on the risks and benefits of MAB treatment. She agreed to giving her father the treatment. The patient was given 25 mg Benadryl IV, 40 mg Solumedrol IV, 0.3 mg Epinephrine IM, 4 mg Zofran IV for nausea and 600 mg Humibid PO. Patient tested positive for COVID-19 with symptom onset in the last 10 days and is at least 12 years old and 40 kg. The patient still has symptoms but doesn't need hospitalization or increased oxygen requirements. The patient does meet eligibility requirement because Patient has COPD and is over 65 years of age which makes them higher risk for complex disease and mAB was recommended. Benefits were reviewed with the patient that includes an estimated 60% decrease in hospitalization and death. Risks were reviewed with patient which includes a reaction to the infusion, which is uncommon and would be treated at the time of the infusion if needed. The patient does consent to receive the monoclonal antibody infusion. The patient was educated that the monoclonal antibodies are a collection of antibodies specifically designed to target the COVID-19 virus. It is used to help the immune system fight off COVID more quickly and make hospitalization and severe illness less likely. There is no direct charge to the patient. A vaccinated patient can receive this infusion without waiting. If the patient is not yet vaccinated, they will wait 90 days from the infusion before getting vaccinated. If getting the infusion, the patient will be scheduled for an outpatient infusion to be administered. The patient was instructed to tell the triage nurse ?they have COVID and were sent from the Hotline to get a COVID antibody infusion and are not to be checked in as a regular patient.? The patient was given a time to arrive and the charge nurse was notified of the patient. The patient is aware it will take about 2-3 hours including prep time and observation afterwards. 1559: Spoke with nursing home staff, who stated that he will be under constant observation and will be in isolation. The patient was updated on his results and the plan of care. Prescription for Mucinex was provided for congestion. The patient was advised to follow up with his primary care physician, Dr. for reevaluation, and to contact their office to schedule an appointment. Return precautions are provided, and he will return here immediately with any new or worsening symptoms. The patient verbalized understanding and agreement, and was discharged home in stable condition. On 11/16/2021 Patient presented again to the to the emergency department with chief complaint of concern for fluctuating pulse oxygenation at the outlying facility. Per EMR there was no reported number associated with the fluctuations. Patient does state that he feels short of breath but denies any additional symptoms. He has had breakfast this morning but has not been drinking as much fluids as he reports he should. He denies any fever, chest pain, nausea or vomiting. He was seen here on 11/26/2021 where diagnosis was confirmed. CMP did not show any significant electrolyte abnormalities with an elevation of his BUN and creatinine to 66 (48) and 3 (1.7) which shows marked significant elevation. For this acute kidney injury do believe he should be admitted for close rehydration and re-evaluation. Troponin was minimally elevated at 0.027 which could likely be because of the acute kidney injury. CBC is unremarkable with no signs of acute anemia or leukocytosis. Magnesium was within normal limits. Procalcitonin was essentially negative. The chest x-ray was reviewed by the ED physician showed no acute pneumonia. Patient to be admitted for further management of AKI on CKD 3. Patient remained stable on RA. Diuretics were on hold and Cr improved to 1.8. Patient to resume lasix on discharge but to discontinue other diuretics. SLP evaluated patient for dysphagia and recommended patient to be on pureed solid and thin liquid diet with meds crushed. PT/OT evaluated patient and recommending post acute therapy. Followed for DC planning and patient was accepted. Patient stable for DC to SNF. Needs f/u with PCP in 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 15,0
Labordaten: Positive COVID 19 test 11/26-11/28/21.
Aktuelle Erkrankungen: -
Vorgeschichte: 9/14/16 Symptomatic cholelithiasis 11-6-15 Calculus of bile duct 8-2015 Pneumonia, organism unspecified(486) Date Unknown Aneurysm of descending thoracic aorta Date Unknown ASHD (arteriosclerotic heart disease) Date Unknown Back pain Date Unknown Bilateral renal cysts Date Unknown CKD (chronic kidney disease) Date Unknown COPD (chronic obstructive pulmonary disease) 2007 about DVT (deep venous thrombosis) Date Unknown GERD (gastroesophageal reflux disease) Date Unknown Hip pain Date Unknown Hypertension Date Unknown Hypothyroid Date Unknown NSTEMI (non-ST elevated myocardial infarction) Date Unknown Pulmonary fibrosis Date Unknown Pulmonary nodule, right
Andere Medikamente: albuterol (VENTOLIN) (2.5 mg/3 mL) 0.083% nebulizer solution albuterol (VENTOLIN) (2.5 mg/3 mL) 0.083% nebulizer solution allopurinol (ZYLOPRIM) 100 MG tablet atorvastatin (LIPITOR) 10 MG tablet Cholecalciferol (VITAMIN D3) 2000 UNIT TABS d
Allergien: Rocephin
Vorherige Impfungen: -

VAERS 2525196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 20.01.2021
Beginn: 24.10.2022
Tage bis Beginn: 642,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Hypoxia Pneumonia aspiration Pyrexia SARS-CoV-2 test positive Sepsis

Symptomtext

Narrative: Patient received four doses COVID 19 vaccine in Jan/Feb/Apr/Oct 2021. The patient tested positive for COVID 19 on 24 Oct 2022. The patient presented to the ED with shortness of breath, cough, and fever. The patient was admitted with aspiration pneumonia, sepsis, and hypoxia. The patient was treated with antibiotics, oxygen, and steroids. The patient was discharged in stable condition on 4 Nov 2022. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2523111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 05.12.2022
Impfdatum: 02.03.2021
Beginn: 28.10.2022
Tage bis Beginn: 605,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Chills Dyspnoea Pyrexia SARS-CoV-2 test positive

Symptomtext

10/28/22 presents to ED for "fever, chills, shortness of breath, weakness". PMHx of "atrial fibrillation, hypertension, hyperlipidemia, hypothyroidism".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 10/29/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2520032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 29.11.2021
Beginn: 01.08.2022
Tage bis Beginn: 245,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Decreased appetite Dyspnoea Fatigue Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I received my first Pfizer booster for COVID-19 on 11/29/2021. In early August 2022, I ended up catching COVID-19. My symptoms were relatively mild. I had fatigue, sore throat, loss of appetite, and headache. The only treatment I received for the virus was monoclonal antibodies. The illness lasted for about a week, and I pretty much resumed my normal activities afterwards, though the sore throat and headache did linger for about a week longer. During my bout with COVID-19, I didn't have any issues with my breathing. However, since having had COVID-19, I have found myself having shortness of breath and a sore throat. These symptoms are not constant, but they do manifest on random occasions. I went to my PCP for some guidance on the matter, and she told me that she didn't really know why I was having these symptoms, but she did advise me to keep an albuterol inhaler on hand. I have had to use the inhaler on occasion, and it usually helps reopen my breathing passages.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Osteoarthritis; Hypertension; High Cholesterol; Bipolar Disorder; Urinary Incontinence; Chronic Pain; Muscle Spasms.
Andere Medikamente: Diltiazem ER; famotidine; oxybutynin; lamotrigine; methadone; lovastatin; omeprazole; topiramate; buspirone; losartan potassium; baclofen; calcium; vitamin B12; multivitamin; lidocaine.
Allergien: Tetracycline; sulfa drugs; codeine; hydrocodone; adhesive tape; milk; peanuts.
Vorherige Impfungen: -

VAERS 2518033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: OH
Alter: 61,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 21.10.2021
Beginn: 01.08.2022
Tage bis Beginn: 284,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation Dyspnoea exertional Echocardiogram Electrocardiogram abnormal Fatigue

Symptomtext

April 2022 I noticed I was getting fatigued much sooner than ever before. By August 2022, I was short of breath after minimal exertion and fatigued after not much physical activity. In September of 2022, I had my annual exam with Medical Center. During my exam, the Dr told me he wanted an EKG after spending a lot of time listening to my heart. The EKG confirmed what he had suspected, there was Arterial Fibrillation. I was given a consult with a Cardiologist and to get an Echocardiogram (ECG) and started on Eliquis. The results of the ECG were not readable do to poor image quality. The diagnosis of A-Fib was confirmed by the Cardiologist on 10/5/2022 and I was advised to continue on Eliquis. advised to follow up with the Medical Center . I made appointments and my Cardiologist appointment is 12/1/2022.

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Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: EKG and 2 ECG's to further explore the condition of my heart and severity of the A-Fib. I have an appointment to discuss results on 12/1/2022. I have no family history of A-Fib.
Aktuelle Erkrankungen: Hypogonadism, Asthma, Seasonal Allergies
Vorgeschichte: Shortness of breath, fatigue began in August 2022.
Andere Medikamente: Montelukast 10mg One tablet daily Testosterone 50mg packet, Apply one packet to each shoulder daily Albuterol Inhaler 200mcg 1-2 puffs every 6 hours as needed for Shortness of Breath (Only as needed) Eliquis 5mg One tablet twice daily (Star
Allergien: No food or drug allergies
Vorherige Impfungen: -

VAERS 2516754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: MI
Alter: 48,0
Geschlecht: F
Eingang: 25.11.2022
Impfdatum: 24.11.2021
Beginn: 30.07.2022
Tage bis Beginn: 248,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

I did not have an adverse reaction to the vaccine. I had a holiday with my family and friends without any problems. After a camping trip with my family in July 2022, I tested positive for COVID-19 on 07/30/2022. I contacted my doctor's office in an email and in database. I had difficulty breathing and congestion. I did not receive a prescription, but I took over the counter medication.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 30JUL2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Migraines; Osteopenia; Hypothyroidism
Andere Medikamente: N/A
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2509467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 19.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: IM / -

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

Autoimmune hypothyroidism Autoimmune thyroiditis Blood pressure abnormal Chest pain Dizziness Dyspnoea Heart rate abnormal Herpes zoster Hypoaesthesia Laboratory test Squamous cell carcinoma of skin Supraventricular tachycardia

Symptomtext

Diagnosed with autoimmune hypothyroidism-Hashimotos on Jan 6, 2022.-Related to immune system Diagnosed with squamous cell skin cancer August 2022-Related to immune system. Diagnosed with shingles Nov 4, 2022 even though I've had 2 shingles vaccines-Related to immune system Cardiac symptoms-SOB, Chest Pain, erratic heart rate and BP, lightheadedness, facial numbness began in Spring of 2022 and intensified in June-September, Diagnosed with SVT but all symptoms not explained.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: Many
Aktuelle Erkrankungen: -
Vorgeschichte: hypoparathyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2489146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 22.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Acupuncture Amenorrhoea Antinuclear antibody Blood test COVID-19 Chest X-ray Computerised tomogram Dyspnoea Erythema Gastric electrical stimulation Gastric emptying study Gastrointestinal disorder Glucocorticoid deficiency Heart rate increased Hormone level abnormal Hyperhidrosis Hypogonadism Impaired gastric emptying

Symptomtext

Four days after booster I had redness in fingers ? red, hardened skin ? and I still have this on my fingers. I also had an itchy scalp with no redness from October 2021 to July 2022. I started having night sweats that drenched the sheets every night and they lasted from October 2021 until August of 2022. COVID-19 and Mononucleosis in January 2022. COVID-19 symptoms were very mild. I was not having my periods since my second dose of Moderna in February of 2021. In January of 2022 we learned of hormonal deficiencies. I had an MRI of my brain to learn more and was diagnosed with Pituitary Micro Adenoma. I saw a rheumatologist and was diagnosed with Anti-Nuclear Antibodies (ANA). This was in April 2022. I was having gastrointestinal issues with regurgitations and was diagnosed with Gastro Perisis in September of 2022. In addition, my heart rate would go very high up to 140 just from standing and 170 when I would go upstairs. I was diagnosed with POTTS by a cardiologist. I saw a pulmonologist for reason of shortness of breath. I began taking Corlanor to reduce tachycardia and responding well. They also found perforation in my nasal septum possibly from COVID-19. There was a 5mm hole that required 7-hour surgery to repair and reconstruct my nose. Acupuncture has resolved night sweats. Electric stimulation and Motegrity for Gastro Paresis. Diagnosis: Long COVID-19; POTTS (Postural Orthostatic Tachycardia Syndrome) ; Gastro Paresis; Hypo Cortosolism; Pituitary Micro Adenoma; Hypogonad Atropric Hypogonadism; Anti-Nuclear Antibodies (ANA)

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Over 100 blood panels; 3 CT scans;6 MRIs; Chest X-Rays; 3 Ultrasounds; Nuclear Gastric Emptying Study; Pulmonary Function Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; ADHD; Depression; Anxiety; PTSD; Endometriosis; Polycystic Ovarian Syndrome; Chronic Active Epstein Barr Virus
Andere Medikamente: Wellbutrin; Adderall; Paxil; Juneau
Allergien: N/A
Vorherige Impfungen: -

VAERS 2481979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 14.10.2021
Beginn: 16.09.2022
Tage bis Beginn: 337,0
Dosis: 3
Route/Site: IM / RA

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

Ageusia Anosmia COVID-19 Discomfort Dysphagia Dyspnoea Feeling abnormal Headache Malaise Mobility decreased Oropharyngeal discomfort Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I was diagnosed on 09/17/2022 with COVID-19 after completing an at home COVID-19 Test. I was quarantined at home for 5 days. I did not feel quite right and when I woke up Saturday morning, that's when I realized I was sick. My fever was 101.3 initially and about an hour later it was up to 103.0. He took me to a doctor after getting the positive result. That did the COVID-19 PCR Test and advised me to get the Monoclonal Infusion Therapy, but I did not take the treatment. I had a terrible sore throat where it was difficult to swallow. I had some difficulty breathing but nothing that was alarming. It just felt like this heaviness so trying to move around was not easy. I lost my taste and smell and ran a fever for about 3 days. I contacted my primary care provider who recommended I take Robitussin DM and take Tylenol. I had a terrible headache. The sore throat eased up but I am still able to feel discomfort. I am still recovering from some symptoms.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 Home -Test 09/17/2022 COVID-19 PCR-Test-09/17/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Crohn's Disease; Depression; Anxiety
Andere Medikamente: Levothyroxine; Wellbutrin; Prilosec; Zofran; Xanax; Trazadone; Zoloft
Allergien: N/A
Vorherige Impfungen: Dose 2-Pfizer-Really sick the next day.

VAERS 2481672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: TN
Alter: 66,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 15.10.2021
Beginn: 15.08.2022
Tage bis Beginn: 304,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Cough Dyspnoea Fatigue Headache Migraine Pyrexia SARS-CoV-2 test positive Sinus headache

Symptomtext

On 08/12/2022 I experienced difficulty breathing, headache, fatigue, low grade fever and cough. I tested positive on the day of my appointment with my doctor on 08/15/2022. My doctor prescribed me with albuterol, dexamethasone for 1 week, and cough medicine promethazine as needed. I have lingering sinus headaches and migraines.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 Test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Depression; Acid reflux
Andere Medikamente: Prozac; Wellbutrin; Lipitor; Gabapentin; Tylenol; Omeprazole;
Allergien: None
Vorherige Impfungen: -

VAERS 2475276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: MI
Alter: 40,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Blood test Cardiac stress test Electrocardiogram Palpitations

Symptomtext

The morning after receiving my third dose, I started to experience heart palpitations. I was thinking that it could be related to POTS, but I was not sure. I contacted a cardiologist through a portal, and they told me to rest and take my medicine. I was diagnosed with A-Fib after visiting the doctor. I do not attribute A-Fib to receiving the vaccine because according to my doctor, I had A-Fib prior to receiving my vaccines.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Blood work; EKG; Stress test
Aktuelle Erkrankungen: No
Vorgeschichte: POTS
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2472914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: CT
Alter: 74,0
Geschlecht: F
Eingang: 09.10.2022
Impfdatum: 19.10.2021
Beginn: 15.02.2022
Tage bis Beginn: 119,0
Dosis: 3
Route/Site: IM / LA

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

Amino acid level Anti-ganglioside antibody negative Blood folate normal Blood magnesium normal Blood test normal Blood thyroid stimulating hormone increased Blood urea nitrogen/creatinine ratio increased Borrelia test negative C-reactive protein normal Computerised tomogram head normal Culture urine negative Differential white blood cell count normal Electrocardiogram normal Electromyogram normal Electrophoresis protein Full blood count normal Humerus fracture Hypoaesthesia

Symptomtext

The symptoms were first noticed in February 2022 but may have been present for longer. The primary symptom is numbness in both feet and a tingling sensation up both legs to just below the knee. I went to Hospital Emergency room on 2/27/2022 because all of a sudden the numbness and tingling traveled up by body and into my face. They did blood work for T4 free, magnesium, a basic metabolic panel, CBC w/auto differential, ecg 12-lead, reflexive urine culture, Urinalysis with reflex to microscopic, CT head without contrast, US Arterial Duplex Leg-Bilateral. Other than Highly sensitive TSH, the results were all negative. I was discharged and referred to a neurologist. My first visit was ordered 4/07/2022 extensive blood work which will be identified in item 19. He also performed or ordered several diagnostic tests to be addressed in item 19. On 6/28/2022 I was again seen in the Emergency Room at Hospital with similar symptoms of numbness and tingling traveling up from my legs into the rest of my body. They tested for TSH (highly sensitive 5.96), Lyme IGG and IGM with reflex to Elisa, Malaria smear, c-reactive protein, Sedimentation rate, automated, comprehensive metabolic panel, CBC w/ auto differential. The Sedimentation rate was slightly elevated at 40. ABS Lymphocytes Auto were slightly low at .91. White blood cell count slightly low at 3.6. BUN/Creatinine Ratio slightly high at 29.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Besides the tests and results at Hospital included in the narrative in #18, Dr. ordered/performed the following labs/tests: On 4/7/2022 the lab work included test for Immuofixation Electrophoresis; Protein Electrophoresis Serum; Free Kappa/Lambda, w/ratio, serum; Ganglioside GD1B Antibody, IGG; Autoimmune Neurology Antibody Comprehensive; Vitamin E; Vitamin B2; Vitamin B12 and Folate; Vitamin B1; Methylmalonic Acid, Serum; Lyme AB IGG/IGM Screen Reflex Western Blot; Test results were all negative. He conducted an EMG on 4/14/2022 and the results were in the normal range. He ordered MRI of the Thoracic Spine without Contrast; result was Thoracic kyphosis. No focal osseous abnormalities, No disc herniation or stenosis. 4/15/2022 MRI of the Cervical Spine without Contrast; result was Developmentally narrow spinal canal. Spondylitic changes throughout the cervical levels. Central and foraminal stenoses throughout cervical levels without cord compression or myelomalacia. 4/15/2022 I saw Dr. on 7/7/2022 for a follow up post the ER visit on 6/28/2022 at Hospital. He ordered an MRI Brain without contrast which was performed on 7/15/2022. The result was stable findings. No active disease. My most recent appointment with Dr. was on 9/6/2022. The final test he can run is an MRI of the Lumbar spine which has been ordered but not performed yet due to a fracture of my left humerus on 9/3/2022. I expect to be able to schedule the test soon. I am reporting this information primarily because the Neurologist has been unable to find any cause or make any diagnosis as to why my feet are numb and my legs tingling. Therefore, I am reporting it as a possible side effect of the Covid vaccine.
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial Fibrilation
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Age 73; 01/26/2021; Covid 19 Pfizer; 1st vaccine in series; severe migraine with Aphasia

VAERS 2472482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: KY
Alter: 50,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 05.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Back pain Inflammation Injected limb mobility decreased Lymphadenopathy Magnetic resonance imaging abnormal Vaginal haemorrhage

Symptomtext

I had a severe lymph node swelling in chest, neck, breast, down to my elbow. I couldn't put my right arm down. I called my doctor to let him know. I had horrific back pain and still going to physical therapy since I had vaccine. I also had vaginal bleeding.

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Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: MRI, Inflammation
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Omeprazole
Allergien: Sulfa drugs
Vorherige Impfungen: Shingles booster, migraine for 24 hrs., fever.

VAERS 2461965

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Staat: RI
Alter: 36,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 11.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Asthenia Chest pain Dyspnoea Fatigue Impaired work ability Laboratory test Weight increased

Symptomtext

extreem fatigue for several days, missed work. Then on October 20th, started getting chest pains. They continued getting worse despite visiting my doctor. Went to the local County Hospital Emergency Room on November 2, 2021 because it felt like I was having a heart attack. This was a vaccine I did NOT want and was done under coercion. I have also experienced significant weight gain despite diet and exercise, lifestyle change and energy has decreased. I also have trouble breathing going up stairs which I have never experienced before in my life. This vaccine has been extremely damaging.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: You can get results from the local County Hospital.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 08.10.2021
Beginn: 17.09.2022
Tage bis Beginn: 344,0
Dosis: 3
Route/Site: - / -

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

Angiogram pulmonary abnormal Antiplatelet therapy Atelectasis Atrial fibrillation CHA2DS2-VASc-score COVID-19 Chemotherapy Chest X-ray Diarrhoea Fatigue Haemodynamic instability Hypokalaemia Hypomagnesaemia Hypotension Hypovolaemia Hypoxia Lactic acidosis Lung infiltration

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 9/17/2022 Discharge Date: 9/25/2022 Clinical Narrative: Patient was admitted with post chemotherapy nausea vomiting and diarrhea. He was quite volume depleted and had a mild lactic acidosis which resolved promptly. He did continue to improve as outlined below. He will be discharged home today with Oncology follow-up on Tuesday. Please see the following problem-list oriented Hospital Course below: Lactic acidosis Assessment & Plan The patient presented emergency department with likely chemotherapy-induced nausea vomiting diarrhea with pancytopenia lactic acidosis. Patient given 2 L bolus in the emergency department lactic acidosis improved in decreased to 1.8 patient still having watery diarrhea in the emergency department. The patient will be admitted will be given IV hydration will be given a dose of hydrocortisone as he is on oral hydrocortisone outpatient his oral dosing will be increased to 20 mg a.m. 10 mg p.m.. Lactic acidosis was likely secondary to the extent of his volume depletion and hemodynamic alteration after his chemotherapy, watery diarrhea, nausea, vomiting. Resolved promptly. * Pancytopenia Assessment & Plan Likely due to his chemotherapy. Improved. Responded to Neupogen. Antibiotics later stopped. Observing. Subsequent leukocytosis secondary to Neupogen therapy. Diarrhea Assessment & Plan Nausea vomiting diarrhea lactic acidosis likely due to chemotherapy does have pancytopenia will be empirically covering him with antibiotics continue hydration will check blood cultures will check stool studies - complicated by nausea and vomiting. Post chemotherapy. Complicated by hypokalemia and hypomagnesemia. Both were repleted. Complicated by lactic acidosis. Improved. Required volume resuscitation. Did well. COVID-19 Assessment & Plan Patient is a pleasant 80-year-old male with history of metastatic colon cancer to the liver is undergoing chemotherapy patient has had nausea vomiting diarrhea was seen in the emergency department on the 12th hydrated and discharged home patient has had persistent symptoms increasing fatigue presented emergency department is COVID positive pancytopenic hypotensive which resolved with fluid lactic acidosis which resolved with fluid. Patient admitted for further care - largely a incidental finding. No corresponding symptoms. The patient did have increasing oxygen needs near discharge but this responded to ambulation, incentive spirometer, and observation. Repeat chest x-rays stable. Recent CT angiogram without evidence of pulmonary embolus. Small bilateral pleural effusions are present but did not require intervention. This is likely residual from his volume resuscitation. Malignant neoplasm of sigmoid colon Assessment & Plan History of colon cancer with metastases to the liver undergoing chemotherapy last dosing was September 6th gets dosing every 2 weeks. Patient with nausea vomiting diarrhea pancytopenia lactic acidosis. The patient admitted for further care Oncology follow-up planned for Tuesday. Discussed. Excellent baseline functional status. Adrenal insufficiency Assessment & Plan History of adrenal insufficiency. Resuscitation on admission hydrocortisone dosing increased in the short-term. Tolerated well. Home on his prior dosing. Abdominal aortic aneurysm (AAA) without rupture Assessment & Plan History of abdominal aortic aneurysm status post stent placement. Continue to follow with PCP/serial observation as needed. Secondary prevention with BP control and lipid management. Atrial fibrillation Assessment & Plan Paroxysmal atrial fibrillation on flecainide (restarted) - continued on Toprol and aspirin Stable at discharge. CHADS Vasc = 2. He has, over time, elected to stay on simple antiplatelet therapy. Hypoxia Assessment & Plan Oxygen needs had increased the day prior to discharge. He required a CT angiogram which the exclude pulmonary embolus. He is noted have bilateral pleural effusions and mild bibasilar infiltrates/atelectasis. He responded to mobilization, incentive spirometer, and cough and deep breathing. Discharge chest x-ray remained stable. No residual oxygen need on discharge. No corresponding symptoms. Atelectasis with shunting. Pleural effusion, bilateral Assessment & Plan Bilateral pleural effusions present. Likely secondary to the extent of volume resuscitation required on admission. Small. Did well without intervention. Atelectasis present. Discharge chest x-ray stable. Exam stable.

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Praegender Schweregrund: Hypotension
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Atrial fibrillation Fatigue Cardiac pacemaker in situ Prostate cancer Idiopathic hypotension SSS (sick sinus syndrome) Abdominal aortic aneurysm (AAA) without rupture Adrenal insufficiency Malignant neoplasm of sigmoid colon Lactic acidosis Pancytopenia COVID-19 Diarrhea Unspecified severe protein-calorie malnutrition Pleural effusion, bilateral Hypoxia
Andere Medikamente: aspirin 325 MG tablet atorvastatin (LIPITOR) 20 MG tablet CENTRUM SILVER (CENTRUM SILVER) tablet flecainide (TAMBOCOR) 100 MG tablet HYDROcodone-acetaminophen (NORCO) 5-325 mg per tablet hydrocortisone (CORTEF) 5 MG tablet hydrocortisone (C
Allergien: None
Vorherige Impfungen: -

VAERS 2459739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 24.09.2022
Impfdatum: 23.07.2022
Beginn: 19.09.2022
Tage bis Beginn: 58,0
Dosis: 3
Route/Site: IM / -

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

Cervical spinal stenosis Fall Fine motor skill dysfunction Hypotension Movement disorder Spinal fusion surgery

Symptomtext

Patient had a sudden fall for the first time at 73 years old. He acquired cervical stenosis requiring a C3-C6 posterior decompression and fusion. He was also having severely low blood pressures requiring a levophed drip. Patient is currently unable to move his lower extremities as well as he has no hand and finger dexterity on either hand.

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Praegender Schweregrund: Hypotension
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: CAD, HTN, HLD, DM type 2
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2450522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

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Staat: FL
Alter: 70,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 28.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Herpes virus infection

Symptomtext

3 days after this COVID vax injection, onset of crop of herpes lesions on right buttock (never had herpes lesions before in this same spot; took Rx acyclovir to lessen severity and duration of lesions. (Note: patient has approx. 50-yr Hx of occasional herpes lesion outbreaks on lower back or buttocks, usually occurring after sun exposure or brought on by stressful situation or illness.)

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: long Hx of herpes 1 and herpes 2 infections with occasional outbreaks
Andere Medikamente: losartan; rosuvastatin; loratadine; calcium; multivitamin
Allergien: tetracycline; metronidazole
Vorherige Impfungen: -

VAERS 2439786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 62,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 01.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Gait disturbance Hypoaesthesia Palpitations Paraesthesia

Symptomtext

I have had numbness and tingling in my left arm every morning; my arm is just going to sleep but it happens every morning; I have had numbness and tingling in my left arm every morning; my arm is just going to sleep but it happens every morning; I have heart palpitations sometimes; I am starting to have difficulty in walking; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 01Nov2021 as dose 3 (booster), single (Lot number: FF2590) at the age of 62 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer, ), for COVID-19 immunization. The following information was reported: HYPOAESTHESIA (non-serious), PARAESTHESIA (non-serious), outcome "not recovered" and all described as "I have had numbness and tingling in my left arm every morning; my arm is just going to sleep but it happens every morning"; PALPITATIONS (non-serious), outcome "unknown", described as "I have heart palpitations sometimes"; GAIT DISTURBANCE (non-serious), outcome "unknown", described as "I am starting to have difficulty in walking". Therapeutic measures were not taken as a result of hypoaesthesia, paraesthesia, palpitations, gait disturbance. Additional Information: The patient stated that she was wondering if having a side effect from the Pfizer vaccine booster or whatever she had the first and second shot last year. The patient had the booster but there was things going on usually she was extremely healthy but lately had numbness and tingling in left arm every morning and also had heart palpitations. The patient stated, thinking it's possible that was a side effect that she was having. The patient do have a doctor appointment on 25Oct to talk to doctor about the numbness and tingling in left arm which she told him once before and he saw that it was that arm was just going to sleep but it happens every morning and the patient concerned about it. Well, it's actually happening now so the numbness and tingling in arm are concern of patient and then had heart palpitations sometimes. The patient started to have difficulty in walking. Now, that's another reason patient going to doctor on 25Oct. The patient hope it was not anything but maybe it could be that hips going out on me she don't know, it could be knee. The patient don't know but having difficulty in walking lately. So, that was the concern of patient but you know she may not have nothing to do with anything other than the normal aging process but we can just, the patient just thought she should report it just in case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
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 2436385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 01.03.2021
Beginn: 04.09.2022
Tage bis Beginn: 552,0
Dosis: 3
Route/Site: - / RA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB, INCREASED HOME O2 NEEDS,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: POSITIVE COVID TEST 9/5/22
Aktuelle Erkrankungen: -
Vorgeschichte: Abscess of temple region Adenocarcinoma of left lung (HCC) Arthritis BPH (benign prostatic hypertrophy) Chronic pain COPD (chronic obstructive pulmonary disease) Emphysema lung (HCC) Hard of hearing Hyperlipidemia Hypertension Inguinal hernia Tobacco use disorder Pure hypercholesterolemia Benign prostatic hyperplasia without lower urinary tract symptoms Positive fecal occult blood test Hyperplastic polyp of ascending colon Hyponatremia Pneumothorax after biopsy Hypo-osmolality and hyponatremia Adenocarcinoma of left lung (HCC) Left upper lobe pulmonary nodule Malignant neoplasm of upper lobe of left lung (HCC) Oxygen dependent Pneumonia, suspected bacterial
Andere Medikamente: acetaminophen (TYLENOL) 500 mg oral tablet albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler atorvastatin (LIPITOR) 10 mg oral tablet cetirizine (ZYRTEC) 10 mg oral tablet FERROUS SULFATE ORAL finasteride (PROSCAR) 5 mg o
Allergien: Voltaren [Diclofenac Sodium]
Vorherige Impfungen: -

VAERS 2433625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 90,0
Geschlecht: U
Eingang: 08.09.2022
Impfdatum: 18.01.2021
Beginn: 27.08.2022
Tage bis Beginn: 586,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

08/27/22 presents to EC ED for "chest pain". PMHx of "CAD, DM, lower extremity edema, and arthritis"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 08/27/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2435983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 94,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 12.01.2021
Beginn: 23.04.2022
Tage bis Beginn: 466,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury COVID-19 COVID-19 pneumonia Cough Decreased appetite Hyperglycaemia Malaise SARS-CoV-2 test positive Wheezing

Symptomtext

Narrative: Patient received three doses of Pfizer COVID 19 Vaccine. The patient tested positive for COVID 19 on 23 April 2022. The patient presented to the ED with cough, malaise, wheezing and decreased appetite. The patient was admitted to the hospital with acute kidney injury, covid pneumonia, and hyperglycemia. The patient was treated with supportive care, antitussives, and bronchodilators. The patient was discharged on 2 May 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2401450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injected limb mobility decreased Injection site pain Pain Paraesthesia

Symptomtext

Point tenderness at the injection site that grew increasingly worse over time. Continued pain at the injection site. Right shoulder, bicep and tricep pain. Limited range of motion .Tingling to the right wrist and thumb that is resolving. Constant ache in the arm and shoulder pain increases with certain movements. Currently I have had several physical therapy appointments - Therapist is thinking a SIRVA injury or shoulder pain from guarding. Therapy for several months

Weitere VAERSDATA-Felder

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

VAERS 2391220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IL
Alter: 60,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 20.04.2022
Beginn: 19.07.2022
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia Blood test Cough Dysphonia Dyspnoea Electrocardiogram Heart rate irregular Influenza virus test Laboratory test Malaise Nasopharyngitis Nervousness Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Symptoms were mild and similar to a common cold. I was at a conference between the 12th and the 16th of July. It started with a mild cough. I felt fine. I thought it was allergies. By the 18th of July the symptoms were getting stronger so I took an at home test and it came back negative. On the 19th of July, I had a cough and congestion and 2 days later it developed to weakness, shaky, and I had trouble breathing. My smart watch was saying my heart rate was weirdly up as if my body was fighting something. Then I went to urgent care but they turned me away and I had to go to the ER and they did an EKG and lab work, which included the swab for COVID and that came back positive. They gave me Paxlovid and sent me home. I feel a lot better now although my voice is still a little hoarse and I have a bit of a cough, but nothing to severe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG; blood panel; covid test; flu test
Aktuelle Erkrankungen: None
Vorgeschichte: diabetes type 2; moderate asthma; high cholesterol, GERD
Andere Medikamente: Metformin; gradience; singular; ezetimibe; vitamin D; calcium; multi vitamin; biotin; inhaler
Allergien: penicillin; sulfa
Vorherige Impfungen: -

VAERS 2373973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: FL
Alter: 94,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 16.11.2021
Beginn: 14.07.2022
Tage bis Beginn: 240,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea

Symptomtext

Pt presented with covid and shortness of breath. Treated with remdesivir, and doxycycline. IV dexamethasone given. pt discharged to snf.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHF, afib, htn, hld,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2368774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IA
Alter: 54,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 21.12.2021
Beginn: 08.07.2022
Tage bis Beginn: 199,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Cardioversion Dyspnoea Malaise Palpitations

Symptomtext

Emergency Services to inpatient- Cardio Palm Sx: palpitations, SOB, N, "generally not feeling well" - in ER: afib RVR - chemical conversion but continues to no feel well.

Weitere VAERSDATA-Felder

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

VAERS 2341762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: GA
Alter: 73,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 19.10.2021
Beginn: 16.01.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Back pain Mobility decreased Neck pain Pain in extremity X-ray

Symptomtext

I am still seeing the Dr. I started seeing him in February and it is a ongoing treatment. I was having pain that started in my left arm and I didn't give it a second thought and went to my back and this was a course over three weeks and I thought it was gas. It moved to my back, stomach and now it has settled back to my arm and my neck where it left me I can hardly move my neck to the left. The chiropractor is manipulating my bones and deep tissue massage. He has a license to do that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-Ray of area- preexisting condition no new abnormal results
Aktuelle Erkrankungen: N/A
Vorgeschichte: Deep Vein Thrombosis; Pulmonary Embolisms; Atrial Fibrillation; Degenerative Arthritis; Baker's Cyst Knee; Lung nodules
Andere Medikamente: Tylenol; Vitamin D6; Vitamin D3; Folic Acid; Vitamin B6;Claritin
Allergien: Pantoprazole Sodium; Plaquenil; Allopurinol; Ulrica Febuxostat; Codeine; Lactate Acid; Nylon; Latex; Mold
Vorherige Impfungen: -

VAERS 2335894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 74,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Anger Antibody test abnormal Aortic valve replacement Arthralgia Asthenia Back pain Balance disorder Blood test abnormal Dizziness Dyspnoea Emotional distress Fatigue Feeling abnormal Inflammation Mobility decreased Pain Pain in extremity Protein total increased

Symptomtext

I had fever later on that day on October 11th, fatigue and body aches, these symptoms lasted about 36 hours. The pain in my arm from the shot lasted over a week. Body aches and joint pain, lower back pain that is excruciating, I never had any of this before the shot. The lower back pain is very dibilitating. I get dizzy and I get a foggy head, I feel unbalance like. I am seeing eye floaters. I had to have my aortic valve replaced (TAVR procedure) on 10.28.22. I experienced shortness of breath. I cant continue with cardio rehab. I had bloodwork done, that showed inflamation in my body. But it's not like anything like arthritis. But I have inflammation without explanation. Emotionally this is effecting me, an emotional nightmare. With the blood work, it showed inflammation and my spike protien was over 12000 and my antibodies were over 800. I did not have this problem before the shot. It's so bad I can hardly get out of bed. Spike protein has come down to 10000, but antibodies are still high. I am really upset and angry about this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Bloodwork
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: On first report
Allergien: Penicillin, Shellfish
Vorherige Impfungen: -

VAERS 2331756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 26.01.2021
Beginn: 17.05.2022
Tage bis Beginn: 476,0
Dosis: 3
Route/Site: - / -

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

Dyspnoea

Symptomtext

Patient present to ED due to concerns with shortness of breath for past 10 days. Patient denies chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: aspirin (ECOTRIN) 81 MG PO Tablet Delayed Response atorvastatin (LIPITOR) 40 MG PO Tab losartan (COZAAR) 100 MG PO Tab metoprolol (TOPROL XL) 100 MG PO TABLET SR 24 HR rivaroxaban (XARELTO) 20 MG PO Tab torsemide (DEMADEX) 20 MG PO Tab
Allergien: -
Vorherige Impfungen: -

VAERS 2327056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 03.03.2021
Beginn: 15.06.2022
Tage bis Beginn: 469,0
Dosis: 3
Route/Site: IM / UN

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

COVID-19 Cough Dizziness Dyspnoea Laboratory test Positive airway pressure therapy Productive cough SARS-CoV-2 test positive Sepsis

Symptomtext

Pt to ED 6/15 for cough and sob, positive at home COVID test. COVID+ upon admission 6/15, maintained on Decadron. 6/16 pt reporting SOB and dizziness. Sepsis BPA fired score of 5. RRT not activated. VSS on 2L NC. ID on consult. Started on remdesivir. 6/18 pt remains A&Ox4 and showing no s/s of distress. Oxygen remains at 2L via NC and patient using home CPAP machine. Productive cough noted overnight. 6/19 pt remains A&Ox4 and showing no s/s of distress. 6/19 pt discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: OSA (obstructive sleep apnea) Chronic obstructive pulmonary disease Chronic respiratory failure with hypoxia, on home O2 therapy Rhinitis, chronic IFG (impaired fasting glucose) Secondary hyperparathyroidism Lymphedema S/P splenectomy Nocturnal enuresis Pulmonary hypertension Occlusion of celiac artery CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min Seborrheic eczema Varicose veins of lower extremity Right ureteral calculus Peripheral vascular disease Venous ulcer History of colonoscopy Ureteral stone with hydronephrosis Gout Right nephrolithiasis Venous insufficiency of both lower extremities Onychomycosis Cellulitis of right lower leg Cellulitis of leg Obesity (BMI 35.0-39.9 without comorbidity) Leg pain, bilateral Celllitis and abscess of left leg Cellulitis of right lower extremity Bilateral renal cysts Wound infection COVID-19 Cellulitis of right lower extremity Polycythemia
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln amoxicillin-potassium clavulanate (AUGMENTIN) 875-125 MG PO Tab budesonide-formoterol (Symbicort) 160-4.5 MCG/ACT INHAL inhaler bumetanide (Bumex) 1 MG PO Tab
Allergien: Adhesive tape
Vorherige Impfungen: -

VAERS 2323275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 99,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 02.12.2021
Beginn: 14.06.2022
Tage bis Beginn: 194,0
Dosis: 3
Route/Site: UN / UN

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

Asthenia Atelectasis Blood culture negative Blood lactic acid C-reactive protein increased COVID-19 Chest X-ray abnormal Cough Degenerative bone disease Dysphagia Dyspnoea Fatigue Hiatus hernia Hypoxia Lung opacity Malaise Metabolic function test normal Oropharyngeal pain

Symptomtext

Patient is a 100 y.o. female who presented to the emergency department on 6/14/22 with fatigue, cough and shortness of breath. She began feeling ill on 06/12/2022 with main complaints of fatigue, weakness, cough, fever, shortness of breath, and sore throat. She tested positive for COVID-19 via home test prior to presentation. In the ER she was found to be mildly hypoxic and subsequently placed on 2 L oxygen nasal cannula. Labs reveal relatively unremarkable CMP, CRP of 36.3, procalcitonin 0.07, lactic acid 1.4, WBC 8.16. Positive COVID-19 confirmed. Chest x-ray showed mild interstitial prominence likely chronic and less likely due to mild congestion, mild right perihilar and right medial opacity likely due to atelectasis. She was given 6 mg of dexamethasone in the ER. She was admitted to the hospitalist service for ongoing management evaluation of COVID-19 hypoxia. During hospital course, dexamethasone was continued and Remdesivir was initiated. PT/OT evaluations were completed due to generalized weakness. Patient does reside at home with family. Medications for hypertension and prior stroke continued. Dysphagia evaluation completed. Diagnosed with mild pharyngeal phase dysphagia. Recommending mildly thick (nectar-thick) liquids, minced and moist (dysphagia mechanically altered), liquids via cup and straw (cup with handle/mug easiest for pt's self-feeding). Today, she is sitting in a chair in no acute distress. Is on room air. Has no complaints of shortness of breath, chest pain. Is at her mental baseline. Appetite is intact. She is requesting discharge home. Son in laws at the bedside and states that family is ready for her discharge. As she is on room air, will discontinue dexamethasone at this time. Home physical, occupational therapies arranged with home health RN. Patient is stable for discharge home to the care of her family at this time. They are agreeable with the plan of care. All questions and concerns were addressed. Please see discharge instructions for further information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: DR CHEST SINGLE VIEW Collected: 06/14/22 1654 Order Status: Completed Updated: 06/14/22 1656 Narrative: EXAMINATION: Single View Chest EXAM DATE: 6/14/2022 4:20 PM TECHNIQUE: Single view chest INDICATION: COVID dyspnea COMPARISON: January 2022. ENCOUNTER: Not applicable _________________________ FINDINGS: There is no evidence of pneumothorax. Interstitial prominence is seen. Mild opacity in the right medial lung base. Cardiac and mediastinal silhouette again shows a moderate to large sized hiatal hernia. Bony structures show degenerative changes.. _________________________ Impression: 1. No evidence of pneumothorax. Mild interstitial prominence likely chronic and less likely due to mild congestion. Mild right perihilar and right medial opacity likely due to atelectasis and less likely evolving infiltrate. Electronically signed by: doctor on 6/14/2022 4:55 PM. Procedure Component Value Ref Range Date/Time Peripheral Blood Culture Collected: 06/14/22 1606 Order Status: Completed Specimen: Blood, Venous Updated: 06/16/22 1703 Cult Blood Peripheral No Growth 48 hours Peripheral Blood Culture Collected: 06/14/22 1540 Order Status: Completed Specimen: Blood, Venous Updated: 06/16/22 1603 Cult Blood Peripheral No Growth 48 hours COVID-19 PCR - Rapid (Abnormal) Collected: 06/14/22 1543 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 06/14/22 1605 COVID-19 PCR Detected Abnormal Not Detected
Aktuelle Erkrankungen: -
Vorgeschichte: Circulatory Essential hypertension Digestive Dysphagia Infectious/Inflammatory COVID-19 Other Generalized weakness History of CVA (cerebrovascular accident) Type 2 diabetes
Andere Medikamente: Bacillus Coagulans-Inulin (PROBIOTIC FORMULA PO) benzonatate (TESSALON) 100 MG capsule calcium carbonate (TUMS) 500 MG chewable tablet Cholecalciferol (VITAMIN D-3 PO) clopidogrel (PLAVIX) 75 MG tablet cyanocobalamin 1000 MCG tablet furosem
Allergien: Darvon [Propoxyphene]
Vorherige Impfungen: -

VAERS 2298863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 72,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 27.04.2022
Beginn: 07.05.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain upper Bacterial test negative Chest pain Flatulence Ultrasound biliary tract

Symptomtext

Gas, chest pains, stomach pain. Dr checking for gall bladder and ulcer and heart disease

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ulcer bacteria negative, gall bladder ultrasound results not back
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: claaritan, lisinpril
Allergien: sulfa, hay fever(grasses, weeds, trees)
Vorherige Impfungen: -

VAERS 2296605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MT
Alter: 19,0
Geschlecht: M
Eingang: 26.05.2022
Impfdatum: 22.10.2021
Beginn: 17.04.2022
Tage bis Beginn: 177,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Influenza A virus test Influenza B virus test Pneumonia bacterial Respiratory syncytial virus test SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

Case was vaccinated and boosted as of October 2021, then was hospitalized for Covid in April 2022 Hospitalized at: Medical Center Case was hospitalized with cough, shortness of breath, O2 sats in the 20's (!), and recent history of bacterial pneumonia. Was treated with Dexamethasone, and DVT prophylaxis, and discharged home after 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: Ordered Test: FLUABV+SARS-CoV-2+RSV RNA Pnl Resp NAA+p (SARS CoV2-Flu-RSV PCR) Ordered Test Codes: Status: Final Accession Number: Specimen Source: Nasopharynx Specimen Site: Specimen Collection Date/Time: 2022-04-17 12:33:00.0 * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe (SARS CoV-2 PCR (COVID-19)) Coded Result: Positive (LOCAL) Numeric Result: Units: Text Result: Reference Range From: Negative Reference Range To: Performing Facility Details: Date/Time: Performing Facility: Med Cntr Facility ID:(FI) Interpretation: Abnormal Result Method: (Xpert Xpress SARS-Co) Status: Final Test Code: Result Code: (SCT/Positive (L LOCAL) Result Comments: Positive results are indicative of active infection with SARS-CoV-2. Positive results do not rule out bacterial infection or co-infection with other viruses.
Aktuelle Erkrankungen: Pneumonia of right lower lobe due to infectious organism Fetal alcohol syndrome Attention deficit disorder with hyperactivity(314.01) Decreased left ventricular systolic function GERD (gastroesophageal reflux disease) Duchenne muscular dystrophy
Vorgeschichte: Pneumonia of right lower lobe due to infectious organism Fetal alcohol syndrome Attention deficit disorder with hyperactivity(314.01) Decreased left ventricular systolic function GERD (gastroesophageal reflux disease) Duchenne muscular dystrophy
Andere Medikamente: ARIPiprazole (ABILIFY) 10 mg tablet (Taking) Take 10 mg by mouth nightly. Calcium Carbonate (CALCIUM 600 PO) (Taking) Take 600 mg by mouth Daily. carvedilol (COREG) 12.5 mg tablet (Taking) Take 1.5 tablets by mouth 2 times daily (with b
Allergien: Penicillins, Tylenol
Vorherige Impfungen: -

VAERS 2295945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: -
Geschlecht: M
Eingang: 26.05.2022
Impfdatum: 30.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Condition aggravated Joint noise

Symptomtext

Popping in both elbows; It has worsened over time; 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 male patient received BNT162b2 (BNT162B2), on 30Oct2021 as dose 2, single (Lot number: FF2590) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (First Dose: , Lot: 301358A), administration date: 09Oct2021, for COVID-19 immunization. The following information was reported: JOINT NOISE (non-serious), outcome "not recovered", described as "Popping in both elbows"; CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "It has worsened over time". Therapeutic measures were not taken as a result of joint noise, condition aggravated. Additional information: Caller would not provide any identifiers except phone number. Caller received the first dose of the Pfizer COVID-19 on 09Oct2021 and the second dose on 30Oct2021. He has noticed "popping in both elbows" since he received the vaccine and it has worsened over time. Caller would like to know if this is a side effect of the Pfizer COVID-19 vaccine and how long it may last. Caller clarifies that he does have popping in both elbows. Caller declines to provide any patient identifiers other than his phone number. Caller states it started whenever he got the vaccine shots, well not too long after he got his Pfizer Vaccine Shots. Caller later states he thinks it might have started after his second one and it has gotten worse. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
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 2294771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MT
Alter: 46,0
Geschlecht: M
Eingang: 25.05.2022
Impfdatum: 28.10.2021
Beginn: 16.03.2022
Tage bis Beginn: 139,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Decreased appetite Diarrhoea Dyspnoea Gastrointestinal haemorrhage Headache Polyuria Pyrexia Respiratory symptom SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

Case completed primary Covid series in October 20212, then was hospitalized for Covid in March 2022. Medical record review indicates case was symptomatic for Covid (fever, cough, headache, SOB, diarrhea, loss of appetite), along with GI bleed, and respiratory symptoms which improved with diuresis. Other treatments contraindicated due to other health issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: vOrdered Test: SARS-CoV-2 RNA Resp Ql NAA+probe Ordered Test Codes: 94500-6 (LN LOINC)/ Status: Final Specimen Source: SOFT TISSUE SAMPLE Specimen Site: ENTIRE NASOPHARYNX Specimen Collection Date/Time: 2022-03-05 14:06:00.0 Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe Coded Result: DETECTED Numeric Result: Units: Text Result: Reference Range From: Not Detected Reference Range To: Performing Facility Details: Date/Time: 2022-03-05 15:03:28.0 Interpretation: Very abnormal Result Method: LAB DEVICE: CEPHEID GENEXPERT DX SYSTEM Status: Final Test Code: 94500-6 (LN LOINC)/ Result Code: 260373001 (SCT/
Aktuelle Erkrankungen: Cirrhossis with alcoholism GERD
Vorgeschichte: Cirrhossis with Alcoholism GERD
Andere Medikamente: acetaminophen (TYLENOL) 325 mg tablet Take 2 tablets by mouth every 6 hours as needed. furosemide (LASIX) 40 mg tablet Take 1 tablet by mouth Daily. gabapentin (GRALISE) 300 mg tablet Take 1 tablet by mouth nightly. gabapentin (
Allergien: Sulfa antibiotics
Vorherige Impfungen: -

VAERS 2284807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 27.10.2021
Beginn: 28.04.2022
Tage bis Beginn: 183,0
Dosis: 3
Route/Site: UN / UN

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

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

Symptomtext

congestion, cough, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 4/18/22 +covid test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2273246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 42,0
Geschlecht: F
Eingang: 12.05.2022
Impfdatum: 07.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / RA

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

Blood pressure increased Blood test Dehydration Dizziness Electrocardiogram Electrocardiogram ambulatory normal Heart rate increased Hypotension

Symptomtext

Rapid heart rate (120 bpm) as measured via smart watch. Steady and would not drop - even when at rest. Went to urgent care - blood pressure was elevated. Urgent care sent me to the ER. ER said it was dehydration and gave fluids; heart rate/blood pressure still did not drop. Followed up with primary care on 11/15/22. She prescribed Lisinopril (5 mg/1x day). Seemed to help. At the end of January/beginning of April, began to feel lightheaded. Went to primary care on 3/2/22 to see if Lisinopril was still needed. Primary care insisted that it was still needed. Bought a home blood pressure machine - blood pressures were low. Went to cardiologist on 3/23/22. He instructed me to stop taking Lisinopril - did not think I had high blood pressure based on visit and my tracked blood pressure. After I stopped Lisinopril, no more light headedness and blood pressure returned to normal. Did a 24 hour Holter Monitor on 4/6/22 - 4/7/22 - no issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: EKGs on 11/11/22 and 3/2/22. 24 hour Holter monitor from 4/6/22 - 4/7/22. Bloodwork on 11/11/22 and 3/2/22.
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's disease and PCOS
Andere Medikamente: Levothyroxine (50mcg/1x day), Metformin HCL (500 mg/2x day), women's multivitamin, calcium/d3, B12 (1000)
Allergien: None
Vorherige Impfungen: -

VAERS 2270975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 30.01.2021
Beginn: 29.01.2022
Tage bis Beginn: 364,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

01/29/22 presents to ED for "chest pain". "no significant PMH"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01/29/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2328539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 13.01.2021
Beginn: 20.01.2022
Tage bis Beginn: 372,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Cough Dyspnoea Respiratory failure SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received three doses of Pfizer COVID 19 Vaccine. The patient tested positive for COVID 19 on 20 Jan 2022. The patient presented to the ED with shortness of breath, cough, and wad admitted in another hospital for COVID pneumonia. The patient was treated with remdesivir and dexamethasone. The patient was discharged, but the patient was readmitted to the hospital on 6 February 2022 with cough and shortness of breath. The patient was admitted with COVID pneumonia and respiratory failure. The patient was treated with antibiotics. The patient was discharged 10 Feb 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2269345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 11.11.2021
Beginn: 09.04.2022
Tage bis Beginn: 149,0
Dosis: 3
Route/Site: IM / RA

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

Atrial flutter Condition aggravated

Symptomtext

My atrial flutter was corrected by an ablation in 2014 and had not returned. It suddenly returned on April 9, 2022. My cardiologist claims that it is very unusual for atrial flutter to return that long after an ablation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial flutter
Andere Medikamente: Lisinopril, Carvedilol, Lovastatin, Aspirin, CoQ10, Vitamin D3, Flaxseed Oil, Multivitamin
Allergien: Pollen and mold
Vorherige Impfungen: -

VAERS 2268814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 32,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / AR

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

Ankle fracture Balance disorder Blood test normal Condition aggravated Dizziness Dyspnoea Dyspnoea exertional Electroencephalogram normal Fall Hypoaesthesia Impaired driving ability Magnetic resonance imaging normal Malaise Paraesthesia oral Photophobia Pyrexia Vision blurred

Symptomtext

11/6/2021 Later that evening I had a fever. My blurred vision from my previous vaccination became worse. I felt really sick. Ever since then, I have seen my PCP and a Neurologist because of the blurred vision, light headedness, dizziness, light sensitivity, numbness, tingling around my mouth, off balance and shortness of breath with activity. All symptoms get worse with heat and when I get up and move around. The blurred vision gets so bad that I cannot drive. At the end of November, I fell and broke my ankle. Bloodwork, EEG, MRI were all normal. I see a Cardiologist at the end of this month. I still have not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Bloodwork: Normal MRI: Normal EEG: Normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2263563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Alopecia Chest pain Fatigue Injury Malaise Muscle spasms Myalgia Pyrexia Rash Swelling

Symptomtext

I was feeling sick, I had a low grade fever. By Friday I developed an arm rash and swelling. It started to fade after 3 days. I would also say fatigue, muscle aches, also I had some achiness in my chest. I also noticed a change where I started to have more orthopedic type injuries. 2 of my fingers started to get an arthritic rhythm-that never happened before until after I received the booster. I've also noticed some hair loss but not sure where that came from.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Vitamins Amlodipine
Allergien: Penicillin medication
Vorherige Impfungen: -

VAERS 2262989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 03.10.2021
Beginn: 01.04.2022
Tage bis Beginn: 180,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain Chills Cough Dyspnoea Headache Nasal congestion Pyrexia SARS-CoV-2 test Vaccination failure

Symptomtext

COVID-19; COVID-19; fever; chills; cough; congestion; headache; difficulty breathing; chest pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27Jan2021 as dose 1, single (Lot number: EL9261), on 17Feb2021 as dose 2, single (Lot number: EN6200) and on 03Oct2021 as dose 3 (booster), single (Lot number: ff2590) at the age of 66 years for covid-19 immunization. The patient's relevant medical history included: "Thyroid" (unspecified if ongoing), notes: Other Medical History: Thyroid; "esophagitis" (unspecified if ongoing), notes: Other medical History: esophagitis. Concomitant medication(s) included: LEVOTHYROXINE, start date: 01Jan2019, stop date: 30Apr2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Apr2022, outcome "not recovered" and all described as "COVID-19"; CHEST PAIN (non-serious) with onset 2022, outcome "not recovered"; CHILLS (non-serious) with onset 2022, outcome "not recovered"; NASAL CONGESTION (non-serious) with onset 2022, outcome "not recovered", described as "congestion"; COUGH (non-serious) with onset 2022, outcome "not recovered"; DYSPNOEA (non-serious) with onset 2022, outcome "not recovered", described as "difficulty breathing"; PYREXIA (non-serious) with onset 2022, outcome "not recovered", described as "fever"; HEADACHE (non-serious) with onset 2022, outcome "not recovered". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (29Apr2022) Negative; (30Apr2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Additional information: The patient taking any other medications/products within 2 weeks of starting COVID-19 treatment. The relapse of covid on 30Apr2022 after taking Paxlovid. Tested negative yesterday, then positive today with all symptoms returning fever, chills, cough, serious congestion, difficulty breathing, headache, chest pain. As I have compromised lungs, I am concerned I will end up in the hospital. No Paxlovid this time. Known allergies was reported as no. Device Date was reported as 30Apr2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220429; Test Name: SARS-CoV-2 test; Test Result: Negative ; Test Date: 20220430; Test Name: SARS-CoV-2 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Esophagitis (Other medical History: esophagitis); Thyroid disorder (Other Medical History: Thyroid)
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2262004

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NJ
Alter: 25,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 07.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: SYR / AR

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

Bronchitis Chest X-ray abnormal Chest pain Cough Decreased appetite Somnolence Throat irritation

Symptomtext

I didn't have any reactions to the vaccine. On the first day of catching COVID-19 I had an itchy throat. Then on day 2 or 3 I developed a cough. On day 5 or 6, I went to an urgent care because I had chest pain. I was prescribed benzoate. They told me to rest as much as possible because I was getting early signs of bronchitis. I was drowsy and had a little bit of loss of appetite, but I was still able to eat. After about 10 days, I felt pretty normal again. My throat stayed itchy the entire time. I had a cough for a total of about 25 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Chest x-ray- showed early signs of bronchitis.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C Women's Multivitamin
Allergien: None
Vorherige Impfungen: (April 30, 2021) After the 2nd dose of the COVID-19 vaccine I got sick with a fever, and I vomited once or twice. The fever last

VAERS 2260512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NM
Alter: 62,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 01.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / RA

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

Burning sensation Herpes zoster Mobility decreased Nerve injury Neuralgia Pain

Symptomtext

I started to get well, Since my mobility is limited, sometimes I sleep in the recliner, I thought I was getting a pressure sore on my back around the belt line. It started going down the right side to the hip and down to about the knee. It was a burning sensation that felt like someone dumped gas on me and lit it in fire. I'd get this sensation up to four times per hour when I would eat the wrong things. The medical people have done a terrible job with shingles. The pain hit when I was in the doctor's office and the staff was freaking out because I was in so much pain. The doctor gave me medications that would tale 45 to 55 minutes before it would work. I am still having nerve pain. No medical tests were done. The nerve damage is done, I am not screaming like I used to. I am afraid to take any medications because we do not know what causes it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: COPD
Andere Medikamente: Oxycodone #10, Tramadol, Albuterol Sulfate, Turmerol, Inhalers
Allergien: High doses of Ibuprofen and Tylenol, Short Haired Cats, Horses
Vorherige Impfungen: -

VAERS 2260209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: ME
Alter: 59,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Fear Feeling abnormal Glycosylated haemoglobin increased Immediate post-injection reaction Injection site discomfort Injection site pain Laboratory test normal Lymphoedema Mobility decreased Pain Pain in extremity Peripheral swelling Rash Sleep disorder Tendon rupture

Symptomtext

She had her vaccine, had severe pain immediately, like somebody beat her arms up, punched her in her arms at the location of her injection. She has a Popeye arm when her main tendon from her shoulder to her elbow ruptured and there is nothing they can do to resolve it. She has been doctors and specialists and there is nothing than can be done. The pain was in waves from slight to severe pain. Then her arms became painful everywhere. Then she got a rash on both hands and both feet and swelling started going up her arms and legs. Then the tendon ruptured in her left arm. She has popping noises if she can move her arm, but cannot move them very much. Every time she moves her right arm it pops and doesn't know if the tendon is going to rupture or not. The injection sites feels like somebody took a hot pocker and stuck in her arm. The pain never goes away, has is 24/7. The pain would previously go from bad to worse and would be there, but now it's a hot fire pocker all the time. She tried to get the Lidocaine patches and creams on her arms, but did not help at all. She had similar reactions with the other vaccines as well. The first vaccine when she first got it had the burning feeling and dissipated, but in 2 weeks came back. The 2nd and third vaccines had instant onset of the pain. She went to the doctor after the first vaccine but could not give her any answers. Then she saw Dr. about a month ago and he is the one that diagnosed with her lymphedema. Two days ago she was speaking to a friend of hers that is a nurse and she informed her that there is are cases that have been reported to her where the COVID vaccinations are causing with peoples lymph nodes, and feels it's interesting that she was diagnosed with lymphedema, and now knows it was from the vaccinations. In the past year she has been to her orthopedist, endocrinologist, dermatologist who told her to go to a cardiologist, went to that and did not know what it was, went to her neurologist who did not know what it was. Also went to her pain specialist who did not know who it was, and her prior PCP before Dr. did not know what was causing her symptoms. She now sleeps in a recliner and due to her scoliosis she only gets a few hours of sleep off and on, and really does not sleep much at all. Her arms are so painful as she cannot bend her elbows for any period of time or it starts pounding in pain. She may fall sleep but wakes up in 30 minutes due to the pain. Her feet are also swelling. Has a sleep number bed but cannot lie down due to her arms hurting immensely and feels like there is a football under each armpit. Her PCP has not given her anything as of yet for the lymphedema. He is trying to find out why she has the burning sensation in her right nostril. Her nose runs all the time and looking into that. She asked him for something for the lymphedema, and is waiting to hear back from him for that. One thing that shows in her protein is that it is extremely high. Her other levels are high like her A1C which was 8.5 on the latest check, and her other levels are pretty normal. Her A1C was 7.1 for about a year, then tried to decrease her medication intake and tried controlling it on her own and her A1C is now lower, but does have a check up soon for more blood work. She is scared and lives alone and feels like she is dying and that the vaccines will kill her or the effects from it will. Her quality of life is so bad that she cannot get around and does not know what she can do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Extensive blood work in the last year.
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes, neuropathy, rare scoliosis, fibromyalgia, lymphedema, tendonitis both arms, dry eyes, chronic insomnia due to chronic pain.
Andere Medikamente: Glipizide 20 mg daily, Jardiance 25 mg daily, Vitamin D 2000 units, Avapro 300 mg, Prevacid 60 mg daily, Bystolic 40 mg daily, Meloxicam 15 mg per day, 81 mg aspirin, Mirapex 2 mg daily, Hydrocodone 10/325 every 4-6 hours, Hysingla 60 mg da
Allergien: Dust, pollen.
Vorherige Impfungen: In 2009 she got the vaccine for the swine flu/bird flu and suggested that she get that and did not ask if she was allergic to eg

VAERS 2258346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IL
Alter: 56,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 08.11.2021
Beginn: 11.02.2022
Tage bis Beginn: 95,0
Dosis: 3
Route/Site: SYR / AR

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

Asthenia Chest pain Dysgraphia Fatigue Fear Feeling abnormal Gait disturbance Loss of personal independence in daily activities Malaise Mental impairment Mobility decreased Pain Pyrexia SARS-CoV-2 test negative Sinus disorder Somnolence Suspected COVID-19

Symptomtext

The day before, I had a 45 minute exposure to a woman who had COVID-19, unknown at the time and we were not wearing masks. I felt that we were social distancing but I guess not. I got sick suddenly on Friday, and it really hit me hard. I had to lay down and couldn't move. I was completely exhausted. I had a fever. My chest hurt. I had sinus issues. I've never felt this sick and it happened so quick. So I called my doctor and he said to take a COVID-19 test in 3 days. I remember feeling achy, very achy. I just got very sick very fast, miserable. I found out on Sunday that the woman I was with had COVID-19. Her 3 tests came back positive and she was sick also. I think I got my COVID-19 test on Monday at the pharmacy and I got my results Tuesday or Wednesday and I tested negative. I was sick from about that Friday, 24 hours, then got better. I had that exhaustion and fevers too. I was so exhausted, I couldn't walk to the car and couldn't even get to the pharmacy. I was loopy and couldn't think straight. I couldn't do the basic or important things like grocery lists, etc. It was debilitating and I was miserable. I started to feel better in the beginning to mid April. Sometimes I was so tired I couldn't write and couldn't make out my letters. That's why my doctor thought I had COVID-19 because I had the exhaustion and the fevers. I had a GI doctor in the area and she assumed I had COVID-19 as well. I have noted that March 21, I felt loopy. Less exhaustion on March 28 but thinking issues, taking naps. I started taking walks on April 3rd, so I may have started to feel better. I'd say around April 7th, I was incredibly tired. April 8, noted I was miserable. April 10, I noted that I had a lot of energy to do basic things. So I'd say mid-April was when I started feeling better. I could focus on what I needed to do and take walks. It was hard for me to take walks when I was miserable. I couldn't even walk steps. I was exhausted and it was horrible, head felt miserable and I couldn't think straight and I couldn't walk. It was very hard and frightening too. I feel fine now, recently had a 4th dose on April 19, 2022. Felt miserable for 2 days and now I feel fine, like it never happened. I also took a second COVID-19 test on March 15, 2022 and I got the results on March 16 and it was negative. Due to the symptoms, doctors assumed that it was COVID-19 and possibility of false negatives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 test on 02/14/2022 - Negative COVID-19 test on 03/15/2022 - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Fatty Liver Disease (managed) Mild Aortic Stenosis Severe Scoliosis Schizoaffective disorder (managed)
Andere Medikamente: Prempro Levothyroxine 75mcg Risperidone 1mg 2xday Omeprazole 20mg 1xday Lamotrigine 100mg 2xday Latuda 20mg every other day Sonata 10mg PM for sleep Glycine 3g PM for sleep Melatonin 10mg PM for sleep Multivitamin Buspirone Hydrochloride 1
Allergien: Aspirin All Sulfa medication Latex Geodon
Vorherige Impfungen: 1st COVID-19 Pfizer vaccine, April 1, 2021, achiness and soreness at injection site, couldn't bend arm; 4th COVID-19 Pfizer vacc

VAERS 2258297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 28.10.2021
Beginn: 19.01.2022
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Cardiac stress test Chest X-ray Dyspnoea Electrocardiogram Fatigue Oropharyngeal pain Pyrexia

Symptomtext

I had fever sore throat extreme fatigue shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest x-ray ekg ecg stress test blood work up
Aktuelle Erkrankungen: No.
Vorgeschichte: Diabetes Hypothyroid Bipolar IBS
Andere Medikamente: Aripiprazole Dicyclomine Escitalopram Clonazepam Propranolol Dicyclomine metformin Rosuvastatin Lisinopril Synthroid Multivitamin Potassium Vitamin C
Allergien: latex and adhesive
Vorherige Impfungen: -

VAERS 2257512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 26.10.2021
Beginn: 08.01.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Asthma COVID-19 Condition aggravated Cough Fatigue Malaise SARS-CoV-2 test positive Sinusitis

Symptomtext

About 2.5 months after vaccination, I started feeling very tired and had a lot of coughing. I had no energy for several weeks. I was taking my nebulizer at least every 3-4 hours. I tried taking OTC Sudafed. I ended up with a sinus infection. Starting the second week, I called my doctor and I was started on Azithromycin. It helped slightly but my asthma was still out of control. After almost 2 weeks, I ended up having to call my allergist and he prescribed me two different rounds of prednisone before my asthma started getting better. I was sick for a month. I tested positive for Covid 6 months after 3rd vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I Health Covid Home Test positive on April 1, 2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Amitriptyline 20mg at hs, Magnesium OTC daily,
Allergien: Cipro
Vorherige Impfungen: -

VAERS 2256996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 68,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 26.10.2021
Beginn: 04.01.2022
Tage bis Beginn: 70,0
Dosis: 3
Route/Site: SYR / AR

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

Asthma COVID-19 Dyspnoea Headache Nausea SARS-CoV-2 test positive

Symptomtext

01/04/2022 At first, I thought my asthma was getting worse, I was having trouble breathing. I was using my albuterol more. Then the headaches started. I called my neighbor and he had COVID-19. I did a COVID-19 test at my doctor's office and it was positive. He gave me a steroid, cough medicine and anti-nausea. I would get nauseated when I ate. I still have breathing issues. This lasted for about 6 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 Test, Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Fibromyalgia; Chronic Anxiety; Occasional Depression; Spinal stenosis
Andere Medikamente: Tramadol Loratadine Clonazepam Buspirone Propranolol Sertraline Losartan Montelukast Trazadone Pravastatin Albuterol inhaler Vitamin D3 with Calcium Daily Multi Vitamin
Allergien: Shellfish; Cymbalta; Celexa; Codeine; Cats; Trees; Summer; Fall; Grass
Vorherige Impfungen: -

VAERS 2248025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MT
Alter: 37,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 13.10.2021
Beginn: 16.01.2022
Tage bis Beginn: 95,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Condition aggravated Cough Exposure to SARS-CoV-2 Malaise Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Urticarial vasculitis

Symptomtext

On the 16th I had a kiddo who tested positive for Covid, she is also fully vaccinated as I am, I started having symptoms late that night. I went in to to the Dr. to take a test and it showed I was negative. My symptoms were getting worse and I thought that I had to be positive. I tested on the 19th and 21st at home both also showed negative. I did feel better on the 22nd and then had no symptoms on the 23rd but took one last test to be sure that test showed I was positive. Starting the 24th I had horrible symptoms and was out for about 2 weeks with symptoms. Coughing sore throat fever no taste or smell. The Covid did cause a flare up from my existing condition, Urticarial vasculitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: None
Vorgeschichte: Urticarial Vasculitis
Andere Medikamente: Levothyroxine; Vitamin; Allegra
Allergien: Penicillin; Copper; Acacia gum
Vorherige Impfungen: -

VAERS 2246209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 12.10.2021
Beginn: 31.01.2022
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Arthralgia Blood test Palpitations Rectal haemorrhage

Symptomtext

Joint pain and bowel issues. I've also been having heart palpitations. I still have bowel issue and rectal bleeding. I'm not sure if its related to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Osteoporosis
Andere Medikamente: Multivitamin Calcium D3 Alginate
Allergien: Penicillin; Sulfa
Vorherige Impfungen: Flu vaccine.

VAERS 2238717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 30.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia Condition aggravated

Symptomtext

symptoms of polyarthralgia (both hips, both upper legs, both shoulders, both upper arms). Self medication with aleve, advil for 3 months, currently on 15 mg Meloxicam 1/day and by twice monthly PT. Possible PMR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: polyarthralgia (possibly PMR). Severe pain in both hips, upper legs, shoulders and upper arms. Unable to twist, bend, lift, squat or pull without significant pain in muscles and joints.
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 2231447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NM
Alter: 62,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Influenza Pneumonia Vaccine breakthrough infection

Symptomtext

Breakthrough COVID: I was told that I had the flu. Then, they called and told me I also had COVID. The doctor wanted to see me that day in the parking lot. I went and he did more testing. He gave me medication for the flu. He wanted to see me back every day in the parking lot. On the 3rd day, he sent me to the hospital for the monoclonal antibodies. I was at the hospital for about 6 hours while they did that and about 3 or 4 weeks later, I started feeling better. It seems like my health is real my immune system seems to be really down because after that, 2 months later, I got pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: Monoclonal Antibodies 11/08/2021
Aktuelle Erkrankungen: Flu
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2228759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 12.04.2022
Impfdatum: 24.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia Bladder dilatation Blood culture positive Citrobacter sepsis Flank pain Hydronephrosis Hypotension Nephrolithiasis Urinary tract infection

Symptomtext

Severe citrobacter induced sepsis complicating acute complicated UTI, severe due to acute weakness, relative hypotension, slight AKI. Patient who is a direct admission from an outside hospital because of symptomatic left flank pain due to 7 mm mid ureteral stone with left hydroureteronephrosis and a distended urinary bladder, required urology intervention, later turned to have +ve blood culture in outside facility, managed for this, managed for the above acute issues, improved, today he is cleared by all teams to dc, ID called in am, cleared by her to dc on po Cipro for 2 weeks, stable to dc to f/w ID, PMD, urology for further care after dc. Hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2223121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 13.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Asthenia Atrial fibrillation Cystitis Dizziness Dyspnoea Hypophagia International normalised ratio increased

Symptomtext

Atrial fibrillation with rapid ventricular response. Patient who was discharged form the hospital yesterday for atrial fib with RVR reports to the clinic today c/o dizziness. Metoprolol and digoxin where added during her last hospitalizations. Pt states she went home and felt ok. This morning she as had dizziness, worse when sitting up. She denies any chest pain. She occasionally has some shortness of breath. She has not eaten today due to dizziness. Admitted for weakness/Dizziness. But we will for now treat her as Uncomplicated cystitis to complete with Cefdinir X total 5 days. She is refusing PT/OT eval at this time and states she has no problem with Ambulation. Her warfarin dose to be adjusted as INR this am is 3.1, Likely Interaction with Ceftriaxone. ED visit 7 days later for dizziness - treated and released. Hospital admission and ED visit within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2218415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IN
Alter: 23,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Heavy menstrual bleeding Impaired work ability Metabolic function test Mobility decreased Sexually transmitted disease test Smear cervix

Symptomtext

Once I received the dose it was the last day of my period. The next day on 11/20/2021, I had extreme heavy menstrual bleeding. I could no get out of bed and could not go to work, I had heavy menstrual bleeding for 38 days. On 12/10/2021, I went to see the doctor and was prescribed medroxyprogesterone to elevate menstrual bleeding. After 10 days, the bleeding stopped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Metabolic panel, Pap Smear, STD/ STI testing.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2211389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WI
Alter: 61,0
Geschlecht: F
Eingang: 01.04.2022
Impfdatum: 18.10.2021
Beginn: 09.11.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac stress test normal Chest pain Dysgeusia Electrocardiogram normal Fatigue Injection site pain Joint swelling Musculoskeletal chest pain Myalgia Somnolence

Symptomtext

sore injection site day after vaccine, tired/sleepy, muscle aches, metallic taste, then sharp chest pain on 11/9/2021 w/ soreness along the sternum,, on 3/3 & 5/2022 had chest pain soreness along sternum and ribs, swollen joints.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ECG/EKG cardio stress test. Doc said ok.
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, reflux, osteoartheritis
Andere Medikamente: multivitamin, zinc, vit D, vit C, tumeric, famodidine, avorstatin, cetrizine
Allergien: oxycontin, bees, hydrocodone,
Vorherige Impfungen: flu vaccine in my early 30's; temperary hearing loss

VAERS 1815102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Blood pressure measurement Chest pain Depression Hypertension Insomnia Malaise Migraine Movement disorder Restlessness Stress Tinnitus

Symptomtext

ringing in my ear; This ringing in my ear does not let me rest or sleep more than 2 hours in a row; This ringing in my ear does not let me rest or sleep more than 2 hours in a row; High blood pressure; migraines; chest pains; stress; depression; I can't run; I feel horrible every day; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 20Oct2021 12:15 (Lot number: FF2590) at the age of 46 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Covid-19" (unspecified if ongoing), notes: If covid prior vaccination: Yes. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot number: 30135BA, Dose administration time: 12:15 PM, Dose vaccine location: Left leg), administration date: 29Sep2021, when the patient was 46 years old, for Covid-19 immunization. The following information was reported: TINNITUS (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "ringing in my ear"; RESTLESSNESS (disability), INSOMNIA (disability) all with onset 20Oct2021 12:15, outcome "not recovered" and all described as "This ringing in my ear does not let me rest or sleep more than 2 hours in a row"; HYPERTENSION (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "High blood pressure"; MIGRAINE (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "migraines"; CHEST PAIN (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "chest pains"; STRESS (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "stress"; DEPRESSION (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "depression"; MOVEMENT DISORDER (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "I can't run"; MALAISE (disability) with onset 20Oct2021 12:15, outcome "not recovered", described as "I feel horrible every day". The events "ringing in my ear", "this ringing in my ear does not let me rest or sleep more than 2 hours in a row", "this ringing in my ear does not let me rest or sleep more than 2 hours in a row", "high blood pressure", "migraines", "chest pains", "stress", "depression", "i can't run" and "i feel horrible every day" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (20Oct2021) high. Therapeutic measures were taken as a result of tinnitus, restlessness, insomnia, hypertension, migraine, chest pain, stress, depression, movement disorder, malaise which included acupuncture, massage and chiropractor. Clinical course: The patient had no other medications in two weeks. The patient was not tested for covid post vaccination. The patient had no known allergies. The patient had no other medical history. The patient started getting a loud ringing in ear that has not stopped. This ringing in ear does not let her rest or sleep more than 2 hours in a row. The patient was getting secondary side effects due to the ringing in ears: High blood pressure, migraines, chest pains, stress, depression. The patient wished she would have never taken the vaccine. The patient used to run and be fit and now she can't run and felt horrible every day. The patient have tried everything that people recommended and have not been able to resolve the ringing in ears. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20211020; Test Name: Blood pressure; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2199192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 04.10.2021
Beginn: 10.01.2022
Tage bis Beginn: 98,0
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

01/10/22 presents to EC ED for "worsening dyspnea". PMHx of "COPD on 3L home O2, HFrEF (last EF 60% in September), HTN, and pulmonary HTN"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/10/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2194511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 14.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / -

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

Arthralgia Condition aggravated Limb injury Myalgia Neck pain Polymyalgia rheumatica Red blood cell sedimentation rate increased

Symptomtext

I had a PMR (Polymyalgia Rheumatic) flare up the week following my vaccine. Treated with prednisone (with a taper) for two weeks. Helped temporarily. When I came off the prednisone I had a worse flare up. Went on prednisone (with taper) for almost 3 months. Again, there was temporary relief, but as I came off the prednisone, the muscle aches returned. My shoulders are more sore than they have ever been. I've been receiving PT (for shoulder and neck pain), acupuncture, and therapeutic massage. I also have injured my left shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood work (on 12/2) showed elevated sedimentation rate.
Aktuelle Erkrankungen: -
Vorgeschichte: Polymyalgia Rheumatica
Andere Medikamente: Rosuvastatin Calcium, Losartan-HCTZ, Levothyroxine, Fluoxetine, Pantoprazole, Amitriptyline
Allergien: None
Vorherige Impfungen: -

VAERS 2189884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 21.03.2022
Impfdatum: 22.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / RA

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

Pneumonia aspiration

Symptomtext

Patient presented to the ED and was subsequently hospitalized for aspiration pneumonia within 6 weeks of receiving covid booster vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia aspiration
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2187297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 53,0
Geschlecht: M
Eingang: 18.03.2022
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Back pain Chest pain Dyspnoea Fatigue Feeling abnormal Haematoma Inappropriate schedule of product administration Inflammation Pain in extremity SARS-CoV-2 test

Symptomtext

prev dose administration date=14Mar2021, dose number=2 administration date=06Oct2021; Inflammatory Sporadic pain-back, chest hand; Inflammatory Sporadic pain-back, chest hand; Inflammatory Sporadic pain-back, chest hand; Inflammatory Sporadic pain-back, chest hand; Brain Fog; Toe Hematoma; Fatigue; Shortness of breath; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 53 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 06Oct2021 12:15 (Lot number: FF2590) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Hypertension" (unspecified if ongoing); "Hyperlipidemia" (unspecified if ongoing); "Insomnia" (unspecified if ongoing); "Anxiety" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6204, Location of injection: Arm Left, Vaccine Administration Time: 08:30 AM, Verbatim:Inflammatory Sporadic pain-back, chest hand), administration date: 14Mar2021, when the patient was 52 years old, for Covid-19 Immunization, reaction(s): "Inflammatory Sporadic pain-back, chest hand", "Inflammatory Sporadic pain-back, chest hand", "Inflammatory Sporadic pain-back, chest hand", "Inflammatory Sporadic pain-back, chest hand", "Brain Fog", "Toe Hematoma", "Fatigue", "Shortness of breath". The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 06Oct2021, outcome "unknown", described as "prev dose administration date=14Mar2021, dose number=2 administration date=06Oct2021"; INFLAMMATION (non-serious), BACK PAIN (non-serious), CHEST PAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 2021, outcome "unknown" and all described as "Inflammatory Sporadic pain-back, chest hand"; FEELING ABNORMAL (non-serious) with onset 2021, outcome "unknown", described as "Brain Fog"; HAEMATOMA (non-serious) with onset 2021, outcome "unknown", described as "Toe Hematoma"; FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "Fatigue"; DYSPNOEA (non-serious) with onset 2021, outcome "unknown", described as "Shortness of breath". The events "inflammatory sporadic pain-back, chest hand", "inflammatory sporadic pain-back, chest hand", "inflammatory sporadic pain-back, chest hand", "inflammatory sporadic pain-back, chest hand", "brain fog", "toe hematoma", "fatigue" and "shortness of breath" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of inflammation, back pain, chest pain, pain in extremity, feeling abnormal, haematoma, fatigue, dyspnoea. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No hospitalization required or prolonged. No seriousness provided. No known allergies. Prior to vaccination, was the patient diagnosed with COVID-19?:No. Since the vaccination, has the patient been tested for COVID-19?:Yes No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220202; Test Name: PCR; Test Result: Negative ; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Hyperlipidemia; Hypertension; Insomnia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2184192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: CO
Alter: 58,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / AR

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

Back pain Chest X-ray abnormal Chest X-ray normal Chills Condition aggravated Cough Dyspnoea Fatigue Pain Pneumonia Respiratory tract congestion Sinus disorder

Symptomtext

My dad was in the hospital at this point, and around this time he went in for a uti and he contracted covid in the hospital. We all got tested and we came back negative. He had no idea he had covid, he only found out because of the tests done at the doctor. It is said that he contracted it in the hospital. It was stressful, and my mother got her booster a week before I did. I had sinus issues since that point. I felt fine after the booster for several hours but then it hit me that I was tired and I had chills and aches. That happened to me with the 2nd shot as well so I did not think anything of it. I was having a congested cough but it did get worse. The sinuses got worse. I did ignore them because my father was really sick and because of work I didn't have the time. My doctor did order me a chest x ray and I went in January. It was determined I had pneumonia. I was given an inhaler to take 4 times a day. I saw my doctor for a follow up and she extended the anti biotics, but I still have this crazy harsh cough. They had me on what was called Doxycycline 2 times a day. I have not tested positive at all for Covid. I constantly get tested for work and just because my mother is 80. About 3 to 4 weeks ago I ended up in the ER because I had shortness of breath and back pain. I was given a steroid but it resulted in nothing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Chest X ray and determined I had pneumonia. 2nd chest x ray done weeks later that showed no results.
Aktuelle Erkrankungen: Sinus allergies
Vorgeschichte: Allergies
Andere Medikamente: Kertonix 40mg, Linnets 290 capsule, Vexter Generic, Mucinex 1200mg, Tramadol, Suva statin, Tracedon 100mg, Bioidenticals twice a day
Allergien: None
Vorherige Impfungen: -

VAERS 2182381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CT
Alter: 79,0
Geschlecht: M
Eingang: 16.03.2022
Impfdatum: 22.10.2021
Beginn: 26.01.2022
Tage bis Beginn: 96,0
Dosis: 3
Route/Site: IM / LA

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

Computerised tomogram Condition aggravated Follicular lymphoma

Symptomtext

As of Jan. 7, 2022 the Follicular Lymphomas had been spreading and growing since being detected in Dec. 2020 and diagnosed via biopsy in Feb. 2021. However, as of Jan. 26, 2022 there was noticeable shrinkage in the size of the ones at the 4 major sites detected externally. At visit with Dr. on Feb. 22, 2022 he agreed that they were significantly smaller than they were at the previous exam on Nov. 8, 2021. My primary care doc has speculated that the shrinkage may be due to the booster shot in Oct. 2021. She has observed shrinkage to the point of not being detectable by manual exam in a long-standing cyst in a breast of a patient following a booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: A CT scan is scheduled for Apr. 5, 2022 to compare with results of one done in Oct. 2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Follicular Lymhoma
Andere Medikamente: Tamsulosin, multi-vitamin, B-12
Allergien: None
Vorherige Impfungen: -

VAERS 2180168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 01.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Catheterisation cardiac normal Chest pain Intracranial aneurysm Magnetic resonance imaging head abnormal

Symptomtext

Atypical chest pain after COVID-19 vaccination.- resolved and s/p cardiac cath yesterday and negative. MRI, MRA brain with out contract and labs looking for vitamin deficiencies. 11/06 mri/mra done, all unremarkable except a small 3.5mm aneurysm that he will follow up with. Hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2180023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF 2590

moderat

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 01.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Echocardiogram Electrocardiogram Exercise tolerance decreased Loss of personal independence in daily activities Pain Ultrasound Doppler

Symptomtext

CHEST PAIN AND UNABLE TO DO PHYSICAL ACTIVITIES. NO PE AT SCHOOL . NO LIFTING. NO EXCERTION OF ANY TYPE. NO DESIRE TO DO ANYTHING ABSENT FROM SCOOL ALL THE TIME BECAUSE OF PAIN TREATMENT RECOMMEND TYLENOL PATIENT STILL HS CHEST PAIN IT IS NOW 5 MONTHS SINCE THE SECOND VACCINE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: PATIENT WS SEEN BY A CARDIOLOGIST. THEY DID FOLLOWING. ROUTINE EKG USING 12 LEADS, ULTRASOUND EXAMINATION OF CONGENITAL HEART DEFECT, ULTRASOUND EXAMINATION OF HEART INCLUDING COLOR DEPICTED BLOOD FLOW RATE DIRECTION AND VALVE FUNCTION. DOPPLER ULTRASOUND STUDY OF BLOOD FLOW, VALVES AND CHAMBERS. HEART RHYTHM TRACING, ANALYSIS AND INTERPRETATION OD 48-HOUR EKG
Aktuelle Erkrankungen: NONE
Vorgeschichte: GOOD HEALTH
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2179686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 29.10.2021
Beginn: 10.12.2021
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: IM / RA

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

Pneumonia Respiratory failure Sepsis

Symptomtext

Severe sepsis due to PNA with Hypoxic Resp Failure. Patient treated and released to home health care. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2177762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 94,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 03.11.2021
Beginn: 12.12.2021
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: IM / LA

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

Chronic obstructive pulmonary disease Condition aggravated Fall Musculoskeletal stiffness Respiratory failure

Symptomtext

Patient Fall - she was treated for COPD exacerbation with steroids and that has significantly improved she is stiff she has been discharged on 3 L and she is chronically on 2.5 her acute on chronic hypercarbic hypoxemic respiratory failure i.e. hypoxia and hypercapnia improved throughout and she is on a tapering course of prednisone. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2176566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AR
Alter: 50,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Chest pain Cough Dyspnoea

Symptomtext

dry cough; chest pain; you have to catch your breath; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 05Nov2021 (Lot number: FF2590) at the age of 50 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), administered in arm left, administration date 05Nov2021 (Lot number: FK5127) as dos enumber unknown, single for immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose #1 in her right arm in the morning between 08:00 am-10:00am. Lot EN6208.), administration date: 13Mar2021, when the patient was 49 years old, for COVID-19 immunization; Bnt162b2 (Dose #2 in her left arm, unknown time. Lot EP7533), administration date: 03Apr2021, when the patient was 49 years old, for COVID-19 immunization. The following information was reported: COUGH (non-serious) with onset 06Nov2021, outcome "not recovered", described as "dry cough"; CHEST PAIN (non-serious) with onset 06Nov2021, outcome "not recovered", described as "chest pain"; DYSPNOEA (non-serious) with onset 06Nov2021, outcome "not recovered", described as "you have to catch your breath". No follow-up attempts are possible. 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: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: FL
Alter: 30,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: -
Beginn: 09.11.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Arthralgia Back pain Chills Decreased appetite Migraine Musculoskeletal stiffness Pain Pyrexia

Symptomtext

Second dose, chills; fever; body ache; loss of appetite; migraines; joint pain; stiff neck; back aches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30-year-old male patient received bnt162b2 (BNT162B2), administered in arm left (Lot number: Ff2590) at the age of 30 years as dose 2, single for COVID-19 immunization. Relevant medical history included: "COVID-19" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Prednisone for known allergies: Prednisone. Vaccination history included: Bnt162b2 (Previous dose lot number: FF2590, dose administration date: 18Oct2021, dose number: 1, dose vaccine location: Left arm), when the patient was 30 years old, for COVID-19 immunization, reaction(s): "crippling migraines", "back aches", "joint pain", "stiff neck". The following information was reported: CHILLS (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "Second dose, chills"; PYREXIA (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "fever"; PAIN (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "body ache"; DECREASED APPETITE (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "loss of appetite"; MIGRAINE (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "migraines"; ARTHRALGIA (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "joint pain"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "stiff neck"; BACK PAIN (non-serious) with onset 09Nov2021 12:00, outcome "unknown", described as "back aches". Therapeutic measures were not taken as a result of AEs. Additional Information: Patient had no other medical history. Patient did not receive any other vaccine in four weeks nor received any other medications in two weeks. Patient had COVID prior vaccination. Patient had not COVID tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 30,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 18.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Back pain Migraine Musculoskeletal stiffness

Symptomtext

First dose, crippling migraines; back aches; joint pain; stiff neck; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Oct2021 (Lot number: FF2590) at the age of 30 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "If covid tested prior vaccination: Yes" (unspecified if ongoing), notes: If covid tested prior vaccination: Yes. There were no concomitant medications. Past drug history included: Prednisone, reaction(s): "Known allergies: Prednisone", notes: Known allergies: Prednisone. The following information was reported: MIGRAINE (non-serious) with onset Nov2021, outcome "unknown", described as "First dose, crippling migraines"; BACK PAIN (non-serious) with onset Nov2021, outcome "unknown", described as "back aches"; ARTHRALGIA (non-serious) with onset Nov2021, outcome "unknown", described as "joint pain"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset Nov2021, outcome "unknown", described as "stiff neck". Therapeutic measures were not taken as a result of migraine, back pain, arthralgia, musculoskeletal stiffness. Additional information: Other medical history: No. Other medications in two weeks: No. If other vaccine in four weeks: No. If covid prior vaccination: Yes. If covid tested post vaccination: No. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid tested prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2175780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 06.10.2021
Beginn: 06.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Headache Palpitations

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 81 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 06Oct2021 (Lot number: FF2590) at the age of 81 years as dose 3 (booster), single for Covid-19 immunisation. Relevant medical history included: "cancer" (unspecified if ongoing), notes: cancer 2 years ago. I am taking one for bone density and Somatostatin' 40 mg, I only take half 20 mg. Concomitant medication(s) included: ALENDRONATE SODIUM taken for osteoporosis (ongoing); ANASTROZOLE taken for breast cancer; SIMVASTATIN taken for blood cholesterol increased (ongoing). Vaccination history included: Flu shot (Route: Muscular, Anatomical site of injection: Arm), administration date: 27Sep2021, when the patient was 81 years old, for immunization; Bnt162b2 (Dose: 1, morning, Anatomical Site of injection: Left upper arm, Route: intramuscular, Batch/lot number: EI9262), administration date: 30Jan2021, when the patient was 81 years old, for COVID-19 immunization; Bnt162b2 (Dose: 2, morning, Anatomical Site of injection: Left upper arm. Route: intramuscular, Batch/lot number: EN6200), administration date: 23Feb2021, when the patient was 81 years old, for COVID-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 06Oct2021, outcome "recovered" (07Oct2021), described as "Headache"; PALPITATIONS (non-serious) with onset 06Oct2021, outcome "recovered" (07Oct2021), described as "Heart is racing and it is racing all night". Therapeutic measures were not taken as a result of headache, palpitations. Additional information: My height is 5 feet 3 and it used to be 5 feet 4 or 3 and a half, I am shrunk a little. I did get a Flu Shot (Unspecified Flu Shot) about a week or 2 weeks something like that. Consumer stated, "You know I have done many clinical studies myself. I got a booster yesterday. I was wondering where I can report side effects. Are you keeping a track of all of them at Pfizer? I wanted to find out like I said, I have done clinical studies and always reported the adverse event (Further clarification was unknown) I just wondering are you collecting the booster Shot adverse event or you not collecting them." Consumer added, "So, I had the Pfizer booster (Clarified as Pfizer COVID-19 Vaccine) yesterday and then I got a headache most of the yesterday, even this morning, I have a little bit but much stronger last evening and then also my heart is racing and it is racing all night. So, I just wanted to report those 2 things." Email: # (Not spelled, hence not captured in tab). Consumer stated, "Now I am retired but I used to be in a biotech company. That's why I know we used to report all our adverse event that's why I wanted to report." (Further clarification was unknown, hence captured as consumer or non-health professional by default) Consumer added, "I have no problem with the first two shots, only the booster". Reason for no lot number: of Unspecified Flu Shot: Other: Could not be probed since the medication was Unspecified. Consumer stated, "Well, I was supposed to get it at 11:45. I don't know if I got it 5 minutes later or earlier but around 11:45. I am just checking to see. The time is not written here. "Prior vaccination (4 weeks) consumer stated, "I told you 2 weeks ago I had the flu shot." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer (cancer 2 years ago. I am taking one for bone density and Somatostatin' 40 mg, I only take half 20 mg).
Andere Medikamente: Alendronate Sodium; Anastrozole; Simvastatin
Allergien: -
Vorherige Impfungen: -

VAERS 2170899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 66,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 05.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Alopecia Back pain Cardiac discomfort Dysstasia Fatigue Feeling abnormal Heart rate increased Hyperhidrosis Malaise Muscle fatigue Muscular weakness Myalgia Night sweats Pain Pain in extremity Paraesthesia Rash Rash papular

Symptomtext

The 1st thing I noticed was I had an overall sense of malaise. I then had a rash that started at my neck and then it went all the way down to my ankles. The rash was slightly elevated. The next day I woke up in the night with bad pain in my back. It felt like my heart was being squeezed, and it felt like something was going through it. It then passed. These symptoms went on for awhile. I had a pain in my leg. I woke up in the morning and my leg would just hurt. The muscles around my ankles would hurt too. Then that went away. I would get a tingling feeling in my body that would happen with my arms, legs, and hands. I had a hard time getting up in the morning. When I would get up from my bed and then walk to my kitchen, I would break out in a sweat. I haven't felt right for weeks. My heart feels like it could jump out of my chest. I never had any respiratory symptoms. I had some odd pain. My arm would really hurt and then it would just go away. A lot of my hair fell out. I felt very tired. In the morning my hands, arms, and elbows felt weak. Then it would go away after I got up. I also had some night sweats. One day I could barely pick up my leaf blower. I was also riding a bicycle one day and I felt fatigue in my legs. All of these symptoms lasted up until the end of January 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Complete blood panel-red blood cell counts were slightly elevated but normal
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Valsartan Lorazepam
Allergien: Avocados Sulfa medications and antibiotics
Vorherige Impfungen: -

VAERS 2168157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WI
Alter: 76,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 15.10.2021
Beginn: 08.03.2022
Tage bis Beginn: 144,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Bronchitis COVID-19 Candida infection Cough Dyspnoea Emphysema Fibrin D dimer increased Hypophagia Lung opacity

Symptomtext

Patient presents today with a several day history of increasing SOB and non productive cough. She reports recently taking doxycycline and prednisone for bronchitis and subsequently being treated for thrush yesterday. She has known COPD and monitors her 02 sats at home. Over the past couple of days her sats have been in the low 80's (83% on admission), usually in the low to mid 90's. No fever or chills. Her oral intake has been poor the last couple of days. No nausea, vomiting or other abdominal symptoms. In TEC her Ddimer was elevated at 2086, CTA negative for PE however chronic emphysematous changes and lower opacities consistent with COVID.

Weitere VAERSDATA-Felder

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

VAERS 2162597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WI
Alter: 70,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

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

Arthralgia Crying Dysstasia Gait disturbance Mobility decreased Neck pain Pain

Symptomtext

I was in a lot of pain, I was crying and I couldn't stand up from a sitting position. I couldn't go up any of my stairs, I couldn't get into a car. The pain was in my hip, shoulder and neck. I call my doctor but my PCP doctor had left the practice and I was getting the run around, I needed something for pain. When I do get something for the pain, the PA said that I was having a flare up from the Booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes, COPD, Chronic Respiratory Failure, Pulmonary Embolism and Obesity.
Andere Medikamente: Albuterol HFA 90mg x2, Atorvastatin 40mg, Biotin 1000mcg, Flovent HFA 110mg, Lantus 26 units, Xalatan one drop in both eyes, Lisinopril 20 mg, Metformin 500mg x3, Oxygen 3 Liters, Prednisone, Xarelto 20mg and Trazodone 100mg.
Allergien: Shrimp
Vorherige Impfungen: -

VAERS 2162586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 14.10.2021
Beginn: 25.11.2021
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: IM / RA

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

Pneumonia Urinary tract infection

Symptomtext

Patient was admitted with community-acquired pneumonia and UTI was treated with a week of antibiotics with good resolution. ED visit and hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2162517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 27.10.2021
Beginn: 23.01.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: UN / UN

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

Abdominal pain upper Asthenia COVID-19 Decreased appetite Exposure to SARS-CoV-2 Fatigue Hypoxia Laboratory test normal Mobility decreased Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Date: 1/23/2022 HPI: Patient is a very pleasant 87-year-old male, well-known to my outpatient practice. He presented to the emergency room with abdominal pain, predominantly right upper quadrant and fever. He does report 1 episode of emesis yesterday. Noted with temperature of 102 degrees. Took Tylenol prior to coming in. Patient globally weak. He has had recent anorexia, fatigue. Challenged getting out of bed at home today. He is COVID vaccinated x3. He has had family exposures to COVID illness. Not wearing a mask. Seen in the emergency room setting in which he appears to be comfortable. He did have a brief hypoxic event with a decline In O2 saturation to 88% .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 9,0
Labordaten: COVID19 LABS Lab Results Component Value Date COVID19 Detected (A) 01/23/2022 FLRA Not Detected 01/23/2022 FLRB Not Detected 01/23/2022 FLRR Not Detected 01/23/2022
Aktuelle Erkrankungen: ? Arthritis ? Bladder stone secondary to BOO from BPH ? BPH (benign prostatic hyperplasia) ? Dyslipidemia ? Elevated hemoglobin A1c ? Hypertension ? Kidney calculi ? Nephrolithiasis ? Osteoarthritis ? Retained urethral stent Bilat
Vorgeschichte: ? Arthritis ? Bladder stone secondary to BOO from BPH ? BPH (benign prostatic hyperplasia) ? Dyslipidemia ? Elevated hemoglobin A1c ? Hypertension ? Kidney calculi ? Nephrolithiasis ? Osteoarthritis ? Retained urethral stent Bilat
Andere Medikamente: finasteride (PROSCAR) 5 MG PO Tab TAKE 1 TABLET BY MOUTH EVERY DAY ? hydroCHLOROthiazide (HYDRODIURIL) 25 mg, Oral, DAILY ? losartan (COZAAR) 100 mg, Oral, DAILY ? metFORMIN (GLUCOPHAGE) 500 mg, Oral, TWICE DAILY BEFORE BRKFST & DINNER
Allergien: none
Vorherige Impfungen: -

VAERS 2157635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 44,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 31.10.2021
Beginn: 08.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea exertional Echocardiogram Electrocardiogram ambulatory Extrasystoles Pyrexia

Symptomtext

Within 8 days the patient began having dyspnea upon exertion. Mild fever within 24 hours of booster. Ectopic beats reported. These are all new and temporal to booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: Transthoracic echocardiogram with new LVEF 35%. Holter monitor with no new findings.
Aktuelle Erkrankungen: None
Vorgeschichte: History of recovered cardiomyopathy. Normal LVEF 55% within year (no current symptoms).
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2155547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NJ
Alter: 72,0
Geschlecht: F
Eingang: 26.02.2022
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: nein

Blood test normal Chest X-ray Chills Computerised tomogram normal Dizziness Erythema Fall Fatigue Feeling abnormal Hot flush Hypoaesthesia Illness Magnetic resonance imaging Magnetic resonance imaging head Malaise Migraine Muscle spasms Muscular weakness

Symptomtext

15 minutes after vaccination began with tinnitus, dizziness, nausea. Felt extremely ill for next 11 days. October 26 right leg and arm collapsed and I fell. Went to ER. Checked for stroke or other illness. Nothing found and sent home. One week later right leg went numb, became sicker and almost passed out. Went to ER and admitted for observation. After many tests, nothing found and sent home. Three days later left leg became numb. Got even sicker with blury vision, hot flashes, chills and migraines - no fever. Spent two months using walker. Have since had tinnitus, vestibular problems, leg muscle weakness, sore feet, red toes and toenails have stopped growing, foot cramps, extreme fatigue, foggy head, and have just

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: October 26- CAT scan of brain and bloodwork - nothing found. November 5-6 CAT scan of brain, chest x-ray, MRI of brain and spinal column, ultrasounds of arteries, bloodwork-
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, osteoporosis, high cholesterol, sinus infections
Andere Medikamente: Loratadine, Pulmicort, Famotidine, Serevent, Nasacort, Biotin
Allergien: Tobramycin, Gentamycin, Ciprofloxacin, Phenazopyridine
Vorherige Impfungen: -

VAERS 2146445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: UT
Alter: 38,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Asthma Dizziness Dyspnoea Menstruation irregular Palpitations Wheezing

Symptomtext

Palpitations; Lightheaded; SOB; Asthma; Wheezing; Got my period 2 weeks early; My joints have been super painful; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 11Oct2021 17:00 (Lot number: Ff2590) at the age of 38 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Ehlers danlos syndrome" (unspecified if ongoing). Concomitant medication(s) included: VIT D [VITAMIN D NOS]; IBUPROFEN. The following information was reported: PALPITATIONS (non-serious) with onset 12Oct2021 18:00, outcome "recovering", described as "Palpitations"; DIZZINESS (non-serious) with onset 12Oct2021 18:00, outcome "recovering", described as "Lightheaded"; DYSPNOEA (non-serious) with onset 12Oct2021 18:00, outcome "recovered" (Oct2021), described as "SOB"; ASTHMA (non-serious) with onset 12Oct2021 18:00, outcome "recovering", described as "Asthma"; WHEEZING (non-serious) with onset 12Oct2021 18:00, outcome "recovering", described as "Wheezing "; MENSTRUATION IRREGULAR (non-serious) with onset 12Oct2021 18:00, outcome "recovering", described as "Got my period 2 weeks early"; ARTHRALGIA (non-serious) with onset 12Oct2021 18:00, outcome "recovering", described as "My joints have been super painful". Therapeutic measures were not taken as a result of palpitations, dizziness, dyspnoea, asthma, wheezing, menstruation irregular, arthralgia. Additional Information: Facility type Vaccine: Pharmacy or Drug Store. No other vaccines in four weeks. No covid prior vaccination. No Covid tested post vaccination. No known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Ehlers-Danlos syndrome
Andere Medikamente: VIT D [VITAMIN D NOS]; IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 2140329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 82,0
Geschlecht: M
Eingang: 25.02.2022
Impfdatum: 16.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Confusional state Pyrexia Tachycardia

Symptomtext

Patient woke up confused, febrile (102.7), and tachycardic. Patient received tylenol and IV fluids. Patient was observed and discharged to residing Nursing Home.

Weitere VAERSDATA-Felder

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

VAERS 2139848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 07.10.2021
Beginn: 03.01.2022
Tage bis Beginn: 88,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Dyspnoea Nucleic acid test SARS-CoV-2 test positive

Symptomtext

01/03/22 presents to ED for "SOB". PMHx of "ESRD s/p permacath placement, CAD s/p stent placement"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/03/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2134526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MT
Alter: 67,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 22.10.2021
Beginn: 29.12.2021
Tage bis Beginn: 68,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dyspnoea Hypoxia Influenza A virus test Influenza B virus test Nucleic acid test Respiratory syncytial virus test SARS-CoV-2 test positive

Symptomtext

Case was vaccinated and boosted by 10/22/21, then hospitalized for Covid on 12/31/21. Admitted for shortness of breath and hypoxia. Treated with dexamethosone, and discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: Ordered Test: FLUABV+SARS-CoV-2+RSV RNA Pnl Resp NAA+p (SARS CoV2-Flu-RSV PCR) Ordered Test Codes: Status: Final Accession Number: Specimen Source: Nasopharynx Specimen Site: Specimen Collection Date/Time: 2021-12-29 11:06:00.0 * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe (SARS CoV-2 PCR (COVID-19)) Coded Result: Positive Numeric Result: Units: Text Result: Reference Range From: Negative Reference Range To: Performing Facility Details: Date/Time: 2021-12-29 13:01:54.0 Performing Facility: Facility ID: Interpretation: Abnormal Result Method: (SARS-Co) Status: Final Test Code: Result Code:
Aktuelle Erkrankungen: Stage IV Chronic kidney disease, HTN, Peripheral neuropathy Wegeners Granulomatosis General anxiety disorder Hyperparathyroidism
Vorgeschichte: Stage IV Chronic kidney disease, HTN, Peripheral neuropathy Wegeners Granulomatosis General anxiety disorder Hyperparathyroidism
Andere Medikamente: Vitamin C, Calcitriol, Ferrous sulfate, gabapentin, metoprolol, Vitamin D3, Zofran, Tizanidine PRN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2131242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 22.10.2021
Beginn: 20.02.2022
Tage bis Beginn: 121,0
Dosis: 3
Route/Site: - / -

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

COVID-19 pneumonia

Symptomtext

Covid 19 pna

Weitere VAERSDATA-Felder

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

VAERS 1837424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Blood pressure measurement Blood test Burning sensation Condition aggravated Gait inability Drug ineffective Suspected COVID-19 Gait disturbance Hypoaesthesia Musculoskeletal stiffness Hypertension Myalgia Pain in extremity Movement disorder Neuralgia

Symptomtext

not able to move her right leg.; 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 female patient received bnt162b2 (BNT162B2) (Batch/Lot number: unknown) 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 1, SINGLE), for Covid-19 immunization. The following information was reported: MOVEMENT DISORDER (non-serious), outcome "unknown", described as "not able to move her right leg.". Additional information: Patient was a consumer who received the second dose for Pfizer-BioNTech COVID-19 vaccine 3 months ago and is not able to move her right leg. Patient thought Pfizer is not doing anything about side effects of the vaccine and that other people have been reporting this adverse event on the internet. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2119034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 28.10.2021
Beginn: 06.02.2022
Tage bis Beginn: 101,0
Dosis: 3
Route/Site: IM / -

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

Chest pain Dyspnoea Influenza A virus test Influenza B virus test Palpitations SARS-CoV-2 test

Symptomtext

Palpitations, Chest Pain, SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, CHF, coronary artery disease, and atrial flutter status post ablation
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2119021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 68,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Lip swelling Malaise Mouth swelling Paraesthesia oral Pruritus Swollen tongue Thirst

Symptomtext

Within 5 minutes after the vaccine I developed severe tingling, itching and swelling of my tongue, lips and my entire mouth and I was administered plenty of water and prednisone to stop the symptoms. Was monitored for about 3hrs and released. At home I was so thirsty resulting in me drinking about 9 bottles of water. Self administered myself with levocetirizine 5mg later that evening because I still didn't feel well and fell asleep without eating that entire day and about 4am I woke up and all symptoms had subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Herbal vitamins
Allergien: Aspirin, Tramadol, Morphine, Any inflammatory drugs
Vorherige Impfungen: 2/21-Pfizer COVID-19-2nd dose

VAERS 2113009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: MN
Alter: 45,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 21.10.2021
Beginn: 07.02.2022
Tage bis Beginn: 109,0
Dosis: 3
Route/Site: IM / LA

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

Full blood count Heart rate increased Laboratory test Metabolic function test Sinus tachycardia Supraventricular tachycardia Thyroid function test

Symptomtext

about 3 months and 1 week after booster dose on 2/7/2022 experienced supraventricular tachycardia. This last for 40 min during a project at work at the hospital. Caffeine, stress, physical exertion , poor sleep the night before were all contributing factors at the time. Hooked myself up to a cardiac monitor to see cardiac rhythm in a rate of 210. with regular QRS. Went to the ER and while waiting in the ER self converted. Went to triage obtained vitals and ECG which showed sinus tachycardia with possible left atrial enlargement (which could be stress transient related, never had left atrial enlargement)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: -
Labordaten: on 2/11 visit primary for follow up. Increased lisinopril to 40mg for poor BP control, Zio path for 14 days, oximetry preliminary study, CBC, BMP, and Thyroid labs, and referral to outpatient psychology for stress/possible anxiety.
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril 20mg Ibuprophren 200-400mg Multivitamin
Allergien: NA
Vorherige Impfungen: -

VAERS 2112913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 10.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: SYR / RA

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

Anaemia Blood test Dyspnoea Oedema Oedema peripheral X-ray

Symptomtext

I started having shortness of breath while walking. It has been gradually been increasing. I started getting edema in my stomach, legs, and feet. I went to the doctor and they don't have a diagnosis yet, but they said that I am anemic. I was prescribed Lasix and an Advair inhaler, but it has not really helped yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood Panel- normal Liver- normal Gallbladder- normal X-ray of lungs & heart- normal
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multivitamin Vitamin D Vitamin C Zoloft
Allergien: none
Vorherige Impfungen: -

VAERS 2109400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WI
Alter: 44,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 26.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Electrocardiogram Fatigue Palpitations

Symptomtext

Received Pfizer booster as I had received previous 2 Pfizer vaccine doses. Shortly after began having heart palpitations and severe fatigue that I have now had for nearly 4 months. As a mental health professional I initially thought I had anxiety but quickly ruled that out. Pounding/strong heartbeat hundreds of times/day, sometimes less. Feel like I have to take a nap every afternoon. This is completely unlike me. Never had any heart issues, very healthy, don't nap often at all typically. No chest pain with this. EKG normal, blood tests normal, awaiting heart monitoring. I have read thousands of posts from others online that have similar experience in younger, healthy, never experienced this before people. AND constant dismissal by medical providers that this is related to vaccine despite all of the evidence. AND many people being diagnosed with and prescribed medications for anxiety only to find it is not anxiety. Found out by chance that my father has experienced the exact same symptoms as me..could it be DNA, certain biological make-up in people where this is occurring?

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG and blood tests normal (mid January/beginning Feb 2022). Pending heart monitoring (Feb 2022)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish oil, Lipitor, Lysine, Celexa
Allergien: None
Vorherige Impfungen: -

VAERS 2107371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MA
Alter: 43,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Abdominal pain Body temperature Chills Decreased appetite Dizziness Dry eye Eye pain Headache Hyperhidrosis Lethargy Migraine Mobility decreased Pain Pain in extremity Pyrexia Vaccination site pain

Symptomtext

Temperature 100 for 3 days so far; unable to get out of bed; Body aches/ Extremely sharp shooting pain on left sided of head; constant headache; chills; sweats; pain at injection site as well as down the left side of abdomen and unable to get; pain at injection site as well as down the left side of abdomen; eye pain; Lethargy; Dizziness; Migraine; Severe dry eyes; no appetite; Sore arm; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 43 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 08Oct2021 (Lot number: FF2590) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "HTN" (ongoing); "high cholesterol" (ongoing); "sulfonamide allergy" (unspecified if ongoing), notes: known allergies: Sulfa; "Depression" (ongoing); "Anxiety" (ongoing); "Increased blood pressure" (ongoing). Concomitant medication(s) included: LAMICTAL taken for depression, anxiety (ongoing); OXCARBAZEPINE taken for depression, anxiety (ongoing); LEXAPRO taken for depression, anxiety (ongoing); BUSPAR taken for depression, anxiety (ongoing); ATORVASTATIN taken for blood cholesterol increased (ongoing); VALSARTAN HCTZ taken for blood pressure increased (ongoing). Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: RL1283, Location of injection: Arm Right, Route of administration: Intramuscular), administration date: 14Jan2021, when the patient was 43 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL9264, Location of injection: Arm Left, Route of administration: Intramuscular), administration date: 04Feb2021, when the patient was 43 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "Temperature 100 for 3 days so far"; MOBILITY DECREASED (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "unable to get out of bed"; PAIN (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "Body aches/ Extremely sharp shooting pain on left sided of head"; HEADACHE (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "constant headache"; CHILLS (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "chills"; HYPERHIDROSIS (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "sweats"; VACCINATION SITE PAIN (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "pain at injection site as well as down the left side of abdomen and unable to get"; ABDOMINAL PAIN (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "pain at injection site as well as down the left side of abdomen"; EYE PAIN (non-serious) with onset 09Oct2021 07:30, outcome "recovering", described as "eye pain"; PAIN IN EXTREMITY (non-serious) with onset 08Oct2021, outcome "recovering", described as "Sore arm"; LETHARGY (non-serious) with onset 09Oct2021, outcome "recovering", described as "Lethargy"; DIZZINESS (non-serious) with onset 09Oct2021, outcome "recovering", described as "Dizziness"; MIGRAINE (non-serious) with onset 09Oct2021, outcome "recovering", described as "Migraine"; DRY EYE (non-serious) with onset 09Oct2021, outcome "recovering", described as "Severe dry eyes"; DECREASED APPETITE (non-serious) with onset 09Oct2021, outcome "recovering", described as "no appetite". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia. Therapeutic measures were not taken as a result of mobility decreased, pain, headache, chills, hyperhidrosis, vaccination site pain, abdominal pain, eye pain, pain in extremity, lethargy, dizziness, migraine, dry eye, decreased appetite. Additional information: No Prolonged Hospitalization and no treatment was received. Facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. The 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. Since the vaccination, the patient has not been tested for COVID-19, Device Date :10Oct2021. It was reported No treatment was required for the event for the initiation of new medication/other treatment/Procedure. Beginning the night of vaccine patient began w/a sore arm of the start of a headache. The following morning 09Oct was unable to get out of bed this continued 10Oct and 11Oct. Patient had a temp of ever 100 degree chills, eye pain, lethargy, dizziness, sweats, pain at the injection site that travelled down the side of the body left side, no appetite, severe dry eyes, migraine. On 12Oct felt better out continued to have a migraine that felt like an extremely sharp shooting pain on the left side of my head that woke me up even night coupled with severe left eye pain. No OTC meds provided any relief (nor did they for the temp - that continued to remain at 100 for 3 days). On 15 Oct was the first day patient woke up to no shooting pain. In addition to the above patient had dry eyes (as if they were covered in sand) with no relief. Patient has never experienced this has subsided as well. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20211009; Test Name: Temperature; Result Unstructured Data: Test Result:100; Comments: Temperature 100 for 3 days so far
Aktuelle Erkrankungen: Anxiety; Depression; High cholesterol; Hypertension; Increased blood pressure
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy (known allergies: Sulfa)
Andere Medikamente: LAMICTAL; OXCARBAZEPINE; LEXAPRO; BUSPAR; ATORVASTATIN; VALSARTAN HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 2105498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 81,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 08.10.2021
Beginn: 01.12.2021
Tage bis Beginn: 54,0
Dosis: 3
Route/Site: - / RA

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

Anticoagulant therapy Dyspnoea Echocardiogram Ultrasound Doppler Ventilation/perfusion scan

Symptomtext

Around the end of December 2021, I experienced shortness of breath, which continued to worsen. On 12/29/2021, I went to the hospital. I was then admitted into the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: VQ Scan, Ultrasound on my legs, Echocardiogram, Blood thinner by IV.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Bronchiectasis; High blood pressure; Sleep Apnea; Peripheral Neuropathy; Pernicious Anemia
Andere Medikamente: Alopurinol; azelastine nasal spray; clonidine; clopidogrel; diltiazem; levothyroxine; lisinopril; Lyrica; montelukast; Symbicort inhaler; Spiriva inhaler; vitamin B12 injection
Allergien: Aspirin; penicillin; iodine solution; Levaquin; hydralazine; aspergillosis
Vorherige Impfungen: -

VAERS 2102008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IN
Alter: 41,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 08.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Neck pain Paraesthesia Peripheral swelling

Symptomtext

Stated that One hour after receiving the injection she started having pain in right shoulder and up into neck that got progressively worse through the day. The following morning she stated the pain was much worse (8-9 on 0-10 scale) and now has swelling and tingling in her right hand and fingers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Referred to Ortho
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: Metoprolol 25 mg po daily
Allergien: PCN = hives
Vorherige Impfungen: -

VAERS 2093387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 13.10.2021
Beginn: 01.02.2022
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: IM / RA

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

Blood bilirubin normal Blood lactic acid normal COVID-19 Chest X-ray normal Chest pain Electrocardiogram abnormal Fibrin D dimer increased Haemoglobin normal Headache Hypoxia Laboratory test Lipase normal Liver function test increased SARS-CoV-2 test positive Sinus tachycardia Tachycardia Troponin normal Urine analysis normal

Symptomtext

02/01/2022 - 55-year-old woman with history of schizophrenia, chronic urinary retention requiring Foley catheter, seizure disorder presents with headache and chest pain. Initial vital signs significant for oxygen saturation 89% and tachycardia to 125. Oxygenation improved to mid 90s with 2 L by nasal cannula. EKG shows sinus tachycardia with rate 105, normal axis, normal intervals, no ST elevations or depressions, initial troponin negative. Chest x-ray without evidence of pneumonia. Labs show no leukocytosis, hemoglobin normal not suggestive of acute blood loss, slight LFT elevation but at baseline, normal bilirubin and lipase, normal lactate not suggestive of sepsis, urinalysis not strongly suggestive of infection and low suspicion in absence of symptoms. D-dimer is elevated to 1.96. Covid swab is positive. Patient's tachycardia did improve with fluids, making suspicion for pulmonary embolism and lower so CT was deferred. Patient requires admission given her hypoxia and will be started on remdesivir and dexamethasone. 02/01/2022 - Patient arrived to floor from ED at 1605. Transferred self to bed from w/c. O2 saturation 92%RA. Patient placed on oxygen 1L/NC. Admission assessment completed. Patient received Remdesivir, and evening dose of Phenobarbital, Keppra, and Potassium 40 mEq now dose at 1730. 02/06/2022 - Patient discharged from facility following covid-19/hypoxia

Weitere VAERSDATA-Felder

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

VAERS 2090149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 38,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chills Hypoaesthesia Inappropriate schedule of product administration Insomnia Migraine Muscle spasms Myalgia Nausea Pyrexia SARS-CoV-2 test Vaccination site movement impairment Vaccination site pain Vaccination site swelling Vaccination site warmth Vomiting

Symptomtext

Numbness in arm and hand of left arm (injection arm); Intense pain at injection site with swelling and heat; Intense pain at injection site with swelling and heat; Intense pain at injection site with swelling and heat; Chills; fever; Muscular pain throughout whole body; Intense Migraine & muscle spasms; Intense Migraine & muscle spasms; Nausea; vomiting; Insomnia; Inability to lift of move injection arm; administration date 04Sep2021(dose number 1) and administration date 24Oct2021 (for dose number 2); This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 24Oct2021 (Lot number: FF2590) at the age of 38 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Sjogren's Syndrome" (unspecified if ongoing), notes: Sjogren's Syndrome; "Hashimoto's Thyroid" (unspecified if ongoing), notes: Hashimoto's Thyroid; "Migraines" (unspecified if ongoing), notes: Migraines; "IBS" (unspecified if ongoing), notes: Irritable bowel syndrome; "Rheumatoid Arthritis" (unspecified if ongoing), notes: Rheumatoid Arthritis; "Known allergies: Yes" (unspecified if ongoing), notes: Allergies. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FC3184, Location of injection: Left Arm), administration date: 04Sep2021, when the patient was 38 years old, for COVID-19 Immunization. The following information was reported: HYPOAESTHESIA (non-serious) with onset 24Oct2021, outcome "not recovered", described as "Numbness in arm and hand of left arm (injection arm)"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE SWELLING (non-serious), VACCINATION SITE WARMTH (non-serious) all with onset 24Oct2021, outcome "not recovered" and all described as "Intense pain at injection site with swelling and heat"; CHILLS (non-serious) with onset 24Oct2021, outcome "not recovered", described as "Chills"; PYREXIA (non-serious) with onset 24Oct2021, outcome "not recovered", described as "fever"; MYALGIA (non-serious) with onset 24Oct2021, outcome "not recovered", described as "Muscular pain throughout whole body"; MIGRAINE (non-serious), MUSCLE SPASMS (non-serious) all with onset 24Oct2021, outcome "not recovered" and all described as "Intense Migraine & muscle spasms"; NAUSEA (non-serious) with onset 24Oct2021, outcome "not recovered", described as "Nausea"; VOMITING (non-serious) with onset 24Oct2021, outcome "not recovered", described as "vomiting"; INSOMNIA (non-serious) with onset 24Oct2021, outcome "not recovered", described as "Insomnia"; VACCINATION SITE MOVEMENT IMPAIRMENT (non-serious) with onset 24Oct2021, outcome "not recovered", described as "Inability to lift of move injection arm"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 24Oct2021, outcome "unknown", described as "administration date 04Sep2021(dose number 1) and administration date 24Oct2021 (for dose number 2)". The events "numbness in arm and hand of left arm (injection arm)", "intense pain at injection site with swelling and heat", "intense pain at injection site with swelling and heat", "intense pain at injection site with swelling and heat", "chills", "fever", "muscular pain throughout whole body", "intense migraine & muscle spasms", "intense migraine & muscle spasms", "nausea", "vomiting", "insomnia" and "inability to lift of move injection arm" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of hypoaesthesia, vaccination site pain, vaccination site swelling, vaccination site warmth, chills, pyrexia, myalgia, migraine, muscle spasms, nausea, vomiting, insomnia, vaccination site movement impairment. Additional information: Treatment with tylonel, rest, heat, fluids, re-evaluate was given. Prior to vaccination, patient was not diagnosed with COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Test Date: 20211025; Test Name: binax; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy NOS (Allergies); Hashimoto's thyroiditis (Hashimoto's Thyroid); Irritable bowel syndrome; Migraine (Migraines); Rheumatoid arthritis; Sjogren's syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2088074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: SC
Alter: 27,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Blood test Hypoaesthesia Nasopharyngitis Pain in extremity Palpitations X-ray

Symptomtext

I STARTED FEELING LIKE A BAD COLD WAS COMING ON, I HAD LEFT ARM PAIN AND THEN IT WENT NUMB. I WAS HAVING HEART PALPATATIONS, I FELT WEAK & SO I WENT TO ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: BLOOD WORK, CHEST X-RAY.
Aktuelle Erkrankungen: NONE
Vorgeschichte: BLOOD PLALET FUNCTION DEFECT, EXERCISE INDUCED ASTHMA
Andere Medikamente: Birth Control, Tretinoin, Tazorac, Multi Vitamin, Flax Seed Oil, Zyrtec, Benadryl, Albuterol Inhaler, Trazadone
Allergien: PENICILLIN, SULFA, IBUPROFEN, PEANUTS, ALMONDS
Vorherige Impfungen: -

VAERS 2082762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: SD
Alter: 54,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 02.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Headache Tinnitus Vaccine positive rechallenge

Symptomtext

Actually started after my initial two doses which were given on 12/22/2021 and 01/12/2021. After these doses I started getting headaches and eventually ringing in my ears (tinnitus). These symptoms lasted for months and I had a doctors visit on July 6, 2021 about the headaches and I mentioned the tinnitus. In about October the headaches seemed to subside and the tinnitus had diminished. Then on November 2, 2021 I received the third shot (booster) and a few days later the headaches came back and the tinnitus came back as well. Today the headaches have subsided but the tinnitus is always present with some days it being more intense than others. The COVID19 (Pfizer-BioNTech) shots I received in December and January of 2021 have the following lot numbers (EK9231) and (EL3246).

Weitere VAERSDATA-Felder

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

VAERS 2068829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: WA
Alter: 37,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 27.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Blood pressure increased Chest X-ray normal Computerised tomogram normal Echocardiogram normal Headache Hypertension Laboratory test normal

Symptomtext

Sever Headache started on Sunday 10/31 following the vaccination and continued for multiple days. I did not think to check my Blood pressure until a doctor checked it on 11/2 and it was 170s/110s. It onto us to rise on 11/2/21 and I went to emergency room for treatment on 11/2 evening and 11/3 evening. This is now onset acute hypertension. Medication was needed to control and maintain the blood pressure . By three months following the booster I am no longer in medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Labs were normal. Ct scan was normal. Echo was normal. X-ray of chest was normal. No reason could be found as to why the blood pressure was raised.
Aktuelle Erkrankungen: None
Vorgeschichte: Heart valve replacement in 2016 Epilepsy, controlled with medication
Andere Medikamente: Aspirin 81 mg Zonisamide 200 mg
Allergien: Lamictal
Vorherige Impfungen: -

VAERS 2068819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 26.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram Hypoaesthesia Magnetic resonance imaging Paraesthesia Raynaud's phenomenon

Symptomtext

Raynaud's Phenomenon, numbness and tingling on my entire left side 1 week after my 2nd shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Went to urgent care, they thought I was having a stroke. Went to Emergency room for CT scan on November 4, 2021. They wanted to do blood work and thought an MRI might show more. However after waiting 6 hours I voluntarily left after MRI was completed.
Aktuelle Erkrankungen: Seasonal allergies
Vorgeschichte: Sjogren's syndrome, Fibromyalgia, ADHD
Andere Medikamente: Adderall, birth control pill, Tylenol
Allergien: -
Vorherige Impfungen: -

VAERS 2062646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MO
Alter: 47,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 21.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / -

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

Condition aggravated Migraine

Symptomtext

Debilitating migraine 2 days after, which continued for 8 days. I then got another one two weeks later for 7 days. It's continued in this pattern. Today is a migraine day. They are now every 2 weeks for 10 days. I have 10 out of 30 good days since my booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine. Usually every other month for 7-10 days. Can be monthly for 10 days. Now it's twice a month for 7-10 days as well as the intensity has increased.
Andere Medikamente: Lisinopril 5mg (twice a day for migraine prevention); Ubrelvy (as needed for migraine) and Sumatriptan (nasal spray as needed to break migraine)
Allergien: Cherries, Emgality, soaps
Vorherige Impfungen: -

VAERS 2062334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 38,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 07.04.2021
Beginn: 12.01.2022
Tage bis Beginn: 280,0
Dosis: 3
Route/Site: - / -

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

Chills Cough Musculoskeletal chest pain Nasal congestion Oropharyngeal pain Sinus congestion Upper-airway cough syndrome

Symptomtext

sore throat (has improved), cough, nonproductive cough, chills, sinus congestion (Improving), nasal congestion, post nasal drainage, some pain in ribs. starting 1/12/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: ?Omega 3 550 MG Capsule as directed Orally ?Probiotic - Capsule as directed Orally ?Vitamin D 400 UNIT Capsule 1 capsule Orally Once a day
Allergien: none
Vorherige Impfungen: -

VAERS 1856937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Lymph node pain Mobility decreased Incorrect route of product administration Magnetic resonance imaging Pain in extremity Peripheral swelling Shoulder injury related to vaccine administration

Symptomtext

patient saying she got the vaccine too high in the arm and pain swelling and per MD she had SIRVA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: MRI patient didn't provide date
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2050666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 30.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: SYR / LA

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

Dyspnoea Palpitations

Symptomtext

Heart palpitations, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: Turkey tail mushroom, vitamin d3, zinc, magnesium
Allergien: -
Vorherige Impfungen: -

VAERS 2034842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: KY
Alter: 72,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 10.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Condition aggravated Confusional state Hypercalcaemia Malaise Mental status changes SARS-CoV-2 test positive

Symptomtext

Per History and physical on 1/10/22: "patient is a 72 y.o. female with a history of Sick Sinus syndrome s/p pacemaker placement, diastolic CHF, hypertension, Diabetes Mellitus, hyperlipidemia, hypercalcemia (follows nephrology), and anxiety who presents to ED with complaint of generalized weakness, malaise, and worsening confusion. Was recently admitted on 12/20/21-1/05/22 for altered mental status and hypercalcemia. Scheduled to see Nephrology next month. Covid-19 positive on admission today." Patient later had possible TIA.

Weitere VAERSDATA-Felder

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

VAERS 2028024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 69,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 06.02.2021
Beginn: 08.01.2022
Tage bis Beginn: 336,0
Dosis: 3
Route/Site: - / -

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

Cold sweat Cough Dysphonia Dyspnoea Feeling hot Headache Nausea Pain in extremity Squamous cell carcinoma of skin Stress echocardiogram normal Upper-airway cough syndrome Vitamin D deficiency

Symptomtext

post nasal drainage, cough, hoarse voice, nausea,, slight headache, hot and clammy, shortness of breath, legs ache. starting 1/8/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Elevated cholesterol. Hypothyroid. Osteopenia-Osteoporosis. Hx of phlebitis. Shingles x 3. Vitamin D deficiency 3/10. Remote history of impaired fasting glucose. Squamous cell- face 3/10. Hx of Parotitis/sailadentiis. Hearing loss. Stress echo 6/11: normal . Tobacco use. Chronic middle ear effusions- recommended for tubes 3/14. Sinus surgery planned 4/14. Hx of mastoiditis, s/p surgery. Cholesteatoma of mastoid on the right. Environmental allergies. Patient wakes up during surgical procedures, requires careful anesthesiology, perhaps more aggressive. Elevated blood pressure reading without diagnosis of hypertension. Polyarthritis. Adenomatous colon polyp. Family history of colon cancer. S/P colostomy and colostomy take down due to severe diverticulitis (had ruptured diverticulitis in early 2015). . Family history of colon cancer. SBO 4/2018, treated conservatively. Question of left trigeminal neuralgia. Elevated cholesterol. Hypothyroid. Osteopenia-Osteoporosis. Hx of phlebitis. Shingles x 3. Vitamin D deficiency 3/10. Remote history of impaired fasting glucose. Squamous cell- face 3/10. Hx of Parotitis/sailadentiis. Hearing loss. Stress echo 6/11: normal . Tobacco use. Chronic middle ear effusions- recommended for tubes 3/14. Sinus surgery planned 4/14. Hx of mastoiditis, s/p surgery. Cholesteatoma of mastoid on the right. Environmental allergies. Patient wakes up during surgical procedures, requires careful anesthesiology, perhaps more aggressive. Elevated blood pressure reading without diagnosis of hypertension. Polyarthritis. Adenomatous colon polyp. Family history of colon cancer. S/P colostomy and colostomy take down due to severe diverticulitis (had ruptured diverticulitis in early 2015). . Family history of colon cancer. SBO 4/2018, treated conservatively. Question of left trigeminal neuralgia.
Andere Medikamente: ?Ondansetron 4 MG Tablet Disintegrating 1 tablet on the tongue and allow to dissolve Orally two times a day as needed for nausea, Notes: prn ?Accu-Chek Nano SmartView w/Device Kit as directed - 1 kit ?Vitamin D3 50 MCG (2000 UT) Table
Allergien: Actonel: heartburn - Side Effects Evista: heartburn - Side Effects Fosamax: heartburn - Side Effects Lipitor: myalgia - Side Effects Lovastatin: myalgia - Side Effects Crestor: myalgias at higher doses - Side Effects
Vorherige Impfungen: -

VAERS 2025145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 21.10.2021
Beginn: 30.11.2021
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: - / -

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

Dyspnoea exertional

Symptomtext

Dyspnea on exertion. ED visit and hospital admission. This visit was within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2024872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NJ
Alter: 81,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 30.10.2021
Beginn: 10.01.2022
Tage bis Beginn: 72,0
Dosis: 3
Route/Site: IM / -

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

Arrhythmia COVID-19 Chest X-ray normal Fall SARS-CoV-2 test positive Troponin

Symptomtext

81 year old male with hx PAF, s/p watchmans, HTN, COPD, current lifelong smoker, bladder ca, ETOH abuse, RBBBB, HLD, hypothyroidsm, presents for a fall, he states he was placing the garbage cans out and lost his footing and was walking backwards and slid on the ground onto his right shoulder. NO syncope or dizziness, no chest pain or changes in breathing, no fever or chills. He is positive COVID 19 in the ED. Otherwise his chest xray is clear, no nausea or other changes in taste or smell or any loose stools. He is vaccinated x 3 with pfizer. Plan to admit to telemetry for arrhtymia monitoring and due to mild tropnin leak. Cardilogist is Hynes. Chest xray is negative for infiltrates or effusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: 1,0
Labordaten: 01/10/2022 - SARS-COV-2 Antigen (++)
Aktuelle Erkrankungen: -
Vorgeschichte: Paroxysmal atrial fibrillation Hypertension Hyperlipidemia COPD BPH Bladder cancer GERD Barrots esophagus. Significant Surg Hx As Listed Addt'l Surgical History; Bladder surgery, watchmans procedure. Smoking Status Daily Smoker.
Andere Medikamente: "ACTIVE - ASPIRIN 81MG BY MOUTH DAILY (AT BEDTIME)" "ACTIVE - BREO ELLIPTA 1 PUFF BY INHALATION DAILY" "ACTIVE - COLACE 300MG BY MOUTH DAILY (AT BEDTIME)" "ACTIVE - FLOMAX 0.4MG BY MOUTH DAILY; AT 2PM" "ACTIVE - MULTIVITAMIN FORMULAS 1 TABL
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2018304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 64,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Blood pressure measurement Blood test Computerised tomogram Dehydration Dizziness Immunisation Investigation Speech disorder

Symptomtext

booster; dizziness; dehydrated; couldnt speak; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 07Oct2021 14:00 (Lot number: FF2590) at the age of 64 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Pancreatis", start date: 2015 (ongoing), notes: No symptoms doing good; "Skin Cancer" (ongoing), notes: Onset date: At least 30 years, Doing good; "BP" (ongoing), notes: Onset date: Last 20 years, Normal losartan; "Cholesterol" (ongoing), notes: Onset date: 20 years, Normal, Pravastatin. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1st, Date: 06Jan2021, Time (24 hrs): 2 PM, Site and Route of Injection: Right Arm, Batch/Lot Number: EK4176, DOSE 1, SINGLE), administration date: 06Jan2021, when the patient was 63 years old, for COVID-19 Immunization; Bnt162b2 (Dose: 2nd, Date: 21Jan2021, Time (24 hrs): 1-2 PM, Site and Route of Injection: Right Arm, Batch/Lot Number: 8N5318, DOSE 2, SINGLE), administration date: 21Jan2021, when the patient was 63 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 07Oct2021 14:00, outcome "unknown", described as "booster"; DIZZINESS (non-serious) with onset 07Oct2021, outcome "recovering", described as "dizziness"; DEHYDRATION (non-serious) with onset 07Oct2021, outcome "recovering", described as "dehydrated"; SPEECH DISORDER (non-serious) with onset 07Oct2021, outcome "recovering", described as "couldnt speak". The event "dizziness" was evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: No prior Vaccination. On 28Jan2021, the lab tests CT, Blood and BP were normal. It was reported that vaccine in middle of day but work requires. That night dizzy, dehydrated and couldn't speak. Sent home 3 hours later, doing good. Test Normal. Dehydrated, better. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 20210128; Test Name: BP; Result Unstructured Data: Test Result:Normal; Test Date: 20210128; Test Name: Blood; Result Unstructured Data: Test Result:Normal; Test Date: 20210128; Test Name: CT; Result Unstructured Data: Test Result:Normal; Test Name: Test; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: BP (Onset date: Last 20 years Normal losartan); Cholesterol (Onset date: 20 years Normal, Pravastatin); Pancreatitis (No symptoms doing good); Skin cancer (Onset date: At least 30 years Doing good)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2659669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: -
Beginn: 21.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chills Dyspnoea Exposure to SARS-CoV-2 Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/26, Pfizer, dose #1 03/19, Pfizer, dose #2 10/14, Pfizer, dose #3 12/22 COVID swab, result: detected 12/22 SARS-COV-2 Variant Sequencing: pending 12/21 pt cc: chills, sore throat, rhinorrhea, dyspnea, congestion & sneezing exposure wife 12/28 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/22 COVID swab, result detected 12/22 SARS-COV-2 Variant Sequencing: pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014234

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MO
Alter: 65,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 12.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Influenza virus test negative Injection site pain Mobility decreased Muscle disorder Muscular weakness Pain Respiratory syncytial virus test negative SARS-CoV-2 test negative Sleep disorder

Symptomtext

He woke up at 2:00 in the morning on 10/13/21 with generalized fatigue, body aches, severe left upper arm pain, muscle weakness, decreased joint mobility. He was seen virtually in clinic at on 10/27/21 due to his symptoms and again on 11/22/21. He has taken OTC medication for pain, heat, ice, rest. He is still having a lot of pain in the shoulder joint with movement and resistance training. He believes he has lost muscle mass in his deltoid region as well. He was instructed to contact his insurance company to see if an MRI would be covered to further evaluate his condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: negative COVID, Flu, RSV tests on 10/27/21. MRI for further evaluation to be ordered once insurance will approve it
Aktuelle Erkrankungen: None
Vorgeschichte: Elevated Cholesterol Hypothyroidism
Andere Medikamente: Lovastatin 10mg Synthroid 25mcg
Allergien: None
Vorherige Impfungen: -

VAERS 2001089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 76,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Dyspnoea Mobility decreased Pneumonia Sepsis

Symptomtext

started with a "Parkinson's freeze" the same day, next day developed trouble breathing and admitted for bilateral pneumonia and sepsis.

Weitere VAERSDATA-Felder

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

VAERS 1995395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Condition aggravated Erythema Immunisation Rash Drug ineffective Interchange of vaccine products Off label use SARS-CoV-2 test Urticaria Vaccination failure

Symptomtext

covid test result: Positive; covid test result: Positive; rashes in different areas of body; hives in different areas of body; redness in different areas of body; Interchange of vaccine products; off label use; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 01Dec2021 19:00 (Lot number: FF2590) at the age of 31 years as dose 3 (booster), single for covid-19 immunisation; covid-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), administered in arm left, administration date 01Apr2021 11:15 (Lot number: 007B21A) as dose 1, single and administered in arm left, administration date 29Apr2021 16:15 (Lot number: 005C21A) as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant) all with onset 13Dec2021, outcome "unknown" and all described as "covid test result: Positive"; INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 01Dec2021, outcome "unknown", described as "Interchange of vaccine products"; OFF LABEL USE (medically significant) with onset 01Dec2021, outcome "unknown", described as "off label use"; RASH (non-serious) with onset 01Dec2021 20:00, outcome "not recovered", described as "rashes in different areas of body"; URTICARIA (non-serious) with onset 01Dec2021 20:00, outcome "not recovered", described as "hives in different areas of body"; ERYTHEMA (non-serious) with onset 01Dec2021 20:00, outcome "not recovered", described as "redness in different areas of body". The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (13Dec2021) positive. Therapeutic measures were not taken as a result of covid-19, drug ineffective, rash, urticaria, erythema. Patient did not receive any other vaccine in four weeks and any other medications in two weeks. Patient has no reported allergies. Patient did not have covid prior to vaccination and tested for covid post No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211213; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1985197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MA
Alter: 66,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 17.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation Cardiomyopathy Dyspnoea Ejection fraction decreased

Symptomtext

On 11/27/2021 The patient begin to experience episodes of shortness of breath. Which progressively became worse overtime, resulting in hospital admission on 12/10/2021. When discharge from hospital she was newly diagnosed with Atrial Fibrillation and cardiomyopathy with reduced ejection fraction. She was discharged home with several medications; Digoxin, Furosemide, Lisinopril, Spironolactone, Warfarin, Carvedilol

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: On 11/27/2021 The patient begin to experience episodes of shortness of breath. Which progressively became worse overtime, resulting in hospital admission on 12/10/2021. When discharge from hospital she was newly diagnosed with Atrial Fibrillation and cardiomyopathy with reduced ejection fraction. She was discharged home with several medications; Digoxin, Furosemide, Lisinopril, Spironolactone, Warfarin, Carvedilol
Vorgeschichte: -
Andere Medikamente: No Medications were being taken at the time this event occurred
Allergien: No Known Drug Allergies
Vorherige Impfungen: -

VAERS 1984634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: CO
Alter: 39,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Chest pain Dyspnoea Fatigue

Symptomtext

Significant chest pain, shortness of breath, fatigue, continuing for over 3 weeks, worse shortly after vaccine, worse after exercise. Recommended to seek EKG/diagnostics by medical provider (unable to afford diagnostics)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: unable to afford diagnostics
Aktuelle Erkrankungen: none
Vorgeschichte: celiac
Andere Medikamente: none
Allergien: gluten
Vorherige Impfungen: Regular fevers after flu vaccines

VAERS 1929298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: MA
Alter: 63,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 28.10.2021
Beginn: 04.12.2021
Tage bis Beginn: 37,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Computerised tomogram thorax abnormal Dyspnoea Lung opacity Neutropenia SARS-CoV-2 test positive

Symptomtext

Patient was admitted prior to this admission for covid 19 infection iso neutropenia and tested positive for covid on 11/27/21. Patient presented to Hospital on 12/4/21 with worsening SOB and was started on 5 days of remdesivir. Patient was also continued on home oncologic treatment. Patient is fully vaccinated for covid. Patient was discharged on 12/10/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: covid positive on 12/5/21. 12/4 CT chest impression: No evidence for PE. small peripheral pulmonary groundglass opacities and consolidations likely related to patient's known covid 19 infection
Aktuelle Erkrankungen: N/A
Vorgeschichte: mantle cell lymphoma c/b babesia
Andere Medikamente: acalabrutinib, acyclovir, allopurinol, vitamin d3, melatonin, venetoclax
Allergien: penicillin G, benzathin, procain
Vorherige Impfungen: -

VAERS 1971433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 68,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 20.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Cellulitis Condition aggravated Lymphoedema Peripheral venous disease SARS-CoV-2 test negative

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient admitted to hospital with right lower extremity cellulitis, chronic venous stasis, and lymphedema. Received antibiotics, improved, and discharged to home medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 10,0
Labordaten: SARS-CoV-2: negative
Aktuelle Erkrankungen: right arm pain
Vorgeschichte: chronic venous insufficiency, hypertension, history of recurrent DVT, hypothyroidism, GERD< cirrhosis, anemia, shoulder pain, psoriasis, lymphedema, cervical radiculopathy
Andere Medikamente: albuterol, warfarin, diclofenac topical, gabapentin, levothyroxine, lidocaine patch, oxycodone, pantoprazole
Allergien: vancomycin, lactose
Vorherige Impfungen: -

VAERS 1970773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MD
Alter: 48,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 13.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: - / LA

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

Dyspnoea Epistaxis HLA marker study Inflammation Migraine SARS-CoV-2 test

Symptomtext

migraine headache; difficulty breathing / I was able to breath in but not out; nose bleeds; acute inflammation in entire body; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Oct2021 10:15 (Lot number: FF2590) at the age of 48 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "genetic marker HLA-B27 positive" (unspecified if ongoing); "history of ankloysing spondinitis" (unspecified if ongoing); "known allergies: Shellfish" (unspecified if ongoing). Concomitant medication(s) included: HUMIRA. Past drug history included: Mesalamine, reaction(s): "allergies". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FC3184, Location of injection: Arm Left, Vaccine Administration Time: 10:15 AM), administration date: 22Sep2021, when the patient was 47 years old, for Covid-19 immunization. The following information was reported: MIGRAINE (hospitalization) with onset 23Oct2021, outcome "recovering", described as "migraine headache"; DYSPNOEA (hospitalization) with onset 23Oct2021, outcome "recovering", described as "difficulty breathing / I was able to breath in but not out"; EPISTAXIS (hospitalization) with onset 23Oct2021, outcome "recovering", described as "nose bleeds"; INFLAMMATION (hospitalization) with onset 23Oct2021, outcome "recovering", described as "acute inflammation in entire body". The patient was hospitalized for migraine, dyspnoea, epistaxis, inflammation (start date: 29Oct2021, discharge date: 03Nov2021, hospitalization duration: 5 day(s)). The events "migraine headache", "difficulty breathing / i was able to breath in but not out", "nose bleeds" and "acute inflammation in entire body" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: hla marker study: (unspecified date) positive; sars-cov-2 test: (30Oct2021) negative, notes: covid test type post vaccination=Blood test, covid test name post vaccination=Hospital did it. Therapeutic measures were taken as a result of migraine, dyspnoea, epistaxis, inflammation which included antibiotics. Clinical course: Within 1 week after 2nd dose, she had migraine headache, difficulty breathing, nose bleeds. She was able to breath in but not out. Ended up in hospital 29Oct-03Nov with acute inflammation in entire body. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: Test Name: genetic marker HLA-B27; Test Result: Positive ; Test Date: 20211030; Test Name: Covid test; Test Result: Negative ; Comments: covid test type post vaccination=Blood test, covid test name post vaccination=Hospital did it
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Ankylosing spondylitis; HLA-B*27 positive; Shellfish allergy
Andere Medikamente: HUMIRA
Allergien: -
Vorherige Impfungen: -

VAERS 1968448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: HI
Alter: 55,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 28.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / -

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

Arthralgia Blood test Cardiac stress test normal Echocardiogram normal Exercise electrocardiogram Palpitations Troponin increased

Symptomtext

Joint pain and heart palpitations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Blood work, 2- treadmill stress tests and 3- echocardiograms. Blood work found Troponin levels elevated. All other tests (treadmill tests and echocardiograms) didn?t detect any heart damage.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1963893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Blood magnesium normal Blood test Blood thyroid stimulating hormone normal Computerised tomogram head Electrocardiogram Full blood count normal Glycosylated haemoglobin Hypertension Immediate post-injection reaction Insomnia Metabolic function test Metabolic function test normal Panic attack Thyroxine free normal Tri-iodothyronine normal Urine analysis

Symptomtext

Immediately following my shot, which was a booster as I was fully vacinnated with Moderna back in January 2021, I developed hypertension and extreme anxiety. I also began to have panic attacks and had great difficulty sleeping. All of these symptoms are highly unusual for me. I am now seven weeks since receiving the Pfizer Booster and I am still suffering these symptoms and don't know what to do as my numerous doctors' visits since the shot have not been able to conclusively identify a reason.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: EKQ, complete bloodpanel, CT on brain, and a urinalysis. The bloodpanel tests looked at: T3 Total, T4 Free, Thyroid stimulating hormone, complete blood count, comprehensive metabolic panel, magnesium, hemaglobin A1C, TSH (3rd generation). None of the tests showed any results out of normal range.
Aktuelle Erkrankungen: hemorrhoids
Vorgeschichte: none
Andere Medikamente: None
Allergien: dust
Vorherige Impfungen: -

VAERS 1963329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: GA
Alter: 47,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dyspnoea Headache Lymphadenopathy Pain Palpitations Pyrexia Throat irritation

Symptomtext

Heart racing felt short of breath on 12/18/2021 when I went to the ER early morning but later that afternoon I started having fever body aches and noticed slight swelling in left under arm pit On 12/19/2021 still had slight swelling under arm pit and had a headache. 12/20/2021 no more swelling under arm pit still have a headache and throat is a little itchy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: History of palpitations and elevated blood pressure and Graves? disease
Andere Medikamente: Methimazole 10mg, Pantoprazole 40mg, Loratadine10mg, metoprolol 25 mg, 81mg Aspirin, Women multivitamin, Emergen-C 1000 mg, Elderberry Linzess 72
Allergien: -
Vorherige Impfungen: 1/8/2021

VAERS 1954946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 06.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: IM / -

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

Atrial fibrillation Bundle branch block Cardiac failure Cardiac failure congestive Cardiac pacemaker insertion Catheterisation cardiac normal Electrocardiogram Implantable defibrillator insertion Magnetic resonance imaging heart Sinus tachycardia Ultrasound scan Ventricular arrhythmia Ventricular dysfunction

Symptomtext

Otherwise healthy male in shape and active. In a few weeks ends up two hopsitals with substantial Cardiac problems. I had no prior history of heart issues and testing done by school medical rules out other diseases that sponsor heart failure. My cardiac heart failure includes sinus tachycardia, ventricular arrhythmia, atrial fib, ventricular dysfunction, bundled branch etc. I had to have a Pacemaker and Defibulator surgically implanted. Cath Review of the heart showed no blockages or related vascular complications. Congestive heart failure that I feel is likely related to me taking the third shot of the Pizer Covid19 Vaccination.

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Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: 12,0
Labordaten: EKG, Ultrasound, Cardialc MRI, Cath Review Of Heart
Aktuelle Erkrankungen: None
Vorgeschichte: None. Diabetes Type 2
Andere Medikamente: Metformin, Allegra
Allergien: None
Vorherige Impfungen: -

VAERS 1950775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Blood pressure increased Blood pressure measurement Burning sensation Chest pain Coagulation time Dizziness Electrocardiogram Gait disturbance Pallor SARS-CoV-2 test Speech disorder Ultrasound scan Vaccination site pain

Symptomtext

Within a few minute I received the shot on my left arm, I felt burning sensation spreading from there to left heart area, left chest then moved to right arm area, to both legs; I felt burning sensation spreading from there to left heart area, left chest then moved to right arm area, to both legs.; I got so pale; Right headed, almost fainting; Couldn't walk; Difficulty to talk and answer doctor's question; After the shot, my blood pressure elevated from 100-110's to 140-160 , at that time 150/100 around for 2 weeks; All night long, I had a left chest pain and thought I will have a heart attack or not.; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 29Oct2021 at 12:30 (Lot number: FF2590) at the age of 51 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Pituitary tumour" (unspecified if ongoing); "Pituitary cyst" (unspecified if ongoing) and "Allergy to antibiotic" (unspecified if ongoing), notes: Known allergies: one antibiotic. There were no concomitant medications. Past drug history included: Atropine, reaction: "Drug allergy", notes: Known allergies: Atropine. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 29Oct2021 at 12:30, outcome "recovering", described as "Within a few minute I received the shot on my left arm, I felt burning sensation spreading from there to left heart area, left chest then moved to right arm area, to both legs"; BURNING SENSATION (non-serious) with onset 29Oct2021 at 12:30, outcome "recovering", described as "I felt burning sensation spreading from there to left heart area, left chest then moved to right arm area, to both legs"; PALLOR (non-serious) with onset 29Oct2021 at 12:30, outcome "recovering", described as "I got so pale"; DIZZINESS (non-serious) with onset 29Oct2021 at 12:30, outcome "recovering", described as "Right headed, almost fainting"; GAIT DISTURBANCE (non-serious) with onset 29Oct2021 at 12:30, outcome "recovering", described as "Couldn't walk"; SPEECH DISORDER (non-serious) with onset 29Oct2021 at 12:30, outcome "recovering", described as "Difficulty to talk and answer doctor's question"; CHEST PAIN (non-serious) with onset 29Oct2021, outcome "recovering", described as "All night long, I had a left chest pain and thought I will have a heart attack or not"; BLOOD PRESSURE INCREASED (non-serious) with onset 29Oct2021 at 12:30, outcome "recovering", described as "After the shot, my blood pressure elevated from 100-110's to 140-160 , at that time 150/100 around for 2 weeks". The event "All night long, I had a left chest pain and thought I will have a heart attack or not." was evaluated at the emergency room visit. The events "Within a few minute I received the shot on my left arm, I felt burning sensation spreading from there to left heart area, left chest then moved to right arm area, to both legs.", "I felt burning sensation spreading from there to left heart area, left chest then moved to right arm area, to both legs.", "I got so pale", "Right headed, almost fainting", "Couldn't walk", "Difficulty to talk and answer doctor's question" and "After the shot, my blood pressure elevated from 100-110's to 140-160 , at that time 150/100 around for 2 weeks" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of vaccination site pain, burning sensation, pallor, dizziness, gait disturbance, speech disorder, chest pain and blood pressure increased. Additional Information: The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. It was reported that the doctors came to make the patient sit on a wheelchair and gave the patient 10 bottle of water to drink, also 3 strawberries and three hours later, the patient felt better and could walk out from hospital herself. The patient had almost called for ambulance due to left chest pain. The following day, the patient went to an Urgent care to do EKG (result was normal). The left chest pain continued for 2 weeks. The patient went to see cardiologist 2 times to do another EKG, ultra sound and blood clot test since she had the chest pain; the results were ok except high blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood clot test; Result Unstructured Data: Test Result:The results were ok; Test Date: 2021; Test Name: Ultra sound; Result Unstructured Data: Test Result:The results were ok; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:The results were ok; Test Date: 20211030; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20211029; Test Name: Blood pressure; Result Unstructured Data: Test Result:150/100; Test Date: 20211029; Test Name: Blood pressure; Result Unstructured Data: Test Result:140-160; Comments: Blood pressure elevated from 100-110's to 140-160; Test Date: 20211115; Test Name: PCR; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic (Known allergies: one antibiotic); Pituitary cyst; Pituitary tumour.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1948231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 62,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Diarrhoea Migraine Nausea Vertigo

Symptomtext

Shot #1 Migraine, Nausea, Spins, Upset Stomach lasting 8-10 days Shot #2 Migraine, Nausea, Spins, Diarrhea lasting 6 days

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None; Stayed in Bed, had to stay laying down
Aktuelle Erkrankungen: Migraine Headache, Nausea, Spins
Vorgeschichte: Girdlestone
Andere Medikamente: Cymbalta, Sertraline, Alendronate, Lisinopril, Morphine
Allergien: None
Vorherige Impfungen: -

VAERS 1947000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: ID
Alter: 68,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 21.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / RA

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

Chest pain Discomfort Feeling abnormal Hypoacusis Immunisation Joint range of motion decreased Pain Pleurisy Pulmonary pain Vaccination site pain

Symptomtext

Chest pain (Rt lateral mid chest) with movement; Sitting up + deep breaths increase discomfort; some pain around the injection site; Booster; I have like pleurisy in my right lung lateral chest; lining of my lungs are painful like if we cough or if you are going to just lay on and move or try to sit up so I am going to call it pleurisy type feeling; I laid pretty low this whole time; little hard of hearing; Increased pain and movement worses; Do not reach with Rt arm; This is a spontaneous report received from a contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 68-year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 21Oct2021 10:09 (Lot number: FF2590, Expiration Date: 31Mar2022) at the age of 68 years as dose 3 (booster), single for covid-19 immunization. Relevant medical history included: "broken rib" (unspecified if ongoing), notes: I have had a broken rib before; "Depression" (ongoing); "Leg jerks" (ongoing); "Hormone replacement" (ongoing). Concomitant medication(s) included: BUPROPION HCL XL taken for depression (ongoing); PROGESTERONE taken for hormone replacement therapy (ongoing); CARB/LEVO ER taken for dyskinesia (ongoing). Vaccination history included: Bnt162b2 (Dose :1 , No events reported, Anatomical site of injection: Right upper arm, Route of administration: Intramuscular, Batch/Lot number: ER8727), administration date: 19Mar2021, when the patient was 67 years old, for Covid-19 Immunization; Bnt162b2 (Dose : 2, No events reported, Anatomical site of injection: Right upper arm, Route of administration: Intramuscular, Batch/Lot number: EP7533), administration date: 09Apr2021, when the patient was 67 years old, for Covid-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 21Oct2021 22:30, outcome "recovering", described as "some pain around the injection site"; PLEURISY (non-serious) with onset Oct2021, outcome "recovering", described as "I have like pleurisy in my right lung lateral chest"; PULMONARY PAIN (non-serious) with onset Oct2021, outcome "recovering", described as "lining of my lungs are painful like if we cough or if you are going to just lay on and move or try to sit up so I am going to call it pleurisy type feeling"; FEELING ABNORMAL (non-serious) with onset Oct2021, outcome "recovering", described as "I laid pretty low this whole time"; HYPOACUSIS (non-serious) with onset Oct2021, outcome "recovering", described as "little hard of hearing"; CHEST PAIN (non-serious) with onset 22Oct2021, outcome "recovering", described as "Chest pain (Rt lateral mid chest) with movement"; DISCOMFORT (non-serious) with onset 22Oct2021, outcome "recovering", described as "Sitting up + deep breaths increase discomfort"; PAIN (non-serious) with onset 2021, outcome "recovering", described as "Increased pain and movement worses"; JOINT RANGE OF MOTION DECREASED (non-serious) with onset 2021, outcome "recovering", described as "Do not reach with Rt arm"; IMMUNISATION (non-serious) with onset 21Oct2021 10:09, outcome "unknown", described as "Booster". Therapeutic measures were taken as a result of vaccination site pain, pleurisy, pulmonary pain, feeling abnormal, hypoacusis. Additional information included: The patient concomitant medications included: Bupropion Hydrochloride (BUPROPION HCL XL) via oral route at 300 mg, daily at AM for Depression; Progesterone (capsule) via oral route at 100 mg, once a day, one at bedtime for Hormone replacement. The patient stated that she did have some pain around the injection site, but she had like pleurisy in her right lung lateral chest, and she wanted it to report, and it was finally better today, like at 4 O' clock it started getting better. The patient pressed on her ribs, and she have had a broken rib before (Intent history). This just felt like lining of her lungs were painful like if we cough or if you were going to just lay on and move or try to sit up, so she was going to call it pleurisy type feeling and that happened the next day Friday and she went to get like around 3 and laid pretty low this whole time and now was finally feeling better. Anyway, she looked up the symptoms and did not saw that as a symptom of a typical reaction. She did some yard work on Thursday, and she thought may be that caused it but it was never caused it before. The patient was just little hard of hearing (further not clarified). She put some CBD oil on the site for pain and took some CBD last night under her tongue. The patient did not receive any vaccine Prior to 4 weeks of COVID vaccine. The patient underwent lab tests, and she does not know the results of them as they have been a little while ago (three months ago). She just hoped they were all normal and it was like to check for arthritis, for rheumatoid arthritis (further clarification unknown). On 21Oct2021, 10:09 Am right upper lateral arm injection aching at site and area around it around 10:30 pm. She slept on left side to protect it. Next day she had chest pain (Rt lateral mid chest) with movement. Sitting up and deep breaths increased discomfort. she pressed on ribs, not tender at 3:00 pm and she got to bed because of increased pain and movement worsened it. she spent Saturday in bed till 4:00 pm. The patient had slowly improved enough to get up. she moved slowly and did not reach with Right arm. The patient slowly improved and by Thursday only a slight awareness. She continued to notice an ache with twisting or turning, a deep breath or some reaching. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Depression; Hormone replacement therapy; Jerkiness.
Vorgeschichte: Medical History/Concurrent Conditions: Rib injury (I have had a broken rib before.)
Andere Medikamente: BUPROPION HCL XL; PROGESTERONE; CarB/Levo ER.
Allergien: -
Vorherige Impfungen: -

VAERS 1944605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 22.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Joint swelling Laboratory test Magnetic resonance imaging head Neuralgia Neurological examination Paraesthesia Peripheral swelling Ultrasound scan Urine analysis

Symptomtext

I got the vaccine on Friday 10/22. On Monday 10/25 my feet and legs (primarily calves and just above my knees) were both very swollen. I read that swollen legs could be a severe reaction so I went to urgent care and they sent me to the ER. The ER was overcrowded so they did some bloodwork to check my kidneys I think and said to follow up with my primary care doctor. The next day, Tuesday 10/26, I started feeling "pins and needles" in my hands, feet, and face. The swelling went away after about five days. The nerve pain has not gone away although it has gotten slightly lesser in intensity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: On 11/12 I had an ultrasound of my legs. On 11/18 I had blood and urine labs done. On 12/8 I saw a neurologist who did a neurological exam and then ordered MRIs of my brain and thoracic and cervical spines. I'm getting those MRIs done on 12/16 and then following up with my neurologist on 12/18.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: symbicort
Allergien: celiac disease (gluten), eugenol, latex
Vorherige Impfungen: -

VAERS 1942852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: WI
Alter: 63,0
Geschlecht: M
Eingang: 12.12.2021
Impfdatum: 05.11.2021
Beginn: 08.12.2021
Tage bis Beginn: 33,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Diarrhoea Fatigue Headache Nausea

Symptomtext

Chest pain, Fatigue, Nausea, Headache, DIARRHERA Took baby aspirin at about 2 hours after 10 hours of pain started to feel better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High blood Pressure
Andere Medikamente: centrum silver multivitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1940692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: KS
Alter: 70,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 29.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / -

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

Anaemia Angiogram cerebral normal Aplastic anaemia Asthenia Biopsy bone marrow Blood albumin normal Blood bilirubin increased Blood calcium decreased Blood creatinine normal Blood smear test abnormal Blood urea normal Bone marrow failure Cerebral ischaemia Chest X-ray normal Computerised tomogram head abnormal Cytogenetic abnormality Cytopenia Dyspepsia

Symptomtext

covid vaccines 1/28/2021, 2/18/2021, and 10/29/2021, all pfizer, had rapid decline and progression of dyspnea and profound cytopenias 1 wk after booster, ultimately dx'd w/ MDS-U, hypoplastic, on tx, all seemed to rapidly decline 1 wk post booster Patient is a 70 y.o. male with bone marrow failure, who has been referred for consultation regarding allogeneic transplant. He presented to outside hospital on 11/12/21 with right sided paraesthesia, and was found to have a left subarrachanoid frontal lobe hemorrhage. He was profoundly cytopenic at presentation, with a plt count of 4, hgb of 7, and WBC of 1.8. He has been very active throughout his life, and was riding his bike 60 miles a week. He felt that his endurance started to decline around a month prior to presentation. He did not require surgical intervention for his bleed, and was managed with aggressive platelet transfusions. He had a bone marrow biopsy on 11/12/21 which showed a hypocellular marrow (10%), with severely decreased hematopoiesis, no dysplasia, and numerous small mature lymphocytes. NGS unremarkable and cytogenetics showed isolated 13q deletion. Repeat bone marrow bx on 11/23/21 showed an aplastic marrow without dysplasia. He received a trial of IVIG and dexamethasone x 4 days with no response. He started hATG x 4 days, promacta, cyclosporin and prednisone on 11/25. Outpatient promacta currently on hold pending medication copay assistance. He feels well today and has no acute complaints. No new neurological complaints or headaches. Denies any infections symptoms. Cancer Staging No matching staging information was found for the patient. Diagnosis: MDS APPOINTMENT: 12/2/21 Dr. REFERRING PHYSICIAN: Dr. Allergies: Penicillins and Sulfa (sulfonamide antibiotics) Family Hx: Father: Bone Cancer (Deceased) Mother/Mat. Grandmother: Alzheimer's(Both deceased), GPA/MPA father, hashimoto's thyroiditis daughter, henoch-schonlein purpura daughter He has 2 brothers, age 75 and 58. Two daughters age 35 and 31. Medical Hx: Essential HTN, GERD, a fib, iron deficiency anemia, hypothyroidism, prediabetes, ED Surgical Hx: Cardiac ablation (10/30/20), colonoscopy, knee replacement, upper GI endoscopy, s/p placement of implantable loop recorder. Social Hx: Married, retired school superintendent, former smoker (1ppd; 7 pack-years) quit at age 26, ETOH use, no current drug use Patient is a 70 y.o. gentleman with a PMH for hypertension, hypothyroidism, atrial fibrillation s/p ablation in 2020 who presented to Facility following right-sided paresthesias. Patient reported experiencing mild headaches and significant decrease in energy which is unusual because he is very athletic. Lab work at Facility indicated patient was pancytopenic with a platelet count of 4K. He was transferred to higher level of care for further evaluation. Patient was found to have profound thrombocytopenia, anemia, concerning for aplastic anemia. Ultimately, patient was transferred to inpatient hematology to begin treatment. Patient underwent a BMBX on 11/12/21 that showed markedly hypocellular bone marrow (10%) with near absent trilineage hematopoiesis, less than 1% blasts, and numerous small mature lymphocytes in the aspirate smears. FISH was negative. Repeat BMBX indicated markedly hypocellular bone marrow (<5%) with nearly absent trilineage hematopoiesis and 1% blasts. Due to concern for aplastic anemia with ongoing frequent transfusion requirements, patient started hATG x 4 days, eltrombopag, cyclosporine, and prednisone on 11/25. Patient presents today following hospital discharge for follow-up. Timeline of Events: Aplastic anemia (HCC) 11/10/2021 Imaging CT LMH Small amount of subrachnoid hemorrhage of uncertain etiology overlying the high left frontal lobe posteriorly. 11/12/2021 Pertinent Labs LMH WBC: 1.8 RBC: 2.22 HGB: 7.0 HCT: 19.5 PLT: 4 ANC: 162 11/12/2021 Pertinent Labs WBC: 0.8 RBC: 1.40 HGB: 4.4 HCT: 12.9 RDW: 15.1 PLT: 82 ANC: 0.11 Lymphocytes: 82 A. Peripheral blood, flow cytometry: Minor PNH clone identified in both WBCs and RBCs. Interpretation: Flow cytometric analysis shows a minor PNH clone within the granulocytes (0.25%), monocytes (0.07%) and a minor PNH clone in the RBCs (0.04%). The clinical significance of the small populations with GPI deficiency is uncertain. Small PNH clones have been reported in cases of myelodysplastic syndrome and aplastic anemia. 11/12/2021 Biopsy BMBX KU Bone marrow, left iliac crest, aspirate, biopsy, clot, and touch prep: Markedly hypocellular bone marrow (10%) with near absent trilineage hematopoiesis, less than 1% blasts, and numerous small mature lymphocytes in the aspirate smears. Peripheral blood smear: Pancytopenia with severe normocytic anemia, leukopenia with neutropenia, and marked thrombocytopenia. Flow cytometry: Bone Marrow, flow cytometry: Negative phenotypic study. Cytogenetics: 46,XY,del(13)(q14q22)[cp3]/46,XY[12] FISH: NGS: Pending TP53 PCR Array: Not Detected 11/12/2021 Imaging X-ray-Chest KU No consolidation or pleural effusion. 11/12/2021 Imaging CTA Head 1. Mild increase in subarachnoid hemorrhage at the left frontal lobe. 2. No intracranial arterial stenosis, aneurysm, vascular malformation, or large vessel occlusion identified. 3. Very mild white matter disease, likely secondary to chronic microvascular ischemic changes. 11/12/2021 Imaging MRI Head MR brain: 1. Stable localized subarachnoid hemorrhage along the left frontal cerebral convexity (superimposed superficial siderosis could also be present). Superimposed linear leptomeningeal enhancement, likely reflecting incidental reactive benign vascular engorgement, though, conventional cerebral arteriogram may be beneficial to exclude subtle arteriovenous malformation-fistula. 2. Mild patchy supratentorial white matter FLAIR hyperintensities, likely due to chronic microvascular ischemic changes. 3. Small right mastoid effusion. MRV brain: Normal MRV of the brain. 11/17/2021 Pertinent Labs Peripheral Blood A. Peripheral blood, flow cytometry: Negative immunophenotypic study. 11/23/2021 Biopsy BMBX KU Bone marrow, left iliac crest, aspirate, biopsy, clot, and touch prep: Markedly hypocellular bone marrow (<5%) with nearly absent trilineage hematopoiesis and 1% blasts. Peripheral blood smear: Pancytopenia Comment: Rare erythroid and myeloid elements are present for evaluation. Megakaryocytes are absent. There is no morphologic evidence of dysplasia or increase in blasts. The presence of deletion of 13q in the previous marrow is noted. The overall morphologic and cytogenetic findings are consistent with myelodysplastic syndrome, unclassifiable (hypoplastic myelodysplastic syndrome). Flow cytometry: Not done Cyto/FISH: Not done 11/29/2021 Imaging CT Head WO Contrast 1. Decreased conspicuity of left frontal subarachnoid hemorrhage. No new areas of hemorrhage identified. 2. Mild patchy supratentorial white matter hypodensities, likely sequela of chronic microvascular signal changes. 11/30/2021 Pertinent Labs WBC: 0.3 RBC: 2.23 HGB: 7.1 HCT: 19.5 RDW: 15.3 PLT: 26 BUN: 15 Creat: 0.73 Alb: 3.5 Ca: 8.0 TP: 6.5 Tbilli: 2. Review of Systems Constitutional: Positive for activity change. HENT: Negative for congestion. Eyes: Negative. Respiratory: Positive for shortness of breath (exertional). Cardiovascular: Negative for leg swelling. Gastrointestinal: Heartburn Skin: Positive for pallor. Allergic/Immunologic: Positive for immunocompromised state. Neurological: Positive for headaches (mild, intermittent. None today ). Negative for speech difficulty. Hematological: Bruises/bleeds easily. Psychiatric/Behavioral: Negative for agitation and confusion. Objective: ? acetaminophen (TYLENOL EXTRA STRENGTH) 500 mg tablet Take 500 mg by mouth every 8 hours as needed for Pain. Max of 4,000 mg of acetaminophen in 24 hours. ? acyclovir (ZOVIRAX) 800 mg tablet Take one tablet by mouth twice daily. Indications: infection prophylaxis, medical ? amLODIPine (NORVASC) 5 mg tablet Take one tablet by mouth daily. ? calcium carbonate/vitamin D-3 (OSCAL-500+D) 1250 mg/200 unit tablet Take 1 tablet by mouth daily. Calcium Carb 1250mg delivers 500mg elemental Ca ? cycloSPORINE modified (CYCLOSPORINE) 100 mg capsule Take two capsules by mouth twice daily. Take with one 25 mg capsule for a total of 225 mg twice daily. Indications: Aplastic Anemia ? cycloSPORINE modified (CYCLOSPORINE) 25 mg capsule Take one capsule by mouth twice daily. Take with two 100 mg capsules for a total of 225 mg twice daily. Indications: Aplastic anemia ? eltrombopag (PROMACTA) 75 mg tablet Take two tablets by mouth daily. Take on an empty stomach, at least 1 hour before or 2 hours after food. Separate from antacids by at least 4 hours. ? fluconazole (DIFLUCAN) 200 mg tablet Take two tablets by mouth daily. Indications: infection prophylaxis, medical ? levoFLOXacin (LEVAQUIN) 750 mg tablet Take one tablet by mouth daily. Indications: infection prophylaxis, medical ? levothyroxine (SYNTHROID) 88 mcg tablet Take 88 mcg by mouth daily. ? melatonin (MELATIN) 5 mg tablet Take 5 mg by mouth at bedtime daily. ? multivitamin with minerals (MULTIVITAMIN & MINERAL FORMULA PO) Take 1 tablet by mouth daily. ? omeprazole DR (PRILOSEC) 20 mg capsule Take 20 mg by mouth daily before breakfast. ? predniSONE (DELTASONE) 10 mg tablet Take seven tablets by mouth daily for 4 days, THEN 5.5 tablets daily for 3 days, THEN 3.5 tablets daily for 3 days, THEN two tablets daily for 3 days, THEN one tablet daily for 3 days. ? sildenafil (REVATIO) 20 mg tablet Take 1-3 tablets by mouth as Needed. ? trimethoprim/sulfamethoxazole (BACTRIM DS) 160/800 mg tablet Take one tablet by mouth twice daily twice weekly. Take AM and PM on Mondays and Thursdays only Indications: infection prophylaxis, medical BP 125/71 (BP Source: Arm, Left Upper, Patient Position: Sitting) | Pulse 93 | Temp 36.5 ?C (97.7 ?F) (Oral) | Resp 16 | Wt 72.1 kg (159 lb) | SpO2 100% | BMI 22.81 kg/m? Wt Readings from Last 5 Encounters: 12/08/21 72.1 kg (159 lb) 12/07/21 71.2 kg (156 lb 14.4 oz) 12/05/21 71.9 kg (158 lb 9.6 oz) 12/04/21 71.2 kg (157 lb) 12/02/21 71.3 kg (157 lb 3.2 oz) Body mass index is 22.81 kg/m?. Pain Score: Zero Fatigue Scale: 4 Pain Addressed: N/A Karnofsky Scale: 70% Cares for self; unable to do normal activity, or active work BMT Assessment & Plan Diagnosis: MDS-U Cytogenetics: 13q deletion NGS: No variants detected High Risk - R-IPPS 5 at diagnosis Patient is a 70 y/o male with bone marrow failure due to MDS-U with 13q deletion. His clinical course has been complicated by a subarachnoid hemorrhage due to severe thrombocytopenia, from which he has now clinically recovered. He is being treated with triple IST with hATG, cyclosporin and promacta (staring 11/25/21), based on a retrospective study. He has had no response so far, remains profoundly pancytopenic and requiring transfusions multiple times a week. He has high risk MDS per R-IPSS, and we now have prospective randomized data from BMT CTN 1102 which shows a clear survival benefit in patients with intermediate and high risk MDS. I discussed the case in BMT multi-disciplinary conference, and this was the consensus recommendation. I discussed the logistics, adverse effects associated with allo-HCT, and patient wants to proceed with transplant workup. Patient has been HLA typed and a donor search is ongoing. Cyclosporin level being managed per pharmacy Heme: Transfuse for hgb < 7, plt < 10 (inpatient), plt < 20 (outpatient). Recent subarachnoid hemorrhage. Plt transfusion to be given 12/8/21 - Restart eltrombopag 150 mg qday as soon as medication copay assistance approved Upon physical exam, patient currently meets criteria to exceed standard TACO rates Endo: Started on prednisone taper inpatient as part of IST. On taper to finish on 12/17/21. Closely monitor glucose. Infectious disease: Remains profoundly immunosuppressed. On ppx with acyclovir, fluconazole, levofloxacin, bactrim. Subarachnoid hemorrhage -Observed on CT head prior to admission, Concern for dAVF on CTA and MRI -Cerebral angiogram on 11/16 without any evidence of AVM, dAVF, or aneurysm -No indication for neurosurgical intervention at this time -S/p Keppra 11/12 through 11/19 -Repeat CT head 11/29 mild resolution of previously seen SAH, no new intracranial hemorrhage. Plan: > Follow-up with neurosurgery with repeat imaging on 12/12 >Amlodipine discontinued by nephrology on 12/7/21. Patient to monitor blood pressures at home. If SBP consistently > 140, restart amlodipine given recent SAH. FEN/Renal: - Mild hyponatremia. Being managed by nephrology, seen on 12/7/21 HTN > Titrate amlodipine to SBP < 140 Hypothyroidism -PTA levothyroxine 88 mcg, continuing during admission History of A. Fib -S/p ablation 2020 -Previously on Eliquis but discontinued after 3 months RTC: Labs 3x a week (due to transfusion needs). Provider weekly

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Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: melatonin, MV
Allergien: PCN
Vorherige Impfungen: -

VAERS 1939644

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 10.12.2021
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: ja ER: unbekannt Erholt: nein

Blood test normal Burning sensation Fatigue Gait disturbance Hyperhidrosis Hypoaesthesia Myalgia Pain in extremity Paraesthesia Pyrexia Sleep disorder

Symptomtext

Night of day of vaccination: fever with sweating. Day after vaccine: fever with significant leg muscle soreness making walking difficult. Night of day after vaccine: in middle of night, waking me up with a start, sharp intense burning pain in both feet effecting identical area in each feet: approx. 5 inch band around top of foot and around bottom of foot. Pain eventually dissipated leaving both feet numb with pins and needles, affecting the entire foot. For 2 weeks numbness and pins and needles during the day, extreme burning pain at night. Third week extreme burning pain all day relieved only by soaking feet in ice water. Fourth week and this week taking Feverfew for pain and wearing ice booties to bed. help. I don't have insurance. Also, I have lost confidence in the competence of my current medical provider. Thought I could ride this out myself, but it's taking too long, the pain is too bad, the numbness is spreading to my ankles and hands, and I think I'm in trouble. I never had any nerve or foot problems previous to this event. My annual blood labs from 5 months ago indicated normal blood sugar levels. Being a former competitive swimmer, I have stayed fit all my life and work out almost every day. I experienced no adverse reactions to the first two Covid-19 Pfizer vaccines, just a few days of fatigue after 2nd one. They were done in March 2021.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Routine annual blood tests done 5 months previous indicated normal blood sugar levels.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Armour Thyroid 2 gr ; multi-vitamin:Thorne Advanced Nutrients
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1938669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 12.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Balance disorder Condition aggravated Immunisation Limb discomfort

Symptomtext

losing his balance; Seem to be losing balance was reported as worsened; booster; feet are a little crooked; 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 72 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Nov2021 (Lot number: FF2590, Expiration Date: 31Dec2021) at the age of 72 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 (First dose, Date of administration-05Mar2021, lot: ENG199 or EN6199, caller clarifies he does think the lot is EN6199., Route of administration: Left Upper arm), administration date: 05Mar2021, when the patient was 72 years old, for COVID-19 immunization; Bnt162b2 (Second dose: 02APR2021, lot number: EP6955, NDC: Unknown, Expiration: Unknown, Route of administration: Left or right upper arm), administration date: 02Apr2021, when the patient was 72 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 12Nov2021, outcome "unknown", described as "booster"; BALANCE DISORDER (non-serious) with onset 13Nov2021, outcome "not recovered", described as "losing his balance"; CONDITION AGGRAVATED (non-serious) with onset 13Nov2021, outcome "unknown", described as "Seem to be losing balance was reported as worsened"; LIMB DISCOMFORT (non-serious) with onset Nov2021, outcome "unknown", described as "feet are a little crooked". Additional information: The patient had no side effects after receiving the first and second dose Pfizer Covid 19 Vaccine. He got his first and second dose of the covid vaccine without experiencing any side effects. He said he got his booster dose last 12Nov2021 and a day after, he started losing his balance and "getting a little bit worse" so far. Follow-up attempts are completed. No further information is expected.

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

VAERS 1936277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Anxiety Condition aggravated Electrocardiogram Injection site reaction Nausea Panic attack Rash Rash erythematous

Symptomtext

PT received Pfizer booster on 11/22/21 within 24 hours developed a red painful non raised non pruritic ring around the injection site; nausea; anxiety with panic attacks PT states he tolerated the first two injection without the above sxs PMHx significant for MDD and GAD, however states prior anxiety was controlled and no panic attacks meds: lamotrigine, fluoetine, buspiron, tylenol

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: ekg
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Buspirone 10mg tablet Fluoxetine 20mg capsule LamoTrLgine 200mg tablet
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1933599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 65,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Dehydration Headache Pyrexia Tinnitus

Symptomtext

Fever, chills, headache, dehydration, ringing in the ears.

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Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cold 3 weeks prior
Vorgeschichte: None
Andere Medikamente: Sertraline HLC 100 MG Lisinopril 40MG
Allergien: None
Vorherige Impfungen: Same as above

VAERS 1931557

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 12,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal discomfort Abdominal pain Arthralgia Chest pain Decreased appetite Dehydration Dizziness Fatigue Feeling cold Full blood count normal Headache Hot flush Hypoaesthesia Loss of personal independence in daily activities Muscle fatigue Oropharyngeal pain Pain in extremity Paraesthesia

Symptomtext

Initial intense arm pain. Started sore throat with red lesions/bumps later that day and bilateral arm pain and odd numbness and tingling. Muscle fatigue and overall joint pain started that evening. GI upset. Hot and cold flashes. Sandpaper rash over torso, groin, and back. Extreme fatigue with any effort, then dizziness. Headache, then later severe headache with visual disturbances like tiny colorful lights and later dark spots. Chest pain localized to middle and abdominal pain. Dehydration and lack of appetite until today, 8 days later. Telehealth with family doctor twice, one office visit with normal CBC and ESR according to report on phone. Doctor recommended round the clock Benadryl and ibuprofen. Ruled out strep at a minute clinic to be sure about the rash and sore throat. All are related to the vaccine. No other illness reported. Missed school all week so far.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CBC and ESR on Friday. Physician's office reported normal results via phone. I'm taking him to hospital for a second opinion on treatment and further evaluation due to escalation of symptoms tomorrow or tonight.
Aktuelle Erkrankungen: Long haul covid symptomatic (smell and taste disturbance, fatigue, body aches, excess weight loss) since mid December 2020
Vorgeschichte: Unsure. Autism, ADHD.
Andere Medikamente: Buspirone, fluoxetine, famotidine, occasionally melatonin or vitamin d
Allergien: Penicillin/amoxicillin
Vorherige Impfungen: Kindergarten vaccine series. Fever for several days then strange behaviors, lost known words, and chewing on things. Unsure of l

VAERS 1929249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MD
Alter: 48,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 13.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Chest scan Dyspnoea Epistaxis Inflammation Lumbar puncture Malaise Migraine Viral test negative White blood cell count increased X-ray

Symptomtext

One week after receiving my 2nd dose of the Pfizer vaccine, I experienced migraine headache, difficulty breathing & nose bleeds. Went to my doctor on 10/26 who did bloodwork & sent me home on bed rest. Later put me on antibiotics due to elevated WBC; by 10/29 I was so sick and couldn't breath I was admitted to the hospital where I stayed until 11/3/21. They ran several test and showed that my body was inflamed but couldn't find any virus, discharged me. Went to neurologist on 12/1/21 who determined that I had an adverse reaction to the vaccine.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: 5,0
Labordaten: Several blood test, x-rays, chest scan, spinal tap.
Aktuelle Erkrankungen: -
Vorgeschichte: Diagnosed with genetic marker HLA-B27 positive (ankylosing spondylitis)
Andere Medikamente: Humira (weekly); singular 10mg, baclofen 10mg, zyrtec (5mg), folic acid 800, Vitamin D2, topiramate 50mg,
Allergien: Shellfish, mesalamine, cosentex
Vorherige Impfungen: -

VAERS 1925130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WI
Alter: 79,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Chills Confusional state Cough Decreased appetite Diarrhoea Fatigue Feeling abnormal Gait disturbance Headache Initial insomnia Injection site pain Injection site pruritus Nausea Oropharyngeal pain Pain Somnolence Tremor

Symptomtext

Trouble sleeping Day 1; sleeping 12 or more hrs for couple of days; itch and pain at vaxx injection; chills and tremors; high temps Day 2 (102.2-102.7); nausea; vomiting; diarrhea; headache and fog; physical fatigue; "dry" cough; body aches; weakness; trouble walking; loss of appetite. This was information given to the doctor's office. They advised reporting to this agency. Since those first 5 or 6 days following vaxx and ongoing, I've randomly been having a sore throat and fatigue and fog/confusion. This is debilitating because of caregiving responsibilities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none -- felt well until vaxx
Vorgeschichte: Arthritis, depression
Andere Medikamente: Levothyroxin, Ezetimibe, Effexor, Atorvastatin, Dorzolamide/Timolol, Latanaprost Multi vitamin, turmeric, Zyrtec, acetaminophen Vit C, Vit D3, Folic Acid
Allergien: -
Vorherige Impfungen: Vaxx #2 resulted in heavy fatigue one day following injection

VAERS 1924013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 10,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Bone pain Headache Injected limb mobility decreased Nasal congestion Nausea Pain in extremity Pyrexia

Symptomtext

Two hours after the shot, my son felt nauseous and his arm hurt and was hard to move. This lasted for one and a half days. Seven hours after the shot, my son had a fever for two hours. 21 hours after the shot, my son got a sore throat and stuff nose. This lasted for one hour. 25 hours after the shot, my son got a headache. This lasted for 9 hours. Two and a half days after the shot, my son got a pain in his armpit bone which lasted for four days.

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Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: seizures, hypoglycaemia
Andere Medikamente: Vimpat, multivitamin, vit D, probiotic
Allergien: none
Vorherige Impfungen: -

VAERS 1923916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WI
Alter: 74,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 28.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Paraesthesia

Symptomtext

Tingling in all 4 limbs on and off since 1 week post vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zinc carnosine, Niacin, MK-4, Glycine, Glucosamine, L-lysine, Betafood, Berberine, Selenium, Manuka honey, Milk thistle, Lutein- zeaxanthin, Gastro health
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1923704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 38,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Chest discomfort Chest pain Injection site pain

Symptomtext

About 2:30am the next morning after the vaccine I was woken up to a slight painful tightness in my chest I went to Care Urgent but nothing was done and I was released. This persisted for about 8hrs and finally went away. My shoulder joint was painful the next day which caused me to have to use a heating pad for about a day or so and my arm at the injection site was sore for a few days also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Hypothyroidism, Depression, ADHD, Obese
Andere Medikamente: Omeprazole 20mg, Fluoxetine Hydrochloride, Wellbutrin 200mg, Aspirin 81mg, Levothyroxine 100 mcg, Loratadine 10mg, Melatonin 10mg, Adderall 20mg.
Allergien: Cat
Vorherige Impfungen: -

VAERS 1923122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 34,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Bursitis Hypoaesthesia Impaired work ability Injection site erythema Injection site pain Injection site swelling Limb injury Nerve injury Paraesthesia

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: Pt was given vaccine too high in the arm and developed tingling and numbness, nerve damage, bursa as diagnosed with an MRI by the doctor. She has had many doctor appointments and has to have physical therapy for months as well as missing work for doctor appointments.

Weitere VAERSDATA-Felder

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

VAERS 1920600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: IL
Alter: 35,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 18.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Chest X-ray normal Chest pain Electrocardiogram normal Myocardial necrosis marker normal

Symptomtext

Chest pain started 11/20/21, 2 days after receiving the vaccine. Patient did not seek medical treatment until the Wednesday after, 11/24/2021. Patient was instructed by his primary care physician to go to nearest emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: While in the emergency room, 11/24/2021, an EKG was performed (normal results), blood work to test for enzymes was performed (normal results), x-ray to check for fluid around heart and/or lungs (no fluid detected).
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: amoxicillin, penicillin -- hives
Vorherige Impfungen: -

VAERS 1913007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TN
Alter: 32,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Diplopia Dizziness Dyspnoea Feeling hot

Symptomtext

chest tightness, dizziness, double vision, shortness of breath, "warm feeling" Patient was given 40 mg of PO Pepcid and 4 mg of PO Decadron at 10:15 am. Reaction lasted about 20 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Crohn's disease
Andere Medikamente: Methadone
Allergien: Amoxicillin, Tramadol
Vorherige Impfungen: -

VAERS 1912899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: GA
Alter: 40,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 09.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Injection site pain Pain Pain in extremity

Symptomtext

After receiving my 2nd Shot 4/29/2021, in my right Deltoid, I began to experience stiffness and pain at the injection site about 2-3 weeks post-vaccine. As the time has progressed the pain has not subsided and is localized to my right Deltoid and has shooting pain if the arm is raised over the head or reach behind the back causing a limiting range of motion without pain. My PCP suggested in August 2021 an anti-inflammatory pain medication( Naproxen) and topical analgesics as a suggestion for pain relief. In August 2021 I went to the chiropractor to see if an adjustment would relieve the pain in my arm and pain still persists. After receiving 3rd shot on 11/9/2021 in my right Deltoid I have continued to have pain. I have intermittent pain in the right deltoid and downside of the arm when moved in certain positions (raise the arm up overhead and if I reach behind my back, put on a coat or book bag.). On 11/30/2021. I went back to the chiropractor to see if there was something I could do and was referred to the place I received injection as any adjustment would not help with the pain. When I completed my daily symptom tracker VSAFE I noted the issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 1 diabetes
Andere Medikamente: Humalog Kwik Pen 4-6 units with meals Tresiba Flextouch Insulin degludec injection 26 units at night
Allergien: Latex, hay fever
Vorherige Impfungen: -

VAERS 2572884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 21.01.2021
Beginn: 24.10.2021
Tage bis Beginn: 276,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 COVID-19 pneumonia Headache Hypoxia SARS-CoV-2 test positive Sepsis

Symptomtext

Narrative: Patient received two Pfizer vaccine doses in Feb/Mar 21 and a 3rd dose on 22 Oct 21. The patient tested positive for COVID 19 on 24 Oct 21 (two days later) and was hospitalized with Sepsis, hypoxia, weakness, headache, and COVID pneumonia. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2571908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 20.10.2021
Beginn: 22.09.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Ageusia Anosmia COVID-19 Chills Cough Diarrhoea Dyspnoea Fatigue Headache Myalgia Nausea Oropharyngeal pain Pyrexia Rhinorrhoea SARS-CoV-2 test positive Vomiting

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/17, Pfizer, dose #1 03/10, Pfizer, dose #2 10/20, Pfizer, dose #3 09/19 10/15 COVID swab, result: NOT detected 09/22 pt cc: chills, cough, diarrhea, fatigue, fever, headache, loss of taste or smell, myalgias, nausea, rhinorrhea dyspnea, sore throat vomiting exposure: unknown 09/22 COVID swab, result: detected 10/12 COVID swab, result: NOT detected 10/15 COVID swab, result: NOT detected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/19 10/15 COVID swab, result: NOT detected 09/22 COVID swab, result: detected 10/12 COVID swab, result: NOT detected 10/15 COVID swab, result: NOT detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1910077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: RI
Alter: 55,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 14.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Echocardiogram Electrocardiogram abnormal Laboratory test normal Palpitations Ventricular extrasystoles

Symptomtext

Persistent PVCs that began within days of vaccine but didn't make immediate connection so not sure of exact start date. Ongoing daily symptoms (palpitations) which I have never had before. Documented by EKG. Further cardiac evaluation is in progress.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG 11/9/21 Echocardiogram 11/30/21 Holter monitor scheduled 12/3/21 Routine lab tests normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: gadolinium
Vorherige Impfungen: -

VAERS 1906165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: VA
Alter: 101,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 28.10.2021
Beginn: 29.11.2021
Tage bis Beginn: 32,0
Dosis: UNK
Route/Site: - / -

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

Balance disorder Dysstasia Muscle rigidity Tremor

Symptomtext

Patient experienced loss of balance and inability to stand up. Body became rigid while lying on floor with tremors in extremities.

Weitere VAERSDATA-Felder

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

VAERS 2570401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 14.10.2021
Beginn: 07.11.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Cough Dyspnoea Fatigue Headache Myalgia Pyrexia SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/09, Pfizer, dose #1 03/02, Pfizer, dose #2 10/14, Pfizer, dose #3 11/08 COVID swab, result: detected 11/07 pt cc: cough, fatigue, fever, headache, loss of taste or smell, myalgias, dyspnea exposure: unknown 11/08 SARS-COV-2 Variant Sequencing result: pending 11/17 clinically resolved

Weitere VAERSDATA-Felder

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

VAERS 1896804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 25,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Cough Dyspnoea Echocardiogram normal Myalgia Nausea Palpitations Pyrexia Vaccination complication Vomiting

Symptomtext

I received the Pfizer vaccine on November 12. A day after I received the vaccine I started noticing some chest pains and heart palpitations. Each day that passed I noticed they were getting a little bit stronger. On the 18th I woke up with severe chest pain, SOB, fever, cough. The pain was so bad I started to vomit. Just couldn?t seem to catch my breath at all. Went to the ER and my pulse ranged anywhere from 112-146 .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Echocardiogram conducted 11/19/21 and was negative for any cardiac etiology per echocardiogram report. Physician documented in discharge assessment that pain and muscle aches as well as nausea/vomiting is due to the recent covid vaccine that you received after having previously developed antibodies to covid.
Aktuelle Erkrankungen: seen on 11/4 at urgen care due to fever and not feeling well. was prescribed prednisone and amoxicillin at this time.
Vorgeschichte: anxiety
Andere Medikamente: paroxetine, prednisone and amoxicillin.
Allergien: vancomycin - red man syndrome
Vorherige Impfungen: -

VAERS 1894467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 23.11.2021
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: ja Erholt: unbekannt

Aptyalism Chest X-ray Cough Dry mouth Dysphagia Dyspnoea Ear pain Electrocardiogram Eye pain Fatigue Headache Hypertension Oxygen saturation decreased Pain Photophobia Pyrexia Tremor Wheezing

Symptomtext

On Friday November 19th at approximately 9:30am at the Hospital Covid vaccine clinic, I received the Pfizer Covid vaccine 1st dose, within 5 minutes of receiving the vaccine, my hands started shaking, then followed up with mouth getting dry and no saliva, I was provided water to drink, drinking water didn?t help and now starting a wheezing cough, the cough became more constant and unable to take a moderate breath without coughing or talking without coughing, and shortness of breath, then started having difficulty swallowing. The nurse was evaluating me during this time as I gave the nurse notice of a possible reaction can occur due to current medical conditions. After an estimated 20 minutes I was at the Emergency Department being admitted and IV started, with IV push meds were given. Xray chest AP portable was used, EKG 9 performed, and blood work. Clinical Impressions as of November 19 2021, Allergic reaction, initial encounter ? to Covid vaccination. After hospital treatment, wheezing cough, fever 100 degrees, severe headaches, throbbing left and right eye pain and light sensitive, throbbing left and right ear pain, low oxygen saturation at times, lowest at 92 sat with pulse 115 resting, high blood pressure 168/82 pulse 109, Spiroflow Peak Flow meter at 425 which is very low, at my critical zone, and fatigue. I had Epi pens available while recovering at home in case symptoms reoccurred and needed to return to Hospital. Prescribed Hydroxyzine and Prednisone - 60 mg daily for 5 days. Provided message to primary care an hour after leaving hospital, notifying specialty doctors (Pulmonologist, Allergist, Nephrologist) on 11-22-21 for possible follow up visits. I submitted a request # UR0206840 and assigned to HRIT Operations to provide information on my health condition and recommended by primary and specialty doctors to have Covid vaccine at the Hospital and immediately taken to Emergency Department to be monitored for reactions.

Weitere VAERSDATA-Felder

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

VAERS 1893324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CT
Alter: 56,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 08.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Paraesthesia Sensory loss Vaccination site paraesthesia

Symptomtext

Pins and needle tingling at injection site; Pins and needle tingling at injection site and radiating to left fingertips / Tingling in the left face from earlobe to nose; loss of tactile feeling in the left cheek; This is a spontaneous report from a contactable consumer, the patient. A 56-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590) via an unspecified route of administration in the left arm on 08Nov2021 at 14:00 (at the age of 56-year-old), as a single dose for COVID-19 immunisation. The patient had no medical history and no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. Concomitant medications included lisinopril (MANUFACTURER UNKNOWN) and rosuvastatin calcium (CRESTOR); both for unspecified indication from unknown date and unknown if ongoing. On 08Nov2021 at 14:00, the patient experienced pins and needle tingling at injection site and radiating to left fingertips, tingling in the left face from earlobe lobe to nose and currently it was loss of tactile feeling in the left cheek. The events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events pins and needle, tingling at injection site, tingling in the left face from earlobe lobe to nose and loss of tactile feeling in the left cheek was not resolved at the time of this report.

Weitere VAERSDATA-Felder

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

VAERS 1893260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 69,0
Geschlecht: U
Eingang: 23.11.2021
Impfdatum: 15.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Arthralgia Body temperature Chills Fatigue Immunisation Pain Pyrexia Tremor

Symptomtext

severe tremors; aches; joint pain; 101.7 fever; chills; BNT162b2 dose 3 (booster); extreme fatigue; This is a spontaneous report received from a contactable consumer (patient). This consumer reported events after the first, second, and third dose of vaccine. This is the third of three reports (dose 3). A 69-year-old female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number FF2590) intramuscular in left arm on 15Oct2021 01:00 PM (at the age of 69-year-old) as dose 3 (booster), single for COVID-19 immunisation. Vaccination facility type for third dose was reported as hospital or drug store. The patient did not received any prior vaccinations within 4 weeks. The patient's medical history included high blood pressure from unspecified date and ongoing. The patient's concomitant medications included valsartan/hydrochlorothiazide (HCT), oral from unspecified date and ongoing for high blood pressure. The patient previously received BNT162b2 (lot number EL3247), intramuscular in left arm on 18Jan2021 08:30 AM as dose 1, single for COVID-19 immunization and she did not experience any reaction other than a sore arm for a day or two. She also previously received BNT162b2 (lot number EL9264), intramuscular in left arm on 08Feb2021 08:30 AM (at the age of 69-year-old) as dose 2, single for COVID-19 immunization and by 10 PM (08Feb2021), she began experiencing chills, body aches, joint pain and 101.9 fever. This lasted for 4 days followed by 100-degree fever for another day and extreme tiredness for several weeks. In light of this reaction, she was hesitant to obtain a booster shot without discussing this with a professional medical adviser. Her concern was that this was not a typical response and that she was experiencing a hyperimmune or autoimmune response. Also, Guillain-Barre syndrome crossed her mind. At that time, she did not consider that the product was defective, but rather that something in her immune system might be amiss. On 27Sep2021, while at a well-care visit, she discussed this reaction with her physician. She recommended that perhaps she could delay taking the booster if she checked her antibody titers. She was not comfortable with putting off the inevitable, taking a booster, since she was over 65 years old. The following day, she called the facility to obtain reassurance that her reaction was normal and it would be safe to make an appointment for a booster shot. She spoke to (privacy) in the medical division. She advised her to speak to her physician which she had already done and she read off a list of common reactions. She did not experience a rash, hives, low grade fever, or any other anaphylaxis event. With no clear on whether or not the booster would be safe for her to take, she made the decision to take a booster at (privacy) on 15Oct2021 at 01:00 PM. It was reported that by 10 PM that night (15Oct2021) she once again had severe tremors, chills, aches, joint pain and 101.7 fever which lasted for three days followed by extreme fatigue (Oct2021). She was currently relieved that she was as protected as possible from COVID-19, but concerned that she will have to obtain a yearly booster shot for the disease. She asked if it was not safe for her to do so and if her reaction was abnormal. Booster dose due to high risk of frequent institutional or occupational exposure to coronavirus (and at risk of serious covid-19 complications): over 65. The patient took paracetamol (TYLENOL) oral for fever and aches on 08Feb2021, 12Feb2021, 15Oct2021 and 19Oct2021. No relevant test was reported. The outcome of the events was resolved on 19Oct2021 for "101.7 fever" and unknown for all other events. Follow-up (11Nov2021): Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER_INC-202101546711 same drug and patient, different event and drug dose;US-PFIZER INC-202101281664 same drug and patient, different event and drug dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20211015; Test Name: body temperature; Result Unstructured Data: Test Result:101.7 Fahrenheit
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: -
Andere Medikamente: VALSARTAN HCT
Allergien: -
Vorherige Impfungen: -

VAERS 1891014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WI
Alter: 63,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 29.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / AR

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

Asthma Condition aggravated

Symptomtext

Asthma became worse, Preznol Oral Therapy Nebulizer - never used nebulizer and rarely used rescue inhaler, which now is used regularly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 11/14 doctor's appointment - Pulmonologist
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism Acid Reflux Chronic Kidney Disease Congestive Heart Failure Major Depressive Disorder Asthma
Andere Medikamente: Hypothyroidism 2 meds Acid Reflux 2 meds Chronic Kidney Disease 2 meds Congestive Heart Failure 4 meds Major Depressive Disorder 2 meds Asthma 5 meds Vitamin B12 Vitamin C Zinc Ceambetro
Allergien: Topical Thimerosal Preservative in Flu/Pneumonia Vaccine Z-pack Macrocytes Prevacid
Vorherige Impfungen: Thiomersal Preservative in Flu/Pneumonia vaccine 09/22/2014, within 5 mins of receiving developed swelling in left arm, hot, 30

VAERS 1890607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AK
Alter: 16,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / LA

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

Blood test normal Conjunctivitis Feeding disorder Headache Insomnia Migraine Nausea Paranasal sinus discomfort Visual impairment Vomiting X-ray normal

Symptomtext

2nd does of vaccine was received Tuesday November 9, 2021. On Thursday the 11th patient woke up at approximately 3pm and had decreased vision in her right eye. On Monday November 15th the patient woke up with a minor headache. When she returned from school at approximately 2:15 the headache had become a migraine, she complained of sinus pressure, nausea, and vomiting. On Tuesday November 16 the patient complained that the migraine, nausea and pressure was getting worse and vision had not gotten better. On Wednesday the 17th the patient continued to complain the symptoms were getting worse. Mother called primary care physician who instructed her to take child to emergency room to rule out blood clots. Patient arrived in the emergency room where tests were run to rule out blood clots. Patient was diagnosed with a migraine and conjunctivitis. Patient followed up with primary care physician on November 22 at 9:45 am. Patients vision was returning with the use of eye drops. However, headache and nausea remained. Patient has noted that it has been difficult to eat or drink due to nausea and headache. In addition patient complains that she is unable to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Blood work - 11/17/21 - normal Xrays - 11/17/21 - normal Eye Exam - 11/17/21 Conjunctivitis in both eyes
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma and Irritable Bowel Syndrome
Andere Medikamente: None
Allergien: Penicillan
Vorherige Impfungen: -

VAERS 1890372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 22.11.2021
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

Ear discomfort Electrocardiogram Headache Palpitations Peripheral swelling Ultrasound scan normal Vaccine positive rechallenge

Symptomtext

After first dose, experience chest pain, discomfort from left side of neck on top of shoulder into arm, sore arm for 4 days, red and swelling. High Heart rate for a day, chest pain/discomfort for two days. After second dose, same reaction as first with pain on left side, even though administered in right arm this time. Sudden fullness in ears as if I was on a plane. Increase heart rate and resting pulse-current. Headache, swelling of right foot, chest pain intermittingly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Dr visit on 11/15, for palpitations, Cardiology on 11/16/21 EKG was done. Ultrasound done of leg extremities, negative. 11/16/21- Second dose was given 11/12/21.
Aktuelle Erkrankungen: Covid in September
Vorgeschichte: -
Andere Medikamente: Vitamin D MuliVitamin
Allergien: none
Vorherige Impfungen: -

VAERS 1890144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: KY
Alter: 91,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 22.10.2021
Beginn: 19.11.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Lung infiltration Mental status changes SARS-CoV-2 test positive

Symptomtext

admitted with COVID PNA requiring supplemental oxygen family reported altered mental status and cough pt started on decadron and remdesivir

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: COVID + 11/19 CXR - Bilateral pulmonary infiltrates.
Aktuelle Erkrankungen: -
Vorgeschichte: CLL
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1889505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: KY
Alter: 30,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypoaesthesia Paraesthesia

Symptomtext

Health department went to Nursing Home on 11/18/21 to vaccinate employees/residents as needed. Client received 1st pfizer vaccine. Client called and left message 11/19/21; tried to call back; no answer left message. Made contact with client 11/22/21. Client reported after vaccination on 11/18/21 developed numbness and tingling of the right side of her face, neck, down to shoulder. She reports started shortly after vaccination and resolved midday 11/19/21. Reports she has notified her PCP. Denies any issues at this time. As of our conversation on 11/22/21, client reports feels fine with no issues.

Weitere VAERSDATA-Felder

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

VAERS 1888923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: PA
Alter: 36,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 11.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure increased Chills Heart rate increased Oxygen saturation decreased Palpitations

Symptomtext

approx 30-45 minutes after administration, pt complained of racing heart/chills. Pt placed on O2 & monitored. BP was elevated, pulse was elevated & O2 was low. EMS was contacted & pt was taken to ER. After vaccination, patient noted she had previously experienced substantial side effects from previous COVID Vaccine administrations. Pt also has extensive allergy history including Benadryl & oral steroids.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Pt noted extensive allergy history after receiving vaccine.
Vorherige Impfungen: -

VAERS 1888372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MA
Alter: 83,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Injection site paraesthesia Paraesthesia

Symptomtext

Patient received a covid booster on 11/10/21. Patient came in today complaining of numbness and tingling that began one day after receiving the vaccine and has not subsided for the last 10 days. she explains the tingling starts at the injection site and radiates down into her palm and all fingers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: unknown
Allergien: none reported
Vorherige Impfungen: -

VAERS 1888277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: WY
Alter: 36,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Back pain Chest pain Electrocardiogram abnormal Musculoskeletal pain

Symptomtext

About 24 hours after the shot, the soreness began to reach around to my shoulder blade, with in a few hours of that I started to get pain in both the front of my chest and back pains.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: They did a ECG and it came back abnormal, still waiting to get approval for a echo, I'm told won't happen til next week. I was given no medication for treatment.
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes
Andere Medikamente: Levemir, atorvastatin, fenofibrate, metformin
Allergien: -
Vorherige Impfungen: -

VAERS 1887831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Hypoaesthesia Migraine Nausea Sensory loss

Symptomtext

This is a spontaneous report from a contactable consumer, the patient. A 60-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590) via an unspecified route of administration in the left arm on 09Nov2021 at 12:30 (at the age of 60-years-old) as a single dose for COVID-19 immunisation. Medical history included known allergy to penicillin. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient did not receive any other medications within two weeks of vaccination. The patient previously took codeine (MANUFACTURER UNKNOWN) and experienced drug allergy. On 09Nov2021 at 13:00, the patient experienced severe migraines, nausea, neurological problems - numbness and loss of sensation in hands- intermittent but severe when it occurred. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event severe migraines, nausea, neurological problems - numbness and loss of sensation in hands- intermittent but severe when it occurs were not resolved at the time of this report.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (known allergies: penicillin.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1885779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Bone pain Dyspnoea Heart rate increased Injection site pain Injection site swelling Injection site urticaria Injection site warmth Lymphadenopathy Neck pain Pain Skin warm

Symptomtext

Soreness at injection site. Soreness became a painful burning sensation. Pain the injection site. Then, progress to a radiating pain extending from shoulder to neck. Collarbone area sensitive to touch. Lymph nodes swelled to ping-pong ball size. Injection site swelled to softball size. Hives around injection site, warm at injection site and along neckline. Increased heart rate, shortness of breath.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Basic physical, told this a a typical Booster reaction, advised to take Ibuprofen for swelling in arm, told that lymph node should "settle down" within the next day to two.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, High blood pressure, High Cholesterol, Menopause
Andere Medikamente: Metformin, Losartan, Amlodipine, Rosuvastatin, Gabapentin
Allergien: IV iodine
Vorherige Impfungen: -

VAERS 1885340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MO
Alter: 76,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest X-ray normal Chest pain Dyspnoea Electrocardiogram normal Swollen tongue Troponin normal

Symptomtext

15 minutes after vaccine given patient had feeling of tongue swelling and chest pain with some shortness of breath. Was brought from the clinic in the hospital to the emergency department. Upon arrival in the emergency department the patient had near complete resolution of symptoms. No significant abnormalities seen or found on exam. Given 12.5 mg of benadryl IV. EKG normal. CXR normal. Trop negative x 2. MOnitored for 3 hrs in the ED and had complete resolution of all symptoms and patient was feeling "normal". discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Given 12.5 mg of benadryl IV. EKG normal. CXR normal. Trop negative x 2. MOnitored for 3 hrs in the ED and had complete resolution of all symptoms and patient was feeling "normal". 11/19/2021
Aktuelle Erkrankungen: -
Vorgeschichte: GERD, Seasonal Allergies, Migraine, Peptic ulcer disease
Andere Medikamente: Tylenol, Calcium carbonate, pepcid, neurontin, L-Lysine, Melatonin, ultram
Allergien: Lansoprazole, milk, peanut, preservative, red food color, wasp venom, codeine, sumatriptan, conjugated estrogens
Vorherige Impfungen: influenza

VAERS 1882660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OR
Alter: 74,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 13.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / RA

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

Dizziness Electrocardiogram abnormal Extra dose administered Heart rate increased Hypertension Induration Lymphadenopathy Sinus tachycardia

Symptomtext

Booster dose received on the morning of Nov 13. Blood pressure and pulse were normal at approximately 112/70 the week before the vaccination and the day following vaccination. High pulse rate 101bpm, high blood pressure 188/89, dizziness on the afternoon of Nov 15. On the afternoon of the 15th, the lymph node at the right base of the skull was swollen and hard. Symptoms recurred to a lesser extent on the 16th and 18th with exercise/stress. bp and pulse return to slightly elevated after 1 hour rest period.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: self monitoring of bp and pulse; Sinus tachycardia ECG
Aktuelle Erkrankungen: None
Vorgeschichte: Aortic valve replacement March 2018
Andere Medikamente: Baby aspirin, Vitamin C, Adult multivitamin, B-complex, Vitamin D, AREDS-2, Magnesium
Allergien: Contact skin dermatitis from handling raw shell fish
Vorherige Impfungen: -

VAERS 1881192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IN
Alter: 44,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Influenza Lymphadenopathy Mobility decreased Pain Pyrexia Swelling

Symptomtext

Day after injection I felt as if I had the flu. Feverish and chills. The most significant reaction has been the lymph node(s) in my left armpit. Swelling, stabbing pain, pain with movement. This pain increased throughout the day 11/17/2021. Taking acetaminophen and ibuprofen with heat applications has provided little relief. Today 11/18/2021 pain has reduced from 11/17/2021 but is still having effects on my physical ability to move and rest.

Weitere VAERSDATA-Felder

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

VAERS 1881150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Dyspnoea Feeling jittery Panic attack

Symptomtext

REPORTED SOME SHORTNESS OF BREATH 24 HRS AFTER DOSE ADMINISTRATION, DESCRIBED IT AS A FEELING OF COFFEE JITTERS OR THE BEGINNING OF A PANIC ATTACK.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: NONE AT THIS TIME
Aktuelle Erkrankungen: NONE GIVEN
Vorgeschichte: GOOD
Andere Medikamente: NOT GIVEN
Allergien: PENICILLINS, SULFA MEDICATIONS
Vorherige Impfungen: -

VAERS 1880588

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FF2590

moderat

Staat: CO
Alter: 42,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Interchange of vaccine products Migraine Pruritus Rash SARS-CoV-2 test negative Swelling of eyelid Throat irritation

Symptomtext

My first two shots were through Moderna. I had a mild/moderate reaction, (previously reported), so under the care of my PA, I switched to Pfizer for the booster and pretreated with 50mg of benadryl. Within an hour, I began to feel a slight itching under my skin all over, but mostly in the arms and torso. My throat also felt 'fuzzy', like when a body part is waking up after fally asleep. No airway obstruction. As I neared the four hour mark when I could take benadryl again, the symptoms intensified. This cycle continued for the first two days. I continued to take 50mg of benadryl every four hours for the first 48 hours, and then decreased to 25 mg. By day two, I developed a rash on my chest and torso. Days three and four, I felt dizzy, light headed, and developed a severe migraine. On day five, my eyes swelled to the point they could not be opened. I went to urgent care and was given a steroid injection, which decreased the swelling. I am continuing to treat with prednisone and benadryl for the next few days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Covid-19 test was negative
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Hypothyroidism
Andere Medikamente: Advair 100/50 Albuterol PRN Levothyroxin 100 mcg Vitamin D 5000 iu Lorezapam PRN
Allergien: Seasonal and pet allergies
Vorherige Impfungen: Moderna 04/26/21

VAERS 1879643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chills Decreased appetite Dyspnoea Immunisation Lymphadenitis Malaise Pain Sinusitis

Symptomtext

Left lymph node within the armpit, extremely inflamed; Malaise; While I did not have a fever, chills and could not stay warm; Almost felt like a sinus infection; Whole body ached; Difficult breathing, like running in the winter, or hiking in higher elevations than accustomed to; "0" appetite; The patient received the third/booster dose of BNT162b2; This is a spontaneous report from a contactable consumer, the patient. A 59-year-old non-pregnant female patient received third dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590) via an unspecified route of administration on 10Nov2021 (at the age of 59-years-old) as a single dose for COVID-19 immunisation. Medical history included migraines. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications were not reported. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6205) via an unspecified route of administration on 12Mar2021 (at the age of 58-years-old) and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: CK8734) via an unspecified route of administration on 03Apr2021 as a single dose for COVID-19 immunisation. The patient previously also received tetracycline (MANUFACTURER UNKNOWN), for unknown indication from an unknown date and experienced drug allergy. On 11Nov2021, the patient experienced extreme inflammation of left lymph node within the armpit and malaise, while she did not have a fever but chills and could not stay warm. The patient almost felt like a sinus infection, whole body ached, "0" appetite, difficult breathing, like running in the winter or hiking in higher elevations than accustomed to. For first two doses, the patient not had one side effect, not even a sore arm. Since the vaccination, the patient had not been tested for COVID-19. No therapeutic measures were taken as a result of the events. The clinical outcome of the events left lymph node within the armpit, extremely inflamed, malaise, while she did not have a fever, chills and could not stay warm, almost felt like a sinus infection, whole body ached, "0" appetite, difficult breathing, like running in the winter or hiking in higher elevations than accustomed to was resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine (Migraines)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1879569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: GA
Alter: 74,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Abdominal discomfort Abdominal pain upper Asthenia Balance disorder Blood immunoglobulin M Blood test Chills Dizziness Dyspnoea Fatigue Feeling abnormal Feeling cold Immunisation Irritable bowel syndrome Mobility decreased Muscular weakness Pain in extremity Pyrexia

Symptomtext

extreme fatigue/ fatigue and weakness; Muscle weakness; sort of dizziness that made her feel off balance; sort of dizziness that made her feel off balance; Stomach ache; Chills; Shortness of breath; leg weakness; can't lift like she did before this; lost 3 pounds through this; Upset stomach; was miserable for almost 3 weeks; it triggered IBS symptoms as well; freezing; felt like she had a fever but she didn't have a thermometer to check her temperature; fatigue and weakness; sore arm; Booster; This is a spontaneous report from a contactable consumer. This consumer (patient) reported that the 74-year-old female patient received bnt162b2 (BNT162B2), dose 3 via an unspecified route of administration, administered in Arm Right on 14Oct2021 14:00 (Batch/Lot Number: FF2590) at the age of 74-year-old as dose 3 (BOOSTER), single for covid-19 immunisation. Medical history included immunodeficiency from an unknown date and unknown if ongoing. No Family Medical History and she does not know. Concomitant medication included influenza vaccine (FLU VACCINE VII) taken for immunisation from Sep2021 to Sep2021. The patient previously took first dose of bnt162b2 (Pfizer Covid shot) on 19Jan2021 (LOT: looks like EL3246) in right arm and second dose of bnt162b2 (Pfizer Covid shot) on 12Feb2021 (LOT: EL9264) in right arm for covid-19 immunization. The patient experienced had every one of the typical covid symptoms on 15Oct2021 with outcome of unknown, extreme fatigue/ fatigue and weakness on 15Oct2021 with outcome of recovering , muscle weakness on 15Oct2021 with outcome of recovering, sort of dizziness that made her feel off balance on 15Oct2021 with outcome of recovering, sort of dizziness that made her feel off balance on 15Oct2021 with outcome of recovering , stomach ache on 15Oct2021 with outcome of recovering , chills on 15Oct2021 with outcome of recovering, shortness of breath on 15Oct2021 with outcome of not recovered , leg weakness on 15Oct2021 with outcome of not recovered, can't lift like she did before this on 15Oct2021 with outcome of recovering, lost 3 pounds through this on 15Oct2021 with outcome of recovering, upset stomach on 15Oct2021 with outcome of recovering, was miserable for almost 3 weeks on 15Oct2021 with outcome of recovering, it triggered ibs symptoms as well on 15Oct2021 with outcome of recovering, freezing on 15Oct2021 with outcome of recovering , felt like she had a fever but she didn't have a thermometer to check her temperature on 15Oct2021 with outcome of recovering , fatigue and weakness on 15Oct2021 with outcome of recovering , still feeling weak on 15Oct2021 with outcome of recovering, sore arm on 15Oct2021 with outcome of recovering. The patient underwent lab tests and procedures which included blood immunoglobulin m: unknown results (She did an IMG which is supposed to be immediate in finding out if any infections are present). They got the results today, blood test: unknown results (PA also did a blood test to find out if she had the infection. She has not had the infection), sars-cov-2 test: negative (More information available (Y/N): No), thyroid function test: unknown results (She was supposed to go have her thyroid checked every 6 months), weight: 105 pounds. Therapeutic measures were taken as a result of had every one of the typical covid symptoms, extreme fatigue/ fatigue and weakness, muscle weakness, sort of dizziness that made her feel off balance, sort of dizziness that made her feel off balance, stomach ache, chills, shortness of breath, leg weakness, can't lift like she did before this (mobility decreased) , lost 3 pounds through this, upset stomach, was miserable for almost 3 weeks, it triggered ibs symptoms as well, freezing, felt like she had a fever but she didn't have a thermometer to check her temperature, fatigue and weakness, still feeling weak, sore arm. The clinical course was reported as follows: She states that her physician's assistant who is actually her regular physician, told her to call Pfizer because she considered this as an adverse reaction. Caller states that she took the first shot and second shot and had no side effects, no sore arm, nothing. Then, she had the Covid booster 14Oct2021 and it is now 3Nov2021. Yesterday was the first day the side effects started to go away. She had every one of the typical Covid symptoms, except loss of taste and smell. She was miserable for almost 3 weeks. Her PA even did additional blood work to find out because she had so many symptoms. She had them for so long and the PA also did a blood test to find out if she had the infection. She has not had the infection. Clarified that the caller was referring to the Covid infection. Caller states that she did not want anybody else to go through this. She was so happy with the first 2. Weight: She thinks about 105 pounds. She lost 3 pounds through this. She had an upset stomach as well which also triggered and it lasted so long it triggered IBS symptoms as well. Caller states that her physician's assistant knows that she called and she is wonderful. She just talked to her this morning when she got the lab results from the blood test. She did an IMG which is supposed to be immediate in finding out if any infections are present. They got the results today. Caller states that she got a negative Covid test Sunday and then she had a blood test that took a little longer. The PA wanted to narrow it down because she was getting so many symptoms. The symptoms started the next day after the dose, on 15Oct2021. She had extreme fatigue, muscle weakness, a sort of dizziness that made her feel off balance, stomach ache and chills. Chills: The chills were on and off and she would feel them just rush through her body. Two minutes later, she would be freezing and was putting on a jacket on and off and on and off. She does not know if she had a fever because when she had those kind of chills, it felt like she had a fever but she didn't have a thermometer to check her temperature. Clarified that all of the symptoms mentioned, the extreme fatigue, muscle weakness, a sort of dizziness that made her feel off balance, stomach ache and chills all started around the same time on 15Oct2021. She states that she does not know what time of day that they occurred, she was just hanging on. Outcome: For 18 days, she had most of these symptoms. Chills: The chills are lessening and she does not recall if she had those on day 18. The fatigue and weakness, she thinks that it accumulative and she is one who goes on the treadmill every other day. She does circuit training and interval training. She usually does silver sneakers, like weigh training and stuff, 2 or 3 times a week. Caller state she had another symptom, shortness of breath. Shortness of breath: Clarified that it started the same date as the other symptoms on 15Oct2021 but she then states that she thinks she noticed it later because she has a new puppy and she was walking on just a little bit of an incline. She was huffing and puffing and she usually does the treadmill for an hour and does not experience any of that. She could feel her legs getting weak, walking up the hill. She still has the shortness of breath, but not as much leg weakness. At work, part of her job is to lift boxes that are pretty heavy. Now, she can't lift like she could before this. Leg weakness: Outcome: It is hard to tell. It hasn't gotten better yet. She thinks the chills have gone down the past several days. She is still feeling weak. Today is the first day she has felt a little more back to normal. She just went out to walk the dog. Her legs are weak and she is usually pretty strong. Her PA that is tracking this, she has a population more the caller's age group and they are calling about their symptoms. Caller has a friend that had them and only lasted at most 3 or 4 days. The PA has considered that there might be other auto immune diseases and did a sed rate, there was nothing, no infection. Caller states that is why she had to call. Treatment: No. About 3 days ago, she still had the symptoms and she thought she would maybe just try a dose of Tylenol, like acetaminophen. Ibuprofen can upset the stomach and she didn't want that. She tried the 2 tablets of acetaminophen and didn't notice any difference. She went to (withheld) where they had a need for care, which gave a whole list of things and didn't give anything to do about side effects. They didn't give any indication that she should be taking anything for muscle weakness or shortness of breath, nothing. There was nothing on the (withheld) site under needs for care. It just hit her like a ton of bricks. Caller states that with flu shots, she never had a sore arm or problem until the Pfizer vaccine. Concomitant medications: Caller states she has medications she has taken for years and there is nothing new. Nothing has changed. No further details regarding medications were provided. Test results: She was supposed to go have her thyroid checked every 6 months. She was supposed to go in for that Monday and she had to wait for a Covid test to come back negative before she could go in. Once she got the Covid test, she had the thyroid test and that is when they saw the kinds of things they would test for to know if there was any infection. Vaccination Facility Type was Pharmacy/Drug Store. No additional Vaccines Administered on Same Date of the Pfizer Suspect. AE(s) require a visit to Physician Office not to Emergency Room. Prior Vaccinations (within 4 weeks): She thinks she had a flu shot around mid Sep2021 but does not know if she has the date. She knows she had it at (withheld). They might have that information.AE(s) following prior vaccinations was none. That is why this is such a surprise. If she would have known, she would not have taken it. She had a negative Covid test Sunday. Clarified that the caller had taken Tylenol and it did not help. She states that she does not usually use it but nobody was telling her what to do. Clarified that it was acetaminophen that she had taken, the generic form of Tylenol and it was the Equate brand. Provided LOT: 5KR0276. EXP: She states she is sure it expired because she never uses it. Provided EXP as Jul2018. NDC: 49035-975-83. Caller states that she did not take those 2 tablets until after having the symptoms for probably 14 days. States that the dose was 500mg. From what Pfizer knows about having this happen, what is the recommendation for taking another booster? If she has to have another booster yearly, like when the flu shot comes, is she ok to take it? There is not enough data and they are like the beta tests for the product. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101509832 Same reporter/vaccine/event, different patients

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: IMG; Result Unstructured Data: Test Result:Unknown results; Comments: She did an IMG which is supposed to be immediate in finding out if any infections are present. They got the results today; Test Name: blood test; Result Unstructured Data: Test Result:Unknown results; Comments: PA also did a blood test to find out if she had the infection. She has not had the infection.; Test Name: Covid test; Test Result: Negative ; Comments: More information available (Y/N): No; Test Name: thyroid test; Result Unstructured Data: Test Result:Unknown results; Comments: She was supposed to go have her thyroid checked every 6 months; Test Name: Weight; Result Unstructured Data: Test Result:105 pounds
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Immunocompromised
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1878056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 38,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 20.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Burning sensation Chills Condition aggravated Decreased appetite Diarrhoea Fatigue Feeling abnormal Feeling hot Heart rate irregular Impaired driving ability Impaired work ability Injection site pain Joint range of motion decreased Loss of personal independence in daily activities Malaise Nervousness Pain

Symptomtext

My first dose I had a dead arm of 2 days? meaning I had reduced ROM and couldn?t lift my arm above my head with assistance of using my right arm. General soreness to injection site. I slept 14 hours the day after my injection and had no appetite for a few days. Fatigue and these onset of symptoms occurred 12 hours after my shot. My 2nd dose similar symptoms.. not as sore or dead of an arm as the first dose. Again general malaise that lasted a few days. Fatigue, Foggy and didn?t drive or even go on a walk as I was too weak and couldn?t think straight. My husband had to make me meals and I stayed in bed for a few days. Thankfully I didn?t have to work. My booster shot was on a Wednesday. Again sore arm and fatigue. No appetite. My symptom hit me hard on that Friday when I was at work and had to leave early from my shift. I had worsening of these intermittent irregular heart rate and rhythm. Foggy, couldn?t tolerate bright lights, nervousness, diarrhea. A new symptom was this burning sensation at the base of my skull in my cervical spine. It was warm and aching. My spine ached. I felt out of control and couldn?t get comfortable. I bathed and put pajamas on and went to bed. I had chills. I slept? I had to call off of work for that Saturday 10/13 and 10/14 because I was so weak. I had no appetite. I made myself eat and hydrate. My heart just kept acting up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I eventually went to the ED and was diagnosed with PVC?s and am now on atenolol 12.5mg daily? Today is 11/17/21 and I?m Just now feeling better. I still can?t run due to fatigue but I can slowly get back to work again.
Aktuelle Erkrankungen: *I?ve been feeling intermittent irregular heart rate/rhythm over the past year This was my booster shot of pfiser FF2590 10/20/21 I received my initial vaccination of pfiser 12/21/20 ELO140 I received my 2nd dose of pfiser 1/7/21 EL3246
Vorgeschichte: None
Andere Medikamente: Vitamin d, c, fish oil, calcium +d
Allergien: Rifampin, sulfa
Vorherige Impfungen: -

VAERS 1877413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 66,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Fatigue Headache Malaise Migraine

Symptomtext

Felt unwell, tired, then headache which transitioned to a migraine with a total of 3 more days of symptoms including some mental confusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Various vitamin supplements including Vit D, C, K2 B6. Calcium, Magnesium, Omega 3
Allergien: Gluten, Augmentin
Vorherige Impfungen: -

VAERS 1876614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / UN

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

Dyspnoea Extra dose administered Laboratory test normal

Symptomtext

Got Booster on 11/11/21, developed SOB on 11/14/21. Went to ER on 11/14/21, work-up negative. Discharged home under stable condition with prescription for inhaler PRN

Weitere VAERSDATA-Felder

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

VAERS 1875942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CT
Alter: 55,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

Within 4 minutes of receiving the dose I had tingling in my left facial cheek area, left orbital socket and towards the left ear; I can not feel it; This is a spontaneous report from a contactable consumer, the patient. A 55-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590) via an unspecified route of administration in the left arm on 08Nov2021 at 14:00 (at the age of 55-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included lisinopril (MANUFACTURER UNKNOWN) and rosuvastatin calcium (CRESTOR); both from an unknown date for an unknown indication and unknown if ongoing. On 08Nov2021 at 14:04, within 4 minutes of receiving the dose the patient had tingling in his left facial cheek area, left orbital socket and towards the left ear. It felt like "novacaine" was wearing off from the dentist office. He could move his face, smile frown etc. But he could not feel. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events within 4 minutes of receiving the dose he had tingling in his left facial cheek area, left orbital socket and towards the left ear and he could not feel was resolving at the time of report.

Weitere VAERSDATA-Felder

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

VAERS 2574889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 20.10.2021
Beginn: 08.09.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Blood fibrinogen normal COVID-19 Chest X-ray normal Cough Diarrhoea Dyspnoea Fibrin D dimer Myalgia Nasal congestion Pyrexia Rhinorrhoea SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/02, Pfizer, dose #1 02/24, Pfizer, dose #2 10/20, Pfizer, dose #3 09/08 pt cc: cough, fever, diarrhea, myalgais, rhinorrhea, nasal congestion, dyspnea exposure: unknown 09/16 SARS-COV-2 Variant Sequencing result: pending 09/16 09/27 COVID swab, result: detected 09/17 CXR impression: No acute disease in the chest. 09/17 FIBRINOGEN: 371 09/17 DDIMER: 0.27 09/27 COVID swab, result: detected 09/30 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/16 SARS-COV-2 Variant Sequencing result: pending 09/16 09/27 COVID swab, result: detected 09/17 CXR impression: No acute disease in the chest. 09/17 FIBRINOGEN: 371 09/17 DDIMER: 0.27 09/27 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 18.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

Pt developed numbness/tingling in all of her toes on her L foot 3 days following vaccination. She was evaluated by 2 providers as symptoms persisted until 11/16/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: mild asthma, hx of herpes zoster
Andere Medikamente: sertraline, albuterol
Allergien: None
Vorherige Impfungen: -

VAERS 1873753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Arrhythmia Bradycardia Condition aggravated Heart rate abnormal Tachycardia Ventricular extrasystoles Ventricular tachycardia

Symptomtext

Frequent arrhythmia episodes (PVCs, non-sustained V-tach). Transient tachycardia alternating with transient bradycardia (HR fluctuating from 130s to 50s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: PVCs, non-sustained V-tach
Andere Medikamente: 2.5 - 5 mg Melatonin HS, PRN
Allergien: NKA
Vorherige Impfungen: Possibly. Cardiac arrhythmia related hospitalization and work disability (already reported in VAERS). Age 27. Date of vaccinati

VAERS 1873684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 03.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: SYR / -

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

Condition aggravated Tinnitus

Symptomtext

Approximately 9 days after injection, Existing Tinnutis (from 2008 after a bout of Labrynthitis, and hearing loss), became extremely loud. Previous Tinnitus fluctuates in tone, but this at least tripled the volume suddenly, and has not gone down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Exam and Hearing Test- 11/2/2021
Aktuelle Erkrankungen: Ear Infection
Vorgeschichte: Vacuolar interface dermatitis, Arthralgia of both hands, Subacute cutaneous lupus erythematosus, Systolic dysfunction, Peripheral polyneuropathy, Lyme disease, acute, Atherosclerosis of coronary artery, Prior stent to RCA, Left Bundle Branch Block, Labrynthitis-Left Ear Hearing loss & Tinnitus
Andere Medikamente: Clopidogril, Carvedilol, Bumetanide, Aspirin, Allegra, Simvastatin, Lisinopril, Diazepam, B12 injections, Dupixent injections,
Allergien: Sulfa, Cipro
Vorherige Impfungen: -

VAERS 1873001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: MO
Alter: 70,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 28.10.2021
Beginn: 07.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray Chest pain Electrocardiogram

Symptomtext

{Note - my first two Covid 19 Vaccination shots were Moderna 2/18/2021 and 3/17/2021} Pain around the right side of the chest from below the right nipple around the flank to below the scapular on the right shoulder (5-6 ) and left side flank (2-3)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2 view Chest X Ray 12 lead EKG pain is diminishing from 11/12 /2021
Aktuelle Erkrankungen: none
Vorgeschichte: atheroschlerosis, post herpetic neuralgia costochondritis Hypertension
Andere Medikamente: 1. Aspirin 162 mg EC tablet (*) Take 162 mg by mouth every morning (suspended from August 25 to August 01 2020) 2. Cholecalciferol 1000 unit tablet (*) Commonly known as: VITAMIN D-3 Take 1,000 units by mouth nightly 3. ClopidogreL 75
Allergien: fentanyl latex grass pollen tree pollen iodinated IV cath dye mouse protein lentils capsaicin oi
Vorherige Impfungen: -

VAERS 1872317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 05.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Arthralgia Asthenia Body temperature Chills Dyspnoea Fatigue Headache Immunisation Lymphadenopathy Migraine Myalgia Nausea Pain in extremity Paranasal sinus discomfort Paranasal sinus hypersecretion Pyrexia Sinus congestion

Symptomtext

Headache; Sinus congestion, pressure and drainage; Sinus congestion, pressure and drainage; Sinus congestion, pressure and drainage; Muscle and joint aches; Muscle and joint aches; Fatigue; Chills; Fever/Fever ranged to 102.1; Nausea; Swollen lymph nodes; Weakness; Sore arm; The patient received third/booster dose of BNT162b2; There were periods of perceived difficulty breathing.; These lasted approximately 36 hours with the exception that the headache became an intractable migraine that lasted 4 days.; This is a spontaneous report from a non-contactable consumer, the patient. A 61-year-old non-pregnant female patient received third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590) via an unspecified route of administration in the left arm on 05Nov2021 at 10:15 (at the age of 61-years-old) as a single dose for COVID-19 immunisation. The medical history included migraines, non-alcoholic fatty liver, obesity, endometriosis and known allergy to sulfa drugs. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient received other vaccine within four weeks prior to the vaccination which included influenza vaccine (MANUFACTURER UNKNOWN) for an unknown indication in the left arm. The concomitant medications included levothyroxine (MANUFACTURER UNKNOWN), acetylsalicylic acid/caffeine/paracetamol (EXCEDRIN MIGRAINE) and diphenhydramine hydrochloride (BENADRYL), all for unknown indications from unknown dates and unknown if ongoing. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6202) via an unspecified route of administration in the left arm on 09Mar2021 (at the age of 60-years-old) and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8733) via an unspecified route of administration in the left arm on 30Mar2021 (at the age of 60-years-old) as a single dose for COVID-19 immunisation. The patient previously received hydrocodone bitartrate/paracetamol (VICODIN) and experienced allergy. On 05Nov2021 at 23:00, the patient began with sore arm. On 06Nov2021,approximately 12 hours later, the patient experienced headache, sinus congestion, pressure and drainage, muscle and joint aches, fatigue and chills. Approximately 6 hours after that, the patient developed fever, nausea and swollen lymph nodes and weakness. The fever ranged to 102.1 (units unspecified). On an unknown date in Nov2021, there were periods of perceived difficulty breathing. The events lasted approximately 36 hours with the exception that the headache became an intractable migraine that lasted 4 days. On 06Nov2021, the patient underwent body temperature test and the result was found to be 102.1(unspecified units). The adverse events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events difficulty breathing, intractable migraine, sore arm, headache, sinus congestion, pressure and drainage, muscle and joint aches, fatigue, chills, fever/fever ranged to 102.1, nausea, swollen lymph nodes and weakness were resolved on an unknown date in Nov2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211106; Test Name: Body temperature; Result Unstructured Data: Test Result:Fever ranged to 102.1
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Endometriosis; Migraine (Migraines); Non-alcoholic fatty liver; Obesity; Sulfonamide allergy (Known allergies: sulfa drugs)
Andere Medikamente: INFLUENZA VACCINE; LEVOTHYROXINE; EXCEDRIN MIGRAINE; BENADRYL
Allergien: -
Vorherige Impfungen: -

VAERS 1870663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 40,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test normal Breast pain Burning sensation Chest pain Contusion Dizziness Electrocardiogram normal Fatigue Hot flush Hyporeflexia Immediate post-injection reaction Mobility decreased Muscle tightness Nausea Neck pain Neuralgia Night sweats Pain

Symptomtext

After the first shot, my throat got tight and I had to take benadryl. I also had night sweats and hot flashes. After the second shot, the pain in my arm started immediately. It felt like fire spreading to my fingers. About an hour later, swelling started in my left shoulder, arm, and hand. The next day the swelling and pain spread to my collar bone and neck. Collar bone felt bruised. Neck muscles became tight and painful. Each day this fire and pain and tight muscles spread further down the left side of my body. It became difficult to move my left arm and shoulder. Some chest pain, left side, left breast as well. Nauseous and dizzy often. Extreme fatigue. I saw the Nurse on 11/12/2021 for these issues. She gave me Prednisose and Gabepentin. She listed Hyporeflexia, Neuropathic pain, and racing heart. I am still undergoing treatment for these symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/12/2021 EKG was fine. Bloodwork looked good.
Aktuelle Erkrankungen: -
Vorgeschichte: Eosinophilic Esophagitis, bone lesion, fatty liver
Andere Medikamente: fluticasone propionate 220 mcg/actuation inhaler, famotidine 20 mg tablet, cetirizine 10 mg tablet, pantoprazole 40 mg EC tablet,
Allergien: penicillins (hives), Hydroxyzine HCL (rash), dairy, wheat, tree nuts, sunflower, tomato, potato, peanut butter
Vorherige Impfungen: -

VAERS 1870074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 28,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 31.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Nasopharyngitis Paraesthesia Peroneal nerve palsy

Symptomtext

pt had severe cold symptoms, and on the second day, work to parasthesia of right lower extremity, with drop foot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Urgent care visit on 11/10/2021 ordering neurology consult
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1870061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: MO
Alter: 55,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Confusional state Dizziness Pruritus Tremor Urticaria Vision blurred

Symptomtext

Within 1 hour complaint of hives, itching, blurred vision, dizziness, confusion, weakness, shakiness. All resolved except itchiness remains and shakiness remains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none listed
Vorgeschichte: thyroid disorder depression anxiety
Andere Medikamente: levothyroxine, clonazepam, buproprion
Allergien: nka
Vorherige Impfungen: -

VAERS 1869248

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 40,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Neuropathy peripheral Tremor

Symptomtext

neuropathy( numbness, tingling, weakness) - that began in the upper extremities bilaterally the first week and now migrated to my lower extremities. Hand tremor as well

Weitere VAERSDATA-Felder

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

VAERS 1869036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: FL
Alter: 79,0
Geschlecht: M
Eingang: 15.11.2021
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

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 1868267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 40,0
Geschlecht: U
Eingang: 14.11.2021
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: unbekannt

Asthenia Axillary pain Breast pain Chest pain Chills Dizziness Dyspnoea Ear pain Fatigue Headache Hyperhidrosis Hypersomnia Injected limb mobility decreased Lymph node pain Lymphadenopathy Myalgia Pain Pyrexia

Symptomtext

Fever, headaches, chest pain, shortness of breath, body aches and weakness, dizziness, extreme pain and swelling in my lymph nodes left side and left breast - nodes swollen that I couldn't put my left arm down, chills, sweating and extreme tiredness, sleeping for longer than usual periods (more than 8 hours), swollen lymph nodes in my neck causing pain in my ears and ringing, eating and drinking is difficult, muscle pain and weakness in entire body. This has been ongoing for 10 day after the vaccine and I am still experiencing dizziness, ringing in my ears, chest pain daily, pain in left underarm, weakness and left breast pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Coronary Artery Disease
Vorgeschichte: Diabetes, Lower Pulmonary Function due to Covid 19 infection in 03/2020
Andere Medikamente: Metformin Insulin Ranexa, Plavix Aspirin Statin Metoprolol
Allergien: Penicillin, Okra, Eggplant
Vorherige Impfungen: -

VAERS 1868076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 32,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Back pain Blood test Computerised tomogram Diarrhoea Gait disturbance Migraine Pain Pain in extremity Pyrexia Urine analysis Vomiting

Symptomtext

Fever, vomiting, diarrhea, chronic migraine, body aches, and extreme back and leg pain that impaired the ability to walk.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Urine tests (11/10/21 and 11/11/21), CT scan at ER (11/11/21), and blood work at ER (11/11/21).
Aktuelle Erkrankungen: N/A
Vorgeschichte: Celiac disease, endometriosis, ovarian cysts, fatty liver, and pre-diabetic.
Andere Medikamente: Citalopram 10mg, Prazosin 1mg, Tylenol or Ibuprofen as needed, Vitamin D3, and Iron supplement.
Allergien: Azithromycin, zofran, and gluten.
Vorherige Impfungen: -

VAERS 1867711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 70,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 25.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Laboratory test Urinary tract infection Vaccine positive rechallenge

Symptomtext

Urinary Tract Infection, treated with Cephalexin for 5 days, symptoms stopped. However, I received two additional doses of Pfizer and came down with UTI within days after. First vaccine was 2/20/21. Second was 3/13/2021. Booster was 10/25/2021. I am still on antibiotics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Lab test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: Penicillin, Sulfa, Macrobid,
Vorherige Impfungen: All prior Covid vaccinations

VAERS 1867592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: CA
Alter: 22,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Blood pressure increased Dizziness Heart rate increased Hypertension Injection site pruritus Lymph node pain Lymphadenopathy Palpitations Pruritus Tachycardia Throat irritation Tremor

Symptomtext

Site: Itching at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Dizziness / Lightheadness-Mild, Systemic: Hypertension-Mild, Systemic: Lymph Node Swelling-Medium, Systemic: Shakiness-Severe, Systemic: Tachycardia-Mild, Additional Details: Approx 5 min after vaccine adminstration patient reported burning/itching sensation in throat, racing heartbeat, dizziness and anxiety regarding vaccine. BP and HR were elevated (144/90, 91). Throat, tongue, face negative for swelling. Patient declined difficulty breathing, tongue feeling swollen/heavy. Patient reports that burning/itching sensation in throat persists and took 25mg benadryl. Also reported swelling/tender lymph nodes. Monitored x45min and called in afternoon - symptoms resolved

Weitere VAERSDATA-Felder

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

VAERS 1862528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NJ
Alter: 40,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Asthenia Dizziness Heart rate increased Injection site pain Insomnia Migraine Nausea Pain in extremity

Symptomtext

As soon as the injection occurred, I had intense pain not just at the injection site but throughout my left arm. I also felt that my pulse was very fast. This continued through the next week. The next day, I had a migraine in the evening and could not sleep. Earlier in the day, I started to have incredible dizziness and weakness. On the 3rd day in the afternoon, I became so nauseous when standing outside, that I wasn't able to go back into the house on my own. I was dizzy and weak. These symptoms kept coming in waves. I also still felt the adrenaline-type rush. I was so weak that I had to rest. These symptoms continued for a total of a week and a half.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: multivitamins
Allergien: NKA - I got jaundice after the Hepatitis B vaccine (1999) and difficulty breathing after the flu vaccine (2008)
Vorherige Impfungen: Hepatitis B (1999) and flu vaccine (2008)

VAERS 1862382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CT
Alter: 54,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 15.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / RA

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

Paraesthesia

Symptomtext

Pins and needles feeling in fingers and feet. Treatment with low dose sertraline to promote circulation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ulcerative colitis hoshimotto thyroid asthma
Andere Medikamente: Levothyroxine, mesalamine dr, metoprolol, montelukast sodium, fish oil multivitamin, d3,magnesium, probiotic
Allergien: Erythromycin fresh pineapple
Vorherige Impfungen: -

VAERS 1861459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 73,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Bronchospasm Chest discomfort Dyspnoea Fatigue Headache Somnolence

Symptomtext

extreme fatigue, shortness of breath, sleepiness, headache , chest tightness and brochoconstriction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Asthma
Vorgeschichte: RA and CAD
Andere Medikamente: Lipitor, aspirin, vitamin D3, hydroxycloroquine . Valacyclovir, multivitamin
Allergien: Penicillin
Vorherige Impfungen: Pfizer

VAERS 1860942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 44,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Abdominal pain Blood test normal Chest pain Chills Dyspnoea Feeling abnormal Feeling hot Headache Inflammation Limb discomfort Mobility decreased Myalgia Paraesthesia Sensory disturbance X-ray normal

Symptomtext

The next day after receiving the vaccine I felt like I got hit really hard in the arm. Then I started to experience abdominal pain and headaches. I would get chills and feel hot in the head area, but when I checked my temperature, I would not have a fever. I started getting some chest pains starting from the left side going in towards the center. I would get a tingling sensation from head to toe, it did not make me feel right. I did not feel like myself. It felt like something was wrong. Along the left side of my back, I would get some muscle pain on the side that the vaccine was injected. Along with abdominal pain I would get a really weird feeling in my stomach. I ended up going to the ER on 11/7/2021, at hospital because the abdominal pain got so bad to where it was starting to be difficult to breath. Through the IV they gave me fluids and medicine to help with inflammation. The doctors did test but everything came back normal. They just said they do not know what it is. I have an appointment with my PCP today. This has been going on since then but it is slowly going away. There are days that I would not do anything because I did not feel good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Bloodwork Normal 11/7/2021 X Ray Normal 11/7/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Cervical Dystonia POS (Unknown)
Andere Medikamente: Amlodipine 2.5mg 1xday Botox injections 2 rounds of in neck, chest, and shoulder areas Advil as needed Tylenol as needed Omeprazole 10mg 1xday
Allergien: Penicillin Amoxicillin ZPak Bactrim Marcaine DTap Shot
Vorherige Impfungen: DTap: When I was a kid I instantly swelled up and my throat had closed up.

VAERS 1858405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: ME
Alter: 42,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Back pain Chest pain Hypoaesthesia Impaired work ability Injection site erythema Injection site swelling Joint range of motion decreased Limb discomfort Musculoskeletal chest pain Pain Pain in extremity Skin discolouration

Symptomtext

24 hours after administered, right deltoid had quarter sized red spot and I started to have general achiness. 48 hours after administered, red spot has doubled in size and deltoid is quite swollen. Last 3-4 days, I have had severe pain to right shoulder, deltoid, pain in my chest and ribs and back. Yesterday, my right hand started turning purple at times and I am having heaviness to hand and arm. Today, I?m having great difficulty moving right arm due to numbness and pain. I have had to call in sick today and for tomorrow. My deltoid is still swollen and slightly red. I am taking Prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: No tests yet
Aktuelle Erkrankungen: Unknown disorder causing pain to chest and abdomen and right side and around umbilicus since cholecystectomy on 11/19/2019
Vorgeschichte: ADHD, pain and creepy crawly sensation to chest, abdomen, right side and back, sometimes around umbilicus since cholecystectomy on 11/19/19, acid reflux or indigestion
Andere Medikamente: Adderall XR, Pregabalin, Librax, Claritin, Pepcid, Ibuprofen, Excedrin
Allergien: Adverse reactions to all SSRIs
Vorherige Impfungen: Hives off and on for about 4 weeks, severe body aches, Moderna COVID-19 vaccine on 12/30/2020..I was age 41

VAERS 1855896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 09.11.2021
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

Arthralgia Body temperature increased Condition aggravated Extra dose administered Hemiplegia Hypoaesthesia Monoplegia Pain Pain in extremity

Symptomtext

On Friday, October 29, 2021 at approximately 8:00 AM, I experienced similar arm pain as I had in the previous two Pfizer vaccinations. At approximately 6:00 PM, I started to experience partial paralysis of my left hand. I would have to physically manipulate my left hand with my right. On Saturday, October 30, 2021, I woke up at approximately 3:00 AM with significant arm pain from my left rear shoulder radiatiing down my left arm, wrapping around my forearm to my hand. The paralysis had stopped and my complete left hand was numb. To date (Tuesday, November 9, 2021 at 7:50 PM), there has been no improvement. I did take three vidocin over a 18 hour period w/o any relief. I have been taking 600mg ibuprofen for three days w/o any relief. I went to a chiropractor on Monday, November 8, 2021 at 2:05 PM hoping it was a nerve that an adjustment would help. I went a second time to my chiropractor on Tuesday, November 9, 2021 at 2:20 PM. As of now I have no relief, with significant left rear shoulder and left arm pain that radiates from the shoulder. I still have complete numbness of my left hand.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Pantoprazole 40mg every third day
Allergien: None
Vorherige Impfungen: For Pfizer shot #1 & 2, 103 temperature and hallucinations. 104 temp for booster shot #3 without hallucinations.

VAERS 1854726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: GA
Alter: 41,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Body temperature fluctuation Chest discomfort Chest pain Chills Dyspnoea Flushing Headache Hyperhidrosis Hypertension Injection site swelling Lymphadenopathy Tachycardia

Symptomtext

Site: Swelling at Injection Site-Severe, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Chills-Severe, Systemic: unable to regulate body temperature-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Headache-Severe, Systemic: Hypertension-Severe, Systemic: Lymph Node Swelling-Severe, Systemic: Tachycardia-Severe

Weitere VAERSDATA-Felder

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

VAERS 1854516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 15.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Mobility decreased Pain Underdose

Symptomtext

At the moment of injection on Oct. 15, 2021, Patient verbalized he felt liquid dropping down to his elbow and rested there at the elbow and didn't go past there. On the 18, he woke up in the morning and could not lift his hand and bring his arm/hand to his chest or lift his arm up. Had to support his elbow with his other hand in order to support his left arm upwards. Reports sharp pain 8/10 states constant even while resting slipping. Any little movement triggers the pain. States pain is relieved by gradually bending arm over across chest and bending elbow. States he also has to guide his arm to an extended position when on his back. Reports that he is unable to lift an object up from the ground nor is he able to hold an object with his arm extended, such as a bag , etc. States as he is speaking to me, the pain is a stinging pain, constant. He has to lean in to the left side to hold the car's steering wheel.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic back pain High Blood Pressure Hepatitis B
Andere Medikamente: No dietary supplements or herbal remedies Ibuprofen once in a while for chronic back pain Propanolol for blood pressure Metformin PO daily Levothyroxine PO daily Entecavir PO daily Simvastatin PO daily Rizatriptan as needed for migraine
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1853837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TN
Alter: 35,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Arthralgia Condition aggravated Fatigue Headache Myalgia Nausea Pain Pyrexia

Symptomtext

High fever, increased to as high as 102.4 F Severe body aches, muscles, joint pain, headache Nausea, fatigue, stomach pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: spondylolisthesis dermatitis
Andere Medikamente: -
Allergien: animal protein, dairy, almonds flu shots
Vorherige Impfungen: Excused from flu shots due to similar severe side effects

VAERS 1853654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NH
Alter: 48,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Chills Feeling hot Headache Hypertension Hypoaesthesia Immunodeficiency Pain Pyrexia

Symptomtext

Tuesday evening - severe headache and body aches. Wednesday morning better - then complete numbness in left upper leg quadricep area, pain in mid back on the left side, but no headache. Went to nurse at employer just to check things out. Took vitals - I had a fever of 99.9 degrees F, my BP was very high for me at 135/95, and my pulse was 111. Took some deep breaths and drank some water, rested for ~ 5 minutes. Retook vitals and the results were nearly the same (slightly lower but not by much.) That evening after traveling home I went to bed at 6:15 pm. I had the chills and felt very feverish (my neck, face and forehead were VERY hot, while the rest of me was very cold.) I do not have a thermometer at home so could not take temperature. The next morning when I woke up I felt much better. Then only remaining pain in my left arm for two more days. Now I'm feeling myself again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Simply the vitals taken in the nurse's office on 03NOV2021. Temp 99.9, BP 135/95, Pulse 111. No other tests were taken.
Aktuelle Erkrankungen: none
Vorgeschichte: sinusitis, depression/anxiety, endometriosis
Andere Medikamente: Armour Thyroid, Methylphenidate, Rosuvistatin, Amitriptyline, Escitalopram, Ferrous Gluconate
Allergien: amoxicillin, prednisone
Vorherige Impfungen: -

VAERS 1853261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IL
Alter: 30,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chest pain Headache Insomnia Pain

Symptomtext

chest pain; No sleep whole night.; pain; Feeling severe head ache; This is a spontaneous report from a contactable consumer (patient) reported for himself. A 30-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2 via an unspecified route of administration, administered in arm left on 24Oct2021 12:00 (Lot Number: FF2590) (age at vaccination 30-year-old) as dose 2, single for covid-19 immunisation at Pharmacy or Drug Store. The patient had no allergies. The patient relevant medical history and concurrent conditions was reported as no. There were no concomitant medications. The patient received historical vaccine (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) (age at vaccination 30-year-old) dose 1 via an unspecified route of administration, administered in arm left on 30Sep2021 at 06:00 pm (Lot Number: 301308A) as dose 1, single for covid-19 immunisation. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient did not received any other medications the patient received within 2 weeks of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient had no known allergies. The patient experienced chest pain, no sleep whole night, pain and feeling severe headache on 24Oct2021 at 14:00. It was reported that feeling severe headache and chest pain. No sleep whole night. Took tylenol but no use. Not slept whole night and still pain is continuing. He don't know what to do. Seriousness criteria were reported as no. The patient did not received treatment for events. Therapeutic measures were taken as a result of chest pain and feeling severe headache. The outcome of the events was not recovered. No follow-up attempts are possible. 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: Relevant medical history and concurrent conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1853253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 77,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 20.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

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

Anxiety Blood pressure abnormal Blood pressure measurement Condition aggravated Heart rate Heart rate increased Panic attack

Symptomtext

heart rate over 100 beats per minute; panic, anxiety attack lasting 1/2-1 hour; panic, anxiety attack lasting 1/2-1 hour; Blood pressure reading 142 over 100; Panic/Anxiety attack lasting 1/2-1 hour with elevated heart rate over 100 beats per minute, reaching 144 beats per minutes at it's worse; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient (not pregnant) received the third dose of BNT162B2 (PFIZER COVID) via an unspecified route of administration on the left arm on 20Oct2021 at 11:00 AM (Lot Number: FF2590) at the age of 77-year-old as single dose for COVID-19 immunization. Medical history included atrial fibrillation and high blood pressure. The patient didn't received other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, the patient hadn't been tested for COVID-19. Known allergy was none. Concomitant medications included rivaroxaban (XARELTO), nebivolol hydrochloride (BYSTOLIC), amlodipine, olmesartan medoxomil (OLMESAR) and atorvastatin. The patient previously received the second dose and the first dose of BNT162B2, the second dose on 26Feb2021 at 11:00 AM (Batch/Lot Number: EN6203), the first dose on 05Feb2021 at 11:00 AM (Batch/Lot Number: EL9265), both via an unspecified route of administration on the left arm at the age of 77-year-old as single dose for COVID-19 immunization. On 23Oct2021 at 19:30, the patient experienced panic, anxiety attack lasting 1/2-1 hour with elevated heart rate over 100 beats per minute, reaching 144 beats per minutes at it's worse, blood pressure reading 142 over 100. Hospitalization prolonged was none. Treatment was received included Clonazepam 0.5 mg & Amlodipine Besylate 2.5mg. The outcome of events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 20211023; Test Name: blood pressure; Result Unstructured Data: Test Result: 142 over 100; Test Date: 20211023; Test Name: heart rate; Result Unstructured Data: Test Result: 100 beats per minute; Test Date: 20211023; Test Name: heart rate; Result Unstructured Data: Test Result: 144 beats per minute.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Blood pressure high.
Andere Medikamente: Xarelto; Bystolic; Amlodipine; Olmesar; Atorvastatin
Allergien: -
Vorherige Impfungen: -

VAERS 1852037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IN
Alter: 56,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest X-ray normal Chills Culture urine negative Differential white blood cell count normal Electrocardiogram normal Extra dose administered Fatigue Feeling hot Full blood count normal Heart rate increased Hypertension Metabolic function test Nausea Pain in extremity Paraesthesia Pruritus Rash Urine analysis normal

Symptomtext

The evening of the vaccine (approximately three hours following) I experienced a rash on neck and wrist with itching. The following day, November 5th, the itching continued but the rash had subsided. At approximately 6PM I felt tired and experienced chills. At approximately 9 PM my Watch alerted me to a rapid heartbeat - which reached 120 bpm at one point. My blood pressure was high also. I also experienced pain in the right arm and tingling in hands. I became hot and nauseous at about 11PM. The symptoms continued and my husband transported me to the emergency room at 12:15AM November 6th. A series of lab tests was done which mostly came back normal. I was put on a saline IV and was given Zofran for the nausea. By 4AM I was feeling better and was able to be released.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Urine culture CBC with differential UA w Rflx microscopic Basic metabolic panel ECG 12 lead Chest Xray Information on specific lab results were not provided. Physician stated for most part everything came back normal or close to normal.
Aktuelle Erkrankungen: Eustachian tube disorder (chronic Eustachian salpingitis, bilateral)
Vorgeschichte: None
Andere Medikamente: Flonase 50 mcg/actuation nasal spray Singulair (10 mg) Zyrtec 10mg capsule Multivitamin, stress formula
Allergien: Food - onion, garlic, asparagus, rice, fish Amoxicillin
Vorherige Impfungen: After 2d Pfizer dose on 3/27/21 I experienced chills, fever, and body aches that subsided within 24 hours. I was 56 at the time

VAERS 1851397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IL
Alter: 50,0
Geschlecht: M
Eingang: 08.11.2021
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: unbekannt ER: unbekannt Erholt: ja

Blood pressure diastolic increased Dizziness Headache Interchange of vaccine products Palpitations

Symptomtext

Patient previously vaccinated with Moderna vaccine asked to received the Pfizer booster . Patient reported that he felt weak heart palpitations and dizzy right after. Patient has a hx of HTN which is evident in vitals assessed by covid vaccine clinic staff. Vitals were as follows 165/85 86bpm 97% on RA 18rr. Patient states "I didn't take my medicine today and I didn't have any thing to eat since about 130am." pt was given a light snack and allowed to rest Vitals were assessed again after an hr and showed no change. Patient stated he felt better and proceeded to get up but he experienced a headache and had to sit back down and wait for his Wife to come to pick him up. vitals were assessed again in an hr and the diastolic pressure had risen to 100. patient refused medical attention outside of the vital assessment and stated he will be fine after he takes his meds and eat. Pt's wife arrived and he left the facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: N/A
Vorgeschichte: hypertension Hyperlipidemia PreDM
Andere Medikamente: Lisinopril
Allergien: Iodine
Vorherige Impfungen: -

VAERS 1850857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: KY
Alter: 84,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 09.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 Dyspnoea Immunodeficiency Malaise SARS-CoV-2 test positive

Symptomtext

84 yr old immunocompromised by MTX and a biologic agent, is vaccinated against COVID but developed symptoms and tested positive 2 days prior to admission. Came to ED for progressive dyspnea and generalized weakness, unable to manage at home. Records only indicate 1 dose of Pfizer series.

Weitere VAERSDATA-Felder

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

VAERS 1849372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: FL
Alter: 68,0
Geschlecht: M
Eingang: 07.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Deafness unilateral Dyspnoea Tinnitus

Symptomtext

patient said they had difficulty breathing the night of the third. felt like they had to think about breathing to make sure they were. Felt like their body was not doing it on their own. then on 11/4/21 they said they lost hearing in their left ear.. They said it buzzes when a sound is heard, like a "broken speaker". the lack of hearing is still going on. its obviously 4 days after so it is unknown whether is is permanent or not

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

VAERS 1849059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 06.11.2021
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: unbekannt

Discomfort Dyspnoea Heart rate decreased Oxygen saturation decreased Palpitations

Symptomtext

feels like my heart is racing, and i was short of breath, but when I check my heart rate was actually low, it was 59, and my oxygen level was 90, after some time it went back up, then it dropped again, then it went back up, both, it feels very uncomfortable, I have never had this feeling in my chest, and my heart rate has never been that low in my life

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: still waiting to hear back from the on call doctor to see if I should be seen in a hospital, my symptoms are getting worse each day that goes by, each occurrence is getting longer, and more intense
Aktuelle Erkrankungen: fibromyalgia, seasonal allergies
Vorgeschichte: fibromyalgia, acute asthma
Andere Medikamente: none
Allergien: sulfa, flonase, some laxatives, percocet, lactose, scallops, flucstisone proponate cream
Vorherige Impfungen: -

VAERS 1848527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 16.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Chills Dizziness Headache Immunisation Orthostatic hypotension Pyrexia

Symptomtext

Severe chills; Fevers went up to 103 deg. F; Postural hypotension; faintness and lightheadedness; Headache; administered with dose 3 or booster shot; This is a spontaneous report from a contactable pharmacist (patient). A 55-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Lot number: FF2590; Expiration date was not reported), via an unspecified route of administration in the left arm on 16Oct2021 03:00 PM (at the age of 55-years-old) as dose 3 (booster), single for COVID-19 immunisation. The facility where the most recent COVID-19 vaccine was administered was at a pharmacy or drug store. The patient has no relevant medical history. Concomitant medication included influenza vaccine (FLU) via unspecified route of administration in the left arm on 05Oct2021 as single dose for influenza immunization. The patient was previously vaccinated with BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) on 21Jan2021 (at the age of 54-years-old; Lot number: El1283; Expiration date was not reported) as dose 2, single and on 31Dec2020 (at the age of 54-years-old; Lot number: Ej1685; Expiration date was not reported) as dose 1, single, both via an unspecified route of administration in the left arm and for COVID-19 immunisation. It was reported that the patient did not have any reaction to the first 2 Pfizer-BioNTech vaccines. The patient previously took Aspirin and experienced drug allergy. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 16Oct2021 03:00 PM, the patient was administered with dose 3 or booster shot of BNT162B2. On 17Oct2021 03:00 AM, 12 hrs after the booster shot, the patient experienced severe chills, fevers went up to 103 degrees Fahrenheit, postural hypotension leading to faintness and lightheadedness lasting 48hrs and headache lasting 72 hrs. Fevers lasted 3 days despite acetaminophen and ibuprofen round the clock. Events were reported as non-serious by the reporter. Treatment with acetaminophen and ibuprofen round the clock was taken for event fevers went up to 103 degrees Fahrenheit and no treatment was taken for the other events. The outcome of event severe chills was recovered on an unspecified date in Oct2021, outcome of event fevers went up to 103 degrees Fahrenheit was recovered on 20Oct2021, outcome of events postural hypotension leading to faintness and lightheadedness was recovered on 19Oct2021 03:00 AM and outcome of event headache was recovered on 20Oct2021 03:00 AM.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: -
Labordaten: Test Date: 20211017; Test Name: Body temperature; Result Unstructured Data: Test Result:103 degrees Fahrenheit; Comments: fevers
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: GA
Alter: 27,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Abdominal discomfort Abdominal pain upper Blood test Cough Dyspnoea Fatigue Headache Influenza virus test negative Injection site pain Malaise Nasal congestion Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test negative Sneezing White blood cell count increased

Symptomtext

Soreness at injection site, fatigue, headache day for about a week long. Friday 10/22 I went to the ER because I was having difficulty breathing and felt some stomach tightness/ pain close to my left chest area. I recovered the next day. Saturday 10/30 I experienced covid like symptoms such as coughing, sneezing, runny and stuffy nose along with headache and body aches. Majority of those symptoms lasted until Thursday 11/4. On 11/ 4 I went to the doctor and took a covid-19 test and flu test. Both came out negative, however my WBC count was still high so the doctor took some blood work to further investigate. Today , I feel better but still experiencing sore throat cough and nasal drainage which cause me to have to blow my nose sometimes. I?d like to add that because of my allergies blowing my nose often isn?t uncommon. However, the sore throat and coughing is.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/4 Covid 19 test - negative 11/4 Flu test - negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Amitriptylin
Allergien: Contrast
Vorherige Impfungen: -

VAERS 1795540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 55,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 08.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / LA

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

Anxiety Blood pressure increased Blood test normal Burning sensation Chest pain Blood test Chest X-ray Computerised tomogram head Decreased appetite Emotional distress Crying Emotional disorder Fatigue Fear Migraine Pain Tension headache Feeling abnormal

Symptomtext

body burn/ burning pain in her arm that was sometimes in her chest and up the back of her head that made her felt like her body was on fire/ body burned so bad; muscle spasms; doctor thought it was due to the fact that she received the flu shot and the Pfizer COVID-19 vaccine together and her reaction was "so extreme"; feeling lethargic; increase in blood pressure/ has never had her blood pressure that high; loss of appetite; changes in her mental clarity; weak in her legs; fatigue/ very tired; severe headaches; received her Pfizer COVID-19 booster; pain was so bad; she couldn't move, she couldn't get out of bed or function; anxiety; getting woke up in the middle of the night; uncontrollably cry; This is a spontaneous report from a contactable consumer (patient herself). A 55-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in the arm on 08Oct2021 at the age of 55 years old (Batch/Lot Number: FF2590, Expiration date: unknown) as dose 3 (booster), single for COVID-19 immunization and influenza vaccine (FLU, Solution for injection), via an unspecified route of administration, administered in the arm on 08Oct2021 (Batch/Lot number and Expiration date were unknown), as dose number unknown, single for immunization. Relevant medical history included problem with her elbow and had a naturally low blood pressure (normally, it was 100-115 for the higher number and the lower number was always in the 60s), both from an unknown date and unknown if ongoing. There were no concomitant medications. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), administered on 28Jan2021 at the age of 55 years old (Batch/Lot number: EL9265, Expiration date: unknown) as dose 1, single, and then administered on 25Feb2021 at the age of 55 years old (Batch/Lot number: EN6203, Expiration date: unknown) as dose 2, single for COVID-19 immunization. On Friday 08Oct2021, the patient received her Pfizer COVID-19 booster and her flu shot. Since 12Oct2021, the patient had been experiencing muscle spasms, so bad that her body burn; an increase in blood pressure; fatigue; loss of appetite; and changes in her mental clarity. The patient was looking for someone to help her figure out what had happened and if this was due to the booster, and if it would eventually stop as her life had been frightening since those shots. The patient added that she had spoken to her doctor, who thought that it was due to the fact that she received the flu shot and the Pfizer COVID-19 vaccine together and her reaction was "so extreme." The patient had also spoke with other people who had the same experience and stated that she was doing better, but was still having issues. It was further reported that the patient received the booster of the Pfizer COVID-19 vaccine on 08Oct2021 and on the same day she did receive a flu shot as well; it was unknown which flu vaccine was given. The patient got the Pfizer COVID-19 vaccine booster dose, because it was needed; she had health conditions and a lot of health problems. The patient stated that she had severe headaches that Friday night when her shot was given, on 08Oct2021. She said on Saturday, 09Oct2021, her headache was better, she was very tired and especially weak in her legs. She said on Sunday, 10Oct2021, she felt fine, and then Monday, 11Oct2021, she definitely didn't. She said that from that time on, it progressed until when she got to Friday, 15Oct2021, and she had to go to the emergency room (ER) because the pain was so bad. She said her headache was severe, but the thing that was really bad was the burning pain in her arm that was sometimes in her chest and up the back of her head that made her felt like her body was on fire. She said she was still having that problem. She said that one other thing that was so bad was with whatever was going on, it made her very emotional, she had an overwhelming sense of fear come over her, and would uncontrollably cry on an unspecified date in Oct2021. She said that on the Saturday (16Oct2021) after her first ER visit, she felt really good and thought that it's over. She said on Sunday, 17Oct2021, she couldn't move, she couldn't get out of bed or function. She said one other thing was early in the week, her appetite left her completely; she would put food in her mouth and then she didn't want it. She said on this past Monday, on 18Oct2021, she was feeling lethargic too, and it actually frightened her, she couldnt get out of bed, and her body burned so bad that it frightened her. She clarified that when she came home the second time she went to the ER, they had kept her in ER overnight for observation and because she was having trouble. She clarified this was this past Monday, on the 18Oct2021 that she went to the ER and she came home on the 19Oct2021. For the increased blood pressure, it all happened when she was at a doctor's appointment for an unrelated thing, which was a problem with her elbow. She said they checked her blood pressure and it was 161/84 on an unspecified date in 2021, which she had never had her blood pressure that high. She said it remained in the 140s on the top, and was in the mid to upper 80s for the bottom. She said sometimes this would break and it would come back down, and she would also feel a little relief from the other problems. She said that in the ER, they said her blood pressure was not high enough to treat. Therapeutic measures were taken as a result of all the events. For the treatment, the patient stated that the first time she went to the emergency room on that Friday, they gave her a prescription for Gabapentin, but before she got home, she felt better and never took the Gabapentin. She said they gave her Gabapentin and an anxiety medication, and it did work, it did help, though she didn't like to have to take them. The patient said she did start taking the Gabapentin, because she was desperate. She said they gave her 300 mg capsules, and she was supposed to take two at night since she came home from the ER. The patient said that Gabapentin indication depends on who she talks to. She said some people at the ER said they didn't think it was the vaccine and some thought it was from getting the flu vaccine and booster together. The patient said her family doctor thought it was because she did flu and booster together, and said that probably it wasn't a good idea, but by now she should be better. She said she didn't think they knew what to do. She said they did a bunch blood work on an unspecified date in Oct2021, and there was nothing wrong with her other than her body was on fire. She said they gave her the Gabapentin and anxiety medication to try to help. The patient clarified that the anxiety medication was lorazepam 1 mg. She said that on the night she came home, she took a whole pill, and then that Tuesday night or last night, she took a quarter of it because she kept getting woke up in the middle of the night having episodes feeling like her body was on fire on an unspecified date in Oct2021. She clarified that last night, she was fine when she went to bed, then at 1:00 AM, she woke up burning like crazy on the upper part of her body, so she took a quarter of the anxiety pill. She said she had gone to bed after she took only 300 mg of Gabapentin, not the full 600 mg, so she took another one when she woke up and that did help. The patient said after she took the Gabapentin and the quarter pill of the anxiety medication, she was able to go back to sleep. The patient said she didn't know if the Gabapentin was doing anything or if her problems were getting better, though she was still having waves of burning and high blood pressure, at least her mental clarity was better and she felt like herself again. The patient was prescribed to take Gabapentin 600 mg at bedtime by mouth nightly and lorazepam for anxiety, 1 mg tablet by mouth as needed. When she had went to the ER on Monday, the first thing they gave her was Benadryl and Valium, which did nothing. The patient further said that it was so bizarre, she went to the ER on Monday, because she was in such pain that she told people that she wished she could die, which was not normal for her, and she had lots of health problems and had been through worse things before and never felt that way before. The patient didn't remember what her thyroid labs (unknown results) were when they were run, she got those done whenever anything weird was going on. The patient was hospitalized for "muscle spasms, so bad that her body burn/ burning pain in her arm that was sometimes in her chest and up the back of her head that made her felt like her body was on fire/ body burned so bad" from 18Oct2021 to 19Oct2021. The events resulted in emergency room visit. The patient was recovering from the changes in her mental clarity, the outcome of the events "feeling lethargic, anxiety, getting woke up in the middle of the night, uncontrollably cry, weak in her legs" was unknown, and the patient was not recovered from the rest of the events at the time of the report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 1,0
Labordaten: Test Name: Blood Pressure; Result Unstructured Data: Test Result:100-115 higher number; lower number always 60s; Comments: normally, it was 100-115 for the higher number and the lower number was always in the 60s; Test Date: 2021; Test Name: Blood Pressure; Result Unstructured Data: Test Result:161/84; Test Date: 20211012; Test Name: Blood Pressure; Result Unstructured Data: Test Result:increased; Test Date: 202110; Test Name: blood work; Result Unstructured Data: Test Result:nothing wrong; Test Name: thyroid labs; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Elbow injury; Low blood pressure (normally, it was 100-115 for the higher number and the lower number was always in the 60s)
Andere Medikamente: Pfizer, Inc. EUA 027034; FLU
Allergien: -
Vorherige Impfungen: -

VAERS 1846874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 05.11.2021
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: nein

Chest pain Exposure during pregnancy Peripheral swelling

Symptomtext

At time of vaccination, I was 21weeks2days pregnant. EDD is 3.8.2022 AEs: 1) 10/27/21: intermittent sharp, short chest pain (over heart) lasting a few seconds per episode; started within 1.5 hrs of vaccine, resolve by the next morning. No sob. 2) 10/28/21 - ongoing: swelling of all my fingers (this was common for me prior to becoming g pregnant d.t CREST syndrome, but had resolved during my pregnancy, only to be retriggered after the vaccination).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Hashimoto's CREST syndrome - not on medication
Andere Medikamente: Levothyroxine Vit C Vit D Folic Acid
Allergien: Nkda
Vorherige Impfungen: -

VAERS 1846756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MT
Alter: 31,0
Geschlecht: M
Eingang: 05.11.2021
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: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chills Dyspnoea Fatigue Heart rate abnormal Hypoaesthesia Injection site pain Nausea Pain Pyrexia

Symptomtext

Fever, fatigue, nausea, chills, tiredness, joint pain, body aches, numbness distal to injection site, rapid heart rate, difficulty breathing, abnormal heart rate, pain in injection site, soreness at injection sight.

Weitere VAERSDATA-Felder

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

VAERS 1846551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 56,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cyanosis Dyspnoea Nausea

Symptomtext

About 10 minute post injection patient starting feeling nauseous, a minute late patient reports difficulty breathing, I provided water and monitored her, she continued to struggle and lips started turning blue. I administered an Epipen and called 911

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: anxiety and depression
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1846236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 17.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

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

Atrial flutter Hypoaesthesia Paraesthesia Peripheral swelling

Symptomtext

I woke up in the middle of the night with R hand numbness, tingling, and significant swelling in the pointer and middle finger. The numbness lasted several hours. During this time of wakefulness, I also experienced the feeling of pins and needles in waves over my body--mostly in my torso and upper body. I experienced a tingling/nerve response in my intestines as well. The next morning, the swelling in my fingers had gone down but had not resolved. That day, I also experienced numbness in my feet--mostly in my heels and the feeling of atrial fluttering. The fluttering lasted no more than a few seconds but happened numerous times that day. I had lingering but lessing episodes of numbness/tingling/pins and needles throughout my body for several days until they wholly resolved without intervention about 3 days after the onset.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: n/a
Vorgeschichte: Lupus (SLE) Reynaud's IBS pharmacogenetic mutations delayed gastric emptying scoliosis
Andere Medikamente: Biotin Jolessa Zyrtec Dicylomine GasEx Advil
Allergien: Legumes--lentils, chickpeas, peanuts, etc. soy corn sunflower scopolamine cephalaspores
Vorherige Impfungen: -

VAERS 1808079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 16.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Burning sensation Cough Diarrhoea Ear swelling Erythema Impaired work ability Fatigue Lip swelling Nausea Paraesthesia Peripheral swelling Rash Pruritus Skin warm Swelling face Rash pruritic Tenderness Vomiting

Symptomtext

Narrative: ***NOTE: previously reported to VAERS; VAERS ID 1808079 E-Report Number 687643 date 10/22/21; please review both reports*** The patient reported the morning after COVID vaccine on 10/16/21 his face and upper lip and behind both ears were very swollen, tender and hot. Later that day his L arm was swollen, hot and red. He also reported that he had a bad rash to his face, behind ears, neck arms, chest and groin with itching and progressive worsening the next day. Pt also reported he was nauseated, with vomiting and diarrhea on the dat after the vaccine, which continued; he requested something for nausea on 10/22/21. He reports that he had to take off work on 10/18/21 and 10/19/21, and worked from home on 10/20/21. On 10/22/21 he stated he had a burning sensation to face, neck, chest, arms and genitals. Reported cold showers and cetirizine twice daily had been providing some relief. Denied shortness of breath, wheezing, coughing, dizziness and/or lightheadedness, difficulty swallowing.On physical exam 10/22/21, ear lobes erythemic and swollen, hot and tender to touch. No swelling to tongue. Erythema and swelling to face, eyelids, earlobes, chest, neck, bilateral upper arms, with L arm > R arm, and chest with warmth to touch. On 10/26/21, patient symptoms improved, but still with rash to arms, face, and chest. Still with headache, fatigue, and diarrhea. Had dry cough and tingling feelings in his arms. On 10/29/21, patient stated ace and ears better - no longer red, hot, tingling or swelling, but L Arm and L side of chest - although improving daily - still a little red with some warmth. On physical exam, mild erythema/warmth to Left upper arm/Left side of chest. He started feeling better after taking the steroids within 46-72 hours.

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

VAERS 1843835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 65,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Arthralgia Back pain Blood test normal Chest X-ray normal Chills Computerised tomogram normal Dyspnoea Electrocardiogram normal Eructation Extra dose administered Fatigue Influenza virus test negative Injected limb mobility decreased Insomnia Migraine Musculoskeletal pain Nausea

Symptomtext

About 12 hours after receiving my 3rd dose. I started having neck pain. I woke with chills and fever around midnight. I felt the same the next day, but with fatigue. This lasted for a week. My left arm didn't hurt at first, but then I couldn't lift it hardly at all. My back pain went across my shoulders and down around my buttocks, right leg and to my heel. Along with this, I started getting a rash that started on my fingers and toes. I noticed there was a little on my chest, but not much. Then the migraines came. It was awful. I started having issues with my breathing and with stomach pain. The pain was starting around my esophagus to my left side. I have been only able to sleep for about 10-15 minutes per night for the past few weeks. I did get 3 hours last night. I went to two ER hospitals, and they gave me morphine (which I'm allergic to) and that added welts to my rash and pain I already had. I kept myself from eating and drinking anything for a while. I had ice chips and started to become nauseous and vomit a bit, but it wasn't much because all I consumed were ice chips. I've noticed, for about a week now, I've been belching a lot. The migraine, chills and fever have subsided, but everything else remains. I was told that I need to have an endoscopy because the pains are not going away. I'm trying to schedule an appointment. I have been in complete exhaustion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Ultrasounds 2 CAT scan Flu test COVID-19 test Blood work EKG Chest x-ray Everything came back with normal results
Aktuelle Erkrankungen: I was not experiencing any illness
Vorgeschichte: I do not have any chronic or long-standing health conditions
Andere Medikamente: Sertraline Levothyroxine sodium Atorvastatin Vitamin D3 Multivitamin
Allergien: Morphine Dilaudid
Vorherige Impfungen: -

VAERS 1843566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: ME
Alter: 56,0
Geschlecht: F
Eingang: 04.11.2021
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

Balance disorder Cough Dizziness Feeling abnormal Hot flush Hyperhidrosis Injection site pain Insomnia Joint range of motion decreased Palpitations

Symptomtext

Within 10 minutes started coughing, which for me is a sign of sensitivity as that is how I discovered I was allergic to peanuts. The person at the pharmacy called across the room to ask if I was alright and I told her no. I had immediate diaphoresis, became flush and the aid offered me a water. I became lightheaded and dizzy, which to date is still present and I often loose my balance and have fallen in my home one time, only because I try to make sure there is something around to hold onto. I also had a very strange feeling that came down my left arm into my inside elbow that felt swollen and odd in my vein. I do have factor V clotting disorder in my family but was not allowed a medical exemption. I loss use of my left arm for three days. I could not lift my arm and had extreme difficulty sleeping. Pain is still present in my upper left arm,, lightheadeness continues to date, I generally check my heart rate to be 80-110 bpm and have occasional heart palpitations. I waited to file the report in hopes these events would clear. I am due for my second shot next week and I am extremely worried.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None as it seems an uphill battle to get any attention to this matter.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Peanuts
Vorherige Impfungen: -

VAERS 1843396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 32,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Condition aggravated Nausea Oral pruritus Throat irritation Throat tightness

Symptomtext

Approximately 2 minutes after dose throat felt like it was tightening up really bad. Could still breathe, took Claritin preemptively from similar reaction to the first COVID shot but this was much quicker. Tightening kept happening in waves, felt nauseous, and some itching in mouth and throat. Was still happening while leaving ~45 min after the shot but agreed to let me go home and monitor and keep taking antihistamines and have epi pen just in case I got after my first shot.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Checked vitals - HR, O2, BP all stable
Aktuelle Erkrankungen: None
Vorgeschichte: POTS, MCAS, Ehlers danlos
Andere Medikamente: Tylenol, Pepcid, Claritin
Allergien: Morphine, xifaxin, cefaclor, omeprazole Sensitivity to eggs, beef, dairy
Vorherige Impfungen: Pfizer 1st dose, started flushing, felt nauseous and felt like throat was getting really tight, mouth started itching a bit.

VAERS 1843320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 04.11.2021
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: ja

Chest pain Dyspnoea Fatigue Headache Lymphadenopathy Nausea Pain Pyrexia SARS-CoV-2 test negative

Symptomtext

I had lymph nodes in my left arm were swollen from the 28th to 31st of October. I had a fever; I didn't check it on Thursday, but I did have it on the 29th and 30th. I had a headache from the 28th the 29th. From the 28th to 30 of Oct, I had aches and nausea on the 29th. I had chest pain and shortness of breath. I also had fatigue. I still have shortness of breath. It mainly occurs when I had to step out of the apartment. I had a COVID-19 test done on Friday and it came back negative. I took Tylenol to help with the pain and the complications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 Test-29th of October- negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hyperthyroid GERD Diabetes Type 2
Andere Medikamente: Levothyroxine Nexium Allegra
Allergien: N/A
Vorherige Impfungen: First covid-19 vaccine

VAERS 1842840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 49,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Chills Condition aggravated Fatigue Influenza like illness Myalgia Pyrexia

Symptomtext

I began having Flu like symptoms of shivering,fever,muscle aches, fatigue and joint pains around 10:30 am on 11-2-2021 and they lasted til around 8 am on 11-3-2021

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: Type 2 Diabetes, High Blood pressure,Cholesteral
Andere Medikamente: Metformin ,Farxiga ,Simvastatin ,Omeprazole ,D3 vitamin
Allergien: NONE
Vorherige Impfungen: symptoms of shivering,fever,muscle aches, fatigue and joint pains ,49,10/11/2021,Covid-19, Pfizer

VAERS 1842233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 46,0
Geschlecht: F
Eingang: 04.11.2021
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

Back pain Body temperature Crying Depression Dysphagia Eye pain Facial pain Headache Immunisation Insomnia Muscle tightness Myalgia Nausea Neck pain Paraesthesia Pyrexia Tremor Vomiting

Symptomtext

Headache; Nausea; Running a fever / temp is 100 degrees; Severe muscle pain in whole body; Tingling in arms and legs; Neck hurts; Jaw tight; Pain behind eyes; Having trouble keeping food down; Depressed; Crying; Face pain; Shaking; Back pain; Unable to stay asleep; Throwing up; The patient received the third/booster dose of BNT162b2; This is a spontaneous report from a contactable consumer, the patient. A 46-year-old non-pregnant female patient received the third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590) via an unspecified route of administration in the right arm on 28Oct2021 at 15:45 (at the age of 46-years-old) as a single dose for COVID-19 immunisation. Medical history included narcolepsy and depression. The patient was allergic to powder on latex gloves. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications were not reported. The patient previously received cefalexin (CEPHALEXIN) and escitalopram oxalate (LEXAPRO) and experienced drug allergy. The patient previously received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EW0172) via an unspecified route of administration in the right arm on 30Apr2021 at 15:30 (at the age of 45-years-old) and also received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EW0162) via an unspecified route of administration in the right arm on 09Apr2021 at 16:30 (at the age of 45-years-old) as a single dose for COVID-19 immunisation. On 29Oct2021 at 12:00, the patient experienced headache, nausea, running a fever, severe muscle pain in whole body, tingling in arms and legs, neck hurts, jaw tight, pain behind eyes, temperature was 100 degrees, having trouble keeping food down, depressed, crying, face pain, shaking, back pain, unable to stay asleep and throwing up. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. On 29Oct2021, the patient underwent body temperature test and the result was 100 degrees (unspecified units). Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events headache, nausea, running a fever, severe muscle pain in whole body, tingling in arms and legs, neck hurts, jaw tight, pain behind eyes, temperature was 100 degrees, having trouble keeping food down, depressed, crying, face pain, shaking, back pain, unable to stay asleep and throwing up were unknown at the time of this report.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20211029; Test Name: Body temperature; Result Unstructured Data: Test Result:100 degrees; Comments: Time: 12:00, temp is 100 degrees
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Latex allergy (Known allergies: Powder on latex gloves); Narcolepsy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1840379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 13.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chest pain Painful respiration Palpitations

Symptomtext

Intermittent palpitations on 11/2/2021 followed by chest pain/discomfort on inspiration on 11/3/2021. Increased water intake and rested.

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

VAERS 1840295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NV
Alter: 41,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Hypoaesthesia oral Immediate post-injection reaction Lip swelling Paraesthesia oral Pruritus Urticaria

Symptomtext

Approximately 3-4 minutes after receiving the injection I experience itching all over my body. Approximately 5 minutes later I experience a numb tingling sensation toward the first 1/3 of my tongue. My lips became puffy shortly thereafter. Approximately 10 minutes after the injection, a few hives appeared on my face. It took about 45 minutes to an hour for for the majority of the symptoms to subside.

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Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Total thyroidectomy (1998)
Andere Medikamente: Synthroid, Adderall, Xanax, Losartan. Loratadine, Multi vitamin.
Allergien: Augmentin, IVP Dyes
Vorherige Impfungen: -

VAERS 1839614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: MD
Alter: 29,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Hypotension Vomiting

Symptomtext

Systemic: Hypotension-Mild, Systemic: Vomiting-Medium, Additional Details: Patient received vaccination within 10 minutes, she felt lightheaded and fell to the ground. She did not fiant, but did vomit.

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

VAERS 1838069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Angina pectoris Arthralgia Back pain Blood test normal Brain natriuretic peptide Chest X-ray normal Chest discomfort Chest pain Differential white blood cell count Electrocardiogram normal Electroencephalogram Fear Full blood count Gait disturbance Hypoaesthesia Immediate post-injection reaction Injury Metabolic function test

Symptomtext

The Pfizer covid vaccine was given in the afternoon and immediately after the vaccine, he had tingling and numb feeling on right arm and leg. The next day he had pain in his heart. The pain increased to a severe level and he felt like his heart was being constricted. He continued to have severe pain in my his heart, back and should and continued to feel numb and tingling all over arms and legs. He was very afraid he was having a heart attack, so we called 911 and they came and did an EKG, which had a normal result. He decided to still go into ER, where they did blood work, chest X-ray and another EKG, all tests came back with normal results, so he went home. That night, he was up the entire night with severe pain in his heart and pain all over his body, but the pain was concentrated in his heart and chest. He said he thought he was dying. He could not think clearly and could hardly walk or function, so early the next morning, I took him back to the ER and they admitted him to the hospital. He stayed overnight in the hospital and they repeated all the previous tests and did an EEG as well because he felt like he could not think clearly and felt something was neurologically wrong, it was hard for him to explain. He was also having frequent panic attacks because of the trauma of the heart pain and not knowing what was wrong. I am reporting this a week after the event and at this time he still has tingling/numbness and a small amount of pain, but it is much less than at onset.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: Automated differential BNP B-type Natriutetic Peptide CBC with Differential Comprehensive Metabolic Panel Troponin 1 (CTNI) performed 2 times Chest Xray
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1837701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 19.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / -

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

Arrhythmia Chest pain Dizziness Dyspnoea

Symptomtext

intermittent chest pain, shortness of breath, dizziness, and arrhythmia starting 3 days after receipt of Pfizer Covid vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Office visit 11/2/2021
Aktuelle Erkrankungen: chronic nocturnal polyuria, left renal vein nutcracker anatomy, pelvic venous congestion, cervical spondylosis, lumbar spondylosis, osteoporosis, chronic memory impairment secondary to chronic sleep disturbance from chronic nocturnal polyuria
Vorgeschichte: as above
Andere Medikamente: None
Allergien: Latex LatexOther (See Comments)Allergy/Hypersensitivity CHEST TIGHTNESS AND RED FACEDeletion Reason: Mestinon [Pyridostigmine Bromide] Mestinon [Pyridostigmine Bromide]Other (See Comments)Allergy/Hypersensitivity twitchy cough, excessive/ frequent urination, leakage, dizziness, ineffective at 4 hours, ineffective with vertical exertion.Deletion Reason: Midodrine MidodrineOther (See Comments)Allergy/Hypersensitivity ?elevated BP, no effect on HR, head pain, head pressure, dizzinessDeletion Reason: Penicillins PenicillinsHives, SwellingAllergy/Hypersensitivity swelling of face; Converted from Generic Allergy: Penicillin SWELLING & HIVES Deletion Reason: Symbicort [Budesonide-formoterol] Symbicort [Budesonide-formoterol]Other (See Comments)Allergy/Hypersensitivity hoarsenessDeletion Reason: Actonel [Risedronate] Actonel [Risedronate]leg pain, elevated BPDeletion Reason: Azelastine Azelastinepossibly dizzinessDeletion Reason: Ddavp [Desmopressin] Ddavp [Desmopressin]HyponatremiaDeletion Reason: Eliquis [Apixaban] Eliquis [Apixaban]DizzinessDeletion Reason: Famotidine FamotidineAgitation, paresthesias, depressed mood (likely through potentiation of tizanidine effect through concurrent usage of both medications)Deletion Reason: Hyoscyamine Hyoscyamineocular migraineDeletion Reason: Theratears [Carboxymethylcellulose Sodium] Theratears [Carboxymethylcellulose Sodium]skin irritation of L cheekDeletion Reason: Zyrtec [Cetirizine] Zyrtec [Cetirizine]DizzinessDeletion Reason: Gabapentin GabapentinDizziness, FatigueDeletion Reason: Phs Other Free Text-see Phs Viewer Phs Other Free Text-see Phs ViewerEnvironmental Allergies, MiscDeletion Reason: Wrong allergy selectedAdverse Reactions/Drug Intolerances Montelukast MontelukastOther (See Comments)IntolerancePossibly caused laryngitisDeletion Reason: Fosamax [Alendronate] Fosamax [Alendronate]Other (See Comments)IntoleranceSevere leg painDeletion Reason: Oxybutynin OxybutyninOther (See Comments)Intolerancedry mouth, dizziness, constipation (also wasn't effective)Deletion Reason: Reclast [Zoledronic Acid-mannitol-water] Reclast [Zoledronic Acid-mannitol-water]Other (See Comments) Intolerance Severe eye pain (iritis versus uveitis) Deletion Reason: Myrbetriq [Mirabegron] Myrbetriq [Mirabegron]Other (See Comments) Intolerance fatigue, back pain Deletion Reason: Erroneous Entry Prolia [Denosumab] Prolia [Denosumab] Other (See Comments) IntoleranceMight have lowered her BP. Might be potentially contributing to or worsening POTS syndrome.
Vorherige Impfungen: Pfizer Covid vaccine

VAERS 1836987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Fatigue Lethargy Nausea Tachycardia

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Nausea-Mild, Additional Details: Upon pt reported tachycardia/"pounding heart," RPh went out to vaccine waiting area and checked pt's vitals. BP came out 128/87 and pulse was at 86. Offered pt some water and advised to relax. Closely monitored pt every 3 minutes for initial 15 minutes and had a conversation. Pt requested to recheck her vital, and it came out 125/81 and pulse was at 75. Monitored 15 more minutes and got confirmation from Pt directly that she's ok to walk/leave.

Weitere VAERSDATA-Felder

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

VAERS 1836478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: MN
Alter: 36,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling of body temperature change Hyperhidrosis Malaise Paraesthesia Somnolence

Symptomtext

Patient felt unwell and had to sit. Felt extremely dizzy and hot/cold (alternating). Patient was sweating profusely and very drowsy. Recovered after sitting and drinking Peidalyte. Patient is still having tingling in limbs the day after the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1833928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Angiogram abnormal Chest X-ray Chills Cough Cyanosis Fibrin D dimer increased Hypopnoea Laboratory test Pulmonary fibrosis Pyrexia Respiratory tract congestion Tremor

Symptomtext

fever, cough, congestion, chills, shaking, fingers turning blue, shallow breathing, pulmonary fibrosis - occurred same day as vaccination leading to ER visit on 10/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: labwork, CXR, CTA 10/22 elevated d-dimer and CTA showed pulmonary fibrosis repeat CTA on 10/28 showed pulmonary fibrosis
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1833193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: RI
Alter: 36,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Dry eye Ear pruritus Headache Malaise Muscle twitching Paraesthesia Pruritus Rhinorrhoea Throat irritation

Symptomtext

Within 12-15mins of getting vaccine, I started to feel tingling under my skin, then prickly itching all over my body including the back of my throat and inside ears, dry eyes, also small random muscle twitches. I also experienced the other common side effects of severe headache, runny nose, and feeling mailaise. reported it to Pharmacists and nurse. I was recommended to take Benadryl. I took it that night and the side effects decreased but lasted pretty intensely for about 3 days. The symptoms have decreased over time but remain mildy even till this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Took Bendaryl PRN Do not have PCP, currently looking for one.
Aktuelle Erkrankungen: None
Vorgeschichte: positive lupus anticoagulant antibody
Andere Medikamente: None
Allergien: NKFA/NKDA
Vorherige Impfungen: -

VAERS 1833072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CO
Alter: 35,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 18.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain upper Appendicitis Dehydration Drug hypersensitivity Exposure during pregnancy Full blood count Magnetic resonance imaging abdominal abnormal Pruritus Vomiting White blood cell count increased

Symptomtext

I am 35 and was 33 weeks pregnant at the time of my vaccination on Monday morning, 10/18/21. The night of Wednesday, 10/21/21, I woke up with severe stomach pain and eventually started vomiting. I proceeded to experience the pain and vomiting through the next day (10/22/21) and it was so severe, I couldn't even keep water down. The pain changed from my entire abdomen to just the right side sometime Thursday afternoon. I decided to go to the hospital to get checked out at their Labor and Delivery department. They gave me an IV for hydration because I was very dehydrated at this point and ran blood work. My white blood cell count came back high so they proceeded to do an MRI to check for appendicitis. They found early appendicitis on the MRI and decided to treat me with antibiotics instead of surgery until I get a little further along in pregnancy. While in the hospital, I developed a reaction to one of the antibiotics, which I have never had reactions to medications before, and I am still experiencing the pain from appendicitis as well as severe itching from the antibiotics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 4,0
Labordaten: CBC panels daily while in the hospital from 10/21/21-10/24/21 MRI on 10/21/21
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: 100 mg Pristiq and a pre-natal vitamin and 4 mg of Zofran as needed for pregnancy related nausea
Allergien: Developed an allergic reaction to antibiotic after adverse event started
Vorherige Impfungen: -

VAERS 1832620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 20,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Lymphadenopathy Metastases to lymph nodes Neck pain Pain in extremity Rash Swelling

Symptomtext

intermittent shortness of breath occurring a few hours after vaccination, followed by the onset of an area of swelling above left collarbone (appears consistent with left supraclavicular lymphadenopathy/Virchow Node), left neck pain, onset of rash on bilateral cheeks, temporary left deltoid soreness. Patient has taken OTC advil and symptoms are improving, but lymphadenopathy and rash have not yet fully resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: latex, yeast
Vorherige Impfungen: -

VAERS 1832254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 45,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Injected limb mobility decreased Shoulder injury related to vaccine administration

Symptomtext

Potential SIRVA. Patient experiencing left shoulder pain and reduced range of motion. Recommended patient take NSAID therapy and if symptoms continue to get worse to seek treatment by a physician. Patient did see a nurse practitioner and started a 3 day course of prednisone 30 mg.

Weitere VAERSDATA-Felder

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

VAERS 1829859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 21.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Headache Pyrexia

Symptomtext

Patient received her second dose at 14 days instead of 21 days. Her symptoms included fever, headache, shortness of breath and tightness in her chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: depression/anxiety
Vorgeschichte: none
Andere Medikamente: Potassium chloride er 10 meq cap sertraline 50mg tab betamethasone valerate cream 0.1%
Allergien: no known allergies
Vorherige Impfungen: sore arm

VAERS 1829285

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: UT
Alter: 67,0
Geschlecht: F
Eingang: 29.10.2021
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: unbekannt Erholt: ja

Blood magnesium Blood potassium decreased Chest X-ray Differential white blood cell count Fibrin D dimer increased Full blood count Laboratory test Metabolic function test Pulmonary imaging procedure Tachycardia Troponin I Ultrasound scan

Symptomtext

3 hrs after booster (3rd shot) @ 1:15pm HR 130 taken manually at carotid, tachycardia. Relaxed, deep breathing; HR slowed and BP returned to normal after 15 minutes. I didn't call Dr. or seek medical treatment at that time. 5 days later Wednesday 10/20 at 3:55pm tachycardia again with BP of 164/104 HR 97, 98. I called my clinic and RN told me to report to ER. I arrived about 4:30-5:00pm, was admitted gave urine and blood sample.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: 10/20/21 at IMC ER : CBC with auto diff; CMP; DDimer, Mg+; thyroid stem hormone with reflex free T4; troponin-I; XGRYIM; XUAYI; blood test indicated low K+ and Hi D-dimer. US lower extremities, NM lung perfusion imaging and XR chest showed no clots.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: estradiol .5mg; loratadine 10mg;Vit E 180mg; Red yeast rice 600 mg; Fish Oil 1000mg; Kirkland Mature Adult 50+ multivitamins & minerals; Glucosamine Hal 1500mg with MSM 1500mg; Calcium 600mg with Vit D3 400IU.
Allergien: sulfa meds; iodine imaging contrast dye
Vorherige Impfungen: -

VAERS 1829196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Extra dose administered Injection site pain Lymphadenopathy Pain

Symptomtext

Mild body aches 10/28 and pain at the injection site as well as swollen lymph nodes. However, 10/29 sweeping of lymph nodes under left arm much worse, extending into left chest and left bicep

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Possible post Covid reaction last week in September. Coughing up thick yellow/green mucous, cough, and sinus pressure. Positive for Covid early august
Vorgeschichte: Anxiety, IBS, migraines
Andere Medikamente: Birth control pills, lexapro 20mg
Allergien: Keflex, codeine, neosporin
Vorherige Impfungen: 2nd dose of COVID 1/12/21 has mildly swollen lymph nodes under arm

VAERS 1829047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 61,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dyspnoea exertional

Symptomtext

Shortness of breath with activity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: none at this time
Aktuelle Erkrankungen: none
Vorgeschichte: Thyroid insufficiency, Heart blockage. History of cancer.
Andere Medikamente: Lipitor 10mg, Synthroid 112 mcg, Estradiol 25 mg, ASAP 325mg,
Allergien: IV contrast Severe. Marcaine, Severe
Vorherige Impfungen: -

VAERS 1827534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: RI
Alter: 62,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood test Body temperature Chills Computerised tomogram Dyspnoea Extra dose administered Fatigue Headache Hyperhidrosis Illness Nausea Off label use Pain Pain in extremity Pyrexia SARS-CoV-2 test Supraventricular extrasystoles Vomiting

Symptomtext

PAC; Shortness of breath; Sore arm; Chills; Nausea; Vomiting; Fever / fever went to 103.6; Sweating; Extreme Headache; fatigue; complete body ache; illness; Third dose was administered; Third dose was administered; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received the third dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 08Oct2021 13:00 (Batch/Lot Number: FF2590) (at the age of 62 years old) as dose 3 (booster), single dose for Covid-19 immunisation. Medical history included hypothyroidism and fibromyalgia. The patient had no known allergies. The patient was not pregnant at the time of vaccination. The patient did not have Covid-19 prior to vaccination. The first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) was administered on 09Mar2021 at 09:15am (Batch/Lot No: Pfizer EN6199) (at the age of 61 years old) in left arm, second dose on 25Mar2021 at 10:15am (Batch/Lot No: Pfizer ER8732) (at the age of 61 years old) in left arm, both for Covid-19 immunisation. Concomitant medication included unspecified prescription medication. Third dose was administered on 08Oct2021 at 13:00. The following day, 09Oct2021 at 10:00, the patient experienced shortness of breath, sore arm, chills, nausea, vomiting, fever/fever went to 103.6, sweating, PAC's (premature atrial contraction), extreme headache, fatigue, complete body ache, and illness. They lasted for 6 days (as reported), fever going lower and lower. Patient had two ER visits and visit with her own personal internist doctor. Treatment received: Tylenol and potassium. The events resulted in emergency room visit and physician office visit. The patient underwent lab tests and procedures which included body temperature: 103.6 on 09Oct2021 at 10:00; Cat Scan, Blood Work, and X-ray in Oct2021 with unknown results; Covid-19 PCR/Nasal swab: negative on 10Oct2021. Outcome of the events was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 202110; Test Name: Blood Work; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211009; Test Name: fever; Result Unstructured Data: Test Result:103.6; Comments: 10:00; Test Date: 202110; Test Name: Cat Scan; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211010; Test Name: Covid-19 PCR/ Nasal swab; Test Result: Negative ; Test Date: 202110; Test Name: xray; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fibromyalgia; Hypothyroidism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1794900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TN
Alter: 53,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Dysphagia Dyspnoea Nausea Pain in extremity Swelling Musculoskeletal pain Neck pain Pain Palatal swelling Pharyngeal swelling Sinus disorder Vomiting

Symptomtext

Extreme soreness in arm; Swelling of sinus tissue; difficulty in breathing; difficulty in swallowing; Nausea; This is a spontaneous report from a contactable consumer (patient). A 53-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590), via an unspecified route of administration, administered in left arm on 15Oct2021 at 09:15 (at the age of 53-years-old) as dose 1, single for COVID-19 immunisation. Medical history included high cholesterol (hereditary) and COVID-19 (prior vaccination). The patient had known allergies to Penicillin, Codeine, Sulfates. Concomitant medication included pravastatin taken for an unspecified indication, start and stop date were not reported. On 15Oct2021 at 10:45 the patient experienced swelling of sinus tissue and at the back of the roof of her mouth causing difficulty in breathing and swallowing, extreme soreness in arm that radiated all the way across shoulder blade and up the left side of her neck and nausea. The patient took a Benadryl at 11:00 am and again at 10:00 pm. The outcome of events was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (prior vaccination); High cholesterol; Penicillin allergy
Andere Medikamente: PRAVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1794900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TN
Alter: 53,0
Geschlecht: F
Eingang: 29.10.2021
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: unbekannt Erholt: nein

Dysphagia Dyspnoea Nausea Pain in extremity Swelling Musculoskeletal pain Neck pain Pain Palatal swelling Pharyngeal swelling Sinus disorder Vomiting

Symptomtext

Extreme soreness in arm; Swelling of sinus tissue; difficulty in breathing; difficulty in swallowing; Nausea; This is a spontaneous report from a contactable consumer (patient). A 53-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2590), via an unspecified route of administration, administered in left arm on 15Oct2021 at 09:15 (at the age of 53-years-old) as dose 1, single for COVID-19 immunisation. Medical history included high cholesterol (hereditary) and COVID-19 (prior vaccination). The patient had known allergies to Penicillin, Codeine, Sulfates. Concomitant medication included pravastatin taken for an unspecified indication, start and stop date were not reported. On 15Oct2021 at 10:45 the patient experienced swelling of sinus tissue and at the back of the roof of her mouth causing difficulty in breathing and swallowing, extreme soreness in arm that radiated all the way across shoulder blade and up the left side of her neck and nausea. The patient took a Benadryl at 11:00 am and again at 10:00 pm. The outcome of events was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (prior vaccination); High cholesterol; Penicillin allergy
Andere Medikamente: PRAVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1794184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Cardiac fibrillation Diarrhoea Fatigue Immunisation Insomnia Malaise Myalgia Palpitations Off label use

Symptomtext

Muscle pain everywhere; Very tired; Heart Fibrillations; Could not sleep for 12 hours; 3rd single booster dose; 3rd single booster dose; Diarrhea; This is a spontaneous report from a contactable consumer (patient). An 82-year-old female patient received BNT162b2 (COMIRNATY), via an unspecified route of administration, on 12Oct2021 (Lot Number: FF2590), at the age of 82 years old, as 3rd single booster dose, for COVID-19 immunisation. Medical history included high blood pressure, and allergy. Concomitant medications included amlodipine for hypertension, and montelukast sodium (SINGULAIR) for allergy. The patient received the 1st single dose of BNT162b2 on 27Jan2021 (lot# EL9261) and the 2nd single dose on 01Feb2021 (lot# EL9205), both at the age of 82 years old. The patient had no side effects after the 1st and 2nd doses of BNT162b2. The patient stated that in the evening of 13Oct2021, she could not sleep for 12 hours and when she woke up, she had muscle pain everywhere (on 14Oct2021). She had like heart fibrillations and it took her a long half an hour to get under control. She was very tired the whole day and then that night (unspecified if on 13Oct2021 or 14Oct2021) she had diarrhea for 6 hours. On 15Oct2021 she was feeling fine and she was also fine at the time of the reporting on 16Oct2021. The patient recovered from fibrillation on 13Oct2021, from diarrhea on 14Oct2021, and from all the remaining events on 15Oct2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1794184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac fibrillation Diarrhoea Fatigue Immunisation Insomnia Malaise Myalgia Palpitations Off label use

Symptomtext

Muscle pain everywhere; Very tired; Heart Fibrillations; Could not sleep for 12 hours; 3rd single booster dose; 3rd single booster dose; Diarrhea; This is a spontaneous report from a contactable consumer (patient). An 82-year-old female patient received BNT162b2 (COMIRNATY), via an unspecified route of administration, on 12Oct2021 (Lot Number: FF2590), at the age of 82 years old, as 3rd single booster dose, for COVID-19 immunisation. Medical history included high blood pressure, and allergy. Concomitant medications included amlodipine for hypertension, and montelukast sodium (SINGULAIR) for allergy. The patient received the 1st single dose of BNT162b2 on 27Jan2021 (lot# EL9261) and the 2nd single dose on 01Feb2021 (lot# EL9205), both at the age of 82 years old. The patient had no side effects after the 1st and 2nd doses of BNT162b2. The patient stated that in the evening of 13Oct2021, she could not sleep for 12 hours and when she woke up, she had muscle pain everywhere (on 14Oct2021). She had like heart fibrillations and it took her a long half an hour to get under control. She was very tired the whole day and then that night (unspecified if on 13Oct2021 or 14Oct2021) she had diarrhea for 6 hours. On 15Oct2021 she was feeling fine and she was also fine at the time of the reporting on 16Oct2021. The patient recovered from fibrillation on 13Oct2021, from diarrhea on 14Oct2021, and from all the remaining events on 15Oct2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1825080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 25.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Fatigue Headache Paraesthesia Spinal pain

Symptomtext

Fatigue-mild headache 10/25 & 10/26 Spine pain 10/27 Pins and needles left arm on and off 10/28

Weitere VAERSDATA-Felder

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

VAERS 1825047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 21.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Headache Pain Pyrexia Tremor

Symptomtext

About 10 hours after the vacinne I had shakes similar to coming out of anesthesia. This lasted one hour. I thought I was going to chip a tooth, I was shaking so badly. I had no fever at this time. About an hour later I had 102 fever which lasted about 12 hours. Body and headache also lasting about 12 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: hydroxyzine 25mg
Allergien: demeral
Vorherige Impfungen: -

VAERS 1824869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 41,0
Geschlecht: M
Eingang: 28.10.2021
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: ja

Blood glucose increased Condition aggravated Diabetes mellitus

Symptomtext

Persistent high blood sugar (350-450 mg/dL) lasting from ~24 until ~36 hours after shot. Did not respond typically to additional insulin. I administered an additional ~20 units of insulin over the course of the night. Typically, dosage is 1 unit per 35-50 mg/dL reduction, so 5-7 units would be needed to correct from 450 to 100 mg/dL. No issues noted with insulin pump or infusion set.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Type 1 diabetes, Crohn's
Andere Medikamente: Novolog insulin via pump, Budesinide, multivitamin, melatonin
Allergien: none
Vorherige Impfungen: -

VAERS 1823587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 79,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Blood pressure increased Blood pressure measurement Condition aggravated

Symptomtext

spike in his blood pressure readings from his normal of 130/80/48 to 152/85/58; spike in his blood pressure readings from his normal of 130/80/48 to 152/85/58; This is a spontaneous report from a contactable consumer (patient). A 79-year-old male patient received booster (third dose) of BNT162B2 (brand=Pfizer), via an unspecified route of administration (right arm) on 11Oct2021 14:45 as single dose for COVID-19 immunization. Facility type vaccine: military base. The patient previously received the first dose on 24Jan2021 09:15 AM (lot number: EL9263) and second dose on 14Feb2021 09:30 AM (lot number: EN6200), both in the right arm at 78 years of age for COVID-19 immunization. Medical history included known allergies to lisinopril, ongoing high blood pressure, and 1 heart blockage 20yrs ago (from 2001). No Covid prior to vaccination. Concomitant medications were not reported. No other vaccine in four weeks. With other medications in two weeks (unspecified). The patent experienced a spike in his blood pressure readings from his normal of 130/80/48 to 152/85/58 on 12Oct2021. No treatment the event. No Covid test post vaccination. The patient recovered from the event on an unspecified date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:130/80/48; Test Date: 20211012; Test Name: blood pressure; Result Unstructured Data: Test Result:152/85/58
Aktuelle Erkrankungen: Blood pressure high
Vorgeschichte: Medical History/Concurrent Conditions: Heart block
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1821937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: TX
Alter: 64,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Malaise Pallor

Symptomtext

Patient came in to receive 2nd dose of pfizer, she warned me that with her first dose she had a reaction where she broke out in hives. I let patient know the risks of receiving the second dose but she wanted the vaccine anyway due to not wanting to lose her job. After receiving the second dose she waited around for the 15 minute time requirement in which she started to feel unwell. She became short of breath, and pale. I gave her some water to drink and placed a fan in front of her while she sat in the lobby. After about 15 minutes of not doing well, we made the decision to call ems. Patient left with ems.

Weitere VAERSDATA-Felder

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

VAERS 1821933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MA
Alter: 35,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Ageusia Anosmia Breast pain COVID-19 Chest pain Cough Diarrhoea Dysmenorrhoea Fatigue Headache Malaise Menstrual disorder Nausea Pain Pulmonary pain Pyrexia SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on Monday, the 25th. I had the symptoms starting on the 20th. On the 25th, I had a fever of 103.8. Severe body aches, lungs and chest hurt. Headache that won't go away. Severe diarrhea right now - something I have never experienced ever. I have fatigue and nausea. I lost my taste and smell today. I can't taste or smell anything today at all. I have a cough. My left breast is super, super, super painful. It's very, very painful. It's more by the areola. It's something that I have never experienced ever. It's so, so painful. Last night, I had what felt like what were menstrual like cramps. I have a Merina IUD. I started bleeding this morning, but it's not time for my period. the cramping subsided but I'm taking 800 mg Motrin. The breast pain has not gone away and is very intense. And I'm not having any vaginal bleeding right now, but it was bright, red full blown period this morning. Very odd. At the Urgent Center, they just told me to take OTC medications for the symptoms. My doctor has offered me the monoclonal infusions but I'm waiting to see how I do. I don't have a fever right now but I'm on Motrin around the clock with Tylenol in-between. Phone call with Primary Care doctor, too.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: October 25th - Urgent Center - COVID-19 test - rapid and the PCR. I'm still waiting for the PCR but the rapid is positive. They didn't give any other tests.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1821393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 40,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chills Confusional state Headache Injection site pain Injection site swelling Migraine Nausea Pain

Symptomtext

S/S started 6 hours after receiving second dose. Including headache, confusion, full body aches, chills, nausea, migraine, sore and swollen arm at injection site. S|S were constant, lasting for about 4 days. Felt better as of 10-27-2021 morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, Iron deficiency anemia
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1819403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AL
Alter: 33,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 08.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Dysmenorrhoea Lymphadenopathy Menstrual disorder Mobility decreased Pain Pelvic pain

Symptomtext

Initially after getting second dose I experienced swollen lymph nodes, body aches, and inability to move which subsided in about 2 days. I started experiencing severe cramping, pain in pelvis, and abnormal bleeding which has yet to subside as of this date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Pending at this time.
Aktuelle Erkrankungen: None
Vorgeschichte: May Thurners Syndrome
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1819390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration Listless Malaise Mobility decreased Nausea Pyrexia

Symptomtext

Symptoms: Fever of 103F for four days, onset one day after vaccination. Nausea, listlesness, generally ill and bedridden

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none. Received a seasonal flu vaccine about 05 Oct 2021
Vorgeschichte: None
Andere Medikamente: Baby Asprin 81mg Hydrochlorathiazide 12.5mg Methimazole 5mg, Lisinopril 20mg. Krill Oil 750mg Schiff MegaRed
Allergien: None
Vorherige Impfungen: -

VAERS 1819200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 29,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Dizziness Dyspnoea Nausea Sensation of foreign body Throat tightness

Symptomtext

Pt at clinic for initial Covid Pfizer vaccine, pt. denies allergies , she did state she had her flu vaccine last week and had no problem with it . Pfizer information reviewed, patient stated she had no further questions. Vaccine given at 1605 in right arm , within mins patient stated that she felt a tightness in her throat and that it felt like she had lump in it that wasn?t going away, Patient was holding her throat and said if feels like the pressure is now in my chest also, she also complained of dizziness like she felt she was ?going to pass out? and felt nauseous like she was ?going to vomit?, Extra staff called to bring epi kit in case needed, RN arrived and assessed patient again, pt again stated she felt she had a tightness in her throat and pressure in her chest, Adult dose epipen given in R thigh at 1607, vital signs were obtained and were stable, patient felt improvement in her symptoms and no longer had the tightness in her throat, 7 minutes later she felt the tightness in her throat and pressure down in the chest return as well as shortness of breath, a second dose of adult dose epipen was administered in the right thigh. Oxygen was delivered via nonrebreather. She was transferred into a chair with her feet elevated. EMS had arrived within 15 minutes after start of the event. Patient?s symptoms had again improved however patient did state she still felt nauseous. Vital signs were stable and patient was alert and oriented throughout event. Patient was then transferred to local hospital via EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Documented history of dermatofibroma
Andere Medikamente: Unknown
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1818775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: WI
Alter: 47,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood magnesium Blood thyroid stimulating hormone Electrocardiogram Full blood count Laboratory test Palpitations

Symptomtext

Received Covid injection at 1530 and at 1800 the patient started having heart palpitations that lasted approximately 1.5 hours. At 1400 the day after the injection (10/26/2021) heart palpitations returned and lasted approximately 30 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: CBC, Chemistry, TSH, magnesium level and EKG on 10/26/2021
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Took aspirin 325 mg on 10/26
Allergien: none
Vorherige Impfungen: -

VAERS 1818455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 08.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac flutter Palpitations Ventricular extrasystoles Vertigo

Symptomtext

palpitations, runs of cardiac flutter, vertigo

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: apple watch recording multiple PVCs via ECG app
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1817975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: NY
Alter: 25,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dizziness Immediate post-injection reaction Pharyngeal paraesthesia Pruritus

Symptomtext

Immediately after I felt dizzy, the back of my throat started to tingle. I experienced slight chest pain. I started itching as with the 1st dose. Breathing remained within normal limits. Today is day 4 after dose 2 administration, I'm itching even more from head (scalp) to toe. It is becoming unbearable. I just took 2 25mg Benadryl PO tablets as per pharmacist. Will continue to monitor

Weitere VAERSDATA-Felder

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

VAERS 1817963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Dizziness Fatigue Hypersensitivity Unresponsive to stimuli

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: Allergic Reaction Received first dose of Pfizer vaccine on 10/23/2021. Patient presented to the ED following an episode of dizziness and subjective fatigue after receiving the COVID vaccine. The office gave the patient a single dose of epinephrine and no other medications. The patient was not observed to have a decrease in BP, tachycardia, or decreased SpO2. The patient has not verbally responded while in transport. The patient was was observed for >3 hours with improvement in her subjective symptoms and stable clinical findings. Patient was provided with detailed return precautions and was agreeable to discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Bipolar 1 disorder, Chronic Back pain, chronic constipation, depression, dizziness, GERD, Migraines, Obesity, OSA, Peripheral neuropathy, Recurrent UTI, Sciatica of left side, Urinary incontinence, vertigo.
Andere Medikamente: Calcium Carbonate / Vitamin D 500 mg / 200 units QD, Hydroxyzine 25 mg Q6H prn, Macrodantin 100 mg UD, Pnatoprazole 40 mg QD, Epipen PRN.
Allergien: Dexamethasone (Anxiety / Palpitations), Droperidol (anaphylaxis) , Fluticasone (Rash), Flowers (Dyspnea), Lavender (Itch / SOB), Morphine (Hives / SOB), Sulfa (Swelling), Wellbutrin (Anxiety), Ketchup (Headache), Prochlorperazine (Akathisa, Nausea, Vomiting, Dizziness, SOB), DHE (Worsening of Migraines).
Vorherige Impfungen: -

VAERS 1793543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: VA
Alter: 71,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 14.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Rash Wheezing Extra dose administered Furuncle

Symptomtext

I spoke with patient via phone on 10/26/21. Patient called to inform us that after her COVID vaccine on 10/14/21, she experienced two small rashes on her neck and face the morning after her vaccination. She treated these with rubbing alcohol and they were resolved. Further, the patient reported wheezing, breathing problems and a slight fever (98.8) beginning 3-4 days after her vaccination. Her symptoms have persisted. She denies COPD, emphysema, and asthma. I asked her to call her primary care provider and make an appointment. I will plan on checking on her on Thursday 10/28/21 via phone.

Weitere VAERSDATA-Felder

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

VAERS 1815656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
Alter: 49,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 18.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain upper Arthralgia Asthma Chest pain Condition aggravated Dyspnoea Fatigue Headache Myalgia Pain Painful respiration Wheezing

Symptomtext

The day of and after I had severe muscle and joint pain, tired, headache and stomach pain. A week later I developed chest pain on the right side of my chest, wheezing and breathlessness. Deep breaths hurt. I had to take my asthma pump. I almost never use it and have never had a flare up like this. I am still achy and have joint pain but it is better than earlier in the week. The chest pain and breathing issues are new and concerning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Claritin
Allergien: Sulfa, Penicillin, seasonal
Vorherige Impfungen: -

VAERS 1815137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: IL
Alter: 38,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 24.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / RA

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

Hypoaesthesia oral Lip swelling Paraesthesia oral

Symptomtext

Lips tingly, lips swelled, tongue tingly/numb, roof of mouth numb. Took 50 mg of Benedryl. Symptoms resolved within 20 minutes of taking meds.

Weitere VAERSDATA-Felder

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

VAERS 1814873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthma Bordetella test negative Condition aggravated Dyspnoea Extra dose administered Human metapneumovirus test Human rhinovirus test Influenza virus test negative Respiratory syncytial virus test negative SARS-CoV-2 test negative

Symptomtext

47 year old Female history of asthma (hx of intubation), LE DVT 2011 on xarelto and DM2 presenting with dyspnea. Admitted with asthma exacerbation triggerd by covid 19 booster 10/8/21. Responded to steroids and nebs. Pulm consulted. Patient weaned to room air and symptoms resolved. Plan to taper prednisone with pulm f/u as outpatient. Discussed with Dr and patient stable for discharge home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: SARS-COV-2 MOLECULAR, COVID-19(RAPID-ABBOTT) Collection Time: 10/08/21 1:52 PM Result Value Ref Range Spec Source THROAT COVID-19 (SARS CoV-2, Molecular) Negative Negative RESPIRATORY VIRUS PANEL BY PCR(INCLUDES SARS COV-2) Collection Time: 10/08/21 4:30 PM Result Value Ref Range PCR RP Interp See Note Adenovirus (RVP) Not Detected Not Detected Coronavirus 229E (NOT COVID-19) Not Detected Not Detected Coronavirus HKU1 (NOT COVID-19) Not Detected Not Detected Coronavirus NL63 (NOT COVID-19) Not Detected Not Detected Coronavirus OC43 (NOT COVID-19) Not Detected Not Detected COVID-19 (SARS COV-2 RNA,RT PCR) Not Detected Not Detected Human Metapneumovirus (RVP) Not Detected Not Detected Human Rhinovirus/Enterovirus (RVP) Not Detected Not Detected Influenza A (RVP) Not Detected Not Detected Influenza B (RVP) Not Detected Not Detected Parainfluenza Virus 1 Not Detected Not Detected Parainfluenza Virus 2 Not Detected Not Detected Parainfluenza Virus 3 Not Detected Not Detected Parainfluenza Virus 4 Not Detected Not Detected Respiratory Syncytial Virus (RVP) Not Detected Not Detected Bordetella parapertussis (IS1001) Not Detected Not Detected Bordetella pertussis (ptxP) Not Detected Not Detected Chlamydia pneumoniae (RVP) Not Detected Not Detected Mycoplasma pneumoniae (RVP) Not Detected Not Detected Spec Source NASOPHARYNGEAL SWAB
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Class 3 severe obesity due to excess calories with serious comorbidity in adult Morbid obesity
Andere Medikamente: sertraline (ZOLOFT) 50 mg Tablet predniSONE (ORASONE, DELTASONE) 10 mg Tablet metFORMIN (GLUCOPHAGE) 500 mg Tablet ascorbic acid, vitamin C, (Vitamin C) 500 mg Tablet pyridoxine, vitamin B6, (VITAMIN B6) 100 mg Tablet MULTIVITAMIN ORAL
Allergien: Asa [Aspirin]Hives Biaxin [Clarithromycin]Other Nucala [Mepolizumab]Shortness of Breath Pfizer Covid-19 Vaccine (Eua) [Covid-19 Vacc,mrna(pfizer)(pf)]Anaphylaxis Xolair [Omalizumab]Shortness of Breath
Vorherige Impfungen: COVID-19

VAERS 1814349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dyspnoea Erythema Extra dose administered Flushing Hyperhidrosis Livedo reticularis Rash Skin discolouration

Symptomtext

Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: unclear if allergic reaction, as this was 3rd covid dose & pt has had flu vaccine in past. Pt reported flushed face. Upon observation cheeks turned bright red, skin mottled & face and neck pink. No s/sx of breathing trouble, no local reaction at injection sites. Patient sat in observation for 1 hour total, drank cool water & redness/pink/mottled skin slowly diminished over the hour, remaining slight pink at 1:15hr after dose w/o any s/sx of anaphylaxis

Weitere VAERSDATA-Felder

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

VAERS 1813848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MA
Alter: 56,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injection site bruising Injection site erythema Injection site pain Injection site swelling Injection site vesicles Pharyngeal paraesthesia

Symptomtext

Site: Bruising at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Additional Details: Pt said the injection site has a little blister there and it broke and little swelling and also a little brusing at the site. And also when pt is waiting for the 15minutes she felt tingling in her throat.

Weitere VAERSDATA-Felder

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

VAERS 1813436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 34,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Flushing Hyperhidrosis Paraesthesia

Symptomtext

Systemic: Left sided arm and head tingling-Mild, Systemic: Flushed / Sweating-Medium

Weitere VAERSDATA-Felder

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

VAERS 1813233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NJ
Alter: 47,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 13.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Axillary pain Chest X-ray Chest pain Electrocardiogram Flank pain Headache Hypoaesthesia Musculoskeletal pain Nerve stimulation test Pain Pain in extremity Paraesthesia Sciatica

Symptomtext

10/13/21 1pm Pharmacy got Pfizer shot 10/13/21 mild headache within 2 hours 10/14/21 bad headache the entire day. No arm soreness. 10/15 teaching all day and felt pain on right side. 10/16-10/17 still pain on right side and armpit 10/18 teaching all day With the pain 10/18 5pm feeling pain down back of right leg down through heal. Tingling. Numbness. Deep tissue pain right but cheek. 10/19 called dr 3x to tell of pain. No call back 10/20 9:00am. Primary dr sent me to emergency room for Nerve tests/scans. Ekg, chest X-ray, given Valume amd toroidal given. Dr release Me ans said it was muscular. I strained my sciatica somehow he said. He would not discuss with me if it could hane possible been due to vaccine a few days prior. 600mg iniprophen given as prescription amd a muscle relaxer as well Today is 10/23/21. I still have pain on right side that radiates from arm pit through chest and parricularly painful Down right leg. Increasing in severity to a 10 At times

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: See above in item number 18
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Rusavatastin (crestor), Vitamin d3, Vitamin C, Zinc, One a day multivitamin, Co Q10, Xanax
Allergien: None known
Vorherige Impfungen: -

VAERS 1813230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 24,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Axillary pain Back pain Chest discomfort Chest pain Cough Lymphadenopathy Musculoskeletal stiffness

Symptomtext

Armpit swelling and pain lasting longer than 24hours. Advil providing relief. Chest and upper back pain and tightness. No relief from standard otc medicine like Advil or NyQuil. Coughing when trying to take deep breaths.

Weitere VAERSDATA-Felder

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

VAERS 1808757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 35,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Chest discomfort Chest pain Chills Dizziness Nausea

Symptomtext

Patient received first dose of Pfizer at 1410. RN sat with patient for observation because of anaphylactic reaction to hydrocodone. 1428 patient patient given water and juice. 1430 patient feeling nauseated, assisted to wheelchair then to gurney and laid down. 1440 blood pressure 190/100 HR 101 oxygen saturation 98 .1442 blood pressure 192/118 patient denies history of hypertension complains of tightness in chest, reports history of anxiety ?this is how it felt before I think it?s my anxiety ?1450 medicated with Benadryl 25 mg wife arrived at 1445 to be at bedside informed of status. 1454 sat patient up on side of gurney BP 160/ 98 HR 93 O2sat 96%. Patient continues to feel tight in middle of chest pointing to his mid sternum. Patient became dizzy and chills after drinking cold water. 1510 laid patient back down on gurney complain of 3/ 10 pain mid sternum. At 15 03 BP 158/94 HR 80 O2 sat 99%1518 EMS called 1528 EMS arrived evaluation done, patient refused EMS transport wife drove patient to ER at 1542

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: Antihistamine for seasonal allergies Antidepressant
Allergien: Hydrocodone - anaphylactic
Vorherige Impfungen: -

VAERS 1808449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: VA
Alter: 53,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 14.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: IM / LA

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

Colitis ulcerative Condition aggravated

Symptomtext

Patient reports Pfizer #1/2 on 10/14/21, worsened ulcerative colitis flare 10/18/21. Managed by GI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Office visit with PCP 10/22/21
Aktuelle Erkrankungen: Ulcerative colitis Vestibular migraines
Vorgeschichte: Ulcerative colitis Vestibular migraines TMJD Allergic rhinitis Coronary artery disease
Andere Medikamente: Aspirin 81mg qd Budesonide 90mg qd Effexor XR 37.5mg qd Propranolol 20mg TID Progesterone 200mg qd Omeprazole 40mg qd Pepcid 40mg HS Symbicort 80mcg-40.5mcg 2 puffs BID Albuterol PRN Xyzal 5mg HS Nasonex PRN Fioricet with codeine P
Allergien: Benadryl Mesalamine Singulair
Vorherige Impfungen: -

VAERS 1808010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: TX
Alter: 69,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 20.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Back pain Chills Dyspnoea Headache Pyrexia

Symptomtext

Fever, shivers, hard breathing, back ache, headache. Shivers & hard breathing lasted 10 - 15 minutes Fever peaked at 101

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lisinopril 10mg Doxazosin 4mg
Allergien: No
Vorherige Impfungen: -

VAERS 1807246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: RI
Alter: 50,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 19.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Axillary pain Breast pain Breast swelling Chest pain Lymphadenopathy Swelling

Symptomtext

Having pain and swelling on left side of chest, left underarm and left side of left breast. Painful to light touch. Started in the early morning hours on 10/21/21. Have not been seen by PCP yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: Vicodin and tetanus vaccine
Vorherige Impfungen: Tetanus vaccine, approximately in year of 1980

VAERS 1804814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MO
Alter: 41,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 17.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Condition aggravated Inflammation Rash Rash pruritic Urticaria

Symptomtext

My doctor had me start Allegra several days before reviving the injection and then continue taking it for up to 2 weeks after injection.. I was instructed to take Benedryl 2 hours before the injection and continue every 6 hours for a 24 hour period. The pharmacist suggested ibuprofen for inflammation, so I took that as needed. Continued Allegra as instructed. When I woke up on Tuesday, October 19th, the itchy hives rash was observed on my neck, chest, stomach, back, arms, thighs and pelvic area. Benedryl was started again. Hydrocortisone was used as needed. Thursday, October 21st- rash is practically gone. But still itchy. Hydrocortisone used as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Benedryl
Allergien: Cefdinir Augmentin Decongestants
Vorherige Impfungen: 02/25/2021 itchy/hives rash reaction to 1st Pfizer vaccine. Also had a rash when I had COVID-19 in December 2020

VAERS 1804442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: CT
Alter: 73,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

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 1801231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IL
Alter: 31,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 18.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Dyspepsia Dyspnoea Extra dose administered Palpitations

Symptomtext

After 2nd shot (Feb 11, 2021) had severe chest pain and was in ER, they thought it was heart burn, took a Pepcid and eventually it went away. Symptoms were racing heart, trouble breathing, extreme chest pain in waves. Recently got 3rd shot thinking would be better, around 12:30 am woke up with chest pain, and it grew to extreme levels. Treated it with a Pepcid and ibuprofen, after about 2 hours the pain eventually subsided. Didn't go to ER because I thought it was just heart burn from the last time I had it. Based on recent studies, we think it may be Myocarditis or Pericarditis which they say can be a side effect of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, raynaud's syndrome
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1800952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 54,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 17.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Hypertension Impaired work ability Pyrexia Tachycardia

Symptomtext

Patient reports after receiving second shot in COVID vaccine series she developed tachycardia, HR ranging from 108-119, HTN 180s/97, and high fevers of 103. Patient states her symptoms started throughout the night after receiving the vaccine. Report she attempted to go to work, but had to leave due to her symptoms. Reports she was evaluated by Hospital and was sent home to rest, treat symptoms, and monitor HR and BP. Patient states she rested and took Tylenol for her symptoms. Reports she had a fever of 99-103 until 10/20/21. Stated on 10/20/21 her symptoms started to improve, HR 84, blood pressure 130/81. Reports she had tachycardia, hypertension, and febrile for 3 days post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: evaluation on 10/18/21 at Hospital.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Mobic as needed ibuprofen as needed
Allergien: seasonal allergies prednisone
Vorherige Impfungen: -

VAERS 1800783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NY
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

Blood test normal Brain scan normal Electrocardiogram normal Eye irritation Feeling abnormal Feeling hot Headache Muscle tightness Neck pain Paraesthesia Paraesthesia ear Paraesthesia oral Pruritus Sensory disturbance

Symptomtext

15 minutes after the vaccination, I felt something hot in my neck and it went up to the middle of my head, with pain, very ugly and my neck felt tense but it happened. The next day my neck felt tense again and at night at 11:30PM my mouth felt strange and my face, ears, lips, nose felt asleep-the whole face was sleep. At 12am I went to sleep. I woke up and face was no longer asleep, but 2 hours later (8:30am) the face was asleep again, the sleepiness of the face came and went, From #PM I felt the whole face asleep and I wen to the emergency room. They did a head scan (they ruled out a facial effusion) they gave me medicine for my headache, as I had a mild headache, they did an electrocardiogram and it was normal. They sent me to a Neurologist (I have and appt Oct 26). 3 days ago I felt a tight neck taking TYLENOL. 3 days ago I also felt like an anthill on the fingers of my right and and itching on both hands. Immediately after the vaccine I felt burning in my eyes, but it passed quickly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 10/16/2021 - Blood test were normal. Electro normal, scan normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Thyroid; Acid Reflux; Heart Palpitations
Andere Medikamente: Vitamin D; Vitamin flax
Allergien: Pollen
Vorherige Impfungen: Flu vaccine, 40-45 yrs. For a week I was always on bed sick worst than a flu. With pain.

VAERS 1798933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Dizziness Heart rate increased Throat tightness Tremor

Symptomtext

fast heartbeat, lightheaded, shakes, chills, felt like throat was closing. Gave patient diphenhydramine 50 mg and had her sit with her head down. Patient felt she was well enough to drive home and throat closing felt better. Time course was over 1 hour.

Weitere VAERSDATA-Felder

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

VAERS 1798481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: PA
Alter: 49,0
Geschlecht: M
Eingang: 19.10.2021
Impfdatum: 14.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Dyspnoea Hyperhidrosis

Symptomtext

10/15/2021-shortness of breath, chest pain, sweating

Weitere VAERSDATA-Felder

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

VAERS 1798385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: WA
Alter: 62,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Eye movement disorder Fall Palpitations Unresponsive to stimuli

Symptomtext

RN sitting with patient talking to her. At 10:25 she received her first dose of Pfizer. At 10:27 patient reporting filling her heart racing ,feeling woozy feeling like she was going to faint. Patient went limp in the chair with her eyes rolled in the back top of her head unresponsive for 20 to 30 seconds. Patient came to and said she was nervous about the vaccine since all of her family reacts this way. Assisted transfer to wheelchair then transferred to gurney. At 10:32 AM BP 105/66 heart rate 63. At 10:37 BP 120/80 heart rate 62 respirations 20 oxygen saturation 98% temperature 98.0. Because of history with seizures and not taking seizure medication EMT was called. 1042 EMT arrived and did their assessment. At that time patient was sitting up and ambulating without dizziness. Patient called friend to pick her up in private auto at 11:17 to take her home and reported he could stay with her for the next couple of hours for observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient reported a bladder infection one month ago and received antibiotics for it. She reported that she completed the medication a week ago.
Vorgeschichte: Patient reports having had seizures and has a prescription for seizure medication but could not name what the medication. She also states she has she does not currently take the medication.
Andere Medikamente: Vitamin D, vitamin B12, zinc. Patient reports taking a seizure medication but does not know the name of it.
Allergien: Patient says she reacts to pills but could not name any of the medications.
Vorherige Impfungen: -

VAERS 1798037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ff2590

moderat

Staat: VA
Alter: 50,0
Geschlecht: F
Eingang: 19.10.2021
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: ja

Dyspnoea Paraesthesia

Symptomtext

Severe numbness and tingling in both hands for a couple of hours along with shortness of breath beginning the day after I received the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lexapro, Levothyroxine, Vitamin C (500Mg) , Bi Yan Pian. One a Day Multi Vitamin
Allergien: Sesame Seeds, pumpkin seeds, poppy seeds and wool
Vorherige Impfungen: -

VAERS 1797801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

Within approximately 5 minutes of injection had numbness and tingling from left upper arm all the way down to fingertips. Told the nurse about it and she said oh, that has happened to some people. When I asked how long it lasts she said it should go away but not within the 15 minutes. The nurse asked if I wanted to stay longer. Then the nurse said if it doesn't go away to call and let your Doctor know. Then she sent me on my way like it was no big deal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Thrive, Claritin D
Allergien: No
Vorherige Impfungen: -

VAERS 1797717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 19.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Chest pain Dizziness Heart rate increased Hypertension Nausea Palpitations Throat tightness

Symptomtext

Following vaccination, patient experienced chest pain, throat tightness, dizziness, nauseous, heart racing, initially hypertensive with elevated pulse. Transported the the emergency department.

Weitere VAERSDATA-Felder

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

VAERS 1796186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: MO
Alter: 53,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain

Symptomtext

About 30 seconds after administering patient's booster shot, she started complaining of a squeezing feeling in her chest and then started calling it chest pain. Called 911 and patient's husband came into immunization room. 911 Operator wanted pt to take an 325mg Aspirin while ambulance in root. Pt did not report arm pain, no sweats, or other symptoms of heart attack. BP by paramedics was 142/94. Pt was taken to hospital across the street to be checked out. Follow up call to husband at 8pm, he reported that EKG in ambulance appeared to be normal per paramedics. Pt and husband got tired of waiting in hospital ER and checked her out after wasn't seen 'quick enough' and was 'feeling better' and chest pain went away. Said they'll follow up with her MD next morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: DM Type 2
Andere Medikamente: no listed in our pharmacy system
Allergien: no reported allergies prior to vaccination
Vorherige Impfungen: -

VAERS 1795085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 19,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 13.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Chest pain Dyspnoea Nausea

Symptomtext

Experiencing shortness of breath, chest pain, and pressure. Also feeling of nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: had COVID in Aug 2021 and anxiety
Andere Medikamente: birth control
Allergien: no
Vorherige Impfungen: -

VAERS 1794036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MD
Alter: 69,0
Geschlecht: M
Eingang: 17.10.2021
Impfdatum: 15.10.2021
Beginn: 15.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Migraine

Symptomtext

Booster shot, I had a Migraine like headache for 30 hours. I was unable to take any medicine as I am having a prostate examination on Thursday October 21, at the request of the doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NO
Vorgeschichte: No
Andere Medikamente: This is a list of the medications I am taking daily as of 9/30/2021 Centrum Silver vit tabs Allopurinol 300 mg for Gout Fluoxetine20 mg for anxiety OLM MED/AMLO 40-10-25mg for Blood Pressure Metoprolol Succinate 50mg for Blood Pressure Doxa
Allergien: No
Vorherige Impfungen: -

VAERS 1794031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: KS
Alter: 47,0
Geschlecht: F
Eingang: 17.10.2021
Impfdatum: 15.10.2021
Beginn: 16.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Lymphadenopathy Musculoskeletal chest pain Pain in extremity Vaccine positive rechallenge

Symptomtext

Swollen lymph nodes in left arm. Lump the size of a softball. Extreme pain in armpit, arm, hand and ribcage. Happened after second and third shots, but not first.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Metoprolol, Escitalopram, Estatylla, Nexium
Allergien: None
Vorherige Impfungen: Covid #2, same symptoms, 4/15/2021

VAERS 1793707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: VA
Alter: 13,0
Geschlecht: F
Eingang: 16.10.2021
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: ja

Dyspnoea

Symptomtext

Systemic: Allergic: Difficulty Breathing-Medium

Weitere VAERSDATA-Felder

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

VAERS 1788740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 73,0
Geschlecht: F
Eingang: 15.10.2021
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: unbekannt Erholt: ja

Chills Pyrexia Tremor

Symptomtext

severe chills and shaking which started suddenly about 11pm and lasted about 3 hours. slight fever of 99.3 to 100.2. i don't know the exact name of the flu shot i got. it just said Senior-dose flu shot. i guessed on the exact type

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: surgery on ruptured patella tendon in right knee on Sept 13, 2021
Vorgeschichte: diabetes type 2, high blood pressure, high cholesterol, restless legs, anxiety
Andere Medikamente: Gabapentin, Pramipexole Dihydrochloride ER, Fluoxetine Hcl, Glyburide, Metformin ER, atorvastatin, 81 mg aspirin, invokana, hydrochlorothiazide, trulicity, omeprazole,
Allergien: Sulfa, Tequin, Levequin, Cipro, Humira
Vorherige Impfungen: -

VAERS 1788684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: IA
Alter: 42,0
Geschlecht: F
Eingang: 15.10.2021
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

Chest discomfort Cough Crying Dysphonia Hypertension Tearfulness Throat irritation

Symptomtext

10:50 - Patient complained of itchy throat, reports this is the same reaction she had to the first two shots, took a benadryl and dose of albuterol inhaler last time and it went away. 10:55 - 25mg of Benadryl taken per patient request. Given by school nurse. SpO2 99% RA, HR 104, RR - 21, unlabored, BP 136/78, patient reports BP high for her. Reports itchy throat, no trouble breathing, cough, raspy voice noted, 2 RN's monitoring patient, patient refusing epinephrine. 11:00 - Patient tearful, reportedly due to "attention", No trouble breathing, however is still having cough, raspy voice, itchy throat. Continues to refuse epinephrine. "I know when I need epi and I'm no where close to that." Spo2 96% RA, HR 99, RR 26 - crying. No swelling noted to tongue. 11:05 - Patient agreeable to epinephrine, RN told patient that once epinephrine was given, ambulance needs to be called or patient needs to go to ED. Patient adamently refused ambulance/ED and then refused epi again. Husband brought patient her inhaler, took 2 puffs off albuterol inhaler - reports this is what she does for allergic reactions. Both RNs continued counseling patient on dangers of allergic reactions and subsequent exposures being worse, that previous interventions may not work this time, swelling could return, albuterol won't help the reaction itself, continued encouraging epinephrine and ambulance?ED. Patient continued to refuse. SpO2 just prior to albuterol 93-94% RA, RR 22 unlabored, HR-99, voice still raspy. 11:08 - Post albuterol, patient SpO2 99%, HR 93, RR 21 unlabored, BP 117/72. Continues to refuse epi despite education and encouragement from nurses. Reports she is feeling better - itchiness still present but improved, adament on attending her personal development for teachers that was occurring at that time, reporting, "there's a whole library full of people to watch me." This RN walked her down to library where her table was informed of her status and told to notify RN immediately upon changes in coughing, breathing, appearance, or reported by patient. 11:48 - Reports chest tightness, raspy voice, but reports improvement in itchiness. Continues to refuse epi, ambulance, or ED. SpO2 99% Ra, HR 93, BP 116/72, RR 18.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: Unknown
Allergien: Remicaid, sulfa
Vorherige Impfungen: Reported itchy throat after first two doses as well.

VAERS 1788431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 48,0
Geschlecht: M
Eingang: 15.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Flushing Hyperhidrosis Hypotension

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Mild, Additional Details: Pt received the flu shot and Pfizer 3rd dose on 10/14/2021. after vaccine administration during the 15min wait time, pt became dizzy and light headed. Vital signs taken Bp 100/60 HR 70, SP02 99% on room air, FSBS 87, patient placed in siting position and verbalized that he started feeling better, and he stated that he usually vasovagals after blood draws and he suffers from hypertension. Patient also verbalized his father died from covid 1 week prior. EMS arrived and transported patient.

Weitere VAERSDATA-Felder

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

VAERS 1788407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MT
Alter: 74,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 05.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Bradycardia Condition aggravated Dizziness

Symptomtext

Bradycardia and Light Headed; History of bradycardia episodes.

Weitere VAERSDATA-Felder

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

VAERS 1786199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Hypotension Immunisation Lymphocyte count decreased Lymphocyte percentage decreased Nausea Neutrophil count decreased Neutrophil percentage increased Pyrexia Tremor

Symptomtext

At 02:30 pm on 10/12/21 (20 hours after the injections), I began shaking uncontrollably. I developed nausea and sever light headedness. The paramedics called, and I was taken to the hospital and admitted for fever and low blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Blood pressure: 90/60. Fever: 99. Absolute Lymphocytes: 0.6. Absolute Neutrophil/Ab Lymph. Ratio: 13.1. Neutrophils: 88.8. Lymphs: 6.6.
Aktuelle Erkrankungen: Stopped skin treatment 9/3/2021 (Accutane)
Vorgeschichte: Depression, anxiety, migraines, skin inflammation (unspecified)
Andere Medikamente: Sertraline 50mg; Buspirone 22mg; Trazodone 50mg; Multivitamin; Probiotic vitamin
Allergien: Clarithromycin; Miconazole; Neosporin; Adhesive; fruit preserves; lactose intolerance
Vorherige Impfungen: Flu vaccine 2018. Low blood pressure; possible fever. No hospitalization/ER required.

VAERS 1785548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: FL
Alter: 33,0
Geschlecht: M
Eingang: 14.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Anxiety Blood test Chest X-ray Dyspnoea Electrocardiogram Feeling abnormal Headache Heart rate decreased Immediate post-injection reaction Palpitations

Symptomtext

Immediate palpitation and shortness of breath upon second dose. One day after I went to the hospital for extreme palpitations, and slow heart rate under 59bpm. Very high anxiety since vaccination. Also headache and brain fog.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG, Chest X-ray, blood work
Aktuelle Erkrankungen: Anxiety, palpitations, sleep apnea
Vorgeschichte: Anxiety, palpitations, sleep apnea
Andere Medikamente: Fish oil, multivitamin, ashwagandha, b complex
Allergien: No
Vorherige Impfungen: -

VAERS 1785420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 38,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 14.10.2021
Beginn: 14.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Paraesthesia oral Rash Throat irritation

Symptomtext

left arm and neck rash, throat itching, tongue felt "funny"

Weitere VAERSDATA-Felder

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

VAERS 1785377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 13.10.2021
Beginn: 13.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Dyspnoea Injection site bruising Pain

Symptomtext

Site: Bruising at Injection Site-Mild, Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Additional Details: called 911 for pt. who had chest tightness after getting the covid shot. pt recovered after being seen by paramadics

Weitere VAERSDATA-Felder

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

VAERS 1783072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: CA
Alter: 75,0
Geschlecht: M
Eingang: 13.10.2021
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: unbekannt Erholt: ja

Dyspnoea

Symptomtext

pt reported feeling shortness of breath 5 hours after receiving the 3rd dose Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 3rd dose Pfizer vaccine
Aktuelle Erkrankungen: none
Vorgeschichte: bp, dm cholesterol asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1782722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: KS
Alter: 27,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Axillary pain Chest pain Dizziness Heart rate increased Injection site erythema Injection site swelling Musculoskeletal chest pain Pain in extremity Palpitations Pyrexia

Symptomtext

Multiple reactions: Dizzy/Lightheadedness Fast beating heart/heart palpitations Sharp pains in chest near heart Fever Pain in arm, armpit, and down ribs Swelling and redness at injection site

Weitere VAERSDATA-Felder

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

VAERS 1782589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: ME
Alter: 41,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Cardiac flutter Chest pain Dyspnoea

Symptomtext

Sharp chest pain without prior exertion. Heart flutters, and inability to take a deep breath. Intermittent chest pains come when sitting, lying, or walking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: waiting, have contacted my cardiologist
Aktuelle Erkrankungen: none
Vorgeschichte: Qualitative platelet disorder - bleeding disorder like Von Willabrands Ehlers Danlos Syndrome Heart irregular beats History of SVT Influenza vaccine allergy
Andere Medikamente: no medication taken at time of vaccination but taken BID QD Bariatric Fusion MVI Wellbutrin Ritalin Cymbalta Chantix Salsalate nexium turmeric -Bioperine Clonazepam PRN Colace HS Gabapentin HS
Allergien: Any NSAIDS, Aspirin PCN, Keflex, Influenza vaccine allergy, and fresh pineapple, iodine.
Vorherige Impfungen: -

VAERS 1782239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 13.10.2021
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

Arthralgia Injury Joint injury Paraesthesia Product administration error

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 1779313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dysphagia Paraesthesia

Symptomtext

Patient said he was experiencing difficulty swallowing about every 3 swallow and some facial tingling.

Weitere VAERSDATA-Felder

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

VAERS 1779206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

moderat

Staat: CT
Alter: 26,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 11.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Injection site pain Muscle tightness Pain in extremity Paraesthesia

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Joint Pain-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: jaw tightness and leg pain, resolved with time

Weitere VAERSDATA-Felder

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

VAERS 1779133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AZ
Alter: 45,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Pharyngeal paraesthesia

Symptomtext

Vaccinator went to check on pt at the end of the 15 mins wait post-Pfizer COVID vaccine 3rd dose. Pt reported "tingling" in throat, but denied swelling, itching, difficulty breathing. HR 74. O2 98%. Had pt wait for full 30 mins. Pt reported symptoms resolved, denied any other symptoms, and he went home. Advised to go to ED for any worsening symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: none listed in medical record
Andere Medikamente: unknown
Allergien: morphine - unknown reaction
Vorherige Impfungen: -

VAERS 1779023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: NC
Alter: 28,0
Geschlecht: F
Eingang: 12.10.2021
Impfdatum: 05.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Pain Pain in extremity Paraesthesia

Symptomtext

Pain in entire arm; numbness/tingling in lower left arm into hand. Unable to grip anything without pain going through arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Beta thalessemia
Andere Medikamente: Birth control Nortryptaline
Allergien: Topamax
Vorherige Impfungen: -

VAERS 1776748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MT
Alter: 24,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Chest discomfort Dyspnoea Electrocardiogram abnormal Fatigue Myalgia Pyrexia Ventricular extrasystoles

Symptomtext

Fever, fatigue, severe muscle aches for 2 days. 2 days after vaccine, became short of breath and felt chest tightness,.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG done-Trigeminal PVCS. will be following up with a provider
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1776418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: PA
Alter: 80,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dyspnoea Fatigue Pyrexia

Symptomtext

Pt. states that after receiving the 3rd dose Booster of Phizer 10/08/2021, started experiencing symptoms 10/09/2021 of fever (101.0), chills, fatigue, shortness of breath *Inhaler Use (Lasting 2 days). Self-treating with Tylenol, no noted Primary visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Aspirin, Pennicillin, Fentanyl
Vorherige Impfungen: -

VAERS 1775140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MD
Alter: 45,0
Geschlecht: M
Eingang: 09.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Paraesthesia

Symptomtext

Patient reported feeling dizzy, light headed and a feeling of pins and needles after his first covid pfizer vaccine. His blood pressure was monitored and readings were as follows: approx 30 min after vaccine 149/92 hr 69, 2:00pm 148/85 HR 67, 205pm 162/105 HR 74 208pm 166/94 HR 71. 1 dose of Epinephrine autoinjector 0.3mg was given at 210pm. 212pm: 154/85 HR 71, 216pm 145/86 HR 86 EMS was called at 2:10pm after epeneprine. EMS arrived and transported patient to hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes type 2
Andere Medikamente: metformin
Allergien: shrimp, cats, dogs
Vorherige Impfungen: -

VAERS 1772621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: MI
Alter: 22,0
Geschlecht: F
Eingang: 08.10.2021
Impfdatum: 08.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Paraesthesia Peripheral swelling

Symptomtext

Patient said arm felt "tingly" and patient said hand appeared to be swelling. Patient was observed for over the 15 minute appropriate wait time. She was given water and the option of Benadryl. After over 30 minutes of observation, the patient said she was fine and was okay to leave. Once the patient informed me that her arm felt 'tingly' and that her hand look swollen, I had her sit down in the observation zone for another 15 minutes. I contacted my coordinator to see what steps I should take next. I offered the patient water and Benadryl. After sitting for 15 minutes, I asked the patient if she was experiencing any shortness of breath or any other symptom that warranted EMT presence. The patient said she was feeling fine and that she was okay to leave. I made sure to counsel the patient and let her know that if she started to have any a serious reaction, she should head to the ER immediately.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None known of.
Andere Medikamente: None known of.
Allergien: None.
Vorherige Impfungen: -

VAERS 1769678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: AL
Alter: 42,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 07.10.2021
Beginn: 07.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Cough Lip swelling Malaise Oropharyngeal discomfort Paraesthesia oral Pruritus Rash

Symptomtext

Patient began to complain of "itching all over" about 20 minutes after receiving her vaccination. Shortly after that, she complained of feeling unwell. BP was 152/100. Patient began to complain of tingling around her mouth. Rph observed mild swelling on bottom edge of lower lip. Pt began to cough and kept trying to clear her throat. EPI 0.3 was administered. Paramedics arrived 4 minutes and 30 seconds afterward. Patient had developed a pink rash on arms that was noted by EMS and Rph.. Patient taken to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: recent flu vaccine with anaphylaxis
Vorgeschichte: -
Andere Medikamente: -
Allergien: Patient stated allergic to Compazine and had recently had an allergic reaction to her FLU vaccine
Vorherige Impfungen: per pt- two other times she has had reactions to a FLU shot

VAERS 1764978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

moderat

Staat: OH
Alter: 36,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 04.10.2021
Beginn: 05.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac flutter Chest pain Fatigue

Symptomtext

Chest started hurting. Feeling of heart fluttering and tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2727376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: MN
Alter: 51,0
Geschlecht: F
Eingang: 26.12.2023
Impfdatum: 27.09.2022
Beginn: 22.12.2023
Tage bis Beginn: 451,0
Dosis: 3
Route/Site: UN / UN

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

Oropharyngeal pain SARS-CoV-2 test

Symptomtext

Sore throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Home COVID Test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2720029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: MN
Alter: 62,0
Geschlecht: M
Eingang: 01.12.2023
Impfdatum: 16.04.2021
Beginn: 02.12.2021
Tage bis Beginn: 230,0
Dosis: 3
Route/Site: IM / RA

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

Oropharyngeal pain

Symptomtext

12/2/2021-sore throat

Weitere VAERSDATA-Felder

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

VAERS 2442733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: MN
Alter: 59,0
Geschlecht: F
Eingang: 22.11.2023
Impfdatum: 22.10.2021
Beginn: 22.11.2023
Tage bis Beginn: 761,0
Dosis: 3
Route/Site: IM / LA

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

Chills Pain Pyrexia COVID-19 SARS-CoV-2 test positive

Symptomtext

Fever, body aches, chills

Weitere VAERSDATA-Felder

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

VAERS 2646380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: ID
Alter: 61,0
Geschlecht: F
Eingang: 16.06.2023
Impfdatum: 01.12.2021
Beginn: 07.08.2022
Tage bis Beginn: 249,0
Dosis: 3
Route/Site: IM / RA

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

Ageusia Arthralgia COVID-19 Chills Decreased appetite Fatigue Headache Malaise Nausea Pyrexia SARS-CoV-2 test positive

Symptomtext

On 8/7/2022, I had fever, joint pain, nausea, headache, fatigue, and chills. Just a few days later, I lost my sense of taste. I also lost my appetite and had a headache at one point. The only medicine I took to relieve my symptoms was ALEVE, which helped some. I was pretty sick for about ten days. However, I was back to normal (for the most part) within three weeks, though I did have fatigue for about a month longer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 08AUG2022 home antigen test positive result
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estradiol (vaginal); multivitamin; vitamin D3; lutein; vitamin K2; relieve and repair quercetin complex; magnesium; omega 3; milk thistle
Allergien: None
Vorherige Impfungen: -

VAERS 2643195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: OR
Alter: 45,0
Geschlecht: M
Eingang: 08.06.2023
Impfdatum: 04.01.2021
Beginn: 17.06.2021
Tage bis Beginn: 164,0
Dosis: 3
Route/Site: SYR / AR

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

Autoimmune thyroiditis Blood thyroid stimulating hormone Cervical spinal stenosis Hypothyroidism Intervertebral disc degeneration Magnetic resonance imaging spinal abnormal Muscle atrophy Musculoskeletal stiffness Pain Thyroxine Tri-iodothyronine

Symptomtext

In June of 2021 pain, stiffness, and muscle wasting on my left upper body resulted in a doctor visit. I underwent MRI and was diagnosed with mild to severe spinal stenosis and disc degeneration in my cervical spine. The following year I was diagnosed with hypothyroidism and Hashimoto?s. Please note that I do not suspect that the vaccine caused these conditions. When I reported these conditions on the VSafe survey, I was encouraged to report this information on VAERS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: I underwent an MRI for my neck in June 2021. I underwent repeated TSH, T3, and T4 blood tests in November and December 2022.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin C, fish oil
Allergien: Lactose intolerance
Vorherige Impfungen: -

VAERS 2633316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: FL
Alter: -
Geschlecht: F
Eingang: 18.05.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Arthralgia Blood test Dysstasia Gait disturbance Insomnia Malaise Myalgia Pain in extremity Vitamin D Vitamin D decreased

Symptomtext

She is not well; Bilateral leg pain/severe leg pain./pain went to the right arm/pain went to her left arm; calf and thigh muscles (pain); also the joints (pain); having trouble walking; couldn't sleep; couldn't stand the sheet on her leg; for Vitamin D3, which was low; This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 78-year-old female patient received BNT162b2 (BNT162B2), in 2021 as dose 3 (booster), single (Lot number: FF2590, Expiration Date: 31Dec2021), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications.She doesn't take any other medications other than vitamins. She took magnesium thinking it would help; took 500mg tablets of Magnesium. Magnesium didn't help the pain. Was already a daily multi-vitamin. Clarified all of her vitamins are over the counter. She does not have any prescription medications. Vaccination history included: BNT162b2 (Dose 1, Time: morning, 10AM, LOT: PFR EN6204, Anatomical Site of injection: Left upper arm), administration date: 08Mar2021, when the patient was 76-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, Time: 7:59AM, LOT: PFR EP6955, Anatomical Site of injection: left upper arm), administration date: 29Mar2021, when the patient was 76-year-old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (disability) with onset 2021, outcome "unknown", described as "Bilateral leg pain/severe leg pain./pain went to the right arm/pain went to her left arm"; MALAISE (disability) with onset 2021, outcome "unknown", described as "She is not well"; ARTHRALGIA (disability) with onset 2021, outcome "unknown", described as "also the joints (pain)"; MYALGIA (disability) with onset 2021, outcome "unknown", described as "calf and thigh muscles (pain)"; INSOMNIA (disability) with onset 2021, outcome "unknown", described as "couldn't sleep"; DYSSTASIA (disability) with onset 2021, outcome "unknown", described as "couldn't stand the sheet on her leg"; VITAMIN D DECREASED (disability) with onset 2021, outcome "unknown", described as "for Vitamin D3, which was low"; GAIT DISTURBANCE (disability) with onset 2021, outcome "unknown", described as "having trouble walking". The events "she is not well", "bilateral leg pain/severe leg pain./pain went to the right arm/pain went to her left arm", "calf and thigh muscles (pain)", "also the joints (pain)", "having trouble walking", "couldn't sleep", "couldn't stand the sheet on her leg" and "for vitamin d3, which was low" required physician office visit. Patient is not well and is very concerned about it. She didn't have a doctor for 10 years until she went a couple months ago because of the severe leg pain. She couldn't sleep, couldn't stand the sheet on her leg. She has been on feet her whole life. Was a hospital and surgical nurse. Then she did read a blurp about side effects and never thought about that. The more she thought, she did go to a primary care doctor. Her lab work was good except for Vitamin D3, which was low, not excruciatingly low. She now takes 5,000mg of vitamin D3 a day. Her doctor was going to write a prescription but she already takes vitamin D3 so she advised her doctor she'll just take more of it. Attempted to clarify dose of 5,000mg but caller would not reclarify. She has a follow up appointment on 01Jun2023, but she doesn't feel any better. Is having trouble walking. The pain went to her left arm, the middle of arm for 3-4 days. Then the left arm got better, but the pain went to the right arm. Her legs are still terrible. She doesn't know and all she is doing is asking questions because when she goes to see her primary care doctor. She is not a big doctor fan. If she's no better by 01Jun2023, primary doctor is going to send her to an orthopedic doctor for knee replacements. Caller states she doesn't need knee replacements. Seriousness criteria: Disabling at times. Always manages to get up in the night, just to get to the bathroom, but the paint is terrible then. It's excruciating, it's awful. During the day, she can tolerate it and not be in such terrible pain. The patient underwent the following laboratory tests and procedures: Blood test: good, notes: Her lab work was good; Vitamin D: low, not excruciatingly low, notes: Her lab work was good except for Vitamin D3, which was low, not excruciatingly low. Therapeutic measures were taken as a result of malaise, pain in extremity, myalgia, arthralgia, gait disturbance, insomnia, dysstasia, vitamin d decreased.; Sender's Comments: As there is limited information in the case provided, the causal association between the reported events and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate. ,Linked Report(s) : US-PFIZER INC-202300192113 Same reporter/patient/drug, different AE.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: lab work/bloodwork; Result Unstructured Data: Test Result:good; Comments: Her lab work was good; Test Name: Vitamin D3; Result Unstructured Data: Test Result:low, not excruciatingly low; Comments: Her lab work was good except for Vitamin D3, which was low, not excruciatingly low
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2619364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: FL
Alter: 82,0
Geschlecht: F
Eingang: 22.04.2023
Impfdatum: 03.02.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Fatigue Therapeutic response unexpected

Symptomtext

happy unexpected improvement; general fatigue; The initial case was missing the following minimum criteria: unspecified product, unspecified adverse event and unspecified number of patients. Upon receipt of follow-up information on (17Apr2023), this case now contains all required information to be considered valid. This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID: (005570). An 84-year-old female patient received BNT162b2 (BNT162B2), on 03Feb2022 as dose 3 (booster), single (Lot number: FF2590) at the age of 82 years for covid-19 immunisation. The patient's relevant medical history included: "vascular dementia alzheimers and parkinsons" (unspecified if ongoing); "vascular dementia alzheimers and parkinsons" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE , Lot: EL3246), administration date: 07Jan2021, when the patient was 81-year-old, for COVID-19 immunization, reaction(s): "cognitive improvement", "general fatigue"; BNT162b2 (DOSE 2, SINGLE , Lot: EL3246), administration date: 28Jan2021, when the patient was 81-year-old, for COVID-19 immunization, reaction(s): "cognitive improvement", "general fatigue". The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "happy unexpected improvement"; FATIGUE (non-serious), outcome "unknown", described as "general fatigue". Additional information: This is not an adverse negative reaction but rather a positive side effect. At both initial vaccines patient (reporter's mother) experienced a (Illegible word) cognitive improvement. More alert and responsive as if to suggest an arresting of disease process. She had vascular dementia alzheimers and parkinsons. Both of which degrade overall awareness and interactive responsiveness. Beyond a pronounced general fatigue which is the understood effect of any vaccine on the body, the happy unexpected improvement which seems to occurred with any revaccination of pfizer covid vaccine. Reporter reported for the record that research may result. One or more of the chemicals or chemistry of this product could prove useful in the fight of both alzheimers and parkinsons.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Dementia Alzheimer's type; Parkinson's disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2612938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 20.07.2022
Beginn: 01.12.2022
Tage bis Beginn: 134,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Chest X-ray normal Chills Fall Fatigue Fibrin D dimer SARS-CoV-2 test positive Spinal fusion surgery White blood cell count decreased

Symptomtext

12/1/2022- Presents to ED, fall at rehab s/p spinal fusion surgery. C/o fatigue and chills. T-99, BP-139/94. Spo2 96% on RA. Covid + test. CXR- no infiltrates. Ordered bebtelovimab, IV ceftriaxone given in ED, IV decadron and IV remdesivir. Admit generalized weakness l/t mechanical fall Covid. WBC-7.0, D Dimer 345. 12/4/2022-WBC-3.7, continue doxy and ceftriaxone. Spo2-95% on RA. 12/6/2022- WBC-9.7, completed 5 day course remdesivir. Maintained sat of above 95% on RA. Continue deadon Po for 6 more days. Was on ceftriaxone and doxy, will take cefdinir and doxy at home. Discharge to Home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, High cholesterol,
Andere Medikamente: -
Allergien: Bacitracin and Sulfamethoxazole-trimethoprim
Vorherige Impfungen: -

VAERS 2610180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 02.09.2022
Beginn: 22.01.2023
Tage bis Beginn: 142,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Chills Cough Pain Pyrexia SARS-CoV-2 test positive Sinus congestion

Symptomtext

I tested positive for Covid 19 on Jan 22, 2023 - home test. +fever, +chills, cough, sinus congestion, +body aches, I was treated with Lageviro capsules. 48 hours after starting the Lageviro - I started feeling markedly improved. I am back to my health base line. But, I still have decreased sense of taste/smell from the first time I had Covid 19 in November of 2020.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Home Covid test
Aktuelle Erkrankungen: No Acute illness at the time of vaccination
Vorgeschichte: Hx Factor Leiden Deficiency, Chronic thromboembolic pulmonary hypertension, Diastolic Heart Failure, Venous Insufficiency, hypertension, pre-diabetic, hx DVT, Severe OSA- cpap, GERD, hx pulmonary embolism
Andere Medikamente: Xarelto 20 mg QD, Omeprazole 20 mg QD, Furosemide 40/20mg MWF/S,T,Th,Sa, Spironolactone 25 mg QD, Vitamin B12 1000 mg QD, Vitamin D 500 IU QD, Multivitamin QD, Calcium Citrate 400 mg QD, Glucosamine 1500 mg qd,
Allergien: NKA
Vorherige Impfungen: -

VAERS 2596215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: AK
Alter: 76,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 17.03.2022
Beginn: 04.06.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: SYR / UN

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

Asthenia COVID-19 Cough Fatigue Lethargy Malaise SARS-CoV-2 test positive

Symptomtext

I had my vaccination on 03/17/2022. I started to feel unwell on 06/07/2022 with low energy coughing lethargic fatigue. On 06/09/2023 I tested COVID-19 positive at home. I contacted my physician on 06/09/2022 but I had fallen out of the timeline of prescription. I was provided advice for over-the-counter treatment. I did not work for 3 weeks as I was still COVID-19 positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 06/09/2022 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arrhythmia; Elevated Cholesterol; Headaches on occasion
Andere Medikamente: ELIQUIS; pravastatin; rizatriptan; vitamin D3; vitamin C; multivitamin B12; zinc; fiber
Allergien: N/A
Vorherige Impfungen: -

VAERS 2589260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 28.10.2021
Beginn: 14.02.2023
Tage bis Beginn: 474,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

02/14/23 presents to ED for "fatigue". PMHx of "chronic back pain with prior history of lumbar spinal stenosis and lumbar radiculopathy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 02/14/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2579395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FF2590

mild

Staat: OH
Alter: 65,0
Geschlecht: F
Eingang: 10.02.2023
Impfdatum: 11.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Balance disorder Blood test Diarrhoea Dizziness Gait disturbance Nausea Walking aid user

Symptomtext

Dizziness issues and her dizziness sometimes debilitating the point she has to use the walker; Dizziness issues and her dizziness sometimes debilitating the point she has to use the walker; Balance issues; Somedays she is barely able to walk and other day she can't walk; Nausea; Diarrhea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 66-year-old female patient received BNT162b2 (BNT162B2), on 11Jan2022 as dose 3 (booster), single (Lot number: FF2590) at the age of 65 years for covid-19 immunisation. The patient's relevant medical history included: "Cholesterol" (ongoing), notes: Cholesterol. Concomitant medication(s) included: ATORVASTATIN taken for blood cholesterol. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Date: 04Mar2021, LOT#: EN6199), administration date: 04Mar2021, when the patient was 64-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Date: 30Mar2021, LOT#: ER8733), administration date: 30Mar2021, when the patient was 64-year-old, for COVID-19 immunization. The following information was reported: DIZZINESS (non-serious), WALKING AID USER (non-serious), outcome "unknown" and all described as "Dizziness issues and her dizziness sometimes debilitating the point she has to use the walker"; BALANCE DISORDER (non-serious), outcome "unknown", described as "Balance issues"; GAIT DISTURBANCE (non-serious), outcome "unknown", described as "Somedays she is barely able to walk and other day she can't walk"; NAUSEA (non-serious), outcome "unknown"; DIARRHOEA (non-serious), outcome "unknown", described as "Diarrhea". The events "dizziness issues and her dizziness sometimes debilitating the point she has to use the walker" and "balance issues" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of dizziness, walking aid user, balance disorder, gait disturbance, nausea, diarrhoea. Additional Information: Concern: Reporter stated, "My wife Withheld and I both were received the initial two Pfizer shots like a year and a half ago and then we were both booster glass spring and shortly after my wife got the booster, she started having dizziness issues and her dizziness sometimes debilitating the point she has to use the walker and we got numerous, we have been to the higher state university the Withheld, the vaccination center at Withheld where we saw a Neurologist, a ear nose and throat specialist for balance, an eye specialists, thinking that may be a part of her dizziness and nobody was able to help us so then our family Physician send us to the Withheld it's near in withheld where we saw a brain surgeon again and a Neurologist, they after clean they could find nothing wrong with my wife and had no idea other than it could possibly be the Booster side effect of the vaccine, so we have been doing physical therapy which says to just, my wife is working with a lady and she is working on her Vestibular system which just part of ear and in brain I guess, trying to correct her balance but we didn't know, we just felt like we need too report this because none of the Doctors, none of the tests that we have taken to find any reason at all for here balance issues. We both got the Booster shots. Concern was paraphrased. Reporter stated, "Somedays she is barely able to walk and other day she can't walk she also has nausea and sometimes she has diarrhea also." Reporter was informed about the role of Pfizer Drug Safety. Lab Work: Reporter stated, "Not the last two but we had extensive blood work done at withheld states at the withheld in the Vaccination Center, not the last two weeks, no." Facility Details: Name: Reporter stated, "Withheld." Mailing Address and Telephone#: Reporter stated, "Well, I don't see the address of the facility right here." Treatment: Reporter stated, "No."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:Unknown results; Comments: Lab Work: Reporter stated, "Not the last two but we had extensive blood work done
Aktuelle Erkrankungen: Cholesterol (Cholesterol)
Vorgeschichte: -
Andere Medikamente: ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2568710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ff2590

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 19.10.2021
Beginn: 26.01.2023
Tage bis Beginn: 464,0
Dosis: 1
Route/Site: IM / LA

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

Pyrexia

Symptomtext

Patient went to ER 10 hours after getting a vaccination because she had a fever of 107F.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: no test
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: n/a
Allergien: nka
Vorherige Impfungen: -